王同华

个人信息Personal Information

教授

博士生导师

硕士生导师

任职 : 现任大连理工大学化工学院教授、博士生导师。同时担任“膜科学与技术”期刊编委,膜学会理事(筹),膜工业协会工程与应用专业委员会及特种分离膜专业委员会委员、中国兵工学会活性炭测试分析与应用研究分会委员等。

性别:男

毕业院校:大连工学院

学位:硕士

所在单位:化工学院

学科:化学工艺. 膜科学与技术. 功能材料化学与化工

办公地点:化工综合楼A201

联系方式:微信/电话 13500711370

电子邮箱:wangth@dlut.edu.cn

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Enhanced removal ability of phenol from aqueous solution using coal-based carbon membrane coupled with electrochemical oxidation process

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论文类型:期刊论文

发表时间:2018-03-05

发表刊物:COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS

收录刊物:SCIE、EI

卷号:540

页面范围:186-193

ISSN号:0927-7757

关键字:Phenol; Carbon membrane; Electrochemical oxidation; Degradation; GC-MS

摘要:A treatment system combining the coal-based carbon membrane with electrochemical oxidation process was designed for the enhanced phenol removal ability. The effects of various parameters including electric voltage, phenol concentration, solution pH, rotate speed, electrolyte type and concentration, and electrode distance on the permeate flux and removal efficiency of the treatment system were carried out. The degradation intermediates of phenol were detected by gas chromatography-mass spectrometry (GC-MS). The results showed the phenol removal ability of carbon membrane was significantly improved by coupling with electrochemical oxidation process. High phenol concentration usually increased the load of the treatment system, resulting in low permeate flux and removal efficiency because of limited decomposition ability. When the initial pH increased from 4.0 to 10.0, the enhanced permeate flux and removal efficiency were observed. The permeate flux displayed a decrease trend with the increase of electrode distance, while the removal efficiency showed an opposite trend. The optimum operation parameters of 2.0 V electric voltage, 7.5 r/min pump rotate speed, and 2.50 g/L Na2SO4 were recommended. During the degradation process, the reactive free radicals and H2O2 attacked the benzene ring of phenol to produce catechol, hydroquinone and resorcinol. And then, hydroquinone was degraded to benzoquinone, which was further decomposed to organic acids such as maleic, fumaric, and oxalic acids. Finally, these organic acids were oxidized into CO2 and H2O.