个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:中国科学院大连化学物理研究所
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:大连理工大学西部校区环境楼B623
联系方式:tanf@dlut.edu.cn
Efficient degradation of methyl orange in water via both radical and non-radical pathways using Fe-Co bimetal-doped MCM-41 as peroxymonosulfate activator
点击次数:
论文类型:期刊论文
发表时间:2021-01-10
发表刊物:CHEMICAL ENGINEERING JOURNAL
卷号:402
ISSN号:1385-8947
关键字:FeCo-MCM-41; Methyl orange; Peroxymonosulfate activation; Heterogeneous catalysis; Singlet oxygen; Degradation pathways
摘要:Cobalt-mediated activation of peroxymonosulfate (PMS) has been widely investigated for the effective oxidation of organic contaminants in wastewater. Herein, monometal- and bimetal-doped MCM-41 catalysts (Fe-MCM-41, Co-MCM-41, and FeCo-MCM-41) were synthesized by using one-pot hydrothermal method and attempted to degrade artificial methyl orange (MO) dye wastewater via PMS activation. The influences of initial PMS concentration, pH, catalyst dosage and reaction temperature on the degradation efficiency of MO were systematically examined. Compared with the contrasting catalysts, FeCo-MCM-41 exhibited extremely higher activity and lower amount of metal leaching in the degradation process. The excellent catalytic activity of FeCo-MCM-41 was ascribed to the high dispersion of metals and the synergistic effects of Co2+/Co3+ and Fe2+/Fe3+ redox cycles. A series of radical inhibition and electron paramagnetic resonance experiments revealed that both radical and non-radical pathways were involved in the degradation of MO. Singlet oxygen (O-1(2)) was unveiled to be the dominant reactive oxygen species in the FeCo-MCM-41/PMS system. The possible degradation pathways were proposed based on the identification of intermediate products generated in the degradation process by LC-MS analyses.