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聚苯胺/石墨导电复合材料的制备与表征
引用本文:李侃社,邵水源,闫兰英,任华苗.聚苯胺/石墨导电复合材料的制备与表征[J].高分子材料科学与工程,2002,18(5):92-95.
作者姓名:李侃社  邵水源  闫兰英  任华苗
作者单位:西安科技学院材料工程系,陕西,西安,710054
摘    要:根据石墨的层状结构,以可膨胀石墨(KP)或膨胀石墨(EP)为模板,应用原位聚合法成功制备了聚苯胺(PANi)石墨导电复合材料。通过FT-IR、XRD、SEM和电导率测量等手段表征了其结构和性能。结果表明,PANi/EP的电导率与单一组分相比,都有大幅度提高,而PANi/KP的电导率介于两组分之间,PANi/EP的电导率高于PANi/KP复合材料4-5倍。XRD证明,膨胀石墨与聚苯胺复合大大提高了聚苯胺的结晶度,改善了聚苯胺的结构缺陷。FT-IR表明聚苯胺的特征吸收峰发生了位移,表明KP或EP的表面官能团与聚苯胺之间发生了氢键或共轭作用。

关 键 词:聚苯胺  石墨  导电复合材料  制备  表征  膨胀石墨  电导率  原位聚合
文章编号:1000-7555(2002)05-0092-04
修稿时间:2002年1月20日

PREPARATION AND CHARACTERIZATION OF POLYANILINE/GRAPHITE COMPOSITES
LI Kan she,SHAO Shui yuan,YAN Lan ying,REN Hau miao.PREPARATION AND CHARACTERIZATION OF POLYANILINE/GRAPHITE COMPOSITES[J].Polymer Materials Science & Engineering,2002,18(5):92-95.
Authors:LI Kan she  SHAO Shui yuan  YAN Lan ying  REN Hau miao
Abstract:Polyaniline (PANi)/graphite conducting composites were prepared by in situ polymerization of aniline based on expandable graphite (KP) or expanded graphite (EP) according to their layered structure. Structures and properties of PANi/KP and PANi/EP composites were characterized through FT IR, XRD, SEM and measurement of the electrical conductivity. Results show that the electrical conductivity of PANi/EP composites powders greatly increases compared with neat polyaniline or expanded graphite and it of PANi/KP composites varies from neat polyaniline to expandable graphite, then the conductivity of PANi/EP is 4~5 times higher than PANi/KP. XRD proves that the crystallinity of polyaniline in PANi/EP composites greatly increases and crystal structure disfigurements of polyaniline are greatly improved because of coordinated interaction between polyaniline and EP and crystallinity of polyaniline in PANi/KP composites a little decreases. FT IR shows that there are many oxygen containing groups in KP surface and strong hydrogen bond between polyaniline and KP, but a little in between polyaniline and EP.
Keywords:expanded graphite  polyaniline  polyaniline/graphite composites  electrical conductivity  in  situ polymerization
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