IP Library Granted Patent US 7,396,370
Granted Patent B2
US 7,396,370 · App. 10/517,234 · Granted Jul 8, 2008

Method of dyeing or printing synthetic polyamide fibre materials using reactive dyes

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Quick Facts
Patent No.
US 7,396,370
App. No.
10/517,234
Granted
Jul 8, 2008
Kind
B2
Abstract

A method of dyeing or printing synthetic polyamide fiber materials, wherein (a) the fiber material is dyed or printed with at least one reactive dye, and (b) the dyed or printed fiber material is subjected to after-treatment with a reducing agent, the fiber material not being treated with polycondensable or polymerizable compounds for fixing the dye on the fiber, results in dyeings and printings that are distinguished by good fastness properties.

Claims (32)

1. A method of dyeing or printing synthetic polyamide fibre materials, wherein

(a) the fibre material is dyed or printed with at least one reactive dye, and

(b) the dyed or printed fibre material is subjected to after-treatment with a reducing agent,

the fibre material not being treated with polycondensable or polymerisable compounds for fixing the dye on the fibre, and

wherein blend fibres of polyester and polyamide are excluded,

and wherein the at least one reactive dye is a reactive dye of formula

wherein

R 1 is hydrogen or unsubstituted or substituted C 1 -C 4 alkyl,

X is halogen,

A is the radical of a monoazo, disazo, polyazo, metal complex azo, anthraquinone, phthalocyanine, formazan or dioxazine dye, and

V is a non-fibre-reactive substituent or is a fibre-reactive substituent of formula

wherein

R 2 is hydrogen or unsubstituted or substituted C 1 -C 4 alkyl or a radical

wherein R 3 is as defined below,

R 3 is hydrogen, hydroxy, sulfo, sulfato, carboxy, cyano, halogen, C 1 -C 4 alkoxycarbonyl, C 1 -C 4 alkanoyloxy, carbamoyl or a group —SO 2 —Y,

R 4 is hydrogen or C 1 -C 4 alkyl,

alk and alk 1 are each independently of the other linear or branched C 1 -C 6 alkylene,

arylene is a phenylene or naphthylene radical which is unsubstituted or substituted by sulfo, carboxy, hydroxy, C 1 -C 4 alkyl, C 1 -C 4 alkoxy or by halogen,

Y is vinyl or a radical —-CH 2 —CH 2 -U and U is a leaving group,

Y 1 is a group —CH(Hal)-CH 2 (Hal) or —C(Hal)=CH 2 wherein Hal is chlorine or bromine,

W is a group —SO 2 —NR 4 —, —CONR 4 — or —NR 4 CO— wherein R 4 is as defined above,

Q is a radical —O— or —NR 4 — wherein R 4 is as defined above, and

n is a number 0 or 1.

2. A method according to claim 1 , wherein

R 1 is hydrogen.

3. A method according claim 1 , wherein

X is chlorine.

4. A method according to claim 1 , wherein

V is a fibre-reactive substituent of formula (2a), (2b), (2c), (2d), (2e) or (2f) wherein R 2 , R 3 , R 4 , alk, alk 1 , arylene, Y, Y 1 , W, Q and n are as defined in claim 1 .

5. A method according to claim 1 , wherein

hydrosulfite is used as reducing agent.

6. A method according to claim 1 , wherein the after-treatment is carried out at a pH of from 7 to 12 and at a temperature of from 30 to 100° C.

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 Jul 25, 2005
From: GRUNER, FRANZ; SCHMIEDL, JURGEN; FEMBACHER, ULRICH; STRAHM, ULRICH
To: CIBA SPECIALTY CHEMICALS CORP.
Reel/Frame 016792/0865 →