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投稿时间:2016-09-05 修订日期:2016-09-14 录用日期:2016-09-18 网络发布日期:2016-12-21
投稿时间:2016-09-05 修订日期:2016-09-14 录用日期:2016-09-18 网络发布日期:2016-12-21
中文摘要: 采用失重法、恒电流极化、EIS、CV和CP等方式研究了不同Cl-浓度下Pb-0.1?-1.5%Sn阳极的析氧行为和腐蚀行为。研究表明,在电解过程中引入Cl-,多出现了一个氧化峰(Cl-→Cl2)。随着Cl-的加入,阳极的析氧过电位先升高后降低,自腐蚀电流先升高后降低,腐蚀速率也先增大后降低。恒电流极化12 h后,阳极表面主要由PbO2、PbSO4和PbO?PbSO4组成。Cl-也可以抑制恒电流极化条件下PbO?PbSO4的生成,促进PbO2和PbSO4的生成,加速阳极的腐蚀。
Abstract:Oxygen and corrosion behavior of Pb-0.1?-1.5%Sn anode under different concentrations of Cl- were studied by weight-loss method, galvanostatic polarization, EIS, CV, and CP. The results show that one more oxidation peak (Cl-→Cl2) emerged upon introduction of Cl- in electrolytic process. With increase of Cl-, oxygen evolution potential, self-corrosion current, and corrosion rate first rise then drop in Pb-0.1?-1.5%Sn anode. Surface of Pb-0.1?-1.5%Sn anode is mainly composed of PbO2, PbSO4 and PbO?PbSO4 after galvanostatic polarizating for 12 h. PbO?PbSO4 of Pb-0.1?-1.5%Sn anode under condition of galvanostatic polarization is effectively suppressed by Cl-, which promotes generation of PbO2 and PbSO4, and accelerates corrosion of anode.
文章编号: 中图分类号: 文献标志码:
基金项目:贵州省高层次创新型人才培养计划项目(黔科合人才[2016]4019号)
| 作者 | 单位 | |
| 张弘梨 | 贵州大学 | 491968769@qq.com |
| 苏向东* | 贵州理工学院 | suxiangdong@sina.com |
| 李勇 | 贵州省过程工业技术研究中心 | |
| 林齐 | 贵州省过程工业技术研究中心 | |
| 丁元发 | 贵州省过程工业技术研究中心 |
| Author Name | Affiliation | |
| zhanghongli | Guizhou University | 491968769@qq.com |
| suxiangdong | suxiangdong@sina.com | |
| LI Yong | ||
| LIN Qi | ||
| DING Yuan-fa |
引用文本:
张弘梨,苏向东,李勇,林齐,丁元发.Cl-对Pb-0.1%Ca-1.5%Sn阳极在硫酸锌溶液中电化学性能的影响[J].有色金属(冶炼部分),2017(1):11-16.
zhanghongli,suxiangdong,LI Yong,LIN Qi,DING Yuan-fa.Effect of Cl- on Electrochemical Behavior of Pb-0.1?-1.5%Sn Anode in Zinc Sulfate Solution[J].Nonferrous Metals (Extractive Metallurgy),2017(1):11-16.
张弘梨,苏向东,李勇,林齐,丁元发.Cl-对Pb-0.1%Ca-1.5%Sn阳极在硫酸锌溶液中电化学性能的影响[J].有色金属(冶炼部分),2017(1):11-16.
zhanghongli,suxiangdong,LI Yong,LIN Qi,DING Yuan-fa.Effect of Cl- on Electrochemical Behavior of Pb-0.1?-1.5%Sn Anode in Zinc Sulfate Solution[J].Nonferrous Metals (Extractive Metallurgy),2017(1):11-16.

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