DE2146761C3 - Verfahren zur Herstellung ichtechter Färbungen auf synthetischen Fasern - Google Patents
Verfahren zur Herstellung ichtechter Färbungen auf synthetischen FasernInfo
- Publication number
- DE2146761C3 DE2146761C3 DE19712146761 DE2146761A DE2146761C3 DE 2146761 C3 DE2146761 C3 DE 2146761C3 DE 19712146761 DE19712146761 DE 19712146761 DE 2146761 A DE2146761 A DE 2146761A DE 2146761 C3 DE2146761 C3 DE 2146761C3
- Authority
- DE
- Germany
- Prior art keywords
- carrier
- dyeing
- dyeings
- dye
- production
- 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
Links
- 238000004043 dyeing Methods 0.000 title claims description 30
- 238000000034 method Methods 0.000 title claims description 15
- 229920002994 synthetic fiber Polymers 0.000 title claims description 5
- 239000012209 synthetic fiber Substances 0.000 title claims description 5
- 238000004519 manufacturing process Methods 0.000 title claims description 3
- 239000000975 dye Substances 0.000 claims description 22
- 239000000835 fiber Substances 0.000 claims description 14
- 239000000463 material Substances 0.000 claims description 10
- 239000000126 substance Substances 0.000 claims description 10
- 229920000728 polyester Polymers 0.000 claims description 8
- 239000000654 additive Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims 1
- 239000004753 textile Substances 0.000 claims 1
- LLEMOWNGBBNAJR-UHFFFAOYSA-N biphenyl-2-ol Chemical group OC1=CC=CC=C1C1=CC=CC=C1 LLEMOWNGBBNAJR-UHFFFAOYSA-N 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 7
- 238000004140 cleaning Methods 0.000 description 7
- GSVLCKASFMVUSW-UHFFFAOYSA-N decyl(dimethyl)phosphine oxide Chemical compound CCCCCCCCCCP(C)(C)=O GSVLCKASFMVUSW-UHFFFAOYSA-N 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 230000002829 reductive effect Effects 0.000 description 6
- 239000003995 emulsifying agent Substances 0.000 description 5
- 150000002903 organophosphorus compounds Chemical class 0.000 description 5
- 238000004383 yellowing Methods 0.000 description 5
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 235000010292 orthophenyl phenol Nutrition 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 125000006267 biphenyl group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 3
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 235000013162 Cocos nucifera Nutrition 0.000 description 2
- 244000060011 Cocos nucifera Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 150000001733 carboxylic acid esters Chemical class 0.000 description 2
- 238000010411 cooking Methods 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- NJGCRMAPOWGWMW-UHFFFAOYSA-N octylphosphonic acid Chemical compound CCCCCCCCP(O)(O)=O NJGCRMAPOWGWMW-UHFFFAOYSA-N 0.000 description 2
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 2
- 125000004430 oxygen atom Chemical group O* 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
- 238000010186 staining Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FQACWXQAPCNZNP-UHFFFAOYSA-N 1-[bis(2-methylpropoxy)phosphoryl]hexane Chemical compound C(C(C)C)OP(OCC(C)C)(=O)CCCCCC FQACWXQAPCNZNP-UHFFFAOYSA-N 0.000 description 1
- JPGXOMADPRULAC-UHFFFAOYSA-N 1-[butoxy(butyl)phosphoryl]oxybutane Chemical compound CCCCOP(=O)(CCCC)OCCCC JPGXOMADPRULAC-UHFFFAOYSA-N 0.000 description 1
- PVKVYEPLFYSUEL-UHFFFAOYSA-N 1-[butyl(methyl)phosphoryl]decane Chemical compound C(CCCCCCCCC)P(CCCC)(C)=O PVKVYEPLFYSUEL-UHFFFAOYSA-N 0.000 description 1
- HFZNAKHLQWAGSB-UHFFFAOYSA-N 1-[ethoxy(methyl)phosphoryl]dodecane Chemical compound C(C)OP(=O)(CCCCCCCCCCCC)C HFZNAKHLQWAGSB-UHFFFAOYSA-N 0.000 description 1
- YXKURXKHPLONNO-UHFFFAOYSA-N 1-[methyl(2-methylpropoxy)phosphoryl]decane Chemical compound C(C(C)C)OP(=O)(CCCCCCCCCC)C YXKURXKHPLONNO-UHFFFAOYSA-N 0.000 description 1
- VVUJWLDQIIFQHI-UHFFFAOYSA-N 1-diethoxyphosphorylhexane Chemical compound CCCCCCP(=O)(OCC)OCC VVUJWLDQIIFQHI-UHFFFAOYSA-N 0.000 description 1
- CXRUQTPIHDKFTG-UHFFFAOYSA-N 1-diethylphosphoryldodecane Chemical compound CCCCCCCCCCCCP(=O)(CC)CC CXRUQTPIHDKFTG-UHFFFAOYSA-N 0.000 description 1
- PMGZGGRJTZYVLL-UHFFFAOYSA-N 1-diethylphosphoryloctane Chemical compound CCCCCCCCP(=O)(CC)CC PMGZGGRJTZYVLL-UHFFFAOYSA-N 0.000 description 1
- SIDULKZCBGMXJL-UHFFFAOYSA-N 1-dimethylphosphoryldodecane Chemical compound CCCCCCCCCCCCP(C)(C)=O SIDULKZCBGMXJL-UHFFFAOYSA-N 0.000 description 1
- OCBOQSGCZXEWIH-UHFFFAOYSA-N 1-dimethylphosphorylhexane Chemical compound CCCCCCP(C)(C)=O OCBOQSGCZXEWIH-UHFFFAOYSA-N 0.000 description 1
- LSCHYBAAWCZBDM-UHFFFAOYSA-N 1-dimethylphosphoryloctane Chemical compound CCCCCCCCP(C)(C)=O LSCHYBAAWCZBDM-UHFFFAOYSA-N 0.000 description 1
- ZELXQOMIZMDPHB-UHFFFAOYSA-N 1-dodecyl-1-oxidopiperidin-1-ium Chemical compound CCCCCCCCCCCC[N+]1([O-])CCCCC1 ZELXQOMIZMDPHB-UHFFFAOYSA-N 0.000 description 1
- UASZLWRRHYPIAS-UHFFFAOYSA-N 2-methyl-1-[methyl(propyl)phosphoryl]oxypropane Chemical compound CCCP(C)(=O)OCC(C)C UASZLWRRHYPIAS-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- LKWMVIXIVCCTMS-UHFFFAOYSA-N C(CCCCC)P(CCCC)(C)=O Chemical compound C(CCCCC)P(CCCC)(C)=O LKWMVIXIVCCTMS-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229920002284 Cellulose triacetate Polymers 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical class OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 230000000740 bleeding effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- -1 chloroethyl ester Chemical class 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- PATIESKUYYXOQY-UHFFFAOYSA-N dodecyl(methyl)phosphinic acid Chemical compound CCCCCCCCCCCCP(C)(O)=O PATIESKUYYXOQY-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 150000002169 ethanolamines Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000009413 insulation Methods 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 239000000434 metal complex dye Substances 0.000 description 1
- OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
- 229940095102 methyl benzoate Drugs 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 description 1
- RSVIRMFSJVHWJV-UHFFFAOYSA-N n,n-dimethyloctan-1-amine oxide Chemical compound CCCCCCCC[N+](C)(C)[O-] RSVIRMFSJVHWJV-UHFFFAOYSA-N 0.000 description 1
- ONLRKTIYOMZEJM-UHFFFAOYSA-N n-methylmethanamine oxide Chemical compound C[NH+](C)[O-] ONLRKTIYOMZEJM-UHFFFAOYSA-N 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 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
- 150000002989 phenols Chemical class 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical class O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 150000003008 phosphonic acid esters Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 210000002268 wool Anatomy 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
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/34—Material containing ester groups
- D06P3/52—Polyesters
- D06P3/54—Polyesters using dispersed dyestuffs
-
- 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
- D06P1/6428—Compounds containing aminoxide groups
-
- 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
- D06P1/667—Organo-phosphorus compounds
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Coloring (AREA)
Priority Applications (10)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE788960D BE788960A (fr) | 1971-09-18 | Procede de realisation de teintures et impressions solides a lalumiere sur des fibres synthetiques | |
| DE19712146761 DE2146761C3 (de) | 1971-09-18 | 1971-09-18 | Verfahren zur Herstellung ichtechter Färbungen auf synthetischen Fasern |
| CH1349472A CH559809A (de) | 1971-09-18 | 1972-09-14 | Verfahren zur herstellung lichtechter faerbungen auf synthetischen fasern. |
| CH1349472D CH1349472A4 (enrdf_load_stackoverflow) | 1971-09-18 | 1972-09-14 | |
| CA151,794A CA980061A (en) | 1971-09-18 | 1972-09-15 | Process for the production of dyeings and prints fast to light on synthetic fibers |
| GB4295372A GB1408304A (en) | 1971-09-18 | 1972-09-15 | Process for the production of deyings and prints fast to light on synthetic fibres |
| AT792272A AT336540B (de) | 1971-09-18 | 1972-09-15 | Verfahren zur ausbildung von in ihrer lichtechtheit durch farbebeschleuniger (carrier) nicht beeintrachtigten farbungen mit dispersionsfarbstoffen auf synthetischen fasermaterialien |
| IT2932172A IT967564B (it) | 1971-09-18 | 1972-09-16 | Procedimento per la preparazione di tinture e stampe solide alla luce su fibre sintetiche |
| JP47092258A JPS4839778A (enrdf_load_stackoverflow) | 1971-09-18 | 1972-09-16 | |
| FR7232995A FR2153093B1 (enrdf_load_stackoverflow) | 1971-09-18 | 1972-09-18 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712146761 DE2146761C3 (de) | 1971-09-18 | 1971-09-18 | Verfahren zur Herstellung ichtechter Färbungen auf synthetischen Fasern |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2146761A1 DE2146761A1 (de) | 1973-04-05 |
| DE2146761B2 DE2146761B2 (de) | 1975-02-20 |
| DE2146761C3 true DE2146761C3 (de) | 1975-10-02 |
Family
ID=5819985
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19712146761 Expired DE2146761C3 (de) | 1971-09-18 | 1971-09-18 | Verfahren zur Herstellung ichtechter Färbungen auf synthetischen Fasern |
Country Status (9)
| Country | Link |
|---|---|
| JP (1) | JPS4839778A (enrdf_load_stackoverflow) |
| AT (1) | AT336540B (enrdf_load_stackoverflow) |
| BE (1) | BE788960A (enrdf_load_stackoverflow) |
| CA (1) | CA980061A (enrdf_load_stackoverflow) |
| CH (2) | CH1349472A4 (enrdf_load_stackoverflow) |
| DE (1) | DE2146761C3 (enrdf_load_stackoverflow) |
| FR (1) | FR2153093B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1408304A (enrdf_load_stackoverflow) |
| IT (1) | IT967564B (enrdf_load_stackoverflow) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS585939B2 (ja) * | 1975-04-08 | 1983-02-02 | 三菱化学株式会社 | ポリエステルナンネンセイソセイブツ |
| AU4944896A (en) * | 1995-03-15 | 1996-10-02 | Ciba Specialty Chemicals Holding Inc. | Improving the light-fastness of dyes on polyamide fibres |
| BR112013026857B8 (pt) * | 2011-04-20 | 2023-05-16 | Huntsman Adv Mat Switzerland | Método para tingir material têxtil contendo poliéster |
-
0
- BE BE788960D patent/BE788960A/xx unknown
-
1971
- 1971-09-18 DE DE19712146761 patent/DE2146761C3/de not_active Expired
-
1972
- 1972-09-14 CH CH1349472D patent/CH1349472A4/xx unknown
- 1972-09-14 CH CH1349472A patent/CH559809A/xx not_active IP Right Cessation
- 1972-09-15 CA CA151,794A patent/CA980061A/en not_active Expired
- 1972-09-15 GB GB4295372A patent/GB1408304A/en not_active Expired
- 1972-09-15 AT AT792272A patent/AT336540B/de not_active IP Right Cessation
- 1972-09-16 IT IT2932172A patent/IT967564B/it active
- 1972-09-16 JP JP47092258A patent/JPS4839778A/ja active Pending
- 1972-09-18 FR FR7232995A patent/FR2153093B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA980061A (en) | 1975-12-23 |
| FR2153093B1 (enrdf_load_stackoverflow) | 1976-08-13 |
| ATA792272A (de) | 1976-09-15 |
| GB1408304A (en) | 1975-10-01 |
| IT967564B (it) | 1974-03-11 |
| CH559809A (de) | 1975-03-14 |
| JPS4839778A (enrdf_load_stackoverflow) | 1973-06-11 |
| DE2146761A1 (de) | 1973-04-05 |
| BE788960A (fr) | 1973-03-19 |
| FR2153093A1 (enrdf_load_stackoverflow) | 1973-04-27 |
| CH559809B5 (enrdf_load_stackoverflow) | |
| CH1349472A4 (enrdf_load_stackoverflow) | 1974-08-15 |
| DE2146761B2 (de) | 1975-02-20 |
| AT336540B (de) | 1977-05-10 |
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| Date | Code | Title | Description |
|---|---|---|---|
| C3 | Grant after two publication steps (3rd publication) | ||
| E77 | Valid patent as to the heymanns-index 1977 | ||
| EHJ | Ceased/non-payment of the annual fee |