Electrochemical Behaviors and Properties of Zn-Ni Alloys Obtained from Alkaline Non-Cyanide Bath Using 5,5′-Dimethylhydantoin as Complexing Agent

被引:35
|
作者
Feng, Zhongbao [1 ]
Li, Qingyang [1 ]
Zhang, Jinqiu [1 ]
Yang, Peixia [1 ]
An, Maozhong [1 ]
机构
[1] Harbin Inst Technol, Sch Chem Engn & Technol, State Key Lab Urban Water Resource & Environm, Harbin 150001, Peoples R China
关键词
ZINC-NICKEL ALLOYS; CORROSION-RESISTANCE; SULFATE ELECTROLYTES; IONIC LIQUID; ELECTRODEPOSITION BEHAVIOR; CHLORIDE BATH; CD COATINGS; DEPOSITION; CODEPOSITION; TEMPERATURE;
D O I
10.1149/2.0121509jes
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Zn-Ni alloys were prepared in an alkaline bath with 5,5'-dimethylhydantoin (DMH) and Na4P2O7 center dot 10H(2)O as the complexing agents. The electrochemical behaviors of Zn-Ni alloy and Zn only on Pt and glassy carbon (GC) electrodes were investigated by cyclic voltammetry (CV), chromoamperometry (CA) and cathode polarization. Results show that DMH is the main complexing agent in the bath. Different behaviors of CV curves on Pt and GC electrodes were observed. The effects of Ni2+/Zn2+ ratio and bath temperature on CV curves were investigated. The transfer coefficient (alpha) and diffusion coefficient (D) were also calculated. The nucleation growth processes of Zn-Ni alloy and Zn only show an agreement with three-dimensional progressive growth. Zn-Ni alloy coatings were also characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), potentiodynamic polarization curves and electrochemical impedance spectroscopy (EIS). The morphology of deposits is rectangular pyramid. The grain size decreases with the extension of the electrodepositing time and the decrease in the deposition potential can also lead to the decrease of grain size in deposits. The phase structure changes from the mixture of eta and gamma phases to single gamma phase with (411) orientation and the corrosion resistance of deposits increases by decreasing the deposition potential. (C) The Author(s) 2015. Published by ECS. All rights reserved.
引用
收藏
页码:D412 / D422
页数:11
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