EP0592466B1 - Verdickung für textildruckpasten - Google Patents
Verdickung für textildruckpasten Download PDFInfo
- Publication number
- EP0592466B1 EP0592466B1 EP92911776A EP92911776A EP0592466B1 EP 0592466 B1 EP0592466 B1 EP 0592466B1 EP 92911776 A EP92911776 A EP 92911776A EP 92911776 A EP92911776 A EP 92911776A EP 0592466 B1 EP0592466 B1 EP 0592466B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- fatty acid
- glycerol
- acid ester
- parts
- 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.)
- Expired - Lifetime
Links
- 230000008719 thickening Effects 0.000 title abstract description 27
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 80
- 239000000194 fatty acid Substances 0.000 claims abstract description 41
- -1 fatty-acid ester Chemical class 0.000 claims abstract description 40
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 38
- 229930195729 fatty acid Natural products 0.000 claims abstract description 38
- 239000000203 mixture Substances 0.000 claims abstract description 38
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 22
- 150000001720 carbohydrates Chemical class 0.000 claims abstract description 19
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000003381 stabilizer Substances 0.000 claims abstract description 13
- 239000004753 textile Substances 0.000 claims description 15
- 239000002562 thickening agent Substances 0.000 claims description 11
- 235000011187 glycerol Nutrition 0.000 abstract description 24
- 235000014633 carbohydrates Nutrition 0.000 description 12
- 239000000975 dye Substances 0.000 description 11
- 239000000463 material Substances 0.000 description 9
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 229920000742 Cotton Polymers 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- LIBWRRJGKWQFSD-UHFFFAOYSA-M sodium;2-nitrobenzenesulfonate Chemical compound [Na+].[O-][N+](=O)C1=CC=CC=C1S([O-])(=O)=O LIBWRRJGKWQFSD-UHFFFAOYSA-M 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 4
- 235000010443 alginic acid Nutrition 0.000 description 4
- 229920000615 alginic acid Polymers 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 235000010413 sodium alginate Nutrition 0.000 description 4
- 239000000661 sodium alginate Substances 0.000 description 4
- 229940005550 sodium alginate Drugs 0.000 description 4
- FKOKUHFZNIUSLW-UHFFFAOYSA-N 2-Hydroxypropyl stearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(C)O FKOKUHFZNIUSLW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 229920000297 Rayon Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000003925 fat Substances 0.000 description 3
- 150000004665 fatty acids Chemical group 0.000 description 3
- 229940093625 propylene glycol monostearate Drugs 0.000 description 3
- 235000012424 soybean oil Nutrition 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 229920000926 Galactomannan Polymers 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000006887 Ullmann reaction Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 235000019426 modified starch Nutrition 0.000 description 2
- 235000011837 pasties Nutrition 0.000 description 2
- 235000010987 pectin Nutrition 0.000 description 2
- 239000001814 pectin Substances 0.000 description 2
- 229920001277 pectin Polymers 0.000 description 2
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- QIZPVNNYFKFJAD-UHFFFAOYSA-N 1-chloro-2-prop-1-ynylbenzene Chemical compound CC#CC1=CC=CC=C1Cl QIZPVNNYFKFJAD-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000106483 Anogeissus latifolia Species 0.000 description 1
- 235000011514 Anogeissus latifolia Nutrition 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 244000201986 Cassia tora Species 0.000 description 1
- 244000037364 Cinnamomum aromaticum Species 0.000 description 1
- 235000014489 Cinnamomum aromaticum Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000303965 Cyamopsis psoralioides Species 0.000 description 1
- 239000001922 Gum ghatti Substances 0.000 description 1
- 229920000161 Locust bean gum Polymers 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 241000083869 Polyommatus dorylas Species 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229930006000 Sucrose Natural products 0.000 description 1
- 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
- 238000003854 Surface Print Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000007171 acid catalysis Methods 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
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000010980 cellulose Nutrition 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- NKLPQNGYXWVELD-UHFFFAOYSA-M coomassie brilliant blue Chemical compound [Na+].C1=CC(OCC)=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=C1 NKLPQNGYXWVELD-UHFFFAOYSA-M 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 210000000416 exudates and transudate Anatomy 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 235000019314 gum ghatti Nutrition 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 230000003165 hydrotropic effect Effects 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 150000003903 lactic acid esters Chemical class 0.000 description 1
- 235000010420 locust bean gum Nutrition 0.000 description 1
- 239000000711 locust bean gum Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 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
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- NCAIGTHBQTXTLR-UHFFFAOYSA-N phentermine hydrochloride Chemical compound [Cl-].CC(C)([NH3+])CC1=CC=CC=C1 NCAIGTHBQTXTLR-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 150000004804 polysaccharides Chemical class 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- COEZWFYORILMOM-UHFFFAOYSA-M sodium 4-[(2,4-dihydroxyphenyl)diazenyl]benzenesulfonate Chemical compound [Na+].OC1=CC(O)=CC=C1N=NC1=CC=C(S([O-])(=O)=O)C=C1 COEZWFYORILMOM-UHFFFAOYSA-M 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-N sodium;hydron;carbonate Chemical compound [Na+].OC(O)=O UIIMBOGNXHQVGW-UHFFFAOYSA-N 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000010025 steaming Methods 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 229940035023 sucrose monostearate Drugs 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- YXZRCLVVNRLPTP-UHFFFAOYSA-J turquoise blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Cu+2].NC1=NC(Cl)=NC(NC=2C=C(NS(=O)(=O)C3=CC=4C(=C5NC=4NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)NC=4NC(=C6C=C(C=CC6=4)S([O-])(=O)=O)NC=4[N-]C(=C6C=CC(=CC6=4)S([O-])(=O)=O)N5)C=C3)C(=CC=2)S([O-])(=O)=O)=N1 YXZRCLVVNRLPTP-UHFFFAOYSA-J 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 210000002268 wool Anatomy 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
- D06P1/64—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using insoluble pigments or auxiliary substances, e.g. binders using compositions containing low-molecular-weight organic compounds without sulfate or sulfonate groups
- D06P1/651—Compounds without nitrogen
- D06P1/65106—Oxygen-containing compounds
- D06P1/65125—Compounds containing ester 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
- D06P5/00—Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
- D06P5/001—Special chemical aspects of printing textile materials
Definitions
- the invention relates to mixtures containing a glycerol-C6 ⁇ 22 fatty acid ester hydrate with a water content between 5 and 30 wt .-% and a monoglyceride content, based on glycerol fatty acid ester, between 50 and 95 wt .-%, a stabilizer and a carbohydrate, and the use of such a mixture as a thickener in textile printing pastes.
- Textile printing pastes contain thickening as an important component.
- Thickenings are those parts of the printing paste which, mainly composed of thickening agents, give an aqueous, dye and chemical-containing liquor a printable, pasty consistency.
- thickened portions are called stock thickenings (Ullmanns Encyklopadie der Technische Chemie, Volume 22, pages 583-587, Verlag Chemie Weinheim (1982)).
- the Brookfield viscosity of a stock thickening at 20 ° C is typically between 35,000 and 50,000 mPas.
- thickeners are powdery or granular substances or viscous concentrates with a pronounced swelling capacity in water. They form colloidal systems with water and can therefore increase the viscosity of dye and chemical solutions.
- the thickeners must be compatible with the dyes and chemicals intended for printing pastes, must not react with them and should not be stained themselves, if possible, or only evenly. Only a few thickeners, such as alginates, satisfactorily meet these requirements. However, due to the limited and fluctuating availability of this polysaccharide, there is a need for an equivalent replacement that is always available in sufficient quantities.
- glycerol soya oil fatty acid esters with a monoglyceride content of 34 and 40% by weight is known.
- These glycerin fatty acid esters are used as water-containing, pasty pressure thickeners in reactive and dispersion printing and are characterized by good washability, good color depth and the absence of hardening after washing the textile material.
- the print image obtained on the textile material with a paste containing glycerol soybean oil fatty acid ester has a poor contour level.
- the production of a printing paste containing glycerol fatty acid esters requires temperatures between 60 and 90 ° C.
- the use of mixtures of glycerol soya oil fatty acid esters with a monoglyceride content of up to 40% by weight and sodium alginate leads to a deterioration in the color depth.
- the object underlying the invention was to develop thickenings for textile printing pastes, which are always available in sufficient quantities and with those in printing pastes containing dyes and auxiliaries are compatible and do not react with them, have a high storage stability at temperatures between 18 and 25 ° C and can be processed to thickened stocks at temperatures between 18 and 25 ° C. Furthermore, the textile materials which are treated with a printing paste which contains such a thickening and can be produced at temperatures between 18 and 25 ° C. should have an excellent printed image and a very good depth of color.
- the high demands placed on the thickenings to be developed are met by mixtures containing a glycerol-C6 ⁇ 22 fatty acid ester hydrate with a water content of between 5 and 30% by weight and a monoglyceride content, based on glycerine fatty acid esters, of between 50 and 95% by weight. , a stabilizer and a carbohydrate in certain amounts.
- the object of the invention is accordingly a mixture that 30 - 85 parts by weight of a glycerol-C6 ⁇ 22-fatty acid ester hydrate with a water content between 5 and 30% by weight and a monoglyceride content, based on glycerol fatty acid esters, between 50 and 95% by weight, 5 - 35 parts by weight of a stabilizer and Contains 10 - 50 parts by weight of a carbohydrate.
- a mixture containing 40-85 parts by weight of a glycerol-C Gly22 fatty acid ester hydrate is preferred. 5 - 30 parts by weight of a stabilizer and Contains 10 - 40 parts by weight of a carbohydrate.
- Glycerol-C6 ⁇ 22-fatty acid ester hydrates with a water content between 5 and 30 wt .-% and a monoglyceride content, based on glycerol fatty acid esters, between 50 and 95 wt .-% are known compounds, for example according to EP-A-63 468 by mixing Glycerol fatty acid esters with a monoglyceride content between 50 and 95 wt .-% and water at temperatures between 20 ° C and the temperature of the melted glycerol ester are accessible.
- Suitable monoglyceride-containing glycerol fatty acid esters have iodine numbers ⁇ 10, preferably ⁇ 5 and fatty acid residues with preferably 12-22 carbon atoms, particularly preferably 16-22 carbon atoms.
- Glycerol fatty acid esters with a monoglyceride content between 50 and 95% by weight are produced by known methods by disproportional transesterification of fats and oils, for example beef tallow, hardened lard, hardened rapeseed oil, palm fat and / or coconut fat, with glycerin in the presence of a preferably alkaline catalyst at temperatures between 160 and 250 ° C or by reacting fatty acids, for example stearic and / or palmitic acid, with glycerol under acid catalysis (Ullmanns Encyklopadie der Technische Chemie, 4th edition, volume 22, pages 494-495, Verlag Chemie Weinheim 1982 ).
- a mixture according to the invention is preferably prepared in such a way that a stabilizer during the preparation of the monoglyceride-containing glycerol C6 ⁇ 22 fatty acid ester hydrate or directly the glycerol C6 ⁇ 22 fatty acid ester hydrate with a water content of between 5 and 30% by weight and a monoglyceride content , based on glycerol fatty acid esters, between 50 and 95 wt .-% is added at temperatures between 18 and 25 ° C. The mixture obtained is then mixed with a carbohydrate at temperatures between 18 and 25 ° C.
- Suitable stabilizers are C12 ⁇ 18 fatty acid esters of propylene glycol, such as propylene glycol monostearate, C12 ⁇ 18 fatty acid esters of sucrose, such as sucrose monostearate, and / or acetic acid and / or lactic acid esters of monoglycerides.
- Suitable carbohydrates in a mixture according to the invention are carbohydrates from the group of pectins, alkali alginates, alginic acid, starch ethers and esters, celluloses and carbohydrates from the group of exudates, for example gum ghatti, galactomannans, such as guar, locust bean gum, Tora and Cassia.
- the carbohydrates can be chemically modified. Under "chemically modified" changes to the carbohydrate structure, z. B. by oxidative or hydrolytic degradation, as well as changes to the carbohydrate structure while maintaining the polymer chain, for. B. understood by alkoxylation or carboxymethylation.
- Alkali alginates, carboxymethyl celluloses, pectins and / or optionally chemically modified galactomannans are preferably used as carbohydrates.
- a mixture according to the invention can contain 0-10 parts by weight of an additive from the group C8 ⁇ 22 fatty acids in the form of their alkali metal salts and / or C8 ⁇ 22 fatty alcohols.
- the additive is preferably added to the glycerol fatty acid ester hydrate together with a stabilizer directly or during its production.
- Another object of the invention is the use of a mixture that 30 - 85 parts by weight of a glycerol-C6 ⁇ 22-fatty acid ester hydrate with a water content between 5 and 30% by weight and a monoglyceride content, based on glycerol fatty acid esters, between 50 and 95% by weight, 5 - 35 parts by weight of a stabilizer and 10 - 50 parts by weight of a carbohydrate contains, as a thickening in textile printing pastes.
- a mixture to be used according to the invention is used as such or after dilution with water as a thickening stock, preferably as a thickening stock with dyes and auxiliaries necessary for textile printing, such as organic acids or alkalis, for example citric acid or sodium bicarbonate, sodium hydroxide solution and / or soda, oxidizing agents, for example Ludigol R , hydrotropic substances, for example urea, fixing accelerators and / or water softeners, processed to a printing paste at temperatures between 18 and 25 ° C. If the printing paste is used for surface printing, the Brookfield viscosity of the printing paste at 20 ° C. is preferably between 4,500 and 7,000 mPas.
- the printing paste When used for printing contours, the printing paste has a Brookfield viscosity at 20 ° C., preferably between 7,000 and 10,000 mPas.
- the stock thickening is produced in a manner known per se at a temperature between 18 and 25 ° C. by stirring a mixture according to the invention in water. The amount of water is chosen so that the Brookfield viscosity of the resulting thickening at 20 ° C after one hour is between 25,000 and 50,000 mPas.
- the printing pastes containing a mixture according to the invention as a thickening are applied to the textile material in a manner known per se using printing rollers or doctor blades.
- the dye is fixed washable on the textile material.
- the mixture to be used as a thickener according to the invention has a high storage stability, which means that such a thickening even after 12 months of storage at temperatures between 18 and and 25 ° C can be processed to a trunk thickening at room temperature.
- the printing pastes suitable for reactive, dispersion and acid printing and containing a mixture according to the invention as a thickener are distinguished by good washability and a high color yield.
- the print has a very good levelness and a very good contour level.
- the textile materials treated with a printing paste containing a mixture according to the invention as a thickening, such as cotton, viscose, rayon, wool, silk, polyamide, polyester and mixtures of cotton and polyester, have a soft feel.
- the viscosities were measured on a Brookfield RVT rotary viscometer at 20 ° C.
- parts means parts by weight.
- Propylene glycol monostearate was added to a glycerol fatty acid ester hydrate at 20 ° C. and the resulting mixture was then mixed with a carbohydrate at 20 ° C.
- propylene glycol monostearate was added to a glycerol fatty acid ester hydrate at 20 ° C.
- the compositions of the mixtures prepared are given in Table 1.
- the mixtures according to the invention were stirred into 1000 g of water at 20 ° C. using a high-speed stirrer.
- the amounts of the mixtures according to the invention used and the viscosities of the stock thickenings measured after one hour are summarized in Table 2.
Landscapes
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Coloring (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4120050A DE4120050A1 (de) | 1991-06-18 | 1991-06-18 | Verdickung fuer textildruckpasten |
| DE4120050 | 1991-06-18 | ||
| PCT/EP1992/001286 WO1992022700A1 (de) | 1991-06-18 | 1992-06-09 | Verdickung für textildruckpasten |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0592466A1 EP0592466A1 (de) | 1994-04-20 |
| EP0592466B1 true EP0592466B1 (de) | 1995-05-24 |
Family
ID=6434195
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP92911776A Expired - Lifetime EP0592466B1 (de) | 1991-06-18 | 1992-06-09 | Verdickung für textildruckpasten |
Country Status (6)
| Country | Link |
|---|---|
| EP (1) | EP0592466B1 (da) |
| AT (1) | ATE123086T1 (da) |
| DE (2) | DE4120050A1 (da) |
| DK (1) | DK0592466T3 (da) |
| ES (1) | ES2073927T3 (da) |
| WO (1) | WO1992022700A1 (da) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19717828A1 (de) * | 1997-04-26 | 1998-10-29 | Arnold Prof Dr Wartenberg | Verfahren zur Herstellung von Pigmenten aus Textilfarbstoffen und partikulierter Cellulose und Verwendung dieser Pigmente zur Herstellung von Farben, vorzugsweise von Künstlerfarben |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR582957A (fr) * | 1924-06-19 | 1925-01-03 | Procédé pour l'obtention des matières colorantes épaisses pour l'impression sur tissus | |
| JPS6047393B2 (ja) * | 1977-12-26 | 1985-10-21 | 花王株式会社 | 捺染用染色助剤 |
| AU8169082A (en) * | 1981-04-20 | 1982-10-28 | C.J. Patterson Co. | High solids monoglyceride hydrate |
-
1991
- 1991-06-18 DE DE4120050A patent/DE4120050A1/de not_active Withdrawn
-
1992
- 1992-06-09 AT AT92911776T patent/ATE123086T1/de not_active IP Right Cessation
- 1992-06-09 EP EP92911776A patent/EP0592466B1/de not_active Expired - Lifetime
- 1992-06-09 ES ES92911776T patent/ES2073927T3/es not_active Expired - Lifetime
- 1992-06-09 DK DK92911776.0T patent/DK0592466T3/da active
- 1992-06-09 DE DE59202362T patent/DE59202362D1/de not_active Expired - Fee Related
- 1992-06-09 WO PCT/EP1992/001286 patent/WO1992022700A1/de not_active Ceased
Also Published As
| Publication number | Publication date |
|---|---|
| DE4120050A1 (de) | 1992-12-24 |
| EP0592466A1 (de) | 1994-04-20 |
| DK0592466T3 (da) | 1995-10-16 |
| WO1992022700A1 (de) | 1992-12-23 |
| DE59202362D1 (de) | 1995-06-29 |
| ES2073927T3 (es) | 1995-08-16 |
| ATE123086T1 (de) | 1995-06-15 |
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