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111.
Polyaniline (PANI) is one of the most investigated intrinsically conducting polymers. Copolymerization of aniline with aniline derivatives was considered one of the most effective and promising ways of improving the properties of PANI. In this work, firstly ethyl 3‐aminobenzoate and butyl 3‐aminobenzoate were synthesized from 3‐aminobenzoic acid by direct esterification. Then the copolymerization of 3‐amino benzoic acid, ethyl 3‐aminobenzoate, and butyl 3‐aminobenzoate with aniline was carried out by sonochemical polymerization in aqueous hydrochloric acid using ammonium persulfate (APS) as an initiator. The effects of variation in the molar ratio of the two monomers on chain structure, conductivity, and the redox properties of the copolymer are discussed. The prepared polymers are characterized by 1H NMR spectroscopy, X‐ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT‐IR). Thermal behavior of the prepared copolymers was studied by differential scanning calorimetry. The copolymers were doped with HCl and their conductivity was measured. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
112.
Facile synthesis and optimization of conductive copolymer nanoparticles and nanocomposite films from aniline with sulfodiphenylamine 总被引:1,自引:0,他引:1
A new series of electrically conductive pure copolymer nanoparticles was facilely synthesized by using oxidative polymerization of aniline (AN) and sodium diphenylamine-4-sulfonate (SDP) in acidic media in the absence of stabilizer. The variation of the structure of the copolymer particles was comprehensively studied by carefully choosing several important parameters, such as the comonomer ratio, oxidant/monomer ratio, polymerization time and temperature, monomer concentration, acidic medium, and oxidant species. Analytical techniques used include IR and UV-visible spectroscopy, X-ray diffraction, laser particle analysis, atomic force microscopy, and transmission electron microscopy. It was found that the particle size varied significantly with the above-mentioned polymerization parameters, only changes in the salt concentration in the aqueous testing solution had no noticeable effect. The polymerization conditions were optimized for the formation of copolymer nanoparticles with sought-after properties. The doped copolymer particles of AN/SDP (50:50) at an oxidant/monomer molar ratio of 0.5 exhibit a minimum length of 50 nm and a minimum diameter of 44 nm. The bulk electrical conductivity of the copolymer particles increases greatly from 5.90x10(-4) to 1.15x10(-2) S cm(-1) with increasing AN content. Compared with barely soluble polyaniline, the copolymers exhibit a remarkably enhanced solubility in most solvents, including NH4OH and even water, due to the presence of the hydrophilic sulfonic groups. Nanocomposite films of the nanoparticles and cellulose diacetate exhibit a percolation threshold of down to 0.1 wt %, at which the film retains 98% of the transparency, 94% of the strength, and 5x10(7) times the conductivity of a pure cellulose diacetate film. 相似文献
113.
采用动力学方法研究了MnO2颗粒物对TiO2光催化降解苯胺活性的影响,对比考察了光催化降解过程中苯胺溶液的UV吸收光谱的变化,并用HPLC方法鉴别了中间产物.结果表明,少量MnO2颗粒物就能使TiO2光催化降解苯胺的活性受到明显的抑制,不同结构的二氧化锰致毒效应由大到小的顺序为:δ-MnO2α-MnO2β-MnO2;降解不同时间后溶液的UV吸收光谱的变化也反映了MnO2颗粒物具有同样的致毒效应;MnO2颗粒物不改变TiO2光催化降解苯胺的途径,但对生成中间产物的基元步骤的抑制程度不同。 相似文献
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UV cured transparent films containing non‐aqueous conductive microgels coated with poly(aniline)/dodecyl benzenesulfonic acid(DBSA) were obtained. The conductive microgels were prepared by interface polymerization of aniline/DBSA in the presence of non‐aqueous polymeric microgels. The electrical conductivity and the particle size of the prepared conductive microgel were 0.5 S/cm and 58 nm, respectively. The prepared conductive microgels were easily blended with a UV curable coating formulation, and then were cured to make highly optically transparent films. For the UV cured film containing about 35 wt% of the conductive microgels, a surface resistance in the range of 107 to 108 Ω/square was obtained. In a polar cosolvent, such as NMP and m‐cresol, the critical volume was shifted to the lower range, with a value of 10 wt%. The UV cured films containing the conductive microgels exhibited good electrical stability against the thermal aging and humidity. Copyright © 2002 John Wiley & Sons, Ltd. 相似文献
116.
Electrochemical polymerization of aniline and 3-methylthiophene has been accomplished in 1-methylimidazium tetrafluoroborate (HMIMBF4) ionic liquid. Homopolymer and copolymers of aniline and 3-methylthiophene were obtained successfully. The copolymer was studied by cyclic voltammetry and electrochemical impedance spectroscopy. The formation of copolymer has been confirmed by FT-IR and UV spectra. The atomic force microscope (AFM) was used for microstructural analysis. Both the homopolymer and the copolymer had the catalytic activity for the hydroquinone. 相似文献
117.
Chang Yuan HU Feng Yi LI Rong Bin ZHANG Li HUA 《中国化学快报》2006,17(1):109-112
Carbon nanotubes (CNTs) are severely bundled and essentially insoluble in solvent. These properties are generally considered as a significant barrier toward the practical uses of CNTs. Therefore, the functionalization and solubilization of CNTs have recei… 相似文献
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Poly(aniline) (PANi) and poly(γ-glutamic acid) (γ-PGA) have been synthesized by enzymatic catalysis and natural bacterial reactions, respectively. Layer-by-layer films have been prepared on glass or quartz slides by alternative immersions of the substrate in dilute solutions of γ-PGA and PANi, with several rinsing in between each deposition. UV-vis spectroscopy has been used to follow the evolution of the self-assembly process as well as to characterize the oxidative states of PANi. The linear dependence of the absorbance vs. the number of layers indicates a constant increase of thickness layer-by-layer. The morphology of the multilayer films, analyzed by atomic force microscopy, is granular type. Enzymatically synthesized PANi nanofilms present good electrical conductivity while γ-PGA acts as an insulating material. These differences in electrical properties and the possibility to obtain alternated multilayered films permit the construction of entirely “biological” nanocapacitors. 相似文献
120.