US20020006757A1 - Gas permeable fabric - Google Patents
Gas permeable fabric Download PDFInfo
- Publication number
- US20020006757A1 US20020006757A1 US09/904,208 US90420801A US2002006757A1 US 20020006757 A1 US20020006757 A1 US 20020006757A1 US 90420801 A US90420801 A US 90420801A US 2002006757 A1 US2002006757 A1 US 2002006757A1
- Authority
- US
- United States
- Prior art keywords
- gas permeable
- permeable fabric
- aramid
- fabric according
- fluoropolymer
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 239000004744 fabric Substances 0.000 title claims abstract description 32
- 239000000203 mixture Substances 0.000 claims abstract description 44
- 239000000758 substrate Substances 0.000 claims abstract description 26
- 229920002313 fluoropolymer Polymers 0.000 claims abstract description 22
- 239000004811 fluoropolymer Substances 0.000 claims abstract description 22
- 239000000463 material Substances 0.000 claims abstract description 12
- 239000004962 Polyamide-imide Substances 0.000 claims description 19
- 229920002312 polyamide-imide Polymers 0.000 claims description 19
- 239000000835 fiber Substances 0.000 claims description 15
- 229920003235 aromatic polyamide Polymers 0.000 claims description 13
- -1 polytetrafluoroethylene Polymers 0.000 claims description 11
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 11
- 229920001343 polytetrafluoroethylene Polymers 0.000 claims description 10
- 239000010445 mica Substances 0.000 claims description 8
- 229910052618 mica group Inorganic materials 0.000 claims description 8
- 239000002245 particle Substances 0.000 claims description 7
- 239000004642 Polyimide Substances 0.000 claims description 6
- 239000004760 aramid Substances 0.000 claims description 6
- 239000011521 glass Substances 0.000 claims description 6
- 229920001721 polyimide Polymers 0.000 claims description 6
- 239000004952 Polyamide Substances 0.000 claims description 4
- 230000015556 catabolic process Effects 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 238000006731 degradation reaction Methods 0.000 claims description 4
- 229920002647 polyamide Polymers 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 229920000742 Cotton Polymers 0.000 claims description 3
- 239000004696 Poly ether ether ketone Substances 0.000 claims description 3
- 239000000919 ceramic Substances 0.000 claims description 3
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000000049 pigment Substances 0.000 claims description 3
- 229920001652 poly(etherketoneketone) Polymers 0.000 claims description 3
- 229920002239 polyacrylonitrile Polymers 0.000 claims description 3
- 229920002530 polyetherether ketone Polymers 0.000 claims description 3
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 2
- 229920000297 Rayon Polymers 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 claims description 2
- 229920002480 polybenzimidazole Polymers 0.000 claims description 2
- 229920000728 polyester Polymers 0.000 claims description 2
- 229920001601 polyetherimide Polymers 0.000 claims description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 claims 3
- 239000004693 Polybenzimidazole Substances 0.000 claims 1
- 239000004697 Polyetherimide Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000004809 Teflon Substances 0.000 description 6
- 229920006362 Teflon® Polymers 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- XPFVYQJUAUNWIW-UHFFFAOYSA-N furfuryl alcohol Chemical compound OCC1=CC=CO1 XPFVYQJUAUNWIW-UHFFFAOYSA-N 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 4
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical compound C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000219146 Gossypium Species 0.000 description 2
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 2
- 229920000784 Nomex Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000004763 nomex Substances 0.000 description 2
- 229920005575 poly(amic acid) Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BWHOZHOGCMHOBV-BQYQJAHWSA-N trans-benzylideneacetone Chemical compound CC(=O)\C=C\C1=CC=CC=C1 BWHOZHOGCMHOBV-BQYQJAHWSA-N 0.000 description 2
- BZPCMSSQHRAJCC-UHFFFAOYSA-N 1,2,3,3,4,4,5,5,5-nonafluoro-1-(1,2,3,3,4,4,5,5,5-nonafluoropent-1-enoxy)pent-1-ene Chemical compound FC(F)(F)C(F)(F)C(F)(F)C(F)=C(F)OC(F)=C(F)C(F)(F)C(F)(F)C(F)(F)F BZPCMSSQHRAJCC-UHFFFAOYSA-N 0.000 description 1
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical compound CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 description 1
- 229920000271 Kevlar® Polymers 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004936 P-84 Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229920006231 aramid fiber Polymers 0.000 description 1
- 150000004984 aromatic diamines Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 230000000593 degrading effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000011152 fibreglass Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 150000004679 hydroxides Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004761 kevlar Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007761 roller coating Methods 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/12—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins
- D06N3/125—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. gelatine proteins with polyamides
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/08—Filter cloth, i.e. woven, knitted or interlaced material
- B01D39/083—Filter cloth, i.e. woven, knitted or interlaced material of organic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/08—Filter cloth, i.e. woven, knitted or interlaced material
- B01D39/086—Filter cloth, i.e. woven, knitted or interlaced material of inorganic material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B5/00—Layered 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
- B32B5/18—Layered 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 of foamed material
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
- C08L79/04—Polycondensates having nitrogen-containing heterocyclic rings in the main chain; Polyhydrazides; Polyamide acids or similar polyimide precursors
- C08L79/08—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
-
- D—TEXTILES; PAPER
- D04—BRAIDING; LACE-MAKING; KNITTING; TRIMMINGS; NON-WOVEN FABRICS
- D04H—MAKING TEXTILE FABRICS, e.g. FROM FIBRES OR FILAMENTARY MATERIAL; FABRICS MADE BY SUCH PROCESSES OR APPARATUS, e.g. FELTS, NON-WOVEN FABRICS; COTTON-WOOL; WADDING ; NON-WOVEN FABRICS FROM STAPLE FIBRES, FILAMENTS OR YARNS, BONDED WITH AT LEAST ONE WEB-LIKE MATERIAL DURING THEIR CONSOLIDATION
- D04H1/00—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres
- D04H1/40—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties
- D04H1/58—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives
- D04H1/64—Non-woven fabrics formed wholly or mainly of staple fibres or like relatively short fibres from fleeces or layers composed of fibres without existing or potential cohesive properties by applying, incorporating or activating chemical or thermoplastic bonding agents, e.g. adhesives the bonding agent being applied in wet state, e.g. chemical agents in dispersions or solutions
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M11/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising
- D06M11/77—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with inorganic substances or complexes thereof; Such treatment combined with mechanical treatment, e.g. mercerising with silicon or compounds thereof
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
- D06M15/256—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/347—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated ethers, acetals, hemiacetals, ketones or aldehydes
- D06M15/353—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated ethers, acetals, hemiacetals, ketones or aldehydes containing fluorine
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/59—Polyamides; Polyimides
- D06M15/592—Polyamides; Polyimides made from polymerised unsaturated fatty acids and polyamines
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/0056—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the compounding ingredients of the macro-molecular coating
- D06N3/0063—Inorganic compounding ingredients, e.g. metals, carbon fibres, Na2CO3, metal layers; Post-treatment with inorganic compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/04—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06N3/047—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof with macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds with fluoropolymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
- B01D2239/0471—Surface coating material
- B01D2239/0478—Surface coating material on a layer of the filter
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/04—Additives and treatments of the filtering material
- B01D2239/0471—Surface coating material
- B01D2239/0485—Surface coating material on particles
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D2239/00—Aspects relating to filtering material for liquid or gaseous fluids
- B01D2239/12—Special parameters characterising the filtering material
- B01D2239/1291—Other parameters
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
Definitions
- the present invention relates to gas permeable fabrics, more particularly to gas permeable fabrics which are formable into desired shapes and made rigid, and to their use in industrial environments, such as filters.
- Shapeable, rigidizable gas permeable fabrics are used in a variety of industrial and environmental applications. Of primary interest is their use as filter media. In certain applications, such filters must be able to withstand continuous exposure to extremely high temperatures (up to 280° C.) without degrading.
- a filter can be formed into a desired shape, and thereafter made rigid and durable. For example, it is often desirable to maximize the surface area of a filter while minimizing the volume of space it occupies. Thus, filters are often pleated into “accordion” type configurations.
- a disadvantage of the prior art gas permeable fabrics is that the polymer treatment is difficult to distribute uniformly onto the fabric, resulting in spotwise blinding and uneven fabric strengths. In addition, the tongue tear strength tends to be reduced.
- the present invention provides a gas permeable fabric made from a porous substrate that is treated with a composition comprising a fluoropolymer and a rigidizing, film-forming material. More specifically, the present invention provides a gas permeable fabric that is treated with a mixture of a fluoropolymer and a polyamideimide to provide a shapeable, rigidizable substrate which is formed into a desired configuration, and subsequently rigidized, to yield a temperature resistant, durable fabric suitable for various industrial and environmental end-uses.
- End-uses for the fabric of the present invention may be divided into two categories: “high temperature end-uses” refer to those requiring resistance to degradation at temperatures of about 200° C. to 280° C. for extended periods of time, and resistance at temperatures of about 280° C. to 365° C. for periods up to about 10 minutes.
- Moderate temperature end-uses refer to those requiring resistance to degradation at temperatures of up to about 200° C. for extended periods of time, and resistance at temperatures of about 200° C. to 280° C. for periods up to about 10 minutes.
- Porous substrates for use in the present invention may be woven or nonwoven, and may be made from a plurality of different fibers.
- suitable fibers include meta-aramids. para-aramids, aramid copolymers, polyamideimides, polyoxadiazoles, polyimides, polyetheretherketones, polyetherketoneketones, polybenzimidazoles, polytetrafluorethylenes (PTFE), glasses, ceramics, and blends thereof.
- Preferred substrates include those made from meta-aramids (e.g. NOMEX), para-aramids (e.g KEVLAR), PTFE (e.g. TEFLON), PTFE-glass blends (e.g. TEFAIRE), all of which are available from the DuPont Company, and polymides (e.g. P-84, available from Lenzing, Austria).
- the fabric can be made from fibers such as polyamides, polyacrylonitriles, polyesters, polyphenylensulfides, polyetherimides, viscoses, cottons, modified cellulosics and blends thereof.
- fibers for making moderate temperature resistant substrates are polyacrylonitriles, cotton or modified cellulosics.
- fluoropolymers are, per se, known in the art, and give the fabrics of the present invention chemical protection and lubricity under end-use operating conditions.
- suitable fluoropolymers for use in the present invention are polytetrafluoroethylenes (PTFE) and copolymers of tetrafluoroethylene (TFE) with one or more of 1) a perfluorinated vinyl ether, 2) perfluorinated ethylene-propylene, 3) hexafluoropropylene and 4) vinylidene fluoride; and blends thereof (cf. U.S. Pat. No. 4,252,859).
- TEFLON TEFLON
- TEFLON PFA a copolymer of TFE and ca. 1.5% perfluoro-propyl-vinyl-ether
- TEFLON FEP a copolymer of TFE and ca. 10 to 12% perfluoronated ethylene-propylene
- fluoropolymer in water For moderate temperature end-uses, common, commercially available dispersions of fluoropolymer in water are suitable, such as OLEOPHOBOL (Pfersee), ZEPEL (DuPont) and SCOTCHGUARD (3M).
- OLEOPHOBOL Pfersee
- ZEPEL DuPont
- SCOTCHGUARD 3M
- a preferred such fluoropolymer is OLEOPHOBOL.
- the fluoropolymer is provided in the form of an aqueous dispersion, and the water introduced into the composition with the fluoropolymer also serves as a carrier for the composition.
- organic liquids such as alcohols (e.g. furfuryl alcohol), ketones. aliphatic and aromatic hydrocarbons (e.g. N-methyl pyrrolidone), or mixtures thereof, can be used.
- the fluoropolymer is preferably present in the composition for treating the porous substrate in an amount ranging from 1 to 30% by weight, more preferably to 20% by weight.
- “Rigidizing film forming materials” are known in the art, and, as their name implies, give the fabrics of the present invention dimensional stability, i.e. rigidity. They should be capable of forming a film at or below the fusion temperature of the fluoropolymer used in the present invention. Suitable film forming materials, and methods for making them, are described in U.S. Pat. No. 4,087,394. Such film forming materials include acrylic polymers, nitrocellulose, polyamides, polyvinyl chloride and derivatives of epoxy resins (polymeric quaternary hydroxides) blended with nitrogen resins for moderate temperature resistance applications; and polyamide or polyamic acid salts (precursors of polyimides and polyamideimides) for high temperature resistance applications.
- Preferred rigidized films in the present invention are polyamideimides (PAI), which are the reaction products of polyamic acid salts, such as trimellitic anhydride, and aromatic diamines such as 4,4′-methylendianiline or bis(4-aminophenyl)methane.
- PAI polyamideimides
- Compositions for preparing PAI will, typically, also contain triethylamine, diethylethanolamine, furfuryl alcohol, methylpyrrolidone and water.
- the rigidizing film forming materials are preferably present in the composition for treating the porous substrate in an amount ranging from 1 to 30% by weight, more preferably 3 to 10% by weight.
- “Mica particles, mica particles coated with pigment or metal flake; and blends thereof” are commercially available; they are described in U.S. Pat. No. 4,123,401. They may be present in the composition containing the fluoropolymer and film forming agent in amounts up to 10% by weight, and are preferably present in amounts ranging from 3 to 6% by weight.
- compositions for treating porous substrates according to the present invention will contain fluoropolymer and film forming material, and optionally may contain other components such as the aforementioned mica-based particles, as well as conventional additives such as antioxidants, flow control agents, surfactants, plasticizers, antistats and the like. These additives will be used in conventional amounts, depending upon the ultimate end-use of the fabric of the present invention.
- compositions can be made by simply mixing together appropriate amounts of the proper components.
- compositions will be governed by the substrate to which the compositions are to be applied, the method of application, the curing procedures and like factors.
- the compositions will be formed as aqueous dispersions, containing 1-80% by weight of solids.
- compositions may be applied in any of the usual ways, such as spraying, roller-coating, dipping and doctor-blading.
- compositions are typically applied to the substrate on a dry weight basis at a rate of 3-30% of the weight of the substrate, according to end-use.
- the coated substrate is then formed into a desired shape or configuration, e.g. is pleated or convoluted, and the resulting article is baked at a temperature and for a time sufficient to cure the fluoropolymer and the film forming material of the composition.
- the baking and shaping steps may be reversed.
- porous substrate a commercially available 500 g/m 2 needle felt of NOMEX aramid fiber (available from the DuPont Company) is cut into strips having dimensions of 800 mm ⁇ 500 mm. Two grades of felt are used: quality (A) is loom state needled (referred to below as substrate “A”); quality (B) is singed (open flame treatment at 40 m/minute) and caelered (215° C./10 kg/cm) (referred to below as substrate “B”).
- dispersions set forth in Table 1 are formed according to the procedures prescribed in U.S. Pat. No. 4,087,394. TABLE 1 Compositions I) PAI solution* [18.7% solids], II) PAI solution*/TEFLON FEP [23% solids (7.7%/15.3%) aqueous dispersion], III) PAI solution*/TEFLON FEP/Mica [25.5% solids (7%/14%/4.6%) aqueous dispersion]
- the needle felt porous substrate samples are impregnated with compositions I, II and III on a BENZ laboratory padder with a pick-up between 150 and 250% (based on weight of dried sample), dried on a mini-tenter frame (BENZ) at 200° C. for 3 minutes, followed by baling for 3 minutes at 300° C.
- Half of the samples treated with composition 1) are not baked as they do not contain fluoropolymer which provides high chemical protection and lubricity.
- Application rates are given in Table 2, wherein “owf” stands for “on weight fabric” (dry basis).
- the substrates obtained from the previous step are then pleated on conventional equipment at temperatures between 200° C. and 250° C. for periods ranging between 30 and 60 seconds under hand pressure. All samples prepared are pleatable at all test temperatures, although at lower temperatures the pleating time is longer.
- compositions I, II and III provide a rigidized needle felt structure with adequate air permeability.
- composition I leads to a decrease in tongue tear strength (as measured according to DIN 53849/4) of the needle felt as compared with untreated needle felt, whereas treatment with compositions II and III maintain or improve tongue tear strength.
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Abstract
A gas permeable fabric made from a porous substrate that is treated with a composition comprising a fluoropolymer and a rigidizing, film-forming material is disclosed.
Description
- The present invention relates to gas permeable fabrics, more particularly to gas permeable fabrics which are formable into desired shapes and made rigid, and to their use in industrial environments, such as filters.
- Shapeable, rigidizable gas permeable fabrics are used in a variety of industrial and environmental applications. Of primary interest is their use as filter media. In certain applications, such filters must be able to withstand continuous exposure to extremely high temperatures (up to 280° C.) without degrading.
- In addition, it is desirable that a filter can be formed into a desired shape, and thereafter made rigid and durable. For example, it is often desirable to maximize the surface area of a filter while minimizing the volume of space it occupies. Thus, filters are often pleated into “accordion” type configurations.
- Typical filter substrates, though durable and heat resistant, tend to be difficult to mold into and to retain various desired configurations. Thus, in the past, it has been proposed to impregnate filter substrates with various polymers, which lend to the filter substrates the properties of moldability and retention of shape. C.f. U.S. Pat. No. 3,918,943, DE 41 37 627 C2, which describe filters made from fiberglass paper that is treated with a polyimide binder, and sheets formed from glass or quartz fibers that are treated with a fluoropolymer.
- A disadvantage of the prior art gas permeable fabrics is that the polymer treatment is difficult to distribute uniformly onto the fabric, resulting in spotwise blinding and uneven fabric strengths. In addition, the tongue tear strength tends to be reduced.
- The present invention provides a gas permeable fabric made from a porous substrate that is treated with a composition comprising a fluoropolymer and a rigidizing, film-forming material. More specifically, the present invention provides a gas permeable fabric that is treated with a mixture of a fluoropolymer and a polyamideimide to provide a shapeable, rigidizable substrate which is formed into a desired configuration, and subsequently rigidized, to yield a temperature resistant, durable fabric suitable for various industrial and environmental end-uses.
- As used herein, and unless otherwise noted, the following terms have the meanings indicated below.
- End-uses for the fabric of the present invention may be divided into two categories: “high temperature end-uses” refer to those requiring resistance to degradation at temperatures of about 200° C. to 280° C. for extended periods of time, and resistance at temperatures of about 280° C. to 365° C. for periods up to about 10 minutes.
- “Moderate temperature end-uses” refer to those requiring resistance to degradation at temperatures of up to about 200° C. for extended periods of time, and resistance at temperatures of about 200° C. to 280° C. for periods up to about 10 minutes.
- “Porous substrates” for use in the present invention may be woven or nonwoven, and may be made from a plurality of different fibers. For high temperature end-uses, suitable fibers include meta-aramids. para-aramids, aramid copolymers, polyamideimides, polyoxadiazoles, polyimides, polyetheretherketones, polyetherketoneketones, polybenzimidazoles, polytetrafluorethylenes (PTFE), glasses, ceramics, and blends thereof. Preferred substrates include those made from meta-aramids (e.g. NOMEX), para-aramids (e.g KEVLAR), PTFE (e.g. TEFLON), PTFE-glass blends (e.g. TEFAIRE), all of which are available from the DuPont Company, and polymides (e.g. P-84, available from Lenzing, Austria).
- For moderate temperature end-uses, the fabric can be made from fibers such as polyamides, polyacrylonitriles, polyesters, polyphenylensulfides, polyetherimides, viscoses, cottons, modified cellulosics and blends thereof. Preferred fibers for making moderate temperature resistant substrates are polyacrylonitriles, cotton or modified cellulosics.
- “Fluoropolymers” are, per se, known in the art, and give the fabrics of the present invention chemical protection and lubricity under end-use operating conditions. For high temperature end-uses, suitable fluoropolymers for use in the present invention are polytetrafluoroethylenes (PTFE) and copolymers of tetrafluoroethylene (TFE) with one or more of 1) a perfluorinated vinyl ether, 2) perfluorinated ethylene-propylene, 3) hexafluoropropylene and 4) vinylidene fluoride; and blends thereof (cf. U.S. Pat. No. 4,252,859). Preferred such fluoropolymers are TEFLON (PTFE), TEFLON PFA (a copolymer of TFE and ca. 1.5% perfluoro-propyl-vinyl-ether) and TEFLON FEP (a copolymer of TFE and ca. 10 to 12% perfluoronated ethylene-propylene), all of which are available from the DuPont Company.
- For moderate temperature end-uses, common, commercially available dispersions of fluoropolymer in water are suitable, such as OLEOPHOBOL (Pfersee), ZEPEL (DuPont) and SCOTCHGUARD (3M). A preferred such fluoropolymer is OLEOPHOBOL.
- Commonly, the fluoropolymer is provided in the form of an aqueous dispersion, and the water introduced into the composition with the fluoropolymer also serves as a carrier for the composition. However, if desired, organic liquids such as alcohols (e.g. furfuryl alcohol), ketones. aliphatic and aromatic hydrocarbons (e.g. N-methyl pyrrolidone), or mixtures thereof, can be used.
- The fluoropolymer is preferably present in the composition for treating the porous substrate in an amount ranging from 1 to 30% by weight, more preferably to 20% by weight.
- “Rigidizing film forming materials” are known in the art, and, as their name implies, give the fabrics of the present invention dimensional stability, i.e. rigidity. They should be capable of forming a film at or below the fusion temperature of the fluoropolymer used in the present invention. Suitable film forming materials, and methods for making them, are described in U.S. Pat. No. 4,087,394. Such film forming materials include acrylic polymers, nitrocellulose, polyamides, polyvinyl chloride and derivatives of epoxy resins (polymeric quaternary hydroxides) blended with nitrogen resins for moderate temperature resistance applications; and polyamide or polyamic acid salts (precursors of polyimides and polyamideimides) for high temperature resistance applications.
- Preferred rigidized films in the present invention are polyamideimides (PAI), which are the reaction products of polyamic acid salts, such as trimellitic anhydride, and aromatic diamines such as 4,4′-methylendianiline or bis(4-aminophenyl)methane. Compositions for preparing PAI will, typically, also contain triethylamine, diethylethanolamine, furfuryl alcohol, methylpyrrolidone and water.
- The rigidizing film forming materials are preferably present in the composition for treating the porous substrate in an amount ranging from 1 to 30% by weight, more preferably 3 to 10% by weight.
- “Mica particles, mica particles coated with pigment or metal flake; and blends thereof” are commercially available; they are described in U.S. Pat. No. 4,123,401. They may be present in the composition containing the fluoropolymer and film forming agent in amounts up to 10% by weight, and are preferably present in amounts ranging from 3 to 6% by weight.
- Compositions for treating porous substrates according to the present invention will contain fluoropolymer and film forming material, and optionally may contain other components such as the aforementioned mica-based particles, as well as conventional additives such as antioxidants, flow control agents, surfactants, plasticizers, antistats and the like. These additives will be used in conventional amounts, depending upon the ultimate end-use of the fabric of the present invention.
- The compositions can be made by simply mixing together appropriate amounts of the proper components.
- The amount of total solids in the composition will be governed by the substrate to which the compositions are to be applied, the method of application, the curing procedures and like factors. In the usual case, the compositions will be formed as aqueous dispersions, containing 1-80% by weight of solids.
- The compositions may be applied in any of the usual ways, such as spraying, roller-coating, dipping and doctor-blading.
- The compositions are typically applied to the substrate on a dry weight basis at a rate of 3-30% of the weight of the substrate, according to end-use. The coated substrate is then formed into a desired shape or configuration, e.g. is pleated or convoluted, and the resulting article is baked at a temperature and for a time sufficient to cure the fluoropolymer and the film forming material of the composition. Alternatively, the baking and shaping steps may be reversed.
- Unless otherwise indicated, all percentages given are on a weight basis.
- As porous substrate, a commercially available 500 g/m2 needle felt of NOMEX aramid fiber (available from the DuPont Company) is cut into strips having dimensions of 800 mm×500 mm. Two grades of felt are used: quality (A) is loom state needled (referred to below as substrate “A”); quality (B) is singed (open flame treatment at 40 m/minute) and calandered (215° C./10 kg/cm) (referred to below as substrate “B”).
- As treatment compositions, dispersions set forth in Table 1 are formed according to the procedures prescribed in U.S. Pat. No. 4,087,394.
TABLE 1 Compositions I) PAI solution* [18.7% solids], II) PAI solution*/TEFLON FEP [23% solids (7.7%/15.3%) aqueous dispersion], III) PAI solution*/TEFLON FEP/Mica [25.5% solids (7%/14%/4.6%) aqueous dispersion] - The needle felt porous substrate samples are impregnated with compositions I, II and III on a BENZ laboratory padder with a pick-up between 150 and 250% (based on weight of dried sample), dried on a mini-tenter frame (BENZ) at 200° C. for 3 minutes, followed by baling for 3 minutes at 300° C. Half of the samples treated with composition 1) are not baked as they do not contain fluoropolymer which provides high chemical protection and lubricity. Application rates are given in Table 2, wherein “owf” stands for “on weight fabric” (dry basis).
TABLE 2 Application Rates g/l of Composition pick up substrate final amount on felt 140 g/l of I 155% B 2.5% owf (2.5 PAI) 150 g/l of II 192% B 6.8% owf (2.3 PAI) 300 g/l of III 145% B 10.8% owf (3 PAI) 140 g/l of I 235% A 6% owf (6 PAI) 500 g/l of I 244% A 23% owf (23 PAI) 300 g/l of II 168% A 11.7% owf (3.9 PAI) 300 g/l of III 169% A 20% owf (5.4 PAI) - The substrates obtained from the previous step are then pleated on conventional equipment at temperatures between 200° C. and 250° C. for periods ranging between 30 and 60 seconds under hand pressure. All samples prepared are pleatable at all test temperatures, although at lower temperatures the pleating time is longer.
- Each of compositions I, II and III provide a rigidized needle felt structure with adequate air permeability. However, composition I leads to a decrease in tongue tear strength (as measured according to DIN 53849/4) of the needle felt as compared with untreated needle felt, whereas treatment with compositions II and III maintain or improve tongue tear strength.
Claims (14)
1. A gas permeable fabric comprising a porous substrate treated with a composition comprising a fluoropolymer and a rigidizing film forming material.
2. A gas permeable fabric according to claim 1 , wherein the film forming material is a polyamideimide.
3. A gas permeable fabric according to claim 1 or 2, wherein the composition further comprises mica particles, mica particles coated with pigment or metal flake; and blends thereof.
4. A gas permeable fabric according to any one of claims 1 to 3 wherein the fluoropolymer is a polytetrafluoroethylene or a copolymer of tetrafluoroethylene with one or more of 1) a perfluorinated vinyl ether, 2) perfluoronated ethylenepropylene, 3) hexafluoropropylene and 4) vinylidene fluoride; and blends thereof.
5. A gas permeable fabric according to any one of claims 1 to 4 wherein the fabric is made from fibers selected from a meta-aramid, a para-aramid, an aramid copolymer, a polyamideimide, a polyoxadiazole, a polyimide, a polyetheretherketone, a polyetherketoneketone, a polybenzimidazole, a polytetrafluorethylene, a glass, a ceramic, and blends thereof.
6. A gas permeable fabric according to claim 1 or 2 wherein the fabric is made from fibers selected from a polyamide, a polyacrylonitrile, a polyester, a polyphenylensulfide, a polyetherimide, a viscose, a cotton or a modified cellulosic, and blends thereof.
7. A gas permeable fabric according to claim 6 wherein the fluoropolymer is dispersed in water.
8. A gas permeable fabric according to any one of the preceding claims wherein the fabric is formed into a desired shape.
9. A gas permeable fabric according to claim 8 , wherein the fabric is a filter.
10. A method of making a gas permeable fabric according to any one of the preceding claims comprising applying a composition containing a fluoropolymer and a film forming material to a porous substrate, forming the substrate into a desired shape, and curing the composition.
11. A fiber having resistance to degradation at a temperature in the range of 280° C. to 365° C. for a period of 10 minutes comprising a gas permeable fabric of a porous substrate made from fibers capable of withstanding degradation in said temperature range for said time period, said fibers treated with a composition comprising fluoropolymer and a rigidizing film forming material.
12. The fiber of claim 11 wherein the fibers are selected from the group consisting of meta-aramid, para-aramid, aramid copolymer, polyamideimide, polyoxadiazole, polyimide, polyetheretherketone, polyetherketoneketone, polybenimidazole, polytetrafluoroethylene, glass, ceramic, and blends thereof.
13. The fiber of claim 12 wherein the fibers are selected from the group consisting of meta-aramid, para-aramid, polytetrafluoroethylene, polytetrafluoroethylene-glass blend, and polyimide.
14. The fiber of claim 11 wherein the composition further comprises mica particles, mica particles coated with pigment or metal flake; and blends thereof.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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US09/904,208 US20020006757A1 (en) | 1995-02-10 | 2001-07-13 | Gas permeable fabric |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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EP95200320A EP0726348A1 (en) | 1995-02-10 | 1995-02-10 | Gas permeable fabric |
EP95200320.0 | 1995-02-10 | ||
US87596897A | 1997-08-07 | 1997-08-07 | |
US09/904,208 US20020006757A1 (en) | 1995-02-10 | 2001-07-13 | Gas permeable fabric |
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US87596897A Continuation | 1995-02-10 | 1997-08-07 |
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US09/904,208 Abandoned US20020006757A1 (en) | 1995-02-10 | 2001-07-13 | Gas permeable fabric |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6734122B1 (en) * | 2001-11-16 | 2004-05-11 | Bgf Industries, Inc. | Fabric for high-temperature gaseous filtration applications |
US20040261616A1 (en) * | 2003-06-26 | 2004-12-30 | Jorgensen Betty S. | Cross-linked polybenzimidazole membrane for gas separation |
US20060021502A1 (en) * | 2004-07-28 | 2006-02-02 | Young Jennifer S | Cross-linked polybenzimidazole membrane for gas separation |
US9446351B2 (en) | 2013-11-25 | 2016-09-20 | Milliken & Company | Filtration medium and process for filtering a fluid stream |
-
2001
- 2001-07-13 US US09/904,208 patent/US20020006757A1/en not_active Abandoned
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6734122B1 (en) * | 2001-11-16 | 2004-05-11 | Bgf Industries, Inc. | Fabric for high-temperature gaseous filtration applications |
US20040261616A1 (en) * | 2003-06-26 | 2004-12-30 | Jorgensen Betty S. | Cross-linked polybenzimidazole membrane for gas separation |
US6946015B2 (en) * | 2003-06-26 | 2005-09-20 | The Regents Of The University Of California | Cross-linked polybenzimidazole membrane for gas separation |
US20060021502A1 (en) * | 2004-07-28 | 2006-02-02 | Young Jennifer S | Cross-linked polybenzimidazole membrane for gas separation |
US6997971B1 (en) * | 2004-07-28 | 2006-02-14 | The Regents Of The University Of California | Cross-linked polybenzimidazole membrane for gas separation |
US9446351B2 (en) | 2013-11-25 | 2016-09-20 | Milliken & Company | Filtration medium and process for filtering a fluid stream |
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