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个人信息Personal Information
副教授
博士生导师
硕士生导师
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:环境学院
学科:环境科学. 环境工程
办公地点:环境楼B509
联系方式:13889406768
电子邮箱:zhguoquan@dlut.edu.cn
Efficient Adsorption and Combined Heterogeneous/Homogeneous Fenton Oxidation of Amaranth Using Supported Nano-FeOOH As Cathodic Catalysts
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论文类型:期刊论文
发表时间:2012-02-09
发表刊物:JOURNAL OF PHYSICAL CHEMISTRY C
收录刊物:SCIE、EI、Scopus
卷号:116
期号:5
页面范围:3623-3634
ISSN号:1932-7447
摘要:Iron oxyhydroxide (FeOOH) as heterogeneous catalyst has been widely used in Fenton-like advanced oxidation processes due to its attractive properties such as wide-operating pH range and controllable iron leaching into solution. However, little is known about the Fe3+/Fe2+ transformation of supported FeOOH catalyst under the external electrical field condition, which is of the essence in electro-Fenton-like oxidation reactions. In this study, activated carbon-supported nano-FeOOH (FeOOH/AC) catalysts were prepared by the air oxidation of ferrous hydroxide suspension method. The as-prepared catalyst was characterized with various characterization techniques and identified as goethite and lepidocrocite mixed crystals. Adsorption and electrochemically assisted oxidation of amaranth with the FeOOH/AC heterogeneous catalysts were investigated at pH 4.0 using graphite felt as cathode. Under weak acidic and external electric field conditions, the supported nano-FeOOH catalyst undergoes proton-promoted dissolution and electrochemical reductive dissolution processes, which facilitates Fe3+/Fe2+ transformation and produces a beneficial enhancement of the heterogeneous/homogeneous electro-Fenton reaction rates. Experimental results demonstrated that the FeOOH/AC heterogeneous catalyst possesses admirable adsorbability, and the electrochemically assisted oxidation of amaranth takes place not only through the heterogeneous Fenton reaction on catalyst/solution interface but also through the homogeneous Fenton reaction in bulk solution due to iron liberation from the supported nano-FeOOH. In addition, a possible electrochemically assisted oxidation mechanism is also proposed.