SE308290B - - Google Patents

Info

Publication number
SE308290B
SE308290B SE5764/65A SE576465A SE308290B SE 308290 B SE308290 B SE 308290B SE 5764/65 A SE5764/65 A SE 5764/65A SE 576465 A SE576465 A SE 576465A SE 308290 B SE308290 B SE 308290B
Authority
SE
Sweden
Prior art keywords
cross
linking
acid
condensation products
weight
Prior art date
Application number
SE5764/65A
Inventor
Bonin W Von
G Berndt
Original Assignee
Bayer Ag
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 Bayer Ag filed Critical Bayer Ag
Publication of SE308290B publication Critical patent/SE308290B/xx

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/21Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/263Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof
    • D06M15/267Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of unsaturated carboxylic acids; Salts or esters thereof of unsaturated carboxylic esters having amino or quaternary ammonium groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/0008Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/0025Crosslinking or vulcanising agents; including accelerators

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
  • Phenolic Resins Or Amino Resins (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Paints Or Removers (AREA)

Abstract

Solvent-resistant textile coatings are prepared by applying to a textile a solution of a copolymer in an organic solvent, which copolymer contains 90 to 99% by weight of an ester of acrylic acid with a monohydric alcohol having 2 to 4 carbon atoms, 0.5 to 5% by weight of 2-hydroxy-n-propyl methacrylate and 0.5 to 5% by weight of acrylic acid and/or methacrylic acid in polymerized form and which solution contains a cross-linking agent which is able to react with the hydroxyl and/or carboxylic acid groups of the polymer to form a cross-linked product, and then reacting the polymer and cross-linking agent with each other. The copolymers used are preferably prepared by copolymerizing the appropriate monomers in solution in an organic solvent below 85 DEG C. using as initiator azodiisobutyronitrile, benzoyl peroxide, lauroyl peroxide, dichlorobenzoyl peroxide, t-butyl perisobutyrate, dicyclohexyl peroxy-dicarbonate or mixtures thereof, e.g. azodiisobutyronitrile plus benzoyl peroxide. Suitable cross-linking agents include condensation products of formaldehyde with urea, thiourea, ethylene or propylene urea, aminotriazines, e.g. melamine, guanamines and ethers thereof; di- and poly-isocyanates; masked isocyanates; polymers or copolymers containing optionally etherified N - methylol - acrylamide groupings; and phenol-formaldehyde condensation products. Cross-linking is preferably completed, during or after evaporation of the solvent, at 30 DEG to 150 DEG C. When formaldehyde condensation products are used for cross-linking, a free acid such as oxalic or maleic acid may be included in the coating compositions. The compositions may be pigmented with organic pigments or inorganic pigments, e.g. kaolin, titanium dioxide, iron oxide, chromium oxide and silica.ALSO:Solvent-resistant textile coatings are prepared by applying to a textile a solution of a copolymer in an organic solvent, which copolymer contains 90 to 99% by weight of an ester of acrylic acid with a monohydric alcohol having 2 to 4 carbon atoms, 0.5 to 5% by weight of 2-hydroxy-n-propyl methacrylate and 0.5 to 5% by weight of acrylic acid and/or methacrylic acid in polymerized form and which solution contains a cross-linking agent which is able to react with the hydroxyl and/or carboxylic acid groups of the polymer to form a cross-linked product, and then reacting the polymer and cross-linking agent with each other. Suitable cross-linking agents include condensation products of formaldehyde with urea, thiourea, ethylene or propylene urea, amino-triazines, e.g. melamine, quanamines and ethers thereof; di- and poly-isocyanates; masked isocyanates; polymers or copolymers containing optionally etherified N-methylol-acrylamide groupings; and phenol-formaldehyde condensation products. Cross-linking is preferably completed, during or after evaporation of the solvent, at 30 to 150 DEG C., for example by passing the coated fabric through an optionally heated drying panel. When formaldehyde condensation products are used for cross-linking, a free acid such as oxalic acid or maleic acid may be included in the coating compositions. The compositions may be pigmented with organic pigments or inorganic pigments, e.g. kaolin, titanium dioxide, iron oxide, chromium oxide and silica. Textiles which may be treated include cotton, polyamide, polyester and polyester-cotton fabrics, which may be coated with the polymer solutions by means of a floating knife or rubber blanket coater. More than one coating may be applied, and cotton or blended cotton fabrics may be calendered before or after the first coat is applied. The treated textiles may subsequently be coated with hydrophobic agents, e.g. silicone-based impregnating agents, and those based on paraffin or perfluorocarboxylic acid/chromium complexes, or hydrophobic agents modified by masked isocyanates.
SE5764/65A 1964-05-19 1965-05-03 SE308290B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF42913A DE1247259B (en) 1964-05-19 1964-05-19 Process for the production of solvent-resistant textile coatings

Publications (1)

Publication Number Publication Date
SE308290B true SE308290B (en) 1969-02-10

Family

ID=7099317

Family Applications (1)

Application Number Title Priority Date Filing Date
SE5764/65A SE308290B (en) 1964-05-19 1965-05-03

Country Status (9)

Country Link
AT (1) AT252865B (en)
BE (1) BE662797A (en)
DE (1) DE1247259B (en)
DK (1) DK109637C (en)
ES (1) ES313006A1 (en)
FR (1) FR1433012A (en)
GB (1) GB1037367A (en)
NL (1) NL6506308A (en)
SE (1) SE308290B (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3327016C2 (en) * 1983-07-27 1986-09-25 Mechanische Leinenweberei Laichingen Dr. R. Woernle GmbH & Co, 7903 Laichingen Tarpaulin fabric and process for its manufacture
US4797176A (en) * 1987-08-10 1989-01-10 Desoto, Inc. Thermosetting size press composition
CN114438774A (en) * 2022-03-08 2022-05-06 罗莱生活科技股份有限公司 Self-cleaning cotton fiber and preparation method thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1124465B (en) * 1957-05-18 1962-03-01 Roehm & Haas Gmbh Process for synthetic resin finishing of textile structures

Also Published As

Publication number Publication date
DK109637C (en) 1968-05-27
ES313006A1 (en) 1966-02-01
FR1433012A (en) 1966-03-25
AT252865B (en) 1967-03-10
NL6506308A (en) 1965-11-22
DE1247259B (en) 1967-08-17
BE662797A (en) 1965-08-17
GB1037367A (en) 1966-07-27

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