Miscibility and ferroelectric behavior in blends of poly(vinylidene fluoride/trifluoroethylene) and poly(vinyl acetate)

被引:5
作者
Tang, YW [1 ]
Scheinbeim, J [1 ]
机构
[1] Rutgers State Univ, Dept Chem & Biochem Engn, Polymer Electroproc Lab, Piscataway, NJ 08855 USA
关键词
poly(vinylidene fluoride/trifluoroethylene); poly(vinyl acetate); blends; miscibility; ferroelectricity; VINYLIDENE FLUORIDE; POLYMER BLENDS; COPOLYMERS; TRIFLUOROETHYLENE; CRYSTALLIZATION; TRANSITION; POINT;
D O I
10.1002/polb.10447
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The blend system containing a poly(vinylidene fluoride/trifluoroethylene) [P(VDF/TrFE)] copolymer (68/32 mol %) and poly(vinyl acetate) (PVAc) was miscible from the results of differential scanning calorimetry (DSC) studies that exhibit the presence of a single, composition-dependent glass transition temperature (T-g) and a strong melting point depression for the semicrystalline P(VDF/TrFE) component. However, differences between the DSC and dielectric measurements, which showed a separate P(VDF/TrFE) T-g peak, suggests that the P(VDF/TrFE)/PVAc blends are actually partially miscible. Because of the lower dielectric constant of PVAc and the reduced sample crystallinity caused by the addition of PVAc, both the dielectric constant and the remanent polarization of the copolymer blends decrease with increasing PVAc content. The presence of a small amount of PVAc stabilized the anomalous ferroelectric behavior of ice-water-quenched P(VDF/TrFE), and the blend portrayed normal polarization reversal behavior after adding only 1 wt % PVAc. The piezoelectric response suggests small changes with an increasing number of poling cycles. It is believed that PVAc affects the D-E hysteresis behavior at the interface between crystalline and amorphous phases, although much work remains to be done to confirm this hypothesis. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:927 / 935
页数:9
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