CA2073580A1 - Process for printing and photochemically stabilising polyester fibre materials - Google Patents

Process for printing and photochemically stabilising polyester fibre materials

Info

Publication number: CA2073580A1
Authority: CA; Canada
Prior art keywords: absorber; formula; c5alkyl; hydrogen; c5alkoxy
Prior art date: 1991-07-12
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.): Abandoned

Application number

CA002073580A

Other languages

English (en)

French (fr)

Inventor

Rudolf Rommel

Peter Liechti

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.)

BASF Schweiz AG

Original Assignee

Individual

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.)

1991-07-12

Filing date

1992-07-10

Publication date

1993-01-13

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=4225570&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2073580(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1992-07-10 Application filed by Individual filed Critical Individual

1993-01-13 Publication of CA2073580A1 publication Critical patent/CA2073580A1/en

Status Abandoned legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 36
239000000463 material Substances 0.000 title claims abstract description 29
229920000728 polyester Polymers 0.000 title claims abstract description 20
238000007639 printing Methods 0.000 title claims abstract description 20
239000000835 fiber Substances 0.000 title claims abstract description 18
230000003019 stabilising effect Effects 0.000 title claims abstract description 7
239000006096 absorbing agent Substances 0.000 claims abstract description 37
239000000986 disperse dye Substances 0.000 claims abstract description 10
238000010438 heat treatment Methods 0.000 claims abstract description 5
-1 chloro, hydroxy Chemical group 0.000 claims description 35
229910052739 hydrogen Inorganic materials 0.000 claims description 20
239000001257 hydrogen Substances 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 14
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
229910052736 halogen Inorganic materials 0.000 claims description 10
150000002367 halogens Chemical class 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000001424 substituent group Chemical group 0.000 claims description 5
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 3
NJCDRURWJZAMBM-UHFFFAOYSA-N 6-phenyl-1h-1,3,5-triazin-2-one Chemical group OC1=NC=NC(C=2C=CC=CC=2)=N1 NJCDRURWJZAMBM-UHFFFAOYSA-N 0.000 claims description 2
125000004423 acyloxy group Chemical group 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
125000005647 linker group Chemical group 0.000 claims description 2
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
125000003944 tolyl group Chemical group 0.000 claims description 2
125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical group C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims 1
RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical group C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims 1
239000012965 benzophenone Substances 0.000 claims 1
239000012964 benzotriazole Substances 0.000 claims 1
125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 1
230000002708 enhancing effect Effects 0.000 claims 1
238000000859 sublimation Methods 0.000 claims 1
230000008022 sublimation Effects 0.000 claims 1
125000005023 xylyl group Chemical group 0.000 claims 1
239000000975 dye Substances 0.000 description 18
239000004744 fabric Substances 0.000 description 13
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 12
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 10
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
239000002253 acid Substances 0.000 description 8
239000000203 mixture Substances 0.000 description 8
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
239000006185 dispersion Substances 0.000 description 6
QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 6
150000002431 hydrogen Chemical class 0.000 description 5
239000002562 thickening agent Substances 0.000 description 5
238000010023 transfer printing Methods 0.000 description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 4
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 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
238000009835 boiling Methods 0.000 description 4
239000003795 chemical substances by application Substances 0.000 description 4
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 4
239000000976 ink Substances 0.000 description 4
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
239000003755 preservative agent Substances 0.000 description 4
239000011734 sodium Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000004753 textile Substances 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
238000009472 formulation Methods 0.000 description 3
125000000623 heterocyclic group Chemical group 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
150000003254 radicals Chemical class 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000005406 washing Methods 0.000 description 3
IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 2
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
YEJRWHAVMIAJKC-UHFFFAOYSA-N 4-Butyrolactone Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000007798 antifreeze agent Substances 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
229920001222 biopolymer Polymers 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000002738 chelating agent Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000010276 construction Methods 0.000 description 2
MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000004665 fatty acids Chemical class 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
150000004676 glycans Chemical class 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
238000003801 milling Methods 0.000 description 2
239000011707 mineral Substances 0.000 description 2
RKISUIUJZGSLEV-UHFFFAOYSA-N n-[2-(octadecanoylamino)ethyl]octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(=O)NCCNC(=O)CCCCCCCCCCCCCCCCC RKISUIUJZGSLEV-UHFFFAOYSA-N 0.000 description 2
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
239000002736 nonionic surfactant Substances 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 2
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 2
229920001282 polysaccharide Polymers 0.000 description 2
239000005017 polysaccharide Substances 0.000 description 2
230000002829 reductive effect Effects 0.000 description 2
229920002545 silicone oil Polymers 0.000 description 2
239000000661 sodium alginate Substances 0.000 description 2
235000010413 sodium alginate Nutrition 0.000 description 2
229940005550 sodium alginate Drugs 0.000 description 2
JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
230000008719 thickening Effects 0.000 description 2
239000003799 water insoluble solvent Substances 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 description 1
BGJSXRVXTHVRSN-UHFFFAOYSA-N 1,3,5-trioxane Chemical compound C1OCOCO1 BGJSXRVXTHVRSN-UHFFFAOYSA-N 0.000 description 1
LNBSDTJULOKQCT-UHFFFAOYSA-N 2-(4,6-diethyl-1,3,5-triazin-2-yl)-4,5-dimethylphenol Chemical compound CCC1=NC(CC)=NC(C=2C(=CC(C)=C(C)C=2)O)=N1 LNBSDTJULOKQCT-UHFFFAOYSA-N 0.000 description 1
RJBNOOYPPQJCJT-UHFFFAOYSA-N 2-(4,6-dimethyl-1,3,5-triazin-2-yl)-4,6-dimethylphenol Chemical compound CC1=CC(C)=C(O)C(C=2N=C(C)N=C(C)N=2)=C1 RJBNOOYPPQJCJT-UHFFFAOYSA-N 0.000 description 1
DUUPYWGBKXYZIZ-UHFFFAOYSA-N 2-(4,6-dimethyl-1,3,5-triazin-2-yl)-4-methylphenol Chemical compound CC1=CC=C(O)C(C=2N=C(C)N=C(C)N=2)=C1 DUUPYWGBKXYZIZ-UHFFFAOYSA-N 0.000 description 1
OJADXDOGYHVWDN-UHFFFAOYSA-N 2-(4,6-dimethyl-1,3,5-triazin-2-yl)phenol Chemical compound CC1=NC(C)=NC(C=2C(=CC=CC=2)O)=N1 OJADXDOGYHVWDN-UHFFFAOYSA-N 0.000 description 1
OFJFRCRFNOCFPW-UHFFFAOYSA-N 2-(4,6-dioctyl-1,3,5-triazin-2-yl)phenol Chemical compound CCCCCCCCC1=NC(CCCCCCCC)=NC(C=2C(=CC=CC=2)O)=N1 OFJFRCRFNOCFPW-UHFFFAOYSA-N 0.000 description 1
IGFDJZRYXGAOKQ-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-ethoxyphenol Chemical compound OC1=CC(OCC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 IGFDJZRYXGAOKQ-UHFFFAOYSA-N 0.000 description 1
UUINYPIVWRZHAG-UHFFFAOYSA-N 2-(4,6-diphenyl-1,3,5-triazin-2-yl)-5-methoxyphenol Chemical compound OC1=CC(OC)=CC=C1C1=NC(C=2C=CC=CC=2)=NC(C=2C=CC=CC=2)=N1 UUINYPIVWRZHAG-UHFFFAOYSA-N 0.000 description 1
VQTWLUCKWLXPPS-UHFFFAOYSA-N 2-(4,6-dipropyl-1,3,5-triazin-2-yl)phenol Chemical compound CCCC1=NC(CCC)=NC(C=2C(=CC=CC=2)O)=N1 VQTWLUCKWLXPPS-UHFFFAOYSA-N 0.000 description 1
YSSYJGUBRBPHBC-UHFFFAOYSA-N 2-(4,6-ditert-butyl-1,3,5-triazin-2-yl)phenol Chemical compound CC(C)(C)C1=NC(C(C)(C)C)=NC(C=2C(=CC=CC=2)O)=N1 YSSYJGUBRBPHBC-UHFFFAOYSA-N 0.000 description 1
FJGQBLRYBUAASW-UHFFFAOYSA-N 2-(benzotriazol-2-yl)phenol Chemical compound OC1=CC=CC=C1N1N=C2C=CC=CC2=N1 FJGQBLRYBUAASW-UHFFFAOYSA-N 0.000 description 1
SXFBMPJPLXXFFN-UHFFFAOYSA-N 2-[4,6-di(heptadecyl)-1,3,5-triazin-2-yl]phenol Chemical compound CCCCCCCCCCCCCCCCCC1=NC(CCCCCCCCCCCCCCCCC)=NC(C=2C(=CC=CC=2)O)=N1 SXFBMPJPLXXFFN-UHFFFAOYSA-N 0.000 description 1
JSZKRKKTFWXMQZ-UHFFFAOYSA-N 2-[4,6-di(nonyl)-1,3,5-triazin-2-yl]phenol Chemical compound CCCCCCCCCC1=NC(CCCCCCCCC)=NC(C=2C(=CC=CC=2)O)=N1 JSZKRKKTFWXMQZ-UHFFFAOYSA-N 0.000 description 1
IEZGLQLYKGRESO-UHFFFAOYSA-N 2-[4-butoxy-6-(4-ethoxy-2-hydroxyphenyl)-1,3,5-triazin-2-yl]-5-ethoxyphenol Chemical compound N=1C(OCCCC)=NC(C=2C(=CC(OCC)=CC=2)O)=NC=1C1=CC=C(OCC)C=C1O IEZGLQLYKGRESO-UHFFFAOYSA-N 0.000 description 1
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
125000006040 2-hexenyl group Chemical group 0.000 description 1
BZSXEZOLBIJVQK-UHFFFAOYSA-N 2-methylsulfonylbenzoic acid Chemical compound CS(=O)(=O)C1=CC=CC=C1C(O)=O BZSXEZOLBIJVQK-UHFFFAOYSA-N 0.000 description 1
125000006024 2-pentenyl group Chemical group 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
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
AFJWMGOTLUUGHF-UHFFFAOYSA-N 4,5,6,7-tetrahydroisoindole-1,3-dione Chemical compound C1CCCC2=C1C(=O)NC2=O AFJWMGOTLUUGHF-UHFFFAOYSA-N 0.000 description 1
AKYAMTDRHCBNQV-UHFFFAOYSA-N 4,5-dihydroisoindole-1,3-dione Chemical compound C1CC=CC2=C1C(=O)NC2=O AKYAMTDRHCBNQV-UHFFFAOYSA-N 0.000 description 1
NEQFBGHQPUXOFH-UHFFFAOYSA-N 4-(4-carboxyphenyl)benzoic acid Chemical class C1=CC(C(=O)O)=CC=C1C1=CC=C(C(O)=O)C=C1 NEQFBGHQPUXOFH-UHFFFAOYSA-N 0.000 description 1
NUBZGQQHTISWLZ-UHFFFAOYSA-N 4-chloro-2-(4,6-dimethyl-1,3,5-triazin-2-yl)phenol Chemical compound CC1=NC(C)=NC(C=2C(=CC=C(Cl)C=2)O)=N1 NUBZGQQHTISWLZ-UHFFFAOYSA-N 0.000 description 1
ZPECLGVYJKUVTC-UHFFFAOYSA-N 4-ethoxytriazine Chemical compound CCOC1=CC=NN=N1 ZPECLGVYJKUVTC-UHFFFAOYSA-N 0.000 description 1
ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical class COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 description 1
BWZQLVJQEQFOLU-UHFFFAOYSA-N 4-tert-butyl-2-(4,6-dimethyl-1,3,5-triazin-2-yl)phenol Chemical compound CC1=NC(C)=NC(C=2C(=CC=C(C=2)C(C)(C)C)O)=N1 BWZQLVJQEQFOLU-UHFFFAOYSA-N 0.000 description 1
CARJPEPCULYFFP-UHFFFAOYSA-N 5-Sulfo-1,3-benzenedicarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(S(O)(=O)=O)=C1 CARJPEPCULYFFP-UHFFFAOYSA-N 0.000 description 1
GJIRUFVYMWSAMO-UHFFFAOYSA-L C(C)(C)=C(CC(OC1=CC=CC=C1)OC1=CC=CC=C1)S(=O)(=O)[O-].[Na+].[Na+].C(C)(C)=C(CC(OC1=CC=CC=C1)OC1=CC=CC=C1)S(=O)(=O)[O-] Chemical compound C(C)(C)=C(CC(OC1=CC=CC=C1)OC1=CC=CC=C1)S(=O)(=O)[O-].[Na+].[Na+].C(C)(C)=C(CC(OC1=CC=CC=C1)OC1=CC=CC=C1)S(=O)(=O)[O-] GJIRUFVYMWSAMO-UHFFFAOYSA-L 0.000 description 1
OBAFGQADKPXCST-UHFFFAOYSA-M C(O)C(COC(CC)S(=O)(=O)[O-])C(C)CO.[Na+] Chemical compound C(O)C(COC(CC)S(=O)(=O)[O-])C(C)CO.[Na+] OBAFGQADKPXCST-UHFFFAOYSA-M 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
235000013912 Ceratonia siliqua Nutrition 0.000 description 1
240000008886 Ceratonia siliqua Species 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000001856 Ethyl cellulose Substances 0.000 description 1
ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
BRJVGSBQJZCIIN-UHFFFAOYSA-N OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCCOCC.OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCC Chemical compound OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCCOCC.OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCC BRJVGSBQJZCIIN-UHFFFAOYSA-N 0.000 description 1
XDLLDYCBXVKOHX-UHFFFAOYSA-N OC1=C(C=CC(=C1)OCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCC)O)OCCOCCOCC.OC1=C(C=CC(=C1)OCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCC)O)OCCOCC Chemical compound OC1=C(C=CC(=C1)OCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCC)O)OCCOCCOCC.OC1=C(C=CC(=C1)OCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCC)O)OCCOCC XDLLDYCBXVKOHX-UHFFFAOYSA-N 0.000 description 1
SNFQFCNAPMWWSH-UHFFFAOYSA-N OC1=C(C=CC(=C1)OCCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCCC)O)OCCOC.OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCCC Chemical compound OC1=C(C=CC(=C1)OCCC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OCCC)O)OCCOC.OC1=C(C=CC(=C1)OC)C1=NC(=NC(=N1)C1=C(C=C(C=C1)OC)O)OCCOCCC SNFQFCNAPMWWSH-UHFFFAOYSA-N 0.000 description 1
229930040373 Paraformaldehyde Natural products 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
229920002472 Starch Polymers 0.000 description 1
229910000831 Steel Inorganic materials 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
YIMQCDZDWXUDCA-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol Chemical compound OCC1CCC(CO)CC1 YIMQCDZDWXUDCA-UHFFFAOYSA-N 0.000 description 1
QTRNDORTMVTOEG-UHFFFAOYSA-N [O-][N+](=O)OS(=O)(=O)[N+]([O-])=O Chemical compound [O-][N+](=O)OS(=O)(=O)[N+]([O-])=O QTRNDORTMVTOEG-UHFFFAOYSA-N 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001409 amidines Chemical class 0.000 description 1
239000001000 anthraquinone dye Substances 0.000 description 1
239000002518 antifoaming agent Substances 0.000 description 1
239000013011 aqueous formulation Substances 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
125000001204 arachidyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
OSNDUYDDOHEKEE-UHFFFAOYSA-N azepane-2,7-dione Chemical compound O=C1CCCCC(=O)N1 OSNDUYDDOHEKEE-UHFFFAOYSA-N 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
239000011805 ball Substances 0.000 description 1
239000011324 bead Substances 0.000 description 1
150000008366 benzophenones Chemical class 0.000 description 1
150000001565 benzotriazoles Chemical class 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
230000008033 biological extinction Effects 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
125000005569 butenylene group Chemical group 0.000 description 1
229930188620 butyrolactone Natural products 0.000 description 1
239000001768 carboxy methyl cellulose Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000008112 carboxymethyl-cellulose Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
125000000490 cinnamyl group Chemical group C(C=CC1=CC=CC=C1)* 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000009833 condensation Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 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
230000001419 dependent effect Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 1
229910000397 disodium phosphate Inorganic materials 0.000 description 1
235000019800 disodium phosphate Nutrition 0.000 description 1
229920001249 ethyl cellulose Polymers 0.000 description 1
235000019325 ethyl cellulose Nutrition 0.000 description 1
150000002193 fatty amides Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
238000009998 heat setting Methods 0.000 description 1
239000007970 homogeneous dispersion Substances 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
101150058567 moaA gene Proteins 0.000 description 1
101150112330 moaA1 gene Proteins 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
229910000403 monosodium phosphate Inorganic materials 0.000 description 1
235000019799 monosodium phosphate Nutrition 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
239000001005 nitro dye Substances 0.000 description 1
229940099990 ogen Drugs 0.000 description 1
239000003921 oil Substances 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229920002866 paraformaldehyde Polymers 0.000 description 1
KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920005646 polycarboxylate Polymers 0.000 description 1
150000007519 polyprotic acids Polymers 0.000 description 1
239000011970 polystyrene sulfonate Substances 0.000 description 1
229920005749 polyurethane resin Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
KCXFHTAICRTXLI-UHFFFAOYSA-M propane-1-sulfonate Chemical compound CCCS([O-])(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-M 0.000 description 1
125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
238000010022 rotary screen printing Methods 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
229930195734 saturated hydrocarbon Natural products 0.000 description 1
238000007650 screen-printing Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
239000002904 solvent Substances 0.000 description 1
241000894007 species Species 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000010959 steel Substances 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
150000003504 terephthalic acids Chemical class 0.000 description 1
235000007586 terpenes Nutrition 0.000 description 1
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/642—Compounds containing nitrogen
- D06P1/6426—Heterocyclic compounds
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/44—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/651—Compounds without nitrogen
- D06P1/65106—Oxygen-containing compounds
- D06P1/65112—Compounds containing aldehyde or ketone groups

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Coloring (AREA)
Chemical Or Physical Treatment Of Fibers (AREA)
Artificial Filaments (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Printing Plates And Materials Therefor (AREA)
Treatment Of Fiber Materials (AREA)
Polyesters Or Polycarbonates (AREA)

CA002073580A 1991-07-12 1992-07-10 Process for printing and photochemically stabilising polyester fibre materials Abandoned CA2073580A1 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH208691		1991-07-12
CH2086/91-5		1991-07-12

Publications (1)

Publication Number	Publication Date
CA2073580A1 true CA2073580A1 (en)	1993-01-13

Family

ID=4225570

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002073580A Abandoned CA2073580A1 (en)	1991-07-12	1992-07-10	Process for printing and photochemically stabilising polyester fibre materials

Country Status (9)

Country	Link
EP (1)	EP0523006B1 (de)
JP (1)	JPH05209374A (de)
AT (1)	ATE130883T1 (de)
BR (1)	BR9202579A (de)
CA (1)	CA2073580A1 (de)
DE (1)	DE59204472D1 (de)
DK (1)	DK0523006T3 (de)
ES (1)	ES2080473T3 (de)
GR (1)	GR3018250T3 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0657577A1 (de) *	1993-12-06	1995-06-14	Ciba-Geigy Ag	Verfahren zur photochemischen und thermischen Stabilisierung von ungefärbten und gefärbten oder bedruckten Polyesterfasermaterialien
ATE200478T1 (de) *	1995-03-17	2001-04-15	Ciba Sc Holding Ag	Liposomogene uv-absorber
EP0864687A3 (de) *	1997-03-11	1999-11-24	Ciba SC Holding AG	Verfahren zur Verbesserung der photochemischen Stabilität von Färbungen und Drucken auf Polyesterfasern
JP2009030214A (ja) *	2007-07-27	2009-02-12	Senka Kk	繊維製品の耐光堅牢度向上剤及び耐光堅牢度向上方法
JP5072496B2 (ja) *	2007-09-11	2012-11-14	小松精練株式会社	リサイクル用のぼり旗の脱色方法およびのぼり旗のリサイクル方法
DE102007046745A1 (de) *	2007-09-28	2009-04-02	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Dispersionsfarbstoff und/oder UV-Absorber enthaltende Präparationen
EP2387600B1 (de)	2009-01-19	2014-04-02	Basf Se	Organische schwarzpigmente und ihre herstellung
DE102011082078A1 (de) *	2011-09-02	2013-03-07	Carl Stahl Gmbh & Co. Kg	Verfahren zum Bedrucken eines Gurtbands

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE630546A (de) *	1961-06-16
DE3417782A1 (de) *	1983-05-23	1984-11-29	Sandoz-Patent-GmbH, 7850 Lörrach	Faerbereihilfsmittel
US4775386A (en) *	1986-05-05	1988-10-04	Ciba-Geigy Corporation	Process for photochemical stabilization of undyed and dyed polyamide fibre material and blends thereof with other fibres: copper complex and light stabilizer treatment
US4831068A (en) *	1987-02-27	1989-05-16	Ciba-Geigy Corporation	Process for improving the photochemical stability of dyeings on polyester fibre materials
DE58906867D1 (de) *	1988-05-31	1994-03-17	Ciba Geigy	Wässrige Dispersion von 2-(2'-Hydroxyphenyl-)benzotriazolen.
ES2074688T5 (es) *	1990-07-23	1998-11-01	Ciba Geigy Ag	Dispersion acuosa de absorbentes de uv poco solubles.

1992
- 1992-07-03 ES ES92810511T patent/ES2080473T3/es not_active Expired - Lifetime
- 1992-07-03 EP EP92810511A patent/EP0523006B1/de not_active Expired - Lifetime
- 1992-07-03 AT AT92810511T patent/ATE130883T1/de not_active IP Right Cessation
- 1992-07-03 DK DK92810511.3T patent/DK0523006T3/da active
- 1992-07-03 DE DE59204472T patent/DE59204472D1/de not_active Expired - Fee Related
- 1992-07-10 BR BR929202579A patent/BR9202579A/pt not_active IP Right Cessation
- 1992-07-10 JP JP4206280A patent/JPH05209374A/ja active Pending
- 1992-07-10 CA CA002073580A patent/CA2073580A1/en not_active Abandoned
1995
- 1995-11-30 GR GR950403168T patent/GR3018250T3/el unknown

Also Published As

Publication number	Publication date
GR3018250T3 (en)	1996-02-29
DK0523006T3 (da)	1995-12-27
JPH05209374A (ja)	1993-08-20
BR9202579A (pt)	1993-03-16
ES2080473T3 (es)	1996-02-01
ATE130883T1 (de)	1995-12-15
EP0523006B1 (de)	1995-11-29
DE59204472D1 (de)	1996-01-11
EP0523006A1 (de)	1993-01-13

Legal Events

Date	Code	Title	Description
2000-07-10	FZDE	Discontinued

Publication	Publication Date	Title
US5298030A (en)	1994-03-29	Process for the photochemical and thermal stabilization of undyed and dyed or printed polyester fiber materials
US4427413A (en)	1984-01-24	Dye mixture, and its use in transfer printing
KR950007820B1 (ko)	1995-07-20	폴리에스테르 섬유재료 염색물의 광화학적 안정성을 향상시키는 방법
EP0112120B1 (de)	1989-10-25	Verwendung von 2-(2'Hydroxyaryl)-2H-Benzotriazolsulfonaten als photostabilisierende Mittel für natürliche und synthetische Fasern
AU653350B2 (en)	1994-09-29	Aqueous dispersions of sparingly soluble UV absorbers
EP0345219B1 (de)	1994-02-02	Wässrige Dispersion von 2-(2'-Hydroxyphenyl-)benzotriazolen
EP0523006B1 (de)	1995-11-29	Verfahren zum Bedrucken und photochemischen Stabilisieren von Polyesterfasermaterialien
CA2137212A1 (en)	1995-06-07	Process for the photochemical and thermal stabilisation of undyed and dyed or printed polyester fibre materials
AU3498899A (en)	1999-12-23	Process for improving the photochemical and thermal stability of dyeings and prints on polyester fibre materials
KR920000745B1 (ko)	1992-01-21	모노아조 염료 조성물 및 이의 제조방법
GB1572080A (en)	1980-07-23	Disperse dyestuffs their preparation and their application to the colouration of semi-synthetic or synthetic materials
US4124355A (en)	1978-11-07	Transfer dyeing with 1-amino-4-anilinoanthraquinone dyes
US5984976A (en)	1999-11-16	Process for improving the photochemical stability of dyeings and prints on polyester fibres
US4306874A (en)	1981-12-22	Process for printing synthetic, hydrophobic fiber material in accordance with the principle of transfer printing
US4274831A (en)	1981-06-23	Process for dyeing or printing synthetic fiber materials by means of disperse dyes, and colorant compositions utilizable for this purpose
GB2041390A (en)	1980-09-10	Alpha-hydrazone alpha-phenyl acetonitriles their preparation and their application as disperse dyestuffs for the colouration of artificial or synthetic materials
KR100832223B1 (ko)	2008-05-23	분산 염료로서 안료의 용도
US3409385A (en)	1968-11-05	Anthraquinone dyed polypropylene fibers
US4200570A (en)	1980-04-29	5-Halo-2-trifluoromethylphenylazo-pyrazolones
US4087241A (en)	1978-05-02	Printing inks for transfer printing
US4128395A (en)	1978-12-05	Transfer printing with carboxylic dyes
US3927964A (en)	1975-12-23	6-Anilino-1,4,5-trihydroxyanthraquinones
EP0316731B1 (de)	1993-05-19	Azofarbstoffe auf der Basis von 2-Hydrazinothiazolen, deren Verwendung zum Färben und Bedrucken von Fasermaterialien sowie für den Sublimationstransferdruck
EP1366230A1 (de)	2003-12-03	Verwendung von pigmentfarbstoffen zur dispersionsfärbung aus wässrigen medien
GB1569937A (en)	1980-06-25	Dyes and their use in transfer printing