首页> 外文期刊>Journal of Applied Polymer Science >Blends of Poly(hydroxyether of bisphenol A) and Polycarbonate: In Situ Polymerization Preparation, Miscibility, and Transreaction
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Blends of Poly(hydroxyether of bisphenol A) and Polycarbonate: In Situ Polymerization Preparation, Miscibility, and Transreaction

机译:聚(双酚A的羟基醚)与聚碳酸酯的共混物:原位聚合制备,互溶性和反式反应

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摘要

In the presence of polycarbonate (PC), the polymerization of diglycidyl ether of bisphenol A (DGEBA) and bisphenol A in the melt was initiated to prepare blends of poly(hydroxyether of bisphenol A) (phenoxy) and PC. The polymerization reaction started from hte initially homogeneous ternary mixture consisting of DGEBA, bisphenol A, and PC; phenoxy/PC blends with PC content up to 20 wt % were obtained. Differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) were employed to characterize the miscibility of the as-polymerized blends. All the blends displayed separate glass transition temperatures (T_g's), that is, the blends were phase-separated. The formation of a two-phase structure is considered to result from phase separation induced by polymerization. This result is consistent with the immiscibility established through solution- and melt-blending approaches. The insolubility of the as-polymerized blends showed that crosslinking between the components occurred. Both Fourier-transform infrared (FTIR) and solid ~13C-nuclear magnetic resonance (~13C-NMR) spectroscopic studies demonstrated a transreaction between the components and in situ polymerization of DGEBA and bisphenol A in the presence of PC, which yielded a phase-separated, transreacted material. The results of this work provide a contrast to those of hte transreacted phenoxy-PC blends based on conventional blending methods; however, the transreaction in the present case occurred at a much lower temperature (180deg C), at which polymerization blending was carried out.
机译:在聚碳酸酯(PC)的存在下,引发双酚A的二缩水甘油醚(DGEBA)和双酚A在熔体中的聚合,以制备聚(双酚A的羟基醚)(苯氧基)和PC的共混物。聚合反应从最初由DGEBA,双酚A和PC组成的均相三元混合物开始;获得了PC含量高达20重量%的苯氧基/ PC共混物。差示扫描量热法(DSC)和动态力学分析(DMA)用于表征聚合共混物的混溶性。所有共混物均显示出独立的玻璃化转变温度(T_g),也就是说,共混物已被相分离。认为两相结构的形成是由于聚合引起的相分离。该结果与通过溶液和熔融共混方法建立的不溶性相一致。聚合共混物的不溶性表明组分之间发生了交联。傅立叶变换红外(FTIR)和固体〜13C核磁共振(〜13C-NMR)光谱研究均表明,在PC的存在下,DGEBA和双酚A的组分之间发生了反应,并进行了原位聚合,产生了分离的反式反应物质。这项工作的结果与基于常规共混方法的反式苯氧基-PC共混物形成对比。然而,目前的反应是在较低的温度(180℃)下进行的,在该温度下进行聚合共混。

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