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
  • D06P1/52—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 synthetic macromolecular substances
  • D06P1/5207—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • D06P1/525—Polymers of unsaturated carboxylic acids or functional derivatives thereof
  • D06P1/5257—(Meth)acrylic acid
• • D—TEXTILES; PAPER
  • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
  • D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
  • D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
  • D06P3/58—Material containing hydroxyl groups
  • D06P3/60—Natural or regenerated cellulose
  • D06P3/66—Natural or regenerated cellulose using reactive dyes
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S8/00—Bleaching and dyeing; fluid treatment and chemical modification of textiles and fibers
  • Y10S8/916—Natural fiber dyeing
  • Y10S8/918—Cellulose textile

Definitions

• the present invention relates to a process for the block dyeing of web-shaped textiles which consist of or contain cellulose fibers, preferably of knitted tubular fabrics, with reactive dyes after a cold dwell process.
• the knitted tube is double when padding in the pinch joint of the foulard, which means that the pinch edges receive less liquor than the rest of the material in the double layer. If there is no effective compensation, the pinch edges are clearly marked as lighter vertical stripes. The coloring of the double layer (and the individual threads) is also impaired, which has the effect that the inside of the tube is colored lighter and more unevenly than the outside. The entire product image is often restless. Such goods are unsaleable, which has led to recommendations to use devices that enable edge displacement or air blowing. However, this has not always led to complete success.
• the block cold dwelling process of cellulose fiber tubular knitted fabrics with reactive dyes is known per se, e.g. B. from TEXTILBETRIEB, 7-8, 1976, pages 43-45.
• sheet-like textiles consisting of or containing cellulose fibers, preferably tubular knitted fabrics, are block-dyed with aqueous liquors while avoiding the difficulties mentioned in terms of levelness and dyeing after a cold dwell process at temperatures between about 5 ° C. and about 40 ° C.
• the liquor containing reactive dyes, fixing alkalis and wetting agents, characterized in that the liquor is additionally added to polymers or copolymers of an acrylic acid amide in an amount of 0.4 to 5 g / l in the form of aqueous solutions.
• the padded liquors behave favorably during the residence process on the material, likewise to the surprise of the person skilled in the art.
• the liquid on the docked goods tends to "sag" much less when lingering without rotation or when stacking (accumulation of the liquor in the lower part of the goods under the influence of gravity) than when one increases wanted to force the fleet up to values above 120% without reducing these products by reducing the roller pressure of the foulard.
• the increased fleet intake in turn has two surprising effects. First of all, as has already been shown, it leads to the unevenness which the textile material exhibits immediately after leaving the foulard by diffusion, ie during the dwell process the liquor with dye migrates to the places where Squeezing less of it. The second effect is that it is proportional to the fleets more absorption also increases the color depth.
• all sheet-like textiles consisting of or containing cellulose are suitable for the process according to the invention, ie woven or knitted fabrics, but preferably tubular knitted fabrics in which the levelness is particularly important.
• woven or knitted fabrics ie woven or knitted fabrics, but preferably tubular knitted fabrics in which the levelness is particularly important.
• tubular knitted fabrics in which the levelness is particularly important.
• the organic dyes known under this term come into consideration as reactive dyes.
• This class of dyes is referred to in the COLOR INDEX, 3rd edition 1971 as "reactive dyes". These are predominantly those dyes which contain at least one group which is reactive with polyhydroxyl fibers, a precursor therefor or a substituent which is reactive with the polyhydroxyl fiber.
• Particularly suitable as the basic body of the organic dyes are those from the series of the azo, anthraquinone and phthalocyanine dyes, it being possible for the azo and phthalocyanine dyes to be both metal-free and metal-containing.
• reactive groups and precursors which form such reactive groups are epoxy groups, the ethyleneimine group, the vinyl grouping in the vinylsulfone or in the acrylic acid residue, also called the ⁇ -sulfatoethylsulfone group, the ß-chloroethylsulfone group, the ß-phosphatoethylsulfone group, or the ⁇ -dialkylaminoethylsulfone group.
• derivatives of the tetrafluorocyclobutyl series e.g. B. the tetrafluorocyclobutyl acrylic acid in question.
• the reactive substituents in reactive dyes are those that are easily removable and leave an electrophilic residue. Examples of suitable substituents are 1 to 3 halogen atoms on the following ring systems: quinoxaline, triazine, pyrimidine, phthalazine, pyridazine and pyridazone. Dyes with several identical or different reactive groups can also be used.
• the padding liquors are first prepared without alkali by hot dissolving of the dye, the wetting agent and the intended polymeric acrylic acid amide product, the selected alkali is metered into the chassis by means of a metering device and the cellulose tubular fabric is applied padded in a foulard at 5 - 40 ° C, docked straight to the edge or plate and covered with foil.
• a mixture of water glass and sodium hydroxide solution has proven very useful as an alkali (cf. the known water glass process according to DE-PS 1 619 510 and DE-PS 1 619 513), since this prevents the exposed edges of the material from becoming brighter on the ball.
• the aftertreatment is carried out in the usual way by rinsing well and neutral soaping.
• a raw tubular knitted fabric made of cotton is padded on a special pad for jersey at a roller pressure of 1 bar / cm 2 and at room temperature with a liquor which contains 45 g of the reactive dye Reactive Black 5 (COLOR INDEX No. 20 505) 15 g in liters of the reactive dye of the formula 8 of a commercially available anionic wetting agent and 30 g of linear polyacrylic acid (padding auxiliary) in the form of its g 4.3 weight percent aqueous solution (molecular weight 1.4. 10 6).
• the fleet intake achieved here is 183%.
• the aftertreatment is carried out in the customary manner by thorough rinsing and hot neutral soaping with a nonionic detergent (0.5 g / l of the addition product of 8 mol of ethylene oxide and 1 mol of nonylphenol) at 90 ° C. for 20 minutes.
• a nonionic detergent 0.5 g / l of the addition product of 8 mol of ethylene oxide and 1 mol of nonylphenol
• the cotton jersey has an unusually rich black color that is level in every respect.
• Untreated cotton jersey (interlock) is padded on a special pad for knitted fabrics at a roller pressure of 1 bar / cm 2 and at 22 ° C with an aqueous liquor, which contains 21 g of the reactive dye Reactive Orange 16 (COLOR INDEX No. 17 757) , 40 g of the reactive dye of the formula
• the fleet intake achieved here is 171%.
• the dyeing is carried out as described above, but with omission of the acrylic acid amide copolymer, after padding and squeezing, a liquor absorption of only 104% is achieved at the same squeezing pressure.
• the coloring achieved here differs in the color depth of the value obtained with the addition of the acrylic acid amide copolymer by a value proportional to the various fleet recordings and is uneven (edge marking).
• Bleached terry toweling made of cotton is padded on a padder at a squeezing pressure of 1 bar / cm 2 and a temperature of 24 ° C. with an aqueous liquor which contains 22 g of the reactive dye of the formula in liters 25 g of the reactive dye of the formula 15 g of the reactive dye of the formula 8 g of a commercially available anionic wetting agent and 30 g of the copolymer (padding aid) made from acrylic acid amide and acrylamidopropionesulfonic acid in a weight ratio of 1: 0.1 (based on the acrylic acid amide) in the form of its 4.3% aqueous solution (molecular weight of the copolymer mentioned 1.90. 10 6 ).
• the required fixing alkali is by means of a D o - sierpumpe in the chassis metered in an amount of 1 20 cm 3 of a hanaels choir sodium silicate solution of specific gravity 1.41 (42 ° Be), in which the ratio Na 2 0: SiO 2 1: 2 , 5 is, and 20 cm 3 of caustic soda 32.5 percent by weight per liter of padding liquor.
• the fleet intake is 167%. After the blocked goods have been removed and covered, they are left to linger. The aftertreatment is carried out as described in Examples 1 and 2. A full, level bordo dyeing with very good coloration is obtained.
• An untreated tubular knitted fabric made from a mixed yarn of 50% cotton and 50% polyacrylonitrile fibers is padded on a pad at a roller pinch pressure of 1 bar / cm 2 at 22 ° C. with an aqueous liquor which contains 3.8 g of the liter Reactive Dye Reactive Black 5 (COLOR INDEX No. 20 505), 15.0 g of the reactive dye of the formula 8 of a commercially available wetting agent g (anionic) and 40 g of branched polyacrylic acid amide (padding auxiliary) in the form of its 4.3 percent by weight aqueous L ö- solution (molecular weight 1.4. 10 6).
• the required alkali is metered in via a metering device in an amount of 120 cm 3 of a commercially available water glass solution with a specific weight of 1.41 (42 ° Be) in which the ratio Na 2 O: Si0 2 is 1: 2.5 and 16 cm 3 32.5% sodium hydroxide solution per liter of padding liquor.
• the fleet intake achieved here is 113%.
• a full and level navy blue dyeing is obtained on the cellulose fiber portion of the knitted fabric without any edge marking. If the addition of the said polyacrylic acid amide is omitted and the rest of the procedure is as described above, a liquor absorption of only 78% and a lighter color corresponding to the lower liquor absorption are obtained with the same roller pressure.
• the fleet intake achieved here is 123%.
• the dyes are fixed within 6 hours by lingering at room temperature.
• the cotton portion is dyed in a full and perfectly level red shade.
• the ceiling of the polyester fiber portion is made on the winch by a carrier dyeing with dyes D ispersions- at boiling temperature following a Rinsing process.
• Raw raw cotton interlock knitted fabric in tubular form is padded on a tricot pad at a roller pressure of 1 bar / cm 2 and at room temperature with a liquor which contains 30 g of the reactive dye of the formula in liters 30 g of the reactive dye of the formula 7 g of a commercially available anionic wetting agent, 40 g of the padding aid described in Example 5 and 80 g of urea.
• the required fixing alkali is added to the chassis in a quantity of 8 cm 3 sodium hydroxide solution 32.5% and 10 g sodium carbonate anhydrous using a dosing device Liters of dye liquor dosed.
• the fleet intake is 171%.
• a tubular knitted fabric made of cotton is padded at a pressure of 1 bar / cm 2 and at room temperature with an aqueous liquor on a pad, which contains 60 g of the reactive dye of the formula in liters 6 g of a commercially available anionic wetting agent and 40 g of K described in Example 1 lotzosstoffs in the form of a 4.3% aqueous solution contains.
• the required fixing alkali is introduced into the chassis in an amount of 30 g sodium carbonate anhydrous per liter of padding liquor using a metering pump. siert.
• the fleet intake is 173%.
• the liquor absorption is then only 105% (with the same roller pressure).
• the color depth corresponds to the lower liquor absorption.

Landscapes

• Engineering & Computer Science (AREA)
• Textile Engineering (AREA)
• Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Coloring (AREA)

Priority Applications (1)

Applications Claiming Priority (2)

Publications (2)

Family

ID=6070266

Family Applications (1)

Country Status (11)

Cited By (9)

Families Citing this family (8)

Citations (8)

Family Cites Families (6)

• 1979
  • 1979-05-09 DE DE19792918607 patent/DE2918607A1/de not_active Withdrawn
• 1980
  • 1980-05-06 AT AT80102447T patent/ATE4467T1/de not_active IP Right Cessation
  • 1980-05-06 EP EP80102447A patent/EP0019188B1/fr not_active Expired
  • 1980-05-06 DE DE8080102447T patent/DE3064569D1/de not_active Expired
  • 1980-05-07 US US06/147,595 patent/US4304567A/en not_active Expired - Lifetime
  • 1980-05-07 AR AR280929A patent/AR222226A1/es active
  • 1980-05-08 AU AU58218/80A patent/AU533170B2/en not_active Expired
  • 1980-05-08 MX MX182243A patent/MX150868A/es unknown
  • 1980-05-08 CA CA000351473A patent/CA1140304A/fr not_active Expired
  • 1980-05-08 BR BR8002843A patent/BR8002843A/pt unknown
  • 1980-05-08 JP JP6004980A patent/JPS55152876A/ja active Granted
  • 1980-05-08 PT PT71206A patent/PT71206B/pt unknown

Patent Citations (8)

Also Published As

Similar Documents

Legal Events