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Use of Hydroxyl Functionalized (Meth)acrylic Cross‐Linked Polymer Microparticles as Chain Transfer Agent in Cationic Photopolymerization of Cycloaliphatic Epoxy Monomer, 1
Author(s) -
Valette Ludovic,
Pascault JeanPierre,
Magny Benoît
Publication year - 2003
Publication title -
macromolecular materials and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.913
H-Index - 96
eISSN - 1439-2054
pISSN - 1438-7492
DOI - 10.1002/mame.200300034
Subject(s) - photopolymer , cationic polymerization , materials science , comonomer , chain transfer , monomer , polymer chemistry , acrylate , epoxy , polymer , dynamic mechanical analysis , butyl acrylate , radical polymerization , chemical engineering , composite material , engineering
In the case of cationic‐type photopolymerized epoxy networks, a new type of chain transfer agent based on hydroxyl functional acrylic cross‐linked polymer microparticles (CPM, also called microgels) has been tested. The CPM functionality was obtained through hydroxyethyl acrylate (HEA) monomer, used as comonomer with butyl acrylate (BA) and hexane diol diacrylate (HDDA). Stabilizing monomers were also required for the synthesis of CPM. In order to compare their particular effects, 4 sets of CPM were synthesized with 4 different stabilizing agents, either hydroxyl functional or not. Consequently, two types of OH groups were present in the particles: primary groups coming from HEA and preferentially located in the particles, and optional hydroxyl groups due to the hydroxyl functional stabilizing agents which were mainly placed onto the particles' surface. The viscoelastic properties of the photopolymerized films have been used to obtain information about the chain transfer reaction and the network microstructure. In all cases, the rubber modulus, $E'_{\rm r}$ was improved because of the decrease of the number of dangling epoxy chains in the epoxy network. When hydroxyl groups were only present in the particles, the mobility of the linkages was assumed to be low, and the mechanical relaxation temperature, T α , strongly increased. However, CPM aggregation occurred at high CPM concentrations, lowering $E'_{\rm r}$ and T α . On the contrary, when OH groups were located both on the surface as well as inside the particles, no large CPM aggregation took place, even with [CPM] = 40 wt.‐%. Nevertheless, the presumably higher mobility of the linkages on the particles' surface prevented any T α increase. The water absorption of all systems based on CPM was very low, around 2% whatever the concentration of chain transfer agent.Schematic description of the transfer reaction between a propagating cationic‐type epoxy chain and a hydroxyl functional CPM.