JPH04226342A - Heat-resistant, flame-retardant film member - Google Patents
Heat-resistant, flame-retardant film memberInfo
- Publication number
- JPH04226342A JPH04226342A JP12035891A JP12035891A JPH04226342A JP H04226342 A JPH04226342 A JP H04226342A JP 12035891 A JP12035891 A JP 12035891A JP 12035891 A JP12035891 A JP 12035891A JP H04226342 A JPH04226342 A JP H04226342A
- Authority
- JP
- Japan
- Prior art keywords
- heat
- resistant
- flame
- fibers
- inorganic
- 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.)
- Granted
Links
- 239000003063 flame retardant Substances 0.000 title claims abstract description 53
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 48
- 239000004744 fabric Substances 0.000 claims abstract description 74
- 239000000835 fiber Substances 0.000 claims abstract description 61
- 229920005989 resin Polymers 0.000 claims abstract description 31
- 239000011347 resin Substances 0.000 claims abstract description 31
- 150000002484 inorganic compounds Chemical class 0.000 claims abstract description 23
- 229910010272 inorganic material Inorganic materials 0.000 claims abstract description 23
- 239000011247 coating layer Substances 0.000 claims abstract description 21
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 19
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 19
- 239000000654 additive Substances 0.000 claims abstract description 16
- 239000012784 inorganic fiber Substances 0.000 claims abstract description 15
- 230000000996 additive effect Effects 0.000 claims abstract description 9
- 239000010445 mica Substances 0.000 claims abstract description 6
- 229910052618 mica group Inorganic materials 0.000 claims abstract description 6
- 239000002585 base Substances 0.000 claims description 48
- 239000012528 membrane Substances 0.000 claims description 35
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 16
- 239000003365 glass fiber Substances 0.000 claims description 15
- 239000000779 smoke Substances 0.000 claims description 12
- 229920002994 synthetic fiber Polymers 0.000 claims description 11
- 239000012209 synthetic fiber Substances 0.000 claims description 11
- 239000000377 silicon dioxide Substances 0.000 claims description 8
- 239000010425 asbestos Substances 0.000 claims description 7
- 229910052895 riebeckite Inorganic materials 0.000 claims description 7
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 claims description 6
- 238000002844 melting Methods 0.000 claims description 6
- 230000008018 melting Effects 0.000 claims description 6
- 239000003638 chemical reducing agent Substances 0.000 claims description 5
- 239000012796 inorganic flame retardant Substances 0.000 claims description 4
- 229910052751 metal Inorganic materials 0.000 claims description 4
- 239000002184 metal Substances 0.000 claims description 4
- 229920000049 Carbon (fiber) Polymers 0.000 claims description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 2
- 239000003513 alkali Substances 0.000 claims description 2
- 239000004917 carbon fiber Substances 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- 238000005979 thermal decomposition reaction Methods 0.000 claims description 2
- 238000009958 sewing Methods 0.000 abstract description 9
- 239000000203 mixture Substances 0.000 abstract description 6
- 239000000463 material Substances 0.000 description 12
- 238000000576 coating method Methods 0.000 description 11
- 238000005452 bending Methods 0.000 description 10
- 239000011248 coating agent Substances 0.000 description 10
- 239000000843 powder Substances 0.000 description 10
- -1 polyethylene terephthalate Polymers 0.000 description 9
- 239000011342 resin composition Substances 0.000 description 8
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 7
- 238000000354 decomposition reaction Methods 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910000831 Steel Inorganic materials 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 5
- 230000001070 adhesive effect Effects 0.000 description 5
- 238000005520 cutting process Methods 0.000 description 5
- 230000014759 maintenance of location Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000004014 plasticizer Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 239000010959 steel Substances 0.000 description 5
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 4
- 239000004760 aramid Substances 0.000 description 4
- 229920003235 aromatic polyamide Polymers 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000945 filler Substances 0.000 description 4
- 229920002681 hypalon Polymers 0.000 description 4
- 229920000271 Kevlar® Polymers 0.000 description 3
- YKTSYUJCYHOUJP-UHFFFAOYSA-N [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] Chemical compound [O--].[Al+3].[Al+3].[O-][Si]([O-])([O-])[O-] YKTSYUJCYHOUJP-UHFFFAOYSA-N 0.000 description 3
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000005038 ethylene vinyl acetate Substances 0.000 description 3
- 239000012210 heat-resistant fiber Substances 0.000 description 3
- 239000004761 kevlar Substances 0.000 description 3
- 239000002075 main ingredient Substances 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 230000002265 prevention Effects 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 238000010998 test method Methods 0.000 description 3
- 239000002759 woven fabric Substances 0.000 description 3
- 150000003752 zinc compounds Chemical class 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 229940037003 alum Drugs 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001642 boronic acid derivatives Chemical class 0.000 description 2
- 239000004566 building material Substances 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 239000010440 gypsum Substances 0.000 description 2
- 229910052602 gypsum Inorganic materials 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000009413 insulation Methods 0.000 description 2
- 150000002506 iron compounds Chemical class 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000123 paper Substances 0.000 description 2
- 229920001084 poly(chloroprene) Polymers 0.000 description 2
- 239000002893 slag Substances 0.000 description 2
- 239000006104 solid solution Substances 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- 229920002972 Acrylic fiber Polymers 0.000 description 1
- NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical group C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- ZVFDTKUVRCTHQE-UHFFFAOYSA-N Diisodecyl phthalate Chemical compound CC(C)CCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC(C)C ZVFDTKUVRCTHQE-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- PMVSDNDAUGGCCE-TYYBGVCCSA-L Ferrous fumarate Chemical compound [Fe+2].[O-]C(=O)\C=C\C([O-])=O PMVSDNDAUGGCCE-TYYBGVCCSA-L 0.000 description 1
- 244000043261 Hevea brasiliensis Species 0.000 description 1
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229920000784 Nomex Polymers 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 229920002302 Nylon 6,6 Polymers 0.000 description 1
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004962 Polyamide-imide Substances 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 241000270295 Serpentes Species 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- 230000004308 accommodation Effects 0.000 description 1
- 229920006221 acetate fiber Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000005263 alkylenediamine group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 229940058905 antimony compound for treatment of leishmaniasis and trypanosomiasis Drugs 0.000 description 1
- 150000001463 antimony compounds Chemical class 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004069 aziridinyl group Chemical group 0.000 description 1
- XBJJRSFLZVLCSE-UHFFFAOYSA-N barium(2+);diborate Chemical compound [Ba+2].[Ba+2].[Ba+2].[O-]B([O-])[O-].[O-]B([O-])[O-] XBJJRSFLZVLCSE-UHFFFAOYSA-N 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- ZFMQKOWCDKKBIF-UHFFFAOYSA-N bis(3,5-difluorophenyl)phosphane Chemical compound FC1=CC(F)=CC(PC=2C=C(F)C=C(F)C=2)=C1 ZFMQKOWCDKKBIF-UHFFFAOYSA-N 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000000920 calcium hydroxide Substances 0.000 description 1
- 229910001861 calcium hydroxide Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KRGNPJFAKZHQPS-UHFFFAOYSA-N chloroethene;ethene Chemical group C=C.ClC=C KRGNPJFAKZHQPS-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000005034 decoration Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 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 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- MIMDHDXOBDPUQW-UHFFFAOYSA-N dioctyl decanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCCC(=O)OCCCCCCCC MIMDHDXOBDPUQW-UHFFFAOYSA-N 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229920001038 ethylene copolymer Polymers 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000011773 ferrous fumarate Substances 0.000 description 1
- 235000002332 ferrous fumarate Nutrition 0.000 description 1
- 229960000225 ferrous fumarate Drugs 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 239000002657 fibrous material Substances 0.000 description 1
- 230000009970 fire resistant effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 229910001701 hydrotalcite Inorganic materials 0.000 description 1
- 229960001545 hydrotalcite Drugs 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000001841 imino group Chemical group [H]N=* 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011490 mineral wool Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 229920003052 natural elastomer Polymers 0.000 description 1
- 229920001194 natural rubber Polymers 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000004763 nomex Substances 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 239000002367 phosphate rock Substances 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000011295 pitch Substances 0.000 description 1
- 229920002312 polyamide-imide Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 229920002803 thermoplastic polyurethane Polymers 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 description 1
- VLCLHFYFMCKBRP-UHFFFAOYSA-N tricalcium;diborate Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]B([O-])[O-].[O-]B([O-])[O-] VLCLHFYFMCKBRP-UHFFFAOYSA-N 0.000 description 1
- NFMWFGXCDDYTEG-UHFFFAOYSA-N trimagnesium;diborate Chemical compound [Mg+2].[Mg+2].[Mg+2].[O-]B([O-])[O-].[O-]B([O-])[O-] NFMWFGXCDDYTEG-UHFFFAOYSA-N 0.000 description 1
- 239000003981 vehicle Substances 0.000 description 1
- 238000009941 weaving Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Landscapes
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
Abstract
Description
【0001】0001
【産業上の利用分野】本発明は耐熱難燃性膜体に関する
ものであり、更に詳しく述べるならば、耐熱難燃性にす
ぐれ、かつ、縫製性および耐屈曲性にすぐれた繊維膜体
に関するものである。[Field of Industrial Application] The present invention relates to a heat-resistant and flame-retardant membrane, and more specifically, to a fiber membrane that has excellent heat-resistant and flame-retardant properties, as well as excellent sewing and bending resistance. It is.
【0002】0002
【従来の技術】近年、建築材料、内装材等の素材、車両
、船舶、航空機等の各種用品、電気器具等に使用される
合成樹脂の不燃化、難燃化が強く要望されており法令に
よる使用規制も強化されている。[Prior Art] In recent years, there has been a strong demand for synthetic resins used in building materials, interior decoration materials, various items for vehicles, ships, aircraft, electrical appliances, etc. to be made nonflammable and flame retardant, and this is required by law. Regulations on its use have also been strengthened.
【0003】その対策の1つとして、例えば特公昭55
−25055号公報には、ガラス繊維クロスの表面上に
クロルスルフォン化ポリエチレンを主剤とする被膜層を
形成した不燃性膜体が開示されている。しかし、クロル
スルフォン化ポリエチレンが高価であるため、この不燃
性膜体は実用化されていない。近年耐熱難燃化被膜主剤
としてシリコーン樹脂、又は弗素樹脂を用いたものが種
々開発されているが何れも、前記クロルスルフォン化ポ
リエチレンにくらべて更に高価であり、その上シリコー
ン樹脂は架橋、被膜形成に長時間を要し、弗素樹脂は作
業性が悪く実用的な加工材料としては使用に難がある。
上記の理由により耐熱難燃化被膜主剤としては、樹脂自
体が難燃性であり、かつ汎用性のあるポリ塩化ビニル樹
脂を使用することが好ましい。[0003] As one of the countermeasures, for example,
Japanese Patent No. 25055 discloses a nonflammable film body in which a coating layer containing chlorosulfonated polyethylene as a main ingredient is formed on the surface of a glass fiber cloth. However, because chlorosulfonated polyethylene is expensive, this nonflammable membrane has not been put into practical use. In recent years, various types of heat-resistant and flame-retardant coatings using silicone resins or fluororesins as the main ingredient have been developed, but they are all more expensive than the chlorosulfonated polyethylene mentioned above, and in addition, silicone resins are difficult to crosslink and form a coating. It takes a long time to process, and fluororesin has poor workability, making it difficult to use as a practical processing material. For the above reasons, it is preferable to use polyvinyl chloride resin, which is flame retardant itself and has versatile properties, as the main ingredient for the heat-resistant and flame-retardant coating.
【0004】被覆材料として最も一般的なポリ塩化ビニ
ル樹脂については、燃焼時多量の発煙を伴って火災現場
に居合せた人及び消防活動者を呼吸困難にさせ死傷者を
出すことがあるなどの問題があり、このためポリ塩化ビ
ニル樹脂の不燃化を一層高め、さらに、燃焼時の発煙を
可及的減少せしめることが課題となっている。[0004] Polyvinyl chloride resin, which is the most common coating material, produces a large amount of smoke when burned, making it difficult for people present at the fire scene and firefighters to breathe, which can result in casualties. Therefore, it has become a challenge to further improve the nonflammability of polyvinyl chloride resin and to further reduce smoke generation during combustion as much as possible.
【0005】特公昭55−4582号公報には、塩化ビ
ニル樹脂にホウ酸塩、亜鉛化合物又は鉄化合物の1種又
は2種以上と、水酸化アルミニウム及び又は硫酸バリウ
ムを加えてなる組成物を不燃性基布上に均一に被覆して
なる不燃性膜体を開示している。この膜体は火炎が近づ
いても殆んど燃焼することがなく、また、たとえ着火し
た場合にも殆んど発煙せず、さらに、所望の防水性及び
強度を備えたシート状物として広範な用途に供しうるも
のである。[0005] Japanese Patent Publication No. 55-4582 discloses that a composition consisting of a vinyl chloride resin, one or more of borate, zinc compound or iron compound, and aluminum hydroxide and/or barium sulfate is used as a non-combustible material. The present invention discloses a nonflammable membrane formed by uniformly coating a base fabric. This membrane hardly combusts even when a flame approaches, and even if it ignites, it emits almost no smoke.Furthermore, it can be widely used as a sheet-like material with the desired waterproofness and strength. It can be used for various purposes.
【0006】しかし、この膜体は、基布として不燃性ガ
ラス繊維布帛を用いているため、その不燃性はすぐれて
いるが、その重量(目付)は大きくて使用や取扱いに不
便があり、また縫製しにくく、また耐屈曲性が低いため
、使用間に折損しやすく、ミシン目から裂けやすいなど
の問題があった。However, since this membrane uses nonflammable glass fiber fabric as the base fabric, although its nonflammability is excellent, its weight (fabric weight) is large, making it inconvenient to use and handle. Since it is difficult to sew and has low bending resistance, it has problems such as being easily broken during use and easily tearing from perforations.
【0007】従って、実用上十分な耐熱難燃性を保持し
、かつ、はげしい振動、はためき、或は繰り返えし屈曲
に十分耐え、縫製容易でミシン目からの裂断のない耐熱
難燃性膜体の出現が強く望まれている。[0007] Therefore, a heat-resistant and flame-retardant material that maintains sufficient heat-resistance and flame retardancy for practical use, can withstand strong vibrations, flapping, or repeated bending, is easy to sew, and does not tear from perforations. The appearance of a membranous body is strongly desired.
【0008】[0008]
【発明が解決しようとする課題】本発明は満足すべき耐
熱難燃性を有し、しかも縫製しやすく、耐屈曲性が良好
で、かつ、ミシン目からの裂断の生じにくい耐熱難燃性
膜体を提供する。[Problems to be Solved by the Invention] The present invention has satisfactory heat and flame retardant properties, is easy to sew, has good bending resistance, and is resistant to tearing from perforations. Provides a membrane body.
【0009】[0009]
【課題を解決するための手段】本発明の耐熱難燃性膜体
は、無機繊維と、有機繊維とを含んでなる基布と、この
基布の少くとも1面上に形成され、かつ、塩化ビニル樹
脂とを含んでなる耐熱難燃被覆層とを有し、前記基布中
の無機繊維の有機繊維に対する混用重量比が、10:9
0〜99.5:0.5の範囲内にあることを特徴とする
ものである。[Means for Solving the Problems] The heat-resistant and flame-retardant membrane of the present invention comprises a base fabric containing inorganic fibers and organic fibers, and formed on at least one surface of the base fabric, and a heat-resistant and flame-retardant coating layer comprising a vinyl chloride resin, and the weight ratio of inorganic fiber to organic fiber in the base fabric is 10:9.
It is characterized by being within the range of 0 to 99.5:0.5.
【0010】0010
【作用】本発明の耐熱難燃性膜体の基布に用いられる無
機繊維は、石綿繊維、セラミック繊維、シリカ繊維、ガ
ラス繊維、カーボン繊維および金属繊維から選ぶことが
できる。[Function] The inorganic fibers used for the base fabric of the heat-resistant and flame-retardant membrane of the present invention can be selected from asbestos fibers, ceramic fibers, silica fibers, glass fibers, carbon fibers and metal fibers.
【0011】また基布に用いられる有機繊維は、天然繊
維、例えば、木綿、麻など、再生繊維、例えば、ビスコ
ースレーヨン、キュプラなど、半合成繊維、例えば、ジ
−およびトリ−アセテート繊維など、及び合成繊維、例
えば、ナイロン6、ナイロン66、ポリエステル(ポリ
エチレンテレフタレート等)繊維、芳香族ポリアミド繊
維、アクリル繊維、ポリ塩化ビニル繊維、ポリオレフィ
ン繊維および不溶化又は難溶化されたポリビニルアルコ
ール繊維など、から選ぶことができる。The organic fibers used for the base fabric include natural fibers such as cotton and linen, regenerated fibers such as viscose rayon and cupro, semi-synthetic fibers such as di- and tri-acetate fibers, etc. and synthetic fibers, such as nylon 6, nylon 66, polyester (polyethylene terephthalate, etc.) fibers, aromatic polyamide fibers, acrylic fibers, polyvinyl chloride fibers, polyolefin fibers, and insoluble or poorly soluble polyvinyl alcohol fibers. I can do it.
【0012】基布中の繊維は通常の糸条、例えば短繊維
紡績糸条、長繊維糸条、スプリットヤーン、テープヤー
ンおよびバルキーヤーンなどのいずれの形状のものでも
よく、また基布は織物、編物又は不織布或いはこれらの
複合布のいずれであってもよい。しかし、縫製部分の強
度や耐屈曲性を考慮すれば、基布としては織物又は編物
が好ましく、織物がより好ましい。また、繊維の形態と
しては、ストレスに対する伸びが少ない長繊維(フィラ
メント)の形状のものが好ましく、且つ平織布を形成し
ていることが好ましい。しかし、編織組織やその形態に
ついては特に限定はない。有機繊維は、得られる耐熱難
燃性膜体の機械的強度を高いレベルに維持するために有
用である。[0012] The fibers in the base fabric may be in any form such as ordinary yarns, such as short fiber spun yarns, long fiber yarns, split yarns, tape yarns and bulky yarns, and the base fabric may be woven fabrics, It may be a knitted fabric, a nonwoven fabric, or a composite fabric thereof. However, in consideration of the strength and bending resistance of the sewn portion, a woven or knitted fabric is preferable as the base fabric, and a woven fabric is more preferable. Further, as for the form of the fibers, it is preferable that the fibers are in the form of long fibers (filaments) which have little elongation under stress, and are preferably in the form of a plain woven fabric. However, there are no particular limitations on the weaving structure or its form. Organic fibers are useful for maintaining the mechanical strength of the resulting heat-resistant and flame-retardant membrane at a high level.
【0013】また有機糸条の破断伸度は10%以下、好
ましくは7%以下、5〜0.5%程度のものが無機繊維
の伸度性能とバランスして破断強力利用率を向上させ破
断強力を高めるために更に好ましい。[0013] Furthermore, the elongation at break of the organic yarn is 10% or less, preferably 7% or less, and an elongation of about 5 to 0.5% balances the elongation performance of the inorganic fiber and improves the breaking strength utilization rate. More preferred for increasing strength.
【0014】ガラス繊維が用いられる場合、その種類や
太さなどに格別の限定はないが、一般に、太さ約2〜1
0μm、特に3μm程度のベーターヤーンと称されてい
るものが賞用されている。[0014] When glass fiber is used, there are no particular limitations on its type or thickness, but it generally has a thickness of about 2 to 1
Beta yarns with a diameter of about 0 μm, particularly about 3 μm, are widely used.
【0015】基布中における無機繊維と有機繊維との混
用形態に格別の限定はなく、混紡糸、混交織編物、混交
撚糸、混交バルキーヤーン或いは異種繊維糸条の引揃え
糸などのいづれであってもよく、或いは無機繊維と有機
繊維とをそれぞれ別々に織成もしくは編成等した後にそ
れらをいっしょに用いて基布としてもよい。[0015] There is no particular limitation on the form in which the inorganic fibers and organic fibers are mixed in the base fabric, and they may be mixed yarns, mixed woven or knitted fabrics, mixed twisted yarns, mixed bulky yarns, or drawn yarns of different types of fiber yarns. Alternatively, inorganic fibers and organic fibers may be woven or knitted separately and then used together to form a base fabric.
【0016】本発明の耐熱難燃性膜体において、基布に
含まれる有機繊維が 300℃以上の融点、又は、加熱
分解点を有する耐熱性有機合成繊維を含むことが好まし
い。
このような高融点、又は高分解点繊維を形成するポリマ
ーとしては表1〜5に示すようなものがある。[0016] In the heat-resistant and flame-retardant membrane of the present invention, it is preferable that the organic fibers contained in the base fabric include heat-resistant organic synthetic fibers having a melting point of 300°C or higher or a thermal decomposition point. Examples of polymers that form such high melting point or high decomposition point fibers include those shown in Tables 1 to 5.
【表1】[Table 1]
【表2】[Table 2]
【表3】[Table 3]
【表4】[Table 4]
【表5】[Table 5]
【0017】表1〜5に示された耐熱性ポリマーのうち
では、特にポリメタフェニレンイソフタルアミド及びポ
リパラフェニレンテレフタルアミドが一般的であり、前
記以外のパラ系アラミド繊維として帝人(株)の「HM
−50 」等も使用できる。Among the heat-resistant polymers shown in Tables 1 to 5, polymetaphenylene isophthalamide and polyparaphenylene terephthalamide are particularly common. H.M.
-50'' etc. can also be used.
【0018】かかる繊維に有用な芳香族ポリアミドは、
また、少なくとも50モル%の下記式(I)及び(II
):Aromatic polyamides useful in such fibers include:
In addition, at least 50 mol% of the following formulas (I) and (II)
):
【化1】
で示される単位から選ばれる少くとも1種を主反復単位
として有するものであるのが好ましい。Preferably, it has at least one type of unit selected from the following as the main repeating unit.
【0019】上記式(I)及び(II)において、 A
r1及びAr2で表わされる二価の芳香族基は、下記式
:In the above formulas (I) and (II), A
The divalent aromatic group represented by r1 and Ar2 has the following formula:
【化2】
で示される芳香族残基群から選ばれるのが好ましい。こ
れらの芳香族残基ハロゲン、アルキル基、ニトロ基など
の不活性置換基を含んでいてもよい。Preferably, it is selected from the group of aromatic residues represented by the following formula. These aromatic residues may contain inert substituents such as halogen, alkyl groups, and nitro groups.
【0020】一般に、芳香族ポリアミドとしては、下記
式:Generally, the aromatic polyamide has the following formula:
【化3】
で示される反復単位を主成分として有するものが更に好
ましい。これらの耐熱性有機合成繊維の破断伸度は一般
に10%以下であり、しかも高強度を示すので耐熱性の
面からのみならず膜体の強力利用率の向上の面からも高
強力膜体を得るために極めて好ましいものである。It is more preferable to have a repeating unit represented by the following formula as a main component. The elongation at break of these heat-resistant organic synthetic fibers is generally 10% or less, and they also exhibit high strength. Therefore, high-strength membranes are required not only from the standpoint of heat resistance but also from the standpoint of improving the strength utilization rate of the membrane. It is extremely preferable to obtain
【0021】耐熱性有機合成繊維としては、以上のもの
のほか、融点又は分解点が 300℃以上のものであれ
ば、弗素系繊維やその他の繊維を用いることもできる。In addition to the above-mentioned heat-resistant organic synthetic fibers, fluorine-based fibers and other fibers can also be used as long as they have a melting point or decomposition point of 300° C. or higher.
【0022】本発明の基布中の無機繊維の有機繊維に対
する混用重量比は、10:90〜99.5:0.5の範
囲内にある。無機繊維の含有率が、10重量%未満にな
ると、得られる膜体の難燃性が不十分となり、有機繊維
の含有率が0.5重量%未満になると、得られる膜体の
屈曲強度が不十分となる。また、有機繊維中には、少く
とも25重量%の前記耐熱性有機合成繊維が含まれるこ
とが好ましく、その含有率が30〜 100重量%であ
ることがより好ましく、50〜100 重量%であるこ
とが更に一層好ましい。The weight ratio of inorganic fiber to organic fiber in the base fabric of the present invention is within the range of 10:90 to 99.5:0.5. If the content of inorganic fibers is less than 10% by weight, the flame retardancy of the obtained membrane will be insufficient, and if the content of organic fibers is less than 0.5% by weight, the flexural strength of the obtained membrane will be insufficient. It becomes insufficient. Further, the organic fiber preferably contains at least 25% by weight of the heat-resistant organic synthetic fiber, more preferably 30 to 100% by weight, and more preferably 50 to 100% by weight. It is even more preferable.
【0023】また、基布と耐熱難燃被覆層との接着性そ
の他の性能を助長するために、有機繊維中に 300℃
よりも低い融点又は分解点を有する低耐熱性繊維を含ん
でいてもよい。この場合、混用される低耐熱性繊維に格
別の限定はない。しかし、混用される低耐熱性繊維の混
用率が、基布内繊維の合計重量に対し70%以下である
ことが好ましく、50%以下であることが更に好ましい
。[0023] In addition, in order to promote adhesion and other properties between the base fabric and the heat-resistant and flame-retardant coating layer, the organic fibers are heated at 300°C.
It may also contain low heat resistant fibers having a lower melting point or decomposition point. In this case, there are no particular limitations on the low heat resistant fibers to be mixed. However, the mixing rate of the low heat resistant fibers to be mixed is preferably 70% or less, more preferably 50% or less, based on the total weight of the fibers in the base fabric.
【0024】無機繊維と有機繊維の混合比が99.5:
0.5〜70:30の範囲内にあるとき、得られる膜体
の難燃性が顕著にすぐれている。有機繊維は耐熱性有機
合成繊維から選ばれることが好ましいが、しかしこれに
限定されるものではない。無機繊維と有機繊維との混合
重量比が70:30〜10:90の範囲にあるとき、得
られる膜体の難燃性は良好であり、上記重量比が50:
50〜10:90の範囲では、有機繊維の混用比が高く
なった場合、有機繊維として耐熱性有機合成繊維を用い
、その使用量の比率を増大させることが好ましく、無機
繊維の有機繊維に対する混用率が20:80よりも小さ
い場合、有機繊維の 100%が耐熱有機合成繊維であ
ることがより好ましい。耐熱難燃被覆層は後に述べる配
合剤をポリ塩化ビニル樹脂に配合してもよい。[0024] The mixing ratio of inorganic fiber and organic fiber is 99.5:
When the ratio is within the range of 0.5 to 70:30, the flame retardance of the resulting membrane is significantly excellent. The organic fibers are preferably selected from heat-resistant organic synthetic fibers, but are not limited thereto. When the mixing weight ratio of inorganic fibers and organic fibers is in the range of 70:30 to 10:90, the resulting membrane has good flame retardancy, and the above weight ratio is 50:
In the range of 50 to 10:90, when the mixing ratio of organic fibers becomes high, it is preferable to use heat-resistant organic synthetic fibers as the organic fibers and increase the ratio of the amount used. When the ratio is less than 20:80, it is more preferable that 100% of the organic fibers are heat-resistant organic synthetic fibers. The heat-resistant and flame-retardant coating layer may be formed by blending the compounding agents described later with the polyvinyl chloride resin.
【0025】本発明において、耐熱難燃被覆層を形成す
るために用いられるポリ塩化ビニル樹脂は、例えば、塩
化ビニル単独重合体、および、塩化ビニル−酢酸ビニル
共重合体、塩化ビニル−エチレン共重合体、塩化ビニル
−エチレン−酢酸ビニル共重合体に塩化ビニルをグラフ
ト重合した共重合体などの塩化ビニル共重合体が挙げら
れる。In the present invention, the polyvinyl chloride resin used to form the heat-resistant and flame-retardant coating layer includes, for example, vinyl chloride homopolymer, vinyl chloride-vinyl acetate copolymer, and vinyl chloride-ethylene copolymer. Examples include vinyl chloride copolymers such as a copolymer obtained by graft polymerizing vinyl chloride onto a vinyl chloride-ethylene-vinyl acetate copolymer.
【0026】本発明に適用される塩化ビニル樹脂には、
例えばホウ酸塩、亜鉛化合物等の減煙剤、及び水酸化ア
ルミニウム、三(五)酸化アンチモン、硫酸バリウムな
どの従来公知の難燃剤のほか、通常使用される可塑剤(
特に難燃性可塑剤)、安定剤、防炎剤、充填剤、顔料そ
の他の添加物を添加してもよい。[0026] The vinyl chloride resin applied to the present invention includes:
For example, in addition to smoke reducing agents such as borates and zinc compounds, and conventionally known flame retardants such as aluminum hydroxide, antimony tri(5) oxide, and barium sulfate, commonly used plasticizers (
In particular, flame retardant plasticizers), stabilizers, flame retardants, fillers, pigments and other additives may also be added.
【0027】減煙剤に使用されるホウ酸塩では、ホウ酸
カルシウム、ホウ酸マグネシウム、ホウ酸バリウム等が
、また、亜鉛化合物では酸化亜鉛、炭酸亜鉛等が、さら
に、鉄化合物では、シュウ酸第1鉄、フマール酸第1鉄
、黒色酸化鉄等が適当である。Borates used in smoke reducing agents include calcium borate, magnesium borate, barium borate, etc., zinc compounds include zinc oxide, zinc carbonate, etc., and iron compounds include oxalate, etc. Ferrous iron, ferrous fumarate, black iron oxide, etc. are suitable.
【0028】また、可塑剤としては、ジオクチルフタレ
ート、ジイソデシルフタレート、ジブチルフタレート等
のフタール酸エステル類、ジオクチルアジペート、ジオ
クチルセバケート等の脂肪族2塩基酸エステル類からな
る難燃性可塑剤、又はエポキシ化大豆油、エポキシ化ア
マニ油等のエポキシ可塑剤等が用いられる。[0028] As a plasticizer, flame-retardant plasticizers consisting of phthalate esters such as dioctyl phthalate, diisodecyl phthalate, and dibutyl phthalate, aliphatic dibasic acid esters such as dioctyl adipate and dioctyl sebacate, or epoxy Epoxy plasticizers such as epoxidized soybean oil and epoxidized linseed oil are used.
【0029】また、防炎剤には、塩化パラフィン、脂肪
族、環状脂肪族又は芳香族系のハロゲン化合物類、トリ
クレジルホスフェート、トリス−2,3−ジブロムプロ
ピルホスフェート、トリス−2,3−ジクロルプロピル
ホスフェート等が用いられ、充填剤には、炭酸カルシウ
ム、シリカ、珪酸アルミニウム等が適当である。In addition, flame retardants include chlorinated paraffin, aliphatic, cycloaliphatic or aromatic halogen compounds, tricresyl phosphate, tris-2,3-dibromopropyl phosphate, tris-2,3 - Dichloropropyl phosphate, etc. are used, and calcium carbonate, silica, aluminum silicate, etc. are suitable as fillers.
【0030】基布に施工される塩化ビニル樹脂組成物は
、ペースト、フィルム等として用いられることが好まし
く、ペーストは樹脂組成物を不燃性有機溶剤を用いて希
釈しこれを基布に含浸し、或は、ナイフコーティング、
ロールコーティング等を用いて塗布し、また、フィルム
は主としてカレンダー機を用いて基布に貼着する。
通常ペーストを基布に含浸、又は塗布固着せしめたのち
、この基布の片面又は両面にフィルムを貼着し、基布に
施工される樹脂全量を 100〜300g/m2 に規
制することが好ましい。The vinyl chloride resin composition applied to the base fabric is preferably used as a paste, film, etc. The paste is prepared by diluting the resin composition with a nonflammable organic solvent and impregnating the base fabric with the diluted resin composition. Or knife coating,
It is applied using roll coating or the like, and the film is mainly attached to the base fabric using a calendar machine. It is usually preferable to impregnate or apply and fix the paste onto a base fabric and then affix a film to one or both sides of the base fabric so that the total amount of resin applied to the base fabric is regulated to 100 to 300 g/m 2 .
【0031】ペーストは均一に基布に含浸、塗布され、
糸条中に十分に浸透せしめたのち約100℃〜 150
℃で約1〜5分間乾燥させ、さらに、 150℃〜 2
00℃の高温雰囲気中で熱処理してゲル化せしめられる
。The paste is uniformly impregnated and applied to the base fabric,
After sufficiently permeating into the yarn, the temperature is about 100°C to 150°C.
Dry at ℃ for about 1 to 5 minutes, and then dry at 150℃ to 2
It is gelled by heat treatment in a high temperature atmosphere of 00°C.
【0032】また、通常基布片面又は両面に、同一の樹
脂組成物フィルムを貼着する。フィルムは0.04〜0
.20mm程度の均厚のもので、カレンダー機を用いて
加熱加圧して基布に貼着せしめられる。基布全体に固着
される樹脂組成物重量は 100〜 300g/m2
の範囲にあることが好ましい。 100g/m2 未満
では、基布を完全に被覆することが難しく、また、 3
00g/m2 を超えると、基布に対する樹脂分が過剰
となってかえって、燃焼時発煙及び発熱量の増大を招く
危険がある。[0032] Also, the same resin composition film is usually attached to one or both sides of the base fabric. Film is 0.04~0
.. It has a uniform thickness of about 20 mm and is attached to the base fabric by heating and pressing using a calendar machine. The weight of the resin composition fixed to the entire base fabric is 100 to 300 g/m2
It is preferable that it is in the range of . If it is less than 100g/m2, it is difficult to completely cover the base fabric, and 3
If it exceeds 00 g/m2, the resin content will be excessive with respect to the base fabric, and there is a danger that it will cause smoke generation and an increase in calorific value during combustion.
【0033】このようにして得られた耐熱難燃性膜体は
、燃焼時の発煙、発熱量が低く、JIS−A−1321
(1975)に規定されている「建築物の内装材料及び
工法の難燃性試験法」における表面試験で発煙係数が
120以下であり、60以下、又は30以下のものもあ
る。また、基布を連続フィルムをもって均一に被覆する
ので、少なくとも1500mm水柱の水圧に耐えられ、
また適度の強度を有して良好な耐熱難燃性膜体が得られ
る。The thus obtained heat-resistant and flame-retardant film exhibits low smoke emission and calorific value during combustion, and meets JIS-A-1321.
(1975), the smoke generation coefficient is
It is 120 or less, some 60 or less, or 30 or less. In addition, since the base fabric is uniformly covered with a continuous film, it can withstand water pressure of at least 1500 mm of water column.
Further, a film body having appropriate strength and good heat resistance and flame retardancy can be obtained.
【0034】本発明に係る膜体の防炎性判定、防水性試
験は下記により行なわれる。イ)防炎性判定JIS−A
−1321(1975)に示す難燃性試験法に基づいて
基材試験及び表面試験を行う。(建築基準法施行令、準
不燃、難燃、表面試験、建設省公告3415号)。表面
試験における試験体に溶融、亀裂がなく、変形、有毒ガ
スの発生がなく、残炎時間が30秒未満で、排気温度曲
線が標準温度曲線を超えず、単位面積当りの発煙係数(
CA)で判定した。[0034] The flame retardant property judgment and waterproof test of the membrane according to the present invention are carried out as follows. b) Flame retardant judgment JIS-A
A base material test and a surface test are conducted based on the flame retardancy test method shown in J.-1321 (1975). (Enforcement Ordinance of the Building Standards Act, semi-flammable, flame retardant, surface test, Ministry of Construction Public Notice No. 3415). The specimen in the surface test has no melting, no cracks, no deformation, no generation of toxic gas, afterflame time is less than 30 seconds, the exhaust temperature curve does not exceed the standard temperature curve, and the smoke generation coefficient per unit area (
CA).
【0035】ロ)防水性JIS−L−1079化学繊維
織物試験方法の5.24.1.A法を用い試験片の裏側
の3ケ所から水滴が出たときの水位(mm)を測定した
。B) Waterproof JIS-L-1079 Chemical Fiber Fabric Test Method 5.24.1. Using Method A, the water level (mm) when water droplets appeared from three locations on the back side of the test piece was measured.
【0036】耐熱難燃被覆層は、上記のようなポリ塩化
ビニル樹脂を主成分として形成されるが、チタン酸アル
カリを除く耐熱無機添加剤をポリ塩化ビニル樹脂の重量
に対し好ましくは1〜 300%、より好ましくは10
〜250 %の添加量で含んでいることが好ましい。無
機添加剤としては、無機減煙剤、無機難燃剤、シリカ系
添加剤、石綿繊維、雲母、および、高屈折率無機化合物
、或は、吸熱型無機化合物などから選ぶことができる。The heat-resistant and flame-retardant coating layer is formed using the above-mentioned polyvinyl chloride resin as a main component, and preferably contains a heat-resistant inorganic additive other than alkali titanate in an amount of 1 to 300% by weight based on the weight of the polyvinyl chloride resin. %, more preferably 10
It is preferable that it is added in an amount of ~250%. Inorganic additives can be selected from inorganic smoke reducers, inorganic flame retardants, silica additives, asbestos fibers, mica, high refractive index inorganic compounds, endothermic inorganic compounds, and the like.
【0037】上記無機添加剤はポリ塩化ビニル層の補強
作用を果たすもので、例えば、酸化チタン、マイカ、ア
ルミナ、タルク、ガラス繊維粉末、岩綿微細繊維、シリ
カ粉末、クレイ等の各種無機物を含んでいてもよい。得
られるシートに表面平滑性を具備せしめたい場合には、
シートの表面平滑性を損うことのないように、無機添加
剤として、一般に50μm以下の微粉末状のものを使用
するのが好ましい。The above-mentioned inorganic additives serve to reinforce the polyvinyl chloride layer, and include various inorganic substances such as titanium oxide, mica, alumina, talc, glass fiber powder, rock wool fine fibers, silica powder, and clay. It's okay to stay. If you want the resulting sheet to have surface smoothness,
In order not to impair the surface smoothness of the sheet, it is generally preferable to use a fine powder of 50 μm or less as the inorganic additive.
【0038】更に、本発明の耐熱難燃被覆層には上記の
ように高屈折率無機化合物又は吸熱型無機化合物が含ま
れていてもよい。高屈折率無機化合物は輻射熱に対する
遮断性能に優れ、また吸熱型無機化合物は溶接又は溶断
時のスラグと直接接触した場合、この接触面において加
熱され、その分解時に吸熱反応が起こり、スラグの温度
を低下させる。従って上記の無機化合物は、本発明の被
覆層の崩壊や貫通破壊をおさえ、更には膜体基材を保護
することが出来るものである。Furthermore, the heat-resistant and flame-retardant coating layer of the present invention may contain a high refractive index inorganic compound or an endothermic inorganic compound as described above. High refractive index inorganic compounds have excellent shielding performance against radiant heat, and when endothermic inorganic compounds come into direct contact with slag during welding or fusing, they are heated at this contact surface, and an endothermic reaction occurs during decomposition, lowering the temperature of the slag. lower. Therefore, the above-mentioned inorganic compound can suppress the collapse and penetration failure of the coating layer of the present invention, and can further protect the membrane base material.
【0039】本発明に有用な高屈折率無機化合物は屈折
率1.5以上のものであれば良いが、特に比重2.8以
上のものが好適であり、その例としては、下記のような
ものがある。
等の天然又は合成鉱物の破砕品の粉末。2)フリット又
は高屈折ガラスもしくは燐鉱石と蛇鉱石との固溶体とし
て得られる熔成燐肥その他の類似の固溶体の微細粉末も
しくは粒状物、繊維状物質又は発泡体など。[0039] The high refractive index inorganic compound useful in the present invention may have a refractive index of 1.5 or more, but those with a specific gravity of 2.8 or more are particularly suitable; examples thereof include the following: There is something. Powder of crushed natural or synthetic minerals such as 2) Fine powders or granules, fibrous materials or foams of frit or high refractive glass or molten phosphorus fertilizer obtained as a solid solution of phosphorite and snake ore or other similar solid solutions.
【0040】また吸熱型無機化合物としては、焼石膏、
明ばん、炭酸カルシウム、水酸化アルミニウム、ハイド
ロサルサイト系ケイ酸アルミニウム等、結晶水放出型、
炭酸ガス放出型、分解吸熱型及び相転換型等の吸熱型無
機化合物を例示することができる。[0040] Also, examples of endothermic inorganic compounds include calcined gypsum,
Alum, calcium carbonate, aluminum hydroxide, hydrosalcite aluminum silicate, etc., crystal water releasing type,
Examples include endothermic inorganic compounds such as carbon dioxide releasing type, decomposition endothermic type, and phase conversion type.
【0041】本発明において、シリカ系添加剤、石綿繊
維、雲母、高屈折率無機化合物、及び/又は吸熱型無機
化合物をポリ塩化ビニル樹脂中に混合分散せしめると、
本発明に係る膜体構造用の好ましい被覆用混合物が得ら
れる。混合分散の調製方法としては、公知の手段がすべ
て利用されうる。この他、上記被覆用混合物中には、各
成分を均質に分散させるための分散剤や脱泡剤、色や機
械強度等を調整するための着色剤、樹脂粉末、難燃剤、
金属粉、その他各種充填剤を自由に混入し得る。尚、銅
粉、ニッケル粉、黄銅粉、アルミニウム粉等の金属粉の
混入は、表面熱反射効果、貫通抑制効果の向上の点から
好ましい。In the present invention, when silica additives, asbestos fibers, mica, high refractive index inorganic compounds, and/or endothermic inorganic compounds are mixed and dispersed in polyvinyl chloride resin,
A preferred coating mixture for membrane structures according to the invention is obtained. All known means can be used to prepare the mixed dispersion. In addition, the above-mentioned coating mixture includes a dispersant and a defoaming agent for homogeneously dispersing each component, a coloring agent for adjusting color and mechanical strength, etc., resin powder, flame retardant,
Metal powder and various other fillers can be mixed freely. Incidentally, it is preferable to mix metal powder such as copper powder, nickel powder, brass powder, aluminum powder, etc. from the viewpoint of improving the surface heat reflection effect and the penetration suppressing effect.
【0042】基布の表面を、耐熱難燃被覆層で被覆する
方法としては、基布の表面に被覆用混合物をスプレー塗
装、刷毛塗り、ロールコート等の塗工による方法、或は
被覆用混合物を成型加工したフィルムを基布の表面に貼
着する方法又は基布を被覆用混合物中に浸漬し含浸加工
する方法がある。また、これらの方法の二以上を併用し
てもよい。[0042] The surface of the base fabric can be coated with a heat-resistant and flame-retardant coating layer by applying a coating mixture to the surface of the base fabric by spraying, brushing, roll coating, or the like; There is a method in which a film formed by molding is adhered to the surface of a base fabric, or a method in which the base fabric is immersed in a coating mixture and impregnated. Furthermore, two or more of these methods may be used in combination.
【0043】ポリ塩化ビニル樹脂と高屈折率無機化合物
、無機減煙剤、無機難燃剤、シリカ系添加剤、石綿繊維
、雲母、及び/又は吸熱型無機化合物等との配合割合は
、使用するポリ塩化ビニル樹脂及び無機化合物の種類及
び粒度により異なるが、一般に高屈折率無機化合物およ
び/又は吸熱型無機化合物の含有率が高くなると、得ら
れる被覆層の耐熱難燃性が向上する。しかしポリ塩化ビ
ニル樹脂の含有率が少なすぎると、被覆層の強度が不足
する結果、耐熱難燃性膜体として用いたとき被覆層に亀
裂を生じたり又は被覆層が基布から剥離したりする等の
欠点が生ずる。The blending ratio of polyvinyl chloride resin and high refractive index inorganic compound, inorganic smoke reducing agent, inorganic flame retardant, silica additive, asbestos fiber, mica, and/or endothermic inorganic compound, etc. depends on the polyvinyl chloride resin used. Although it varies depending on the type and particle size of the vinyl chloride resin and the inorganic compound, in general, as the content of the high refractive index inorganic compound and/or endothermic inorganic compound increases, the heat resistance and flame retardance of the resulting coating layer improves. However, if the content of polyvinyl chloride resin is too low, the strength of the coating layer will be insufficient, resulting in cracks in the coating layer or peeling of the coating layer from the base fabric when used as a heat-resistant and flame-retardant membrane. Such disadvantages arise.
【0044】従って、本発明ではポリ塩化ビニル樹脂
100重量部(以下重量部を部と略す。)に対して耐熱
無機添加剤を配合する場合は 400部を限度に配合で
きるが、普通1〜 300部の範囲が好ましい。尚、こ
れら耐熱無機添加剤の一部又は全量を一般に常用されて
いる無機質顔料、無機質の増量用充填剤、難燃性を付与
する無機粉末等にかえることが出来るが、その使用量は
ポリ塩化ビニル樹脂 100部に対し 400部以下で
あることが好ましく、より好ましくは 300部以下で
ある。Therefore, in the present invention, polyvinyl chloride resin
When blending a heat-resistant inorganic additive to 100 parts by weight (hereinafter referred to as parts by weight), up to 400 parts can be blended, but a range of 1 to 300 parts is generally preferred. In addition, some or all of these heat-resistant inorganic additives can be replaced with commonly used inorganic pigments, inorganic bulking fillers, inorganic powders that impart flame retardancy, etc., but the amount used is limited to polychloride. It is preferably at most 400 parts, more preferably at most 300 parts, based on 100 parts of the vinyl resin.
【0045】本発明の効果をより優れたものにするため
難燃剤を併用してもよい。ここで使用される難燃剤につ
いては特に限定されるものではないが、例えば、リン酸
エステル型、有機ハロゲン化合物型、ホスファゼン化合
物型などの有機難燃剤、焼石膏、明ばん、炭酸カルシウ
ム、水酸化アルミニウム、ハイドロタルサイト系ケイ酸
アルミニウムなどの結晶水放出型、炭酸ガス放出型、分
解吸熱型および相転換型などの無機化合物からなる吸熱
分解型無機化合物やアンチモン化合物(三(五)酸化ア
ンチモン)等の無機難燃剤等がある。A flame retardant may be used in combination to further enhance the effects of the present invention. The flame retardants used here are not particularly limited, but include, for example, organic flame retardants such as phosphate ester type, organic halogen compound type, and phosphazene compound type, calcined gypsum, alum, calcium carbonate, and hydroxide. Endothermic decomposition type inorganic compounds such as aluminum, hydrotalcite-based aluminum silicate, crystal water release type, carbon dioxide gas release type, decomposition endothermic type and phase conversion type inorganic compounds and antimony compounds (tri(5) antimony oxide) There are inorganic flame retardants such as
【0046】基布と被覆層との接着及び耐久性を向上さ
せる目的で、両者間に接着性物質を介在させてもよい。
この場合、接着力の向上を図る以上に特に厚く介在させ
る必要はない。接着性物質は被膜形成のために用いられ
るのではなく、従って接着剤として公知の物質を用いる
ことができる。例えば、アミノ基、イミノ基、エチレン
イミン残基、アルキレンジアミン残基を含むアクリレー
ト、アジリジニル基を含有するアクリレート、アミノエ
ステル変性ビニル重合体−芳香族エポキシ接着剤、アミ
ノ窒素含有メタクリレート重合体、その他の接着剤を併
用してもよい。またポリアミドイミド、ポリイミド等の
繊維基布を構成する樹脂と同質の樹脂やRFL変性物質
等を任意に選択することもできる。[0046] In order to improve the adhesion and durability between the base fabric and the coating layer, an adhesive substance may be interposed between the two. In this case, there is no need to interpose the layer thicker than to improve adhesive strength. Adhesive substances are not used for film formation; therefore substances known as adhesives can be used. For example, acrylates containing amino groups, imino groups, ethyleneimine residues, alkylene diamine residues, acrylates containing aziridinyl groups, amino ester-modified vinyl polymer-aromatic epoxy adhesives, amino nitrogen-containing methacrylate polymers, etc. An adhesive may also be used. Further, a resin having the same quality as the resin constituting the fiber base fabric, such as polyamideimide or polyimide, or an RFL modified substance, etc. can be arbitrarily selected.
【0047】被覆層の重量や厚さには格別の限定はない
が、一般に10〜1000g/m2 、好ましくは50
〜 300g/m2 の重量が好ましい。There are no particular limitations on the weight or thickness of the coating layer, but it is generally 10 to 1000 g/m2, preferably 50 g/m2.
A weight of ~300 g/m2 is preferred.
【0048】本発明の耐熱難燃性膜体において、耐熱難
燃被覆層は片面のみに形成されてもよいが、基布の耐候
性の低さ等を補填するために両面に形成されてもよく、
使用状況によっては両面形成が必須の条件になることも
ある。また、他の片面には、膜体に要求される性能によ
り、天然ゴム、ネオプレンゴム、クロロプレンゴム、シ
リコーンゴム、弗素ゴム、ハイパロンその他の合成ゴム
、又はエチレン−酢酸ビニルコポリマー(EVA) 樹
脂、アクリル樹脂、シリコーン樹脂、弗素樹脂、ウレタ
ン樹脂、ポリエステル樹脂その他の合成樹脂を用いるこ
ともできる。この場合、これらの樹脂は難燃化されてい
る必要がある。In the heat-resistant and flame-retardant film body of the present invention, the heat-resistant and flame-retardant coating layer may be formed only on one side, but it may be formed on both sides to compensate for the low weather resistance of the base fabric. often,
Depending on the usage situation, double-sided formation may be an essential condition. Depending on the performance required of the membrane, the other side may be made of natural rubber, neoprene rubber, chloroprene rubber, silicone rubber, fluorine rubber, Hypalon or other synthetic rubber, ethylene-vinyl acetate copolymer (EVA) resin, acrylic. Resin, silicone resin, fluororesin, urethane resin, polyester resin and other synthetic resins can also be used. In this case, these resins need to be flame retardant.
【0049】本発明の耐熱難燃性膜体は、テープ状、又
は短冊状に形成されてもよいし、或は、広巾の膜体をテ
ープ状、または短冊状に切断してもよい。また、本発明
の耐熱難燃性膜体は、他の材料、例えば発泡体、マット
或はネットなどと組合せて用いられてもよい。本発明の
耐熱難燃性膜体は、保護すべき材料、例えば、電線など
に被覆又は巻きつけられてもよい。The heat-resistant and flame-retardant film of the present invention may be formed into a tape or strip, or a wide film may be cut into a tape or strip. Furthermore, the heat-resistant and flame-retardant membrane of the present invention may be used in combination with other materials such as foam, mat, or net. The heat-resistant and flame-retardant membrane of the present invention may be coated or wrapped around a material to be protected, such as an electric wire.
【0050】[0050]
【実施例】本発明の耐熱難燃性膜体を実施例により更に
説明する。[Example] The heat-resistant and flame-retardant membrane of the present invention will be further explained with reference to Examples.
【0051】実施例1〜5および比較例1〜2比較例に
おいては、下記組織の布帛を基布として用いた。比較例
1の布帛
布帛A:ガラス繊維使用 トルコ朱子織:DE150
1/2 3.3S 54本
/25.4mm×51本/25.4mm比較例2の布帛
布帛B:ポリエステル紡績糸平織物Examples 1 to 5 and Comparative Examples 1 to 2 In the comparative examples, fabrics having the following structure were used as base fabrics. Fabric of Comparative Example 1 Fabric A: Turkish satin weave using glass fiber: DE150
1/2 3.3S 54 pieces/25.4mm x 51 pieces/25.4mm Fabric of Comparative Example 2 Fabric B: Polyester spun yarn plain fabric
【0052】実施例1の布帛(布帛1):布帛Aのガラ
ス繊維布帛において、25.4mmに1本の割合でガラ
ス繊維糸をポリエステルフィラメント 1000d/1
48fの糸条により代替した。実施例2の布帛(布帛2
):布帛Aの組織をガラス繊維糸条10本、ポリエステ
ル糸条1本の順に並べて布帛とした。実施例3の布帛(
布帛3):
布帛Aの組織において、ガラス繊維糸条2本/ポリエス
テル糸条1本/ガラス繊維糸条2本/芳香族ポリアミド
繊維(ケブラー)糸条(1000d/148f) 1本
の順に並べて布帛とした。Fabric of Example 1 (Fabric 1): In the glass fiber fabric of Fabric A, polyester filament 1000d/1 was replaced with glass fiber thread at a ratio of one thread per 25.4 mm.
It was replaced with a 48f thread. Fabric of Example 2 (Fabric 2
): The structure of Fabric A was arranged in the order of 10 glass fiber threads and 1 polyester thread to prepare a fabric. Fabric of Example 3 (
Fabric 3): In the structure of fabric A, two glass fiber threads/one polyester thread/two glass fiber threads/one aromatic polyamide fiber (Kevlar) thread (1000d/148f) are arranged in the order of the fabric. And so.
【0053】実施例4の布帛(布帛4):布帛Aの組織
においてガラス繊維糸条と、ケブラー糸条とを交互に並
べて構成した。実施例5の布帛(布帛5):
布帛Aの組織においてガラス繊維糸条2本、ケブラー糸
条8本の順に並べて構成した。Fabric of Example 4 (Fabric 4): In the structure of Fabric A, glass fiber threads and Kevlar threads were arranged alternately. Fabric of Example 5 (Fabric 5): In the structure of Fabric A, two glass fiber threads and eight Kevlar threads were arranged in this order.
【0054】以上の各基布を下記の樹脂組成物で処理し
た。Each of the above base fabrics was treated with the following resin composition.
【0055】上記樹脂組成物のペーストをトリクレンで
希釈し、この希釈液を浸漬法により基布に含浸し、しぼ
り、 150℃で2分間乾燥して希釈剤を飛散せしめた
のち、 185℃で1分間熱処理し、基布に対し樹脂を
70g/m2 の割合に固着せしめた。次に、ストレー
トPVCを用い、上記と同じ樹脂組成物からなるフィル
ムをカレンダーで作成し、これをPVC樹脂含浸固着基
布の片面に貼着し、基布に保持され全樹脂量を 200
g/m2 とした。得られた各種膜体の性能を評価した
結果を表6に示す。[0055] The paste of the above resin composition was diluted with trichlene, this diluted liquid was impregnated into a base fabric by a dipping method, wrung out, dried at 150°C for 2 minutes to scatter the diluent, and then soaked at 185°C for 1 hour. The resin was heat-treated for a minute to adhere the resin to the base fabric at a rate of 70 g/m2. Next, using straight PVC, a film made of the same resin composition as above was created using a calendar, and this was pasted on one side of the PVC resin-impregnated fixing base fabric, so that the total resin content was reduced to 200% by being retained by the base fabric.
g/m2. Table 6 shows the results of evaluating the performance of the various membrane bodies obtained.
【0056】[0056]
【表6】
表6の註:
*1−判定基準:
*2−耐折強さ:JIS−P−8115(1976
)、「紙および板紙のMIT型試験器による耐折強さ試
験方法」に準拠した。*3−殆んど無限大[Table 6] Notes for Table 6: *1-Judgment criteria: *2-Folding strength: JIS-P-8115 (1976
), "Folding strength test method using MIT type tester for paper and paperboard". *3 - Almost infinite
【0057】*4−縫製結合部の引張強度保存率:シン
ガー112W−115工業用ミシン(2本針、本縫糸送
り、テント用)を用い、縫糸としてノーメックスマルチ
フィラメント糸(500d)を使用し、本縫、直線2本
縫いにより、第2表記載の運針数で縫製し、その縫製結
合部を観察し、かつ、その引張強度を測定し、未縫製部
の強力に比較してその保存率を算出した。*4 - Tensile strength retention rate of sewn joint: Using a Singer 112W-115 industrial sewing machine (two needles, lockstitch thread feed, tent use), Nomex multifilament thread (500d) was used as the sewing thread, Sewing was performed using lockstitch and two straight stitches at the number of stitches listed in Table 2, the sewn joint was observed, and its tensile strength was measured, and the retention rate was determined by comparing it with the strength of the unsewn part. Calculated.
【0058】*5−縫製中に結合部が裂断した。
*6−耐熱性:特開昭58−130183号に記載され
ている耐火断熱試験に準拠し次の基準で評価した。*5-The joint was torn during sewing. *6-Heat resistance: Evaluated according to the following criteria based on the fire resistance and insulation test described in JP-A-58-130183.
【0059】評価基準
耐火断熱性能の評価は以下の5種に級別した。
A種:厚さ9mmの火花発生用鋼板を溶断する時、発生
する火花に対し発炎及び防火上有害な貫通孔がないこと
。
B種:厚さ4.5mmの火花発生用鋼板を溶断する時、
発生する火花に対し発炎及び防火上有害な貫通孔がない
こと。
C種:厚さ3.2mmの火花発生用鋼板を溶断する時、
発生する火花に対し発炎及び防火上有害な貫通孔がない
こと。
D種:厚さ3.2mmの火花発生用鋼板を溶断する時、
防火上有害な貫通孔が発生。
E種:厚さ3.2mmの火花発生用鋼板を溶断する時、
発炎。(市販アスベスト紙(3A級)は、E種であった
。)Evaluation Criteria The fire resistance and heat insulation performance was graded into the following five categories. Class A: When cutting a 9mm thick spark-generating steel plate, there should be no through-holes that are harmful to the sparks that are generated and are harmful to fire prevention. Class B: When cutting a spark-generating steel plate with a thickness of 4.5 mm,
There shall be no through-holes that are harmful to sparks and cause fire prevention. Class C: When cutting a spark-generating steel plate with a thickness of 3.2 mm,
There shall be no through-holes that are harmful to sparks and cause fire prevention. Class D: When cutting a spark-generating steel plate with a thickness of 3.2 mm,
Penetration holes that are harmful to fire safety occur. Class E: When cutting a spark-generating steel plate with a thickness of 3.2 mm,
Inflammation. (Commercially available asbestos paper (Class 3A) was Class E.)
【0060】表6に明示されているように従来の有機繊
維 100%の場合(比較例1)は、耐熱難燃被膜層を
形成してもその防炎性は不十分であり不合格である。ガ
ラス繊維100%の場合は、不燃性であるが折り曲げや
縫製結合部の引張強度保存率が低い。有機繊維を併用す
ると耐折り曲げ性が向上し、また縫製結合部の引張強度
保存率も向上する。通常膜体は縫製されて使用に供され
るものなので、この特性は極めて好ましく、実用的価値
のあるものとなる。As clearly shown in Table 6, in the case of 100% conventional organic fiber (Comparative Example 1), even if a heat-resistant and flame-retardant coating layer was formed, its flame retardancy was insufficient and it was rejected. . In the case of 100% glass fiber, it is nonflammable, but the tensile strength retention rate at the folded or sewn joint is low. When organic fibers are used in combination, the bending resistance is improved and the tensile strength retention rate of the sewn joints is also improved. Since membrane bodies are usually sewn before use, this characteristic is extremely desirable and has practical value.
【0061】また、表6が明らかに示すように、比較例
1の従来の不燃性膜体は耐折強さが低く、折り曲げのは
げしい用途、振動やはためきなどをはげしく受ける用途
には適していない。しかも、その縫製性も低く、縫製結
合部の引張強度を大きくするために運針数を約25ピッ
チ/10cmより大きくすると、結合部の引張強度が低
下し、やがてミシン針により裂断されてしまう。Furthermore, as Table 6 clearly shows, the conventional nonflammable membrane of Comparative Example 1 has low bending strength, and is not suitable for applications that require heavy bending or applications that are subject to severe vibrations or flapping. . Moreover, its sewing properties are poor, and if the number of stitches is increased to more than about 25 pitches/10 cm in order to increase the tensile strength of the sewn joint, the tensile strength of the joint decreases and it will eventually be torn by the sewing machine needle.
【0062】しかし、本発明の耐熱難燃性膜体(実施例
1〜5)は、良好な難燃、不燃性、耐折強さおよび縫製
性、縫製結合部の引張強度保存率を示した。However, the heat-resistant and flame-retardant membranes of the present invention (Examples 1 to 5) showed good flame retardancy, non-combustibility, folding strength, seamability, and retention of tensile strength at sewn joints. .
【0063】[0063]
【発明の効果】本発明に係る耐熱難燃性膜体は、良好な
耐熱難燃性を示し、しかも、軽量で強靱であって、耐繰
り返えし折り曲げ性や、縫製性、特に縫合部のミシン目
の裂断防止においてもすぐれている。このため、本発明
の耐熱難燃性膜体は、耐火服、火災が予想される体育館
、倉庫、マーケット、遊技場、工場、駐車場、各種宿泊
施設等の建築材料、内装材料に、さらに、テント、日除
け、ブラインド、シート類、間仕切等の素材その他の折
り曲げ、振動、はためきなどをはげしく受ける用途に適
している。Effects of the Invention The heat-resistant and flame-retardant film body according to the present invention exhibits good heat-resistant and flame-retardant properties, is lightweight and strong, and has excellent resistance to repeated bending and sewing properties, especially at seams. It is also excellent in preventing tearing at the perforations. Therefore, the heat-resistant and flame-retardant film body of the present invention can be used as fire-resistant clothing, building materials and interior materials for gymnasiums, warehouses, markets, playgrounds, factories, parking lots, various accommodation facilities, etc. where fire is expected, and Suitable for materials such as tents, awnings, blinds, sheets, partitions, etc., and other applications that are subject to significant bending, vibration, flapping, etc.
Claims (7)
基布と、この基布の少なくとも1面上に形成され、かつ
ポリ塩化ビニル樹脂とを含んでなる耐熱難燃被覆層とを
有し、前記基布中の無機繊維の有機繊維に対する混用重
量比が10:90〜99.5:0.5の範囲内にある、
ことを特徴とする耐熱難燃性膜体。1. A base fabric comprising an inorganic fiber and an organic fiber, and a heat-resistant and flame-retardant coating layer formed on at least one surface of the base fabric and comprising a polyvinyl chloride resin. and the weight ratio of inorganic fiber to organic fiber in the base fabric is within the range of 10:90 to 99.5:0.5.
A heat-resistant and flame-retardant film body characterized by:
繊維、シリカ繊維、ガラス繊維、カーボン繊維および金
属繊維から選ばれる、請求項1に記載の膜体。2. The membrane body according to claim 1, wherein the inorganic fibers are selected from asbestos fibers, ceramic fibers, silica fibers, glass fibers, carbon fibers and metal fibers.
、又は、加熱分解点を有する耐熱性有機合成繊維を含む
、請求項1に記載の膜体。3. The membrane body according to claim 1, wherein the organic fiber includes a heat-resistant organic synthetic fiber having a melting point or thermal decomposition point of 300° C. or higher.
の前記耐熱性有機合成繊維を含む、請求項3に記載の膜
体。4. The organic fiber comprises at least 25% by weight.
The membrane body according to claim 3, comprising the heat-resistant organic synthetic fiber.
酸アルカリを除く耐熱無機添加剤を含む、請求項1に記
載の膜体。5. The membrane body according to claim 1, wherein the heat-resistant and flame-retardant coating layer further contains a heat-resistant inorganic additive excluding alkali titanate.
添加剤を更に含み、無機減煙剤、無機難燃剤が、シリカ
系添加剤、石綿繊維、雲母、硫酸バリウム高屈折率無機
化合物および吸熱型無機化合物から選ばれる、請求項5
に記載の膜体。6. The heat-resistant and flame-retardant coating layer further includes a heat-resistant inorganic additive, and the inorganic smoke reducing agent and inorganic flame retardant are silica-based additives, asbestos fibers, mica, and barium sulfate high refractive index inorganic compounds. and an endothermic inorganic compound.
Membrane body described in.
塩化ビニル樹脂の重量に対し1〜 300%の範囲内に
ある、請求項5に記載の膜体。7. The membrane body according to claim 5, wherein the content of the heat-resistant inorganic additive is within a range of 1 to 300% based on the weight of the polyvinyl chloride resin.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3120358A JPH0712645B2 (en) | 1991-05-24 | 1991-05-24 | Heat resistant flame retardant film |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3120358A JPH0712645B2 (en) | 1991-05-24 | 1991-05-24 | Heat resistant flame retardant film |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6856785A Division JPS61227047A (en) | 1985-04-02 | 1985-04-02 | Heat-resistant flame-retardant film body |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8138970A Division JP2812671B2 (en) | 1996-05-31 | 1996-05-31 | Heat-resistant and flame-retardant film |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH04226342A true JPH04226342A (en) | 1992-08-17 |
| JPH0712645B2 JPH0712645B2 (en) | 1995-02-15 |
Family
ID=14784234
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3120358A Expired - Fee Related JPH0712645B2 (en) | 1991-05-24 | 1991-05-24 | Heat resistant flame retardant film |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0712645B2 (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5580648A (en) * | 1992-12-01 | 1996-12-03 | Avco Corporation | Reinforcement system for mastic intumescent fire protection coatings |
| CN102501410A (en) * | 2011-10-21 | 2012-06-20 | 浙江师范大学 | Preparation method for flame-retardant and antistatic pipeline with high strength |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4833160A (en) * | 1971-09-02 | 1973-05-08 | ||
| JPS5777336A (en) * | 1980-10-27 | 1982-05-14 | Hitachi Ltd | Composite fiber product |
-
1991
- 1991-05-24 JP JP3120358A patent/JPH0712645B2/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4833160A (en) * | 1971-09-02 | 1973-05-08 | ||
| JPS5777336A (en) * | 1980-10-27 | 1982-05-14 | Hitachi Ltd | Composite fiber product |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5580648A (en) * | 1992-12-01 | 1996-12-03 | Avco Corporation | Reinforcement system for mastic intumescent fire protection coatings |
| CN102501410A (en) * | 2011-10-21 | 2012-06-20 | 浙江师范大学 | Preparation method for flame-retardant and antistatic pipeline with high strength |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0712645B2 (en) | 1995-02-15 |
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