Synthesis,characterization, and redox and electrochromic behaviors of poly(3-n-octyloxythiophene)

Poly(3-n-octyloxythiophene), a conjugated polymer, which possessed solubility in common organic solvents, was synthesized by electrochemical polymerization in the presence of lithium perchlorate as the supporting electrolyte and sodium dodecyl sulfate as the surfactant in an aqueous medium. Characterizations of the intermediate, monomer, and polymer were performed by NMR spectroscopy, Fourier transform infrared spectroscopy, ultraviolet–visible spectroscopy, and gel permeation chromatography. The process of electrochemical polymerization and the electrochemical redox behaviors were investigated by cyclic voltammetry and the potentiostatic method. A poly(3-n-octyloxythiophene) film that was deposited on a platinum electrode was found to exhibit electrochromic behaviors, and it switched electrochemically between blue–green oxidized and dark red reduced states. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

Ti_3Al金属间化合物的熔盐热腐蚀

采用电化学方法并结合扫描电镜、X 射线衍射、电子探针和能谱等物相分析技术研究了 Ti_3Al 金属间化合物在800℃熔融 NaCl-(Na,K)_2SO_4体系中的腐蚀行为。结果表明,Ti_3Al 合金耐熔盐腐蚀性能远低于 Ni 基 IN738合金。腐蚀时在合金表面形成外层为 TiO_2;内层为富 Nb 的Nb_2O_5,Al_2O_3,TiO_2的混合层和中间层为富 Al 的 TiO_2,Al_2O_3混合层的多层腐蚀层结构。Ti 快速向外扩散和氧向内扩散使合金表面腐蚀产物层迅速增厚。腐蚀产物内层的富 Nb 氧化物破坏了膜层与合金基体的粘附性。     

Novel polymeric aromatic lithium sulfonylimides as salts for polymer electrolytes

Three new polymeric aromatic lithium sulfonylimides were used as salts in high molecular weight poly(ethylene oxide) (PEO) electrolytes. Their conductivity and electrochemical stability behaviors were investigated. The electrolytes with lithium poly[4,4′‐(hexafluoroisopropylidene)diphenoxy]sulfonylimide (LiPHFIPSI) showed a better conductive performance compared with the other two lithium salts. The best conductivity was obtained for PEO/LiPHFIPSI EO/Li = 16 (1.90 × 10^?4 S/cm at 60°C). Thermal analysis indicated that the salts effectively decreased the crystallinity of PEO. Moreover, the electrolytes also had good electrochemical stability and their oxidative potential was to 5.5 V versus Li/Li⁺. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 85: 1802–1805, 2002     

钢筋混凝土结构内的钢筋腐蚀监测

用钢筋混凝土修建的建筑物和构筑物，因受外界因素的影响，其内部钢筋可能会受到腐蚀而生锈，锈蚀严重者将危及安全。根据钢筋在混凝土内的锈蚀是一个电化学过程的特点，在不损伤钢筋混凝土结构的条件下，利用腐蚀监测仪，测量钢筋混凝的电化学特性值，并以此特性值绘制等值线图，利用该图能正确评估混凝土内钢筋受腐蚀的情况。     

基于两电极体系的水质检测分析平台设计

为实现对水质的多参数检测,设计了一个基于两电极体系的水质检测分析平台。该检测平台通过最小化极化电流的思想,采用辅助电极面积远大于工作电极的电极参数,设计了基于两电极体系的集成电极和软硬件系统,摈弃了传统三电极体系的参比电极,同时克服了传统三电极体系容易污染样品的缺点,能实现电化学工作站的诸多功能。本研究在该检测平台上开展了水样的电导率(EC)、pH和重金属浓度的检测研究,获得了较好的结果,可用于实验室及工业现场的水质监测。     

重金属强化含金矿石的氰化浸出

通过分析铊、铋、汞和铅等重金属强化金氰化溶解的电化学原理,对含金氧化物矿石和难浸硫化物金精矿进行了重金属强化浸金研究.结果表明:重金属对金氰化溶解的阳极过程有显著的强化作用,但在常规供氧条件下,金的溶解速率并未显著提高;只有同时采用阴极强化措施,才能使重金属起到显著提高金溶解速率的作用;对于含金氧化物矿石,单独采用重金属强化即可明显提高浸金速率,如果在过氧化氢助浸的基础上添加重金属,金的浸出速率会有更大幅度的提高;对硫化物金精矿而言,单独采用重金属无明显强化效果,只有在添加过氧化氢作为辅助氧化剂的基础上,重金属对金的浸出才能起到强化的作用,该体系中过氧化氢起到了强化阴极过程和氧化硫化物的双重作用.     

时效对2195铝锂合金腐蚀行为的影响

研究了2195铝锂合金在不同时效状态下的晶间腐蚀和剥落腐蚀行为.结果表明:2195合金在自然时效状态下具有较好的抗晶间腐蚀和剥落腐蚀能力,但随着在160℃时效时间的延长,其晶间腐蚀与剥落腐蚀倾向逐渐增加;在剥落腐蚀溶液中进行的极化曲线测试也表现出相同的趋势.透射电镜观察发现:2195合金主要析出相为T1相;随着时效时间延长,T1相逐渐粗化,在晶界处还会出现无析出带及平衡相.模拟相实验证实,由于T1相和无析出带的开路电位都明显低于铝基体的,在腐蚀性介质中作为阳极相优先溶解,从而导致2195合金产生晶间腐蚀及剥落腐蚀.过时效状态与峰时效状态相比,晶界平衡相增多,无析出带变宽,晶间腐蚀及剥落腐蚀程度将更加严重.     

电化学方法研究碳钢高温水体系中的氢扩散和渗透

本文应用Devanathan渗透装置的原理,设计了一套能用于测量碳钢-高温水体系中氢在碳钢中的扩散和渗透的实验装置,找出了该装置用于测量的最佳工作参数,并用该装置测量了373—473K下氢在碳钢中的扩散系数和扩散速率,讨论了氢在碳钢上还原的机理。     

Characterization of conducting poly(3‐methylthiophene) films prepared under sono‐electrochemical conditions

Poly(3‐methlthiophene) films were prepared under “silent” and “sono‐electrochemical” potentiostatic (SEP) conditions. A three‐electrode one‐compartment sono‐cell was used with a working platinum disc electrode. The sono‐electrochemically formed polymer films were deposited with different working electrode‐to‐horn distances. The composition, electrochemical, spectroscopic, and morphological characteristics of the resulting polymer films were determined. Elemental analysis, FTIR‐spectra, and X‐ray photoelectron spectroscopy (XPS) data proved that the polymer films prepared under SEP conditions have predominant α‐α′‐couplings between the 3MT units, and the aromatic ring integrity is maintained in the film. Scanning electron microscopy showed that those films are more compact and less porous compared to the films prepared under silent conditions. The use of sono‐irradiation during electropolymerization enhanced the diffusion of the monomer units towards the electrode surface and resulted in relatively less doped polymers with less conductivity. Electrochemical impedance spectroscopy (EIS) data for films prepared under silent and SEP conditions were collected in a monomer‐free solution. The results show that the impedance of SEP films is relatively higher than those prepared under silent conditions, and a combination of charge transfer kinetics with diffusion‐controlled conduction mechanism within the films. The diffusion was found to be a function of the porosity of the film. Conductivity measurements are in good agreement with EIS, elemental analysis, and XPS data. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 2416–2425, 2006     

三价铬电镀用氧化物涂层钛电极的电化学行为

采用极化曲线、循环伏安曲线及钝化曲线研究了三价铬电镀用含IrO2涂层钛电极的电化学行为.电极表面的扫描电镜照片表明,部分IrO2分散在针状结晶中,其余则分散在非晶相中.分析了三价铬镀铬过程中产生六价铬的原因.所研制的I型氧化物涂层钛电极具有高的析氧活性,其电催化活性与国外某公司的钛电极相当.在三价铬镀铬过程中,采用该电极连续电解120 A·h后,镀液中无Cr(Ⅵ)产生.