IP Library Granted Patent US 7,026,499
Granted Patent B2
US 7,026,499 · App. 10/772,166 · Granted Apr 11, 2006

Linear carboxy-functional organosiloxanyl derivatives and the use thereof for the treatment of the surfaces of leather

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Quick Facts
Patent No.
US 7,026,499
App. No.
10/772,166
Granted
Apr 11, 2006
Kind
B2
Abstract

The invention relates to linear carboxy-functional organosiloxane compounds of the general formula (I) in which a is from 1 to 200, R 1 are identical or different aliphatic or aromatic hydrocarbon radicals and R 2 is —(Y)[O(C 2 H 4-b (R 3 ) b O) c (C d H 2d O) e ] f X, and the use thereof for the treatment of the surface of leather.

Claims (63)

1. A linear carboxy-functional organosiloxane compound of the general formula (I)

in which

a is from 1 to 200,

R 1 are identical or different aliphatic or aromatic hydrocarbon radicals,

R 2 is —(Y)[O(C 2 H 4-b (R 3 ) b O) c (C d H 2d O) e ] f X,

where

Y is an (f+1)-valent, optionally branched hydrocarbon radical having 3 to 12 C atoms,

b is from 1 to 3,

c is from 0 to 20,

d is from 2 to 4,

e is from 0 to 20,

f is from 1 to 4,

R 3 is R 1 ,

X is C(O)-Z-CO 2 H and

Z is a divalent hydrocarbon radical selected from the group consisting of

where

g is from 1 to 12;

R a is alkyl; and

y is 0 to 4.

2. The linear carboxy-functional organosiloxane as claimed in claim 1 , wherein the radical R 2 is a polyether radical comprising mixed blocks.

3. The linear carboxy-functional organosiloxanes a claimed in claim 1 , wherein R 1 is a C 1 –C 5 aliphatic hydrocarbyl group or a C 6 to C 12 aromatic group.

4. The linear carboxy-functional organosiloxane as claimed in claim 1 , wherein R 1 is H and/or methyl.

5. The linear carboxy-functional organosiloxane as claimed in claim 1 , wherein a has a value of from 10 to 150.

6. The linear carboxy-functional organosiloxane as claimed in claim 1 , wherein z is

7. The linear carboxy-functional organosiloxane as claimed in claim 1 which has the formula

wherein

R a is identical or different and is a C 1 –C 4 -alkyl radical,

R 1 is methyl;

a is from 1 to 150;

z is 3 to 12;

c is from 0 to 4; and

y is from 0 to 4.

8. The linear carboxy-functional organosiloxane as claimed in claim 7 wherein R a is methyl and y is 1.

9. The linear carboxy-functional organosiloxane as claimed in claim 7 wherein

R 1 is CH 3 ;

a is from 1 to 150;

z is 3 or 6; and

c is 0 or 4; and

y is 0.

10. A process for the preparation of linear carboxy-functional polysiloxanes as claimed in claim 1 , which comprises reacting hydroxy-functional siloxanes of the general formula

in which

a is from 1 to 200,

R 1 are identical or different aliphatic or aromatic hydrocarbon radicals,

R 4 is —(Y)[O(C 2 H 4-b (R 3 ) b O) c (C d H 2d O) e ] f H,

where

Y is an (f+1)-valent, optionally branched hydrocarbon radical having 3 to 12 C atoms,

b is from 1 to 3,

c is from 0 to 20,

d is from 2 to 4,

e is from 0 to 20 and

f is from 1 to 4,

with organic carboxylic anhydrides of the general formula

in which

Z is a divalent hydrocarbon radical selected from the group consisting of

where

g is 1 to 12

R a is alkyl;

y is 0 to 4.

11. A leather treatment formulation which comprises from about 0.01 to about 50.0% by weight, based upon total weight of the formulation, of at least one linear carboxy-functional polysiloxane as claimed in claim 1 , a solvent, and optionally an additive.

12. The leather treatment formulation as claimed in claim 11 , wherein the solvent is an aqueous solvent.

13. The leather treatment formulation according to claim 11 wherein the additive is an emulsifier, liquid paraffin or mineral oil.

14. The leather treatment formulation as claimed in claim 11 wherein the amount of carboxy-functional polysiloxane is between about 0.01 to about 20% by weight.

15. A method for providing water repellancy to leather which comprises applying the leather treatment formulation as claimed in claim 11 to the surface of the leather.

Assignments (4)
MERGER Recorded Feb 26, 2014
From: EVONIK GOLDSCHMIDT GMBH
To: EVONIK DEGUSSA GMBH
Reel/Frame 032335/0326 →
CHANGE OF NAME Recorded Feb 22, 2010
From: GOLDSCHMIDT GMBH
To: EVONIK GOLDSCHMIDT GMBH
Reel/Frame 024016/0789 →
CHANGE OF NAME Recorded May 20, 2005
From: GOLDSCHMIDT AG
To: GOLDSCHMIDT GMBH
Reel/Frame 016038/0250 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 2, 2004
From: BUSKIES, HEIKE; KRAKENBERG, MANFRED; OESTREICH, SASCHA; STADTMULLER, STEFAN
To: GOLDSCHMIDT AG
Reel/Frame 014968/0377 →