CS197314B2 - Method of continuously coloring textile fabrics from aromatic polyesters,or cellulose triacetate - Google Patents

Method of continuously coloring textile fabrics from aromatic polyesters,or cellulose triacetate Download PDF

Info

Publication number: CS197314B2
Authority: CS; Czechoslovakia
Prior art keywords: dye; dyes; reactive; textile material; beta
Prior art date: 1977-01-14

Application number

CS78263A

Other languages

Czech (cs)

English (en)

Inventor

Violet Boyd

Brian R Fishwick

Original Assignee

Glover Brian

Korn Steward R

Bostock Susan M

Ici Ltd

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.)

1977-01-14

Filing date

1978-01-13

Publication date

1980-04-30

1978-01-13 Application filed by Glover Brian, Korn Steward R, Bostock Susan M, Ici Ltd filed Critical Glover Brian

1980-04-30 Publication of CS197314B2 publication Critical patent/CS197314B2/cs

Links

239000004753 textile Substances 0.000 title claims abstract description 73
229920000728 polyester Polymers 0.000 title claims abstract description 52
238000000034 method Methods 0.000 title claims abstract description 50
125000003118 aryl group Chemical group 0.000 title claims abstract description 49
229920002284 Cellulose triacetate Polymers 0.000 title claims abstract description 9
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 title claims abstract description 9
238000004040 coloring Methods 0.000 title claims description 14
239000004744 fabric Substances 0.000 title description 48
239000000463 material Substances 0.000 claims abstract description 80
239000000975 dye Substances 0.000 claims abstract description 74
230000008569 process Effects 0.000 claims abstract description 27
229920002678 cellulose Polymers 0.000 claims abstract description 10
239000001913 cellulose Substances 0.000 claims abstract description 10
125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims abstract description 9
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 7
ILJSQTXMGCGYMG-UHFFFAOYSA-N triacetic acid Chemical compound CC(=O)CC(=O)CC(O)=O ILJSQTXMGCGYMG-UHFFFAOYSA-N 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 91
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 63
239000000835 fiber Substances 0.000 claims description 50
238000007639 printing Methods 0.000 claims description 49
239000000985 reactive dye Substances 0.000 claims description 41
239000000986 disperse dye Substances 0.000 claims description 37
239000006185 dispersion Substances 0.000 claims description 35
229920003043 Cellulose fiber Polymers 0.000 claims description 27
239000000049 pigment Substances 0.000 claims description 19
238000010025 steaming Methods 0.000 claims description 14
238000010438 heat treatment Methods 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 8
125000001424 substituent group Chemical group 0.000 claims description 8
125000000623 heterocyclic group Chemical group 0.000 claims description 7
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 6
229910052799 carbon Inorganic materials 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 3
239000000460 chlorine Substances 0.000 claims description 3
229910052731 fluorine Inorganic materials 0.000 claims description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
125000001931 aliphatic group Chemical group 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
238000011437 continuous method Methods 0.000 claims 1
125000001153 fluoro group Chemical group F* 0.000 claims 1
229910052717 sulfur Inorganic materials 0.000 claims 1
239000011593 sulfur Substances 0.000 claims 1
-1 for example by block Substances 0.000 description 93
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 57
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 32
239000007864 aqueous solution Substances 0.000 description 30
239000000126 substance Substances 0.000 description 29
239000000987 azo dye Substances 0.000 description 24
238000005859 coupling reaction Methods 0.000 description 22
239000000243 solution Substances 0.000 description 22
230000008878 coupling Effects 0.000 description 21
238000010168 coupling process Methods 0.000 description 21
229910000029 sodium carbonate Inorganic materials 0.000 description 16
229920000742 Cotton Polymers 0.000 description 15
239000005020 polyethylene terephthalate Substances 0.000 description 15
239000003599 detergent Substances 0.000 description 12
229920004933 Terylene® Polymers 0.000 description 11
239000003513 alkali Substances 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 10
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 9
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 8
239000012670 alkaline solution Substances 0.000 description 8
FFRBMBIXVSCUFS-UHFFFAOYSA-N 2,4-dinitro-1-naphthol Chemical compound C1=CC=C2C(O)=C([N+]([O-])=O)C=C([N+]([O-])=O)C2=C1 FFRBMBIXVSCUFS-UHFFFAOYSA-N 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 7
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 7
239000004202 carbamide Substances 0.000 description 7
150000001875 compounds Chemical class 0.000 description 7
239000002270 dispersing agent Substances 0.000 description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 7
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 6
WMFOQBRAJBCJND-UHFFFAOYSA-M Lithium hydroxide Chemical compound [Li+].[OH-] WMFOQBRAJBCJND-UHFFFAOYSA-M 0.000 description 6
229920000297 Rayon Polymers 0.000 description 6
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
238000001035 drying Methods 0.000 description 6
229920002239 polyacrylonitrile Polymers 0.000 description 6
229910052708 sodium Inorganic materials 0.000 description 6
239000011734 sodium Substances 0.000 description 6
235000010413 sodium alginate Nutrition 0.000 description 6
239000000661 sodium alginate Substances 0.000 description 6
229940005550 sodium alginate Drugs 0.000 description 6
239000000984 vat dye Substances 0.000 description 6
239000003795 chemical substances by application Substances 0.000 description 5
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
LJRGBERXYNQPJI-UHFFFAOYSA-M sodium;3-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC(S([O-])(=O)=O)=C1 LJRGBERXYNQPJI-UHFFFAOYSA-M 0.000 description 5
125000000542 sulfonic acid group Chemical group 0.000 description 5
239000002562 thickening agent Substances 0.000 description 5
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
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
125000001309 chloro group Chemical group Cl* 0.000 description 4
DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
239000000982 direct dye Substances 0.000 description 4
238000004043 dyeing Methods 0.000 description 4
239000003921 oil Substances 0.000 description 4
229920000139 polyethylene terephthalate Polymers 0.000 description 4
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 4
235000019982 sodium hexametaphosphate Nutrition 0.000 description 4
239000000988 sulfur dye Substances 0.000 description 4
239000001577 tetrasodium phosphonato phosphate Substances 0.000 description 4
QPQKUYVSJWQSDY-UHFFFAOYSA-N 4-phenyldiazenylaniline Chemical class C1=CC(N)=CC=C1N=NC1=CC=CC=C1 QPQKUYVSJWQSDY-UHFFFAOYSA-N 0.000 description 3
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical group OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 3
239000002253 acid Substances 0.000 description 3
230000002378 acidificating effect Effects 0.000 description 3
239000003638 chemical reducing agent Substances 0.000 description 3
150000008049 diazo compounds Chemical class 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
238000005470 impregnation Methods 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 3
230000007935 neutral effect Effects 0.000 description 3
239000010665 pine oil Substances 0.000 description 3
238000012545 processing Methods 0.000 description 3
230000002829 reductive effect Effects 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
159000000000 sodium salts Chemical class 0.000 description 3
229920002994 synthetic fiber Polymers 0.000 description 3
239000004758 synthetic textile Substances 0.000 description 3
HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 3
238000005406 washing Methods 0.000 description 3
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 2
RHEVAQGXLUQWBM-UHFFFAOYSA-N 2-(1-amino-9,10-dioxoanthracen-2-yl)naphtho[2,3-f][1,3]benzoxazole-5,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C(C=C2O3)=C1C=C2N=C3C1=C(N)C(C(=O)C2=CC=CC=C2C2=O)=C2C=C1 RHEVAQGXLUQWBM-UHFFFAOYSA-N 0.000 description 2
AKCRQHGQIJBRMN-UHFFFAOYSA-N 2-chloroaniline Chemical compound NC1=CC=CC=C1Cl AKCRQHGQIJBRMN-UHFFFAOYSA-N 0.000 description 2
JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
PNPCRKVUWYDDST-UHFFFAOYSA-N 3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1 PNPCRKVUWYDDST-UHFFFAOYSA-N 0.000 description 2
JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 2
WOXLPNAOCCIZGP-UHFFFAOYSA-N 4-chloro-2-methoxyaniline Chemical compound COC1=CC(Cl)=CC=C1N WOXLPNAOCCIZGP-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
MPERLAKDODPTCL-UHFFFAOYSA-N C(#N)C1=C(C(=C(C=C1)N=NC1=CC=CC=C1)N)C#N Chemical compound C(#N)C1=C(C(=C(C=C1)N=NC1=CC=CC=C1)N)C#N MPERLAKDODPTCL-UHFFFAOYSA-N 0.000 description 2
206010053567 Coagulopathies Diseases 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
BWIDYKYLZYDCHW-UHFFFAOYSA-N NC(C(C#N)=C(C=C1)N=NC2=CC=CC=C2)=C1[N+]([O-])=O Chemical compound NC(C(C#N)=C(C=C1)N=NC2=CC=CC=C2)=C1[N+]([O-])=O BWIDYKYLZYDCHW-UHFFFAOYSA-N 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
125000004442 acylamino group Chemical group 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
125000003277 amino group Chemical group 0.000 description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
125000000129 anionic group Chemical group 0.000 description 2
239000011260 aqueous acid Substances 0.000 description 2
AAKMSGQPNUGLAZ-UHFFFAOYSA-N atic vat brown r Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC(C(C2=C3NC4=C5C=6C(C7=CC=CC=C7C5=O)=O)=O)=C1C(=O)C2=CC=C3C4=CC=6NC(=O)C1=CC=CC=C1 AAKMSGQPNUGLAZ-UHFFFAOYSA-N 0.000 description 2
229950011260 betanaphthol Drugs 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
125000006267 biphenyl group Chemical group 0.000 description 2
125000002843 carboxylic acid group Chemical group 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
230000035602 clotting Effects 0.000 description 2
239000003086 colorant Substances 0.000 description 2
239000006103 coloring component Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000002845 discoloration Methods 0.000 description 2
239000003623 enhancer Substances 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
150000002430 hydrocarbons Chemical class 0.000 description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
125000001841 imino group Chemical group [H]N=* 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 2
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
SURBWPDBSGYCTM-UHFFFAOYSA-N methyl 2-amino-3-nitro-6-phenyldiazenylbenzoate Chemical compound NC=1C(=C(C=CC=1[N+](=O)[O-])N=NC1=CC=CC=C1)C(=O)OC SURBWPDBSGYCTM-UHFFFAOYSA-N 0.000 description 2
VAMXMNNIEUEQDV-UHFFFAOYSA-N methyl anthranilate Chemical compound COC(=O)C1=CC=CC=C1N VAMXMNNIEUEQDV-UHFFFAOYSA-N 0.000 description 2
230000005012 migration Effects 0.000 description 2
238000013508 migration Methods 0.000 description 2
RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 2
GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
239000007800 oxidant agent Substances 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
RZXMPPFPUUCRFN-UHFFFAOYSA-N p-toluidine Chemical compound CC1=CC=C(N)C=C1 RZXMPPFPUUCRFN-UHFFFAOYSA-N 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
229910000027 potassium carbonate Inorganic materials 0.000 description 2
230000009467 reduction Effects 0.000 description 2
239000012266 salt solution Substances 0.000 description 2
238000002791 soaking Methods 0.000 description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
235000017557 sodium bicarbonate Nutrition 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
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
238000010186 staining Methods 0.000 description 2
239000000758 substrate Substances 0.000 description 2
229940006295 sulfonated oleic acid Drugs 0.000 description 2
239000000271 synthetic detergent Substances 0.000 description 2
JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 2
TUHUVPGYYIDKLW-UHFFFAOYSA-N (4-amino-2-chlorophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C(Cl)=C1 TUHUVPGYYIDKLW-UHFFFAOYSA-N 0.000 description 1
FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical compound C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-N 0.000 description 1
GWEHVDNNLFDJLR-UHFFFAOYSA-N 1,3-diphenylurea Chemical group C=1C=CC=CC=1NC(=O)NC1=CC=CC=C1 GWEHVDNNLFDJLR-UHFFFAOYSA-N 0.000 description 1
ZDBJFAWRZSOCMM-UHFFFAOYSA-N 1-(bromomethyl)-2,4-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=C(CBr)C([N+]([O-])=O)=C1 ZDBJFAWRZSOCMM-UHFFFAOYSA-N 0.000 description 1
JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical class NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 description 1
PGYZAKRTYUHXRA-UHFFFAOYSA-N 2,10-dinitro-12h-[1,4]benzothiazino[3,2-b]phenothiazin-3-one Chemical compound S1C2=CC(=O)C([N+]([O-])=O)=CC2=NC2=C1C=C1SC3=CC=C([N+](=O)[O-])C=C3NC1=C2 PGYZAKRTYUHXRA-UHFFFAOYSA-N 0.000 description 1
GVBHCMNXRKOJRH-UHFFFAOYSA-N 2,4,5,6-tetrachloropyrimidine Chemical compound ClC1=NC(Cl)=C(Cl)C(Cl)=N1 GVBHCMNXRKOJRH-UHFFFAOYSA-N 0.000 description 1
NGXMWCHDSDVSJY-UHFFFAOYSA-N 2,4-dibromo-6-methoxyaniline Chemical compound COC1=CC(Br)=CC(Br)=C1N NGXMWCHDSDVSJY-UHFFFAOYSA-N 0.000 description 1
NMGHEOHOYKBWEM-UHFFFAOYSA-N 2,4-dichloro-6-methoxyaniline Chemical compound COC1=CC(Cl)=CC(Cl)=C1N NMGHEOHOYKBWEM-UHFFFAOYSA-N 0.000 description 1
WAEZOSSWRXDWAX-UHFFFAOYSA-N 2,6-dichloropyridin-4-amine Chemical compound NC1=CC(Cl)=NC(Cl)=C1 WAEZOSSWRXDWAX-UHFFFAOYSA-N 0.000 description 1
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 1
WXUAZZARGUDIHU-UHFFFAOYSA-N 2-(ethylamino)-5-sulfobenzoic acid Chemical compound CCNC1=CC=C(S(O)(=O)=O)C=C1C(O)=O WXUAZZARGUDIHU-UHFFFAOYSA-N 0.000 description 1
RIYSFSQPHCAGLS-UHFFFAOYSA-N 2-amino-3,5-dinitrobenzonitrile Chemical compound NC1=C(C#N)C=C([N+]([O-])=O)C=C1[N+]([O-])=O RIYSFSQPHCAGLS-UHFFFAOYSA-N 0.000 description 1
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239000001005 nitro dye Substances 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
VMPITZXILSNTON-UHFFFAOYSA-N o-anisidine Chemical compound COC1=CC=CC=C1N VMPITZXILSNTON-UHFFFAOYSA-N 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
BHAAPTBBJKJZER-UHFFFAOYSA-N p-anisidine Chemical compound COC1=CC=C(N)C=C1 BHAAPTBBJKJZER-UHFFFAOYSA-N 0.000 description 1
125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
ABLZXFCXXLZCGV-UHFFFAOYSA-N phosphonic acid group Chemical group P(O)(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
230000002250 progressing effect Effects 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
239000003352 sequestering agent Substances 0.000 description 1
230000035939 shock Effects 0.000 description 1
150000003377 silicon compounds Chemical class 0.000 description 1
COEZWFYORILMOM-UHFFFAOYSA-M sodium 4-[(2,4-dihydroxyphenyl)diazenyl]benzenesulfonate Chemical compound [Na+].OC1=CC(O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 COEZWFYORILMOM-UHFFFAOYSA-M 0.000 description 1
FDRCDNZGSXJAFP-UHFFFAOYSA-M sodium chloroacetate Chemical compound [Na+].[O-]C(=O)CCl FDRCDNZGSXJAFP-UHFFFAOYSA-M 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
229910052911 sodium silicate Inorganic materials 0.000 description 1
229910052979 sodium sulfide Inorganic materials 0.000 description 1
GRVFOGOEDUUMBP-UHFFFAOYSA-N sodium sulfide (anhydrous) Chemical compound [Na+].[Na+].[S-2] GRVFOGOEDUUMBP-UHFFFAOYSA-N 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
FGDMJJQHQDFUCP-UHFFFAOYSA-M sodium;2-propan-2-ylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=CC2=C(S([O-])(=O)=O)C(C(C)C)=CC=C21 FGDMJJQHQDFUCP-UHFFFAOYSA-M 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000008107 starch Substances 0.000 description 1
235000019698 starch Nutrition 0.000 description 1
PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical group C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
235000021286 stilbenes Nutrition 0.000 description 1
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
238000012360 testing method Methods 0.000 description 1
238000010023 transfer printing Methods 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
HADKRTWCOYPCPH-UHFFFAOYSA-M trimethylphenylammonium hydroxide Chemical compound [OH-].C[N+](C)(C)C1=CC=CC=C1 HADKRTWCOYPCPH-UHFFFAOYSA-M 0.000 description 1
MSBHLDQWHHNCML-UHFFFAOYSA-K trisodium 4-hydroxy-7-[[5-hydroxy-6-[(2-methoxyphenyl)diazenyl]-7-sulfonatonaphthalen-2-yl]carbamoylamino]-3-[(2-methyl-4-sulfonatophenyl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].COc1ccccc1N=Nc1c(O)c2ccc(NC(=O)Nc3ccc4c(O)c(N=Nc5ccc(cc5C)S([O-])(=O)=O)c(cc4c3)S([O-])(=O)=O)cc2cc1S([O-])(=O)=O MSBHLDQWHHNCML-UHFFFAOYSA-K 0.000 description 1
BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
SOBHUZYZLFQYFK-UHFFFAOYSA-K trisodium;hydroxy-[[phosphonatomethyl(phosphonomethyl)amino]methyl]phosphinate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)CN(CP(O)([O-])=O)CP([O-])([O-])=O SOBHUZYZLFQYFK-UHFFFAOYSA-K 0.000 description 1
WTHDKMILWLGDKL-UHFFFAOYSA-N urea;hydrate Chemical compound O.NC(N)=O WTHDKMILWLGDKL-UHFFFAOYSA-N 0.000 description 1
239000002351 wastewater Substances 0.000 description 1
238000005303 weighing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000011592 zinc chloride Substances 0.000 description 1
235000005074 zinc chloride Nutrition 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
- D06P3/36—Material containing ester groups 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
- 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
- D06P3/82—Textiles which contain different kinds of fibres
- D06P3/8204—Textiles which contain different kinds of fibres fibres of different chemical nature
- D06P3/8223—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups
- D06P3/8238—Textiles which contain different kinds of fibres fibres of different chemical nature mixtures of fibres containing hydroxyl and ester groups using different kinds of dye
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S534/00—Organic compounds -- part of the class 532-570 series
- Y10S534/01—Mixtures of azo compounds

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Chemical & Material Sciences (AREA)
Dispersion Chemistry (AREA)
Coloring (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

CS78263A 1977-01-14 1978-01-13 Method of continuously coloring textile fabrics from aromatic polyesters,or cellulose triacetate CS197314B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB1488/77A GB1589478A (en)	1977-01-14	1977-01-14	Process for the continuous coloration of aromatic polyester or cellulose triacetate textile materials and of unions of aromatic polyester with cellulose

Publications (1)

Publication Number	Publication Date
CS197314B2 true CS197314B2 (en)	1980-04-30

Family

ID=9722891

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS78263A CS197314B2 (en)	1977-01-14	1978-01-13	Method of continuously coloring textile fabrics from aromatic polyesters,or cellulose triacetate

Country Status (21)

Country	Link
US (1)	US4169705A (fr)
JP (1)	JPS5390489A (fr)
BE (1)	BE862647A (fr)
BR (1)	BR7800162A (fr)
CS (1)	CS197314B2 (fr)
DD (1)	DD133827A5 (fr)
DE (1)	DE2801397A1 (fr)
DK (1)	DK17678A (fr)
ES (1)	ES465950A1 (fr)
FI (1)	FI780114A7 (fr)
FR (1)	FR2377473A1 (fr)
GB (1)	GB1589478A (fr)
IL (1)	IL53688A0 (fr)
IT (1)	IT1174354B (fr)
NL (1)	NL7800282A (fr)
NO (1)	NO774388L (fr)
OA (1)	OA05848A (fr)
PL (1)	PL105808B1 (fr)
PT (1)	PT67524B (fr)
SE (1)	SE7800365L (fr)
ZA (1)	ZA777540B (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2929763A1 (de) *	1979-07-23	1981-02-19	Basf Ag	Verfahren zum faerben und bedrucken von cellulosehaltigem textilmaterial
DE2931847A1 (de) *	1979-08-06	1981-02-26	Cassella Ag	Verfahren zum bedrucken von synthetischem, hydrophobem fasermaterial nach dem transferdruckprinzip
US4801303A (en) *	1987-06-01	1989-01-31	Sandoz Ltd.	One-bath dyeing of polyester-cellulosic blends using disperse and sulfur dyes
US5603736A (en) *	1992-04-27	1997-02-18	Burlington Chemical Co., Inc.	Liquid alkali for reactive dyeing of textiles
US6530961B1 (en)	1998-03-04	2003-03-11	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Alkaline aqueous solutions and use thereof in processes for dyeing cellulosic textile materials
BRPI0804658B1 (pt) *	2008-08-11	2012-06-26		processo de tingimento têxtil de fibras celulósicas e suas combinações com outras fibras com banhos de tingimentos reutilizados, sem realizar nenhum tratamento de depuração posterior.
US12151498B2 (en)	2020-12-10	2024-11-26	Appvion, Llc	Multi-purpose phenol-free direct thermal recording media
US12115803B2 (en)	2020-12-10	2024-10-15	Appvion, Llc	Fade-resistant water-dispersible phenol-free direct thermal media
KR20250044285A (ko)	2022-08-10	2025-03-31	압비온, 엘엘씨	내유성을 위한 다이아릴우레아 조합을 포함한 직접 감열식 기록 매체

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3125402A (en) *		1964-03-17		Xcx ch
NL302927A (fr)	1959-05-16
NL302926A (fr)	1960-02-02
DE1266272B (de)	1964-03-21	1968-04-18	Bayer Ag	Verfahren zum Faerben hydrophober Fasermaterialien
IL31803A (en) *	1968-03-22	1972-04-27	Ciba Geigy Ag	Transfer printing
JPS5341270B2 (fr)	1972-06-24	1978-11-01
GB1456586A (en)	1974-04-03	1976-11-24	Ici Ltd	Colouration process
AR206168A1 (es) *	1974-10-31	1976-06-30	Ici Ltd	Procedimiento para la coloracion de materiales textiles de triacetato de celulosa y poliester aromatico

1977
- 1977-01-14 GB GB1488/77A patent/GB1589478A/en not_active Expired
- 1977-12-19 ZA ZA00777540A patent/ZA777540B/xx unknown
- 1977-12-20 NO NO774388A patent/NO774388L/no unknown
- 1977-12-20 US US05/862,428 patent/US4169705A/en not_active Expired - Lifetime
- 1977-12-23 IL IL53688A patent/IL53688A0/xx unknown
1978
- 1978-01-04 BE BE184113A patent/BE862647A/fr not_active IP Right Cessation
- 1978-01-10 NL NL7800282A patent/NL7800282A/xx not_active Application Discontinuation
- 1978-01-11 PL PL1978203935A patent/PL105808B1/pl unknown
- 1978-01-11 BR BR7800162A patent/BR7800162A/pt unknown
- 1978-01-12 PT PT67524A patent/PT67524B/pt unknown
- 1978-01-12 DD DD7800203198A patent/DD133827A5/xx unknown
- 1978-01-12 SE SE7800365A patent/SE7800365L/xx unknown
- 1978-01-13 ES ES465950A patent/ES465950A1/es not_active Expired
- 1978-01-13 CS CS78263A patent/CS197314B2/cs unknown
- 1978-01-13 OA OA56366A patent/OA05848A/fr unknown
- 1978-01-13 IT IT19256/78A patent/IT1174354B/it active
- 1978-01-13 DE DE19782801397 patent/DE2801397A1/de not_active Withdrawn
- 1978-01-13 DK DK17678A patent/DK17678A/da not_active Application Discontinuation
- 1978-01-13 JP JP326478A patent/JPS5390489A/ja active Pending
- 1978-01-13 FI FI780114A patent/FI780114A7/fi not_active Application Discontinuation
- 1978-01-13 FR FR7800964A patent/FR2377473A1/fr active Pending

Also Published As

Publication number	Publication date
OA05848A (fr)	1981-05-31
FR2377473A1 (fr)	1978-08-11
IT7819256A0 (it)	1978-01-13
ES465950A1 (es)	1978-09-16
US4169705A (en)	1979-10-02
DK17678A (da)	1978-07-15
BR7800162A (pt)	1978-09-26
PL105808B1 (pl)	1979-11-30
PT67524A (en)	1978-02-01
IT1174354B (it)	1987-07-01
IL53688A0 (en)	1978-03-10
FI780114A7 (fi)	1978-07-15
SE7800365L (sv)	1978-07-15
DD133827A5 (de)	1979-01-24
PT67524B (en)	1979-06-12
JPS5390489A (en)	1978-08-09
ZA777540B (en)	1978-10-25
GB1589478A (en)	1981-05-13
DE2801397A1 (de)	1978-07-20
NO774388L (no)	1978-07-17
PL203935A1 (pl)	1978-08-28
NL7800282A (nl)	1978-07-18
BE862647A (fr)	1978-07-04

Publication	Publication Date	Title
US3066005A (en)	1962-11-27	Process for the treatment of hydroxyl group-containing textile materials
AU652870B2 (en)	1994-09-08	Process for the preparation of a modified fiber material and process for the dyeing of the modified fiber material anionic textile dyes
US4252530A (en)	1981-02-24	Process for dyeing and printing synthetic hydrophobic fiber material
JPH0748781A (ja)	1995-02-21	三色法でセルロース繊維材料を染色または捺染する方法
US3993438A (en)	1976-11-23	Process for coloring aromatic polyester-cellulose unions with a reactive dyestuff and a disperse dyestuff containing at least two carboxylic acid ester groups
CS197314B2 (en)	1980-04-30	Method of continuously coloring textile fabrics from aromatic polyesters,or cellulose triacetate
JPS626592B2 (fr)	1987-02-12
JPS5842316B2 (ja)	1983-09-19	ホウコウゾクポリエステルマタハトリアセチルセルロ−スセンイザイリヨウノセンシヨクホウ
US4065254A (en)	1977-12-27	Process for dyeing and printing
US4153413A (en)	1979-05-08	Coloration process
US2940812A (en)	1960-06-14	New textile treatment process
US3334961A (en)	1967-08-08	Process for dyeing or printing materials of fibrous structure containing cellulose
US4134723A (en)	1979-01-16	Coloration process
US3530111A (en)	1970-09-22	Water-insoluble phenyl-azo-phenyl dyestuffs
US4110071A (en)	1978-08-29	Process for the tone-in-tone printing and pad-dyeing of textile material made from fibre mixtures
US3494716A (en)	1970-02-10	Printing and dyeing of polyester and cellulosic fibers and blends thereof
US5928387A (en)	1999-07-27	Dye mixtures, process for their preparation and their use
US4147510A (en)	1979-04-03	Coloration process
US3085849A (en)	1963-04-16	Process for dyeing and printing cellulose-containing fibres and composition for same
US4654046A (en)	1987-03-31	Continuous process for dyeing cellulose/polyamide blends: thermobol pad liquor containing nonionic surfactant
KR820000296B1 (ko)	1982-03-19	착색법
JPH01111078A (ja)	1989-04-27	エンデイングを起こすことなしにセルロース繊維材料を染色する方法
US3334084A (en)	1967-08-01	Mono azo pyrazolone dyestuff
US3552906A (en)	1971-01-05	Process for dyeing and printing linear polyester fibers and said dyed fibers
DE2612741A1 (de)	1976-10-07	Verfahren zum faerben von textilmaterialien aus aromatischen polyestern