DE2653418B2 - - Google Patents
Info
- Publication number
- DE2653418B2 DE2653418B2 DE2653418A DE2653418A DE2653418B2 DE 2653418 B2 DE2653418 B2 DE 2653418B2 DE 2653418 A DE2653418 A DE 2653418A DE 2653418 A DE2653418 A DE 2653418A DE 2653418 B2 DE2653418 B2 DE 2653418B2
- Authority
- DE
- Germany
- Prior art keywords
- dyes
- dye
- methyl
- blue
- minutes
- Prior art date
- 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.)
- Granted
Links
- 238000000034 method Methods 0.000 claims description 23
- 239000000463 material Substances 0.000 claims description 13
- 239000003513 alkali Substances 0.000 claims description 12
- 238000004043 dyeing Methods 0.000 claims description 12
- 238000007639 printing Methods 0.000 claims description 11
- 239000004753 textile Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 150000002118 epoxides Chemical class 0.000 claims 1
- 239000000975 dye Substances 0.000 description 40
- 239000000460 chlorine Substances 0.000 description 21
- JXYZHMPRERWTPM-UHFFFAOYSA-N hydron;morpholine;chloride Chemical compound Cl.C1COCCN1 JXYZHMPRERWTPM-UHFFFAOYSA-N 0.000 description 19
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 18
- 239000004744 fabric Substances 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 14
- 229920000742 Cotton Polymers 0.000 description 12
- 230000000694 effects Effects 0.000 description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 239000000835 fiber Substances 0.000 description 8
- 239000000049 pigment Substances 0.000 description 8
- 125000000129 anionic group Chemical group 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 6
- 239000000985 reactive dye Substances 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 5
- 150000001450 anions Chemical class 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 229920000297 Rayon Polymers 0.000 description 4
- 239000000982 direct dye Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 150000002924 oxiranes Chemical class 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- OMDQUFIYNPYJFM-XKDAHURESA-N (2r,3r,4s,5r,6s)-2-(hydroxymethyl)-6-[[(2r,3s,4r,5s,6r)-4,5,6-trihydroxy-3-[(2s,3s,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@@H]1OC[C@@H]1[C@@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)[C@H](O)[C@H](O)[C@H](O)O1 OMDQUFIYNPYJFM-XKDAHURESA-N 0.000 description 3
- -1 3-epoxypropyl Chemical group 0.000 description 3
- 229920000926 Galactomannan Polymers 0.000 description 3
- LJWXZQWHULANEO-UHFFFAOYSA-N P(=O)(O)(O)O.C(C)C(C[Na])CCCC Chemical compound P(=O)(O)(O)O.C(C)C(C[Na])CCCC LJWXZQWHULANEO-UHFFFAOYSA-N 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000002657 fibrous material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- STOOUUMSJPLRNI-UHFFFAOYSA-N 5-amino-4-hydroxy-3-[[4-[4-[(4-hydroxyphenyl)diazenyl]phenyl]phenyl]diazenyl]-6-[(4-nitrophenyl)diazenyl]naphthalene-2,7-disulfonic acid Chemical compound OS(=O)(=O)C1=CC2=CC(S(O)(=O)=O)=C(N=NC=3C=CC(=CC=3)C=3C=CC(=CC=3)N=NC=3C=CC(O)=CC=3)C(O)=C2C(N)=C1N=NC1=CC=C([N+]([O-])=O)C=C1 STOOUUMSJPLRNI-UHFFFAOYSA-N 0.000 description 2
- INOIOAWTVPHTCJ-UHFFFAOYSA-N 6-acetamido-4-hydroxy-3-[[4-(2-sulfooxyethylsulfonyl)phenyl]diazenyl]naphthalene-2-sulfonic acid Chemical compound CC(=O)NC1=CC=C2C=C(C(N=NC3=CC=C(C=C3)S(=O)(=O)CCOS(O)(=O)=O)=C(O)C2=C1)S(O)(=O)=O INOIOAWTVPHTCJ-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229920000615 alginic acid Polymers 0.000 description 2
- 235000010443 alginic acid Nutrition 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 239000000834 fixative Substances 0.000 description 2
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 239000001044 red dye Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical group C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 description 2
- 239000000984 vat dye Substances 0.000 description 2
- 230000004584 weight gain Effects 0.000 description 2
- 235000019786 weight gain Nutrition 0.000 description 2
- VZSRBBMJRBPUNF-UHFFFAOYSA-N 2-(2,3-dihydro-1H-inden-2-ylamino)-N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]pyrimidine-5-carboxamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C(=O)NCCC(N1CC2=C(CC1)NN=N2)=O VZSRBBMJRBPUNF-UHFFFAOYSA-N 0.000 description 1
- ADCWDMYESTYBBN-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-3-methyl-4-[(4-nitrophenyl)diazenyl]anilino]ethanol Chemical compound CC1=CC(N(CCO)CCO)=CC=C1N=NC1=CC=C([N+]([O-])=O)C=C1 ADCWDMYESTYBBN-UHFFFAOYSA-N 0.000 description 1
- RZVCEPSDYHAHLX-UHFFFAOYSA-N 3-iminoisoindol-1-amine Chemical compound C1=CC=C2C(N)=NC(=N)C2=C1 RZVCEPSDYHAHLX-UHFFFAOYSA-N 0.000 description 1
- CTRXDTYTAAKVSM-UHFFFAOYSA-N 3-{[ethyl({4-[(4-{ethyl[(3-sulfophenyl)methyl]amino}phenyl)(2-sulfophenyl)methylidene]cyclohexa-2,5-dien-1-ylidene})azaniumyl]methyl}benzene-1-sulfonate Chemical compound C=1C=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C(=CC=CC=2)S(O)(=O)=O)C=CC=1N(CC)CC1=CC=CC(S(O)(=O)=O)=C1 CTRXDTYTAAKVSM-UHFFFAOYSA-N 0.000 description 1
- CXNVOWPRHWWCQR-UHFFFAOYSA-N 4-Chloro-ortho-toluidine Chemical compound CC1=CC(Cl)=CC=C1N CXNVOWPRHWWCQR-UHFFFAOYSA-N 0.000 description 1
- JLHFVIHSWVYOFK-UHFFFAOYSA-M 4-methyl-4-(oxiran-2-ylmethyl)morpholin-4-ium;chloride Chemical compound [Cl-].C1OC1C[N+]1(C)CCOCC1 JLHFVIHSWVYOFK-UHFFFAOYSA-M 0.000 description 1
- LYWVNPSVLAFTFX-UHFFFAOYSA-N 4-methylbenzenesulfonate;morpholin-4-ium Chemical compound C1COCCN1.CC1=CC=C(S(O)(=O)=O)C=C1 LYWVNPSVLAFTFX-UHFFFAOYSA-N 0.000 description 1
- FHVDTGUDJYJELY-UHFFFAOYSA-N 6-{[2-carboxy-4,5-dihydroxy-6-(phosphanyloxy)oxan-3-yl]oxy}-4,5-dihydroxy-3-phosphanyloxane-2-carboxylic acid Chemical compound O1C(C(O)=O)C(P)C(O)C(O)C1OC1C(C(O)=O)OC(OP)C(O)C1O FHVDTGUDJYJELY-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229920003043 Cellulose fiber Polymers 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000002000 Electrolyte additive Substances 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
- FCLZCOCSZQNREK-UHFFFAOYSA-N Pyrrolidine, hydrochloride Chemical compound Cl.C1CCNC1 FCLZCOCSZQNREK-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-O Pyrrolidinium ion Chemical compound C1CC[NH2+]C1 RWRDLPDLKQPQOW-UHFFFAOYSA-O 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 241001584775 Tunga penetrans Species 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 229940072056 alginate Drugs 0.000 description 1
- 239000000783 alginic acid Substances 0.000 description 1
- 229960001126 alginic acid Drugs 0.000 description 1
- 150000004781 alginic acids Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- POJOORKDYOPQLS-UHFFFAOYSA-L barium(2+) 5-chloro-2-[(2-hydroxynaphthalen-1-yl)diazenyl]-4-methylbenzenesulfonate Chemical compound [Ba+2].C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O.C1=C(Cl)C(C)=CC(N=NC=2C3=CC=CC=C3C=CC=2O)=C1S([O-])(=O)=O POJOORKDYOPQLS-UHFFFAOYSA-L 0.000 description 1
- 229940077388 benzenesulfonate Drugs 0.000 description 1
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 1
- 229960001506 brilliant green Drugs 0.000 description 1
- HXCILVUBKWANLN-UHFFFAOYSA-N brilliant green cation Chemical compound C1=CC(N(CC)CC)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](CC)CC)C=C1 HXCILVUBKWANLN-UHFFFAOYSA-N 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- NZFPRFFQXUVQMT-UHFFFAOYSA-L disodium 8-amino-7-[(2-chlorophenyl)diazenyl]-2-[[4-[4-[(4-oxidophenyl)diazenyl]phenyl]phenyl]diazenyl]-3,6-disulfonaphthalen-1-olate Chemical compound C1=CC=C(C(=C1)N=NC2=C(C=C3C=C(C(=C(C3=C2N)[O-])N=NC4=CC=C(C=C4)C5=CC=C(C=C5)N=NC6=CC=C(C=C6)[O-])S(=O)(=O)O)S(=O)(=O)O)Cl.[Na+].[Na+] NZFPRFFQXUVQMT-UHFFFAOYSA-L 0.000 description 1
- 239000000986 disperse dye Substances 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 210000004209 hair Anatomy 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- VEIWYFRREFUNRC-UHFFFAOYSA-N hydron;piperidine;chloride Chemical compound [Cl-].C1CC[NH2+]CC1 VEIWYFRREFUNRC-UHFFFAOYSA-N 0.000 description 1
- 235000019239 indanthrene blue RS Nutrition 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- MTDQTHOKIZBFQQ-UHFFFAOYSA-N methyl sulfate;morpholin-4-ium Chemical compound COS([O-])(=O)=O.C1COCC[NH2+]1 MTDQTHOKIZBFQQ-UHFFFAOYSA-N 0.000 description 1
- XCKKIKBIPZJUET-VYKNHSEDSA-N morphine hydrochloride Chemical compound Cl.O([C@H]1[C@H](C=C[C@H]23)O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4O XCKKIKBIPZJUET-VYKNHSEDSA-N 0.000 description 1
- NXIGDUAONGBUKR-UHFFFAOYSA-N n-(2-ethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide Chemical compound CCOC1=CC=CC=C1NC(=O)C1=CC2=CC=CC=C2C=C1O NXIGDUAONGBUKR-UHFFFAOYSA-N 0.000 description 1
- AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 229920001206 natural gum Polymers 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- ROFVJSWBDQUQGW-UHFFFAOYSA-N piperidin-1-ium;bromide Chemical compound Br.C1CCNCC1 ROFVJSWBDQUQGW-UHFFFAOYSA-N 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000010020 roller printing Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- HUAUNKAZQWMVFY-UHFFFAOYSA-M sodium;oxocalcium;hydroxide Chemical compound [OH-].[Na+].[Ca]=O HUAUNKAZQWMVFY-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229920006304 triacetate fiber Polymers 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 238000003911 water pollution Methods 0.000 description 1
- 239000001043 yellow dye Substances 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
- D06P1/655—Compounds containing ammonium groups
- D06P1/66—Compounds containing ammonium groups containing quaternary ammonium groups
-
- 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
- D06P1/96—Dyeing characterised by a short bath ratio
-
- 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
- D06P5/22—Effecting variation of dye affinity on textile material by chemical means that react with the fibre
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Coloring (AREA)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2653418A DE2653418C3 (de) | 1976-11-24 | 1976-11-24 | Verfahren zum Bedrucken und Färben |
| NL7712143A NL7712143A (nl) | 1976-11-24 | 1977-11-03 | Werkwijze voor het bedrukken en verven van textiel. |
| US05/853,863 US4149849A (en) | 1976-11-24 | 1977-11-22 | Process for printing and dyeing |
| JP13956577A JPS5365478A (en) | 1976-11-24 | 1977-11-22 | Printing and dyeing method |
| GB48606/77A GB1554520A (en) | 1976-11-24 | 1977-11-22 | Process for printing and dyeing |
| FR7735176A FR2372271A1 (fr) | 1976-11-24 | 1977-11-23 | Procede perfectionne pour la teinture et l'impression |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2653418A DE2653418C3 (de) | 1976-11-24 | 1976-11-24 | Verfahren zum Bedrucken und Färben |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| DE2653418A1 DE2653418A1 (de) | 1978-06-01 |
| DE2653418B2 true DE2653418B2 (en:Method) | 1979-06-21 |
| DE2653418C3 DE2653418C3 (de) | 1980-02-21 |
Family
ID=5993880
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2653418A Expired DE2653418C3 (de) | 1976-11-24 | 1976-11-24 | Verfahren zum Bedrucken und Färben |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US4149849A (en:Method) |
| JP (1) | JPS5365478A (en:Method) |
| DE (1) | DE2653418C3 (en:Method) |
| FR (1) | FR2372271A1 (en:Method) |
| GB (1) | GB1554520A (en:Method) |
| NL (1) | NL7712143A (en:Method) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH631589B (de) * | 1976-12-07 | Sandoz Ag | Verfahren zur erhoehung der affinitaet fuer anionische farbstoffe und optische aufheller von textilmaterial. | |
| DE2914142A1 (de) * | 1979-04-07 | 1980-11-13 | Bayer Ag | Verfahren zum einbadigen, einstufigen faerben oder bedrucken von cellulosefasern mit faserreaktiven dispersionsfarbstoffen |
| DE2838274A1 (de) * | 1978-09-01 | 1980-03-13 | Bayer Ag | Verfahren zum faerben und bedrucken von cellulosefasern mit reaktivfarbstoffen |
| FR2470185A1 (fr) * | 1979-11-20 | 1981-05-29 | Protex Manuf Prod Chimiq | Application nouvelle des composes epoxyalkylammonium quaternaire au pretraitement des fibres de polyamide |
| US4421826A (en) * | 1980-05-08 | 1983-12-20 | W. R. Grace & Co. | Polyurethane polymer amine salt as a dyeing aid, particularly for polyolefin fibers |
| US4447243A (en) * | 1981-08-17 | 1984-05-08 | Dixie Yarns, Inc. | Odor scavenging system |
| US4874402A (en) * | 1981-12-01 | 1989-10-17 | Shell Oil Company | Process for purifying and cooling a hot gas |
| JPS60231877A (ja) * | 1984-04-27 | 1985-11-18 | 東洋紡績株式会社 | セルロ−ス系繊維の異色染色法 |
| JPS60231878A (ja) * | 1984-04-27 | 1985-11-18 | 東洋紡績株式会社 | セルロ−ス系繊維の異色染色方法 |
| EP0362138B1 (de) * | 1988-09-29 | 1995-07-19 | Ciba-Geigy Ag | Epoxidharzgemische |
| DE59108072D1 (de) * | 1990-10-04 | 1996-09-19 | Ciba Geigy Ag | Konzentrierte wässrige Lösungen anionischer Disazofarbstoffe |
| JPH0749631B2 (ja) * | 1990-10-09 | 1995-05-31 | 株式会社松井色素化学工業所 | 染色方法及び染色物 |
| US5320646A (en) * | 1992-05-22 | 1994-06-14 | The Dow Chemical Company | Process for improving the dyeability of fabrics and fibers |
| US5330541A (en) * | 1992-12-15 | 1994-07-19 | American Emulsions, Co. | Method for salt-free dyeing |
| JP2672458B2 (ja) * | 1993-11-05 | 1997-11-05 | ツヤック株式会社 | 蛋白繊維製品の低温染色化剤及びこれを用いた染色法 |
| US5698476A (en) * | 1995-03-01 | 1997-12-16 | The Clorox Company | Laundry article for preventing dye carry-over and indicator therefor |
| DE19717764A1 (de) * | 1997-04-26 | 1998-10-29 | Josef Stuhler | Viskoseplüsch |
| US7201778B2 (en) * | 2003-01-13 | 2007-04-10 | North Carolina State University | Ionic cross-linking of ionic cotton with small molecular weight anionic or cationic molecules |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2876217A (en) * | 1956-12-31 | 1959-03-03 | Corn Products Co | Starch ethers containing nitrogen and process for making the same |
| US2995513A (en) * | 1957-12-31 | 1961-08-08 | Corn Products Co | Flocculation by starch ethers |
| FR2146545A6 (fr) * | 1968-08-30 | 1973-03-02 | Inst Textile De France | Jeu educatif permettant de s'initier a la teinture et a l'impression de polymeres polyhydroxyles |
| FR2061533A1 (en) | 1969-04-24 | 1971-06-25 | Protex Manufacture Produ | Alkyl ammonium 2,3-epoxypropyl salts - as dyebath or printing paste additives |
| BE737603A (en:Method) | 1968-09-25 | 1970-02-02 | ||
| FR2041703B1 (en:Method) | 1969-05-12 | 1973-05-25 | Protex Manuf Prod Chimiq | |
| NL170146C (nl) | 1970-11-13 | Hoffmann Staerkefabriken Ag | Werkwijze ter bereiding van glycidyltrialkylammoniumhalogeniden. | |
| DE2117182A1 (en) | 1971-04-08 | 1972-10-12 | Bergmann, Gerhard, 5165 Niederau | Increasing anionic dye receptivity of polyamide fibres - - by treating with amine-conggtg epoxy cpds, and heat-treatment |
| DE2407147A1 (de) * | 1974-02-15 | 1975-08-28 | Bayer Ag | Quartaere n- (2,3-epoxyalkyl)-ammonium- verbindungen |
| FR2303112A1 (fr) * | 1975-03-04 | 1976-10-01 | Protex Manuf Prod Chimiq | Procede de traitement de matieres textiles, notamment en vue de l'amelioration des teintures ou impressions de ces matieres |
-
1976
- 1976-11-24 DE DE2653418A patent/DE2653418C3/de not_active Expired
-
1977
- 1977-11-03 NL NL7712143A patent/NL7712143A/xx not_active Application Discontinuation
- 1977-11-22 US US05/853,863 patent/US4149849A/en not_active Expired - Lifetime
- 1977-11-22 JP JP13956577A patent/JPS5365478A/ja active Pending
- 1977-11-22 GB GB48606/77A patent/GB1554520A/en not_active Expired
- 1977-11-23 FR FR7735176A patent/FR2372271A1/fr active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| GB1554520A (en) | 1979-10-24 |
| NL7712143A (nl) | 1978-05-26 |
| DE2653418C3 (de) | 1980-02-21 |
| US4149849A (en) | 1979-04-17 |
| FR2372271A1 (fr) | 1978-06-23 |
| JPS5365478A (en) | 1978-06-10 |
| DE2653418A1 (de) | 1978-06-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OD | Request for examination | ||
| C3 | Grant after two publication steps (3rd publication) | ||
| 8330 | Complete renunciation |