Monsanto Company

Richard D Chapman

Oscar A Pickett, Jr

Donald A Holmer

James H Saunders

Kurt Moedritzer

Chris E Schwier

James S Ridgway

George A Mortimer

Roger C Ayotte

A process is disclosed for the production of linear amorphous polyamides which results in polyamides having more amine endgroups than acid endgroups. It comprises condensing an aqueous solution of salts comprising at least one aromatic diacid containing from 7 to 20 carbon atoms and a greater than equimolar amount of at least one aliphatic diamine containing from 4 to 20 carbon atoms.

Process for the production of linear amorphous polyamides with excess

Fiber-forming polymers are prepared from a mixture of the hexamethylene diamine salts of terephthalic acid, isophthalic acid, and a small amount of at least one aliphatic dibasic acid (e.g. adipic acid) having from 5 to 12 carbon atoms. The polymers can be prepared in a batch autoclave and extruded therefrom without cleaning the autoclave between successive runs.

Polyamides derived from hexamethylene diamine, terephthalic acid,

Polyamide fibers containing one or more of a certain class of poly(copper phosphinates) have improved resistance to color fading when dyed with disperse dyes and exposed to ozone than do corresponding fibers from which the phosphinate has been omitted.

Polyamide fibers having improved ozone fading resistance

An improvement in the process for preparing random copolyamides by the melt polymerization of a mixture of hexamethylenediammonium terephthalate and hexamethylenediammonium isophthalate is described. The improvement comprises accomplishing the melt polymerization in the presence of a small amount of a certain phosphorus compound, such as benzene phosphinic acid, whereby ammonia formation during polymerization is reduced.

Melt preparation of 6TA/6IA polymers with phosphorus compound to reduce

Dimensionally stable fibers are produced from copolymers prepared from substantially equimolar amounts of hexamethylene diamine and a 50:50 to 80:20 mixture of terephthalic and isophthalic acids by heating essentially amorphous fibers melt spun from the copolymers to a temperature between about 160.degree. C. and 300.degree. C. for a short period of time. The dimensionally stable fibers combine many of the best properties of nylon 66 and poly(ethylene terephthalate) and are particularly useful in tire and textile applications.

Dimensionally stable 6TA/6IA fibers

Copolymers made from hexamethylenediamine and a mixture of tere- and isophthalic acids in which the mixture contains between about 60 and 80 mole percent terephthalic acid are described as well as useful fibers prepared therefrom.

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Pensacola, FL, United States of America

Richard D Chapman