JP7399709B2 - Napped artificial leather and decorated polyurethane moldings - Google Patents
Napped artificial leather and decorated polyurethane moldings Download PDFInfo
- Publication number
- JP7399709B2 JP7399709B2 JP2019236484A JP2019236484A JP7399709B2 JP 7399709 B2 JP7399709 B2 JP 7399709B2 JP 2019236484 A JP2019236484 A JP 2019236484A JP 2019236484 A JP2019236484 A JP 2019236484A JP 7399709 B2 JP7399709 B2 JP 7399709B2
- Authority
- JP
- Japan
- Prior art keywords
- artificial leather
- basic
- napped
- napped artificial
- dye
- 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.)
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Links
- 239000002649 leather substitute Substances 0.000 title claims description 111
- 229920002635 polyurethane Polymers 0.000 title claims description 42
- 239000004814 polyurethane Substances 0.000 title claims description 42
- 238000000465 moulding Methods 0.000 title description 20
- 239000000981 basic dye Substances 0.000 claims description 76
- 239000000835 fiber Substances 0.000 claims description 59
- 238000000034 method Methods 0.000 claims description 37
- 229920000728 polyester Polymers 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 25
- 239000001257 hydrogen Substances 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 21
- 239000000284 extract Substances 0.000 claims description 21
- 125000000524 functional group Chemical group 0.000 claims description 21
- 125000002091 cationic group Chemical group 0.000 claims description 20
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 18
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 13
- 229920001971 elastomer Polymers 0.000 claims description 10
- 239000000806 elastomer Substances 0.000 claims description 10
- 229920001410 Microfiber Polymers 0.000 claims description 9
- 235000015165 citric acid Nutrition 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 150000007524 organic acids Chemical group 0.000 claims description 5
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 4
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims description 4
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 4
- 239000001630 malic acid Substances 0.000 claims description 4
- 235000011090 malic acid Nutrition 0.000 claims description 4
- 239000011975 tartaric acid Substances 0.000 claims description 4
- 235000002906 tartaric acid Nutrition 0.000 claims description 4
- 239000004310 lactic acid Substances 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 238000004043 dyeing Methods 0.000 description 34
- 239000000975 dye Substances 0.000 description 31
- -1 amine compounds Chemical class 0.000 description 26
- 238000002845 discoloration Methods 0.000 description 24
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
- 239000002585 base Substances 0.000 description 23
- 239000000463 material Substances 0.000 description 20
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 18
- 229920005989 resin Polymers 0.000 description 18
- 239000011347 resin Substances 0.000 description 18
- 238000011282 treatment Methods 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 238000004519 manufacturing process Methods 0.000 description 12
- 239000004745 nonwoven fabric Substances 0.000 description 11
- 239000003945 anionic surfactant Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 10
- 239000002994 raw material Substances 0.000 description 10
- KKEYFWRCBNTPAC-UHFFFAOYSA-N terephthalic acid group Chemical group C(C1=CC=C(C(=O)O)C=C1)(=O)O KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 9
- 239000007789 gas Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 8
- IURGIPVDZKDLIX-UHFFFAOYSA-M [7-(diethylamino)phenoxazin-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].C1=CC(=[N+](CC)CC)C=C2OC3=CC(N(CC)CC)=CC=C3N=C21 IURGIPVDZKDLIX-UHFFFAOYSA-M 0.000 description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 7
- 239000004744 fabric Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- DSZCWNRVMXBILR-UHFFFAOYSA-M (2z)-1,3,3-trimethyl-2-[2-(2-methyl-2,3-dihydroindol-1-ium-1-ylidene)ethylidene]indole;chloride Chemical compound [Cl-].CN/1C2=CC=CC=C2C(C)(C)C\1=C/C=[N+]1C2=CC=CC=C2CC1C DSZCWNRVMXBILR-UHFFFAOYSA-M 0.000 description 5
- PXGZQGDTEZPERC-UHFFFAOYSA-N 1,4-cyclohexanedicarboxylic acid Chemical compound OC(=O)C1CCC(C(O)=O)CC1 PXGZQGDTEZPERC-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- YZTJKOLMWJNVFH-UHFFFAOYSA-N 2-sulfobenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1S(O)(=O)=O YZTJKOLMWJNVFH-UHFFFAOYSA-N 0.000 description 4
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000002131 composite material Substances 0.000 description 4
- 238000007334 copolymerization reaction Methods 0.000 description 4
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 4
- 150000001991 dicarboxylic acids Chemical class 0.000 description 4
- 239000000986 disperse dye Substances 0.000 description 4
- 239000013013 elastic material Substances 0.000 description 4
- 230000009477 glass transition Effects 0.000 description 4
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 125000001453 quaternary ammonium group Chemical group 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- VEJIQHRMIYFYPS-UHFFFAOYSA-N (3-phenyl-1,2-oxazol-5-yl)boronic acid Chemical compound O1C(B(O)O)=CC(C=2C=CC=CC=2)=N1 VEJIQHRMIYFYPS-UHFFFAOYSA-N 0.000 description 3
- WMAVHUWINYPPKT-UHFFFAOYSA-M (e)-3-methyl-n-[(e)-(1-methyl-2-phenylindol-1-ium-3-ylidene)amino]-1,3-thiazol-2-imine;chloride Chemical compound [Cl-].C12=CC=CC=C2N(C)C(C=2C=CC=CC=2)=C1N=NC=1SC=C[N+]=1C WMAVHUWINYPPKT-UHFFFAOYSA-M 0.000 description 3
- MHOFGBJTSNWTDT-UHFFFAOYSA-M 2-[n-ethyl-4-[(6-methoxy-3-methyl-1,3-benzothiazol-3-ium-2-yl)diazenyl]anilino]ethanol;methyl sulfate Chemical compound COS([O-])(=O)=O.C1=CC(N(CCO)CC)=CC=C1N=NC1=[N+](C)C2=CC=C(OC)C=C2S1 MHOFGBJTSNWTDT-UHFFFAOYSA-M 0.000 description 3
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000001412 amines Chemical group 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 150000002431 hydrogen Chemical class 0.000 description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
- 238000001746 injection moulding Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- SYHRPJPCZWZVSR-UHFFFAOYSA-M n-benzyl-4-[(2,4-dimethyl-1,2,4-triazol-4-ium-3-yl)diazenyl]-n-methylaniline;bromide Chemical compound [Br-].C=1C=C(N=NC2=[N+](C=NN2C)C)C=CC=1N(C)CC1=CC=CC=C1 SYHRPJPCZWZVSR-UHFFFAOYSA-M 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920005862 polyol Polymers 0.000 description 3
- 150000003077 polyols Chemical class 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 239000005871 repellent Substances 0.000 description 3
- 230000002940 repellent Effects 0.000 description 3
- 238000002791 soaking Methods 0.000 description 3
- PCGDWIWUQDHQLK-UHFFFAOYSA-N 2-morpholin-4-yl-5-nitrobenzaldehyde Chemical compound O=CC1=CC([N+](=O)[O-])=CC=C1N1CCOCC1 PCGDWIWUQDHQLK-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 235000001671 coumarin Nutrition 0.000 description 2
- 229960000956 coumarin Drugs 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 238000005187 foaming Methods 0.000 description 2
- 125000005842 heteroatom Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 239000012948 isocyanate Substances 0.000 description 2
- 150000002513 isocyanates Chemical class 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 2
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 2
- 230000003472 neutralizing effect Effects 0.000 description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
- 238000010107 reaction injection moulding Methods 0.000 description 2
- 239000001044 red dye Substances 0.000 description 2
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000000542 sulfonic acid group Chemical group 0.000 description 2
- 229920005992 thermoplastic resin Polymers 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- XTHLNJJMYLLKPD-UHFFFAOYSA-N 2-aminoethanol;carbonic acid Chemical compound NCCO.OC(O)=O XTHLNJJMYLLKPD-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
- SPWPAFQLIZTXFN-UHFFFAOYSA-M 4-methoxy-n-methyl-n-[(1,3,3-trimethylindol-1-ium-2-yl)methylideneamino]aniline;methyl sulfate Chemical compound COS([O-])(=O)=O.C1=CC(OC)=CC=C1N(C)\N=C\C1=[N+](C)C2=CC=CC=C2C1(C)C SPWPAFQLIZTXFN-UHFFFAOYSA-M 0.000 description 1
- CARJPEPCULYFFP-UHFFFAOYSA-N 5-Sulfo-1,3-benzenedicarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(S(O)(=O)=O)=C1 CARJPEPCULYFFP-UHFFFAOYSA-N 0.000 description 1
- LCVNGSHJQQOSDB-UHFFFAOYSA-M 7-(diethylamino)-3-(1,3-dimethylbenzimidazol-3-ium-2-yl)chromen-2-one;chloride Chemical compound [Cl-].CN1C2=CC=CC=C2[N+](C)=C1C1=CC2=CC=C(N(CC)CC)C=C2OC1=O LCVNGSHJQQOSDB-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- NFZAWWHHOOFKTN-UHFFFAOYSA-K C(CCC)[P+](CCCC)(CCCC)CCCC.S(=O)(=O)([O-])C1=C(C(=O)[O-])C=CC=C1C(=O)[O-].C(CCC)[P+](CCCC)(CCCC)CCCC.C(CCC)[P+](CCCC)(CCCC)CCCC Chemical group C(CCC)[P+](CCCC)(CCCC)CCCC.S(=O)(=O)([O-])C1=C(C(=O)[O-])C=CC=C1C(=O)[O-].C(CCC)[P+](CCCC)(CCCC)CCCC.C(CCC)[P+](CCCC)(CCCC)CCCC NFZAWWHHOOFKTN-UHFFFAOYSA-K 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- 239000004970 Chain extender Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 241001584775 Tunga penetrans Species 0.000 description 1
- UOKMUTMXUMSRKM-UHFFFAOYSA-M [6-(diethylamino)-9-(2-ethoxycarbonylphenyl)xanthen-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].CCOC(=O)C1=CC=CC=C1C1=C2C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C21 UOKMUTMXUMSRKM-UHFFFAOYSA-M 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 229920000800 acrylic rubber Polymers 0.000 description 1
- 239000012790 adhesive layer Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 230000003373 anti-fouling effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000003429 antifungal agent Substances 0.000 description 1
- 229940121375 antifungal agent Drugs 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- HWYNRVXFYFQSID-UHFFFAOYSA-M benzo[a]phenoxazin-9-ylidene(dimethyl)azanium;chloride Chemical compound [Cl-].C1=CC=C2C(N=C3C=CC(C=C3O3)=[N+](C)C)=C3C=CC2=C1 HWYNRVXFYFQSID-UHFFFAOYSA-M 0.000 description 1
- HIFVAOIJYDXIJG-UHFFFAOYSA-N benzylbenzene;isocyanic acid Chemical class N=C=O.N=C=O.C=1C=CC=CC=1CC1=CC=CC=C1 HIFVAOIJYDXIJG-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000004067 bulking agent Substances 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000015271 coagulation Effects 0.000 description 1
- 238000005345 coagulation Methods 0.000 description 1
- 239000006258 conductive agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- QYQADNCHXSEGJT-UHFFFAOYSA-N cyclohexane-1,1-dicarboxylate;hydron Chemical class OC(=O)C1(C(O)=O)CCCCC1 QYQADNCHXSEGJT-UHFFFAOYSA-N 0.000 description 1
- 229960002887 deanol Drugs 0.000 description 1
- 230000001877 deodorizing effect Effects 0.000 description 1
- 125000001142 dicarboxylic acid group Chemical group 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000003063 flame retardant Substances 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
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- 239000012634 fragment Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 238000009981 jet dyeing Methods 0.000 description 1
- 239000010985 leather Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000010446 mirabilite Substances 0.000 description 1
- SHXOKQKTZJXHHR-UHFFFAOYSA-N n,n-diethyl-5-iminobenzo[a]phenoxazin-9-amine;hydrochloride Chemical compound [Cl-].C1=CC=C2C3=NC4=CC=C(N(CC)CC)C=C4OC3=CC(=[NH2+])C2=C1 SHXOKQKTZJXHHR-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920006306 polyurethane fiber Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 150000003297 rubidium Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- RSIJVJUOQBWMIM-UHFFFAOYSA-L sodium sulfate decahydrate Chemical compound O.O.O.O.O.O.O.O.O.O.[Na+].[Na+].[O-]S([O-])(=O)=O RSIJVJUOQBWMIM-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- BJQWBACJIAKDTJ-UHFFFAOYSA-N tetrabutylphosphanium Chemical group CCCC[P+](CCCC)(CCCC)CCCC BJQWBACJIAKDTJ-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- HNONEKILPDHFOL-UHFFFAOYSA-M tolonium chloride Chemical compound [Cl-].C1=C(C)C(N)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 HNONEKILPDHFOL-UHFFFAOYSA-M 0.000 description 1
- 239000002341 toxic gas Substances 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000009976 warp beam dyeing Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000002759 woven fabric Substances 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Images
Landscapes
- Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)
- Laminated Bodies (AREA)
- Coloring (AREA)
Description
本発明は、塩基性染料で染色された立毛人工皮革、及びその用途に関する。 The present invention relates to napped artificial leather dyed with a basic dye and uses thereof.
立毛面を有する立毛人工皮革は、加飾成形体の樹脂成形体の表面を加飾する部材として用いられている。立毛人工皮革を用いた加飾成形体の製造方法としては、例えば、樹脂成形体を成形するための金型のキャビティ表面に立毛人工皮革を配置し、キャビティに樹脂又は樹脂原料を注入し、キャビティ内で樹脂又は樹脂原料を硬化させることにより樹脂成形体を成形する方法により製造される。また、別の製造方法としては、予め成形された樹脂成形体の表面に、立毛人工皮革を接着剤で貼りあわせる方法も挙げられる。 A napped artificial leather having a napped surface is used as a member for decorating the surface of a resin molded object of a decorative molded object. As a method for manufacturing a decorative molded object using napped artificial leather, for example, napped artificial leather is placed on the cavity surface of a mold for molding a resin molded object, resin or resin raw material is injected into the cavity, and It is manufactured by a method of molding a resin molded article by curing a resin or resin raw material within a chamber. Another manufacturing method includes a method in which napped artificial leather is bonded to the surface of a preformed resin molded body using an adhesive.
一般的な立毛人工皮革は、不織布等の繊維構造体と高分子弾性体とを含み、染料で染色されている。立毛人工皮革に含まれる繊維構造体を形成する繊維としては、耐熱性や成形性に優れる点からポリエステル繊維が好ましく用いられている。立毛人工皮革に含まれるポリエステル繊維を染色する染料としては、発色性に優れる点から分散染料が広く用いられていた。しかし、分散染料で染色された立毛人工皮革は、加飾成形を製造する際に付与される熱により分散染料が昇華して他の物品に移る昇華移行や、接着剤に含まれる有機溶剤により立毛人工皮革に含まれる分散染料が遊離して他の物品を汚染する問題があった。 Typical napped artificial leather includes a fibrous structure such as a nonwoven fabric and an elastic polymer, and is dyed with a dye. Polyester fibers are preferably used as fibers forming the fiber structure included in napped artificial leather because of their excellent heat resistance and moldability. Disperse dyes have been widely used as dyes for dyeing the polyester fibers contained in napped artificial leather because of their excellent color development. However, raised artificial leather dyed with disperse dyes does not undergo sublimation transfer due to the heat applied during the manufacturing of decorative moldings, causing the disperse dyes to sublimate and transfer to other products, or due to the raising due to organic solvents contained in adhesives. There has been a problem that disperse dyes contained in artificial leather are liberated and contaminate other articles.
上述のような問題を解決すべく、塩基性染料に対する染着座を分子中に有するカチオン可染ポリエステル繊維からなる不織布を含む立毛人工皮革であって、塩基性染料で染色された立毛人工皮革も知られている。例えば、下記特許文献１は、明度Ｌ*値≦５０の表面を有し、カチオン可染ポリエステル繊維の不織布と不織布に付与された高分子弾性体とを含む繊維基材を含み、少なくとも１種の塩基性染料（カチオン染料）で染色された立毛人工皮革を開示する。引用文献１は、塩基性染料で染色された立毛人工皮革によれば、人工皮革に積層した樹脂層や、樹脂成形体等の他の部材と接触した状態にあっても、樹脂層や樹脂成形体が染料で汚染されにくい、濃色に着色された立毛人工皮革が得られることを開示する。 In order to solve the above-mentioned problems, raised artificial leather containing a nonwoven fabric made of cationic dyeable polyester fibers having dye sites for basic dyes in the molecule, and raised artificial leather dyed with basic dyes, is also known. It is being For example, Patent Document 1 below includes a fiber base material having a surface with a lightness L * value ≦50 and including a nonwoven fabric of cationically dyeable polyester fibers and a polymeric elastic material imparted to the nonwoven fabric, and includes at least one type of A raised artificial leather dyed with a basic dye (cationic dye) is disclosed. Cited document 1 states that, according to the raised artificial leather dyed with basic dye, even if it is in contact with the resin layer laminated on the artificial leather or other members such as the resin molding, the resin layer or the resin molding It is disclosed that a deeply colored napped artificial leather whose body is not easily contaminated with dyes can be obtained.
ところで、例えば、下記特許文献２は、ｐＨが６．０～６．９５である、塩基性染料で染色されている塩基性染料可染型繊維と、セルロース繊維とポリウレタン繊維とを混用した消臭性布帛を開示する。そして、カチオン染料を用いて染色仕上げした布帛のｐＨを６．０～６．９５の範囲内に維持しておけば、製品での保管時に変色や黄変が極めて起き難いという効果や繰り返し洗濯による変褪色が小さいという効果があることが記載されている。
By the way, for example,
上述のように、立毛人工皮革は、加飾成形体の樹脂成形体の表面を加飾する部材として用いられている。塩基性染料で染色された立毛人工皮革を樹脂成形体の表面に一体化した加飾成形体を製造した場合、熱や圧力を掛けられた部分が変色することがあった。本発明は、塩基性染料で染色された立毛人工皮革において、変色しにくい立毛人工皮革を提供することを課題とする。 As mentioned above, the raised artificial leather is used as a member for decorating the surface of a resin molded body of a decorative molded body. When producing a decorative molded article in which raised artificial leather dyed with a basic dye is integrated onto the surface of a resin molded article, the areas exposed to heat or pressure may discolor. An object of the present invention is to provide a napped artificial leather dyed with a basic dye that is resistant to discoloration.
本件出願人らは、塩基性染料で染色された立毛人工皮革の、熱や圧力を掛けられた部分が変色する事例について分析したところ、アミン系化合物と接したり、塩基性ガスに接したりした場合に、立毛人工皮革が変色しやすくなるという知見を得た。そして、このような知見に基づいて、塩基性染料で染色された立毛人工皮革が変色することを抑制する手段を鋭意検討した結果、本発明に想到するに至った。 The applicants analyzed cases where the areas of napped artificial leather dyed with basic dyes changed color when heat or pressure was applied, and found that when it came into contact with amine compounds or basic gases, In addition, we obtained the knowledge that napped artificial leather becomes more susceptible to discoloration. Based on these findings, the inventors of the present invention have intensively studied means for suppressing discoloration of napped artificial leather dyed with basic dyes, and as a result, have arrived at the present invention.
すなわち、本発明の一局面は、カチオン可染ポリエステル繊維である繊度０．９ｄｔｅｘ以下の極細繊維からなる繊維構造体と、高分子弾性体とを含み、少なくとも一面の極細繊維が立毛された立毛人工皮革であって、少なくとも１種の塩基性染料で染色されており、JIS L 1096 8.37（抽出液のｐＨ）のＡ法に規定された方法に拠って測定された、抽出液のｐＨが３．５～６．５である立毛人工皮革である。このような立毛人工皮革によれば、アミン系化合物と接したり、塩基性ガスに接したりした場合の変色を抑制することができる。抽出液のｐＨが３．５未満の場合には、酸性度が高すぎるために使用者の肌に刺激を与える懸念や、立毛人工皮革を構成するカチオン可染ポリエステルやポリウレタン等の樹脂の劣化が促進されたりしやすくなる懸念がある。また、ｐＨが６．５を超える場合には、塩基を中和して塩基性染料の構造変化を抑制する効果が小さくなる。 That is, one aspect of the present invention is a napped artificial fiber structure including a fiber structure made of ultrafine fibers having a fineness of 0.9 dtex or less, which are cationic dyeable polyester fibers, and a polymeric elastic material, and in which at least one side of the ultrafine fibers is napped. The leather is dyed with at least one basic dye, and the pH of the extract as measured by method A of JIS L 1096 8.37 (pH of extract) is 3. It is a raised artificial leather with a rating of 5 to 6.5. According to such napped artificial leather, it is possible to suppress discoloration when it comes into contact with an amine compound or a basic gas. If the pH of the extract is less than 3.5, there is a risk of irritation to the user's skin due to the high acidity, and deterioration of the resins such as cationic dyeable polyester and polyurethane that make up the napped artificial leather. There are concerns that this could easily be promoted. Moreover, when the pH exceeds 6.5, the effect of neutralizing the base and suppressing structural changes of the basic dye becomes small.
また、塩基性染料は、共役系に活性水素を有する官能基を有しない塩基性染料分子を含むことが、とくに変色しにくい点から好ましい。後述するように、塩基性染料が発色団及び助色団を含む共役系に１級または２級アミノ基や水酸基などの活性水素を含む官能基や、アゾ基あるいは複素環のヘテロ原子等に結合した水素のような活性水素を有する構造を有する場合、アミン系化合物と接したり、塩基性ガスに接したりするような、塩基性雰囲気において、該官能基から活性水素が脱離して、塩基性染料の発色に寄与していた共役系が変化する。そのために、塩基性染料が変色する。そのために、共役系に活性水素を有する官能基を含まない塩基性染料分子で染色された立毛人工皮革である場合においては、変色を抑制する効果がとくに高くなる。このような共役系に活性水素を有する官能基を含まない塩基性染料分子としては、例えば、C.I.Basic Blue 3，C．I．Basic Red 29，C．I．Basic Yellow 21が挙げられる。 Further, it is preferable that the basic dye contains a basic dye molecule that does not have a functional group having an active hydrogen in the conjugated system, especially from the viewpoint of being less likely to discolor. As described below, basic dyes are bonded to conjugated systems containing chromophores and auxochromes, to functional groups containing active hydrogen such as primary or secondary amino groups and hydroxyl groups, to azo groups or heteroatoms of heterocycles, etc. When the functional group has a structure with active hydrogen such as hydrogen, in a basic atmosphere such as in contact with an amine compound or a basic gas, the active hydrogen is detached from the functional group and becomes a basic dye. The conjugated system that contributed to the color changes. This causes the basic dye to change color. Therefore, in the case of napped artificial leather dyed with a basic dye molecule that does not contain a functional group having an active hydrogen in the conjugated system, the effect of suppressing discoloration is particularly high. Examples of basic dye molecules that do not contain a functional group having active hydrogen in the conjugated system include C.I.Basic Blue 3, C.I.Basic Blue 3, C.I. I. Basic Red 29, C. I. Basic Yellow 21 is an example.
また、立毛人工皮革は、クエン酸，リンゴ酸，乳酸，酒石酸，マロン酸からなる群から選ばれる少なくとも１種の有機酸を含有することが、抽出液のｐＨを３．５～６．５になるように調整しやすい点から好ましい。 In addition, the raised artificial leather contains at least one organic acid selected from the group consisting of citric acid, malic acid, lactic acid, tartaric acid, and malonic acid to adjust the pH of the extract to 3.5 to 6.5. This is preferable because it is easy to adjust so that
また、本発明の他の一局面は、ポリウレタン成形体の一面に、上記何れかの立毛人工皮革を一体化させてなる加飾ポリウレタン成形体である。ポリウレタン成形体は、ウレタン原料としてアミン系の鎖伸長剤を用いたり、アミン系触媒を用いたりすることが多い。また、ポリウレタン接着剤にもアミン系化合物が配合されていることが多い。そして、従来、加飾ポリウレタン成形体の製造の際に、塩基性染料で染色された立毛人工皮革はアミン系化合物と接触した場合には、立毛人工皮革は変色しやすかった。本発明に係る加飾ポリウレタン成形体は、製造の際に、アミン系化合物と接したり、塩基性ガスに接したりした場合であっても、変色しにくい。 Another aspect of the present invention is a decorated polyurethane molded body, which is formed by integrating any of the above-mentioned napped artificial leathers onto one surface of the polyurethane molded body. Polyurethane molded articles often use an amine chain extender or an amine catalyst as a urethane raw material. Furthermore, polyurethane adhesives often contain amine compounds. Conventionally, when a napped artificial leather dyed with a basic dye comes into contact with an amine compound during the production of a decorated polyurethane molded article, the napped artificial leather tends to discolor. The decorated polyurethane molded article according to the present invention is not easily discolored even when it comes into contact with an amine compound or a basic gas during production.
本発明によれば、塩基性染料で染色された立毛人工皮革において、変色しにくい立毛人工皮革が得られる。 According to the present invention, a napped artificial leather dyed with a basic dye that is resistant to discoloration can be obtained.
はじめに、本発明に係る立毛人工皮革の一実施形態を詳しく説明する。 First, one embodiment of the napped artificial leather according to the present invention will be described in detail.
本実施形態の立毛人工皮革は、カチオン可染ポリエステル繊維である繊度０．９ｄｔｅｘ以下の極細繊維からなる繊維構造体と、高分子弾性体とを含み、少なくとも一面の極細繊維が立毛されており、少なくとも１種の塩基性染料で染色されている。そして、立毛人工皮革は、JIS L 1096 8.37（抽出液のｐＨ）のＡ法に規定された方法に拠って測定された、抽出液のｐＨが３．５～６．５である。 The napped artificial leather of the present embodiment includes a fiber structure made of ultrafine fibers having a fineness of 0.9 dtex or less, which are cationic dyeable polyester fibers, and a polymeric elastic body, and the ultrafine fibers on at least one side are napped, Dyed with at least one basic dye. The raised artificial leather has an extract having a pH of 3.5 to 6.5, as measured by method A of JIS L 1096 8.37 (pH of extract).
カチオン可染ポリエステル繊維とは、ポリエステルに、塩基性染料による染色を可能にするためのスルホン酸基等のアニオン性官能基を導入することにより、塩基性染料による可染性を付与されたポリエステルの繊維である。詳しくは、例えば、下記式(I)で表される成分を１．５～３モル％含み、テレフタル酸を主成分とするジカルボン酸成分と、エチレングリコールを主成分とするグリコール成分とを含む共重合モノマーを共重合させて得られるカチオン染料可染性ポリエチレンテレフタレートが挙げられる。 Cationically dyeable polyester fibers are polyester fibers that have been made dyeable with basic dyes by introducing anionic functional groups such as sulfonic acid groups into the polyester to enable dyeing with basic dyes. It is a fiber. Specifically, for example, a compound containing 1.5 to 3 mol% of the component represented by the following formula (I), a dicarboxylic acid component whose main component is terephthalic acid, and a glycol component whose main component is ethylene glycol. Examples include cationic dye-dyeable polyethylene terephthalate obtained by copolymerizing polymer monomers.
［上記式(I)中、Ｒは水素、炭素数１～１０個のアルキル基又は２－ヒドロキシエチル基を表し、Ｘは金属イオン、４級ホスホニウムイオン又は４級アンモニウムイオンを表す。］ [In the above formula (I), R represents hydrogen, an alkyl group having 1 to 10 carbon atoms, or a 2-hydroxyethyl group, and X represents a metal ion, a quaternary phosphonium ion, or a quaternary ammonium ion. ]
式(I)で表される化合物としては、５－スルホイソフタル酸のアルカリ金属塩（リチウム塩、ナトリウム塩、カリウム塩、ルビジウム塩、セシウム塩）や、５－テトラブチルホスホニウムスルホイソフタル酸，５－エチルトリブチルホスホニウムスルホイソフタル酸などの５－テトラアルキルホスホニウムスルホイソフタル酸や、５－テトラブチルアンモニウムスルホイソフタル酸，５－エチルトリブチルアンモニウムスルホイソフタル酸などの５－テトラアルキルアンモニウムスルホイソフタル酸等が挙げられる。式(I)で表される化合物は単独で用いても、２種以上を組み合わせて用いてもよい。これらの中では、式(I)で表される化合物が、４級ホスホニウムイオン又は４級アンモニウムイオンであるＸを含む化合物を含むことが、機械的特性及び高速紡糸性に優れるカチオン染料可染性ポリエステルが得られる点から好ましい。好ましくは式(I)で表される化合物、とくにはＸが４級ホスホニウムイオン又は４級アンモニウムイオンである式(I)で表される化合物を１．５～３モル％含み、テレフタル酸を主成分とするジカルボン酸成分と、エチレングリコールを主成分とするグリコール成分とを含む共重合モノマーを共重合させることにより得られるカチオン染料可染性ポリエステルが溶融紡糸性にも優れる点から好ましい。 Examples of the compound represented by formula (I) include alkali metal salts of 5-sulfoisophthalic acid (lithium salt, sodium salt, potassium salt, rubidium salt, cesium salt), 5-tetrabutylphosphonium sulfoisophthalic acid, 5- Examples include 5-tetraalkylphosphonium sulfoisophthalic acids such as ethyltributylphosphonium sulfoisophthalic acid, and 5-tetraalkylammonium sulfoisophthalic acids such as 5-tetrabutylammonium sulfoisophthalic acid and 5-ethyltributylammonium sulfoisophthalic acid. The compounds represented by formula (I) may be used alone or in combination of two or more. Among these, the compound represented by formula (I) containing a compound containing X, which is a quaternary phosphonium ion or a quaternary ammonium ion, has excellent mechanical properties and high-speed spinnability, and is dyeable with cationic dyes. This is preferable since polyester can be obtained. It preferably contains 1.5 to 3 mol% of a compound represented by formula (I), particularly a compound represented by formula (I) in which X is a quaternary phosphonium ion or a quaternary ammonium ion, and contains terephthalic acid as the main A cationic dye-dyeable polyester obtained by copolymerizing a copolymerizable monomer containing a dicarboxylic acid component and a glycol component whose main component is ethylene glycol is preferred because it also has excellent melt spinnability.
ここで、テレフタル酸を主成分とするとは、共重合モノマーに含有されるジカルボン酸成分のうち５０モル％以上がテレフタル酸であることを意味する。ジカルボン酸成分のうちテレフタル酸の含有割合は、７５モル％以上であることが好ましい。また、塩基性染料による染色堅牢性を向上させ、高速紡糸性を向上させ、また、立毛人工皮革を成形用途に使う場合の賦形性を向上させるために、ガラス転移温度を低下させることを目的として、ジカルボン酸成分として、式(I)で表される化合物を除く、その他のジカルボン酸を含んでもよい。その他のジカルボン酸成分の具体例としては例えば、イソフタル酸等の芳香族ジカルボン酸や、１，４－シクロヘキサンジカルボン酸などのシクロへキサンジカルボン酸や、アジピン酸などの脂肪族ジカルボン酸等のその他のジカルボン酸又はその誘導体を含んでもよい。これらの中では、イソフタル酸、または、１，４－シクロヘキサンジカルボン酸とアジピン酸との組み合わせ、又はその誘導体を用いることが機械的特性と高速紡糸性に優れる点からとくに好ましい。 Here, terephthalic acid as the main component means that 50 mol% or more of the dicarboxylic acid component contained in the copolymerization monomer is terephthalic acid. The content of terephthalic acid in the dicarboxylic acid component is preferably 75 mol% or more. In addition, the aim is to improve the fastness of dyeing with basic dyes, improve high-speed spinnability, and lower the glass transition temperature in order to improve the formability when using napped artificial leather for molding purposes. As a dicarboxylic acid component, other dicarboxylic acids other than the compound represented by formula (I) may be included. Specific examples of other dicarboxylic acid components include aromatic dicarboxylic acids such as isophthalic acid, cyclohexane dicarboxylic acids such as 1,4-cyclohexane dicarboxylic acid, and other aliphatic dicarboxylic acids such as adipic acid. It may also contain a dicarboxylic acid or a derivative thereof. Among these, it is particularly preferable to use isophthalic acid, a combination of 1,4-cyclohexanedicarboxylic acid and adipic acid, or a derivative thereof from the viewpoint of excellent mechanical properties and high-speed spinnability.
その他のジカルボン酸の共重合割合は、２～１２モル％、さらには３～１０モル％であることが好ましい。その他のジカルボン酸の共重合割合が２モル％未満の場合には、ガラス転移温度が充分に低下せず、繊維内部における非晶部位の配向度が高くなるために染色性が低下する傾向がある。一方、その他のジカルボン酸の共重合割合が１２モル％を超える場合には、ガラス転移温度が低下しすぎて、繊維内部における非晶部位の配向度が低くなるために繊維強度が低下する傾向がある。なお、その他のジカルボン酸単位としてイソフタル酸単位を含有する場合には、イソフタル酸単位を１～６モル％、さらには２～５モル％含有することが機械的特性と高速紡糸性に優れる点から好ましい。また、１，４－シクロヘキサンジカルボン酸単位とアジピン酸単位とを含有する場合には、１，４－シクロヘキサンジカルボン酸単位及びアジピン酸単位をそれぞれ１～６モル％、さらには２～５モル％含有することが機械的特性と高速紡糸性に優れるカチオン可染ポリエステルが得られる点から好ましい。 The copolymerization ratio of other dicarboxylic acids is preferably 2 to 12 mol%, more preferably 3 to 10 mol%. If the copolymerization ratio of other dicarboxylic acids is less than 2 mol%, the glass transition temperature will not be lowered sufficiently and the degree of orientation of amorphous sites within the fiber will increase, resulting in a tendency for dyeability to decrease. . On the other hand, if the copolymerization ratio of other dicarboxylic acids exceeds 12 mol%, the glass transition temperature will drop too much and the degree of orientation of amorphous sites inside the fiber will decrease, resulting in a tendency for fiber strength to decrease. be. In addition, when containing isophthalic acid units as other dicarboxylic acid units, it is preferable to contain 1 to 6 mol%, and even 2 to 5 mol%, of isophthalic acid units from the viewpoint of excellent mechanical properties and high-speed spinnability. preferable. In addition, when containing 1,4-cyclohexanedicarboxylic acid units and adipic acid units, it contains 1 to 6 mol%, more preferably 2 to 5 mol%, of 1,4-cyclohexanedicarboxylic acid units and adipic acid units, respectively. It is preferable to do so because a cationically dyeable polyester having excellent mechanical properties and high-speed spinnability can be obtained.
また、エチレングリコールを主成分とするとは、共重合モノマーに含有されるグリコール成分のうち５０モル％以上がエチレングリコールであることを意味する。グリコール成分のうちエチレングリコールの含有割合は、７５モル％以上、さらには９０モル％以上であることが好ましい。また、その他の成分としては、例えば、ジエチレングリコールやポリエチレングリコール等が挙げられる。 Moreover, ethylene glycol as a main component means that 50 mol% or more of the glycol components contained in the copolymerized monomer is ethylene glycol. The content of ethylene glycol among the glycol components is preferably 75 mol% or more, more preferably 90 mol% or more. Moreover, examples of other components include diethylene glycol and polyethylene glycol.
また、カチオン可染ポリエステルには、本発明の効果を損なわない範囲で、カーボンブラック等の着色剤、耐候剤、防黴剤等を必要に応じて、配合してもよい。 Further, the cationic dyeable polyester may be blended with a coloring agent such as carbon black, a weathering agent, a fungicide, etc., as necessary, within a range that does not impair the effects of the present invention.
本実施形態におけるカチオン可染ポリエステル繊維の繊度は、０．９ｄｔｅｘ以下であり、０．０９～０．９ｄｔｅｘ、さらには０．１～０．５ｄｔｅｘであることが、変色を抑制する効果が顕著になる点から好ましい。０．９ｄｔｅｘ以下である極細繊維は、繊度の高い繊維に比べて表面積が大きいために、アミン系化合物や塩基性ガス等の変色を引き起こす化合物に接して変色が起こりやすくなるために、変色を抑制する効果が顕著になる。また、０．９ｄｔｅｘを超える場合には、外観や表面のタッチや外観の品位が低くなる。なお、繊度は、立毛人工皮革の断面の走査型電子顕微鏡（ＳＥＭ）写真を３０００倍で撮影し、繊維の断面をランダムに１０個選んで断面積を測定し、その断面積の平均値を算出し、カチオン可染ポリエステル繊維の密度から換算して算出される。 The fineness of the cationic dyeable polyester fiber in this embodiment is 0.9 dtex or less, 0.09 to 0.9 dtex, and more preferably 0.1 to 0.5 dtex, so that the effect of suppressing discoloration is remarkable. It is preferable from this point of view. Ultra-fine fibers with a diameter of 0.9 dtex or less have a larger surface area than fibers with higher fineness, so discoloration is more likely to occur when they come into contact with compounds that cause discoloration, such as amine compounds and basic gases, so discoloration can be suppressed. The effect of Moreover, if it exceeds 0.9 dtex, the quality of appearance, surface touch, and appearance will be degraded. The fineness is determined by taking a scanning electron microscope (SEM) photograph of the cross section of the napped artificial leather at 3000x magnification, randomly selecting 10 fiber cross sections, measuring the cross-sectional area, and calculating the average value of the cross-sectional area. It is calculated based on the density of cationic dyeable polyester fiber.
繊維構造体としては、不織布，織物，編物等が特に限定なく用いられる。これらの中では、極細繊維を絡合させた不織布が好ましい。 As the fiber structure, non-woven fabrics, woven fabrics, knitted fabrics, etc. can be used without particular limitation. Among these, a nonwoven fabric in which ultrafine fibers are entangled is preferred.
本実施形態の立毛人工皮革には、繊維構造体にポリウレタン等の高分子弾性体が含浸付与されている。高分子弾性体の具体例としては、例えば、ポリウレタン，アクリロニトリルエラストマー，オレフィンエラストマー，ポリエステルエラストマー，ポリアミドエラストマー，アクリルエラストマー等が挙げられる。これらの中では、ポリウレタンが好ましい。 In the napped artificial leather of this embodiment, the fiber structure is impregnated with a polymer elastic material such as polyurethane. Specific examples of the polymeric elastomer include polyurethane, acrylonitrile elastomer, olefin elastomer, polyester elastomer, polyamide elastomer, and acrylic elastomer. Among these, polyurethane is preferred.
なお、高分子弾性体は、本発明の効果を損なわない範囲で、カーボンブラック等の顔料や染料などの着色剤、凝固調節剤、酸化防止剤、紫外線吸収剤、蛍光剤、防黴剤、浸透剤、消泡剤、滑剤、撥水剤、撥油剤、増粘剤、増量剤、硬化促進剤、発泡剤、ポリビニルアルコールやカルボキシメチルセルロースなどの水溶性高分子化合物、無機微粒子、導電剤などをさらに含有してもよい。 The polymeric elastomer may contain pigments such as carbon black, coloring agents such as dyes, coagulation regulators, antioxidants, ultraviolet absorbers, fluorescent agents, antifungal agents, and penetrating agents, to the extent that the effects of the present invention are not impaired. We further add additives, antifoaming agents, lubricants, water repellents, oil repellents, thickeners, bulking agents, curing accelerators, foaming agents, water-soluble polymer compounds such as polyvinyl alcohol and carboxymethyl cellulose, inorganic fine particles, conductive agents, etc. May be contained.
高分子弾性体の含有割合としては、カチオン可染ポリエステル繊維との合計量に対して、０．１～５０質量％、さらには３～４０質量％、とくには５～２５質量％、ことには１０～１５質量％であることが、充実感としなやかさ等のバランスに優れた立毛人工皮革が得られる点から好ましい。 The content of the polymeric elastomer is 0.1 to 50% by mass, more preferably 3 to 40% by mass, particularly 5 to 25% by mass, especially 5 to 25% by mass, based on the total amount of cationic dyeable polyester fiber A content of 10 to 15% by mass is preferable from the standpoint of obtaining napped artificial leather with an excellent balance of fullness and suppleness.
そして、カチオン可染ポリエステル繊維の繊維構造体に高分子弾性体を含浸付与してなる繊維基材の少なくとも一面を、好ましくは１２０～６００番手、さらに好ましくは３２０～６００番手程度のサンドペーパーやエメリーペーパーを用いてバフィングして起毛処理を施すことにより、一面の極細繊維が立毛されたスエード調やヌバック調の立毛面が形成された繊維基材が得られる。 Then, at least one side of a fiber base material made by impregnating a fiber structure of cationic dyeable polyester fibers with a polymeric elastic material is coated with sandpaper or emery paper of preferably about 120 to 600 grit, more preferably about 320 to 600 grit. By performing the raising treatment by buffing with paper, a fiber base material having a suede-like or nubuck-like raised surface in which ultrafine fibers are raised on one side can be obtained.
そして、立毛面が形成された繊維基材を塩基性染料で染色することにより、塩基性染料で染色された立毛人工皮革が得られる。塩基性染料としては、従来から知られている塩基性染料であればとくに限定なく用いられる。なお、塩基性染料は染料液中で溶解してカチオン性を示し、例えば４級アンモニウム基等を有する染料イオンとなってカチオン可染ポリエステル繊維のスルホン酸基等のアニオン性官能基にイオン結合する。このような塩基性染料は一般的には、塩素イオン等のアニオンと塩を形成している。 Then, by dyeing the fiber base material on which the napped surface is formed with a basic dye, a napped artificial leather dyed with the basic dye is obtained. As the basic dye, any conventionally known basic dye can be used without particular limitation. Note that the basic dye exhibits cationic properties when dissolved in the dye solution, and becomes a dye ion having, for example, a quaternary ammonium group, which ionically bonds to an anionic functional group such as a sulfonic acid group of the cationically dyeable polyester fiber. . Such basic dyes generally form salts with anions such as chloride ions.
塩基性染料の具体例としては、C.I.Basic Blue 3，C.I. Basic Blue 6，C.I. Basic Blue 10，C.I. Basic Blue 12，C.I.Basic Blue75，C.I. Basic Blue 96等のオキサジン系青色塩基性染料；C.I.Basic Blue 54やC.I.Basic Blue 159等のアゾ系青色塩基性染料；C．I．Basic Yellow 21やC．I．Basic Yellow 12等のメチン系染料； C．I．Basic Blue 17等のフェノチアジン系塩基性染料；C．I．Basic Yellow 40等のクマリン系染料、C．I．Basic Yellow 28等のアゾメチン系染料； C．I．Basic Red 29やC．I．Basic Red 46等のアゾ系赤色染料； C．I．Basic Violet 11 等のキサンテン系染料が挙げられる。これらは単独で用いても、２種以上を組み合わせて用いてもよい。
Specific examples of basic dyes include oxazine blue basic dyes such as C.I.Basic Blue 3, C.I. Basic Blue 6, C.I.
これらの中では、とくに、共役系に活性水素を有する官能基を有しない塩基性染料分子を含むことが、とくに変色しにくい点から好ましい。ここで、「共役系に活性水素を有する官能基を有しないカチオン染料」とは、カチオン染料のうち、発色団及び助色団を含む共役系に活性水素を有する構造を有さないカチオン染料を意味する。共役系に１級または２級アミノ基や水酸基などの活性水素を含む官能基や、アゾ基あるいは複素環のヘテロ原子等に結合した水素のような活性水素を含む構造を有する塩基性染料の場合、アミン系化合物と接したり、塩基性ガスに接したりするような塩基性雰囲気において、共役系から活性水素が脱離して、塩基性染料の発色に寄与していた共役系が変化する。そのために、塩基性染料が変色する。そのために、共役系に活性水素を有する官能基を有しない塩基性染料分子で染色された立毛人工皮革である場合においては、変色を抑制する効果がとくに高くなる。このような共役系に活性水素を有する官能基を有しない塩基性染料分子としては、例えば、C.I.Basic Blue 3，C．I．Basic Red 29，C．I．Basic Yellow 21などが挙げられる。 Among these, it is particularly preferable that the conjugated system contains a basic dye molecule that does not have a functional group having active hydrogen, since it is particularly resistant to discoloration. Here, "a cationic dye that does not have a functional group that has an active hydrogen in its conjugated system" refers to a cationic dye that does not have a structure that has an active hydrogen in its conjugated system that includes a chromophore and an auxochrome. means. In the case of basic dyes that have a conjugated system containing active hydrogen-containing functional groups such as primary or secondary amino groups or hydroxyl groups, or active hydrogen-containing structures such as hydrogen bonded to azo groups or heteroatoms of heterocycles. In a basic atmosphere such as contact with an amine compound or basic gas, active hydrogen is removed from the conjugated system, and the conjugated system that contributed to the color development of the basic dye changes. This causes the basic dye to change color. Therefore, in the case of napped artificial leather dyed with a basic dye molecule that does not have a functional group having active hydrogen in the conjugated system, the effect of suppressing discoloration is particularly high. Examples of basic dye molecules having no functional group having active hydrogen in the conjugated system include C.I.Basic Blue 3, C.I.Basic Blue 3, C.I. I. Basic Red 29, C. I. Examples include Basic Yellow 21.
染色方法は特に限定されないが、例えば、液流染色機、ビーム染色機、ジッガーなどの染色機を用いて染色する方法が挙げられる。染色加工の条件としては、染色温度としては１００～１３５℃、さらには９０～１２０℃で染色することが環境負荷も低く、染色コストを低減できる点から好ましい。また、染色の際に、酢酸や芒硝のような染色助剤を用いてもよい。 Although the dyeing method is not particularly limited, examples thereof include a method of dyeing using a dyeing machine such as a jet dyeing machine, a beam dyeing machine, or a jigger. As for the conditions for the dyeing process, it is preferable to dye at a dyeing temperature of 100 to 135°C, more preferably 90 to 120°C, since this has a low environmental impact and can reduce dyeing costs. Further, during dyeing, a dyeing aid such as acetic acid or Glauber's salt may be used.
染料液中の塩基性染料の濃度は目的とする色に応じて適宜調整されるが、例えば、立毛人工皮革の基材に対し、０．５～２０％ｏｗｆ、さらには、１．０～１５％ｏｗｆ、となるような範囲が挙げられる。 The concentration of the basic dye in the dye solution is adjusted appropriately depending on the desired color, but for example, the concentration of the basic dye in the dye solution is 0.5 to 20% owf, more preferably 1.0 to 15% owf, based on the base material of napped artificial leather. %owf.
本実施形態においては、塩基性染料により染色された立毛人工皮革を、アニオン系界面活性剤を含有する湯浴中で洗浄処理することにより、結合力の低い塩基性染料を除去することが好ましい。このような洗浄処理により、高分子弾性体に吸収された塩基性染料が充分に除去されて、染色された立毛人工皮革から塩基性染料が他の部材に移行しにくくなる。アニオン系界面活性剤の具体例としては、例えば、日成化成（株）製のソルジンＲ，センカ（株）製のセンカノールＡ－９００，明成化学工業（株）製のメイサノールＫＨＭ等が挙げられる。 In this embodiment, it is preferable to remove the basic dye with low binding strength by washing the napped artificial leather dyed with the basic dye in a hot water bath containing an anionic surfactant. Such washing treatment sufficiently removes the basic dye absorbed by the polymeric elastomer, making it difficult for the basic dye to migrate from the dyed napped artificial leather to other members. Specific examples of anionic surfactants include Soljin R manufactured by Nissei Kasei Co., Ltd., Senkanol A-900 manufactured by Senka Co., Ltd., and Maysanol KHM manufactured by Meisei Chemical Industry Co., Ltd., and the like.
アニオン系界面活性剤を含有する湯浴中での洗浄処理は、５０～１００℃、さらには６０～８０℃の湯浴で行うことが好ましい。また、湯浴の槽としては、染色処理を行った染色機を用いることが、製造工程が簡略化できる点から好ましい。 The washing treatment in a water bath containing an anionic surfactant is preferably carried out at a temperature of 50 to 100°C, more preferably 60 to 80°C. Furthermore, it is preferable to use a dyeing machine that has undergone a dyeing process as the hot water bath because the manufacturing process can be simplified.
洗浄時間としては、得られる染色された立毛人工皮革のＪＩＳ法（ＪＩＳ Ｌ ０８４６）による水堅牢度の綿汚染の判定が４－５級以上になるような時間であることが好ましく、具体的には、１０～３０分間、さらには、１５～２０分間程度であることが好ましい。また、この洗浄を１回以上、好ましくは２回以上繰り返してもよい。このように染色及び洗浄処理された立毛人工皮革は乾燥される。 The washing time is preferably such that the resulting dyed napped artificial leather has a water fastness rating of 4-5 or higher for cotton staining according to the JIS method (JIS L 0846). is preferably about 10 to 30 minutes, more preferably about 15 to 20 minutes. Further, this washing may be repeated one or more times, preferably two or more times. The raised artificial leather dyed and washed in this way is dried.
立毛人工皮革には、必要に応じて、各種仕上げ処理が施される。仕上げ処理としては、柔軟化処理、毛ブラシによるブラッシング処理、防汚処理、撥水化処理、滑剤処理、柔軟剤処理、酸化防止剤処理、紫外線吸収剤処理、蛍光剤処理、難燃剤処理等が挙げられる。 The napped artificial leather is subjected to various finishing treatments as necessary. Finishing treatments include softening treatment, brushing with a bristle brush, antifouling treatment, water repellent treatment, lubricant treatment, softener treatment, antioxidant treatment, ultraviolet absorber treatment, fluorescent agent treatment, flame retardant treatment, etc. Can be mentioned.
そして、本実施形態の立毛人工皮革は、JIS L 1096 8.37（抽出液のｐＨ）のＡ法に規定された方法に拠って測定された、抽出液のｐＨが３．５～６．５になるように調整されている。立毛人工皮革は、高分子弾性体に含まれる添加剤や、仕上げ処理に用いられる各種薬剤、アニオン系界面活性剤による洗浄により、塩基性を帯びやすい。本実施形態の立毛人工皮革においては、立毛人工皮革の抽出液のｐＨが３．５～６．５になるように調整されている。このような立毛人工皮革によれば、アミン系化合物と接したり、塩基性ガスに接したりした場合の変色を顕著に抑制することができる。 The raised artificial leather of this embodiment has a pH of 3.5 to 6.5 as measured by method A of JIS L 1096 8.37 (pH of extract). It has been adjusted as follows. Napped artificial leather tends to become basic when washed with additives contained in the polymeric elastomer, various chemicals used in finishing treatments, and anionic surfactants. In the napped artificial leather of this embodiment, the pH of the napped artificial leather extract is adjusted to 3.5 to 6.5. According to such napped artificial leather, discoloration when coming into contact with an amine compound or a basic gas can be significantly suppressed.
抽出液のｐＨを３．５～６．５になるように立毛人工皮革を調整する方法は特に限定されないが、例えば、クエン酸，リンゴ酸，乳酸，酒石酸，マロン酸のような有機酸の水溶液に、ｐＨ未調整の塩基性染料で染色された立毛人工皮革を浸漬し、乾燥することにより、立毛人工皮革を酸性～弱酸性に処理する方法が挙げられる。 There are no particular limitations on the method for adjusting the nape artificial leather so that the pH of the extract is 3.5 to 6.5, but examples include aqueous solutions of organic acids such as citric acid, malic acid, lactic acid, tartaric acid, and malonic acid. Another method includes a method in which the napped artificial leather is treated to be acidic to weakly acidic by soaking the napped artificial leather dyed with a pH-unadjusted basic dye and drying it.
塩基性染料で染色されたｐＨ未調整の立毛人工皮革のｐＨは、６．５を超える。このようなｐＨ６．５を超えるｐＨ未調整の立毛人工皮革を抽出液のｐＨを３．５～６．５になるように立毛人工皮革を調整することにより、立毛人工皮革中の酸性成分が塩基を中和し、アミン系化合物と接したり、塩基性ガスに接したりした場合の塩基と塩基性染料との反応を防ぎ、変色を顕著に抑制することができる。 The pH of non-pH-adjusted raised artificial leather dyed with a basic dye exceeds 6.5. By adjusting the pH of the extract of unadjusted napped artificial leather with a pH exceeding 6.5 to 3.5 to 6.5, the acidic components in the napped artificial leather are converted into bases. It is possible to neutralize the dye, prevent the reaction between the base and the basic dye when it comes into contact with an amine compound or a basic gas, and significantly suppress discoloration.
有機酸の水溶液に浸漬して乾燥することによって、塩基性染料で染色された立毛人工皮革のｐＨを調整する場合、ｐＨ調整後の立毛人工皮革に含まれる有機酸の含有割合は、例えば、２００～８０００ｐｐｍ、さらには、５００～５０００ｐｐｍ、であることが好ましい。 When adjusting the pH of napped artificial leather dyed with a basic dye by immersing it in an aqueous solution of an organic acid and drying it, the content ratio of the organic acid contained in the napped artificial leather after pH adjustment is, for example, 200. ~8000 ppm, more preferably 500 ~ 5000 ppm.
このようにして調整された立毛人工皮革の抽出液のｐＨは、３．５～６．５であり、好ましくは、４．０～６．０である。抽出液のｐＨが３．５未満の場合には、酸性度が高すぎて使用者の肌へ刺激を与えたり、立毛人工皮革を構成するカチオン可染ポリエステルやポリウレタン等の樹脂の劣化が促進されやすくなったりする。また、ｐＨが６．５を超える場合には、塩基を中和することにより塩基性染料の構造変化を抑制する効果が小さくなる。 The pH of the thus-adjusted napped artificial leather extract is 3.5 to 6.5, preferably 4.0 to 6.0. If the pH of the extract is less than 3.5, the acidity is too high and may irritate the user's skin, or accelerate the deterioration of the cationically dyeable polyester, polyurethane, and other resins that make up the napped artificial leather. It might become easier. Moreover, when the pH exceeds 6.5, the effect of suppressing structural changes of the basic dye by neutralizing the base becomes small.
上述したような本実施形態の塩基性染料で染色された立毛人工皮革は、従来知られた立毛人工皮革の各用途に好ましく用いられるが、これらの中でも、とくには、加飾成形体の表皮材として用いられる用途、具体的には、成形体の一面に、本実施形態の立毛人工皮革を直接一体化させてなる加飾成形体の用途に特に好ましく用いられる。また、このような用途において、とくには、ポリウレタン成形体の一面に立毛人工皮革を直接一体化させてなる加飾成形体の製造においては、製造時に立毛人工皮革がアミン系化合物と接したり、塩基性ガスに接したりしやすく、その場合には、塩基性染料で染色された立毛人工皮革が変色しやすかった。本実施形態の塩基性染料で染色された立毛人工皮革を用いることにより、このような変色を低減することができる。 The raised artificial leather dyed with the basic dye of the present embodiment as described above is preferably used for various purposes of conventionally known raised artificial leather, but among these, it is particularly suitable for use as a skin material for decorative molded articles. Specifically, it is particularly preferably used in applications where the napped artificial leather of the present embodiment is directly integrated into one surface of the molded product. In addition, in such applications, especially in the production of decorated molded products in which napped artificial leather is directly integrated onto one surface of a polyurethane molded product, the napped artificial leather may come into contact with amine compounds or be exposed to bases during manufacturing. It is easy to come into contact with toxic gases, and in that case, the napped artificial leather dyed with basic dyes is prone to discoloration. By using the napped artificial leather dyed with the basic dye of this embodiment, such discoloration can be reduced.
図１は、本実施形態の立毛人工皮革１を含む加飾成形体１０の模式断面図である。加飾成形体１０は、成形体２の一面に本実施形態の立毛人工皮革１が直接一体化されている。なお、直接一体化とは、射出成形を用いたインモールド成形において、射出成形機に搭載された金型のキャビティ表面に立毛人工皮革の断片を配し、金型を密閉して、密閉された金型内に流動状態の樹脂又は樹脂原料を注入し、金型内で、成形体を硬化させることにより、成形体の一面を覆うように立毛人工皮革が配された加飾成形体であることを意味し、成形体の表面に接着剤による接着層を介して立毛人工皮革を接着する形態と区別される。
FIG. 1 is a schematic cross-sectional view of a decorative molded
また、本実施形態の立毛人工皮革を用いた加飾成形体としては、とくには、リム（Reaction Injection Molding）成形を用いて製造された、ポリウレタン成形体の一面に立毛人工皮革を直接一体化させてなる加飾ポリウレタン成形体がとくに好ましい。 In addition, as a decorative molded body using the napped artificial leather of this embodiment, in particular, the napped artificial leather is directly integrated on one surface of a polyurethane molded body manufactured using rim (reaction injection molding) molding. Particularly preferred are decorated polyurethane molded products.
リム成形は、反応射出成形とも称され、密閉された金型内にポリウレタン原料を射出し、金型内に注入されたポリウレタン原料を急速に反応させて硬化させることにより、ポリウレタン成形体を成形する方法である。詳しくは、射出成形機に搭載された、リム成形用金型のキャビティ形成面に立毛人工皮革を配置して型締めする工程と、型締めされて形成されたキャビティにポリウレタン原料を注入して加熱することにより、ポリウレタン原料を反応させて硬化させることにより、ポリウレタン成形体の一面に立毛人工皮革を直接一体化させる工程と、を含む加飾ポリウレタン成形体の製造方法である。 Rim molding, also known as reaction injection molding, involves injecting a polyurethane raw material into a sealed mold and rapidly reacting and hardening the polyurethane raw material injected into the mold to form a polyurethane molded body. It's a method. The details include the process of placing the raised artificial leather on the cavity forming surface of the rim molding die mounted on the injection molding machine and clamping the mold, and the process of injecting polyurethane raw material into the cavity formed by clamping the mold and heating it. This is a method for producing a decorated polyurethane molded body, which includes a step of directly integrating napped artificial leather on one surface of the polyurethane molded body by reacting and curing the polyurethane raw materials.
リム成形を用いた加飾ポリウレタン成形体の製造においては、キャビティ形成面に配された立毛人工皮革にポリウレタン原料に含有されたアミン系の化合物や原料に由来する塩基性ガスに接触することが多い。そのために、従来、塩基性染料で染色された立毛人工皮革をリム成形を用いた加飾成形に用いた場合には、変色しやすかった。上述したような塩基性染料で染色された立毛人工皮革を用いることにより、リム成形を用いてポリウレタン成形体の一面に立毛人工皮革を直接一体化させた加飾成形体を製造する場合においても、変色が抑制される。このような加飾ポリウレタン成形体は、例えば、ポリウレタン成形体をソール部とする靴の主要部の製造に好ましく用いられる。 In the production of decorated polyurethane molded bodies using rim molding, the raised artificial leather placed on the cavity forming surface often comes into contact with amine compounds contained in polyurethane raw materials and basic gases derived from raw materials. . For this reason, conventionally, when napped artificial leather dyed with basic dyes was used for decorative molding using rim molding, it was prone to discoloration. By using the raised artificial leather dyed with the above-mentioned basic dye, even when manufacturing a decorative molded object in which the raised artificial leather is directly integrated on one surface of the polyurethane molded object using rim molding, Discoloration is suppressed. Such a decorated polyurethane molded body is preferably used, for example, in manufacturing the main part of a shoe whose sole portion is made of a polyurethane molded body.
以下、本発明を実施例によりさらに具体的に説明する。なお、本発明の範囲は実施例により何ら限定されるものではない。 Hereinafter, the present invention will be explained in more detail with reference to Examples. Note that the scope of the present invention is not limited in any way by the examples.
はじめに、本実施例で用いた評価方法をまとめて説明する。 First, the evaluation method used in this example will be summarized and explained.
（立毛人工皮革の抽出液のｐＨ）
JIS L 1096(２０１０) 8.37（抽出液のｐＨ）のＡ法に規定された方法に従って、立毛人工皮革の抽出液のｐＨを測定した。具体的には、立毛人工皮革から５．０ｇ±０．１ｇの試験片を採取し、約１０ｍｍ×１０ｍｍの断片にした。一方、ガラス栓付きの２００ｍＬフラスコに５０ｍＬの蒸留水を入れ、２分間静かに煮沸した後、フラスコを熱源から遠ざけ、上記の断片試料をフラスコに入れ、フラスコに栓をして３０分間放置した。この間ときどき栓を緩めてフラスコを振とうした。そして、３０分後抽出液を２５℃±２℃に調節し、JIS Z8805に規定する ｐＨ測定器で抽出液のｐＨを測定した。試験は、２個の試験片について行い、その平均値を算出し、小数点以下１けたに丸めた。
(pH of extract of napped artificial leather)
The pH of the extract of napped artificial leather was measured according to the method specified in Method A of JIS L 1096 (2010) 8.37 (pH of extract). Specifically, a 5.0 g ± 0.1 g test piece was taken from the napped artificial leather and cut into pieces of about 10 mm x 10 mm. On the other hand, 50 mL of distilled water was placed in a 200 mL flask with a glass stopper, and after gently boiling for 2 minutes, the flask was moved away from the heat source, the above fragment sample was placed in the flask, and the flask was stoppered and left for 30 minutes. During this time, the stopper was occasionally loosened and the flask was shaken. After 30 minutes, the temperature of the extract was adjusted to 25°C±2°C, and the pH of the extract was measured using a pH meter specified in JIS Z8805. The test was conducted on two test pieces, and the average value was calculated and rounded to one decimal place.
（加飾成形による変色性評価）
加飾成形前の立毛人工皮革と加飾成形後の立毛人工皮革との色差ΔＥcmcを求めた。具体的には、分光光度計（（株）日立ハイテクノロジーズ製：Ｕ－３０１０）を用いて、加飾成形をする前後の立毛人工皮革の立毛面のΔＥcmcを測定した。なお、値は、試験片から平均的な位置を万遍なく選択して測定された３点の平均値である。
(Evaluation of discoloration by decorative molding)
The color difference ΔE cmc between the napped artificial leather before decorative molding and the napped artificial leather after decorative molding was determined. Specifically, using a spectrophotometer (manufactured by Hitachi High-Technologies Corporation: U-3010), ΔE cmc of the napped surface of the napped artificial leather before and after decorative molding was measured. Note that the value is the average value of three points measured by uniformly selecting average positions from the test piece.
（外観）
立毛人工皮革を縦３０ｃｍ×横２０ｃｍに切りだしたサンプルを調製した。そして、当業者３名により以下の基準で外観を判定した。
Ａ：立毛面が均一できめ細かいスエード調の立毛感を有する
Ｂ：立毛面が粗く、スエード調の外観に乏しい
(exterior)
A sample was prepared by cutting the raised artificial leather into a size of 30 cm in length and 20 cm in width. The appearance was evaluated by three persons skilled in the art based on the following criteria.
A: The raised surface is uniform and has a fine suede-like appearance. B: The raised surface is rough and the suede-like appearance is poor.
［実施例１］
海成分の熱可塑性樹脂としてエチレン変性ポリビニルアルコール（ＰＶＡ）、島成分の熱可塑性樹脂としてスルホイソフタル酸のテトラブチルホスホニウム塩で変性されたポリエチレンテレフタレート（ＣＤ‐ＰＥＴ）を含み、海成分と島成分との質量比が海成分／島成分＝２５／７５である、海島型複合繊維を三次元絡合させた不織布を製造した。なお、ＣＤ‐ＰＥＴは、スルホイソフタル酸のテトラブチルホスホニウム塩単位１．７モル％，１，４－シクロヘキサンジカルボン酸単位５モル％，アジピン酸単位５モル％含有する、ガラス転移温度６２℃の変性ＰＥＴであった。
[Example 1]
Contains ethylene-modified polyvinyl alcohol (PVA) as the thermoplastic resin for the sea component, and polyethylene terephthalate (CD-PET) modified with tetrabutylphosphonium salt of sulfoisophthalic acid as the thermoplastic resin for the island component. A nonwoven fabric was produced in which sea-island composite fibers were three-dimensionally entangled in a mass ratio of sea component/island component = 25/75. CD-PET is a modified film with a glass transition temperature of 62°C, containing 1.7 mol% of sulfoisophthalic acid tetrabutylphosphonium salt units, 5 mol% of 1,4-cyclohexanedicarboxylic acid units, and 5 mol% of adipic acid units. It was PET.
そして、海島型複合繊維を三次元絡合させた不織布に、ポリウレタンのエマルジョンを含浸させ、１５０℃の乾燥炉で乾燥することによりポリウレタンを付与した。なお、ポリウレタンのエマルジョンは、ポリカーボネート／エーテル系ポリウレタンを主体とするポリウレタンの固形分濃度３０％のエマルジョンであった。そして、ポリウレタンを付与された海島型複合繊維を三次元絡合させた不織布を９５℃の熱水中に２０分間浸漬することにより海島型複合繊維に含まれる海成分を抽出除去し、１２０℃の乾燥炉で乾燥した。このようにして、ポリウレタンを含浸付与された、繊度０．２ｄｔｅｘのＣＤ‐ＰＥＴの繊維の不織布を含む繊維基材の原反を得た。得られた繊維基材の原反は、ＣＤ‐ＰＥＴの繊維／ポリウレタンの質量比が８８／１２であった。そして、得られた繊維基材の原反をスライスして２分割し、スライス面を６００番手のサンドペーパーでバフィングして立毛面を形成した。このようにして、立毛面が形成された厚さ１ｍｍの立毛繊維基材を得た。 Then, a nonwoven fabric in which sea-island composite fibers were three-dimensionally entangled was impregnated with a polyurethane emulsion and dried in a drying oven at 150°C to impart polyurethane. The polyurethane emulsion was a polyurethane emulsion containing polycarbonate/ether polyurethane as its main component and having a solid content concentration of 30%. Then, the sea component contained in the sea-island composite fibers is extracted and removed by immersing the nonwoven fabric in which the sea-island composite fibers coated with polyurethane are three-dimensionally entangled in hot water at 95°C for 20 minutes. Dry in a drying oven. In this way, an original fabric of a fiber base material containing a nonwoven fabric of CD-PET fibers with a fineness of 0.2 dtex and impregnated with polyurethane was obtained. The resulting fiber base material had a CD-PET fiber/polyurethane mass ratio of 88/12. Then, the obtained raw fiber base material was sliced into two parts, and the sliced surface was buffed with 600-grit sandpaper to form a raised surface. In this way, a napped fiber base material with a thickness of 1 mm on which a napped surface was formed was obtained.
そして、塩基性染料として、オキサジン系青色塩基性染料であるC.I.Basic Blue 3を含むNichilon Blue 7G （日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、濃青色に染色した。なお、C.I.Basic Blue 3は、共役系に活性水素を有する官能基を含まない塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。そして、ソーピング後、乾燥することにより、染色されたスエード調の立毛面を有する立毛人工皮革を得た。 As a basic dye, Nichilon Blue 7G (manufactured by Nissei Kasei Co., Ltd.) containing 2% owf containing C.I.Basic Blue 3, an oxazine blue basic dye, and 1 g/L of 90% acetic acid as a dyeing aid. The napped fiber base material was immersed in a dyeing bath containing a dye solution at 120° C. at a bath ratio of 1:30 for 30 minutes to dye it deep blue. C.I.Basic Blue 3 is a basic dye molecule that does not contain a functional group having active hydrogen in its conjugated system. Then, in the same dyeing bath, the process of soaping at 70° C. using a hot water bath containing 2 g/L of Sorgin R as an anionic surfactant was repeated twice. Then, after soaping and drying, a raised artificial leather having a dyed suede-like raised surface was obtained.
ソーピング後に染色浴に常温水を張りクエン酸を見掛け０．２％濃度で投入し染色生地を２０分間程度走行させた後、生地を取り出し拡布し乾燥することにより酸性化された立毛人工皮革を得た。 After soaping, fill the dye bath with room temperature water, add citric acid at an apparent concentration of 0.2%, run the dyed fabric for about 20 minutes, then take out the fabric, spread it out and dry it to obtain acidified napped artificial leather. Ta.
このようにして、繊度０．２ｄｔｅｘのカチオン可染ポリエステル繊維の絡合不織布を含む、塩基性染料で染色された濃青色の立毛人工皮革を得た。 In this way, a deep blue raised artificial leather dyed with a basic dye was obtained, which included an entangled nonwoven fabric of cationic dyeable polyester fibers with a fineness of 0.2 dtex.
そして、得られた立毛人工皮革を用いて、次のようにして、加飾ポリウレタン成形体を製造した。ポリオキシエチレン系ポリエーテルポリオール（水酸基価２８ｍｇＫＯＨ/ｇ、１３００ｍＰａ・s）に、アミン系触媒（ジメチルアミノエタノール） ０．５質量％、整泡剤（Evonik社Tegostab B8736LF2）１．０質量％、発泡剤（モノエタノールアミン炭酸塩）５．０質量％を配合した高分子ポリオール組成物を準備した。また、ポリオール変性ジフェニルメタンジイソシアネート（ＮＣＯ率２６．７%、１４０ｍＰ・ｓ（25℃））を有機イソシアネートとして準備した。そして、ＲＩＭ成形機である高圧発泡機に搭載された１４０℃に加熱された金型のキャビティ内に、立毛人工皮革をその立毛面がキャビティ表面に対向するように配置した。そして、高分子ポリオール組成物と有機イソシアネートとをそれぞれ、５０℃に加熱した状態でＮＣＯ Ｉｎｄｅｘが１．０５になる比率で、金型のキャビティ内に射出した。そして、１４０℃で５分間保持することにより、発泡及び硬化させたポリウレタン成形体を成形した。そして、冷却し、金型を開くことにより、ポリウレタン成形体の一面に、立毛人工皮革を直接一体化させてなる加飾ポリウレタン成形体を製造した。 Using the obtained raised artificial leather, a decorated polyurethane molded article was produced in the following manner. Polyoxyethylene polyether polyol (hydroxyl value 28 mgKOH/g, 1300 mPa・s), 0.5% by mass of amine catalyst (dimethylaminoethanol), 1.0% by mass of foam stabilizer (Evonik Tegostab B8736LF2), foaming. A polymer polyol composition containing 5.0% by mass of an agent (monoethanolamine carbonate) was prepared. In addition, polyol-modified diphenylmethane diisocyanate (NCO rate 26.7%, 140 mP·s (25°C)) was prepared as an organic isocyanate. Then, the napped artificial leather was placed in the cavity of a mold heated to 140°C mounted on a high-pressure foaming machine, which is a RIM molding machine, so that its napped side faced the cavity surface. Then, the polymer polyol composition and the organic isocyanate were each injected into the cavity of a mold at a ratio that gave an NCO Index of 1.05 while being heated to 50°C. Then, a foamed and cured polyurethane molded product was molded by holding at 140° C. for 5 minutes. Then, by cooling and opening the mold, a decorated polyurethane molded body was manufactured by directly integrating napped artificial leather onto one surface of the polyurethane molded body.
そして、得られた立毛人工皮革または加飾ポリウレタン成形体を上述のようにして評価した。結果を下記表１に示す。 The resulting raised artificial leather or decorated polyurethane molded article was evaluated as described above. The results are shown in Table 1 below.
［実施例２］
実施例１において、クエン酸含有量を表１に示すように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
[Example 2]
Napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the citric acid content was changed as shown in Table 1. The results are shown in Table 1.
［実施例３～４］
実施例１において、クエン酸に代えて、表１に示すようにリンゴ酸または酒石酸に変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
[Examples 3-4]
Napped artificial leather was produced and evaluated in the same manner as in Example 1, except that citric acid was replaced with malic acid or tartaric acid as shown in Table 1. The results are shown in Table 1.
［実施例５］
実施例１において、立毛繊維基材の染色工程を次のように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
（染色工程）
塩基性染料として、アゾ系赤色染料であるC．I．Basic Red 46を含むNichilon Red-GRL（日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、濃赤色に染色した。なお、C．I．Basic Red 46は、共役系に活性水素を有する官能基を含まない塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。
[Example 5]
In Example 1, a napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the dyeing process of the napped fiber base material was changed as follows. The results are shown in Table 1.
(dying process)
C., an azo red dye, is used as a basic dye. I. Nichilon Red-GRL (manufactured by Nissei Kasei Co., Ltd.) containing Basic Red 46 Napped fibers were placed in a dyeing bath containing a dye solution at 120°C containing 2% owf and 1 g/L of 90% acetic acid as a dyeing aid. The substrate was dyed deep red by immersing it in a bath ratio of 1:30 for 30 minutes. In addition, C. I. Basic Red 46 is a basic dye molecule that does not contain a functional group with active hydrogen in its conjugated system. Then, in the same dyeing bath, the process of soaping at 70° C. using a hot water bath containing 2 g/L of Sorgin R as an anionic surfactant was repeated twice.
［実施例６］
実施例１において、立毛繊維基材の染色工程を次のように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
（染色工程）
塩基性染料として、メチン系黄色染料であるC．I．Basic Yellow 21を含むNichilon Yellow7GL（日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、黄色に染色した。なお、C．I．Basic Yellow 21は、共役系に活性水素を有する官能基を含まない塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。
[Example 6]
In Example 1, napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the dyeing process of the napped fiber base material was changed as follows. The results are shown in Table 1.
(dying process)
C., a methine yellow dye, is used as a basic dye. I. Nichilon Yellow 7GL (manufactured by Nissei Kasei Co., Ltd.) containing
［実施例７］
実施例１において、立毛繊維基材の染色工程を次のように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
（染色工程）
塩基性染料として、クマリン系黄色染料であるC．I．Basic Yellow 40を含むNichilon Flavine 10GFF（日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、黄色に染色した。なお、C．I．Basic Yellow 40は、共役系に活性水素を有する官能基を含まない塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。
[Example 7]
In Example 1, napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the dyeing process of the napped fiber base material was changed as follows. The results are shown in Table 1.
(dying process)
C., a coumarin-based yellow dye, is used as a basic dye. I. Nichilon Flavine 10GFF containing Basic Yellow 40 (Nichilon Kasei Co., Ltd.) 2% owf, 120°C dye solution containing 90% acetic acid 1g/L as a dyeing aid was stored in a dyeing bath containing napped fiber base. The material was dyed yellow by soaking it in a bath ratio of 1:30 for 30 minutes. In addition, C. I. Basic Yellow 40 is a basic dye molecule that does not contain a functional group with active hydrogen in its conjugated system. Then, in the same dyeing bath, the process of soaping at 70° C. using a hot water bath containing 2 g/L of Sorgin R as an anionic surfactant was repeated twice.
［実施例８］
実施例１において、立毛繊維基材の染色工程を次のように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
（染色工程）
塩基性染料として、キサンテン系紫色染料であるC．I．Basic Violet 11を含むNichilon Pink CP（日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、ピンク色に染色した。なお、C．I．Basic Violet 11は、共役系に活性水素を有する官能基を含まない塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。
[Example 8]
In Example 1, a napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the dyeing process of the napped fiber base material was changed as follows. The results are shown in Table 1.
(dying process)
As a basic dye, C. I. Nichilon Pink CP (manufactured by Nissei Kasei Co., Ltd.) containing Basic Violet 11 Napped fiber base The material was dyed pink by soaking it in a bath ratio of 1:30 for 30 minutes. In addition, C. I. Basic Violet 11 is a basic dye molecule that does not contain a functional group with active hydrogen in its conjugated system. Then, in the same dyeing bath, the process of soaping at 70° C. using a hot water bath containing 2 g/L of Sorgin R as an anionic surfactant was repeated twice.
［実施例９］
実施例１において、立毛繊維基材の染色工程を次のように変更した以外は、実施例１と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
（染色工程）
塩基性染料として、オキサジン系青色塩基性染料であるC.I.Basic Blue75を含むNichilon Blue350（日成化成（株）製） ２％owf、染色助剤として９０％酢酸１ｇ／Lを含有する１２０℃の染料液を貯留した染色浴中に、立毛繊維基材を、浴比１：３０の割合で３０分間浸漬して、濃青色に染色した。なお、C.I.Basic Blue75は、共役系に活性水素を有する官能基を有する塩基性染料分子である。そして、同一染色浴で、アニオン系界面活性剤としてソルジンＲ ２g/Lを含有する湯浴を用いて７０℃でソーピングする工程を２回繰り返した。
[Example 9]
In Example 1, napped artificial leather was produced and evaluated in the same manner as in Example 1, except that the dyeing process of the napped fiber base material was changed as follows. The results are shown in Table 1.
(dying process)
Nichilon Blue350 (manufactured by Nissei Kasei Co., Ltd.) containing CIBasic Blue75, an oxazine-based blue basic dye, as a basic dye, 2% owf, and a dye solution at 120°C containing 1 g/L of 90% acetic acid as a dyeing aid. The napped fiber base material was immersed for 30 minutes in the dyeing bath containing the dye at a bath ratio of 1:30 to dye it deep blue. Note that CIBasic Blue75 is a basic dye molecule that has a functional group having active hydrogen in its conjugated system. Then, in the same dyeing bath, the process of soaping at 70° C. using a hot water bath containing 2 g/L of Sorgin R as an anionic surfactant was repeated twice.
［比較例１～６］
酸処理工程を省略した以外は、それぞれ、実施例１，５，６，７，８及び９と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
[Comparative Examples 1 to 6]
Napped artificial leathers were produced and evaluated in the same manner as in Examples 1, 5, 6, 7, 8, and 9, except that the acid treatment step was omitted. The results are shown in Table 1.
［比較例７］
比較例６において、繊度０．２ｄｔｅｘのカチオン可染ポリエステル繊維の代わりに、繊度１．５ｄｔｅｘのカチオン可染ポリエステル繊維を形成した以外は、比較例６と同様にして立毛人工皮革を製造し、評価した。結果を表１に示す。
[Comparative Example 7]
In Comparative Example 6, raised artificial leather was produced and evaluated in the same manner as in Comparative Example 6, except that cationically dyeable polyester fibers with a fineness of 1.5 dtex were formed instead of cationically dyeable polyester fibers with a fineness of 0.2 dtex. did. The results are shown in Table 1.
表１を参照すれば、抽出液のｐＨが３．５～６．５の範囲である実施例１～７の立毛人工皮革は、何れもΔＥcmcが小さく、変色しにくかった。なお、共役系に活性水素を有する官能基を有する塩基性染料分子を含む染料で染色した実施例９は、やや変色が大きかった。一方、抽出液のｐＨが６．５を超える比較例１～６の立毛人工皮革は、何れもΔＥcmcが大きく、顕著に変色した。なお、繊度１．５ｄｔｅｘのカチオン可染ポリエステル繊維を用いた比較例７で得られた立毛人工皮革は、ΔＥcmcが小さく、変色しなかった。しかし、繊度１．５ｄｔｅｘの繊維で構成されており、外観品位が悪かった。 Referring to Table 1, the napped artificial leathers of Examples 1 to 7 in which the pH of the extract was in the range of 3.5 to 6.5 all had small ΔE cmc and were resistant to discoloration. In addition, Example 9, which was dyed with a dye containing a basic dye molecule having a functional group having an active hydrogen in the conjugated system, had a slightly large discoloration. On the other hand, the napped artificial leathers of Comparative Examples 1 to 6 in which the pH of the extract exceeded 6.5 all had large ΔE cmc and significant discoloration. The napped artificial leather obtained in Comparative Example 7 using cationic dyeable polyester fibers with a fineness of 1.5 dtex had a small ΔE cmc and did not change color. However, it was composed of fibers with a fineness of 1.5 dtex, and its appearance quality was poor.
１ 立毛人工皮革
２ 成形体
１０ 加飾成形体
1 Napped
Claims (4)
少なくとも１種の塩基性染料で染色されており、
JIS L 1096 8.37（抽出液のｐＨ）のＡ法に規定された方法に拠って測定された、抽出液のｐＨが３．５～６．５であることを特徴とする立毛人工皮革。 A napped artificial leather comprising a fiber structure made of ultrafine fibers having a fineness of 0.9 dtex or less, which are cationic dyeable polyester fibers, and a polymeric elastomer, and in which at least one side of the ultrafine fibers is napped,
dyed with at least one basic dye,
A raised artificial leather characterized in that the pH of the extract is 3.5 to 6.5, as measured by the method specified in Method A of JIS L 1096 8.37 (pH of the extract).
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| JP2003247165A (en) | 2002-02-19 | 2003-09-05 | Kuraray Co Ltd | Fabric for shoes |
| JP2013227685A (en) | 2012-04-24 | 2013-11-07 | Toray Ind Inc | Flame retardant artificial leather, method for producing the same, and flame retardant agent for artificial leather |
| JP2018048435A (en) | 2016-09-14 | 2018-03-29 | 株式会社クラレ | Artificial leather substrate, napped artificial leather, shoes and artificial leather with resin layer |
| WO2018101016A1 (en) | 2016-11-30 | 2018-06-07 | 株式会社クラレ | Dyed leather-form sheet and fiber structure |
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| JP2003247165A (en) | 2002-02-19 | 2003-09-05 | Kuraray Co Ltd | Fabric for shoes |
| JP2013227685A (en) | 2012-04-24 | 2013-11-07 | Toray Ind Inc | Flame retardant artificial leather, method for producing the same, and flame retardant agent for artificial leather |
| JP2018048435A (en) | 2016-09-14 | 2018-03-29 | 株式会社クラレ | Artificial leather substrate, napped artificial leather, shoes and artificial leather with resin layer |
| WO2018101016A1 (en) | 2016-11-30 | 2018-06-07 | 株式会社クラレ | Dyed leather-form sheet and fiber structure |
| US20190323173A1 (en) | 2016-11-30 | 2019-10-24 | Kuraray Co., Ltd. | Dyed leather-like sheet and fiber structure |
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