JP3165475B2 - Fiber bleach dyeing method - Google Patents
Fiber bleach dyeing methodInfo
- Publication number
- JP3165475B2 JP3165475B2 JP25021891A JP25021891A JP3165475B2 JP 3165475 B2 JP3165475 B2 JP 3165475B2 JP 25021891 A JP25021891 A JP 25021891A JP 25021891 A JP25021891 A JP 25021891A JP 3165475 B2 JP3165475 B2 JP 3165475B2
- Authority
- JP
- Japan
- Prior art keywords
- bleaching
- dyeing
- bath
- acid
- bleach
- 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.)
- Expired - Fee Related
Links
- 239000007844 bleaching agent Substances 0.000 title claims description 37
- 238000004043 dyeing Methods 0.000 title claims description 35
- 239000000835 fiber Substances 0.000 title claims description 24
- 238000000034 method Methods 0.000 title claims description 14
- 238000004061 bleaching Methods 0.000 claims description 49
- 150000003839 salts Chemical class 0.000 claims description 17
- 238000007599 discharging Methods 0.000 claims description 6
- 229910021645 metal ion Inorganic materials 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
- 229920003043 Cellulose fiber Polymers 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 3
- 150000004967 organic peroxy acids Chemical class 0.000 claims description 3
- 238000000354 decomposition reaction Methods 0.000 claims 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 36
- 239000000975 dye Substances 0.000 description 26
- 239000002253 acid Substances 0.000 description 24
- 230000000052 comparative effect Effects 0.000 description 21
- 239000004115 Sodium Silicate Substances 0.000 description 19
- 235000019795 sodium metasilicate Nutrition 0.000 description 19
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 19
- 229910052911 sodium silicate Inorganic materials 0.000 description 19
- 239000000203 mixture Substances 0.000 description 18
- 229910000029 sodium carbonate Inorganic materials 0.000 description 18
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 14
- 238000010186 staining Methods 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 11
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 239000004744 fabric Substances 0.000 description 10
- 238000002845 discoloration Methods 0.000 description 8
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 6
- 239000005708 Sodium hypochlorite Substances 0.000 description 6
- -1 halogen ion Chemical group 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 6
- 239000011780 sodium chloride Substances 0.000 description 5
- 229920000742 Cotton Polymers 0.000 description 4
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000005562 fading Methods 0.000 description 4
- 239000000985 reactive dye Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 2
- WZFUQSJFWNHZHM-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 WZFUQSJFWNHZHM-UHFFFAOYSA-N 0.000 description 2
- JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 2
- YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 2
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000009991 scouring Methods 0.000 description 2
- 239000000565 sealant Substances 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- AYRVGWHSXIMRAB-UHFFFAOYSA-M sodium acetate trihydrate Chemical compound O.O.O.[Na+].CC([O-])=O AYRVGWHSXIMRAB-UHFFFAOYSA-M 0.000 description 2
- 239000001488 sodium phosphate Substances 0.000 description 2
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 2
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 2
- 235000019801 trisodium phosphate Nutrition 0.000 description 2
- KZEVSDGEBAJOTK-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[5-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CC=1OC(=NN=1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O KZEVSDGEBAJOTK-UHFFFAOYSA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- RTLULCVBFCRQKI-UHFFFAOYSA-N 1-amino-4-[3-[(4,6-dichloro-1,3,5-triazin-2-yl)amino]-4-sulfoanilino]-9,10-dioxoanthracene-2-sulfonic acid Chemical compound C1=2C(=O)C3=CC=CC=C3C(=O)C=2C(N)=C(S(O)(=O)=O)C=C1NC(C=1)=CC=C(S(O)(=O)=O)C=1NC1=NC(Cl)=NC(Cl)=N1 RTLULCVBFCRQKI-UHFFFAOYSA-N 0.000 description 1
- XYPISWUKQGWYGX-UHFFFAOYSA-N 2,2,2-trifluoroethaneperoxoic acid Chemical compound OOC(=O)C(F)(F)F XYPISWUKQGWYGX-UHFFFAOYSA-N 0.000 description 1
- QWQITSDOHAMJJW-UHFFFAOYSA-N 2,4-dichlorobenzenecarboperoxoic acid Chemical compound OOC(=O)C1=CC=C(Cl)C=C1Cl QWQITSDOHAMJJW-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- IHCCLXNEEPMSIO-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)CC(=O)N1CC2=C(CC1)NN=N2 IHCCLXNEEPMSIO-UHFFFAOYSA-N 0.000 description 1
- YJLUBHOZZTYQIP-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=N2 YJLUBHOZZTYQIP-UHFFFAOYSA-N 0.000 description 1
- GLVYLTSKTCWWJR-UHFFFAOYSA-N 2-carbonoperoxoylbenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1C(O)=O GLVYLTSKTCWWJR-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-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
- 244000025254 Cannabis sativa Species 0.000 description 1
- 235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
- 235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical group CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- BAVYZALUXZFZLV-UHFFFAOYSA-O Methylammonium ion Chemical compound [NH3+]C BAVYZALUXZFZLV-UHFFFAOYSA-O 0.000 description 1
- MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- CVXHBROPWMVEQO-UHFFFAOYSA-N Peroxyoctanoic acid Chemical compound CCCCCCCC(=O)OO CVXHBROPWMVEQO-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical group CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
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- 229910052782 aluminium Inorganic materials 0.000 description 1
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- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- LBAYFEDWGHXMSM-UHFFFAOYSA-N butaneperoxoic acid Chemical compound CCCC(=O)OO LBAYFEDWGHXMSM-UHFFFAOYSA-N 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 238000003421 catalytic decomposition reaction Methods 0.000 description 1
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- 229910052801 chlorine Inorganic materials 0.000 description 1
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- 238000000605 extraction Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
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- 150000002367 halogens Chemical class 0.000 description 1
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- 229910052742 iron Inorganic materials 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
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- 229910052759 nickel Inorganic materials 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- CZPZWMPYEINMCF-UHFFFAOYSA-N propaneperoxoic acid Chemical compound CCC(=O)OO CZPZWMPYEINMCF-UHFFFAOYSA-N 0.000 description 1
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- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical group CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical group CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Landscapes
- Treatment Of Fiber Materials (AREA)
- Coloring (AREA)
Description
【0001】[0001]
【産業上の利用分野】本発明は繊維の漂白染色法に関す
る。FIELD OF THE INVENTION The present invention relates to a method for bleaching and dyeing fibers.
【0002】[0002]
【従来の技術】木綿、麻、レーヨン等のセルロース繊維
の染色は、特に鮮明度を得るため精練のあと、次亜塩素
酸ナトリウムや過酸化水素等の塩素系または酸素系の漂
白剤を用いて下晒しをしたあと、還元、中和ないしは水
洗により漂白剤を除去しその後で染色するという工程が
通常行なわれている。そしてこの方法では、下晒しおよ
び漂白剤の除去並びに反応性染料による染色後のソーピ
ング工程に多大の時間とエネルギーを必要としている。2. Description of the Related Art Cellulose fibers such as cotton, hemp, rayon, etc. are dyed using a chlorine-based or oxygen-based bleach such as sodium hypochlorite or hydrogen peroxide, after scouring to obtain sharpness. It is a common practice to remove the bleaching agent by reducing, neutralizing, or washing with water after exposing underneath, followed by dyeing. In this method, a great deal of time and energy is required for removing the bleaching agent and the bleaching agent and for the soaping step after dyeing with the reactive dye.
【0003】[0003]
【発明が解決しようとする課題】反応性染料による染色
の前に繊維の漂白を行うことにより漂白効果を得ると共
に、同浴に於いて染色を行うことにより工程の簡略化、
工程短縮を行うことにあり、またこれを可能にならしめ
るため新規な方法と繊維の漂白染色剤が求められてい
る。The bleaching effect is obtained by bleaching the fiber before dyeing with the reactive dye, and the process is simplified by dyeing in the same bath.
In order to shorten the process, a new method and a bleaching dye for fibers are required to make this possible.
【0004】[0004]
【課題を解決するための手段】本発明者等は、すでに染
料は破壊せずに繊維中の不純物からなる色のみを漂白で
きる漂白剤を見いだし、染色漂白剤及び染色漂白法とし
て特許申請している(特願平2−325442)が、こ
の特許記載の方法では使用出来る染料に制限がある。Means for Solving the Problems The present inventors have already found a bleaching agent capable of bleaching only the color consisting of impurities in fibers without destroying the dye, and have applied for a patent as a dye bleaching agent and a dye bleaching method. (Japanese Patent Application No. 2-325442), but there are limitations on the dyes that can be used in the method described in this patent.
【0005】染色に入る前に、漂白剤を完全に無くして
しまえば漂白剤の影響が無くなり、使用出来る染料に制
限なく同浴で染色に入れ、漂白液の抜取り、漂白剤の洗
浄という工程が省け、合理化が出来ると考えて鋭意研究
の結果、ある特定の染色漂白剤とある特定の添加剤との
組合せにより、この目的を達成出来ることを見出し本発
明に到った。If the bleaching agent is completely eliminated before dyeing, the effect of the bleaching agent disappears, and the dyeing in the same bath without limitation on the usable dyes, the extraction of the bleaching solution, and the washing of the bleaching agent are performed. As a result of earnest studies, it has been found that a combination of a specific dye bleaching agent and a specific additive can achieve this object, leading to the present invention.
【0006】即ち本発明は次の(1)及び(2)からな
る。 (1)繊維を染色するに際し、下記一般式(1)で表わ
される有機過酸またはそれらの塩もしくは錯体からなる
漂白剤で漂白し、引き続き下記一般式(2)で表わされ
る塩を使用して漂白剤を分解し、漂白後浴を排出するこ
となく、引き続いて染色を施すことを特徴とする繊維の
漂白染色法。 一般式(1)That is, the present invention comprises the following (1) and (2). (1) When dyeing a fiber, the fiber is bleached with a bleach comprising an organic peracid represented by the following general formula (1) or a salt or complex thereof, and subsequently, a salt represented by the following general formula (2) is used. A method for bleach-dyeing a fiber, comprising decomposing a bleaching agent and subsequently performing dyeing without discharging the bath after bleaching. General formula (1)
【0007】[0007]
【化2】 Embedded image
【0008】(但し、Rは置換または非置換のアルキル
基、アリル基またはアラルキル基、nは1〜6の自然数
を示す。) 一般式(2) R1 X (但し、R1 は金属イオン又は置換または非置換の4級
アンモニウム基を示し、Xはハロゲンイオンを示す。)(Where R is a substituted or unsubstituted alkyl group, allyl group or aralkyl group, and n is a natural number of 1 to 6.) General formula (2) R 1 X (where R 1 is a metal ion or X represents a substituted or unsubstituted quaternary ammonium group, and X represents a halogen ion.)
【0009】(2)繊維がセルロース繊維単独またはそ
の他の繊維と混合したセルロース繊維である(1)記載
の繊維の漂白染色法。(2) The method for bleach-dyeing fibers according to (1), wherein the fibers are cellulose fibers alone or mixed with other fibers.
【0010】本発明の繊維の染色漂白剤である一般式
(1)で表わされる有機過酸またはその塩(金属塩又は
アンモニウム塩)の具体例としては過蟻酸、過酢酸、過
プロピオン酸、過クロル酢酸、過トリフルオロ酢酸、過
ブチル酸、過カプリル酸、過ラウリン酸、ジ過こはく
酸、ジ過グルタル酸、ジ過アジピン酸、モノ過ノナン二
酸、ジ過ノナン二酸、モノ過デカン二酸、ジ過デカン二
酸、モノ過ドデカン二酸、ジ過ドデカン二酸、モノ過ウ
ンデカン二酸、ジ過ウンデカン二酸、ジ過フタル酸、ジ
過テレフタル酸、過安息香酸、m−クロロ過安息香酸、
2,4−ジクロロ過安息香酸、モノ過フタル酸、モノ過
フタル酸マグネシウム、モノ過こはく酸、モノ過こはく
酸マグネシウム、モノ過マレイン酸、モノ過マレイン酸
カルシウム、モノ過グルタル酸、モノ過グルタル酸マグ
ネシウム、過トリメリット酸、過ピロメリット酸等が挙
げられる。特に好ましくはモノ過フタル酸マグネシウム
及びジ過ドデカン二酸である。Specific examples of the organic peracid or its salt (metal salt or ammonium salt) represented by the general formula (1), which is a dye bleaching agent for fibers of the present invention, include formic acid, peracetic acid, perpropionic acid, Chloroacetic acid, pertrifluoroacetic acid, perbutyric acid, percaprylic acid, perlauric acid, disuccinic acid, diperglutaric acid, diperadipic acid, monopernonanedioic acid, dipernonanedioic acid, monoperdecane Diacid, diperdecandioic acid, monoperdodecandioic acid, diperdodecandioic acid, monoperoundecanoic acid, diperoundecanoic acid, diperphthalic acid, diperterephthalic acid, perbenzoic acid, m-chloro Perbenzoic acid,
2,4-dichloroperbenzoic acid, monoperphthalic acid, magnesium monoperphthalate, monopersuccinic acid, magnesium monopersuccinate, monopermaleic acid, calcium monopermaleate, monoperglutaric acid, monoperglutarate Magnesium acid, pertrimellitic acid, perpyromellitic acid and the like. Particularly preferred are magnesium monoperphthalate and diperdodecandioic acid.
【0011】漂白浴中の漂白剤の濃度は、有効活性酸素
量で好ましくは0.05〜10% o.w.f. 特に好ましく
は0.3〜5% o.w.f. である。The concentration of the bleaching agent in the bleaching bath is preferably 0.05 to 10% owf, particularly preferably 0.3 to 5% owf in terms of active oxygen content.
【0012】pHは好ましくは1〜14、特に好ましく
は2〜10である。漂白浴の温度は好ましくは20〜1
10℃特に好ましくは40〜90℃である。The pH is preferably from 1 to 14, particularly preferably from 2 to 10. The temperature of the bleaching bath is preferably 20-1.
10 ° C is particularly preferably 40 to 90 ° C.
【0013】漂白剤を分解する塩の金属イオンとなる金
属は、ナトリウム、カリウム、リチウム、銅、アルミニ
ウム、マグネシウム、カルシウム、亜鉛、バリウム、
錫、鉄、コバルト、ニッケル等であり、漂白剤を分解す
る塩の置換または非置換の4級アンモニウム基は、アン
モニウム基、モノメチルアンモニウム基、ジメチルアン
モニウム基、トリメチルアンモニウム基、テトラメチル
アンモニウム基、モノエチルアンモニウム基、ジエチル
アンモニウム基、トリエチルアンモニウム基、モノメチ
ルトリエチルアンモニウム基、テトラエチルアンモニウ
ム基等のアンモニウム基であり、更に高級のアルキル
基、アリル基またはアラルキル基で置換されていてもよ
いアンモニウム基である。漂白剤を分解する塩のハロゲ
ンイオンは、フッ素イオン、塩素イオン、臭素イオン、
沃素イオンである。また4級アンモニュウム基とハロゲ
ンイオンの塩は置換又は非置換アミンとハロゲン酸とか
ら作られてもよい。特に好ましい塩は、食塩、臭化カリ
ウム、塩化アンモニウム等である。The metal which becomes the metal ion of the salt that decomposes the bleach is sodium, potassium, lithium, copper, aluminum, magnesium, calcium, zinc, barium,
Substituted or unsubstituted quaternary ammonium groups of salts that decompose bleach, such as tin, iron, cobalt, nickel, etc. include ammonium, monomethylammonium, dimethylammonium, trimethylammonium, tetramethylammonium, An ammonium group such as an ethylammonium group, a diethylammonium group, a triethylammonium group, a monomethyltriethylammonium group, and a tetraethylammonium group, and an ammonium group which may be substituted with a higher alkyl group, an allyl group or an aralkyl group. Halogen ions of salts that decompose bleach are fluorine ions, chloride ions, bromine ions,
Iodine ion. The salt of a quaternary ammonium group and a halogen ion may be formed from a substituted or unsubstituted amine and a halogen acid. Particularly preferred salts are sodium chloride, potassium bromide, ammonium chloride and the like.
【0014】漂白剤を分解するに際し、使用される塩の
濃度は0.05〜10重量%であり、特に好ましくは
0.3〜5重量%である。In decomposing the bleach, the concentration of the salt used is 0.05 to 10% by weight, particularly preferably 0.3 to 5% by weight.
【0015】漂白剤を分解するに際し、使用される温度
は20〜110℃特に好ましくは40〜90℃である。In decomposing the bleaching agent, the temperature used is 20 to 110 ° C., preferably 40 to 90 ° C.
【0016】本発明に適用される染料は一般に市販され
ている種々の染料が挙げられ、特に反応性染料が好まし
く、使用量及び染色法はそれら市販品の摘要基準にした
がって行う。代表的な反応性染料の例としては、カヤシ
オン(日本化薬)、レマゾール(ヘキスト)、プロシオ
ン(ICI)、ダイアミラ(三菱化成)、セルマゾール
(三井東圧化学)、スミフィックス(住友化学)、シバ
クロン(CIBA)、レバフィックス(バイエル)、フ
ィクサゾール(大東化学)等が挙げられる。The dyes applicable to the present invention include various commercially available dyes, particularly reactive dyes, and the amount used and the dyeing method are determined in accordance with the standards for those commercially available products. Examples of typical reactive dyes include Kayashion (Nippon Kayaku), Remazol (Hoechst), Procion (ICI), Daimira (Mitsubishi Kasei), Sermazol (Mitsui Toatsu Chemical), Sumifix (Sumitomo Chemical), Cibacron. (CIBA), Levafix (Bayer), Fixazole (Daito Chemical) and the like.
【0017】本発明の漂白剤及び漂白剤を分解する塩は
使用時におけるpHを有効成分の最適pH域に保つため
のpH調節剤例えば、酢酸、メタケイ酸ナトリウム、炭
酸ナトリウム又は炭酸水素ナトリウムを好ましくは0〜
40%、有効成分の水中金属イオンによる接触分解を抑
制するための金属イオン封止剤例えばカヤキレーターC
−1000、エチレンジアミン四酢酸又はディクエスト
2010(三菱モンサント化成(株)製)を好ましくは
0〜1%、染色助剤例えば食塩又は硫酸ナトリウムを好
ましくは0〜98%及び取り扱いや安定性を良くするた
めの希釈剤例えば水、有機溶剤、セライト又は超微粒子
状無水シリカを漂白剤1部及び/又は漂白剤を分解する
塩1部に対し好ましくは0〜100部含むことができ
る。The bleaching agent and the salt capable of decomposing the bleaching agent of the present invention are preferably pH adjusters for keeping the pH in use at the optimum pH range of the active ingredient, for example, acetic acid, sodium metasilicate, sodium carbonate or sodium hydrogen carbonate. Is 0
40%, a metal ion sealant for suppressing catalytic decomposition of active ingredients by metal ions in water, such as Kayachelator C
-1000, preferably ethylenediaminetetraacetic acid or Dequest 2010 (manufactured by Mitsubishi Monsanto Kasei Co., Ltd.) at 0 to 1%, and a dyeing aid such as sodium chloride or sodium sulfate preferably at 0 to 98% to improve handling and stability. For example, water, an organic solvent, celite or ultrafine anhydrous silica may be contained in an amount of 0 to 100 parts per part of the bleaching agent and / or 1 part of the salt that decomposes the bleaching agent.
【0018】本発明の漂白剤及び漂白剤を分解する塩は
染色法に応じて溶液、懸濁液、ペーストあるいは粉末状
等どのような形態でもとることができる。The bleaching agent and the salt for decomposing the bleaching agent of the present invention can be in any form such as a solution, a suspension, a paste or a powder depending on the dyeing method.
【0019】[0019]
【作 用】本発明の染色漂白剤及び漂白剤を分解する塩
を使用すれば繊維の染色漂白に当たって漂白を先に行
い、漂白後漂白剤を分解する事により排出操作或いはす
すぎ洗い操作を省いて染色することが可能である。通常
の下晒し後染色する方法と同等もしくはそれ以上の漂白
効果を得ることが可能である。[Operation] If the dye bleaching agent of the present invention and the salt that decomposes the bleaching agent are used, bleaching is performed first in dyeing and bleaching of the fiber, and after bleaching, the bleaching agent is decomposed to eliminate the discharging operation or the rinsing operation. It is possible to stain. It is possible to obtain a bleaching effect equivalent to or more than that of the method of dyeing after ordinary under-exposure.
【0020】[0020]
【実施例】次に本発明をより充分に理解せしめるために
実施例を示すが、これらの実施例は例証のためのもので
あって、本発明を限定するものではない。The present invention will now be described in more detail with reference to the following Examples, which are for illustrative purposes only and do not limit the present invention.
【0021】まず実施例1では、最も一般的な漂白剤で
ある過酸化水素(比較例1−1)及び次亜塩素酸ナトリ
ウム(比較例1−2)と比較することにより本発明の漂
白剤の漂白能及び染色に与える影響を評価した。First, in Example 1, the bleaching agent of the present invention was compared with hydrogen peroxide (Comparative Example 1-1) and sodium hypochlorite (Comparative Example 1-2), which are the most common bleaching agents. Was evaluated for its bleaching ability and its effect on dyeing.
【0022】実施例2において他種属の染料による例を
示した。また実施例3〜4に混紡についての例を示し
た。In Example 2, an example using another kind of dye was shown. Examples of blending are shown in Examples 3 and 4.
【0023】実施例1.精練後晒しをしていない未染色
の木綿布(以後未染色布と表記する)をまず最初に以下
に示す実施例1−1〜4に示した組成をもつ浴中で80
℃の温度で20分間処理し漂白した。引き続いて浴を排
出することなく食塩10g/lを加え90℃に昇温し2
0分間処理した。更に浴を排出することなく80℃に下
げ次の染色薬剤のうち染料と無水硫酸ナトリウムを加え
て同温度で10分間処理した。続いて炭酸ナトリウムを
加えて同温度で1時間染色した。染色後すすぎ洗いし、
ついで98℃の石鹸水で15分間洗浄した。浴中の繊維
対漂白浴及び染色浴の比はいずれも1:15である。Embodiment 1 FIG. An undyed cotton cloth which has not been exposed after scouring (hereinafter referred to as an undyed cloth) is first placed in a bath having the composition shown in Examples 1-1 to 4 below.
Bleached by processing at a temperature of 20 ° C for 20 minutes. Subsequently, 10 g / l of sodium chloride was added without discharging the bath, and the temperature was raised to 90 ° C.
Treated for 0 minutes. Further, the temperature was lowered to 80 ° C. without draining the bath, and a dye and anhydrous sodium sulfate were added among the following dyeing agents, followed by treatment at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and staining was performed at the same temperature for 1 hour. Rinse after dyeing,
Then, it was washed with a soap water at 98 ° C. for 15 minutes. The ratio of the fibers in the bath to the bleaching and dyeing baths is 1:15.
【0024】 カヤシオンブルーE−CN 2 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/lKayashion Blue E-CN 2% o. w. f. Anhydrous sodium sulfate 100 g / l sodium carbonate 20 g / l
【0025】実施例1−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l (日本化薬(株)製金属イオン封止剤) 40%過酢酸 2 g/lExample 1-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l (Metal ion sealant manufactured by Nippon Kayaku Co., Ltd.) 40% peracetic acid 2 g / L
【0026】実施例1−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 1-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecandioic acid 2.3 g / l
【0027】実施例1−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/l (日本パーオキサイド(株)製モノ過フタル酸マグネシ
ウム、有効酸素4.9%)Example 1-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l (manufactured by Nippon Peroxide Co., Ltd., magnesium monoperphthalate, active oxygen 4.0 g / l) 9%)
【0028】実施例1−4 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 過安息香酸 1 g/lExample 1-4 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l Perbenzoic acid 1 g / l
【0029】比較例1.未染色布を実施例1と同じく比
較例1−1及び比較例1−2に示した組成の漂白浴中
で、実施例1と同一条件で漂白した。引き続いて実施例
1と同一の染色薬剤を用いて、実施例1と同一条件で染
色処理を施した。Comparative Example 1 The undyed cloth was bleached in a bleaching bath having the composition shown in Comparative Examples 1-1 and 1-2 in the same manner as in Example 1 under the same conditions as in Example 1. Subsequently, using the same staining agent as in Example 1, a staining treatment was performed under the same conditions as in Example 1.
【0030】比較例1−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 1-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l
【0031】比較例1−2 12%次亜塩素酸ナトリウム 0.9g/lComparative Example 1-2 12% sodium hypochlorite 0.9 g / l
【0032】比較例2.未染色布を実施例1−2と同一
条件で漂白し、その後90℃での食塩処理を行うことな
く、引き続いて実施例1と同一の染色薬剤を用いて、実
施例1と同一条件で染色処理を施した。(特願平2−3
25442の方法に相当する。)Comparative Example 2 The undyed cloth is bleached under the same conditions as in Example 1-2, and subsequently dyed under the same conditions as in Example 1 using the same dyeing agent as in Example 1 without performing salt treatment at 90 ° C. Processing was performed. (Japanese Patent Application No. 2-3
25442. )
【0033】 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちあり[0033] Bleaching ability ○: Sufficient bleaching ability △: Insufficient bleaching ability ×: Almost no bleaching ability XX: No bleaching ability at all Clarity ○: Practical use △: Slight discoloration ×: Severe discoloration × ×: marked color fading
【0034】比較例3.未染色布をまず最初に次の組成
を持つ浴中で80℃の温度で20分間処理し漂白した。 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/l 漂白後、浴を排出しそして繊維材料を冷水で注意深くす
すぎ洗いし、その後次の染色薬剤組成のうち染料と無水
硫酸ナトリウムを加えた浴中で80℃の温度で10分間
処理した。続いて炭酸ナトリウムを加えて同じく同温度
で1時間染色した。Comparative Example 3 The undyed fabric was first treated and bleached in a bath having the following composition at a temperature of 80 ° C. for 20 minutes. Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l After bleaching, the bath is drained and the textile material is carefully rinsed with cold water, Thereafter, treatment was carried out at a temperature of 80 ° C. for 10 minutes in a bath containing the dye and anhydrous sodium sulfate in the following dyeing chemical composition. Subsequently, sodium carbonate was added, and staining was performed at the same temperature for 1 hour.
【0035】 カヤシオンブルーE−CN 2 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後すすぎ洗いし、ついで98℃の石鹸水で15分間
洗浄した。なお繊維対漂白浴及び染色浴の比はいずれも
1:15である。通常の優れた染色物が得られた。Kayashion Blue E-CN 2% o. w. f. After dyeing, anhydrous sodium sulfate 100 g / l sodium carbonate 20 g / l was rinsed, and then washed with 98 ° C. soapy water for 15 minutes. The ratio of fiber to bleaching bath and dyeing bath was 1:15. The usual excellent dyeings are obtained.
【0036】実施例2.未染色布をまず最初に以下に示
す実施例2−1〜3に示した組成をもつ浴中で80℃の
温度で30分間処理し漂白した。引き続いて浴を排出す
ることなく臭化カリウム(KBr)10g/lを加え9
0℃に昇温し20分間処理した。更に引き続いて浴を排
出することなく60℃にし次の染色薬剤のうち染料と無
水硫酸ナトリウムを加えて同温度で10分間処理した。
続いて結晶リン酸三ナトリウムを加えて同温度で1時間
染色した。染色後注意深く水洗し陰干しして乾燥した。
浴中の繊維対漂白浴及び染色浴の比はいずれも1:15
である。 ダイヤミラターキスブルーG 2 %o.w.f. 無水硫酸ナトリウム 50 g/l 結晶リン酸三ナトリウム 20 g/lEmbodiment 2 FIG. The undyed fabric was first treated in a bath having the composition shown in Examples 2-1 to 3 below at a temperature of 80 ° C. for 30 minutes and bleached. Subsequently, 10 g / l of potassium bromide (KBr) was added without draining the bath.
The temperature was raised to 0 ° C and the treatment was performed for 20 minutes. Subsequently, the temperature was raised to 60 ° C. without draining the bath, and the dyeing agent and anhydrous sodium sulfate were added to the next dyeing agent, followed by treatment at the same temperature for 10 minutes.
Subsequently, crystalline trisodium phosphate was added and staining was performed at the same temperature for 1 hour. After dyeing, it was carefully washed with water, dried in the shade and dried.
The ratio of the fiber in the bath to the bleaching bath and the dyeing bath was 1:15.
It is. Diamond Mira Turkey Blue G 2% o. w. f. Anhydrous sodium sulfate 50 g / l crystalline trisodium phosphate 20 g / l
【0037】実施例2−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 2-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l
【0038】実施例2−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 2-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecandioic acid 2.3 g / l
【0039】実施例2−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 2-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l
【0040】比較例4.未染色布を実施例2と同じく比
較例4−1及び比較例4−2に示した組成の漂白浴中
で、実施例2と同一条件で漂白した。引き続いて実施例
2と同一の染色薬剤を用いて、実施例2と同一条件で染
色処理を施した。Comparative Example 4 The undyed cloth was bleached in the same manner as in Example 2 in a bleaching bath having the composition shown in Comparative Examples 4-1 and 4-2 under the same conditions as in Example 2. Subsequently, using the same staining agent as in Example 2, a staining treatment was performed under the same conditions as in Example 2.
【0041】比較例4−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 4-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l
【0042】比較例4−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちありComparative Example 4-2 12% sodium hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Insufficient bleaching ability ×: Almost no bleaching ability XX: No bleaching ability at all Clarity ○: Practical use △: Slight discoloration ×: Severe discoloration × ×: marked color fading
【0043】実施例3 未染色の木綿とアクリルの50:50の混紡の布(以後
未染色アクリル混紡布と表記する)をまず最初に次に示
す染色薬剤組成の浴中で98℃で1時間染色した。 カヤクリルライトブルー4GSL−ED 1 %o.w.f. 酢酸 0.5 g/l Example 3 A 50:50 blend of undyed cotton and acrylic (hereinafter referred to as undyed acrylic blended fabric) was first prepared at 98 ° C. for 1 hour in a bath of the following dyeing agent composition. Stained. Kayacryl Light Blue 4GSL-ED 1% o. w. f. Acetic acid 0.5 g / l
【0044】次いで浴を排出することなく80℃まで降
温し、以下に示す実施例3−1〜3に示した組成をもつ
浴中で80℃の温度で20分間処理し漂白した。引き続
いて浴を排出することなく食塩10g/lを加え90℃
に昇温し20分間処理した。更に引き続いて浴を排出す
ることなく80℃に下げ次の染色薬剤のうち染料と無水
硫酸ナトリウムを加えて同温度で10分間処理した。続
いて炭酸ナトリウムを加えて同温度で1時間染色した。 カヤシオンターキスE−A 1 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後水洗し、ついで80℃のデモールN 2g/l
(株式会社花王の製品)の浴で15分間洗浄した。浴中
の繊維対漂白浴及び染色浴の比はいずれも1:15であ
る。Then, the temperature was lowered to 80 ° C. without discharging the bath, and the mixture was treated in a bath having the composition shown in Examples 3-1 to 3 below at a temperature of 80 ° C. for 20 minutes to bleach. Subsequently, 10 g / l of sodium chloride was added without draining the bath, and 90 ° C.
And heated for 20 minutes. Subsequently, the temperature was lowered to 80 ° C. without draining the bath, and a dye and anhydrous sodium sulfate were added to the next dyeing agent, followed by treatment at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and staining was performed at the same temperature for 1 hour. Kayashi On Turkey EA 1% o. w. f. Anhydrous sodium sulfate 100 g / l Sodium carbonate 20 g / l After dyeing, washing with water and then 80 g of Demol N 2 g / l
(A product of Kao Corporation) for 15 minutes. The ratio of the fibers in the bath to the bleaching and dyeing baths is 1:15.
【0045】実施例3−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 3-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l
【0046】実施例3−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 3-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecandioic acid 2.3 g / l
【0047】実施例3−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 3-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l
【0048】比較例5.未染色アクリル混紡布を実施例
3と同じくカヤクリルライトブルー4GSL−EDで染
色し、比較例4−1及び比較例4−2に示した組成の漂
白浴中で、実施例3と同一条件で漂白した。引き続いて
実施例3と同一の染色薬剤を用いて、実施例3と同一条
件で染色処理を施した。Comparative Example 5 The undyed acrylic blended fabric is dyed with Kayacryl Light Blue 4GSL-ED in the same manner as in Example 3 and in a bleach bath having the composition shown in Comparative Examples 4-1 and 4-2, under the same conditions as in Example 3. Bleached. Subsequently, a staining treatment was performed using the same staining agent as in Example 3 under the same conditions as in Example 3.
【0049】比較例5−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 5-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l
【0050】比較例5−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちありComparative Example 5-2 12% sodium hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Insufficient bleaching ability ×: Almost no bleaching ability XX: No bleaching ability at all Clarity ○: Practical use △: Slight discoloration ×: Severe discoloration × ×: marked color fading
【0051】実施例4.未染色の木綿とポリエステルの
50:50の混紡の布(以後未染色ポリエステル混紡布
と表記する)をまず最初に耐圧容器中次に示す染色薬剤
組成の浴中で130℃で1時間染色した。 カヤセロンターキスE−GL 1 %o.w.f. 酢酸 0.45 g/l 酢酸ナトリウム(3水塩) 0.55 g/lEmbodiment 4 FIG. A 50:50 blend of undyed cotton and polyester (hereinafter referred to as undyed polyester blend) was first dyed in a pressure vessel at 130 ° C. for 1 hour in a bath of the following dyeing agent composition. Kayaceron Turkish E-GL 1% o. w. f. Acetic acid 0.45 g / l Sodium acetate (trihydrate) 0.55 g / l
【0052】次いで浴を排出することなく80℃まで降
温し、以下に示す実施例4−1〜3に示した組成をもつ
浴中で80℃の温度で20分間処理し漂白した。引き続
いて浴を排出することなく食塩10g/lを加え90℃
に昇温し20分間処理した。更に引き続いて浴を排出す
ることなく80℃に下げ次の染色薬剤のうち染料と無水
硫酸ナトリウムを加えて同温度で10分間処理した。続
いて炭酸ナトリウムを加えて同温度で1時間染色した。 カヤシオンターキスE−A 1 %o.w.f. 無水硫酸ナトリウム 100 g/l 炭酸ナトリウム 20 g/l 染色後水洗し、ついで98℃の石鹸水で15分間洗浄し
た。浴中の繊維対漂白浴及び染色浴の比はいずれも1:
15である。Next, the temperature was lowered to 80 ° C. without discharging the bath, and the mixture was treated in a bath having the composition shown in Examples 4-1 to 3 below at a temperature of 80 ° C. for 20 minutes to bleach. Subsequently, 10 g / l of sodium chloride was added without draining the bath, and 90 ° C.
And heated for 20 minutes. Subsequently, the temperature was lowered to 80 ° C. without draining the bath, and a dye and anhydrous sodium sulfate were added to the next dyeing agent, followed by treatment at the same temperature for 10 minutes. Subsequently, sodium carbonate was added and staining was performed at the same temperature for 1 hour. Kayashi On Turkey EA 1% o. w. f. After dyeing with anhydrous sodium sulfate 100 g / l sodium carbonate 20 g / l, it was washed with water, and then washed with soap water at 98 ° C. for 15 minutes. The ratio of the fibers in the bath to the bleaching and dyeing baths was 1:
Fifteen.
【0053】実施例4−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 40%過酢酸 2 g/lExample 4-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 40% peracetic acid 2 g / l
【0054】実施例4−2 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l 27%ジ過ドデカン二酸 2.3g/lExample 4-2 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l 27% diperdodecandioic acid 2.3 g / l
【0055】実施例4−3 メタケイ酸ナトリウム 4 g/l カヤキレーターC−1000 10 g/l H−48 15.6g/lExample 4-3 Sodium metasilicate 4 g / l Kayachelator C-1000 10 g / l H-48 15.6 g / l
【0056】比較例6.未染色ポリエステル混紡布をま
ず最初に耐圧容器中次に示す染色薬剤組成の浴中で13
0℃で1時間染色した。 カヤセロンターキスE−GL 1 %o.w.f. 酢酸 0.45 g/l 酢酸ナトリウム(3水塩) 0.55 g/l 次いで浴を排出することなく80℃まで降温し、実施例
4と同じく比較例5−1及び比較例5−2に示した組成
の漂白浴中で、実施例4と同一条件で漂白した。引き続
いて実施例4と同一の染色薬剤を用いて、実施例4と同
一条件で染色処理を施した。Comparative Example 6 The undyed polyester blended fabric is first placed in a pressure vessel and then into a bath of the following dyeing agent composition.
Stained for 1 hour at 0 ° C. Kayaceron Turkish E-GL 1% o. w. f. Acetic acid 0.45 g / l Sodium acetate (trihydrate) 0.55 g / l Then, the temperature was lowered to 80 ° C. without draining the bath, and the same as in Example 4, Comparative Example 5-1 and Comparative Example 5-2 Bleaching was carried out in a bleaching bath of the indicated composition under the same conditions as in Example 4. Subsequently, using the same staining agent as in Example 4, a staining treatment was performed under the same conditions as in Example 4.
【0057】比較例6−1 メタケイ酸ナトリウム 4 g/l 炭酸ナトリウム 20 g/l カヤキレーターC−1000 10 g/l 30%過酸化水素 2.7g/lComparative Example 6-1 Sodium metasilicate 4 g / l Sodium carbonate 20 g / l Kayachelator C-1000 10 g / l 30% hydrogen peroxide 2.7 g / l
【0058】比較例6−2 12%次亜塩素酸ナトリウム 0.9g/l 漂白能○:充分な漂白能あり △:漂白能不充分 ×:漂白能ほとんどなし ××:漂白能全くなし 鮮明度○:実用に耐える △:僅かに色落ちあ
り ×:かなりの色落ちあり ××:著しい色落ちありComparative Example 6-2 12% sodium hypochlorite 0.9 g / l Bleaching ability ○: Sufficient bleaching ability △: Insufficient bleaching ability ×: Almost no bleaching ability XX: No bleaching ability at all Clarity ○: Practical use △: Slight discoloration ×: Severe discoloration × ×: marked color fading
【0059】[0059]
【発明の効果】本発明の染色漂白剤を使用すると繊維の
漂白工程と染色工程との間に従来必要であった排出操作
及び/又は洗浄の回数を減らし且つ水及び加熱のための
熱量の節約、洗浄及び/又は排出に要する時間の節約、
水処理に関する改善などを得ることができる。The use of the dye bleach of the present invention reduces the number of discharge operations and / or washes conventionally required between the fiber bleaching and dyeing steps and saves water and heat for heating. Saving the time required for cleaning and / or draining,
Improvements in water treatment can be obtained.
───────────────────────────────────────────────────── フロントページの続き (58)調査した分野(Int.Cl.7,DB名) D06P 5/00 D06B 21/00 D06L 3/02 ──────────────────────────────────────────────────続 き Continued on the front page (58) Field surveyed (Int. Cl. 7 , DB name) D06P 5/00 D06B 21/00 D06L 3/02
Claims (2)
で表わされる有機過酸またはそれらの塩もしくは錯体か
らなる漂白剤で漂白し、引き続き下記一般式(2)で表
わされる塩を使用して漂白剤を分解し、漂白後浴を排出
することなく、引き続いて染色を施すことを特徴とする
繊維の漂白染色法。 一般式(1) 【化1】 (但し、Rは置換または非置換のアルキル基、アリル基
またはアラルキル基、nは1〜6の自然数を示す。) 一般式(2) R1 X (但し、R1 は金属イオン又は置換または非置換の4級
アンモニウム基を示し、Xはハロゲンイオンを示す。)1. When dyeing a fiber, the following general formula (1)
, Bleaching with a bleach comprising an organic peracid or a salt or complex thereof, followed by decomposition of the bleach using a salt represented by the following general formula (2), and without discharging the bath after bleaching. Bleaching and dyeing of fibers, characterized by successively dyeing. General formula (1) (However, R represents a substituted or unsubstituted alkyl group, allyl group or aralkyl group, and n represents a natural number of 1 to 6.) General formula (2) R 1 X (where R 1 is a metal ion or substituted or unsubstituted) X represents a substituted quaternary ammonium group, and X represents a halogen ion.)
繊維と混合したセルロース繊維である第1項記載の繊維
の漂白染色法。2. The method for bleach-dyeing fibers according to claim 1, wherein the fibers are cellulose fibers alone or mixed with other fibers.
Priority Applications (1)
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JP25021891A JP3165475B2 (en) | 1991-09-04 | 1991-09-04 | Fiber bleach dyeing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP25021891A JP3165475B2 (en) | 1991-09-04 | 1991-09-04 | Fiber bleach dyeing method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0571082A JPH0571082A (en) | 1993-03-23 |
JP3165475B2 true JP3165475B2 (en) | 2001-05-14 |
Family
ID=17204592
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WO2000017437A1 (en) * | 1998-09-19 | 2000-03-30 | A. Monforts Textilmaschinen Gmbh & Co. | Process for preparative and reactive dyeing of cellulose material |
CN103541169B (en) * | 2013-09-26 | 2015-06-17 | 浙江大港印染有限公司 | Method for producing computer cross-stitch printed and dyed cloth |
CN103981740A (en) * | 2014-05-16 | 2014-08-13 | 苏州市吴中区大明针织漂染有限公司 | Pad dyeing staining method |
CN104328615A (en) * | 2014-11-19 | 2015-02-04 | 南充嘉美印染有限公司 | Batik fabric pretreatment device and method |
CN108708119A (en) * | 2018-06-21 | 2018-10-26 | 浙江美欣达纺织印染科技有限公司 | Based on the elastic polyurethane fiber cloth production process for evaporating shrinking process |
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