JP2016121417A - Non-flammable film material for building structure - Google Patents
Non-flammable film material for building structure Download PDFInfo
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- JP2016121417A JP2016121417A JP2014261708A JP2014261708A JP2016121417A JP 2016121417 A JP2016121417 A JP 2016121417A JP 2014261708 A JP2014261708 A JP 2014261708A JP 2014261708 A JP2014261708 A JP 2014261708A JP 2016121417 A JP2016121417 A JP 2016121417A
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- film material
- resin
- base fabric
- aya
- flame retardant
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- 239000000463 material Substances 0.000 title claims abstract description 98
- 239000004744 fabric Substances 0.000 claims abstract description 115
- 229920005989 resin Polymers 0.000 claims abstract description 79
- 239000011347 resin Substances 0.000 claims abstract description 79
- 239000003063 flame retardant Substances 0.000 claims abstract description 60
- 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 claims abstract description 58
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 19
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 claims description 13
- 239000000835 fiber Substances 0.000 claims description 10
- 239000003365 glass fiber Substances 0.000 claims description 10
- 239000000377 silicon dioxide Substances 0.000 claims description 9
- 229920002050 silicone resin Polymers 0.000 claims description 8
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 7
- 239000011737 fluorine Substances 0.000 claims description 7
- 229910052731 fluorine Inorganic materials 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 6
- 239000002759 woven fabric Substances 0.000 claims description 6
- 230000008520 organization Effects 0.000 claims description 3
- 230000002087 whitening effect Effects 0.000 abstract description 20
- 238000000034 method Methods 0.000 abstract description 11
- 239000011248 coating agent Substances 0.000 abstract description 8
- 238000000576 coating method Methods 0.000 abstract description 8
- 238000010276 construction Methods 0.000 abstract description 7
- 230000008569 process Effects 0.000 abstract description 7
- 238000009958 sewing Methods 0.000 abstract description 7
- 230000004888 barrier function Effects 0.000 abstract description 5
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- 238000005192 partition Methods 0.000 abstract description 4
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- 238000009792 diffusion process Methods 0.000 abstract description 3
- 239000002585 base Substances 0.000 description 84
- 239000010410 layer Substances 0.000 description 53
- 239000012528 membrane Substances 0.000 description 27
- 239000011521 glass Substances 0.000 description 18
- 239000000203 mixture Substances 0.000 description 17
- -1 platinum group compound Chemical class 0.000 description 17
- 238000012360 testing method Methods 0.000 description 16
- 238000007667 floating Methods 0.000 description 15
- 238000009472 formulation Methods 0.000 description 14
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 230000005540 biological transmission Effects 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 229920002379 silicone rubber Polymers 0.000 description 9
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- 239000000178 monomer Substances 0.000 description 7
- 229920001296 polysiloxane Polymers 0.000 description 7
- 231100000241 scar Toxicity 0.000 description 7
- 230000037387 scars Effects 0.000 description 7
- 238000007259 addition reaction Methods 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 229920001971 elastomer Polymers 0.000 description 6
- 239000000806 elastomer Substances 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 239000002245 particle Substances 0.000 description 6
- 239000004925 Acrylic resin Substances 0.000 description 5
- 229920000178 Acrylic resin Polymers 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 5
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- 150000002148 esters Chemical class 0.000 description 5
- 239000011342 resin composition Substances 0.000 description 5
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- 239000004566 building material Substances 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
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- 239000004014 plasticizer Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000012508 resin bead Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 238000006482 condensation reaction Methods 0.000 description 3
- 125000000524 functional group Chemical group 0.000 description 3
- 150000002484 inorganic compounds Chemical class 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 238000002834 transmittance Methods 0.000 description 3
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 2
- 235000019826 ammonium polyphosphate Nutrition 0.000 description 2
- 229920001276 ammonium polyphosphate Chemical class 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000011247 coating layer Substances 0.000 description 2
- 238000002788 crimping Methods 0.000 description 2
- 150000007973 cyanuric acids Chemical class 0.000 description 2
- 239000004205 dimethyl polysiloxane Substances 0.000 description 2
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 2
- 238000007720 emulsion polymerization reaction Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 238000007641 inkjet printing Methods 0.000 description 2
- ZQKXQUJXLSSJCH-UHFFFAOYSA-N melamine cyanurate Chemical compound NC1=NC(N)=NC(N)=N1.O=C1NC(=O)NC(=O)N1 ZQKXQUJXLSSJCH-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005862 polyol Polymers 0.000 description 2
- 150000003077 polyols Chemical class 0.000 description 2
- 229920005990 polystyrene resin Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 150000003377 silicon compounds Chemical class 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 1
- ADTHJEKIUIOLBX-UHFFFAOYSA-N 1,1,3,4,4,5,5,6,6,6-decafluoro-3-(trifluoromethyl)hex-1-ene Chemical compound FC(C(F)(F)F)(C(C(C(F)(F)F)(C=C(F)F)F)(F)F)F ADTHJEKIUIOLBX-UHFFFAOYSA-N 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- GZVHEAJQGPRDLQ-UHFFFAOYSA-N 6-phenyl-1,3,5-triazine-2,4-diamine Chemical compound NC1=NC(N)=NC(C=2C=CC=CC=2)=N1 GZVHEAJQGPRDLQ-UHFFFAOYSA-N 0.000 description 1
- 239000004114 Ammonium polyphosphate Chemical class 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 239000006087 Silane Coupling Agent Substances 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- RJDOZRNNYVAULJ-UHFFFAOYSA-L [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[F-].[F-].[Mg++].[Mg++].[Mg++].[Al+3].[Si+4].[Si+4].[Si+4].[K+] RJDOZRNNYVAULJ-UHFFFAOYSA-L 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000410 antimony oxide Inorganic materials 0.000 description 1
- SHLNMHIRQGRGOL-UHFFFAOYSA-N barium zinc Chemical compound [Zn].[Ba] SHLNMHIRQGRGOL-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- HORIEOQXBKUKGQ-UHFFFAOYSA-N bis(7-methyloctyl) cyclohexane-1,2-dicarboxylate Chemical compound CC(C)CCCCCCOC(=O)C1CCCCC1C(=O)OCCCCCCC(C)C HORIEOQXBKUKGQ-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical class OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 150000001649 bromium compounds Chemical class 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical compound OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- QSAWQNUELGIYBC-UHFFFAOYSA-N cyclohexane-1,2-dicarboxylic acid Chemical compound OC(=O)C1CCCCC1C(O)=O QSAWQNUELGIYBC-UHFFFAOYSA-N 0.000 description 1
- 230000032798 delamination Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000004806 diisononylester Substances 0.000 description 1
- 125000005388 dimethylhydrogensiloxy group Chemical group 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- 238000001879 gelation Methods 0.000 description 1
- 229920000578 graft copolymer Polymers 0.000 description 1
- 238000007646 gravure printing Methods 0.000 description 1
- 150000002357 guanidines Chemical class 0.000 description 1
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 1
- 125000006038 hexenyl group Chemical group 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
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- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
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- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- VTRUBDSFZJNXHI-UHFFFAOYSA-N oxoantimony Chemical compound [Sb]=O VTRUBDSFZJNXHI-UHFFFAOYSA-N 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- QQVIHTHCMHWDBS-UHFFFAOYSA-N perisophthalic acid Natural products OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 125000004437 phosphorous atom Chemical group 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000000088 plastic resin Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920001228 polyisocyanate Polymers 0.000 description 1
- 239000005056 polyisocyanate Substances 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000012763 reinforcing filler Substances 0.000 description 1
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- 239000002904 solvent Substances 0.000 description 1
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Landscapes
- Building Environments (AREA)
- Laminated Bodies (AREA)
- Woven Fabrics (AREA)
Abstract
Description
本発明は、無機織物を基材とする不燃性膜材料に関するものであり、更に詳しくは不燃性、可撓性及び適度な光の拡散性を有し、特に膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、膜材料の外観及び光透過外観において白化痕筋の発現が効果的に抑止される建築構造用不燃膜材に関する。 The present invention relates to a non-combustible film material based on an inorganic fabric, and more particularly has non-combustibility, flexibility, and appropriate light diffusibility, especially the sewing process and construction handling of the film material. In some cases, the present invention relates to a non-combustible film material for a building structure in which the appearance of whitening scars is effectively suppressed in the appearance of the film material and the light transmission appearance even if the film material is bent or inadvertently bent.
特許文献1にはガラス繊維織物と熱硬化性樹脂層とからなる透明不燃性シートが開示され、この透明不燃シートは、ガラス繊維織物と樹脂層との屈折率の差を小さくすることで優れた透明性を確保している。しかしシートを強く折り曲げてしまうと、折れ部分のガラス繊維と含浸被覆樹脂とに微細な剥離と隙間を生じ、それが屈折乱反射することで白化痕筋となって外観を悪くする欠点があり、しかも白化痕筋が消えない問題を有していた。そこで特許文献2ではガラス繊維織物と熱硬化性樹脂層との構成に熱可塑性樹脂層を追加して屈曲折り曲げによる白化発生を起し難いよう改善したものであるが、熱硬化性樹脂層と熱可塑性樹脂層との接着性に劣るため、屈曲折り曲げによって層間剥離し易い問題を新たに発生するものであった。このようにガラス繊維織物に対する熱硬化性樹脂加工では、根本的にガラス素材と樹脂との接着の相性に劣り、屈曲歪により白化痕筋を生じ易いものであった。 Patent Document 1 discloses a transparent incombustible sheet composed of a glass fiber fabric and a thermosetting resin layer, and this transparent incombustible sheet is excellent by reducing the difference in refractive index between the glass fiber fabric and the resin layer. Transparency is ensured. However, if the sheet is bent strongly, fine peeling and gaps will be generated between the glass fiber and the impregnated coating resin at the folded part, and it has the disadvantage that it becomes whitened traces due to refracted reflection, which deteriorates the appearance. There was a problem that the whitening traces did not disappear. Therefore, in Patent Document 2, a thermoplastic resin layer is added to the configuration of the glass fiber fabric and the thermosetting resin layer to improve the occurrence of whitening due to bending and bending, but the thermosetting resin layer and the thermosetting resin layer are improved. Since the adhesiveness with the plastic resin layer is inferior, a new problem of easy delamination due to bending and bending occurs. As described above, in the thermosetting resin processing for the glass fiber fabric, the compatibility between the glass material and the resin is fundamentally inferior, and whitening traces are easily generated due to bending strain.
本発明は、不燃性、可撓性及び適度な光の拡散性を有し、特に膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、膜材料の外観及び光透過外観において白化痕筋の発現が効果的に抑止されるなど、取り扱い性に優れた建築材料用の膜材料であって、間仕切り、防煙垂壁、光壁膜、光天井膜などに適した建築構造用不燃膜材の提供をしようとするものである。 The present invention has non-flammability, flexibility, and moderate light diffusibility. Even when the membrane material is folded or inadvertently bent, especially when the membrane material is sewn or handled, the appearance of the membrane material In addition, it is a film material for building materials that has excellent handleability, such as effectively suppressing the appearance of whitening traces in the light-transmitting appearance, such as partitions, smoke barriers, light wall films, and light ceiling films. It is intended to provide a suitable non-combustible film material for building structures.
上記課題を解決するために、無機マルチフィラメントヤーンを経糸及び緯糸とする織物を基材布帛として、この基材布帛の片面以上に、樹脂被覆難燃層を設け、基材布帛の表側及び裏側の完全組織に経糸及び緯糸の浮き跨ぎ構造とすることによって、膜材料に折り曲げの負荷が加えられても、浮き跨ぎ構造が歪変位を吸収緩和する作用を発現し、得られる膜材料の外観や光透過外観に白化痕筋が発生し難いことを見出して本発明を完成するに至った。 In order to solve the above-mentioned problems, a woven fabric having an inorganic multifilament yarn as warp and weft is used as a base fabric, and a resin-coated flame retardant layer is provided on one or more sides of the base fabric, and the front and back sides of the base fabric are provided. By adopting a warp and weft floating straddle structure in the complete structure, even if a bending load is applied to the membrane material, the float straddle structure exhibits the action of absorbing and relaxing strain displacement, and the appearance and light of the obtained film material The present invention was completed by finding that whitening scars hardly occur in the transparent appearance.
すなわち本発明の建築構造用不燃膜材は、無機マルチフィラメントヤーンを経糸及び緯糸とする織物を基材布帛として、この基材布帛の片面以上に、樹脂被覆難燃層を設けてなる光拡散透過性積層体であって、前記基材布帛の表側及び裏側の完全組織において、経糸による緯糸の浮き跨ぎ本数、及び緯糸による経糸の浮き跨ぎ本数が、3本、4本、及び5本、の何かとするルーズ構造を有することが好ましい。経糸及び緯糸の浮き跨ぎ本数が3本、4本、及び5本、の何かとするルーズ構造を有することにより、膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、ルーズ構造が外力による歪変位を吸収緩和し、膜材料の外観及び光透過外観において白化痕筋の発現を効果的に抑止することができる。 That is, the non-combustible film material for building structure of the present invention is a light diffusing and transmitting material in which a fabric having inorganic multifilament yarn as warp and weft is used as a base fabric, and a resin-coated flame retardant layer is provided on at least one side of the base fabric. In the complete structure on the front side and back side of the base fabric, the number of weft float straddles by warps, and the number of warp float struts by wefts is 3, 4, and 5. It is preferable to have a loose structure. By having a loose structure with three, four, and five warp and weft floats, the membrane material is bent or accidentally bent during the sewing process or construction handling of the membrane material However, the loose structure absorbs and relaxes the strain displacement due to the external force, and can effectively suppress the appearance of whitening scars in the appearance of the film material and the light transmission appearance.
本発明の建築構造用不燃膜材は、前記完全組織を構成する基本組織が、3/1斜文(四枚綾)、3/1破れ斜文(四枚綾)、3/2斜文(五枚綾)、4/1斜文(五枚綾)、5/1斜文(六枚綾)、4/2斜文(六枚綾)、1・3/1・1斜文(六枚綾)、2飛び4/1朱子(五枚朱子)、3飛び4/1朱子(五枚朱子)、2飛び3/2朱子(五枚朱子)、3飛び3/2朱子(五枚朱子)から選ばれた1種であることが好ましい。このように経糸または緯糸の浮き跨ぎ本数が3本、4本、及び5本、の何かとするルーズ構造を有することにより、膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、ルーズ構造が外力による歪変位を吸収緩和し、膜材料の外観及び光透過外観において白化痕筋の発現を効果的に抑止することができる。 In the non-combustible film material for building structure of the present invention, the basic structure constituting the complete structure is 3/1 oblique (4 sheets Aya), 3/1 broken oblique (4 sheets Aya), 3/2 oblique ( 5 Aya), 4/1 Akira (5 Aya), 5/1 Akira (6 Aya), 4/2 Akira (6 Aya), 1/3/1, 1 Akira (6) Aya) 2 Jump 4/1 Akuko (5 sheets Auko), 3 Jump 4/1 Akuko (5 sheets Auko), 2 Jump 3/2 Auko (5 sheets Auko), 3 Jump 3/2 Auko (5 sheets Auko) It is preferable that it is 1 type chosen from. By having a loose structure with three, four and five warp or weft floating struts in this way, the membrane material can be bent or inadvertently handled during the sewing process or construction of the membrane material. Even if it is bent, the loose structure absorbs and relaxes strain displacement due to external force, and can effectively suppress the appearance of whitening traces in the appearance of the film material and the light transmission appearance.
本発明の建築構造用不燃膜材は、前記無機マルチフィラメントヤーンが、ガラス繊維、シリカ繊維、アルミナ繊維、シリカアルミナ繊維から選ばれた1種以上であることが好ましい。これによってISO5660Part1に規定の不燃特性に適合することができる。 In the incombustible film material for building structure of the present invention, the inorganic multifilament yarn is preferably at least one selected from glass fiber, silica fiber, alumina fiber, and silica alumina fiber. This makes it possible to meet the non-flammable characteristics specified in ISO 5660 Part 1.
本発明の建築構造用不燃膜材は、前記樹脂被覆難燃層が、シリコーン系樹脂、フッ素系樹脂、及び塩化ビニル系樹脂から選ばれた1種以上を含むことが好ましい。これによってISO5660Part1に規定の不燃特性に適合することができる。 In the incombustible film material for building structures of the present invention, it is preferable that the resin-coated flame retardant layer contains one or more selected from silicone resins, fluorine resins, and vinyl chloride resins. This makes it possible to meet the non-flammable characteristics specified in ISO 5660 Part 1.
本発明によれば、ISO5660Part1に規定の燃焼特性に適合し、さらに可撓性及び適度な光の拡散性を有し、特に膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、膜材料の外観及び光透過外観において白化痕筋の発現が効果的に抑止されるように極めて取り扱い性に優れたものであるので、建築構造用不燃膜材として、間仕切り、防煙垂壁、光壁膜、光天井膜などの建築材料用途に広く用いることができる。 According to the present invention, it conforms to the combustion characteristics specified in ISO 5660 Part 1 and has flexibility and appropriate light diffusibility. In particular, the membrane material can be bent or inadvertently handled during the sewing process and construction of the membrane material. Even if it is bent, it is extremely easy to handle so that the appearance of whitening traces is effectively suppressed in the appearance of the film material and the light transmission appearance, so as a non-combustible film material for building structures, It can be widely used for building material applications such as smoke barriers, light wall films, and light ceiling films.
本発明の建築構造用不燃膜材は、無機マルチフィラメントヤーン(好ましくはガラス繊維、シリカ繊維)を経糸及び緯糸とする綾織物(例えば四枚綾、五枚綾、六枚綾)、又は朱子織物(例えば五枚朱子)を基材布帛として、この基材布帛の片面以上に、樹脂被覆難燃層(好ましくはシリコーン系樹脂、フッ素系樹脂、塩化ビニル系樹脂)を設け、基材布帛の表側及び裏側の完全組織(1区間の組織を基礎とし、これを繰り返して構成される織物における、この1区間の単位組織)に、経糸及び緯糸による特定の浮き跨ぎ構造(例えば、浮き跨ぎ本数3本、4本、5本)を有するものである。このような経糸による緯糸の浮き跨ぎ本数及び、緯糸による経糸の浮き跨ぎ本数が、3本、4本、及び5本、の何かとするルーズ構造を有することにより、膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、ルーズ構造が外力による歪変位を吸収緩和し、膜材料の外観及び光透過外観において白化痕筋の発現を効果的に抑止することができる。浮き跨ぎ本数が2本以下では白化痕筋発現の抑止効果が不十分となり、浮き跨ぎ本数が6本以上ではルーズ構造が過剰となって建築構造用の不燃膜材として用いたときの寸法安定性を悪くする弊害を招くことがある。 The non-combustible film material for building structures of the present invention is a twill fabric (for example, four twills, five twills, six twills) or a satin fabric using inorganic multifilament yarns (preferably glass fibers, silica fibers) as warps and wefts. (For example, five sheets of satin) is used as a base fabric, and a resin-coated flame retardant layer (preferably silicone resin, fluorine resin, vinyl chloride resin) is provided on one side or more of the base fabric, and the front side of the base fabric And the back side complete structure (unit structure of this 1 section in the woven fabric constructed by repeating this structure based on the structure of 1 section), and a specific floating straddle structure with warp and weft (for example, 3 floating structures) 4 and 5). By having such a loose structure that the number of weft floats by warps and the number of warp floats by wefts is 3, 4, or 5, it has a loose structure, so that the sewing process and construction of membrane materials are handled. Sometimes, even if the membrane material is bent or accidentally bent, the loose structure absorbs and relaxes strain displacement due to external force, and can effectively suppress the appearance of whitening scars in the appearance and light transmission appearance of the membrane material. . When the number of floating straddles is 2 or less, the effect of inhibiting whitening scars is insufficient, and when the number of floating straddles is 6 or more, the loose structure becomes excessive and the dimensional stability when used as a non-combustible film material for building structures May cause adverse effects.
本発明の建築構造用不燃膜材に用いる基材布帛は、無機マルチフィラメントヤーンを経糸及び緯糸とし、基材布帛の完全組織において、経糸及び緯糸の浮き跨ぎ本数が3本、4本、及び5本、の何かとするルーズ構造を有する布帛である。無機マルチフィラメントヤーンは、ガラス繊維、シリカ繊維、アルミナ繊維、シリカアルミナ繊維から選ばれた1種以上で構成され、これらはフィラメント直径が3〜10μm、繊度138〜2223dtex、特に277〜1112dtexのマルチフィラメントで、フィラメント数50〜500本、特に100〜300本で集束してなるヤーンである。ガラス繊維としては、E(無アルカリ)ガラス、C(アルカリ含)ガラス、Gガラス、Aガラス、Sガラス、Dガラス、DEガラスなど何れのガラス組成であってもよい。これらの無機マルチフィラメントヤーンは単糸に撚りを掛けて、あるいは撚りを掛けずに使用、あるいは単糸2本を合撚した双糸で、単糸の断面が略円形、楕円、または扁平のヤーンである。基材布帛は完全組織を構成する基本組織が、3/1斜文(四枚綾)、3/1破れ斜文(四枚綾)、3/2斜文(五枚綾)、4/1斜文(五枚綾)、5/1斜文(六枚綾)、4/2斜文(六枚綾)、1・3/1・1斜文(六枚綾)、2飛び4/1朱子(五枚朱子)、3飛び4/1朱子(五枚朱子)、2飛び3/2朱子(五枚朱子)、3飛び3/2朱子(五枚朱子)から選ばれた何れか1種である。基材布帛は経糸と緯糸との織交点に生じる空隙の総和が8%以下の空隙率の布帛が好ましく、経糸、及び緯糸の打ち込み密度を各々、277〜1112dtexのヤーンを30〜100本/1インチとするものである。空隙率が8%を越えると、膜材表面にピンホールを発生し易くなり、ISO5660Part1に規定の燃焼特性に適合できなくなることがある。またこれらの基材布帛には、シランカップリング剤による表面改質処理が施されていることが樹脂被覆難燃層との密着性向上の観点において好ましい。 The base fabric used for the non-combustible film material for building structures of the present invention uses an inorganic multifilament yarn as warp and weft. In the complete structure of the base fabric, the number of floating straddles of warp and weft is 3, 4, and 5 It is a fabric having a loose structure as a book. The inorganic multifilament yarn is composed of at least one selected from glass fiber, silica fiber, alumina fiber, and silica alumina fiber, and these are multifilaments having a filament diameter of 3 to 10 μm and a fineness of 138 to 2223 dtex, particularly 277 to 1112 dtex. Thus, it is a yarn formed by converging with 50 to 500 filaments, particularly 100 to 300 filaments. The glass fiber may have any glass composition such as E (non-alkali) glass, C (containing alkali) glass, G glass, A glass, S glass, D glass, and DE glass. These inorganic multifilament yarns are twisted or untwisted single yarns, or double yarns in which two single yarns are twisted together. The single yarn has a substantially circular, elliptical or flat cross section. It is. The base fabric that forms the complete structure of the base fabric is 3/1 oblique (4 sheets Aya), 3/1 broken oblique (4 sheets Aya), 3/2 oblique (5 sheets Aya), 4/1 Syllabary (5 sheets of Aya), 5/1 Syllabary (6 sheets of Aya), 4/2 Syllabary (6 sheets of Aya), 1/3/1. Any one selected from Ako (5 sheets Auko), 3 jump 4/1 Auko (5 sheets Auko), 2 jump 3/2 Auko (5 sheets Auko), 3 jump 3/2 Auko (5 sheets Auko) It is. The base fabric is preferably a fabric having a porosity of 8% or less of the total voids generated at the intersection of the warp and the weft. The warp and weft driving density is 30 to 100 yarns of 277 to 1112 dtex / 100 yarns / 1, respectively. Inch. If the porosity exceeds 8%, pinholes are likely to be generated on the surface of the membrane material, and it may not be possible to conform to the combustion characteristics specified in ISO 5660 Part 1. These base fabrics are preferably subjected to a surface modification treatment with a silane coupling agent from the viewpoint of improving adhesion with the resin-coated flame retardant layer.
本発明の建築構造用不燃膜材において、樹脂被覆難燃層は、シリコーン系樹脂、フッ素系樹脂、及び塩化ビニル系樹脂から選ばれた何れか1種による単層構造、もしくはこれらの樹脂の組み合わせによる複層構造による樹脂被覆難燃層で、樹脂被覆難燃層の形成は表裏合計で、基材布帛の質量に対して25〜150質量%、特に50〜100質量%である。樹脂被覆難燃層の質量が25質量%未満だと得られる膜材料の形態安定性が不十分となることがあり、150質量%を越えるとISO5660Part1に規定の燃焼特性に適合できなくなることがある。シリコーン系樹脂としては、付加反応硬化型シリコーンエラストマー、縮合反応硬化型シリコーンエラストマー、ラジカル(パーオキサイド架橋)反応硬化型シリコーンエラストマーなど、柔軟性を有するものが使用でき、特にトルエン等で希釈してコーティングが可能で、しかも低温硬化ができる付加反応硬化型シリコーンエラストマーが好ましい。付加反応硬化型シリコーンエラストマーは、2種類のオルガノポリシロキサン中の官能基が付加反応により結合して架橋しエラストマー化するもので、これらは例えば、ビニル基やヘキセニル基のような脂肪族不飽和基を含有するオルガノポリシロキサン、オルガノハイドロジェンポリシロキサンおよび白金族化合物系触媒からなる組成物が挙げられる。脂肪族不飽和基含有オルガノポリシロキサンとしては、両末端ビニルジメチルシロキシ基封鎖ジメチルポリシロキサン、両末端ビニルジメチルシロキシ基封鎖ジメチルシロキサン・メチルビニルシロキサン共重合体、両末端ビニルメチルフェニルシロキシ基封鎖ジメチルシロキサン・メチルフェニルシロキサン共重合体が挙げられる。オルガノハイドロジェンポリシロキサンとしては、両末端トリメチルシロキシ基封鎖メチルハイドロジェンポリシロキサン、両末端トリメチルシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、両末端ジメチルハイドロジェンシロキシ基封鎖ジメチルシロキサン・メチルハイドロジェンシロキサン共重合体、メチルハイドロジェンシクロポリシロキサンが挙げられる。縮合反応硬化型シリコーンエラストマーは、2種類のオルガノポリシロキサン中の官能基、またはオルガノポリシロキサンとシリカやシラン等のケイ素化合物中の官能基が縮合反応により結合して架橋しエラストマー化するもの、ラジカル反応硬化型シリコーンエラストマーは、オルガノポリシロキサン、補強性充填剤および有機過酸化物によりエラストマー化するものである。これらのシリコーンエラストマーには、増量充填剤、難燃剤、有機顔料、無機顔料、有機溶剤などを含有することができる。 In the non-combustible film material for building structures of the present invention, the resin-coated flame retardant layer is a single-layer structure of any one selected from silicone resins, fluorine resins, and vinyl chloride resins, or a combination of these resins. In the resin-coated flame retardant layer having a multilayer structure, the formation of the resin-coated flame retardant layer is 25 to 150% by mass, particularly 50 to 100% by mass, based on the total mass of the base fabric. If the mass of the resin-coated flame retardant layer is less than 25% by mass, the resulting film material may have insufficient shape stability, and if it exceeds 150% by mass, it may not be able to meet the combustion characteristics specified in ISO 5660 Part 1. . As the silicone resin, those having flexibility such as addition reaction curable silicone elastomer, condensation reaction curable silicone elastomer, radical (peroxide crosslinking) reaction curable silicone elastomer can be used. An addition reaction curable silicone elastomer that can be cured at low temperature is preferable. Addition reaction curable silicone elastomers are those in which functional groups in two types of organopolysiloxane are bonded by an addition reaction to be crosslinked and formed into an elastomer. These include, for example, aliphatic unsaturated groups such as vinyl groups and hexenyl groups. And a composition comprising an organopolysiloxane, an organohydrogenpolysiloxane, and a platinum group compound catalyst. Aliphatic unsaturated group-containing organopolysiloxanes include vinyl dimethylsiloxy group-blocked dimethylpolysiloxane at both ends, vinyldimethylsiloxy group-blocked dimethylsiloxane / methylvinylsiloxane copolymer at both ends, and vinylmethylphenylsiloxy group-blocked dimethylsiloxane at both ends. -A methylphenylsiloxane copolymer is mentioned. Examples of the organohydrogenpolysiloxane include trimethylsiloxy group-capped methylhydrogen polysiloxane at both ends, trimethylsiloxy group-capped dimethylsiloxane / methylhydrogensiloxane copolymer, dimethylhydrogensiloxy group-capped dimethylsiloxane / methylhydrol at both ends. Examples include a disiloxane copolymer and methylhydrogencyclopolysiloxane. Condensation reaction curable silicone elastomers are functional groups in two types of organopolysiloxanes, or those in which organopolysiloxanes and functional groups in silicon compounds such as silica and silane are bonded by a condensation reaction to crosslink and become elastomers. The reaction curable silicone elastomer is made into an elastomer by an organopolysiloxane, a reinforcing filler and an organic peroxide. These silicone elastomers can contain an expanding filler, a flame retardant, an organic pigment, an inorganic pigment, an organic solvent, and the like.
また、樹脂被覆難燃層に用いるフッ素系樹脂には、フッ化ビニル、ビニリデンフルオライド、トリフルオロエチレン、テトラフルオロエチレン、クロロトリフルオロエチレン、ヘキサフルオロプロピレンから選ばれた1種のモノマーを単独重合してなるフッ素系ポリマー、またはこれらの2種以上のモノマーを共重合してなるフッ素系エラストマー、またはこれらの1種以上のモノマーをビニルモノマーと共重合してなるフッ素系エラストマーなど、柔軟性を有するものが使用できる。また、樹脂被覆難燃層に用いる塩化ビニル系樹脂は、塩化ビニルモノマーの単独重合体(乳化重合タイプ、懸濁重合タイプで重合度が700〜3800のもの)の他、塩化ビニルモノマーと共重合し得る他のモノマー類との共重合体、及びグラフト重合体を含む。塩化ビニル系樹脂は、可塑剤を含む軟質塩化ビニル樹脂が柔軟性に優れ好ましく、可塑剤として、アジピン酸ジアルキルエステル類、セバシン酸ジアルキルエステル類、フタル酸ジアルキルエステル類、イソまたはテレフタル酸ジアルキルエステル類,シクロヘキサンジカルボン酸ジアルキルエステル類、芳香族リン酸エステル類、塩素化パラフィン類、ポリエステルオリゴマー類などを樹脂被覆難燃層に対して10〜50質量%含有するもの、接着剤としてポリイソシアネート化合物及びポリオール化合物、その他、難燃剤、充填剤、金属複合安定剤、着色剤、紫外線吸収剤などを含有するものが例示できる。 The fluororesin used for the resin-coated flame retardant layer is a homopolymer of one monomer selected from vinyl fluoride, vinylidene fluoride, trifluoroethylene, tetrafluoroethylene, chlorotrifluoroethylene, and hexafluoropropylene. Such as a fluorine-containing polymer, a fluorine-based elastomer obtained by copolymerizing two or more of these monomers, or a fluorine-based elastomer obtained by copolymerizing one or more of these monomers with a vinyl monomer. What you have can be used. The vinyl chloride resin used for the resin-coated flame retardant layer is a copolymer of vinyl chloride monomer in addition to a vinyl chloride monomer homopolymer (emulsion polymerization type, suspension polymerization type having a polymerization degree of 700 to 3800). Copolymers with other monomers that can be made, and graft polymers. As the vinyl chloride resin, a soft vinyl chloride resin containing a plasticizer is preferable because of its excellent flexibility. As the plasticizer, adipic acid dialkyl esters, sebacic acid dialkyl esters, phthalic acid dialkyl esters, iso or terephthalic acid dialkyl esters , Cyclohexanedicarboxylic acid dialkyl esters, aromatic phosphate esters, chlorinated paraffins, polyester oligomers and the like containing 10-50% by mass of the resin-coated flame retardant layer, polyisocyanate compounds and polyols as adhesives Examples include compounds, flame retardants, fillers, metal composite stabilizers, colorants, ultraviolet absorbers and the like.
樹脂被覆難燃層には難燃剤を含むことが好ましく、難燃剤は具体的に、a).金属リン酸塩、金属有機リン酸塩、リン酸誘導体、ポリリン酸アンモニウム、及びポリリン酸アンモニウム誘導体化合物などのリン原子含有化合物、b).(イソ)シアヌレート系化合物、(イソ)シアヌル酸系化合物、グアニジン系化合物、尿素系化合物、及び、これらの誘導体化合物などの窒素原子含有化合物(メラミンシアヌレート)、c).ケイ素化合物、金属水酸化物、金属酸化物、金属炭酸塩化合物、金属硫酸塩化合物、ホウ酸化合物、及び無機系化合物複合体などの無機系化合物、d).有機臭素化物、有機塩素化物から選ばれた1種以上であり、樹脂被覆難燃層を構成する樹脂(エラストマー)100質量部に対して、10〜150質量部、好ましくは30〜100質量部使用することで、これら難燃剤を光拡散剤代わりとして光源位置の隠蔽目的としても活用することができる。 The resin-coated flame retardant layer preferably contains a flame retardant, and the flame retardant is specifically a). Phosphorus atom-containing compounds such as metal phosphates, metal organic phosphates, phosphate derivatives, ammonium polyphosphates, and ammonium polyphosphate derivative compounds, b). Nitrogen-containing compounds (melamine cyanurate) such as (iso) cyanurate compounds, (iso) cyanuric acid compounds, guanidine compounds, urea compounds, and derivative compounds thereof, c). Inorganic compounds such as silicon compounds, metal hydroxides, metal oxides, metal carbonate compounds, metal sulfate compounds, boric acid compounds, and inorganic compound complexes; d). 10 to 150 parts by mass, preferably 30 to 100 parts by mass, based on 100 parts by mass of resin (elastomer) that is one or more selected from organic bromides and organic chlorinated compounds. By doing so, these flame retardants can be used for the purpose of concealing the light source position instead of the light diffusing agent.
また、樹脂被覆難燃層には光拡散性粒子として、平均粒子径が1〜30μmの乳白色〜透明の、球状または不定形粒子状の無機系化合物、高分子化合物などを、樹脂被覆難燃層に対して、0.1〜20質量%、好ましくは1〜10質量%含んでいてもよく、これらの光拡散性粒子は例えば、ガラスビーズ、中空ガラスビーズ、ガラス粉、シリカ(酸化ケイ素)、天然雲母粉末、合成雲母粉末、シリコーン樹脂ビーズ、シリコーン樹脂粉末、(架橋)アクリル系樹脂ビーズ、(架橋)アクリル系樹脂粉末、(架橋)ポリスチレン系樹脂ビーズ、(架橋)ポリスチレン系樹脂粉末、(高密度)ポリエチレン系樹脂ビーズ、(高密度)ポリエチレン系樹脂粉末、エポキシ樹脂ビーズ、エポキシ樹脂粉末、ベンゾグアナミン樹脂ビーズ、ベンゾグアナミン樹脂粉末などである。 In addition, the resin-coated flame retardant layer is made of a light-diffusing particle, such as a milky white to transparent, spherical or amorphous particulate inorganic compound or polymer compound having an average particle diameter of 1 to 30 μm. The light diffusing particles may contain, for example, glass beads, hollow glass beads, glass powder, silica (silicon oxide), 0.1 to 20% by mass, preferably 1 to 10% by mass. Natural mica powder, synthetic mica powder, silicone resin beads, silicone resin powder, (crosslinked) acrylic resin beads, (crosslinked) acrylic resin powder, (crosslinked) polystyrene resin beads, (crosslinked) polystyrene resin powder, (high Density) polyethylene resin beads, (high density) polyethylene resin powder, epoxy resin beads, epoxy resin powder, benzoguanamine resin beads, benzoguana Down resin powder and the like.
樹脂被覆難燃層を基材布帛上に形成し、光拡散透過性積層体を得る方法としては、例えば、有機溶剤に溶解させた樹脂組成物(塗料)、樹脂エマルジョン(ラテックス)による樹脂組成物(塗料)、軟質ポリ塩化ビニル樹脂を主体とするペーストゾル、などを用いて、公知の塗工方法、例えばディッピング(基材布帛への両面加工)、コーティング(基材布帛への片面加工、または両面加工)などの含浸(基材布帛内部に樹脂組成物が含浸しているが、基材布帛表面には樹脂組成物による被覆層が形成されていない状態)、及び含浸被覆(基材布帛内部に樹脂組成物が含浸し、かつ、基材布帛表面に樹脂組成物による被覆層が形成される状態)が例示できる。また基材布帛上に、カレンダー成型、Tダイス押出法により成形した0.01〜0.3mmのフィルムを、接着剤を介して、あるいは熱ラミネートにより積層する方法であってもよい。本発明の建築構造用不燃膜材(光拡散透過性積層体)の可視光透過率(JIS Z8722)が10〜50%であることが光天井膜の用途において、光を透過すると同時に光源位置を隠蔽する効果に最適となる。 As a method for forming a resin-coated flame retardant layer on a base fabric and obtaining a light diffusive transparent laminate, for example, a resin composition (paint) dissolved in an organic solvent, a resin composition using a resin emulsion (latex) (Paint), paste sol mainly composed of soft polyvinyl chloride resin, and the like, for example, dipping (double-sided processing on base fabric), coating (single-sided processing on base fabric, or Impregnation such as double-sided processing (in which the resin composition is impregnated inside the base fabric, but a coating layer is not formed on the surface of the base fabric), and impregnation coating (inside the base fabric) And the resin composition is impregnated and a coating layer of the resin composition is formed on the surface of the base fabric. Moreover, the method of laminating | stacking the film of 0.01-0.3 mm shape | molded on the base material fabric by the calendar | calender shaping | molding and the T-die extrusion method through an adhesive agent or a thermal lamination may be sufficient. In the use of the optical ceiling film, the visible light transmittance (JIS Z8722) of the non-combustible film material for building structure (light diffusive transparent laminate) of the present invention is 10 to 50%. Best suited for concealment effects.
本発明の建築構造用不燃膜材には、樹脂被覆難燃層に印刷を施すことによって、昼夜を通じて外観表示及び光透過による行灯表示を可能とする。印刷は公知の印刷、例えばグラビア印刷、スクリーン印刷、転写印刷、インクジェット印刷の何れも可能であるが、本発明の建築構造用不燃膜材においては、光透過性及び発色性とのバランスにおいて、インク塗布量が少ないインクジェット印刷が適している。 The incombustible film material for building structure according to the present invention can be printed on the resin-coated flame retardant layer, thereby enabling appearance display and display of light by light transmission throughout the day and night. The printing can be any known printing, such as gravure printing, screen printing, transfer printing, and ink jet printing. However, in the non-combustible film material for building structure of the present invention, the ink is balanced in light transmittance and color development. Inkjet printing with a small coating amount is suitable.
本発明の建築構造用不燃膜材は、コーンカロリーメーター試験法(ISO5660Part1)において、建築構造用不燃膜材(光拡散透過性積層体)に対して輻射電気ヒ−タ−による輻射熱を、50kW/m2で照射した時に、加熱開始後20分間の総発熱量が8MJ/m2以下であり、且つ加熱開始後20分間、10秒以上継続して最高発熱速度が200kW/m2を超えない燃焼特性を満たすものである。 The non-combustible film material for building structure of the present invention is radiated by a radiant electric heater with respect to the non-combustible film material for building structure (light diffusive laminate) in a cone calorimeter test method (ISO5660Part1). when irradiated m 2, and the gross calorific value of the heating start after 20 minutes is at 8 MJ / m 2 or less, and the heating start after 20 minutes, the highest heat release rate continues for 10 seconds or more not exceeding 200 kW / m 2 combustion It satisfies the characteristics.
以下、本発明について実施例を挙げて具体的に説明するが、本発明はこれらに限定されるものではない。先ずは本発明の建築構造用不燃膜材の評価方法を述べる。
〈可視光透過率〉
分光側色計CM3600d(コニカミノルタ社製)を使用し、JIS Z8722に従って測定した。
〈燃焼試験〉(ASTM-E1354:コーンカロリーメーター試験法)
輻射電気ヒーターによる50kW/m2の輻射熱を膜材面に20分間照射し、この発熱性試験において、20分間の総発熱量と発熱速度を測定し、試験後の膜材外観を観察した。
(a)総発熱量:8MJ/m2以下のものを適合とした。
(b)発熱速度:10秒以上継続して200kW/m2を超えないものを適合とした。
(c)外観観察:直径0.5mmを超えるピンホール陥没痕の発生がないものを適合と
した。
〈耐屈曲性試験(1)〉10cm(タテ)×10cm(ヨコ)の正方形の膜材片を、タテ5cmの位置で2つ折りしたものを、さらにヨコ5cmの位置で2つ折りした5cm(タテ)×5cm(ヨコ)の4つ折り畳み体を試験片とした。この試験片を10cm×10cmの2枚のガラス板に挟み、5kgの錘を乗せた状態で20℃×30分間放置した後、試験片を拡げ、折り痕を透過光で観察し白化痕の有無及び状態を確認した。
1 :白化痕の発生を認めない
2 :白化痕の発生が軽微である
3 :白化痕の発生が顕著である
〈耐屈曲性試験(2)〉上記試験(1)の試験片を用い、(1)で行った2つ折りの部分を反転した2つ折りとして試験(1)と同様に4つ折り畳み体を試験片として試験(1)と同じ試験及び評価を行った。
〈耐屈曲性試験(3)〉スコット形屈曲往復摩耗試験(JIS L1096 8.19.2B法)
膜材から長さ25mm×幅120mmの試料を採取し、スコット形試験機に装着し、1kgf荷重の負荷で50回の往復屈曲を行い、試験後の基材布帛面の状態を観察し、摩耗耐久性を下記のように判定した。
1:基材布帛の織組織に異常を認めない
2:基材布帛の織組織にズレが認められる
3:基材布帛の織組織に顕著な乱れを認められる
EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated concretely, this invention is not limited to these. First, a method for evaluating a non-combustible film material for building structures according to the present invention will be described.
<Visible light transmittance>
A spectroscopic color meter CM3600d (manufactured by Konica Minolta Co., Ltd.) was used, and measurement was performed according to JIS Z8722.
<Combustion test> (ASTM-E1354: Corn calorimeter test method)
The surface of the film material was irradiated with 50 kW / m 2 of radiant heat from a radiant electric heater for 20 minutes. In this exothermic test, the total heat generation amount and the heat generation rate for 20 minutes were measured, and the appearance of the film material after the test was observed.
(A) Total calorific value: 8 MJ / m 2 or less was regarded as suitable.
(B) heating speed: 10 seconds or more continuously to the Relevant not exceed 200 kW / m 2.
(C) Appearance observation: Applicable to those with no pinhole depression exceeding 0.5 mm in diameter.
<Bend Resistance Test (1)> A 10 cm (vertical) × 10 cm (horizontal) square film material piece folded in two at a vertical 5 cm position and further folded in two at a horizontal 5 cm position (vertical) A four-fold body of 5 cm (horizontal) was used as a test piece. The test piece is sandwiched between two 10 cm × 10 cm glass plates and left standing at 20 ° C. for 30 minutes with a 5 kg weight placed on it. Then, the test piece is expanded, the fold marks are observed with transmitted light, and there is no whitening mark. And the state was confirmed.
1: No whitening marks are observed
2: The occurrence of whitening marks is slight
3: The occurrence of whitening marks is remarkable <Bend resistance test (2)> Using the test piece of the above test (1), the two-fold portion performed in (1) was inverted and tested as a double fold (1) In the same manner as above, the same test and evaluation as in test (1) were performed using four folded bodies as test pieces.
<Bend resistance test (3)> Scott type bending reciprocating wear test (JIS L1096 8.19.2B method)
A sample 25 mm long x 120 mm wide was taken from the membrane material, mounted on a Scott type tester, bent 50 times under a load of 1 kgf, and observed the condition of the substrate fabric surface after the test to wear Durability was determined as follows.
1: No abnormality in the woven structure of the base fabric
2: Deviation is recognized in the woven structure of the base fabric
3: Remarkable disorder is recognized in the woven structure of the base fabric
〔実施例1〕
〈基材布帛1〉
Eガラスのマルチフィラメントヤーン(フィラメント径9μm、フィラメント数400本:75dtexの扁平糸条)を基材布帛の経糸及び緯糸とする空隙率1%の四枚綾織物で、表側及び裏側の完全組織において、経糸の緯糸に対する浮き跨ぎ本数及び、緯糸の経糸に対する浮き跨ぎ本数が、各々3本のルーズ構造を有する3/1破れ斜文、経糸打込密度52本/1インチ、緯糸打込密度40本/1インチ、質量250g/m2、ヒートクリーニング布帛を用いた。
〈樹脂被覆難燃層〉
樹脂被覆難燃層形成用に下記配合1の軟質塩化ビニル樹脂ペースト組成物を用いた。この配合1のペーストを基材布帛1の幅方向に均一に垂らし、ドクターブレードによる圧着部を通過させて、基材布帛1の片表面に配合1のペーストによる濡塗膜を均一に形成し、180℃×3分間電気炉加熱してゲル化処理を行い、基材布帛1の片表面に樹脂被覆難燃層が50g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛1の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は300g/m2であった。
〔配合1〕塩化ビニル系樹脂による樹脂被覆難燃層
乳化重合塩化ビニル樹脂(重合度1700) 100質量部
1,2−シクロヘキサンジカルボン酸ジイソノニル(可塑剤) 60質量部
※商品名:ヘキサモールDINCH(BASF社製)
リン酸クレジルジフェニル(防炎可塑剤) 10質量部
(別名CDP:クレジルジフェニルフォスフェート)
酸化アンチモン(難燃剤) 15質量部
酸化モリブデン(難燃剤) 5質量部
架橋アクリル系樹脂ビーズ(光拡散剤)粒子径15μm 5質量部
バリウム亜鉛複合化合物(安定剤) 2質量部
イソシアヌレート変性トリイソシアネート(TDIの3量体) 3質量部
ジエチレングリコール(ポリオール) 3質量部
※イソシアヌレート変性トリイソシアネートの付加反応により、基材布帛1との密着性を向上すると同時に、ジエチレングリコールとの重合により軟質塩化ビニル樹脂内部にポリウレタン構造を生成することで、より基材布帛1との密着性を強固とする。
[Example 1]
<Base material fabric 1>
A 4% twill woven fabric with a porosity of 1% using E glass multifilament yarn (filament diameter 9 μm, 400 filaments: flat yarn with 75 dtex) as the warp and weft of the base fabric, in the complete structure on the front and back sides The number of floating striations for warp and weft and the number of floating striations for weft for warp are 3/1 broken oblique lines each having three loose structures, warp threading density 52/1 inch, weft threading density 40 / 1 inch, mass 250 g / m 2 , heat cleaning fabric was used.
<Resin-coated flame retardant layer>
A soft vinyl chloride resin paste composition of the following formulation 1 was used for forming a resin-coated flame retardant layer. This formulation 1 paste is uniformly hung in the width direction of the base fabric 1, and is passed through a pressure-bonding portion by a doctor blade, so that a wet coating film with the formulation 1 paste is uniformly formed on one surface of the base fabric 1, Gelation treatment was performed by heating in an electric furnace at 180 ° C. for 3 minutes to obtain a film material in which 50 g / m 2 of a resin-coated flame retardant layer was provided on one surface of the base fabric 1. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 1, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 300 g / m 2 .
[Formulation 1] Resin-coated flame retardant layer with vinyl chloride resin emulsion polymerization vinyl chloride resin (degree of polymerization 1700) 100 parts by mass 1,2-cyclohexanedicarboxylic acid diisononyl (plasticizer) 60 parts by mass * Product name: Hexamol DINCH ( (Made by BASF)
Cresyl diphenyl phosphate (flameproof plasticizer) 10 parts by mass (also known as CDP: cresyl diphenyl phosphate)
Antimony oxide (flame retardant) 15 parts by weight Molybdenum oxide (flame retardant) 5 parts by weight Cross-linked acrylic resin beads (light diffusing agent) particle size 15 μm 5 parts by weight Barium zinc composite compound (stabilizer) 2 parts by weight Isocyanurate-modified triisocyanate (TDI trimer) 3 parts by weight Diethylene glycol (polyol) 3 parts by weight * Adhesion of isocyanurate-modified triisocyanate improves adhesion to the base fabric 1 and at the same time, soft vinyl chloride resin by polymerization with diethylene glycol. By forming a polyurethane structure inside, the adhesiveness with the base fabric 1 is further strengthened.
〔実施例2〕
実施例1の配合1を下記配合2に変更した以外は実施例1と同様として、この配合2の溶液を基材布帛1の幅方向に均一に垂らし、ドクターブレードによる圧着部を通過させて、基材布帛1の片表面に配合2の溶液による濡塗膜を均一に形成し、予備乾燥でトルエンを除去した後、160℃×3分間電気炉加熱して付加反応硬化を行い、基材布帛1の片表面に樹脂被覆難燃層が40g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛1の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は290g/m2であった。
〔配合2〕シリコーン系樹脂による樹脂被覆難燃層
※付加反応硬化型シリコーンエラストマー(下記2液を使用)
両末端ビニルジメチルシロキシ基封鎖ジメチルポリシロキサン 50質量部
両末端トリメチルシロキシ基封鎖メチルハイドロジェンポリシロキサン 50質量部
白金族化合物(触媒) 0.2質量部
架橋アクリル系樹脂ビーズ(光拡散剤)粒子径15μm 5質量部
メラミンシアヌレート(難燃剤) 10質量部
水酸化アルミニウム(難燃剤) 10質量部
トルエン(希釈剤) 100質量部
[Example 2]
Except that the formulation 1 of Example 1 was changed to the following formulation 2, as in Example 1, the solution of this formulation 2 was evenly hung in the width direction of the base fabric 1, and the crimping part by a doctor blade was passed through. A wet coating with the solution of Formulation 2 is uniformly formed on one surface of the base fabric 1, and toluene is removed by preliminary drying, followed by addition reaction curing by heating in an electric furnace at 160 ° C. for 3 minutes. A film material having a resin-coated flame retardant layer of 40 g / m 2 on one surface was obtained. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 1, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 290 g / m 2 .
[Formulation 2] Resin-coated flame retardant layer with silicone resin * Addition reaction curable silicone elastomer (using the following two liquids)
Both ends vinyldimethylsiloxy group-capped dimethylpolysiloxane 50 parts by mass Both ends trimethylsiloxy group-capped methylhydrogenpolysiloxane 50 parts by mass Platinum group compound (catalyst) 0.2 parts by mass Crosslinked acrylic resin beads (light diffusing agent) particle size 15 μm 5 parts by weight Melamine cyanurate (flame retardant) 10 parts by weight Aluminum hydroxide (flame retardant) 10 parts by weight Toluene (diluent) 100 parts by weight
〔実施例3〕
実施例1の配合1を下記配合3に変更した以外は実施例1と同様として、この配合3の溶液を基材布帛1の幅方向に均一に垂らし、ドクターブレードによる圧着部を通過させて、基材布帛1の片表面に配合3の溶液による濡塗膜を均一に形成し、120℃×3分間電気炉加熱して溶剤除去を行い、基材布帛1の片表面に樹脂被覆難燃層が46g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛1の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は296g/m2であった。
〔配合3〕フッ素系樹脂による樹脂被覆難燃層
軟質フッ素樹脂
(四フッ化エチレン−六フッ化プロピレン−フッ化ビニリデン三元共重合体樹脂)
100質量部
架橋アクリル系樹脂ビーズ(光拡散剤)粒子径15μm 5質量部
三酸化アンチモン(難燃剤) 10質量部
水酸化アルミニウム(難燃剤) 10質量部
ジメチルホルムアミド(希釈剤) 50質量部
メチルエチルケトン(希釈剤) 50質量部
トルエン(希釈剤) 50質量部
Example 3
Except that the formulation 1 of Example 1 was changed to the following formulation 3, as in Example 1, the solution of this formulation 3 was uniformly suspended in the width direction of the base fabric 1, and the crimping part by a doctor blade was passed through. A wet coating with a solution of Formulation 3 is uniformly formed on one surface of the base fabric 1, and the solvent is removed by heating in an electric furnace at 120 ° C. for 3 minutes, and a resin-coated flame retardant layer is formed on one surface of the base fabric 1. There was obtained 46 g / m 2 provided with film material. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 1, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 296 g / m 2 .
[Formulation 3] Resin-coated flame retardant layer with fluororesin Soft fluororesin (tetrafluoroethylene-hexafluoropropylene-vinylidene fluoride terpolymer resin)
100 parts by mass Crosslinked acrylic resin beads (light diffusing agent) particle size 15 μm 5 parts by mass Antimony trioxide (flame retardant) 10 parts by mass Aluminum hydroxide (flame retardant) 10 parts by mass Dimethylformamide (diluent) 50 parts by mass Methyl ethyl ketone ( Diluent) 50 parts by mass Toluene (diluent) 50 parts by mass
〔実施例4〕
実施例1の基材布帛1を下記基材布帛2に変更した以外は実施例1と同様として、基材布帛2の片表面に樹脂被覆難燃層が50g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛2の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は300g/m2であった。
〈基材布帛2〉
Eガラスのマルチフィラメントヤーン(フィラメント径9μm、フィラメント数400本:75dtexの扁平糸条)を基材布帛の経糸及び緯糸とする空隙率1%の五枚朱子織物で、表側及び裏側の完全組織において、経糸の緯糸に対する浮き跨ぎ本数及び、緯糸の経糸に対する浮き跨ぎ本数が、各々4本のルーズ構造を有する3飛び4/1朱子、経糸打込密度52本/1インチ、緯糸打込密度40本/1インチ、質量250g/m2、ヒートクリーニング布帛を用いた。
Example 4
A film material in which a resin-coated flame retardant layer is provided at 50 g / m 2 on one surface of the base fabric 2 is the same as in Example 1 except that the base fabric 1 of Example 1 is changed to the following base fabric 2. Obtained. A part of the resin-coated flame retardant layer was formed in the base fabric 2 in an impregnated state, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 300 g / m 2 .
<Base material fabric 2>
5% satin fabric with a porosity of 1% using E glass multifilament yarn (filament diameter 9 μm, 400 filaments: flat yarn with 75 dtex) as the warp and weft of the base fabric, in the complete structure on the front and back sides The number of floating struts for the warp and the weft and the number of float straddles for the warp of the weft are 3 jumps 4/1 satin each having a loose structure, warp driving density 52/1 inch, weft driving density 40 / 1 inch, mass 250 g / m 2 , heat cleaning fabric was used.
〔実施例5〕
実施例2の基材布帛1を基材布帛2に変更した以外は実施例2と同様として、基材布帛2の片表面に樹脂被覆難燃層が40g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛2の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は290g/m2であった。
Example 5
A film material in which a resin-coated flame retardant layer is provided at 40 g / m 2 on one surface of the base fabric 2 is obtained in the same manner as in Example 2 except that the base fabric 1 is changed to the base fabric 2. It was. A part of the resin-coated flame retardant layer was formed in the base fabric 2 in an impregnated state, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 290 g / m 2 .
〔実施例6〕
実施例2の基材布帛1を下記基材布帛3に変更した以外は実施例2と同様として、基材布帛3の片表面に樹脂被覆難燃層が40g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛3の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は290g/m2であった。
〈基材布帛3〉
Eガラスのマルチフィラメントヤーン(フィラメント径9μm、フィラメント数400本:75dtexの扁平糸条)を基材布帛の経糸及び緯糸とする空隙率1%の五枚朱子織物で、表側及び裏側の完全組織において、経糸の緯糸に対する浮き跨ぎ本数及び、緯糸の経糸に対する浮き跨ぎ本数が、各々4本のルーズ構造を有する2飛び4/1朱子、経糸打込密度52本/1インチ、緯糸打込密度40本/1インチ、質量250g/m2、ヒートクリーニング布帛を用いた。
Example 6
A film material having a resin-coated flame retardant layer of 40 g / m 2 provided on one surface of the base fabric 3 is the same as Example 2 except that the base fabric 1 of Example 2 is changed to the following base fabric 3. Obtained. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 3, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 290 g / m 2 .
<Base material fabric 3>
5% satin fabric with a porosity of 1% using E glass multifilament yarn (filament diameter 9 μm, 400 filaments: flat yarn with 75 dtex) as the warp and weft of the base fabric, in the complete structure on the front and back sides The number of floats over the weft of the warp and the number of floats over the warp of the weft are 4 jumps 4/1 satin each having a loose structure, warp driving density 52/1 inch, weft driving density 40 / 1 inch, mass 250 g / m 2 , heat cleaning fabric was used.
実施例1〜6の膜材は、いずれもISO5660Part1に規定の燃焼特性に適合する不燃性を有し、可撓性及び適度な光の拡散性を有するなど、間仕切り、防煙垂壁、光壁膜、光天井膜などの建築材料用途に適し、特に基材布帛に特定の浮き跨ぎ構造を有することにより、膜材料を折り曲げても、浮き跨ぎ構造が歪変位を吸収緩和することで膜材料の外観及び光透過外観に白化痕筋の発現が効果的に抑止された取り扱い性に優れた膜材料であった。 The film materials of Examples 1 to 6 all have non-flammability that conforms to the combustion characteristics specified in ISO 5660 Part 1, have flexibility and moderate light diffusion properties, etc., such as partitions, smoke barriers, and light walls. Suitable for building material applications such as membranes and optical ceiling membranes, especially by having a specific floating straddle structure on the base fabric, so that even if the membrane material is bent, the floating strut structure absorbs and relaxes strain displacement. It was a film material excellent in handleability in which appearance of whitening scars was effectively suppressed in appearance and light transmission appearance.
〔比較例1〕
実施例2の基材布帛1を下記基材布帛4に変更した以外は実施例2と同様として、基材布帛4の片表面に樹脂被覆難燃層が40g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛4の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は290g/m2であった。
〈基材布帛4〉
Eガラスのマルチフィラメントヤーン(フィラメント径9μm、フィラメント数400本:75dtexの扁平糸条)を基材布帛の経糸及び緯糸とする空隙率1%の平織物で、表側及び裏側の完全組織において、経糸の緯糸に対する浮き跨ぎ本数及び、緯糸の経糸に対する浮き跨ぎ本数が、各々1本の構造を有し、経糸打込密度52本/1インチ、緯糸打込密度40本/1インチ、質量250g/m2、ヒートクリーニング布帛を用いた。
[Comparative Example 1]
A film material in which a resin-coated flame retardant layer is provided at 40 g / m 2 on one surface of the base fabric 4 except that the base fabric 1 of Example 2 is changed to the base fabric 4 described below. Obtained. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 4, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 290 g / m 2 .
<Base material fabric 4>
A plain woven fabric with a porosity of 1% using a multifilament yarn of E glass (filament diameter 9 μm, 400 filaments: flat yarn with 75 dtex) as the warp and weft of the base fabric. The number of floating struts for each weft and the number of float straddles for the warp of wefts has one structure, and a warp driving density of 52/1 inch, a weft driving density of 40/1 inch, and a mass of 250 g / m. 2. A heat cleaning fabric was used.
〔比較例2〕
実施例2の基材布帛1を下記基材布帛5に変更した以外は実施例2と同様として、基材布帛5の片表面に樹脂被覆難燃層が40g/m2設けられた膜材を得た。樹脂被覆難燃層の一部は基材布帛5の内部に含浸状態で形成され、これによって樹脂被覆難燃層が基材布帛1と接着していた。得られた膜材料の質量は290g/m2であった。
〈基材布帛5〉
Eガラスのマルチフィラメントヤーン(フィラメント径9μm、フィラメント数400本:75dtexの扁平糸条)を基材布帛の経糸及び緯糸とする空隙率1%の十枚朱子織物で、表側及び裏側の完全組織において、経糸の緯糸に対する浮き跨ぎ本数及び、緯糸の経糸に対する浮き跨ぎ本数が、各々9本の構造を有する七飛び9/1朱子、経糸打込密度52本/1インチ、緯糸打込密度40本/1インチ、質量250g/m2、ヒートクリーニング布帛を用いた。
[Comparative Example 2]
A film material having a resin-coated flame retardant layer of 40 g / m 2 provided on one surface of the base fabric 5 is the same as Example 2 except that the base fabric 1 of Example 2 is changed to the following base fabric 5. Obtained. A part of the resin-coated flame retardant layer was formed in an impregnated state inside the base fabric 5, whereby the resin-coated flame retardant layer was adhered to the base fabric 1. The mass of the obtained film material was 290 g / m 2 .
<Base material fabric 5>
A 10% satin woven fabric with a porosity of 1% using E glass multifilament yarn (filament diameter 9 μm, 400 filaments: flat yarn with 75 dtex) as the warp and weft of the base fabric, in the complete structure on the front and back sides The number of floats over the weft of the warp and the number of floats over the warp of the weft has 9 structures, respectively, 7 jump 9/1 satin, warp driving density 52/1 inch, weft driving density 40 / One inch, a mass of 250 g / m 2 , and a heat cleaning fabric were used.
比較例1と2の膜材は、不燃性、可撓性及び適度な光の拡散性を有していた。しかし比較例1の膜材は、基材布帛4(平織物)を用いたことで、経糸及び緯糸の浮き跨ぎ本数が各々1本の構造となり、膜材料を折り曲げた時に、歪変位の吸収緩和が十分に発現されないことで基材布帛と樹脂被覆難燃層との界面に微細な剥離を生じることによる乱反射を生じ、これが白化痕筋となって目視されることで膜材料の外観及び光透過外観を悪いものとした。また比較例2の膜材は、基材布帛5(十枚朱子織物)を用いたことで、経糸及び緯糸の浮き跨ぎ本数9本を有するルーズ構造を有し、膜材料を折り曲げた時に、歪変位の吸収緩和作用が十分になされ、白化痕筋発生が抑止されたものであったが、しかし経糸及び緯糸の浮き跨ぎ本数9本のルーズ構造は、基材布帛の織組織の形態保持性が脆弱となり、膜材裏面を擦ったときに、織組織に顕著な乱れを発生するなど、実用耐久性に乏しいものであった。 The film materials of Comparative Examples 1 and 2 had incombustibility, flexibility, and appropriate light diffusibility. However, the membrane material of Comparative Example 1 has a structure in which the number of warp and weft floats is one each because the base material fabric 4 (plain fabric) is used, and when the membrane material is bent, the strain displacement is absorbed and reduced. Is not fully expressed, it causes irregular reflection due to fine peeling at the interface between the base fabric and the resin-coated flame retardant layer, and this is visually observed as whitening traces, so that the appearance and light transmission of the film material Appearance was bad. Further, the membrane material of Comparative Example 2 has a loose structure having nine floating warps and weft yarns by using the base material fabric 5 (ten-leaf satin fabric), and when the membrane material is bent, the membrane material is distorted. Although the effect of absorbing and absorbing displacement was sufficiently achieved and the occurrence of whitening scars was suppressed, the loose structure with nine floating warps and wefts has a shape retention of the woven structure of the base fabric. It became brittle, and when it was rubbed on the back side of the membrane material, it was poor in practical durability, such as significant disturbance in the woven structure.
本発明によれば、ISO5660Part1に規定の燃焼特性に適合し、さらに可撓性及び適度な光の拡散性を有し、特に膜材料の縫製工程や施工の取り扱い時に、膜材料を折り曲げたり、不慮に折れ曲がったとしても、膜材料の外観及び光透過外観において白化痕筋の発現が効果的に抑止されるので、建築構造用不燃膜材として、間仕切り、防煙垂壁、光壁膜、光天井膜などの建築材料用途に広く用いることができる。 According to the present invention, it conforms to the combustion characteristics specified in ISO 5660 Part 1 and has flexibility and appropriate light diffusibility. In particular, the membrane material can be bent or inadvertently handled during the sewing process and construction of the membrane material. Even if it is bent, the appearance of whitening traces is effectively suppressed in the appearance of the film material and the light transmission appearance, so as a non-combustible film material for building structures, partitions, smoke barriers, light wall films, light ceilings It can be widely used for building materials such as membranes.
1:無機マルチフィラメントヤーン(経)
2:無機マルチフィラメントヤーン(緯)
3:3/1破れ斜文(四枚綾織物)
4:3飛び4/1朱子(五枚朱子織物)
5:2飛び4/1朱子(五枚朱子織物)
6:完全組織
1: Inorganic multifilament yarn (warp)
2: Inorganic multifilament yarn (lat)
3: 3/1 broken tears (four-sheet twill fabric)
4: 3 Jump 4/1 Akuko (Five Ako Fabric)
5: 2 jump 4/1 Akuko (Five sheets Akiko fabric)
6: Complete organization
Claims (4)
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Cited By (2)
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KR102032391B1 (en) * | 2019-05-28 | 2019-10-15 | 재단법인 한국탄소융합기술원 | Flame retarding sheet for sheet molding compound and molded article having the flame retarding sheet |
KR102174023B1 (en) * | 2019-10-04 | 2020-11-04 | 주식회사 한국선진철도시스템 | Method for manufacturing SMC product using the flame retardant sheet for railroad cars |
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KR102594053B1 (en) * | 2021-06-18 | 2023-10-25 | 희성폴리머 주식회사 | Coating Composition of Building Membrane Structures with improved fire resistance, contamination, durability, and weather resistance |
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