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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Isothermal crystallization behavior of isotactic polypropylene blended with small loading of polyhedral oligomeric silsesquioxane
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Isothermal crystallization behavior of isotactic polypropylene blended with small loading of polyhedral oligomeric silsesquioxane

机译:等规聚丙烯与少量多面体低聚倍半硅氧烷共混的等温结晶行为

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摘要

The isothermal crystallization kinetics and morphology development of isotactic polypropylene (iPP) blended with small loading of nanostructure of polyhedral oligomeric silsesquioxane (POSS) were studied with differential scanning calorimetry (DSC), polarized optical microscopy (POM), and wide-angle X-ray diffraction (WAXD). The crystallization behaviors of iPP/POSS composites presented an unusual crystallization behavior during isothermal and nonisothermal crystallization conditions. The exothermic morphologies of isothermal and nonisothermal crystallization of iPP/POSS composites changed remarkably with increasing POSS. Moreover, the developments of spherulitic morphology for iPP/POSS composites showed that the major dispersed POSS molecules became nanocrystals first and then aggregated together forming thread- or network-like morphologies, respectively, depending on POSS content, which was observed. It implies that these major POSS nanocrystals' morphologies appeared as an effective nucleating agent and promoted the nucleation rate of iPP, whereas the minor dispersed POSS molecules that had slight miscibility between iPP retarded the nucleation and growth rates of iPP in the remaining bulk region. Therefore, the isothermal crystallization showed a single exothermic peak at pure iPP and POSS-1.0, whereas at POSS-2.0 and POSS-3.0, displayed the multi-exothermic peaks during isothermal crystallization. These faces indicated that POSS molecules were both influence on the transport of iPP chain in the melted state and on the free-energy of formation the critical nuclei of iPP assisted by the POSS structures were observed. Therefore, we postulated that the crystallization mechanisms of multi-exothermic peaks in isothermal crystallization may proceed to combine the "nucleating agent inducing nucleation of iPP event assisted by the POSS domains" that the nucleation of iPP does occur preferentially on the surfaces of the POSS "threads" or "networks" structures, and "nucleation and growth of iPP in the remaining bulk melted iPP region retarded by dispersed POSS molecules". Therefore, effects of POSS content on the isothermal and nonisothermal crystallization behaviors of iPP/POSS composites due to the POSS molecules partially miscible with iPP, at very small loading of POSS molecules, promoted or retarded the rates of nucleation and growth of iPP depending on the POSS content and crystallization temperature were discussed. (c) 2007 Elsevier Ltd. All rights reserved.
机译:用差示扫描量热法(DSC),偏振光学显微镜(POM)和广角X射线研究了等规聚丙烯(iPP)的等温结晶动力学和形貌发展,该混合物共混有少量纳米结构低聚倍半硅氧烷(POSS)的纳米结构。衍射(WAXD)。 iPP / POSS复合材料的结晶行为在等温和非等温结晶条件下均表现出异常的结晶行为。 iPOS / POSS复合材料的等温和非等温结晶的放热形态随POSS的增加而显着变化。此外,iPP / POSS复合材料球状形态的发展表明,主要分散的POSS分子首先变成纳米晶体,然后聚集在一起形成线状或网状形态,具体取决于POSS含量。这表明这些主要的POSS纳米晶体的形态表现为有效的成核剂,并促进了iPP的成核速率,而在iPP之间具有微溶性的少量分散的POSS分子则阻碍了其余主体区域中iPP的成核和生长速率。因此,等温结晶在纯iPP和POSS-1.0处显示一个放热峰,而在POSS-2.0和POSS-3.0处,在等温结晶过程中显示多个放热峰。这些面表明,POSS分子在熔融状态下均会影响iPP链的运输,并且在形成的自由能上也受到POSS结构辅助的iPP关键核的影响。因此,我们推测等温结晶中多放热峰的结晶机制可能会继续结合“成核剂诱导由POSS域协助的iPP事件成核”,即iPP的成核确实优先发生在POSS表面上。线”或“网络”结构,以及“ iPP在剩余的大块熔融iPP区域中被分散的POSS分子阻滞的iPP的形核和生长”。因此,由于POSS分子与iPP部分混溶,在很小的POSS分子负载下,POSS含量对iPP / POSS复合材料的等温和非等温结晶行为的影响促进或阻碍了iPP的成核和生长速率,具体取决于讨论了POSS含量和结晶温度。 (c)2007 Elsevier Ltd.保留所有权利。

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