基于溶出伏安法的水质重金属自动监测系统

基于线性扫描溶出伏安法研制了一套水质重金属自动监测系统,实现了水中铅、锌、砷、锑重金属元素的自动监测.介绍了系统的硬、软件设计,详细阐述了数据采集中虚假点识别和纠正算法、定量分析方法和富集电位等参数的配置.实验表明,该仪器具有检出限低、响应快、自动化程度高等优点,具有一定应用前景.     

cdSe_xTe_(1-x)薄膜电极光溶解性能的研究

用循环伏安法对半导体Cdse_xTe_(1-x)薄膜电池的光溶解性能进行了研究。在1mol/L KCl溶液中测量光溶解产物的阴极还原特性,考察了在多硫化钠,多硫化钾及铁氰化钾溶液中的光腐蚀行为。用此方法还研究了薄膜电极表面的光刻蚀过程和pH的影响,并用X射线光电子能谱分析光刻进行不同时间后,电极表面发生的变化。     

阴极溶出伏安法测定黄原酸盐

提出了一种测定微量有机硫化合物的方法一阴极溶出伏安法测定黄原酸盐，研究了它的溶出伏安性质和测试条件，此化合物在酸性溶液中，在电位-0．45V附近出现溶出峰。溶出峰高度与浓度在10^-6-10^-8mol／L范围内具有良好的线性关系。     

冰花镀锡工艺探讨

阐述冰花镀锡的工艺流程、要点，以及不良镀层的退除。     

锂离子电池负极材料 Na2Li2Ti6O14的嵌脱锂过程动力学研究

为了研究钛酸钠锂(Na2Li2Ti6O14)负极材料嵌脱锂的动力学行为,用溶胶-凝胶法合成 Na2Li2Ti6O14负极材料,采用 X 射线衍射法(XRD)和电子显微镜(SEM)分别对材料进行物相分析和微观形貌的观察.采用恒流充放电测试、循环伏安法(CV)和恒电流间歇滴定法(GITT)研究了 Na2Li2Ti6O14的电化学性能和嵌脱锂过程动力学.研究结果表明,制备的 Na2Li2Ti6O14材料纯度高,结晶度良好,循环稳定性好;由不同扫描速率的循环伏安法测出的 Na2Li2Ti6O14中锂离子在氧化、还原峰对应的化学扩散系数 Da和 Dc分别为7.3×10-11和7.8×10-11cm2/s;由恒电流间歇滴定技术测得的锂离子在 Na2Li2Ti6O14电极中的扩散系数为10-11~10-8cm2/s.     

Effects of current density on the corrosion behaviour of anodized aluminum alloy in FeCl3 solution

In the present study,2024 aluminum alloy specimen was anodized in acetic acid and oxalic acid electrolytcs.Effects of the currcnt dcnsity on thc microstructure and corrosion resistance of anodic oxide ...     

纳米TiO2管电化学生物传感器用于测定水体中微囊藻毒素

制作了辣根过氧化物酶和溶胶-凝胶结合Nafion-TiO2修饰石墨电化学传感器,用示差脉冲伏安法研究了该修饰电极的电化学性质,并优化了微囊藻毒素-LR(MC-LR)的测定条件.结果表明,在pH=6.5柠檬酸-NaOH-HCl缓冲溶液中,采用该修饰电极示差脉冲伏安法测定MC-LR,质量浓度在10-5～1μg/L范围内呈良好的线性关系,脉冲伏安法测定微囊藻毒素线性方程为100Δi=0.142 2logC+0.799 7,相关系数为0.995 0,最低检测限达10-6μg/L.电极的重现性及稳定性较好,连续测定10次,相对标准偏差为2.5%;4℃下储存28d后示差脉冲信号无明显变化;应用于饮用水中MC-LR的测定,样品的回收率为99.3%～102.9%.该传感器灵敏度高、稳定性好.     

Characterisation of a thiosulphate-sulphite gold electrodeposition process

Electrodeposition of soft gold is an important process in the fabrication of micro devices for electronics, optics etc. Traditional gold electroplating is based on a gold cyanide process which is not applicable for the stringent requirements in state of the art micro device manufacture. Newcastle University has been involved in the development of an industrial process based on a mixed ligand electrolyte—the gold thiosulphate-sulphite system. Here we present methods for the formulation of this electrolyte in the laboratory which ensure bath stability and process compatibility. In addition, we have carried out spectrophotometry to elucidate the possible reasons of its chemical stability. Standard rotating disk and cyclic voltammetry has been carried out to determine the electrochemical behaviour of the gold thiosulphate-sulphite system. The changes in electrochemical behaviour as the bath ages are also discussed.     

Trichloroacetic acid‐imprinted polypyrrole film and its property in piezoelectric quartz crystal microbalance and electrochemical sensors to application for determination of haloacetic acids disinfection by‐product in drinking water

A molecularly trichloroacetic acid (TCAA) imprinted non‐crosslinked polypyrole (TCAA‐MIPpy) has been successfully prepared and evaluated in its properties for both piezoelectric quartz crystal microbalance (QCM) and electrochemical means of detection, and application of such sensors for determination of haloacetic acid concentrations in water. Haloacetic acid selectivity was demonstrated in gravimetric or in electrochemical sensors via either cyclic voltammetric or inter‐digitated conductometric (IDC) analyses studies upon comparison with nonimprinted polypyrrole and TCAA‐imprinted polypyrrole. The measurement results with all these systems revealed that the prepared molecularly imprinted polymer can recognize TCAA well from structurally similar compounds. The TCAA‐MIPpy incorporated with only the IDC transduction system produced the specific signal for TCAA detection in aqueous environment, which is useful for the quantifying TCAA disinfection by‐product in water. The analytical application for determination of TCAA in real‐life samples was readily achieved with the incorporation of TCAA‐MIPpy in the IDC analysis system, the results revealing the high sensitivity and selectivity of the method. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Comparison between cyclic voltammetry and chronoamperometry when coupled with EQCM for the study of the SEI on a carbon film electrode

Cyclic voltammetry (CV) and chronoamperometry have been conducted with the electrochemical quartz crystal microbalance (EQCM) to characterize electron-beam deposited carbon film electrodes in LiClO₄-containing mixed electrolytes of ethylene carbonate (EC) and dimethyl carbonate (DMC). For a system whose electrolyte viscosity changes in the course of experiments, such as the above combination of electrode and electrolyte, the mass change per mole of electrons transferred (MPE) of the species on quartz crystals depends on the potential scan rate of CV. Chronoamperometry with a short period is more desirable for the estimation of the MPE of the solid electrolyte interphase (SEI) because the viscosity-induced frequency change, which hinders the correct MPE estimation, constitutes a small portion of the measured frequency change under this experimental condition.