JPS6354835B2 - - Google Patents

Info

Publication number: JPS6354835B2
Authority: JP; Japan
Prior art keywords: acid; dyed; nickel; light; leather
Prior art date: 1984-07-31
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.): Expired

Application number

JP59162614A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6141381A (ja

Inventor

Nobuhiro Kuramoto

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

OOSAKAFU

Original Assignee

OOSAKAFU

Priority date (The priority date 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 date listed.)

1984-07-31

Filing date

1984-07-31

Publication date

1988-10-31

1984-07-31 Application filed by OOSAKAFU filed Critical OOSAKAFU

1984-07-31 Priority to JP59162614A priority Critical patent/JPS6141381A/ja

1986-02-27 Publication of JPS6141381A publication Critical patent/JPS6141381A/ja

1988-10-31 Publication of JPS6354835B2 publication Critical patent/JPS6354835B2/ja

Status Granted legal-status Critical Current

Links

239000010985 leather Substances 0.000 claims description 36
150000001875 compounds Chemical class 0.000 claims description 19
238000004043 dyeing Methods 0.000 claims description 17
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 16
239000000835 fiber Substances 0.000 claims description 14
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical compound C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 claims description 10
-1 aromatic sulfonic acids Chemical class 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
229910052759 nickel Inorganic materials 0.000 claims description 9
239000002253 acid Substances 0.000 claims description 8
238000004040 coloring Methods 0.000 claims description 8
125000000217 alkyl group Chemical group 0.000 claims description 7
239000002184 metal Chemical class 0.000 claims description 7
229910052751 metal Inorganic materials 0.000 claims description 7
150000002815 nickel Chemical class 0.000 claims description 7
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
229910017052 cobalt Inorganic materials 0.000 claims description 4
239000010941 cobalt Substances 0.000 claims description 4
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 4
229910052725 zinc Inorganic materials 0.000 claims description 4
239000011701 zinc Substances 0.000 claims description 4
LXFQSRIDYRFTJW-UHFFFAOYSA-N 2,4,6-trimethylbenzenesulfonic acid Chemical compound CC1=CC(C)=C(S(O)(=O)=O)C(C)=C1 LXFQSRIDYRFTJW-UHFFFAOYSA-N 0.000 claims description 3
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 claims description 3
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 3
229940092714 benzenesulfonic acid Drugs 0.000 claims description 3
GPUMPJNVOBTUFM-UHFFFAOYSA-N naphthalene-1,2,3-trisulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC2=C1 GPUMPJNVOBTUFM-UHFFFAOYSA-N 0.000 claims description 3
YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 claims description 3
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 claims description 3
KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical compound C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 claims description 3
239000003960 organic solvent Substances 0.000 claims description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
150000007513 acids Chemical class 0.000 claims 2
239000010953 base metal Substances 0.000 claims 2
239000000975 dye Substances 0.000 description 39
239000000049 pigment Substances 0.000 description 23
239000004744 fabric Substances 0.000 description 22
230000000694 effects Effects 0.000 description 20
239000004611 light stabiliser Substances 0.000 description 20
239000000243 solution Substances 0.000 description 17
238000005562 fading Methods 0.000 description 10
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
229920000742 Cotton Polymers 0.000 description 8
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 8
239000007864 aqueous solution Substances 0.000 description 7
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
229910052799 carbon Inorganic materials 0.000 description 6
150000003839 salts Chemical class 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000000980 acid dye Substances 0.000 description 5
239000000982 direct dye Substances 0.000 description 5
229910052760 oxygen Inorganic materials 0.000 description 5
239000007921 spray Substances 0.000 description 5
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 4
SJEYSFABYSGQBG-UHFFFAOYSA-M Patent blue Chemical compound [Na+].C1=CC(N(CC)CC)=CC=C1C(C=1C(=CC(=CC=1)S([O-])(=O)=O)S([O-])(=O)=O)=C1C=CC(=[N+](CC)CC)C=C1 SJEYSFABYSGQBG-UHFFFAOYSA-M 0.000 description 4
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
RDAWAFGWUCQBNF-UHFFFAOYSA-L nickel(2+);2,4,6-trimethylbenzenesulfonate Chemical compound [Ni+2].CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1.CC1=CC(C)=C(S([O-])(=O)=O)C(C)=C1 RDAWAFGWUCQBNF-UHFFFAOYSA-L 0.000 description 4
239000001301 oxygen Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
IBVWKDVFDAWRFU-UHFFFAOYSA-L benzenesulfonate;nickel(2+) Chemical compound [Ni+2].[O-]S(=O)(=O)C1=CC=CC=C1.[O-]S(=O)(=O)C1=CC=CC=C1 IBVWKDVFDAWRFU-UHFFFAOYSA-L 0.000 description 3
NLMHXPDMNXMQBY-UHFFFAOYSA-L chembl260999 Chemical compound [Na+].[Na+].C1=CC(NC(=O)C)=CC=C1N=NC(C(=CC1=C2)S([O-])(=O)=O)=C(O)C1=CC=C2NC(=O)NC1=CC=C(C(O)=C(N=NC=2C=CC=CC=2)C(=C2)S([O-])(=O)=O)C2=C1 NLMHXPDMNXMQBY-UHFFFAOYSA-L 0.000 description 3
NKLPQNGYXWVELD-UHFFFAOYSA-M coomassie brilliant blue Chemical compound [Na+].C1=CC(OCC)=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=C1 NKLPQNGYXWVELD-UHFFFAOYSA-M 0.000 description 3
229920006239 diacetate fiber Polymers 0.000 description 3
FPAYXBWMYIMERV-UHFFFAOYSA-L disodium;5-methyl-2-[[4-(4-methyl-2-sulfonatoanilino)-9,10-dioxoanthracen-1-yl]amino]benzenesulfonate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1S([O-])(=O)=O FPAYXBWMYIMERV-UHFFFAOYSA-L 0.000 description 3
125000002524 organometallic group Chemical group 0.000 description 3
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 3
239000000985 reactive dye Substances 0.000 description 3
238000012360 testing method Methods 0.000 description 3
OLSOUGWNONTDCK-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3OC)C=3C=C(C(=CC=3)N=NC=3C(=CC4=CC(=CC(N)=C4C=3O)S([O-])(=O)=O)S([O-])(=O)=O)OC)=C(O)C2=C1N OLSOUGWNONTDCK-UHFFFAOYSA-J 0.000 description 3
SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 3
OXLITIGRBOEDEZ-UHFFFAOYSA-N 1,5-diamino-4,8-dihydroxy-2-(4-hydroxyphenyl)anthracene-9,10-dione Chemical compound C=1C(O)=C2C(=O)C=3C(N)=CC=C(O)C=3C(=O)C2=C(N)C=1C1=CC=C(O)C=C1 OXLITIGRBOEDEZ-UHFFFAOYSA-N 0.000 description 2
AQXYVFBSOOBBQV-UHFFFAOYSA-N 1-amino-4-hydroxyanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2N AQXYVFBSOOBBQV-UHFFFAOYSA-N 0.000 description 2
CJTBLQAAOUUAHX-UHFFFAOYSA-N 3h-1,3-benzothiazole-2-thione;nickel Chemical compound [Ni].C1=CC=C2SC(S)=NC2=C1 CJTBLQAAOUUAHX-UHFFFAOYSA-N 0.000 description 2
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000000654 additive Substances 0.000 description 2
238000007605 air drying Methods 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
DSSYKIVIOFKYAU-UHFFFAOYSA-N camphor Chemical compound C1CC2(C)C(=O)CC1C2(C)C DSSYKIVIOFKYAU-UHFFFAOYSA-N 0.000 description 2
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 2
HNBQFKZSMFFZQY-UHFFFAOYSA-L chembl1559341 Chemical compound [Na+].[Na+].C1=CC(C)=CC=C1S(=O)(=O)OC1=CC=C(N=NC=2C(=CC(=CC=2)C=2C=C(C)C(N=NC=3C4=C(C=C(C=C4C=CC=3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=2)C)C=C1 HNBQFKZSMFFZQY-UHFFFAOYSA-L 0.000 description 2
DYKLIOJHWZQJBH-UHFFFAOYSA-K chembl258542 Chemical compound [Na+].[Na+].[Na+].N=1C(Cl)=NC(NC=2C3=C(O)C(N=NC=4C(=CC(C)=CC=4)S([O-])(=O)=O)=C(C=C3C=C(C=2)S([O-])(=O)=O)S([O-])(=O)=O)=NC=1N(C)C1=CC=CC=C1 DYKLIOJHWZQJBH-UHFFFAOYSA-K 0.000 description 2
238000011161 development Methods 0.000 description 2
238000007865 diluting Methods 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
JCGDEGCAEZOBSD-UHFFFAOYSA-L disodium 2-[4-[(2-hydroxynaphthalen-1-yl)diazenyl]-2-sulfonatophenyl]-5-[(3-methyl-5-oxo-1-phenyl-4H-pyrazol-4-yl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].CC1=NN(C(=O)C1N=Nc1ccc(-c2ccc(cc2S([O-])(=O)=O)N=Nc2c(O)ccc3ccccc23)c(c1)S([O-])(=O)=O)c1ccccc1 JCGDEGCAEZOBSD-UHFFFAOYSA-L 0.000 description 2
SVSHEAJPDAGGCC-UHFFFAOYSA-L disodium 7-hydroxy-8-[[4-[4-[[4-(4-methylphenyl)sulfonyloxyphenyl]diazenyl]phenyl]phenyl]diazenyl]naphthalene-1,3-disulfonate Chemical compound CC1=CC=C(C=C1)S(=O)(=O)OC2=CC=C(C=C2)N=NC3=CC=C(C=C3)C4=CC=C(C=C4)N=NC5=C(C=CC6=CC(=CC(=C65)S(=O)(=O)O)S(=O)(=O)[O-])[O-].[Na+].[Na+] SVSHEAJPDAGGCC-UHFFFAOYSA-L 0.000 description 2
SLZCDQVDTBWJND-UHFFFAOYSA-L disodium 8-[[4-[4-[(4-ethoxyphenyl)diazenyl]-3-methylphenyl]-2-methylphenyl]diazenyl]-7-hydroxynaphthalene-1,3-disulfonate Chemical compound CCOC1=CC=C(C=C1)N=NC2=C(C=C(C=C2)C3=CC(=C(C=C3)N=NC4=C(C=CC5=CC(=CC(=C54)S(=O)(=O)O)S(=O)(=O)[O-])[O-])C)C.[Na+].[Na+] SLZCDQVDTBWJND-UHFFFAOYSA-L 0.000 description 2
ZRYQXQUPWQNYSX-UHFFFAOYSA-L disodium;5-[(3-methyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]-2-[4-[(3-methyl-5-oxo-1-phenyl-4h-pyrazol-4-yl)diazenyl]-2-sulfonatophenyl]benzenesulfonate Chemical compound [Na+].[Na+].CC1=NN(C=2C=CC=CC=2)C(=O)C1N=NC(C=C1S([O-])(=O)=O)=CC=C1C(C(=C1)S([O-])(=O)=O)=CC=C1N=NC(C1=O)C(C)=NN1C1=CC=CC=C1 ZRYQXQUPWQNYSX-UHFFFAOYSA-L 0.000 description 2
239000000986 disperse dye Substances 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
238000002474 experimental method Methods 0.000 description 2
229910052748 manganese Inorganic materials 0.000 description 2
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
229920001778 nylon Polymers 0.000 description 2
239000003921 oil Substances 0.000 description 2
ZQBAKBUEJOMQEX-UHFFFAOYSA-N phenyl salicylate Chemical compound OC1=CC=CC=C1C(=O)OC1=CC=CC=C1 ZQBAKBUEJOMQEX-UHFFFAOYSA-N 0.000 description 2
230000000704 physical effect Effects 0.000 description 2
HFIYIRIMGZMCPC-YOLJWEMLSA-J remazole black-GR Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]S(=O)(=O)C1=CC2=CC(S([O-])(=O)=O)=C(\N=N\C=3C=CC(=CC=3)S(=O)(=O)CCOS([O-])(=O)=O)C(O)=C2C(N)=C1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 HFIYIRIMGZMCPC-YOLJWEMLSA-J 0.000 description 2
DHHGSXPASZBLGC-VPMNAVQSSA-L remazole orange-3R Chemical compound [Na+].[Na+].OC=1C2=CC(NC(=O)C)=CC=C2C=C(S([O-])(=O)=O)C=1\N=N\C1=CC=C(S(=O)(=O)CCOS([O-])(=O)=O)C=C1 DHHGSXPASZBLGC-VPMNAVQSSA-L 0.000 description 2
239000012047 saturated solution Substances 0.000 description 2
RIJLWEYDGZAVGC-UHFFFAOYSA-M sodium;5-methyl-2-[[4-(methylamino)-9,10-dioxoanthracen-1-yl]amino]benzenesulfonate Chemical compound [Na+].C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(NC)=CC=C1NC1=CC=C(C)C=C1S([O-])(=O)=O RIJLWEYDGZAVGC-UHFFFAOYSA-M 0.000 description 2
238000005507 spraying Methods 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
NLXFWUZKOOWWFD-UHFFFAOYSA-N 1-(2-hydroxyethylamino)-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(NCCO)=CC=C2NC NLXFWUZKOOWWFD-UHFFFAOYSA-N 0.000 description 1
ICVRBKCRXNVOJC-UHFFFAOYSA-N 1-amino-4-(methylamino)anthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(N)=CC=C2NC ICVRBKCRXNVOJC-UHFFFAOYSA-N 0.000 description 1
KHUFHLFHOQVFGB-UHFFFAOYSA-N 1-aminoanthracene-9,10-dione Chemical class O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2N KHUFHLFHOQVFGB-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
IDYLMOYUCOPIRT-UHFFFAOYSA-L 4-methylbenzenesulfonate;nickel(2+) Chemical compound [Ni+2].CC1=CC=C(S([O-])(=O)=O)C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 IDYLMOYUCOPIRT-UHFFFAOYSA-L 0.000 description 1
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 1
229920001747 Cellulose diacetate Polymers 0.000 description 1
239000004129 EU approved improving agent Substances 0.000 description 1
235000000177 Indigofera tinctoria Nutrition 0.000 description 1
229910021586 Nickel(II) chloride Inorganic materials 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
238000005299 abrasion Methods 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
239000003963 antioxidant agent Substances 0.000 description 1
XFWCDQMDZATIEY-UHFFFAOYSA-L benzenesulfonate;nickel(2+);hexahydrate Chemical compound O.O.O.O.O.O.[Ni+2].[O-]S(=O)(=O)C1=CC=CC=C1.[O-]S(=O)(=O)C1=CC=CC=C1 XFWCDQMDZATIEY-UHFFFAOYSA-L 0.000 description 1
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
239000012964 benzotriazole Substances 0.000 description 1
239000013522 chelant Substances 0.000 description 1
230000009920 chelation Effects 0.000 description 1
JSAKRLDIZOGQTN-UHFFFAOYSA-N chembl122275 Chemical compound C1=CC=C2C(N=NC3=C4C=CC=CC4=CC=C3O)=CC=C(S(O)(=O)=O)C2=C1 JSAKRLDIZOGQTN-UHFFFAOYSA-N 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
239000003086 colorant Substances 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
150000004696 coordination complex Chemical class 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
230000001934 delay Effects 0.000 description 1
238000007598 dipping method Methods 0.000 description 1
PBOIUUROGJVVNC-UHFFFAOYSA-L disodium 2-hydroxy-5-[[4-[[2-methoxy-4-[(3-sulfonatophenyl)diazenyl]phenyl]carbamoylamino]phenyl]diazenyl]benzoate Chemical compound [Na+].[Na+].COc1cc(ccc1NC(=O)Nc1ccc(cc1)N=Nc1ccc(O)c(c1)C([O-])=O)N=Nc1cccc(c1)S([O-])(=O)=O PBOIUUROGJVVNC-UHFFFAOYSA-L 0.000 description 1
PHBXSOKXCTZJBO-UHFFFAOYSA-L disodium 7-amino-4-hydroxy-3-[[4-[4-[(1-hydroxy-4-sulfonatonaphthalen-2-yl)diazenyl]-3-methoxyphenyl]-2-methoxyphenyl]diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].COc1cc(ccc1N=Nc1cc(c2ccccc2c1O)S([O-])(=O)=O)-c1ccc(N=Nc2c(O)c3ccc(N)cc3cc2S([O-])(=O)=O)c(OC)c1 PHBXSOKXCTZJBO-UHFFFAOYSA-L 0.000 description 1
PHOZXQMVPWPNAP-UHFFFAOYSA-L disodium 8-[[4-[4-[(4-ethoxyphenyl)diazenyl]phenyl]phenyl]diazenyl]-7-hydroxynaphthalene-1,3-disulfonate Chemical compound [Na+].[Na+].CCOc1ccc(cc1)N=Nc1ccc(cc1)-c1ccc(cc1)N=Nc1c(O)ccc2cc(cc(c12)S([O-])(=O)=O)S([O-])(=O)=O PHOZXQMVPWPNAP-UHFFFAOYSA-L 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
235000019253 formic acid Nutrition 0.000 description 1
229940097275 indigo Drugs 0.000 description 1
KHLVKKOJDHCJMG-QDBORUFSSA-L indigo carmine Chemical compound [Na+].[Na+].N/1C2=CC=C(S([O-])(=O)=O)C=C2C(=O)C\1=C1/NC2=CC=C(S(=O)(=O)[O-])C=C2C1=O KHLVKKOJDHCJMG-QDBORUFSSA-L 0.000 description 1
COHYTHOBJLSHDF-UHFFFAOYSA-N indigo powder Natural products N1C2=CC=CC=C2C(=O)C1=C1C(=O)C2=CC=CC=C2N1 COHYTHOBJLSHDF-UHFFFAOYSA-N 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
239000000991 leather dye Substances 0.000 description 1
SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical compound [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 1
239000000463 material Substances 0.000 description 1
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
229910052753 mercury Inorganic materials 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
PCPDOIKJFCRPEA-UHFFFAOYSA-L naphthalene-1,2-disulfonate nickel(2+) Chemical compound C=1(C(=CC=C2C=CC=CC12)S(=O)(=O)[O-])S(=O)(=O)[O-].[Ni+2] PCPDOIKJFCRPEA-UHFFFAOYSA-L 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
VYZBOZAQWHMWLL-UHFFFAOYSA-L naphthalene-1-sulfonate;nickel(2+) Chemical compound [Ni+2].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1.C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 VYZBOZAQWHMWLL-UHFFFAOYSA-L 0.000 description 1
150000002816 nickel compounds Chemical class 0.000 description 1
QMMRZOWCJAIUJA-UHFFFAOYSA-L nickel dichloride Chemical compound Cl[Ni]Cl QMMRZOWCJAIUJA-UHFFFAOYSA-L 0.000 description 1
IWDCLRJOBJJRNH-UHFFFAOYSA-N p-cresol Chemical compound CC1=CC=C(O)C=C1 IWDCLRJOBJJRNH-UHFFFAOYSA-N 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
229960000969 phenyl salicylate Drugs 0.000 description 1
230000000176 photostabilization Effects 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
238000007639 printing Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
238000010791 quenching Methods 0.000 description 1
230000000171 quenching effect Effects 0.000 description 1
TVRGPOFMYCMNRB-UHFFFAOYSA-N quinizarine green ss Chemical compound C1=CC(C)=CC=C1NC(C=1C(=O)C2=CC=CC=C2C(=O)C=11)=CC=C1NC1=CC=C(C)C=C1 TVRGPOFMYCMNRB-UHFFFAOYSA-N 0.000 description 1
235000012752 quinoline yellow Nutrition 0.000 description 1
FZUOVNMHEAPVBW-UHFFFAOYSA-L quinoline yellow ws Chemical compound [Na+].[Na+].O=C1C2=CC=CC=C2C(=O)C1C1=NC2=C(S([O-])(=O)=O)C=C(S(=O)(=O)[O-])C=C2C=C1 FZUOVNMHEAPVBW-UHFFFAOYSA-L 0.000 description 1
238000011160 research Methods 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
230000009291 secondary effect Effects 0.000 description 1
238000002791 soaking Methods 0.000 description 1
CKMPIIPZKJISCU-UHFFFAOYSA-M sodium;4,8-diamino-1,5-dihydroxy-9,10-dioxoanthracene-2-sulfonate Chemical compound [Na+].O=C1C2=C(N)C=C(S([O-])(=O)=O)C(O)=C2C(=O)C2=C1C(O)=CC=C2N CKMPIIPZKJISCU-UHFFFAOYSA-M 0.000 description 1
239000010421 standard material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
MPCYPRXRVWZKGF-UHFFFAOYSA-J tetrasodium 5-amino-3-[[4-[4-[(8-amino-1-hydroxy-3,6-disulfonatonaphthalen-2-yl)diazenyl]phenyl]phenyl]diazenyl]-4-hydroxynaphthalene-2,7-disulfonate Chemical compound [Na+].[Na+].[Na+].[Na+].C1=C(S([O-])(=O)=O)C=C2C=C(S([O-])(=O)=O)C(N=NC3=CC=C(C=C3)C3=CC=C(C=C3)N=NC3=C(C=C4C=C(C=C(C4=C3O)N)S([O-])(=O)=O)S([O-])(=O)=O)=C(O)C2=C1N MPCYPRXRVWZKGF-UHFFFAOYSA-J 0.000 description 1
239000004753 textile Substances 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
150000004961 triphenylmethanes Chemical class 0.000 description 1
210000002268 wool Anatomy 0.000 description 1
230000037303 wrinkles Effects 0.000 description 1
BOXSVZNGTQTENJ-UHFFFAOYSA-L zinc dibutyldithiocarbamate Chemical compound [Zn+2].CCCCN(C([S-])=S)CCCC.CCCCN(C([S-])=S)CCCC BOXSVZNGTQTENJ-UHFFFAOYSA-L 0.000 description 1

Landscapes

Coloring (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

JP59162614A 1984-07-31 1984-07-31 染色繊維又は染色皮革の着色色素の耐光堅牢化方法 Granted JPS6141381A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP59162614A JPS6141381A (ja)	1984-07-31	1984-07-31	染色繊維又は染色皮革の着色色素の耐光堅牢化方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP59162614A JPS6141381A (ja)	1984-07-31	1984-07-31	染色繊維又は染色皮革の着色色素の耐光堅牢化方法

Publications (2)

Publication Number	Publication Date
JPS6141381A JPS6141381A (ja)	1986-02-27
JPS6354835B2 true JPS6354835B2 (de)	1988-10-31

Family

ID=15757943

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP59162614A Granted JPS6141381A (ja)	1984-07-31	1984-07-31	染色繊維又は染色皮革の着色色素の耐光堅牢化方法

Country Status (1)

Country	Link
JP (1)	JPS6141381A (de)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5190576B2 (ja) *	2009-08-25	2013-04-24	株式会社ピラミッド	合成樹脂及び合成樹脂製品の耐光性向上方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1035769A (en) *	1973-11-29	1978-08-01	Wendell F. Smith (Jr.)	Stabilized dyes
JPS58134174A (ja) *	1982-02-02	1983-08-10	Mitsubishi Paper Mills Ltd	劣化防止剤

1984
- 1984-07-31 JP JP59162614A patent/JPS6141381A/ja active Granted

Also Published As

Publication number	Publication date
JPS6141381A (ja)	1986-02-27

Publication	Publication Date	Title
JP3051494B2 (ja)	2000-06-12	ポリアミド繊維染色物の安定化方法
US4950304A (en)	1990-08-21	Process for quenching or suppressing the fluorescence of substrates treated with fluorescent whitening agents
JP3051461B2 (ja)	2000-06-12	ポリアミド繊維染色物の安定化方法
JPH0284555A (ja)	1990-03-26	しみ防止剤で加工されたポリアミド繊維材料の黄変を防止する方法
JPH03185186A (ja)	1991-08-13	ポリアミド基質を染色する方法
US4455147A (en)	1984-06-19	Transfer printing
CA1267490A (en)	1990-04-03	Dyeing and printing fibres
US7018429B1 (en)	2006-03-28	Process for coloring a textile substrate
CA1229205A (en)	1987-11-17	Process for dyeing or printing polyamide fibres
NL8302986A (nl)	1984-03-16	Werkwijze voor het verbeteren van de echtheidseigenschappen van anionogene kleurstoffen en optische bleekmiddelen.
US2890094A (en)	1959-06-09	Dyeing composition and method
JPS6354835B2 (de)	1988-10-31
US5904738A (en)	1999-05-18	Gas-fade inhibition
JPS63309680A (ja)	1988-12-16	染料の堅牢度を改良するための安定剤
US3945793A (en)	1976-03-23	Process for the colouration of acid-modified synthetic textile fibers and acrylic fibers
BE1006499A5 (fr)	1994-09-13	Procede de stabilisation de teintures sur des fibres de polyamide et teintures sur fibres de polyamide traitees selon ce procede.
RU2362851C1 (ru)	2009-07-27	Способ крашения арамидного волокна
PT1668079E (pt)	2011-11-09	Corantes dispersos preto e marinho sem (aox) de halogénio orgânico adsorvível
JPH03287873A (ja)	1991-12-18	着色繊維布帛の耐塩素性向上方法
US7527656B2 (en)	2009-05-05	Process for the thermal and photochemical stabilization of dyed polyamide fiber material
US3960479A (en)	1976-06-01	Coloring of organic materials with asymmetric thioindigoid compounds
TWI415995B (zh)	2013-11-21	改善熱穩定性的方法
US3597149A (en)	1971-08-03	Inhibition of gas-fume fading of dyed cellulose acetate material
US2533100A (en)	1950-12-05	Nylon immunized against dyes by
CH523377A (fr)	1972-01-31	Procédé de teinture, d'impression, de rongeage et/ou de blanchiment optique des matières textiles à base d'acétate de cellulose