EP0801165B1 - Prétraitement de textiles - Google Patents

Prétraitement de textiles Download PDF

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Publication number
EP0801165B1
EP0801165B1 EP97103334A EP97103334A EP0801165B1 EP 0801165 B1 EP0801165 B1 EP 0801165B1 EP 97103334 A EP97103334 A EP 97103334A EP 97103334 A EP97103334 A EP 97103334A EP 0801165 B1 EP0801165 B1 EP 0801165B1
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EP
European Patent Office
Prior art keywords
acid
weight
compositions according
glucose
acids
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EP97103334A
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German (de)
English (en)
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EP0801165A2 (fr
EP0801165A3 (fr
Inventor
Herbert Dr. Bachus
Andrea Fischer
Silvia Held-Beller
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CHT Germany GmbH
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CHT R Beitlich GmbH
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Classifications

    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L1/00—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods
    • D06L1/12—Dry-cleaning or washing fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods using aqueous solvents
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06L—DRY-CLEANING, WASHING OR BLEACHING FIBRES, FILAMENTS, THREADS, YARNS, FABRICS, FEATHERS OR MADE-UP FIBROUS GOODS; BLEACHING LEATHER OR FURS
    • D06L4/00—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs
    • D06L4/10—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen
    • D06L4/12—Bleaching fibres, filaments, threads, yarns, fabrics, feathers or made-up fibrous goods; Bleaching leather or furs using agents which develop oxygen combined with specific additives
    • D—TEXTILES; PAPER
    • D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/01—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural macromolecular compounds or derivatives thereof
    • D06M15/03—Polysaccharides or derivatives thereof

Definitions

  • the invention relates to compositions for the treatment of textile fiber material, a process for the preparation of the composition and the use thereof for finishing textile material.
  • the pretreatment of textile fiber material serves to remove unwanted accompanying substances.
  • Cellulosic substrates in particular contain a number of classes of compounds which may otherwise interfere with subsequent processing steps.
  • Surfactant formulations are used to remove fats in washing processes, complexing agents and dispersants are added to the treatment bath to remove unwanted hardness agents and heavy metals. If complexes of complexing agents are already acid-buffered formulations, their effect can be optimized by an improved acid solubility of alkaline earth or heavy metal salts.
  • complexing agents and dispersants non-biodegradable phosphonates and polyacrylates are used today, especially in commercial formulations.
  • Example 1 is a mixture of citric acid, sodium gluconate and small amounts of mineral acid, in Example a) 5% hydrochloric acid without concentration, described for acidic demineralization.
  • hydrochloric acid can act corrosive on textile machines and, if after pH change without deflation is subsequently bleached, neither Hardness is still hydrogen peroxide stabilized.
  • bleaching additionally produces 10 ml / l of a peroxide stabilizer and hardness dispersing agent, since neither citric acid nor gluconic acid in the pH range of 10 to 13 at high temperatures have sufficient dispersing action on insoluble hardening salts or stabilization to hydrogen peroxide.
  • Alkylpolyglycosides are described as auxiliaries in textile pretreatment.
  • the alkyl polyglycosides have a very high resistance to chemicals and temperatures, which is a mandatory requirement in pretreatment processes such as alkaline decoction, desizing, acid demineralization and bleaching.
  • pretreatment processes such as alkaline decoction, desizing, acid demineralization and bleaching.
  • Examples 2 and 3 it is described to add to the processes Alkaline boiling and bleaching commercial phosphonates to achieve a stabilizing effect of the peroxide and a dispersing action of hardness.
  • the disadvantage of such a procedure is seen in the use of two products and in the use of non-biodegradable phosphonates and polyacrylates.
  • DE-A-4344029 refers to copolymers of unsaturated carboxylic acids with other unsaturated compounds and their blends as sequestering agents, complexing agents and cobuilders in the detergents and cleaning agents industry and as auxiliaries in textile finishing.
  • a stabilizer may be added, which may be a phosphonic acid.
  • DE 43 44 357 A2 describes a liquid washing and cleaning agent which, in addition to nonionic surfactants, especially alkylpolyglycosides, a soil release polymer and organic builders, such as citric acid and water-soluble organic polymers as in DE 42 21 381 C1 , contains. This mixture is used as a washing and cleaning agent.
  • WO 93/13256 describes the use of lipases to remove hydrophobic fatty acid esters from textiles.
  • DE 43 12 010 A1 describes an enzymatic detergent containing as enzymatic components lipases, amylases, proteases and cellulases.
  • anionic, nonionic, cationic and / or amphoteric surfactant and up to 40% of inorganic or organic builders are contained.
  • EP 0 289 895 B1 By contrast, it was already possible in EP 0 289 895 B1 produce well biodegradable Zuckeracrylklarepolymere, wherein capable of enolate-capable saccharides are polymerized in alkaline solution with unsaturated carboxylic acids.
  • This class of substance is described as a complexing agent and co-builder in detergents and cleaners.
  • DE 43 44 029 A1 are special copolymers with saccharides capable of enolate formation, whose EP 0 289 895 B1 Blends described with other complexing agents and their textile applications described.
  • Water glass is a cheap and COD-free hydrogen peroxide stabilizer and alkali buffer. In the application, however, alkaline earth metal ions can lead to deposits on textile goods and machine parts which are no longer removable even with mineral acids.
  • EP 0 585 038 A1 mixtures of water glass are described with complexing agents, wherein the phosphonic acids, aminocarboxylic acids and polyacrylic acids contained therein are not based on renewable resources and are not biodegradable.
  • the polyacrylic acid Alcosperse ® 175 is described only in a narrow SiO 2 / Na 2 O weight ratio (LVN: weight ratio number) storage-stable miscible.
  • Glucose-free in the context of the present invention comprises low-glucose polymers having a glucose content of less than 1% by weight, based on the polymer.
  • a second embodiment of the invention relates to alkaline water glass-buffered compositions having a pH greater than 11.5 for the treatment of textile fiber material, in each case based on the composition 30 to 2 parts by weight (based on dry matter) of a polymer of acrylic acid and enolisierbaren monosaccharides, oligosaccharides and / or polysaccharides prepared in the alkaline pH range, 10 to 95 parts by weight of one or more additives of (i) 10 to 40% by weight (based on dry matter) of water glasses, (j) 0 to 20% by weight. % of a further complexing agent, in particular alkali metal and / or alkaline earth metal salts of gluconic acid or glucoheptonic acid, preferably sodium gluconate.
  • a further complexing agent in particular alkali metal and / or alkaline earth metal salts of gluconic acid or glucoheptonic acid, preferably sodium gluconate.
  • the compositions contain 20 to 80 parts by weight of water, based on 80 to 20 parts by weight of the polymers or of the mixtures of polymer and additive.
  • mixtures according to the invention also have the advantage that they can be diluted with water and thus low-viscosity and thus better pumpable mixtures can be represented.
  • biodegradable dispersing complexing agents can be synergistically supported by the addition of further biodegradable complexing agents such as, for example, sodium gluconate.
  • further biodegradable complexing agents such as, for example, sodium gluconate.
  • the polymers according to the invention which are known per se, despite their polyelectrolyte character, are well suited for formulation with surfactants and do not tend to cause the instability of the mixture even at low pH values. Furthermore, it has surprisingly been found that these blends are outstandingly suitable for the treatment of fiber material in various process stages of textile finishing, in particular pretreatment.
  • polymers of acrylic acid and enolisable monosaccharides, oligosaccharides and / or polysaccharides in the alkaline pH range from 7 to 10. These polymers are expressis verbis in EP 0 289 895 B1 described.
  • Saccharides capable of enolate formation do not necessarily have to be used directly as a raw material as such. These can also be prepared by acidic, alkaline or enzymatic processes before or during polymerization from oligosaccharides or polysaccharides.
  • EP 0 289 895 B1 brings the advantage of the properties the surfactant, wetting and penetration of the textiles with liquor and removing sizings, preparations and accompanying substances of all kinds, with the properties of a polyacrylate, dispersion of hardness and particle dirt, positive to connect while maintaining an environmentally friendly and biodegradable textile auxiliaries.
  • the enzymes are preferably selected from amylases, catalases, cellulases, lipases, pectinases, proteases and / or glucose oxidases.
  • compositions of the invention especially for use, require a greater or lesser amount of water. This depends in particular on the desired application of the compositions.
  • low molecular weight organic and inorganic acids are not particularly limited. Accordingly, it is particularly preferred to select the low molecular weight organic acids from low molecular weight mono- or polycarboxylic acids, in particular citric acid, tartaric acid, lactic acid, gluconic acid and / or glucoheptonic acid.
  • Phosphonic acids for the purposes of the present invention which are preferably used as additives, are preferably selected from HEDP, ATMP, DTPMP and / or HDTMP.
  • the inorganic acids are preferably selected from mineral acids, in particular hydrochloric acid and sulfuric acid, and furthermore amidosulfonic acid.
  • compositions for the treatment of textile fiber material usually contain surfactant-containing constituents.
  • surfactant-containing constituents Particularly preferred in The meaning of the present invention are anionic surfactants, nonionic surfactants and / or alkylpolyglycosides.
  • the anionic surfactants are preferably selected from linear or branched C 8 -C 20 -alkanesulfonates, alkanesulfates, alkanecarboxylates or alkanethercarboxylic acids and also alkylbenzenesulfonates and soaps (maximum 20% by weight).
  • Nonionic surfactants for the purposes of the present invention are in particular selected from linear or branched C 8 -C 20 fatty alcohol alkoxylates.
  • a further embodiment of the present invention consists in a process for the preparation of the above-defined glucose-free compositions, wherein the polymers of acrylic acid and saccharides containing glucose as raw material or reaction product are treated with glucose oxidase. As a result, a glucose-free or low-glucose product is obtained, which can be used particularly advantageously.
  • compositions according to the invention can be used according to processes known per se for refining textile material.
  • a special process of textile finishing are in particular the binding of polyvalent metal ions, the inhibition of water hardness, the dispersion of pigments and the use in washing, bleaching and dyeing liquors, especially for the aftertreatment of dyeings of textile materials mentioned.
  • the polymer was brown in color and clear. It had, as indicated, a viscosity of 40 mPas. There were 4% free glucose and 4% free fructose. The determination of the total elimination, which resulted from biological degradation and elimination by adsorption, generally resulted in values below 40% for several series of measurements according to OECD 302B.
  • acrylic acid was within 2 hours, hydrogen peroxide was metered for 30 minutes longer. The mixture was then stirred at 90 ° C for 30 minutes.
  • the polymer had a viscosity of 400 mPas and contained 1.2% free glucose.
  • compositions for textile finishing were compiled in analogy to the above instructions, the composition of which is shown in the table below.
  • the data in the following Table 1 are in each case for percentages by weight. ⁇ u> Table 1 ⁇ / u> Examples 2 3 4 5 6 7 Polymer according to Reference Example 2 15 15 15 Polymer according to Example 1 30 4 10 gluconic; 50% 10 10 10 10 Citric acid * H 2 O 5 5 5 5 Sulfuric acid conc.
  • compositions for textile finishing were compiled in analogy to the above instructions, the composition of which is shown in the table below.
  • the SiO 2 / Na 2 O weight ratio in Table 2 was adjusted by dissolving solid sodium hydroxide in 38 ° Be (GVZ 3.3) waterglass, but may also be made by mixing with commercially available lower GVZ waterglasses.
  • Example A 1 Acidic Demineralization - Discontinuous Process
  • Raw cotton fabric was treated for 30 minutes at 70 ° C and a liquor ratio of 1:10 with a liquor containing 5 g / l of the mixture according to Example 4. After treatment, the tissue was washed off warm and cold. The result was a textile material that was very well demineralized and could be used for all other treatments.
  • the total hardness on the fabric was reduced by 60%, the iron content by 50%, a treatment with 5 g / l of the polymer according to Reference Example 1 or Reference Example 2 alone reduced the total hardness by only 30% and the iron content by 20% and 30, respectively %.
  • Raw cotton fabric was treated as in Example A1 for 30 minutes at 70 ° C and a liquor ratio of 1:10 with a liquor containing 5 g / l of the mixture according to Example 4. Thereafter, 6 g / l sodium hydroxide solution was 50% without intermediate rinsing the liquor added 8 ml / l 35% hydrogen peroxide and 0.8 g / l of a high affinity fluorescent whitening agent (trade name "VA Tuboblanc ® fl.”). Thereafter, hot and cold rinsed.
  • a high affinity fluorescent whitening agent trade name "VA Tuboblanc ® fl.”
  • the product reached a base white of 81 and a fluorescence of 72 Berger units.
  • a liquor was padded containing 6 g / l of the mixture according to Example 2 and 4 g / l of a wetting agent (trade name "Subitol DM").
  • the liquor pickup was 100%
  • the liquor temperature was 60 ° C
  • the residence time was 30 minutes
  • the residence temperature was also 60 ° C.
  • the textile material was well demineralized and could be subjected to further treatment steps. That's how it became the total hardness on the fabric reduced by 50% and the iron content by 40%, which was not achievable with less acidic complexing agents alone.
  • the degree of desizing according to TEGEWA was 9.
  • a green cotton fabric was impregnated with the following liquor: 0.2 g / l Epsom salt, 7 ml / l of the combination product mentioned in Example 5, 30 g / l sodium hydroxide solution 50%, 10 ml / l water glass 38 ° Bé, 40 ml / l hydrogen peroxide 35 %.
  • the liquor pickup was 100%.
  • the product was left for 24 hours at room temperature according to the KKV method, then washed, rinsed and dried.
  • the basic white rose from 18 to 82 Berger units.
  • the same formulation with 10 ml / l mixture according to Example 9 instead of water glass 38 Be gave 83. Even without 7 ml / l product according to Example 5 here still 81 Berger units were reached.
  • An experiment according to Example D without water glass gave only 75 Berger units.
  • a raw cotton fabric with a base white of 18 Berger units was impregnated with the following liquor: 0.2 g / l of Epsom salt, 2 or 6 ml / l of the product mentioned in Table 3 below, 20 g / l of sodium hydroxide solution 50%, 40 ml / l of hydrogen peroxide 35%. The liquor pickup was 100%. Subsequently, the product was steamed at 102 ° C for 30 minutes, washed, rinsed and dried by pad steam method.
  • a raw cotton fabric was treated with a liquor containing 3 g / l of the combination product of Example 7 and 1 g / l of soda.
  • the liquor ratio was 1:10, the temperature was 95 ° C and the washing time was 30 minutes. Subsequently, hot and cold were washed out.
  • a raw cotton fabric was treated with a liquor containing 3 g / l of the combination product of Example 7 and 3 g / l of soda.
  • the liquor ratio was 1:20, the temperature 90 ° C and the washing time 30 minutes. Subsequently, hot and cold were washed out. The accompanying substances were removed completely and the textile corresponded in its properties the standard of a washing process.
  • Reference Example 1 showed no grease-removing effect and the fabric pattern remained hydrophobic.
  • Example F2 Washing process with standardized EMPA dirt cotton fabric
  • the test fabric was treated with a liquor containing 2 g / l of the combination product of Example 7 and 1 g / l of soda.
  • the liquor ratio was 1:40, the temperature 60 ° C and the washing time was 30 minutes. Subsequently, hot and cold were washed out.
  • the whiteness increased from 19 to 31 Berger units.
  • Raw cotton fabric was boiled at a liquor ratio of 1:10 in the presence of 5 g / l of the combination product according to Example 7 and 20 g / l NaOH 100% for 30 minutes at 98 ° C.
  • the whiteness of the goods rose from 22 to 39 Berger units.
  • Example I Testing for alkaline earth dispersing in the presence of iron ions
  • Example H It was tested as in Example H, but additionally added 25 ° dH calcium ions (calcium chloride) and 10 ° dH magnesium ions (from magnesium sulfate) of the test solution. Residue-free filters received the rating 1, coarse-grained residues such as when using water glass without dispersing agent received the grade 6. ⁇ u> Table 5: ⁇ / u> product grade Water glass GV 3.3 6 Water glass GV 1.6 6 Example 9 3 Example 10 2 Example 11 2 Comparative Example 3 6 Comparative Example 4 5

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  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Detergent Compositions (AREA)
  • Chemical Or Physical Treatment Of Fibers (AREA)

Claims (20)

  1. Compositions conçues pour le traitement de matériaux en fibres textiles, contenant, par rapport à la composition dans chaque cas, 99 à 1 parties en poids, en substance sèche, d'un produit de polymérisation à base d'acide acrylique et d'oses, oligosides et/ou polyosides énolisables, préparé en milieu à pH alcalin, et 1 à 99 parties en poids, en substance sèche,
    a) d'un adjuvant consistant en jusqu'à 40 % en poids d'acides libres organiques et minéraux de faible poids moléculaire, dont les protons acides, dans l'ensemble, sont neutralisés à moins de 50 %, et au moins un ou plusieurs adjuvants choisis parmi les suivants :
    b) 0 à 60 % en poids de tensio-actifs non-ioniques,
    c) 0 à 40% en poids d'alkyl-polyglycosides,
    d) 0 à 40 % en poids de tensio-actifs anioniques,
    e) 0 à 20 % en poids d'auxiliaires de désaération,
    f) 0 à 20 % en poids d'auxiliaires de démoussage,
    g) 0 à 70 % en poids de solvants organiques, excepté les hydrocarbures halogénés,
    h) et 0 à 10 % en poids d'enzymes,
    chacun de ces pourcentages étant rapporté à la quantité totale d'adjuvants.
  2. Compositions conformes à la revendication 1, caractérisées en ce qu'elles contiennent des produits de polymérisation d'acide acrylique et d'osides qui contenaient du glucose, en tant que produit de départ ou produit de réaction, et qui en ont été débarrassés.
  3. Compositions conformes à la revendication 1 ou 2, comprenant 2 à 30 parties en poids, en substance sèche, du produit de polymérisation et 70 à 98 parties en poids, en substances sèches, d'adjuvants.
  4. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce qu'on a remplacé 0 à 100 % des produits de polymérisation à base d'acide acrylique et d'osés, oligosides et/ou polyosides énolisables, préparés en milieu alcalin, par des produits de polymérisation d'acide acrylique et d'osides qui contenaient du glucose, en tant que produit de départ ou produit de réaction, et qui en ont été débarrassés.
  5. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que l'acide organique à faible poids moléculaire est choisi parmi les acides monocarboxyliques et polycarboxyliques, en particulier les acides citrique, tartrique, lactique, gluconique et/ou glucoheptonique.
  6. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que l'acide organique est choisi parmi les acides phosphoniques, en particulier les acides HEDP, ATMP, DTPMP et/ou HDTMP.
  7. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que l'acide inorganique est choisi parmi les acides minéraux, en particulier les acides chlorhydrique et sulfurique, et l'acide amidosulfonique.
  8. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que le constituant tensio-actif est choisi parmi les tensio-actifs anioniques, les tensio-actifs non-ioniques et/ou les alkyl-polyglycosides.
  9. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que le tensio-actif anionique est choisi parmi les alcane-sulfonates, alcane-sulfates, alcane-carboxylates et/ou acides alkyl-éther-carboxyliques en C8-20, à chaîne linéaire ou ramifiée, et les alkylbenzènesulfonates.
  10. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que le tensio-actif non-ionique est choisi parmi les produits d'alcoxylation d'alcools gras en C8-20 à chaîne linéaire ou ramifiée.
  11. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que l'alkyl-polyglycoside est choisi parmi les polyglycosides (n = 1 - 3) à groupe alkyle en C8-20 à chaîne linéaire ou ramifiée.
  12. Compositions conformes à l'une des revendications 1 à 3, caractérisées en ce que les enzymes sont choisies parmi les amylases, catalases, cellulases, lipases, pectinases, protéases et/ou glucose-oxydases.
  13. Compositions conformes à l'une des revendications 1 à 3, dont le pH est supérieur à 11,5, caractérisées en ce que les adjuvants sont aussi choisis parmi
    i) 10 à 40 % en poids, en substance sèche, de verre soluble,
    j) 0 à 20 % en poids d'un agent complexant,
    et de l'eau pour le complément à 100 % en poids.
  14. Compositions conformes à la revendication 13, caractérisées en ce que l'agent complexant est choisi parmi les sels de métaux alcalins et/ou alcalino-terreux de l'acide gluconique ou de l'acide glucoheptonique.
  15. Compositions conformes à l'une ou plusieurs des revendications 1 à 14, qui contiennent 20 à 80 parties en poids d'eau, pour 80 à 20 parties en poids des produits de polymérisation ou des mélanges de produit de polymérisation et d'adjuvant(s).
  16. Procédé de préparation des compositions conformes à l'une ou plusieurs des revendications 1 à 15, caractérisé en ce qu'on traite, avec une glueose-oxydase, des produits de polymérisation d'acide acrylique et d'osides qui contiennent du glucose, en tant que produit de départ ou produit de réaction.
  17. Procédé de préparation des compositions conformes à l'une ou plusieurs des revendications 1 à 15, dans lequel on prépare les osides énolisables in situ, avant et/ou pendant la réaction de polymérisation, à partir d'oligosides et/ou de polyosides, par hydrolyse.
  18. Procédé de préparation des compositions conformes à l'une ou plusieurs des revendications 1 à 15, dans lequel on prépare en milieu à pH de 7 à 10 les produits de polymérisation à base d'acide acrylique et d'oses, oligosides et/ou polyosides énolisables.
  19. Procédé d'ennoblissement de matériaux textiles, en particulier de matériaux en fibres cellulosiques, caractérisé en ce que l'on traite un tel matériau avec un mélange conforme à l'une ou plusieurs des revendications 1 à 15.
  20. Procédé conforme à la revendication 19, caractérisé en ce qu'on utilise 0,2 à 50 mL, et de préférence 1 à 20 mL, de composition par litre de bain de traitement.
EP97103334A 1996-04-13 1997-02-28 Prétraitement de textiles Expired - Lifetime EP0801165B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19614628 1996-04-13
DE19614628A DE19614628A1 (de) 1996-04-13 1996-04-13 Vorbehandlung von Textilien

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EP0801165A2 EP0801165A2 (fr) 1997-10-15
EP0801165A3 EP0801165A3 (fr) 1997-12-10
EP0801165B1 true EP0801165B1 (fr) 2007-08-29

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AT (1) ATE371764T1 (fr)
DE (2) DE19614628A1 (fr)

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CN109371667A (zh) * 2018-12-27 2019-02-22 福建省健为医疗用品有限公司 一种纯棉非织造布煮练试剂及漂煮方法和纯棉非织造布
CN109371667B (zh) * 2018-12-27 2021-05-14 福建省健为医疗用品有限公司 一种纯棉非织造布煮练试剂及漂煮方法和纯棉非织造布

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ATE371764T1 (de) 2007-09-15
EP0801165A2 (fr) 1997-10-15
DE19614628A1 (de) 1997-10-16
EP0801165A3 (fr) 1997-12-10

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