Synthesis of Poly(methyl methacrylate-g-glycidyl azide) Graft Copolymers Using N, N-Dithiocarbamate-Mediated Iniferters

被引:8
作者
Al-Kaabi, Khalifa [1 ]
Van Reenen, Albert J. [1 ]
机构
[1] Univ Stellenbosch, Dept Chem & Polymer Sci, ZA-7602 Matieland, South Africa
关键词
macrophotoinitiator; photopolymerization; graft copolymer; azide polymers; poly(methyl methacrylate-g-glycidyl azide); LIVING RADICAL POLYMERIZATION; THERMAL CHARACTERIZATION; METHYL-METHACRYLATE; VINYL MONOMERS; N; N-DIETHYLDITHIOCARBAMATE; POLYEPICHLOROHYDRIN; EPICHLOROHYDRIN; POLYMERS;
D O I
10.1002/app.30522
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A glycidyl azide polymer with pendent N, N-diethyl dithiocarbamate groups (GAP-DDC) was prepared by the reaction of poly(epichlorohydrin) (PECH) with pendent N, N-diethyl dithiocarbamate groups (PECH-DDC) and sodium azide (NaN3) in dimethylformamide (DMF). It was then used as a macro-photoinitiator for the graft polymerization of methyl methacrylate (MMA). Photopolymerization was carried out in a photochemical reactor at a wavelength greater than 300 nm. Conversion was determined gravimetrically and first-order time conversion plot for the polymerization system showed linear increase with the polymerization time indicating that polymerization proceed in controlled fashion. The molecular weight distribution (M-w/M-n) was in the range of 1.4-1.6 during polymerization. The formation of poly(methyl methacrylate-g-glycidyl azide) (PMMA-g-GAP) graft copolymer was characterized by gel permeation chromatography, FT-IR spectroscopy, Thermogravimetric analysis, and differential scanning calorimetry. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 114: 398-403, 2009
引用
收藏
页码:398 / 403
页数:6
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