WO2004094556A1 - Methods, aqueous well treating fluids and friction reducers therefor - Google Patents

Methods, aqueous well treating fluids and friction reducers therefor Download PDF

Info

Publication number
WO2004094556A1
WO2004094556A1 PCT/GB2004/001640 GB2004001640W WO2004094556A1 WO 2004094556 A1 WO2004094556 A1 WO 2004094556A1 GB 2004001640 W GB2004001640 W GB 2004001640W WO 2004094556 A1 WO2004094556 A1 WO 2004094556A1
Authority
WO
WIPO (PCT)
Prior art keywords
weight
amount
present
copolymer
treating fluid
Prior art date
Application number
PCT/GB2004/001640
Other languages
French (fr)
Inventor
Karen L. King
David E. Mcmechan
Jiten Chatterji
Original Assignee
Halliburton Energy Services, Inc.
Wain, Christopher, Paul
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., Wain, Christopher, Paul filed Critical Halliburton Energy Services, Inc.
Priority to CA002523090A priority Critical patent/CA2523090C/en
Publication of WO2004094556A1 publication Critical patent/WO2004094556A1/en

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F17STORING OR DISTRIBUTING GASES OR LIQUIDS
    • F17DPIPE-LINE SYSTEMS; PIPE-LINES
    • F17D1/00Pipe-line systems
    • F17D1/08Pipe-line systems for liquids or viscous products
    • F17D1/16Facilitating the conveyance of liquids or effecting the conveyance of viscous products by modification of their viscosity
    • F17D1/17Facilitating the conveyance of liquids or effecting the conveyance of viscous products by modification of their viscosity by mixing with another liquid, i.e. diluting
    • 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
    • C09K8/02Well-drilling compositions
    • C09K8/04Aqueous well-drilling compositions
    • C09K8/06Clay-free compositions
    • C09K8/12Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
    • 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
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/62Compositions for forming crevices or fractures
    • C09K8/66Compositions based on water or polar solvents
    • C09K8/68Compositions based on water or polar solvents containing organic compounds
    • 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
    • C09K8/60Compositions for stimulating production by acting on the underground formation
    • C09K8/84Compositions based on water or polar solvents
    • C09K8/86Compositions based on water or polar solvents containing organic compounds
    • C09K8/88Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S507/00Earth boring, well treating, and oil field chemistry
    • Y10S507/922Fracture fluid

Definitions

  • the present invention relates to friction pressure reducers for use in aqueous treating fluids.
  • aqueous well treating fluids are often pumped through tubular goods disposed in well bores.
  • friction pressure reducing additives have heretofore been combined with the aqueous treating fluids.
  • a treatment commonly utilized for stimulating hydrocarbon production from a subterranean zone penetrated by a well bore is hydraulic fracturing.
  • an aqueous treating fluid referred to in the art as a pad fluid is pumped through tubular goods disposed in the well bore into the subterranean zone to be stimulated at a rate and pressure such that fractures are formed and extended in the subterranean zone.
  • a viscosified aqueous fluid having proppant particles suspended therein is pumped into the fractures so that the proppant particles suspended therein are deposited in the fractures when the viscous aqueous fluid is broken and recovered.
  • the proppant particles function to prevent the fractures from closing whereby conductive channels are formed through which produced fluids can flow to the well bore.
  • friction pressure reducers While the aqueous pad fluids and other aqueous well treating fluids containing friction pressure reducers utilized heretofore have been used successfully, the friction pressure reducers have been suspended in a hydrocarbon-water emulsion and as a result they have been toxic and detrimental to the environment. Thus, there are needs for improved friction pressure reducers which are non-toxic and environmentally acceptable.
  • a method of this invention for treating a subterranean zone penetrated by a well bore comprises the following steps.
  • An aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer is prepared or provided.
  • the friction pressure reducer comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2- [(l,oxo-2-propenyl)oxy]-chloride. Thereafter, the aqueous treating fluid is pumped into the subterranean zone.
  • An aqueous well treating fluid of this invention is basically comprised of water and a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanarninium,N,N,N-trimethyl-2-[(l,oxo- 2-propenyl)oxy] -chloride.
  • a non-toxic environmentally acceptable water friction pressure reducer of this invention comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.
  • the present invention provides methods of treating a subterranean zone penetrated by a well bore comprising the steps of preparing or providing an aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer and then pumping the aqueous treating fluid into the subterranean zone.
  • An aqueous well treating fluid is also provided comprising water and a non-toxic environmentally acceptable friction pressure reducer as is the friction pressure reducer.
  • the water utilized in the aqueous treating fluid can be fresh water or salt water.
  • salt water is used herein to mean unsaturated salt solutions, saturated salt solutions and brines.
  • the non-toxic environmentally acceptable friction pressure reducer of this invention comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.
  • the acrylamide is present in the copolymer in an amount in the range of from about 90 weight % to about 95 weight % and the dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the copolymer in an amount in the range of from about 5 weight % to about 10 weight %.
  • the acrylamide is present in the copolymer in an amount of about 93 weight % and the dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the copolymer in an amount of about 7 weight %.
  • the copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the mixture in an amount of about 96 weight % and the stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy-chloride is present in the mixture in an amount of about 4 weight %.
  • the friction pressure reducer mixture is included in the aqueous treating fluid in an amount in the range of from about 0.1 gallon to about 10 gallons per 1000 gallons of water therein, more preferably in an amount of about 2 gallons per 1000 gallons.
  • a method of this invention for treating a subterranean zone penetrated by a well bore comprises the following steps.
  • An aqueous treating fluid that comprises water and a nontoxic environmentally acceptable friction pressure reducer is prepared or provided.
  • the friction pressure reducer is comprised of a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]- chloride.
  • the aqueous treating fluid is pumped into the subterranean zone.
  • the aqueous well treating fluid of this invention is comprised of water and the nontoxic environmentally acceptable friction pressure reducer described above.
  • the non-toxic environmentally acceptable water friction pressure reducer of this invention is comprised of the mixture described above.
  • a preferred method of this invention for treating a subterranean zone penetrated by a well bore comprises the steps of: (a) preparing or providing an aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride; and (b) pumping the aqueous treating fluid into the subterranean zone.
  • a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2
  • a preferred aqueous well treating fluid of this invention comprises: water; and a nontoxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo- 2-propenyl)oxy] -chloride.
  • a preferred non-toxic environmentally acceptable water friction pressure reducer comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.
  • the friction pressure reducer of this invention was prepared as follows. A three- necked flask equipped with a stirrer, an inlet nitrogen purging tube and a condensor was charged with 52 grams of deionized water. To the water, 18 grams of ammonium sulfate, 7.5 grams of sodium sulfate and 2 grams of glycerol were added. The salt solution formed was continuously agitated.
  • 0.1 gram of napthol ethyl ether surfactant and less than 0.1 grams of vazo initator, i.e., lH-imidazole J 2,2'-(azobis91- methylethylidene)bis(4,5-dihydro-dihydrochloride) were then added to the stirring solution.
  • the solution was maintained at a temperature of from about 40°C to about 45°C with continuous nitrogen purging. When the oxygen was completely displaced, the polymerization initiated as indicated by the increasing viscosity of the solution and the production of exothermic heat.
  • the solution was held at in the range of from 75° to 80°C for about two hours.
  • the reaction was terminated by raising the temperature to 95 °C and holding that temperature for one hour.
  • the copolymer and homopolymer product mixture had a specific gravity of 1.15 plus or minus 0.05 at 60°F and the liquid product had a milky white appearance.
  • Portions of the above described friction pressure reducer product were added to portions of fresh water, a 2% KC1 solution, a 10% NaCl solution and synthetic brine and tested for friction pressure reduction.
  • a small scale friction pressure reduction measurement apparatus was used comprised of a transducer connected to a 6 foot long pipe. The inlet of the transducer was 2 feet from the inlet end of the pipe. The inside diameter of the measurement tube connected between the pipe and the transducer was 0.48 inches.
  • the outlet end of the 6 foot long pipe (4 feet) was attached to a reservoir tank through a nipple which had a diameter of 1 inch.
  • the reservoir tank held a total of 10 liters of the base liquid to which the friction pressure reducing mixture would be added. Two preliminary pressure measurements of the base fluid were required before the friction reduction agent was tested.
  • the first measurement (Ph) was taken with the pump stopped for 10 seconds. The pump was then started and the second base fluid measurement (Pb) was made to establish a 0% reduction. After 60 seconds, the friction pressure reducer terpolymer was introduced into the base fluid and the pressure (Ps) was monitored for a total test time of 20 minutes after which the test was terminated.
  • the friction pressure reduction (FR) obtained was calculated as a function of time in accordance with the equation below.
  • Pb FR Meter gage indication while pumping the base fluid.
  • Ps FR Meter gage indication while pumping the fluid sample which contains the friction pressure reducer terpolymer.
  • Ph FR Meter gage indication with the pump stopped which represents the hydrostatic pressure.
  • Example 2 The tests described in Example 1 above were repeated utilizing a 2% by weight solution of potassium chloride in fresh water. The results of these tests are given in Table II below.
  • EXAMPLE 3 The tests described in Example 1 were repeated utilizing a 10% by weight solution of sodium chloride in fresh water. The results of these tests are set forth in Table III below.
  • EXAMPLE 4 The tests described in Example 1 above were repeated utilizing a synthetic brine solution.
  • the synthetic brine solution utilized was comprised of 10 liters of fresh water having the following compounds dissolved therein in the following amounts: sodium chloride - 1591.1 grams; calcium chloride - 635.48 grams; magnesium chloride - 50.27 grams; potassium chloride - 39.8 grams; barium chloride - 0.288 grams; strontium sulfate - 4.6 grams; strontium chloride - 21.9 grams; and sodium carbonate - 0.3 grams.
  • the synthetic brine had a pH of 5.42. The results of these tests are given in Table IV below.

Abstract

The present invention relates to methods, aqueous treating fluids and friction pressure reducers for the treating fluids. A treating fluid of the invention comprises water and a non­toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.

Description

METHODS, AQUEOUS WELL TREATING FLUIDS AND FRICTION REDUCERS THEREFOR
BACKGROUND OF THE INVENTION
1. FIELD OF THE INVENTION
The present invention relates to friction pressure reducers for use in aqueous treating fluids.
2. DESCRIPTION OF THE PRIOR ART
In the drilling, completion and stimulation of oil and gas wells, aqueous well treating fluids are often pumped through tubular goods disposed in well bores. In order to reduce the friction between the aqueous treating fluid and the tubular goods during pumping whereby the pressure at the pump is reduced, friction pressure reducing additives have heretofore been combined with the aqueous treating fluids.
For example, a treatment commonly utilized for stimulating hydrocarbon production from a subterranean zone penetrated by a well bore is hydraulic fracturing. In most hydraulic fracturing treatments, an aqueous treating fluid referred to in the art as a pad fluid is pumped through tubular goods disposed in the well bore into the subterranean zone to be stimulated at a rate and pressure such that fractures are formed and extended in the subterranean zone. Thereafter, a viscosified aqueous fluid having proppant particles suspended therein is pumped into the fractures so that the proppant particles suspended therein are deposited in the fractures when the viscous aqueous fluid is broken and recovered. The proppant particles function to prevent the fractures from closing whereby conductive channels are formed through which produced fluids can flow to the well bore.
While the aqueous pad fluids and other aqueous well treating fluids containing friction pressure reducers utilized heretofore have been used successfully, the friction pressure reducers have been suspended in a hydrocarbon-water emulsion and as a result they have been toxic and detrimental to the environment. Thus, there are needs for improved friction pressure reducers which are non-toxic and environmentally acceptable.
SUMMARY OF THE INVENTION
The present invention provides improved methods of treating subterranean zones penetrated by well bores, improved aqueous well treating fluids and non-toxic environmentally acceptable friction reducers which meet the needs described above and overcome the deficiencies of the prior art. A method of this invention for treating a subterranean zone penetrated by a well bore comprises the following steps. An aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer is prepared or provided. The friction pressure reducer comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2- [(l,oxo-2-propenyl)oxy]-chloride. Thereafter, the aqueous treating fluid is pumped into the subterranean zone.
An aqueous well treating fluid of this invention is basically comprised of water and a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanarninium,N,N,N-trimethyl-2-[(l,oxo- 2-propenyl)oxy] -chloride.
A non-toxic environmentally acceptable water friction pressure reducer of this invention comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.
The objects, features and advantages of the present invention will be readily apparent to those skilled in the art upon a reading of the description of preferred embodiments which follows.
DESCRIPTION OF PREFERRED EMBODIMENTS
As mentioned above, the present invention provides methods of treating a subterranean zone penetrated by a well bore comprising the steps of preparing or providing an aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer and then pumping the aqueous treating fluid into the subterranean zone. An aqueous well treating fluid is also provided comprising water and a non-toxic environmentally acceptable friction pressure reducer as is the friction pressure reducer.
The water utilized in the aqueous treating fluid can be fresh water or salt water. The term "salt water" is used herein to mean unsaturated salt solutions, saturated salt solutions and brines.
The non-toxic environmentally acceptable friction pressure reducer of this invention comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride. The acrylamide is present in the copolymer in an amount in the range of from about 90 weight % to about 95 weight % and the dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the copolymer in an amount in the range of from about 5 weight % to about 10 weight %. More preferably, the acrylamide is present in the copolymer in an amount of about 93 weight % and the dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the copolymer in an amount of about 7 weight %. The copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride is present in the mixture in an amount of about 96 weight % and the stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy-chloride is present in the mixture in an amount of about 4 weight %.
The friction pressure reducer mixture is included in the aqueous treating fluid in an amount in the range of from about 0.1 gallon to about 10 gallons per 1000 gallons of water therein, more preferably in an amount of about 2 gallons per 1000 gallons.
A method of this invention for treating a subterranean zone penetrated by a well bore comprises the following steps. An aqueous treating fluid that comprises water and a nontoxic environmentally acceptable friction pressure reducer is prepared or provided. The friction pressure reducer is comprised of a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]- chloride. Thereafter, the aqueous treating fluid is pumped into the subterranean zone.
The aqueous well treating fluid of this invention is comprised of water and the nontoxic environmentally acceptable friction pressure reducer described above.
The non-toxic environmentally acceptable water friction pressure reducer of this invention is comprised of the mixture described above.
A preferred method of this invention for treating a subterranean zone penetrated by a well bore comprises the steps of: (a) preparing or providing an aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride; and (b) pumping the aqueous treating fluid into the subterranean zone.
A preferred aqueous well treating fluid of this invention comprises: water; and a nontoxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo- 2-propenyl)oxy] -chloride.
A preferred non-toxic environmentally acceptable water friction pressure reducer comprises a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride.
In order to further illustrate the methods and fracturing fluids of the present invention, the following examples are given.
EXAMPLE 1
The friction pressure reducer of this invention was prepared as follows. A three- necked flask equipped with a stirrer, an inlet nitrogen purging tube and a condensor was charged with 52 grams of deionized water. To the water, 18 grams of ammonium sulfate, 7.5 grams of sodium sulfate and 2 grams of glycerol were added. The salt solution formed was continuously agitated. 15.35 grams of acrylamide, 1.15 grams of dimethylaminoethyl acrylate quaternized with benzyl chloride and 4 grams of a stabilizing and dispersing homopolymer of ethanamimum,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride were then added to the salt solution while the solution was being stirred. 0.1 gram of napthol ethyl ether surfactant and less than 0.1 grams of vazo initator, i.e., lH-imidazoleJ2,2'-(azobis91- methylethylidene)bis(4,5-dihydro-dihydrochloride) were then added to the stirring solution. The solution was maintained at a temperature of from about 40°C to about 45°C with continuous nitrogen purging. When the oxygen was completely displaced, the polymerization initiated as indicated by the increasing viscosity of the solution and the production of exothermic heat. The solution was held at in the range of from 75° to 80°C for about two hours. Thereafter, the reaction was terminated by raising the temperature to 95 °C and holding that temperature for one hour. The copolymer and homopolymer product mixture had a specific gravity of 1.15 plus or minus 0.05 at 60°F and the liquid product had a milky white appearance. Portions of the above described friction pressure reducer product were added to portions of fresh water, a 2% KC1 solution, a 10% NaCl solution and synthetic brine and tested for friction pressure reduction. A small scale friction pressure reduction measurement apparatus was used comprised of a transducer connected to a 6 foot long pipe. The inlet of the transducer was 2 feet from the inlet end of the pipe. The inside diameter of the measurement tube connected between the pipe and the transducer was 0.48 inches. The outlet end of the 6 foot long pipe (4 feet) was attached to a reservoir tank through a nipple which had a diameter of 1 inch. The reservoir tank held a total of 10 liters of the base liquid to which the friction pressure reducing mixture would be added. Two preliminary pressure measurements of the base fluid were required before the friction reduction agent was tested.
The first measurement (Ph) was taken with the pump stopped for 10 seconds. The pump was then started and the second base fluid measurement (Pb) was made to establish a 0% reduction. After 60 seconds, the friction pressure reducer terpolymer was introduced into the base fluid and the pressure (Ps) was monitored for a total test time of 20 minutes after which the test was terminated. The friction pressure reduction (FR) obtained was calculated as a function of time in accordance with the equation below.
Pb - Ps
FR % = X 100
Pb - Ph wherein:
Pb = FR Meter gage indication while pumping the base fluid.
Ps = FR Meter gage indication while pumping the fluid sample which contains the friction pressure reducer terpolymer.
Ph = FR Meter gage indication with the pump stopped which represents the hydrostatic pressure.
The results of the tests utilizing fresh water as the base fluid is set forth in Table I below. TABLE I FRICTION PRESSURE REDUCTION OF FRESH WATER
Figure imgf000007_0001
EXAMPLE 2
The tests described in Example 1 above were repeated utilizing a 2% by weight solution of potassium chloride in fresh water. The results of these tests are given in Table II below.
TABLE II FRICTION PRESSURE REDUCTION OF 2% KC1
Figure imgf000007_0002
EXAMPLE 3 The tests described in Example 1 were repeated utilizing a 10% by weight solution of sodium chloride in fresh water. The results of these tests are set forth in Table III below.
TABLE III FRICTION PRESSURE REDUCTION OF 10% NaCl
Figure imgf000007_0003
EXAMPLE 4 The tests described in Example 1 above were repeated utilizing a synthetic brine solution. The synthetic brine solution utilized was comprised of 10 liters of fresh water having the following compounds dissolved therein in the following amounts: sodium chloride - 1591.1 grams; calcium chloride - 635.48 grams; magnesium chloride - 50.27 grams; potassium chloride - 39.8 grams; barium chloride - 0.288 grams; strontium sulfate - 4.6 grams; strontium chloride - 21.9 grams; and sodium carbonate - 0.3 grams. The synthetic brine had a pH of 5.42. The results of these tests are given in Table IV below.
TABLE IV FRICTION PRESSURE REDUCTION OF BRINE SOLUTION
Figure imgf000008_0001
From the results set forth in Tables I - IV above it can be seen that the friction pressure reducer of the present invention provided excellent friction pressure reduction in fresh water, a 2% solution of potassium chloride, a 10% solution of sodium chloride and a synthetic brine solution.
Thus, the present invention is well adapted to carry out the objects and attain the ends and advantages mentioned as well as those which are inherent therein. While numerous changes may be made by those skilled in the art, such changes are encompassed within the spirit of this invention as defined by the appended claims.

Claims

What is claimed is:
1. A method of treating a subterranean zone penetrated by a well bore comprising the steps of:
(a) preparing or providing an aqueous treating fluid that comprises water and a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo- 2-propenyl)oxy] -chloride; and
(b) pumping said aqueous treating fluid into said subterranean zone.
2. The method of claim 1 wherein said water is selected from the group consisting of fresh water and salt water.
3. The method of claim 1 wherein said acrylamide is present in said copolymer in an amount in the range of from about 90 weight % to about 95 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said copolymer in an amount in the range of from about 5 weight % to about 10 weight %.
4. The method of claim 1 wherein said acrylamide is present in said copolymer in an amount of about 93 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said copolymer in an amount of about 7 weight %.
5. The method of claim 1 wherein said copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said mixture in an amount of about 96 weight % and said stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy]-chloride is present in said mixture in an amount of about 4 weight %.
6. The method of claim 1 wherein said friction pressure reducer is present in said aqueous treating fluid in an amount in the range of from about 0.1 gallon to about 10 gallons per 1000 gallons of water therein.
7. The method of claim 1 wherein said friction pressure reducer is present in said aqueous treating fluid in an amount of about 2 gallons per 1000 gallons of water therein.
8. The method of claim 1 wherein said aqueous treating fluid is a pad fluid utilized in a subterranean zone fracturing treatment.
9. An aqueous well treating fluid comprising:
water; and
a non-toxic environmentally acceptable friction pressure reducer comprising a mixture of a copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l ,oxo-2-propenyl)oxy] -chloride.
10. The treating fluid of claim 9 wherein said water is selected from the group consisting of fresh water and salt water.
11. The treating fluid of claim 9 wherein said acrylamide is present in said copolymer in an amount in the range of from about 90 weight % to about 95 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said copolymer in an amount in the range of from about 5 weight % to about 10 weight %.
12. The treating fluid of claim 9 wherein said acrylamide is present in said copolymer in an amount of about 93 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said terpolymer in an amount of about 7 weight %.
13. The treating fluid of claim 9 wherein said copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said mixture in an amount of about 96 weight % and said stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy] -chloride is present in said mixture in an amount of about 4 weight %.
14. The treating fluid of claim 9 wherein said friction pressure reducer is present in said aqueous treating fluid in an amount in the range of from about 0.1 gallon to about 10 gallons per 1000 gallons of water therein.
15. The treating fluid of claim 9 wherein said friction pressure reducer is present in said aqueous treating fluid in an amount of about 2 gallons per 1000 gallons of water therein.
16. The treating fluid of claim 9 wherein said aqueous treating fluid is a pad fluid utilized in a subterranean zone fracturing treatment.
17. A non-toxic environmentally acceptable friction pressure reducer comprising a mixture of copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride and a stabilizing and dispersing homopolymer of ethanaminium,N,N,N- trimethyl-2-[( 1 ,oxo-2-propenyl)oxy]-chloride.
18. The friction pressure reducer of claim 17 wherein said acrylamide is present in said copolymer in an amount in the range of from about 90 weight % to about 95 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said copolymer in an amount in the range of from about 5 weight % to about 10 weight %.
19. The friction pressure reducer of claim 17 wherein said acrylamide is present in said copolymer in an amount of about 93 weight % and said dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said copolymer in an amount of about 7 weight %.
20. The friction pressure reducer of claim 17 wherein said copolymer of acrylamide and dimethylaminoethyl acrylate quaternized with benzyl chloride is present in said mixture in an amount of about 96 weight % and said stabilizing and dispersing homopolymer of ethanaminium,N,N,N-trimethyl-2-[(l,oxo-2-propenyl)oxy] -chloride is present in said mixture in an amount of about 4 weight %.
PCT/GB2004/001640 2003-04-21 2004-04-15 Methods, aqueous well treating fluids and friction reducers therefor WO2004094556A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CA002523090A CA2523090C (en) 2003-04-21 2004-04-15 Methods, aqueous well treating fluids and friction reducers therefor

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10/419,455 2003-04-21
US10/419,455 US6784141B1 (en) 2003-04-21 2003-04-21 Methods, aqueous well treating fluids and friction reducers therefor

Publications (1)

Publication Number Publication Date
WO2004094556A1 true WO2004094556A1 (en) 2004-11-04

Family

ID=32908368

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2004/001640 WO2004094556A1 (en) 2003-04-21 2004-04-15 Methods, aqueous well treating fluids and friction reducers therefor

Country Status (4)

Country Link
US (1) US6784141B1 (en)
AR (1) AR042566A1 (en)
CA (1) CA2523090C (en)
WO (1) WO2004094556A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009098668A1 (en) * 2008-02-08 2009-08-13 Schlumberger Canada Limited Use of relative permeability modifiers in treating subterranean formations

Families Citing this family (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7405184B2 (en) * 2001-12-11 2008-07-29 Southwest Research Institute Anti-traction, mobility denial methods and products
US7625848B2 (en) * 2001-12-11 2009-12-01 Southwest Research Institute Anti-traction compositions
AU2003285254A1 (en) * 2002-12-02 2004-06-23 Genesis International Oilfield Services Inc. Drilling fluid and methods of use thereof
US7465360B2 (en) 2005-05-02 2008-12-16 Southwest Research Institute Methods for removing a dispersed lubricious coating from a substrate
US7004254B1 (en) 2005-06-17 2006-02-28 Halliburton Energy Services, Inc. Subterranean treatment fluids, friction reducing copolymers, and associated methods
US7232793B1 (en) 2005-12-13 2007-06-19 Halliburton Energy Services, Inc. Water-based polymers for use as friction reducers in aqueous treatment fluids
US7271134B2 (en) * 2005-12-13 2007-09-18 Halliburton Energy Services, Inc. Water-based polymers for use as friction reducers in aqueous treatment fluids
US8697613B2 (en) * 2006-03-03 2014-04-15 Halliburton Energy Services, Inc. Treatment fluids comprising friction reducers and antiflocculation additives and associated methods
US7806185B2 (en) * 2006-03-03 2010-10-05 Halliburton Energy Services, Inc. Treatment fluids comprising friction reducers and antiflocculation additives and associated methods
CA2658696C (en) * 2006-08-16 2012-07-24 Halliburton Energy Services, Inc. Subterranean treatment fluids, friction reducing copolymers, and associated methods
US7311146B1 (en) 2006-08-16 2007-12-25 Halliburton Energy Services, Inc. Subterranean treatment fluids, friction reducing copolymers, and associated methods
US7504366B2 (en) 2006-08-16 2009-03-17 Halliburton Energy Services, Inc. Subterranean treatment fluids, friction reducing copolymers, and associated methods
US8640774B1 (en) 2007-02-16 2014-02-04 Wsp Chemicals & Technology, Llc Method of treating a formation
US7846878B2 (en) * 2007-07-17 2010-12-07 Halliburton Energy Services, Inc. Friction reducer performance in water containing multivalent ions
US7579302B2 (en) * 2007-07-17 2009-08-25 Halliburton Energy Services, Inc. Friction reducer performance by complexing multivalent ions in water
US20090298720A1 (en) * 2008-05-27 2009-12-03 Halliburton Energy Services, Inc. Methods for maintaining fracture conductivity
US20100200239A1 (en) * 2009-02-09 2010-08-12 Kemira Chemicals, Inc. Friction reducing compositions for well treatment fluids and methods of use
MX358434B (en) 2011-01-31 2018-08-06 Halliburton Energy Services Inc Increasing fracture complexity in ultra-low permeable subterranean formation using degradable particulate.
US9796900B2 (en) 2011-06-22 2017-10-24 Halliburton Energy Services, Inc. Alkaline persulfate for low-temperature breaking of polymer viscosified fluid
US20140148369A1 (en) 2012-11-28 2014-05-29 Halliburton Energy Services, Inc. Methods of Treating a Subterranean Formation with Friction Reducing Clays
US9932513B2 (en) 2013-01-23 2018-04-03 Haliburton Energy Services, Inc. Treatment fluids comprising stabilized heteropolysaccharides and related methods
US9422420B2 (en) 2013-02-01 2016-08-23 Halliburton Energy Services, Inc. Low-temperature breaker for well fluid viscosified with a polyacrylamide
CN104974298B (en) * 2014-04-10 2017-04-26 中国石油化工股份有限公司 Resistance reducing agent for fracture and preparation method thereof
CN104974737B (en) * 2014-04-10 2018-09-21 中国石油化工股份有限公司 A kind of pressure break friction reducer and preparation method thereof
WO2017058245A1 (en) 2015-10-02 2017-04-06 Halliburton Energy Services, Inc. Methods of controlling well bashing

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4152274A (en) * 1978-02-09 1979-05-01 Nalco Chemical Company Method for reducing friction loss in a well fracturing process
EP0501776A1 (en) * 1991-02-28 1992-09-02 Halliburton Company Stabilization of subterranean formations
US5197544A (en) * 1991-02-28 1993-03-30 Halliburton Company Method for clay stabilization with quaternary amines
US20030191030A1 (en) * 2002-04-03 2003-10-09 Blair Cecil C. Use of dispersion polymers as friction reducers in aqueous fracturing fluids

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3758406A (en) 1971-10-22 1973-09-11 Halliburton Co Flow of hydrocarbon liquids methods and compositions for reducing frictional pressure loss in the
US3748266A (en) 1971-11-01 1973-07-24 Halliburton Co Methods and compositions for reducing frictional pressure loss in theflow of hydrocarbon liquids
US4024040A (en) * 1974-02-26 1977-05-17 Hercules Incorporated Polymerization of unsaturated monomers with radiation in the presence of salts
US4626363A (en) * 1984-08-29 1986-12-02 National Starch And Chemical Corporation Cationic acrylamide emulsion polymer brine thickeners
US4861499A (en) * 1987-10-13 1989-08-29 American Cyanamid Company Water-dispersible hydrophobic thickening agent
US20020165307A1 (en) * 1996-10-03 2002-11-07 Sun-Yi Huang Aqueous dispersions
US5762140A (en) 1996-11-04 1998-06-09 Halliburton Energy Services, Inc. High viscosity low friction pressure loss well treating fluids and methods
US6169058B1 (en) * 1997-06-05 2001-01-02 Bj Services Company Compositions and methods for hydraulic fracturing
GB2342110B (en) * 1998-10-01 2000-11-15 Baker Hughes Inc Shale stabilizing drilling fluids comprising calcium chloride and low molecular weight low charge cationic polyacrylamide copolymers
US6398967B2 (en) * 2000-04-20 2002-06-04 Nalco Chemical Company Method of clarifying water using low molecular weight cationic dispersion polymers
US6413433B1 (en) * 2000-08-31 2002-07-02 Nalco Chemical Company Method for dewatering of sludge
US6627719B2 (en) * 2001-01-31 2003-09-30 Ondeo Nalco Company Cationic latex terpolymers for sludge dewatering
US6702044B2 (en) * 2002-06-13 2004-03-09 Halliburton Energy Services, Inc. Methods of consolidating formations or forming chemical casing or both while drilling

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4152274A (en) * 1978-02-09 1979-05-01 Nalco Chemical Company Method for reducing friction loss in a well fracturing process
EP0501776A1 (en) * 1991-02-28 1992-09-02 Halliburton Company Stabilization of subterranean formations
US5197544A (en) * 1991-02-28 1993-03-30 Halliburton Company Method for clay stabilization with quaternary amines
US20030191030A1 (en) * 2002-04-03 2003-10-09 Blair Cecil C. Use of dispersion polymers as friction reducers in aqueous fracturing fluids

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009098668A1 (en) * 2008-02-08 2009-08-13 Schlumberger Canada Limited Use of relative permeability modifiers in treating subterranean formations

Also Published As

Publication number Publication date
CA2523090A1 (en) 2004-11-04
AR042566A1 (en) 2005-06-29
US6784141B1 (en) 2004-08-31
CA2523090C (en) 2009-09-08

Similar Documents

Publication Publication Date Title
CA2523090C (en) Methods, aqueous well treating fluids and friction reducers therefor
CA2725112C (en) Subterranean treatment fluids, friction reducing copolymers, and associated methods
US4152274A (en) Method for reducing friction loss in a well fracturing process
US7271134B2 (en) Water-based polymers for use as friction reducers in aqueous treatment fluids
US7232793B1 (en) Water-based polymers for use as friction reducers in aqueous treatment fluids
RU2404223C2 (en) Bored well processing compositions containing foam filler and methods of using said compositions
US6555505B1 (en) Foamed acidizing fluids, additives and methods of acidizing subterranean zones
CN113646381B (en) Reverse emulsion for hydraulic fracturing
US6844297B2 (en) Fracturing method using aqueous or acid based fluids
RU2590914C2 (en) Fluid for well servicing
CN112521560A (en) Efficient salt-resistant one-agent dual-purpose thickening agent and preparation method and application thereof
EP1973982B1 (en) Water-based polymers for use as friction reducers in aqueous treatment fluids
CN111763511B (en) Preparation and liquid preparation method of integrated self-crosslinking thickener modified polymer for fracturing
CN108138035B (en) Friction reducing agents, well treatment fluids and improvements relating thereto
US7806185B2 (en) Treatment fluids comprising friction reducers and antiflocculation additives and associated methods
US8697613B2 (en) Treatment fluids comprising friction reducers and antiflocculation additives and associated methods
US11618848B2 (en) Reverse emulsion for hydraulic fracturation
EP0130732B1 (en) Anionic polymer composition and its use for stimulating a subterranean formation
CN116410402A (en) Resistance reducing agent for fracturing and preparation method thereof
CN112126421B (en) Drag reducer for chemical fracturing and preparation method thereof
RU2816318C2 (en) Reverse emulsion for hydraulic fracturing
RU2698784C2 (en) Thickener of an aqueous acid solution, a method of thickening an aqueous acid solution and an oil recovery method using said thickener, a set of components for thickening an aqueous acid solution and a composition for carrying out acidic hydraulic fracturing of the formation, including said thickener
MX2014009475A (en) Method of fracturing using ultra lightweight proppant suspensions and gaseous streams.
CN113969159A (en) Weighted slickwater fracturing fluid and preparation method thereof

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
ENP Entry into the national phase

Ref document number: 2523090

Country of ref document: CA

122 Ep: pct application non-entry in european phase