首页> 外文OA文献 >Enhanced Photoelectrocatalytic Decomplexation of Cu-EDTA and Cu Recovery by Persulfate Activated by UV and Cathodic Reduction
【2h】

Enhanced Photoelectrocatalytic Decomplexation of Cu-EDTA and Cu Recovery by Persulfate Activated by UV and Cathodic Reduction

机译:紫外光活化和阴极还原过硫酸盐增强铜-EDTA的光电催化分解和铜的回收

摘要

In order to enhance Cu-EDTA decomplexation and copper cathodic recovery via the photoelectrocatalytic (PEC) process, S2O82- was introduced into the PEC system with a TiO2/Ti photoanode. At a current density of 0.2 mA/cm(2) and initial solution pH of 3.0, the decomplexation ratio of Cu complexes was increased from 47.5% in the PEC process to 98.4% with 5 mM S2O82- addition into the PEC process (PEC/S2O82-). Correspondently, recovery percentage of Cu was increased to 98.3% from 47.4% within 60 min. It was observed that nearly no copper recovery occurred within the initial reaction period of 10 min. Combined with the analysis of ESR and electrochemical LSV curves, it was concluded that activation of S2O82- into SO4- radicals by cathodic reduction occurred, which was prior to the reduction of liberated Cu2+ ions. UV irradiation of S2O82- also led to the production of SO4-. The generated SO4- radicals enhanced the oxidation of Cu-EDTA. After the consumption of S2O82-, the Cu recovery via cathodic reduction proceeded quickly. Acidification induced by the transformation of SO4- to OH. favored the copper cathodic recovery. The combined PEC/S2O82- process was also efficient for the TOC removal from a real electroplating wastewater with the Cu recovery efficiency higher than 80%.
机译:为了通过光电催化(PEC)工艺增强Cu-EDTA的分解和铜阴极的回收率,将S2O82-引入具有TiO2 / Ti光电阳极的PEC系统中。在电流密度为0.2 mA / cm(2)和初始溶液pH为3.0的情况下,在PEC过程中添加5 mM S2O82-(PEC / S2O82-)。相应地,铜的回收率在60分钟内从47.4%提高到98.3%。观察到在10分钟的初始反应时间内几乎没有铜的回收。结合对ESR和电化学LSV曲线的分析,得出的结论是,在还原释放的Cu2 +离子之前,通过阴极还原将S2O82-活化为SO4-自由基。 S2O82-的紫外线照射也导致了SO4-的产生。产生的SO4-自由基增强了Cu-EDTA的氧化。消耗S2O82-后,通过阴极还原进行的Cu回收迅速进行。由SO4-转化为OH引起的酸化。有利于铜阴极回收。结合的PEC / S2O82-工艺对于从真正的电镀废水中去除TOC也是有效的,Cu的回收率高于80%。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号