Image from Google Jackets

Sulfur vulcanization of simple model olefins, Part IV : Vulcanizations of 2,3-dimethyl-2-butene with TMTD and activated zinc dithiocarbamate/xanthate accelerators at different temperatures

By: Contributor(s): Material type: TextTextPublication details: Rubber Chemistry and Technology 1995Description: 563-572Subject(s): Summary: The mechanism of the accelerated sulfur vulcanization of rubber was studied by the use of 2,3-dimethyl-2-butene (C6H12, TME) as a simple, low-molecular model alkene. Treatment of TME with a mixture of ZnO, S8 and the classical accelerator TMTD at temperatures above 100 C yields a mixture of addition products (C6H11-Sn-C6H11). In the temperature range of 50 up to 100 C only interrmediate products, C6H11-Sn-S(s)CN(CH3)2 are obtained. Room temperature vulcanization is feasible using highly reactive accelerators, such as xanthate derivatives. These derivatives result in formation of the crosslink precursors which are converted to the actual crosslink in the presence of zinc dithiocarbamates. The addition of (secondary) amines enhances the solubility of the dithiocarbamates, and therefore the reactivity of the xanthate/zinc dithiocarbamate combination.
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Vol info Status
Journals Journals RRII Library Rubber chemistry Volume 68, Issue 4 Journals
Total holds: 0

The mechanism of the accelerated sulfur vulcanization of rubber was studied by the use of 2,3-dimethyl-2-butene (C6H12, TME) as a simple, low-molecular model alkene. Treatment of TME with a mixture of ZnO, S8 and the classical accelerator TMTD at temperatures above 100 C yields a mixture of addition products (C6H11-Sn-C6H11). In the temperature range of 50 up to 100 C only interrmediate products, C6H11-Sn-S(s)CN(CH3)2 are obtained. Room temperature vulcanization is feasible using highly reactive accelerators, such as xanthate derivatives. These derivatives result in formation of the crosslink precursors which are converted to the actual crosslink in the presence of zinc dithiocarbamates. The addition of (secondary) amines enhances the solubility of the dithiocarbamates, and therefore the reactivity of the xanthate/zinc dithiocarbamate combination.

There are no comments on this title.

to post a comment.
Share