Surface modification of thermally expandable microspheres by grafting poly(glycidyl methacrylate) using ARGET ATRP

被引:78
作者
Jonsson, Magnus [1 ,2 ]
Nystrom, Daniel [1 ]
Nordin, Ove [2 ]
Malmstrom, Eva [1 ]
机构
[1] Royal Inst Technol, Sch Chem Sci & Engn, KTH Fibre & Polymer Technol, SE-10044 Stockholm, Sweden
[2] Eka Chem AB, SE-85013 Sundsvall, Sweden
基金
瑞典研究理事会;
关键词
Expandable microspheres; Grafting from; Glycidyl methacrylate (GMA); ARGET ATRP; TRANSFER RADICAL POLYMERIZATION; GLYCIDYL METHACRYLATE; AMBIENT-TEMPERATURE; METHYL-METHACRYLATE; CONTROLLED GROWTH; BLOCK-COPOLYMERS; POLYMERS; BRUSHES; CATALYST; NANOPARTICLES;
D O I
10.1016/j.eurpolymj.2009.05.002
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This study demonstrates the surface modification of thermally expandable core/shell microspheres by grafting glycidyl methacrylate (GMA) using activators regenerated by electron transfer (ARGET) ATRP. To retain the expansion properties it was essential to minimize the shear forces, use solvents compatible with the microspheres and keep the reaction times short (three hours or less). Using microspheres with hydroxyl groups on the surface, it was found that after converting these to alpha-bromo esters, GMA could be grafted by ARGET ATRP using only 50 ppm of copper catalyst in toluene at 30 degrees C. Decent control of the polymerization was achieved with PMDETA as ligand reaching PDIs of 1.4 for the solution polymerization of GMA. When microspheres were present, the polymerization was less controlled with higher PDIs. The epoxide groups of the grafted microspheres were hydrolyzed by HCl in THF providing a hydrophilic surface of the microsphere. The expansion property of the microspheres was studied after each reaction step by thermal mechanical analysis, and it was found that the expansion capacity was well preserved with only limited negative effect on the microspheres. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2374 / 2382
页数:9
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