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1.
聚乙烯/聚并苯复合材料室温电阻率变化规律研究   总被引:3,自引:1,他引:2  
以新型导电材料聚并苯替代碳黑作为导电填料制备聚乙烯/聚并苯复合物.确定了复合物渗流转变区,并解释渗流转变现象的产生机理.从聚并苯含量和热处理过程,对聚乙烯/聚并苯复合物室温电阻率变化规律进行讨论.结果表明,聚并苯质量分数在20%~40%之间是聚乙烯/聚并苯复合物渗流转变区;热处理有利于聚乙烯晶区完善排列,也有利于导电链形成;以聚并苯作为导电填料所制备的复合物具有较高的PTC强度;辐射交联可以提高聚乙烯/聚并苯复合物PTC强度,抑制NTC效应.  相似文献   

2.
聚乙烯/炭黑复合材料导电体系的结构形态   总被引:4,自引:0,他引:4  
沈烈  益小苏 《高分子学报》2001,28(1):130-133
将导电填料(例如炭黑)加入绝缘的聚合物基体即得到导电复合材料,两组混全物的电阻率随导电填料体积分数的变化而改变,电阻率与导电填料体积分数的关系称为渗流曲线,可分为三个主要区域:低导电填料含量区域,复合材料的电阻率很大,聚合物的电阻率占主导;渗流区域,导电填料含量少量的增加会引起复合材料电阻率很大的提高;高导电填料区域,复合材料电阻率很大的提高;高导电填料区域,复合材料电阻率主要由导电填料的电阻率决定,对于导电复合材料已有大量的实验和理论工作来解释导电复合材料已有大量的实验和理论工作来解释导电填料含量和复合材料各组分的形貌对电性能的影响,其中有效介质普适方程(GEM方程)已经对大量的渗流曲线进行了精确的拟合。聚乙烯/炭黑复合材料中由于炭黑的大量分布很难观测其微观形貌,本文对不同辐照交联程度和不同环境温度下聚乙烯/炭黑复合材料的渗流曲线进行分析,试图找出GEM方程各参数与复合材料各组分形貌的关系,为导电复合材料的设计和制备提供理论基础。  相似文献   

3.
用Haake转矩流变仪制备了聚对苯二甲酸乙二酯-聚乙烯-炭黑(PET-PE-CB)复合材料.通过溶解性试验、扫描电镜测试对CB在PET-PE多相体系中的选择性分散进行了研究,考察了CB分布对电性能的影响.结果表明:CB倾向于分布在PET相,改变CB填充量、基体配比以及加料次序对CB微观分布的影响不大.当m(CB)/m(PET-PE)=0.07时,出现渗滤现象.固定炭黑含量,当PET的质量分数由20%增加到60%时,材料的体积电阻率下降了6个数量级,一次性加料更有利于形成导电通路,可以获得较低的体积电阻.  相似文献   

4.
以双酚A二缩水甘油醚(DGEBA)环氧树脂(Epoxy Resin,EP)为基体、甲基六氢苯酐(MHHPA)为固化剂、以多壁碳纳米管(MWCNTs)为添加剂制备了环氧树脂/碳纳米管纳米复合材料。通过对微观结构、玻璃化转变温度(Tg)、热失重、热导率和锥形量热测试结果分析,研究了质量分数少于1.5%的MWCNTs对环氧树脂的导热和阻燃性能影响,结果表明,MWCNTs质量分数为1.5%时,复合材料发生团聚;纳米复合材料随着MWCNTs质量分数的增加Tg值先增加后降低;失重5%时,对应的温度先增加后降低,残炭量增加;样品的热导率呈现先升高后降低的趋势,当MWCNTs质量分数为1%时,复合材料的热导率最大;MWCNTs加入后环氧树脂的总释热量减少,释烟量增加,阻燃性得到一定程度的提高。  相似文献   

5.
以4,4'-二羟甲基-1,4-庚二炔功能单体作为扩链剂制备了端炔基功能化聚氨酯,与叠氮基改性纳米蒙脱土(MMT-N3)、纳米氢氧化铝(ATH-N3)和纳米氢氧化镁(MH-N3)通过Click反应制备了水性聚氨酯(WPU)阻燃纳米复合材料.采用红外光谱(FTIR)、核磁氢谱(1H NMR)和扫描电子显微镜(SEM)对WPU阻燃纳米复合材料的结构进行了表征,对比研究了纳米阻燃剂配比和制备方法对WPU阻燃纳米复合材料的氧指数、动态燃烧行为和热稳定性的影响.阻燃性能研究结果表明,当MMT-N3,MH-N3和ATH-N3的质量分数分别为7%,2%和1%时,采用Click反应制备的复合材料的氧指数比纯WPU高7%,点燃时间从10 s延长到29 s,峰值热释放速率和烟释放速率分别降低了41%和42%.热失重分析结果表明,当MMT-N3质量分数为10%时,与WPU相比,采用Click反应制备的MMT/WPU复合材料在热失重50%时的温度提高了21℃.复合材料断面和燃烧后残渣的SEM分析证明在聚合物基体中Click反应是分散纳米材料的一种有效方法.  相似文献   

6.
选用硅烷偶联剂KH570对纳米Al_2O_3进行表面改性处理,并用改性后的Al_2O_3对双酚A环氧丙烯酸酯进行复合改性,研究了纳米Al_2O_3含量(1%(wt)~5%(wt))对树脂性能的影响。结果表明:改性纳米Al_2O_3质量分数为5%时的复合材料的体积收缩率最小,为6.48%;粒子质量分数为2%时,树脂的凝胶率最大,为88.3%;热失重测试结果表明,改性纳米Al_2O_3提高了树脂的热稳定性;拉伸性能显示,随着改性纳米Al_2O_3质量分数的增加,复合材料的拉伸强度先升高后下降,当改性纳米Al_2O_3质量分数为3%时,复合树脂拉伸强度最大,为34.74MPa,与未改性树脂相比,拉伸强度提高了108.27%。本文所制备的改性光敏树脂可适用于3D打印环境。  相似文献   

7.
利用界面能原理使CB选择性分布于HDPE中成为复合导电相,固定CB在HDPE中的质量分数(20 wt%),控制CB/HDPE导电相在iPP中的含量,制备出一系列三元(iPP/HDPE/CB)导电复合材料,并研究其导电逾渗和流变逾渗行为.结果表明,在复合导电相含量为20 wt%时复合材料内即形成导电网络,在复合导电相含量30 wt%时出现流变网络.只有当复合导电相在材料中形成连续相时(60 wt%),损耗因子在频率扫描中才出现峰值.  相似文献   

8.
以碳纤维(CF)为填料,聚偏氟乙烯(PVDF)为基体,通过熔融共混法制备PVDF/CF导电复合材料.所得复合材料具有显著的正温度系数(PTC)效应,温度上升到聚合物熔点附近时,电阻率对温度变化敏感.在转折温度区间(155.5~171.0oC,(35)(28)15.5oC)内,其体积电阻率的增加速率约为1.3×105?cm K-1.在不同CF含量下,复合材料表现出不同的PTC行为.随着CF含量的增加,其峰值电阻略有下降.高导电粒子含量下,无负温度系数(NTC)效应.在冷却循环过程,导电网络的重构性良好.复合材料即使经过多次热循环,依然表现出良好的PTC特性重现性.  相似文献   

9.
通过共挤出包覆-热压法制备了具有隔离结构的聚丙烯(PP)/碳纳米管(CNTs)电磁屏蔽复合材料。 其中,CNTs随机分布于PP基体中形成导电相,该导电复合物作为包覆层包敷在纯PP颗粒表面,形成包覆复合粒子,经热压后形成隔离导电网络。 结果表明,所制备的隔离结构复合材料呈现良好的导电性能,可获得较低的导电逾渗值0.28%(体积分数);在CNTs质量分数为5.6%时,该复合材料电磁屏蔽性能达到25.6 dB,同时具有良好的力学性能。 本文结果表明,共挤出包覆-热压法制备隔离结构导电复合材料方法简单可控、绿色环保,对开发高性能电磁屏蔽复合材料具有重要指导意义。  相似文献   

10.
采用熔融共混及模压的方法制备了碳纳米管(CNT)-高密度聚乙烯(HDPE)复合材料,并用介电谱仪研究了逾渗值附近的导电填料对复合材料体系在不同温度、频率条件下的介电常数、介电损耗、交流电阻率的变化规律。结果表明:复合材料的介电常数、介电损耗均随CNT质量分数增加而逐渐增大;在频率为103~106 Hz,温度为40~130℃时,HDPE基体的介电常数随频率和温度的变化较小,而添加CNT填料的复合材料的介电常数随频率和温度的增加而略微降低。当w(CNT)0.5%时,复合材料的交流电阻率表现出对频率的强烈依赖性;而当w(CNT)0.5%时,在低频处表现出直流特性,在高频处显示出交流电阻率的降低。  相似文献   

11.
随着导电填料含量的增加,聚合物导电复合材料的电导率呈现非连续的递增.当填料含量达到渗流阈值并导致渗流现象出现时,导电填料相互聚集并形成网络,体系电导率急剧增大,关于此类电渗流现象已有很多报道[1~4].填充类导电复合材料的结构和性能与其粘弹性密切相关.近年来,由于炭黑填充使得许多光学方法失效,流变学方法受到了广泛重视.最新的研究发现,非均相结构的出现和演化对浓度的依赖性有着特征流变响应,是一种粘弹渗流现象[5~7].  相似文献   

12.
A carbon black (CB)/polypropylene (PP)/ultrahigh-molecular-weight polyethylene (UHMWPE) composite with a segregated structure was fabricated by using binary polymer granules as matrices. In preparation, an ethanol-assisted dispersion method was employed to disperse CB particles on the surface of the two polymer granules. The segregated conductive network was then constructed by hot compaction based on the volume exclusion effect of the polymer matrices. The conductive composite shows an ultralow percolation threshold of 0.34 vol.%. In temperature-resistivity test, a double positive temperature coefficient (PTC) effect was observed. In addition, the negative temperature coefficient (NTC) effect was eliminated significantly. These interesting temperature-resistivity behaviors were ascribed to the introduction of the binary polymer matrices and the mobility limitation of CB particles located at the PP/UHMWPE interface. These characteristics were probed by in situ morphology observation in heating process. The present paper provides a novel route for preparing conductive composites with an ultralow percolation threshold, a wider PTC region, and a zero NTC effect.  相似文献   

13.
The electrical conductivity of polymer/multi-walled carbon nanotubes (MWCNTs) composites in a powder and in a hot-pressed compacted state, prepared by mechanical mixing, was studied. The semicrystalline ultrahigh molecular weight polyethylene (UHMWPE) was used as a polymer matrix. The data clearly evidence the presence of a percolation threshold φc at a very small volume fraction of the MWCNTs φ in a polymer matrix, φc ≈ 0.0004-0.0007. The ultralow percolation threshold in UHMWPE/MWCNTs thermoplastic composites was explained by high aspect ratio of the nanotubes and their segregated distribution inside the polymer matrix. The method of composite preparation effects the values of percolation threshold concentration φc and critical exponent t. A noticeable positive temperature coefficient of resistivity (PTC effect) was observed in the region of temperatures higher than melting point. It was explained by influence of thermal expansion of the polymer matrix and independence from the melting process that is a result of specific structure of conductive phase.  相似文献   

14.
多壁碳纳米管/聚乙烯复合材料的制备及其导电行为   总被引:2,自引:0,他引:2  
李文春  沈烈  孙晋  郑强 《应用化学》2006,23(1):64-0
多壁碳纳米管/聚乙烯复合材料的制备及其导电行为;碳纳米管;高密度聚乙烯;渗流阈值;导电行为;V-PTC特性  相似文献   

15.
A methodology for improving antistatic property of polyetherimide (PEI) composite using polyaniline (PANI) grafted multi‐walled carbon nanotubes (MWNTs) as conductive medium was proposed. First, the MWNTs grafted with PANI (PANI‐g‐MWNTs) were prepared by in‐situ polymerization in an emulsion system. Subsequently, PANI‐g‐MWNTs were blended with PEI using N‐methyl‐2‐pyrrolidone as solvent. After removing the solvent, the PEI/PANI‐g‐MWNT composite was prepared. As assisted conductive medium, the grafted PANI molecular chains on MWNT surface were dispersed in the PEI matrix to decrease the percolation value of the antistatic composites. The structure and morphology of PANI‐g‐MWNTs were characterized by Fourier transform infrared spectroscopy, transmission electron microscope, thermogravimetric analysis, and X‐ray powder diffraction, respectively. The dispersion of PANI‐g‐MWNTs in PEI matrix was studied by scanning electron microscope. The electrical performance was characterized by highly resistant meter. The volume resistivity of the conductivity percolation threshold was 1.781 × 10?8 S/cm when the loading of PANI‐g‐MWNTs was 1.0 wt%. The conductivity of PANI‐g‐MWNTs/PEI composites was found to be higher than that of pristine MWNTs/PEI composite. Copyright © 2012 John Wiley & Sons, Ltd.  相似文献   

16.
This paper reports the structural, electrical, dielectric and mechanical properties of the Styrene-acrylonitrile (SAN)/graphite sheets (GS) composites. The composites were prepared by in situ polymerization. The variation of electrical conductivity, dielectric constant and ac conductivity as a function of volume fraction of GS was found to follow the power law model. The dielectric constant and dissipation factor of SAN/GS composites increased significantly near the percolation. The frequency dependence of dielectric constant, dissipation factor and ac conductivity was also analyzed. Nearly ohmic behavior of current density with electric field was observed above the percolation threshold. The composite was found to possess the hardness of pure polymer at the threshold value of GS.  相似文献   

17.
A novel ionic liquid containing phosphorus ([PCMIM]Cl) was synthesized and characterized by FTIR, 1H NMR, 13C NMR and 31P NMR. Moreover, a new intumescent flame retardant (IFR) system, which was composed of [PCMIM]Cl and ammonium polyphosphate (APP), was used to impart flame retardancy and dripping resistance to polypropylene (PP). The flammability and thermal behaviors of intumescent flame‐retarded PP (PP/IFR) composites were evaluated by limiting oxygen index (LOI), UL‐94 test, thermogravimetric analysis (TGA) and cone calorimeter test. It was found that there was an obvious synergistic effect between [PCMIM]Cl and APP. When the weight ratio of [PCMIM]Cl and APP was 1:5 and the total amount of IFR was kept at 30 wt%, LOI value of PP/IFR composite reached 31.8, and V‐0 rating was obtained. Moreover, both the peak heat release rate and the peak mass loss rate of PP/IFR composites decreased significantly relative to PP and PP/APP composite from cone calorimeter analysis. The TGA curves suggested that [PCMIM]Cl had good ability of char formation, and when combined with APP, it could greatly promote the char formation of PP/IFR composites, hence improved the flame retardancy. Additionally, the rheological behaviors and mechanical properties of PP/IFR composites were also investigated, and it was found that [PCMIM]Cl could also serve as an efficient lubricant and compatibilizer between APP and PP, endowing the materials with satisfying processability and mechanical properties. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

18.
It is known that the electrical volume resistivity of insulating polymers filled with conductive fillers suddenly decreases at a certain content of filler. This phenomenon is called percolation. Therefore, it is known that controlling resistivity in the semi-conductive region for carbon black (CB) filled composites is very difficult. When poly (ethylene-co-vinyl acetate) (EVA) is used as a matrix, the percolation curve becomes gradual because CB particles disperse well in EVA. In this study, the relationship between the dispersion state of CB particles and electrical resistivity for EVA/poly (L-lactic acid) (PLLA) filled with CB composite was investigated. The apparent phase separation was seen in the SEM photograph. It was predicted that the CB particles located into the EVA phase in the light of thermodynamical consideration, which was estimated from the wetting coefficient between polymer matrix and CB particles. The total surface area per unit mass of dispersed CB particles in the polymer blend matrix was estimated from small-angle X-ray scattering and the volume resistivity decreased with increasing CB content. The values of the surface area of CB particles in CB filled EVA/PLLA (25/75 wt%) and EVA/PLLA (50/50 wt%) polymer blends showed a value similar to that of the CB filled EVA single polymer matrix. In electrical volume resistivity measurement, moreover, the slopes of percolation curves of EVA/PLLA (25/75 wt%) and EVA/PLLA (50/50 wt%) filled with CB composite are similar to that of EVA single polymer filled with CB composite. As a result, it was found that CB particles selectively locate in the EVA phase, and then the particle forms conductive networks similar to the networks in the case of EVA single polymer used as a matrix.  相似文献   

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