JPS6220309B2 - - Google Patents

Info

Publication number: JPS6220309B2
Authority: JP; Japan
Prior art keywords: parts; dye; bath; minutes; dyeing
Prior art date: 1977-10-21
Legal status (The legal status 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 status listed.): Expired

Application number

JP53127941A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5468475A (en

Inventor

Reeman Borufuganku

Hirudeburanto Deiitaa

Binfuriito Hendoritsukusu Udo

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer 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.)

1977-10-21

Filing date

1978-10-19

Publication date

1987-05-06

1978-10-19 Application filed by Bayer AG filed Critical Bayer AG

1979-06-01 Publication of JPS5468475A publication Critical patent/JPS5468475A/ja

1987-05-06 Publication of JPS6220309B2 publication Critical patent/JPS6220309B2/ja

Status Granted legal-status Critical Current

Links

239000000975 dye Substances 0.000 claims description 36
229920000768 polyamine Polymers 0.000 claims description 20
238000000034 method Methods 0.000 claims description 17
230000007062 hydrolysis Effects 0.000 claims description 16
238000006460 hydrolysis reaction Methods 0.000 claims description 16
239000004952 Polyamide Substances 0.000 claims description 12
229920002647 polyamide Polymers 0.000 claims description 12
125000001302 tertiary amino group Chemical group 0.000 claims description 12
239000000985 reactive dye Substances 0.000 claims description 11
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 claims description 10
239000007864 aqueous solution Substances 0.000 claims description 9
229920002396 Polyurea Polymers 0.000 claims description 8
239000004814 polyurethane Substances 0.000 claims description 5
229920003043 Cellulose fiber Polymers 0.000 claims description 4
239000002657 fibrous material Substances 0.000 claims description 4
229920003226 polyurethane urea Polymers 0.000 claims 1
239000000047 product Substances 0.000 description 33
238000004043 dyeing Methods 0.000 description 26
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
229920000742 Cotton Polymers 0.000 description 20
238000011282 treatment Methods 0.000 description 18
238000005406 washing Methods 0.000 description 18
238000009835 boiling Methods 0.000 description 17
239000000835 fiber Substances 0.000 description 17
150000001875 compounds Chemical class 0.000 description 13
239000000243 solution Substances 0.000 description 13
-1 N-β-cyanoethylethylenediamino Chemical group 0.000 description 12
239000007788 liquid Substances 0.000 description 12
150000001412 amines Chemical class 0.000 description 10
238000004140 cleaning Methods 0.000 description 9
125000003277 amino group Chemical group 0.000 description 8
239000004744 fabric Substances 0.000 description 8
125000001931 aliphatic group Chemical group 0.000 description 7
239000007795 chemical reaction product Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
238000012360 testing method Methods 0.000 description 7
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
238000004045 reactive dyeing Methods 0.000 description 6
XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 5
239000007859 condensation product Substances 0.000 description 5
238000010186 staining Methods 0.000 description 5
239000004753 textile Substances 0.000 description 5
125000003368 amide group Chemical group 0.000 description 4
239000004202 carbamide Substances 0.000 description 4
235000013351 cheese Nutrition 0.000 description 4
JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 description 4
238000010409 ironing Methods 0.000 description 4
KMBPCQSCMCEPMU-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-methylpropane-1,3-diamine Chemical compound NCCCN(C)CCCN KMBPCQSCMCEPMU-UHFFFAOYSA-N 0.000 description 4
229920002635 polyurethane Polymers 0.000 description 4
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
KRPRVQWGKLEFKN-UHFFFAOYSA-N 3-(3-aminopropoxy)propan-1-amine Chemical compound NCCCOCCCN KRPRVQWGKLEFKN-UHFFFAOYSA-N 0.000 description 3
RPNUMPOLZDHAAY-UHFFFAOYSA-N Diethylenetriamine Chemical compound NCCNCCN RPNUMPOLZDHAAY-UHFFFAOYSA-N 0.000 description 3
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
229920000297 Rayon Polymers 0.000 description 3
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
125000002723 alicyclic group Chemical group 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
229920002678 cellulose Polymers 0.000 description 3
235000010980 cellulose Nutrition 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
238000012805 post-processing Methods 0.000 description 3
229910000029 sodium carbonate Inorganic materials 0.000 description 3
SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 2
XAZDZMUGHYYPQM-UHFFFAOYSA-N 1-chloro-3-(3-chloro-2-hydroxypropoxy)propan-2-ol Chemical compound ClCC(O)COCC(O)CCl XAZDZMUGHYYPQM-UHFFFAOYSA-N 0.000 description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 description 2
NOWKCMXCCJGMRR-UHFFFAOYSA-N Aziridine Chemical compound C1CN1 NOWKCMXCCJGMRR-UHFFFAOYSA-N 0.000 description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
229920002873 Polyethylenimine Polymers 0.000 description 2
239000002253 acid Substances 0.000 description 2
WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
230000001153 anti-wrinkle effect Effects 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000004432 carbon atom Chemical group C* 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 2
AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
238000003825 pressing Methods 0.000 description 2
KIDHWZJUCRJVML-UHFFFAOYSA-N putrescine Chemical compound NCCCCN KIDHWZJUCRJVML-UHFFFAOYSA-N 0.000 description 2
229960001124 trientine Drugs 0.000 description 2
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
238000010626 work up procedure Methods 0.000 description 2
239000002759 woven fabric Substances 0.000 description 2
238000009970 yarn dyeing Methods 0.000 description 2
JEQDSBVHLKBEIZ-REOHCLBHSA-N (2s)-2-chloropropanoyl chloride Chemical compound C[C@H](Cl)C(Cl)=O JEQDSBVHLKBEIZ-REOHCLBHSA-N 0.000 description 1
HFBHOAHFRNLZGN-LURJTMIESA-N (2s)-2-formamido-4-methylpentanoic acid Chemical compound CC(C)C[C@@H](C(O)=O)NC=O HFBHOAHFRNLZGN-LURJTMIESA-N 0.000 description 1
125000006702 (C1-C18) alkyl group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
PAAZPARNPHGIKF-UHFFFAOYSA-N 1,2-dibromoethane Chemical compound BrCCBr PAAZPARNPHGIKF-UHFFFAOYSA-N 0.000 description 1
KNKRKFALVUDBJE-UHFFFAOYSA-N 1,2-dichloropropane Chemical compound CC(Cl)CCl KNKRKFALVUDBJE-UHFFFAOYSA-N 0.000 description 1
VYMPLPIFKRHAAC-UHFFFAOYSA-N 1,2-ethanedithiol Chemical compound SCCS VYMPLPIFKRHAAC-UHFFFAOYSA-N 0.000 description 1
DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 1
YHRUOJUYPBUZOS-UHFFFAOYSA-N 1,3-dichloropropane Chemical compound ClCCCCl YHRUOJUYPBUZOS-UHFFFAOYSA-N 0.000 description 1
QRMPKOFEUHIBNM-UHFFFAOYSA-N 1,4-dimethylcyclohexane Chemical group CC1CCC(C)CC1 QRMPKOFEUHIBNM-UHFFFAOYSA-N 0.000 description 1
OVISMSJCKCDOPU-UHFFFAOYSA-N 1,6-dichlorohexane Chemical compound ClCCCCCCCl OVISMSJCKCDOPU-UHFFFAOYSA-N 0.000 description 1
FYBFGAFWCBMEDG-UHFFFAOYSA-N 1-[3,5-di(prop-2-enoyl)-1,3,5-triazinan-1-yl]prop-2-en-1-one Chemical compound C=CC(=O)N1CN(C(=O)C=C)CN(C(=O)C=C)C1 FYBFGAFWCBMEDG-UHFFFAOYSA-N 0.000 description 1
PVBMXMKIKMJQRK-UHFFFAOYSA-N 1-chloro-4-(4-chlorobutoxy)butane Chemical compound ClCCCCOCCCCCl PVBMXMKIKMJQRK-UHFFFAOYSA-N 0.000 description 1
VUSYFNXNYLAECV-UHFFFAOYSA-N 2,3-bis(chloromethyl)oxirane Chemical compound ClCC1OC1CCl VUSYFNXNYLAECV-UHFFFAOYSA-N 0.000 description 1
HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 1
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
POGBEGTVYWWXSF-UHFFFAOYSA-N 2-[bis(3-aminopropyl)amino]ethanol Chemical compound NCCCN(CCO)CCCN POGBEGTVYWWXSF-UHFFFAOYSA-N 0.000 description 1
SVDDJQGVOFZBNX-UHFFFAOYSA-N 2-chloroethyl carbonochloridate Chemical compound ClCCOC(Cl)=O SVDDJQGVOFZBNX-UHFFFAOYSA-N 0.000 description 1
YZOXPLQWARQVEJ-UHFFFAOYSA-N 2-methylsulfonyl-1,3-benzothiazole Chemical compound C1=CC=C2SC(S(=O)(=O)C)=NC2=C1 YZOXPLQWARQVEJ-UHFFFAOYSA-N 0.000 description 1
OIGXNHYFKZCTCH-UHFFFAOYSA-N 2-methylsulfonylpyrimidine Chemical compound CS(=O)(=O)C1=NC=CC=N1 OIGXNHYFKZCTCH-UHFFFAOYSA-N 0.000 description 1
QPIOXOJERGNNMX-UHFFFAOYSA-N 3-(3-aminopropylsulfanyl)propan-1-amine Chemical compound NCCCSCCCN QPIOXOJERGNNMX-UHFFFAOYSA-N 0.000 description 1
RNLHGQLZWXBQNY-UHFFFAOYSA-N 3-(aminomethyl)-3,5,5-trimethylcyclohexan-1-amine Chemical compound CC1(C)CC(N)CC(C)(CN)C1 RNLHGQLZWXBQNY-UHFFFAOYSA-N 0.000 description 1
USNBVHYUYWSPNK-UHFFFAOYSA-N 3-[3-(3-aminopropoxy)-2,2-dimethylpropoxy]propan-1-amine Chemical compound NCCCOCC(C)(C)COCCCN USNBVHYUYWSPNK-UHFFFAOYSA-N 0.000 description 1
CJCOYIXVZLLXHJ-UHFFFAOYSA-N 3-[4-(3-aminopropoxy)phenoxy]propan-1-amine Chemical compound NCCCOC1=CC=C(OCCCN)C=C1 CJCOYIXVZLLXHJ-UHFFFAOYSA-N 0.000 description 1
INUNLMUAPJVRME-UHFFFAOYSA-N 3-chloropropanoyl chloride Chemical compound ClCCC(Cl)=O INUNLMUAPJVRME-UHFFFAOYSA-N 0.000 description 1
MCSXGCZMEPXKIW-UHFFFAOYSA-N 3-hydroxy-4-[(4-methyl-2-nitrophenyl)diazenyl]-N-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound Cc1ccc(N=Nc2c(O)c(cc3ccccc23)C(=O)Nc2cccc(c2)[N+]([O-])=O)c(c1)[N+]([O-])=O MCSXGCZMEPXKIW-UHFFFAOYSA-N 0.000 description 1
IHDBZCJYSHDCKF-UHFFFAOYSA-N 4,6-dichlorotriazine Chemical group ClC1=CC(Cl)=NN=N1 IHDBZCJYSHDCKF-UHFFFAOYSA-N 0.000 description 1
LFEAJBLOEPTINE-UHFFFAOYSA-N 4-(chloromethyl)-1,3-dioxolan-2-one Chemical compound ClCC1COC(=O)O1 LFEAJBLOEPTINE-UHFFFAOYSA-N 0.000 description 1
SZINXEOBIAOWBV-UHFFFAOYSA-N 4-methylsulfonyltriazine Chemical compound CS(=O)(=O)C1=CC=NN=N1 SZINXEOBIAOWBV-UHFFFAOYSA-N 0.000 description 1
ALEBYBVYXQTORU-UHFFFAOYSA-N 6-hydrazinyl-6-oxohexanoic acid Chemical compound NNC(=O)CCCCC(O)=O ALEBYBVYXQTORU-UHFFFAOYSA-N 0.000 description 1
ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 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
KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical class NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
VGCXGMAHQTYDJK-UHFFFAOYSA-N Chloroacetyl chloride Chemical compound ClCC(Cl)=O VGCXGMAHQTYDJK-UHFFFAOYSA-N 0.000 description 1
ZFIVKAOQEXOYFY-UHFFFAOYSA-N Diepoxybutane Chemical compound C1OC1C1OC1 ZFIVKAOQEXOYFY-UHFFFAOYSA-N 0.000 description 1
239000004593 Epoxy Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
240000002129 Malva sylvestris Species 0.000 description 1
235000006770 Malva sylvestris Nutrition 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
FDLQZKYLHJJBHD-UHFFFAOYSA-N [3-(aminomethyl)phenyl]methanamine Chemical compound NCC1=CC=CC(CN)=C1 FDLQZKYLHJJBHD-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000001361 adipic acid Substances 0.000 description 1
235000011037 adipic acid Nutrition 0.000 description 1
239000002168 alkylating agent Substances 0.000 description 1
229940100198 alkylating agent Drugs 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
150000001491 aromatic compounds Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
125000005392 carboxamide group Chemical group NC(=O)* 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000004132 cross linking Methods 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
VKIRRGRTJUUZHS-UHFFFAOYSA-N cyclohexane-1,4-diamine Chemical compound NC1CCC(N)CC1 VKIRRGRTJUUZHS-UHFFFAOYSA-N 0.000 description 1
238000003795 desorption Methods 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
125000005442 diisocyanate group Chemical group 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
229940052303 ethers for general anesthesia Drugs 0.000 description 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
238000000605 extraction Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000011487 hemp Substances 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
238000009981 jet dyeing Methods 0.000 description 1
GKQPCPXONLDCMU-CCEZHUSRSA-N lacidipine Chemical compound CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1C1=CC=CC=C1\C=C\C(=O)OC(C)(C)C GKQPCPXONLDCMU-CCEZHUSRSA-N 0.000 description 1
150000003951 lactams Chemical class 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
239000000203 mixture Substances 0.000 description 1
QMXSDTGNCZVWTB-UHFFFAOYSA-N n',n'-bis(3-aminopropyl)propane-1,3-diamine Chemical compound NCCCN(CCCN)CCCN QMXSDTGNCZVWTB-UHFFFAOYSA-N 0.000 description 1
HUWUUMUEMQWJKZ-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-benzylpropane-1,3-diamine Chemical compound NCCCN(CCCN)CC1=CC=CC=C1 HUWUUMUEMQWJKZ-UHFFFAOYSA-N 0.000 description 1
CMDGBXZMCXCQFG-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-butylpropane-1,3-diamine Chemical compound CCCCN(CCCN)CCCN CMDGBXZMCXCQFG-UHFFFAOYSA-N 0.000 description 1
ZKKMLXOYLORBLV-UHFFFAOYSA-N n'-(3-aminopropyl)-n'-ethylpropane-1,3-diamine Chemical compound NCCCN(CC)CCCN ZKKMLXOYLORBLV-UHFFFAOYSA-N 0.000 description 1
LSHROXHEILXKHM-UHFFFAOYSA-N n'-[2-[2-[2-(2-aminoethylamino)ethylamino]ethylamino]ethyl]ethane-1,2-diamine Chemical compound NCCNCCNCCNCCNCCN LSHROXHEILXKHM-UHFFFAOYSA-N 0.000 description 1
ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
238000004806 packaging method and process Methods 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920000962 poly(amidoamine) Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
AOHJOMMDDJHIJH-UHFFFAOYSA-N propylenediamine Chemical compound CC(N)CN AOHJOMMDDJHIJH-UHFFFAOYSA-N 0.000 description 1
239000002964 rayon Substances 0.000 description 1
239000004627 regenerated cellulose Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
239000000979 synthetic dye Substances 0.000 description 1
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
125000003396 thiol group Chemical group [H]S* 0.000 description 1
239000010981 turquoise Substances 0.000 description 1
229960000834 vinyl ether Drugs 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/02—After-treatment
- D06P5/04—After-treatment with organic compounds
- D06P5/08—After-treatment with organic compounds macromolecular
- 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
- D06P3/58—Material containing hydroxyl groups
- D06P3/60—Natural or regenerated cellulose
- D06P3/66—Natural or regenerated cellulose using reactive dyes

Landscapes

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

JP12794178A 1977-10-21 1978-10-19 Postttreating of reactive dyestuff Granted JPS5468475A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19772747358 DE2747358C2 (de)	1977-10-21	1977-10-21	Verfahren zur Nachbehandlung von Reaktivfärbungen

Publications (2)

Publication Number	Publication Date
JPS5468475A JPS5468475A (en)	1979-06-01
JPS6220309B2 true JPS6220309B2 (de)	1987-05-06

Family

ID=6021986

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP12794178A Granted JPS5468475A (en)	1977-10-21	1978-10-19	Postttreating of reactive dyestuff

Country Status (3)

Country	Link
JP (1)	JPS5468475A (de)
DE (1)	DE2747358C2 (de)
GB (1)	GB2006279B (de)

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NL187688C (nl) *	1980-02-22	1991-12-16	Sandoz Ag	In water oplosbaar produkt, werkwijze voor het bereiden van een preparaat voor het behandelen van textielmaterialen en werkwijze voor het verbeteren van de natte echtheidseigenschappen van een kleurstof.
JPS56136204A (en) *	1980-03-26	1981-10-24	Nippon Steel Corp	Highly efficient cold rolling method
DE3129562C2 (de) *	1980-07-29	1994-10-06	Kao Corp	Farbvertiefendes Mittel
NL8104330A (nl) *	1980-09-24	1982-04-16	Sandoz Ag	Werkwijze voor het wasecht maken van cellulose-bevattend textiel en daarbij te gebruiken stoffen.
JPS58115183A (ja) *	1981-12-29	1983-07-08	大日本製薬株式会社	染色された綿繊維製品の塩素堅牢度増進剤及びその増進方法
US4424061A (en) *	1981-02-27	1984-01-03	Dainippon Pharmaceutical Co., Ltd.	Color fastness of dyed cotton textiles to chlorinated water and process for improving the color fastness of dyed cotton textiles to chlorinated water
CH669081GA3 (de) *	1981-05-14	1989-02-28
CH673195B5 (de) *	1981-05-14	1990-08-31	Sandoz Ag
US4436524A (en)	1981-05-16	1984-03-13	Sandoz Ltd.	After treating composition for direct or reactive dyeings on cellulose
FR2513279B1 (fr) *	1981-05-18	1985-10-18	Sandoz Sa	Procede de post-traitement de substrats contenant des groupes hydroxy
FR2513278A1 (en) *	1981-06-15	1983-03-25	Sandoz Sa	Treating dyed cellulosic fibrous substrates with precondensate - to improve wet fastness and crease resistance
JPS5824453A (ja) *	1981-08-06	1983-02-14	Nippon Senka Kogyo Kk	湿式転写捺染方法
DE3329029A1 (de) *	1983-08-11	1985-02-28	Cassella Ag, 6000 Frankfurt	Verfahren zur herstellung von faerbungen mit reaktivfarbstoffen
FR2557603B1 (fr) *	1984-01-03	1988-02-19	Sandoz Sa	Procede de teinture et de post-traitement de substrats textiles
US4718918A (en) *	1984-01-03	1988-01-12	Sandoz Ltd.	Treatment of textile materials to improve the fastness of dyeings made thereon and polymers useful therefor
DE3446284A1 (de) *	1984-01-03	1985-07-11	Sandoz-Patent-GmbH, 7850 Lörrach	Faerbeverfahren
CH674786B5 (de) *	1984-01-03	1991-01-31	Sandoz Ag
DE3416693A1 (de) *	1984-05-05	1985-11-07	Bayer Ag, 5090 Leverkusen	Verfahren zur behandlung von cellulosischen fasermaterialien
JPS6134292A (ja) *	1984-07-20	1986-02-18	株式会社日本触媒	染色物処理方法
DE3526101A1 (de) *	1985-07-22	1987-01-22	Basf Ag	Verfahren zur nachbehandlung von faerbungen mit reaktivfarbstoffen auf cellulose-fasermaterialien
DE3537458A1 (de) *	1985-10-22	1987-04-23	Basf Ag	Verfahren zur nachbehandlung von reaktivfaerbungen auf cellulosefasern
DE3607963A1 (de) *	1986-03-11	1987-09-17	Bayer Ag	Kondensationsprodukte und verfahren zur nachbehandlung von gefaerbten polyamiden
DE3609984A1 (de) *	1986-03-25	1987-10-01	Bayer Ag	Verfahren zur behandlung von fasermaterialien
DE3709766A1 (de) *	1987-03-25	1988-10-06	Hoechst Ag	Verfahren zum alkali-freien faerben mit reaktivfarbstoffen
DE3816699A1 (de) *	1988-05-17	1989-11-30	Bayer Ag	Verfahren zur nachbehandlung von gefaerbten textilmaterialien
DE3831139A1 (de) *	1988-09-13	1990-03-15	Hoechst Ag	Verfahren zum ungleichmaessigen, alkali-freien faerben von cellulosefasern
AU633066B2 (en) *	1989-03-08	1993-01-21	Commonwealth Scientific And Industrial Research Organisation	Modification of the properties of textile fibres and keratinous materials
WO1990010747A1 (en) *	1989-03-08	1990-09-20	Commonwealth Scientific And Industrial Research Organisation	Modification of the properties of textile fibres and keratinous materials
DE4413007A1 (de) *	1994-04-15	1995-10-19	Bayer Ag	Neue Farbstoffe und ihre Verwendung in Tinten für ink-jet-Druckverfahren
FR2746808B1 (fr) *	1996-03-27	1998-05-07	Protex Manuf Prod Chimiq	Agent et procede d'amelioration de la solidite au frottement de teintures ou d'impressions
GB9608505D0 (en) *	1996-04-25	1996-07-03	Zeneca Ltd	Compositions processes and uses
EP0963478A1 (de) *	1997-02-26	1999-12-15	Textil Color Ag	Carbamat modifizierte niedermolekulare polymere verbindung und deren verwendung zur nachbehandlung von gefärbtem oder bedrucktem cellulose textilmaterial
BRPI0416400B1 (pt) *	2003-11-11	2014-12-30	Ciba Sc Holding Ag	Método para tingimento ou impressão de materiais de fibras têxteis usando corantes reativos
DE102004045861B4 (de) *	2004-09-20	2008-05-08	Dystar Textilfarben Gmbh & Co. Deutschland Kg	Verfahren zur Ringfärbung von textilen Flächengebilden aus cellulosischen Fasern und Mischmaterialien enthaltend cellulosische Fasern und danach hergestellte ringgefärbte Gewebe und Mischmaterialien
CN102330368B (zh) *	2011-06-30	2013-02-13	北京泛博化学股份有限公司	一种媒介染色后处理剂、其制备方法及应用
CN102493054B (zh) *	2011-11-24	2015-07-29	无锡市天然绿色纤维科技有限公司	一种混纺可拔染色纺纱线的加工方法

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JPS4993680A (de) *	1972-11-24	1974-09-05

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GB879980A (en) *	1959-08-04	1961-10-11	Ici Ltd	Textile colouration process

1977
- 1977-10-21 DE DE19772747358 patent/DE2747358C2/de not_active Expired
1978
- 1978-10-18 GB GB7840934A patent/GB2006279B/en not_active Expired
- 1978-10-19 JP JP12794178A patent/JPS5468475A/ja active Granted

Patent Citations (1)

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Publication number	Priority date	Publication date	Assignee	Title
JPS4993680A (de) *	1972-11-24	1974-09-05

Also Published As

Publication number	Publication date
GB2006279A (en)	1979-05-02
GB2006279B (en)	1982-10-06
DE2747358C2 (de)	1986-12-04
DE2747358A1 (de)	1979-04-26
JPS5468475A (en)	1979-06-01

Publication	Publication Date	Title
JPS6220309B2 (de)	1987-05-06
US6679924B2 (en)	2004-01-20	Dye fixatives
EP0315477B1 (de)	1993-08-18	Verfahren zur Behandlung von Wolle
Shore	1996	Advances in direct dyes
US4599087A (en)	1986-07-08	Treatment of textile materials to improve the fastness of dyeings made thereon
US4718918A (en)	1988-01-12	Treatment of textile materials to improve the fastness of dyeings made thereon and polymers useful therefor
JPS6052687A (ja)	1985-03-25	反応性染料を用いて染色物を製造する方法
JPH0127189B2 (de)	1989-05-26
JPH0381324A (ja)	1991-04-05	新規ポリマー及びプレポリマー及び羊毛処理方法におけるそれらの用途
US5512064A (en)	1996-04-30	Process for modifying and dyeing modified fiber materials
CN105220528B (zh)	2017-07-28	一种纤维素纤维成衣无水无盐的染色方法
EP0151370B1 (de)	1990-03-14	Färben und Bedrucken von Fasern
JPH0152516B2 (de)	1989-11-09
US4775384A (en)	1988-10-04	Process for treating fibre materials
WO2002059416A2 (en)	2002-08-01	Production of dyed lyocell garments
US5131913A (en)	1992-07-21	Production of pattern effects when dyeing or printing textile material in the absence of alkali or reducing agents: cationization and oxidized in a pattern before dyeing
JPH08113821A (ja)	1996-05-07	アミノ化された再生セルロース繊維およびその製造方法
JPS6220312B2 (de)	1987-05-06
US20230089849A1 (en)	2023-03-23	Pad-steam cationization of textiles
JPS63120172A (ja)	1988-05-24	織物の処理方法
Gutjahr et al.	1994	Direct print coloration
EP0938515B1 (de)	2001-08-08	Polykondensationsprodukte sowie deren verwendung als färbereihilfsmittel
JPS63256777A (ja)	1988-10-24	繊維材料の染色または捺染方法
US4592757A (en)	1986-06-03	Production of dyed or undyed wool with an antifelting finish: quaternized piperazine condensate
US4787910A (en)	1988-11-29	Condensation products and processes for the after-treatment of dyed polyamides