CH555934A - Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths - Google Patents

Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths

Info

Publication number: CH555934A
Authority: CH; Switzerland
Prior art keywords: sep; dye; dyeing; formula; azopyridone
Prior art date: 1972-11-16

Application number

CH1673072A

Other languages

German (de)

English (en)

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.)

1972-11-16

Filing date

1972-11-16

Publication date

1974-11-15

1972-11-16 Application filed filed Critical

1972-11-16 Priority to CH1673072D priority Critical patent/CH1673072A4/xx

1972-11-16 Priority to CH1673072A priority patent/CH555934A/de

1973-10-31 Priority to AU62047/73A priority patent/AU6204773A/en

1973-11-02 Priority to GB5104473A priority patent/GB1454755A/en

1973-11-12 Priority to US05/415,282 priority patent/US4015934A/en

1973-11-14 Priority to DE2356864A priority patent/DE2356864A1/de

1973-11-14 Priority to IT53680/73A priority patent/IT997805B/it

1973-11-15 Priority to ZA738745A priority patent/ZA738745B/xx

1973-11-15 Priority to FR7340603A priority patent/FR2207213B1/fr

1973-11-16 Priority to JP48129113A priority patent/JPS4980381A/ja

1973-11-16 Priority to BE137787A priority patent/BE807371A/fr

1974-11-15 Publication of CH555934A publication Critical patent/CH555934A/de

Links

239000000975 dye Substances 0.000 title claims abstract description 64
229920000728 polyester Polymers 0.000 title claims description 12
238000010016 exhaust dyeing Methods 0.000 title 1
150000005826 halohydrocarbons Chemical class 0.000 title 1
125000000217 alkyl group Chemical group 0.000 claims abstract description 16
125000003118 aryl group Chemical group 0.000 claims abstract description 10
125000005842 heteroatom Chemical group 0.000 claims abstract description 9
125000003342 alkenyl group Chemical group 0.000 claims abstract description 6
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 6
229910052736 halogen Inorganic materials 0.000 claims abstract description 5
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 5
238000000034 method Methods 0.000 claims description 41
238000004043 dyeing Methods 0.000 claims description 32
239000000463 material Substances 0.000 claims description 26
CYTYCFOTNPOANT-UHFFFAOYSA-N Perchloroethylene Chemical group ClC(Cl)=C(Cl)Cl CYTYCFOTNPOANT-UHFFFAOYSA-N 0.000 claims description 16
229950011008 tetrachloroethylene Drugs 0.000 claims description 16
KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 claims description 15
239000002202 Polyethylene glycol Substances 0.000 claims description 14
229920001223 polyethylene glycol Polymers 0.000 claims description 14
239000006185 dispersion Substances 0.000 claims description 13
239000004744 fabric Substances 0.000 claims description 13
-1 β-hydroxyethyl group Chemical group 0.000 claims description 13
230000001419 dependent effect Effects 0.000 claims description 12
239000001257 hydrogen Substances 0.000 claims description 12
229910052739 hydrogen Inorganic materials 0.000 claims description 12
150000008282 halocarbons Chemical class 0.000 claims description 10
125000004093 cyano group Chemical group *C#N 0.000 claims description 8
229920002994 synthetic fiber Polymers 0.000 claims description 8
238000009835 boiling Methods 0.000 claims description 7
238000005562 fading Methods 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
239000004758 synthetic textile Substances 0.000 claims description 7
239000004753 textile Substances 0.000 claims description 7
239000005662 Paraffin oil Substances 0.000 claims description 6
230000003197 catalytic effect Effects 0.000 claims description 6
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
239000000835 fiber Substances 0.000 claims description 5
239000002657 fibrous material Substances 0.000 claims description 5
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
239000000203 mixture Substances 0.000 claims description 5
150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 4
150000005840 aryl radicals Chemical class 0.000 claims description 4
239000001913 cellulose Substances 0.000 claims description 4
229920002678 cellulose Polymers 0.000 claims description 4
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
229910052757 nitrogen Inorganic materials 0.000 claims description 4
239000002245 particle Substances 0.000 claims description 4
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
229920002284 Cellulose triacetate Polymers 0.000 claims description 3
239000004952 Polyamide Substances 0.000 claims description 3
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 claims description 3
239000002253 acid Substances 0.000 claims description 3
150000007513 acids Chemical class 0.000 claims description 3
150000008280 chlorinated hydrocarbons Chemical class 0.000 claims description 3
229920002647 polyamide Polymers 0.000 claims description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
150000001298 alcohols Chemical class 0.000 claims description 2
239000001046 green dye Substances 0.000 claims description 2
230000008878 coupling Effects 0.000 abstract description 6
238000010168 coupling process Methods 0.000 abstract description 6
238000005859 coupling reaction Methods 0.000 abstract description 6
229910052801 chlorine Inorganic materials 0.000 abstract description 5
150000001412 amines Chemical class 0.000 abstract description 4
125000005843 halogen group Chemical group 0.000 abstract description 3
125000000623 heterocyclic group Chemical group 0.000 abstract 1
LVWZTYCIRDMTEY-UHFFFAOYSA-N metamizole Chemical compound O=C1C(N(CS(O)(=O)=O)C)=C(C)N(C)N1C1=CC=CC=C1 LVWZTYCIRDMTEY-UHFFFAOYSA-N 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
239000000460 chlorine Substances 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 5
239000000194 fatty acid Substances 0.000 description 5
229930195729 fatty acid Natural products 0.000 description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
150000004665 fatty acids Chemical class 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
229910052794 bromium Inorganic materials 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
YRGYYQCOWUULNF-UHFFFAOYSA-N 2-hydroxy-4-methyl-6-oxo-1h-pyridine-3-carbonitrile Chemical compound CC1=CC(=O)NC(O)=C1C#N YRGYYQCOWUULNF-UHFFFAOYSA-N 0.000 description 2
FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
239000000987 azo dye Substances 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229910052731 fluorine Inorganic materials 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
238000004519 manufacturing process 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
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 2
239000001788 mono and diglycerides of fatty acids Substances 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N n-hexadecanoic acid Natural products CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
239000001267 polyvinylpyrrolidone Substances 0.000 description 2
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
239000000047 product Substances 0.000 description 2
150000005846 sugar alcohols Polymers 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
XVOUMQNXTGKGMA-OWOJBTEDSA-N (E)-glutaconic acid Chemical class OC(=O)C\C=C\C(O)=O XVOUMQNXTGKGMA-OWOJBTEDSA-N 0.000 description 1
GETTZEONDQJALK-UHFFFAOYSA-N (trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=CC=C1 GETTZEONDQJALK-UHFFFAOYSA-N 0.000 description 1
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
AVGQTJUPLKNPQP-UHFFFAOYSA-N 1,1,1-trichloropropane Chemical compound CCC(Cl)(Cl)Cl AVGQTJUPLKNPQP-UHFFFAOYSA-N 0.000 description 1
AJDIZQLSFPQPEY-UHFFFAOYSA-N 1,1,2-Trichlorotrifluoroethane Chemical compound FC(F)(Cl)C(F)(Cl)Cl AJDIZQLSFPQPEY-UHFFFAOYSA-N 0.000 description 1
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 1
RQXXCWHCUOJQGR-UHFFFAOYSA-N 1,1-dichlorohexane Chemical compound CCCCCC(Cl)Cl RQXXCWHCUOJQGR-UHFFFAOYSA-N 0.000 description 1
UWTUEMKLYAGTNQ-UHFFFAOYSA-N 1,2-dibromoethene Chemical group BrC=CBr UWTUEMKLYAGTNQ-UHFFFAOYSA-N 0.000 description 1
KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
KJDRSWPQXHESDQ-UHFFFAOYSA-N 1,4-dichlorobutane Chemical compound ClCCCCCl KJDRSWPQXHESDQ-UHFFFAOYSA-N 0.000 description 1
VFWCMGCRMGJXDK-UHFFFAOYSA-N 1-chlorobutane Chemical compound CCCCCl VFWCMGCRMGJXDK-UHFFFAOYSA-N 0.000 description 1
YZNQITSGDRCUKE-UHFFFAOYSA-N 1-chloropropane Chemical compound [CH2]CCCl YZNQITSGDRCUKE-UHFFFAOYSA-N 0.000 description 1
CBRUQZUHJAXNHS-UHFFFAOYSA-M 1-hexadecylpyridin-1-ium;acetate Chemical compound CC([O-])=O.CCCCCCCCCCCCCCCC[N+]1=CC=CC=C1 CBRUQZUHJAXNHS-UHFFFAOYSA-M 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
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
ZZLCFHIKESPLTH-UHFFFAOYSA-N 4-Methylbiphenyl Chemical compound C1=CC(C)=CC=C1C1=CC=CC=C1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 description 1
YIYBPEDZAUFQLO-UHFFFAOYSA-N 4-amino-3-chlorobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1Cl YIYBPEDZAUFQLO-UHFFFAOYSA-N 0.000 description 1
QLWHQJCFTMNUPX-UHFFFAOYSA-N 4-amino-3-cyano-n-cyclohexyl-n-methylbenzamide Chemical compound C=1C=C(N)C(C#N)=CC=1C(=O)N(C)C1CCCCC1 QLWHQJCFTMNUPX-UHFFFAOYSA-N 0.000 description 1
YLKLDLKLEXDSJY-UHFFFAOYSA-N 4-amino-3-nitrobenzamide Chemical compound NC(=O)C1=CC=C(N)C([N+]([O-])=O)=C1 YLKLDLKLEXDSJY-UHFFFAOYSA-N 0.000 description 1
229940090248 4-hydroxybenzoic acid Drugs 0.000 description 1
JLLYLQLDYORLBB-UHFFFAOYSA-N 5-bromo-n-methylthiophene-2-sulfonamide Chemical compound CNS(=O)(=O)C1=CC=C(Br)S1 JLLYLQLDYORLBB-UHFFFAOYSA-N 0.000 description 1
UFFRSDWQMJYQNE-UHFFFAOYSA-N 6-azaniumylhexylazanium;hexanedioate Chemical compound [NH3+]CCCCCC[NH3+].[O-]C(=O)CCCCC([O-])=O UFFRSDWQMJYQNE-UHFFFAOYSA-N 0.000 description 1
XZIIFPSPUDAGJM-UHFFFAOYSA-N 6-chloro-2-n,2-n-diethylpyrimidine-2,4-diamine Chemical compound CCN(CC)C1=NC(N)=CC(Cl)=N1 XZIIFPSPUDAGJM-UHFFFAOYSA-N 0.000 description 1
AYYACMVBGCDRQV-UHFFFAOYSA-N 6-hydroxy-5-(2-hydroxyethyl)-4-methyl-2-oxo-1h-pyridine-3-carbonitrile Chemical compound CC=1C(CCO)=C(O)NC(=O)C=1C#N AYYACMVBGCDRQV-UHFFFAOYSA-N 0.000 description 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
240000002129 Malva sylvestris Species 0.000 description 1
235000006770 Malva sylvestris Nutrition 0.000 description 1
VCUFZILGIRCDQQ-KRWDZBQOSA-N N-[[(5S)-2-oxo-3-(2-oxo-3H-1,3-benzoxazol-6-yl)-1,3-oxazolidin-5-yl]methyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C1O[C@H](CN1C1=CC2=C(NC(O2)=O)C=C1)CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F VCUFZILGIRCDQQ-KRWDZBQOSA-N 0.000 description 1
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HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
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CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
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150000001408 amides Chemical class 0.000 description 1
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239000012736 aqueous medium Substances 0.000 description 1
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OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
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125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000001045 blue dye Substances 0.000 description 1
150000003857 carboxamides Chemical class 0.000 description 1
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AMFIJXSMYBKJQV-UHFFFAOYSA-L cobalt(2+);octadecanoate Chemical compound [Co+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O AMFIJXSMYBKJQV-UHFFFAOYSA-L 0.000 description 1
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IPCSVZSSVZVIGE-UHFFFAOYSA-M hexadecanoate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
ALBYIUDWACNRRB-UHFFFAOYSA-N hexanamide Chemical compound CCCCCC(N)=O ALBYIUDWACNRRB-UHFFFAOYSA-N 0.000 description 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
ULYZAYCEDJDHCC-UHFFFAOYSA-N isopropyl chloride Chemical compound CC(C)Cl ULYZAYCEDJDHCC-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000004898 kneading Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
235000019960 monoglycerides of fatty acid Nutrition 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
229940049964 oleate Drugs 0.000 description 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
235000021313 oleic acid Nutrition 0.000 description 1
239000011368 organic material Substances 0.000 description 1
150000002918 oxazolines Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
230000008929 regeneration Effects 0.000 description 1
238000011069 regeneration method Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
238000007363 ring formation reaction Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
239000011555 saturated liquid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
229940035044 sorbitan monolaurate Drugs 0.000 description 1
235000011067 sorbitan monolaureate Nutrition 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
125000000565 sulfonamide group Chemical group 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
239000012209 synthetic fiber Substances 0.000 description 1
NBRKLOOSMBRFMH-UHFFFAOYSA-N tert-butyl chloride Chemical compound CC(C)(C)Cl NBRKLOOSMBRFMH-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
239000002351 wastewater Substances 0.000 description 1
239000001993 wax Substances 0.000 description 1

Classifications

- 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
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/34—Monoazo dyes prepared by diazotising and coupling from other coupling components
- C09B29/36—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds
- C09B29/3604—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom
- C09B29/3617—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom
- C09B29/3621—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring
- C09B29/3626—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O)
- C09B29/363—Monoazo dyes prepared by diazotising and coupling from other coupling components from heterocyclic compounds containing only a nitrogen as heteroatom containing a six-membered heterocyclic with only one nitrogen as heteroatom from a pyridine ring from a pyridine ring containing one or more hydroxyl groups (or = O) from diazotized amino carbocyclic rings
- 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
- D06P1/90—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 dyes dissolved in organic solvents or aqueous emulsions thereof
- D06P1/92—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 dyes dissolved in organic solvents or aqueous emulsions thereof in organic solvents
- D06P1/922—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 dyes dissolved in organic solvents or aqueous emulsions thereof in organic solvents hydrocarbons
- D06P1/924—Halogenated hydrocarbons

Landscapes

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

CH1673072A 1972-11-16 1972-11-16 Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths CH555934A (en)

Priority Applications (11)

Application Number	Priority Date	Filing Date	Title
CH1673072D CH1673072A4 (fr)	1972-11-16	1972-11-16
CH1673072A CH555934A (en)	1972-11-16	1972-11-16	Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths
AU62047/73A AU6204773A (en)	1972-11-16	1973-10-31	Synthetic textile material
GB5104473A GB1454755A (en)	1972-11-16	1973-11-02	Process for the dyeing of syntheetic textile material
US05/415,282 US4015934A (en)	1972-11-16	1973-11-12	Process for the dyeing of synthetic textile material
DE2356864A DE2356864A1 (de)	1972-11-16	1973-11-14	Verfahren zum faerben von synthetischem textilmaterial
IT53680/73A IT997805B (it)	1972-11-16	1973-11-14	Procedimento per tingere materiale tessile sintetico in particolare poliestereo
ZA738745A ZA738745B (en)	1972-11-16	1973-11-15	Process for the dyeing of synthetic textile material
FR7340603A FR2207213B1 (fr)	1972-11-16	1973-11-15
JP48129113A JPS4980381A (fr)	1972-11-16	1973-11-16
BE137787A BE807371A (fr)	1972-11-16	1973-11-16	Procede de teinture de textiles synthetiques

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1673072A CH555934A (en)	1972-11-16	1972-11-16	Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths

Publications (1)

Publication Number	Publication Date
CH555934A true CH555934A (en)	1974-11-15

Family

ID=4419736

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CH1673072A CH555934A (en)	1972-11-16	1972-11-16	Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths
CH1673072D CH1673072A4 (fr)	1972-11-16	1972-11-16

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
CH1673072D CH1673072A4 (fr)	1972-11-16	1972-11-16

Country Status (3)

Country	Link
BE (1)	BE807371A (fr)
CH (2)	CH555934A (fr)
ZA (1)	ZA738745B (fr)

1972
- 1972-11-16 CH CH1673072A patent/CH555934A/de unknown
- 1972-11-16 CH CH1673072D patent/CH1673072A4/xx unknown
1973
- 1973-11-15 ZA ZA738745A patent/ZA738745B/xx unknown
- 1973-11-16 BE BE137787A patent/BE807371A/fr unknown

Also Published As

Publication number	Publication date
ZA738745B (en)	1974-09-25
CH1673072A4 (fr)	1974-05-31
BE807371A (fr)	1974-05-16

Publication	Publication Date	Title
DE1295115B (de)	1969-05-14	Verfahren zur Herstellung von Monoazofarbstoffen
DE1644328C3 (de)	1974-03-14	Verfahren zur Herstellung von Monoazofarbstoffen
DE1644103B2 (de)	1977-04-28	Basische kationische azofarbstoffe
DE2356864A1 (de)	1974-05-30	Verfahren zum faerben von synthetischem textilmaterial
CH468073A (de)	1969-01-31	Elektrische Schaltervorrichtung
CH555934A (en)	1974-11-15	Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths
DE1927416C3 (de)	1978-09-28	Basische Azofarbstoffe, Verfahren zu ihrer Herstellung und ihre Verwendung
CH555935A (en)	1974-11-15	Exhaust dyeing of textured polyester knits - yellow shades with known azopyridone dyes from halohydrocarbon baths
EP0013892B1 (fr)	1982-05-26	Procédé de teinture de matières fibreuses synthétiques par le procédé d'extraction
DE1644351B2 (de)	1973-10-18	Blaue Disazofarbstoffe und deren Verwendung zum Farben von Mischgeweben aus Polyester und Baumwollfasern
CH653973A5 (it)	1986-01-31	Apparecchio per la accumulazione e l'alimentazione di fili, fettucce, nastri per uso tessile a macchine utilizzatrici.
DE2422033A1 (de)	1974-11-28	Ausziehverfahren zum faerben von synthetischem, organischem textilmaterial
DE1928372A1 (de)	1970-02-19	Wasserunloesliche Monoazofarbstoffe
DE2425842A1 (de)	1975-01-02	Ausziehverfahren zum faerben von synthetischem, organischem textilmaterial
DE2238339C3 (de)	1975-03-20	Verfahren zum kontinuierlichen Färben von synthetischen Fasermaterialien aus organischen Lösemitteln
DE2642664C3 (de)	1978-12-21	Wasserunlösliche Monoazofarbstoffe, Verfahren zu deren Herstellung und ihre Verwendung zum Färben und Bedrucken
DE2811067C3 (de)	1981-12-03	Monoazofarbstoffe, Verfahren zu deren Herstellung und Verwendung
DE1810063C (de)	1971-09-02	In Wasser schwer lösliche Azoverbm düngen
DE4238231A1 (fr)	1993-05-19
CH642091A5 (de)	1984-03-30	Disperse anthrachinonfarbstoffe.
DE2209247B2 (de)	1974-02-28	Verfahren zur Herstellung echter Färbungen oder Drucke auf synthetischen Fasermaterialien
DE1644094C3 (de)	1976-10-28	Wasserunlösliche Azofarbstoffe
DE1619567C (de)	1973-05-17	Verwendung von Iminocumannverbin düngen zum Farben und Bedrucken von synthetischen Faserstoffen
DE1644104C3 (de)	1977-03-10	Besiehe Monoazofarbstoffe
CH554403A (de)	1974-09-30	Verfahren zur herstellung von faserreaktiven azofarbstoffen.