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Controlled polymerization of aniline at sub-zero temperatures [Review]

机译:零以下温度下苯胺的受控聚合[综述]

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Aniline is polymerized by oxidation with ammonium persulfate in aqueous hydrochloric acid solutions at sub-zero temperatures down to -43 degrees C in the presence of LiCl and ethanol. The polymerization is controlled by concomitant potential, temperature and pH profiling. The concentrations of LiCl and ethanol are so determined to enable complete dissolution of the reactants in solution and to prevent freezing. Six polymerization steps were identified at low temperatures. The reduction of primarily synthesized pernigraniline to emeraldine with FeCl2 is investigated. The as-synthesized and deprotonated emeraldine is purified by extraction with chloroform. The polyaniline is characterized by viscosity, gel permeation chromatography (GPC), UV-Vis-NIR spectroscopy, conductivity, X-ray diffraction and chlorine analysis. High molecular weight polyanilines are synthesized at temperatures lower than -25 degrees C having inherent viscosities within 2.0-2.15 dl/g, M-n = 30 000 g/mol, M-w= 140 000-170 000 g/mol, with M-w/M-n = 2-3. The polymers in the emeraldine base form dissolved in NMP-0.5% LiCl show a more planar conformation as indicated by the wavelength of the exciton peak reaching 680 nm. An enhanced crystallinity in terms of structural perfection is observed by means of X-ray diffraction spectra. The UW-Vis-NIR spectra of polyanilines reduced with FeCl2, protonated with (+/-)-10-camphorsulfonic acid (CSA), in m-cresol show a smeared polaron peak shifted into the UV. They show a broad convex NIR band peaking far beyond 2700 nm indicating an enhanced polaron delocalization. The conductivity of the films of emeraldine protonated by CSA cast from m-cresol are higher than 300 S/cm for polymers with inherent viscosities exceeding 1.8 dl/g and show an enhanced resistance to ageing. The purification of the emeraldine base by extraction with chloroform increases the molecular weight of the polymers and leads to an enhanced conductivity of the films. Polymers synthesized at low temperatures with FeCl2 reduction have better physical properties probably on account of less branching. (C) 1998 Elsevier Science S.A. All rights reserved. [References: 103]
机译:在过氯酸和乙醇的存在下,通过过硫酸铵在盐酸水溶液中于零下温度降至-43摄氏度下氧化,从而使苯胺聚合。聚合反应是通过伴随的电势,温度和pH曲线来控制的。确定LiCl和乙醇的浓度以使反应物完全溶解在溶液中并防止冻结。在低温下鉴定出六个聚合步骤。研究了用FeCl2将最初合成的肾上腺素减少为翡翠。通过用氯仿萃取纯化合成和去质子化的翡翠。聚苯胺的特征在于粘度,凝胶渗透色谱(GPC),UV-Vis-NIR光谱,电导率,X射线衍射和氯分析。高分子量聚苯胺是在低于-25摄氏度的温度下合成的,固有粘度在2.0-2.15 dl / g之间,Mn = 30 000 g / mol,Mw = 140 000-170 000 g / mol,Mw / Mn = 2 -3。溶解在NMP-0.5%LiCl中的翡翠碱形式的聚合物表现出更平坦的构象,如激子峰的波长达到680 nm所示。通过X射线衍射光谱观察到在结构完善性方面增强的结晶度。在间甲酚中,用FeCl2还原的聚苯胺的UW-Vis-NIR光谱用(+/-)-10-樟脑磺酸(CSA)质子化,显示涂污的极化子峰移向UV。它们显示出一个宽的凸NIR峰,其峰远超过2700 nm,表明极化子离域增强。对于固有粘度超过1.8 dl / g的聚合物,由间甲酚浇铸的CSA质子化翡翠膜的电导率高于300 S / cm。通过用氯仿萃取提纯翡翠碱,可增加聚合物的分子量,并提高薄膜的电导率。在低温下通过还原FeCl2合成的聚合物可能具有更好的物理性能,这可能是由于支化程度较低。 (C)1998 Elsevier Science S.A.保留所有权利。 [参考:103]

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