本文采用差示扫描量热(DSC)从等温结晶和非等温结晶动力学两方面研究了5种不同添加剂的 PET(聚对苯二甲酸乙二醇酯)体系的结晶行为和对形态的影响.结果表明:有机酸盐比金属氢氧化物具有更明显的成核效果.较明显地加快了结晶速率,减小晶...本文采用差示扫描量热(DSC)从等温结晶和非等温结晶动力学两方面研究了5种不同添加剂的 PET(聚对苯二甲酸乙二醇酯)体系的结晶行为和对形态的影响.结果表明:有机酸盐比金属氢氧化物具有更明显的成核效果.较明显地加快了结晶速率,减小晶体尺寸和增加结构均匀性.在 DSC 曲线上,熔融结晶峰(T_(mc))和冷结晶峰(T_(cc))的差值比未改性的 PET 增加了14℃,扩大了结晶温度范围,有利于改进现有 PET 薄膜的加工性,这已为东方绝缘材料厂的中试所验证.展开更多
The drawn copper wires have been analyzed by differential scanning calorimeter(DSC) and a new method, which uses DSC measurements to determine the Johnson-Mehl-Avrami-Kolmogorov(JMAK) exponent via introducing Arrheniu...The drawn copper wires have been analyzed by differential scanning calorimeter(DSC) and a new method, which uses DSC measurements to determine the Johnson-Mehl-Avrami-Kolmogorov(JMAK) exponent via introducing Arrhenius behavior and modifying the baseline of DSC curves, has been proposed. The results show that JMAK exponent and recrystallization activation energy of the drawn copper wires with a strain of 2.77 are about 2.39 and 125 k J/mol, respectively. The line linking the tangency points of DSC curve hypotenuse can be used as the baseline when calculating recrystallization fraction. The JMAK exponent obtained by the DSC method is in a good agreement with that obtained by microhardness measurements. Compared to traditional methods to measure the exponent, the proposed method is faster and less labor intensive.展开更多
A significant enhancement in isothermal crystallization kinetics of biodegradable polylactide(PLA) in its immiscible blends can be accomplished through blending it with a comb-like copolymer. PLA was blended with poly...A significant enhancement in isothermal crystallization kinetics of biodegradable polylactide(PLA) in its immiscible blends can be accomplished through blending it with a comb-like copolymer. PLA was blended with poly(ethylene glycol) methyl ether acrylate(PEGA) and poly[poly(ethylene glycol) methyl ether acrylate](PPEGA, a comb-like copolymer), respectively. The results measured from phase contrast optical microscopy(PCOM) and differential scanning calorimetry(DSC) indicate that PLA and PEGA components are miscible, whereas PLA and PPEGA components are immiscible. The study of crystallization kinetics for PLA/PEGA and PLA/PPEGA blends by means of polarized optical microscopy(POM) and DSC indicates that both PEGA and PPEGA significantly increase the PLA spherulitic growth rates, G, although PLA/PPEGA blends are immiscible and the glass transition temperatures of PLA only have slight decreases. PPEGA component enhances nucleation for PLA crystallization as compared with PEGA component owing to the heterogeneous nucleation effect of PPEGA at the low composition of 20 wt%, while PLA crystallization-induced phase separation for PLA/PEGA blend might cause further nucleation at the high composition of 50 wt%. DSC measurement further demonstrates that isothermal crystallization kinetics can be relatively more enhanced for PLA/PPEGA blends than for PLA/PEGA blends. The "abnormal" enhancement in G for PLA in its immiscible blends can be explained by local interfacial interactions through the densely grafted PEGA side chains in the comb-like PPEGA, even though the whole blend system(PLA/PPEGA blends) represents an immiscible one.展开更多
文摘本文采用差示扫描量热(DSC)从等温结晶和非等温结晶动力学两方面研究了5种不同添加剂的 PET(聚对苯二甲酸乙二醇酯)体系的结晶行为和对形态的影响.结果表明:有机酸盐比金属氢氧化物具有更明显的成核效果.较明显地加快了结晶速率,减小晶体尺寸和增加结构均匀性.在 DSC 曲线上,熔融结晶峰(T_(mc))和冷结晶峰(T_(cc))的差值比未改性的 PET 增加了14℃,扩大了结晶温度范围,有利于改进现有 PET 薄膜的加工性,这已为东方绝缘材料厂的中试所验证.
基金Projects(51171135,51371132,51471123) supported by the National Natural Science Foundation of ChinaProjects(2012K07-08,2013KJXX-61) supported by Key Science and Technology Program of Shaanxi Province,ChinaProject(2013JC14) supported by the Education Department Foundation of Shaanxi Province,China
文摘The drawn copper wires have been analyzed by differential scanning calorimeter(DSC) and a new method, which uses DSC measurements to determine the Johnson-Mehl-Avrami-Kolmogorov(JMAK) exponent via introducing Arrhenius behavior and modifying the baseline of DSC curves, has been proposed. The results show that JMAK exponent and recrystallization activation energy of the drawn copper wires with a strain of 2.77 are about 2.39 and 125 k J/mol, respectively. The line linking the tangency points of DSC curve hypotenuse can be used as the baseline when calculating recrystallization fraction. The JMAK exponent obtained by the DSC method is in a good agreement with that obtained by microhardness measurements. Compared to traditional methods to measure the exponent, the proposed method is faster and less labor intensive.
基金supported by the National Basic Research Program of China (2012CB025901)the National Natural Science Foundation of China (21174139)the Open Research Fund of State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences
文摘A significant enhancement in isothermal crystallization kinetics of biodegradable polylactide(PLA) in its immiscible blends can be accomplished through blending it with a comb-like copolymer. PLA was blended with poly(ethylene glycol) methyl ether acrylate(PEGA) and poly[poly(ethylene glycol) methyl ether acrylate](PPEGA, a comb-like copolymer), respectively. The results measured from phase contrast optical microscopy(PCOM) and differential scanning calorimetry(DSC) indicate that PLA and PEGA components are miscible, whereas PLA and PPEGA components are immiscible. The study of crystallization kinetics for PLA/PEGA and PLA/PPEGA blends by means of polarized optical microscopy(POM) and DSC indicates that both PEGA and PPEGA significantly increase the PLA spherulitic growth rates, G, although PLA/PPEGA blends are immiscible and the glass transition temperatures of PLA only have slight decreases. PPEGA component enhances nucleation for PLA crystallization as compared with PEGA component owing to the heterogeneous nucleation effect of PPEGA at the low composition of 20 wt%, while PLA crystallization-induced phase separation for PLA/PEGA blend might cause further nucleation at the high composition of 50 wt%. DSC measurement further demonstrates that isothermal crystallization kinetics can be relatively more enhanced for PLA/PPEGA blends than for PLA/PEGA blends. The "abnormal" enhancement in G for PLA in its immiscible blends can be explained by local interfacial interactions through the densely grafted PEGA side chains in the comb-like PPEGA, even though the whole blend system(PLA/PPEGA blends) represents an immiscible one.
