DD204277A5 - Verfahren zum kontinuierlichen faerben von fasergut - Google Patents

Verfahren zum kontinuierlichen faerben von fasergut Download PDF

Info

Publication number: DD204277A5
Authority: DD; German Democratic Republic
Prior art keywords: dye; general formula; dyeing; items; anhydrobases
Prior art date: 1981-10-16

Application number

DD82243984A

Other languages

German (de)

English (en)

Inventor

Manfred Haehnke

Wolfgang Teige

Original Assignee

Hoechst Ag

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.)

1981-10-16

Filing date

1982-10-14

Publication date

1983-11-23

1982-10-14 Application filed by Hoechst Ag filed Critical Hoechst Ag

1983-11-23 Publication of DD204277A5 publication Critical patent/DD204277A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 54
239000011152 fibreglass Substances 0.000 title 1
239000000975 dye Substances 0.000 claims abstract description 92
230000008569 process Effects 0.000 claims abstract description 34
229920000642 polymer Polymers 0.000 claims abstract description 30
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 29
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 23
239000000203 mixture Substances 0.000 claims abstract description 15
239000000981 basic dye Substances 0.000 claims abstract description 12
239000002657 fibrous material Substances 0.000 claims abstract description 12
239000003960 organic solvent Substances 0.000 claims abstract description 9
238000010014 continuous dyeing Methods 0.000 claims abstract description 8
238000009987 spinning Methods 0.000 claims description 26
239000002904 solvent Substances 0.000 claims description 22
-1 xanthene compound Chemical class 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 11
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 10
150000001875 compounds Chemical class 0.000 claims description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
229920001577 copolymer Polymers 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
150000005840 aryl radicals Chemical class 0.000 claims description 6
QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 6
125000001424 substituent group Chemical group 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 4
125000001769 aryl amino group Chemical group 0.000 claims description 4
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims description 3
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
238000004519 manufacturing process Methods 0.000 claims description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 2
238000006798 ring closing metathesis reaction Methods 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
125000003710 aryl alkyl group Chemical group 0.000 claims 1
229910052739 hydrogen Inorganic materials 0.000 claims 1
239000001257 hydrogen Substances 0.000 claims 1
150000002790 naphthalenes Chemical class 0.000 claims 1
125000004430 oxygen atom Chemical group O* 0.000 claims 1
125000003107 substituted aryl group Chemical group 0.000 claims 1
238000004043 dyeing Methods 0.000 abstract description 59
239000000835 fiber Substances 0.000 abstract description 32
230000015271 coagulation Effects 0.000 abstract description 27
238000005345 coagulation Methods 0.000 abstract description 27
229920002239 polyacrylonitrile Polymers 0.000 abstract description 15
150000001450 anions Chemical class 0.000 abstract description 12
150000003839 salts Chemical class 0.000 abstract description 10
230000002378 acidificating effect Effects 0.000 abstract description 6
125000000129 anionic group Chemical group 0.000 abstract description 4
239000000470 constituent Substances 0.000 abstract description 3
239000003795 chemical substances by application Substances 0.000 abstract 1
238000007380 fibre production Methods 0.000 abstract 1
230000003993 interaction Effects 0.000 abstract 1
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 33
239000002585 base Substances 0.000 description 20
238000004040 coloring Methods 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 6
239000002253 acid Substances 0.000 description 6
239000000463 material Substances 0.000 description 6
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
230000015572 biosynthetic process Effects 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
238000012986 modification Methods 0.000 description 5
230000004048 modification Effects 0.000 description 5
238000005406 washing Methods 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
150000001768 cations Chemical class 0.000 description 4
239000007788 liquid Substances 0.000 description 4
238000002166 wet spinning Methods 0.000 description 4
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
238000001035 drying Methods 0.000 description 3
238000001802 infusion Methods 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000011084 recovery Methods 0.000 description 3
238000010186 staining Methods 0.000 description 3
OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 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
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 2
230000008901 benefit Effects 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Chemical group 0.000 description 2
230000008859 change Effects 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
238000005260 corrosion Methods 0.000 description 2
238000002788 crimping Methods 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
238000004821 distillation Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
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 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
230000007935 neutral effect Effects 0.000 description 2
229920000058 polyacrylate Polymers 0.000 description 2
229920002959 polymer blend Polymers 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
238000010025 steaming Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 2
OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 description 1
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
FCYVWWWTHPPJII-UHFFFAOYSA-N 2-methylidenepropanedinitrile Chemical compound N#CC(=C)C#N FCYVWWWTHPPJII-UHFFFAOYSA-N 0.000 description 1
XEEYSDHEOQHCDA-UHFFFAOYSA-N 2-methylprop-2-ene-1-sulfonic acid Chemical compound CC(=C)CS(O)(=O)=O XEEYSDHEOQHCDA-UHFFFAOYSA-N 0.000 description 1
AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
SGHZXLIDFTYFHQ-UHFFFAOYSA-L Brilliant Blue Chemical compound [Na+].[Na+].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 SGHZXLIDFTYFHQ-UHFFFAOYSA-L 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
ZMJPCIAEJKVKMQ-UHFFFAOYSA-M [4-[[4-[benzyl(methyl)amino]phenyl]-[4-(dimethylamino)phenyl]methylidene]cyclohexa-2,5-dien-1-ylidene]-dimethylazanium;chloride Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC(=CC=1)N(C)CC=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 ZMJPCIAEJKVKMQ-UHFFFAOYSA-M 0.000 description 1
150000008360 acrylonitriles Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
238000013475 authorization Methods 0.000 description 1
POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical group [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 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
GSCLMSFRWBPUSK-UHFFFAOYSA-N beta-Butyrolactone Chemical compound CC1CC(=O)O1 GSCLMSFRWBPUSK-UHFFFAOYSA-N 0.000 description 1
230000000740 bleeding effect Effects 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
MKUWVMRNQOOSAT-UHFFFAOYSA-N but-3-en-2-ol Chemical compound CC(O)C=C MKUWVMRNQOOSAT-UHFFFAOYSA-N 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
230000001112 coagulating effect Effects 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000010276 construction Methods 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
230000001627 detrimental effect Effects 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
238000005108 dry cleaning Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
238000001125 extrusion Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
239000012458 free base Substances 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
238000007654 immersion Methods 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
150000004893 oxazines Chemical class 0.000 description 1
230000035515 penetration Effects 0.000 description 1
239000003495 polar organic solvent Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
UIIIBRHUICCMAI-UHFFFAOYSA-N prop-2-ene-1-sulfonic acid Chemical compound OS(=O)(=O)CC=C UIIIBRHUICCMAI-UHFFFAOYSA-N 0.000 description 1
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
238000004064 recycling Methods 0.000 description 1
238000012552 review Methods 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
239000000758 substrate Substances 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000007704 transition Effects 0.000 description 1
AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
238000003466 welding Methods 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/06—Dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/10—Amino derivatives of triarylmethanes
- C09B11/24—Phthaleins containing amino groups ; Phthalanes; Fluoranes; Phthalides; Rhodamine dyes; Phthaleins having heterocyclic aryl rings; Lactone or lactame forms of triarylmethane dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B11/00—Diaryl- or thriarylmethane dyes
- C09B11/04—Diaryl- or thriarylmethane dyes derived from triarylmethanes, i.e. central C-atom is substituted by amino, cyano, alkyl
- C09B11/26—Triarylmethane dyes in which at least one of the aromatic nuclei is heterocyclic
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B17/00—Azine dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B19/00—Oxazine dyes
- 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
- D06P3/70—Material containing nitrile groups
- D06P3/702—Material containing nitrile groups dyeing of material in the gel state
- 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
- Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
- Y10S8/92—Synthetic fiber dyeing
- Y10S8/927—Polyacrylonitrile fiber

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Dispersion Chemistry (AREA)
Manufacturing & Machinery (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Coloring (AREA)
Artificial Filaments (AREA)

DD82243984A 1981-10-16 1982-10-14 Verfahren zum kontinuierlichen faerben von fasergut DD204277A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813141082 DE3141082A1 (de)	1981-10-16	1981-10-16	Verfahren zum kontinuierlichen faerben von fasergut von aus organischen loesemitteln versponnenen acrylnitril-polymerisaten im gelzustand

Publications (1)

Publication Number	Publication Date
DD204277A5 true DD204277A5 (de)	1983-11-23

Family

ID=6144219

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82243984A DD204277A5 (de)	1981-10-16	1982-10-14	Verfahren zum kontinuierlichen faerben von fasergut

Country Status (4)

Country	Link
US (1)	US4445904A (fr)
EP (1)	EP0077514A3 (fr)
DD (1)	DD204277A5 (fr)
DE (1)	DE3141082A1 (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IT1153962B (it) *	1982-12-31	1987-01-21	Snia Fibre	Procedimento per la produzione di fibre tinte in linea a base di acrilonitrile
US4944806A (en) *	1987-12-28	1990-07-31	Basf Corporation	Rigmentary salt of a triphenylmethane compound and process for making same
WO2004101709A1 (fr)	2003-05-09	2004-11-25	Applera Corporation	Colorants de phenyle xanthene
US7432298B2 (en) *	2003-05-09	2008-10-07	Applied Biosystems Inc.	Fluorescent polymeric materials containing lipid soluble rhodamine dyes
JP6086885B2 (ja) *	2013-09-30	2017-03-01	富士フイルム株式会社	着色組成物、硬化膜、カラーフィルタ、カラーフィルタの製造方法、固体撮像素子、画像表示装置および化合物

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH522047A (de) *	1969-12-23	1972-04-30	Ciba Geigy Ag	Verfahren zur Färbung von im Nass-Spinnverfahren hergestellten Fasern
JPS5633512B1 (fr) *	1970-06-29	1981-08-04
ES432223A1 (es) *	1973-11-29	1977-03-01	Hoechst Ag	Procedimiento para la tincion en hilatura de polimeros o copolimeros de acrilonitrilo modificados con acidos.
DE2438544C3 (de) *	1974-08-10	1979-08-02	Bayer Ag, 5090 Leverkusen	Verfahren zur Herstellung gefärbter Fäden aus vollaromatischen Polyamiden
DE2606906A1 (de) *	1976-02-20	1977-08-25	Hoechst Ag	Verfahren zur herstellung von faerbungen und drucken auf polyacrylnitril- bzw. sauer modifizierten polyester-fasermaterialien und mittel zu seiner durchfuehrung
IT1114708B (it) *	1978-03-02	1986-01-27	Yorkshire Chemicals Ltd	Procedimento per la colorazione di fibre di polimeri e copolimeri di acrilonitrile
DE3026948A1 (de) *	1980-07-16	1982-02-11	Hoechst Ag, 6000 Frankfurt	Verfahren zum faerben von fasergut aus nassgesponnenen acrylnitril-polymerisaten im gelzustand

1981
- 1981-10-16 DE DE19813141082 patent/DE3141082A1/de not_active Withdrawn
1982
- 1982-10-11 EP EP82109379A patent/EP0077514A3/fr not_active Withdrawn
- 1982-10-14 DD DD82243984A patent/DD204277A5/de unknown
- 1982-10-14 US US06/434,374 patent/US4445904A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
EP0077514A2 (fr)	1983-04-27
DE3141082A1 (de)	1983-04-28
EP0077514A3 (fr)	1984-06-06
US4445904A (en)	1984-05-01

Publication	Publication Date	Title
EP0044059B1 (fr)	1986-03-12	Procédé de teinture à l'état de gel d'articles fibreux en polymères d'acrylonitrile filés au mouillé
EP0376086B1 (fr)	1994-11-30	Mélanges de colorants de dispersion azoiques
DE2438546B2 (de)	1978-11-30	Verfahren zur Herstellung gefärbter Fäden aus vollaromatischen Polyamiden
DE1942409A1 (de)	1970-08-27	Faerbeverfahren
DD204277A5 (de)	1983-11-23	Verfahren zum kontinuierlichen faerben von fasergut
DE2438545C3 (de)	1979-08-09	Verfahren zur Herstellung gefärbter Fäden aus vollaromatischen Polyamiden
DE1014962B (de)	1957-09-05	Verfahren zum Faerben und Bedrucken von geformten Gebilden aus hydrophoben, organischen Hochpolymeren, die Estergruppen enthalten
EP0222696B1 (fr)	1990-05-23	Procédé de post-traitement de matière cellulosique teinte avec des colorants contenant des groupes sulfoniques
DE1469087A1 (de)	1969-01-30	Faerbeverfahren
EP0044061A1 (fr)	1982-01-20	Procédé de teinture à l'état de gel d'articles fibreux filés à partir de solutions de polymères d'acrylonitrile dissous dans des solvants organiques
DE2548009C3 (de)	1980-09-18	Verfahren zum egalen Trichromiefärben von langsam- normal- oder schnellziehenden Polyacrylnitrilmaterialien
DE1494667A1 (de)	1970-12-03	Verfahren zur Verbesserung der Anfaerbbarkeit von Faeden oder Fasern aus synthetischen linearen Polymerisaten,insbesondere Acrylpolymerisaten,durch basische Farbstoffe
EP0044062A1 (fr)	1982-01-20	Procédé de teinture à l'état de gel d'articles fibreux en polymères d'acrylonitrile filés à sec
DE1252846B (de)	1967-10-26	Verfahren zum kontinuierlichen Färben von Fäden und Faserkabeln aus hochmolekularen, linearen Polyestern
DE3781445T2 (de)	1993-03-11	Verfahren zur herstellung von waehrend des spinnverfahrens gefaerbten acrylfasern.
EP0273300A2 (fr)	1988-07-06	Procédé de teinture en un seul bain et une seule étape de mélanges de fibres en polyester pouvant être teintes sans véhiculeur et de fibres cellulosiques
DE3321658A1 (de)	1983-12-15	Verfahren zum faerben von polycapronamid-textilfabrikationsartikeln
EP0099111A1 (fr)	1984-01-25	Procédé de teinture à haute température de matériaux en polyester
EP0057457B1 (fr)	1985-08-21	Procédé pour teindre de façon égale, en deux et trois couleurs, des matières en polyacrylonitrile
DE2504997A1 (de)	1975-08-21	Verfahren zur faerbung in der masse von acrylfasern
DE1669418C3 (fr)	1974-12-19
DE2438543B2 (de)	1978-11-16	Verfahren zur Herstellung gefärbter Fäden aus vollaromatischen Polyamiden
AT208500B (de)	1960-04-11	Verfahren zur Herstellung von synthetischen Fasern aus Polyacrylnitrilpolymerisaten oder Mischpolymerisaten mit überwiegendem Anteil an Acrylnitril
DE1669388C3 (de)	1977-02-24	Verfahren zum Herstellen von Acrylnitrilpolymerisatfasern
DE2018689A1 (de)	1970-11-19	Verfahren zum Färben von synthetischen Superpolyamiden in der Spinnmasse