|
个人信息Personal Information
教授
博士生导师
硕士生导师
主要任职:Professor
性别:男
毕业院校:奥地利University of Graz
学位:博士
所在单位:环境学院
学科:环境工程. 环境科学. 水科学与技术
办公地点:大连理工大学环境学院
联系方式:
电子邮箱:
Preferable utilization of in-situ produced H2O2rather than externally added for efficient deposition of tungsten and molybdenum in microbial fuel cells
点击次数:
论文类型:期刊论文
发表时间:2017-09-01
发表刊物:Electrochimica Acta
收录刊物:SCIE、Scopus、CPCI-S、EI
卷号:247
页面范围:880-890
ISSN号:00134686
关键字:microbial fuel cell; in-situ H2O2; tungsten; molybdenum; deposition
摘要:In-situ H2O2production at the cathode in microbial fuel cells (MFCs) has been well documented to be useful for removal of recalcitrant pollutants based on its reductive and oxidative characteristics. However, the advantages of in-situ produced H2O2, rather than using an exogenous source of this chemical has not been previously examined for removal and cathodic deposition of metals. Greater percentages of W and Mo were deposited on the cathodes of MFCs with in-situ produced H2O2compared to that achieved with chemical addition to the solution through either intermittent multiple-time or one-time modes. A high oxygen supply with in-situ produced H2O2reached deposition of 67.2? ?3.1% of W and 86.4? ?1.9% of Mo, and a coulombic efficiency of 66.4%? ?3.1%, which were 2.4, 1.3 and 3.1 times, respectively as those in the no oxygen control. These metals removals were appreciably higher than the maximum achieved with chemical H2O2of 80?mg/L externally added through either intermittent multiple-time or one-time modes for W deposition, although there was a negligible difference for Mo deposition. More acidic pHs and a lower external resistance were favorable for W and Mo deposition. This study provides a new approach for efficient W and Mo deposition, where in-situ produced H2O2resulted in more complete metal removal than that obtained with an externally intermittent multiple-time or one-time added source of this oxidizer. ? 2017 Elsevier Ltd
