WO2013009780A1 - Settable compositions comprising interground perlite and hydraulic cement - Google Patents

Settable compositions comprising interground perlite and hydraulic cement Download PDF

Info

Publication number
WO2013009780A1
WO2013009780A1 PCT/US2012/046117 US2012046117W WO2013009780A1 WO 2013009780 A1 WO2013009780 A1 WO 2013009780A1 US 2012046117 W US2012046117 W US 2012046117W WO 2013009780 A1 WO2013009780 A1 WO 2013009780A1
Authority
WO
WIPO (PCT)
Prior art keywords
cement
perlite
additive
hydraulic cement
periite
Prior art date
Application number
PCT/US2012/046117
Other languages
French (fr)
Inventor
Jeffrey Karcher
Chad Brenneis
Craig W. Roddy
James R. Benkley
Original Assignee
Halliburton Energy Services, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Halliburton Energy Services, Inc. filed Critical Halliburton Energy Services, Inc.
Priority to CN2012800051623A priority Critical patent/CN103459348A/en
Priority to BR112013016242A priority patent/BR112013016242A2/en
Priority to RU2013129542/03A priority patent/RU2584431C2/en
Priority to AU2012282775A priority patent/AU2012282775B2/en
Priority to CA2821931A priority patent/CA2821931C/en
Priority to MX2013007395A priority patent/MX2013007395A/en
Priority to EP12735761.4A priority patent/EP2651849A1/en
Priority to NZ612235A priority patent/NZ612235B2/en
Publication of WO2013009780A1 publication Critical patent/WO2013009780A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • C09K8/473Density reducing additives, e.g. for obtaining foamed cement compositions
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B20/00Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
    • C04B20/02Treatment
    • C04B20/026Comminuting, e.g. by grinding or breaking; Defibrillating fibres other than asbestos
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/021Ash cements, e.g. fly ash cements ; Cements based on incineration residues, e.g. alkali-activated slags from waste incineration ; Kiln dust cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/06Aluminous cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/08Slag cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/14Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing calcium sulfate cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/18Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing mixtures of the silica-lime type
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • C09K8/48Density increasing or weighting additives
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/42Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells
    • C09K8/46Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement
    • C09K8/467Compositions for cementing, e.g. for cementing casings into boreholes; Compositions for plugging, e.g. for killing wells containing inorganic binders, e.g. Portland cement containing additives for specific purposes
    • C09K8/487Fluid loss control additives; Additives for reducing or preventing circulation loss
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2111/00Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
    • C04B2111/10Compositions or ingredients thereof characterised by the absence or the very low content of a specific material
    • C04B2111/1037Cement free compositions, e.g. hydraulically hardening mixtures based on waste materials, not containing cement as such
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Definitions

  • the present invention relates to cementing operations and, more particularly, in certain embodiments, to methods and compositions that comprise ink-rground periite and hydraulic cement,
  • m general, well treatments include a wide variet of methods that may be performed in oil gas, geotheroial and/Or water wells, such as drilling, completion and workover methods.
  • the drilling, completion and wo.rk.over methods may include, but are not limited to, drilling, fracturing, acidizing, logging, cementing, gravel packing, perforating and conformance methods.
  • Many of these well treatments are designed to enhance and/or facilitate the recovery of desirable fluids from a subterranean well.
  • settable composition refers to a eomposition.(s) that hydraaK.cal.ly sets or otherwise develops compressive strength.
  • Settable compositions may be used in primary cementing operations whereby pipe strings, such as casing and liners, are cemented in well bores.
  • a se table composition may be pumped, into an annulus between a subterranean formation and the pipe string disposed in the subterranean formation.
  • the settable composition should set in the annul us, thereby .forming an annular sheath of hardened cement (e.g., a cement sheath) that should support and position, the pipe string in the well bore and bond the exterior surface of the pipe string to the walls of the well bore.
  • Settable compositions also may be used in remedial cementing methods, such as the placement of eement plugs, and in. squeeze cementing for sealing voids in a pipe string, cement sheath, gravel pack, formation, and the like.
  • the present invention relates to cementing operations and, more particularly, in certain embodiments, to methods and compositions that comprise interground periite and hydraulic cement,
  • An embodiment provides a method of cementing comprising: providing a settable composition comprising periite, hydraulic cement, and water, wherein the periite and hydraulic cement are interground prior to combination with the water to form the settable composition; and allowing the settable composition to set.
  • Another embodiment provides a method of cementing comprising: providing a settable composition comprising unexpended periite, hydraulic cement, and water, wherein the unexpanded periite and hydraulic cement are interground prior to combination with the water to form the settable composition; introducing the settable composition into a well bore; and allowing the settable composition to set
  • Embodiments of the settable compositions of the present invention may comprise periite.
  • Periite suitable for use in embodiments of the present invention includes expanded periite and unexpanded periite.
  • the settable composition may comprise periite interground with a hydraulic cement.
  • the settable compositions may comprise unexpanded periite with cement kiln dust ("CK.O"), pumieite, or a combination thereof.
  • CK.O cement kiln dust
  • One of the many potential advantages of embodiments, of the present invention is thai the inclusion of the unexpanded periite in embodiments of the settable composition may increase the compressive strength of the settable composition after setting.
  • Another potential advantage of embodiments of the present invention is that the CRD, unexpanded periite, pumieite, or a combination thereof may be used to reduce the amount of a higher cost component, such as Portland cement, resulting in a more economical settable composition.
  • a higher cost component such as Portland cement
  • Periite is an ore and generally refers to a naturally occurring volcanic, amorphous siliceous rock comprising mostly silicon dioxide and aluminum oxide.
  • a characteristic of periite is that, it may expand to form a cellular, high-porosity particle or hollow sphere containing multi-cellular cores when exposed to high temperatures due to the sudden vaporization of water within the periite.
  • the expanded periite may be used as a density- reducing additive for making lightweight settable compositions.
  • Periite suitable for use in embodiments of the present invention includes expanded periite and unexpended periite. In some embodiments, the periite may comprise unexpanded periite.
  • unexpanded periite to settable compositions comprising CKD and/or pumicite may provide unexpected increases in compressive strengths.
  • the unexpanded periite may be used to increase the compressive strength of settable compositions comprising CKD and/or pumicite.
  • unexpanded periite can increase the compressive strength of settable compositions comprising Portland cement.
  • the unexpanded periite may be particularly suited for use at elevated well bore temperatures in accordance with embodiments of the present invention, such as at temperatures greater than, about 80 C F, alternatively greater than about 12.0 C' F, and alternatively greater than about i.40°F,
  • unexpanded periite may be used, among other tilings, to replace higher cost eementitious components, such as Portland cement, resulting in more economical settable compositions.
  • substitution of the Portland cement for the unexpanded periite should result in a settable composition with a reduced carbon footprint
  • the periite can be ground, to any size suitable fo use in cementing operations.
  • the periite is ground to a mean particle size of about I micron to about 400 microns, alternatively, about 1 micron to about 100 microns and, alternatively, abou 1 micron to about 25 microns.
  • the mean particle size corresponds to dSO values as measured by commercially available particle size analyzers such as those manufactured by Malvern instruments, Worcestershire, United Kingdom.
  • the periite has a particle size distribution of about 1 micron to about 1 ,000 microns with a mean particle size of about 1 micron to about 100 microns.
  • the particle size distribution corresponds to the maximum and minimum sizes allowed in the distribution.
  • An example of a suitable ground periite tha is unexpanded is available from Hess Pumice Products, Inc., Maiad City, Idaho, under the tradename lsv!-325 with a mesh size of 325.
  • the perlite may he included in the settable compositions in an amount -sufficient to provide the desired compressive strength, density, cost reduction, and/or reduced carbon footprint, in some embodiments, the perlite may be present in the sellable compositions of the present invention in an amount in the range of .from about 1 % to about 75% by weight of cementitious components.
  • cementitious components include those components or combinations of components of the settable compositions that hydrauSicaily set, or otherwise harden, to develop compressive strength, including, for example, perlite, C D, fly ash, pumicite, slag, lime, shale, and the like.
  • the perlite may be present in an amount ranging between any of and/or including an of about 5%, about 10%, about .15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or about 70%.
  • the perlite may be present in the settable compositions in an amount in the range of from about 5% to about 50% b weight ofcementitious components, in another embodiment, the perlite may be present in an amount in the range of from about 10% to about 40% by weight of cementitious components. In yet another embodiment, the perlite may be present in an amount in the range of from about 20% to about 30% by weight of cementitious components.
  • the perlite can be interground with hydraulic cement.
  • the hydraulic cement may be a Portland cement, such as those classified as ASTM Type V cement
  • the perlite can be mterground with hydraulic cement and pumicite.
  • the perlite can be interground with hydraulic cement and CKD.
  • ground or "irttergri tiding” as used herein means using a grinder (e.g., bail mill, rod mill, etc.) to reduce the particle size of the specified components. It is believed that intergrindsng the perlite and hydraulic cement ma improve the properties of the subsequent settable composition.
  • the inierground perlite and hydraulic cement may comprise perlite in an amount of about 0.1 % to about 99% by weight of the interground perlite and hydraulic cement and hydraulic cement in an amount of about. 0.1% to about 99% by weight of the interground perlite and hydraulic cement.
  • the perlite may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of the mterground perlite and hydraulic cement.
  • the hydraulic cement may be present m an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of the interground perlite and hydraulic* cement.
  • the hydraulic cement and perlite may be combined and ground to any size suitable tor use in cementing operations.
  • the hydraulic cement and/or perlite may be ground prior t combination, in yet another embodiment, the perlite may be ground to a first particle size and then interground with the hydraulic cement to a second particle size.
  • the interground perlite and hydrauli cement has a.
  • the interground perlite and hydraulic cement may have a mean particle size of about 0,5 microns to about 50 microns.
  • the interground perlite and hydraulic cement may have a mean particle size of about 0,5 microns to about 10 microns.
  • the interground perlite and hydraulic cement may have a bimodal particle size distribution.
  • the interground perlite and hydraulic cement may have a bimodal particle size distribution with a first peak from about I microns to about 7 microns and a second peak from about 7 microns to about 15 microns, alternatively, a first peak from about 3 microns to about 5 microns and a second peak from about 9 microns to about i 1 microns, and alternatively, a first peak of about 4 microns and a second peak of about .10 microns.
  • the interground. perlite and hydraulic cement may be present in an amount in the range of from about 0.1% to about 1 0% by weight of cemendtious components in the mallahle composition.
  • the interground perlite and hydraulic cement may be present in an amount ranging between any of and or including .any of about 5%, about 1.0%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%,. about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of cememitious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the mterground perltte and hydraulic cement to include for a chosen, application.
  • Embodiments of the lettable compositions further may comprise hydraulic cement.
  • the hydraulic cement rosy be mterground with the perlite in accordance with certain embodiments.
  • Any of a variety of hydraulic cements suitable for use in subterranean cementing operations may be used in accordance with embodiments of the present invention. Suitable examples include hydraulic cements that comprise calcium, aluminum, silicon., oxygen and/or sulfur, which set and harden by reaction with water.
  • Such hydraulic cements include, but are not limited to, Portland cements, pozzolana cements, gypsum cements, high-alumina-content cements, slag cements, silica lime cements and combinations thereof.
  • the hydraulic ceme t may comprise a Portland cement.
  • cements suitable for use in the present invention are classified as Class A, C, H and G cements according to American Petroleum Institute, Recommended Practice for ' Testing We ' ll Cements, API Specification 10B-2 (ISO 10426-2), First edition, July 2005.
  • cements suitable for use in the present invention ma include cements classified as ASTM Type 1, II, 111, IV, or V.
  • the hydraulic cement may be included in the settable compositions in an amount sufficient for a particular application.
  • the hydraulic cement m be present in the settable compositions in an amount in the range of from about 0.1 % to about 99% by weight of eenientitious components.
  • the hydraulic cement may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 1.5%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of cementiiious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the hydraulic cement to include for a chosen application.
  • Embodiments of the settable compositions generally further may comprise CKD.
  • embodiments of the present invention also may encompass intergrinding the CKD with the perlite and the hydraulic cement.
  • GKD Usually, large quantities of GKD are collected in the production of cement that are commonly disposed of as waste. Disposal of the waste CKD can add undesirable costs to the manufacture of the cement, as well as the environmental concerns associated with its disposal
  • the chemical analysis of CKD from various cement manufactures varies depending on a number of factors, including the particular kiln feed, the efficiencies of the cement production operation, and the associated dust collection systems.
  • CKD generally may comprise a variety of oxides, such as Si0 2 , AbCh, Fe 2 Ch, CaO, MgO, SO,, Na 2 0, and K 2 0.
  • the CKD generally may exhibit cementitious properties, in that it may set and harden in the presence of water. Irs accordance with embodiments of the present invention, the CKD may be used, among other things, to replace higher cost cementitious components, such as Portland cement, resultin in mo e economical sellable compositions. In addition, substitution of the Portland cement for the CKD can result in a settable composition with a reduced, carbon footprint.
  • the CKD may be included in the sellable compositions in an amount sufficient io provide the desired compressive strength, density, cost reduction, and/or reduced carbon footprint, in some embodiments, the CKD may be present in the mallable- compositions of the present invention in an amount in the range of from about 1% to about 95% by weight of cementitious components.
  • the CKD may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, or about 90%.
  • the CKD may be present in the sellable compositions in an amount in the range of from about 5% to about 95% by weight of cementitious components. In another embodiment, the CKD may be present in. an. amount in. the .range of from about 50% to about 90% by weight of cementitious components, hi yet another embodiment, the CKD may be present in an amount in the range of from about 60% to about 80% by weight of cementitious components.
  • One of ordinary skill, in the art, with the benefit of this disclosure, will recognize the appropriate amount of CKD to include for a chosen application.
  • Embodiments of the hereable compositions further may comprise pumicite.
  • pumicite is a volcanic rock that exhibits cementitious properties, in that it may set and harden i the presence of hydrated lime and water. Hydrated lime may be used in combination with the pumicite, for example, to provide sufficient calcium, ions for die pumicite to set.
  • the pumicite may be used, among other things, to replace higher cost eementitious components, such as Portland cement, resulting i .more economical sellable compositions. As previously mentioned, replacement of the Portland cement should also result in a sellable composition with a reduced carbon footprint.
  • the pumicite may be included in an amount sufficient to provide the desired compressive strength, density, cost reduction and/or reduced carbon footprint for a particular application, hi some embodiments, the pumicite may be present in the sellable compositions of the present invention in an amount in the range of from about 1% to about 95% by weight of eementitious components.
  • the pumicite may be present in an amount ranging between any of and/or including any of about 5%, about .10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about. 55%, about 60%, about 65%, about 70%, about 75%, about 80%, or about 90% by weight of eementitious components.
  • the pumicite may be present in the sellable compositions of the present invention in an amount i the range of from about 5% to about 95% by weight of eementitious components. In another embodiment, the pumicite may be present in an amount in the range of from about 5% to about 80% by weight of eementitious components. In yet another embodiment, the pumicite may be present in an amount in the range of from about 10% to about 50% by weight of eementitious components. In yet another embodiment, the pumicite may be present in an amount in the range of from about 25% to about 50% by weight of eementitious components.
  • One of ordinary skill in the ait with the benefit of this disclosure, will recognize the appropriate amount of the pumicite to include for a chosen application,
  • the sellable compositions further may comprise lime.
  • the lime may be hydrated lime.
  • the iime may be included in embodiments of the settab!e compositions, for example, to form a hydraulic composition with other components of the sellable compositions, such as the pumicite, fly ash, slag, and/or shale.
  • the lime may be included in the sellable composition in an amount sufficient for a particular application.
  • the lime may be present in an amount in the range of from about 1 % to about 40% by weight of eementitious components.
  • the lime may be present in an amount ranging between any of and/or including any of about.
  • the lime may be present in an amount in the range of from about 5% to about 20% by weight of eementitious components.
  • the appropriate amount of the lime to include for a chosen application.
  • a mixture of pumicite and hydraulic cement, such as Portland cement may be included in the settable composition, in an embodiment, the cement/pumicite mixture contains hydraulic cement in an amount of about 25% to about 75% by weight of the .mixture and pumicite i n an amount of about 25% to about 75% by weight of the mixture, hi an embodiment, the cemeut/pumicite mixture contains about 40% hydraulic cement by weight and about 60% pumicite b weight, hi an embodiment, the ceroent/pumieiie mixture may comprise hydraulic cement interground with pumicite.
  • the cement/pumicite mixture contains hydraulic cement in an amount of about 25% to about 75% by weight of the .mixture and pumicite i n an amount of about 25% to about 75% by weight of the mixture
  • the cemeut/pumicite mixture contains about 40% hydraulic cement by weight and about 60% pumicite b weight
  • the ceroent/pumieiie mixture may comprise hydraulic cement interground with pumicite.
  • the hydraulic cement may comprise Portland cement classified as ASTM Type V cement, in accordance with embodiments, the Portland cement, and pumicite may be combined and ground to any size suitable for use in cementing operations, in another embodiment, the Portland cement and pumicite may be ground prior to combination, in an embodiment, the cenient/puroicite mixture of Portland cement and pumicite has a mean particle size of about 0.1 microns to about 400 microns, alternatively, about 0,5 microns to about 50 microns, and alternatively, about 0,5 microns to about. .10 microns.
  • the mean particle size corresponds to dSO values as measured by commercially available particle size analyzers such as those manufactured by Mal ern instruments, Worcestershire, United Kingdom.
  • An example of a sui table cement/pumicite mixture is available from Halliburton. Energy Services, Inc., under the trade name FhieCem. 'M 925 cement.
  • hydraulic cement interground with pumicite when used in a settable composition .in combination with unespanded perlite may provide synergistic effects.
  • the combination of unexpended perlite and the cement/pumicite mixture may provide significantly higher compressive strength, particularly at elevated well bore temperatures.
  • the combination of unexpended perlite and the cement/pumicite mixture may be particularly suited for use in settable compositions at elevated well bore temperatures, such as at temperatures greater than about S T, alternatively greater man about 120°F, and alternatively greater than about 14QT.
  • Embodiments of the settable compositions further may comprise fly ash.
  • fly ashes may be suitable, including fly ash classified as Class C and Class F fly ash according to American Petroleum institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Pifih Ed., July I , 1990.
  • Class C fly ash comprises both silica and lime so that, when mixed with water, it should set to form a hardened mass.
  • Class F fly ash generally does not contain sufficient lime, so an additional source of calcium ions is typically required for the Class F fly ash. to form a hydraulic composition.
  • lime may be mixed with Class F fly ash in an .amount in the range of about 0, 1% to about 25% by weight of the fly ash, in some instances, the lime may be hydrated lime.
  • fly ash include, but are not limited to, POZMtX* ' A cement additive, commercially available from Halliburton Energy Services, inc.
  • the fly ash generally may be included in the settable compositions in an. amount sufficient to provide the desired compressive strength, density, and/or cost, hi some embodiments, the fly ash may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 75% by weight of cementitious. components.
  • the fly ash may be. present in an amount ranging between any of and/or including any of about 3%, about .10%, about 20%, about 30%, about 40%, about 50%, about 60%, or about 70% by weight of cementitious components, in specific embodiments, the fly ash. may be present in an amount in the range of about .10% to about 60% by weight of cementitious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the fly ash to include for a. chosen application.
  • Embodiments of the settable compositions further may comprise slag cement.
  • a slag cement that may be suitable for use may comprise slag.
  • Slag generally does not contain sufficient basic material, so slag cement further ma comprise a base to produce a hydraulic composition that may react with water to set to form a hardened mass,
  • suitable sources of bases include, but are not limited to, sodium hydroxide, sodium bicarbonate, sodium carbonate, lime, and combinations thereof.
  • the slag cement generally may be included, in the settable compositions in an. amount sufficient to provide the desired conipressive strength, density, and/or cost
  • the slag cement may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 75% by weight of cementitious components.
  • the slag cement ma be present in an. amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about. 40%, about 50%, about 60%, or about 70% by weigh of cementitious components, in specific embodiments, the slag cement ma be present in an amount in the range of about 5% to about 50% by weight of cementitious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the slag cement to include for a chosen application.
  • Embodiments of the settable compositions further may comprise metakaolin.
  • metakaolin. is a white pozzoian that may be prepared by heating kaolin clay, for example, to temperatures m the range of about 6Q0°C to about 800°C.
  • the metakaolin may be present in the settable compositions of the present invention in an amount in the range of about S % to about 75% by weight of cementitious components.
  • the metakaolin may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, or about 70% by weight of cementitious components, in spec ific embodiments, the metakaolin may be present, in an amount in the range of about 10% to about 50% b weight of cementitious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the metakaolin to include for a chosen, application.
  • Embodiments of the sellable compositions further may comprise shale.
  • shale included in the settable compositions may react with excess lime to form, a suitable cementing material, for example, calcium silicate hydrate.
  • a variety of shales may be suitable, including those comprising silicon, aluminum, calcium, and/or magnesium.
  • a example of a suitable shale comprises vitrified shale. Suitable examples of vitrified shale include, but are not limited to, PRESSUR-SBAL FINE LCM material and PRESSUR-SEAL COARSE LCM material which are commercially available from TXl Energ Services, Inc.
  • the shale may have any particle size distribution as desired for a particular application. In certain embodiments, the shale may have a particle size distribution in the range of about 37 micrometers to about 4,750 micrometers.
  • the shale may be included in the settable compositions of the present invention in an amount sufficient to provide the desired compressive strength, density, and/or cost.
  • the shale may be present in the settable compositions of the present invention, in a amount in the range of about 1% t about 75% by weight of cementitious components.
  • the shale may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, of about 70% by weight of cementitious components, in specific embodiments, the shale may be present in an amount in the range of about 10% to about 35% by weight of cementitious components.
  • One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the shale to include or a chose application..
  • Embodiments of the settable compositions further may comprise zeolite.
  • Zeolites generall are porous aiumino-sHicate minerals that may be either a natural or synthetic material. Synthetic zeolites are based on the same type of structural cell as natural zeolites, and may comprise alommosilicate hydrates. As used herein, the term "zeolite” refers to all natural and synthetic- forms of zeolite. Examples of suitable zeolites are described in more detail in U.S. Patent No. 7,445,669.
  • the zeolite may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 65% by weight of eementifious components.
  • the zeolite may be present in an amount ranging between an of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, or about 60% by weight of cemeniitious components, in -specific embodiments, the zeolite may be present in an amount in the range of about 10% to about 40% by weight of cemeniitious components.
  • One of ordinary skill in the art, with the benefit, of this disclosure, will recognize the appropriate amount of the zeolite to include for a chosen application.
  • Embodiments of the settable compositions further may comprise a set retarding additive.
  • set retarding additive refers to an additive that retards the setting of the settable compositions of the present invention.
  • suitable set retarding additives include, but are not limited to, ammonium, alkali metals, alkaline earth metals, metal salts of suifoalkylated lign us, organic acids (e.g., hydrosycarboxy acids), copolymers that comprise acrylic acid or ma!eic acid, and combinations thereof.
  • a suitable suifoalkylated lignin comprises a su!fomethyiated lignin.
  • Suitable set retarding additives are disclosed in more detail in United States Patent No, Re, 3 1 , 190, the entire disclosure of which is incorporated herein by reference. Suitable set retarding additives are commercially available, from Halliburton Energy Services, Inc. under the trademarks fill* 4, BR* 5, HR* 7, HR* 12, HR 3 ⁇ 4 I 5, HR*2S, HR ® 60I f SCRTM 100, and SCRTM 500 retarders. Generally, where used, the set retarding additive may be included in the settable compositions of the present invention in an amount sufficient to provide the desired set retardation. In some embodiments, the set retarding additive may be present in the settable compositions of the present invention an amount in the range of about.
  • cemeniitious components including an amount ranging between any of and or including any of about 0.5%, about i %, about 2%, about 3%, or about 4% by weight of cemeniitious. components.
  • One of ordinary skill in the art, with the benefit, of this disclosure, will recognize the appropriate amount of the set retarding additive to include for chosen application.
  • Embodiments of the settable compositions further may include water.
  • the water that may be used in embodiments of the settable compositions include, for example, freshwater, saltwater (e.g., water containing one or more salts dissolved therein), brine
  • the water may be from any source, provided that the water does not contain an excess of compounds that may undesirably affect other components in the settable composition.
  • the water may be included in an amount sufficient to form a pumpable slurry.
  • the water may be included in the settable compositions of the present invention in an amount in the .range of about 40% to about 200% by weight of cementitious components.
  • the water may be present in an amount ranging between an of and/or including any of about 50%, about 75%, about 100%, about 1.25%, about 1.50%, or about 175% by weight of cementitious components.
  • the water may be included in an amount in the range of about 40% to about 150% b weight of cementitious components.
  • additives may be added to the settable compositions of the present invention as deemed appropriate by one skilled .in the art, with the benefit of this disclosure.
  • additives include, but are not limited to, strength- retrogression additives, set accelerators, weighting agents, lightweight additives, gas- generating additives, mechanical property enhancing additives, lost-circulation materials, filtration-control additives, dispersants, fluid loss control additives, defoaming agents, foaming agents, oil-swel fable particles, water-swellable particles, thixoiropie additives, and combinations thereof.
  • additives include crystalline silica, amorphous silica, fumed silica, salts, fibers, hydratahle clays, microspheres, rice husk, ash, elastomers, efastomeric particles, resins, latex, combinations thereof, and the like.
  • a person having ordinary skill in the art, with the benefit of this disclosure, will readily be able to determine the type and amount of additive useful for a particular application and desired result.
  • Embodiments of the settable compositions may be foamed and/or extended as desired by those of ordinary skill in the art.
  • the settable compositions of the present invention should have a density suitable for a particular application as desired by those of ordinary skill in the art, with the benefit of this disclosure.
  • the settable compositions may have a density in the range of from about 8 pounds per gallon ("lb/gal") to about 16 lb/gal.
  • the settable compositions may be foamed to a density in the range of from about. 8 lb/gal to about 13 lb/gal.
  • embodiments of the settable compositions may be used in a variety of subterranean applications, including primary and remedial cementing.
  • the settable compositions of the present invention also may be used in surface applications, for example, construction cementing.
  • Embodiments ma include providing a settable composition and allowing the settable composition to set in some embodiments, the settable composition may be allowed to set in a locationo that is above ground, for example, in construction cementing.
  • the settable composition may be introduced into a well bore and allowed to set.
  • the settable composition may be placed into a space between a subterranean formation and a conduit located in the well bore.
  • Embodiments of the settable compositions may comprise, for example, water and one or more of perlite, CKD, or pumkite.
  • Embodiments of the settable compositions may comprise, for example, perlite interground with hydraulic cement (e.g., Portland cement).
  • a settable composition may be introduced into a space between a subterranean formation and a conduit (e.g., pipe strings, .liners) located in the well bore.
  • the settable composition m y be allowed to set to form an annular sheath of hardened cement in the space between the subterranean formation and the conduit.
  • the set settable composition may form a barrier, preventing the migration of fluids in the well bore.
  • the set settable composition also may, for example, support the conduit in the well bore.
  • a settable composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs.
  • the settable composition may be placed in a well bore to plug a void or crack in the formation, in a gravel pack, hi the conduit, in the cement sheath, and/or a microannu!us between the cement sheath and the conduit.
  • a series of samples were prepared and subjected to 24-hour crush strength tests in accordance with API Specification .10 to analyze force .resistance propertie of settable compositions that comprise unexpanded perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for twenty-four hours. immediately alter removal from the water bath, crush strengths were determined using a Ttnius Olsen tester. The results of the crush strength tests are set forth in the table below.
  • Test Nos. I ⁇ 6 were performed on samples with a 14.2 ppg and containing water, Portland class H cement, ground unexpanded perlite, lime, and water, as indicated in the table below.
  • the ground unexpanded perlite was 1M-3.25 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
  • Test Nos. 7-8 were performed on samples with a density of 14,2 ppg and containing water, Portland class H cement, pumieite, and lime, as indicated in the table below.
  • the pumictte was about 200 U.S. Standard Mesh in size.
  • Test Nos, 9-14 were performed on samples with a density of 14.2 ppg and containing water, a ground eement pumicite mixture (FineCem' * 925 cement), unexpended perlite, time, and water, as indicated in the table below.
  • the ground cenient/pumicite mixture comprised Portland Type V cement (about4Q% by weight) interground with pumieite (about60% by weight).
  • the ground cement pumicite raixture had a mean particle size in the range of about 1 to about 4 microns.
  • the ground unexpanded perlite was ⁇ -325 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
  • percent by weight is based on the weight of the Portland cement, cement/pumicite mixture, pumieite, and unexpanded perlite in the sample
  • gallons per sack is based on a 94-ponnd sack of the Portland cement, eentent/purmcite mixture, pumieite, and unexpanded perlite.
  • Example 1 thus indicates that replacement of at least a portion of the Portland cement with unexpanded perlite may increase the crush strength of the settahie compositions.
  • the Test Nos. 2 and 4 with unexpanded perlite had crush strengths of 886 psi and 777 psi as compared to a crush .strength of 674 psi for Test No. I with 1 G03 ⁇ 4 Portland cement by weight
  • Example 1 further indicates that the ground pumicite/eement mixture in combination with the unexpended perlite may have synergistic effects on the settah ' le composition, in thai this combination may provide increased crush strengths at elevated temperatures. At 140° F, for example. Test Nos. 12 and 14 with the ground pumieite/ce-ment mixture and unexpanded perlite had crush strengths of 2740 psi and 2610 psi.
  • sample sellable compositions were prepared and tested to analyze the force resistance properties of sellable compositions that comprise CKD and unexpanded perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for either 24 or 72 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester. Hie results of the crush strength tests are set forth in the table below.
  • Test Nos. 15-28 were performed on samples with a density of 14,2 ppg and containing water, CKD, ground unexpanded perlite, and lime, as indicated in the table below.
  • the samples further contained a cement set retarder (CFR ⁇ 3 '3 ⁇ 4 cement set retarder, Halliburton Energy Services, Inc.) in an amount of about 0,4% by weight.
  • the ground unexpanded perlite was ⁇ -325 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
  • percent by weight is based on the weight of the CKD and unexpanded perlite in the sample, and gallons per sack, (gal sfc) is based on a 94-pound sack of the CK D and unexpanded perlite.
  • Example 2 thus indicates that unexpanded perlite may be used to enhance the crush strength of CKD-containing compositions. in addition, this: effect is particularly pronounced at increased temperatures. At .140° F, for example. Test No. 22 with 75% CKD and 25% unexpanded perlite had a 72-hour crush strength of 1 04 pss as compared to a 72-hour crush strength of 457 psi for Test No. .18 with 100% CKD.
  • sample settable compositions were prepared and tested to further analyze the force resistance properties of settable -compositions that comprise CKD and unexpanded perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours.
  • crush strengths were determined using a Tiniits Olsen tester. The results of the crush strength tests are set forth in the table below.
  • Test Nos. 29-37 were performed on samples with a density of 1.4.2 ppg and containing water, CKD. ground unexpanded. perlite. and lime, as indicated in the table below.
  • the samples further contained a cement dispersani in an amount of about 0,4% by weight
  • the ground unexpanded perlite was lM-325 from Hess Pumice Products with a particle size of about 325 U .S. Standard Mesh.
  • percent by weight is based on the weight of the CKD and unexpended perhte in the sample, and gallons per sack (ga! sk) is based on a 94-pound sack of the CKD and unexpended perlite.
  • Example 3 thus indicates that unexpended perlite may be used to enhance the crush strength of CKD-coniaining compositions.
  • the crush strength of the samples steadily increased as the concentration of unexpended perlite in the sample was increased from 0% by weight to 40% by weight,
  • sample settable compositions were prepared and tested to further analyze the force resistance properties of settable compositions that comprise CKD and unexpended perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester. The results of the crush strength tests are set forth in the table below.
  • Test Nos, 38-43 were performed on samples with a density of 14.2 ppg and containing water, CKD, perlite, and lime, as indicated in the table below. The samples further contained a cement dLspersant in an amo unt of about 0.4% by weight.
  • Test Nos, 38 and 39 contained a ground unexpanded perlite (IN4-325) from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
  • Test Nos. 40 and 1 contained unground perlite ore having a mean particle size (dSO) of about 1 0 microns.
  • Test Nos, 42 and 43 contained expanded perlite.
  • percent by weight is based on the weight of the CKD and perlite in the sample
  • gallons per sack ga ' l/sk
  • Example 4 thus indicates that unexpanded perlite provides superior strength enhancement to KD ⁇ containiog compositions when compared lo unground perlite ore and expended perlite. indeed, the sample with the expanded perlite could not even be tested due to mixability problems.
  • sample settable compositions were prepared and tested to further analyze settable compositions that comprise CKD and unexpanded -perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours.
  • crush, strengths were determined using a Tinius Oisen tester. The results of the crush strength tests are set forth in the table below.
  • the thickening time for each sample was also determined at 140 *3 F in accordance with API Specification 10.
  • Test Nos, 44-56 were performed on samples with a density of 12.5 ppg and containing CKD, perlite, and lime, as indicated in the table below.
  • the samples further contained a cement dispersant in a amount of about 0.4% by weight and a cement set retarder (HR* -' 5 cement retarder, Halliburton Energy Services, Inc.).
  • Test Nos. 45, 48, 5.1, and 54 contained a ground unexpanded perlite (i -325) from Hess Pumice Products with a particle size of about 314 U.S. Standard Mesh.
  • Test Nos, 46, 49, 52, and 55 contained unground perlite ore having a mean particle size (d50) of about 190.
  • Test Nos. 47, 50, 53, and 56 contained expanded perlite.
  • Example 5 thus indicates that unexpanded perlite provides enhanced sirenglh to CKD-contaming compositions when compared to unground perlite ore and expanded perlite.
  • the samples with expanded perlit could not even be tested due to mixability problems,
  • sample sellable compositions were prepared and tested to further analyze settable compositions that comprise CKD and unexpanded perlite.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours.
  • crush, strengths were determined using a Tinius Olsen tester. The results of the crush strength tests are set forth in the table below.
  • Test No, 57 was performed on a sample will), a density of . 2.5 ppg and containing water, Portland Type V cement, CKD, unground perlite ore, and purnicite, as indicated in the table below.
  • the unground perlite ore had a. mean particle size (d50) of about S 90.
  • the pum telle had a mean particle size (d50) of about.4 .microns.
  • Test No. 58 was performed on a sample with a density of 12.5 ppg and containing water, ground cement pumicite mixture pomicite, CKD, and ground unexpanded perlite.
  • the ground cementfpumieite mixture comprised Portland Type V cement (about 40% by weight) ioterground with purnicite (about 60% by weight).
  • the ground eement pumicite mixture had a mean particle size of about I -4 microns.
  • the ground unexpanded perlite was IM-325 front Hess Pumice Products with a particle size of about 325 U.S.
  • Standard Mesh in the following table, percent by weight is based on the weight of the CKD, cement, perlite, pumicite, and/or pumicite/cemenl mixture in the sample, and gallons per sack (ga!/sk) is based on a 94-pound sack of the CKD, cement, perlite, pumicite, and/or pumicite eenient mixture in the sample.
  • Example 6 thus indicates that unexpanded perlite in combination with ground pumicite provides enhanced strength to CKD-co.otat.ning compositions in comparison to compositions with standard cement, pumicite, and unground peri he ore.
  • the sample sellable compositions were formed by mixing the components in the amounts set forth in the table below.
  • the interground pumicite and cement comprised pumicite (about 60% by weight) and Portland ' Type V cement (about 40% by weight) and had a mean particle size of about 1-4 microns.
  • the interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name FmeCem' M 925 cement.
  • the interground perlite and cement comprised ground unexpended perlite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a himodal particle size distribution with peak particle sizes of about 4 microns and about 10 microns.
  • the interground perlite and cement was obtained from Hess Pumice Products, Malad City, Idaho.
  • the lime was hydrated lime, obtained from Univar USA.
  • sample compositions were subjected to 24-hour crush strength tests in accordance with API Specification iO.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours. Immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester.
  • % bwc refers to b weight of cement, which in this example is ei her by weight of the interground pumicite and cement or by weight of the interground perlite and cement.
  • Example 7 thus indicates that interground perlite and hydraulic cement generally provides enhances compressive sirength development as compared to interground pumicite and hydraulic cement. It should be noted that the CF -3 'S ' included in Test No. 60 retarded the setting resulting in the lower 24-hour crush strength as compared to Test No. 59 with the interground punucKe and cement.
  • the sample sellable compositions were formed by mixing the components in the amounts set forth in the table below.
  • the interground pumicite and cement comprised pumicite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a mean particle size of about 1 -4 microns.
  • the interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name I' iieCeni " 925 cement.
  • the interground perlite and cement comprised ground unexpended perlite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a bimodal particle size distribution with peak particle sizes of about 4 microns and about 10 .microns.
  • the interground periite and cement was obtained from Hess Pumice Products, aiad City, Idaho.
  • sample compositions were subjected to 24-hour crush strength tests in accordance with API Specification 10.
  • the sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester.
  • the thickening time .for each sample was also determined at 140" F in accordance with API Specification 10.
  • the abbreviation '*% bwc refers to by weight of cement, which in this example is either by weight of the interground pumicite and cement or by weight of the interground periite and cement,
  • Example 8 thus indicates that sellable compositions comprising interground periite and hydraulic cement may have acceptable thickening times for use in subterranean applications.
  • Example 8 further indicates that interground periite and hydraulic cement generally provides enhanced compressive strength development and can be similarly controlled with retarders as compared to interground pumicite and hydraulic cement.
  • EXAMPLE 9
  • the sample mallable compositions were formed by mixing the components in the amounts set forth in the table below.
  • the interground pumicite and cement comprised pumicite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a mean particie size of about ! -4 microns.
  • the interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name FineCeni' M 925 cement.
  • the interground periite and cement comprised ground unexpended periite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a bimodal particie size distribution, with peak particie sizes of about 4 microns and about 10 microns.
  • the interground periite and cement was obtained from Hess Pumice Products, Ma!ad City. Idaho.
  • API Specification 10 The tree water data is set forth in the table below.
  • the abbreviation * '% bwc refers to by weight of cement, which in this exam pi e is either by weight of the interground pumicite and cement or by weight of the interground periite and cement.
  • Example 9 thus indicates that settable compositions comprisin interground periite and hydraulic cement may have provide lower levels of free water as compared to interground pumicite and hydraulic cement.
  • compositions and methods are described in terms of “comprising,” “containing,” or “including” various components or steps, the compositions, and methods can also “consist essentially of or “consist of the various components and steps.
  • ranges from any lower lira it may be combined with any upper limit to recite a range not explicitly recited, as well as, ranges from any lower limit may be combined with any other lower limit to recite a range not explicitly recited, in the same way, ranges from any upper limit may be combined with any other upper limit to recite a range not explicitly recited.
  • any numerical range with a lower limit and an upper limit any number and any included range falling within the. range is specifically disclosed.
  • every range of values (of the form, "from about a to about b,” or, equivatingly, “from approximately a to h,” or, equivalent ⁇ , “from approximately a-h") disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values even if not explicitly recite.
  • every point or individual value ma serve as its own lower or upper limit combined with any other point or individual value or an other lower or upper limit, to recite a .range not explicitl recited.

Abstract

Methods and compositions are disclosed that comprise interground perlite and hydraulic cement. An embodiment provides a method of cementing comprising: providing a settable composition comprising perlite, hydraulic cement, and water, wherein the perlite and hydraulic cement are interground prior to combination with the water to form the settable composition; and allowing the settable composition to set.

Description

SETT ABLE COMPOSITIONS COMPRISING INTERGROU I) PERLITE AND
HYDRAULIC CEMENT
BACKGROUND
The present invention relates to cementing operations and, more particularly, in certain embodiments, to methods and compositions that comprise ink-rground periite and hydraulic cement,
m general, well treatments include a wide variet of methods that may be performed in oil gas, geotheroial and/Or water wells, such as drilling, completion and workover methods. The drilling, completion and wo.rk.over methods may include, but are not limited to, drilling, fracturing, acidizing, logging, cementing, gravel packing, perforating and conformance methods. Many of these well treatments are designed to enhance and/or facilitate the recovery of desirable fluids from a subterranean well.
In cementing methods, such as well construction and remedial cementing, seitable compositions are commonly utilized. As used herein, the term "settable composition" refers to a eomposition.(s) that hydraaK.cal.ly sets or otherwise develops compressive strength. Settable compositions may be used in primary cementing operations whereby pipe strings, such as casing and liners, are cemented in well bores. In performing primary cementing, a se table composition may be pumped, into an annulus between a subterranean formation and the pipe string disposed in the subterranean formation. The settable composition should set in the annul us, thereby .forming an annular sheath of hardened cement (e.g., a cement sheath) that should support and position, the pipe string in the well bore and bond the exterior surface of the pipe string to the walls of the well bore. Settable compositions also may be used in remedial cementing methods, such as the placement of eement plugs, and in. squeeze cementing for sealing voids in a pipe string, cement sheath, gravel pack, formation, and the like.
The hydration of the eement. in these cementing methods is a complex process because several phases may take part in the reaction simultaneously. In order to control the reaction processes to render the compositions suitable for well cementing, various additives such as retarders, strength enhancers, and accelerators may be added. However, the operatin conditions for wells are becoming more challenging and demanding, and the search for new materials continues to meet these challenges, for instance, cement slurries used in well cementing often encounter problems of gaining sufficient strength in a reasonable amount of time for well operations to continue. The costs associated with wait- on-cement ("WQC") play an important role in we'll cementing. SUMMARY
The present invention relates to cementing operations and, more particularly, in certain embodiments, to methods and compositions that comprise interground periite and hydraulic cement,
An embodiment provides a method of cementing comprising: providing a settable composition comprising periite, hydraulic cement, and water, wherein the periite and hydraulic cement are interground prior to combination with the water to form the settable composition; and allowing the settable composition to set.
Another embodiment provides a method of cementing comprising: providing a settable composition comprising unexpended periite, hydraulic cement, and water, wherein the unexpanded periite and hydraulic cement are interground prior to combination with the water to form the settable composition; introducing the settable composition into a well bore; and allowing the settable composition to set
Yet another embodiment provides a composition comprising Interground periite and hydraulic cement
The features and advantages of the present invention will be readily apparent to those skilled in the art. While numerous changes may b made by those skilled in the art, such changes are within the spirit of the invention.
DESCRIPTION OF PREFERRED EMBODIMEN S
Embodiments of the settable compositions of the present invention may comprise periite. Periite suitable for use in embodiments of the present invention includes expanded periite and unexpanded periite. I some embodiments, the settable composition may comprise periite interground with a hydraulic cement. In some embodiments, the settable compositions may comprise unexpanded periite with cement kiln dust ("CK.O"), pumieite, or a combination thereof. There may be several potential advantages to the methods and compositions of the present invention, only some of which may be alluded to herein. One of the many potential advantages of embodiments, of the present invention is thai the inclusion of the unexpanded periite in embodiments of the settable composition may increase the compressive strength of the settable composition after setting. Another potential advantage of embodiments of the present invention is that the CRD, unexpanded periite, pumieite, or a combination thereof may be used to reduce the amount of a higher cost component, such as Portland cement, resulting in a more economical settable composition. Yet anothe potential, advantage of embodiments of the present. In vention is that reduction of the amount of Portland cement can reduce the carbon footprint of the cementing operation. Periite is an ore and generally refers to a naturally occurring volcanic, amorphous siliceous rock comprising mostly silicon dioxide and aluminum oxide. A characteristic of periite is that, it may expand to form a cellular, high-porosity particle or hollow sphere containing multi-cellular cores when exposed to high temperatures due to the sudden vaporization of water within the periite. The expanded periite may be used as a density- reducing additive for making lightweight settable compositions. Periite suitable for use in embodiments of the present invention includes expanded periite and unexpended periite. In some embodiments, the periite may comprise unexpanded periite.
It has recently been discovered the addition, of unexpanded periite to settable compositions comprising CKD and/or pumicite may provide unexpected increases in compressive strengths. In accordance with embodiments of the present Invention, the unexpanded periite may be used to increase the compressive strength of settable compositions comprising CKD and/or pumicite. In addition, unexpanded periite can increase the compressive strength of settable compositions comprising Portland cement. It is believed that, the unexpanded periite may be particularly suited for use at elevated well bore temperatures in accordance with embodiments of the present invention, such as at temperatures greater than, about 80CF, alternatively greater than about 12.0C'F, and alternatively greater than about i.40°F,
In one embodiment, unexpanded periite may be used, among other tilings, to replace higher cost eementitious components, such as Portland cement, resulting in more economical settable compositions. In addition, substitution of the Portland cement for the unexpanded periite should result in a settable composition with a reduced carbon footprint In present embodiments, the periite can be ground, to any size suitable fo use in cementing operations. In an embodiment, the periite is ground to a mean particle size of about I micron to about 400 microns, alternatively, about 1 micron to about 100 microns and, alternatively, abou 1 micron to about 25 microns. The mean particle size corresponds to dSO values as measured by commercially available particle size analyzers such as those manufactured by Malvern instruments, Worcestershire, United Kingdom. In another embodiment, the periite has a particle size distribution of about 1 micron to about 1 ,000 microns with a mean particle size of about 1 micron to about 100 microns. The particle size distribution corresponds to the maximum and minimum sizes allowed in the distribution. An example of a suitable ground periite tha is unexpanded is available from Hess Pumice Products, Inc., Maiad City, Idaho, under the tradename lsv!-325 with a mesh size of 325. The perlite may he included in the settable compositions in an amount -sufficient to provide the desired compressive strength, density, cost reduction, and/or reduced carbon footprint, in some embodiments, the perlite may be present in the sellable compositions of the present invention in an amount in the range of .from about 1 % to about 75% by weight of cementitious components. Cementitious components include those components or combinations of components of the settable compositions that hydrauSicaily set, or otherwise harden, to develop compressive strength, including, for example, perlite, C D, fly ash, pumicite, slag, lime, shale, and the like. For example, the perlite may be present in an amount ranging between any of and/or including an of about 5%, about 10%, about .15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, or about 70%. In specific embodiments, the perlite may be present in the settable compositions in an amount in the range of from about 5% to about 50% b weight ofcementitious components, in another embodiment, the perlite may be present in an amount in the range of from about 10% to about 40% by weight of cementitious components. In yet another embodiment, the perlite may be present in an amount in the range of from about 20% to about 30% by weight of cementitious components. One of ordinary skill in the art, with, the benefit of this disclosure, will, recognize the appropriate amount of perlite to include for a chosen application.
In one particular embodiment, the perlite can be interground with hydraulic cement. In one embodiment, the hydraulic cement may be a Portland cement, such as those classified as ASTM Type V cement In another embodiment, the perlite can be mterground with hydraulic cement and pumicite. In another embodiment, the perlite can be interground with hydraulic cement and CKD. The term "interground" or "irttergri tiding" as used herein, means using a grinder (e.g., bail mill, rod mill, etc.) to reduce the particle size of the specified components. It is believed that intergrindsng the perlite and hydraulic cement ma improve the properties of the subsequent settable composition. Fo example, it is believed that tritergrhiding the perlite and hydraulic cement may provide accelerated strength development, in the subsequent settable compositions, as compared to mtergrinding pumicite and hydraulic cement By way of further example, it is believed that intergrinding the perlite and hydraulic cement may provide increased strength properties of the subsequent settable compositions, as compared to blending separately ground material. in some embodiments, the inierground perlite and hydraulic cement may comprise perlite in an amount of about 0.1 % to about 99% by weight of the interground perlite and hydraulic cement and hydraulic cement in an amount of about. 0.1% to about 99% by weight of the interground perlite and hydraulic cement. For example, the perlite may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of the mterground perlite and hydraulic cement. By way of further example, the hydraulic cement may be present m an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of the interground perlite and hydraulic* cement.
in -accordance with embodiments, the hydraulic cement and perlite may be combined and ground to any size suitable tor use in cementing operations. n another embodiment, the hydraulic cement and/or perlite may be ground prior t combination, in yet another embodiment, the perlite may be ground to a first particle size and then interground with the hydraulic cement to a second particle size. In an embodiment, the interground perlite and hydrauli cement has a. mean particle s ze of about 0.1 micron to about 400 microns, including an amount ranging between an of and/or including any of about 0,5 microns, about 1 micron, about 2 microns, about 5 microns, about 10 microns, about 25 microns, about 50 microns, about 75 microns, about 100 microns, about 150 microns, about 200 microns, about 250 microns, about 300 microns, or about 350 microns, For example, the interground perlite and hydraulic cement may have a mean particle size of about 0,5 microns to about 50 microns. By way of further example, the interground perlite and hydraulic cement may have a mean particle size of about 0,5 microns to about 10 microns. The mean particle size corresponds to d50 values, as measured b commercially available particle size analyzers such as those manufactured by Malvern instruments, Worcestershire, United Kingdom. In some embodiments, the interground perlite and hydraulic cement may have a bimodal particle size distribution. For example, the interground perlite and hydraulic cement may have a bimodal particle size distribution with a first peak from about I microns to about 7 microns and a second peak from about 7 microns to about 15 microns, alternatively, a first peak from about 3 microns to about 5 microns and a second peak from about 9 microns to about i 1 microns, and alternatively, a first peak of about 4 microns and a second peak of about .10 microns.
n some embodiments, the interground. perlite and hydraulic cement may be present in an amount in the range of from about 0.1% to about 1 0% by weight of cemendtious components in the seitahle composition. For example, the interground perlite and hydraulic cement may be present in an amount ranging between any of and or including .any of about 5%, about 1.0%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%,. about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of cememitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the mterground perltte and hydraulic cement to include for a chosen, application.
Embodiments of the lettable compositions further may comprise hydraulic cement. As previously mentioned, the hydraulic cement rosy be mterground with the perlite in accordance with certain embodiments. Any of a variety of hydraulic cements suitable for use in subterranean cementing operations may be used in accordance with embodiments of the present invention. Suitable examples include hydraulic cements that comprise calcium, aluminum, silicon., oxygen and/or sulfur, which set and harden by reaction with water. Such hydraulic cements, include, but are not limited to, Portland cements, pozzolana cements, gypsum cements, high-alumina-content cements, slag cements, silica lime cements and combinations thereof. In certain embodiments, the hydraulic ceme t may comprise a Portland cement. The Portland cements that may be suited for use in embodiments of the present invention are classified as Class A, C, H and G cements according to American Petroleum Institute, Recommended Practice for 'Testing We'll Cements, API Specification 10B-2 (ISO 10426-2), First edition, July 2005. In addition, in some- embodiments* cements suitable for use in the present invention ma include cements classified as ASTM Type 1, II, 111, IV, or V.
The hydraulic cement may be included in the settable compositions in an amount sufficient for a particular application. In some embodiments, the hydraulic cement m be present in the settable compositions in an amount in the range of from about 0.1 % to about 99% by weight of eenientitious components. For example, the hydraulic cement may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 1.5%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, about 85%, about 90%, or about 95% by weight of cementiiious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the hydraulic cement to include for a chosen application.
Embodiments of the settable compositions generally further may comprise CKD. it should be understood that embodiments of the present invention also may encompass intergrinding the CKD with the perlite and the hydraulic cement. Usually, large quantities of GKD are collected in the production of cement that are commonly disposed of as waste. Disposal of the waste CKD can add undesirable costs to the manufacture of the cement, as well as the environmental concerns associated with its disposal The chemical analysis of CKD from various cement manufactures varies depending on a number of factors, including the particular kiln feed, the efficiencies of the cement production operation, and the associated dust collection systems. CKD generally may comprise a variety of oxides, such as Si02, AbCh, Fe2Ch, CaO, MgO, SO,, Na20, and K20.
The CKD generally may exhibit cementitious properties, in that it may set and harden in the presence of water. Irs accordance with embodiments of the present invention, the CKD may be used, among other things, to replace higher cost cementitious components, such as Portland cement, resultin in mo e economical sellable compositions. In addition, substitution of the Portland cement for the CKD can result in a settable composition with a reduced, carbon footprint.
The CKD may be included in the sellable compositions in an amount sufficient io provide the desired compressive strength, density, cost reduction, and/or reduced carbon footprint, in some embodiments, the CKD may be present in the seitable- compositions of the present invention in an amount in the range of from about 1% to about 95% by weight of cementitious components. For example, the CKD may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about 55%, about 60%, about 65%, about 70%, about 75%, about 80%, or about 90%. In specific embodiments, the CKD may be present in the sellable compositions in an amount in the range of from about 5% to about 95% by weight of cementitious components. In another embodiment, the CKD may be present in. an. amount in. the .range of from about 50% to about 90% by weight of cementitious components, hi yet another embodiment, the CKD may be present in an amount in the range of from about 60% to about 80% by weight of cementitious components. One of ordinary skill, in the art, with the benefit of this disclosure, will recognize the appropriate amount of CKD to include for a chosen application.
Embodiments of the seitable compositions further may comprise pumicite. it should be understood that embodiments of the present invention also may encompass intergrindtng the pumicite with the periite and the hydraulic cement. Generally, pumicite is a volcanic rock that exhibits cementitious properties, in that it may set and harden i the presence of hydrated lime and water. Hydrated lime may be used in combination with the pumicite, for example, to provide sufficient calcium, ions for die pumicite to set. In accordance with embodiments of the present invention, the pumicite may be used, among other things, to replace higher cost eementitious components, such as Portland cement, resulting i .more economical sellable compositions. As previously mentioned, replacement of the Portland cement should also result in a sellable composition with a reduced carbon footprint.
Where present, the pumicite may be included in an amount sufficient to provide the desired compressive strength, density, cost reduction and/or reduced carbon footprint for a particular application, hi some embodiments, the pumicite may be present in the sellable compositions of the present invention in an amount in the range of from about 1% to about 95% by weight of eementitious components. Far example, the pumicite may be present in an amount ranging between any of and/or including any of about 5%, about .10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50%, about. 55%, about 60%, about 65%, about 70%, about 75%, about 80%, or about 90% by weight of eementitious components. In specific embodiments, the pumicite may be present in the sellable compositions of the present invention in an amount i the range of from about 5% to about 95% by weight of eementitious components. In another embodiment, the pumicite may be present in an amount in the range of from about 5% to about 80% by weight of eementitious components. In yet another embodiment, the pumicite may be present in an amount in the range of from about 10% to about 50% by weight of eementitious components. In yet another embodiment, the pumicite may be present in an amount in the range of from about 25% to about 50% by weight of eementitious components. One of ordinary skill in the ait, with the benefit of this disclosure, will recognize the appropriate amount of the pumicite to include for a chosen application,
.Embodiments of the sellable compositions further may comprise lime. In certain, embodiments, the lime may be hydrated lime. The iime may be included in embodiments of the settab!e compositions, for example, to form a hydraulic composition with other components of the sellable compositions, such as the pumicite, fly ash, slag, and/or shale. Where present, the lime may be included in the sellable composition in an amount sufficient for a particular application. In some embodiments, the lime may be present in an amount in the range of from about 1 % to about 40% by weight of eementitious components. For example, the lime may be present in an amount ranging between any of and/or including any of about. 5%, about 10%, about 15%, about 20%, about 25%, about 30%, or about 35%. In specific embodiments, the lime ma be present in an amount in the range of from about 5% to about 20% by weight of eementitious components. One of ordinary skill: in the art, with the benefit of this disclosure, will recognize the appropriate amount of the lime to include for a chosen application. In accordance with certain embodiments, a mixture of pumicite and hydraulic cement, such as Portland cement may be included in the settable composition, in an embodiment,, the cement/pumicite mixture contains hydraulic cement in an amount of about 25% to about 75% by weight of the .mixture and pumicite i n an amount of about 25% to about 75% by weight of the mixture, hi an embodiment, the cemeut/pumicite mixture contains about 40% hydraulic cement by weight and about 60% pumicite b weight, hi an embodiment, the ceroent/pumieiie mixture may comprise hydraulic cement interground with pumicite. In one embodiment, the hydraulic cement may comprise Portland cement classified as ASTM Type V cement, in accordance with embodiments, the Portland cement, and pumicite may be combined and ground to any size suitable for use in cementing operations, in another embodiment, the Portland cement and pumicite may be ground prior to combination, in an embodiment, the cenient/puroicite mixture of Portland cement and pumicite has a mean particle size of about 0.1 microns to about 400 microns, alternatively, about 0,5 microns to about 50 microns, and alternatively, about 0,5 microns to about. .10 microns. The mean particle size corresponds to dSO values as measured by commercially available particle size analyzers such as those manufactured by Mal ern instruments, Worcestershire, United Kingdom. An example of a sui table cement/pumicite mixture is available from Halliburton. Energy Services, Inc., under the trade name FhieCem.'M 925 cement.
It is believed that hydraulic cement interground with pumicite when used in a settable composition .in combination with unespanded perlite may provide synergistic effects. For example, it is believed that the combination of unexpended perlite and the cement/pumicite mixture ma provide significantly higher compressive strength, particularly at elevated well bore temperatures. Accordingly, the combination of unexpended perlite and the cement/pumicite mixture may be particularly suited for use in settable compositions at elevated well bore temperatures, such as at temperatures greater than about S T, alternatively greater man about 120°F, and alternatively greater than about 14QT.
Embodiments of the settable compositions further may comprise fly ash. A variety of fly ashes may be suitable, including fly ash classified as Class C and Class F fly ash according to American Petroleum institute, API Specification for Materials and Testing for Well Cements, API Specification 10, Pifih Ed., July I , 1990. Class C fly ash comprises both silica and lime so that, when mixed with water, it should set to form a hardened mass. Class F fly ash generally does not contain sufficient lime, so an additional source of calcium ions is typically required for the Class F fly ash. to form a hydraulic composition. In some embodiments* lime may be mixed with Class F fly ash in an .amount in the range of about 0, 1% to about 25% by weight of the fly ash, in some instances, the lime may be hydrated lime. Suitable examples of fly ash include, but are not limited to, POZMtX*' A cement additive, commercially available from Halliburton Energy Services, inc.
Where present, the fly ash generally may be included in the settable compositions in an. amount sufficient to provide the desired compressive strength, density, and/or cost, hi some embodiments, the fly ash may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 75% by weight of cementitious. components. For example, the fly ash may be. present in an amount ranging between any of and/or including any of about 3%, about .10%, about 20%, about 30%, about 40%, about 50%, about 60%, or about 70% by weight of cementitious components, in specific embodiments, the fly ash. may be present in an amount in the range of about .10% to about 60% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the fly ash to include for a. chosen application.
Embodiments of the settable compositions further may comprise slag cement. In some embodiments, a slag cement that may be suitable for use may comprise slag. Slag generally does not contain sufficient basic material, so slag cement further ma comprise a base to produce a hydraulic composition that may react with water to set to form a hardened mass, Examples of suitable sources of bases include, but are not limited to, sodium hydroxide, sodium bicarbonate, sodium carbonate, lime, and combinations thereof.
Where present, the slag cement generally may be included, in the settable compositions in an. amount sufficient to provide the desired conipressive strength, density, and/or cost, in some embodiments, the slag cement may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 75% by weight of cementitious components. For example, the slag cement ma be present in an. amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about. 40%, about 50%, about 60%, or about 70% by weigh of cementitious components, in specific embodiments, the slag cement ma be present in an amount in the range of about 5% to about 50% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the slag cement to include for a chosen application.
Embodiments of the settable compositions further may comprise metakaolin. Generally, metakaolin. is a white pozzoian that may be prepared by heating kaolin clay, for example, to temperatures m the range of about 6Q0°C to about 800°C. In some embodiments, the metakaolin may be present in the settable compositions of the present invention in an amount in the range of about S % to about 75% by weight of cementitious components. For example, the metakaolin may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, or about 70% by weight of cementitious components, in spec ific embodiments, the metakaolin may be present, in an amount in the range of about 10% to about 50% b weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the metakaolin to include for a chosen, application.
Embodiments of the sellable compositions further may comprise shale. Among other things, shale included in the settable compositions may react with excess lime to form, a suitable cementing material, for example, calcium silicate hydrate. A variety of shales may be suitable, including those comprising silicon, aluminum, calcium, and/or magnesium. A example of a suitable shale comprises vitrified shale. Suitable examples of vitrified shale include, but are not limited to, PRESSUR-SBAL FINE LCM material and PRESSUR-SEAL COARSE LCM material which are commercially available from TXl Energ Services, Inc. Generally, the shale may have any particle size distribution as desired for a particular application. In certain embodiments, the shale may have a particle size distribution in the range of about 37 micrometers to about 4,750 micrometers.
Where present, the shale may be included in the settable compositions of the present invention in an amount sufficient to provide the desired compressive strength, density, and/or cost. In some embodiments, the shale may be present in the settable compositions of the present invention, in a amount in the range of about 1% t about 75% by weight of cementitious components. For example, the shale may be present in an amount ranging between any of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, of about 70% by weight of cementitious components, in specific embodiments, the shale may be present in an amount in the range of about 10% to about 35% by weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of the shale to include or a chose application..
Embodiments of the settable compositions further may comprise zeolite. Zeolites generall are porous aiumino-sHicate minerals that may be either a natural or synthetic material. Synthetic zeolites are based on the same type of structural cell as natural zeolites, and may comprise alommosilicate hydrates. As used herein, the term "zeolite" refers to all natural and synthetic- forms of zeolite. Examples of suitable zeolites are described in more detail in U.S. Patent No. 7,445,669. An example of a suitable source of zeolite is available from the C2C Zeolite Corporation of Calgary, Canada, in some embodiments, the zeolite may be present in the settable compositions of the present invention in an amount in the range of about 1% to about 65% by weight of eementifious components. For example, the zeolite may be present in an amount ranging between an of and/or including any of about 5%, about 10%, about 20%, about 30%, about 40%, about 50%, or about 60% by weight of cemeniitious components, in -specific embodiments, the zeolite may be present in an amount in the range of about 10% to about 40% by weight of cemeniitious components. One of ordinary skill in the art, with the benefit, of this disclosure, will recognize the appropriate amount of the zeolite to include for a chosen application.
Embodiments of the settable compositions further may comprise a set retarding additive. As used herein, the term, "set retarding additive" refers to an additive that retards the setting of the settable compositions of the present invention. Examples of suitable set retarding additives include, but are not limited to, ammonium, alkali metals, alkaline earth metals, metal salts of suifoalkylated lign us, organic acids (e.g., hydrosycarboxy acids), copolymers that comprise acrylic acid or ma!eic acid, and combinations thereof. One example of a suitable suifoalkylated lignin comprises a su!fomethyiated lignin. Suitable set retarding additives are disclosed in more detail in United States Patent No, Re, 3 1 , 190, the entire disclosure of which is incorporated herein by reference. Suitable set retarding additives are commercially available, from Halliburton Energy Services, Inc. under the trademarks fill* 4, BR* 5, HR* 7, HR* 12, HR¾ I 5, HR*2S, HR®60I f SCR™ 100, and SCR™ 500 retarders. Generally, where used, the set retarding additive may be included in the settable compositions of the present invention in an amount sufficient to provide the desired set retardation. In some embodiments, the set retarding additive may be present in the settable compositions of the present invention an amount in the range of about. 0.1 % to about 5% by weight of cemeniitious components, including an amount ranging between any of and or including any of about 0.5%, about i %, about 2%, about 3%, or about 4% by weight of cemeniitious. components. One of ordinary skill in the art, with the benefit, of this disclosure, will recognize the appropriate amount of the set retarding additive to include for chosen application.
Embodiments of the settable compositions further may include water. The water that may be used in embodiments of the settable compositions include, for example, freshwater, saltwater (e.g., water containing one or more salts dissolved therein), brine
(e.g., saturated saltwater produced from subterranean formations), seawater, or combinations thereof Generally, the water may be from any source, provided that the water does not contain an excess of compounds that may undesirably affect other components in the settable composition. In some embodiments, the water may be included in an amount sufficient to form a pumpable slurry. In some embodiments, the water may be included in the settable compositions of the present invention in an amount in the .range of about 40% to about 200% by weight of cementitious components. For example, the water may be present in an amount ranging between an of and/or including any of about 50%, about 75%, about 100%, about 1.25%, about 1.50%, or about 175% by weight of cementitious components. In specific embodiments, the water may be included in an amount in the range of about 40% to about 150% b weight of cementitious components. One of ordinary skill in the art, with the benefit of this disclosure, will recognize the appropriate amount of water to include for a chosen application.
Optionally, other additional, additives may be added to the settable compositions of the present invention as deemed appropriate by one skilled .in the art, with the benefit of this disclosure. Examples of such additives include, but are not limited to, strength- retrogression additives, set accelerators, weighting agents, lightweight additives, gas- generating additives, mechanical property enhancing additives, lost-circulation materials, filtration-control additives, dispersants, fluid loss control additives, defoaming agents, foaming agents, oil-swel fable particles, water-swellable particles, thixoiropie additives, and combinations thereof. Specific examples of these, and other, additives include crystalline silica, amorphous silica, fumed silica, salts, fibers, hydratahle clays, microspheres, rice husk, ash, elastomers, efastomeric particles, resins, latex, combinations thereof, and the like. A person having ordinary skill in the art, with the benefit of this disclosure, will readily be able to determine the type and amount of additive useful for a particular application and desired result. Embodiments of the settable compositions may be foamed and/or extended as desired by those of ordinary skill in the art.
The settable compositions of the present invention should have a density suitable for a particular application as desired by those of ordinary skill in the art, with the benefit of this disclosure. In some embodiments, the settable compositions may have a density in the range of from about 8 pounds per gallon ("lb/gal") to about 16 lb/gal. In other embodiments, the settable compositions may be foamed to a density in the range of from about. 8 lb/gal to about 13 lb/gal.
As will be appreciated by those of ordinary skill in the art, embodiments of the settable compositions may be used in a variety of subterranean applications, including primary and remedial cementing. The settable compositions of the present invention also may be used in surface applications, for example, construction cementing. Embodiments ma include providing a settable composition and allowing the settable composition to set in some embodiments, the settable composition may be allowed to set in a locatio that is above ground, for example, in construction cementing. In other embodiments, the settable composition may be introduced into a well bore and allowed to set. For example, the settable composition may be placed into a space between a subterranean formation and a conduit located in the well bore. Embodiments of the settable compositions may comprise, for example, water and one or more of perlite, CKD, or pumkite. Embodiments of the settable compositions may comprise, for example, perlite interground with hydraulic cement (e.g., Portland cement).
In primary cementing embodiments, for example, a settable composition may be introduced into a space between a subterranean formation and a conduit (e.g., pipe strings, .liners) located in the well bore. The settable composition m y be allowed to set to form an annular sheath of hardened cement in the space between the subterranean formation and the conduit. Among othe things, the set settable composition may form a barrier, preventing the migration of fluids in the well bore. The set settable composition also may, for example, support the conduit in the well bore.
In remedial cementing embodiments, a settable composition may be used, for example, in squeeze-cementing operations or in the placement of cement plugs. B way of example, the settable composition may be placed in a well bore to plug a void or crack in the formation, in a gravel pack, hi the conduit, in the cement sheath, and/or a microannu!us between the cement sheath and the conduit.
To facilitate a better understanding of the present invention, the following examples of certain, aspects of some embodiments are given, in no wa should the following examples be read to limit, or define, the scope of the invention. EXAMPLE 1
A series of samples were prepared and subjected to 24-hour crush strength tests in accordance with API Specification .10 to analyze force .resistance propertie of settable compositions that comprise unexpanded perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for twenty-four hours. immediately alter removal from the water bath, crush strengths were determined using a Ttnius Olsen tester. The results of the crush strength tests are set forth in the table below.
Test Nos. I ~6 were performed on samples with a 14.2 ppg and containing water, Portland class H cement, ground unexpanded perlite, lime, and water, as indicated in the table below. The ground unexpanded perlite was 1M-3.25 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
Test Nos. 7-8 were performed on samples with a density of 14,2 ppg and containing water, Portland class H cement, pumieite, and lime, as indicated in the table below. The pumictte was about 200 U.S. Standard Mesh in size.
Test Nos, 9-14 were performed on samples with a density of 14.2 ppg and containing water, a ground eement pumicite mixture (FineCem'* 925 cement), unexpended perlite, time, and water, as indicated in the table below. The ground cenient/pumicite mixture comprised Portland Type V cement (about4Q% by weight) interground with pumieite (about60% by weight). The ground cement pumicite raixture had a mean particle size in the range of about 1 to about 4 microns. The ground unexpanded perlite was Ϊ -325 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
in the following table, percent by weight is based on the weight of the Portland cement, cement/pumicite mixture, pumieite, and unexpanded perlite in the sample, and gallons per sack (gal/sk) is based on a 94-ponnd sack of the Portland cement, eentent/purmcite mixture, pumieite, and unexpanded perlite.
TABLE I
Crush Strength Tests
Figure imgf000016_0001
Example 1 thus indicates that replacement of at least a portion of the Portland cement with unexpanded perlite may increase the crush strength of the settahie compositions. At J40c F, for example, the Test Nos. 2 and 4 with unexpanded perlite had crush strengths of 886 psi and 777 psi as compared to a crush .strength of 674 psi for Test No. I with 1 G0¾ Portland cement by weight
Example 1 further indicates that the ground pumicite/eement mixture in combination with the unexpended perlite may have synergistic effects on the settah'le composition, in thai this combination may provide increased crush strengths at elevated temperatures. At 140° F, for example. Test Nos. 12 and 14 with the ground pumieite/ce-ment mixture and unexpanded perlite had crush strengths of 2740 psi and 2610 psi. This crush, strength is markedly higher than the crush strengths for compositions with 100% Portland cement (674 psi at 140°F) and compositions with Portland cement and pumtcite that were not ground to fine particle sizes (835 psi and 734 psi at 140 ), This increased compressive strength for combinations of ground puraicite/cement mixture and unexpanded perlite cannot be attributed solely to the addition of expanded perlite as the combination had significantly higher crush strength than seen with additio of unexpended perlite to Portland cement (777 psi and 886 psi at 140° ). in addition, this increased compressive strength for combinations of ground pumicite/cement. mixture- and unexpended perlite cannot be attributed solely to the addition of expanded perlite as the combination had significantly higher crush strength than seen with the ground pumicite/cement mixture alone ( 1877 at. 140°F).
EXAMPLE 2
An additional series of sample sellable compositions were prepared and tested to analyze the force resistance properties of sellable compositions that comprise CKD and unexpanded perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for either 24 or 72 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester. Hie results of the crush strength tests are set forth in the table below.
Test Nos. 15-28 were performed on samples with a density of 14,2 ppg and containing water, CKD, ground unexpanded perlite, and lime, as indicated in the table below. The samples further contained a cement set retarder (CFR~3 cement set retarder, Halliburton Energy Services, Inc.) in an amount of about 0,4% by weight. The ground unexpanded perlite was ΪΜ-325 from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh.
In the following table, percent by weight is based on the weight of the CKD and unexpanded perlite in the sample, and gallons per sack, (gal sfc) is based on a 94-pound sack of the CK D and unexpanded perlite. TABLE 2
Crush Strength
Figure imgf000018_0001
Example 2 thus indicates that unexpanded perlite may be used to enhance the crush strength of CKD-containing compositions. in addition, this: effect is particularly pronounced at increased temperatures. At .140° F, for example. Test No. 22 with 75% CKD and 25% unexpanded perlite had a 72-hour crush strength of 1 04 pss as compared to a 72-hour crush strength of 457 psi for Test No. .18 with 100% CKD.
EXAMPLE 3
An additional series of sample settable compositions were prepared and tested to further analyze the force resistance properties of settable -compositions that comprise CKD and unexpanded perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours. Immediately after removal from the water bath, crush strengths were determined using a Tiniits Olsen tester. The results of the crush strength tests are set forth in the table below.
Test Nos. 29-37 were performed on samples with a density of 1.4.2 ppg and containing water, CKD. ground unexpanded. perlite. and lime, as indicated in the table below. The samples further contained a cement dispersani in an amount of about 0,4% by weight The ground unexpanded perlite was lM-325 from Hess Pumice Products with a particle size of about 325 U .S. Standard Mesh. In the following table, percent by weight is based on the weight of the CKD and unexpended perhte in the sample, and gallons per sack (ga! sk) is based on a 94-pound sack of the CKD and unexpended perlite.
TABLE 3
Crush Strength Tests
Figure imgf000019_0001
Example 3 thus indicates that unexpended perlite may be used to enhance the crush strength of CKD-coniaining compositions. For example, as indicated in the table above, the crush strength of the samples steadily increased as the concentration of unexpended perlite in the sample was increased from 0% by weight to 40% by weight,
EXAMPLE 4
An additional series of sample settable compositions were prepared and tested to further analyze the force resistance properties of settable compositions that comprise CKD and unexpended perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester. The results of the crush strength tests are set forth in the table below.
Test Nos, 38-43 were performed on samples with a density of 14.2 ppg and containing water, CKD, perlite, and lime, as indicated in the table below. The samples further contained a cement dLspersant in an amo unt of about 0.4% by weight. Test Nos, 38 and 39 contained a ground unexpanded perlite (IN4-325) from Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh. Test Nos. 40 and 1 contained unground perlite ore having a mean particle size (dSO) of about 1 0 microns. Test Nos, 42 and 43 contained expanded perlite. in the following table, percent by weight is based on the weight of the CKD and perlite in the sample, and gallons per sack (ga'l/sk) is based on a 94-pound sack of the CKD and perlite.
TABLE 4
rush Strengt Tests
Figure imgf000020_0001
Example 4 thus indicates that unexpanded perlite provides superior strength enhancement to KD~containiog compositions when compared lo unground perlite ore and expended perlite. indeed, the sample with the expanded perlite could not even be tested due to mixability problems.
EXAMPLE 5
An additional series of sample settable compositions were prepared and tested to further analyze settable compositions that comprise CKD and unexpanded -perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours. Immediately after removal from the water bath, crush, strengths were determined using a Tinius Oisen tester. The results of the crush strength tests are set forth in the table below. The thickening time for each sample was also determined at 140*3 F in accordance with API Specification 10.
Test Nos, 44-56 were performed on samples with a density of 12.5 ppg and containing CKD, perlite, and lime, as indicated in the table below. The samples further contained a cement dispersant in a amount of about 0.4% by weight and a cement set retarder (HR*-' 5 cement retarder, Halliburton Energy Services, Inc.). Test Nos. 45, 48, 5.1, and 54 contained a ground unexpanded perlite (i -325) from Hess Pumice Products with a particle size of about 314 U.S. Standard Mesh. Test Nos, 46, 49, 52, and 55 contained unground perlite ore having a mean particle size (d50) of about 190. Test Nos. 47, 50, 53, and 56 contained expanded perlite.
V) In the following table, percent by weight is based on the weight of the CKD and perlite in the sample, and gallons per sack (ga'l/sk) is based on a 94-pound sack of the CKD and per! He,
TABLE 5
Crush Strengt 8»<S T ickemRg Time Tests
Figure imgf000021_0001
Example 5 thus indicates that unexpanded perlite provides enhanced sirenglh to CKD-contaming compositions when compared to unground perlite ore and expanded perlite. In a similar manner to the preceding example, the samples with expanded perlit could not even be tested due to mixability problems,
EXAMPLE 6
An additional series of sample sellable compositions were prepared and tested to further analyze settable compositions that comprise CKD and unexpanded perlite. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours. Immediately after removal from the water bath, crush, strengths were determined using a Tinius Olsen tester. The results of the crush strength tests are set forth in the table below.
Test No, 57 was performed on a sample will), a density of . 2.5 ppg and containing water, Portland Type V cement, CKD, unground perlite ore, and purnicite, as indicated in the table below. The unground perlite ore had a. mean particle size (d50) of about S 90. The pum telle had a mean particle size (d50) of about.4 .microns.
Test No. 58 was performed on a sample with a density of 12.5 ppg and containing water, ground cement pumicite mixture pomicite, CKD, and ground unexpanded perlite. The ground cementfpumieite mixture comprised Portland Type V cement (about 40% by weight) ioterground with purnicite (about 60% by weight). The ground eement pumicite mixture had a mean particle size of about I -4 microns. The ground unexpanded perlite was IM-325 front Hess Pumice Products with a particle size of about 325 U.S. Standard Mesh, in the following table, percent by weight is based on the weight of the CKD, cement, perlite, pumicite, and/or pumicite/cemenl mixture in the sample, and gallons per sack (ga!/sk) is based on a 94-pound sack of the CKD, cement, perlite, pumicite, and/or pumicite eenient mixture in the sample.
TABLE 6
Crush Strength Tests
1 Port ί an Ground
d Type Pumieit
1 v e C Perlit j 24-Hr (. emen Pumicit. Cement D Ground e Ore | Crush
Tes Water j t e Mixture (% Unexpaiide (% j Tem Strengt t (gal/sk J (% by (% by (% by by d Perlite by 1 h ~
No, ) 1 wt) wt) wt) t) (% by wt) t) j (psi)
57 0.52 [ 20 30 25 25 j 140 2 1
58 9.72 1 - 50 25 25 1 - 1 140 1086
Example 6 thus indicates that unexpanded perlite in combination with ground pumicite provides enhanced strength to CKD-co.otat.ning compositions in comparison to compositions with standard cement, pumicite, and unground peri he ore.
EXAMPLE 7
An additional series of sample suitable compositions were prepared and tested to analyze sellable compositions that comprised interground perlite and hydraulic cement.
The sample sellable compositions were formed by mixing the components in the amounts set forth in the table below. The interground pumicite and cement comprised pumicite (about 60% by weight) and Portland 'Type V cement (about 40% by weight) and had a mean particle size of about 1-4 microns. The interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name FmeCem'M 925 cement. The interground perlite and cement comprised ground unexpended perlite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a himodal particle size distribution with peak particle sizes of about 4 microns and about 10 microns. The interground perlite and cement was obtained from Hess Pumice Products, Malad City, Idaho. The lime was hydrated lime, obtained from Univar USA.
The sample compositions were subjected to 24-hour crush strength tests in accordance with API Specification iO. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours. Immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester.
The results of the crush strength tests are set forth in the table below.
TABLE 7
rush Strength Tests
j 1 Interground interground j 24-Hr
1 Pumiciie and Perlite and j Crush
Test Density Water | Cement Cement j Lime Temp. Strength No, (ib/ga!) (% bwc!) j (% bwc) (% bwe) ! 0 >¾ bwc } C'F) I (psi)
59 5.4.2 I 52.46 j . 00 ! — 140 1 2870
60" 14.2 52.46 j loo i — 140 1 1998
61 12,5 92,49 j 100 i 5 140 128?
62 12,5 92.49 ! mo j 5 140 J 1489
63 12.5 I 88.9 1 50 50 i — 140 j i e i
64 12.5 1 92.49 1 50 | 50 | 5 140 1023
65 1 1 1 159,58 j 100 i 140 31 1
66 I t I 159.58 1 100 j — 140 j 408
67 10.5 204.84 i00 ! — 140 105.9
68 10.5 j 204.84 j loo j — "140 j 185.1
¾e term " % bwc" refers to b weight of cement, which in this example is ei her by weight of the interground pumicite and cement or by weight of the interground perlite and cement.
2 1.2 grams of CFR.-3'*" friction reducer were added to the sample seitable composition for Test No. 60.
Example 7 thus indicates that interground perlite and hydraulic cement generally provides enhances compressive sirength development as compared to interground pumicite and hydraulic cement. It should be noted that the CF -3'S' included in Test No. 60 retarded the setting resulting in the lower 24-hour crush strength as compared to Test No. 59 with the interground punucKe and cement.
EXAMPLE 8
An additional series of sample seitable compositions were prepared and tested to further analyze sellable compositions that comprised interground perlite and hydraulic cement.
The sample sellable compositions were formed by mixing the components in the amounts set forth in the table below. The interground pumicite and cement comprised pumicite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a mean particle size of about 1 -4 microns. The interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name I' iieCeni " 925 cement. The interground perlite and cement comprised ground unexpended perlite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a bimodal particle size distribution with peak particle sizes of about 4 microns and about 10 .microns. The interground periite and cement was obtained from Hess Pumice Products, aiad City, Idaho.
The sample compositions were subjected to 24-hour crush strength tests in accordance with API Specification 10. The sample compositions were allowed to cure in a water bath at the temperature indicated in the table below for 24 hours, immediately after removal from the water bath, crush strengths were determined using a Tinius Olsen tester. The thickening time .for each sample was also determined at 140" F in accordance with API Specification 10.
The results of the crush strength and thickening time tests are set forth in the table below.
TABLE 8
Crush Strength and Thickening Time Tests
Figure imgf000024_0001
The abbreviation '*% bwc" refers to by weight of cement, which in this example is either by weight of the interground pumicite and cement or by weight of the interground periite and cement,
2 The abbreviation "Be" refers to Bearden units of consistency.
Example 8 thus indicates that sellable compositions comprising interground periite and hydraulic cement may have acceptable thickening times for use in subterranean applications. Example 8 further indicates that interground periite and hydraulic cement generally provides enhanced compressive strength development and can be similarly controlled with retarders as compared to interground pumicite and hydraulic cement. EXAMPLE 9
An additional series of sample sellable compositions were prepared and tested to further analyze sellable compositions that comprised intergrouiid periite and hydraulic cement,
The sample seitable compositions were formed by mixing the components in the amounts set forth in the table below. The interground pumicite and cement comprised pumicite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a mean particie size of about ! -4 microns. The interground pumicite and cement are available from Halliburton Energy Services, Inc., under the trade name FineCeni'M 925 cement. The interground periite and cement comprised ground unexpended periite (about 60% by weight) and Portland Type V cement (about 40% by weight) and had a bimodal particie size distribution, with peak particie sizes of about 4 microns and about 10 microns. The interground periite and cement was obtained from Hess Pumice Products, Ma!ad City. Idaho.
Free water data was then gathered for each sample composition in accordance with
API Specification 10. The tree water data is set forth in the table below.
TABLE 9
:-ree Water Data
Figure imgf000025_0001
! The abbreviation * '% bwc" refers to by weight of cement, which in this exam pi e is either by weight of the interground pumicite and cement or by weight of the interground periite and cement.
* The abbreviation "ce" refers to cubic centimeters.
Example 9 thus indicates that settable compositions comprisin interground periite and hydraulic cement may have provide lower levels of free water as compared to interground pumicite and hydraulic cement.
it should be understood that the compositions and methods are described in terms of "comprising," "containing," or "including" various components or steps, the compositions, and methods can also "consist essentially of or "consist of the various components and steps.
For the sake of brevity, only certain ranges are explicitly disclosed herein. However, ranges from any lower lira it may be combined with any upper limit to recite a range not explicitly recited, as well as, ranges from any lower limit may be combined with any other lower limit to recite a range not explicitly recited, in the same way, ranges from any upper limit may be combined with any other upper limit to recite a range not explicitly recited. Additionally, whenever a numerical range with a lower limit and an upper limit is disclosed, any number and any included range falling within the. range is specifically disclosed. In particuiar, every range of values (of the form, "from about a to about b," or, equivaiently, "from approximately a to h," or, equivalent^, "from approximately a-h") disclosed herein is to be understood to set forth every number and range encompassed within the broader range of values even if not explicitly recite. Thus, every point or individual value ma serve as its own lower or upper limit combined with any other point or individual value or an other lower or upper limit, to recite a .range not explicitl recited.
Therefore, the present invention is well adapted to attain the ends and advantages mentioned as well as those that are inherent therein. The particular embodiments disclosed, above are illustrative only, as the present invention may he modified and practiced in different but equivalent manners apparent to those skilled in the art having the benefit of the teachings herein. Although individual embodiment are discussed, the invention covers all combinations of all those embodiments. Furthermore, no limitations are intended to the details of construction or design herein shown, other than as described in the claims below. Also, the terms in the claims have their plain, ordinary meaning unless otherwise explicitly and clearly defined by the patentee. It is therefore evident that the particular illustrative embodiments disclosed above may be altered or modified and all such variations are considered within the scope and spirit of the present, invention.

Claims

What is claimed is:
1 - A method of cementing comprising:
providing a settabie composition comprising periite, hydraulic cement, and water, wherein the periite and hydraulic cement are interground prior to combination with the water to form the sellable composition; and
allowing the settabie composition to set
2. The method of claim I wherein the periite comprises unexpended periite.
3. The method of claim I wherein the periite and the hydraulic cement were interground to a mean particle about 0, 1 microns to about 400 microns.
4. The method of claim 1 wherein the periite and the hydraulic cement were interground to a mean particle about 0.5 microns to about 10 .microns.
5. The method of claim 1 wherein the periite is present in an amount of about 40% to about 80% by weight of the periite and hydraulic cement, and wherein the hydraulic cement is present, in an amount, of about 20% to about 60% by weight of the periite and hydraulic cement.
6. The method of claim i wherein the hydraulic cement comprises at least one cement selected from the group consisting of a Portland cement, a pozzo!ana cement,, gypsum cement, a high-aiuniina-content cement, a slag cement, a silica/lime cement, and any combination thereof.
7. The method of claim .! wherein the hydraulic cement comprises a Portland cement.
8. The method of claim 1 wherein the periite and the hydraulic cement were interaround with at least one additional component selected from the group consisting of cement kiln dust and purnieite.
9. The method of claim I wherein the settabie composition further comprises cement kiln dust.
10. The method of claim ί wherein the settabie composition further comprises pumicite.
11. The method of claim .1 wherein the settabie composition further comprises at least one additive selected from the group consisting of lime, fly ash, slag cement, metakaolin, shale, zeolite, crystalline silica, amorphous silica, fumed silica, salt, fiber, hydratah!e clay, microsphere, rice husk ash, elastomer, elastonieric particle, resin, latex,, and any combination thereof
12. The method of claim I wherein the settabie composition further comprises at least one additive selected from the group consisting of a set retarding additive, a strength- retrogression additive, a set accelerator, a weighting agent, a lightweight additive, a gas- generating additive, a mechanical property enhancing additive, a lost-circulation material, a filtration-control additive, a dispetsant, a fluid loss control additive, a detoaming agent, a foaming agent, an oii-sweilabie particle, a water-swe!labie particle, thixotropic additive, and any combination thereof
1.3. The method of claim 1 further comprising introducing the settabie composition into a well bore,
14, The method of claim 13 wherein the settabie composition is allowed to set in the well bore in an annulus between a subterranean formation and a conduit in the we'll bore,
15. The method of claim 13 further comprising squeezing the settabie composition in an opening, the opening comprising at least one opening selected from the group consisting of an opening in a subterranean formation, an opening in a gravel pack, an opening in a conduit, and a. microaiuiulus between a cement sheath and a conduit.
S 6, A method of cementing comprising:
providing a settabie composition comprising unexpanded perlite, hydraulic cement, and water, wherein the unexpended, perlite and hydraulic cement are intergronnd prior to combination with the water to form the sellable composition;
introducing the settabie composition into a well bore; and
allowing the settabie composition to set,
17. The method of claim 16 wherein the perlite and hydraulic cement were interground to a mean particle about 0.5 microns to about 10 microns,
18. The method of claim 1 wherein the perlite is present in an amount of about 40% to about 80% by weight of the perlite and hydraulic cement, and wherein the hydraulic cement in an amount of about 20% to about 60% by weight of the perlite and hydraulic cemen ,
1 . The method of claim 16 wherein the hydraulic cement comprises at least one cement selected from the group consisting of a Portland cement, a pozzolan cement, a gypsum, cement, a high-alumina-content cement, a slag cement, a siticadime cement, and any combi nation thereo
20. The method of claim 16 wherein the hydraulic cement comprises a Portland cement.
21. The method of claim. 16 wherein the perlite and the hydraulic cement were interaround with at least one additional component selected from the group consisting of cement kiln dust and pumicite.
22. The method of claim 16 wherein the settable composition further comprises cement kiln dust.
23. The method of claim 16 wherein the settable composition further comprises pumicite.
24. The method of claim 16 wherein the settable composition -further comprises at least one additive selected from the group consisting of lime, fly ash, slag cement, metakaoliu, shale, zeolite, crystalline silica, amorphous silica, fumed silica, salt, fiber, hydratable clay, microsphere, rice husk ash, elastomer, elastomeric particle, resin, latex, and any combination, thereof,
25. The method of claim 16 wherein, the settable composition further comprises at least one additive selected from the group consisting of a set retarding additive, a strength- retrogression additive, a set accelerator, a weighting aaent, a light-weight additive, a. gas- generating additive, a mechanical property enhancing additive, a lost-circulation material, a filtration-control additive, 3 dispersani, a fluid, loss control additive, a defoaming agent, a foaming agent, an oif-sweUable particle, a water-swellabie panicle, a thix tropic additive, and any combination thereof
26. I'he method of claim 16 wherein the settable composition is allowed to set in the well bore in an annulus between subterranean formation and a conduit in the well. bore.
27. The method of claim 16 further comprising squeezing the settable composition in an opening, the opening comprising at least one opening selected from the group consisting of an opening in a subterranean formation, an opening in a gravel pack, an opening in a conduit, and a .raicroannulus between a cement sheath and. a conduit
28. A composition comprising;
interground perlite and hydraulic cement
PCT/US2012/046117 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement WO2013009780A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
CN2012800051623A CN103459348A (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement
BR112013016242A BR112013016242A2 (en) 2011-07-11 2012-07-10 cementation method and, cementation composition
RU2013129542/03A RU2584431C2 (en) 2011-07-11 2012-07-10 Curable compositions containing co-milled pearlite and hydraulic cement
AU2012282775A AU2012282775B2 (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement
CA2821931A CA2821931C (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement
MX2013007395A MX2013007395A (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement.
EP12735761.4A EP2651849A1 (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement
NZ612235A NZ612235B2 (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US13/180,238 US8672028B2 (en) 2010-12-21 2011-07-11 Settable compositions comprising interground perlite and hydraulic cement
US13/180,238 2011-07-11

Publications (1)

Publication Number Publication Date
WO2013009780A1 true WO2013009780A1 (en) 2013-01-17

Family

ID=46514844

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2012/046117 WO2013009780A1 (en) 2011-07-11 2012-07-10 Settable compositions comprising interground perlite and hydraulic cement

Country Status (11)

Country Link
US (2) US8672028B2 (en)
EP (1) EP2651849A1 (en)
CN (1) CN103459348A (en)
AR (1) AR087113A1 (en)
AU (1) AU2012282775B2 (en)
BR (1) BR112013016242A2 (en)
CA (1) CA2821931C (en)
MX (1) MX2013007395A (en)
MY (1) MY170430A (en)
RU (1) RU2584431C2 (en)
WO (1) WO2013009780A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106150428A (en) * 2015-03-27 2016-11-23 中国石油化工股份有限公司 Split type exempting from bores plug completion tubular column and completion method thereof
US11236902B2 (en) * 2020-04-27 2022-02-01 Rheem Manufacturing Company Frustoconical combustion chamber for a fluid heating device and methods for making the same

Families Citing this family (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9150773B2 (en) 2005-09-09 2015-10-06 Halliburton Energy Services, Inc. Compositions comprising kiln dust and wollastonite and methods of use in subterranean formations
US9023150B2 (en) 2005-09-09 2015-05-05 Halliburton Energy Services, Inc. Acid-soluble cement compositions comprising cement kiln dust and/or a natural pozzolan and methods of use
US8522873B2 (en) 2005-09-09 2013-09-03 Halliburton Energy Services, Inc. Spacer fluids containing cement kiln dust and methods of use
US8950486B2 (en) 2005-09-09 2015-02-10 Halliburton Energy Services, Inc. Acid-soluble cement compositions comprising cement kiln dust and methods of use
US8403045B2 (en) 2005-09-09 2013-03-26 Halliburton Energy Services, Inc. Settable compositions comprising unexpanded perlite and methods of cementing in subterranean formations
US9676989B2 (en) 2005-09-09 2017-06-13 Halliburton Energy Services, Inc. Sealant compositions comprising cement kiln dust and tire-rubber particles and method of use
US9051505B2 (en) 2005-09-09 2015-06-09 Halliburton Energy Services, Inc. Placing a fluid comprising kiln dust in a wellbore through a bottom hole assembly
US8327939B2 (en) 2005-09-09 2012-12-11 Halliburton Energy Services, Inc. Settable compositions comprising cement kiln dust and rice husk ash and methods of use
US8281859B2 (en) 2005-09-09 2012-10-09 Halliburton Energy Services Inc. Methods and compositions comprising cement kiln dust having an altered particle size
US8609595B2 (en) 2005-09-09 2013-12-17 Halliburton Energy Services, Inc. Methods for determining reactive index for cement kiln dust, associated compositions, and methods of use
US8297357B2 (en) * 2005-09-09 2012-10-30 Halliburton Energy Services Inc. Acid-soluble cement compositions comprising cement kiln dust and/or a natural pozzolan and methods of use
US8505630B2 (en) 2005-09-09 2013-08-13 Halliburton Energy Services, Inc. Consolidating spacer fluids and methods of use
US8307899B2 (en) 2005-09-09 2012-11-13 Halliburton Energy Services, Inc. Methods of plugging and abandoning a well using compositions comprising cement kiln dust and pumicite
US8505629B2 (en) 2005-09-09 2013-08-13 Halliburton Energy Services, Inc. Foamed spacer fluids containing cement kiln dust and methods of use
US9006155B2 (en) 2005-09-09 2015-04-14 Halliburton Energy Services, Inc. Placing a fluid comprising kiln dust in a wellbore through a bottom hole assembly
US8672028B2 (en) 2010-12-21 2014-03-18 Halliburton Energy Services, Inc. Settable compositions comprising interground perlite and hydraulic cement
US9809737B2 (en) 2005-09-09 2017-11-07 Halliburton Energy Services, Inc. Compositions containing kiln dust and/or biowaste ash and methods of use
US8555967B2 (en) 2005-09-09 2013-10-15 Halliburton Energy Services, Inc. Methods and systems for evaluating a boundary between a consolidating spacer fluid and a cement composition
NO334970B1 (en) * 2011-06-01 2014-08-11 Elkem As cement Compositions
US9346711B2 (en) 2012-08-16 2016-05-24 Halliburton Energy Services, Inc. Geopolymer cement compositions and methods of use
US8557036B1 (en) 2012-11-09 2013-10-15 Halliburton Energy Services, Inc. Settable compositions comprising wollastonite and pumice and methods of use
US8899329B2 (en) 2013-04-30 2014-12-02 Halliburton Energy Services, Inc. Pumice-containing remedial compositions and methods of use
CA2936003C (en) * 2014-02-28 2018-05-08 Halliburton Energy Services, Inc. Settable compositions and methods of use
AU2015392944B2 (en) * 2015-04-28 2018-07-12 Halliburton Energy Services, Inc. Synthetic hectorite in glass bead suspensions
US20180251403A1 (en) * 2015-09-04 2018-09-06 Imerys Oilfield Minerals Inc. Compositions and methods for well cementing
CN106565383B (en) * 2015-10-13 2019-09-20 中国石油化工股份有限公司 A kind of composite particles, preparation method and application
US11655186B2 (en) 2015-10-23 2023-05-23 Roman Cement, Llc Activitation of natural pozzolans
US11746048B2 (en) 2015-10-23 2023-09-05 Roman Cement, Llc Cement-SCM compositions and methods and systems for their manufacture
US10155695B2 (en) 2016-10-04 2018-12-18 Romeo Ilarian Ciuperca Manufactured natural pozzolan, improved manufactured natural pozzolan-based cement and method of making and using same
CN106810182B (en) * 2017-02-19 2019-03-12 广东广利建设集团有限公司 Cement base bubble partition board
CA3063548A1 (en) * 2017-05-15 2018-11-22 Romeo Ilarian Ciuperca Hyaloclastite, sideromelane or tachylite pozzolan, cement and concrete using same and method of making and using same
US11236018B2 (en) 2017-05-15 2022-02-01 Romeo Ilarian Ciuperca Hyaloclastite, sideromelane or tachylite pozzolan-based geopolymer cement and concrete and method of making and using same
US9822037B1 (en) 2017-05-15 2017-11-21 Romeo Ilarian Ciuperca Hyaloclastite pozzolan, hyaloclastite based cement, hyaloclastite based concrete and method of making and using same
EP3483132A1 (en) * 2017-11-14 2019-05-15 Services Pétroliers Schlumberger Methods for cementing thermal wells
US10450494B2 (en) 2018-01-17 2019-10-22 Bj Services, Llc Cement slurries for well bores
WO2019168690A1 (en) 2018-03-02 2019-09-06 Pörner Ingenieurgesellschaft M.B.H. Sustainable silicates and methods for their extraction
KR20210024001A (en) * 2018-06-15 2021-03-04 사로드 그린백 엘엘피 Engineered concrete binder composition containing mechanical-chemically modified components and method for manufacturing the same
CA3125963A1 (en) * 2019-01-08 2020-07-16 Roman Cement, Llc Activation of natural pozzolan and use thereof
US10752823B1 (en) * 2019-09-06 2020-08-25 Halliburton Energy Services, Inc. Wellbore servicing composition with controlled gelation of cement kiln dust and methods of making and using same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2455446A (en) * 2005-02-09 2009-06-17 Halliburton Energy Serv Inc Method of cementing a wellbore with a composition comprising perlite
US20110100626A1 (en) * 2005-09-09 2011-05-05 Halliburton Energy Services, Inc. Settable Compositions Comprising Unexpanded Perlite and Methods of Cementing in Subterranean Formations
US20120152539A1 (en) * 2010-12-21 2012-06-21 Halliburton Energy Services, Inc. Settable Compositions Comprising Interground Perlite and Hydraulic Cement

Family Cites Families (405)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2021956A (en) 1932-07-25 1935-11-26 Marshall S Hanrahan Cellular aggregate and process
US1931921A (en) 1932-12-01 1933-10-24 Valley Forge Cement Company Manufacture of cement
US2133622A (en) 1934-06-12 1938-10-18 Yosemite Portland Cement Corp Cement process and product
US2045899A (en) 1935-04-30 1936-06-30 Texas Co Method of increasing production from wells
US2094316A (en) 1936-03-06 1937-09-28 Kansas City Testing Lab Method of improving oil well drilling muds
US2144254A (en) 1936-09-24 1939-01-17 Separation Process Company Cement manufacture
US2193807A (en) 1938-01-04 1940-03-19 Dow Chemical Co Cementing practice for earth wells
US2193775A (en) 1938-06-18 1940-03-12 Texaco Development Corp Method of treating a well
US2214715A (en) 1938-06-30 1940-09-10 Separation Process Company Cement manufacture
US2329940A (en) 1940-12-12 1943-09-21 Missouri Portland Cement Co Manufacture of cement
US2592468A (en) 1947-12-06 1952-04-08 Standard Oil Dev Co Manufacture of cement
US2848051A (en) 1954-03-22 1958-08-19 Atlantic Refining Co Method for improving well cementing jobs
US2772739A (en) 1954-09-24 1956-12-04 Shell Dev Method of temporarily closing portion of well and composition therefor
US2880096A (en) 1954-12-06 1959-03-31 Phillips Petroleum Co Cement compositions and process of cementing wells
US2844361A (en) 1955-06-28 1958-07-22 Fuller Co Method and apparatus for blending pulverulent material
US2871133A (en) 1956-12-10 1959-01-27 Peerless Cement Corp Inorganic dust treatment process
US2842205A (en) 1956-12-24 1958-07-08 Exxon Research Engineering Co Method of servicing wells
US2945769A (en) 1957-08-08 1960-07-19 Bj Service Inc Cement composition
US3024125A (en) 1959-02-13 1962-03-06 Pennsalt Chemicals Corp Cement composition
US3066031A (en) 1959-10-21 1962-11-27 Joseph J Coney Cementitious material and method of preparation thereof
US3168139A (en) 1961-05-08 1965-02-02 Great Lakes Carbon Corp Converting drilling muds to slurries suitable for cementing oil and gas wells
US3320077A (en) 1966-01-19 1967-05-16 William L Prior Inorganic plastic cements and process for the preparation thereof
US3467193A (en) 1966-04-04 1969-09-16 Mobil Oil Corp Method for achieving turbulence in cementing wells
US3411580A (en) 1966-09-28 1968-11-19 Byron Jackson Inc Mud removal method
US3473939A (en) 1967-04-10 1969-10-21 Kaiser Aluminium Chem Corp Direct-bonded periclase refractories and process of preparing same
FR1535495A (en) 1967-04-28 1968-08-09 Rice husk treatment process and material obtained by this process
US3454095A (en) 1968-01-08 1969-07-08 Mobil Oil Corp Oil recovery method using steam stimulation of subterranean formation
US3421703A (en) 1968-04-04 1969-01-14 Nat Gypsum Co Kiln feed control
US3574113A (en) 1968-04-18 1971-04-06 Owens Corning Fiberglass Corp Method of producing calcium silicate type high temperature thermal insulation materials
US3499491A (en) 1968-06-28 1970-03-10 Dresser Ind Method and composition for cementing oil well casing
US3557876A (en) 1969-04-10 1971-01-26 Western Co Of North America Method and composition for drilling and cementing of wells
US3628973A (en) * 1970-11-20 1971-12-21 Ass Portland Cement Modified portland cement and process
US3876005A (en) 1972-01-24 1975-04-08 Halliburton Co High temperature, low density cementing method
US3748159A (en) 1972-04-20 1973-07-24 Halliburton Co High temperature cementing compositions containing a lignosulfonic acid salt and a pentaboric acid salt
US3749173A (en) 1972-05-30 1973-07-31 Dow Chemical Co Displacement of drilling fluids from boreholes
US3959007A (en) 1972-07-28 1976-05-25 Structural Materials Process for the preparation of siliceous ashes
NL7306868A (en) 1973-05-17 1974-11-19
US3921717A (en) 1973-07-12 1975-11-25 Solomon Isaakovic Danjushevsky Method for cementing wells
US4105459A (en) 1974-01-28 1978-08-08 The Regents Of The University Of California Siliceous ashes and hydraulic cements prepared therefrom
US3863718A (en) 1974-03-27 1975-02-04 Shell Oil Co Cementing procedure for avoiding mud channeling
US3887009A (en) 1974-04-25 1975-06-03 Oil Base Drilling mud-cement compositions for well cementing operations
US4018619A (en) 1974-09-23 1977-04-19 Iu Technology Corporation Highly activated mixtures for constructing load bearing surfaces and method of making the same
US4036301A (en) 1974-10-29 1977-07-19 Standard Oil Company (Indiana) Process and composition for cementing casing in a well
US4032353A (en) * 1975-04-21 1977-06-28 Westvaco Corporation Low porosity aggregate-containing cement composition and process for producing same
US4031184A (en) 1976-01-14 1977-06-21 Donald L. Christensen Process for reclaiming cement kiln dust and recovering chemical values therefrom
USRE31190E (en) 1976-02-02 1983-03-29 Halliburton Company Oil well cementing process
US4101332A (en) 1976-02-02 1978-07-18 Nicholson Realty Ltd. Stabilized mixture
US4018617A (en) 1976-02-02 1977-04-19 Nicholson Realty Ltd. Mixture for pavement bases and the like
JPS542984Y2 (en) 1976-03-02 1979-02-09
US4141843A (en) 1976-09-20 1979-02-27 Halliburton Company Oil well spacer fluids
US4083407A (en) 1977-02-07 1978-04-11 The Dow Chemical Company Spacer composition and method of use
US4160674A (en) * 1978-01-30 1979-07-10 Lone Star Industries Early high-strength portland cement and method of manufacture
US4176720A (en) 1978-07-27 1979-12-04 Atlantic Richfield Company Well cementing in permafrost
JPS5527881U (en) 1978-08-14 1980-02-22
US4268316A (en) 1979-07-27 1981-05-19 Martin Marietta Corporation Masonry cement composition
US4304300A (en) 1979-08-09 1981-12-08 Halliburton Company Method of using gelled aqueous well treating fluids
US4274881A (en) 1980-01-14 1981-06-23 Langton Christine A High temperature cement
US4341562A (en) 1980-03-21 1982-07-27 N-Viro Energy Systems, Ltd. Lightweight aggregate
US4423781A (en) 1980-04-01 1984-01-03 Standard Oil Company Method of using a spacer system in brine completion of wellbores
US4333764A (en) 1981-01-21 1982-06-08 Shell Oil Company Nitrogen-gas-stabilized cement and a process for making and using it
DE3131548A1 (en) 1981-08-08 1983-02-24 Otavi Minen Ag, 6000 Frankfurt "LIGHTWEIGHT MATERIAL AND METHOD FOR THE PRODUCTION THEREOF"
DE3132928C1 (en) 1981-08-20 1983-01-13 Degussa Ag, 6000 Frankfurt Process for accelerating the setting of hydraulic cement mixtures
US4436850A (en) 1981-10-19 1984-03-13 Allied Corporation Stabilizing SBR latex in cement formulations with low molecular weight polymers
WO1983001443A1 (en) 1981-10-26 1983-04-28 Standard Concrete Material Inc Improvements in cements, mortars and concretes
US4407677A (en) 1982-04-05 1983-10-04 Martin Marietta Corporation Concrete masonry units incorporating cement kiln dust
US4400474A (en) 1982-04-26 1983-08-23 Uss Engineers & Consultants, Inc. Basic refractory cementitious material and components thereof
US4460292A (en) 1982-07-15 1984-07-17 Agritec, Inc. Process for containment of liquids as solids or semisolids
US4432800A (en) 1982-08-16 1984-02-21 N-Viro Energy Systems Ltd. Beneficiating kiln dusts utilized in pozzolanic reactions
US4440576A (en) 1982-09-27 1984-04-03 Corning Glass Works Hydraulic cements prepared from glass powders
US4470463A (en) 1983-01-27 1984-09-11 The Dow Chemical Company Well treating process and composition
US4494990A (en) 1983-07-05 1985-01-22 Ash Grove Cement Company Cementitious composition
US4515635A (en) 1984-03-23 1985-05-07 Halliburton Company Hydrolytically stable polymers for use in oil field cementing methods and compositions
US4555269A (en) 1984-03-23 1985-11-26 Halliburton Company Hydrolytically stable polymers for use in oil field cementing methods and compositions
US4519452A (en) 1984-05-31 1985-05-28 Exxon Production Research Co. Method of drilling and cementing a well using a drilling fluid convertible in place into a settable cement slurry
US4668128A (en) 1984-07-05 1987-05-26 Soli-Tech, Inc. Rigidification of semi-solid agglomerations
US4676832A (en) 1984-10-26 1987-06-30 Halliburton Company Set delayed cement compositions and methods of using the same
US4741782A (en) 1984-11-07 1988-05-03 Resource Technology, Inc. Process for forming a light-weight aggregate
US4624711A (en) 1984-11-07 1986-11-25 Resource Technology, Inc. Light-weight aggregate
US4614599A (en) 1985-04-01 1986-09-30 Texaco Inc. Encapsulated lime as a lost circulation additive for aqueous drilling fluids
US4633950A (en) 1985-05-28 1987-01-06 Texaco Inc. Method for controlling lost circulation of drilling fluids with hydrocarbon absorbent polymers
GB8531866D0 (en) 1985-12-30 1986-02-05 Shell Int Research Forming impermeable coating on borehole wall
US4676317A (en) 1986-05-13 1987-06-30 Halliburton Company Method of reducing fluid loss in cement compositions which may contain substantial salt concentrations
SU1373781A1 (en) 1986-05-15 1988-02-15 Брянский технологический институт Method of producing prestrained ferroconcrete articles
US5183506A (en) 1987-08-19 1993-02-02 Zhang Zhong M Modified flux composition for cement
US4883125A (en) 1987-12-11 1989-11-28 Atlantic Richfield Company Cementing oil and gas wells using converted drilling fluid
US4829107A (en) 1988-02-24 1989-05-09 W. R. Grace & Co.-Conn. Rice hull ash concrete admixture
US5266111A (en) 1988-08-08 1993-11-30 Barbour Ronald L Class F. fly ash containing settable composition for general purpose concrete having high early strength and method of making same
US5520730A (en) 1988-08-08 1996-05-28 Barbour; Ronald L. Settable composition for general purpose concrete and method of making same
US4992102A (en) 1988-08-08 1991-02-12 Barbour Ronald L Synthetic class C fly ash and use thereof as partial cement replacement in general purpose concrete
US5098612A (en) 1988-12-10 1992-03-24 Rowsell Farrell D Method of preparing solidified and stabilized hazardous or radioactive liquids
US4941536A (en) 1989-06-27 1990-07-17 Halliburton Company Set retarded cement compositions and methods for well cementing
US5049288A (en) 1989-06-27 1991-09-17 Halliburton Company Set retarded cement compositions and methods for well cementing
US5030366A (en) 1989-11-27 1991-07-09 Atlantic Richfield Company Spacer fluids
US5113943A (en) 1989-11-27 1992-05-19 Atlantic Richfield Company Spacer fluids
US5673753A (en) 1989-12-27 1997-10-07 Shell Oil Company Solidification of water based muds
US5423379A (en) 1989-12-27 1995-06-13 Shell Oil Company Solidification of water based muds
US5058679A (en) 1991-01-16 1991-10-22 Shell Oil Company Solidification of water based muds
US5515921A (en) 1989-12-27 1996-05-14 Shell Oil Company Water-base mud conversion for high tempratice cementing
US5464060A (en) 1989-12-27 1995-11-07 Shell Oil Company Universal fluids for drilling and cementing wells
US5346548A (en) 1990-06-25 1994-09-13 The Regents Of The University Of California Highly durable cement products containing siliceous ashes
US5127473A (en) 1991-01-08 1992-07-07 Halliburton Services Repair of microannuli and cement sheath
US5086850A (en) 1991-01-08 1992-02-11 Halliburton Company Well bore drilling direction changing method
US5125455A (en) 1991-01-08 1992-06-30 Halliburton Services Primary cementing
US5121795A (en) 1991-01-08 1992-06-16 Halliburton Company Squeeze cementing
US5238064A (en) 1991-01-08 1993-08-24 Halliburton Company Squeeze cementing
US5123487A (en) 1991-01-08 1992-06-23 Halliburton Services Repairing leaks in casings
AU1762692A (en) 1991-03-29 1992-11-02 Raymond S. Chase Silica-containing cement and concrete composition
CA2064682A1 (en) 1991-04-02 1992-10-03 Kirk L. Harris Well bore drilling direction changing method
US5382290A (en) 1991-04-26 1995-01-17 Shell Oil Company Conversion of oil-base mud to oil mud-cement
US5213160A (en) 1991-04-26 1993-05-25 Shell Oil Company Method for conversion of oil-base mud to oil mud-cement
US5542782A (en) 1991-06-24 1996-08-06 Halliburton Nus Environmental Corp. Method and apparatus for in situ installation of underground containment barriers under contaminated lands
NL9101655A (en) 1991-10-01 1993-05-03 Pelt & Hooykaas FIXING AGENT FOR MIXED ORGANIC AND INORGANICALLY CONTAMINATED MATERIALS AND METHOD FOR PREPARING AND USING THE SAME
US5215585A (en) 1991-10-25 1993-06-01 W. R. Grace & Co.-Conn. Hydration retarder
DK49592D0 (en) 1992-04-13 1992-04-13 Aalborg Portland As CEMENT COMPOSITION
US5290355A (en) 1992-04-16 1994-03-01 Jakel Karl W Roofing shingle composition, method of formulation, and structure
US5183505A (en) 1992-05-27 1993-02-02 Concrete Technology, Inc. Cellular concrete
US5641584A (en) 1992-08-11 1997-06-24 E. Khashoggi Industries Highly insulative cementitious matrices and methods for their manufacture
RU2026959C1 (en) 1992-08-19 1995-01-20 Волго-Уральский научно-исследовательский и проектный институт по добыче и переработке сероводородсодержащих газов Grouting mortar for cementing oil and gas wells
US5252128A (en) 1992-09-04 1993-10-12 Basf Corporation Additive composition for oil well cementing formulations
EP0587383A1 (en) 1992-09-10 1994-03-16 Halliburton Company A method of making a cement agglomeration.
US5536311A (en) 1992-10-02 1996-07-16 Halliburton Company Set retarded cement compositions, additives and methods
US5476144A (en) 1992-10-15 1995-12-19 Shell Oil Company Conversion of oil-base mud to oil mud-cement
MY112090A (en) 1992-10-22 2001-04-30 Shell Int Research Method for drilling and cementing a well
US5314022A (en) 1992-10-22 1994-05-24 Shell Oil Company Dilution of drilling fluid in forming cement slurries
US5327968A (en) 1992-12-30 1994-07-12 Halliburton Company Utilizing drilling fluid in well cementing operations
US5316083A (en) 1992-12-31 1994-05-31 Shell Oil Company Blast furnace slag spacer
US5305831A (en) 1993-02-25 1994-04-26 Shell Oil Company Blast furnace slag transition fluid
US5478391A (en) * 1993-03-26 1995-12-26 Cement Technology Corporation Cementitious materials and method of making the same
US5383521A (en) 1993-04-01 1995-01-24 Halliburton Company Fly ash cementing compositions and methods
US5339902A (en) 1993-04-02 1994-08-23 Halliburton Company Well cementing using permeable cement
US5372641A (en) 1993-05-17 1994-12-13 Atlantic Richfield Company Cement slurries for wells
US5361841A (en) 1993-05-27 1994-11-08 Shell Oil Company Drilling and cementing with blast furnace slag/polyalcohol fluid
US5358044A (en) 1993-05-27 1994-10-25 Shell Oil Company Drilling and cementing with blast furnace slag/soluble/insoluble alcohol
US5361842A (en) 1993-05-27 1994-11-08 Shell Oil Company Drilling and cementing with blast furnace slag/silicate fluid
US5352288A (en) 1993-06-07 1994-10-04 Dynastone Lc Low-cost, high early strength, acid-resistant pozzolanic cement
US5337824A (en) 1993-06-28 1994-08-16 Shell Oil Company Coal slag universal fluid
US5439056A (en) 1993-06-28 1995-08-08 Shell Oil Company Coal slag solidification of drilling fluid
US5866516A (en) 1993-08-17 1999-02-02 Costin; C. Richard Compositions and methods for solidifying drilling fluids
US5456751A (en) 1993-09-03 1995-10-10 Trustees Of The University Of Pennsylvania Particulate rubber included concrete compositions
US5370185A (en) 1993-09-08 1994-12-06 Shell Oil Company Mud solidification with slurry of portland cement in oil
US5368103A (en) 1993-09-28 1994-11-29 Halliburton Company Method of setting a balanced cement plug in a borehole
US5398758A (en) 1993-11-02 1995-03-21 Halliburton Company Utilizing drilling fluid in well cementing operations
GB9402581D0 (en) 1994-02-10 1994-04-06 British Tech Group Membrane with anti-viral properties
US5421409A (en) 1994-03-30 1995-06-06 Bj Services Company Slag-based well cementing compositions and methods
US5518996A (en) 1994-04-11 1996-05-21 Dowell, A Division Of Schlumberger Technology Corporation Fluids for oilfield use having high-solids content
US5529624A (en) 1994-04-12 1996-06-25 Riegler; Norbert Insulation material
US5417759A (en) 1994-06-23 1995-05-23 Nalco Chemical Company Set retarding additive for cement slurries
CA2153372A1 (en) 1994-07-08 1996-01-09 Patrick Brown Zeolite-hydraulic cement containment medium
US5458195A (en) 1994-09-28 1995-10-17 Halliburton Company Cementitious compositions and methods
US5585333A (en) 1994-10-12 1996-12-17 Halliburton Company Hydrocarbon base cementitious drilling fluids and methods
US5626665A (en) 1994-11-04 1997-05-06 Ash Grove Cement Company Cementitious systems and novel methods of making the same
US5472051A (en) 1994-11-18 1995-12-05 Halliburton Company Low temperature set retarded well cement compositions and methods
US5484019A (en) 1994-11-21 1996-01-16 Halliburton Company Method for cementing in a formation subject to water influx
US5499677A (en) 1994-12-23 1996-03-19 Shell Oil Company Emulsion in blast furnace slag mud solidification
US5718759A (en) * 1995-02-07 1998-02-17 National Gypsum Company Cementitious gypsum-containing compositions and materials made therefrom
US5529123A (en) 1995-04-10 1996-06-25 Atlantic Richfield Company Method for controlling fluid loss from wells into high conductivity earth formations
US5681384A (en) 1995-04-24 1997-10-28 New Jersey Institute Of Technology Method for increasing the rate of compressive strength gain in hardenable mixtures containing fly ash
US5554352A (en) 1995-05-09 1996-09-10 Construction Material Resources Processed silica as a natural pozzolan for use as a cementitious component in concrete and concrete products
FR2735465B1 (en) 1995-06-13 1997-08-29 Schlumberger Cie Dowell CEMENTING COMPOSITIONS AND APPLICATION THEREOF FOR CEMENTING OIL WELLS OR THE LIKE
US5494513A (en) 1995-07-07 1996-02-27 National Research Council Of Canada Zeolite-based lightweight concrete products
US5728654A (en) 1995-08-25 1998-03-17 Texas United Chemical Company, Llc. Stabilized fluids containing soluble zinc
US5571318A (en) 1995-08-31 1996-11-05 Halliburton Company Well cementing methods and compositions for use in cold environments
US5716910A (en) 1995-09-08 1998-02-10 Halliburton Company Foamable drilling fluid and methods of use in well drilling operations
WO1997009281A1 (en) 1995-09-08 1997-03-13 Fmc Corporation Cement compositions for controlling alkali-silica reactions in concrete and processes for making same
US5588489A (en) 1995-10-31 1996-12-31 Halliburton Company Lightweight well cement compositions and methods
DE19540996A1 (en) 1995-11-03 1997-05-15 Paul Loerke Process for the thermal treatment of fine-grained material, in particular for the production of cement clinker
WO1997021637A1 (en) 1995-12-13 1997-06-19 Henkel Corporation Method of making blended cement compositons
US5711383A (en) 1996-04-19 1998-01-27 Halliburton Company Cementitious well drilling fluids and methods
MY119906A (en) 1996-06-18 2005-08-30 Sofitech Nv Cementing compositions and applications of such compositions to cementing oil (or similar) wells.
FR2749844B1 (en) 1996-06-18 1998-10-30 Schlumberger Cie Dowell CEMENTING COMPOSITIONS AND APPLICATION THEREOF FOR CEMENTING OIL WELLS OR THE LIKE
US5866517A (en) 1996-06-19 1999-02-02 Atlantic Richfield Company Method and spacer fluid composition for displacing drilling fluid from a wellbore
US5874387A (en) 1996-06-19 1999-02-23 Atlantic Richfield Company Method and cement-drilling fluid cement composition for cementing a wellbore
US5789352A (en) 1996-06-19 1998-08-04 Halliburton Company Well completion spacer fluids and methods
US5795924A (en) 1996-07-01 1998-08-18 Halliburton Company Resilient well cement compositions and methods
US5688844A (en) 1996-07-01 1997-11-18 Halliburton Company Resilient well cement compositions and methods
FR2753963B1 (en) 1996-09-30 1998-12-24 Schlumberger Cie Dowell GROUT CEMENT AND METHOD OF DESIGNING A FORMULATION
JPH10110487A (en) 1996-10-07 1998-04-28 Nishikawa Norimichi Block
US6060434A (en) 1997-03-14 2000-05-09 Halliburton Energy Services, Inc. Oil based compositions for sealing subterranean zones and methods
US5913364A (en) 1997-03-14 1999-06-22 Halliburton Energy Services, Inc. Methods of sealing subterranean zones
US6258757B1 (en) 1997-03-14 2001-07-10 Halliburton Energy Services, Inc. Water based compositions for sealing subterranean zones and methods
US5968255A (en) 1997-04-14 1999-10-19 Halliburton Energy Services, Inc. Universal well cement additives and methods
CN1054620C (en) 1997-04-29 2000-07-19 枣庄矿务局水泥厂 Fire-fighting soaking prevention and leaking stoppage expansion powder for grouting coal abscission layer zone
TR199902849T2 (en) * 1997-05-26 2000-06-21 Sobolev Konstantin Production of complex additives and cement-based materials.
US5897699A (en) 1997-07-23 1999-04-27 Halliburton Energy Services, Inc. Foamed well cement compositions, additives and methods
AU738096B2 (en) 1997-08-15 2001-09-06 Halliburton Energy Services, Inc. Light weight high temperature well cement compositions and methods
US5900053A (en) 1997-08-15 1999-05-04 Halliburton Energy Services, Inc. Light weight high temperature well cement compositions and methods
US6796378B2 (en) 1997-08-15 2004-09-28 Halliburton Energy Services, Inc. Methods of cementing high temperature wells and cement compositions therefor
US5873413A (en) 1997-08-18 1999-02-23 Halliburton Energy Services, Inc. Methods of modifying subterranean strata properties
US5988279A (en) 1997-11-05 1999-11-23 Fritz Industries, Inc. Method for control of fluid loss and gas migration in well cementing
US6145591A (en) 1997-12-12 2000-11-14 Bj Services Company Method and compositions for use in cementing
US6230804B1 (en) 1997-12-19 2001-05-15 Bj Services Company Stress resistant cement compositions and methods for using same
US6555307B2 (en) 1997-12-24 2003-04-29 Fuji Photo Film, Co., Ltd. Silver halide photographic emulsion and silver halide photographic light-sensitive material containing the emulsion
GC0000046A (en) 1998-02-26 2004-06-30 Shell Int Research Compositions for use in well construction, repair and/or abandonment.
US6409819B1 (en) 1998-06-30 2002-06-25 International Mineral Technology Ag Alkali activated supersulphated binder
US6098711A (en) 1998-08-18 2000-08-08 Halliburton Energy Services, Inc. Compositions and methods for sealing pipe in well bores
FR2784095B1 (en) 1998-10-06 2001-09-21 Dowell Schlumberger Services CEMENTING COMPOSITIONS AND APPLICATION THEREOF FOR CEMENTING OIL WELLS OR THE LIKE
CA2350545C (en) 1998-11-13 2008-02-26 Schlumberger Canada Limited Cementation product and use for cementing oil wells or the like
US6245142B1 (en) 1999-01-12 2001-06-12 Halliburton Energy Services, Inc. Flow properties of dry cementitious materials
US6170575B1 (en) 1999-01-12 2001-01-09 Halliburton Energy Services, Inc. Cementing methods using dry cementitious materials having improved flow properties
US6379456B1 (en) 1999-01-12 2002-04-30 Halliburton Energy Services, Inc. Flow properties of dry cementitious and non-cementitious materials
US6660080B2 (en) 1999-01-12 2003-12-09 Halliburton Energy Services, Inc. Particulate flow enhancing additives
US6184287B1 (en) 1999-01-26 2001-02-06 Omnova Solutions Inc. Polymeric latexes prepared in the presence of 2-acrylamido-2-methylpropanesulfonate
US6328106B1 (en) 1999-02-04 2001-12-11 Halliburton Energy Services, Inc. Sealing subterranean zones
FR2790258B1 (en) 1999-02-25 2001-05-04 Dowell Schlumberger Services CEMENTING PROCESS AND APPLICATION OF THIS METHOD TO REPAIR CEMENTINGS
US6063738A (en) 1999-04-19 2000-05-16 Halliburton Energy Services, Inc. Foamed well cement slurries, additives and methods
GB2351986B (en) 1999-07-13 2002-12-24 Sofitech Nv Latex additive for water-based drilling fluids
CA2316059A1 (en) 1999-08-24 2001-02-24 Virgilio C. Go Boncan Methods and compositions for use in cementing in cold environments
US6277189B1 (en) 1999-08-31 2001-08-21 The Board Of Trustees Of Southern Illinois University Coal combustion by-products-based lightweight structural materials and processes for making them
CA2318703A1 (en) 1999-09-16 2001-03-16 Bj Services Company Compositions and methods for cementing using elastic particles
US6308777B2 (en) 1999-10-13 2001-10-30 Halliburton Energy Services, Inc. Cementing wells with crack and shatter resistant cement
US6138759A (en) 1999-12-16 2000-10-31 Halliburton Energy Services, Inc. Settable spotting fluid compositions and methods
JP2001226155A (en) 2000-01-27 2001-08-21 Dow Corning Corp Method for manufacturing fluid clay slurry
WO2001058823A1 (en) 2000-02-08 2001-08-16 Rha Technology, Inc. Method for producing a blended cementitious composition
SE522352C2 (en) 2000-02-16 2004-02-03 Sandvik Ab Elongated element for striking rock drilling and use of steel for this
US6244343B1 (en) 2000-03-09 2001-06-12 Halliburton Energy Services, Inc. Cementing in deep water offshore wells
MXPA02008921A (en) 2000-03-14 2004-10-15 James Hardie Res Pty Ltd Fiber cement building materials with low density additives.
US6502634B1 (en) 2000-03-17 2003-01-07 Halliburton Energy Services, Inc. Interface monitoring placement system
FR2806717B1 (en) 2000-03-23 2002-05-24 Dowell Schlumberger Services CEMENTING COMPOSITIONS AND APPLICATION THEREOF FOR CEMENTING OIL WELLS OR THE LIKE
FR2808794B1 (en) 2000-05-15 2002-06-28 Dowell Schlumberger Services PERMEABLE CEMENT, PROCESS FOR OBTAINING SAME AND APPLICATION OF SAME IN OIL WELLS OR THE LIKE
ATE444077T1 (en) 2000-06-30 2009-10-15 Tokyo Metropolitan Inst Of Ger PREVENTIVES AND THERAPEUTICS FOR DEMYELINIZATION-ASSOCIATED DISEASES
US6416574B1 (en) 2000-07-12 2002-07-09 Southern Ionica Incorporated Method and apparatus for recycling cement kiln dust
US6402833B1 (en) 2000-07-13 2002-06-11 Lafarge Canada Inc. Binder for mine tailings
US6716282B2 (en) 2000-07-26 2004-04-06 Halliburton Energy Services, Inc. Methods and oil-based settable spotting fluid compositions for cementing wells
US6668929B2 (en) 2000-07-26 2003-12-30 Halliburton Energy Services, Inc. Methods and oil-based settable spotting fluid compositions for cementing wells
US6666268B2 (en) 2000-07-26 2003-12-23 Halliburton Energy Services, Inc. Methods and oil-based settable drilling fluid compositions for drilling and cementing wells
US6315042B1 (en) 2000-07-26 2001-11-13 Halliburton Energy Services, Inc. Oil-based settable spotting fluid
EP1325897B1 (en) 2000-09-13 2012-03-14 Denki Kagaku Kogyo Kabushiki Kaisha Cement composition
US6457524B1 (en) 2000-09-15 2002-10-01 Halliburton Energy Services, Inc. Well cementing compositions and methods
US6562122B2 (en) 2000-09-18 2003-05-13 Halliburton Energy Services, Inc. Lightweight well cement compositions and methods
FR2814459B1 (en) 2000-09-22 2002-12-06 Lafarge Platres SURFACTANT COMPOSITION FOR PLASTERBOARDS
US6220354B1 (en) 2000-10-24 2001-04-24 Halliburton Energy Services, Inc. High strength foamed well cement compositions and methods
US6367550B1 (en) 2000-10-25 2002-04-09 Halliburton Energy Service, Inc. Foamed well cement slurries, additives and methods
US6767398B2 (en) 2000-10-30 2004-07-27 James H. Trato Cementitious compositions and cementitious slurries for permanently plugging abandoned wells and processes and methods therefor
NL1016892C2 (en) 2000-12-15 2002-06-19 Mega Tech Holding Bv Composition intended as an additive for cement.
CA2370875A1 (en) 2001-02-15 2002-08-15 B.J. Services Company High temperature flexible cementing compositions and methods for using same
EP1236701A1 (en) 2001-02-15 2002-09-04 Schlumberger Technology B.V. Very low-density cement slurry
US20020117090A1 (en) 2001-02-20 2002-08-29 Richard Ku Super high strength concrete
CA2443222C (en) 2001-04-13 2009-09-15 Co2 Solution Inc. A process and a plant for the production of portland cement clinker
US7627870B1 (en) 2001-04-28 2009-12-01 Cisco Technology, Inc. Method and apparatus for a data structure comprising a hierarchy of queues or linked list data structures
US7004263B2 (en) 2001-05-09 2006-02-28 Schlumberger Technology Corporation Directional casing drilling
US6706108B2 (en) 2001-06-19 2004-03-16 David L. Polston Method for making a road base material using treated oil and gas waste material
US6561273B2 (en) 2001-06-19 2003-05-13 Halliburton Energy Services, Inc. Oil based compositions and method for temporarily sealing subterranean zones
US20030116887A1 (en) 2001-08-10 2003-06-26 Scott J. Blake Incorporation of drilling cuttings into stable load-bearing structures
US6645290B1 (en) 2001-10-09 2003-11-11 Ronald Lee Barbour Settable composition containing cement kiln dust
US6749679B2 (en) 2002-01-23 2004-06-15 Advanced Materials Technologies, Llc Composition of materials for production of acid resistant cement and concrete and methods thereof
US6755905B2 (en) 2002-02-15 2004-06-29 Lafarge Canada Inc. Use of high carbon coal ash
US6644405B2 (en) 2002-03-21 2003-11-11 Halliburton Energy Services, Inc. Storable water-microsphere suspensions for use in well cements and methods
US6702044B2 (en) 2002-06-13 2004-03-09 Halliburton Energy Services, Inc. Methods of consolidating formations or forming chemical casing or both while drilling
US6565647B1 (en) 2002-06-13 2003-05-20 Shieldcrete Ltd. Cementitious shotcrete composition
US6840318B2 (en) 2002-06-20 2005-01-11 Schlumberger Technology Corporation Method for treating subterranean formation
US6641658B1 (en) * 2002-07-03 2003-11-04 United States Gypsum Company Rapid setting cementitious composition
US6516884B1 (en) 2002-07-23 2003-02-11 Halliburton Energy Services, Inc. Stable well cementing methods and compositions
US6516883B1 (en) 2002-07-25 2003-02-11 Halliburton Energy Services, Inc. Methods of cementing pipe in well bores and low density cement compositions therefor
MXPA05002057A (en) 2002-08-23 2005-09-12 James Hardie Int Finance Bv Synthetic hollow microspheres.
US6869474B2 (en) * 2002-08-29 2005-03-22 United States Gypsum Company Very fast setting cementitious composition
US7156173B2 (en) 2002-11-08 2007-01-02 Bj Services Company Cement compositions useful in oil and gas wells
US6708760B1 (en) 2002-11-19 2004-03-23 Halliburton Energy Services, Inc. Methods and cement compositions for cementing in subterranean zones
US6964302B2 (en) 2002-12-10 2005-11-15 Halliburton Energy Services, Inc. Zeolite-containing cement composition
US7048053B2 (en) 2002-12-10 2006-05-23 Halliburton Energy Services, Inc. Zeolite compositions having enhanced compressive strength
US7140439B2 (en) 2002-12-10 2006-11-28 Halliburton Energy Services, Inc. Zeolite-containing remedial compositions
US7140440B2 (en) 2002-12-10 2006-11-28 Halliburton Energy Services, Inc. Fluid loss additives for cement slurries
US7147067B2 (en) 2002-12-10 2006-12-12 Halliburton Energy Services, Inc. Zeolite-containing drilling fluids
US6989057B2 (en) 2002-12-10 2006-01-24 Halliburton Energy Services, Inc. Zeolite-containing cement composition
US7544640B2 (en) 2002-12-10 2009-06-09 Halliburton Energy Services, Inc. Zeolite-containing treating fluid
US7150321B2 (en) 2002-12-10 2006-12-19 Halliburton Energy Services, Inc. Zeolite-containing settable spotting fluids
EP1431368A1 (en) 2002-12-18 2004-06-23 Eliokem Fluid loss reducer for high temperature high pressure water-based mud application
US20040171499A1 (en) 2003-01-24 2004-09-02 Halliburton Energy Services, Inc. Cement compositions with improved mechanical properties and methods of cementing in a subterranean formation
US6874353B2 (en) 2003-01-30 2005-04-05 Halliburton Energy Services, Inc. Yield point adaptation for rotating viscometers
RU2239049C1 (en) * 2003-02-25 2004-10-27 ДФГУП Западно-Сибирский научно-исследовательский и проектно-конструкторский институт технологии глубокого разведочного бурения Lightened cementing solution
US6962201B2 (en) 2003-02-25 2005-11-08 Halliburton Energy Services, Inc. Cement compositions with improved mechanical properties and methods of cementing in subterranean formations
US6983799B2 (en) 2003-02-27 2006-01-10 Halliburton Energy Services, Inc. Method of using a swelling agent to prevent a cement slurry from being lost to a subterranean formation
CN1254457C (en) 2003-02-27 2006-05-03 穆桢子 High-strength light concrete and its production method
US6889767B2 (en) 2003-02-28 2005-05-10 Halliburton E{umlaut over (n)}ergy Services, Inc. Cementing compositions and methods of cementing in a subterranean formation using an additive for preventing the segregation of lightweight beads.
US6668927B1 (en) 2003-03-21 2003-12-30 Halliburton Energy Services, Inc. Well completion foamed spacer fluids and methods
US7143827B2 (en) 2003-03-21 2006-12-05 Halliburton Energy Services, Inc. Well completion spacer fluids containing fibers and methods
US20040187740A1 (en) 2003-03-27 2004-09-30 Research Incubator, Ltd. Cementitious composition
US7217441B2 (en) 2003-03-28 2007-05-15 Halliburton Energy Services, Inc. Methods for coating pipe comprising using cement compositions comprising high tensile strength fibers and/or a multi-purpose cement additive
US7147055B2 (en) 2003-04-24 2006-12-12 Halliburton Energy Services, Inc. Cement compositions with improved corrosion resistance and methods of cementing in subterranean formations
US6904971B2 (en) 2003-04-24 2005-06-14 Halliburton Energy Services, Inc. Cement compositions with improved corrosion resistance and methods of cementing in subterranean formations
WO2004101952A1 (en) 2003-05-14 2004-11-25 Services Petroliers Schlumberger Self adaptive cement systems
US20070137528A1 (en) 2003-05-14 2007-06-21 Sylvaine Le Roy-Delage Self adaptive cement systems
WO2004108627A1 (en) 2003-06-04 2004-12-16 Isg Resources, Inc. Cementitious mixtures and methods of use thereof
US6689208B1 (en) 2003-06-04 2004-02-10 Halliburton Energy Services, Inc. Lightweight cement compositions and methods of cementing in subterranean formations
US6908508B2 (en) 2003-06-04 2005-06-21 Halliburton Energy Services, Inc. Settable fluids and methods for use in subterranean formations
US7073585B2 (en) 2003-06-27 2006-07-11 Halliburton Energy Services, Inc. Cement compositions with improved fluid loss characteristics and methods of cementing in surface and subterranean applications
US20050034864A1 (en) 2003-06-27 2005-02-17 Caveny William J. Cement compositions with improved fluid loss characteristics and methods of cementing in surface and subterranean applications
US7198104B2 (en) 2003-08-12 2007-04-03 Halliburton Energy Services, Inc. Subterranean fluids and methods of cementing in subterranean formations
US6832652B1 (en) 2003-08-22 2004-12-21 Bj Services Company Ultra low density cementitious slurries for use in cementing of oil and gas wells
US7055603B2 (en) 2003-09-24 2006-06-06 Halliburton Energy Services, Inc. Cement compositions comprising strength-enhancing lost circulation materials and methods of cementing in subterranean formations
US6899177B2 (en) 2003-10-10 2005-05-31 Halliburton Energy Services, Inc. Methods of cementing subterranean zones with cement compositions having enhanced compressive strengths
CA2445675A1 (en) 2003-10-20 2005-04-20 Yanzhong Wu Composition and method for forming a sprayable materials cover
US6869475B1 (en) 2003-10-28 2005-03-22 Bnz Materials, Inc. Calcium silicate insulating material containing blast furnace slag cement
US7073584B2 (en) 2003-11-12 2006-07-11 Halliburton Energy Services, Inc. Processes for incorporating inert gas in a cement composition containing spherical beads
RU2262497C2 (en) 2003-12-15 2005-10-20 Зубехин Сергей Алексеевич Method of manufacture of foam concrete and installation for its realization
US7413014B2 (en) 2003-12-19 2008-08-19 Halliburton Energy Services, Inc. Foamed fly ash cement compositions and methods of cementing
US20060166834A1 (en) 2004-02-10 2006-07-27 Halliburton Energy Services, Inc. Subterranean treatment fluids comprising substantially hydrated cement particulates
US9512346B2 (en) 2004-02-10 2016-12-06 Halliburton Energy Services, Inc. Cement compositions and methods utilizing nano-hydraulic cement
US7341104B2 (en) 2004-02-10 2008-03-11 Halliburton Energy Services, Inc. Methods of using substantially hydrated cement particulates in subterranean applications
US7445669B2 (en) 2005-09-09 2008-11-04 Halliburton Energy Services, Inc. Settable compositions comprising cement kiln dust and additive(s)
US7607482B2 (en) 2005-09-09 2009-10-27 Halliburton Energy Services, Inc. Settable compositions comprising cement kiln dust and swellable particles
US7096944B2 (en) 2004-03-02 2006-08-29 Halliburton Energy Services, Inc. Well fluids and methods of use in subterranean formations
US7137446B2 (en) 2004-03-22 2006-11-21 Halliburton Energy Services Inc. Fluids comprising reflective particles and methods of using the same to determine the size of a wellbore annulus
US7607483B2 (en) 2004-04-19 2009-10-27 Halliburton Energy Services, Inc. Sealant compositions comprising colloidally stabilized latex and methods of using the same
US7297664B2 (en) 2004-07-28 2007-11-20 Halliburton Energy Services, Inc. Cement-free zeolite and fly ash settable fluids and methods therefor
US7409990B1 (en) 2004-09-09 2008-08-12 Burts Jr Boyce D Downhole mixing of encapsulated plug components for abandoning a well
US7182137B2 (en) 2004-09-13 2007-02-27 Halliburton Energy Services, Inc. Cementitious compositions containing interground cement clinker and zeolite
US8029618B2 (en) 2004-09-21 2011-10-04 Saudi Arabian Oil Company Manufacture of Portland cement using spent claus catalyst
US7219733B2 (en) 2004-09-29 2007-05-22 Halliburton Energy Services, Inc. Zeolite compositions for lowering maximum cementing temperature
US7293609B2 (en) 2004-10-20 2007-11-13 Halliburton Energy Services, Inc. Treatment fluids comprising vitrified shale and methods of using such fluids in subterranean formations
US20100044057A1 (en) 2004-10-20 2010-02-25 Dealy Sears T Treatment Fluids Comprising Pumicite and Methods of Using Such Fluids in Subterranean Formations
US7303008B2 (en) 2004-10-26 2007-12-04 Halliburton Energy Services, Inc. Methods and systems for reverse-circulation cementing in subterranean formations
US7488705B2 (en) 2004-12-08 2009-02-10 Halliburton Energy Services, Inc. Oilwell sealant compositions comprising alkali swellable latex
US7655088B2 (en) 2005-01-14 2010-02-02 Alkemy, Ltd. Synthetic aggregates comprising sewage sludge and other waste materials and methods for producing such aggregates
CA2637107A1 (en) 2005-01-14 2006-07-20 Alkemy, Ltd. Synthetic aggregates comprising sewage sludge and other waste materials and methods for producing such aggregates
US7404855B2 (en) 2005-02-04 2008-07-29 Halliburton Energy Services, Inc. Resilient cement compositions and methods of cementing
US7022755B1 (en) 2005-02-04 2006-04-04 Halliburton Energy Services, Inc. Resilient cement compositions and methods of cementing
CA2538196C (en) 2005-02-28 2011-10-11 Weatherford/Lamb, Inc. Deep water drilling with casing
US9150773B2 (en) 2005-09-09 2015-10-06 Halliburton Energy Services, Inc. Compositions comprising kiln dust and wollastonite and methods of use in subterranean formations
US7395860B2 (en) 2005-09-09 2008-07-08 Halliburton Energy Services, Inc. Methods of using foamed settable compositions comprising cement kiln dust
US8297357B2 (en) 2005-09-09 2012-10-30 Halliburton Energy Services Inc. Acid-soluble cement compositions comprising cement kiln dust and/or a natural pozzolan and methods of use
US7077203B1 (en) 2005-09-09 2006-07-18 Halliburton Energy Services, Inc. Methods of using settable compositions comprising cement kiln dust
US8505629B2 (en) 2005-09-09 2013-08-13 Halliburton Energy Services, Inc. Foamed spacer fluids containing cement kiln dust and methods of use
US8505630B2 (en) 2005-09-09 2013-08-13 Halliburton Energy Services, Inc. Consolidating spacer fluids and methods of use
US9676989B2 (en) 2005-09-09 2017-06-13 Halliburton Energy Services, Inc. Sealant compositions comprising cement kiln dust and tire-rubber particles and method of use
US20070056479A1 (en) 2005-09-09 2007-03-15 Gray Lonnie J Concrete mixtures incorporating high carbon pozzolans and foam admixtures
US8522873B2 (en) 2005-09-09 2013-09-03 Halliburton Energy Services, Inc. Spacer fluids containing cement kiln dust and methods of use
US7631692B2 (en) 2005-09-09 2009-12-15 Halliburton Energy Services, Inc. Settable compositions comprising a natural pozzolan and associated methods
US7617870B1 (en) 2008-05-14 2009-11-17 Halliburton Energy Services, Inc. Extended cement compositions comprising oil-swellable particles and associated methods
US7213646B2 (en) * 2005-09-09 2007-05-08 Halliburton Energy Services, Inc. Cementing compositions comprising cement kiln dust, vitrified shale, zeolite, and/or amorphous silica utilizing a packing volume fraction, and associated methods
US8555967B2 (en) 2005-09-09 2013-10-15 Halliburton Energy Services, Inc. Methods and systems for evaluating a boundary between a consolidating spacer fluid and a cement composition
US7174962B1 (en) 2005-09-09 2007-02-13 Halliburton Energy Services, Inc. Methods of using lightweight settable compositions comprising cement kiln dust
US8333240B2 (en) 2005-09-09 2012-12-18 Halliburton Energy Services, Inc. Reduced carbon footprint settable compositions for use in subterranean formations
US8281859B2 (en) 2005-09-09 2012-10-09 Halliburton Energy Services Inc. Methods and compositions comprising cement kiln dust having an altered particle size
US7353870B2 (en) 2005-09-09 2008-04-08 Halliburton Energy Services, Inc. Methods of using settable compositions comprising cement kiln dust and additive(s)
US7478675B2 (en) 2005-09-09 2009-01-20 Halliburton Energy Services, Inc. Extended settable compositions comprising cement kiln dust and associated methods
US8950486B2 (en) 2005-09-09 2015-02-10 Halliburton Energy Services, Inc. Acid-soluble cement compositions comprising cement kiln dust and methods of use
US8307899B2 (en) 2005-09-09 2012-11-13 Halliburton Energy Services, Inc. Methods of plugging and abandoning a well using compositions comprising cement kiln dust and pumicite
US8609595B2 (en) 2005-09-09 2013-12-17 Halliburton Energy Services, Inc. Methods for determining reactive index for cement kiln dust, associated compositions, and methods of use
RU2404143C2 (en) 2005-09-09 2010-11-20 Хэллибертон Энерджи Сервисиз, Инк. Method of borehole cementation
US9809737B2 (en) 2005-09-09 2017-11-07 Halliburton Energy Services, Inc. Compositions containing kiln dust and/or biowaste ash and methods of use
US7789150B2 (en) 2005-09-09 2010-09-07 Halliburton Energy Services Inc. Latex compositions comprising pozzolan and/or cement kiln dust and methods of use
US7607484B2 (en) 2005-09-09 2009-10-27 Halliburton Energy Services, Inc. Foamed cement compositions comprising oil-swellable particles and methods of use
US8327939B2 (en) 2005-09-09 2012-12-11 Halliburton Energy Services, Inc. Settable compositions comprising cement kiln dust and rice husk ash and methods of use
US20120328377A1 (en) 2005-09-09 2012-12-27 Halliburton Energy Services, Inc. Resin-Based Sealant Compositions Comprising Cement Kiln Dust and Methods of Use
US9023150B2 (en) 2005-09-09 2015-05-05 Halliburton Energy Services, Inc. Acid-soluble cement compositions comprising cement kiln dust and/or a natural pozzolan and methods of use
US7743828B2 (en) 2005-09-09 2010-06-29 Halliburton Energy Services, Inc. Methods of cementing in subterranean formations using cement kiln cement kiln dust in compositions having reduced Portland cement content
US8733440B2 (en) 2009-07-02 2014-05-27 Halliburton Energy Services, Inc. Well cement compositions comprising biowaste ash and methods of use
US7335252B2 (en) 2005-09-09 2008-02-26 Halliburton Energy Services, Inc. Lightweight settable compositions comprising cement kiln dust
CA2624834C (en) 2005-10-11 2016-02-16 Mud King Drilling Fluids (2001) Ltd. Water-based polymer drilling fluid and method of use
US7381263B2 (en) 2005-10-24 2008-06-03 Halliburton Energy Services, Inc. Cement compositions comprising high alumina cement and cement kiln dust
US7337842B2 (en) 2005-10-24 2008-03-04 Halliburton Energy Services, Inc. Methods of using cement compositions comprising high alumina cement and cement kiln dust
WO2007048999A1 (en) 2005-10-24 2007-05-03 Halliburton Energy Services, Inc. Cement compositions comprising high alumina cement and cement kiln dust and method of using them
US7199086B1 (en) 2005-11-10 2007-04-03 Halliburton Energy Services, Inc. Settable spotting compositions comprising cement kiln dust
US7284609B2 (en) 2005-11-10 2007-10-23 Halliburton Energy Services, Inc. Methods of using settable spotting compositions comprising cement kiln dust
CA2577564C (en) 2006-02-15 2011-07-12 Lafarge Canada Inc. Binder for mine tailings, alluvial sand and rock fill, or combinations thereof
CN100344723C (en) * 2006-02-24 2007-10-24 西南石油学院 Comprehensive performace regulator for well cementing cement slurry and its prepn
US7325611B2 (en) 2006-03-09 2008-02-05 Halliburton Energy Services, Inc. Cement compositions for reducing gas or water migration and methods of using the same
US7338923B2 (en) 2006-04-11 2008-03-04 Halliburton Energy Services, Inc. Settable drilling fluids comprising cement kiln dust
US7204310B1 (en) 2006-04-11 2007-04-17 Halliburton Energy Services, Inc. Methods of use settable drilling fluids comprising cement kiln dust
CA2650630C (en) 2006-05-03 2013-01-08 Halliburton Energy Services, Inc. Lightweight settable compositions comprising cement kiln dust and methods of using them
US7341105B2 (en) 2006-06-20 2008-03-11 Holcim (Us) Inc. Cementitious compositions for oil well cementing applications
EP1876154A1 (en) * 2006-06-29 2008-01-09 Services Pétroliers Schlumberger Cement slurry with low water to cement ratio
US20080032901A1 (en) 2006-08-07 2008-02-07 Hull John H Subsurface reactive sealant product
US20080066652A1 (en) 2006-09-14 2008-03-20 Michael Fraser Low density cements for use in cementing operations
US20080169130A1 (en) 2007-01-12 2008-07-17 M-I Llc Wellbore fluids for casing drilling
US9096466B2 (en) 2007-03-22 2015-08-04 Halliburton Energy Services, Inc. Particulate flow enhancing additives and associated methods
US8162055B2 (en) 2007-04-02 2012-04-24 Halliburton Energy Services Inc. Methods of activating compositions in subterranean zones
US8342242B2 (en) 2007-04-02 2013-01-01 Halliburton Energy Services, Inc. Use of micro-electro-mechanical systems MEMS in well treatments
US7712527B2 (en) 2007-04-02 2010-05-11 Halliburton Energy Services, Inc. Use of micro-electro-mechanical systems (MEMS) in well treatments
US7784542B2 (en) 2007-05-10 2010-08-31 Halliburton Energy Services, Inc. Cement compositions comprising latex and a nano-particle and associated methods
US8586512B2 (en) 2007-05-10 2013-11-19 Halliburton Energy Services, Inc. Cement compositions and methods utilizing nano-clay
US8586508B2 (en) 2007-05-30 2013-11-19 Halliburton Energy Services, Inc. Polysaccharide based cement additives
US20090038801A1 (en) 2007-08-08 2009-02-12 Ravi Krishna M Sealant Compositions and Methods of Use
US8276666B2 (en) 2007-08-08 2012-10-02 Halliburton Energy Services Inc. Sealant compositions and methods of use
US7993451B2 (en) 2007-08-13 2011-08-09 Texas Industries, Inc. Cement stabilization of soils using a proportional cement slurry
US7612021B2 (en) 2007-08-24 2009-11-03 Halliburton Energy Services, Inc. Methods and compositions utilizing lost-circulation materials comprising composite particulates
US7665523B2 (en) 2007-10-16 2010-02-23 Halliburton Energy Services, Inc. Compositions and methods for treatment of well bore tar
CA2641472C (en) 2007-10-22 2014-11-25 Sanjel Limited Partnership Pumice containing compositions for cementing a well
WO2009071962A2 (en) 2007-12-04 2009-06-11 Holcim Technology Ltd. Cementitious compositions for oilwell cementing applications
US7963323B2 (en) 2007-12-06 2011-06-21 Schlumberger Technology Corporation Technique and apparatus to deploy a cement plug in a well
EP2075303A1 (en) 2007-12-18 2009-07-01 PRAD Research and Development N.V. Spacer fluid additive
BRPI0821515A2 (en) 2007-12-28 2019-09-24 Calera Corp co2 capture methods
US7741841B2 (en) 2007-12-28 2010-06-22 Schlumberger Technology Corporation Time-lapsed diffusivity logging for monitoring enhanced oil recovery
US7530396B1 (en) * 2008-01-24 2009-05-12 Halliburton Energy Services, Inc. Self repairing cement compositions and methods of using same
US7919064B2 (en) 2008-02-12 2011-04-05 Michigan Technological University Capture and sequestration of carbon dioxide in flue gases
US7748454B2 (en) 2008-04-28 2010-07-06 Halliburton Energy Services, Inc. Gelation inhibiting retarders for highly reactive calcium silicate based binder compositions and methods of making and using same
US7740070B2 (en) 2008-06-16 2010-06-22 Halliburton Energy Services, Inc. Wellbore servicing compositions comprising a density segregation inhibiting composite and methods of making and using same
US7708071B2 (en) 2008-08-14 2010-05-04 Halliburton Energy Services, Inc. Cement compositions comprising aluminum chloride and associated methods
US7815880B2 (en) 2008-09-30 2010-10-19 Calera Corporation Reduced-carbon footprint concrete compositions
US7939336B2 (en) 2008-09-30 2011-05-10 Calera Corporation Compositions and methods using substances containing carbon
TW201026597A (en) 2008-09-30 2010-07-16 Calera Corp CO2-sequestering formed building materials
US7757766B2 (en) 2008-11-19 2010-07-20 Halliburton Energy Services, Inc. Density-matched suspensions and associated methods
US20100258035A1 (en) 2008-12-24 2010-10-14 Brent Constantz Compositions and methods using substances containing carbon
US7762329B1 (en) 2009-01-27 2010-07-27 Halliburton Energy Services, Inc. Methods for servicing well bores with hardenable resin compositions
AU2010200978A1 (en) 2009-02-03 2010-08-19 Calera Corporation CO2 sequestering soil stabilization composition
CA2703604C (en) 2009-05-22 2017-06-20 Lafarge Low density cementitious compositions
WO2011012922A1 (en) 2009-07-29 2011-02-03 SERVICES PETROLIERS SCHLUMBERGER, dénommée SLB Compositions and methods for servicing subterranean wells
US8143198B2 (en) 2009-08-25 2012-03-27 Hallilburton Energy Services Inc. Radiation-induced triggering for set-on-command compositions
US8186457B2 (en) 2009-09-17 2012-05-29 Tesco Corporation Offshore casing drilling method
WO2011056086A2 (en) 2009-11-05 2011-05-12 Google Inc. Statistical stemming
AU2010337357B2 (en) 2009-12-31 2013-11-28 Arelac, Inc. Methods and compositions using calcium carbonate
US8540025B2 (en) 2010-06-08 2013-09-24 Halliburton Energy Services, Inc. Wellbore servicing compositions and methods of making and using same
US8627888B2 (en) 2011-05-13 2014-01-14 Halliburton Energy Services, Inc. Settable compositions containing metakaolin having reduced portland cement content
CA2795818C (en) 2011-11-16 2015-03-17 Weatherford/Lamb, Inc. Managed pressure cementing
US20130126159A1 (en) 2011-11-18 2013-05-23 Hnatiuk Bryan Method and composition for cementing a casing in a wellbore

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2455446A (en) * 2005-02-09 2009-06-17 Halliburton Energy Serv Inc Method of cementing a wellbore with a composition comprising perlite
US20110100626A1 (en) * 2005-09-09 2011-05-05 Halliburton Energy Services, Inc. Settable Compositions Comprising Unexpanded Perlite and Methods of Cementing in Subterranean Formations
US20120152539A1 (en) * 2010-12-21 2012-06-21 Halliburton Energy Services, Inc. Settable Compositions Comprising Interground Perlite and Hydraulic Cement

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106150428A (en) * 2015-03-27 2016-11-23 中国石油化工股份有限公司 Split type exempting from bores plug completion tubular column and completion method thereof
US11236902B2 (en) * 2020-04-27 2022-02-01 Rheem Manufacturing Company Frustoconical combustion chamber for a fluid heating device and methods for making the same

Also Published As

Publication number Publication date
CA2821931A1 (en) 2013-01-17
NZ612235A (en) 2016-02-26
MX2013007395A (en) 2013-12-02
RU2584431C2 (en) 2016-05-20
AU2012282775B2 (en) 2014-10-09
CN103459348A (en) 2013-12-18
US9376609B2 (en) 2016-06-28
AU2012282775A1 (en) 2013-07-11
MY170430A (en) 2019-07-31
US20120152539A1 (en) 2012-06-21
US8672028B2 (en) 2014-03-18
BR112013016242A2 (en) 2016-09-27
CA2821931C (en) 2016-02-16
RU2013129542A (en) 2015-01-10
AR087113A1 (en) 2014-02-12
AU2012282775A8 (en) 2013-07-25
US20140123879A1 (en) 2014-05-08
EP2651849A1 (en) 2013-10-23

Similar Documents

Publication Publication Date Title
US9376609B2 (en) Settable compositions comprising interground perlite and hydraulic cement
CA2821573C (en) Settable compositions comprising unexpanded perlite and methods of cementing in subterranean formations
EP2585552B1 (en) Methods for using acid-soluble cement compositions comprising cement kiln dust and/or a natural pozzolan
US8281859B2 (en) Methods and compositions comprising cement kiln dust having an altered particle size
EP2585551A1 (en) Methods of plugging and abandoning a well using compositions comprising cement kiln dust and pumicite
MX2015005351A (en) Settable compositions comprising wollastonite and pumice and methods of use.
EP2814787B1 (en) Methods and compositions comprising cement kiln dust having an altered particle size
EP2888335A1 (en) Acid-soluble cement compositions comprising cement kiln dust and methods of use
NZ612235B2 (en) Settable compositions comprising interground perlite and hydraulic cement

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 12735761

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2821931

Country of ref document: CA

REEP Request for entry into the european phase

Ref document number: 2012735761

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: 2012735761

Country of ref document: EP

WWE Wipo information: entry into national phase

Ref document number: MX/A/2013/007395

Country of ref document: MX

ENP Entry into the national phase

Ref document number: 2013129542

Country of ref document: RU

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 2012282775

Country of ref document: AU

Date of ref document: 20120710

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112013016242

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 112013016242

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20130624