TWI434976B - 增進熱安定性之方法 - Google Patents
增進熱安定性之方法 Download PDFInfo
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- TWI434976B TWI434976B TW096114178A TW96114178A TWI434976B TW I434976 B TWI434976 B TW I434976B TW 096114178 A TW096114178 A TW 096114178A TW 96114178 A TW96114178 A TW 96114178A TW I434976 B TWI434976 B TW I434976B
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- alkyl
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- 238000000034 method Methods 0.000 title claims description 18
- 239000000203 mixture Substances 0.000 claims description 45
- -1 alkali metal cation Chemical class 0.000 claims description 30
- 239000002657 fibrous material Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 17
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 11
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 9
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 9
- 150000002431 hydrogen Chemical class 0.000 claims description 8
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 7
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 239000000126 substance Substances 0.000 claims description 7
- 229920002994 synthetic fiber Polymers 0.000 claims description 7
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 6
- GJVFBWCTGUSGDD-UHFFFAOYSA-L pentamethonium bromide Chemical compound [Br-].[Br-].C[N+](C)(C)CCCCC[N+](C)(C)C GJVFBWCTGUSGDD-UHFFFAOYSA-L 0.000 claims description 6
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 5
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 150000007524 organic acids Chemical class 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 239000004758 synthetic textile Substances 0.000 claims description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-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
- 239000002253 acid Substances 0.000 claims description 4
- 239000003945 anionic surfactant Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 239000000434 metal complex dye Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
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- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- 239000007787 solid Substances 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 3
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 150000001412 amines Chemical group 0.000 claims description 3
- 125000000129 anionic group Chemical group 0.000 claims description 3
- 235000015165 citric acid Nutrition 0.000 claims description 3
- 150000004696 coordination complex Chemical class 0.000 claims description 3
- 239000000986 disperse dye Substances 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 235000006408 oxalic acid Nutrition 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 235000002906 tartaric acid Nutrition 0.000 claims description 3
- 239000011975 tartaric acid Substances 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000000980 acid dye Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000005577 anthracene group Chemical group 0.000 claims description 2
- 239000004305 biphenyl Substances 0.000 claims description 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 2
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 claims description 2
- 125000000542 sulfonic acid group Chemical group 0.000 claims 2
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims 1
- 239000004753 textile Substances 0.000 description 21
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- 239000000243 solution Substances 0.000 description 5
- 210000002268 wool Anatomy 0.000 description 5
- 239000007864 aqueous solution Substances 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000009998 heat setting Methods 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 229920002334 Spandex Polymers 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000002087 whitening effect Effects 0.000 description 3
- CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- 241000208202 Linaceae Species 0.000 description 2
- 235000004431 Linum usitatissimum Nutrition 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 150000008051 alkyl sulfates Chemical class 0.000 description 2
- 239000012752 auxiliary agent Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 239000006081 fluorescent whitening agent Substances 0.000 description 2
- 229940093915 gynecological organic acid Drugs 0.000 description 2
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 238000000465 moulding Methods 0.000 description 2
- GXELTROTKVKZBQ-UHFFFAOYSA-N n,n-dibenzylhydroxylamine Chemical compound C=1C=CC=CC=1CN(O)CC1=CC=CC=C1 GXELTROTKVKZBQ-UHFFFAOYSA-N 0.000 description 2
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000012209 synthetic fiber Substances 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 150000003628 tricarboxylic acids Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920001174 Diethylhydroxylamine Polymers 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002292 Nylon 6 Polymers 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 210000000077 angora Anatomy 0.000 description 1
- JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960004365 benzoic acid Drugs 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920003086 cellulose ether Polymers 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- FVCOIAYSJZGECG-UHFFFAOYSA-N diethylhydroxylamine Chemical compound CCN(O)CC FVCOIAYSJZGECG-UHFFFAOYSA-N 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
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- 150000002334 glycols Chemical class 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
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- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 210000000050 mohair Anatomy 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- PAZXUKOJTOTKBK-UHFFFAOYSA-N n,n-dibutylhydroxylamine Chemical compound CCCCN(O)CCCC PAZXUKOJTOTKBK-UHFFFAOYSA-N 0.000 description 1
- VMESOKCXSYNAKD-UHFFFAOYSA-N n,n-dimethylhydroxylamine Chemical compound CN(C)O VMESOKCXSYNAKD-UHFFFAOYSA-N 0.000 description 1
- NCLWMRHNDKORFM-UHFFFAOYSA-N n-benzyl-n-methylhydroxylamine Chemical compound CN(O)CC1=CC=CC=C1 NCLWMRHNDKORFM-UHFFFAOYSA-N 0.000 description 1
- 125000006606 n-butoxy group Chemical group 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003506 n-propoxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical compound CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 230000004792 oxidative damage Effects 0.000 description 1
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000002530 phenolic antioxidant Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- PFIOPNYSBSJFJJ-UHFFFAOYSA-M sodium;2-octylbenzenesulfonate Chemical compound [Na+].CCCCCCCCC1=CC=CC=C1S([O-])(=O)=O PFIOPNYSBSJFJJ-UHFFFAOYSA-M 0.000 description 1
- RLJSXMVTLMHXJS-UHFFFAOYSA-M sodium;4-decylbenzenesulfonate Chemical compound [Na+].CCCCCCCCCCC1=CC=C(S([O-])(=O)=O)C=C1 RLJSXMVTLMHXJS-UHFFFAOYSA-M 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 235000018553 tannin Nutrition 0.000 description 1
- 229920001864 tannin Polymers 0.000 description 1
- 239000001648 tannin Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000009997 thermal pre-treatment Methods 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/325—Amines
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Description
本發明係關於一種助劑組成物,以及一種改善未染色、經螢光增白或經染色的天然或合成紡織纖維材料之熱安定性的方法。
在各種紡織處理的步驟中(預處理、螢光增白劑的施用、染色、加工),紡織纖維材料係暴露於熱處理。尤其就未染色且可能已經螢光增白的產品而言,此經常導致不想要的黃化。
在染色之前或之後,熱的作用亦常導致不想要的影響。例如,熱預處理可能導致對聚醯胺的氧化傷害,其自身表露在例如增加的黃化或者張力強度的損失,或者其亦可在染色性上產生負作用。
染色步驟後的熱處理可同樣地導致無法接受的色澤變樣。
已發現上述不利影響可藉特定紡織助劑的使用而實質地減少。
本發明係關於一種組成物,包含(A)以總組成物計,從5至95重量%的至少一種式(1a)或(1b)化合物Y1
-X-Y2
(1a) A1
A2
N-OH (1b)其中X為二價的脂肪族、芳香族、芳脂族或環脂族基,Y1
及Y2
係各彼此獨立為-OH、-CO-OR1
-、NR1
R2
、-CO-NH-NR1
R2
或-NH-CO-NH-NR1
R2
,其中R1
及R2
係各彼此獨立為氫、C1
-C20
烷基、C1
-C20
烷氧基、C5
-C24
環烷基、C5
-C30
芳基或C6
-C36
芳烷基,且該烷基、烷氧基、環烷基、芳基或芳烷基可能為未取代,或被一或多個羥基、胺基、磺酸基或羧基或鹵素原子所取代,A1
及A2
係各彼此獨立為C1
-C20
烷基或C6
-C36
芳烷基;(B)以總組成物計,從0至95重量%的一或多種陰離子或非離子界面活性劑或分散劑;以及(C)以總組成物計,從0至85重量%的固體無機或有機酸;在各例中,組份A+B+C的總量為100重量%。
式(1a)中,脂肪族基X係例如為伸乙基、伸丙基、三亞甲基、丙烷-1,1-二基、四亞甲基、六亞甲基、八亞甲基或十亞甲基,或者直鏈或支鏈的被一或多個氧原子或-NH-、-N-烷基-或-N-伸烷基-NH2
-基團所中斷的伸烷基。
適合的環脂族基X係例如為環己烷-1,2-二基、環己烷-1,3-二基、環己烷-1,4-二基,以及與。
芳香族基X之實例為1,2-伸苯基、1,3-伸苯基、1,4-伸苯基、伸聯苯基、1,2-萘二基、1,3-萘二基、1,4-萘二基、1,5-萘二基、1,6-萘二基、1,8-萘二基、2,3-萘二基、2,6-萘二基、2,7-萘二基,以及與。
二價芳脂族基係例如為及。
作為基團R1
、R2
、A1
或A2
之C1
-C20
烷基可例如為甲基、乙基、正丙基、異丙基、正丁基、異丁基、第二丁基、第三丁基、正戊基、新戊基、正己基、正辛基或者正十二烷基。
作為基團R1
或R2
之C1
-C20
烷氧基實例為甲氧基、乙氧基、正丙氧基、異丙氧基、正丁氧基、異丁氧基、第二丁氧基、第三丁氧基、正戊氧基、新戊氧基、正己氧基、正辛氧基或者正十二烷氧基。
適合的C5
-C24
環烷基係例如為環戊基、環己基及十氫萘基。
作為基團R1
或R2
之C5
-C30
芳基係例如為苯基、甲苯基、2,4,6-三甲基苯基、2,4,6-三異丙基苯基、萘基或蒽基。
適合的C6
-C36
芳烷基係例如為苄基及2-苯基乙基。
較佳者為式(1a)化合物的使用,其中X為伸乙基、伸丙基、三亞甲基、四亞甲基、五亞甲基、六亞甲基、八亞甲基、伸苯基或亞甲基-對-二伸苯基。
較佳者係進一步為式(1a)化合物,其中Y1
及Y2
為NR1
R2
、-CO-NH-NR1
R2
或-NH-CO-NH-NR1
R2
,其中R1
及R2
為氫、C1
-C12
烷基或C5
-C24
芳基。
尤其較佳者為式(1a)化合物,其中Y1
及Y2
為NR1
R2
、-CO-NH-NR1
R2
或-NH-CO-NH-NR1
R2
,其中R1
及R2
為氫、甲基或苯基。
適合的通式(1a)化合物之實例為式(101)-(105)之化合物:
式(1a)化合物為已知,且可藉已知方法合成。
適合的式(1b)化合物為N,N-二甲基羥基胺、N,N-二乙基羥基胺、N,N-二正丁基羥基胺、N,N-二苄基羥基胺,及N-苄基-N-甲基羥基胺。
原則上,任何陰離子或非離子界面活性劑或分散劑皆可在根據本發明之組成物中用作組份B。
適合的陰離子界面活性劑實例為烷基磺酸鹽、烷基苯磺酸鹽、烷基萘磺酸鹽、烷基硫酸鹽、烷基醚硫酸鹽、乙氧化或丙氧化的芳基硫酸鹽、乙氧化或丙氧化的芳基磷酸鹽、乙氧化或丙氧化的芳烷基硫酸鹽,及乙氧化或丙氧化的芳烷基磷酸鹽。
適合的非離子界面活性劑係例如為脂肪醇聚乙二醇醚、烷基酚聚乙二醇醚、脂肪酸去水山梨醇酯、脂肪酸聚乙二醇酯、氧化乙烯/氧化丙烯嵌段聚合物,以及脂肪酸聚甘油酯。
根據本發明之組成物中,作為組份B,較佳者為式(2)化合物之使用:R-Z-SO3
M (2)其中Z為二價芳香族基,R1
為C1
-C20
烷基、C1
-C20
烷氧基、C5
-C24
環烷基、C5
-C30
芳基、C6
-C36
芳烷基、-NHR3
、-NR4
R5
、-NHCOR6
或-NR7
COR8
,其中R3
、R4
、R5
、R6
、R7
及R8
係各彼此獨立為C1
-C20
烷基、C1
-C20
烷氧基、C5
-C24
環烷基、C5
-C30
芳基或C6
-C36
芳烷基,該烷基、烷氧基、環烷基、芳基或芳烷基可能為未取代,或被一或多個羥基,胺基、磺酸基或羧基或鹵素原子所取代,且M為氫、鹼金屬陽離子或未取代的銨離子,或被一或多個C1
-C20
烷基所取代的銨離子。
式(2)中,Z係較佳為伸苯基或伸萘基,且R係較佳為C1
-C20
烷基。
尤其較佳之組份B為式(2a)、(2b)、(2c)及(2d)化合物,
其中R9
為C1
-C20
烷基,R10
、R11
、R12
、R13
、R14
及R15
係各彼此獨立為氫或C1
-C20
烷基,n為從1至10之數字,且M係如前文所定義。
適合的式(2a)化合物係例如為辛基苯磺酸鈉、壬基苯磺酸鈉,以及十二烷基苯磺酸鈉。
在根據本發明之組成物中,作為組份B,較佳者為烷基苯磺酸鹽或烷基硫酸鹽之使用。
在本發明上下文中,適合作為根據本發明之組成物的組份C之固體無機或有機酸,應理解為具有熔點F>40℃的化合物。
多元鹼無機酸及其酸式鹽兩者,例如H3
PO4
、NaH2
PO4
、H4
P2
O7
、Na2
H2
P2
O7
及Na2
H4
P3
O10
,以及未取代或取代的有機單、二元或三元羧酸或磺酸,皆適合用於該目的。
適合的固體有機酸之實例為單羧酸,例如苯甲酸、水楊酸、抗壞血酸及甲苯甲酸;二元羧酸,例如草酸、丙二酸、丁二酸、戊二酸、己二酸、庚二酸、辛二酸、壬二酸、癸二酸、順丁烯二酸、反丁烯二酸、杏仁酸、蘋果酸、酒石酸、檸檬酸及消旋酒石酸;以及三元羧酸,例如偏苯三甲酸。
適合作為本發明上下文中的組份C之額外有機酸,為分子量(重量平均)Mw>200的含羧基寡聚物或聚合物,例如不飽和羧酸如丙烯酸、甲基丙烯酸或丁烯酸的同元或共聚物。
α-羥基羧酸係較佳用作組份C。
特別較佳者為酒石酸、草酸、己二酸及檸檬酸。
根據本發明之組成物中,組份A、B及C的量可在廣範圍內變化。
較佳者為以總組成物計,包含從10至50重量%,尤其是從20至40重量%的組份A,從44至85重量%,尤其是從55至75重量%的組份B,以及從0至75重量%,尤其是從10至60重量%的組份C之組成物。
本發明係關於一種改善未染色、經螢光增白或經反應性酸、金屬錯合物或分散性染料染色的天然或合成紡織纖維材料之熱安定性的方法,其中該纖維材料係以包含一種包含上述組份A、B及C的組成物之藥液處理。
可使用根據本發明之方法處理的紡織纖維材料可為天然或合成纖維,且亦可為其混合物。天然纖維之實例為植物纖維,例如棉花、黏液纖維、亞麻、嫘縈或亞麻;以及動物纖維,例如羊毛、馬海羊毛、喀什米爾羊毛、安哥拉羊毛以及絲。合成纖維係例如為聚酯、聚醯胺、聚胺甲酸酯,以及聚丙烯腈纖維。
根據本發明之方法尤其適合用於聚醯胺纖維材料之處理。
作為聚醯胺纖維材料,可考慮天然的聚醯胺纖維材料,例如羊毛或絲;或者合成的聚醯胺纖維材料,例如聚醯胺6或聚醯胺6.6;或者纖維混合物,例如羊毛/纖維素、聚醯胺/纖維素、聚醯胺/羊毛、聚醯胺/聚酯,或尤其是聚醯胺/彈性纖維混合物。該纖維材料係較佳為合成的聚醯胺纖維材料。
紡織材料可以任何型式使用,例如以纖維、紗、編織纖維或針織纖維之型式。
用於根據本發明之方法、包含定義於上的組份A、B、C之助劑組成物,係有利地以從0.1克/升至100克/升,較佳從0.5克/升至50克/升,且尤其是從1.0克/升至40克/升的量存在於藥液中。
根據本發明之組成物可藉常用的染色或印花方法施用至紡織纖維材料,例如藉噴灑施用或泡沫施用、藉染料吸盡法,或者較佳藉壓染法。
特殊裝置並非為必須。舉例來說,可使用常用的染色裝置,例如開放浴、繩狀染槽、交捲染色機,或者漿翼式、噴射或循環裝置。
除了包含水及根據本發明之紡織助劑外,藥液可包含額外的添加劑,例如潤濕劑、抗發泡劑、均染劑、螢光增白劑,或可影響紡織材料性質的藥劑,例如軟化劑、防火劑或防塵、水及油劑,亦及軟水劑及天然或合成稠化劑,例如褐藻酸鹽及纖維素醚。
如上所述,根據本發明之方法可有利地用於可能已使用螢光增白劑處理的未染色紡織纖維材料(增白織物)以及已染色的紡織纖維材料兩者之熱安定化。
至於未染色或經螢光增白的紡織纖維材料,因熱定型期間(熱風)或模製程序期間(接觸熱)之熱處理導致的黃化被預防或降低。
根據本發明之方法在經螢光增白的紡織纖維材料之處理中尤其有效。
在經染色的紡織纖維材料之熱安定化中,根據本發明之組成物可在染色之前、期間或之後施用。
當組成物在染色之前使用時,可預防或降低未染色產品在所謂預定型期間之黃化。
根據本發明之組成物係較佳在紡織纖維材料經反應性酸、金屬錯合物或分散性染料染色後施用。
使用根據本發明之紡織助劑的經染色紡織纖維材料之後處理,尤其在後定型(熱定型)期間引起了某種程度的纖維保護作用,且有效地降低在該處理步驟中常發生的色澤改變,亦即色澤維持不變,且無消光及色彩強度的損失。
至於未染色或經螢光增白的紡織纖維材料,在使用根據本發明之組成物處理後,未觀察到可見的白度降低。
令人驚訝地,已發現使用根據本發明之組成物處理紡織纖維材料亦引起耐臭氧、NOx
及氯堅牢度之改善。
本發明相應地亦關於一種改善未染色、經螢光增白或經反應性酸、金屬錯合物或分散性染料染色的天然或合成紡織纖維材料之耐臭氧、NOx
及氯堅牢度之方法,其中該纖維材料係以包含一種包含上述組份A、B及C的組成物之藥液處理。
所謂的儲存黃化,亦即在紡織材料儲存期間發生的黃化,出乎意料地亦可藉根據本發明之組成物處理而有效地降低。對儲存黃化的抵抗性一般係使用Courtauld黃化測試而測量。
由Courtauld公司開發且進一步由Mark&Spencer發展的Courtauld測試,為一種在紡織工業中已建立用於評估對由酚抗氧化劑所導致黃化之敏感性的測試。
以根據本發明之組成物處理的紡織纖維材料具有高的Courtauld堅牢度。
根據本發明之組成物可包含例如潤濕劑、分散劑或pH調節劑作為額外的添加劑。
以下實施例係用以解釋本發明。除非另有指示,溫度係以攝氏度數提供,”份”及”重量份”以及”百分率”係相關於”重量百分率”。”重量份”以公斤對公升的同樣比例相關於”體積份”。
(a)漂白方法以含2.0% UvitexNFW液(螢光增白劑,汽巴(Ciba)特用化學)及1.0克/升UltravonEL(分散劑,汽巴特用化學)的藥液水溶液,藉染料吸盡法處理聚醯胺6.6締捲經編物。以醋酸調整pH至4.5。
藥液比1:20,30分鐘/95℃。
(b)助劑的施用以包含表1規定的助劑組成物之藥液水溶液,藉壓染法處理增白織物。
藥液浸吸量100%;在70℃下乾燥根據Ganz之白度:230
接著將該織物進行熱定型測試(60秒/210℃)以及模製測試(60秒/210℃);與未處理材料相比之結果列於表2:
以pH 4.5、含1.7% LanasetBlue 2R(汽巴特用化學)及1.0% LanasetViolet B(汽巴特用化學)之藥液水溶液,以染料吸盡法將聚醯胺6.6/彈性纖維織物(82:18)染色。
在各例中,以含30克/升由30%己二醯二肼與70%IrgasolDAM(分散劑,汽巴特用化學)(實施例14),或30%己二醯二肼與70% TamolNN 904(分散劑)(實施例15),或30%己二醯二肼與70%十二烷基苯磺酸鈉(實施例16)組成之助劑組成物的藥液水溶液,以壓染法(藥液浸吸量約70%)在70℃下將以該方法預染色的織物處理2分鐘,然後熱定型(60秒/180℃)。接著對染色的織物進行氯水浴測試(100 ppm Cl2
)。表3顯示與參照物相比(未處理的染色織物)之色澤偏差(DEF值)。
Claims (13)
- 一種組成物,其包含:(A)以總組成物計,從5至95重量%的至少一種式(1a)或(1b)化合物Y1 -X-Y2 (1a) A1 A2 N-OH (1b)其中X為二價的脂肪族、芳香族、芳脂族或環脂族基,Y1 及Y2 係各彼此獨立為-OH、-CO-OR1 -、NR1 R2 、-CO-NH-NR1 R2 或-NH-CO-NH-NR1 R2 ,其中R1 及R2 係各彼此獨立為氫、C1 -C20 烷基、C1 -C20 烷氧基、C5 -C24 環烷基、C5 -C30 芳基或C6 -C36 芳烷基,且該烷基、烷氧基、環烷基、芳基或芳烷基可能為未取代,或被一或多個羥基、胺基、磺酸基或羧基或鹵素原子所取代,A1 及A2 係各彼此獨立為C1 -C20 烷基或C6 -C36 芳烷基;(B)以總組成物計,從0至95重量%的一或多種式(2)化合物作為陰離子或非離子界面活性劑或分散劑,R-Z-SO3 M (2)其中Z為二價芳香族基,R1 為C1 -C20 烷基、C1 -C20 烷氧基、C5 -C24 環烷基、C5 -C30 芳基、C6 -C36 芳烷基、-NHR3 、-NR4 R5 、-NHCOR6 或-NR7 COR8 ,其中R3 、R4 、R5 、R6 、R7 及R8 係各彼此獨立為C1 -C20 烷基、C1 -C20 烷氧基、C5 -C24 環烷基、C5 -C30 芳基或C6 -C36 芳烷基, 該烷基、烷氧基、環烷基、芳基或芳烷基係可能為未取代,或被一或多個羥基、胺基、磺酸基或羧基或鹵素原子所取代,且M為氫、鹼金屬陽離子或未取代的銨離子,或者被一或多個C1 -C20 烷基所取代的銨離子;以及(C)以總組成物計,從0至85重量%的固體無機或有機酸;且在各例中,組份A+B+C的總量為100重量%。
- 如申請專利範圍第1項之組成物,其包含式(1a)化合物作為組份A,其中X為伸乙基、伸丙基、三亞甲基、四亞甲基、五亞甲基、六亞甲基、八亞甲基、伸苯基,或者亞甲基-對-二伸苯基。
- 如申請專利範圍第1項之組成物,其包含式(1a)化合物作為組份A,其中Y1 及Y2 為NR1 R2 、-CO-NH-NR1 R2 或-NH-CO-NH-NR1 R2 ,其中R1 及R2 為氫、C1 -C12 烷基或C5 -C24 芳基。
- 如申請專利範圍第1項之組成物,其包含式(1a)化合物作為組份A,其中Y1 及Y2 為NR1 R2 、-CO-NH-NR1 R2 或-NH-CO-NH-NR1 R2 ,其中R1 及R2 為氫、甲基或苯基。
- 如申請專利範圍第1項之組成物,其包含式(101)-(105)化合物作為組份A:
- 如申請專利範圍第1項之組成物,其包含式(1b)化合物作為組份A,其中A1 及A2 為乙基。
- 如申請專利範圍第1項之組成物,其包含式(2)化合物作為組份B,其中Z為伸苯基或伸萘基,且R為C1 -C20 烷基。
- 如申請專利範圍第1項之組成物,其包含式(2a)、(2b)、(2c)或(2d)化合物作為組份B,
- 如申請專利範圍第1項之組成物,其包含烷基苯磺酸鹽作為組份B。
- 如申請專利範圍第1項之組成物,其包含α-羥基羧酸作為組份C。
- 如申請專利範圍第1項之組成物,其包含酒石酸、草酸、己二酸或檸檬酸作為組份C。
- 一種方法,其係改善未染色、經螢光增白或經反應性酸、金屬錯合物或分散性染料染色的天然或合成紡織纖維材料之熱安定性,其中該纖維材料係以一種包含如申請專利範圍第1項之組成物的藥液處理。
- 一種方法,其係改善未染色、經螢光增白或經反應性酸、金屬錯合物或分散性染料染色的天然或合成紡織纖維材料耐臭氧、NOx 及氯堅牢度,其中該纖維材料係以一種包含如申請專利範圍第1項之組成物的藥液處理。
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