Electrode reaction during electrochemical chloride extraction of reinforced concrete 电化学除盐过程中钢筋表面发生的电极反应
And the effect of ultrasonic-aided condition on the electrode reaction and the mechanism of ultrasonic-aided leaching gold from refractory gold ores are analyzed. 并由此分析了超声波对金矿浸出的作用机理和对电极反应的影响。
Since the electrode reaction has been changed, The voltage of the electrolyzer has been reduced by about1V. 这改变了电极反应,使电解槽的槽电压降低1.0伏左右。
The speed of electrode reaction is affected by the sizes of hole and grain of cathode. 阴极的孔隙大小和颗粒尺寸会影响电极反应的速度。
And the degradation of thiram by Cu2+ was also studied by spectrophotometry. Furthermore, its electrode reaction mechanism was proposed in this paper. 同时还结合分光光度法研究了Cu~(2+)对福美双的降解行为,并探讨了该极谱波的电极过程机理。
A new method was established for the direct determination of trace amount Sc in pure Yttria. Furthermore, the polarographic behaviour and the electrode reaction mechanism was studied. 用此方法测定了纯氧化钇中的微量钪,并探讨了该极谱波的性质和电极反应机制。
Tourmaline's Surface Absorption and Its Electrode Reaction Research 电气石的表面吸附与电极反应研究
Moreover, the kinetics parameters of electrode reaction are investigated by multi electrochemical techniques. 此外,还研究了电极反应的动力学参数。
METHODS: The electrochemical behavior of theophylline was studied with multi semi differential electrochemical instrument, the reversibility of electrode reaction and the electro reduction mechanism were investigated with cyclic voltammetry and UV spectrometry, respectively. 方法:多阶半微分电化学方法研究茶碱的电化学还原行为,循环伏安和紫外光谱法研究其可逆性和电还原机理。
Mechanism of the electrode reaction was also discussed briefly. 讨论了电极的响应机理。
The process of U(ⅵ) electro-reduction is mainly electrode reaction controlled. 在本文实验范围内,U(Ⅵ)电还原过程由电极反应控制。
Effect coefficients ( Ψ a and Ψ c) of hydrodynamic factor on electrode reaction were defined and then analyzed. 定义了流体力学因素对电极反应的作用系数(Ψa和Ψc),并进行了计算与分析。
Moreover, by means of cyclic voltammetry the electrode reaction has been studied. 此外,还用循环伏安法研究了电极反应的可逆性。
The theory of semidifferential cyclic voltammetry for simple electrode reaction at hemispherical microelectrode has been described. 介绍了超微半球电极上具有简单电极反应时的半微分循环伏安理论。
Effects of formation of complexing ions in electroplating on cathodic electrode reaction, standard electrode potential, overpotential and metal deposition potential are also discussed, therefore providing im-portant theoretic basis for alloy electroplating. 阐述了络离子的形成对阴极电极反应、标准电极电位、过电位和电镀时金属析出电位的重要影响,从而为合金电镀提供了重要的理论依据。
The electrode reaction process had been investigated in detail by lots of electrochemistry techniques, and its dynamics parameters had been obtained. Also, the determined methods for 8-AG, which was sensitive and fast has been performed. 电极反应过程利用多种电化学技术进行了详细研究,求得了对应的动力学参数,建立了灵敏、快速的8-AG的检测方法。
Preliminary studies on the kinetic process of electrode reaction in full Li/ LiMn2O4 battery system were also conducted by CV and EIS. 通过实验电池的循环伏安特性和交流阻抗谱测量,对Li/LiMn2O4电池体系的电极反应动力学过程进行了初步研究。
We studied trivalence chromium ion electrode reaction on three different surface state by cyclic voltammetry, discussed electrode activation influence on electrode reaction, and analysed the mechanism of electrode reaction. 应用循环伏安法考察了三价铬离子在三种不同表面状态石墨电极上的电极反应,探讨了电极表面活化处理对三价铬离子的电极反应的影响,并分析了电极反应的机理;
The current character, the reversibility and the mechanism of electrode reaction etc. were also studied. 文中对体系的电流特性,电极反应过程的可逆性,电极反应机理等也进行了研究。
The kinetics of the electrode reaction is preliminarily studied by linear potential sweep technique and electrochemical impedance while electrodepositing Ni for high aspect ratio structures. 采用线性电位扫描和电化学交流阻抗等电化学测量技术,对高深宽比掩膜条件下微电铸镍的电极反应动力学过程进行了初步研究。
Obvious electrochemical oscillations in Daniell cell, including electromotive force oscillation and its electrode reaction oscillation, were found as adding emulsion to form electrolytic emulsion. 将大量乳液加入丹尼尔电池中,形成电解质乳状液,由此产生了明显的电化学振荡,包括电池电动势振荡和电极反应的振荡。
The properties of the polarographic wave was discussed with direct current polarography and voltammetry in this paper. It is a adsorptive complex wave with catalysis. The complex ratio is 2:1. The electrode reaction is reversible. 用直流极谱法和循环伏安法对该波的电化学性质进行了研究,表明该极谱波是一具有催化作用的络合吸附波,络合比为2∶1;
The reversibility of the electrode reaction of poly ( N methyl) aniline was inspected by cyclic voltammetry. 用循环伏安法考察了聚(N-甲基)苯胺电极反应可逆性;
The different modification, methods of electrode surface have different effects on the electrode reaction of Cyto-C. 电极表面的修饰方法不同对细胞色素C的电极反应有很大影响。
The reversibility of electrode process, the character of adsorption and the mechanism of electrode reaction were investigated. A Series of constants and parameters were calculated. 研究了电极过程的可逆性、吸附特性及电极反应机制,求得一系列常数和参数。
It was observed by cyclic voltammogram that the electrode reaction is irreversible. 循环伏安法证明其电极反应是不可逆的。
Moreover, the electrochemical behavior, the complexity, the current character and the electrode reaction mechanism of this heteropoly acid were investigated in details. 文中还详细研究了该杂多酸的电化学行为、络合性、电流特性和电极反应机理。
The results of Tafel curves showed the additive decrease the exchange current density values and electrode reaction rate constant. Tafel曲线表明,添加剂降低了银电沉积过程的交换电流密度和电化学反应速度常数。
The kinetics parameters were measured by cyclic voltammetry ( CV) and chronocoulometry. The mechanism of electrode reaction was also discussed. 利用循环伏安法、计时库仑法对动力学参数进行了测定,并探讨了电极反应机理。
The electrochemical oscillation is phenomenon in time and space when a parameter in the system of electrode reaction is far from the equilibrium, which is composed of electrode and electrolyte multiphase oscillation. 电化学震荡现象是电极反应体系某个参数远离平衡时产生在时间和空间上具有某种顺序的现象,是由电极和电解液共同组成的多相震荡。