共查询到18条相似文献,搜索用时 125 毫秒
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以EVA为高分子聚合物,采用不同级别的导电炭黑,研究了导电炭黑填充高分子聚合物的导电性,讨论了不同级别和不同用量的导电炭黑在聚合物中的分散性,以及对高分子聚合物导电性的影响。实验结果表明,导电炭黑高分子聚合物的导电性主要取决于不同级别的导电炭黑的表面性和结构等特性、炭黑的不同用量以及导电炭黑的聚集体在高分子聚合物的分散程度。 相似文献
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从本质上说,人们大约在30年前发现了导电聚合物(ICP),但只是在过去的十年来它们的用途才被广泛地开发出来。本文讨论导电聚合物的性能和应用,主要是讨论了聚吡咯沉积在不同基体上的情况。通过在基体如纺织品上涂覆一薄层导电聚合物,产品能够避免许多纯导电聚合物的加工问题。例如,如果在织物上涂覆一层导电聚合物,就能得到坚固、柔韧、弹性较大的易加工导电材料。薄层涂覆物没有改变基础材料的机械性能。 相似文献
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导电高分子材料的研究概况 总被引:5,自引:0,他引:5
戈明亮 《现代塑料加工应用》2002,14(4):43-46
综合介绍了导电聚合物的种类及其合成的方法,列举了导电聚合物在不同领域的应用情况,同时对导电聚合物未来的发展提出了一些看法。 相似文献
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炭黑是最常用的导电添加剂。导电的添加剂加入绝缘聚合物基体后,能在特定的体积浓度闽值下生成一个导电网络。炭黑和聚合物的特征共同决定了这个临界浓度。开发新型导电炭黑的主要任务就是降低此突增界限。与其它导电添加剂相比,导电炭黑具有很显著的优点,因为它和聚合物有相容性,对聚合物机械性能的影响较小。 相似文献
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耐折高导电聚吡咯/聚硫橡胶复合膜马文石,贾振斌,龚克成(华南理工大学高聚物结构与性能改性研究室,广州,510641)将导电聚合物与绝缘聚合物复合,是改善导电聚合物性能的良好方法之一。Wang等[1~3]采用二步法将聚吡咯(PPy)与聚苯乙烯、聚碳酸酯... 相似文献
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综述了建筑用传统节能型高分子材料和新型节能型高分子材料在建筑工程中的应用,其中传统型节能型高分子材料包括聚氨酯、聚苯乙烯、酚醛树脂和相变材料等直接节能保温材料,以及抗菌材料、防潮材料等间接节能材料;新型节能型高分子材料则包括太阳能电池、环境敏感型高分子材料等。直接型节能材料利用自身的保温性能降低建筑物的能耗,而间接型节能材料则通过延长自身使用寿命来降低建筑成本;新型节能材料可以利用清洁能源为建筑物供能,或是通过改变自身性能来适应环境,降低建筑能耗。 相似文献
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The antibacterial activity of insoluble pyridinium‐type polymers with different structures against Escherichia coli suspended in sterilized and distilled water was investigated by a colony count method. The results show that the antibacterial activity of insoluble pyridinium‐type polymers, except for one containing I−, is characterized by an ability to capture bacterial cells in a living state by adsorption or adhesion, with the process of capturing bacterial cells being at least partially irreversible. This feature differs from the antibacterial activity of the corresponding soluble polymers, which is characterized by the ability to kill bacterial cells in water. In addition, insoluble pyridinium‐type polymers can also capture dead bacterial cells. This implies that insoluble pyridinium‐type polymers possess broad prospects for development in new water treatment techniques and whole‐cell immobilization techniques. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 676–684, 2000 相似文献
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A general overview of the optoelectronic properties of π‐conjugated polymers is presented. Two types of polymer are discerned: interchangeable structures of the same energy (degenerate), such as polyacetylene; and non‐degenerate polymers, such as poly(para‐phenylene). The band structures of degenerate and non‐degenerate polymers are related to their conductivities in doped and non‐doped states. In both cases, disorder and impurities play an important role in conductivity. Polarons, bipolarons and excitons are detailed with respect to doping and charge transfers. Given the fibrillic nature of these materials, the variable range hopping (VRH) law for semiconducting polymers is modified to account for metallic behaviours. Optoelectronic properties—electroluminescence and photovoltaic activity—are explained in terms of HOMO and LUMO bands, polaron‐exciton and charge movement over one or more molecules. The properties of H‐ or J‐type aggregates and their effects on transitions are related to target applications. Device structures of polymer light‐emitting diodes are explicitly linked to optimising polaron recombinations and overall quantum efficiencies. The particularly promising use of π‐conjugated polymers in photovoltaic devices is discussed. Copyright © 2004 Society of Chemical Industry 相似文献
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As the ubiquity and complexity of optical devices grows, our technology becomes more dependent on specialized functional materials. One area of continued interest is in high refractive index polymers as lightweight, processable and inexpensive alternatives to silicon and glass. In addition to a high refractive index, optical applications require these polymers to be transparent and have a low optical dispersion. Both nanocomposite and intrinsic high refractive index polymers offer particular advantages and disadvantages. While nanocomposite high refractive index polymers have refractive indices above 1.80, the nanoparticle type, content and size can negatively affect storage stability and processability. Alternatively, intrinsic high refractive index polymers are prepared by introducing an atom or substituent with a high molar refraction into a polymer chain; the resultant polymers are easier to store, transport, tune and process. Polymers containing aromatic groups, halogens (except fluorine), phosphorus, silicon, fullerenes and organometallic moieties have all shown significant promise. Many factors can affect intrinsic high refractive index polymer performance including molecular packing, molar volume, chain flexibility and substituent content. This mini‐review summarizes the principles behind and recent developments in intrinsic high refractive index polymers. © 2014 Society of Chemical Industry 相似文献
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The copolymers of 4‐vinylpyridine (4VP), styrene (St) and divinylbenzene (DVB) with varied compositions, P(4VP‐St‐DVB), were synthesized by suspension polymerization using 2,2′‐azobisisobutyronitrile (AIBN) as an initiator. The insoluble (crosslinked) pyridinium‐type polymers in benzyl–pyridinium bromide form, which possess various macromolecular chain compositions, were prepared by the reaction of each P(4VP‐St‐DVB) with benzyl bromide (BzBr), respectively. By using different halohydrocarbon RX in the quaternization of P(4VP‐St‐DVB), the insoluble pyridinium‐type polymers with various pyridinium group structures were obtained. The structures of P(4VP‐St‐DVB) and its quaternized product Q‐P(4VP‐St‐DVB) were identified by FTIR. The 4VP content in each copolymer P(4VP‐St‐DVB) was measured by nonaqueous titration; and the pyridinium group content (Cq) in each Q‐P(4VP‐St‐DVB) sample was determined by means of the back titration manner in argentometry and/or the elemental analysis method, respectively. In addition, the particle structure and the surface morphology of the thus‐prepared polymer were observed using SEM. According to a series of experimental results, the preparation and characterization of insoluble pyridinium‐type polymers are analyzed and discussed. This work can prepare the ground for a study on the antibacterial activity of insoluble pyridinium‐type polymers. © 2000 John Wiley & Sons, Inc. J Appl Polym Sci 78: 668–675, 2000 相似文献