Polymerization of vinyl monomers initiated by zwitterionic polymer in aqueous solution
✍ Scribed by Der-Jang Liaw; Kueir-Rarn Lee
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 540 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0959-8103
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The polymerization of vinyl monomers, mainly styrene and methyl methacrylate, initiated by zwitterionic poly[3‐dimethyl(methacryloyloxy‐ethyl)ammonium propane sulfonate], [poly(DMAPS)], in aqueous solution was studied under vacuum at 85°C. An initiation mechanism involving hydrogen atom transfer is proposed. The effects of the efficiency of grafting. pH, water content and betaine polymer content on the polymerization were investigated. The conversion of vinyl monomers in poly(DMAPS) is lower than that in poly [3‐dimethyl(acryloyloxyethyl)ammonium propane sulfonate], which may be due to steric hindrance of the methyl group on the α‐carbon of the former.
📜 SIMILAR VOLUMES
## Abstract Es wird die Kinetik der Polymerisation von Vinylmonomeren in wäßriger Lösung beschrieben, die bei Photo‐Intiierung durch die Radikale C~2~O~4~^·−^ und HCitr^·−^ aus den Ionenpaaren FeC~2~O~4~+ und FeHCitr^+^ erfolgt. Über die spektrophotometrischen Untersuchungen der Formeln und Stabili
Almtract--It is found that the interaction of geminal bis-sulphides with acyl(aroyl)peroxides forms systems which initiate polymerization in non-aqueous media. The mechanism of the reaction of benzoyl peroxide with bis(amylthio)methane was studied. The initiation is shown to result form the products
Homopolymerization of styrene and methyl methacrylate was carried out a t 60-130°C in the presence of a mono-captodatively (cd) substituted ethane bearing nitrile and ethylsulfenyl substituents on the same carbon atom. It was found that the cd-ethane accelerated both styrene and methyl methacrylate