GB983908A - Process for the treatment of leather - Google Patents

Process for the treatment of leather

Info

Publication number
GB983908A
GB983908A GB8763A GB8763A GB983908A GB 983908 A GB983908 A GB 983908A GB 8763 A GB8763 A GB 8763A GB 8763 A GB8763 A GB 8763A GB 983908 A GB983908 A GB 983908A
Authority
GB
United Kingdom
Prior art keywords
esters
carbon atoms
methyl
alcohols containing
butyl
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
Application number
GB8763A
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.)
Bayer AG
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 GB983908A publication Critical patent/GB983908A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C14SKINS; HIDES; PELTS; LEATHER
    • C14CCHEMICAL TREATMENT OF HIDES, SKINS OR LEATHER, e.g. TANNING, IMPREGNATING, FINISHING; APPARATUS THEREFOR; COMPOSITIONS FOR TANNING
    • C14C11/00Surface finishing of leather
    • C14C11/003Surface finishing of leather using macromolecular compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)
  • Paints Or Removers (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

Leather is finished by treatment with aqueous copolymer dispersions prepared in the absence of emulsifying agents and comprising, on a weight basis, at least 50% of esters of acrylic acid with alcohols containing 1 to 20 carbon atoms and/or esters of methacrylic acid with alcohols containing 4 to 20 carbon atoms, at least 10% of acrylamide and/or its b - or N substitution products, and optionally halogen-free compounds copolymerizable with the foregoing ester(s) and amide(s), e.g. acrylonitrile, acrylic acid, methacrylic acid and its esters with alcohols containing 1 to 3 carbon atoms, di- and semi-esters of maleic and fumaric acids, vinyl esters of carboxylic acids styrene, vinyl toluene, and conjugated dienes such as 1,3-butadiene and its 2-methyl and 2,3-dimethyl derivatives. Suitable esters of acrylic or methacrylic acid include methyl-, ethyl-, isopropyl, b -hydroxy propyl-, n-butyl, octyl, hexadecyl and octadecyl acrylates and butyl, dodecyl and octadecyl methacrylate. Examples of a - or N-substitution products of acrylamide include: methacrylamide, a -ethylacrylamide, a -chloroacrylamide, a -cyanoacrylamide, a -carboxyacrylamide, N-methylacrylamide, N-methylmethacrylamide, N,N-dimethylacrylamide, N,N-diethylacrylamide, N - tert. - butylacrylamide and N,N-di-n-butylmethacrylamide. The dispersions, which may be prepared by known methods, may incorporate protective colloids, thickeners, stabilizers or softeners, e.g. polyvinyl chloride, polyacrylamide, alkali metal polyacrylates, methyl cellulose, alginates, gums, gelatine, linseed oil, castor oil, turkey red oil, fatty acids, polyalkylene oxides; water-miscible organic liquids such as formamide, acetamide, alcohols, glycerol, glycols cyclic esters, e.g. dioxan and tetrahydrofuran; compounds which react with carboxylamide groups in the copolymers such as formaldehyde, glyoxal (with or without casein), and preliminary condensation products of formaldehyde with urea, dicyanodiamide or melamine.ALSO:Leather is finished by treatment with aqueous copolymer dispersions prepared in the absence of emulsifying agents and comprising, on a weight basis, at least 50% of esters of acrylic acid with alcohols containing 1-20 carbon atoms and/or esters of methacyrlic acid with alcohols containing 4-20 carbon atoms, at least 10% of acrylamide and/or its a - or N-substitution products, and optionally halogen-free compounds copolymerizable with the foregoing ester(s) and amide(s), e.g. acrylonitrile, acrylic acid, methacrylic acid and its esters with alcohols containing 1-3 carbon atoms, di- and semi-esters of maleic and fumaric acids, vinyl esters of carboxylic acids, styrene, vinyl toluene, and conjugated dienes such as 1,3-butadiene and its 2-methyl and 2,3-dimethyl derivatives. Suitable esters of acrylic or methacrylic acid include methyl-, ethyl-, isopropyl, b -hydroxy propyl, n-butyl, octyl, hexadecyl and octadecyl acrylates and butyl, dodecyl and octadecyl methacrylate. Examples of a - or N-substitution products of acrylamide include methacrylamide, a -ethylacrylamide, a -chloroacrylamide, a -cyanoacrylamide, a -carboxyacrylamide, N-methylacrylamide, N-methyl methacrylamide, N,N-dimethylacrylamide, N,N-diethylacrylamide, N-tert.-butylacrylamide, and N,N-di-n-butyl methacrylamide. The dispersion, which may be prepared by known methods, may incorporate protective colloids, thickeners, stabilizers or softeners, e.g. polyvinyl chloride, polyacrylamide, alkali metal polyacrylates, methyl cellulose, alginates, gums, gelatine, linseed oil, castor oil, Turkey Red oil, fatty acids, polyalkylene oxides; water-miscible organic liquids such as formamide, acetamide, alcohols, glycerol, glycols, cyclic esters, e.g. dioxan and tetrahydrofuran; compounds which react with carboxylamide groups in the copolymers such as formaldehyde, glyoxal (with or without casein), and preliminary condensation products of formaldehyde with urea, dicyanodiamide or melamine. The dispersions may be applied repeatedly to the leather, which may then be dried and pressed. A colour may then be applied, e.g. together with a casein solution or a wax or polymer emulsion.
GB8763A 1962-01-11 1963-01-01 Process for the treatment of leather Expired GB983908A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF35751A DE1235496B (en) 1962-01-11 1962-01-11 Process for treating leather

Publications (1)

Publication Number Publication Date
GB983908A true GB983908A (en) 1965-02-17

Family

ID=7096138

Family Applications (1)

Application Number Title Priority Date Filing Date
GB8763A Expired GB983908A (en) 1962-01-11 1963-01-01 Process for the treatment of leather

Country Status (3)

Country Link
CH (1) CH430031A (en)
DE (1) DE1235496B (en)
GB (1) GB983908A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5676707A (en) * 1994-04-15 1997-10-14 Canon Kabushiki Kaisha Leather coloring process comprising jetting ink onto a treated leather

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5348807A (en) * 1991-02-05 1994-09-20 Rohm And Haas Company Polymeric retan fatliquor for low fogging upholstery leather

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB651420A (en) * 1948-02-16 1951-04-04 Vinyl Products Ltd Improvements in or relating to emulsions of copolymers of methyl methacrylate and tothe use of such emulsions
GB785113A (en) * 1953-09-22 1957-10-23 United Gas Industries Ltd Improvements in and relating to the treatment of leather diaphragms and the like

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5676707A (en) * 1994-04-15 1997-10-14 Canon Kabushiki Kaisha Leather coloring process comprising jetting ink onto a treated leather

Also Published As

Publication number Publication date
DE1235496B (en) 1967-03-02
CH430031A (en) 1967-02-15

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