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非共价键合杂化体系中聚己内酯的非等温结晶动力学

Nonisothermal Crystallization Kinetics of Poly(ε-caprolactone) in Non-covalently Coupled Hybrid Materials

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【作者】 聂康明庞文民鲁非朱清仁

【Author】 NIE Kang-Ming~(a,b*),PANG Wen-Min~(b),LU Fei~(b),ZHU Qing-Ren~(b)(~(a)College of Chemistry and Chemical Engineering,Anhui University,Hefei 230039;~(b)Structure Research Laboratory,University of Science and Technology of China,Hefei 230026)

【机构】 安徽大学化学化工学院材料系中国科学技术大学结构分析重点实验室中国科学技术大学结构分析重点实验室 合肥230039中国科学技术大学结构分析重点实验室合肥230026合肥230026合肥230026

【摘要】 运用差示扫描量热法(DSC)分析研究了聚己内酯(PCL)结晶高分子在新型PCL/S iO2非共价键合有机-无机杂化体系中的非等温结晶动力学特性。结果显示,杂化体系中PCL非等温结晶的成核和生长机制与杂化材料的组成和结构微环境效应相关。在相同结晶度下,m(TEOS)∶m(PCL)=60∶40杂化样品的F(T)值为7.42 K.m inn/(m-1),结晶速率最大。其非等温结晶动力学行为受无机纳米S iO2的成核加速作用的影响,也受杂化体系分子间氢键键合作用及无机非晶组分抑制结晶的影响。

【Abstract】 The nonisothermal crystallization kinetics of poly(ε-caprolactone)(PCL) in PCL/silica(SiO2) non-covalently coupled organic-inorganic hybrids was investigated by means of differential scanning calorimetry(DSC).The results show that the mechanism of the nucleation and growth of the PCL nonisothermal crystallization in the hybrids are related to the composition of the hybrids and their structural(micro-)environmental effect.Under the same crystallinity,the F(T) value of a 60∶[KG-*3/5]40(mass fraction) TEOS/PCL hybrid(sample) was 7.42 K·minn/(m-1),whose crystallization rate was the highest.On the one hand,the(inorganic) nano-component(viz.SiO2) could act as a nucleating agent to facilitate the crystallization of PCL in the hybrids.On the other hand,the intermolecular hydrogen bonding and the SiO2 network in the hybrids also confine the crystallization of PCL.

【基金】 安徽省自然科学基金资助项目(03044801)
  • 【文献出处】 应用化学 ,Chinese Journal of Applied Chemistry , 编辑部邮箱 ,2005年10期
  • 【分类号】O631.3;
  • 【被引频次】1
  • 【下载频次】147
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