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Harold E. Hager 《Journal of Applied Electrochemistry》1986,16(2):189-195
Despite growing interest in pulse current electroplating, published theories have not evolved beyond treatments of simple, single-step reaction kinetics. This omission of multiple-step kinetics and associated reaction pseudocapacitance is responsible for the inability to interpret mechanistically several key pulse current electrodeposition process characteristics.A complex kinetics charge transfer model is developed to describe the enhanced geometric control of deposit thickness achievable with judiciously chosen pulse current control conditions. This semiquantitative analysis demonstrates that deposit thickness levelling is primarily the result of the strong potential dependence of the reaction pseudocapacitance, together with proper choices of pulse current control variables. For any system of interest, a well defined on-time current,I
A, and on-time and off-time periods,t
A andt
B, are optimum for minimizing relative deposit thickness variation. 相似文献
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The kinetics of the intercalation of graphite was investigated by measuring the c-face surface profiles during the intercalation of Br2 into highly-oriented pyrolytic graphite cylindrical discs at room temperature. A sharp intercalate front was observed to advance while the surface profile evolved from a bucket-shape to a V-shape, as predicted by the model of interface-controlled intercalation proposed by the authors [11]. The average magnitude of the steady velocity of the front was ~ 15 Å/see; the initial period was marked by a larger velocity attributed to an edge effect. The same behavior was observed during ICI intercalation at room temperature. During desorption, inverted surface profiles were obtained, indicating that desorption may be the reverse of intercalation. In the case of HNO3 intercalation at room temperature, bowl-shaped surface profiles were observed. Preliminary profile measurements were made during ICI intercalation at 50°C, at which the intercalate layers are known to be disordered. 相似文献
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We investigate the effects of denatonium benzoate (Bitrex) on the electrodeposition of copper films from a boric acid bath using scanning electron microscopy, cyclic voltammetry, electrochemical quartz microbalance (EQCM) measurements and corrosion studies. In the absence of Bitrex, pure copper films grown by this method are optically black owing to the appearance of complex surface nanostructures. The addition of Bitrex acts as a levelling agent preventing the formation of these nanostructures even for concentrations as low as 0.02 mM producing a lustrous film with low surface roughness. Bitrex is also found to improve the corrosion resistance by up to a factor of 20 and increase the current efficiency by over a factor of two. Bitrex is hypothesised to act directly on the cathode, partially inhibiting the growth or lowering the deposition current. 相似文献
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电镀集中区电镀废水的处理 总被引:6,自引:0,他引:6
废水处理是电镀集中区建设成功的关键.提出了搞好电镀集中区中电镀废水处理的一些前提与方法:首先要按清洁生产的要求对入驻集中区的企业进行审核,同时要认真剖析集中区内电镀废水的特点,运用循环经济的理念对不同电镀废水进行分类收集,采用最佳的废水处理技术,并根据"集散控制模式"进行处理,以达到回用废水及回收废水中有价值的重金属的理想效果.对各种先进的处理技术(包括化学法、膜分离技术、螯合沉淀法、HR型除铬机、生化法和高压脉冲电凝加硅藻土整合技术)进行了对比.推荐采用国外某公司的重金属捕捉剂. 相似文献
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A sensor based on limiting current density characteristics of a wire tip electrode has been shown to be capable of measuring local variations of agitation and its effect on coating thickness variations during electrodeposition. The effectiveness of agitation is expressed as an enhancement factor. 相似文献
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针对工业园区电镀废水处理中生化指标达标难的问题,采用新型聚四氟乙烯(PTFE)膜组件构建膜生物反应器(MBR),通过现场试验研究了MBR工艺处理电镀废水的实际效果。结果表明,通过合理的维护管理,MBR膜通量能稳定维持在16.67L/(m2·h)左右,对COD的去除率可达到50%以上,出水COD质量浓度稳定在80mg/L以下,但对氨氮的去除效果受水力停留时间(HRT)、温度、系统负荷等因素的影响较大。与传统的生物接触氧化工艺相比,基于新型膜材料的MBR工艺可以大大提高污泥量,避免结垢和出水跑泥等问题,提高了处理效果。从投资运行费用来看,采用MBR工艺的总投资费用高于普通生化处理工艺,运行费用约为2元/t。 相似文献
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The electrode reaction mechanism of electrolytical coating by nickel on paraffin impregnated graphite electrode (PIGE) was investigated by cyclic voltammetry (CV) and elimination voltammetry with linear scan (EVLS). The EVLS, a relatively new method of processing electrochemical signals obtained by voltammetry, is able to eliminate some individual chosen currents from total voltammetric currents measured at different scan rates. During the electrodeposition of metals on the graphite electrode, hydrogen evolved from aqueous acidic solutions interferes with the plating process. The elimination of kinetic current arising due to hydrogen evolution enables one to study other processes proceeding at the electrode. Cyclic voltammograms for metal coating deposition/dissolution on the graphite electrode were measured at three scan rates (12.5, 25 and 50 mV/s) and the EVLS functions were calculated for one or two eliminated currents. The results indicate the occurrence of surface reactions with the adsorption of intermediates on graphite. The application of EVLS provides deeper insight into the mechanism of electrode reaction during metal deposition. 相似文献
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