IP Library Granted Patent US 7,090,704
Granted Patent B2
US 7,090,704 · App. 10/497,364 · Granted Aug 15, 2006

Method of treating natural or synthetic polyamide fibre materials

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Quick Facts
Patent No.
US 7,090,704
App. No.
10/497,364
Granted
Aug 15, 2006
Kind
B2
Abstract

A method of improving the resistance of dyes on natural or synthetic polyamnide fiber materials to the action of ozone and NO x , which comprises treating the fiber material, before, during or after dyeing, with a liquor comprising a terpolymer containing structural repeating units of formulae (I), (II) and (III) in which R is a radical of formula (IV) wherein A 1 and A 2 are independently of one another a direct bond, C 1 –C 8 alkylene or —CO—NH—C 1 –C 8 alkylene, E is vinyl or —OSH 3 H and n denotes 0 or 1. The dyeings and prints obtained are distinguished by improved ozone fastness properties without the shade, color yield and other fastness properties, for example fastness to light, being affected

Claims (14)

1. A method of improving the resistance of a dye on a natural or synthetic polyamide fibre material to the action of ozone and NO x , which comprises treating the fibre material, before, during or after dyeing, with a liquor comprising a terpolymer containing structural repeating units of formulae (I), (II) and (III)

in which R is a radical of formula (IV)

wherein A 1 and A 2 are independently of one another a direct bond, C 1 –C 8 alkylene or —CO—NH—C 1 –C 8 alkylene, E is vinyl or —OSO 3 H and n denotes 0 or 1.

2. A method according to claim 1 , wherein a terpolymer containing structural repeating units of formula (II) is used in which R is a radical of formula (IVa) to (IVf)

3. A method according to claim 1 , wherein a terpolymer containing structural repeating units of formula (II) is used in which R is a radical of formula (IVg) to (IVi)

4. A method according to claim 1 , wherein the terpolymer contains from 30 to 70 mol % of structural repeating units of formula (I), from 1 to 30 mol % of structural repeating units of formula (II) and from 15 to 50 mol % of structural repeating units of formula (III).

5. A method according to claim 1 , wherein the terpolymer has an average molecular weight (weight average M w ) of from 1000 to 70,000.

6. A method according to claim 1 , wherein the amount of terpolymer present in the liquor is from 0.05 to 10% by weight, based on the weight of the polyamide fibre material.

7. A method according to claim 1 , wherein the fibre material is treated during or after the dyeing operation.

8. A method according to claim 7 , wherein the treatment with the liquor comprising the terpolymer is carried out at a pH value of from 2 to 9.

9. A method according to claim 7 , wherein the treatment with the liquor comprising the terpolymer is carried out at a temperature of from 50 to 100° C.

10. A method according to claim 1 , wherein the treatment with the liquor comprising the terpolymer is carried out according to the padding or exhaust method.

11. A method according to claim 1 , wherein the fibre material is synthetic polyamide fibre material.

12. A method according to claim 1 , wherein the dye is an anthraquinone dye.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 2, 2007
From: CIBA SPECIALTY CHEMICALS CORPORATION
To: HUNTSMAN INTERNATIONAL LLC
Reel/Frame 019140/0871 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2006
From: OUZIEL, PHILIPPE
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 017695/0278 →