期刊文献+

Effects of Br^- and I^- concentrations on Zn electrodeposition from ammoniacal electrolytes 被引量:2

Effects of Br^- and I^- concentrations on Zn electrodeposition from ammoniacal electrolytes
下载PDF
导出
摘要 The effects of Br- and I- concentrations on the cell voltage, anodic polarization, current efficiency (CE), and energy consumption (EC) of zinc electrodeposition from ammoniacal ammonium chloride solutions were investigated. The surface morphology of zinc deposits was also examined. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to characterize the morphology of zinc deposits and the phase of anodic sediments produced during electrolysis. The results clearly showed that the CE slightly increased from approximately 95.12% in the absence of F and Br- to 97.08% in the presence of 10 g·L-1 Br; in contrast, the CE significantly decreased to less than 83% in the presence of 10 g·L-1 I- . The addition of Br and I- positively affected the EC, which decreased from 2514 kW·h·t-1 to approximately 2300 kW·h·t-1. The results of anodic polarization measurements showed that the voltage drops were 130 and 510 mV when the concentrations of Br- and I- were 10 g·L-1 at a eUlTent density of 400 A·m2, respectively. SEM images showed that the addition of Br- and I- caused different crystal growth mechanisms, which resulted in the production of compact and smooth zinc deposits. The anodic reactions of I were also studied. The effects of Br- and I- concentrations on the cell voltage, anodic polarization, current efficiency (CE), and energy consumption (EC) of zinc electrodeposition from ammoniacal ammonium chloride solutions were investigated. The surface morphology of zinc deposits was also examined. Scanning electron microscopy (SEM) and X-ray diffraction (XRD) were used to characterize the morphology of zinc deposits and the phase of anodic sediments produced during electrolysis. The results clearly showed that the CE slightly increased from approximately 95.12% in the absence of F and Br- to 97.08% in the presence of 10 g·L-1 Br; in contrast, the CE significantly decreased to less than 83% in the presence of 10 g·L-1 I- . The addition of Br and I- positively affected the EC, which decreased from 2514 kW·h·t-1 to approximately 2300 kW·h·t-1. The results of anodic polarization measurements showed that the voltage drops were 130 and 510 mV when the concentrations of Br- and I- were 10 g·L-1 at a eUlTent density of 400 A·m2, respectively. SEM images showed that the addition of Br- and I- caused different crystal growth mechanisms, which resulted in the production of compact and smooth zinc deposits. The anodic reactions of I were also studied.
出处 《International Journal of Minerals,Metallurgy and Materials》 SCIE EI CAS CSCD 2015年第7期682-687,共6页 矿物冶金与材料学报(英文版)
基金 supported by the National Basic Research Program of China (No. 2014CB643404) the National Natural Science Foundation of China (Nos. 51274094 and 51374254)
关键词 ZINC ELECTRODEPOSITION BROMIDE IODIDE ammonium chloride current efficiency energy consumption zinc electrodeposition bromide iodide ammonium chloride current efficiency energy consumption
  • 相关文献

参考文献2

二级参考文献22

  • 1柳艳修,宋华,李锋.绿色多功能无机材料高铁酸盐的应用[J].无机盐工业,2006,38(7):6-8. 被引量:5
  • 2Yu X,Licht s.Advances in Fe(Ⅵ)charge storage Part Ⅰ:Primary alkaline super-iron batteries[J].J.Power Sources,2007,171:966-980.
  • 3Yu X,Licht S.Advances in Fe(Ⅵ)charge storage Part Ⅱ:Reversible alkaline super-iron batteries and nonaqueous super-iron batteries[J].J.Power Sources,2007,171:1010-1022.
  • 4Wang S Q,Yang Z H,Liu D R,et al.Evaluation of potassium ferrate(Ⅵ)cathode material coated with 2,3-naphthalocyanine for alkaline super iron battery[J].Electrochem.Commun.,2010,12(3):367-370.
  • 5He W C,Wang J M,Shao H B,et al.Novel KOH electrolyte for one-step electrochemical synthesisof high purity solid K2FeO4:Comparison with NaOH[J].Electrochem.Commun.,2005,7(6):607-610.
  • 6Xu Z H,Wang J M,Mao W Q,et al.The effects of ultrasound on the direct electrosynthesis of solid K2 FeO4 and the anodic behaviorsof Fe in 14 M KOH solution[J].J.Solid State Electrochem.,2007,11(3):413-420.
  • 7Jiang J Q, Barry L, Luminita Q. Preparation and evaluation of potassium ferrate as an oxidant and coagulant for potable water treatment [ J]. Environmental Engineering Science, 2001, 18: 323.
  • 8Delaude L, Laszlo P. A novel oxidizing reagent based on potassium ferrate ( VI ) [ J ]. Journal of Organic Chemistry, 1996, 61: 6360.
  • 9Mathieu D K, Daniel B. The electrochemical generation of ferrate at pressed iron powder electrode: comparison with a foil electrode [ J ]. Electrochimica Acta, 2003, 48 : 1435.
  • 10Karel B, Henry B. Comparison of pure and white cast iron dissolution kinetics in highly alkaline electrolyte [J]. Corrosion Science, 1999,41 : 2113.

共引文献1

同被引文献31

引证文献2

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部