4.2 Article

EDTA enhanced heterogeneous Fenton oxidation of dimethyl phthalate catalyzed by Fe3O4: Kinetics and interface mechanism

期刊

JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL
卷 408, 期 -, 页码 179-188

出版社

ELSEVIER
DOI: 10.1016/j.molcata.2015.07.030

关键词

Heterogeneous Fenton; Chelating agent; Reaction kinetic; Interface mechanism

资金

  1. National Basic Research Program of China (973 Program) [2011CB933704]
  2. National Natural Science Foundation of China [21107125, 51221892, 41201498]
  3. National Natural Science Funds for Distinguished Young Scholar [51025830]

向作者/读者索取更多资源

It has been noticed that some chelating agents can enhance heterogeneous Fenton reactions, as well as homogeneous Fenton reactions. However, the mechanism of the enhanced heterogeneous Fenton reactions remains speculative, due to the ambiguous concurrence of homogeneous and heterogeneous reactions. In the present work, ethylene diamine tetraacetic acid (EDTA) was introduced to study the role of the chelating agent in the oxidation of dimethyl phthalate (DMP) in nano-Fe3O4/H2O2 system. The addition of EDTA in solution dramatically accelerated DMP removal partly due to the induced homogeneous Fenton reaction by enhanced dissolution of Fe3O4. Meanwhile, the adsorbed EDTA on the catalyst could also enhance DMP removal. Effects of EDTA surface loadings, initial H2O2 concentrations, initial DMP concentrations, and initial pHs on the reaction kinetics in EDTA modified Fe3O4/H2O2 system were investigated, together with the reusability of the EDTA modified Fe3O4. Results showed that the surface complexed EDTA ( Fe-II/III-EDTA) inhibited H2O2 decomposition by competition for surface active sites. However, the generation of (OH)-O-center dot and HO2 center dot/O-2(-center dot) was not suppressed according to the ESR results. The enhanced DMP removal by Fe-II/III-EDTA was probably due to the efficient use of reactive oxygen species (ROS). A possible EDTA enhanced heterogeneous Fenton mechanism was further proposed. (C) 2015 Published by Elsevier B.V.

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