GB960499A - Finishing of leather - Google Patents

Finishing of leather

Info

Publication number
GB960499A
GB960499A GB842962A GB842962A GB960499A GB 960499 A GB960499 A GB 960499A GB 842962 A GB842962 A GB 842962A GB 842962 A GB842962 A GB 842962A GB 960499 A GB960499 A GB 960499A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
formula
radicals
olefinically unsaturated
methacrylamide
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
GB842962A
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 GB960499A publication Critical patent/GB960499A/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

Abstract

Leather is dressed with a dispersion or solution of a copolymer prepared from olefinically unsaturated compounds which include between 0,5 to 25% of monomers of the general formula: <FORM:0960499/B1-B2/1> in which formulae R1 and R2, which may be the same or different, represent hydrogen atoms, or alkyl radicals containing from 1 to 6 carbon atoms, or aryl radicals, R3 represents a saturated or unsaturated aliphatic hydrocarbon radical containing from 1 to 8 carbon atoms, R4 and R5, which may be the same or different, represent hydrogen atoms, alkyl radicals containing from 1 to 6 carbon atoms or aryl radicals, and R6 and R7, which may be the same or different, represent alkyl radicals preferably containing 1 to 5 carbon atoms, cycloalkyl radicals, aralkyl radicals, or radicals which together with the adjacent nitrogen atom form a heterocyclic ring system. The olefinically unsaturated monomers include 2-10% of monomers of formula I and/or formula II. As compounds of general formula I the reaction product of acryl and methacryl amides with aliphatic alcohols of 1-8 carbon atoms are employed. As compounds of formula II those prepared from (a) formaldehyde, (b) acryl or methacrylamide, and (c) aliphatic secondary amines, the alkyl groups present containing up to 5 carbon atoms, are employed. A copolymer may be used in which the olefinically unsaturated monomers include from 1 to 10% by weight of acrylic acid, methacrylic acid, acrylamide and/or methacrylamide. A copolymer may be used in which the olefinically unsaturated monomers comprise more than 40% of acrylic and/or methacrylic acid esters, 1-10% of acrylic acid and/or methacrylc acid, and 0,5-20% of monomers of the formulae I and/or II. The copolmers are prepared by copolymerization in the presence of anionic, cationic and/or non-ionic emulsifiers. The compound of formula I employed may be methacrylamide methylol methyl ether and this is used in an amount between 2 and 10%. The compound of formula II may be the reaction product of methacrylamide, formaldehyde and dimethylamine or morpholine. Examples of copolymerizable olefinically unsaturated monomers are given. The emulsion polymerization may be activated by addition of organic and inorganic per-compounds, e.g. redox catalysts, or radical forming substance. The coating may contain thickeners, plasticizers, emulsifiers, matting agents, dyestuffs, polyamide dispersions, urea- and melamine-formaldehyde resins, and colloids, e.g. polyvinyl alcohol, partially saponified polyvinyl esters, cellulose ethers and derivatives thereof. Specifications 792,874 and 898,967 are referred to.
GB842962A 1961-05-30 1962-03-05 Finishing of leather Expired GB960499A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEF34052A DE1182769B (en) 1961-05-30 1961-05-30 Process for dressing leather

Publications (1)

Publication Number Publication Date
GB960499A true GB960499A (en) 1964-06-10

Family

ID=7095390

Family Applications (1)

Application Number Title Priority Date Filing Date
GB842962A Expired GB960499A (en) 1961-05-30 1962-03-05 Finishing of leather

Country Status (6)

Country Link
AT (1) AT239429B (en)
BE (1) BE618099A (en)
CH (1) CH427108A (en)
DE (1) DE1182769B (en)
DK (1) DK106811C (en)
GB (1) GB960499A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1278064B (en) * 1965-12-28 1968-09-19 Bayer Ag Process for dressing leather

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1302991B (en) * 1955-02-24 Ppg Industries Inc
US2940945A (en) * 1957-02-13 1960-06-14 Pittsburgh Plate Glass Co Resinous compositions comprising an aldehyde-modified amide interpolymer and an alkyd resin
NL107417C (en) * 1957-04-10

Also Published As

Publication number Publication date
AT239429B (en) 1965-04-12
CH427108A (en) 1966-12-31
DE1182769B (en) 1964-12-03
DK106811C (en) 1967-03-20
BE618099A (en) 1962-09-17

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