共查询到19条相似文献,搜索用时 93 毫秒
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采用化学氧化聚合法,以石墨烯(RGO)为掺杂剂,吡咯(Py)和二苯胺磺酸(SD)共聚制备了导电复合材料。通过正交实验和分散性实验确定了最佳合成条件为:以FeCl3・6H2O为氧化剂,氧化剂与单体的摩尔比为1:1,Py与SD的摩尔比为7:3(总量为0.01 mol),RGO添加量为0.05 g;在此条件下制备的复合材料电导率为12.05 S/cm,且具有良好的水分散性。用傅里叶变换红外(FTIR)光谱和X射线衍射(XRD)对其结构进行了表征,并使用热重分析仪(TGA)对复合材料的热稳定性进行了测试。结果表明,SD结构单元成功嵌入聚吡咯(PPy)的分子链中,RGO的掺杂使复合材料电导率和热稳定性都有了明显提升。将复合材料作为导电填料加入到水性聚氨酯中,考察了涂层的抗静电性能和机械性能,在添加量为4%时,涂层的综合性能较好,涂层表面电阻率可达8.65×107 Ω。 相似文献
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分别采用物理球磨混合法、化学原位聚合法和化学原位聚合-还原法制备了聚吡咯/氧化石墨烯混合物、聚吡咯/氧化石墨烯(PPy/GO)和聚吡咯/还原氧化石墨烯(PPy/RGO)复合材料。通过三电极测试其电化学性能(循环伏安、恒流充放电和交流阻抗)。结果表明,通过化学原位聚合法制备的PPy/GO(304. 5 F/g)比电容远高于物理混合(16 F/g)和聚吡咯/还原氧化石墨烯(126. 4 F/g)。化学法原位聚合法制备PPy/GO最佳条件是冰浴条件下和加入表面活性剂对羟基苯磺酸钠。并通过X射线衍射(XRD)和扫描电子显微镜(SEM)对化学原位制备的PPy/GO组成、结构和形貌进行了表征。 相似文献
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通过原位聚合法制备出聚吡咯/石墨烯(PPy/GE)复合材料。用红外光谱(FT-IR)、扫描电镜(SEM)、透射电镜(TEM)等分析手段对复合材料的结构和形貌进行表征,发现聚吡咯均匀地包覆在石墨烯表面。循环伏安测试表明复合材料对电极对I-/I3-电解质氧化还原体系具有较好的催化能力。电化学交流阻抗测试结果说明掺入聚吡咯后可有效降低石墨烯对电极的电荷转移阻抗。组装成染料敏化太阳能电池(DSSCs),在AM 1.5(100mW.cm-2)的模拟太阳光照射下,得到4.12%的光电转换效率。 相似文献
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利用超声波的分散、粉碎、活化、引发等多重作用以及吡咯单体与石墨烯的π-π相互作用,在实现石墨烯均匀分散的同时,使吡咯单体在石墨烯表面进行原位聚合反应,制备出聚吡咯/石墨烯(PPy/RGO)纳米复合材料。运用扫描电子显微镜(SEM)、红外光谱(FTIR)、X射线光电子能谱(XPS)等测试手段对PPy/RGO纳米复合材料的表面特性、化学组成及结构等进行了表征。在此基础上,研究了制备过程中的各种因素(如氧化剂、反应温度、石墨烯含量等)对PPy/RGO纳米复合材料产率及导电性能的影响。并采用热重分析(TGA)和导电测试分析了石墨烯含量对其热稳定性及电导率的影响。 相似文献
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以氧化石墨烯(GO)作为前体,通过氨丙基三乙氧基硅烷将氧化锡锑(ATO)锚定到氧化石墨烯片层上,制备得到氧化锡锑-氧化石墨烯纳米复合材料(ATO/GO)。通过XRD,XPS和SEM对其结构进行测试。并研究了ATO/GO含量对水性环氧涂料(AE)防腐及抗静电性能的影响。结果表明:随ATO/GO含量的增加,复合涂料表面电阻降低,ATO/GO含量大于3%时,表面电阻降低至108Ω以下,达到了抗静电的使用要求;当ATO/GO含量为3%时,漆膜水蒸气透过率降低至(62.13g/m2 h),具有最低的腐蚀电流密度(Icorr=3.73E-9 A/cm2)和最高的腐蚀电压(Ecorr=-0.19926v),防腐效率与空白样相比提高了99.95%。 相似文献
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以聚乙烯醇(PVA)和自制的羊毛角蛋白(WK)为原料,硼酸为交联剂,将WK与质量分数为15%的PVA溶液按质量比为2:10混合,制得含固体质量分数约为15%的WK/PVA共混纺丝原液,采用湿法纺丝的方法制备WK/PVA复合纤维,研究了复合纤维的结构与性能。结果表明:WK/PVA复合纤维的表面均出现皱纹,其横截面呈椭圆形;硼酸交联对WK/PVA复合纤维的形貌无明显影响,但使复合纤维的耐水性能得到提升;傅里叶变换红外光谱、X射线衍射光谱和热重分析结果证明了交联的发生,硼酸与WK和PVA大分子的交联改变了复合纤维的结晶结构,增强了大分子间的作用力,却使WK/PVA复合纤维的热稳定性降低。 相似文献
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Graphene oxide (GO) was well dispersed in poly(vinyl alcohol) (PVA) diluted aqueous solution, and then the mixture was electrospun into GO/PVA composite nanofibers. Electron microscopy and Raman spectroscopy on the as‐prepared and calcined samples confirm the uniform distribution of GO sheets in the nanofibers. The thermal and mechanical properties of the nanofibers vary considerably with different GO filler contents. The decomposition temperatures of the GO/PVA composite nanofiber dropped by 38–50°C compared with pure PVA. A very small loading of 0.02 wt % GO increases the tensile strength of the nanofibers by 42 times. A porous 3D structure was realized by postcalcining nanofibers in H2. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 相似文献
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In this study, three sets of different bilayered composite coatings of pyrrole and N-substituted pyrroles were synthesized by a layer-by-layer approach on copper surface and corrosion performances of the synthesized materials were compared. Electrodepositions of poly(N-methylpyrrole), poly(N-phenylpyrrole), and poly(N-methoxyphenylpyrrole) were performed in nonaqueous medium on a poly(pryrrole)-coated copper surface using cyclic voltammetry. The morphologies of the resulting bilayered composite coatings of poly(pyrrole)/poly(N-methylpyrrole), poly(pyrrole)/poly(N-phenylpyrrole), and poly(pyrrole)/poly(N-methoxyphenylpyrrole) were investigated by scanning electron microscopy. Stabilities of a doping-dedoping process of the composites were determined from the cyclic voltammetric study of the bilayer-coated electrodes in a monomer-free solution. Corrosion performances of the bilayer composite-coated and uncoated copper electrodes were investigated in 0.1 M H2SO4 solution using open circuit potential–time (E ocp–t) curves, anodic polarization, and electrochemical impedance spectroscopy. All the investigated bilayered coatings gave significant enhancement in the corrosion resistance of copper, compared to the single poly(pyrrole) coating. Stability and corrosion tests revealed that the composite material poly(pyrrole)/poly(N-methoxyphenylpyrrole) exhibited higher electrochemical stability and corrosion resistant behavior than the other bilayered composite coatings. 相似文献
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Graphene (GE)‐based nanocomposites are emerging as a new class of materials that hold promise for many applications. In this article, we present a general approach for the preparation of GE/poly(vinyl alcohol) (PVA) nanocomposites. The basic strategy involved the preparation of graphite oxide from graphite, complete exfoliation of graphite oxide into graphene oxide sheets, followed by reduction to GE nanosheets, and finally, the preparation of the GE/PVA nanocomposites by a simple solution‐mixing method. The synthesized products were characterized by X‐ray diffraction, field emission scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetry, and differential scanning calorimetry analysis. The GE nanosheets were well dispersed in the PVA matrix, and the restacking of the GE sheets was effectively prevented. Because of the strong interfacial interaction between PVA and GE, which mainly resulted from the hydrogen‐bond interaction, together with the improvement in the PVA crystallinity, the mechanical properties and thermal stability of the nanocomposites were obviously improved. The tensile strength was increased from 23 MPa for PVA to 49.5 MPa for the nanocomposite with a 3.25 wt % GE loading. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010 相似文献
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Composites of thermoplastic polyurethane (TPU) with poly(diphenylamine) (PDPA) were prepared by entrapping diphenylamine (DPA) molecules into the matrix of TPU and polymerizing DPA within the TPU matrix. Swelling rate of the parent TPU and the composites in 1M LiClO4 in propylene carbonate solution were compared to understand the influence of the presence of PDPA in the composite in altering the morphology, conductivity, and electrolyte behavior. The nitrogen atoms in the PDPA interact and are likely to form hydrogen bonding with the carbonyl and ether groups in TPU. As a result, different morphology, thermal, and impedance behavior were witnessed for the composites in comparison to TPU. Results from differential scanning calorimetry, scanning electron microscopy (SEM), thermogravimetric analysis, and ac impedance measurements were obtained as supporting evidences. An increase in glass transition temperature for the composite in comparison to TPU infers the increase in phase mixing of soft and hard segment of TPU. The SEM micrograph shows the presence of fibrillar morphology of PDPA molecules in the composite. The ionic conductivity of the swelled composite was 1‐fold higher than that of pure TPU. A schematic representation showing the interaction of PDPA molecules with TPU is presented. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 611–617, 2006 相似文献
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Poly(pyrrole-co-N-methyl pyrrole) copolymer and poly(pyrrole)/poly(N-methyl pyrrole) bilayer composites were electrochemically synthesized on copper by cyclic voltammetry from aqueous solution of 0.3 M oxalic acid and 0.1 M monomer. Synthesis of copolymers were performed with different monomer feed ratios (pyrrole:N-methyl pyrrole, 8:2, 6:4, 5:5, 4:6 and 2:8) and in order to determine the copolymer, which has the best corrosion performance, anodic polarization was applied to copolymer coated samples. It was found that the performance of coatings was strongly dependent to the monomer feed ratio and the copolymer synthesized with 8:2 concentration ratio showed the most protective property compared to others. Bilayer of poly(pyrrole)/poly(N-methyl pyrrole) was also synthesized to compare the anticorrosive properties. Polymer films were characterized by ATR-FTIR spectroscopy and SEM techniques. Corrosion behavior of polymer composites was investigated in 0.1 M H2SO4 solution by anodic polarization and electrochemical impedance spectroscopy. Different approaches such as phase angle at high frequency and areas under Bode plots were used to evaluate corrosion performances of the coatings. Copolymer and bilayer coatings were found to have higher protection effect than single polypyrrole coatings. Moreover, bilayer coating exhibited better protection efficiency than copolymer coating against corrosion of copper when the obtained results were compared. 相似文献
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采用熔融共缩聚反应法合成聚(丙三醇-癸二酸-柠檬酸)酯(PGSC)弹性体,再采用半原位聚合和研磨分散的方法制备多壁碳纳米管(MWCNT)/PGSC复合材料,并对复合材料的性能进行研究.结果表明,MWCNT对PGSC的玻璃化温度影响不大;随着MWCNT用量的增大,MWCNT/PGSC复合材料的弹性模量和拉伸强度总体增大,溶胀度和吸水率逐渐减小;当MWCNT用量达到或超过1份时,与PGSC相比,MWCNT/PGSC复合材料的弹性模量和拉伸强度较大,降解速率较小. 相似文献