Co-continuous morphology development in partially miscible PMMA/PC blends

被引:88
作者
Marin, N [1 ]
Favis, BD [1 ]
机构
[1] Ecole Polytech, Dept Chem Engn, Ctr Rech Appl Polymeres, Montreal, PQ H3C 3A7, Canada
关键词
polymer blends; co-continuity; partial miscibility;
D O I
10.1016/S0032-3861(02)00280-X
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Poly(methyl methacrylate) (PMMA)/polycarbonate (PC) partially miscible blends were produced via melt blending in an internal mixer over the entire range of composition at two different viscosity ratios. The morphology of this low interfacial tension system was investigated by scanning electron microscopy, solvent extraction/gravimetry and surface area measurement (BET) after selective extraction. The partial miscibility of these blends was evaluated by T-g measurements from dynamic mechanical thermal analysis. The co-continuous morphology development curve obtained from gravimetry is commonly reported in the literature as the %continuity vs. the vol% fraction of the dispersed phase for fully phase separated systems. Such systems possess pure phases of A and B. Partially miscible blends on the other hand demonstrate immiscibility between an A-rich phase and a B-rich phase. Quantitative estimation of the partial composition of the minor components in each respective rich phase was calculated using the Fox equation. Using this data, an approach to correcting the gravimetry results to take into account the partial miscibility of the PMMA/PC system is proposed. The co-continuous morphology development curve is then presented as the %continuity vs. the vol% fraction of the PMA4A-rich phase. This corrected curve demonstrates the features of a highly interacting polymer blend: a low percolation threshold and a broad co-continuity region. The BET technique shows that the pore size of the extracted co-continuous blends is dependent on composition, the pore diameter increases with total PMMA content. Use of a low molecular weight PC shifts the co-continuous morphology development curve to higher volume fraction values of PMMA-rich phase. It is suggested that this is the result of a lower dispersed phase thread stability due to the lower matrix viscosity. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:4723 / 4731
页数:9
相关论文
共 26 条
[11]   Characterizing co-continuous high density polyethylene/polystyrene blends [J].
Li, J ;
Favis, BD .
POLYMER, 2001, 42 (11) :5047-5053
[12]   The role of the blend interface type on morphology in cocontinuous polymer blends [J].
Li, JM ;
Ma, PL ;
Favis, BD .
MACROMOLECULES, 2002, 35 (06) :2005-2016
[13]  
Mekhilef N, 1997, J POLYM SCI POL PHYS, V35, P293, DOI 10.1002/(SICI)1099-0488(19970130)35:2<293::AID-POLB7>3.0.CO
[14]  
2-T
[15]   Phase inversion and dual-phase continuity in polymer blends: Theoretical predictions and experimental results [J].
Mekhilef, N ;
Verhoogt, H .
POLYMER, 1996, 37 (18) :4069-4077
[16]  
METELKIN VI, 1984, COLLOID J USSR+, V46, P425
[17]   ROLE OF SLOW PHASE-SEPARATION IN ASSESSING THE EQUILIBRIUM PHASE-BEHAVIOR OF PC PMMA BLENDS [J].
NISHIMOTO, M ;
KESKKULA, H ;
PAUL, DR .
POLYMER, 1991, 32 (02) :272-278
[18]   POLYMER BLENDS (OR ALLOYS) [J].
PAUL, DR ;
BARLOW, JW .
JOURNAL OF MACROMOLECULAR SCIENCE-REVIEWS IN MACROMOLECULAR CHEMISTRY AND PHYSICS, 1980, C18 (01) :109-168
[19]   INFLUENCE OF SOLVENT CASTING ON THE EVOLUTION OF PHASE MORPHOLOGY OF PC/PMMA BLENDS [J].
SALDANHA, JM ;
KYU, T .
MACROMOLECULES, 1987, 20 (11) :2840-2847
[20]   ON THE VISCOSITY-CONCENTRATION DEPENDENCE OF IMMISCIBLE POLYMER BLENDS [J].
UTRACKI, LA .
JOURNAL OF RHEOLOGY, 1991, 35 (08) :1615-1637