Effects of SiC and Al2O3 particles on the electrodeposition of Zn, Co and ZnCo. I. Electrodeposition in the absence of SiC and Al2O3

被引:10
作者
Tulio, Paulo C. [1 ]
Carlos, Ivani A. [1 ]
机构
[1] Univ Fed Sao Carlos, Dept Chem, BR-13565905 Sao Carlos, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Zn; Co and ZnCo; Electrodeposition; Acid solution; Steel substrate; Electrocomposites; PLUS COBALT ALLOYS; NEUTRAL-ACID MEDIA; ELECTROLYTIC CODEPOSITION; UNDERPOTENTIAL DEPOSITION; POLARIZATION CHARACTERISTICS; ELECTROCHEMICAL NUCLEATION; ZINC ELECTRODEPOSITION; SULFATE ELECTROLYTES; HYDROGEN ABSORPTION; ORGANIC ADDITIVES;
D O I
10.1007/s10800-008-9670-8
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Electrodeposition of Zn, Co and ZnCo from acid sulfate solutions onto steel was investigated in this first part of a study of the effects of SiC or Al2O3 particles on these processes and the formation of ZnCo - SiC and ZnCo - Al2O3 electrocomposites. Zn electrodeposition shows a well-defined pre-bulk region, where the hydrogen evolution reaction (HER) and Zn underpotential deposition (upd) compete. Zn bulk electrodeposition begins with primary nucleation and diffusion-controlled growth, strongly dependent on conditions favoring previous Zn upd against HER. It is assumed that this first bulk process takes place over the upd Zn. Zn bulk electrodeposition is followed by secondary nucleation and growth. Co electrodeposition begins with a slow Co-(aq)(2+) reduction in parallel with HER, followed by a faster Co(aq)(2+) reduction. Zn-(aq)(2+) strongly hinders the initial Co(aq)(2+) reduction. The ZnCo and Zn electrodeposition curves are initially similar, retaining features of pre-bulk and bulk Zn electrodeposition.
引用
收藏
页码:283 / 291
页数:9
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