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Synthesis and Nonisothermal Crystallization Kinetics of Poly(Butylene Terephthalate-

机译:聚(丁二醇酯 - 丁二醇酸酯 - 丁二烯酸丁酯的合成和非热结晶动力学

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摘要

Poly(butylene terephthalate-co-tetramethylene ether glycol) (PBT-co-PTMEG) copolymers with PTMEG ranging from 0 to 40 wt% were synthesized through melt polymerization. The structure and composition were supported by Fourier-transform infrared spectroscopy (FT-IR) and nuclear magnetic resonance spectroscopy (1H NMR). All samples had excellent thermal stability at a Td−5% around 370 °C. Crystallization temperature (Tc) and enthalpy of crystallization (ΔHc) were detected by differential scanning calorimetry (DSC), revealing a decrement from 182.3 to 135.1 °C and 47.0 to 22.1 J g−1, respectively, with the increase in PTMEG concentration from 0 to 40 wt%. Moreover, nonisothermal crystallization was carried out to explore the crystallization behavior of copolymers; the crystallization rate of PBT reduced gradually when PTMEG content increased. Hence, a decrement in the spherulite growth rate was detected in polarizing light microscope (PLM) observation, observing that the PTMEG could enhance the hindrance in the molecular chain to lower the crystallinity of PBT-co-PTMEG copolyester. Moreover, thermal properties and the crystallization rate of PBT-co-PTMEG copolymers can be amended via the regulation of PTMEG contents.
机译:通过熔融聚合合成聚(丁二醇丁二醇酯 - 四亚甲基醚二醇)(PBT-CO-PTMEG)与PTMEG的共聚物,由0-40wt%合成。通过傅里叶变换红外光谱(FT-IR)和核磁共振光谱(1H NMR)支持该结构和组合物。所有样品的热稳定性在TD-5%左右约370℃。通过差示扫描量热法(DSC)检测结晶温度(Tc)和结晶(ΔHc)的焓,露出从182.3至135.1℃和47.0至22.1Jg-1的减少,随着PTMEG浓度为0到40%wt%。此外,进行了非等热结晶以探索共聚物的结晶行为;当PTMEG含量增加时,PBT的结晶速率逐渐减少。因此,在偏振光显微镜(PLM)观察中检测到球骨生长速率的减小,观察到PTMEG可以增强分子链中的障碍,以降低PBT-CO-PTMEG共聚酯的结晶度。此外,PBT-Co-PTMEG共聚物的热性能和结晶速率可以通过调节PTMEG含量进行。

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