
教授 博士生导师 硕士生导师
性别:男
毕业院校:大连工学院
学位:硕士
所在单位:环境学院
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发布时间:2019-03-09
论文类型:期刊论文
发表时间:2009-07-01
发表刊物:JOURNAL OF ELECTROANALYTICAL CHEMISTRY
收录刊物:SCIE
卷号:632
期号:1-2
页面范围:154-161
ISSN号:1572-6657
关键字:Amaranth; Anthraquinonedisulphonate; Electro-Fenton; Hydroxyl radicals; Kinetics; Polypyrrole
摘要:Removal of amaranth from aqueous solutions by Fe2+/H2O2 and Fe3+/H2O2 electro-oxidation systems was comparatively studied in an undivided electrochemical cell with anthraquinonedisulfonate (AQDS)/polypyrrole (PPy) composite film modified graphite as cathode. The modified cathode allowed the formation of strong oxidant hydroxyl radical ((OH)-O-center dot) in the medium via Fenton's reaction between cathodically generated H2O2 and added or regenerated Fe2+. The effects of solution pH and iron catalyst concentration on dye degradation by the two systems were studied and compared. Degradation intermediates were analyzed by FTIR and GC-MS, and a tentative reaction pathway is proposed. Dye decay reaction always obeys pseudo-first-order kinetics for Fe3+/H2O2 process, while dye degradation follows a two-stage process with each stage obeying pseudo-first-order kinetics in the case of Fe2+/H2O2 system. In addition, the long-term stability and structural relaxation of the composite film during multiple experimental runs are also examined. (C) 2009 Elsevier B.V. All rights reserved.