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Molecular dynamics of an epoxy resin modified with an epoxidized poly(styrene-butadiene) linear block copolymer during cure and microphase separation processes
被引:19
|作者:
Serrano, E.
[1
]
Kortaberria, G.
[1
]
Arruti, P.
[1
]
Tercjak, A.
[1
]
Mondragon, I.
[1
]
机构:
[1] Univ Pais Vasco Euskal Herriko Unibertsitatea, Escuela Politecn, Mat & Technol Grp, Donostia San Sebastian 20018, Spain
关键词:
Block copolymers;
Epoxy;
Dielectric relaxation spectroscopy;
Molecular dynamics;
Phase;
NANOSTRUCTURED THERMOSETTING SYSTEMS;
DIELECTRIC-SPECTROSCOPY;
SECONDARY RELAXATIONS;
BETA-RELAXATION;
CROSS-LINKING;
BISPHENOL-A;
NETWORK POLYMERIZATION;
MECHANICAL-PROPERTIES;
DIBLOCK COPOLYMER;
ALPHA-RELAXATIONS;
D O I:
10.1016/j.eurpolymj.2008.12.018
中图分类号:
O63 [高分子化学(高聚物)];
学科分类号:
070305 ;
080501 ;
081704 ;
摘要:
Molecular dynamics of diglycidyl ether of bisphenol A (DGEBA) epoxy resin modified with an epoxidized poly(styrene-b-butadiene) (SepB) linear block copolymer has been monitored during cure and microphase separation process by dielectric relaxation spectroscopy (DRS) for wide frequency and temperature ranges. Different primary and secondary relaxation processes have been analyzed for neat components and ternary mixture. Relaxational behaviour has been modelled with Havriliak-Negami, Vogel-Fulcher-Tammann and Arrhenius equations and fitting parameters and their evolution have been obtained. The retention of the epoxidized poly(butadiene) (PepB) block in the epoxy-rich phase during all the polymerization process, previously detected by our group with atomic force and transmission electron microscopies, has been confirmed by dielectric relaxation spectroscopy. The evolution of molecular dynamics during the polymerization process of the epoxy resin in the ternary system indicates a change in the trend of the main relaxation at times that agree with phase separation detected by rheology. (C) 2008 Elsevier Ltd. All rights reserved.
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页码:1046 / 1057
页数:12
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