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Crystallization kinetics and phase transformation of poly(vinylidene fluoride) films incorporated with functionalized baTiO_3 nanoparticles

机译:掺入功能化baTiO_3纳米粒子的聚偏二氟乙烯薄膜的结晶动力学和相变

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摘要

The transformation of α to β-phase in poly(vinylidene fluoride) (PVDF) induced by the addition of tetradecylphosphonic acid (TDPA)-BaTiO_3 nanoparticles and subsequently the isothermal crystallization kinetics of pristine PVDF and its nanocomposites have been investigated. The result of infrared spectra showed that the relative crystalline fraction of β-phase was enhanced greatly after the introduction of TDPA-BaTiO_3 nanoparticles, and reached the peak of 93% when the concentration of nanofillers was 20%. The interaction between TDPA-BaTiO_3 nanoparticles and PVDF macromolecular chains induced the change of conformation from trans-gauche to all-trans crystal structure in PVDF segment. The isothermal crystallization of TDPA-BaTiO_3/PVDF nanocomposites was carried out by the differential scanning calorimetry (DSC). The influence of TDPA-BaTiO_3 nanoparticles concentration on crystallization rate, activate energy, melting enthalpy, and peak temperature were studied. The nanocomposite film loaded 20% TDPA-BaTiO_3 nanoparticles exhibited the highest crystallization rate and activate energy, which decreased after loading more nanofillers in the host because of high volume fraction of nanoparticles leading to steric hindrance and further weakening the mobility of PVDF chains during the crystallization.
机译:研究了通过添加十四烷基膦酸(TDPA)-BaTiO_3纳米颗粒引起的聚偏二氟乙烯(PVDF)中α相向β相的转变,以及原始PVDF及其纳米复合材料的等温结晶动力学。红外光谱结果表明,引入TDPA-BaTiO_3纳米粒子后,β相的相对结晶度大大提高,当纳米填料浓度为20%时,β相的相对结晶度达到93%的峰值。 TDPA-BaTiO_3纳米粒子与PVDF高分子链之间的相互作用导致PVDF片段中构象从反式结构转变为全反式晶体结构。 TDPA-BaTiO_3 / PVDF纳米复合材料的等温结晶是通过差示扫描量热法(DSC)进行的。研究了TDPA-BaTiO_3纳米粒子的浓度对结晶速率,活化能,熔融焓和峰值温度的影响。载有20%TDPA-BaTiO_3纳米复合薄膜的纳米复合材料表现出最高的结晶速率和活化能,在主体中装载更多的纳米填料后下降,因为纳米粒子的高体积分数导致位阻,并进一步削弱了结晶过程中PVDF链的迁移率。

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