IP Library Granted Patent US 7,514,396
Granted Patent B2
US 7,514,396 · App. 10/518,921 · Granted Apr 7, 2009

Method for cleaning textiles

Assignee: Croda International PLC
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Quick Facts
Patent No.
US 7,514,396
App. No.
10/518,921
Granted
Apr 7, 2009
Kind
B2
Abstract

Detergent or micelle free cleaning media based on detergent free and/or micelle free liquid CO 2 and including from 0.01 to 5% by weight of the formulation of a cleaning additive which is at least one multi-ester having a molecular weight of not more than 750 can be used in dry cleaning of textiles. Desirable cleaning additives are of the formula (1): R 1 (XR 2 ) n where X, R 1 , R 2 , and n have defined meanings, particularly to be esters of multi-carboxylic acids and mono-hydroxy alcohols or esters of mono-carboxylic acids and multi-hydroxy alcohols.

Claims (53)

1. A detergent free dry cleaning medium based on liquid CO 2 and including from 0.01 to 5% by weight of the cleaning medium of a cleaning additive which is at least one multi-ester having a molecular weight of not more than 750.

2. A dry cleaning formulation as claimed in claim 1 wherein the multi-ester includes at least one compound of the formula (I):

R 1 (XR 2 ) n   (I)

where

X is —C(O)O— or —OC(O)—; such that

where X is —C(O)O—,

R 1 is a direct bond or the residue of a C 1 to C 10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R 2 is a C 1 to C 10 hydrocarbyl group; and

where X is —OC(O)—,

R 1 is or the residue of C 2 to C 10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R 2 is H or a C 1 to C 10 hydrocarbyl group; and

n is from 2 to 5;

the compound having a molecular weight of not more than 750.

3. A dry cleaning formulation as claimed in claim 2 wherein the multi-ester is of the formula (Ia):

R 1a (XR 2a ) n   (Ia)

where

X is —C(O)O—;

R 1a is a direct bond or the residue of a C 1 to C 10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R 2a is a C 1 to C 10 hydrocarbyl group.

4. A dry cleaning formulation as claimed in claim 3 wherein the multi-ester is a dimethyl ester of adipic, glutaric or succinic acids or a mixture of such esters.

5. A dry cleaning formulation as claimed in claim 1 wherein the average molecular weight of the multi-ester(s) is from 150 to 300.

6. A dry cleaning formulation as claimed in claim 1 wherein the average ratio of oxygen atoms to carbon atoms in the multi-ester(s) is from 1:1 to 1:5.

7. A dry cleaning formulation as claimed in claim 6 wherein the average ratio of oxygen atoms to carbon atoms in the multi-ester(s) is from 1:1 to 1:1.5.

8. A dry cleaning formulation as claimed in claim 1 wherein the amount of cleaning additive multi-ester present in the cleaning medium is from 0.1 to 0.5% by weight of the cleaning medium.

9. A dry cleaning formulation as claimed in claim 1 which additionally includes at least one fragrance, optical brightener, fabric conditioner, enzyme and/or bleach.

10. A method of dry cleaning which includes contacting textile material with a detergent free dry cleaning medium based on liquid CO 2 and including from 0.01 to 5% by weight of the cleaning medium of a cleaning additive which is at least one multi-ester having a molecular weight of not more than 750.

11. A method as claimed in claim 10 wherein the multi-ester includes at least one compound of the formula (I):

R 1 (XR 2 ) n   (I)

where

X is —C(O)O— or —OC(O)—; such that

where X is —C(O)O—,

R1 is a direct bond or the residue of a C1 to C10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R2 is a C1 to C10 hydrocarbyl group; and

where X is —OC(O)—,

R1 is or the residue of C2 to C10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R2 is H or a C1 to C10 hydrocarbyl group; and

n is from 2 to 5;

the compound having a molecular weight of not more than 750.

12. A method as claimed in claim 11 wherein the multi-ester is of the formula (Ia):

R 1a (XR 2a ) n   (Ia)

where

X is —C(O)O—;

R 1a is a direct bond or a C 1 to C 10 hydrocarbyl group from which n hydrogen atoms have been removed; and

R 2a is a C 1 to C 10 hydrocarbyl group.

13. A method as claimed in claim 12 wherein the multi-ester is a dimethyl ester of adipic, glutaric or succinic acids or a mixture of such esters.

14. A method as claimed in claim 10 wherein the average molecular weight of the multi-ester(s) is from 150 to 300.

15. A method as claimed in claim 10 wherein the average ratio of oxygen atoms to carbon atoms in the multi-ester(s) is from 1:1 to 1:1.5.

16. A method as claimed in claim 10 wherein the amount of cleaning additive multi-ester present in the cleaning medium is from 0.1 to 0.5% by weight of the cleaning medium.

17. A method as claimed in claim 10 which additionally includes at least one fragrance, optical brightener, fabric conditioner, enzyme and/or bleach.

18. A method as claimed in claim 10 wherein the multi-ester is pre-mixed with liquid CO 2 before contacting the textiles.

19. A method as claimed in claim 10 wherein the cleaning process is carried out at a temperature of from −5 to 25° C.

20. A method as claimed in claim 19 wherein the temperature is from 5 to 20° C.

21. A method as claimed in claim 20 wherein the temperature is from 12 to 15° C.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2007
From: IMPERIAL CHEMICAL INDUSTRIES, PLC
To: CRODA INTERNATIONAL PLC
Reel/Frame 019965/0235 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2005
From: MOTSON, HAROLD RUSSELL; IRVINE, DEREK JOHN; APPELMAN, ERIC ADRIAAN
To: IMPERIAL CHEMICAL INDUSTRIES PLC
Reel/Frame 016954/0851 →
Continuity (1)
Related Publication 20060178283A1 · Aug 10, 2006