首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >In situ study of nanostructure and morphological development during the crystal-mesophase transition of poly(di-n-hexylsilane) and poly(di-n-butylsilane) by X-ray and hot-stage AFM
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In situ study of nanostructure and morphological development during the crystal-mesophase transition of poly(di-n-hexylsilane) and poly(di-n-butylsilane) by X-ray and hot-stage AFM

机译:X射线和热台原子力显微镜对聚(二正己基硅烷)和聚(二正丁基硅烷)的结晶-中间相转变过程中的纳米结构和形貌发展的原位研究

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摘要

Nanostructure and morphology and their development of poly(di-n-hexylsilane) (PDHS) and poly(di-n-butylsilane) (PDBS) during the crystal-mesophase transition are investigated using small angle X-ray scattering (SAXS), wide angle X-ray diffraction and hot-stage atomic force microscopy. At room temperature, PDHS consists of stacks of lamellae separated by mesophase layers, which can be well accounted using an ideal two-phase model. During the crystal-mesophase transition, obvious morphological changes are observed due to the marked changes in main chain conformation and intermolecular distances between crystalline phase and mesophase. In contrast to PDHS, the lamellae in PDBS barely show anisotropy in dimensions at room temperature. The nonperiodic structure and rather small electronic density fluctuation in PDBS lead to the much weak SAXS. The nonperiodic structure is preserved during the crystal - mesophase transition because of the similarity of main chain conformation and intermolecular distances between crystalline phase and mesophase.
机译:使用小角度X射线散射(SAXS)研究了聚(二正己基硅烷)(PDHS)和聚(二正丁基硅烷)(PDBS)在晶体-中间相转变过程中的纳米结构和形貌及其发展角X射线衍射和热台原子力显微镜。在室温下,PDHS由中间相层分隔的薄片堆叠组成,可以使用理想的两相模型很好地说明这一点。在晶体-中间相转变期间,由于主链构象的显着变化以及结晶相与中间相之间的分子间距离,观察到明显的形态变化。与PDHS相比,PDBS中的薄片在室温下几乎没有各向异性。 PDBS中的非周期性结构和较小的电子密度波动会导致SAXS弱得多。由于主链构象的相似性以及晶相与中间相之间的分子间距离,在晶体-中间相转变期间保留了非周期性结构。

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