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首页> 外文期刊>Journal of Applied Polymer Science >Structure and Properties of Ultra-High Molecular Weight Bisphenol A Polycarbonate Synthesized by Solid-State Polymerization in Amorphous Microlayers
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Structure and Properties of Ultra-High Molecular Weight Bisphenol A Polycarbonate Synthesized by Solid-State Polymerization in Amorphous Microlayers

机译:非晶态微层中固相聚合合成超高分子量双酚A聚碳酸酯的结构和性能

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摘要

The structure and properties of ultrahigh molecular weight polycarbonate synthesized by solid-state polymerization in micro-layers (SSPm) are reported. A low molecular weight prepolymer derived from the melt transesterification of bisphenol A and diphenyl carbonate as a starting material was polymerized to highly amorphous and transparent polycarbonate of molecular weight larger than 300,000 g mol(-1) in the micro-layers of thickness from 50 nm to 20 mu m. It was observed that when the polymerization time in micro-layers was extended beyond conventional reaction time, insoluble polymer fraction increased up to 95%. Through the analysis of both soluble and insoluble polymer fractions of the high molecular weight polycarbonate by H-1 NMR spectroscopy and pyrolysis-gas chromatography mass spectrometry (Py-GC/MS), branches and partially crosslinked structures have been identified. The thermal, mechanical and rheological properties of the ultra-high molecular weight nonlinear polycarbonates synthesized in this study have been measured by differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), and rheometry. The nonlinear chain structures of the polymer have been found to affect the polymer's thermal stability, mechanical strength, shear thinning effect, and elastic properties. (C) 2014 Wiley Periodicals, Inc.
机译:报道了通过固态聚合在微层(SSPm)中合成的超高分子量聚碳酸酯的结构和性能。将双酚A和碳酸二苯酯作为起始原料进行熔融酯交换反应得到的低分子量预聚物在厚度为50 nm的微层中聚合成分子量大于300,000 mol(-1)的高度非晶态和透明的聚碳酸酯到20微米观察到,当在微层中的聚合时间延长到超过常规反应时间时,不溶聚合物分数增加至高达95%。通过H-1 NMR光谱和热解气相色谱质谱法(Py-GC / MS)分析高分子量聚碳酸酯的可溶和不可溶聚合物部分,已确定了支链和部分交联的结构。通过差示扫描量热法(DSC),动态力学分析(DMA)和流变法测量了本研究中合成的超高分子量非线性聚碳酸酯的热,机械和流变性能。已经发现聚合物的非线性链结构会影响聚合物的热稳定性,机械强度,剪切稀化效果和弹性。 (C)2014威利期刊公司

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