DD258628A5 - Verfahren zum faerben von textilem material - Google Patents

Verfahren zum faerben von textilem material Download PDF

Info

Publication number: DD258628A5
Authority: DD; German Democratic Republic
Prior art keywords: item; bis; optionally substituted; polymerizable; cyano
Prior art date: 1985-06-12

Application number

DD86291236A

Other languages

German (de)

English (en)

Inventor

Brian Parton

Original Assignee

��@��@��@��k��

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.)

1985-06-12

Filing date

1986-06-12

Publication date

1988-07-27

1986-06-12 Application filed by ��@��@��@��k�� filed Critical ��@��@��@��k��

1988-07-27 Publication of DD258628A5 publication Critical patent/DD258628A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 36
239000004753 textile Substances 0.000 title claims abstract description 12
239000000463 material Substances 0.000 title claims abstract description 11
229920000642 polymer Polymers 0.000 claims abstract description 22
239000003086 colorant Substances 0.000 claims abstract description 12
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
239000001257 hydrogen Substances 0.000 claims abstract description 12
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
238000004043 dyeing Methods 0.000 claims abstract description 8
125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 7
125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 5
125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
125000004429 atom Chemical group 0.000 claims abstract description 4
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 4
125000000547 substituted alkyl group Chemical group 0.000 claims abstract description 4
125000004423 acyloxy group Chemical group 0.000 claims abstract description 3
125000004414 alkyl thio group Chemical group 0.000 claims abstract description 3
125000005110 aryl thio group Chemical group 0.000 claims abstract description 3
125000004104 aryloxy group Chemical group 0.000 claims abstract description 3
229910052799 carbon Inorganic materials 0.000 claims abstract description 3
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 3
125000005843 halogen group Chemical group 0.000 claims abstract 2
229920000742 Cotton Polymers 0.000 claims description 25
239000000975 dye Substances 0.000 claims description 24
230000008878 coupling Effects 0.000 claims description 13
238000010168 coupling process Methods 0.000 claims description 13
238000005859 coupling reaction Methods 0.000 claims description 13
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 claims description 12
125000001424 substituent group Chemical group 0.000 claims description 9
125000000217 alkyl group Chemical group 0.000 claims description 8
125000002837 carbocyclic group Chemical group 0.000 claims description 7
239000000203 mixture Substances 0.000 claims description 7
229920000728 polyester Polymers 0.000 claims description 7
239000000987 azo dye Substances 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
150000001336 alkenes Chemical class 0.000 claims description 5
229920001577 copolymer Polymers 0.000 claims description 5
125000000623 heterocyclic group Chemical group 0.000 claims description 5
238000010014 continuous dyeing Methods 0.000 claims description 4
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 4
150000001412 amines Chemical class 0.000 claims description 3
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
150000002431 hydrogen Chemical class 0.000 claims description 3
125000003107 substituted aryl group Chemical group 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
125000005415 substituted alkoxy group Chemical group 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 abstract 1
238000005429 filling process Methods 0.000 abstract 1
-1 polyazo Polymers 0.000 description 62
239000000178 monomer Substances 0.000 description 27
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 18
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 16
NMLUEJBAVKPZOQ-UHFFFAOYSA-N 2-chloro-4-nitroaniline Chemical compound C1=CC(=C(C=C1[N+](=O)[O-])Cl)N.C1=CC(=C(C=C1[N+](=O)[O-])Cl)N NMLUEJBAVKPZOQ-UHFFFAOYSA-N 0.000 description 14
239000000835 fiber Substances 0.000 description 12
TYMLOMAKGOJONV-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1 TYMLOMAKGOJONV-UHFFFAOYSA-N 0.000 description 10
238000004040 coloring Methods 0.000 description 10
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 9
239000000243 solution Substances 0.000 description 7
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 6
239000010931 gold Substances 0.000 description 6
229910052737 gold Inorganic materials 0.000 description 6
RILVNLMOTMFTMQ-UHFFFAOYSA-N 2-ethylpyrimidine Chemical compound CCC1=NC=CC=N1 RILVNLMOTMFTMQ-UHFFFAOYSA-N 0.000 description 5
241001024304 Mino Species 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
239000000049 pigment Substances 0.000 description 5
238000006116 polymerization reaction Methods 0.000 description 5
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
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 4
150000004056 anthraquinones Chemical class 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
239000004816 latex Substances 0.000 description 4
229920000126 latex Polymers 0.000 description 4
VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical compound [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
239000010981 turquoise Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
CNCOEDDPFOAUMB-UHFFFAOYSA-N N-Methylolacrylamide Chemical class OCNC(=O)C=C CNCOEDDPFOAUMB-UHFFFAOYSA-N 0.000 description 3
238000005299 abrasion Methods 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
238000007334 copolymerization reaction Methods 0.000 description 3
125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 description 3
125000000524 functional group Chemical group 0.000 description 3
KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical compound ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 description 3
239000003973 paint Substances 0.000 description 3
229920002554 vinyl polymer Polymers 0.000 description 3
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 description 2
125000004514 1,2,4-thiadiazolyl group Chemical group 0.000 description 2
QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 2
MGCGMYPNXAFGFA-UHFFFAOYSA-N 2-amino-5-nitrobenzonitrile Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C#N MGCGMYPNXAFGFA-UHFFFAOYSA-N 0.000 description 2
KWIXNFOTNVKIGM-UHFFFAOYSA-N 2-chloro-5-nitroaniline Chemical compound NC1=CC([N+]([O-])=O)=CC=C1Cl KWIXNFOTNVKIGM-UHFFFAOYSA-N 0.000 description 2
UKAGYRHMXMLMLB-UHFFFAOYSA-N 4,5-dihydroxyocta-1,7-diene-3,6-dione Chemical compound C=CC(=O)C(O)C(O)C(=O)C=C UKAGYRHMXMLMLB-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000007983 Tris buffer Substances 0.000 description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
239000001000 anthraquinone dye Substances 0.000 description 2
125000004391 aryl sulfonyl group Chemical group 0.000 description 2
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
239000003431 cross linking reagent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000004744 fabric Substances 0.000 description 2
RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 2
239000003999 initiator Substances 0.000 description 2
239000000543 intermediate Substances 0.000 description 2
LZXXNPOYQCLXRS-UHFFFAOYSA-N methyl 4-aminobenzoate Chemical compound COC(=O)C1=CC=C(N)C=C1 LZXXNPOYQCLXRS-UHFFFAOYSA-N 0.000 description 2
229960001156 mitoxantrone Drugs 0.000 description 2
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 2
229920002239 polyacrylonitrile Polymers 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
102000004169 proteins and genes Human genes 0.000 description 2
108090000623 proteins and genes Proteins 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 2
229920001567 vinyl ester resin Polymers 0.000 description 2
210000002268 wool Anatomy 0.000 description 2
QLRBNEZOQPLERN-UHFFFAOYSA-N (sulfonylamino)benzene Chemical compound O=S(=O)=NC1=CC=CC=C1 QLRBNEZOQPLERN-UHFFFAOYSA-N 0.000 description 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
125000004520 1,3,4-thiadiazolyl group Chemical group 0.000 description 1
QWXDVWSEUJXVIK-UHFFFAOYSA-N 1,8-diaminoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC(N)=C2C(=O)C2=C1C=CC=C2N QWXDVWSEUJXVIK-UHFFFAOYSA-N 0.000 description 1
YTVNZOABECTEPK-UHFFFAOYSA-N 1-[(2-nitrophenyl)diazenyl]naphthalen-2-ol Chemical compound OC1=CC=C2C=CC=CC2=C1N=NC1=CC=CC=C1[N+]([O-])=O YTVNZOABECTEPK-UHFFFAOYSA-N 0.000 description 1
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 description 1
AZXGXVQWEUFULR-UHFFFAOYSA-N 2',4',5',7'-tetrabromofluorescein Chemical compound OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 AZXGXVQWEUFULR-UHFFFAOYSA-N 0.000 description 1
DUJCPIVNSCGBIH-UHFFFAOYSA-N 2,4,6-trichloropyridin-3-amine Chemical compound NC1=C(Cl)C=C(Cl)N=C1Cl DUJCPIVNSCGBIH-UHFFFAOYSA-N 0.000 description 1
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 1
GDFCZZHSWGWCHP-UHFFFAOYSA-N 2-amino-1,3-benzothiazole-6-carbonitrile Chemical compound C1=C(C#N)C=C2SC(N)=NC2=C1 GDFCZZHSWGWCHP-UHFFFAOYSA-N 0.000 description 1
QTGIFTCDTLWDQE-UHFFFAOYSA-N 2-amino-1,3-thiazole-4,5-dicarbonitrile Chemical compound NC1=NC(C#N)=C(C#N)S1 QTGIFTCDTLWDQE-UHFFFAOYSA-N 0.000 description 1
UAQHVBUYWYKCFB-UHFFFAOYSA-N 2-amino-4,6-bis(trifluoromethyl)benzonitrile Chemical compound NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1C#N UAQHVBUYWYKCFB-UHFFFAOYSA-N 0.000 description 1
KJRBYUWRYRRPKN-UHFFFAOYSA-N 2-amino-4-chloro-1,3-thiazole-5-carbaldehyde Chemical compound NC1=NC(Cl)=C(C=O)S1 KJRBYUWRYRRPKN-UHFFFAOYSA-N 0.000 description 1
WLKYODIBWNIWDK-UHFFFAOYSA-N 2-amino-4-nitrobenzonitrile Chemical compound NC1=CC([N+]([O-])=O)=CC=C1C#N WLKYODIBWNIWDK-UHFFFAOYSA-N 0.000 description 1
CIVQKYPSJGJRGD-UHFFFAOYSA-N 2-amino-5-bromobenzene-1,3-dicarbonitrile Chemical compound NC1=C(C#N)C=C(Br)C=C1C#N CIVQKYPSJGJRGD-UHFFFAOYSA-N 0.000 description 1
TUHHSODDHFDRGR-UHFFFAOYSA-N 2-amino-5-methylbenzene-1,3-dicarbonitrile Chemical compound CC1=CC(C#N)=C(N)C(C#N)=C1 TUHHSODDHFDRGR-UHFFFAOYSA-N 0.000 description 1
ZBEGDHIBRPHOBV-UHFFFAOYSA-N 2-amino-5-nitrobenzene-1,3-dicarbonitrile Chemical compound NC1=C(C#N)C=C([N+]([O-])=O)C=C1C#N ZBEGDHIBRPHOBV-UHFFFAOYSA-N 0.000 description 1
ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 description 1
DXYYSGDWQCSKKO-UHFFFAOYSA-N 2-methylbenzothiazole Chemical compound C1=CC=C2SC(C)=NC2=C1 DXYYSGDWQCSKKO-UHFFFAOYSA-N 0.000 description 1
DHKZCKNBYFNUET-UHFFFAOYSA-N 3-(3-cyano-2-hydroxy-4-methyl-6-oxopyridin-1-yl)propyl prop-2-enoate Chemical compound CC1=CC(=O)N(CCCOC(=O)C=C)C(O)=C1C#N DHKZCKNBYFNUET-UHFFFAOYSA-N 0.000 description 1
SOFRHZUTPGJWAM-UHFFFAOYSA-N 3-hydroxy-4-[(2-methoxy-5-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound COc1ccc(cc1N=Nc1c(O)c(cc2ccccc12)C(=O)Nc1cccc(c1)[N+]([O-])=O)[N+]([O-])=O SOFRHZUTPGJWAM-UHFFFAOYSA-N 0.000 description 1
JDIDEFAHGYQWJD-UHFFFAOYSA-N 3-hydroxynaphthalene-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)=CC(O)=CC2=C1 JDIDEFAHGYQWJD-UHFFFAOYSA-N 0.000 description 1
CLSYWFXMLCQWAG-UHFFFAOYSA-N 3-nitro-2h-oxazine Chemical compound [O-][N+](=O)C1=CC=CON1 CLSYWFXMLCQWAG-UHFFFAOYSA-N 0.000 description 1
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 description 1
LBSXSAXOLABXMF-UHFFFAOYSA-N 4-Vinylaniline Chemical compound NC1=CC=C(C=C)C=C1 LBSXSAXOLABXMF-UHFFFAOYSA-N 0.000 description 1
YLNDNABNWASMFD-UHFFFAOYSA-N 4-[(1,3-dimethylimidazol-1-ium-2-yl)diazenyl]-n,n-dimethylaniline Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=[N+](C)C=CN1C YLNDNABNWASMFD-UHFFFAOYSA-N 0.000 description 1
VFZOPOZDIBQSJG-UHFFFAOYSA-N 4-amino-2,5-dichlorobenzonitrile Chemical compound NC1=CC(Cl)=C(C#N)C=C1Cl VFZOPOZDIBQSJG-UHFFFAOYSA-N 0.000 description 1
RRCAJFYQXKPXOJ-UHFFFAOYSA-N 4-aminobenzene-1,2-dicarbonitrile Chemical compound NC1=CC=C(C#N)C(C#N)=C1 RRCAJFYQXKPXOJ-UHFFFAOYSA-N 0.000 description 1
AGPGQVKEHWTHDI-UHFFFAOYSA-N 4-methyl-5-methylsulfanyl-1,2-thiazol-3-amine Chemical compound CSC=1SN=C(N)C=1C AGPGQVKEHWTHDI-UHFFFAOYSA-N 0.000 description 1
LQAWSWUFSHYCHP-UHFFFAOYSA-N 4-methylpyridine-2-carbonitrile Chemical compound CC1=CC=NC(C#N)=C1 LQAWSWUFSHYCHP-UHFFFAOYSA-N 0.000 description 1
XJEVFFNOMKXBLU-UHFFFAOYSA-N 4-methylsulfonylaniline Chemical compound CS(=O)(=O)C1=CC=C(N)C=C1 XJEVFFNOMKXBLU-UHFFFAOYSA-N 0.000 description 1
XXWXOBCTTXYJLD-UHFFFAOYSA-N 4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1.NC1=CC=C([N+]([O-])=O)C=C1 XXWXOBCTTXYJLD-UHFFFAOYSA-N 0.000 description 1
PJQFZPWSFDVYIF-UHFFFAOYSA-N 5-amino-3-methyl-1,2-thiazole-4-carbonitrile Chemical compound CC1=NSC(N)=C1C#N PJQFZPWSFDVYIF-UHFFFAOYSA-N 0.000 description 1
UBFORUHJOUPFHX-UHFFFAOYSA-N 5-aminobenzene-1,3-dicarbonitrile Chemical compound NC1=CC(C#N)=CC(C#N)=C1 UBFORUHJOUPFHX-UHFFFAOYSA-N 0.000 description 1
XKVUYEYANWFIJX-UHFFFAOYSA-N 5-methyl-1h-pyrazole Chemical compound CC1=CC=NN1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
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244000198134 Agave sisalana Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
229920003043 Cellulose fiber Polymers 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
240000000491 Corchorus aestuans Species 0.000 description 1
235000011777 Corchorus aestuans Nutrition 0.000 description 1
235000010862 Corchorus capsularis Nutrition 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
241000219146 Gossypium Species 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
229920002302 Nylon 6,6 Polymers 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
229920000297 Rayon Polymers 0.000 description 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
UIWQZDKINVCVRN-UHFFFAOYSA-N [(2,2-diphenylhydrazinyl)diazenyl]benzene Chemical compound C=1C=CC=CC=1N(C=1C=CC=CC=1)NN=NC1=CC=CC=C1 UIWQZDKINVCVRN-UHFFFAOYSA-N 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
AHWXCYJGJOLNFA-UHFFFAOYSA-N [1,4]benzoxazino[2,3-b]phenoxazine Chemical compound O1C2=CC=CC=C2N=C2C1=CC1=NC3=CC=CC=C3OC1=C2 AHWXCYJGJOLNFA-UHFFFAOYSA-N 0.000 description 1
ZCPUPHMGAXWYTO-UHFFFAOYSA-N [2-[[4-(2,4-dinitroanilino)phenoxy]methyl]-3-prop-2-enoyloxypropyl] prop-2-enoate Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC=C1NC1=CC=C(OCC(COC(=O)C=C)COC(=O)C=C)C=C1 ZCPUPHMGAXWYTO-UHFFFAOYSA-N 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
239000002253 acid Substances 0.000 description 1
125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
XYLMUPLGERFSHI-UHFFFAOYSA-N alpha-Methylstyrene Chemical compound CC(=C)C1=CC=CC=C1 XYLMUPLGERFSHI-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000005005 aminopyrimidines Chemical class 0.000 description 1
ZOOPTFMVDWNNJH-UHFFFAOYSA-N aniline;4-nitroaniline Chemical compound NC1=CC=CC=C1.NC1=CC=C([N+]([O-])=O)C=C1 ZOOPTFMVDWNNJH-UHFFFAOYSA-N 0.000 description 1
150000004982 aromatic amines Chemical class 0.000 description 1
125000005116 aryl carbamoyl group Chemical group 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
JWAZRIHNYRIHIV-UHFFFAOYSA-N beta-hydroxynaphthyl Natural products C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 1
229950011260 betanaphthol Drugs 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000005282 brightening Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
SKKTUOZKZKCGTB-UHFFFAOYSA-N butyl carbamate Chemical compound CCCCOC(N)=O SKKTUOZKZKCGTB-UHFFFAOYSA-N 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
229910052804 chromium Inorganic materials 0.000 description 1
239000011651 chromium Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
RFMQOHXWHFHOJF-UHFFFAOYSA-N cyano thiocyanate Chemical compound N#CSC#N RFMQOHXWHFHOJF-UHFFFAOYSA-N 0.000 description 1
125000005117 dialkylcarbamoyl group Chemical group 0.000 description 1
150000008049 diazo compounds Chemical class 0.000 description 1
WOGOCIDRKQQKBG-UHFFFAOYSA-N diethyl 4-amino-1,2-thiazole-3,5-dicarboxylate Chemical compound CCOC(=O)C1=NSC(C(=O)OCC)=C1N WOGOCIDRKQQKBG-UHFFFAOYSA-N 0.000 description 1
230000029087 digestion Effects 0.000 description 1
239000000986 disperse dye Substances 0.000 description 1
GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
238000007720 emulsion polymerization reaction Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
VLSAOGJJSUPXEU-UHFFFAOYSA-N ethyl 4-amino-3,5-dicyano-2-methylbenzoate Chemical compound CCOC(=O)C1=CC(C#N)=C(N)C(C#N)=C1C VLSAOGJJSUPXEU-UHFFFAOYSA-N 0.000 description 1
238000011049 filling Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
229960004285 fomepizole Drugs 0.000 description 1
VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
239000011487 hemp Substances 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000000976 ink Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
125000005397 methacrylic acid ester group Chemical group 0.000 description 1
125000005395 methacrylic acid group Chemical class 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
VOQBLPBLKSXCDB-UHFFFAOYSA-N methyl 2-amino-5-nitrobenzoate Chemical compound COC(=O)C1=CC([N+]([O-])=O)=CC=C1N VOQBLPBLKSXCDB-UHFFFAOYSA-N 0.000 description 1
HIQSRSSSCQSJCB-UHFFFAOYSA-N methyl 4-amino-3,5-dicyanobenzoate Chemical compound COC(=O)C1=CC(C#N)=C(N)C(C#N)=C1 HIQSRSSSCQSJCB-UHFFFAOYSA-N 0.000 description 1
210000000050 mohair Anatomy 0.000 description 1
XFCJJPMAGADFQV-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-2-methylprop-2-enamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(=C)C XFCJJPMAGADFQV-UHFFFAOYSA-N 0.000 description 1
XQYPDXASOFTNOU-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-ethenylbenzamide Chemical compound C1=CC(C=C)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O XQYPDXASOFTNOU-UHFFFAOYSA-N 0.000 description 1
YPHQUSNPXDGUHL-UHFFFAOYSA-N n-methylprop-2-enamide Chemical compound CNC(=O)C=C YPHQUSNPXDGUHL-UHFFFAOYSA-N 0.000 description 1
KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000012860 organic pigment Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000003505 polymerization initiator Substances 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920006306 polyurethane fiber Polymers 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 description 1
WLFXSECCHULRRO-UHFFFAOYSA-N pyridine-2,6-diol Chemical compound OC1=CC=CC(O)=N1 WLFXSECCHULRRO-UHFFFAOYSA-N 0.000 description 1
WKSAUQYGYAYLPV-UHFFFAOYSA-N pyrimethamine Chemical compound CCC1=NC(N)=NC(N)=C1C1=CC=C(Cl)C=C1 WKSAUQYGYAYLPV-UHFFFAOYSA-N 0.000 description 1
JQYYPSMCISCIRS-UHFFFAOYSA-N pyrimidin-2-ylmethanethiol Chemical compound SCC1=NC=CC=N1 JQYYPSMCISCIRS-UHFFFAOYSA-N 0.000 description 1
QGKLPGKXAVVPOJ-UHFFFAOYSA-N pyrrolidin-3-one Chemical compound O=C1CCNC1 QGKLPGKXAVVPOJ-UHFFFAOYSA-N 0.000 description 1
125000001453 quaternary ammonium group Chemical group 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
239000007870 radical polymerization initiator Substances 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
239000000985 reactive dye Substances 0.000 description 1
238000007670 refining Methods 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000000758 substrate Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000005406 washing Methods 0.000 description 1
230000003245 working effect Effects 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
- D06P1/52—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 synthetic macromolecular substances
- 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
- C09B69/00—Dyes not provided for by a single group of this subclass
- C09B69/10—Polymeric dyes; Reaction products of dyes with monomers or with macromolecular compounds
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/0056—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres
- D06P1/006—Dyeing with polymeric dyes involving building the polymeric dyes on the fibres by using dyes with polymerisable groups, e.g. dye ---CH=CH2
- 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
- Y10S8/916—Natural fiber dyeing
- Y10S8/918—Cellulose textile

Landscapes

Engineering & Computer Science (AREA)
Textile Engineering (AREA)
Structural Engineering (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Coloring (AREA)

DD86291236A 1985-06-12 1986-06-12 Verfahren zum faerben von textilem material DD258628A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB858514905A GB8514905D0 (en)	1985-06-12	1985-06-12	Colouration process

Publications (1)

Publication Number	Publication Date
DD258628A5 true DD258628A5 (de)	1988-07-27

Family

ID=10580647

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86291236A DD258628A5 (de)	1985-06-12	1986-06-12	Verfahren zum faerben von textilem material

Country Status (10)

Country	Link
US (1)	US4763371A (fr)
EP (1)	EP0205291A3 (fr)
JP (1)	JPS6253483A (fr)
KR (1)	KR870000483A (fr)
BR (1)	BR8602732A (fr)
DD (1)	DD258628A5 (fr)
ES (1)	ES8801854A1 (fr)
GB (2)	GB8514905D0 (fr)
HU (1)	HUT42146A (fr)
ZA (1)	ZA864213B (fr)

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* Cited by examiner, † Cited by third party
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US5188641A (en) *	1985-06-12	1993-02-23	Imperial Chemical Industries Plc	Colored polymers from azo dye monomers containing olefinic groups
US5032670A (en) *	1989-08-30	1991-07-16	Eastman Kodak Company	Copolymerized anthraquinone-polyester color concentrates
US5578419A (en) *	1991-12-12	1996-11-26	Mitsui Toatsu Chemicals, Incorporated	Dyes for color filters, and photosensitive resist resin composition containing the same
US5254655A (en) *	1992-02-05	1993-10-19	Hercules Incorporated	Organosilicon polymers, and dyes, exhibiting nonlinear optical response
DE4218359A1 (de) *	1992-06-04	1993-12-09	Basf Ag	Polymerisate, die Methin- oder Azamethinfarbstoffe enthalten
JPH08503981A (ja) *	1992-11-27	1996-04-30	ゼネカ・リミテッド	染料、その製造および支持体の着色におけるその使用
JP2691499B2 (ja) *	1993-04-14	1997-12-17	大日精化工業株式会社	有色絹糸の製造方法
US5362812A (en) *	1993-04-23	1994-11-08	Minnesota Mining And Manufacturing Company	Reactive polymeric dyes
JP3453741B2 (ja) *	1993-07-08	2003-10-06	日本製紙株式会社	感熱記録体
US5470932A (en) *	1993-10-18	1995-11-28	Alcon Laboratories, Inc.	Polymerizable yellow dyes and their use in opthalmic lenses
US5900445A (en) *	1994-12-20	1999-05-04	Bic Corporation	Erasable ink composition containing a polymer dye obtained from ethylenic monomers and marking instrument containing same
US5876463A (en) *	1995-06-07	1999-03-02	Bristol-Myers Squibb Company	Compositions for coloring keratinous fibers comprising sulfo-containing, water dispersible colored polymers
US5735907A (en) *	1995-06-07	1998-04-07	Clairol, Inc.	Method of coloring hair with sulfo-containing water dispersible colored polymers
US6782176B1 (en)	1999-07-27	2004-08-24	Robert W. Greer	Colored radiation curable coating compositions for identifying telecommunications elements and telecommunications elements coated thereby
US7091257B2 (en)	1999-07-27	2006-08-15	Alcatel	Radiation-curable composition with simultaneous color formation during cure
US6620858B2 (en)	2000-08-07	2003-09-16	Eastman Chemical Company	Colorants containing copolymerizable vinyl groups and sulfonamide linkages
US7197662B2 (en) *	2002-10-31	2007-03-27	Ring Technology Enterprises, Llc	Methods and systems for a storage system
WO2011006946A2 (fr) *	2009-07-15	2011-01-20	Basf Se	Colorants capillaires polymères
WO2011086626A1 (fr) *	2010-01-18	2011-07-21	シャープ株式会社	Appareil de fixation de bande adhésive, appareil de fabrication de dispositif d'affichage à cristaux liquides comportant un appareil de fixation de bande adhésive, et procédé de fixation de bande adhésive
GB2494607B (en) *	2010-07-09	2018-05-02	Merck Patent Gmbh	Semiconducting polymers
KR101982356B1 (ko) *	2010-08-07	2019-09-10	메르크 파텐트 게엠베하	전기영동 디스플레이용 입자
JPWO2017131107A1 (ja) *	2016-01-29	2018-12-27	富士フイルム株式会社	インクジェット捺染方法、インクジェットインク、インクカートリッジ、及び着色布
WO2017146071A1 (fr) *	2016-02-26	2017-08-31	富士フイルム株式会社	Procédé d'impression à jet d'encre sur tissu, composition colorante, encre pour jet d'encre, cartouche d'encre, et polymère de colorant
WO2018043414A1 (fr) *	2016-08-31	2018-03-08	富士フイルム株式会社	Procédé d'impression à jet d'encre sur tissu, procédé de fabrication de tissu coloré, et tissu coloré

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3232691A (en) *	1960-07-12	1966-02-01	Basf Ag	Dyeing with copolymeric dyes and crosslinking the latter
US3344098A (en) *	1961-10-31	1967-09-26	Dainichiseika Color Chem	Method of making a chromogen bonded polymer and products thereof
US3503087A (en) *	1964-04-10	1970-03-31	Basf Ag	Marking fibrous material
DE1266718B (de) *	1964-04-10	1968-04-25	Basf Ag	Verfahren zum voruebergehenden farbigen Signieren von Fasermaterial
GB1141147A (en) *	1964-12-22	1969-01-29	Dainichiseika Color Chem	Fluorescent copolymers
DE1226609B (de) *	1965-02-23	1966-10-13	Basf Ag	Druckpasten zum Bedrucken von Gebilden mit glatter Oberfaleche
FR1526005A (fr) *	1966-02-28	1968-05-24	Dainichiseika Color Chem	Laques de polymères à groupe chromogène ancré
NL6706274A (fr) *	1966-05-24	1967-11-27
FR1546225A (fr) *	1966-12-02	1968-11-15	Basf Ag	Couleurs d'impression
GB1270141A (en) *	1968-04-17	1972-04-12	Ici Ltd	Coloration process
US4132841A (en) *	1974-08-02	1979-01-02	Produits Chimiques Ugine Kuhlmann	Copolymers of dyes and acrylamide
FR2280672A1 (fr) *	1974-08-02	1976-02-27	Ugine Kuhlmann	Copolymeres structurellement colores a base de colorants cyanovinyl-azoiques
GB8514906D0 (en) *	1985-06-12	1985-07-17	Ici Plc	Coloured polymers

1985
- 1985-06-12 GB GB858514905A patent/GB8514905D0/en active Pending
1986
- 1986-05-30 EP EP86304136A patent/EP0205291A3/fr not_active Withdrawn
- 1986-05-30 GB GB868613198A patent/GB8613198D0/en active Pending
- 1986-06-04 US US06/870,544 patent/US4763371A/en not_active Expired - Fee Related
- 1986-06-05 ZA ZA864213A patent/ZA864213B/xx unknown
- 1986-06-11 BR BR8602732A patent/BR8602732A/pt unknown
- 1986-06-11 HU HU862463A patent/HUT42146A/hu unknown
- 1986-06-12 ES ES556007A patent/ES8801854A1/es not_active Expired
- 1986-06-12 KR KR1019860004648A patent/KR870000483A/ko not_active Withdrawn
- 1986-06-12 JP JP61135072A patent/JPS6253483A/ja active Pending
- 1986-06-12 DD DD86291236A patent/DD258628A5/de unknown

Also Published As

Publication number	Publication date
GB8514905D0 (en)	1985-07-17
ES8801854A1 (es)	1988-02-16
ZA864213B (en)	1987-05-27
GB8613198D0 (en)	1986-07-02
BR8602732A (pt)	1987-02-10
EP0205291A3 (fr)	1989-01-25
ES556007A0 (es)	1988-02-16
US4763371A (en)	1988-08-16
KR870000483A (ko)	1987-02-18
EP0205291A2 (fr)	1986-12-17
HUT42146A (en)	1987-06-29
JPS6253483A (ja)	1987-03-09

Publication	Publication Date	Title
DD258628A5 (de)	1988-07-27	Verfahren zum faerben von textilem material
DE1932806C3 (de)	1974-10-10	Wasserunlösliche Monoazofarbstoffe
DE1932809A1 (de)	1970-02-05	Verfahren zum Faerben von synthetischen Textilien
DE2527288A1 (de)	1976-01-08	Polycyclische verbindungen, verfahren zu ihrer herstellung und ihre verwendung zum faerben oder bedrucken von organischem material
US5188641A (en)	1993-02-23	Colored polymers from azo dye monomers containing olefinic groups
DE2416003A1 (de)	1974-10-24	Farbstoffe fuer synthetisches textilmaterial deren herstellung und verwendung
DE1932810C3 (de)	1980-02-14	Wasserunlösliche Monoazofarbstoffe und Verfahren zu deren Herstellung
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