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Structural changes in thermally induced phase transitions of uniaxially oriented delta(e) form of syndiotactic polystyrene investigated by temperature-dependent measurements of X-ray fiber diagrams and polarized infrared spectra

机译:X射线纤维图和偏振红外光谱的温度依赖性测量研究了间同立构聚苯乙烯的单轴取向δ(e)形式的热诱导相变中的结构变化

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摘要

The empty delta (delta(e)) form of uniaxially oriented syndiotactic polystyrene ( sPS) was obtained by extracting the solvent molecules from the delta form of the sPS-solvent complex in acetone and methanol. The X-ray fiber diagrams of the delta(e) form of different solvents like chloroform, toluene, and benzene were found to be appreciably different from each other, probably reflecting the difference in the cavity size after solvent evaporation. Temperature dependence of the X-ray fiber diagram has been measured successfully starting from the uniaxially oriented delta(e) form at various temperatures for the first time. It has been found that the delta(e) form transforms to the intermediate form transiently before transforming into the gamma form. Temperature- dependent polarized FTIR spectra were measured also for the uniaxially oriented delta(e) sample derived from the sPS and chloroform complex. The infrared band intensity characteristic of the T(2)G(2) conformation was found to change drastically in the course of transition from the delta(e) to the intermediate phase and to the gamma phase. On the basis of the X-ray diffraction profile and infrared spectra, the intermediate form is speculated to take the structure of disordered chain packing probably due to the empty cavities present in the original delta(e) form. Thermal data showing an endotherm followed by an exotherm during the transition can be interpreted reasonably using such order-to-disorder-to-order transitions among the delta(e), intermediate, and gamma forms.
机译:通过从丙酮和甲醇中的sPS-溶剂配合物的δ形式中提取溶剂分子来获得单轴取向的间规聚苯乙烯(sPS)的空δ形式。发现不同溶剂(例如氯仿,甲苯和苯)的δ(e)形式的X射线纤维图彼此之间存在明显差异,这可能反映了溶剂蒸发后空腔尺寸的差异。 X射线纤维图的温度依赖性已首次在各种温度下成功地从单轴取向的δ(e)形式开始进行了测量。已经发现,δ(e)形式在转变成γ形式之前会瞬时转变成中间形式。还测量了衍生自sPS和氯仿络合物的单轴取向delta(e)样品的温度依赖性极化FTIR光谱。发现T(2)G(2)构象的红外波段强度特征在从δ(e)过渡到中间相和到γ相的过程中发生了急剧变化。根据X射线衍射图谱和红外光谱,推测中间形式采取无序链堆积的结构,这可能是由于原始delta(e)形式存在的空洞所致。可以使用delta(e),中间体和gamma形式之间的这种从有序到无序到有序的过渡来合理地解释显示过渡过程中吸热继之以放热的热数据。

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