Acceleration by Thiourea and Related Compounds of the Tetramethylthiuram Disulfide Vulcanization of Natural Rubber

Author:

Moore C. G.1,Saville B.1,Watson A. A.1

Affiliation:

1. 1The Natural Rubber Producers Research Association Welwyn Gakden City, Herts., England

Abstract

Abstract It has recently been discovered that thiourea and certain of its N-derivatives and chemically related compounds, accelerate the vulcanization of natural rubber (NR) by tetramethylthiuram disulfide (TMTD)-zinc oxide combinations to such an extent that excellent vulcanizates can be produced at 100° C or lower. A reasonable explanation of this acceleration is now offered, based on a theory of vulcanization by TMTI) and related “sulfurless” curing systems currently being developed here. This theory recognizes the importance of polysulfidic intermediates (I, m>2), formed during the vulcanization process, which subsequently react with the polyisoprene to yield further intermediates (II) which finally react to yield sulfurated crosslinks. The process is broadly schematized as follows:

Publisher

Rubber Division, ACS

Subject

Materials Chemistry,Polymers and Plastics

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