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Tetramethylthiuram disulfide and 2‐mercaptobenzothiazole as binary accelerators in sulfur vulcanization. I. Exchange reactions between the accelerators and sulfur in the absence of rubber
Author(s) -
Giuliani B. V. M. K.,
McGill W. J.
Publication year - 1995
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/app.1995.070571115
Subject(s) - sulfur , vulcanization , chemistry , dimethylamine , polysulfide , sulfide , dissolution , inorganic chemistry , polymer chemistry , natural rubber , organic chemistry , electrode , electrolyte
Exchange reactions between tetramethylthiuram disulfide, 2‐mercaptobenzothizole, and sulfur were studied by heating powdered mixes to vulcanization temperatures at a programmed rate in a DSC. The reaction was stopped at points along the thermal curve and the mixture was analyzed by HPLC. On dissolution, even unheated samples undergo a sulfide exchange reaction leading to a mixed accelerator, while polysulfides of the thiuram and mixed accelerator form in low concentrations. On heating, higher concentrations of these polysulfides are formed, particularly in the presence of elemental sulfur. Dimethyldithiocarbamic acid, formed in the exchange, influences the product spectrum if it remains trapped in the DSC pan. Tetramethylthiourea is formed only at elevated temperatures when dimethylamine, a degradation product of the acid, is trapped in the DSC pan. A series of reactions is proposed to explain the product spectrum obtained under different conditions. © 1995 John Wiley & Sons, Inc.