Facile and Quick Synthesis of Poly(N-Methylolacrylamide)/Polyhedral Oligomeric Silsesquioxane Graft Copolymer Hybrids via Frontal Polymerization

被引:37
作者
Fang, Yuan [1 ]
Chen, Li [1 ]
Chen, Su [1 ]
机构
[1] Nanjing Univ Technol, Coll Chem & Chem Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 210009, Peoples R China
关键词
frontal polymerization (FP); graft copolymers; morphology; nanocomposites; polyhedral oligomeric silsesquioxane (POSS); poly(N-methylolacrylamide) (PNMA); radical polymerization; synthesis; SOLVENT-FREE SYNTHESIS; THERMAL-PROPERTIES; TRAVELING FRONTS; EPOXY-RESIN; NANOCOMPOSITES; POLYURETHANE; POSS; METHACRYLATE; MONOMERS;
D O I
10.1002/pola.23201
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We report on a new strategy for fabricating well-defined POSS-based polymeric materials with and without solvent by frontal polymerization (FP) at ambient pressure. First, we functionalize polyhedral oligomeric silsesquioxane (POSS) with isophorone diisocyanate (IPDI). With these functionalized POSS-containing isocyanate groups, POSS can be easily incorporated into a poly(N-methylolacrylamide) (PNMA) matrix via FP in situ. Constant velocity FP is observed without significant bulk polymerization. The morphology and thermal properties of POSS-based hybrid polymers prepared via FP are comparatively investigated on the basis of scanning electronic microscopy (SEM) and thermogravimetric analysis (TGA). Results show that the as-prepared POSS-based polymeric materials exhibit a higher glass transition temperature than that of pure PNMA, ascribing to modified POSS well-dispersed in these hybrid polymers. Also, the products with different microstructures display different thermal properties. The pure PNMA exhibits a featureless morphology, whereas a hierarchical morphology is obtained for the POSS-based polymeric materials. (C) 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1136-1147, 2009
引用
收藏
页码:1136 / 1147
页数:12
相关论文
共 65 条
[1]  
Bidali S, 2003, E-POLYMERS
[2]   Solvent-free free-radical frontal polymerization:: A new approach to quickly synthesize Poly(N-vinylpyrrolidone) [J].
Cai, Xiaojing ;
Chen, Su ;
Chen, Li .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2008, 46 (06) :2177-2185
[3]  
CHECHILO NM, 1972, DOKL AKAD NAUK SSSR+, V204, P1180
[4]  
Chekanov Y, 1997, J APPL POLYM SCI, V66, P1209
[5]  
Chekanov YA, 2000, J APPL POLYM SCI, V78, P2398, DOI 10.1002/1097-4628(20001220)78:13<2398::AID-APP170>3.3.CO
[6]  
2-B
[7]   First solvent-free synthesis of poly(N-methylolacrylamide) via frontal free-radical polymerization [J].
Chen, Li ;
Hu, Ting ;
Yu, Huan ;
Chen, Su ;
Pojman, John A. .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2007, 45 (18) :4322-4330
[8]   Epoxy resin/polyurethane hybrid networks synthesized by frontal polymerization [J].
Chen, S ;
Tian, Y ;
Chen, L ;
Hu, T .
CHEMISTRY OF MATERIALS, 2006, 18 (08) :2159-2163
[9]   Segmented polyurethane synthesized by frontal polymerization [J].
Chen, S ;
Sui, JJ ;
Chen, L .
COLLOID AND POLYMER SCIENCE, 2005, 283 (08) :932-936
[10]   Polyurethane-nanosilica hybrid nanocomposites synthesized by frontal polymerization [J].
Chen, S ;
Sui, JJ ;
Chen, L ;
Pojman, JA .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 2005, 43 (08) :1670-1680