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1.
静电纺丝法制备聚丙烯腈/聚苯胺复合纳米纤维及其表征   总被引:1,自引:0,他引:1  
利用静电纺丝技术,以聚丙烯腈(PAN)和苯胺(ANI)为前驱物,用过硫酸胺(APS)溶液在低温下缓慢氧化聚合,制备了PAN/PANI复合纳米纤维,直径约500 nm.通过扫描电子显微镜(SEM)、红外光谱(FTIR)、X射线衍射(XRD)和激光拉曼(RAMAN)光谱仪等测试手段对材料的形貌和结构进行了表征.探讨了材料制备过程中影响纤维形貌、尺寸、均匀度的因素和PANI含量对复合纤维导电性能的影响,结果表明,PAN浓度、ANI的加入量和电压是影响纤维特性的主要因素;PANI在PAN基体中呈纳米尺寸分布,复合纳米纤维具有良好的导电性能,导电率可达10-2S/cm.  相似文献   

2.
采用静电纺丝技术将导电聚苯胺(PANI)和铕/铽稀土配合物掺杂到高分子基质聚乙烯吡咯烷酮(PVP)中,制备出荧光导电复合纳米纤维。用扫描电镜(SEM)、荧光光谱仪(FL)、宽频介电松驰谱仪对荧光导电复合纳米纤维的性能进行分析,结果显示,在270nm紫外光激发下,铕系列与铽系列复合纳米纤维分别发出红光和绿光。同时,复合纳米纤维的电导率可以达到1.18×10~(-6) S/cm,两种复合纳米纤维同时具有优异的荧光性能及良好的导电功能。  相似文献   

3.
采用静电纺丝技术将聚苯胺(PANI)和稀土配合物Eu(BA)3phen掺杂到高分子材料聚乙烯吡咯烷酮(PVP)中, 制备出新型的具有光电双功能的Eu(BA)3phen/PANI/PVP复合纳米纤维. 采用扫描电子显微镜、 X射线能量色散谱仪、 荧光光谱仪及宽频介电松弛谱仪对样品进行了表征. 实验结果表明, 复合纳米纤维直径为(270±31) nm. 在275 nm紫外光激发下, Eu(BA)3phen/PANI/PVP复合纳米纤维发射出主峰位于580, 594和617 nm的红光, 对应于Eu3+的 5D0→7F0, 5D0→7F1和5D0→7F2跃迁. 当m[Eu(BA)3phen]:m(PANI):m(PVP)=15:10:100 时, 复合纳米纤维的荧光发射最强. 复合纤维的电导率随PANI含量的增大而升高. 在m(PANI):m(PVP)=50:100时, 其电导率在高频(106 Hz)下达到1.5×10-6 S/cm.  相似文献   

4.
采用静电纺丝技术将聚苯胺(PANI)和稀土配合物[Tb(BA)3phen]掺杂到高分子材料(PVP)中,制备出一类新型的具有光电双功能的Tb(BA)3phen/PANI/PVP复合纳米纤维.用扫描电子显微镜(SEM)、X射线能量色散谱仪(EDS)、荧光光谱仪及宽频介电松弛谱仪对样品进行了表征.结果表明,复合纳米纤维直径为(331±43)nm.在276 nm紫外光激发下,Tb(BA)3phen/PANI/PVP复合纳米纤维发射出主峰位于491,547和585 nm的绿光,对应Tb3+的5D4→7F6,5D4→7F5和5D4→7F4跃迁.当Tb(BA)3phen∶PANI∶PVP的质量比为15∶10∶100时,复合纳米纤维的荧光发射最强,其电导率随PANI含量的增大而升高,在PANI∶PVP为50%(wt%)时,其电导率在高频(106Hz)下达1.531×10-6S/cm.  相似文献   

5.
以不同链长的脂肪酸为配体,1,10-邻菲啰啉为第二配体,通过与发光稀土铕离子进行配位,合成了铕-脂肪酸相变和发光配合物;再采用静电纺丝技术以聚丙烯腈(PAN)为载体基质,铕-脂肪酸为相变和发光材料制备了一种新型的相变和发光纳米纤维.用扫描电镜(SEM)、X射线能量色散谱仪(EDS)、荧光光谱仪(FL)和差示扫描量热仪(DSC)对相变和发光纳米纤维的性能进行分析.研究结果显示,复合纳米纤维的直径在285~600 nm,在280 nm紫外光激发下,复合纳米纤维发射出主峰位于580,593和614 nm的红光,对应Eu3+的5D0-7F0,5D0-7F1及5D0-7F2跃迁.相变和发光纳米纤维具有优异的荧光性能及相变功能,纳米纤维的直径随着铕含量和脂肪酸碳链的增加呈现增大的趋势.  相似文献   

6.
以聚对苯二甲酰对苯二胺(简称芳纶,PPTA)纤维为基材,使用环氧氯丙烷(ECP)对PPTA表面进行有机修饰,得到了ECP改性的PPTA纤维(ECP-PPTA),然后使苯胺单体在ECPPPTA表面接枝聚合,制备了ECP-PPTA/PANI复合导电纤维。用傅里叶变换红外分光光度计(FT-IR)、扫描电子显微镜(SEM)、热重分析仪(TGA)及X射线衍射分析仪(XRD)等分析测试方法对ECP-PPTA及ECP-PPTA/PANI复合导电纤维进行了表征。结果表明:PPTA经ECP改性后,PANI成功接枝在PPTA表面,制备的ECP-PPTA/PANI复合导电纤维的电阻率低于PPTA/PANI纤维的,其室温电阻率最低为0.32MΩ·m。  相似文献   

7.
以不同含水量细菌纤维素为模板,苯胺单体为原料原位聚合生成聚苯胺,制备出不同含水量细菌纤维素/聚苯胺(HBC/PANI、LBC/PANI及DBC/PANI)复合凝胶膜,系统研究了细菌纤维素凝胶膜含水量和反应时间对苯胺原位聚合以及复合凝胶膜微观形貌、电学性能和力学性能的影响.扫描电镜照片表明聚苯胺均匀包覆在BC纤维上形成导电网络结构;四探针测试表明聚合时间90 min时导电率最高;低含水量加快了聚合反应速度,提高了复合凝胶膜的电导率,而完全干燥则使电导率降低;交流阻抗测试也表明低含水量可以明显提高材料的离子导电性;力学性能测试结果表明了BC/PANI复合凝胶膜具有良好的机械性能,抗拉强度可达0.21 MPa,同时低含水量不会降低复合凝胶膜的力学性能.  相似文献   

8.
通过在芳纶浆粕(AP)表面修饰聚苯胺(PANI)制备了聚苯胺-芳纶浆粕(PANI-AP), 然后与碳纤维(CF)共混, 采用湿法抄纸技术制备导电性能优异的纸基材料(PANI-AP/CP). 对其形貌结构、 导电性能及PANI分布均匀性进行了表征, 并研究了环境湿度、 温度、 pH值及放置时间对PANI-AP/CP导电性能的影响. 研究结果表明, PANI-AP表面粗糙度增加, 结晶度增加, 出现含醌式结构的导电PANI的衍射峰, 说明PANI成功修饰于AP表面. 采用该方法制备的PANI-AP/CP导电性能与分布均匀性均得到提高, 相对于碳纤维纸基材(CP), PANI-AP/CP的电导率为3.937 S/cm, 导电性能提高153.5%. 与PANI原位生长于CP(AP/CP-PANI)相比, PANI-AP/CP的导电性能提高34.6%, 总色差值(DE)降低74.9%.  相似文献   

9.
复合乳化剂微乳液法制备聚苯胺及其电化学性能   总被引:1,自引:0,他引:1  
采用复合乳化剂微乳液法合成了导电聚苯胺(PANI),以碳纸负载PANI为工作电极,考察了十二烷基苯磺酸钠(SDBS)和聚乙二醇辛基苯基醚(TX-100)的配比及其复合乳化剂(E)和氧化剂(APS)用量对复合乳化剂微乳液法合成PANI电化学性能(循环伏安、塔费尔)的影响;通过对产物电导率和产率的对比分析,印证了PANI电化学性能表征结果的有效性。结果表明:当SDBS与TX-100的质量比为1/2,E与苯胺(An)单体的质量比为5/3,APS与An的摩尔比为1.2时,PANI的各项性能指标达到最好,且产物的循环伏安峰电流、腐蚀电位和电导率均高于单组分乳化剂SDBS或TX-100微乳液法制备的PANI。  相似文献   

10.
分别采用粉末碳纳米管(CNT)和带连接点的碳纳米管网(CNTN)为模板,通过与聚苯胺(PANI)有限域聚合得到了CNT/PANI和CNTN/PANI 2种复合材料.采用透射电子显微镜和扫描电子显微镜对材料的形貌进行了表征,采用氮气吸附-脱附分析研究了材料的孔结构参数,运用双电四探针测试仪对材料的导电性能进行了测试,利用恒流充放电、循环伏安、循环寿命及交流阻抗等电化学测试手段表征了材料的电化学储能性能.结果表明,CNTN/PANI复合材料比CNT/PANI复合材料表现出更好的导电性能和电化学储能性能,其放电比容量可达到143.2 F/g(有机电解液).  相似文献   

11.
Polyaniline (PANI)/Au composite hollow spheres were successfully synthesized using polystyrene/sulfonated polystyrene core/shell gel particle templates. The PANI shell thickness and the number of Au nanoparticles decorating the PANI could be controlled effectively by adjusting the experimental conditions. The morphology, composition, and optical properties of the resulting products were characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, thermogravimetric analysis, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and ultraviolet-visible absorption spectra. It was found that the electrical conductivity of the PANI/Au composite hollow spheres was more than 3 times higher than that of the pure PANI hollow spheres. Furthermore, PANI/Au composites were immobilized on the surface of a glassy carbon electrode (GCE) and applied to construct a sensor. The obtained PANI/Au-modified GCEs showed one pair of redox peaks and high catalytic activity for the oxidation of dopamine. The possible formation mechanism of the PANI/Au composite hollow spheres was also discussed.  相似文献   

12.
Summary: Composite polyurethane/polyaniline (PU/PANI) films have been chemically prepared by oxidative in-situ polymerization of aniline inside the previously swelled PU film. Swelling kinetic studies have shown that for PU films the swelling degree of aniline is 25 wt.%. The dielectric and electrical properties of the composite films were measured using dielectric relaxation spectroscopy and four-probe method. Dielectric measurements as a function of temperature and frequency revealed the presence of a relaxation process for the composite PU/PANI-HCl film. This relaxation was explained in terms of interfacial polarization due to the double-layered structure of the composite film. The activation energy values found by dielectric and electrical measurements are close and this result confirms the conducting character of the PANI containing layer.  相似文献   

13.
聚苯胺/碳纳米纤维复合材料的制备及电容性能   总被引:1,自引:0,他引:1  
采用原位聚合法制备了聚苯胺/碳纳米纤维(PANI/CNF)复合材料,用傅里叶变换红外(FT-IR)光谱、热重分析(TGA)、扫描电镜(SEM)和孔分布及比表面积测定仪研究了复合材料的表面官能团、组成、表面形貌及比表面积,并运用循环伏安(CV)法和计时电位法测试了PANI/CNF布作为电极材料的电化学性能.研究结果表明:PANI/CNF复合材料具有粗糙的毛刺结构,PANI沿碳纳米纤维均匀分布;PANI/CNF电极氧化还原反应的可逆性良好;在100mA·g-1电流密度下,当PANI含量为44.4%(w)时,复合材料比电容量高达587.1F·g-1,比能量为66.1Wh·kg-1,电流密度为800mA·g-1时比功率可达1014.2W·kg-1;在5A·g-1的电流密度下,1000次循环充放电后,复合材料的比电容量衰减28%.PANI/CNF复合材料具有良好的导电性和快速充放电能力,是一种优良的超级电容器电极材料.  相似文献   

14.
The dielectric investigations of porous synthetic silica gel modified with polyaniline (PANI) and polyethylene glycol (PEG) polyblend at various concentrations are demonstrated in this paper. By using the chemical oxidative process to embed polyaniline (PANI) and polyethylene glycol (PEG) into a silica matrix, conducting gel nanocomposites were synthesized. For various dopant concentrations, the dielectric permittivity (ε′), D.C. conductivity (σdc), loss tangent (tanδ) and dielectric loss (ε″) were investigated. The samples were characterized using differential thermal analysis/thermogravimetric analysis, Fourier transform infrared spectroscopy and high-resolution transmission electron microscopy. Depending on the co-blend content, PANI-PEG modified silica structures produce nanoparticles ranging in size from 9.9 to 48.1 nm. The variation of DC conductivity (σdc) with PANI/PEG content shows Maxwell-Wagner Sillars (MWS) effect confirming the role of the conjugation and the structural order.  相似文献   

15.
In this study, polyamide6 (PA6) nanofiber mats were fabricated through the electrospinning process. The nanofibers were coated by polyaniline (PANI) using the in situ polymerization of aniline in the presence of graphene oxide. The composite of the PANI/graphene oxide–coated nanofiber mat was treated with hydrazine monohydrate to reduce graphene oxide to graphene, and this was followed by the reoxidation of PANI. Field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), wide angle X‐ray diffraction (WAXD), thermal gravimetric analysis (TGA), tensile strength tests, electrical conductivity measurements, cyclic voltammetry (CV), and charge/discharge measurements were conducted on the composite PA6/graphene nanofiber mats. It was found that the surface of the PA6 nanofibers was coated uniformly with the granular PANI and graphene oxide. Besides, the composite nanofibers showed good tensile and thermal properties. Their electrical conductivity and specific capacitance, when used as a separator in the cell, were 1.02 × 10?4 S/cm and 423.28 F/g, respectively. Therefore, the composite PANI/reduced graphene oxide–coated PA6 nanofiber mats could be regarded as suitable candidates for application in energy storage devices.  相似文献   

16.
Polyaniline (PANI) nanocomposites incorporating different loadings of graphene and various other carbon nanostructures including carbon nanotubes (CNTs) and carbon nanofibers (CNFs) have been synthesized using a surface-initiated polymerization (SIP) method. Transmission electron microscopy (TEM) results indicate that the graphene has been exfoliated into a few layers (typically one, two, and three layers) during polymerization and has been uniformly dispersed in the PANI matrix. The graphene layer dispersion degree is quantified by a free-path spacing measurement (FPSM) method based on the TEM microstructures. The SIP method also demonstrates its feasibility for coating PANI on one-dimensional (1D) CNFs and CNTs without introducing additional surface functional groups. The effects of graphene size, loading level, and surface functionality on the electrical conductivity and dielectric permittivity of their corresponding nanocomposites have been systematically studied. The temperature-dependent conductivity behavior revealed a quasi-3D variable range hopping (VRH) electron transport mechanism for all the nanocomposites. Giant magnetoresistance (GMR) at room temperature is observed in pure PANI, which can be enhanced by the incorporation of a high loading of graphene (5%) due to the π-π stacking-induced efficient electron transport at the PANI/graphene interface. More interestingly, negative permittivity is found in each composite which can be easily tuned by adjusting the filler loading, morphology, and surface functionality.  相似文献   

17.
通过真空抽滤的方法制备碳纳米管纸,并对其进行循环伏安电化学氧化处理.以该电化学氧化处理的碳纳米管(CV-CNT)纸为基体,采用电化学聚合沉积聚苯胺(PANI),随后吸附石墨烯(GR),制备具有三明治夹心结构的碳纳米管/聚苯胺/石墨烯(CV-CNT/PANI/GR)复合纳米碳纸.该结构外层为GR,内层由PANI包裹的CNT形成网络骨架,充分发挥三者各自优势构建柔性电极材料.用场发射扫描电镜(FE-SEM)、透射电子显微镜(TEM)、拉曼光谱对其形貌与结构进行表征,并测试其电化学性能.研究发现:PANI呈纳米晶须状,并均匀包裹在CV-CNT表面;该复合碳纸具有良好的电容特性、大电流充放电特性以及良好的循环稳定性能.电流密度为0.5A·g-1时,比电容可达415F·g-1;20A·g-1时仍能保持106F·g-1的比电容.由于GR的保护作用,1000次循环之后较CV-CNT/PANI保持更高的有效比电容.该CV-CNT/PANI/GR复合碳纸展现出在高性能超级电容器柔性电极材料的潜在应用价值.  相似文献   

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