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101.
The electrochemical behaviour of copper has been investigated in different cupric complex solutions by cyclic voltammetry. In pyridinic and picolinic solutions the reduction of cupric complex occurred in two stages leading to Cu(I) and Cu(0), respectively. The electrodeposited copper is oxidized in two steps leading to Cu(I) and Cu(II) as in ammoniacal cupric complex solutions. In glycine, alanine, sulfamic acid and ethylenediamine solutions, the cuprous complex is an intermediate in the cupric complex reduction but it is not detected during the oxidation of the electrodeposited copper in these solutions. In EDTA and triethanolamine solutions, the cuprous complex is not observed. The rate of copper etching was determined in pyridinic and ammoniacal cupric solutions and was shown to be faster in ammoniacal cupric solutions than in the pyridinic solutions. 相似文献
102.
In order to develop an energy-saving copper recycling process from wastes, electrochemical measurements were conducted in ammoniacal alkaline solutions containing Cu(I) ions and an ammonium salt of sulfate, chloride or nitrate. The results of each system were then compared. The polarization measurements suggested that the voltage required for the electrode process is lower in the chloride and nitrate systems than that in the sulfate system. The cathode current efficiency during the copper electrodeposition varied from 39 to 97% and increased with current density in the chloride and sulfate systems. In the nitrate system, the lowest cathode current efficiency of 30% was observed because of nitrate ion reduction. Based on these results, the power consumption required for the electrowinning stage of the copper recycling process was calculated. Among these three systems, the chloride system showed the lowest power consumption of 500 kWh t−1 at the current density of 200 A m−2, which is about 25% of the conventional copper electrowinning process from a copper sulfate-sulfuric acid solution. 相似文献
103.
104.
Nickel-cobalt and nickel-iron electrodeposits were characterized as hydrogen electrodes in alkaline water electrolysis (6 mol/L KOH, 25°C). The nickel-based codeposits were fabricated with different bath compositions and at different current densities. The hydrogen evolution in water electrolysis on the nickel-based codeposits was apparently enhanced as compared with that on nickel. The improvement of the electrocatalytic behaviour of the hydrogen electrodes is attributed to their composition and an increase of their active surface, which are dependent on the electrodeposition conditions. 相似文献
105.
Joan Papavasiliou George Avgouropoulos Theophilos Ioannides 《Applied catalysis. B, Environmental》2007,69(3-4):226-234
Steam reforming of methanol was carried out over a series of doped CuO–CeO2 catalysts prepared via the urea–nitrate combustion method. XRD analysis showed that at least part of the dopant cations enter the ceria lattice. The addition of various metal oxide dopants in the catalyst composition affected in a different way the catalytic performance towards H2 production. Small amounts of oxides of Sm and Zn improved the performance of CuO–CeO2, while further addition of these oxides caused a decrease in catalyst activity. XPS analysis of Zn- and Sm-doped catalysts showed that increase of dopant loading leads to surface segregation of the dopant and decrease of copper oxide dispersion. The addition of oxides of La, Zr, Mg, Gd, Y or Ca lowered or had no effect on catalytic activity, but led to less CO in the reaction products. Noble-metal modified catalysts had slightly higher activity, but the CO selectivity was also significantly higher. 相似文献
106.
107.
K. I. Popov M. G. Pavlovic B. N. Grgur A. T. Dimitrov S. Hadzi Jordanov 《Journal of Applied Electrochemistry》1998,28(8):797-801
The mechanism of compact Ag-film formation by electrolysis from nitrate solution with addition of small amounts of phosphate ions is elucidated. It is shown that the phosphate ions exert their effect by lowering the exchange current density. Consequently, the radii of nucleation exclusion zones also diminishes, thus producing conditions stimulating electrodeposition of continuous thin Ag-film. 相似文献
108.
Polyaniline emeraldine base/epoxy resin (EB/ER) coating was investigated for corrosion protection of mild steel coupled with copper in 3.5% NaCl solution. EB/ER coating with 5-10 wt% EB had long-term corrosion resistance on both uncoupled steel and copper due to the passivation effect of EB on the metal surfaces. During the 150 immersion days, the impedance at 0.1 Hz for the coating increased in the first 1-40 days and subsequently remained constant above 109 Ω cm2, whereas that for pure ER coating fell below 106 Ω cm2 after only 30 or 40 days. Immersion tests on coated steel-copper galvanic couple showed that EB/ER coating offered 100 times more protection than ER coating against steel dissolution and coating delamination on copper, which was mainly attributed to the passive metal oxide films formed by EB blocking both the anodic and cathodic reactions. Salt spray tests showed that 100 μm EB/ER coating protected steel-copper couple for at least 2000 h. 相似文献
109.
110.
采用Gly—GlyOH,4,4'—联吡啶与Cu(NO_3)_2·H_2O在二次水溶液中反应,合成出以4,4'—bpy为中继基,Gly—Glyo为螯环新型双核铜配合物。经X射线单晶结构分析确定该配合物品体的化学结构式:[(H_2NCH_2CONHCH_2COO) Cu(OH) (C_(10)H_8N_2)Cu(OH) (H_2NCH_2CONHCH_2COO)]·9H_2O.晶体属于三斜晶系,P_空间群,晶胞参数a=1.1412nm,b=1.2298nm,C=1.4269nm,α=113.82°,β=101.91°,y=103.64°,V=1.6747nm~3,Z=2。衍射数据是在Nicolet XRD R3型四圆衍射仪上收集,结构参数经块矩阵最小二乘法精修后,最终一致性因子R值为0.068,RW值为0.057。 相似文献