GB1005475A - Improvements in or relating to the treatment of leather - Google Patents

Improvements in or relating to the treatment of leather

Info

Publication number
GB1005475A
GB1005475A GB242864A GB242864A GB1005475A GB 1005475 A GB1005475 A GB 1005475A GB 242864 A GB242864 A GB 242864A GB 242864 A GB242864 A GB 242864A GB 1005475 A GB1005475 A GB 1005475A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
radical containing
weight
leather
aliphatic hydrocarbon
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
GB242864A
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.)
Dow Silicones Corp
Original Assignee
Dow Corning Corp
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 Dow Corning Corp filed Critical Dow Corning Corp
Publication of GB1005475A publication Critical patent/GB1005475A/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
    • C14C9/00Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes
    • C14C9/02Impregnating leather for preserving, waterproofing, making resistant to heat or similar purposes using fatty or oily materials, e.g. fat liquoring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)

Abstract

In fat-liquoring and waterproofing leather, e.g. chrome-tanned leather, it is fat-liquored, in an aqueous medium, with a water-soluble co-polymer prepared by mixing, e.g. in a solvent such as isopropyl, ethyl or methyl alcohol, (a) a silane having the general formula: <FORM:1005475/C6-C7/1> in which R is a divalent aliphatic hydrocarbon radical containing 3-6 carbon atoms, the Z2N. radical is attached to the third, fourth, fifth or sixth carbon atom from the silicon atom and contains not more than 10 carbon atoms, each Z is the same or different and is a hydrogen atom or a monovalent hydrocarbon radical, e.g. amino-substituted, R1 is an alkyl radical containing 1-7 carbon atoms, R11 is an alkyl radical containing 1-3 carbon atoms, e.g. .CH2.CH2.O.CH3 or .CH2.CH2.OH and n is zero or 1, and (b) a liquid hydroxylated polydimethylsiloxane having a viscosity of at least 30 cs. at 25 DEG C., the weight ratio of (a) to (b) being between 1 : 1 and 1 : 20, e.g. 1 : 3. A monocarboxylic having 1-3 carbon atoms in its molecule, e.g. formic, acetic or propionic acid, may be included in the mixture. The leather is then treated with a solution, in a non-aqueous solvent of a water-repellent composition, as described in Specifications 736,378 and 773,347, comprising (1) 15-50% by weight of a titanium compound Ti(OR111)4, or a zirconium compound Zr(OR111)4, or an aliphatic hydrocarbon-soluble partial hydrolysate of such Ti or Zr compound, in which compounds R111 is an aliphatic hydrocarbon radical containing less than 13 carbon atoms and less than 4, e.g. no, hydroxyl groups, (2) 5-70% by weight of a methylpolysiloxane composed essentially of trimethysiloxane units and SiO2 units and having a methyl to Si ratio between 1:1 and 1.5:1, and (3) 15-80% by weight of a polysiloxane having the average unit formula: <FORM:1005475/C6-C7/2> in which R111 is an alkyl or alkenyl radical containing less than 6 carbon atoms, or a monocyclic aryl radical, and average value of m is between 2 and 2.9.ALSO:In fat-liquoring and waterproofing leather, e.g. chrome-tanned leather, it is fat-liquored, in an aqueous medium, with a water-soluble copolymer prepared by mixing, e.g. in a solvent such as isopropyl, ethyl or methyl alcohol (a) a silane having the general formula <FORM:1005475/C3/1> in which R is a divalent aliphatic hydrocarbon radical containing 3 to 6 carbon atoms, the Z2N radical is attached to the third, fourth, fifth or sixth carbon atom from the silicon atom and contains not more than 10 carbon atoms, each Z is the same or different and is a hydrogen atom or a monovalent hydrocarbon or amino-substituted hydrocarbon radical, R1 is an alkyl radical containing 1 to 7 carbon atoms, R11 is an alkyl radical containing 1 to 3 carbon atoms, e.g. CH2.CH2.O.CH3 or CH2.CH2. OH and n is zero or 1, and (b) a liquid hydroxylated polydimethylsiloxane having a viscosity of at least 30 cs. at 25 DEG C., the weight ratio of (a) to )b) being between 1 : 1 and 1 : 20, e.g. 1 : 3. A monocarboxylic having 1 to 3 carbon atoms in its molecule, e.g. formic, acetic or propionic acid, may be included in the mixture. The leather is then treated with a solution, in a non-aqueous solvent, of a water-repellent composition, as described in Specifications 736,378 and 773,347, comprising (1) 15 to 50%, by weight, of a titanium compound Ti(OR111)4, or a zirconium compound Zr(OR111)4, or an aliphatic hydrocarbon-soluble partial hydrolysate of such Ti or Zr compound, in which compounds R111 is an aliphatic hydrocarbon radical containing less than 13 carbon atoms and less than 4, e.g. no, hydroxyl groups (2) 5 to 70% by weight, of a methylpolysiloxane composed essentially of trimethylsiloxane units and SiO2 units and having a methyl to Si ratio between 1 : 1 and 1.5 : 1, and (3) 15 to 80%, by weight, of a polysiloxane having the average unit formula <FORM:1005475/C3/2> in which R1111 is an alkyl or alkenyl radical containing less than 6 carbon atoms, or a monocyclic aryl radical, and the average value of m is between 2 and 2.9.ALSO:In fat-liquoring and waterproofing leather, e.g. chrometanned leather, it is fat-liquored, in an aqueous medium, with a water-soluble copolymer prepared by mixing, e.g. in a solvent such as isopropyl, ethyl or methyl alcohol, (a) a silane having the general formula: <FORM:1005475/D1-D2/1> in which R is a divalent apliphatic hydrocarbon radical containing 3 to 6 carbon atom, the Z2N, radical is attached to the third, fourth, fifth or sixth carbon atom from the silicon atom and contains carbon atom from the silicon atoms, each Z is the same or different and is a hydrogen atom or a monovalent hydrocarbon radical, e.g. amino-substituted, R1 is an alkyl radical containing 1 to 7 carbon atoms, R11 is an alkyl radical containing 1 to 3 carbon atoms, e.g. ,CH2,CH2,O,CH3 or ,CH2,CH2,OH and n i zero or 1, and (b) a liquid hydroxylated polydimethylsiloxane having a viscosity of at least 30 c. at 25\s2C., the weight ratio of (a) to (b) being between 1:1 and 1:20, e.g. 1:3. A monocarboxylic having 1 to 3 carbon atoms in its molecule, e.g. formic, acetic or propionic acid, may be included in the mixture. The leather is then treated with a solution, in a non-aqueous solvent, of a water-repellent composition, as described in Specifications 736,378 and 773, 347, comprising (1) 15 to 50%, by weight, of a titanium compound Ti(OR111)4, or a zirconium compound Zr(OR1114, or an aliphatic hydrocarbon-soluble partial hydrolysate of such Ti or Zr compound, in which compounds R111 is an aliphatic hydrocarbon radical containing less than 13 carbon atoms and less than 4, e.g. no, hydroxyl groups (2) 5 to 70%, by weight, of a methylpolysilozane composed essentially of trimethylsiloxane units and SiO2 units and having a methyl to Si ratio between 1:1 and 1,5:1, and (3) 15 to 80%, by weight, of a polysiloxane having the average unit formula: R1111 <FORM:1005475/D1-D2/2> which R1111 is an alkyl or alkenyl radical containing less than 6 carbon atoms, or a monocylic aryl radical, and the average value of m is between 2 and 2,9.
GB242864A 1963-01-21 1964-01-20 Improvements in or relating to the treatment of leather Expired GB1005475A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US25255363A 1963-01-21 1963-01-21

Publications (1)

Publication Number Publication Date
GB1005475A true GB1005475A (en) 1965-09-22

Family

ID=22956496

Family Applications (1)

Application Number Title Priority Date Filing Date
GB242864A Expired GB1005475A (en) 1963-01-21 1964-01-20 Improvements in or relating to the treatment of leather

Country Status (6)

Country Link
AT (1) AT261101B (en)
BE (1) BE642698A (en)
CH (1) CH476103A (en)
DE (1) DE1444986A1 (en)
GB (1) GB1005475A (en)
NL (1) NL301058A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011147959A2 (en) 2010-05-28 2011-12-01 Momentive Performance Materials Gmbh Hydrophobizing of fibrous materials with polyorganosiloxanes

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3529869A1 (en) * 1985-08-21 1987-02-26 Basf Ag METHOD FOR HYDROPHOBIZING LEATHER AND FURS
NL2027334B1 (en) 2021-01-18 2022-07-25 Stahl Int B V Composition and process for waterproofing leather

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011147959A2 (en) 2010-05-28 2011-12-01 Momentive Performance Materials Gmbh Hydrophobizing of fibrous materials with polyorganosiloxanes

Also Published As

Publication number Publication date
AT261101B (en) 1968-04-10
BE642698A (en) 1964-07-22
CH476103A (en) 1969-07-31
NL301058A (en)
DE1444986A1 (en) 1969-05-22

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