𝔖 Bobbio Scriptorium
✦   LIBER   ✦

ESR and kinetic study of a novel polymerizable photoinitiator comprising the structure of N-phenylmaleimide and benzophenone for photopolymerization

✍ Scribed by Hongyu Wang; Yongtao Shi; Jun Wei; Xuesong Jiang; Jie Yin


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
519 KB
Volume
101
Category
Article
ISSN
0021-8995

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

A novel polymerizable photoinitiator, 4‐[(4‐maleimido)phenoxy]benzophenone (MPBP) comprising the structure of N‐phenylmaleimide and benzophenone was used for the photopolymerization with N,N‐dimethylaminoethyl methacrylate (DMAEMA) as coinitiator. The ESR spectrum of this photoredox system was studied and compared with BP/DMAEMA; the results showed the same signals of them and verified that N‐phenylmaleimide does not generate radicals. The kinetics for photopolymerization of methyl methacrylate (MMA) using such system was studied by dilatometer. It was found that the polymerization rate was proportional to the 0.3172th power of the MPBP concentration, the 0.7669th power and the 0.1765th power of MMA concentration and DMAEMA concentration respectively; the overall apparent activation energy obtained was 31.88 kJ/mol. The polymerization kinetics of 1,6‐hexanediol diacrylate (HDDA) initiated by such system was studied by photo‐DSC. It showed that the increase in the MPBP concentration, light intensity, and temperature leads to increased polymerization rate and final conversion. The apparent activation energy was 11.25 kJ/mol. This polymerizable photoredox system was significantly favorable for reducing the migration of active species but owning high efficiency. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 2347–2354, 2006


📜 SIMILAR VOLUMES


Study of Novel PU-Type Polymeric Photoin
✍ Jun Wei; Hongyu Wang; Xuesong Jiang; Jie Yin 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 170 KB

## Abstract Three PU‐type polymeric photoinitiators containing side‐chain benzophenone and coinitiator amine, PUSBA‐h, PUSBA‐t and PUSBA‐i, were synthesized via polycondensation of 3,5‐diamino‐4′‐thiophenylbenzophenone, different diisocyanates and __N__‐methyldiethanolamine. FT‐IR, ^1^H NMR and GPC