Investigation on synergic activity of N-benzylimine aminothioformamide binary accelerator system in sulfur vulcanization of natural rubber
β Scribed by S. P. Thomas; M. J. Ettolil
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 164 KB
- Volume
- 116
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Abstract
This study explored the possibility of preparing a new thio accelerator, Nβbenzylimine aminothioformamide to investigate its synergic accelerator activity in three conventional binary accelerator systems, Nβcyclohexyl benzothiazyl sulfenamide, mercapto benzothiazyl disulfide, and tetramethylthiuram disulfide in the sulfur vulcanization of natural rubber. Each system was found effective in reduction of cure time as a further proof of the nucleophilic mechanism suggested in the earlier reports. The vulcanizates of the mixes of the three systems were experimented for evaluating their physicomechanical properties. Most of the properties were found better than those of the reference mixes. Crosslinks were also evaluated for correlating the properties. Based on the evaluated properties, optimum dosage of the new binary systems were derived. Β© 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010
π SIMILAR VOLUMES
The synergistic activity of binary accelerator systems in rubber vulcanization is well known. Thiourea and its derivatives are important secondary accelerators in this context. It is suggested that thiourea containing binary systems of rubber vulcanization proceed by a nucleophilic reaction mechanis
## Abstract The synergistic activity of binary accelerator systems in rubber vulcanization is well known. Binary accelerator systems are being widely used in industry and are becoming increasingly popular because of the fact that such mixed systems can effectively prevent prevulcanization, permit t