PA6/POE/黏土纳米复合材料的非等温结晶行为  被引量:4

Nonisothermal Crystallization Behavior of Nylon 6/Ployolefin Elastomer/Clay Nanocomposite

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作  者:张成贵[1] 孙春红[1] 张晓静[1] 李亚东[1] 

机构地区:[1]郑州轻工业学院材料与化学工程学院,河南省表界面材料重点实验室,河南郑州450002

出  处:《塑料》2009年第5期31-33,共3页Plastics

基  金:国家自然科学基金(20804041);河南省教育厅自然科学研究计划项目(2008A430022)

摘  要:采用差示扫描量热仪(DSC)方法研究尼龙6(PA6)及尼龙6/聚烯烃弹性体(POE)/黏土纳米复合材料的非等温结晶及熔融行为,随着降温速率的增加,PA6和PA6/POE/黏土纳米复合材料的结晶峰变宽,结晶峰向低温移动。在相同降温速率下,PA6/POE/黏土纳米复合材料在更高的温度下结晶;PA6和PA6/POE/黏土纳米复合材料中晶体呈三维生长,降温速率的增加和有机黏土的加入会使体系结晶速率增加;PA6/POE/黏土纳米复合材料的结晶活化能低于PA6。Nonisothermal crystallization and melting behavior of nylon 6 ( PA6 ) and nylon 6/ployolefin elastomer(POE) / clay nanocomposite by differential scanning calorimetry (DSC) were mainly investigated. Nonisothermal crystallization curves showed that crystallization exotherms baeame wider and crystallization peak temperatures shifted to a lower temperature with the increasing of cooling rate. Under the same cooling rate, crystallization peak temperature of PA6/POE/elay nanoeomposite was higher than that of PA6. Crystals in PA6 and nanocomposite grew with three-dimensional direction. Increasing cooling rate and organoclay could accelerate the crystallization. The crystallization activation energy of PA6/POE/clay nanocomposite was smaller than that of pure PA6.

关 键 词:尼龙6 纳米复合材料 结晶行为 熔融行为 结晶活化能 

分 类 号:TQ342.11[化学工程—化纤工业] TQ325.1

 

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