首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Spherulitic morphology and crystallization kinetics of melt-miscible blends of poly(3-hydroxybutyrate) with low molecular weight poly(ethylene oxide)
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Spherulitic morphology and crystallization kinetics of melt-miscible blends of poly(3-hydroxybutyrate) with low molecular weight poly(ethylene oxide)

机译:聚(3-羟基丁酸酯)与低分子量聚环氧乙烷的熔融混溶共混物的球状形态和结晶动力学

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The spherulitic morphology and crystallization kinetics of the blends of poly(3-hydroxybutyrate) (PHB) with the low molecular weight poly(ethylene oxide) (PEO) prepared by the solution casting have been investigated by differential scanning calorimetry and polarized optical microscopy. The blend was a crystalline/amorphous system when temperatures lie between the melting point of PEO (T_m~(PEO)=ca. 60 deg C) and that of PHB (T_m~(PHB)=ca. 170 deg C), while it became a crystalline/crystalline system below T_m~(PEO). With PHB crystallization at the crystallization temperature (T_c) of 70 deg C, the blends showed PHB banded spherulitic texture, which could be perturbed by the subsequent PEO crystallization in PEO-rich compositions upon further coooling to room temperature. When PHB and PEO were allowed to crystallize upon quench from melt to room temperature, fairly competitive crystallization emerged where crystallization and segregation of PHB and PEO may occur simultaneously, leading to a complicated spherulitic morphology. As for the results of crystallization kinetics, the PHB crystallization exothermic temperature (T_f~(PHB)) on cooling, PHB spherulitic growth rate (G_(PHB)), and overall crystallization rate of PHB (k_n) exhibited maxima in their dependences of PEO composition. This was attributed to the coupling between enhanced chain mobility and depression in equilibrium melting point (T_m~0), since the low molecular weight PEO has a very low glass transition temperature (T_g) over the T_c range studied, G_(PHB) increased with T_c but k_n was found to decrease. The drop of k_n with increasing T_c was therefore predominately governed by the large depression in nucleation rate at higher T_c.
机译:通过差示扫描量热法和偏光光学显微镜研究了聚(3-羟基丁酸酯)(PHB)与通过溶液流延制备的低分子量聚(环氧乙烷)(PEO)的共混物的球状形态和结晶动力学。当温度介于PEO的熔点(T_m〜(PEO)=大约60摄氏度)和PHB的熔点(T_m〜(PHB)=大约170摄氏度)之间时,共混物为晶体/非晶态体系。在T_m〜(PEO)以下成为晶体/晶体体系。在70℃的结晶温度(T_c)下进行PHB结晶时,共混物显示PHB带状球状织构,当随后进一步冷却至室温时,随后的PEO结晶会在富含PEO的组合物中受到扰动。当PHB和PEO在从熔体到室温淬火后结晶时,出现了相当竞争的结晶,其中PHB和PEO的结晶和偏析可能同时发生,从而导致了复杂的球晶形态。至于结晶动力学的结果,冷却时PHB结晶放热温度(T_f〜(PHB)),PHB球晶生长速率(G_(PHB))和PHB的总体结晶速率(k_n)表现出极大的PEO依赖性。组成。这归因于链迁移率的提高与平衡熔点(T_m〜0)的降低之间的耦合,因为在研究的T_c范围内,低分子量PEO的玻璃化转变温度(T_g)非常低,G_(PHB)随着T_c,但发现k_n减小。因此,随着T_c的增加,k_n的下降主要受较高T_c时成核率大幅度下降的支配。

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