EP0014890A2 - Procédé d'impression de matières textiles volumineuses - Google Patents

Procédé d'impression de matières textiles volumineuses Download PDF

Info

Publication number
EP0014890A2
EP0014890A2 EP80100558A EP80100558A EP0014890A2 EP 0014890 A2 EP0014890 A2 EP 0014890A2 EP 80100558 A EP80100558 A EP 80100558A EP 80100558 A EP80100558 A EP 80100558A EP 0014890 A2 EP0014890 A2 EP 0014890A2
Authority
EP
European Patent Office
Prior art keywords
printing
electrolyte
printed
dye
voluminous
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.)
Withdrawn
Application number
EP80100558A
Other languages
German (de)
English (en)
Other versions
EP0014890A3 (fr
Inventor
Karl Tropschuh
Wolfgang Dr. Schwindt
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.)
BASF SE
Original Assignee
BASF SE
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.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP0014890A2 publication Critical patent/EP0014890A2/fr
Publication of EP0014890A3 publication Critical patent/EP0014890A3/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P3/00Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
    • D06P3/02Material containing basic nitrogen
    • D06P3/04Material containing basic nitrogen containing amide groups
    • D06P3/06Material containing basic nitrogen containing amide groups using acid dyes
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P1/00General 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
    • D06P1/44General 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
    • D06P1/52General 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 synthetic macromolecular substances
    • D06P1/5207Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
    • D06P1/525Polymers of unsaturated carboxylic acids or functional derivatives thereof
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06PDYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
    • D06P5/00Other features in dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form
    • D06P5/001Special chemical aspects of printing textile materials

Definitions

  • Printing pastes are usually used for printing on textile materials, the viscosity of which is adjusted with the aid of a thickener.
  • the printing pastes contain either fiber-affine dyes, which dye the material to be printed in each case, or a pigment dye and additionally a binder which firmly bonds the pigments to the textile material. After the printing process, the dyes are fixed in all cases, and the printed material is washed out and dried. In order, for example, to print woolen ridges, it is necessary to feed the ridges in a spread form to the printing device so that an acceptable through-print is achieved. Nevertheless, the achievable printing leaves something to be desired.
  • the space dyeing (multicolor dyeing) of nylon carpet fibers is currently in first place after the "Knit deknit" - (knitted wind-up) procedural - ren worked.
  • yarns made of textured polyamide carpet fibers are knitted into tubes or ribbons on circular or flat knitting machines and these are first impregnated with the base color using a padder and then printed without intermediate drying.
  • Printing is primarily based on the Rouleau printing process; the pre-padded tapes can also be printed using the Vigoureux printing process. After the paint has been applied, the dyes are fixed to the goods by steaming, washed out in special washing baths and dried. After pulling on the knitting tapes or knitting tubes, the yarns are primarily processed into tufted carpets.
  • Foam formation is extremely damaging, especially on the printing units, because the foam gets into the engravings of the printing rollers instead of the printing pastes and thus causes lighter prints or a very poor printing, since it contains significantly less dye per unit volume than the foam-free printing paste.
  • the foaming can be largely suppressed by adding suitable foam dampers, but better prints and higher processing speeds are also desired here as a result of increased quality requirements for the printed material.
  • the invention has for its object to provide a method for printing voluminous textile materials with printing pastes, in which you get good prints with sharp outlines and thus also achieves an increase in space-time yield with difficult to print materials.
  • Voluminous textile materials within the meaning of the invention are to be understood as ridges, non-woven fabrics, yarn sheets, knitted hoses, terry towels and carpets.
  • the textile materials can consist of natural and / or synthetic fibers or threads or of mixtures of fibers or threads. The process is of particular importance when printing woolen rovings, polyamide carpet yarns in the form of knitted tubes or yarn sheets as well as polyamide tufted carpets.
  • the printing pastes contain either a pigment dye and additionally a binder or fiber-affine dyes which dye the material to be printed in each case, e.g. acid dyes or metal complex dyes containing sulfo groups are used when printing woolen rovings or polyamide carpet yarns, and dispersion dyes are used when printing polyester materials.
  • the printing pastes can contain the usual additives, such as pH regulators, emulsifiers, dispersants, leveling agents, fixing accelerators, foam suppressants, oxidizing agents, reducing agents and agents for high textile finishing. In the latter case, the material is printed and finished at the same time.
  • the textile material is first applied to the entire surface using the above (a) to (c) g treated flat preparations, in such a way that the voluminous textile material is completely impregnated.
  • the voluminous textile material is prepared with a synthetic thickener based on high molecular weight polycarboxylic acids. Synthetic thickeners of this type are commercially available. For example, homopolymers and copolymers of ethylenically unsaturated carboxylic acids with 3 to 5 carbon atoms are suitable.
  • polymers of acrylic acid, methacrylic acid, maleic acid, maleic anhydride, fumaric acid and itaconic acid and copolymers of the carboxylic acids mentioned with one another for example copolymers of acrylic acid with methacrylic acid in a molar ratio of 1: 1 or in a different molar ratio, and copolymers of the carboxylic acids mentioned with other copolymerizable ethylenically unsaturated monomers, such as vinyl esters, acrylic acid esters, methacrylic acid esters, ethylene, styrene, vinyl ethers and amides of ethylenically unsaturated C 3 - to C 5 -carboxylic acids.
  • the copolymers contain at least 40, preferably 75 to 99.5% by weight of an ethylenically unsaturated carboxylic acid.
  • the thickeners are high molecular weight polymers with a molecular weight of more than 200,000 and preferably more than one million. Particularly high molecular weight synthetic thickeners are obtained if the polymerization of the ethylenically unsaturated carboxylic acids is carried out in the presence of monomers which contain two ethylenically unsaturated double bonds. Examples of such monomers are butadiene, divinylbenzene, butanediol diacrylate, divinyldioxane and diallyl phthalate. These monomers make up approximately 0.05 to 5% by weight of the high molecular weight copolymers.
  • bases are, for example, sodium hydroxide solution, potassium hydroxide solution, ammonia and amines, e.g. Triethylamine, butylamine, ethanolamine, triethanolamine, hexamethylenediamine, ethylenediamine, diethylenetriamine, triethylenetetramine and mixtures of ammonia and morpholine or hexamethylenediamine and morpholine.
  • aqueous solutions of the synthetic thickeners are obtained which, at a concentration of 0.25% by weight, a temperature of 25 ° C. and a pH of 7 in accordance with DIN 53 211, measured with a Ford beaker and an outlet nozzle with a diameter of 4 mm, give an outlet time of 30 to 60 s.
  • the neutralized synthetic thickeners in preparations (a) to (c) have a pH in the range from 10 to 6, preferably 9 to 7.
  • the voluminous textile material is prepared by passing it through a bath that contains a dye in addition to a synthetic thickener based on high molecular weight polycarboxylic acids.
  • a dye in addition to a synthetic thickener based on high molecular weight polycarboxylic acids.
  • the usual aids for block staining may also be present in the bathroom, e.g. pH regulators, buffer substances and anti-migration agents.
  • the dyes used for this are used in an electrolyte-free or low-electrolyte form.
  • Preparations (a) and (b) are used in an electrolyte-free or low-electrolyte setting because electrolytes lower the viscosity of the preparation solutions thickened with synthetic thickeners.
  • the voluminous textile material is prepared with an electrolyte-containing padding liquor or an electrolyte-containing printing paste.
  • These padding liquors or printing pastes preferably contain a natural thickener and, in addition to at least one dye, one or more electrolytes, such as organic acids, alkali metal and ammonium salts or water-soluble alkaline earth metal salts of organic or inorganic acids, carboxylic acids and anionic dispersants or their alkali metal salts.
  • electrolytes such as organic acids, alkali metal and ammonium salts or water-soluble alkaline earth metal salts of organic or inorganic acids, carboxylic acids and anionic dispersants or their alkali metal salts.
  • Synthetic thickeners containing carboxyl groups can also be used here, but because of the drop in viscosity of the liquor after the addition of electrolytes, additional thickeners must then be used to increase the viscosity of the liquor.
  • the synthetic thickeners mentioned are sensitive to electrolytes. When Glauber's salt or table salt is added, the viscosity of the thickener solution drops noticeably.
  • the thickener solution can optionally contain a dye to color the textile material. Because of the sensitivity of the synthetic thickeners to electrolytes, low-electrolyte dye solutions or dye formulations are preferably used for this.
  • Process steps (a) to (c) can be carried out, for example, in a padder, as well as by slapping or knife coating.
  • the fleet intake is 60 to 150%.
  • the already neutralized or partially neutralized Ver is used thickener because this saves one operation.
  • the voluminous textile materials in preparations (a), (b) or (c), based on the dry material are loaded with 0.05 to 1% by weight, preferably 0.1 to 0.5% by weight, of solids.
  • the voluminous textile materials prepared in accordance with (a) or (b) are then, optionally after intermediate drying, printed with electrolyte-containing printing pastes which preferably contain an electrolyte-insensitive thickener.
  • the printing paste can be applied using the customary printing methods in gravure, film or spray printing.
  • Electrolyte-insensitive thickeners are, for example, tragacanth, starch ether, core meal ether, alginates, guar meal or locust bean meal ether. These substances are primarily natural products. If electrolyte-sensitive thickeners are used, the printing paste must be thickened after the addition of the electrolyte, which causes the viscosity of the printing paste to drop, by adding a thickening agent again. 1000 g of the finished printing paste contain 2 to 20, preferably 5 to 10 g of the electrolyte-insensitive thickeners.
  • the electrolyte content of the printing paste can vary within a wide range and is between 1 and 20, preferably 5 to 15 g, based on 1000 g of the finished printing paste.
  • the electrolyte content is adjusted either by adding certain substances, such as organic acids, alkali salts of organic or inorganic acids, or by anionic dispersants. Because the commercially available Dyes partly contain alkali salts of anionic dispersants, in many cases a certain electrolyte content is already set in the printing paste by adding a certain commercially available dye. In some cases, this electrolyte content is sufficient to achieve the advantages of the method according to the invention.
  • organic acids, alkali metal or ammonium salts of organic or inorganic acids e.g. using sodium acetate, sodium formate, ammonium chloride, common salt, Glauber's salt, water-soluble alkaline earth metal salts of organic or inorganic acids and sodium salts of anionic dispersants can be obtained, for example, in the condensation of phenols or naphthols with formaldehyde and sodium bisulfite.
  • Low-molecular-weight polymers of acrylic acid or methacrylic acid in partially neutralized or completely neutralized form can be used as anionic dispersants, which also behave like an electrolyte in the printing paste.
  • the polymeric dispersants have molecular weights in the range from about 500 to 10,000.
  • a condition for the use of electrolytes or anionic dispersants in the printing pastes is, of course, that these additives with the other printing paste components do not result in any precipitation. However, this question can by means of a preliminary test easily ge - be clarified.
  • Organic acids for example formic acid, acetic acid, propionic acid, glutaric acid, adipic acid, succinic acid, p-toluenesulfonic acid, sulfosuccinic acid, benzenesulfonic acid and citric acid, are of particular importance as electrolytes.
  • the pH of the electrolyte-containing printing pastes is preferably set to values ⁇ 5.5.
  • the textile materials are printed using the known printing processes. Be particularly highlighted of these printing processes, the Rouleau printing process, the Vigoureux printing and the spray printing process.
  • a wool comb was passed in an undrawn form in 35 bands side by side and 6 cm thick through an aqueous bath containing 0.5 g per liter of a solution neutralized with sodium hydroxide solution and with 0.6% divinyldioxane based on the polymer, crosslinked polyacrylic acid and 0.5 g of a copolymer neutralized with sodium hydroxide solution consisting of 50 mol.% Maleic acid and 50 mol.% Vinyl isobutyl ether, which was crosslinked with 0.8% hexamethylpiperazine, contained on the padder on 100% liquor absorption, based on the weight of the textile product, squeezed off and then printed with an electrolyte-containing printing paste of the following composition using the gravure printing process without intermediate drying:
  • a wool sliver which consisted of 32 ribbons and had a thickness of 6 cm, was passed through an aqueous bath in undrawn form, containing 2 g of a polyacrylic acid neutralized with sodium hydroxide solution and crosslinked with 0.5 divinylbenzene per liter, 2 g of one with ammonia neutralized copolymers of maleic acid and vinyl ethyl ether in a molar ratio of 1: 1, crosslinked with 0.6% hexamethylpiperazine and 10 g of a 25% liquid setting of dye II in equal parts of dimethylformamide and butyl diglycol. It was squeezed to a liquor intake of 100 based on the weight of the textile goods.
  • the goods were then printed without intermediate drying using an electrolyte-containing printing paste of the following composition using the gravure printing process: After printing, the goods are steamed for 30 minutes at 102 ° C in saturated steam, then washed and dried as usual. You get multi-colored effects with good standing and printing.
  • a knitted tube made of polyamide carpet yarns was passed through a bath on a space dye system which contained 2 g of a copolymer of 50 mol% maleic acid and 50 mol% ethylene neutralized with sodium hydroxide solution in liter water, which was mixed with 0.8 mol. % Diallyl phthalate was crosslinked, and 10 g of a low-electrolyte 20% liquid formulation of the dye CI 15 675 contained in equal parts dimethylformamide and butyl diglycol, squeezed on the pad to about 100% liquor absorption, based on the weight of the textile goods, and then without intermediate drying with a electrolytic printing paste of the following composition printed by gravure printing:
  • the voluminous textile material is steamed for 5 minutes at approx. 102 ° C with saturated steam, then washed out and dried as usual.
  • a knitted tube is obtained which, in addition to the sharp state of the prints, has an excellent through-print which is important for later patterning and is free from gray veils.
  • a polyamide tufted carpet was pre-padded with a liquor containing 0.5 g of a high molecular weight polyacrylic acid neutralized with sodium hydroxide solution and crosslinked with 0.8% divinylbenzene in the liter of water, squeezed to a liquor absorption of 80% and then thickened slightly without intermediate drying electrolyte-containing dye liquor of the following composition applied according to the pattern by the spray printing process:
  • the pH of the liquor was adjusted to 4 using acetic acid.
  • the goods were then steamed for 8 minutes at approx. 102 ° C. with saturated steam, washed out and dried.
  • a printed carpet product was obtained which was characterized by sharp contours and good through-printing down to the bottom of the fiber loops.
  • a knitted tube made of polyamide carpet yarn was passed through a bath of the following composition on a space dye system:
  • the goods were then squeezed off on the paddle to about 80% liquor absorption, based on the weight of the textile goods, and then printed without the intermediate drying using a printing paste of the following composition using the gravure printing process:
  • the goods were steamed for 6 minutes at approx. 102 ° C with saturated steam, then washed out and dried as usual.
  • a printed knitted tube was obtained which, in addition to the sharp state of the prints, had an excellent through-print which was important for later patterning, which is particularly important in the case of double-knitted polyamide carpet yarns.
  • Example 5 is repeated with the exception that no dye is used in the printing paste. This gives so-called “negative prints”, which are characterized by lightening in the printed areas.
  • a polyamide tufted carpet fabric was pre-padded with a fleet of the following composition:
  • the fleet can also be poured onto the goods using a paint applicator.

Landscapes

  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Coloring (AREA)
EP80100558A 1979-02-05 1980-02-04 Procédé d'impression de matières textiles volumineuses Withdrawn EP0014890A3 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE2904223 1979-02-05
DE19792904223 DE2904223A1 (de) 1979-02-05 1979-02-05 Verfahren zum bedrucken von voluminoesen textilen materialien

Publications (2)

Publication Number Publication Date
EP0014890A2 true EP0014890A2 (fr) 1980-09-03
EP0014890A3 EP0014890A3 (fr) 1981-01-07

Family

ID=6062158

Family Applications (1)

Application Number Title Priority Date Filing Date
EP80100558A Withdrawn EP0014890A3 (fr) 1979-02-05 1980-02-04 Procédé d'impression de matières textiles volumineuses

Country Status (3)

Country Link
EP (1) EP0014890A3 (fr)
DE (1) DE2904223A1 (fr)
ES (1) ES488251A1 (fr)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0054191A3 (en) * 1980-12-12 1982-11-03 Allied Corporation Wetting solution for use in continuous dyeing of polyamide fabric
EP1072719A1 (fr) * 1999-07-23 2001-01-31 Dainichiseika Color & Chemicals Mfg. Co. Ltd. Procédé de production d'articles imprimés

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2304104A1 (de) * 1972-06-28 1974-01-10 Zimmer Johannes Verfahren zur herstellung eines tiefen oder durchgehenden druckmusters bei dickem textilgut und einrichtung zu dessen durchfuehrung
DE2410155B2 (de) * 1974-03-02 1976-11-11 Schaumdaempfer beim space-dyeing- verfahren
DE2641159A1 (de) * 1975-09-23 1977-03-31 Sandoz Ag Verfahren zum faerben und bedrucken von textilien
DE2801577A1 (de) * 1978-01-14 1979-07-19 Sandoz Ag Textilfaerbeverfahren

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0054191A3 (en) * 1980-12-12 1982-11-03 Allied Corporation Wetting solution for use in continuous dyeing of polyamide fabric
EP1072719A1 (fr) * 1999-07-23 2001-01-31 Dainichiseika Color & Chemicals Mfg. Co. Ltd. Procédé de production d'articles imprimés
US6673394B1 (en) 1999-07-23 2004-01-06 Dainichiseika Color & Chemicals Mfg. Co., Ltd. Process for producing printed articles

Also Published As

Publication number Publication date
ES488251A1 (es) 1980-09-16
DE2904223A1 (de) 1980-08-14
EP0014890A3 (fr) 1981-01-07

Similar Documents

Publication Publication Date Title
DE2700153A1 (de) Verfahren zum faerben von textilmaterial und vorrichtung zur durchfuehrung des verfahrens
DE2214377B2 (de) Verfahren zum kontinuierlichen Färben von flächigem Textilgut
DE3879276T2 (de) Verfahren zum musterfaerben von textilmaterialien.
DE2206983B2 (de) Mittel und Verfahren zum gleichzeitigen antistatischen und schmutzabweisenden Ausrüsten von Fasermateralien
EP0029804B1 (fr) Procédé d'impression ou de teinture par foulardage de matières textiles en fibres cellulosiques ou en mélanges de ces fibres avec des fibres synthétiques, pâtes d'impression ou bains de foulardage pour la mise en oeuvre du procédé
DE2722083A1 (de) Verfahren zur behandlung eines poroesen substrates
DE2947827A1 (de) Cellulosefasern mit verbesserter einfaerbungseigenschaft, verfahren zur herstellung einer solchen faser und verfahren zu aetzdruckbehandlung
EP0014890A2 (fr) Procédé d'impression de matières textiles volumineuses
DE2507905A1 (de) Faerbezusammensetzung und deren verwendung
DE10126244B4 (de) Verfahren zur Herstellung eines cellulosischen Faser- oder Flächengebildes sowie die Verwendung des danach erhaltenen Gewebes, Gestricks oder Vliesstoffs
EP0418214A2 (fr) Procédé de teinture avec des colorants réactifs de surfaces textiles
DE2214409A1 (de) Verfahren zum gleichmaessigen, frostingeffectfreien kontinuierlichen faerben von teppichware aus polyamidfasern mit traegermaterial aus hydrophoben fasern
DE2938766A1 (de) Verfahren zum bedrucken von textilmaterial
DE2120692A1 (de) Verfahren zur Herstellung gesprenkelt gefärbter Textilstoffe
DE2406343A1 (de) Ausruestungsmaterial und dessen verwendung
DE3111277A1 (de) Verfahren zum faerben von polyamidtextilmaterialien, insbesondere zum schnellfaerben von polyamiden
DE1469473A1 (de) Verfahren zur Verbesserung der Aufnahmefaehigkeit bei Cellulosefasern
US3979176A (en) Process for the continuous level processing of poly-acrylonitrile in the hydrated condition
DE899638C (de) Verfahren zum Appretieren von Fasermaterial
AT522744B1 (de) Verfahren zum Bedrucken wenigstens eines textilen Substrats
DE2722082A1 (de) Schaumpraeparat zur behandlung eines poroesen substrates
DE3109373A1 (de) Verfahren zum auftragen von flotte in verschaeumter form auf faseriges material aufweisende ware, wie stueckware oder warenbahnen
DE3632795C2 (fr)
DE2410155A1 (de) Propoxylierte oder butoxylierte verzweigte fettalkohole
DE2133541C3 (de) Verfahren zur Erzeugung vielfarbiger, unregelmäßiger Drucke auf einer Textilbahn

Legal Events

Date Code Title Description
AK Designated contracting states

Designated state(s): AT BE CH DE FR GB IT LU NL SE

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Designated state(s): AT CH DE FR GB IT NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Designated state(s): AT CH DE FR GB IT NL

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN WITHDRAWN

18W Application withdrawn

Withdrawal date: 19810204

RIN1 Information on inventor provided before grant (corrected)

Inventor name: TROPSCHUH, KARL

Inventor name: SCHWINDT, WOLFGANG, DR.