Observations on the thermolytic decomposition of poly(tert-butyl acrylate)
✍ Scribed by Schaefgen, J. R. ;Sarasohn, I. M.
- Publisher
- John Wiley and Sons
- Year
- 1962
- Weight
- 629 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0022-3832
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The thermolytic decomposition of crystalline and amorphous poly(tert‐butyl acrylate) was investigated. At elevated temperatures thin films of polymer were found to evolve isobutylene quantitatively. The weight loss curve has been analyzed, and a mechanism has been suggested involving a slow random decomposition of tert‐butyl ester groups followed by a faster decomposition of ester groups due to neighboring carboxyl groups. The rate and activation energy for isobutylene evolution in both sections of the weightloss curve are not very different for tactic and atactic polymer modifications.
📜 SIMILAR VOLUMES
The high temperature oxidation of ethyl tert-butyl ether (ETBE) with oxygen in argon diluent has been studied in reflected shock waves over the temperature range 1160 to 1830 K, with pressures of 3.5 bar and with varying equivalence ratios from 0.3 to 2.4. Measurements of the ignition delay times, c
To date, most interpenetrating polymer networks (IPNs) are developed for slow processes such as casting or coating. For industrial manufacturing, fast-reactive polymer processing is often required. Simply increasing the amount of catalyst and/or free-radical initiator shows some limitations. Also, i
## Abstract The synthesis of primary amine end‐functional poly(__tert__‐butyl acrylate)s has been achieved by using the Gabriel reaction. Polymerization of __tert__‐butyl acrylate was first achieved by atom transfer radical polymerization using ethyl‐2‐bromoisobutyrate or paramethoxyphenyl‐2‐bromoi