聚苯胺对锌电积用复合惰性阳极材料电化学性能的影响(英文)
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| Published in | 中国有色金属学报:英文版 Vol. 22; no. 7; pp. 1693 - 1700 |
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| Main Author | |
| Format | Journal Article |
| Language | English |
| Published |
2012
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| Subjects | |
| Online Access | Get full text |
| ISSN | 1003-6326 |
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| Bibliography: | composite inert anodes;double pulse electrodeposition;anodic polarization curves;cyclic voltammetry curves;Tafel polarization curves;microstructures ZHAN Peng1,2,XU Rui-dong1,2,HUANG Li-ping3,CHEN Bu-ming1,2,ZHOU Jian-feng1,2 1.Faculty of Metallurgical and Energy Engineering,Kunming University of Science and Technology,Kunming 650093,China;2.State Key Laboratory Breeding Base of Complex Nonferrous Metal Resources Cleaning Utilization in Yunnan Province,Kunming 650093,China;3.Key Laboratory of Inorganic Coating Materials,Chinese Academy of Sciences,Shanghai 200050,China 43-1239/TG In order to search for a suitable anode material used in zinc electrowinning in place of Pb-Ag alloy,Al/Pb-PANI(polyaniline)-WC(tungsten carbide) composite inert anodes were prepared on aluminum alloy substrate by double pulse electrodeposition(DPE) of PANI and WC particles with Pb2+ from an original plating bath.Thereafter,anodic polarization curves,cyclic voltammetry curves and Tafel polarization curves for the composite inert anodes obtained under different PANI concentrations in the original plating bath were measured,and the microstructural features were also investigated by scanning electron microscopy(SEM).The results show that Al/Pb-PANI-WC composite inert anode obtained under PANI concentration of 20 g/L in the original plating bath possesses uniform microstructures and composition distributions,higher electrocatalytic activity,better reversibility of electrode reaction and corrosion resistance in a synthetic zinc electrowinning electrolyte of 50 g/L Zn2+,150 g/L H2SO4 at 35 °C.Compared with Pb-1%Ag alloy,the overpotential of oxygen evolutions for the composite inert anode are decreased by 185 mV and 166 mV,respectively,under 500 A/m2 and 1000 A/m2. |
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| ISSN: | 1003-6326 |