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N,N ′‐Pentamethylenethiuram disulfide‐ and N,N ′‐pentamethylenethiuram hexasulfide‐accelerated sulfur vulcanization. II. Relative stability of N,N ′‐pentamethylenethiuram disulfide and tetramethylthiuram disulfide with respect to amine formation
Author(s) -
ReynekeBarnard C. P.,
Gradwell M. H. S.,
Mcgill W. J.
Publication year - 2000
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/1097-4628(20000919)77:12<2732::aid-app210>3.0.co;2-t
Subject(s) - thiourea , chemistry , sulfur , polymer chemistry , amine gas treating , vulcanization , zinc , thermal stability , organic chemistry , natural rubber
The thermal stability of N , N ′‐dipentamethylenethiuram disulfide (CPTD) and tetramethylthiuram disulfide (TMTD) with respect to thiourea formation was compared. CPTD is stable at 120°C but decomposes to N , N ′‐dipentamethylenethiourea (CPTU) at vulcanization temperatures (140°C), while TMTD is stable to 190°C. These differences do not reside in residual impurities in the compounds. Amines, which catalyze thiourea formation, originate on decomposition of alkyldithiocarbamic acids, and these form more readily in CPTD than in TMTD since the abstraction by thiuram sulfenyl radicals of hydrogen from methylene in CPTD is easier than from methyl in TMTD. ZnO and the zinc‐accelerator complex, zinc bis(pentamethylenedithiocarbamate), inhibit degradation by trapping the alkyldithiocarbamic acid before it can decompose to piperidene, that is, stabilization is achieved when the precursor to the amine, rather than the amine itself, is removed from the system. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 77: 2732–2739, 2000