US20160130747A1 - Coated fabrics - Google Patents
Coated fabrics Download PDFInfo
- Publication number
- US20160130747A1 US20160130747A1 US14/901,139 US201414901139A US2016130747A1 US 20160130747 A1 US20160130747 A1 US 20160130747A1 US 201414901139 A US201414901139 A US 201414901139A US 2016130747 A1 US2016130747 A1 US 2016130747A1
- Authority
- US
- United States
- Prior art keywords
- coated fabric
- fabric
- silicone rubber
- rubber composition
- coating
- 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 120
- 229920002379 silicone rubber Polymers 0.000 claims abstract description 43
- 239000004945 silicone rubber Substances 0.000 claims abstract description 43
- 238000000576 coating method Methods 0.000 claims abstract description 42
- 239000000945 filler Substances 0.000 claims abstract description 42
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 38
- 239000011248 coating agent Substances 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 36
- 239000011256 inorganic filler Substances 0.000 claims abstract description 6
- 229910003475 inorganic filler Inorganic materials 0.000 claims abstract description 6
- 238000011068 loading method Methods 0.000 claims abstract description 5
- 229920001296 polysiloxane Polymers 0.000 claims description 17
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 239000002904 solvent Substances 0.000 claims description 13
- 239000005909 Kieselgur Substances 0.000 claims description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 12
- 239000000853 adhesive Substances 0.000 claims description 11
- 230000001070 adhesive effect Effects 0.000 claims description 11
- 239000002245 particle Substances 0.000 claims description 10
- -1 polysiloxane Polymers 0.000 claims description 10
- 239000007787 solid Substances 0.000 claims description 10
- 238000009472 formulation Methods 0.000 claims description 9
- 239000004952 Polyamide Substances 0.000 claims description 8
- 239000003054 catalyst Substances 0.000 claims description 8
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims description 8
- 229920002647 polyamide Polymers 0.000 claims description 8
- 150000002978 peroxides Chemical class 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 claims description 6
- 239000011148 porous material Substances 0.000 claims description 6
- 239000002318 adhesion promoter Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical class CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 claims description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 claims description 4
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 4
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 229910052697 platinum Inorganic materials 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 230000000704 physical effect Effects 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims description 2
- 229910021502 aluminium hydroxide Inorganic materials 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000292 calcium oxide Substances 0.000 claims description 2
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 claims description 2
- 239000001175 calcium sulphate Substances 0.000 claims description 2
- 235000011132 calcium sulphate Nutrition 0.000 claims description 2
- 239000006229 carbon black Substances 0.000 claims description 2
- 235000019241 carbon black Nutrition 0.000 claims description 2
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 claims description 2
- GDVKFRBCXAPAQJ-UHFFFAOYSA-A dialuminum;hexamagnesium;carbonate;hexadecahydroxide Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Al+3].[Al+3].[O-]C([O-])=O GDVKFRBCXAPAQJ-UHFFFAOYSA-A 0.000 claims description 2
- 229910001701 hydrotalcite Inorganic materials 0.000 claims description 2
- 229960001545 hydrotalcite Drugs 0.000 claims description 2
- 239000000077 insect repellent Substances 0.000 claims description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical group O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052622 kaolinite Inorganic materials 0.000 claims description 2
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims description 2
- 239000000347 magnesium hydroxide Substances 0.000 claims description 2
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims description 2
- 239000000395 magnesium oxide Substances 0.000 claims description 2
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims description 2
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 2
- 239000012621 metal-organic framework Substances 0.000 claims description 2
- 239000010445 mica Substances 0.000 claims description 2
- 229910052618 mica group Inorganic materials 0.000 claims description 2
- 239000000454 talc Substances 0.000 claims description 2
- 229910052623 talc Inorganic materials 0.000 claims description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 claims description 2
- 239000010457 zeolite Substances 0.000 claims description 2
- 239000011787 zinc oxide Substances 0.000 claims description 2
- 150000003961 organosilicon compounds Chemical class 0.000 claims 2
- 229920000742 Cotton Polymers 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- 239000012790 adhesive layer Substances 0.000 claims 1
- 125000003700 epoxy group Chemical group 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 239000012763 reinforcing filler Substances 0.000 claims 1
- 238000000518 rheometry Methods 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- 239000002131 composite material Substances 0.000 description 12
- 239000010410 layer Substances 0.000 description 12
- 239000012528 membrane Substances 0.000 description 11
- 239000004814 polyurethane Substances 0.000 description 10
- 238000010276 construction Methods 0.000 description 9
- 229920002635 polyurethane Polymers 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 229920001971 elastomer Polymers 0.000 description 7
- 239000011159 matrix material Substances 0.000 description 7
- 238000010073 coating (rubber) Methods 0.000 description 6
- 238000002156 mixing Methods 0.000 description 6
- 230000037361 pathway Effects 0.000 description 5
- 239000004677 Nylon Substances 0.000 description 4
- 238000004132 cross linking Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000002808 molecular sieve Substances 0.000 description 4
- 229920001778 nylon Polymers 0.000 description 4
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 4
- 239000004753 textile Substances 0.000 description 4
- 239000004820 Pressure-sensitive adhesive Substances 0.000 description 3
- 239000008199 coating composition Substances 0.000 description 3
- 239000007789 gas Substances 0.000 description 3
- 230000002706 hydrostatic effect Effects 0.000 description 3
- 238000005325 percolation Methods 0.000 description 3
- 230000035699 permeability Effects 0.000 description 3
- 238000010058 rubber compounding Methods 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 239000004447 silicone coating Substances 0.000 description 3
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 238000001354 calcination Methods 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 238000006068 polycondensation reaction Methods 0.000 description 2
- 229920001343 polytetrafluoroethylene Polymers 0.000 description 2
- 239000004810 polytetrafluoroethylene Substances 0.000 description 2
- 239000011527 polyurethane coating Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 230000002028 premature Effects 0.000 description 2
- 238000002203 pretreatment Methods 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- 230000004580 weight loss Effects 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 206010009866 Cold sweat Diseases 0.000 description 1
- 229920000544 Gore-Tex Polymers 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 101100304647 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) RPL39 gene Proteins 0.000 description 1
- NOZAQBYNLKNDRT-UHFFFAOYSA-N [diacetyloxy(ethenyl)silyl] acetate Chemical compound CC(=O)O[Si](OC(C)=O)(OC(C)=O)C=C NOZAQBYNLKNDRT-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000323 aluminium silicate Inorganic materials 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 229920000295 expanded polytetrafluoroethylene Polymers 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 230000009878 intermolecular interaction Effects 0.000 description 1
- 239000008204 material by function Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000012982 microporous membrane Substances 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 229920005573 silicon-containing polymer Polymers 0.000 description 1
- 239000013464 silicone adhesive Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000012301 solution-based formulation Substances 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- 239000012974 tin catalyst Substances 0.000 description 1
- BPSIOYPQMFLKFR-UHFFFAOYSA-N trimethoxy-[3-(oxiran-2-ylmethoxy)propyl]silane Chemical compound CO[Si](OC)(OC)CCCOCC1CO1 BPSIOYPQMFLKFR-UHFFFAOYSA-N 0.000 description 1
- 238000004078 waterproofing Methods 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
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Classifications
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- 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
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- 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
- D06N3/128—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 silicon polymers
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- B32B5/22—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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed
- B32B5/24—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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer
- B32B5/26—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 the presence of two or more layers which are next to each other and are fibrous, filamentary, formed of particles or foamed one layer being a fibrous or filamentary layer another layer next to it also being fibrous or filamentary
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- 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
- D06N2201/00—Chemical constitution of the fibres, threads or yarns
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
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- D06N2201/00—Chemical constitution of the fibres, threads or yarns
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- D—TEXTILES; PAPER
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- 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
- D06N2201/00—Chemical constitution of the fibres, threads or yarns
- D06N2201/04—Vegetal fibres
- D06N2201/042—Cellulose fibres, e.g. cotton
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- 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
- D06N2209/00—Properties of the materials
- D06N2209/12—Permeability or impermeability properties
- D06N2209/121—Permeability to gases, adsorption
- D06N2209/123—Breathable
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- 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
- D06N2209/00—Properties of the materials
- D06N2209/12—Permeability or impermeability properties
- D06N2209/126—Permeability to liquids, absorption
- D06N2209/128—Non-permeable
-
- 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
- D06N2209/00—Properties of the materials
- D06N2209/16—Properties of the materials having other properties
- D06N2209/1671—Resistance to bacteria, mildew, mould, fungi
-
- 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
- D06N3/0086—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique
- D06N3/0095—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by the application technique by inversion technique; by transfer processes
-
- D—TEXTILES; PAPER
- D10—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B—INDEXING SCHEME ASSOCIATED WITH SUBLASSES OF SECTION D, RELATING TO TEXTILES
- D10B2401/00—Physical properties
- D10B2401/02—Moisture-responsive characteristics
Definitions
- the invention relates to coated fabrics and in particular to waterproof, breathable coated textiles that can be used, for example, in the manufacture of protective and leisure clothing, bags and luggage.
- Waterproof, breathable coating and laminates for textiles are well known in the prior art, the terms “waterproof” and “breathable” relating to the coating or laminate being impervious to liquid water and permeable to water vapour respectively. This imparts a high degree of comfort to the wearer, preventing condensation of sweat inside the garment while providing a waterproof barrier to keep the wearer dry in all types of weather.
- GORE-TEX Materials sold under the registered trade mark GORE-TEX are based on an expanded polytetrafluoroethylene membrane (e.g. U.S. Pat. No. 3,953,583) to produce a microporous membrane that can be laminated to a fabric.
- the pores in the membrane are 20,000 times larger than a water molecule allowing the passage of vapour, while the extremely low surface energy of the membrane imparts high waterproofing properties.
- Microporous coatings based on polyurethanes are also known in the art, as described by U.S. Pat. Nos. 4,560,611, 5,520,998, 5,626,950 and 5,692,936. These are produced by direct coating a polyurethane solution onto a fabric, then coagulating the solution to produce a network of micropores in the polymer structure.
- hydrophilic polyurethanes Another group of coatings are based on hydrophilic polyurethanes. These are usually directly coated onto a fabric, and rely on the incorporation of hydrophilic segments in the polymer chains. Water molecules from perspiration are therefore able to diffuse from inside the clothing of the wearer through the polymer layer via a step-wise process and transported to the outside environment.
- the functionality of these hydrophilic layers relies on a humid environment building up inside the breathable garment. The higher the humidity inside the garment, the faster the rate of diffusion of water molecules through the polymeric layer.
- These types of polyurethane coatings usually contain both hydrophilic and hydrophobic segments to incorporate breathability and waterproofness respectively.
- microporous membranes There are a number of problems associated with both the microporous membranes and the hydrophilic coatings.
- the performance of microporous membranes can deteriorate over time due to contamination of the pores by soil, detergents and body oils. Blocking of the pores in this manner reduces the breathability of the membrane and can also alter the surface chemistry of the membrane, resulting in the increased likelihood of liquid water penetration. Gore attempted to resolve this problem by the application of a very thin layer of hydrophilic polyurethane on top of the microporous PTFE as a protective layer to prevent the microporous layer from contaminants.
- hydrophilic based polyurethane breathable coatings There are also problems associated with hydrophilic based polyurethane breathable coatings.
- the main one is their susceptibility to swelling in water. By their very nature, water molecules are attracted to the hydrophilic segments in the polymer. Water molecules are therefore able to “solvate” the hydrophilic segments within the polymer and swell the membrane. This can impart to a “clammy” feeling to the wearer as well as a loss of coating strength. In severe cases it can lead to a loss of adherence to the fabric itself, causing delamination. This is quite common when the garment is subjected to harsh aqueous environments.
- the present invention has been made from a consideration of the above.
- a coated fabric wherein the coating comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour.
- a gas is able to pass through the porous structure via a series of holes or pathways.
- the invention achieves porosity throughout the rubber coating.
- the very nature of the inorganic filler used in the formulation is that of particles containing a plurality of micron and sub-micron pores as an integral part of its structure. In the silicone rubber formulation, below a certain level of filler these particles are not in close proximity to each other. However, when a certain level, or amount of filler is incorporated into the rubber matrix, a mixed matrix compound is achieved where the porous particles are in sufficiently close proximity to each other to allow the passage of water vapour through each porous particle straight through the continuous mixed matrix coating i.e.
- the “percolation threshold” is reached to produce a true percolated structure throughout the mixed rubber/filler matrix.
- the percolation threshold For any given system, below the “percolation threshold” a continuous connected component does not exist, but above the percolation threshold there exists a connected component to scale of the system size.
- the invention tends not to allow the passage of liquid water (up to a hydrostatic head pressure of at least 2000 mm) due to the very hydrophobic nature and low surface energy of the silicone rubber.
- the “percolated structure” of the proposed invention can be described by the interconnectedness of the porous filler particles throughout the mixed matrix compound that gives rise to continuous connected porous pathways to allow the passage of water vapour molecules throughout the rubber matrix, giving rise to its breathability.
- the silicone composite solution can be coated on a natural or synthetic fabric which may be woven, nonwoven or knitted and comprise, for example, polyester or polyamide.
- the coating process may involve direct coating onto the fabric substrate.
- the coated fabric of the invention comprises a waterproof, breathable coated textile that can be used for the manufacture of a variety of articles, such as protective and leisure clothing, bags and luggage.
- Silicone rubber exhibits gas permeability due to the zero energy of rotation about the silicon-oxygen bond in the backbone chain. Together with the plurality of methyl groups on the outside of the polymer chains (which in turn impart water repellent properties), intermolecular interaction is very low causing a large free volume between polymer chains, allowing the diffusion of gas molecules through the polymer matrix.
- the coated fabric of the invention therefore incorporates a porous filler which by creating a percolated structure within the silicone rubber composition, complements the permeable properties of the silicone rubber to produce a truly water-vapour permeable, liquid water impermeable membrane.
- Single texture (2-layer) comprising one fabric (e.g. polyester/polyamide (Nylon)) coated on one side with the silicone composite. This would be the most basic construction, intended for example for use in the manufacture of hiking, walking and camping jackets.
- Double texture (tri-laminate) comprising an outer layer fabric (e.g. polyester/polyamide (Nylon)) laminated to a second, inner liner fabric (polyester) with the silicone composite layer in between. This would be a more durable fabric intended for example for water sport surface suits, dry suits and sailing/yachting suits/jackets. It is envisaged that this durable fabric construction can also be used in heavy duty work wear, for example, for outdoor workers.
- the silicone rubber coating is a solution based formulation that is ideally coated directly onto a fabric.
- the silicone rubber composition contains the following polysiloxane and solid filler.
- the silicone rubber contains any of catalyst, adhesive and/or adhesion promoter and a solvent.
- the various components of the rubber coating may be included as follows:—
- Solvent 200-400 2 1 the above formulation may be based on a condensation, peroxide or addition cured silicone, which will determine the type and quantity of catalyst (organotin, peroxide or platinum type). 2 the solvent level is based on phr of solid rubber to produce a solution of 35-50% solids. A pre mixed silicone polymer solution in toluene may also be used, which would reduce the amount of additional solvent needed
- the breathable silicone rubber coating of the invention has advantages over breathable polyurethane systems in as much that it is non-swelling in aqueous environments with no loss of adhesion in tri-laminate constructions. As it is an inherent property of silicone rubber, the coating also has excellent resistance to ageing (e.g. no hydrolysis, another issue with PU systems) and excellent flexibility and low temperature performance.
- the breathable silicone rubber composite has an extremely porous nature due to the high porosity of the diatomaceous earth filler that is used in the silicone formulation.
- the high porosity and surface area of the composite raises the possibility of extra functionality being designed into the breathable coating. Possibilities include:
- the large internal volume of the porous filler particles may be able to act as a “reservoir” for essential oils that would be released slowly over time to impart antimicrobial properties to the breathable fabric. This would be extremely advantageous for garments that are susceptible to bacterial and fungal growth which causes unpleasant odours.
- insect repellent agents could also be incorporated into the filler particles. This would be advantageous for hiking and camping clothing in areas where a high population of insects is present.
- FIG. 1 which shows a schematic diagram of a tri-laminate waterproof breathable construction of the invention and the water vapour evaporation pathway therethrough.
- a coated fabric 10 comprises a first woven fabric 11 having a plain weave construction made from polyamide. This is direct coated on one side thereof with a silicone rubber composition 12 .
- the silicone rubber composition has the following components:—
- a polysiloxane 13 that can be cross-linked by polyaddition, polycondensation or free radical means catalysed by platinum, organotin or peroxide compounds respectively.
- a porous filler 14 comprises natural diatomaceous earth (or diatomite) which is a soft siliceous sedimentary rock crumbled into a fine powder.
- the porous filler while typically natural diatomaceous earth, may also be calcined and flux-calcined. Calcination is the heat treatment of a material in the presence of air or oxygen. Flux-calcination is the heat treatment of a material in the presence of a fluxing agent.
- (C) a catalyst (not shown), which can be either an organo-tin compound, platinum catalyst or peroxide.
- a catalyst for the current formulation, C14-010, an organo-tin catalyst commercially available from Itac Ltd can be typically used.
- D) additionally (not shown), a mixture of glycidoxypropyltrimethoxysilane and vinyltriacetoxysilane adhesion promoter, such as the commercially available SYL-OFF 297 from Dow Corning. This is also supplied under the product code C14-025 from Itac Ltd.
- a second plain weave fabric 15 also made form polyamide is situated on the other side of the coating such that the silicone coating is sandwiched between the two fabrics.
- the molecular sieve compound needs to be added to the coating formulation and thoroughly mixed and left to stand for not less than two hours before coating onto the fabric.
- a typical molecular sieve compound employed for this purpose is a porous, crystalline aluminosilicate powder such as those marketed under the brand name “Sylosiv”.
- the formulation should be mixed in a mechanical mixing device, such as a Z-blade mixer.
- Components (A) and (B) should be thoroughly mixed in the first instance for 20-30 mins to produce a homogenous “dough” mix, followed by components (C), (D) and (E).
- the complete formulation should then be mixed for a further 20-30 mins until a completely homogenous solution is produced. Measured solids content of the solution should be 35-45%. After the final mix, the formulation will have a useable pot life of 8 hours.
- the water vapour pathway is in the direction of arrows A.
- Tri-Laminate Coated Fabric (as Shown in FIG. 1 )
- the silicone composite solution can be coated on a synthetic woven or knitted fabric e.g. polyester or nylon using direct coating (knife over roller) method.
- a multiple number of passes is required in order to achieve a coating weight of 70-100 gsm.
- a coating weight of around 85 gsm should be achieved. It is usual for at least three coating passes to be needed to achieve this weight.
- It is important to ensure the temperature is at a temperature that enables evaporation of the solvent, but is not too high as to cause premature cross-linking of the silicone composite.
- a temperature of 60-80° C. should be maintained in the heated spreading chest.
- the uncoated side of the fabric will function as the “inner” lining of the waterproof, breathable fabric.
- PSA silicone based pressure sensitive adhesive
- a commercial grade PSA from Dow Corning known as DC7358 (a peroxide cured adhesive) can be used for this purpose.
- Peroxide typically dibenzoyl peroxide
- a light coating of adhesive is then applied over the silicone coating, the solvent is allowed to evaporate through the heated chest (temperature must not be over 75° C. or premature crosslinking of the adhesive will occur).
- the coated fabric is then laminated through two pressurised rollers against a second, uncoated fabric to produce the tri-laminate construction.
- the laminated fabric can then be cured off-line.
- the fabric coating can be cured for 30-45 min at a temperature of 120-140° C. Lower temperatures down to 100° C. can be used for longer curing times of up to 6 hours.
- the tri-laminate water proof breathable fabric can be used (but not limited to) garments for water sport and marine applications such as surface suits, dry suits, sailing garments, etc.
- the single coated fabric is manufactured in a similar way to the tri-laminate.
- the coated fabric serves as the outer fabric shell as opposed to the inner layer fabric, and the fabric is not then laminated to another fabric.
- silicone rubber due to the non-stick properties of silicone rubber, it is necessary to apply a breathable, low melting point thermoplastic top coat on the breathable silicone layer in order to facilitate the adhesion of seam sealing tapes.
- a polyurethane coating solution such as Larithane BTH231 can be used for this purpose. Swelling effects of the polyurethane are not as critical as the fabric is not laminated to another outer fabric, where loss of peel adhesion could become an issue.
- the breathability of the fabric has been internally tested according to BS7209 “Water vapour permeable apparel fabrics”.
- a circular test piece of the fabric is fixed over the rim of a circular aluminium dish that contains a measured amount of distilled water.
- the outside surface of the rim of the dish is then sealed so that the only pathway water vapour can take is through the fabric.
- the total weight of the dish, fabric and water is measured, whereupon the dish is then placed on a circular turntable that rotates to prevent a microclimate of humid air above the surface of the fabric.
- the dish is then left in atmospheric conditions of 65% relative humidity and 20° C. for at least 16 hours.
- the weight of the whole test dish is then measured to calculate the loss of water in the form of vapour through the dish.
- WVTR water vapour transmission rate
- the waterproof breathable fabric as described in this specification will typically have a WVTR of 400-650 g/m2/24 hours, more typically around 500 g/m 2 /24 hours and a WVPI of 50-90%, more typically around 75%.
- test BS3424-26 This is described as the water pressure required to leak (penetrate) through the fabric. This is determined by carrying out test BS3424-26, which subjects a test piece of fabric to pressure from either a column of water or water pressurised from a compressor. Any fabric that can withstand a pressure equivalent to a column height of 1000 mm is deemed “waterproof” although in practice ratings of 2,000-20,000 mm are expected from quality products.
- the waterproof breathable fabric as described in this specification demonstrated a hydrostatic head rating of at least 2,000 mm according to internal tests.
- the peeling strength is simply the force required to peel the laminated fabrics apart, as measured on a tensometer.
- the test piece is a 50 mm wide strip of the fabric with both face and back fabrics delaminated from each other. The force in N/50 mm is then measured that is required to peel the fabrics apart.
- the tri-laminate fabric as described previously typically has a peeling strength of 4-8 N/50 mm, more typically around 6 N/50 mm. The peeling strength will remain unaffected after the test piece has been immersed in a 2% salt water solution for 24 hours.
- the invention contemplates the optional addition of a thixotropic filler such as fumed silica to the base silicone rubber formulation. This would alter the rheological properties by increasing the viscosity of the coating formulation and reduce “strike-through” of the solution through the fabric. This leads to reducing the degree of coating penetration through the fabric leading to a better appearance and handle of the coated fabric.
- a thixotropic filler such as fumed silica
- An improvement in adhesion of silicone rubber to the fabric may optionally be achieved by applying a pre-treatment of an organic silane compound to the fabric prior to applying the rubber coating. The silane pre-treatment would typically be applied by a dipping technique into a silane solution followed by drying to evaporate the solvent.
- the diatomaceous earth filler may be dried prior to mixing into the rubber formulation, as excess moisture present in the filler disrupts the condensation cross-linking reaction.
- the addition of a molecular sieve compound into the rubber/filler solution 2-3 hours prior to coating removes the moisture from within the coating solution, thus eliminating any requirement to pre-dry the filler.
- One or more blowing agents may be used to increase the porosity of the adhesive. Increasing the elastomer content of the adhesive may improve the peel strength.
- the currently preferred porous filler used to create a percolated porous structure is natural diatomaceous earth, there are a range of other porous fillers which may be used in place of or in combination with diatomaceous earth.
- Such fillers may include kaolinite, amorphous silica, zeolites, metal organic frameworks, porous carbon blacks and montmorillonite clay.
- Additional fillers may be incorporated into the composite formulation to improve the physical properties of the composite coating. These include, either alone, or in combination, any of calcium carbonate, barium carbonate, talc, mica, hydrotalcite, calcium sulphate, barium sulphate, aluminium hydroxide, magnesium hydroxide, calcium oxide, magnesium oxide, titanium oxide, and zinc oxide.
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Abstract
A fabric has a coating which comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler. The filler is at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour.
Description
- The invention relates to coated fabrics and in particular to waterproof, breathable coated textiles that can be used, for example, in the manufacture of protective and leisure clothing, bags and luggage.
- Waterproof, breathable coating and laminates for textiles are well known in the prior art, the terms “waterproof” and “breathable” relating to the coating or laminate being impervious to liquid water and permeable to water vapour respectively. This imparts a high degree of comfort to the wearer, preventing condensation of sweat inside the garment while providing a waterproof barrier to keep the wearer dry in all types of weather.
- Materials sold under the registered trade mark GORE-TEX are based on an expanded polytetrafluoroethylene membrane (e.g. U.S. Pat. No. 3,953,583) to produce a microporous membrane that can be laminated to a fabric. The pores in the membrane are 20,000 times larger than a water molecule allowing the passage of vapour, while the extremely low surface energy of the membrane imparts high waterproofing properties.
- Microporous coatings based on polyurethanes are also known in the art, as described by U.S. Pat. Nos. 4,560,611, 5,520,998, 5,626,950 and 5,692,936. These are produced by direct coating a polyurethane solution onto a fabric, then coagulating the solution to produce a network of micropores in the polymer structure.
- Another group of coatings are based on hydrophilic polyurethanes. These are usually directly coated onto a fabric, and rely on the incorporation of hydrophilic segments in the polymer chains. Water molecules from perspiration are therefore able to diffuse from inside the clothing of the wearer through the polymer layer via a step-wise process and transported to the outside environment. The functionality of these hydrophilic layers relies on a humid environment building up inside the breathable garment. The higher the humidity inside the garment, the faster the rate of diffusion of water molecules through the polymeric layer. These types of polyurethane coatings usually contain both hydrophilic and hydrophobic segments to incorporate breathability and waterproofness respectively.
- There are a number of problems associated with both the microporous membranes and the hydrophilic coatings. The performance of microporous membranes can deteriorate over time due to contamination of the pores by soil, detergents and body oils. Blocking of the pores in this manner reduces the breathability of the membrane and can also alter the surface chemistry of the membrane, resulting in the increased likelihood of liquid water penetration. Gore attempted to resolve this problem by the application of a very thin layer of hydrophilic polyurethane on top of the microporous PTFE as a protective layer to prevent the microporous layer from contaminants.
- There are also problems associated with hydrophilic based polyurethane breathable coatings. The main one is their susceptibility to swelling in water. By their very nature, water molecules are attracted to the hydrophilic segments in the polymer. Water molecules are therefore able to “solvate” the hydrophilic segments within the polymer and swell the membrane. This can impart to a “clammy” feeling to the wearer as well as a loss of coating strength. In severe cases it can lead to a loss of adherence to the fabric itself, causing delamination. This is quite common when the garment is subjected to harsh aqueous environments.
- The present invention has been made from a consideration of the above.
- According to the present invention there is provided a coated fabric, wherein the coating comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour.
- In a percolated system a gas is able to pass through the porous structure via a series of holes or pathways. The invention achieves porosity throughout the rubber coating. The very nature of the inorganic filler used in the formulation is that of particles containing a plurality of micron and sub-micron pores as an integral part of its structure. In the silicone rubber formulation, below a certain level of filler these particles are not in close proximity to each other. However, when a certain level, or amount of filler is incorporated into the rubber matrix, a mixed matrix compound is achieved where the porous particles are in sufficiently close proximity to each other to allow the passage of water vapour through each porous particle straight through the continuous mixed matrix coating i.e. the “percolation threshold” is reached to produce a true percolated structure throughout the mixed rubber/filler matrix. For any given system, below the “percolation threshold” a continuous connected component does not exist, but above the percolation threshold there exists a connected component to scale of the system size. Unlike other percolated systems, the invention tends not to allow the passage of liquid water (up to a hydrostatic head pressure of at least 2000 mm) due to the very hydrophobic nature and low surface energy of the silicone rubber.
- In its simplest terms, the “percolated structure” of the proposed invention can be described by the interconnectedness of the porous filler particles throughout the mixed matrix compound that gives rise to continuous connected porous pathways to allow the passage of water vapour molecules throughout the rubber matrix, giving rise to its breathability.
- The silicone composite solution can be coated on a natural or synthetic fabric which may be woven, nonwoven or knitted and comprise, for example, polyester or polyamide. The coating process may involve direct coating onto the fabric substrate. The coated fabric of the invention comprises a waterproof, breathable coated textile that can be used for the manufacture of a variety of articles, such as protective and leisure clothing, bags and luggage.
- Silicone rubber exhibits gas permeability due to the zero energy of rotation about the silicon-oxygen bond in the backbone chain. Together with the plurality of methyl groups on the outside of the polymer chains (which in turn impart water repellent properties), intermolecular interaction is very low causing a large free volume between polymer chains, allowing the diffusion of gas molecules through the polymer matrix. However the level of permeability of silicone rubber alone is not sufficient to produce a water proof, breathable membrane on its own. The coated fabric of the invention therefore incorporates a porous filler which by creating a percolated structure within the silicone rubber composition, complements the permeable properties of the silicone rubber to produce a truly water-vapour permeable, liquid water impermeable membrane.
- For the proposed invention of a waterproof, breathable silicone rubber composite coated onto a textile surface, it is proposed that different construction of coated fabric can be produced according to the end use. Single fabric coated structures are proposed along with multi fabric layer structures. The silicone rubber coating may be provided between adjacent fabrics in a multilayer structure and/or on the exterior of the structure. Some possible embodiments of the invention are mentioned below:—
- 1. Single texture (2-layer) comprising one fabric (e.g. polyester/polyamide (Nylon)) coated on one side with the silicone composite. This would be the most basic construction, intended for example for use in the manufacture of hiking, walking and camping jackets.
2. Double texture (tri-laminate) comprising an outer layer fabric (e.g. polyester/polyamide (Nylon)) laminated to a second, inner liner fabric (polyester) with the silicone composite layer in between. This would be a more durable fabric intended for example for water sport surface suits, dry suits and sailing/yachting suits/jackets. It is envisaged that this durable fabric construction can also be used in heavy duty work wear, for example, for outdoor workers.
3. Double texture (tri-laminate) fabric constructed from an outer fabric and an inner fabric (e.g. polyamide, polyester/polyamide (Nylon)) with the silicone coating in between. This type of construction would be useful for applications where durability and fire retardance are required. - The silicone rubber coating is a solution based formulation that is ideally coated directly onto a fabric. The silicone rubber composition contains the following polysiloxane and solid filler. Optionally the silicone rubber contains any of catalyst, adhesive and/or adhesion promoter and a solvent.
- In one embodiment of the invention the various components of the rubber coating may be included as follows:—
-
Compound Parts (g) (A) Silicone 100 rubber (solid) (B) filler 50-150; optionally 80-120 (C) catalyst 0.5-7.0 (depends on silicone cure system)1 (D) adhesive/adhesion 2.25-4.50 promoter (E) Solvent 200-4002 1the above formulation may be based on a condensation, peroxide or addition cured silicone, which will determine the type and quantity of catalyst (organotin, peroxide or platinum type). 2the solvent level is based on phr of solid rubber to produce a solution of 35-50% solids. A pre mixed silicone polymer solution in toluene may also be used, which would reduce the amount of additional solvent needed - The breathable silicone rubber coating of the invention has advantages over breathable polyurethane systems in as much that it is non-swelling in aqueous environments with no loss of adhesion in tri-laminate constructions. As it is an inherent property of silicone rubber, the coating also has excellent resistance to ageing (e.g. no hydrolysis, another issue with PU systems) and excellent flexibility and low temperature performance.
- The breathable silicone rubber composite has an extremely porous nature due to the high porosity of the diatomaceous earth filler that is used in the silicone formulation. The high porosity and surface area of the composite raises the possibility of extra functionality being designed into the breathable coating. Possibilities include:
- a) incorporation of essential oil anti-microbial agents into the silicone composite. The large internal volume of the porous filler particles may be able to act as a “reservoir” for essential oils that would be released slowly over time to impart antimicrobial properties to the breathable fabric. This would be extremely advantageous for garments that are susceptible to bacterial and fungal growth which causes unpleasant odours.
- b) Similarly, insect repellent agents could also be incorporated into the filler particles. This would be advantageous for hiking and camping clothing in areas where a high population of insects is present.
- The above areas are only possible due to the large porous internal volume of the filler particles. Traditional waterproof, breathable coatings fashioned from microporous PTFE, polyurethane and hydrophilic solid polyurethane membranes do not have this large, internal free volume to act as a reservoir for additional functional materials. This is one other distinct advantage that the present invention has over prior art breathable materials.
- The invention will now be described further by way of example only with reference to the accompanying drawing:—
-
FIG. 1 which shows a schematic diagram of a tri-laminate waterproof breathable construction of the invention and the water vapour evaporation pathway therethrough. - Referring to the drawing a
coated fabric 10 comprises a first wovenfabric 11 having a plain weave construction made from polyamide. This is direct coated on one side thereof with asilicone rubber composition 12. The silicone rubber composition has the following components:— - (A) a
polysiloxane 13 that can be cross-linked by polyaddition, polycondensation or free radical means catalysed by platinum, organotin or peroxide compounds respectively.
(B) aporous filler 14. In one embodiment this comprises natural diatomaceous earth (or diatomite) which is a soft siliceous sedimentary rock crumbled into a fine powder. The porous filler, while typically natural diatomaceous earth, may also be calcined and flux-calcined. Calcination is the heat treatment of a material in the presence of air or oxygen. Flux-calcination is the heat treatment of a material in the presence of a fluxing agent.
(C) a catalyst (not shown), which can be either an organo-tin compound, platinum catalyst or peroxide. For the current formulation, C14-010, an organo-tin catalyst commercially available from Itac Ltd can be typically used.
(D) additionally (not shown), a mixture of glycidoxypropyltrimethoxysilane and vinyltriacetoxysilane adhesion promoter, such as the commercially available SYL-OFF 297 from Dow Corning. This is also supplied under the product code C14-025 from Itac Ltd.
(E) an aromatic or aliphatic solvent (not shown) to adjust the solids content of the coating solution. Toluene is typically used for this purpose, although SPB2 (a mixture of hexane and heptane) can also be used.
The ratio of mixing the components A-E is set out below. -
Compound Parts (g) (A) C14-007 100 (30% solids solution in toluene) (B) Celtix filler 15-45 (C) C14-010 1.75-3.50 (D) C14-025 2.25-4.50 (E) Solvent 10-50 - A second
plain weave fabric 15 also made form polyamide is situated on the other side of the coating such that the silicone coating is sandwiched between the two fabrics. - If using a polycondensation cure silicone rubber such as that mentioned above, excess moisture in the filler should be removed prior to mixing. Natural diatomaceous earth contains around 8% by weight of moisture that is held by the filler. Excessive moisture can interfere with the condensation reaction, leading to insufficient crosslinking and poor physical properties. The diatomaceous earth filler should therefore ideally be dried at temperatures of 100-120° C. for a minimum of 16 hours prior to mixing. Alternatively, a molecular sieve compound can be added to the coating formulation that will remove the moisture from the filler, thus obviating the necessity to pre-dry the filler before mixing the compound. If the latter alternative is to be employed, the molecular sieve compound needs to be added to the coating formulation and thoroughly mixed and left to stand for not less than two hours before coating onto the fabric. A typical molecular sieve compound employed for this purpose is a porous, crystalline aluminosilicate powder such as those marketed under the brand name “Sylosiv”.
- The formulation should be mixed in a mechanical mixing device, such as a Z-blade mixer. Components (A) and (B) should be thoroughly mixed in the first instance for 20-30 mins to produce a homogenous “dough” mix, followed by components (C), (D) and (E). The complete formulation should then be mixed for a further 20-30 mins until a completely homogenous solution is produced. Measured solids content of the solution should be 35-45%. After the final mix, the formulation will have a useable pot life of 8 hours.
- The water vapour pathway is in the direction of arrows A.
- The invention will now be described further with reference to the following examples.
- The silicone composite solution can be coated on a synthetic woven or knitted fabric e.g. polyester or nylon using direct coating (knife over roller) method. A multiple number of passes is required in order to achieve a coating weight of 70-100 gsm. Ideally a coating weight of around 85 gsm should be achieved. It is usual for at least three coating passes to be needed to achieve this weight. It is important to ensure the temperature is at a temperature that enables evaporation of the solvent, but is not too high as to cause premature cross-linking of the silicone composite. As a guide, a temperature of 60-80° C. should be maintained in the heated spreading chest. The uncoated side of the fabric will function as the “inner” lining of the waterproof, breathable fabric.
- After the last coating of the silicone composite has been applied, a final coating of silicone based pressure sensitive adhesive (PSA) is required in order to laminate the coated fabric to an “outer” layer fabric to produce a tri-laminate construction. A commercial grade PSA from Dow Corning known as DC7358 (a peroxide cured adhesive) can be used for this purpose. Peroxide (typically dibenzoyl peroxide) needs to be premixed into the adhesive solution at a level between 0.5-2%. A light coating of adhesive (between 5-20 gsm depending on the level of adhesion required) is then applied over the silicone coating, the solvent is allowed to evaporate through the heated chest (temperature must not be over 75° C. or premature crosslinking of the adhesive will occur). The coated fabric is then laminated through two pressurised rollers against a second, uncoated fabric to produce the tri-laminate construction. The laminated fabric can then be cured off-line. The fabric coating can be cured for 30-45 min at a temperature of 120-140° C. Lower temperatures down to 100° C. can be used for longer curing times of up to 6 hours.
- The tri-laminate water proof breathable fabric can be used (but not limited to) garments for water sport and marine applications such as surface suits, dry suits, sailing garments, etc.
- The single coated fabric is manufactured in a similar way to the tri-laminate. On this occasion the coated fabric serves as the outer fabric shell as opposed to the inner layer fabric, and the fabric is not then laminated to another fabric. There is therefore no need to apply a silicone adhesive layer. However, due to the non-stick properties of silicone rubber, it is necessary to apply a breathable, low melting point thermoplastic top coat on the breathable silicone layer in order to facilitate the adhesion of seam sealing tapes. A polyurethane coating solution such as Larithane BTH231 can be used for this purpose. Swelling effects of the polyurethane are not as critical as the fabric is not laminated to another outer fabric, where loss of peel adhesion could become an issue.
- Water vapour transmission rate (breathability):
- The breathability of the fabric has been internally tested according to BS7209 “Water vapour permeable apparel fabrics”. A circular test piece of the fabric is fixed over the rim of a circular aluminium dish that contains a measured amount of distilled water. The outside surface of the rim of the dish is then sealed so that the only pathway water vapour can take is through the fabric. The total weight of the dish, fabric and water is measured, whereupon the dish is then placed on a circular turntable that rotates to prevent a microclimate of humid air above the surface of the fabric. The dish is then left in atmospheric conditions of 65% relative humidity and 20° C. for at least 16 hours. The weight of the whole test dish is then measured to calculate the loss of water in the form of vapour through the dish. This measurement of weight loss is then calculated to calculate the “water vapour transmission rate” (WVTR) in units of g/m2/24 hours. The weight loss of water vapour through the test fabric is also measured against that from a reference fabric to calculate the water vapour permeability index (WVPI), quoted as a percentage of the reference fabric.
- The waterproof breathable fabric as described in this specification will typically have a WVTR of 400-650 g/m2/24 hours, more typically around 500 g/m2/24 hours and a WVPI of 50-90%, more typically around 75%.
- Hydrostatic Head pressure rating (waterproofness):
- This is described as the water pressure required to leak (penetrate) through the fabric. This is determined by carrying out test BS3424-26, which subjects a test piece of fabric to pressure from either a column of water or water pressurised from a compressor. Any fabric that can withstand a pressure equivalent to a column height of 1000 mm is deemed “waterproof” although in practice ratings of 2,000-20,000 mm are expected from quality products.
- The waterproof breathable fabric as described in this specification demonstrated a hydrostatic head rating of at least 2,000 mm according to internal tests.
- Peeling (adhesion) strength—tri-laminate only.
- The peeling strength is simply the force required to peel the laminated fabrics apart, as measured on a tensometer. The test piece is a 50 mm wide strip of the fabric with both face and back fabrics delaminated from each other. The force in N/50 mm is then measured that is required to peel the fabrics apart.
- The tri-laminate fabric as described previously typically has a peeling strength of 4-8 N/50 mm, more typically around 6 N/50 mm. The peeling strength will remain unaffected after the test piece has been immersed in a 2% salt water solution for 24 hours.
- It is to be understood that the above described embodiments are by way of illustration only. Many modifications and variations are possible.
- Some possible modifications and variations are set out below.
a) The invention contemplates the optional addition of a thixotropic filler such as fumed silica to the base silicone rubber formulation. This would alter the rheological properties by increasing the viscosity of the coating formulation and reduce “strike-through” of the solution through the fabric. This leads to reducing the degree of coating penetration through the fabric leading to a better appearance and handle of the coated fabric.
b) An improvement in adhesion of silicone rubber to the fabric may optionally be achieved by applying a pre-treatment of an organic silane compound to the fabric prior to applying the rubber coating. The silane pre-treatment would typically be applied by a dipping technique into a silane solution followed by drying to evaporate the solvent.
c) As discussed previously the diatomaceous earth filler may be dried prior to mixing into the rubber formulation, as excess moisture present in the filler disrupts the condensation cross-linking reaction. The addition of a molecular sieve compound into the rubber/filler solution 2-3 hours prior to coating removes the moisture from within the coating solution, thus eliminating any requirement to pre-dry the filler.
d) One or more blowing agents may be used to increase the porosity of the adhesive. Increasing the elastomer content of the adhesive may improve the peel strength.
d) While the currently preferred porous filler used to create a percolated porous structure is natural diatomaceous earth, there are a range of other porous fillers which may be used in place of or in combination with diatomaceous earth. Such fillers may include kaolinite, amorphous silica, zeolites, metal organic frameworks, porous carbon blacks and montmorillonite clay.
e) Additional fillers may be incorporated into the composite formulation to improve the physical properties of the composite coating. These include, either alone, or in combination, any of calcium carbonate, barium carbonate, talc, mica, hydrotalcite, calcium sulphate, barium sulphate, aluminium hydroxide, magnesium hydroxide, calcium oxide, magnesium oxide, titanium oxide, and zinc oxide.
Claims (33)
1. A coated fabric, comprising:
a coating comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour.
2. The coated fabric of claim 1 , wherein a fabric is selected from the group consisting of knitted, woven non-woven, and combinations thereof.
3. The coated fabric of claim 1 , wherein a fabric is selected from the group consisting of cotton, polyester, polyamide, and combinations thereof.
4. The coated fabric of claim 1 , wherein the silicone rubber composition is selected from the group consisting of polysiloxane (condensation), peroxide, additional cured silicone, and combinations thereof.
5. The coated fabric of claim 1 , wherein the silicone rubber composition comprises a filler or combination of fillers with a porosity in the range from 2 nm to 1 μm.
6. The coated fabric of claim 5 , wherein the silicone rubber composition comprises a filler or combination of fillers with a mean pore size of substantially −0.5 μm.
7. The coated fabric of claim 1 , wherein the porous filler is selected from the group consisting of kaolinite, amorphous silica, diatomaceous earth, zeolites, metal organic frameworks, porous carbon blacks, montmorillonite clay, and combinations thereof.
8. The coating fabric of claim 1 , wherein the porous filler comprises natural diatomaceous earth.
9. The coating fabric of claim 8 , wherein the porous filler comprises natural diatomaceous earth which is calcined.
10. The coating fabric of claim 8 , wherein the porous filler comprises natural diatomaceous earth which is flux-calcined.
11. The coated fabric of claim 8 , wherein the particle size range of filler is in the range from 5 to 100 μm.
12. The coated fabric of claim 11 , wherein the particle size range of filler is an average pore size of substantially 11 μm.
13. The coated fabric of claim 1 , wherein one or more additional fillers are incorporated into the formulation for improving the rheological properties of the coating compound, and for improving the physical properties of the cured coating itself.
14. The coated fabric of claim 13 , wherein the reinforcing filler or rheology modifying filler is selected from a group consisting of calcium carbonate, barium carbonate, talc, mica, hydrotalcite, calcium sulphate, barium sulphate, aluminium hydroxide, magnesium hydroxide, calcium oxide, magnesium oxide, titanium oxide, zinc oxide, and combinations thereof.
15. The coated fabric of claim 1 , wherein the silicone rubber composition comprises from 50 to 150 parts by weight of porous filler per 100 parts by weight silicone rubber.
16. The coated fabric of claim 1 , wherein the silicone rubber composition comprises catalyst.
17. The coated fabric of claim 16 , wherein the catalyst is selected from a group consisting of organo-tin, platinum, peroxide, and combinations thereof.
18. The coated fabric of claim 16 , wherein the silicone rubber composition comprises from 0.5 to 7.0 parts by weight of the catalyst per 100 parts by weight (solid) silicone rubber.
19. The coated fabric of claim 1 , wherein the silicone rubber composition comprises an adhesion promoter.
20. The coated fabric of claim 19 , wherein the adhesion promoter comprises at least one of an organosilicon compound containing an epoxy group, and an organosilicon compound containing a vinyl acetoxy group.
21. The coated fabric of claim 19 , wherein the silicone rubber composition comprises from 2.25 to 4.5 parts by weight of adhesion promoter per 100 parts by weight silicone rubber.
22. The coated fabric of claim 1 , wherein the silicone rubber composition comprises a solvent.
23. The coated fabric of claim 22 , wherein the solvent comprises an aromatic or aliphatic organic solvent.
24. The coated fabric of claim 22 , wherein the solvent is selected from a group consisting of toluene, xylene, hexane, heptanes, and combinations thereof.
25. The coated fabric of claim 22 , wherein the silicone rubber composition comprises from 200 to 400 parts by weight of solvent per 100 parts by weight (solid) silicone rubber.
26. The coated fabric of claim 1 , wherein the silicone rubber composition comprises at least one anti-microbial agent.
27. The coated fabric of claim 1 , wherein the silicone rubber composition comprises at least one insect repellent agent.
28. The coated fabric of claim 1 , wherein the coated fabric is breathable and waterproof.
29. The coated fabric of claim 1 , having a coating weight of 70-100 gsm of the silicone rubber composition on the fabric.
30. A coated fabric structure, comprising a coated fabric comprising a coating which comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour;
the coated fabric in combination with one or more further fabrics.
31. The coated fabric structure of claim 30 , wherein adhesive is coated onto the coated fabric to laminate a second fabric to produce a trilaminate structure, wherein the adhesive coating has a coating weight of adhesive of 5-20 gsm.
32. A method of making a coated fabric comprising:
providing a coated fabric comprising a coating which comprises an elastomeric, heat curable silicone rubber composition containing a porous inorganic filler at sufficiently high loading to produce a percolated porous structure, the percolated porous structure being permeable to water vapour;
wherein the silicone rubber composition is coated onto the base fabric using a knife-over roller technique.
33. A method of making a coated fabric of claim 32 , wherein a second fabric is laminated to an adhesive layer on the base fabric to provide a trilaminate coated fabric.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1311647.0A GB201311647D0 (en) | 2013-06-28 | 2013-06-28 | Coated fabrics |
| GB1311647.0 | 2013-06-28 | ||
| PCT/GB2014/051928 WO2014207450A1 (en) | 2013-06-28 | 2014-06-24 | Coated fabrics |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20160130747A1 true US20160130747A1 (en) | 2016-05-12 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US14/901,139 Abandoned US20160130747A1 (en) | 2013-06-28 | 2014-06-24 | Coated fabrics |
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| Country | Link |
|---|---|
| US (1) | US20160130747A1 (en) |
| EP (1) | EP3014016A1 (en) |
| CN (1) | CN105518211A (en) |
| AU (1) | AU2014300750A1 (en) |
| GB (2) | GB201311647D0 (en) |
| WO (1) | WO2014207450A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN108078035A (en) * | 2017-12-13 | 2018-05-29 | 仙桃市鼎业劳保用品有限公司 | Protective garment |
| US20180230332A1 (en) * | 2017-02-15 | 2018-08-16 | Gaco Western, LLC | Silicone coatings |
| US10607589B2 (en) | 2016-11-29 | 2020-03-31 | Milliken & Company | Nonwoven composite |
| US11937653B2 (en) * | 2020-07-09 | 2024-03-26 | Vitiprints, LLC | Smart mask |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107163326B (en) * | 2017-05-25 | 2020-02-18 | 际华三五一七橡胶制品有限公司 | Ventilative waterproof adhesive tape compound is glued and adhesive tape raincoat |
| CN108867064B (en) * | 2018-07-20 | 2019-11-26 | 西安科技大学 | A method of cheap stable ultra-hydrophobic fabric is prepared by raw material of magnesia |
| CN109338816B (en) * | 2018-11-21 | 2021-05-14 | 浙江双东装饰材料有限公司 | A kind of wear-resistant soundproof wallpaper and preparation method thereof |
| US11872793B2 (en) * | 2020-04-27 | 2024-01-16 | Patrick Kelly | Method of preparing antimicrobial sheets for articles of manufacture having antimicrobial properties |
| TWI831097B (en) * | 2021-12-09 | 2024-02-01 | 財團法人紡織產業綜合研究所 | Thermal-insulating fabric |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| JPS5920793B2 (en) * | 1982-01-06 | 1984-05-15 | 倉庫精練株式会社 | Durable water-resistant, moisture-permeable, breathable, and anti-melt processing method for synthetic fiber knitted fabrics |
| JPS6197466A (en) * | 1984-10-19 | 1986-05-15 | 東レ株式会社 | Water-proof and moisture pervious processing of synthetic fiber knitted fabric |
| US5789025A (en) * | 1995-12-15 | 1998-08-04 | The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration | Fire resistant, moisture barrier membrane |
| GB9919083D0 (en) * | 1999-08-13 | 1999-10-13 | Dow Corning | Silicone coated textile fabrics |
| FR2835855B1 (en) * | 2002-02-08 | 2005-11-11 | Rhodia Chimie Sa | USE OF REVERSIBLE SILICONE REVERSE EMULSION FOR REALIZING "IMPER-BREATHABLE" COATINGS |
| JP3999987B2 (en) * | 2002-03-14 | 2007-10-31 | 旭化成ワッカーシリコーン株式会社 | Silicone composition for airbag coating |
| GB0302491D0 (en) * | 2003-02-04 | 2003-03-05 | Dow Corning | Coating compositions and textile fabrics coated therewith |
| CN100422430C (en) * | 2005-04-21 | 2008-10-01 | 田文新 | Breathable organic silicon synthetic leather and manufacturing method thereof |
| GB0520145D0 (en) * | 2005-10-04 | 2005-11-09 | Dow Corning Taiwan | A liquid silicone rubber composition for textile coating |
| WO2007097022A1 (en) * | 2006-02-27 | 2007-08-30 | Sumitomo Bakelite Co., Ltd. | Adhesive film |
| CN101501270B (en) * | 2006-08-14 | 2012-08-08 | 陶氏康宁东丽株式会社 | Silicone rubber composition for coating of woven fabric, and coated woven fabric |
| DE102007058358A1 (en) * | 2007-12-03 | 2009-06-10 | Monier Roofing Components Gmbh & Co. Kg | Underlayment, especially for pitched roofs |
| CN102041688B (en) * | 2010-11-01 | 2012-11-14 | 高文源 | Waterproof breathable organic silicon synthetic leather and manufacturing method thereof |
| CN103717645B (en) * | 2011-07-06 | 2016-08-17 | 莫门蒂夫性能材料股份有限公司 | Moisture-curable elastic translucent silicone waterproof coating and method for preparing same |
-
2013
- 2013-06-28 GB GBGB1311647.0A patent/GB201311647D0/en not_active Ceased
-
2014
- 2014-06-24 AU AU2014300750A patent/AU2014300750A1/en not_active Abandoned
- 2014-06-24 CN CN201480037243.0A patent/CN105518211A/en active Pending
- 2014-06-24 EP EP14742572.2A patent/EP3014016A1/en not_active Withdrawn
- 2014-06-24 WO PCT/GB2014/051928 patent/WO2014207450A1/en not_active Ceased
- 2014-06-24 US US14/901,139 patent/US20160130747A1/en not_active Abandoned
- 2014-06-24 GB GB1522041.1A patent/GB2535300A/en not_active Withdrawn
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10607589B2 (en) | 2016-11-29 | 2020-03-31 | Milliken & Company | Nonwoven composite |
| US20180230332A1 (en) * | 2017-02-15 | 2018-08-16 | Gaco Western, LLC | Silicone coatings |
| US10450483B2 (en) * | 2017-02-15 | 2019-10-22 | Firestone Building Products Company, Llc | Method for coating silicone rubber substrate |
| CN108078035A (en) * | 2017-12-13 | 2018-05-29 | 仙桃市鼎业劳保用品有限公司 | Protective garment |
| US11937653B2 (en) * | 2020-07-09 | 2024-03-26 | Vitiprints, LLC | Smart mask |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2014300750A1 (en) | 2016-02-04 |
| WO2014207450A1 (en) | 2014-12-31 |
| GB2535300A (en) | 2016-08-17 |
| CN105518211A (en) | 2016-04-20 |
| GB201311647D0 (en) | 2013-08-14 |
| EP3014016A1 (en) | 2016-05-04 |
| GB201522041D0 (en) | 2016-01-27 |
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Owner name: BRENNAN ENTERPRISE LIMITED, UNITED KINGDOM Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:HARRISON, WAYNE JOHN;REEL/FRAME:037365/0676 Effective date: 20151214 |
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| STCB | Information on status: application discontinuation |
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