EP0198417A2 - Procédé pour teindre uniformément entre les lisières des matériaux fibreux cellulosiques avec des colorants azoiques formés in situ - Google Patents
Procédé pour teindre uniformément entre les lisières des matériaux fibreux cellulosiques avec des colorants azoiques formés in situ Download PDFInfo
- Publication number
- EP0198417A2 EP0198417A2 EP86104881A EP86104881A EP0198417A2 EP 0198417 A2 EP0198417 A2 EP 0198417A2 EP 86104881 A EP86104881 A EP 86104881A EP 86104881 A EP86104881 A EP 86104881A EP 0198417 A2 EP0198417 A2 EP 0198417A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- textile
- dye
- goods
- liquor
- coupling
- 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 title claims abstract description 39
- 230000008569 process Effects 0.000 title claims abstract description 27
- 238000004043 dyeing Methods 0.000 title claims abstract description 17
- 239000000975 dye Substances 0.000 title abstract description 17
- 239000002657 fibrous material Substances 0.000 title description 3
- 239000004753 textile Substances 0.000 claims abstract description 25
- 230000008878 coupling Effects 0.000 claims abstract description 16
- 238000010168 coupling process Methods 0.000 claims abstract description 16
- 238000005859 coupling reaction Methods 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 14
- 239000000835 fiber Substances 0.000 claims abstract description 13
- 238000007598 dipping method Methods 0.000 claims abstract description 11
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims abstract description 10
- -1 diazoamino Chemical group 0.000 claims abstract description 10
- 229920003043 Cellulose fiber Polymers 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 8
- 239000002253 acid Substances 0.000 claims abstract description 7
- 239000007788 liquid Substances 0.000 claims abstract description 4
- 239000000758 substrate Substances 0.000 claims abstract description 4
- 229920002994 synthetic fiber Polymers 0.000 claims abstract description 4
- 239000012209 synthetic fiber Substances 0.000 claims abstract description 4
- 230000009471 action Effects 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims abstract description 3
- 239000004744 fabric Substances 0.000 claims description 11
- 150000001989 diazonium salts Chemical class 0.000 claims description 8
- 238000005470 impregnation Methods 0.000 claims description 8
- 239000000463 material Substances 0.000 abstract description 15
- 239000000987 azo dye Substances 0.000 abstract description 4
- 230000015572 biosynthetic process Effects 0.000 abstract description 3
- 239000003513 alkali Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 26
- 239000000243 solution Substances 0.000 description 25
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 18
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 11
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 7
- 239000006260 foam Substances 0.000 description 7
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 150000004780 naphthols Chemical class 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 5
- 238000007792 addition Methods 0.000 description 5
- GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 4
- 229920000742 Cotton Polymers 0.000 description 4
- XDWATWCCUTYUDE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-hydroxynaphthalene-2-carboxamide Chemical compound C1=C(Cl)C(OC)=CC(OC)=C1NC(=O)C1=CC2=CC=CC=C2C=C1O XDWATWCCUTYUDE-UHFFFAOYSA-N 0.000 description 4
- JACPTQMMZGZAOL-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCN(C)CCS(O)(=O)=O JACPTQMMZGZAOL-KHPPLWFESA-N 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 238000010014 continuous dyeing Methods 0.000 description 3
- 230000009189 diving Effects 0.000 description 3
- 150000007524 organic acids Chemical class 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- ZUVPLKVDZNDZCM-UHFFFAOYSA-N 3-chloro-2-methylaniline Chemical compound CC1=C(N)C=CC=C1Cl ZUVPLKVDZNDZCM-UHFFFAOYSA-N 0.000 description 2
- RLNNKLNZXOUFDY-UHFFFAOYSA-M 3-chlorobenzenediazonium;chloride Chemical compound [Cl-].ClC1=CC=CC([N+]#N)=C1 RLNNKLNZXOUFDY-UHFFFAOYSA-M 0.000 description 2
- YZJSKRBKHCLMQC-UHFFFAOYSA-N 3-hydroxy-n-(3-nitrophenyl)naphthalene-2-carboxamide Chemical compound OC1=CC2=CC=CC=C2C=C1C(=O)NC1=CC=CC([N+]([O-])=O)=C1 YZJSKRBKHCLMQC-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 229920000297 Rayon Polymers 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- VTPSNRIENVXKCI-UHFFFAOYSA-N n-(2,4-dimethylphenyl)-3-hydroxynaphthalene-2-carboxamide Chemical compound CC1=CC(C)=CC=C1NC(=O)C1=CC2=CC=CC=C2C=C1O VTPSNRIENVXKCI-UHFFFAOYSA-N 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 235000002639 sodium chloride Nutrition 0.000 description 2
- 238000010025 steaming Methods 0.000 description 2
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical class NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- KQZBSZUGKSCFBL-UHFFFAOYSA-N 2-phenyldiazenylaniline Chemical class NC1=CC=CC=C1N=NC1=CC=CC=C1 KQZBSZUGKSCFBL-UHFFFAOYSA-N 0.000 description 1
- ALKYHXVLJMQRLQ-UHFFFAOYSA-N 3-Hydroxy-2-naphthoate Chemical compound C1=CC=C2C=C(O)C(C(=O)O)=CC2=C1 ALKYHXVLJMQRLQ-UHFFFAOYSA-N 0.000 description 1
- AQYMRQUYPFCXDM-UHFFFAOYSA-N 3-hydroxy-n-(2-methoxyphenyl)naphthalene-2-carboxamide Chemical compound COC1=CC=CC=C1NC(=O)C1=CC2=CC=CC=C2C=C1O AQYMRQUYPFCXDM-UHFFFAOYSA-N 0.000 description 1
- FBLAHUMENIHUGG-UHFFFAOYSA-N 3-hydroxy-n-(2-methylphenyl)naphthalene-2-carboxamide Chemical compound CC1=CC=CC=C1NC(=O)C1=CC2=CC=CC=C2C=C1O FBLAHUMENIHUGG-UHFFFAOYSA-N 0.000 description 1
- QGZGJNPVHADCFM-UHFFFAOYSA-N 3-hydroxy-n-naphthalen-1-ylnaphthalene-2-carboxamide Chemical compound C1=CC=C2C(NC(=O)C3=CC4=CC=CC=C4C=C3O)=CC=CC2=C1 QGZGJNPVHADCFM-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
- YJKJAYFKPIUBAW-UHFFFAOYSA-N 9h-carbazol-1-amine Chemical class N1C2=CC=CC=C2C2=C1C(N)=CC=C2 YJKJAYFKPIUBAW-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
- 240000006240 Linum usitatissimum Species 0.000 description 1
- 235000004431 Linum usitatissimum Nutrition 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 244000274883 Urtica dioica Species 0.000 description 1
- 235000009108 Urtica dioica Nutrition 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000008043 acidic salts Chemical class 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- PAEJMUPOBGPBPH-UHFFFAOYSA-N aminooxy(oxo)methanesulfonic acid Chemical class NOC(=O)S(O)(=O)=O PAEJMUPOBGPBPH-UHFFFAOYSA-N 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 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
- 239000003788 bath preparation Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 235000009120 camo Nutrition 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 235000005607 chanvre indien Nutrition 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Substances ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000007857 degradation product Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 230000009365 direct transmission Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 239000003292 glue Substances 0.000 description 1
- 239000011487 hemp Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 238000012432 intermediate storage Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 1
- 235000019799 monosodium phosphate Nutrition 0.000 description 1
- MOUVJGIRLPZEES-UHFFFAOYSA-N n-(4-chloro-2,5-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(NC(=O)CC(C)=O)=C(OC)C=C1Cl MOUVJGIRLPZEES-UHFFFAOYSA-N 0.000 description 1
- SLFVYFOEHHLHDW-UHFFFAOYSA-N n-(trifluoromethyl)aniline Chemical class FC(F)(F)NC1=CC=CC=C1 SLFVYFOEHHLHDW-UHFFFAOYSA-N 0.000 description 1
- KUDPGZONDFORKU-UHFFFAOYSA-N n-chloroaniline Chemical class ClNC1=CC=CC=C1 KUDPGZONDFORKU-UHFFFAOYSA-N 0.000 description 1
- VBEGHXKAFSLLGE-UHFFFAOYSA-N n-phenylnitramide Chemical class [O-][N+](=O)NC1=CC=CC=C1 VBEGHXKAFSLLGE-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000004986 phenylenediamines Chemical class 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000017854 proteolysis Effects 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000004627 regenerated cellulose Substances 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000005619 secondary aliphatic amines Chemical class 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 230000003313 weakening 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
- 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
- D06P3/68—Preparing azo dyes on the material
Definitions
- the present invention relates to the dyeing of textile fabrics or web articles made from cellulose fibers or mixtures thereof with synthetic fibers, with coupling component and diazo component in the form of a stabilized diazoamino or tetrazoamino compound or a diazotate on the fiber, by the Dye-forming components are applied continuously and together by direct transfer from an aqueous liquor containing these substances under alkaline conditions to the goods without dipping the textile goods therein, and the subsequent dye development is brought about by the action of acid.
- the foulard technique has primarily been used so far.
- a solution of the same is mechanically pressed (impregnated) onto the spread web by passing the substrate to be dyed through a bath (chassis) filled with treatment liquor and then squeezed off from the excess liquor.
- a primer consists essentially of the alkaline solution of a coupling component (hereinafter also referred to briefly as "naphthol"), in particular of an arylamide of 2-hydroxy-3-naphthoic acid or an arylamide of ketocarboxylic acids.
- naphthol a coupling component
- the dye is developed by treating the previously mentioned primer with a solution of a diazonium compound (Azoic Diazo Component) under acidic conditions.
- the purpose of the present invention is therefore to develop a process which succeeds in eliminating or circumventing the effect of the substantivity of the "naphthols", so that the single-bath continuous operation discussed above without impairing the color tone through the end drain can be realized.
- Such a continuous process should neither include intermediate drying or necessary intermediate storage of the goods loaded with the dye-forming components, nor should special textile auxiliaries be required for wet-on-wet work. * ) and the color depth
- fleet intakes by the Tex - tilgut in the range between 15% and 50% (based on the weight of the dry goods).
- the "naphthol" does not have to be applied hot according to the invention.
- Such a liquor can also be thickened, for example by adding glue, so that a very precise application of dye components can be carried out, which means that no excess dye is used in this way; the wastewater pollution is therefore much lower.
- the process according to the invention is carried out, for example, by impregnating raw or ready-to-dye cellulose fiber fabric with an alkaline, thickened solution which contains a more or less substantive coupling component, a stabilized, non-coupling diazonium compound in the form of a diazoamino or tetrazoamino compound or an antidiazotate and optionally also contains a dispersant and / or a wetting agent.
- the above-described impregnation liquor containing the dye-forming components can advantageously also be used in the form of a fine-pored foam. Due to the inherent consistency of such foams, a certain amount of the thickener can be saved in this variant.
- the stabilized diazonium compound is converted into the couplable form by subsequent treatment of the textile webs, which have been pre-primed in accordance with the process, with acidic agents, which either consist of acidic steaming or an acid passage, so that a pH value between 3 and 6 is established on the goods coupling occurs and with it the formation of dye on the fiber. Finally, the coloring thus produced is then post-treated and finished in the manner customary in accordance with the ice color technique.
- Suitable coupling components in the process according to the invention are predominantly those which have a low to medium substantivity towards cellulose fibers have.
- Suitable compounds are, for example, 2,3-hydroxynaphthoylaminobenzene, 1- (2 ', 3'-hydroxynaphthoylamino) -2-methylbenzene, 1- (2', 3'-hydroxynaphthoylamino) -2-methoxybenzene, 1- (2 ', 3'-hydroxynaphthoylamino) -3-nitrobenzene, 1- (2 ', 3'-hydroxynaphthoylamino) -4-methoxybenzene, 1- (2', 3'-hydroxynaphthoylamino) -2-methyl-4-methoxybenzene, 1- (2 ', 3'-hydroxynaphthoylamino) -2,5-dimethoxybenzene, 1- (2', 3'-hydroxynaphtho
- Coupling components with higher substantivity for example 2- (2 ', 3'-hydroxynaphthoylamino) naphthalene, 1- (2', 3'-hydroxynaphthoylamino) -2-methoxy-4-chloro-5-methylbenzene, 1- (2 ', 3'-hydroxynaphthoylamino) -2,5-dimethoxy-4-chlorobenzene, 2- (2 ', 3'-hydroxynaphthoylamino) -3-methoxy-diphenylene oxide or 1- (2'-hydroxycarbazole-3'-carboylamino) -4- Chlorobenzene can also be used in the process according to the invention. In contrast to other order processes, special measures that counteract substantivity can be dispensed with.
- Diazoamino- or Tetrazoaminoeducationen those from diazotized aromatic or heterocyclic mono-or diamines, such as diazotized chloroanilines, Dichloranilinen, Chlortoluidinen, Chloranisidinen, nitroanilines, Nitrotoluidinen, Nitroanisidinen, Nitroxylidinen, Nitrophenetidinen, Cyantoluidinen, Cyananisidinen, Aminobenzolsulfonklareamiden, Aminobenzolcarbonklaamiden, Aminophenylalkyl-, aryl or aralkyl sulfones, aminodiphenyl ethers, trifluoromethylanilines, monoacylated phenylenediamines, aminoazobenzenes, 4,4'-diaminodiphenyls or amino carbazoles, and primary or secondary aliphatic or aromatic amines, for example N-alkylated aliphatic aminocarboxylic acids or
- Suitable antidiazotates are likewise those compounds obtainable from the above-mentioned primary aromatic amines.
- Suitable dispersants which can also be used in the alkaline impregnation bath are the compounds customary in ice color technology, for example condensation products from higher molecular weight fatty acids and protein degradation products, condensation products of formaldehyde with naphthalenesulfonic acids or purified sulfite cellulose waste liquor.
- Alkyl aryl sulfonates are preferably used as wetting agents.
- the acidic compounds in the development bath are organic acids, for example formic acid, acetic acid, propionic acid, or acidic salts, for example monosodium phosphate.
- organic acids for example formic acid, acetic acid, propionic acid, or acidic salts, for example monosodium phosphate.
- acidic salts for example monosodium phosphate.
- a mixture of a salt of an organic acid and an organic acid for example a mixture of sodium acetate and acetic acid.
- the process according to the invention can be applied to the known cellulosic fibers and mixtures of synthetic fibers, e.g. Polyester fibers, and cellulose fibers are used.
- the cellulose fibers are native fibers such as flax, hemp, linen and cotton, or regenerated fibers such as viscose, rayon and modal fibers.
- solution 2) is stirred into the bath batch and this is filled up with water at 70 ° C. to a total volume of 200 l.
- the dyed material is impregnated by direct transfer without dipping it at 25 ° C. and with a liquor absorption of 40% using a device for minimal application described in European Patent EP-B-0 047 484.
- this liquor is applied to the fabric at 20 ° C. and a liquor application of 40% by direct transfer without dipping it.
- the web thus treated now passes through a chassis with an aqueous development liquor of 80 ° C., which contains.
- the dyed textile material is then subjected to a short passage of air, then rinsed first with hot water, soaped at the boil, rinsed again with water and finally finished.
- a deep Bordo coloration results on the goods.
- solution 2) is stirred into the bath batch and this is filled up with water at 20 ° C. to a total volume of 300 l.
- the cord fabric is impregnated by direct transfer without dipping it at 25 ° C. and with 35% liquor absorption with the aid of a device for minimal dosing as in Example 1. Immediately afterwards, the goods treated in this way are exposed to a short airflow at room temperature.
- the development of the azo dye on the fiber is now carried out by padding the material to be dyed with an acid solution at 80 ° C.
- the impregnated cord is treated on the foulard with 100% liquor absorption, the textile material is then subjected to an air passage of 30 seconds at room temperature and the dyeing obtained in this way is rinsed in a wide washing machine with water at 70 ° C. in the first box.
- the dyed goods are placed in an aqueous bath under the effect of first at 70 ° C and then soaped at the boil, then rinsed again with water and finished.
- a fabric made of regenerated cellulose fibers is impregnated with an aqueous liquor at room temperature and the following composition by direct transfer without dipping it using a minimal application device as in Example 1 with a liquor application of 40%:
- the fabric impregnated in this way is now steamed for 5 minutes at 185 ° C. in the superheated steam for dye development.
- the dyed textile material is then rinsed with water and aftertreated for 10 minutes at 90 ° C. with an aqueous bath with the addition of 1 g / l of an approximately 20-fold ethoxylated nonylphenol.
- the double minimum application of the impregnation liquor can be carried out from the different sides of the textile web in order to achieve a more uniform distribution of the treatment agent on the terry goods and their better penetration.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT86104881T ATE54966T1 (de) | 1985-04-19 | 1986-04-09 | Verfahren zum endengleichen faerben von cellulosefasermaterialien mit azoentwicklungsfarbstoffen. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3514111 | 1985-04-19 | ||
DE19853514111 DE3514111A1 (de) | 1985-04-19 | 1985-04-19 | Verfahren zum endengleichen faerben von cellulosefasermaterialien mit azo-entwicklungsfarbstoffen |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0198417A2 true EP0198417A2 (fr) | 1986-10-22 |
EP0198417A3 EP0198417A3 (en) | 1988-08-24 |
EP0198417B1 EP0198417B1 (fr) | 1990-07-25 |
Family
ID=6268541
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86104881A Expired - Lifetime EP0198417B1 (fr) | 1985-04-19 | 1986-04-09 | Procédé pour teindre uniformément entre les lisières des matériaux fibreux cellulosiques avec des colorants azoiques formés in situ |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0198417B1 (fr) |
AT (1) | ATE54966T1 (fr) |
DE (2) | DE3514111A1 (fr) |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1915390A1 (de) * | 1969-03-26 | 1970-10-01 | Hoechst Ag | Verfahren zum gleichzeitigen Bleichen und Faerben von Textilmaterial aus Cellulosefasern |
DE2145827B2 (de) * | 1970-09-22 | 1976-07-29 | Sandoz Ag, Basel (Schweiz) | Verfahren zur nassbehandlung von poroesem textilgut |
DE2416259B2 (de) * | 1974-04-03 | 1976-12-02 | Hoechst Ag, 6000 Frankfurt | Verfahren zum fixieren von faerbungen oder drucken auf textilgut |
DE2214377B2 (de) * | 1972-03-24 | 1979-08-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zum kontinuierlichen Färben von flächigem Textilgut |
GB2027753A (en) * | 1978-07-27 | 1980-02-27 | Ciba Geigy Ag | Process for the treatment of textile fibre materials with foams |
DE2911166A1 (de) * | 1979-03-22 | 1980-10-02 | Hoechst Ag | Verfahren und vorrichtung zum auftragen geringer fluessigkeitsmengen auf bahnfoermige textile flaechengebilde |
DE2902977C2 (de) * | 1979-01-26 | 1980-12-18 | Hoechst Ag, 6000 Frankfurt | Verfahren zum kontinuierlichen oder halbkontinuierlichen Färben von Mischungen aus Cellulosefasern und synthetischen Polyamidfasern mit Azo-Entwicklungsfarbstoffen |
DE3033478C2 (de) * | 1980-09-05 | 1982-12-30 | Fa. Johannes Zimmer, 9020 Klagenfurt | Foulard mit einer Umschlingungswalze für eine zu behandelnde textile Warenbahn |
-
1985
- 1985-04-19 DE DE19853514111 patent/DE3514111A1/de not_active Withdrawn
-
1986
- 1986-04-09 EP EP86104881A patent/EP0198417B1/fr not_active Expired - Lifetime
- 1986-04-09 AT AT86104881T patent/ATE54966T1/de not_active IP Right Cessation
- 1986-04-09 DE DE8686104881T patent/DE3672874D1/de not_active Expired - Fee Related
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1915390A1 (de) * | 1969-03-26 | 1970-10-01 | Hoechst Ag | Verfahren zum gleichzeitigen Bleichen und Faerben von Textilmaterial aus Cellulosefasern |
DE2145827B2 (de) * | 1970-09-22 | 1976-07-29 | Sandoz Ag, Basel (Schweiz) | Verfahren zur nassbehandlung von poroesem textilgut |
DE2214377B2 (de) * | 1972-03-24 | 1979-08-09 | Hoechst Ag, 6000 Frankfurt | Verfahren zum kontinuierlichen Färben von flächigem Textilgut |
DE2416259B2 (de) * | 1974-04-03 | 1976-12-02 | Hoechst Ag, 6000 Frankfurt | Verfahren zum fixieren von faerbungen oder drucken auf textilgut |
GB2027753A (en) * | 1978-07-27 | 1980-02-27 | Ciba Geigy Ag | Process for the treatment of textile fibre materials with foams |
DE2902977C2 (de) * | 1979-01-26 | 1980-12-18 | Hoechst Ag, 6000 Frankfurt | Verfahren zum kontinuierlichen oder halbkontinuierlichen Färben von Mischungen aus Cellulosefasern und synthetischen Polyamidfasern mit Azo-Entwicklungsfarbstoffen |
DE2911166A1 (de) * | 1979-03-22 | 1980-10-02 | Hoechst Ag | Verfahren und vorrichtung zum auftragen geringer fluessigkeitsmengen auf bahnfoermige textile flaechengebilde |
DE3033478C2 (de) * | 1980-09-05 | 1982-12-30 | Fa. Johannes Zimmer, 9020 Klagenfurt | Foulard mit einer Umschlingungswalze für eine zu behandelnde textile Warenbahn |
Also Published As
Publication number | Publication date |
---|---|
DE3514111A1 (de) | 1986-10-23 |
EP0198417A3 (en) | 1988-08-24 |
DE3672874D1 (de) | 1990-08-30 |
EP0198417B1 (fr) | 1990-07-25 |
ATE54966T1 (de) | 1990-08-15 |
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