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首页> 外文期刊>Journal of Polymer Science, Part B. Polymer Physics >Crystallization and morphology of poly(vinylidene fluoride)/poly(3-hydroxybutyrate) blends. I. Spherulitic morphology and growth by polarized microscopy
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Crystallization and morphology of poly(vinylidene fluoride)/poly(3-hydroxybutyrate) blends. I. Spherulitic morphology and growth by polarized microscopy

机译:聚偏二氟乙烯/聚3-羟基丁酸酯共混物的结晶和形态。 I.偏光显微镜下的球状形态和生长

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The development of the poly(3-hydroxybutyrate) (PHB) morphology in the presence of already existent poly(vinylidene fluoride) (PVDF) spherulites was studied by two-stage solidification with two separate crystallization temperatures. PVDF formed irregular dendrites at lower temperatures and regular, banded spherulites at elevated temperatures. The transition temperature of the spherulitic morphology from dendrites to regular, banded spherulites increased with increasing PVDF content. A remarkable amount of PHB was included in the PVDF dendrites, whereas PHB was rejected into the remaining melt from the banded spherulites. When PVDF crystallized as banded spherulites, PHB could consequently crystallize only around them, if at all. In contrast, PHB crystallized with a common growth front, starting from a defined site in the interfibrillar regions of volume-filling PVDF dendrites. It formed by itself dendritic spherulites that included a large number of PVDF spherulites. For blends with a PHB content of more than 80 wt %, for which the PVDF dendrites were not volume-filling, PHB first formed regular spherulites. Their growth started from outside the PVDF dendrites but could later interpenetrate them, and this made their own morphology dendritic. These PHB spherulites melted stepwise because the lamellae inside the PVDF dendrites melted at a lower temperature than those from outside. This reflected the regularity of the two fractions of the lamellae because that of those inside the dendrites of PVDF was controlled by the intraspherulitic order of PVDF, whereas that from outside was only controlled by the temperature and the melt composition. The described morphologies developed without mutual nucleating efficiency of the components. (C) 2003 Wiley Periodicals, Inc. [References: 40]
机译:通过在两个单独的结晶温度下进行两阶段固化研究了在已经存在的聚偏二氟乙烯(PVDF)球晶存在下聚(3-羟基丁酸酯)(PHB)形态的发展。 PVDF在较低温度下会形成不规则的树枝状晶,在高温下会形成规则的带状球晶。球状形态从树枝状转变为规则的带状球晶的转变温度随PVDF含量的增加而增加。 PVDF树枝状晶体中包含大量的PHB,而PHB从带状球晶中被拒绝进入剩余的熔体中。当PVDF结晶为带状球晶时,PHB因此可能仅在它们周围结晶(如果有的话)。相反,PHB从体积填充的PVDF树突的原纤维间区域中的特定位置开始,以共同的生长前沿结晶。它本身由包括大量PVDF球晶的树枝状球晶形成。对于PHB含量大于80 wt%的共混物(PVDF树枝状晶体未进行体积填充),PHB首先形成规则球晶。它们的生长开始于PVDF树突的外部,但后来可以穿透它们,这使它们自身的形态成为树突。这些PHB球晶逐步熔化,因为PVDF树枝状晶体内部的薄片在比外部的薄片更低的温度下熔化。这反映了薄片的两个部分的规则性,因为PVDF的树突内部的薄片的规则性受PVDF的球内顺序控制,而外部的薄片仅受温度和熔体成分的控制。所描述的形态发展而没有组件的相互成核效率。 (C)2003 Wiley Periodicals,Inc. [参考:40]

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