WO2010054029A2 - Utility materials incorporating a microparticle matrix formed with a setting system - Google Patents

Utility materials incorporating a microparticle matrix formed with a setting system Download PDF

Info

Publication number
WO2010054029A2
WO2010054029A2 PCT/US2009/063323 US2009063323W WO2010054029A2 WO 2010054029 A2 WO2010054029 A2 WO 2010054029A2 US 2009063323 W US2009063323 W US 2009063323W WO 2010054029 A2 WO2010054029 A2 WO 2010054029A2
Authority
WO
WIPO (PCT)
Prior art keywords
core matrix
wallboard
building material
composition
microparticles
Prior art date
Application number
PCT/US2009/063323
Other languages
French (fr)
Other versions
WO2010054029A3 (en
Inventor
Michael D. Kipp
Dilworth L. Pugh
Michael D. Ridges
William T. Mccarvill
Original Assignee
Ashtech Industries, L.L.C.
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 Ashtech Industries, L.L.C. filed Critical Ashtech Industries, L.L.C.
Publication of WO2010054029A2 publication Critical patent/WO2010054029A2/en
Publication of WO2010054029A3 publication Critical patent/WO2010054029A3/en

Links

Classifications

    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04BGENERAL BUILDING CONSTRUCTIONS; WALLS, e.g. PARTITIONS; ROOFS; FLOORS; CEILINGS; INSULATION OR OTHER PROTECTION OF BUILDINGS
    • E04B1/00Constructions in general; Structures which are not restricted either to walls, e.g. partitions, or floors or ceilings or roofs
    • E04B1/62Insulation or other protection; Elements or use of specified material therefor
    • E04B1/74Heat, sound or noise insulation, absorption, or reflection; Other building methods affording favourable thermal or acoustical conditions, e.g. accumulating of heat within walls
    • E04B1/88Insulating elements for both heat and sound
    • E04B1/90Insulating elements for both heat and sound slab-shaped
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B3/00Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form
    • B32B3/26Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B3/00Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form
    • B32B3/26Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer
    • B32B3/30Layered products comprising a layer with external or internal discontinuities or unevennesses, or a layer of non-planar form; Layered products having particular features of form characterised by a particular shape of the outline of the cross-section of a continuous layer; characterised by a layer with cavities or internal voids ; characterised by an apertured layer characterised by a layer formed with recesses or projections, e.g. hollows, grooves, protuberances, ribs
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B5/00Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts
    • B32B5/16Layered products characterised by the non- homogeneity or physical structure, i.e. comprising a fibrous, filamentary, particulate or foam layer; Layered products characterised by having a layer differing constitutionally or physically in different parts characterised by features of a layer formed of particles, e.g. chips, powder or granules
    • 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
    • C04B14/00Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02Granular materials, e.g. microballoons
    • 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
    • C04B14/00Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02Granular materials, e.g. microballoons
    • C04B14/04Silica-rich materials; Silicates
    • C04B14/22Glass ; Devitrified glass
    • C04B14/24Glass ; Devitrified glass porous, e.g. foamed glass
    • 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
    • C04B18/00Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B18/04Waste materials; Refuse
    • C04B18/06Combustion residues, e.g. purification products of smoke, fumes or exhaust gases
    • C04B18/08Flue dust, i.e. fly ash
    • C04B18/081Flue dust, i.e. fly ash from brown coal or lignite
    • 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
    • C04B18/00Use of agglomerated or waste materials or refuse as fillers for mortars, concrete or artificial stone; Treatment of agglomerated or waste materials or refuse, specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B18/04Waste materials; Refuse
    • C04B18/06Combustion residues, e.g. purification products of smoke, fumes or exhaust gases
    • C04B18/08Flue dust, i.e. fly ash
    • C04B18/082Cenospheres
    • 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
    • C04B20/0016Granular materials, e.g. microballoons
    • C04B20/002Hollow or porous granular materials
    • C04B20/0032Hollow or porous granular materials characterised by the gas filling pores, e.g. inert gas or air at reduced pressure
    • 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
    • C04B22/00Use of inorganic materials as active ingredients for mortars, concrete or artificial stone, e.g. accelerators, shrinkage compensating agents
    • C04B22/06Oxides, Hydroxides
    • 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
    • C04B22/00Use of inorganic materials as active ingredients for mortars, concrete or artificial stone, e.g. accelerators, shrinkage compensating agents
    • C04B22/08Acids or salts thereof
    • C04B22/12Acids or salts thereof containing halogen in the anion
    • C04B22/126Fluorine compounds, e.g. silico-fluorine compounds
    • 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
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24Macromolecular compounds
    • C04B24/26Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/2623Polyvinylalcohols; Polyvinylacetates
    • 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
    • C04B24/00Use of organic materials as active ingredients for mortars, concrete or artificial stone, e.g. plasticisers
    • C04B24/24Macromolecular compounds
    • C04B24/28Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C04B24/282Polyurethanes; Polyisocyanates
    • 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
    • C04B28/24Compositions 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 alkyl, ammonium or metal silicates; containing silica sols
    • C04B28/26Silicates of the alkali metals
    • 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
    • C04B38/00Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
    • C04B38/08Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by adding porous substances
    • C04B38/085Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by adding porous substances of micro- or nanosize
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/30Low-molecular-weight compounds
    • C08G18/38Low-molecular-weight compounds having heteroatoms other than oxygen
    • C08G18/3893Low-molecular-weight compounds having heteroatoms other than oxygen containing silicon
    • C08G18/3895Inorganic compounds, e.g. aqueous alkalimetalsilicate solutions; Organic derivatives thereof containing no direct silicon-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L75/00Compositions of polyureas or polyurethanes; Compositions of derivatives of such polymers
    • C08L75/04Polyurethanes
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04CSTRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C2/00Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
    • E04C2/02Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
    • E04C2/04Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres
    • E04C2/043Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials of concrete or other stone-like material; of asbestos cement; of cement and other mineral fibres of plaster
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04CSTRUCTURAL ELEMENTS; BUILDING MATERIALS
    • E04C2/00Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels
    • E04C2/02Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials
    • E04C2/26Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials composed of materials covered by two or more of groups E04C2/04, E04C2/08, E04C2/10 or of materials covered by one of these groups with a material not specified in one of the groups
    • E04C2/284Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials composed of materials covered by two or more of groups E04C2/04, E04C2/08, E04C2/10 or of materials covered by one of these groups with a material not specified in one of the groups at least one of the materials being insulating
    • E04C2/288Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials composed of materials covered by two or more of groups E04C2/04, E04C2/08, E04C2/10 or of materials covered by one of these groups with a material not specified in one of the groups at least one of the materials being insulating composed of insulating material and concrete, stone or stone-like material
    • E04C2/2885Building elements of relatively thin form for the construction of parts of buildings, e.g. sheet materials, slabs, or panels characterised by specified materials composed of materials covered by two or more of groups E04C2/04, E04C2/08, E04C2/10 or of materials covered by one of these groups with a material not specified in one of the groups at least one of the materials being insulating composed of insulating material and concrete, stone or stone-like material with the insulating material being completely surrounded by, or embedded in, a stone-like material, e.g. the insulating material being discontinuous
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B28WORKING CEMENT, CLAY, OR STONE
    • B28BSHAPING CLAY OR OTHER CERAMIC COMPOSITIONS; SHAPING SLAG; SHAPING MIXTURES CONTAINING CEMENTITIOUS MATERIAL, e.g. PLASTER
    • B28B19/00Machines or methods for applying the material to surfaces to form a permanent layer thereon
    • B28B19/0092Machines or methods for applying the material to surfaces to form a permanent layer thereon to webs, sheets or the like, e.g. of paper, cardboard
    • 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
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/0045Polymers chosen for their physico-chemical characteristics
    • C04B2103/0046Polymers chosen for their physico-chemical characteristics added as monomers or as oligomers
    • 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
    • C04B2111/00474Uses not provided for elsewhere in C04B2111/00
    • C04B2111/00612Uses not provided for elsewhere in C04B2111/00 as one or more layers of a layered structure
    • C04B2111/0062Gypsum-paper board like materials
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04FFINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
    • E04F2201/00Joining sheets or plates or panels
    • E04F2201/01Joining sheets, plates or panels with edges in abutting relationship
    • E04F2201/0107Joining sheets, plates or panels with edges in abutting relationship by moving the sheets, plates or panels substantially in their own plane, perpendicular to the abutting edges
    • EFIXED CONSTRUCTIONS
    • E04BUILDING
    • E04FFINISHING WORK ON BUILDINGS, e.g. STAIRS, FLOORS
    • E04F2201/00Joining sheets or plates or panels
    • E04F2201/01Joining sheets, plates or panels with edges in abutting relationship
    • E04F2201/0138Joining sheets, plates or panels with edges in abutting relationship by moving the sheets, plates or panels perpendicular to the main plane
    • 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
    • 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
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/24Structurally defined web or sheet [e.g., overall dimension, etc.]
    • Y10T428/24479Structurally defined web or sheet [e.g., overall dimension, etc.] including variation in thickness
    • Y10T428/24488Differential nonuniformity at margin
    • 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
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249971Preformed hollow element-containing
    • 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
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/249921Web or sheet containing structurally defined element or component
    • Y10T428/249953Composite having voids in a component [e.g., porous, cellular, etc.]
    • Y10T428/249971Preformed hollow element-containing
    • Y10T428/249974Metal- or silicon-containing element
    • 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
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles

Definitions

  • the present invention relates generally to various utility and/or building materials, such as wallboard, sound attenuation materials, shear panels, casting materials, etc., and more particularly to utility and/or building materials incorporating a microparticle-based core matrix. Accordingly, the present invention involves the fields of chemistry, manufacturing engineering, construction, and materials science.
  • the plurality of microparticles has a size from about 10 microns to about 1000 microns. In a further aspect of the present invention, the plurality of microparticles has a size from about 10 microns to about 500 microns.
  • the method further includes coating a contact surface of at least one of the first facing membrane and the second facing membrane with a sodium silicate coating prior to disposing the core matrix therebetween.
  • FIG. 3 illustrates a detailed partial perspective view of a wallboard building material in accordance with another exemplary embodiment of the present invention
  • the composition may then be cured by allowing or causing the evaporation of water present within the composition. Curing may facilitate additional cross-linking of the binder(s) with the microparticles.
  • curing may be done at ambient temperature, which may take between 12 and 48 hours, for example, for a wallboard material having a thickness of about 1 A inch.
  • curing may be accelerated by subjecting the composition to elevated temperatures, such as by heating, for a given period of time. Thus, curing by heating is temperature dependent and is different from curing at ambient temperature.
  • a wallboard building material comprises a core matrix disposed between opposing facing sheets or layers, such as the type of paper common on conventional drywall-type wallboard products.
  • a wallboard building material comprises a core matrix disposed on a single side of a single facing sheet, such that the wallboard has one side with an exposed core matrix face.
  • a wallboard building material comprises one or more facing membranes disposed within the core matrix so the core matrix is on both sides of one or more interior facing membranes, such that both sides of the wallboard have exposed core matrix faces.
  • microp articles contemplated for use herein may comprise many different types, sizes, shapes, constituents, etc.
  • the microparticles used in the present invention wallboard building material will generally have a size ranging between 10 and 1500 microns, or between 10 and 1000 microns, and at times between 10 and 500 microns. Cenospheres sized between 10 and 500 microns are readily available.
  • the bulk density of the microparticles is generally 0.4 - 0.6 g/ml, providing products that are much lighter than conventional wallboard building materials, such as gypsum-based drywall.
  • the size of the microparticles will depend upon the application and the performance characteristics desired.
  • the diameter of the particle can be calculated based on the effective diameter of the particle, using the total area of the cross section of the particle and equating such area to a circumferential area and determining the diameter from that value.
  • the shell thickness can be less than about 20 % of the diameter of the microparticle.
  • the microparticles may comprise hollow, inert, lightweight, naturally occurring, glass particles that are substantially spherical in geometry.
  • ExtendospheresTM is sold under the trademark ExtendospheresTM, which are manufactured and sold by Sphere One Corporation.
  • a hollow interior is preferred as this will reduce the weight of the building material, as well as provide good insulating properties.
  • a composition or core matrix can include from about 25 wt% to about 75 wt% of microparticles based on wet formulation. In another specific example, a composition or core matrix can include from about 50 wt% to about 60 wt% of microparticles based on wet formulation.
  • the present invention further comprises one or more binders operable to couple together the microparticles and to facilitate formation of a core matrix.
  • the binder comprises an inorganic binder, such as sodium silicates in one form or another. This may or may not be combined with an organic binder such as polyvinyl acetate copolymer or ethylene vinyl acetate. A vinyl acetate copolymer may be used, for example, to increase water resistance of a wallboard.
  • a composition can include from about 20 wt% to about 60 wt% of sodium silicate binder based on wet formulation. In another specific example, a composition can include from about 35 wt% to about 45 wt% of sodium silicate binder based on wet formulation.
  • the inorganic binder solution may comprise a ratio of sodium silicate to water of from about 1 :2 to about 2:1, although, higher water content may necessitate a longer curing time. In one embodiment, the ratio of sodium silicate to water is 1 :1.
  • the sodium silicate may be pre-mixed and the solution provided in liquid form, or the sodium silicate may be in powder form and subsequently mixed with water.
  • the core matrix composition does not need to be subjected to elevated temperatures to effectuate initial setting or hardening, and may be cured to produce a suitable end product utility material that will possess the physical and performance properties desired for the particular type of utility material being manufactured.
  • a suitable setting agent such as isocyanate
  • the ratio of binder to setting agent may range between 1 : 1 and 15: 1, and typically between 8:1 and 12:1, depending upon the desired characteristics of the core matrix. Obviously, these ratios may be varied to vary the characteristics of the core matrix. For example, to increase the strength and other characteristics of a utility material, the core matrix may comprise a lower ratio of binder to setting agent (e.g., between 5:1 and 7:1).
  • the core matrix may further comprise one or more additives or fillers.
  • the core matrix may be devoid of further additives and/or fillers. When present, these may be present in an amount between 0.01 and 50% by weight of the total weight of the core matrix in wet mixture.
  • the microparticles may be blended with expanded siliceous inorganic particles, such as perlite, to lower the density of the building material, decrease its weight, and reduce manufacturing costs. Specifically, it is contemplated that expanded siliceous inorganic particles may replace a portion of microparticles in an amount between 1% and 50% by weight of the total weight of the core matrix in wet mixture.
  • This may be done using conventional radiant heating methods, or it may be done using microwaves applied continuously or at various intervals, as well as with microwaves of different intensities.
  • it may be useful to add a limited amount of cross-linking agent to the binder formula in order to increase and/or control the cross-linking.
  • Cross-linking within a building material provides significant advantages over a building material having a composition that is not cross-linked.
  • the binders are generally stronger, they do not absorb water as easily, and the connection between microp articles is much stronger.
  • the building material does not weaken over time.
  • Other advantages may be realized by those skilled in the art. Having said this though, there may be applications where cross- linking is not preferred, and where a non-bonded composition is better suited. This, of course, is contemplated herein.
  • a method of forming a wallboard utility material can include first placing a precut facing sheet, such as a wallboard paper white, face down in an appropriate mold.
  • a formable composition can be formed by mixing microparticles, binder, and the setting agent. The formable composition can be spread over the paper in the mold and can be smoothed using any method.
  • a second facing sheet, such as a brown wallboard paper, can be placed over the mixture.
  • a flat mold lid can be placed on top of the paper and fastened in place. At this point, the core matrix composition may be allowed to initially set via the setting agent.
  • the resulting wallboard product can optionally be subjected to elevated temperatures for a given period of time, such as by heating, or it may be allowed to cure under ambient temperature conditions, although this may take longer.
  • Heat curing can occur at temperatures greater than ambient temperature, preferably less than temperatures required to cause damage or degradation of the paper, mold, or components of the formable composition.
  • all components for the core matrix can be mixed together in a single step or in multiple separate steps in separate mixers.
  • a variety of mixers can be utilized.
  • an auger can be utilized to mix the components for the core matrix.
  • the mixture can be poured into a mold lined with a facing membrane, i.e. paper or aluminum, etc.
  • a conveyor can move the green wallboard to and through an oven.
  • leveling rollers can be utilized to maintain the desired planar shape and thickness of the wallboard during drying.
  • the presence of a metallic facing membrane can allow the method to include exposing the wallboard material to a temperature sufficient to effectuate even more rapid drying and curing of the core matrix.
  • the parameters recited above can be appropriately modified for equipment, variations in core matrix composition, facing membrane types, etc.
  • individual wallboard can be formed and placed in a multi- rack drying oven. Temperature profiles for the oven rack can range depending on the composition of the core matrix and the facing sheets used.
  • a method of forming a wallboard material can include forming a core matrix including mixture of microparticles, sodium silicate binder, and an isocyanate setting agent. This may be followed by disposing the core matrix mixture between a first facing membrane and a second facing membrane and then setting the core matrix.
  • forming the core matrix may comprise forming a first mixture including microparticles and sodium silicate binder and forming a second mixture including microparticles and the isocyanate setting agent. This may be followed by mixing the first mixture with the second mixture to form the core matrix.
  • the method may further include coating a contact surface of at least one of the facing membranes with a sodium silicate coating prior to disposing the core matrix between them.
  • the microparticles, setting agent, binder, and any other components are pre-mixed together in such a way so as to form a semi-rigid utility material.
  • the microparticles are caused to dry or harden, as well as to bond via the binder.
  • the pre-mixed composition may then be placed into a mold and formed into a desired size and shape in accordance with one or more molding methods, examples of which are described below.
  • the pre-mixed composition may be deposited or disposed onto a surface, such as a moving conveyor, and then cut or otherwise formed into the desired size and shape, either before or after the setting and/or curing steps.
  • the utility materials formed to comprise a semi-rigid makeup may be formed into panels of different size, shape, and thickness, such as panels that function as and that have physical characteristics comparable to conventional wallboard.
  • Various backing or containing members may be utilized to support or provide a barrier to the composition.
  • the density of the wallboard building material having the core composition just described can be between 0.4 g/ml and 0.6 g/ml.
  • FIGS. 1 and 2 illustrated is a general perspective view and a detailed perspective view, respectively, of a wallboard building material in accordance with one exemplary embodiment of the present invention. As shown, the wallboard building material 10 is in panel form having a size of approximately 4 ft. in width, and 8 ft.
  • the wallboard building material 10 is shown as comprising a core matrix 14 disposed between opposing facing sheets or layers, namely first facing membrane 34 and second facing membrane 54.
  • first facing membrane 34 and second facing membrane 54 may comprise a single facing membrane, having one side exposed as discussed above.
  • Each of the first facing membrane 34 and the second facing membrane 54 may have a contact surface in contact with the core matrix 14.
  • a contact surface may be any portion of a surface, or an entire surface, of a facing membrane.
  • a contact surface of a facing membrane may be designated as a surface that will come into contact with the core matrix, including an individual component or sub-mixture of select core matrix components, during the process of making a wallboard.
  • a contact surface of a facing membrane may be coated with a sodium silicate coating prior to disposing the core matrix between facing membranes.
  • a contact surface of a facing membrane maybe coated with a sub- mixture of microp articles and sodium silicate binder or coated with a sub-mixture of microparticles and isocyanate setting agent, during the process of making a wallboard.
  • the core matrix 14 is comprised primarily of a plurality of microparticles, at least one binder and a setting agent (isocyanate setting agent) operable with the at least one binder, wherein the microparticles are at least bound or adhered together, and preferably bonded together, by the one or more binders and the setting agent to create a core matrix structure having a plurality of voids defined therein.
  • the voids are formed from the point to point contact between the microparticles.
  • the wallboard building material may further comprise a reinforcing member operable with the core matrix configured to provide enhanced characteristics in one or more areas as compared with the exemplary wallboard building material of FIGS. 1 and 2.
  • the wallboard 110 comprises similar components as discussed above with respect to the wallboard 10 of FIGS. 1 and 2, only the wallboard 110 comprises an additional reinforcing member 174 disposed within the core matrix 114 (sandwiched therein).
  • Reinforcing member 174 is configured to reinforce or enhance one or more properties or characteristics of the wallboard 110.
  • the reinforcing member 174 may be configured to reinforce against (or improve the resistance of) sound transmission, heat transfer or a combination of these.
  • the reinforcing member 174 may also be configured to enhance the overall strength of the wallboard building material 110.
  • the reinforcing member 174 may comprise various types of materials, such as metals, woven or nonwoven fibers or fiber sheets, plastic films, etc., and may comprise any necessary thickness.
  • the reinforcing member 174 comprises an aluminum material disposed within the core matrix.
  • FIG. 4 illustrated is a wallboard building material 10, formed in accordance with one exemplary embodiment of the present invention, just prior to being installed on or hung from a stud wall 2.
  • wallboard building material 10 comprises the same components as that of FIGS. 1 and 2. It should be noted that no specialized installation techniques are required for installing or hanging the wallboard building material 10.
  • the wallboard building material 10 may be installed in a similar manner as conventional drywall or other similar products.
  • FIGS. 5 -A and 5-B illustrate other exemplary embodiments of wallboard building materials that may require one or more special installation techniques. These embodiments are discussed in detail below.
  • FIGS. 5-A and 5-B illustrated are two different examples of coupling and sealing systems, each one being incorporated into a present invention wallboard building material, and each one being configured to couple adjacent wallboard panels together, and to seal or at least partially seal (e.g., not necessarily a strictly airtight seal) the adjacent wallboard panels.
  • the coupling and sealing system is intended to reduce and/or eliminate the flanking path between the adjacent wallboard panels at the joint.
  • the seal may be further enhanced or improved upon nailing, screwing, or otherwise securing the joint to a stud in a stud wall. Indeed, the overlap shown is intended to be positioned about a stud, but this may or may not always be possible.
  • the seal functions to resist sound transmission through the joint, and also to resist heat transfer through the joint, by creating a more complex flanking path for heat transfer and sound transmission, hi other words, the flanking path is intended to be reduced and/or eliminated if possible by the coupling and sealing system of the present invention.
  • first wallboard building material 210-A and a second wallboard building material 210-B, each one formed in a manner as described herein.
  • the first wallboard building material 210-A comprises a protruding or male configuration 218 formed within and along an edge of the core matrix 214-A, which is intended to align and mate with a corresponding recess or female configuration 222 formed within and along an edge of the core matrix 214-B of the second wallboard building material 210-B.
  • the coupling or connection is designed to secure the first and second wallboard building materials 210-A and 210-B, respectively, in a proper position with respect to one another, and to permit the edges of the membranes 234-A and 254-A of the first wallboard building material 210-A to meet the membranes 234-B and 254-B of the second wallboard building material 210-B.
  • the coupling system further helps to maintain proper positioning after installation.
  • the coupling system may be formed about any of the edges of the wallboard building material.
  • FIG. 5-B illustrates partial end views of a first wallboard building material 310-A and a second wallboard building material 310-B, each one formed in a manner as described herein.
  • the first wallboard building material 310-A comprises a notch 326 formed within and along an edge of the core matrix 314-A, with the surface parallel to the surface of the membranes 334-A and 354-A optionally comprising a nub 328, also formed from the core matrix 314-A.
  • the notch 326 is intended to align and mate with a corresponding notch 330 formed in the second wallboard building material 310-B to couple together the first and second wallboard building materials.
  • the notch 326 optionally comprises a recess 332 that receives nub 328 therein when the first and second wallboard building materials are secured or coupled to one another.
  • the coupling system shown in FIG. 5-B is intended to perform a similar function as the coupling system shown in FIG. 5-A. It is noted that the coupling system is integrally formed into the core matrix during manufacture of the wallboard building material. The unique composition of the core matrix provides this capability. The particular size, shape, or configuration of the coupling system may vary, and may be formed in accordance with various different manufacturing techniques. It also contemplated that one or more sealing members or adhesives may be applied to the coupling system to enhance the sealing function achieved by coupling the two wallboard panels together.
  • FIG. 6 illustrated is a detailed perspective view of a wallboard building material formed in accordance with one exemplary embodiment of the present invention.
  • Utility materials can exist in a variety of forms. Much discussion herein is directed to the specific embodiment of wallboard. However, it should be noted that the principles, compositions, and methods discussed apply to a variety of forms of utility materials, and should be interpreted as such.
  • the building material 710 is in panel form, similar to a wallboard panel, having a size of approximately 4 ft. in width, and 8 ft. in length, which is the same size as most conventional wallboard products. Of course, other sizes such 4 ft. by 8 ft. sizes, as well as different thicknesses is also contemplated.
  • the building material 710 is shown as comprising a core matrix 714 disposed about a single facing sheet or layer, namely facing membrane 734.
  • the other side 718 of the building material 710 is exposed, or rather, the other side of the core matrix 714 is exposed, thus exposing a portion of the configuration of microparticles, binder and setting agent.
  • the exposed surface of the core matrix provides and defines a rough, porous surface that is designed and intended to better attenuate sound.
  • the exposed side 718 of the core matrix 714 is intended to face inward as the building material is installed or mounted to a structure, such as a stud wall, with the facing membrane 734 facing out.
  • the density of the building material having the core composition just described is generally between 0.4 g/ml and 0.6 g/ml, although such density can vary greatly depending on the selection and amount of each component, as well as the presence or absence of foaming.
  • the facing membrane 34, and/or 54 shown in FIG. 2 may comprise many different types of materials or combination of materials, and may comprise different properties.
  • facing membranes 34 and/or 54 can each be independently selected.
  • One or both facing membranes can comprises a paper material similar to that found on various wallboard products, such as drywall or the wallboard incorporated by reference herein, as noted above.
  • the facing membrane may comprise metal or a metal alloy.
  • the metal may be quilted, corrugated or otherwise comprise one or more nonplanar surface configurations.
  • one facing membrane can comprise or consist essentially of aluminum or quilted aluminum. In such cases, the aluminum may have a thickness ranging from about .002 in.
  • the metallic facing membrane e.g. an aluminum facing membrane
  • the metallic facing membrane can be embossed or otherwise include a three- dimensional pattern on the surface, or throughout the entire length of the membrane.
  • the core material and facing sheet of the wallboard can be optimized for proper or superior adhesion, thus ensuring the facing sheet will remain secured to the core material.
  • additional binder or binders at the surface level can be utilized to improve adhesion of a facing sheet to the core matrix.
  • a different adhesive agent can be utilized to improve adhesion of a facing sheet to the core matrix.
  • the facing sheet may be eliminated.
  • the core matrix may be configured to be self-supporting, meaning that the building material does not require a facing sheet to maintain its shape and integrity.
  • FIG. 6 further illustrates the exposed side 718 of the core matrix as comprising a multi-elevational surface configuration.
  • a multi-elevational surface configuration may be utilized to reduce weight. Additionally, this configuration may be designed in such a way that enhances the sound attenuation properties of the building material.
  • the purpose of providing a multi-elevational surface configuration formed about one surface, particularly the exposed surface, of the core matrix is at least threefold - 1) to reduce weight, 2) to enhance the sound attenuation or damping properties of the building material, namely to ensure acoustic isolation and absorption over a wide range of frequencies, and 3) to enhance the flex strength of the building material by eliminating shear lines.
  • many different multi-elevational surface configurations are contemplated herein.
  • the multi-elevational surface configuration comprises a waffle pattern, with a plurality of protruding members 718, having a square or rectangular cross-section, defining a plurality of recesses 726.
  • This series of peaks and valleys effectively creates a plurality of surfaces (in this case horizontal surfaces 730 and 734) that are located in different elevations about the overall surface of the core matrix 714.
  • the protruding members 718 maybe configured to provide surfaces oriented at different angles (in this case, the protruding members 718 also define several vertically oriented surfaces 738).
  • a separate mesh facing sheet may or may not be disposed over the exposed multi-elevational surface of the core matrix 714. If used, the mesh facing sheet is preferably configured to be flexible to conform to the multi- elevational surface configuration.
  • the mesh facing sheet may be made from glass, plastics (e.g., extruded plastics), or other materials, depending upon the particular application and need.
  • FIGS. 6 and 14 further illustrate the building material 710 as comprising a plurality of cavities or air pockets 746 strategically formed and located throughout the core matrix 714, and designed to reduce the overall weight of the building material without significantly affecting the strength or other properties of the building material.
  • the cavities 746 are randomly located throughout the core matrix 714, but they may also be arranged in a pre-determined pattern.
  • the cavities 746 may be formed during the manufacture of the building material.
  • the cavities 746 function to define a plurality of voids or air pockets within the core matrix 714 at various locations.
  • the cavities 746 maybe sized to comprise a volume between about 0.2 and about 200 cm , and preferably between about 5 and about 130 cm . These not only help to reduce weight, but also help to increase the overall R value due to the dead air space. In addition, these help to further attenuate sound as these provide additional surfaces that function to absorb sound waves rather than transmit them.
  • building material 810 is similar in many respects to the building material 810 discussed above and shown in FIG. 6.
  • building material 810 comprises a lath 854 disposed or sandwiched within the core matrix 814.
  • the lath 854 comprises a plurality of intersecting members 856 forming a grid having a plurality of openings 858.
  • the lath 854 functions to provide support and stability to the core matrix 814, as well as additional strength.
  • the lath 854 increases the mass of the building material 810, which reduces the potential for vibration, thus contributing to the sound attenuation properties of the building material 810.
  • the lath 854 may comprise many different types and configurations, with the grid and openings being of different sizes and configurations.
  • the lath 854 shown in FIG. 7 is not intended to be limiting in any way.
  • the lath 854 may comprise a metal, fiberglass, or plastic mesh or mesh-like material. This reinforcing lath material provides strength to the building material 810, and further supports the microparticles.
  • the lath 854 may also be made from glass, plastics (e.g., extruded plastics), or other materials, depending upon the particular application and need.
  • the building material 910 comprises a core matrix 914 having a first surface 918.
  • first surface 918 Formed in the first surface 918 is a multi-elevational or nonplanar surface configuration in the form of a repeating pattern of pillow-type protrusions, thus providing multiple different surfaces or surface areas in multiple different elevations.
  • the protrusions may be any desired size, configuration, and height. Therefore, those shown in the drawings are intended to be merely exemplary.
  • FIG. 11 illustrated is a side view of the building material 710 of FIG. 6, having a multi-elevational surface configuration in the form of a repeating waffle-type pattern.
  • the waffle-type configuration extends between the perimeter edges of the building material, and defines a plurality of protrusions 722 and recesses 726.
  • FIG. 9 illustrates a cross-sectional view of a building material wherein the building material 710 comprises a plurality of strategically formed and located cavities or voids 746 in the core matrix 714.
  • FIG. 12 illustrates a detailed side view of another exemplary building material 1010 comprising a core matrix 1014 having a first surface 1018, wherein the first surface 1018 has formed therein a multi-elevational surface configuration comprising a repeating pattern of first protrusions 1022 in the form of pyramids or cones, and a repeating pattern of second protrusions 1024 having an arbitrary shape.
  • the second protrusions 1024 are shown as comprising a primary base protrusion having a square cross -section, upper secondary protrusions 1023, and lateral secondary protrusions 1025, each having a pyramid or cone shape.
  • First and second protrusions 1022 and 1024 define recesses 1026. While the present invention is not intended to be limited to any particular shape of protrusions, FIG. 12 illustrates that arbitrary shapes are at least contemplated.
  • FIG. 13 illustrates a detailed side view of another exemplary building material 1110 comprising a core matrix 1114 having a first surface 1118, wherein the first surface 1118 has formed therein a multi-elevational surface configuration comprising a repeating pattern of first protrusions 1122 and recesses 1126, wherein these form an egg carton-type pattern.
  • FIGS. 8-13 illustrate several different multi-elevational surface configurations. These, however, are not meant to be limiting in any way. Indeed, one skilled in the art will recognize other configurations and/or patterns that may be used to accomplish the designs of the present invention.
  • the building material 1210 comprises a core matrix 1214, a metal lath 1254 disposed or sandwiched within the core matrix 1214, and a facing sheet 1234 comprised of tar paper.
  • the building material 1210 may be used as a finishing material on the exterior of residential or commercial structures, replacing stucco.
  • the building material 1210 comprising pre-formed panels, can be mounted or secured to the exterior walls 1202 of a structure, say a residential home, much in the same way a wallboard is mounted or secured to the interior walls of a home.
  • a stucco finish 1204 commonly known in the art may be applied to the panels to create a finished look.
  • the stucco finish can be applied so as to sufficiently conceal any seams or gaps between adjacent building material panels.
  • such a building material may be applied to shear panels, such as oriented strand board, to shear panels formed after the manner of the present invention, or directly to a stud frame, wherein the building panel may function as the shear panel and also receive the stucco finish directly thereto, thus eliminating the need for a separate shear panel.
  • the heating elements can be configured to concentrate a majority of the heat through the metal facing sheet to the core matrix. In this manner, the heat is better received into the core matrix, steam is removed from the core matrix primarily through the second facing sheet, typically paper, and large steam pockets are not formed.
  • Utility materials as described herein exhibit superior qualities to many utility materials currently available. Furthermore, the superior qualities co-exist, where a material may exhibit both mold resistance and enhanced acoustic properties simultaneously.
  • Wallboards formed of the utility materials are typically lighter than conventional gypsum wallboard by 20% to 30%.
  • An installed R value can be up to about 19.
  • Noise attenuation can be up to about 50 db, depending on the frequency for a /4 inch thick piece of wallboard.
  • the core matrix will not grow mold.
  • Wallboard is water resistant and is still hard after 2 weeks of continuous submersion under water.
  • the material can be formulated to be fire resistant.
  • Wallboard exhibits strong flexural strength up to two times that of conventional gypsum wallboard (e.g., 280 lbs vs. 140 lbs).
  • the wallboard can withstand impacts without crumbling or displacement in surrounding areas such as a corner.
  • Various industry considerations for wallboard performance include, but are not limited to, surface finish, snap and dust, flexural strength, nail pull resistance, dimpling, edge crush, weight, mold growth, water resistance, fire resistance, and R value.
  • the core matrix composition is as follows: the microp articles is 56 wt% of wet core matrix, the sodium silicate binder is 40 wt% of wet core matrix, and the isocyanate setting agent is 4 wt% of wet core matrix.
  • the core matrix is formulated to comprise a two-part mixture. The first part comprising 150 grams microparticles initially mixed with 140 grams sodium silicate Type O from PQ Corporation. The second part comprising 50 grams microparticles (e.g., cenospheres) initially mixed with 14 grams "A" side from Reactamine JS 2:1 of Reactamine Technology, LLC, which is an isocyanate prepolymer.

Abstract

A composition, utility material, and method of making a utility material is disclosed. A composition having an improved setting time may include a plurality of microparticles mixed with a sodium silicate binder and an isocyanate setting agent, where the microparticle composition has a setting time of less than or equal to one hour. A utility material may be a wallboard that includes the composition.

Description

UNITED STATES PATENT APPLICATION
of
Michael D. Kipp Dilworth L. Pugh Michael D. Ridges and William T. Mccarvill
for
UTILITY MATERIALS INCORPORATING A MICROPARTICLE MATRIX FORMED WITH A SETTING AGENT
THORPE NORTH & WESTERN, LLP
ATTORNEYS AT LAW
8180 SOUTH 700 EAST, SUITE 350, SANDY, UTAH 84070 801.566.6633 TELEPHONE 801.566.0750 FACSIMILE UTILITY MATERIALS INCORPORATING A MICROPARTICLE MATRIX FORMED WITH A SETTING AGENT
RELATED APPLICATION
This application claims the benefit of U.S. Provisional Patent Application No. 61/198,554, filed on November 4, 2008, which is incorporated by reference herein in its entirety.
FIELD OF THE INVENTION
The present invention relates generally to various utility and/or building materials, such as wallboard, sound attenuation materials, shear panels, casting materials, etc., and more particularly to utility and/or building materials incorporating a microparticle-based core matrix. Accordingly, the present invention involves the fields of chemistry, manufacturing engineering, construction, and materials science.
BACKGROUND OF THE INVENTION AND RELATED ART
Many different types of building or utility materials, such as wallboard insulation, blown-in insulation, acoustical or sound dampening/absorbing materials, etc., exist in the art. These are all designed to provide a specific function within a structure, hi addition, the composition of ingredients or components making up these utility materials varies greatly. Although there are many different available compositions making up the many different utility materials, relatively few of these incorporate microparticles, such as naturally occurring cenospheres or Extendospheres™, or synthetically manufactured microparticles, into their makeup. In addition, many different types of naturally occurring and artificial microparticles exist. Cenospheres are naturally occurring microparticles found in "fly ash," which is formed during coal combustion. Cenospheres make up a small percentage (l%-4%) of fly ash. They are hollow particles with wall thicknesses about 10% of their diameter. Fly ash also includes small spherical solid particles that have a much higher bulk density than cenospheres. In addition, there are several artificially manufactured microparticles used for a variety of purposes. Although such microparticles tend to be more consistent and uniform in their makeup and structure, they also tend to be extremely expensive and cost prohibitive for many applications. Wallboard is a common utility or building material, which comes in many different types, designs, and sizes. Wallboard can be configured to exhibit many different properties or characteristics, such as different sound absorption, heat transfer and/or fire resistance properties. By far, the most common type of wallboard is drywall or gypsum board. Drywall comprises an inner core of gypsum, the semi- hydrous form of calcium sulphate (CaSO4- 1A H2O), disposed between two facing membranes, typically paper or fiberglass mats.
The most commonly used drywall is one-half- inch thick but can range from one quarter (6.35 mm) to one inch (25 mm) in thickness. For soundproofing or fire resistance, two layers of drywall are sometimes laid at right angles to one another. Drywall provides a thermal resistance, or R value, of 0.32 for three-eighths-inch board, 0.45 for half inch, 0.56 for five-eighths inch, and 0.83 for one-inch board. In addition to increased R- value, thicker drywall has a slightly higher Sound Transmission Class (STC) rating. Conventional interior walls in homes or buildings have opposing sheets of drywall mounted on a stud frame or stud wall. In this arrangement, with the drywall panels having a /4-inch thickness, the interior wall measures an STC of about 33. Adding fiberglass insulation helps, but only increases the STC to 36-39, depending upon the type and quality of insulation, as well as stud and screw spacing. As wallboard is typically comprised of several sheets or panels, the small cracks or gaps between panels, or any other cracks or gaps in the wall structure are referred to as "flanking paths," and will allow sound to transmit more freely, thus resulting in a lower overall STC rating.
SUMMARY OF THE INVENTION
Accordingly, the present invention provides a composition, utility material, and method of making a utility material. In one aspect, for example, a composition having an improved setting time is provided. Such a composition may include a plurality of microp articles mixed with a sodium silicate binder and an isocyanate setting agent. In one aspect, the microparticle composition has a setting time of less than or equal to one hour.
In one aspect of the present invention, the plurality of microparticles is from about 25 wt% to about 75 wt% of wet composition, the sodium silicate is from about 20 wt% to about 60 wt% of wet composition, and the isocyanate setting agent is from about 2 wt% to about 10 wt% of wet composition.
In another aspect of the present invention, the composition includes the sodium silicate binder and the isocyanate setting agent at a ratio of from about 1 : 1 to about 15:1. In yet another aspect of the present invention, the composition includes the sodium silicate binder and the isocyanate setting agent at a ratio of from about 8:1 to about 12:1.
In still another aspect of the present invention, the plurality of microparticles has a size from about 10 microns to about 1000 microns. In a further aspect of the present invention, the plurality of microparticles has a size from about 10 microns to about 500 microns.
In some aspects of the present invention, the composition is a set composition. In a specific aspect, the composition is a cured composition.
In a further aspect of the present invention, the plurality of microparticles contain an inert gas within an internal space.
The present invention additionally provides a utility material. In one aspect, for example, a wallboard is provided. Such a wallboard may include a first facing membrane and a second facing membrane, and a core matrix disposed between the first facing membrane and the second facing membrane. The core matrix includes a composition as described above
The present invention additionally provides a method of making a utility material. In one aspect, for example, a method of making a wallboard having a setting time of less than or equal to one hour is provided. Such a method may include forming a core matrix including a mixture of a plurality of microparticles, a sodium silicate binder, and an isocyanate setting agent, disposing the core matrix between a first facing membrane and a second facing membrane, and setting the core matrix.
In one aspect of the present invention, forming the core matrix further comprises forming a first mixture including a first portion of the plurality of microparticles and the sodium silicate binder, forming a second mixture including a second portion of the plurality of microparticles and the isocyanate setting agent, and mixing the first mixture with the second mixture to form the core matrix.
In another aspect of the present invention, the method further includes coating a contact surface of at least one of the first facing membrane and the second facing membrane with a sodium silicate coating prior to disposing the core matrix therebetween.
In yet another aspect of the present invention, the core matrix is from about 25 wt% to about 75 wt% of wet core matrix, wherein the sodium silicate is from about 20 wt% to about 60 wt% of wet core matrix, and wherein the isocyanate setting agent is from about 2 wt% to about 10 wt% of wet core matrix.
In still another aspect of the present invention, the core matrix includes the sodium silicate binder and the isocyanate setting agent at a ratio of from about 1 : 1 to about 15:1. In a further aspect of the present invention, the core matrix includes the sodium silicate binder and the isocyanate setting agent at a ratio of from about 8: 1 to about 12:1.
In a further aspect of the present invention, the setting time is less than or equal to 30 minutes. In still a further aspect of the present invention, setting the core matrix occurs at ambient temperature. In some aspects of the present invention, the method includes curing the core matrix. In a specific aspect, the method includes actively curing the core matrix by heating. In another specific aspect, the method includes passively curing the core matrix.
There has thus been outlined, rather broadly, various features of the invention so that the detailed description thereof that follows maybe better understood, and so that the present contribution to the art may be better appreciated. Other features of the present invention will become clearer from the following detailed description of the invention, taken with the accompanying claims, or may be learned by the practice of the invention.
BRIEF DESCRIPTION OF THE DRAWINGS
The present invention will become more fully apparent from the following description and appended claims, taken in conjunction with the accompanying drawings. Understanding that these drawings merely depict exemplary embodiments of the present invention they are, therefore, not to be considered limiting of its scope. It will be readily appreciated that the components of the present invention, as generally described and illustrated in the figures herein, could be arranged and designed in a wide variety of different configurations. Nonetheless, the invention will be described and explained with additional specificity and detail through the use of the accompanying drawings in which:
FIG. 1 illustrates a perspective view of a wallboard building material in accordance with one exemplary embodiment of the present invention; FIG. 2 illustrates a detailed partial perspective view of the wallboard building material of FIG. 1 ;
FIG. 3 illustrates a detailed partial perspective view of a wallboard building material in accordance with another exemplary embodiment of the present invention;
FIG. 4 illustrates a perspective view of a wallboard building material just prior to being installed or mounted onto a stud wall;
FIG. 5 -A illustrates a detailed partial end view of a wallboard building material having a coupling system formed therein in accordance with one exemplary embodiment of the present invention;
FIG. 5-B illustrates a detailed partial end view of a wallboard building material having a coupling system formed therein in accordance with another exemplary embodiment of the present invention;
FIG. 6 illustrates a detailed perspective view of a wallboard building material in accordance with one exemplary embodiment of the present invention, wherein the building material comprises a microparticle-based core matrix, a multi-elevational surface configuration formed in one surface of the core matrix, and a facing sheet disposed on an opposing surface of the core matrix;
FIG. 7-A illustrates a detailed perspective view of a wallboard building material in accordance with another exemplary embodiment of the present invention, wherein the building material comprises a microparticle-based core matrix, a lath disposed or sandwiched within the core matrix, a multi-elevational surface configuration formed in one surface of the core matrix, and a facing sheet disposed on an opposing surface of the core matrix;
FIG. 7 -B illustrates a detailed view of the building material of FIG. 7-A;
FIG. 8 illustrates a top view of a building material in accordance with still another exemplary embodiment of the present invention, wherein the building material comprises a patterned pillow-like multi-elevational surface configuration formed in the exposed surface of the core matrix;
FIG. 9 illustrates a cross-sectional side view of the building material of FIG. 8; FIG. 10 illustrates a cross-sectional end view of the building material of FIG. 8;
FIG. 11 illustrates a detailed side view of the building material of FIG. 6;
FIG. 12 illustrates a detailed side view of a building material having a multi- elevational surface configuration in accordance with another exemplary embodiment;
FIG. 13 illustrates a detailed side view of a building material having a multi- elevational surface configuration in accordance with another exemplary embodiment;
FIG. 14 illustrates a cross-sectional side view of a building material in accordance with another exemplary embodiment, wherein the building material comprises a plurality of strategically formed and located cavities or voids; and
FIG. 15 illustrates a building material configured for use as a finishing material on an exterior of a structure.
DETAILED DESCRIPTION OF EXEMPLARY EMBODIMENTS The following detailed description of exemplary embodiments of the invention makes reference to the accompanying drawings, which form a part hereof and in which are shown, by way of illustration, exemplary embodiments in which the invention may be practiced. While these exemplary embodiments are described in sufficient detail to enable those skilled in the art to practice the invention, it should be understood that other embodiments may be realized and that various changes to the invention may be made without departing from the spirit and scope of the present invention. Thus, the following more detailed description of the embodiments of the present invention is not intended to limit the scope of the invention, as claimed, but is presented for purposes of illustration only and not limitation to describe the features and characteristics of the present invention, to set forth the best mode of operation of the invention, and to sufficiently enable one skilled in the art to practice the invention. Accordingly, the scope of the present invention is to be defined solely by the appended claims.
U.S. Patent Application Serial Number 12/077,951 filed on March 21, 2008, is incorporated by reference herein in its entirety. U.S. Patent Application Serial
Number 12/238,399 filed on September 25, 2008, is incorporated by reference herein in its entirety. U.S. Patent Application Serial Number 12/238,367 filed on September 25, 2008, is incorporated by reference herein in its entirety. U.S. Patent Application Serial Number 12/238,379 filed on September 25, 2008, is incorporated by reference herein in its entirety.
The following detailed description and exemplary embodiments of the invention will be best understood by reference to the accompanying drawings, wherein the elements and features of the invention are designated by numerals throughout.
In describing and claiming the present invention, the following terminology will be used in accordance with the definitions set forth below.
The singular forms "a," "an," and, "the" include plural referents unless the context clearly dictates otherwise. Thus, for example, reference to "a wallboard" includes reference to one or more of such wallboards, and reference to "the binder" includes reference to one or more of such binders.
As used herein, "substantially" refers to situations close to and including 100%. Substantially is used to indicate that, though 100% is desirable, a small deviation therefrom is acceptable. For example, substantially free of mold includes situations completely devoid of mold, as well as situations wherein a negligible amount of mold is present, as determined by the particular situation.
As used herein, the term "about" is used to provide flexibility to a numerical range endpoint by providing that a given value may be "a little above" or "a little below" the endpoint.
For purposes of discussion and interpretation of the claims as set forth herein, the terms "utility material," "utility building material," or "building material," as used herein, shall be understood to mean various types of products or materials incorporating a matrix of microparticles (e.g., microspheres) adhered or bound together using one or more components, such as a binder of some kind and a setting agent. The building materials may comprise other additives, components, or constituents, such as setting agents, foaming agents or surfactants, water soluble polymers, and others. The building materials may comprise many different types, embodiments, etc., and may be used in many different applications. The term "microparticle," as used herein, shall be understood to mean any naturally occurring, manufactured, or synthetic particle having an outer surface and an interior space such as a hollow interior. Generally, the microparticles referred to herein comprise a spherical or substantially spherical geometry having a hollow interior, known as microspheres or cenospheres. The term "core matrix," as used herein, shall be understood to mean the combination of microparticles and other constituents used to form the support matrix of the building materials. The microparticles may be combined with one or more binders, setting agents, additives, etc. The terms "core matrix" and "composition" may be used interchangeably in the context of a utility material such as a wallboard. The term "ambient temperature," as used herein, shall be understood to mean the temperature of a surrounding environment when a composition or core matrix becomes set or cured. Unless indicated otherwise, ambient temperature ranges from about 65 degrees F to about 80 degrees F. The term "set composition," as used herein, is a composition that has become firm or hardened, due to a chemical change, sufficient to maintain a substantially self- supporting shape throughout a curing process. A set composition has at least some cross-linking between polymers. The terms "set core matrix" and "set composition" may be used interchangeably in the context of a utility material such as a wallboard. It shall be understood that a composition or core matrix can be set at ambient temperature, above ambient temperature, or below ambient temperature. Unless indicated otherwise, setting shall generally be understood to occur at ambient temperature.
The term "cured composition" is a composition that is substantially devoid of water. The terms "cured core matrix" and "cured composition" may be used interchangeably in the context of a utility material such as a wallboard. A composition or core matrix may become cured at ambient temperature, above ambient temperature, or below ambient temperature. Upon curing, the water content of the wallboard material maybe less then 5%, and can be less than 1%. The term "multi-elevational" shall be understood to describe at least one surface of the core matrix of the building material, wherein the surface has formed therein a series of peaks and valleys (or protrusions and recesses) to provide an overall surface configuration having different surfaces located in different elevations and/or orientations. The multi-elevational surface configuration may be arbitrarily formed or patterned. In addition, the multi-elevational surface may be defined by any arbitrary or geometrically shaped protruding and recessed components.
As used herein, a plurality of items, structural elements, compositional elements, and/or materials may be presented in a common list for convenience. However, these lists should be construed as though each member of the list is individually identified as a separate and unique member. Thus, no individual member of such list should be construed as a de facto equivalent of any other member of the same list solely based on their presentation in a common group without indications to the contrary. Concentrations, amounts, and other numerical data may be expressed or presented herein in a range format. It is to be understood that such a range format is used merely for convenience and brevity and thus should be interpreted flexibly to include not only the numerical values explicitly recited as the limits of the range, but also to include all the individual numerical values or sub-ranges encompassed within that range as if each numerical value and sub-range is explicitly recited. As an illustration, a numerical range of "about 1 to about 5" should be interpreted to include not only the explicitly recited values of about 1 to about 5, but also include individual values and sub-ranges within the indicated range. Thus, included in this numerical range are individual values such as 2, 3, and 4 and sub-ranges such as from 1-3, from 2-4, and from 3-5, etc.
This same principle applies to ranges reciting only one numerical value. Furthermore, such an interpretation should apply regardless of the breadth of the range or the characteristics being described.
The composition of the present invention provides several significant advantages over prior related compositions for utility materials (e.g. wallboard), some of which are recited here and throughout the following more detailed description. First, the present composition is capable of rapidly setting, typically in one hour or less. Second, the set composition of the present invention exhibits properties desirable for a utility material such as a wallboard. For example, the composition gives a wallboard properties that meet at least minimum industry standards such as strength, flexibility, hardness, nail pull resistance, as well as thermal and/or acoustical properties, fire resistant properties, etc.
Each of the above-recited advantages will be apparent in light of the detailed description set forth below, with reference to the accompanying drawings. These advantages are not meant to be limiting in any way. Indeed, one skilled in the art will appreciate that other advantages may be realized, other than those specifically recited herein, upon practicing the present invention.
The present invention describes a composition that may form part of a utility material, such as a wallboard building material, casting material, etc. The composition may include microparticles, an inorganic binder, and a setting agent operable with the inorganic binder, which allows the composition to set under ambient temperature conditions and to possess a desired property once set or cured. It should be noted, however, that the present scope includes compositions that can be set at ambient temperatures, above ambient temperatures, and below ambient temperatures. The time needed to set the composition may depend upon the weight percentages of the various constituents of the core matrix, but may be less than or equal to one hour.
Once set, the composition may then be cured by allowing or causing the evaporation of water present within the composition. Curing may facilitate additional cross-linking of the binder(s) with the microparticles. In one aspect, curing may be done at ambient temperature, which may take between 12 and 48 hours, for example, for a wallboard material having a thickness of about 1A inch. In another aspect, curing may be accelerated by subjecting the composition to elevated temperatures, such as by heating, for a given period of time. Thus, curing by heating is temperature dependent and is different from curing at ambient temperature.
Further, the present invention describes a method of manufacturing a utility material, such as a wallboard building material, shear panel, casting material, etc. As mentioned above, a composition, as described herein, may be a core matrix for a utility material. Thus, the method can include forming a core matrix including microparticles, an inorganic binder, and a setting agent operable with the inorganic binder to set the core matrix and to possess a desired property once set or cured. The core matrix can be deposited within a mold having any desired shape or configuration. The core matrix can then be allowed to set sufficient to form a set composition. Once set, the core matrix may then be cured.
The present invention also describes a method of making a wallboard or other utility material comprising the core matrix discussed herein, and having a setting time of less than or equal to one hour. In one aspect, a wallboard building material comprises a core matrix disposed between opposing facing sheets or layers, such as the type of paper common on conventional drywall-type wallboard products. In another aspect, a wallboard building material comprises a core matrix disposed on a single side of a single facing sheet, such that the wallboard has one side with an exposed core matrix face. In yet another aspect, a wallboard building material comprises one or more facing membranes disposed within the core matrix so the core matrix is on both sides of one or more interior facing membranes, such that both sides of the wallboard have exposed core matrix faces.
The microp articles contemplated for use herein may comprise many different types, sizes, shapes, constituents, etc. Although not limited to this, the microparticles used in the present invention wallboard building material will generally have a size ranging between 10 and 1500 microns, or between 10 and 1000 microns, and at times between 10 and 500 microns. Cenospheres sized between 10 and 500 microns are readily available. The bulk density of the microparticles is generally 0.4 - 0.6 g/ml, providing products that are much lighter than conventional wallboard building materials, such as gypsum-based drywall. The size of the microparticles will depend upon the application and the performance characteristics desired. However, the particles should not be so large as to cause any binder disposed thereon to run off or to not be effective. The size of the microparticles will also function to influence the permeability of the wallboard building material. The microparticles are intended to be compatible with any binders, additives, and/or facing sheets. The shell thickness of the microparticles may be kept to a minimum amount, provided the microparticles maintain structural integrity as desired in the core matrix material. In one aspect, the microparticles can have a shell thickness of less than about 30% of the diameter of the microparticle. Wherein the microparticles are not spherical, the diameter of the particle can be calculated based on the effective diameter of the particle, using the total area of the cross section of the particle and equating such area to a circumferential area and determining the diameter from that value. In a further embodiment, the shell thickness can be less than about 20 % of the diameter of the microparticle. In one exemplary embodiment, the microparticles may comprise hollow, inert, lightweight, naturally occurring, glass particles that are substantially spherical in geometry. One particular type is sold under the trademark Extendospheres™, which are manufactured and sold by Sphere One Corporation. A hollow interior is preferred as this will reduce the weight of the building material, as well as provide good insulating properties. Furthermore, in one aspect, the microspheres or microparticles maintain structural integrity and retain their hollow nature, or original formation to the exclusion of binder or other matrix materials infiltrating the hollow portions of the microparticles. In one aspect of this embodiment, the microparticles may comprise the naturally occurring hollow, inert, glass microspheres obtained from a fly ash byproduct, which microspheres are often referred to as cenospheres. These cenospheres may be separated from the other byproduct components present in the fly ash and further processed, such as to clean and separate these into desired size ranges. Cenospheres are comprised primarily of silica and alumina, and have a hollow interior that is filled with air and/or other gasses. They possess many desirable properties, such as a crush strength between 3000 psi and 5000 psi, low specific gravity and are able to endure extremely high temperatures (above 1800 degrees F). Although they are substantially spherical in overall shape, many are not true spheres, as many are fragmented, or comprise unsmooth surfaces caused by additional silica and/or alumina.
The advantage with having a synthetic material is the uniformity and consistency between microparticles, thus making their behavior and the behavior of the resulting core matrix and building material more predictable. However, these advantages may not be significant enough to justify their use, as synthetic microparticles are extremely expensive to manufacture and can be cost prohibitive in many applications. The use of naturally occurring microparticles over synthetic ones to form a building material may depend on several different factors, such as the intended application, and/or the desired performance properties or characteristics. In some applications, naturally occurring microparticles may be preferred while in others a synthetic type may be more desirable. In one aspect, however, a combination of naturally occurring microparticles and synthetic microparticles can be utilized together in the core matrix. The combination of microparticles can be a homogeneous or heterogeneous distribution throughout the utility material.
Microparticles or microspheres can include an amount of air or other gasses within the hollow interior. Where possible, the composition of the gaseous material within the microparticle can optionally be selected so as to provide enhanced characteristics of the utility material. For example, the hollow interior can include an inert gas or other known insulating gasses to improve the insulating properties of the overall utility material. In one embodiment, a noble gas such as argon may be used.
In one specific example, a composition or core matrix can include from about 25 wt% to about 75 wt% of microparticles based on wet formulation. In another specific example, a composition or core matrix can include from about 50 wt% to about 60 wt% of microparticles based on wet formulation.
The present invention further comprises one or more binders operable to couple together the microparticles and to facilitate formation of a core matrix. In one exemplary embodiment, the binder comprises an inorganic binder, such as sodium silicates in one form or another. This may or may not be combined with an organic binder such as polyvinyl acetate copolymer or ethylene vinyl acetate. A vinyl acetate copolymer may be used, for example, to increase water resistance of a wallboard. In one specific example, a composition can include from about 20 wt% to about 60 wt% of sodium silicate binder based on wet formulation. In another specific example, a composition can include from about 35 wt% to about 45 wt% of sodium silicate binder based on wet formulation.
In many cases, the inorganic binder solution may comprise a ratio of sodium silicate to water of from about 1 :2 to about 2:1, although, higher water content may necessitate a longer curing time. In one embodiment, the ratio of sodium silicate to water is 1 :1. The sodium silicate may be pre-mixed and the solution provided in liquid form, or the sodium silicate may be in powder form and subsequently mixed with water.
The present invention further contemplates one or more constituents of the core matrix comprising a setting agent operable with the one or more binders to cause or enable the core matrix composition to initially set or harden under ambient temperature conditions. In other words, it is contemplated that one or more setting agents may be present within the core matrix composition that will result in a set or hardened core matrix, wherein at least a portion of the setting agent reacts to provide at least some cross linking that gives some structural integrity to the core matrix.
The present invention further comprises a setting agent operable to cause a composition or core matrix to set at a variety of temperatures, including ambient temperature. In one aspect, the setting agent can cause the composition to set in one hour or less. In one embodiment, a setting agent may be an isocyanate material. In a specific embodiment, the isocyanate material may be polymeric. In another aspect, the isocyanate material may be prepolymeric. A prepolymeric isocyanate is an isocyanate polymer chain having a reactive isocyanate terminal group, hi one example, isocyanate molecular weight may be from about 1000 to about 8000. hi another example, isocyanate molecular weight may be from about 2000 to about 5000.
Using a suitable setting agent such as isocyanate, the core matrix composition does not need to be subjected to elevated temperatures to effectuate initial setting or hardening, and may be cured to produce a suitable end product utility material that will possess the physical and performance properties desired for the particular type of utility material being manufactured.
In a specific example, isocyanate setting agent can be present in an amount from about 2% by weight to about 10% by weight of the total weight of the core matrix in wet mixture. In another specific example, isocyanate setting agent can be present in an amount from about 3% by weight to about 6% by weight of the total weight of the core matrix in wet mixture.
The ratio of binder to setting agent may range between 1 : 1 and 15: 1, and typically between 8:1 and 12:1, depending upon the desired characteristics of the core matrix. Obviously, these ratios may be varied to vary the characteristics of the core matrix. For example, to increase the strength and other characteristics of a utility material, the core matrix may comprise a lower ratio of binder to setting agent (e.g., between 5:1 and 7:1).
The ratio of binder to microparticles may vary depending upon the building material to be formed. A higher ratio of binder to microparticles will result in a building material that is more solid and dense than one with a smaller ratio. Indeed, a smaller ratio of binder to microparticles will result in a more porous building material.
The core matrix may further comprise a setting agent in addition to isocyanate, configured or intended to enhance the water resistant properties of the building material, and particularly the core matrix of the building material. In one exemplary embodiment, the setting agent may comprise Class C fly ash. In another exemplary embodiment, the setting agent may comprise zinc oxide, hi still another exemplary embodiment, the setting agent may comprise sodium fluorosilicate. Thus, Class C fly ash, zinc oxide, or sodium fluorosilicate may be used, for example, to increase water resistance of a wallboard.
The core matrix may further comprise one or more additives or fillers. Alternatively, the core matrix may be devoid of further additives and/or fillers. When present, these may be present in an amount between 0.01 and 50% by weight of the total weight of the core matrix in wet mixture. In one exemplary embodiment, the microparticles may be blended with expanded siliceous inorganic particles, such as perlite, to lower the density of the building material, decrease its weight, and reduce manufacturing costs. Specifically, it is contemplated that expanded siliceous inorganic particles may replace a portion of microparticles in an amount between 1% and 50% by weight of the total weight of the core matrix in wet mixture.
It should be noted that fly ash, of any type, can be utilized as a filler material, and/or optionally as a source of cenospheres. In one aspect, Class C fly ash can be one or the only source of microparticles. Class C fly ash can, in one aspect, be included in a core matrix in an amount ranging from about 0.5 wt% to about 50 wt%, in wet mixture form. In one aspect, it can be present in combination with synthetically made microparticles at a ratio of Class C fly ash to synthetic microparticles of about 1 : 15 to about 15: 1. In a further embodiment, Class C fly ash can be present in an amount of less than about 1/3 of the amount of microparticles. The Class C fly ash used can optionally include greater than about 80 wt% calcium aluminum silicates, and less than 2 wt% lime.
Without intending to be bound by any scientific theory, it is believed that upon mixing polymeric isocyanate with sodium silicate in water, a chemical reaction occurs that sets the composition and liberates CO2. The chemical reaction can also cause cross-linking to occur in the composition. It is believed that this cross-linking may be a result of the liberation of CO2. Thus, in one aspect of the present invention, polymeric cross-linking can occur during setting.
By cross-linking the binder(s), a stronger more permanent physical coupling occurs among the binder, thus better physically securing the microspheres. As such, the present invention contemplates using one or more means to effectively cross-link the binders. In one exemplary embodiment, the binders may be cross-linked by setting the core matrix. In another exemplary embodiment, the binders may be cross- linked by curing the core matrix. It should be noted that this cross-linking during curing procedure is in addition to cross-linking that occurs during setting. In another exemplary embodiment, the binders may be cross-linked by elevating the temperatures of the binders to a suitable temperature for a suitable period of time to effectuate polymerization and bonding. This may be done using conventional radiant heating methods, or it may be done using microwaves applied continuously or at various intervals, as well as with microwaves of different intensities. Depending on the binders used, it may be useful to add a limited amount of cross-linking agent to the binder formula in order to increase and/or control the cross-linking.
Cross-linking within a building material provides significant advantages over a building material having a composition that is not cross-linked. For example, with cross-linking, the binders are generally stronger, they do not absorb water as easily, and the connection between microp articles is much stronger. In addition, the building material does not weaken over time. Other advantages may be realized by those skilled in the art. Having said this though, there may be applications where cross- linking is not preferred, and where a non-bonded composition is better suited. This, of course, is contemplated herein.
Curing may facilitate additional polymerization, or cross-linking, beyond what occurred during setting. Curing of the core matrix may be active or passive. Active curing may be subjecting a composition or core matrix to elevated temperatures such as by heating. Passive curing may involve allowing a composition or core matrix to cure for a period of time without significant heating. Acceptable temperatures for curing may depend upon the material of the facing membranes. For example, an upper temperature may be limited by the facing membrane material to prevent damage to the material. In one embodiment, a facing membrane material may comprise paper. In this embodiment, a possible temperature for curing may range from between ambient temperature to about 400 degrees F. A useful temperature for curing, in this embodiment, may range from about ambient temperature to about 300 degrees F. A lower heating temperature, for example, may be about 125 degrees F, with a typical range being from about 150 degrees F to about 300 degrees F.
As noted, a variety of methods can be useful in forming utility materials as presently contemplated. In one aspect, a method of forming a wallboard utility material can include first placing a precut facing sheet, such as a wallboard paper white, face down in an appropriate mold. A formable composition can be formed by mixing microparticles, binder, and the setting agent. The formable composition can be spread over the paper in the mold and can be smoothed using any method. A second facing sheet, such as a brown wallboard paper, can be placed over the mixture. A flat mold lid can be placed on top of the paper and fastened in place. At this point, the core matrix composition may be allowed to initially set via the setting agent. To effectuate curing, the resulting wallboard product can optionally be subjected to elevated temperatures for a given period of time, such as by heating, or it may be allowed to cure under ambient temperature conditions, although this may take longer. Heat curing can occur at temperatures greater than ambient temperature, preferably less than temperatures required to cause damage or degradation of the paper, mold, or components of the formable composition. In one aspect, all components for the core matrix can be mixed together in a single step or in multiple separate steps in separate mixers. A variety of mixers can be utilized. In a specific embodiment, an auger can be utilized to mix the components for the core matrix. The mixture can be poured into a mold lined with a facing membrane, i.e. paper or aluminum, etc. The mold can be placed on a vibrating table so as to encourage proper spread of the mixture onto the membrane. Various other methods are known in the art to properly spread the mixture onto the membrane and are likewise contemplated herein. The second facing membrane can be placed on top of the leveled mixture and the mold can optionally be removed from the green or uncured wallboard. The green wallboard can then be positioned to effectuate initial setting or hardening of the core matrix. Once set, the green wallboard can then be further cured (e.g., such as being placed in an oven). This process can occur in batch, semi-batch, or continuous design.
In a continuous flow, a conveyor can move the green wallboard to and through an oven. Optionally, leveling rollers can be utilized to maintain the desired planar shape and thickness of the wallboard during drying. In one aspect, the presence of a metallic facing membrane can allow the method to include exposing the wallboard material to a temperature sufficient to effectuate even more rapid drying and curing of the core matrix. The parameters recited above can be appropriately modified for equipment, variations in core matrix composition, facing membrane types, etc. In the case of batch formation, individual wallboard can be formed and placed in a multi- rack drying oven. Temperature profiles for the oven rack can range depending on the composition of the core matrix and the facing sheets used.
As noted, a method of forming a wallboard material can include forming a core matrix including mixture of microparticles, sodium silicate binder, and an isocyanate setting agent. This may be followed by disposing the core matrix mixture between a first facing membrane and a second facing membrane and then setting the core matrix. In one aspect of the present invention, forming the core matrix may comprise forming a first mixture including microparticles and sodium silicate binder and forming a second mixture including microparticles and the isocyanate setting agent. This may be followed by mixing the first mixture with the second mixture to form the core matrix. In another aspect, the method may further include coating a contact surface of at least one of the facing membranes with a sodium silicate coating prior to disposing the core matrix between them. In another aspect, a wallboard building material comprises a core matrix disposed on a single side of a single facing sheet, such that the wallboard has one side with an exposed core matrix face. In yet another aspect, a wallboard building material comprises one or more facing membranes disposed within the core matrix so that the core matrix is on both sides of one or more interior facing membranes, such that the wallboard has two sides with exposed core matrix faces.
Once a core matrix is disposed on a facing membrane or between facing membranes, the core matrix can then be permitted to set or harden under normal ambient temperatures sufficient to form a wallboard material having the metallic facing membrane and the second facing membrane attached, adhered, bonded, or otherwise secured to the formed core matrix. The setting or hardening time may be completed in one hour or less, 30 minutes or less, or in 15 minutes or less, with curing (either under ambient temperature conditions or elevated temperature conditions if accelerated drying is desired) taking place thereafter to facilitate evaporation of water present within the core matrix and cross-linking of the binder(s) with the microparticles.
In one aspect, the method can be free from additional steps in-between the mixing, deposition, and setting steps; meaning, the components may be mixed, including water, immediately deposited between facing membranes, and immediately caused to set or harden. In one aspect, the wallboard can be cut before and/or after setting and curing. In a further aspect, one or more leveling rollers can be utilized prior to or during the setting and/or curing steps to maintain a desired shape and level to the wallboard.
In a semi-rigid, molded state, the microparticles, setting agent, binder, and any other components are pre-mixed together in such a way so as to form a semi-rigid utility material. The microparticles are caused to dry or harden, as well as to bond via the binder. In one aspect, the pre-mixed composition may then be placed into a mold and formed into a desired size and shape in accordance with one or more molding methods, examples of which are described below. In another aspect, the pre-mixed composition may be deposited or disposed onto a surface, such as a moving conveyor, and then cut or otherwise formed into the desired size and shape, either before or after the setting and/or curing steps.
The utility materials formed to comprise a semi-rigid makeup may be formed into panels of different size, shape, and thickness, such as panels that function as and that have physical characteristics comparable to conventional wallboard. Various backing or containing members may be utilized to support or provide a barrier to the composition. The density of the wallboard building material having the core composition just described can be between 0.4 g/ml and 0.6 g/ml. With reference to FIGS. 1 and 2, illustrated is a general perspective view and a detailed perspective view, respectively, of a wallboard building material in accordance with one exemplary embodiment of the present invention. As shown, the wallboard building material 10 is in panel form having a size of approximately 4 ft. in width, and 8 ft. in length, and approximately Vi inch thick, which is the same size as most conventional wallboard products. Of course, other sizes such 4 ft. by 12 ft. sizes, as well as different thicknesses is also contemplated. The wallboard building material 10 is shown as comprising a core matrix 14 disposed between opposing facing sheets or layers, namely first facing membrane 34 and second facing membrane 54. Of course, the wallboard building material may comprise a single facing membrane, having one side exposed as discussed above. Each of the first facing membrane 34 and the second facing membrane 54 may have a contact surface in contact with the core matrix 14. A contact surface may be any portion of a surface, or an entire surface, of a facing membrane. Before a core matrix 14 is disposed between opposing facing membranes (or on at least one facing membrane), a contact surface of a facing membrane may be designated as a surface that will come into contact with the core matrix, including an individual component or sub-mixture of select core matrix components, during the process of making a wallboard. For example, a contact surface of a facing membrane may be coated with a sodium silicate coating prior to disposing the core matrix between facing membranes. In another example, a contact surface of a facing membrane maybe coated with a sub- mixture of microp articles and sodium silicate binder or coated with a sub-mixture of microparticles and isocyanate setting agent, during the process of making a wallboard.
The core matrix 14 is comprised primarily of a plurality of microparticles, at least one binder and a setting agent (isocyanate setting agent) operable with the at least one binder, wherein the microparticles are at least bound or adhered together, and preferably bonded together, by the one or more binders and the setting agent to create a core matrix structure having a plurality of voids defined therein. The voids are formed from the point to point contact between the microparticles. With reference to FIG. 3, the wallboard building material may further comprise a reinforcing member operable with the core matrix configured to provide enhanced characteristics in one or more areas as compared with the exemplary wallboard building material of FIGS. 1 and 2. In the exemplary embodiment shown, the wallboard 110 comprises similar components as discussed above with respect to the wallboard 10 of FIGS. 1 and 2, only the wallboard 110 comprises an additional reinforcing member 174 disposed within the core matrix 114 (sandwiched therein). Reinforcing member 174 is configured to reinforce or enhance one or more properties or characteristics of the wallboard 110. For example, the reinforcing member 174 may be configured to reinforce against (or improve the resistance of) sound transmission, heat transfer or a combination of these. The reinforcing member 174 may also be configured to enhance the overall strength of the wallboard building material 110.
The reinforcing member 174 may comprise various types of materials, such as metals, woven or nonwoven fibers or fiber sheets, plastic films, etc., and may comprise any necessary thickness. In the exemplary embodiment shown, the reinforcing member 174 comprises an aluminum material disposed within the core matrix.
With reference to FIG. 4, illustrated is a wallboard building material 10, formed in accordance with one exemplary embodiment of the present invention, just prior to being installed on or hung from a stud wall 2. Specifically, wallboard building material 10 comprises the same components as that of FIGS. 1 and 2. It should be noted that no specialized installation techniques are required for installing or hanging the wallboard building material 10. The wallboard building material 10 may be installed in a similar manner as conventional drywall or other similar products. However, FIGS. 5 -A and 5-B illustrate other exemplary embodiments of wallboard building materials that may require one or more special installation techniques. These embodiments are discussed in detail below.
With reference to FIGS. 5-A and 5-B, illustrated are two different examples of coupling and sealing systems, each one being incorporated into a present invention wallboard building material, and each one being configured to couple adjacent wallboard panels together, and to seal or at least partially seal (e.g., not necessarily a strictly airtight seal) the adjacent wallboard panels. The coupling and sealing system is intended to reduce and/or eliminate the flanking path between the adjacent wallboard panels at the joint. The seal may be further enhanced or improved upon nailing, screwing, or otherwise securing the joint to a stud in a stud wall. Indeed, the overlap shown is intended to be positioned about a stud, but this may or may not always be possible. The seal functions to resist sound transmission through the joint, and also to resist heat transfer through the joint, by creating a more complex flanking path for heat transfer and sound transmission, hi other words, the flanking path is intended to be reduced and/or eliminated if possible by the coupling and sealing system of the present invention.
With specific reference to FIG. 5-A, illustrated are partial end views of a first wallboard building material 210-A and a second wallboard building material 210-B, each one formed in a manner as described herein. The first wallboard building material 210-A comprises a protruding or male configuration 218 formed within and along an edge of the core matrix 214-A, which is intended to align and mate with a corresponding recess or female configuration 222 formed within and along an edge of the core matrix 214-B of the second wallboard building material 210-B. The coupling or connection is designed to secure the first and second wallboard building materials 210-A and 210-B, respectively, in a proper position with respect to one another, and to permit the edges of the membranes 234-A and 254-A of the first wallboard building material 210-A to meet the membranes 234-B and 254-B of the second wallboard building material 210-B. The coupling system further helps to maintain proper positioning after installation. The coupling system may be formed about any of the edges of the wallboard building material.
FIG. 5-B illustrates partial end views of a first wallboard building material 310-A and a second wallboard building material 310-B, each one formed in a manner as described herein. The first wallboard building material 310-A comprises a notch 326 formed within and along an edge of the core matrix 314-A, with the surface parallel to the surface of the membranes 334-A and 354-A optionally comprising a nub 328, also formed from the core matrix 314-A. The notch 326 is intended to align and mate with a corresponding notch 330 formed in the second wallboard building material 310-B to couple together the first and second wallboard building materials. The notch 326 optionally comprises a recess 332 that receives nub 328 therein when the first and second wallboard building materials are secured or coupled to one another. The coupling system shown in FIG. 5-B is intended to perform a similar function as the coupling system shown in FIG. 5-A. It is noted that the coupling system is integrally formed into the core matrix during manufacture of the wallboard building material. The unique composition of the core matrix provides this capability. The particular size, shape, or configuration of the coupling system may vary, and may be formed in accordance with various different manufacturing techniques. It also contemplated that one or more sealing members or adhesives may be applied to the coupling system to enhance the sealing function achieved by coupling the two wallboard panels together.
With reference to FIG. 6, illustrated is a detailed perspective view of a wallboard building material formed in accordance with one exemplary embodiment of the present invention.
Utility materials can exist in a variety of forms. Much discussion herein is directed to the specific embodiment of wallboard. However, it should be noted that the principles, compositions, and methods discussed apply to a variety of forms of utility materials, and should be interpreted as such. As shown in FIG. 6, the building material 710 is in panel form, similar to a wallboard panel, having a size of approximately 4 ft. in width, and 8 ft. in length, which is the same size as most conventional wallboard products. Of course, other sizes such 4 ft. by 8 ft. sizes, as well as different thicknesses is also contemplated. The building material 710 is shown as comprising a core matrix 714 disposed about a single facing sheet or layer, namely facing membrane 734. The other side 718 of the building material 710 is exposed, or rather, the other side of the core matrix 714 is exposed, thus exposing a portion of the configuration of microparticles, binder and setting agent. The exposed surface of the core matrix provides and defines a rough, porous surface that is designed and intended to better attenuate sound. The exposed side 718 of the core matrix 714 is intended to face inward as the building material is installed or mounted to a structure, such as a stud wall, with the facing membrane 734 facing out.
The density of the building material having the core composition just described is generally between 0.4 g/ml and 0.6 g/ml, although such density can vary greatly depending on the selection and amount of each component, as well as the presence or absence of foaming.
The facing membrane 34, and/or 54 shown in FIG. 2, may comprise many different types of materials or combination of materials, and may comprise different properties. In one exemplary embodiment, facing membranes 34 and/or 54 can each be independently selected. One or both facing membranes can comprises a paper material similar to that found on various wallboard products, such as drywall or the wallboard incorporated by reference herein, as noted above. In another exemplary embodiment, the facing membrane may comprise metal or a metal alloy. The metal may be quilted, corrugated or otherwise comprise one or more nonplanar surface configurations. In a further embodiment, one facing membrane can comprise or consist essentially of aluminum or quilted aluminum. In such cases, the aluminum may have a thickness ranging from about .002 in. to about 0.010 in, and more commonly between 0.004 in. and 0.005 in. Optionally, the metallic facing membrane, e.g. an aluminum facing membrane, can be embossed or otherwise include a three- dimensional pattern on the surface, or throughout the entire length of the membrane.
As the final product is desirably a cohesive one, in one aspect, the core material and facing sheet of the wallboard can be optimized for proper or superior adhesion, thus ensuring the facing sheet will remain secured to the core material. As such, additional binder or binders at the surface level can be utilized to improve adhesion of a facing sheet to the core matrix. Alternatively, a different adhesive agent can be utilized to improve adhesion of a facing sheet to the core matrix.
In certain applications, it may be desirable to eliminate the facing sheet altogether. Specifically, to enhance the fire resistant properties of the building material, the facing sheet, particularly if paper, may be eliminated. The core matrix may be configured to be self-supporting, meaning that the building material does not require a facing sheet to maintain its shape and integrity.
FIG. 6 further illustrates the exposed side 718 of the core matrix as comprising a multi-elevational surface configuration. Such a configuration may be utilized to reduce weight. Additionally, this configuration may be designed in such a way that enhances the sound attenuation properties of the building material. The purpose of providing a multi-elevational surface configuration formed about one surface, particularly the exposed surface, of the core matrix is at least threefold - 1) to reduce weight, 2) to enhance the sound attenuation or damping properties of the building material, namely to ensure acoustic isolation and absorption over a wide range of frequencies, and 3) to enhance the flex strength of the building material by eliminating shear lines. As will be described below, many different multi-elevational surface configurations are contemplated herein. Those skilled in the art will recognize the benefits of providing a series of peaks and valleys about a surface to create different surfaces located in different elevations, as well as different surfaces oriented on different inclines, particularly for the specific purpose of attenuating sound. Sound waves incident on these different elevational and/or oriented surfaces are more effectively attenuated. In the specific embodiment shown, the multi-elevational surface configuration comprises a waffle pattern, with a plurality of protruding members 718, having a square or rectangular cross-section, defining a plurality of recesses 726. This series of peaks and valleys effectively creates a plurality of surfaces (in this case horizontal surfaces 730 and 734) that are located in different elevations about the overall surface of the core matrix 714. In addition, the protruding members 718 maybe configured to provide surfaces oriented at different angles (in this case, the protruding members 718 also define several vertically oriented surfaces 738).
It is further contemplated that a separate mesh facing sheet may or may not be disposed over the exposed multi-elevational surface of the core matrix 714. If used, the mesh facing sheet is preferably configured to be flexible to conform to the multi- elevational surface configuration. The mesh facing sheet may be made from glass, plastics (e.g., extruded plastics), or other materials, depending upon the particular application and need.
FIGS. 6 and 14 further illustrate the building material 710 as comprising a plurality of cavities or air pockets 746 strategically formed and located throughout the core matrix 714, and designed to reduce the overall weight of the building material without significantly affecting the strength or other properties of the building material. Preferably, the cavities 746 are randomly located throughout the core matrix 714, but they may also be arranged in a pre-determined pattern. The cavities 746 may be formed during the manufacture of the building material. Essentially, the cavities 746 function to define a plurality of voids or air pockets within the core matrix 714 at various locations. The cavities 746 maybe sized to comprise a volume between about 0.2 and about 200 cm , and preferably between about 5 and about 130 cm . These not only help to reduce weight, but also help to increase the overall R value due to the dead air space. In addition, these help to further attenuate sound as these provide additional surfaces that function to absorb sound waves rather than transmit them.
With reference to FIGS. 7-A and 7-B, shown is a building material formed in accordance with another exemplary embodiment of the present invention. The building material 810 is similar in many respects to the building material 810 discussed above and shown in FIG. 6. However, building material 810 comprises a lath 854 disposed or sandwiched within the core matrix 814. The lath 854 comprises a plurality of intersecting members 856 forming a grid having a plurality of openings 858. The lath 854 functions to provide support and stability to the core matrix 814, as well as additional strength. In addition, the lath 854 increases the mass of the building material 810, which reduces the potential for vibration, thus contributing to the sound attenuation properties of the building material 810. The lath 854 may comprise many different types and configurations, with the grid and openings being of different sizes and configurations. The lath 854 shown in FIG. 7 is not intended to be limiting in any way.
In one aspect, the lath 854 may comprise a metal, fiberglass, or plastic mesh or mesh-like material. This reinforcing lath material provides strength to the building material 810, and further supports the microparticles. The lath 854 may also be made from glass, plastics (e.g., extruded plastics), or other materials, depending upon the particular application and need.
With reference to FIGS. 8-10, illustrated is a building material 910 formed in accordance with another exemplary embodiment of the present invention. In this embodiment, the building material 910 comprises a core matrix 914 having a first surface 918. Formed in the first surface 918 is a multi-elevational or nonplanar surface configuration in the form of a repeating pattern of pillow-type protrusions, thus providing multiple different surfaces or surface areas in multiple different elevations. The protrusions may be any desired size, configuration, and height. Therefore, those shown in the drawings are intended to be merely exemplary.
With reference to FIG. 11, illustrated is a side view of the building material 710 of FIG. 6, having a multi-elevational surface configuration in the form of a repeating waffle-type pattern. The waffle-type configuration extends between the perimeter edges of the building material, and defines a plurality of protrusions 722 and recesses 726. FIG. 9 illustrates a cross-sectional view of a building material wherein the building material 710 comprises a plurality of strategically formed and located cavities or voids 746 in the core matrix 714.
FIG. 12 illustrates a detailed side view of another exemplary building material 1010 comprising a core matrix 1014 having a first surface 1018, wherein the first surface 1018 has formed therein a multi-elevational surface configuration comprising a repeating pattern of first protrusions 1022 in the form of pyramids or cones, and a repeating pattern of second protrusions 1024 having an arbitrary shape. The second protrusions 1024 are shown as comprising a primary base protrusion having a square cross -section, upper secondary protrusions 1023, and lateral secondary protrusions 1025, each having a pyramid or cone shape. First and second protrusions 1022 and 1024 define recesses 1026. While the present invention is not intended to be limited to any particular shape of protrusions, FIG. 12 illustrates that arbitrary shapes are at least contemplated.
FIG. 13 illustrates a detailed side view of another exemplary building material 1110 comprising a core matrix 1114 having a first surface 1118, wherein the first surface 1118 has formed therein a multi-elevational surface configuration comprising a repeating pattern of first protrusions 1122 and recesses 1126, wherein these form an egg carton-type pattern.
FIGS. 8-13 illustrate several different multi-elevational surface configurations. These, however, are not meant to be limiting in any way. Indeed, one skilled in the art will recognize other configurations and/or patterns that may be used to accomplish the designs of the present invention.
Referring now to FIG. 15, illustrated is a building material formed in accordance with another exemplary embodiment. In this particular embodiment, the building material 1210 comprises a core matrix 1214, a metal lath 1254 disposed or sandwiched within the core matrix 1214, and a facing sheet 1234 comprised of tar paper. With this configuration, the building material 1210 may be used as a finishing material on the exterior of residential or commercial structures, replacing stucco. The building material 1210, comprising pre-formed panels, can be mounted or secured to the exterior walls 1202 of a structure, say a residential home, much in the same way a wallboard is mounted or secured to the interior walls of a home. Once secured in place, a stucco finish 1204 commonly known in the art may be applied to the panels to create a finished look. The stucco finish can be applied so as to sufficiently conceal any seams or gaps between adjacent building material panels. Some obvious advantages that result from providing exterior finishing panels is the elimination of the labor intensive task of securing metal lath to the exterior walls, subsequently applying plaster over the metal lath, and then waiting several days for the plaster to dry and set prior to being able to apply the stucco finish. With the pre-formed building panels shown herein, installers can mount the panels and apply the stucco finish immediately, thus significantly reducing labor and costs.
It is contemplated that such a building material may be applied to shear panels, such as oriented strand board, to shear panels formed after the manner of the present invention, or directly to a stud frame, wherein the building panel may function as the shear panel and also receive the stucco finish directly thereto, thus eliminating the need for a separate shear panel.
When the metal facing sheet is used, the heating elements can be configured to concentrate a majority of the heat through the metal facing sheet to the core matrix. In this manner, the heat is better received into the core matrix, steam is removed from the core matrix primarily through the second facing sheet, typically paper, and large steam pockets are not formed.
Utility materials as described herein exhibit superior qualities to many utility materials currently available. Furthermore, the superior qualities co-exist, where a material may exhibit both mold resistance and enhanced acoustic properties simultaneously. Wallboards formed of the utility materials are typically lighter than conventional gypsum wallboard by 20% to 30%. An installed R value can be up to about 19. Noise attenuation can be up to about 50 db, depending on the frequency for a /4 inch thick piece of wallboard. The core matrix will not grow mold. Wallboard is water resistant and is still hard after 2 weeks of continuous submersion under water. The material can be formulated to be fire resistant. Wallboard exhibits strong flexural strength up to two times that of conventional gypsum wallboard (e.g., 280 lbs vs. 140 lbs). Furthermore, the wallboard can withstand impacts without crumbling or displacement in surrounding areas such as a corner. Various industry considerations for wallboard performance include, but are not limited to, surface finish, snap and dust, flexural strength, nail pull resistance, dimpling, edge crush, weight, mold growth, water resistance, fire resistance, and R value.
EXAMPLES
The following examples illustrate embodiments of the invention that are presently known. Thus, these examples should not be considered as limitations of the present invention, but are merely in place to teach how to make the best-known compositions and forms of the present invention based upon current experimental data. Additionally, some experimental test data is included herein to offer guidance in optimizing compositions and forms of the utility material. As such, a representative number of compositions and their method of manufacture are disclosed herein. EXAMPLE 1 - SAMPLE WALLBOARD UTILITY MATERIAL
In one specific example (producing a sample core matrix having dimensions of 8" x 9" x 1A"), the core matrix composition is as follows: the microp articles is 56 wt% of wet core matrix, the sodium silicate binder is 40 wt% of wet core matrix, and the isocyanate setting agent is 4 wt% of wet core matrix. In this example, the core matrix is formulated to comprise a two-part mixture. The first part comprising 150 grams microparticles initially mixed with 140 grams sodium silicate Type O from PQ Corporation. The second part comprising 50 grams microparticles (e.g., cenospheres) initially mixed with 14 grams "A" side from Reactamine JS 2:1 of Reactamine Technology, LLC, which is an isocyanate prepolymer. These two mixtures, once each individually blended, were then blended together and deposited onto one side of a sodium silicate-coated wallboard face paper. A waffle pattern was then pressed into the upper surface of the core matrix composition. A second sodium silicate-coated paper facing sheet was then deposited over the core matrix composition, which second paper facing sheet was held in place under pressure for between 5 -10 minutes, which allowed the core matrix composition to initially set and harden under ambient temperature conditions. The sample was then placed onto a drying rack and allowed to cure under ambient temperature conditions for a 24 hour period.
The foregoing detailed description describes the invention with reference to specific exemplary embodiments. However, it will be appreciated that various modifications and changes can be made without departing from the scope of the present invention as set forth in the appended claims. The detailed description and accompanying drawings are to be regarded as merely illustrative, rather than as restrictive, and all such modifications or changes, if any, are intended to fall within the scope of the present invention as described and set forth herein.
More specifically, while illustrative exemplary embodiments of the invention have been described herein, the present invention is not limited to these embodiments, but includes any and all embodiments having modifications, omissions, combinations (e.g., of aspects across various embodiments), adaptations and/or alterations as would be appreciated by those in the art based on the foregoing detailed description. The limitations in the claims are to be interpreted broadly based on the language employed in the claims and not limited to examples described in the foregoing detailed description or during the prosecution of the application, which examples are to be construed as non-exclusive. For example, in the present disclosure, the term
"preferably" is non-exclusive where it is intended to mean "preferably, but not limited to." Any steps recited in any method or process claims may be executed in any order and are not limited to the order presented in the claims. Means-plus-function or step- plus-function limitations will only be employed where for a specific claim limitation all of the following conditions are present in that limitation: a) "means for" or "step for" is expressly recited; and b) a corresponding function is expressly recited. The structure, material, or acts that support the means-plus function are expressly recited in the description herein. Accordingly, the scope of the invention should be determined solely by the appended claims and their legal equivalents, rather than by the descriptions and examples given above.
What is claimed and desired to be secured by Letters Patent is:

Claims

1. A method of making a wallboard having a setting time of less than or equal to one hour, comprising: forming a core matrix including a mixture of a plurality of microp articles, a sodium silicate binder, and an isocyanate setting agent; disposing the core matrix between a first facing membrane and a second facing membrane; and setting the core matrix.
PCT/US2009/063323 2008-11-04 2009-11-04 Utility materials incorporating a microparticle matrix formed with a setting system WO2010054029A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US19855408P 2008-11-04 2008-11-04
US61/198,554 2008-11-04

Publications (2)

Publication Number Publication Date
WO2010054029A2 true WO2010054029A2 (en) 2010-05-14
WO2010054029A3 WO2010054029A3 (en) 2010-08-26

Family

ID=42153537

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2009/063323 WO2010054029A2 (en) 2008-11-04 2009-11-04 Utility materials incorporating a microparticle matrix formed with a setting system

Country Status (2)

Country Link
US (6) US8591677B2 (en)
WO (1) WO2010054029A2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111075107A (en) * 2019-12-31 2020-04-28 同济大学 Assembled combined concrete external wall board and preparation and installation method thereof

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090239429A1 (en) * 2007-03-21 2009-09-24 Kipp Michael D Sound Attenuation Building Material And System
CA2681528C (en) * 2007-03-21 2018-10-23 Ashtech Industries, Llc Utility materials incorporating a microparticle matrix
US8445101B2 (en) 2007-03-21 2013-05-21 Ashtech Industries, Llc Sound attenuation building material and system
US9388568B2 (en) * 2007-04-06 2016-07-12 Pacific Coast Building Products, Inc. Acoustical sound proofing material with improved fracture characteristics and methods for manufacturing same
US8397864B2 (en) 2007-04-24 2013-03-19 Serious Energy, Inc. Acoustical sound proofing material with improved fire resistance and methods for manufacturing same
US9387649B2 (en) * 2007-06-28 2016-07-12 Pacific Coast Building Products, Inc. Methods of manufacturing acoustical sound proofing materials with optimized fracture characteristics
US7908818B2 (en) * 2008-05-08 2011-03-22 Serious Materials, Inc. Methods of manufacturing acoustical sound proofing materials with optimized fracture characteristics
US8591677B2 (en) * 2008-11-04 2013-11-26 Ashtech Industries, Llc Utility materials incorporating a microparticle matrix formed with a setting agent
US8015848B2 (en) * 2009-01-22 2011-09-13 Electrolux Home Products, Inc. Acoustic panel
US8806832B2 (en) 2011-03-18 2014-08-19 Inotec Global Limited Vertical joint system and associated surface covering system
US10001442B2 (en) * 2013-06-13 2018-06-19 The Regents Of The University Of California Optical fiber-based hybrid SERS platform for in vivo detection of bio-molecules
USD854193S1 (en) * 2017-02-16 2019-07-16 Huntsman International Llc Foam board with facer
USD843019S1 (en) * 2017-02-16 2019-03-12 Huntsman International Llc Foam board with facer
USD844859S1 (en) * 2017-02-16 2019-04-02 Huntsman International Llc Foam board with facer
US11339569B2 (en) * 2017-04-18 2022-05-24 Nexgen Composites Llc Unitized construction panel
EP3470599B1 (en) * 2017-10-13 2019-09-11 SWISS KRONO Tec AG Osb board and use of same
BE1027024B1 (en) * 2019-02-04 2020-09-02 Flooring Ind Ltd Sarl Floor panel and method for its manufacture
DE102019116321A1 (en) * 2019-06-14 2020-12-17 Technische Universität Clausthal Method for producing a sandwich structure
CN112252578B (en) * 2020-11-06 2022-05-20 绍兴宝城建筑工业化制造有限公司 Precast concrete wallboard and assembling method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0475302A1 (en) * 1990-09-10 1992-03-18 Manville Corporation Lightweight building material board
JPH11322880A (en) * 1998-05-18 1999-11-26 Aren:Kk Setting agent for roadbed crushed-stone and stabilization of roadbed
WO2006018904A1 (en) * 2004-08-19 2006-02-23 Minoru Tanaka Earth wall board and method for molding earth wall board
JP2006083048A (en) * 2004-09-15 2006-03-30 Nanbu:Kk Inorganic foamed board

Family Cites Families (375)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1881420A (en) 1930-03-10 1932-10-04 Celotex Company Wallboard and joint made therewith
US1914345A (en) * 1932-07-07 1933-06-13 United States Gypsum Co Wall construction
US3045709A (en) 1959-01-21 1962-07-24 Insul Fil Co Inc Protective casing for pipes and the like
US3501419A (en) 1962-06-07 1970-03-17 Tee Pak Inc Cellulose microspherical product
US3440130A (en) * 1965-11-12 1969-04-22 Dow Chemical Co Large celled material
US3528846A (en) 1967-05-22 1970-09-15 Armstrong Cork Co Back-coated ceramic acoustical product and method of manufacture
US3769770A (en) 1969-01-23 1973-11-06 Sanders Nuclear Corp Thermal super insulation
US3703394A (en) 1969-09-19 1972-11-21 Champion Int Corp Form board coated with a porous polymer film and a form oil,said film characterized by having solid particles distributed therethrough
US3697422A (en) 1970-11-23 1972-10-10 Us Navy Intumescent fillers for paints
US3781170A (en) 1971-07-15 1973-12-25 Kureha Chemical Ind Co Ltd Lightweight metal composite material and process for producing same
US3782985A (en) 1971-11-26 1974-01-01 Cadcom Inc Lightweight,high strength concrete and method for manufacturing the same
GB1410043A (en) 1972-10-19 1975-10-15 Foseco Trading Ag Refractory heat insulating materials
US4083159A (en) 1973-10-29 1978-04-11 Hitco Structural sound absorbing panel for underwater use and methods of making same
US4079162A (en) 1974-03-20 1978-03-14 Aim Associates, Inc. Soundproof structure
US4025686A (en) 1975-06-26 1977-05-24 Owens-Corning Fiberglas Corporation Molded composite article and method for making the article
US3995086A (en) 1975-06-27 1976-11-30 Mark Plunguian Shaped articles of hydraulic cement compositions and method of making same
US4090887A (en) 1975-11-25 1978-05-23 E. I. Du Pont De Nemours And Company Pigmented microporous silica microspheres produced by a water in oil emulsion
US4074482A (en) 1976-01-09 1978-02-21 Klahr Carl N Radiation reflecting building
GB1514239A (en) * 1976-12-07 1978-06-14 Nat Res Dev Fibre-reinforced composites
US4077921A (en) 1977-01-19 1978-03-07 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Sprayable low density ablator and application process
CH629274A5 (en) 1977-02-28 1982-04-15 Augusto Capecchi Plate for indicating electrically arrival of a swimmer in swimming races
US4257710A (en) * 1978-02-08 1981-03-24 Saint Gobain Industries Continuous process mixing of pulverized solids and liquids and mixing apparatus
US4303061A (en) 1978-08-28 1981-12-01 Torobin Leonard B Solar energy collector having hollow microspheres
US4303433A (en) 1978-08-28 1981-12-01 Torobin Leonard B Centrifuge apparatus and method for producing hollow microspheres
JPS57140642A (en) 1978-08-28 1982-08-31 Torobin Leonard B Minute sphere of hollow inorganic film forming material
GB2041384A (en) * 1979-02-10 1980-09-10 Pennington J Improvements in and Relating to Board Products and Mouldings
DE3068776D1 (en) 1979-04-20 1984-09-06 Secr Defence Brit Resin materials, their use and article thereof
US4303729A (en) 1979-07-20 1981-12-01 Torobin Leonard B Hollow plastic microspheres
US4415512A (en) 1979-07-20 1983-11-15 Torobin Leonard B Method and apparatus for producing hollow metal microspheres and microspheroids
US4303736A (en) 1979-07-20 1981-12-01 Leonard Torobin Hollow plastic microspheres
US4303730A (en) 1979-07-20 1981-12-01 Torobin Leonard B Hollow microspheres
US4303732A (en) * 1979-07-20 1981-12-01 Torobin Leonard B Hollow microspheres
US4303431A (en) 1979-07-20 1981-12-01 Torobin Leonard B Method and apparatus for producing hollow microspheres
US4303603A (en) 1979-07-20 1981-12-01 Torobin Leonard B Method and apparatus for producing hollow plastic microspheres
US4760296A (en) 1979-07-30 1988-07-26 General Electric Company Corona-resistant insulation, electrical conductors covered therewith and dynamoelectric machines and transformers incorporating components of such insulated conductors
US4303731A (en) 1979-08-24 1981-12-01 Torobin Leonard B Compressed gaseous materials in a contained volume
US4292348A (en) 1980-01-14 1981-09-29 Johnson Matthey, Inc. Low density ceramic insulating
US4357436A (en) 1980-06-02 1982-11-02 Rm Industrial Products Company, Inc. Composite insulating material and process
GB2081246B (en) 1980-07-25 1984-03-14 Rolls Royce Thermal barrier coating composition
US4377414A (en) 1980-09-04 1983-03-22 A/S Niro Atomizer Shaped cementitious products
DE3100626C2 (en) 1981-01-12 1985-05-15 Schmittmann, Hans-Bernd, Dipl.-Chem. Dr.Rer.Nat., 5620 Velbert Flame-retardant plastics, especially those which can be used as building materials or the like, processes for their production and their use as components
US4568389A (en) 1981-03-18 1986-02-04 Torobin Leonard B Shaped form or formed mass of hollow metal microspheres
US4582534A (en) 1981-03-18 1986-04-15 Torobin Leonard B Metal microspheres, filamented hollow metal microspheres and articles produced therefrom
GB2105341A (en) 1981-09-11 1983-03-23 Shell Int Research Flame retardant thermally insulating material
CA1166392A (en) 1981-12-07 1984-04-24 Otto G. Udvardy Thermoplastic fast-curing powdered resol and novolac resin mixtures
CA1200039A (en) 1981-12-26 1986-01-28 Hiroaki Koyama Resin composition containing granular or powdery phenol-aldehyde resin
US4441944A (en) 1981-12-31 1984-04-10 Pmp Corporation Building board composition and method of making same
US4446177A (en) 1982-03-12 1984-05-01 Munoz George L Reinforced plastic product
US4594368A (en) 1982-06-22 1986-06-10 University Of Dayton Phenol-formaldehyde intumescent coating composition and coating prepared therefrom
US4424196A (en) 1982-06-29 1984-01-03 United States Gypsum Company Phosphohemihydrate process for purification of gypsum
US4659385A (en) 1982-08-23 1987-04-21 Costopoulos Nick G Building material manufacturing from fly ash
US4731389A (en) 1982-09-03 1988-03-15 Air Krete, Inc. Foam insulation and process for producing the same
US4644014A (en) 1982-09-03 1987-02-17 Thomson Donald W Foamed insulation and process for producing the same
US4666960A (en) 1982-12-16 1987-05-19 Spain Raymond G Fire retardant coating for combustible substrates
FR2543536B1 (en) 1983-03-28 1987-05-15 Inst Francais Du Petrole MATERIAL OF HIGH MECHANICAL STRENGTH AND NEARBY DENSITY OF THE UNIT, ITS MANUFACTURE AND ITS USES
US4476258A (en) * 1983-03-30 1984-10-09 National Research Development Corporation Energy absorbing polyurethane compositions
US4504320A (en) 1983-09-26 1985-03-12 Research One Limited Partnership Light-weight cementitious product
JPS6071881A (en) 1983-09-28 1985-04-23 松下電器産業株式会社 Heat-insulating structure
US4502901A (en) 1983-10-19 1985-03-05 National Gypsum Company Manufacture of gypsum board from FGD gypsum
US4687752A (en) 1984-06-21 1987-08-18 Resco Products, Inc. Medium weight abrasion-resistant castable
US4623390A (en) * 1984-07-02 1986-11-18 Old Western Paints, Inc. Insulating paint for interior and exterior of buildings and method of making same
US4741782A (en) 1984-11-07 1988-05-03 Resource Technology, Inc. Process for forming a light-weight aggregate
FR2573064B1 (en) 1984-11-15 1991-10-25 Schlumberger Cie Dowell IMPROVED LIGHT-DUTY CEMENT MILK COMPOSITION FOR CEMENTING OIL WELLS AND GASES
DE3600574A1 (en) 1985-01-11 1986-07-17 Hitachi Metals, Ltd., Tokio/Tokyo EXHAUST DEVICE AND METHOD FOR THEIR PRODUCTION
GB8501196D0 (en) 1985-01-17 1985-02-20 Webco Ltd Pipelines
US4632876A (en) 1985-06-12 1986-12-30 Minnesota Mining And Manufacturing Company Ceramic spheroids having low density and high crush resistance
GB8519654D0 (en) 1985-08-05 1985-09-11 Shell Int Research Insulation material
US4798762A (en) 1985-08-14 1989-01-17 Toray Industries, Inc. Laminate board containing uniformly distributed filler particles and method for producing the same
US4661301A (en) 1985-08-14 1987-04-28 Toray Industries, Inc. Method for producing laminate board containing uniformly distributed filler particles
NO158499C (en) 1985-09-03 1988-09-21 Elkem As HYDRAULIC CEMENT SUSPENSION.
US4661533A (en) 1985-10-28 1987-04-28 The Dow Chemical Company Rigid polyurethane modified polyisocyanurate containing fly ash as an inorganic filler
GB2182323B (en) 1985-11-01 1989-10-25 Coal Ind Settable compositions and methods of use thereof
CH667096A5 (en) 1985-11-22 1988-09-15 Sika Ag METHOD FOR PRODUCING A BUILDING AND / OR CONSTRUCTION MATERIAL.
US4671994A (en) 1986-02-10 1987-06-09 Materials Technology Corporation Method for producing fiber reinforced hollow microspheres
US5218016A (en) 1986-05-16 1993-06-08 Institut Francais Du Petrole Filler and floatability material manufacturing process and tubular units that incorporate this material
FR2598713B1 (en) 1986-05-16 1988-11-10 Inst Francais Du Petrole NEW FILLING AND BUOYANCY MATERIAL. MANUFACTURING METHOD AND TUBULAR ASSEMBLIES INCORPORATING SUCH MATERIAL
US4681788A (en) 1986-07-31 1987-07-21 General Electric Company Insulation formed of precipitated silica and fly ash
US4839394A (en) 1986-10-30 1989-06-13 Watercolour Bath Products, Inc. Fillers for use in casting marble products
US4686244A (en) 1986-12-17 1987-08-11 Dow Corning Corporation Intumescent foamable compositions
US4798753A (en) 1986-12-19 1989-01-17 General Electric Company Insulating panels containing insulating powders and insulating gases
DE3702667A1 (en) 1987-01-27 1988-08-04 Mankiewicz Gebr & Co SHAPE DIMENSIONS
US4940676A (en) 1987-05-15 1990-07-10 Board Of Regents, The University Of Texas System Ceramic compositions and methods employing same
US4885203A (en) 1987-07-01 1989-12-05 Applied Ultralight Technologies, Inc. Lightweight fired building products
US4861097A (en) 1987-09-18 1989-08-29 Essex Composite Systems Lightweight composite automotive door beam and method of manufacturing same
US4901500A (en) 1987-09-18 1990-02-20 Essex Composite Systems Lightweight composite beam
GB8722603D0 (en) 1987-09-25 1987-11-04 Shell Int Research Thermally insulated pipeline
CN1017881B (en) 1987-12-16 1992-08-19 库特·赫尔德·法布里肯特 Apparatus and method for manufacturing wood plank
SE463513B (en) 1988-07-21 1990-12-03 Eka Nobel Ab COMPOSITION FOR PREPARING A HEAT-INSULATING CERAMIC COATING ON A METAL, PROCEDURE FOR ITS PREPARATION, APPLICATION OF THE SAME AND EXHAUST PIPE PROCEDURED WITH A COATING OF SUCH A COMPOSITION
US4904709A (en) 1988-09-28 1990-02-27 Polymer Plastics Corp. Textured exterior surface treatment
US5134179A (en) 1988-11-25 1992-07-28 Armstrong World Industries, Inc. Composite fiberboard and process of manufacture
US5217552A (en) 1989-02-22 1993-06-08 Toyo Linoleum Company Limited Method of installing tile-like floor material
US5019311A (en) 1989-02-23 1991-05-28 Koslow Technologies Corporation Process for the production of materials characterized by a continuous web matrix or force point bonding
US5492696A (en) 1989-04-14 1996-02-20 The Government Of The United States Of America As Represented By The Secretary Of The Navy Controlled release microstructures
DE58904362D1 (en) 1989-06-22 1993-06-17 Freudenberg Carl Fa METHOD FOR PRODUCING A LATENT REACTIVE, PASTOUS MOLD.
US4960184A (en) 1989-11-09 1990-10-02 Bruce Woodward Sound absorbing structure
US5091256A (en) 1989-12-27 1992-02-25 General Electric Company Polyphenylene ether foams from low I.V. polyphenylene ether expandable microparticles
US5126192A (en) 1990-01-26 1992-06-30 International Business Machines Corporation Flame retardant, low dielectric constant microsphere filled laminate
DE4002961C1 (en) 1990-02-01 1991-03-07 Fa. Carl Freudenberg, 6940 Weinheim, De
JPH0413770A (en) 1990-05-01 1992-01-17 Junkosha Co Ltd Insulating material and production thereof
US5064266A (en) 1990-07-05 1991-11-12 Photonic Integration Research, Inc. Circular channel waveguides and lenses formed from rectangular channel waveguides
US5342566A (en) 1990-08-23 1994-08-30 Carl Schenck Ag Method of manufacturing fiber gypsum board
US5256222A (en) 1990-09-10 1993-10-26 Manville Corporation Lightweight building material board
US5098577A (en) 1991-01-09 1992-03-24 Pq Corporation Method for contacting active material with liquids and separating same
US5196240A (en) 1991-03-18 1993-03-23 Stockwell Gregg M Seamless bodysuit and a method for fabricating same
GB9106809D0 (en) 1991-04-02 1991-05-22 Dow Corning Sa Silicone foams
US5211238A (en) 1991-11-08 1993-05-18 Atlantic Richfield Company Method using micro-sphere cement slurries for deviated wells
DK17592A (en) 1992-02-13 1993-08-14 Inge Bodil Elmstroem Soerensen PLASTIC PLATE FOR SOUND ABSORPTION AND PROCEDURE FOR PREPARING SUCH A PLASTIC PLATE
US5393794A (en) 1993-04-19 1995-02-28 Sperber; Henry Insulation material and method using fly ash
US5228494A (en) 1992-05-01 1993-07-20 Rohatgi Pradeep K Synthesis of metal matrix composites containing flyash, graphite, glass, ceramics or other metals
US5679145A (en) 1992-08-11 1997-10-21 E. Khashoggi Industries Starch-based compositions having uniformly dispersed fibers used to manufacture high strength articles having a fiber-reinforced, starch-bound cellular matrix
US5549859A (en) 1992-08-11 1996-08-27 E. Khashoggi Industries Methods for the extrusion of novel, highly plastic and moldable hydraulically settable compositions
US5582670A (en) 1992-08-11 1996-12-10 E. Khashoggi Industries Methods for the manufacture of sheets having a highly inorganically filled organic polymer matrix
US5810961A (en) 1993-11-19 1998-09-22 E. Khashoggi Industries, Llc Methods for manufacturing molded sheets having a high starch content
EP0662029A4 (en) 1992-08-11 1998-04-01 Khashoggi E Ind Hydraulically settable containers.
US5683772A (en) 1992-08-11 1997-11-04 E. Khashoggi Industries Articles having a starch-bound cellular matrix reinforced with uniformly dispersed fibers
US5545297A (en) 1992-08-11 1996-08-13 E. Khashoggi Industries Methods for continuously placing filaments within hydraulically settable compositions being extruded into articles of manufacture
US5506046A (en) 1992-08-11 1996-04-09 E. Khashoggi Industries Articles of manufacture fashioned from sheets having a highly inorganically filled organic polymer matrix
US5830548A (en) 1992-08-11 1998-11-03 E. Khashoggi Industries, Llc Articles of manufacture and methods for manufacturing laminate structures including inorganically filled sheets
US5631097A (en) 1992-08-11 1997-05-20 E. Khashoggi Industries Laminate insulation barriers having a cementitious structural matrix and methods for their manufacture
US5508072A (en) 1992-08-11 1996-04-16 E. Khashoggi Industries Sheets having a highly inorganically filled organic polymer matrix
US5795102A (en) 1992-08-12 1998-08-18 Corbishley; Terrence Jeffrey Marine and submarine apparatus
US5225124A (en) 1992-08-13 1993-07-06 The United States Of America As Represented By The Secretary Of The Navy Method for in-situ casting of fire barrier silicone sheets onto acoustic tiles
US6183852B1 (en) 1992-09-15 2001-02-06 The Boeing Company Refractory fibrous ceramic insulation and process of making same
US5849650A (en) 1992-09-15 1998-12-15 The Boeing Company Slurry for making ceramic insulation
US5604266A (en) 1992-10-15 1997-02-18 Ecomat, Inc. Cured unsaturated polyest-polyurethane highly filled resin materials and process for preparing them
WO1995027752A1 (en) 1992-10-15 1995-10-19 Ecomat, Inc. Cured unsaturated polyester-polyurethane hybrid highly filled resin foams
US5302634A (en) 1992-10-15 1994-04-12 Hoppmann Corporation Cured unsaturated polyester-polyurethane hybrid highly filled resin foams
US5476343A (en) 1992-11-30 1995-12-19 Sumner; Glen R. Offshore pipeline insulated with a cementitious coating
US5543186A (en) 1993-02-17 1996-08-06 E. Khashoggi Industries Sealable liquid-tight, thin-walled containers made from hydraulically settable materials
US5624737A (en) 1993-02-18 1997-04-29 General Electric Company Method for adhering materials having differing expansion properties and articles produced therefrom
US5424099A (en) 1993-03-12 1995-06-13 W.R. Grace & Co.-Conn. High strength pourable gypsum floor underlayments and methods of providing same
US5472760A (en) 1993-06-25 1995-12-05 W. L. Gore & Associates, Inc. Vehicle insulation
AU7092494A (en) 1993-09-21 1995-04-10 W.L. Gore & Associates, Inc. Puffed insulative material and methods for making such material
JO1812B1 (en) 1993-10-15 1995-07-05 ساسول كيميكال اندستريز ليمتد Porous prilled ammonium nitrate
US5492870A (en) 1994-04-13 1996-02-20 The Board Of Trustees Of The University Of Illinois Hollow ceramic microspheres by sol-gel dehydration with improved control over size and morphology
US6168226B1 (en) 1994-05-19 2001-01-02 Henkel Corporation Composite laminate automotive structures
US5884960A (en) 1994-05-19 1999-03-23 Henkel Corporation Reinforced door beam
EP0766720B1 (en) 1994-06-14 2004-04-14 Outlast Technologies, Inc. Energy absorbing fabric coating and manufacturing method
US6207738B1 (en) 1994-06-14 2001-03-27 Outlast Technologies, Inc. Fabric coating composition containing energy absorbing phase change material
US6155305A (en) 1994-08-29 2000-12-05 Sumner; Glen R. Offshore pipeline with waterproof thermal insulation
AU3547895A (en) 1994-09-06 1996-03-27 Thermacell Technologies, Inc. Insulation microspheres and method of manufacture
GB9420791D0 (en) 1994-10-14 1994-11-30 Hunting Eng Ltd Optical windows
US5512324A (en) 1994-11-14 1996-04-30 General Motors Corporation Metal substrate with insulative coating thereon and method of making the same
US5622556A (en) 1994-12-19 1997-04-22 Shulman; David M. Lightweight, low water content cementitious compositions and methods of their production and use
US5725652A (en) 1994-12-19 1998-03-10 Shulman; David M. Lightweight, low water content expanded shale, clay and slate cementitious compositions and methods of their production and use
US5580378A (en) 1994-12-19 1996-12-03 Shulman; David M. Lightweight cementitious compositions and methods of their production and use
US5574561A (en) 1994-12-22 1996-11-12 The Whitaker Corporation Kinematic mounting of optical and optoelectronic elements on silicon waferboard
US5534058A (en) 1995-01-27 1996-07-09 Midway Environmental Associates, Inc. Structural products manufactured from fly ash
CA2243977C (en) 1995-02-17 2002-09-10 Drexel University Fly ash cementitious material and method of making a product
US5600930A (en) 1995-04-10 1997-02-11 Drucker; Ernest R. Construction system using lightweight fire-resistant panels
IL118088A0 (en) 1995-06-07 1996-08-04 Anzon Inc Colloidal particles of solid flame retardant and smoke suppressant compounds and methods for making them
US5711362A (en) 1995-11-29 1998-01-27 Electric Power Research Institute Method of producing metal matrix composites containing fly ash
IT1282373B1 (en) 1996-01-31 1998-03-20 Montell Nort America Inc POLYOLEFIN COMPOSITION FOR COATING METALS WITH FLAME SPRAYING
US5749111A (en) 1996-02-14 1998-05-12 Teksource, Lc Gelatinous cushions with buckling columns
US5766686A (en) 1996-03-01 1998-06-16 North American Refractories Co. Spray insulating coating for refractory articles
US5770267A (en) 1996-04-05 1998-06-23 J. M. Huber Corporation Method and apparatus for smoothing substrate surfaces
US6584742B1 (en) 1996-04-18 2003-07-01 Structural Technologies, Inc. Oriented strand board wall panel system
US6277454B1 (en) 1999-02-24 2001-08-21 Insulation Dimension Corporation Syntactic foam insulated container
US6265040B1 (en) 1996-06-14 2001-07-24 Insulation Dimension Corporation Self-bonding syntactic foam insulated container sleeve
FR2749844B1 (en) 1996-06-18 1998-10-30 Schlumberger Cie Dowell CEMENTING COMPOSITIONS AND APPLICATION THEREOF FOR CEMENTING OIL WELLS OR THE LIKE
CA2208337C (en) 1996-06-22 2002-05-14 Clifford P. Ronden Process for the production of lightweight cellular composites of wood waste and thermoplastic polymers
US5786095A (en) 1996-07-03 1998-07-28 H.B. Fuller Licensing & Financing, Inc. Inorganic based intumescent system
CA2208344C (en) * 1996-07-09 2002-04-16 Clifford P. Ronden Process for the production of composites of co-mingled thermoset resin-bonded wood waste blended with thermoplastic polymers
US5814250A (en) 1996-09-18 1998-09-29 The United States Of America As Represented By The Secretary Of The Navy Method of protecting a structure
US6379497B1 (en) 1996-09-20 2002-04-30 Fort James Corporation Bulk enhanced paperboard and shaped products made therefrom
EP0927231B1 (en) 1996-09-23 2003-11-26 Akzo Nobel N.V. Low density, light weight intumescent coating
US5980980A (en) 1996-10-29 1999-11-09 Mcdonnell Douglas Corporation Method of repairing porous ceramic bodies and ceramic composition for same
US6020062A (en) 1996-11-08 2000-02-01 D.W. Wallcovering Inc. Article having slippable adhesive
US5746932A (en) 1996-11-14 1998-05-05 Solv-Ex Corporation Method for producing thermal insulation from dry-fine oil-sands tailings
DE19653930A1 (en) 1996-12-21 1998-06-25 Wilhelmi Werke Ag Sound absorbing building board
US6362252B1 (en) 1996-12-23 2002-03-26 Vladimir Prutkin Highly filled polymer composition with improved properties
US5862772A (en) 1996-12-26 1999-01-26 Emerson & Cumingcomposite Materials, Inc. Damage control materials for warship construction
US5788184A (en) 1997-01-04 1998-08-04 Eddy; Robert G. Aircraft passenger safety enhanced fuselage insulation blanket
US5754491A (en) 1997-02-24 1998-05-19 Poiesis Research, Inc. Multi-technology acoustic energy barrier and absorber
US6740373B1 (en) 1997-02-26 2004-05-25 Fort James Corporation Coated paperboards and paperboard containers having improved tactile and bulk insulation properties
US6919111B2 (en) 1997-02-26 2005-07-19 Fort James Corporation Coated paperboards and paperboard containers having improved tactile and bulk insulation properties
US6805737B2 (en) * 1997-03-26 2004-10-19 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Lightweight substance molded body, method for the production and use thereof
US6397549B1 (en) 1997-05-08 2002-06-04 Robert A. Baldwin Building block with a wooden attachment layer
US5840179A (en) 1997-06-19 1998-11-24 Jtm Industries, Inc. Ultrasonic conditioning and wet scubbing of fly ash
EP1457467A1 (en) 1997-06-27 2004-09-15 Elk Premium Building Products, Inc. Coated structural articles
US6194051B1 (en) 1997-07-15 2001-02-27 Bradley Corporation Composite structural components for outdoor use
DE19730466A1 (en) 1997-07-16 1999-01-21 Bayer Ag Pressure-resistant and thermally stable insulating coatings for hollow bodies and a process for their production
US6058979A (en) 1997-07-23 2000-05-09 Cuming Corporation Subsea pipeline insulation
CA2239950C (en) 1997-08-11 2007-09-18 Bayer Corporation Syntactic rigid pur/pir foam boardstock
US5817230A (en) 1997-08-29 1998-10-06 University Of Kentucky Research Foundation Method for improving the pozzolanic character of fly ash
US5899256A (en) 1997-10-03 1999-05-04 Electric Power Research Institute, Inc. Metal-fly ash composites and low pressure infiltration methods for making the same
US5913002A (en) 1997-12-31 1999-06-15 The Whitaker Corporation Optical coupling device for passive alignment of optoelectronic devices and fibers
US6103360A (en) 1998-01-09 2000-08-15 Armstrong World Industries, Inc. High light reflectance and durable ceiling board coating
US5983984A (en) 1998-01-12 1999-11-16 Ashland Inc. Insulating sleeve compositions and their uses
DE69924234T2 (en) 1998-01-20 2005-08-04 Kimberly-Clark Worldwide, Inc., Neenah COATING COMPOSITION CONTAINING PARTICLES WITH A HIGH BREAKING NUMBER
FR2775216B1 (en) 1998-02-26 2000-07-13 Snecma SOUNDPROOFING PANEL AND METHOD FOR PRODUCING THE SAME
US6376022B1 (en) 1998-05-14 2002-04-23 Southwest Research Institute Protective coating and method
ATE292165T1 (en) 1998-05-14 2005-04-15 Cww Gerko Akustik Gmbh & Co Kg METHOD FOR PRODUCING A HOT APPLICABLE, ACOUSTICALLY EFFECTIVE, BITUMINOUS MASS, MASS PRODUCED THEREFROM AND USES THEREOF
FR2779716B1 (en) 1998-06-15 2000-08-18 Vesuvius France Sa INSULATING REFRACTORY MATERIAL, PREPARATION METHOD, AND PARTS MADE OF SUCH MATERIAL
WO2000005302A1 (en) 1998-07-22 2000-02-03 Borden Chemical, Inc. Composite proppant, composite filtration media and methods for making and using same
US6582819B2 (en) 1998-07-22 2003-06-24 Borden Chemical, Inc. Low density composite proppant, filtration media, gravel packing media, and sports field media, and methods for making and using same
US6309492B1 (en) 1998-09-16 2001-10-30 Marc A. Seidner Polymer fill coating for laminate or composite wood products and method of making same
US6022912A (en) 1998-09-22 2000-02-08 Bayer Corporation Expansion of polymeric microspheres insitu in a rigid PUR/PIR foam formulation using a twin screw extruder
WO2000022021A1 (en) 1998-10-13 2000-04-20 Mitsui Chemicals, Incorporated Binder composition and process for manufacturing board by using the binder composition
US6165308A (en) 1998-11-06 2000-12-26 Lilly Industries, Inc. In-press process for coating composite substrates
US6251979B1 (en) 1998-11-18 2001-06-26 Advanced Construction Materials Corp. Strengthened, light weight wallboard and method and apparatus for making the same
AU2184100A (en) 1998-12-14 2000-07-03 Hexablock Inc. Building structures
US6187697B1 (en) 1998-12-31 2001-02-13 Alan Michael Jaffee Multiple layer nonwoven mat and laminate
DE60034674T2 (en) 1999-03-19 2008-01-17 Polycem LLC, Grand Haven POLYMER CEMENT COMPOSITES AND METHOD OF MANUFACTURING THE SAME
US6531222B1 (en) 1999-06-30 2003-03-11 Asahi Glass Company, Limited Fine hollow glass sphere and method for preparing the same
CA2283890C (en) 1999-09-27 2007-09-18 Advanced Glazings Ltd. Honeycomb transparent insulation with improved insulating ability
US6444594B1 (en) 1999-11-10 2002-09-03 Milliken & Company Airbag coatings providing improved thermal resistance
US6576574B2 (en) 1999-11-10 2003-06-10 Milliken & Company Airbag coatings comprising microspheres providing improved thermal resistance
AR026461A1 (en) 1999-11-18 2003-02-12 Vesuvius Crucible Co INSULATING REFRACTORY MATERIAL
US6586353B1 (en) 1999-11-30 2003-07-01 Elk Corp. Of Dallas Roofing underlayment
US6990779B2 (en) 1999-11-30 2006-01-31 Elk Premium Building Products, Inc. Roofing system and roofing shingles
US6872440B1 (en) 1999-11-30 2005-03-29 Elk Premium Building Products, Inc. Heat reflective coated structural article
US6673432B2 (en) 1999-11-30 2004-01-06 Elk Premium Building Products, Inc. Water vapor barrier structural article
GB2357111B (en) * 1999-12-10 2003-04-23 Environmental Seals Ltd Fire resistant structures
US6534176B2 (en) 1999-12-10 2003-03-18 Asahi Glass Company, Limited Scaly silica particles and hardenable composition containing them
US6231970B1 (en) 2000-01-11 2001-05-15 E. Khashoggi Industries, Llc Thermoplastic starch compositions incorporating a particulate filler component
JP4180825B2 (en) 2000-01-26 2008-11-12 インターナショナル・ペーパー・カンパニー Low density paperboard articles
US6673144B2 (en) 2000-02-11 2004-01-06 United States Gypsum Company Joint compound providing low dusting and good gloss retention
FR2805025B1 (en) 2000-02-15 2003-05-16 Hutchinson THERMAL INSULATION MATERIAL AND USES THEREOF
US6245842B1 (en) 2000-03-03 2001-06-12 Trus Joist Macmillan A Limited Partnership Flame-retardant coating and building product
MXPA02008921A (en) 2000-03-14 2004-10-15 James Hardie Res Pty Ltd Fiber cement building materials with low density additives.
US20020017224A1 (en) 2000-05-03 2002-02-14 Robert Horton Method for the treatment of pozzolanic materials
EP1156021A1 (en) 2000-05-19 2001-11-21 Asahi Glass Co., Ltd. Hollow aluminosilicate glass microspheres and process for their production
US20040194657A1 (en) 2000-06-22 2004-10-07 Thomas Lally Fire-retardant coating, method for producing fire-retardant building materials
US6713008B1 (en) 2000-06-23 2004-03-30 Darrin Blake Teeter Method for making composite structures
US6630221B1 (en) 2000-07-21 2003-10-07 Dexter Corporation Monolithic expandable structures, methods of manufacture and composite structures
US7037865B1 (en) 2000-08-08 2006-05-02 Moldite, Inc. Composite materials
US6368527B1 (en) 2000-08-18 2002-04-09 Vladimir Gontmakher Method for manufacture of foamed perlite material
WO2002016519A2 (en) 2000-08-25 2002-02-28 J.C. Hempel's Skibsfarve-Fabrik A/S Method for thermally insulating oil and gas pipes and paint compositions for coating the inner surface of oil and gas pipes
AUPR022300A0 (en) 2000-09-19 2000-10-12 James Hardie International Finance B.V. Cement render system
US20020178672A1 (en) 2000-09-25 2002-12-05 Robinson Michael G. Composite hybrid resin panels, molded parts and filler enhanced polymers therefor
US6572736B2 (en) 2000-10-10 2003-06-03 Atlas Roofing Corporation Non-woven web made with untreated clarifier sludge
US6916863B2 (en) 2000-11-14 2005-07-12 Boral Material Technologies, Inc. Filler comprising fly ash for use in polymer composites
JP2002144468A (en) 2000-11-16 2002-05-21 Toyo Aluminium Kk Composite sheet, method for manufacturing the same and panel equipped with composite sheet
US6620487B1 (en) 2000-11-21 2003-09-16 United States Gypsum Company Structural sheathing panels
US6444162B1 (en) 2000-11-27 2002-09-03 The United States Of America As Represented By The United States Department Of Energy Open-cell glass crystalline porous material
US6472579B1 (en) 2000-11-27 2002-10-29 The United States Of America As Represented By The Department Of Energy Method for solidification of radioactive and other hazardous waste
US6545066B1 (en) 2000-11-28 2003-04-08 United States Gypsum Company Lightweight ready-mix joint compound
US6840994B2 (en) 2000-12-20 2005-01-11 Bnz Materials, Inc. Calcium silicate insulating material containing alumina silica microspheres
US20020112648A1 (en) 2000-12-20 2002-08-22 Krowl Thomas R. Calcium silicate insulating material containing alumina silica microspheres
US7090918B2 (en) 2001-01-11 2006-08-15 Vesuvius Crucible Company Externally glazed article
US6758305B2 (en) 2001-01-16 2004-07-06 Johns Manville International, Inc. Combination sound-deadening board
US20020103091A1 (en) 2001-01-29 2002-08-01 Kodali Dharma R. Reactive oil compositions and uses thereof
US20020157573A1 (en) 2001-02-02 2002-10-31 Pellett Alwin W. Hydraulic cement coatings and method of forming and applying the coatings
PL201390B1 (en) 2001-03-02 2009-04-30 James Hardie Int Finance Bv A method and apparatus for forming a laminated sheet material by spattering
US20030057594A1 (en) 2001-03-05 2003-03-27 Anderson Robert Phillip Method of making a sheet of building material
CN1543444A (en) 2001-03-05 2004-11-03 ղķ˹�������о����޹�˾ Low density accelerant and strength enhancing additive for cementitious products and methods of using same
US6743830B2 (en) * 2001-03-07 2004-06-01 Innovative Construction And Building Materials Construction board materials with engineered microstructures
US20040221529A1 (en) 2001-04-03 2004-11-11 Zornes David A. Modular building structure
ITPS20010017A1 (en) 2001-05-24 2002-11-24 Canti & Figli Srl PROCEDURE FOR OBTAINING TILES AND SIMILAR PANELS WITH VARIOUS MINERAL AGGLOMERATES AND POSSIBLE ADDITION OF RUBBER OR PLASTIC MATERIALS
JP2004536172A (en) 2001-05-25 2004-12-02 アパーチェ・プロダクツ・カンパニー Expandable microspheres and methods for foam insulation
CA2447211A1 (en) 2001-06-08 2002-12-19 E.I. Du Pont De Nemours And Company Low gloss free radical powder coatings
DE10129232A1 (en) 2001-06-19 2003-01-02 Basf Ag Process for the production of syntactic polyurethane
FR2828484B1 (en) 2001-08-13 2004-12-10 Schlumberger Services Petrol POLYMERIC ADDITIVES FOR CEMENT COMPOSITIONS FOR IMPROVING INTERFACIAL ACTION AFTER TAKING
DE10139171A1 (en) 2001-08-16 2003-02-27 Basf Ag Use of microcapsules in plasterboard
US6716293B2 (en) 2001-08-30 2004-04-06 Sper-Tech Llc Wallboard with fly ash
CA2459990A1 (en) 2001-09-12 2003-03-20 Apache Products Company Composite foam products and method
US20030056696A1 (en) 2001-09-18 2003-03-27 Fenske John W. Polymer-cement composites including efflorescence-control agent and method of making same
US8017531B2 (en) 2001-09-18 2011-09-13 Elkcorp Composite material
US7517402B2 (en) 2001-10-08 2009-04-14 Xexos Ltd. Composition comprising a phosphate binder and its preparation
US20040003570A1 (en) 2001-10-23 2004-01-08 Phillips Jerry S. Methods of making manufactured housing or modular homes
WO2003046301A1 (en) 2001-11-28 2003-06-05 James Hardie Research Pty Limited Caulkless panelized wall system
US6601647B2 (en) 2001-12-03 2003-08-05 Halliburton Energy Services, Inc. Methods, well cement compositions and lightweight additives therefor
NO339168B1 (en) 2001-12-03 2016-11-14 Halliburton Energy Services Inc Lightweight cement mix and method of sealing around a pipe in a wellbore
AU2002353050A1 (en) 2001-12-05 2003-06-17 Shell Oil Company Syntactic foam
US6901713B2 (en) 2002-01-03 2005-06-07 Erich Jason Axsom Multipurpose composite wallboard panel
US20030175497A1 (en) 2002-02-04 2003-09-18 3M Innovative Properties Company Flame retardant foams, articles including same and methods for the manufacture thereof
US7199168B2 (en) 2002-02-13 2007-04-03 Bayer Materialscience Llc Process for making cellular composites using polymeric isocyanates as binders for hollow filler particles
US6858280B2 (en) 2002-02-26 2005-02-22 Technology Applications, Inc. Microsphere insulation systems
US6659362B1 (en) 2002-03-12 2003-12-09 Gerald Hallissy Composite railroad ties with optional integral conduit
US6644405B2 (en) 2002-03-21 2003-11-11 Halliburton Energy Services, Inc. Storable water-microsphere suspensions for use in well cements and methods
US7074499B2 (en) 2002-03-22 2006-07-11 Holofiber, Llc Polymeric fiber composition and method
US6794449B2 (en) 2002-04-11 2004-09-21 Adco Products, Inc. Hot melt pressure sensitive adhesive composition for attaching roofing membranes
SE0201129L (en) 2002-04-16 2003-10-17 Borealis Tech Oy Syntactic polyolefin composition for pipe coating g
US20050025952A1 (en) 2002-05-15 2005-02-03 Cabot Corporation Heat resistant insulation composite, and method for preparing the same
GB2405112B (en) 2002-06-03 2006-03-01 Chong Hak Tay A fire resistant insulation material
US6699522B2 (en) 2002-06-24 2004-03-02 Takeshi Sakakibara Inorganic insulation coating material
US6939610B1 (en) 2002-07-31 2005-09-06 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Thermal insulating coating for spacecrafts
US6833203B2 (en) 2002-08-05 2004-12-21 United Technologies Corporation Thermal barrier coating utilizing a dispersion strengthened metallic bond coat
US7101607B2 (en) 2002-08-21 2006-09-05 The Research Foundation Of State University Of New York Process for enhancing material properties and materials so enhanced
DE10239631A1 (en) 2002-08-23 2004-03-04 Carcoustics Tech Center Gmbh Insulating structural part for heat and noise insulation, has fire resistant coating, ceramic adhesive, expandable microhollow ceramic spheres and heat expanding propellant
MXPA05002057A (en) 2002-08-23 2005-09-12 James Hardie Int Finance Bv Synthetic hollow microspheres.
US6953129B2 (en) 2002-08-27 2005-10-11 The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration Pressure vessel with impact and fire resistant coating and method of making same
US6960388B2 (en) 2002-09-13 2005-11-01 Gerald Hallissy Electrical distribution system components with fire resistant insulative coating
US20040067352A1 (en) 2002-10-04 2004-04-08 Hagerman Joseph W. Rigid composite building materials and assemblies utilizing porous and non-porous rigid foamed core materials
GB0226773D0 (en) 2002-11-18 2002-12-24 Pyro Technologies Ltd A syntactic phenolic foam composition
CA2507824C (en) 2002-12-13 2012-03-13 G-P Gypsum Corporation Gypsum panel having uv-cured moisture resistant coating and method for making the same
RU2251168C2 (en) 2002-12-24 2005-04-27 Государственное унитарное предприятие Научно-производственное объединение "Радиевый институт им. В.Г. Хлопина" Method for extracting radioactive elements from liquid wastes
US20040123555A1 (en) 2002-12-26 2004-07-01 Cole Jefferson Anthony Pre manufactured structural panel consisting of a flame retardant external crust and an aeroboard core fabricated from laminations of uncompressed cardboard, impregnated by resin solutions recovered from post consumer thermoplastics
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
US20040157961A1 (en) 2003-01-30 2004-08-12 Gordon Tullos Curable coating powders and powder coatings formed therefrom
US20040249005A1 (en) 2003-02-11 2004-12-09 Anna Kron Microspheres
US6902614B2 (en) 2003-03-21 2005-06-07 Slawomir Ratomski Perlited Portland cement plaster joint compound additive with lime
US7435694B2 (en) 2003-03-28 2008-10-14 Johns Manville Nonwoven fibrous mats with good hiding properties and laminate
US6995098B2 (en) 2003-04-15 2006-02-07 National Gypsum Properties, Llc Wallboard containing scrim and matt
SI1622990T1 (en) * 2003-05-15 2008-02-29 Huntsman Int Llc Polyisocyanate-based adhesive formulation for use in sandwich panels
US6739806B1 (en) 2003-06-13 2004-05-25 Halliburton Energy Services, Inc. Cement compositions with improved fluid loss characteristics and methods of cementing in subterranean formations
KR20060056286A (en) 2003-06-24 2006-05-24 디 오리지널 콘크리트 컴퍼니 Pigment paste for concrete and method for making the same
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
US6831876B1 (en) 2003-07-09 2004-12-14 Goodrich Corporation Acoustic window
US7217458B2 (en) 2003-07-16 2007-05-15 Huber Engineered Woods Llc Strength-enhanced, lightweight lignocellulosic composite board materials and methods of their manufacture
US20050019552A1 (en) 2003-07-21 2005-01-27 Jack Wiersma Physical and thermal protective coating
US20070054797A1 (en) 2003-08-09 2007-03-08 Thomas Ronald J Siliceous clay slurry
US7811493B2 (en) 2003-09-23 2010-10-12 Kazak Composites, Incorporated Joiner panel system
US7442248B2 (en) 2003-11-18 2008-10-28 Research Incubator, Ltd. Cementitious composition
US7083758B2 (en) 2003-11-28 2006-08-01 Les Produits Industriels De Haute Temperature Pyrotek Inc. Free flowing dry back-up insulating material
US8287998B2 (en) 2003-12-01 2012-10-16 Anthony David Skelhorn Composition of a thermaly insulating coating system
US7156174B2 (en) 2004-01-30 2007-01-02 Halliburton Energy Services, Inc. Contained micro-particles for use in well bore operations
US7932193B2 (en) 2004-02-17 2011-04-26 Johns Manville Coated mat products, laminates and method
US20050197444A1 (en) 2004-03-08 2005-09-08 Kyte William J. Stain-resistant grout composition, dispenser therefor, and method of use
US7238402B2 (en) 2004-03-10 2007-07-03 Johns Manville Glass fibers and mats having improved surface structures in gypsum boards
AU2004201393A1 (en) 2004-04-05 2005-10-20 Smith, Ken Mr Lightweight Wallboard
US20050256228A1 (en) 2004-04-20 2005-11-17 Zeev Ariel Seamless smooth acoustical ceiling
US7128158B2 (en) 2004-05-25 2006-10-31 Halliburton Energy Services, Inc. Lightweight composite particulates and methods of using such particulates in subterranean applications
US20050281997A1 (en) 2004-06-16 2005-12-22 Sealed Air Corporation (Us) Pitch modulating laminate
US20060216471A1 (en) 2005-03-28 2006-09-28 Cyovac, Inc. Pitch modulating laminate with an apertured acoustic layer
US20050281979A1 (en) 2004-06-17 2005-12-22 Toas Murray S Loose fill insulation product having phase change material therein
US20050288394A1 (en) 2004-06-29 2005-12-29 John Rothman Insulative, emissive and reflective coating
US20050287293A1 (en) 2004-06-29 2005-12-29 John Rothman Coated wallboard process
US7622683B2 (en) 2004-07-26 2009-11-24 Terry Jeffrey Corbishley Marine and submarine pipelines
CA2513969A1 (en) 2004-08-02 2006-02-02 W.R. Grace & Co.-Conn. Method for fastening building materials together
US20060037815A1 (en) 2004-08-18 2006-02-23 Schabel Norman G Jr Particulate insulation materials
US20060040096A1 (en) 2004-08-19 2006-02-23 Rajan Eadara Constrained layer, composite, acoustic damping material
US20060054061A1 (en) 2004-09-13 2006-03-16 Ruddick Douglas H Bacteria and mold resistant wallboard
US9067383B2 (en) 2004-09-16 2015-06-30 United States Gypsum Company Flexible and rollable cementitious membrane and method of manufacturing it
US8586090B2 (en) 2004-10-05 2013-11-19 Albert Einstein College Of Medicine Of Yeshiva University Melanin nanoshells for protection against radiation and electronic pulses
US20060084743A1 (en) 2004-10-20 2006-04-20 Chen John C Composition comprising polymer and silicone rubber
US6974494B1 (en) 2004-10-25 2005-12-13 Karim Zahedi Apparatus and method using an electrified filter bed for removal of pollutants from a flue gas stream
US20060101785A1 (en) 2004-11-01 2006-05-18 Wiercinski Robert A Structural building elements having pressure-sensitive adhesive
US7790796B2 (en) 2004-11-08 2010-09-07 Elmer's Products Inc. Spackling composition containing polyaramid fibers and ceramic microparticles, and methods of repair and attachment
US7473722B2 (en) 2004-11-08 2009-01-06 Certain Teed Corp. Polymer-fiber composite building material with bulk and aesthetically functional fillers
US20060165885A1 (en) 2004-12-28 2006-07-27 Fay Ralph M Method of insulating cavities in a structure using a spray-on method and resultant insulation
TW200635830A (en) 2004-12-29 2006-10-16 Hunter Paine Entpr Llc Composite structural material and method of making the same
US7849648B2 (en) 2004-12-30 2010-12-14 United States Gypsum Company Non-combustible reinforced cementitious lightweight panels and metal frame system for flooring
US7732032B2 (en) 2004-12-30 2010-06-08 United States Gypsum Company Lightweight, fiber-reinforced cementitious panels
US20060188674A1 (en) 2005-01-24 2006-08-24 Mark Fernette Cement-based hydraulic flexible composites and package therefor
US7849650B2 (en) 2005-01-27 2010-12-14 United States Gypsum Company Non-combustible reinforced cementitious lightweight panels and metal frame system for a fire wall and other fire resistive assemblies
US7841148B2 (en) 2005-01-27 2010-11-30 United States Gypsum Company Non-combustible reinforced cementitious lightweight panels and metal frame system for roofing
US7849649B2 (en) 2005-01-27 2010-12-14 United States Gypsum Company Non-combustible reinforced cementitious lightweight panels and metal frame system for shear walls
EP2292894A1 (en) 2005-02-04 2011-03-09 Oxane Materials, Inc. A composition and method for making a proppant
US7538152B2 (en) 2005-02-10 2009-05-26 Construction Research & Technology Gmbh Lightweight structural finish
US20060178453A1 (en) 2005-02-10 2006-08-10 Markus Bohler Lightweight base coating
US7504165B2 (en) * 2005-06-14 2009-03-17 United States Gypsum Company High strength flooring compositions
US20070020475A1 (en) 2005-07-21 2007-01-25 Prince Kendall W Primed substrate and method for making the same
US9315612B2 (en) 2005-07-27 2016-04-19 Certainteed Corporation Composite material including rigid foam with inorganic fillers
US7635731B2 (en) 2005-07-28 2009-12-22 Chemtura Corporation Cellulosic-thermoplastic composite and method of making the same
US20070044397A1 (en) 2005-08-09 2007-03-01 Wiercinski Robert A Skid resistant surfaces
US7658967B2 (en) 2005-08-25 2010-02-09 Pittsburgh Glass Works, Llc Methods for applying sound dampening and/or aesthetic coatings and articles made thereby
US20070048504A1 (en) 2005-08-25 2007-03-01 Dimario Joseph Methods for applying sound dampening and/or aesthetic coatings and articles made thereby
US7174962B1 (en) 2005-09-09 2007-02-13 Halliburton Energy Services, Inc. Methods of using lightweight settable compositions comprising cement kiln dust
US7335252B2 (en) 2005-09-09 2008-02-26 Halliburton Energy Services, Inc. Lightweight settable compositions comprising cement kiln dust
US20070062143A1 (en) 2005-09-21 2007-03-22 Noushad Rafie L Construction products and method of making same
WO2007041272A2 (en) 2005-09-30 2007-04-12 Maxam Industries, Inc. Long lasting natural anti-pest additive
US20070094992A1 (en) 2005-10-13 2007-05-03 Antonic James P Structural wall panel assemblies
US8555589B2 (en) 2005-11-29 2013-10-15 Mos, Llc Roofing system
US20070141316A1 (en) 2005-12-19 2007-06-21 Mcgrath Ralph D Tri-extruded WUCS glass fiber reinforced plastic composite articles and methods for making such articles
US20070148429A1 (en) 2005-12-19 2007-06-28 Mcgrath Ralph D Tri-excluded WUCS glass fiber reinforced plastic composite articles and methods for making such articles
US7845130B2 (en) * 2005-12-29 2010-12-07 United States Gypsum Company Reinforced cementitious shear panels
US20070155859A1 (en) 2006-01-04 2007-07-05 Zhengzhe Song Reactive polyurethane hot melt adhesive
US7900411B2 (en) 2006-02-17 2011-03-08 Antonic James P Shear wall building assemblies
US7318288B2 (en) 2006-03-17 2008-01-15 Karim Zahedi Apparatus and method using an electrified filter bed for removal of pollutants from a flue gas stream
US20070261224A1 (en) 2006-05-11 2007-11-15 Dow Global Technologies Inc. Methods and articles in having a fringed microprotrusion surface structure
US7870698B2 (en) 2006-06-27 2011-01-18 United States Gypsum Company Non-combustible reinforced cementitious lightweight panels and metal frame system for building foundations
US7524386B2 (en) 2006-11-01 2009-04-28 United States Gypsum Company Method for wet mixing cementitious slurry for fiber-reinforced structural cement panels
US7475599B2 (en) 2006-11-01 2009-01-13 United States Gypsum Company Wet slurry thickness gauge and method for use of same
US7513963B2 (en) 2006-11-01 2009-04-07 United States Gypsum Company Method for wet mixing cementitious slurry for fiber-reinforced structural cement panels
US7754052B2 (en) 2006-11-01 2010-07-13 United States Gypsum Company Process and apparatus for feeding cementitious slurry for fiber-reinforced structural cement panels
US20080099133A1 (en) 2006-11-01 2008-05-01 United States Gypsum Company Panel smoothing process and apparatus for forming a smooth continuous surface on fiber-reinforced structural cement panels
US8106105B2 (en) * 2007-01-29 2012-01-31 Interfacial Solutions Ip, Llc Compositions and methods for producing high strength composites
US20090239059A1 (en) 2007-03-21 2009-09-24 Kipp Michael D Wallboard Materials Incorporating a Microparticle Matrix
US20090239429A1 (en) 2007-03-21 2009-09-24 Kipp Michael D Sound Attenuation Building Material And System
CA2681528C (en) * 2007-03-21 2018-10-23 Ashtech Industries, Llc Utility materials incorporating a microparticle matrix
US8445101B2 (en) 2007-03-21 2013-05-21 Ashtech Industries, Llc Sound attenuation building material and system
US8591677B2 (en) * 2008-11-04 2013-11-26 Ashtech Industries, Llc Utility materials incorporating a microparticle matrix formed with a setting agent
JP5269722B2 (en) 2009-08-26 2013-08-21 株式会社東芝 Security design support apparatus and program

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0475302A1 (en) * 1990-09-10 1992-03-18 Manville Corporation Lightweight building material board
JPH11322880A (en) * 1998-05-18 1999-11-26 Aren:Kk Setting agent for roadbed crushed-stone and stabilization of roadbed
WO2006018904A1 (en) * 2004-08-19 2006-02-23 Minoru Tanaka Earth wall board and method for molding earth wall board
JP2006083048A (en) * 2004-09-15 2006-03-30 Nanbu:Kk Inorganic foamed board

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111075107A (en) * 2019-12-31 2020-04-28 同济大学 Assembled combined concrete external wall board and preparation and installation method thereof

Also Published As

Publication number Publication date
US20140205808A1 (en) 2014-07-24
WO2010054029A3 (en) 2010-08-26
US20140079915A1 (en) 2014-03-20
US10508437B2 (en) 2019-12-17
US20170321417A1 (en) 2017-11-09
US9816266B2 (en) 2017-11-14
US20100116405A1 (en) 2010-05-13
US8591677B2 (en) 2013-11-26
US20220010550A1 (en) 2022-01-13
US20200080299A1 (en) 2020-03-12

Similar Documents

Publication Publication Date Title
US20220010550A1 (en) Utility materials incorporating a microparticle matrix formed with a setting agent
EP2132385B1 (en) Utility materials incorporating a microparticle matrix
US20090239059A1 (en) Wallboard Materials Incorporating a Microparticle Matrix
US8440296B2 (en) Shear panel building material
US8445101B2 (en) Sound attenuation building material and system
CA2719088C (en) Wallboard materials incorporating a microparticle matrix
EP3309313B1 (en) Sound attenutation material
WO2009117020A1 (en) Shear panel building material

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: 09825383

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 09825383

Country of ref document: EP

Kind code of ref document: A2