Reaction-induced microphase separation in thermosetting blends of epoxy resin with poly(methyl methacrylate)-block-polystyrene block copolymers:: Effect of topologies of block copolymers on morphological structures

被引:60
作者
Fan, Wenchun [1 ]
Zheng, Sixun [1 ]
机构
[1] Shanghai Jiao Tong Univ, Dept Polymer Sci & Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
epoxy thermosets; block copolymers; nanostructures and topological structures of block copolymer;
D O I
10.1016/j.polymer.2008.05.010
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polystyrene-block-poly(methyl methacrylate) (PS-b-PMMA) block copolymers with linear and tetra-armed star-shaped topological structures were synthesized via sequential atomic transfer radical polymerization (ATRP). With pentaerythritol tetrakis(2-bromoisobutyrate) as the initiator, the star-shaped block copolymers with two sequential structures (i.e., s-PMMA-b-PS and s-PS-b-PMMA) were prepared and the arm lengths and composition of the star-shaped block copolymers were controlled to be comparable with those of the linear PS-b-PMMA (denoted as l-PS-b-PMMA). The block copolymers were incorporated into epoxy resin to access the nanostructures in epoxy thermosets, by knowing that PMMA is miscible with epoxy after and before curing reaction whereas the reaction-induced phase separation occurred in the thermosetting blends of epoxy resin with PS. Considering the difference in miscibility of epoxy with PMMA and/or PS, it is judged that the reaction-induced microphase separation occurred in the systems. The design of these block copolymers allows one to investigate the effect of topological structures of block copolymers on the morphological structures of the thermosets. By means of atomic force microscopy (AFM) and small-angle X-ray scattering (SAXS), the morphology of the thermosets was examined. It is found that the nanostructures were formed in the thermosets containing l-PMMA-b-PS and s-PS-b-PMMA block copolymers. It is noted that the long-range order of the nanostructures in the epoxy thermosets containing l-PMMA-b-PS is obviously higher than that in the system containing s-PS-b-PMMA. However, the macroscopic phase separation occurred in the thermosetting blends of epoxy resin with s-PMMA-b-PS block copolymer. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3157 / 3167
页数:11
相关论文
共 51 条
[1]   Structure-property relationships and melt rheology of segmented, non-chain extended polyureas: Effect of soft segment molecular weight [J].
Das, Sudipto ;
Yilgor, Iskender ;
Yilgor, Emel ;
Inci, Bora ;
Tezgel, Ozgul ;
Beyer, Frederick L. ;
Wilkes, Garth L. .
POLYMER, 2007, 48 (01) :290-301
[2]   Nanostructure toughened epoxy resins [J].
Dean, JM ;
Verghese, NE ;
Pham, HQ ;
Bates, FS .
MACROMOLECULES, 2003, 36 (25) :9267-9270
[3]   INFLUENCE OF STAR-CORE EXCLUSION ON POLYMER POLYMER MISCIBILITY [J].
FAUST, AB ;
STREMCICH, PS ;
GILMER, JW ;
MAYS, JW .
MACROMOLECULES, 1989, 22 (03) :1250-1254
[4]  
Flory P J., PRINCIPLES POLYM CHE
[5]   Hydroxyl terminated poly(ether ether ketone) with pendent methyl group toughened epoxy resin: miscibility, morphology and mechanical properties [J].
Francis, B ;
Thomas, S ;
Jose, J ;
Ramaswamy, R ;
Rao, VL .
POLYMER, 2005, 46 (26) :12372-12385
[6]   Cure kinetics, morphological and dynamic mechanical analysis of diglycidyl ether of bisphenol-A epoxy resin modified with hydroxyl terminated poly(ether ether ketone) containing pendent tertiary butyl groups [J].
Francis, Bejoy ;
Rao, V. Lakshmana ;
Poel, Geert Vanden ;
Posada, Fabrice ;
Groeninckx, Gabriel ;
Ramaswamy, R. ;
Thomas, Sabu .
POLYMER, 2006, 47 (15) :5411-5419
[7]   ENTROPIC CORRECTIONS TO THE FLORY-HUGGINS THEORY OF POLYMER BLENDS - ARCHITECTURAL AND CONFORMATIONAL EFFECTS [J].
FREDRICKSON, GH ;
LIU, AJ ;
BATES, FS .
MACROMOLECULES, 1994, 27 (09) :2503-2511
[8]   A LIQUID-STATE THEORY OF DENSE STAR POLYMER FLUIDS [J].
GRAYCE, CJ ;
SCHWEIZER, KS .
MACROMOLECULES, 1995, 28 (22) :7461-7478
[9]   Effective interaction parameter between topologically distinct polymers [J].
Greenberg, CC ;
Foster, MD ;
Turner, CM ;
Corona-Galvan, S ;
Cloutet, E ;
Butler, PD ;
Hammouda, B ;
Quirk, RP .
POLYMER, 1999, 40 (16) :4713-4716
[10]   Effective interaction parameter between branched and linear polystyrene [J].
Greenberg, CC ;
Foster, MD ;
Turner, CM ;
Corona-Galvan, S ;
Cloutet, E ;
Quirk, RP ;
Butler, PD ;
Hawker, C .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2001, 39 (21) :2549-2561