USRE29724EExpiredUtility

Dyeing process

Priority: Apr 25, 1973Filed: Mar 8, 1977Granted: Aug 8, 1978
Est. expiryApr 25, 1993(expired)· nominal 20-yr term from priority
C09B 5/14C09B 1/20C09B 1/50C09B 1/547C09B 1/585C09B 29/00C09B 62/04C09B 69/00D06P 3/10D06P 3/241D06P 3/248D06P 3/6033D06P 3/8228
2
PatentIndex Score
0
Cited by
5
References
9
Claims

Abstract

Dyeing nylon by applying sulphonated or unsulphonated dyestuffs containing cyclic anhydride groups, anhydride forming dicarboxylic acid groups or half-esters or half-amides thereof, as free acids or as salts with ammonia or volatile amines, and heating the fibre until dyestuff fixation takes place.

Claims

exact text as granted — not AI-modified
We claim: 
     
       1. A process for dyeing nylon fibers by applying thereto a dyestuff of the anthraquinone series containing a dicarboxylic cyclic anhydride grouping or a dicarboxylic acid grouping such that cyclic anhydride formation can occur by loss of water therefrom, or a half-ester or half-amide of such a dicarboxylic acid grouping, any carboxylic acid group in the said dyestuff being present in free acid form or in the form of a salt with ammonia or a volatile amine, said dicarboxylic grouping not being on the anthraquinone nucleus and being either in ortho position on a benzene ring attached to said anthraquinone nucleus or in anhydride-forming position or positioned with one carboxyl group on a carbocyclic aromatic ring attached to said anthraquinone nucleus and the other in anhydride-forming position therewith on an alkyl side chain, and heating the nylon fiber until fixation of the dyestuff takes place. 
     
     
       2. Process according to claim 1 wherein the said dyestuff contains a grouping ##STR70## or ##STR71## wherein R 1  is hydrogen or an alkyl or substituted alkyl group of 1 to 5 carbon atoms or an aryl group, R 2  is hydrogen or an alkyl or substituted alkyl group of 1 to 5 carbon atoms and A represents a molecule of ammonia or a volatile amine. 
     
     
       3. Process according to claim 1 wherein the dyestuff contains at least one sulphonic acid group or salt thereof. 
     
     
       4. Process according to claim 3 wherein the dyestuff additionally contains another type of fibre-reactive grouping. 
     
     
       5. Process according to claim 4 wherein the said fibre-reactive grouping is a halogenotriazinyl grouping. 
     
     
       6. Process according to claim 1 wherein the dyestuff in the form of a water soluble salt is applied to nylon fibre and free acid dyestuff is thereafter liberated by means of mineral or organic acid or a substance with generates an acid on heating. 
     
     
       7. Process according to claim 1 wherein the dyestuff is applied to nylon fibre from an aqueous or non-aqueous liquor or by a printing technique and subsequently baked or steamed at a temperature above 125° C. 
     
     
       8. Process according to claim 7 wherein the dyestuff is in the form of a salt with ammonia or a volatile amine. 
     
     
       9. Process according to claim 7 wherein the temperature is 180° to 210° C. .[.10. Process according to claim 1 wherein the dyestuff is of the azo series..]. .[.11. Process according to claim 1 wherein the 
     
     
        dyestuff is of the anthraduinone series..]. 12. The process of claim 2 wherein said volatile amine is an aliphatic or cycloaliphatic amine.

Join the waitlist — get patent alerts

Track USRE29724E — get alerts on status changes and closely related new filings.

We store only your email — no account needed. See our privacy policy.