CH384530A - Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters - Google Patents

Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters

Info

Publication number: CH384530A
Authority: CH; Switzerland
Prior art keywords: acid; polyamide; dye; dye solution; compound
Prior art date: 1961-08-11

Application number

CH942861A

Other languages

German (de)

English (en)

Other versions

CH942861A4 (fr

Inventor

Schaeuble Alfred

Adolf Dr Raeuchle

Willi Dr Leutenegger

Original Assignee

Geigy Ag J R

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.)

1961-08-11

Filing date

1961-08-11

Publication date

1965-02-15

Priority to NL281972D priority Critical patent/NL281972A/xx

1961-08-11 Application filed by Geigy Ag J R filed Critical Geigy Ag J R

1961-08-11 Priority to CH942761A priority patent/CH381641A/de

1961-08-11 Priority to CH942861A priority patent/CH384530A/de

1962-08-10 Priority to FR906698A priority patent/FR1331094A/fr

1962-08-10 Priority to ES280151A priority patent/ES280151A1/es

1962-08-10 Priority to BE621284A priority patent/BE621284A/fr

1962-08-10 Priority to DEG35696A priority patent/DE1255627B/de

1962-08-10 Priority to GB30714/62A priority patent/GB969701A/en

1962-08-10 Priority to GB30715/62A priority patent/GB975375A/en

1962-08-10 Priority to ES280150A priority patent/ES280150A1/es

1963-07-31 Publication of CH942861A4 publication Critical patent/CH942861A4/xx

1965-02-15 Publication of CH384530A publication Critical patent/CH384530A/de

1966-08-09 Priority to US571194A priority patent/US3468620A/en

Links

239000000975 dye Substances 0.000 title claims description 48
239000004952 Polyamide Substances 0.000 title claims description 34
229920002647 polyamide Polymers 0.000 title claims description 34
238000000034 method Methods 0.000 title claims description 22
238000004043 dyeing Methods 0.000 title claims description 19
239000000835 fiber Substances 0.000 title claims description 15
125000000129 anionic group Chemical group 0.000 title claims description 11
239000000243 solution Substances 0.000 claims description 27
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 16
239000002253 acid Substances 0.000 claims description 13
235000014113 dietary fatty acids Nutrition 0.000 claims description 11
239000002270 dispersing agent Substances 0.000 claims description 11
239000000194 fatty acid Substances 0.000 claims description 11
229930195729 fatty acid Natural products 0.000 claims description 11
150000004665 fatty acids Chemical class 0.000 claims description 11
238000005187 foaming Methods 0.000 claims description 11
150000003839 salts Chemical class 0.000 claims description 11
239000007864 aqueous solution Substances 0.000 claims description 9
239000007859 condensation product Substances 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 7
238000010025 steaming Methods 0.000 claims description 7
239000003795 chemical substances by application Substances 0.000 claims description 6
-1 hydroxyl compound Chemical class 0.000 claims description 6
230000002522 swelling effect Effects 0.000 claims description 6
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 4
125000004432 carbon atom Chemical group C* 0.000 claims description 4
BGLLQCPSNQUDKF-UHFFFAOYSA-N 1,2,3,4-tetrahydronaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)CCCC2=C1 BGLLQCPSNQUDKF-UHFFFAOYSA-N 0.000 claims description 3
238000010521 absorption reaction Methods 0.000 claims description 3
150000001409 amidines Chemical class 0.000 claims description 3
239000002562 thickening agent Substances 0.000 claims description 3
235000010443 alginic acid Nutrition 0.000 claims description 2
229920000615 alginic acid Polymers 0.000 claims description 2
150000004781 alginic acids Chemical class 0.000 claims description 2
238000007654 immersion Methods 0.000 claims description 2
239000004753 textile Substances 0.000 claims description 2
150000001408 amides Chemical class 0.000 claims 2
125000003118 aryl group Chemical group 0.000 claims 2
230000001419 dependent effect Effects 0.000 claims 2
AEOCXXJPGCBFJA-UHFFFAOYSA-N ethionamide Chemical compound CCC1=CC(C(N)=S)=CC=N1 AEOCXXJPGCBFJA-UHFFFAOYSA-N 0.000 claims 2
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 2
239000000783 alginic acid Substances 0.000 claims 1
229960001126 alginic acid Drugs 0.000 claims 1
210000002268 wool Anatomy 0.000 description 18
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 14
239000002657 fibrous material Substances 0.000 description 9
238000005470 impregnation Methods 0.000 description 8
239000000463 material Substances 0.000 description 8
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 7
235000019253 formic acid Nutrition 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000004744 fabric Substances 0.000 description 6
235000011890 sandwich Nutrition 0.000 description 6
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 5
229910052804 chromium Inorganic materials 0.000 description 5
239000011651 chromium Substances 0.000 description 5
229910017052 cobalt Inorganic materials 0.000 description 5
239000010941 cobalt Substances 0.000 description 5
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
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 5
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 4
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 4
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 4
239000000987 azo dye Substances 0.000 description 4
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 4
150000007524 organic acids Chemical class 0.000 description 4
229920000151 polyglycol Polymers 0.000 description 4
239000010695 polyglycol Substances 0.000 description 4
229920006395 saturated elastomer Polymers 0.000 description 4
239000000661 sodium alginate Substances 0.000 description 4
235000010413 sodium alginate Nutrition 0.000 description 4
229940005550 sodium alginate Drugs 0.000 description 4
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 3
244000060011 Cocos nucifera Species 0.000 description 3
235000013162 Cocos nucifera Nutrition 0.000 description 3
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
230000000740 bleeding effect Effects 0.000 description 3
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 3
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
235000005985 organic acids Nutrition 0.000 description 3
230000035515 penetration Effects 0.000 description 3
SQHKJSPPFSVNDF-UHFFFAOYSA-N 1,2,2,3-tetrakis(hydroxymethyl)cyclohexan-1-ol Chemical compound OCC1CCCC(O)(CO)C1(CO)CO SQHKJSPPFSVNDF-UHFFFAOYSA-N 0.000 description 2
KUMMBDBTERQYCG-UHFFFAOYSA-N 2,6-bis(hydroxymethyl)-4-methylphenol Chemical compound CC1=CC(CO)=C(O)C(CO)=C1 KUMMBDBTERQYCG-UHFFFAOYSA-N 0.000 description 2
CTRXDTYTAAKVSM-UHFFFAOYSA-N 3-{[ethyl({4-[(4-{ethyl[(3-sulfophenyl)methyl]amino}phenyl)(2-sulfophenyl)methylidene]cyclohexa-2,5-dien-1-ylidene})azaniumyl]methyl}benzene-1-sulfonate Chemical compound C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S(O)(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 CTRXDTYTAAKVSM-UHFFFAOYSA-N 0.000 description 2
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 2
XDCOQJQVRYQMEB-UHFFFAOYSA-N C1(CCCC2=CC=CC=C12)S(=O)(=O)O.[Na] Chemical compound C1(CCCC2=CC=CC=C12)S(=O)(=O)O.[Na] XDCOQJQVRYQMEB-UHFFFAOYSA-N 0.000 description 2
ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
229920002292 Nylon 6 Polymers 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
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000008043 acidic salts Chemical class 0.000 description 2
238000010014 continuous dyeing Methods 0.000 description 2
FPVGTPBMTFTMRT-UHFFFAOYSA-L disodium;2-amino-5-[(4-sulfonatophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].[Na+].C1=C(S([O-])(=O)=O)C(N)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 FPVGTPBMTFTMRT-UHFFFAOYSA-L 0.000 description 2
238000001035 drying Methods 0.000 description 2
QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 description 2
235000019233 fast yellow AB Nutrition 0.000 description 2
MGJXBDMLVWIYOQ-UHFFFAOYSA-N methylazanide Chemical compound [NH-]C MGJXBDMLVWIYOQ-UHFFFAOYSA-N 0.000 description 2
150000007522 mineralic acids Chemical class 0.000 description 2
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 2
239000011734 sodium Substances 0.000 description 2
150000003460 sulfonic acids Chemical class 0.000 description 2
230000008961 swelling Effects 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
SYRBOMODLUADBZ-RNIAWFEPSA-N 1-[(E)-[(E)-(2-hydroxynaphthalen-1-yl)methylidenehydrazinylidene]methyl]naphthalen-2-ol Chemical compound N(\N=C\C1=C(C=CC2=CC=CC=C12)O)=C/C1=C(C=CC2=CC=CC=C12)O SYRBOMODLUADBZ-RNIAWFEPSA-N 0.000 description 1
ZZXDRXVIRVJQBT-UHFFFAOYSA-N 2,3-dimethylbenzenesulfonic acid Chemical compound CC1=CC=CC(S(O)(=O)=O)=C1C ZZXDRXVIRVJQBT-UHFFFAOYSA-N 0.000 description 1
LSYXXLMBRSSBGS-UHFFFAOYSA-N 2,4,6-tris(hydroxymethyl)phenol Chemical compound OCC1=CC(CO)=C(O)C(CO)=C1 LSYXXLMBRSSBGS-UHFFFAOYSA-N 0.000 description 1
XLXNBJHLHFGROB-UHFFFAOYSA-N 2,6-bis(hydroxymethyl)-4-pentylphenol Chemical compound CCCCCC1=CC(CO)=C(O)C(CO)=C1 XLXNBJHLHFGROB-UHFFFAOYSA-N 0.000 description 1
HUJVUMPYHGYXDS-UHFFFAOYSA-N 2-(2,5-dimethoxy-n-methylsulfonylanilino)-n-[(4-methylphenyl)methyl]acetamide Chemical compound COC1=CC=C(OC)C(N(CC(=O)NCC=2C=CC(C)=CC=2)S(C)(=O)=O)=C1 HUJVUMPYHGYXDS-UHFFFAOYSA-N 0.000 description 1
ZUVDVLYXIZFDRM-UHFFFAOYSA-N 2-(hydroxymethyl)-4-methylphenol Chemical compound CC1=CC=C(O)C(CO)=C1 ZUVDVLYXIZFDRM-UHFFFAOYSA-N 0.000 description 1
VLZVIIYRNMWPSN-UHFFFAOYSA-N 2-Amino-4-nitrophenol Chemical compound NC1=CC([N+]([O-])=O)=CC=C1O VLZVIIYRNMWPSN-UHFFFAOYSA-N 0.000 description 1
LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 description 1
HSKGHUJMBLYPDO-UHFFFAOYSA-N 4-(hydroxymethyl)-2-methylphenol Chemical compound CC1=CC(CO)=CC=C1O HSKGHUJMBLYPDO-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 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
239000005977 Ethylene Substances 0.000 description 1
229920003620 Grilon® Polymers 0.000 description 1
CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 description 1
239000004677 Nylon Substances 0.000 description 1
240000007817 Olea europaea Species 0.000 description 1
239000004959 Rilsan Substances 0.000 description 1
240000002114 Satureja hortensis Species 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
235000011114 ammonium hydroxide Nutrition 0.000 description 1
ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 1
229940075861 ammonium thioglycolate Drugs 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
239000001000 anthraquinone dye Substances 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
159000000007 calcium salts Chemical class 0.000 description 1
239000004202 carbamide Substances 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
239000003086 colorant Substances 0.000 description 1
239000003599 detergent Substances 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 description 1
PCXGGAYBVUZJEZ-UHFFFAOYSA-N dinaphthalen-1-ylmethanediol Chemical compound C1=CC=C2C(C(O)(C=3C4=CC=CC=C4C=CC=3)O)=CC=CC2=C1 PCXGGAYBVUZJEZ-UHFFFAOYSA-N 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
KJADDPWIRVBKPZ-UHFFFAOYSA-N ethyl n-(7-hydroxynaphthalen-1-yl)carbamate Chemical compound C1=C(O)C=C2C(NC(=O)OCC)=CC=CC2=C1 KJADDPWIRVBKPZ-UHFFFAOYSA-N 0.000 description 1
238000009998 heat setting Methods 0.000 description 1
229910001385 heavy metal Inorganic materials 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
239000001005 nitro dye Substances 0.000 description 1
229920001778 nylon Polymers 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
229910000343 potassium bisulfate Inorganic materials 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910000342 sodium bisulfate Inorganic materials 0.000 description 1
IYNDBHDAIOZDQC-UHFFFAOYSA-M sodium;1,2,3,4-tetrahydronaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])CCCC2=C1 IYNDBHDAIOZDQC-UHFFFAOYSA-M 0.000 description 1
ZCOGBQMNWOQJBU-UHFFFAOYSA-M sodium;1,6-dimethylcyclohexa-2,4-diene-1-sulfonate Chemical compound [Na+].CC1C=CC=CC1(C)S([O-])(=O)=O ZCOGBQMNWOQJBU-UHFFFAOYSA-M 0.000 description 1
HIEHAIZHJZLEPQ-UHFFFAOYSA-M sodium;naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 HIEHAIZHJZLEPQ-UHFFFAOYSA-M 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
239000011782 vitamin Substances 0.000 description 1
229940088594 vitamin Drugs 0.000 description 1
229930003231 vitamin Natural products 0.000 description 1
235000013343 vitamin Nutrition 0.000 description 1
150000003722 vitamin derivatives Chemical class 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
- D06P1/649—Compounds containing carbonamide, thiocarbonamide or guanyl groups
- D06P1/6495—Compounds containing carbonamide -RCON= (R=H or hydrocarbons)
- D06P1/6496—Condensation products from carboxylic acids and hydroxyalkyl amine (Kritchewski bases)
- 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
- D06P1/62—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 with sulfate, sulfonate, sulfenic or sulfinic groups
- D06P1/621—Compounds without nitrogen
- D06P1/622—Sulfonic acids or their salts
- D06P1/625—Aromatic
- 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
- D06P1/65118—Compounds containing hydroxyl 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
- D06P1/653—Nitrogen-free carboxylic acids or their salts
- D06P1/6536—Aromatic
- 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
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/06—Material containing basic nitrogen containing amide groups using acid dyes

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Coloring (AREA)

CH942861A 1961-08-11 1961-08-11 Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters CH384530A (de)

Priority Applications (11)

Application Number	Priority Date	Filing Date	Title
NL281972D NL281972A (fr)	1961-08-11
CH942761A CH381641A (de)	1961-08-11	1961-08-11	Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters
CH942861A CH384530A (de)	1961-08-11	1961-08-11	Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters
BE621284A BE621284A (fr)	1961-08-11	1962-08-10	Teinture de fibres en polyamides
ES280151A ES280151A1 (es)	1961-08-11	1962-08-10	Procedimiento para teñir fibras de poliamida
FR906698A FR1331094A (fr)	1961-08-11	1962-08-10	Teinture de fibres de polyamides
DEG35696A DE1255627B (de)	1961-08-11	1962-08-10	Verfahren zum Faerben von natuerlichen oder synthetischen Polyamidfasern
GB30714/62A GB969701A (en)	1961-08-11	1962-08-10	Process for the dyeing of polyamide fibres and dye liquors for use therein
GB30715/62A GB975375A (en)	1961-08-11	1962-08-10	Process for the dyeing of polyamide fibres and dye liquors for use therein
ES280150A ES280150A1 (es)	1961-08-11	1962-08-10	Procedimiento para teñir fibras de poliamida
US571194A US3468620A (en)	1961-08-11	1966-08-09	Process for the dyeing of polyamide fibers

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH942861A CH384530A (de)	1961-08-11	1961-08-11	Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters

Publications (2)

Publication Number	Publication Date
CH942861A4 CH942861A4 (fr)	1963-07-31
CH384530A true CH384530A (de)	1965-02-15

Family

ID=4351869

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH942861A CH384530A (de)	1961-08-11	1961-08-11	Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters

Country Status (4)

Country	Link
BE (1)	BE621284A (fr)
CH (1)	CH384530A (fr)
ES (2)	ES280150A1 (fr)
FR (1)	FR1331094A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3702229A (en) *	1970-12-29	1972-11-07	Ciba Geigy Corp	Printing of anionic dyes on polycarbon-amides of bis(para-aminocyclohexyl)methane and dodecanedioic acid

1961
- 1961-08-11 CH CH942861A patent/CH384530A/de unknown
1962
- 1962-08-10 FR FR906698A patent/FR1331094A/fr not_active Expired
- 1962-08-10 ES ES280150A patent/ES280150A1/es not_active Expired
- 1962-08-10 ES ES280151A patent/ES280151A1/es not_active Expired
- 1962-08-10 BE BE621284A patent/BE621284A/fr unknown

Also Published As

Publication number	Publication date
FR1331094A (fr)	1963-06-28
BE621284A (fr)	1963-02-11
ES280151A1 (es)	1963-05-01
ES280150A1 (es)	1963-05-01
CH942861A4 (fr)	1963-07-31

Publication	Publication Date	Title
DE582101C (de)	1933-08-10	Verfahren zur Verbesserung der Echtheitseigenschaften von mit wasserloeslichen Farbstoffen gefaerbten Textilien
CH531262A (de)	1972-11-30	Flach-Kollektor
DE685124C (de)	1939-12-12	Verfahren zum Faerben von Faserstoffen
DE1290913B (de)	1969-03-20	Verfahren zum Faerben von organischem Fasermaterial
CH384530A (de)	1965-02-15	Verfahren zum Färben und Bedrucken von natürlichen oder synthetischen Polyamidfasern mit Farbstoffen anionischen Charakters
DE1444267B1 (de)	1969-10-16	Verfahren zum Faerben von Polyamidfasern und Faerbereihilfsmittel
DE1255627B (de)	1967-12-07	Verfahren zum Faerben von natuerlichen oder synthetischen Polyamidfasern
DE849992C (de)	1952-09-22	Verfahren zur Herstellung von Faerbungen und Drucken auf Polyamidfasern
DE2108876C3 (de)	1974-01-17	Verfahren zum einbadigen Färben von Mischungen aus Cellulose- und Polyamidfasern nach der Ausziehmethode
AT224597B (de)	1962-11-26	Verfahren zum Färben von Polypeptidfasern
DE1444267C (de)		Verfahren zum Färben von Polyamidfasern und Färbereihilfsmittel
DE402623C (de)	1924-09-16	Neuerung im Verfahren zur Darstellung von Azofarbstoffen aus 2,3-Oxynaphthoesaeurearyliden auf der Faser
DE537126C (de)	1931-10-30	Verfahren zur Darstellung von wasserunloeslichen Azofarbstoffen
DE914245C (de)	1954-06-28	Verfahren zum Faerben oder Bedrucken von Wolle in verschiedenen Schattierungen oder Farben
AT101301B (de)	1925-10-26	Verfahren zur Erzeugung von Färbungen und Drucken mit Küpenfarbstoffen.
DE933022C (de)	1955-09-15	Verfahren zur Herstellung von Effektfaeden enthaltenden Faserverbaenden
DE913285C (de)	1954-06-10	Verfahren zum Faerben mit sauren Farbstoffen und Faerbepraeparate
DE1263677B (de)	1968-03-21	Verfahren zum Faerben von natuerlichen und synthetischen Polyamidfasern
DE641517C (de)	1937-02-03	Verfahren zur Herstellung von wasserunloeslichen Azofarbstoffen auf Wolle
DE371597C (de)	1923-03-16	Verfahren zur Herstellung echter Drucke oder Faerbungen
DE1619569A1 (de)	1970-10-01	Verfahren zum Faerben von organischem Fasermaterial
DE402502C (de)	1924-09-15	Verfahren zur Herstellung waschechter Faerbungen auf pflanzlichen Fasern
AT155964B (de)	1939-04-25	Verfahren zur Herstellung wasserunlöslicher Farbstoffe auf der Faser nach der Eisfarbenmethode.
DE744275C (de)	1944-06-08	Verfahren zum Buntreservieren von Anilinschwarz mit Schwefelsaeureestersalzen von Leukokuepenfarbstoffen oder mit Eisfarbenzubereitungen, die im Saeuredampf entwickelt werden, auf Cellulosefasern
DE395636C (de)	1924-05-21	Verfahren zum Faerben und Drucken von Celluloseacetatseide