首页 | 本学科首页   官方微博 | 高级检索  
     检索      

原位聚合纳米Ni/聚苯乙烯复合材料及其热力学性能
引用本文:廖其龙,熊杰,宁海霞.原位聚合纳米Ni/聚苯乙烯复合材料及其热力学性能[J].强激光与粒子束,2011,23(7).
作者姓名:廖其龙  熊杰  宁海霞
作者单位:西南科技大学 四川省非金属复合与功能材料重点实验室-省部共建国家重点实验室培育基地, 四川 绵阳 621010
基金项目:国家自然科学基金委员会-中国工程物理研究院联合基金,先进建筑材料四川省重点实验室开放基金,四川省教育厅重大培育基金
摘    要: 磁性聚苯乙烯(PS)材料有利于实现惯性约束聚变靶丸在辐射场中的无接触支撑。采用液相还原法制备了粒度为75~200 nm的Ni球形粒子,用原位聚合的方法制备了纳米Ni/PS复合材料。利用X射线衍射仪、傅氏转换红外线光谱分析仪、扫描电子显微镜及热重差示扫描量热仪分别研究了所得纳米Ni的特性、复合材料的结构及掺杂量对纳米Ni/PS复合材料的热力学行为的影响。研究结果表明:纳米Ni的掺杂能提高玻璃转变温度;纳米Ni的掺杂可以增大PS热分解焓变,在掺杂质量分数为1%~2%之间焓变达到最大;纳米Ni的掺杂降低了纳米Ni/PS复合材料热分解的比热容。

关 键 词:纳米Ni  聚苯乙烯  原位聚合  热力学性能
收稿时间:1900-01-01;

Thermodynamics parameters of nano-Ni/PS composites prepared by in situ polymerization method
Liao Qilong,Xiong Jie,Ning Haixia.Thermodynamics parameters of nano-Ni/PS composites prepared by in situ polymerization method[J].High Power Laser and Particle Beams,2011,23(7).
Authors:Liao Qilong  Xiong Jie  Ning Haixia
Institution:(State Key Laboratory Cultivation Base for Nonmetal Composite and Functional Materials, Southwest University of Science and Technology, Mianyang 621010, China)
Abstract:Spherical nickel nanoparticles with about 75~200 nm in size were obtained by a liquid reduction method. The nickel nanoparticles/PS composites were synthesized via in situ polymerization method. XRD, FTIR, SEM and TG-DSC were respectively used to measure the properties of nickel nanoparticles, the microstructure of as-prepared composites samples, the distribution of nickel nanoparticles in PS and the thermodynamic parameters of as-prepared composites. The results show that the nickel nanoparticles will enhance the glass transition temperature of nano-Ni/PS composites. The enthalpy of composites is heightened by increasing of doping dose, and it reaches the top when the doping dose is from 1% to 2%. The specific heat of the composites will reduce with the doping dose of nickel nanoparticles
Keywords:polystyrene  in situ polymerization  thermodynamics parameters
本文献已被 万方数据 等数据库收录!
点击此处可从《强激光与粒子束》浏览原始摘要信息
点击此处可从《强激光与粒子束》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号