Journal Article RAFT-mediated graft polymerization of glycidyl methacrylate in emulsion from polyethylene/polypropylene initiated with γ-radiation

フェルナンデス, マドリッド ジョーダン  ,  ジョーダン  ,  植木, 悠二  ,  Lucille, V. Abad(Philippine Nuclear Research Institute)  ,  山延, 健 (群馬大学)  ,  瀬古, 典明

134 ( 36 )  , pp.45270 (1 of 11) - 45270 (11 of 11) , 2017-09 , Wiley
The successful reversible addition-fragmentation (RAFT)-mediated graft polymerization of glycidyl methacrylate (GMA) in emulsion phase from polyethylene/polypropylene nonwoven fabric using 4-cyano-4-[(phenylcarbonothioyl)thio]pentanoic acid under γ-irradiation at ambient condition is reported. While conventional graft polymerization in emulsion phase yielded grafted materials with low Dg values [<7.5% at 10% (wt/wt) GMA], addition of RAFT agent to the graft polymerization system allowed the synthesis of polyethylene/polypropylene-g-poly(glycidyl methacrylate) (PE/PP-g-PGMA) with more tunable degree of grafting (8% < Dg < 94%) by controlling the grafting parameters. Relatively good control (PDI ~1.2 for selected grafting conditions) during polymerization was attained at 100:1 monomer-to-RAFT agent molar ratio. The number average molecular weight of free PGMA increased as a function of monomer conversion. NMR analyses of the free PGMA homopolymers indicate the presence of dithiobenzoate group from 4-cyano-4-((phenylcarbonothioyl)thio) pentanoic acid on the polymer chain. The reactive pendant oxirane group of the grafted GMA can be modified for various environmental and industrial applications.

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