Chemistry & Chemical Engineering

Catalytic Wet Peroxide Oxidation of Phenol on CeO2 -ZSM-5 Fixed Bed Reactor

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  • School of Chemistry and Chemical Engineering,South China University of Technology,Guangzhou 510640,Guangdong,China
杨逸(1994-),男,博士生,主要从事废水处理研究. E-mail:y.y05@mail.scut.edu.cn

Received date: 2016-07-07

  Revised date: 2016-12-30

  Online published: 2017-05-02

Supported by

 Supported by the National Natural Science Foundation of China(21376101)

Abstract

In this paper,first,CeO2 -ZSM-5 zeolite catalysts were prepared by means of impregnation method and were applied to the catalytic wet peroxide oxidation of phenol in a fixed bed reactor.Then,the phase structure,specific surface area and pore structure of CeO2 -ZSM-5 were characterized via XRD and N2adsorption-desorption.Finally,the effects of temperature,bed height and feed flow rate on the conversion rates of phenol,H2O2 and total organic carbon (TOC),as well as on the cerium leaching concentration and the selectivity of CO2 ,were investiga- ted.Characterization results show that CeO2 -ZSM-5 catalysts are micro-pore materials; and that,after the loading of active components,the crystal form of CeO2 -ZSM-5 almost keeps unchanged but the specific surface area decrea- ses.Moreover,from the activity evaluation results,it is found that (1) the conversion rates of phenol,H2O2 and TOC,as well as the selectivity of CO2 all increase with the increase of temperature and with the decrease of feed flow rate; (2) with the increase of bed height,the conversion rates of phenol,H2O2 and TOC all increase,while the selectivity of CO2 decreases; (3) the cerium leaching concentration is small under all conditions,which means that the catalysts possess good stability; and (4) no by-products are observed in the process of CWPO.

Cite this article

YANG Yi ZHANG Hui-ping YAN Ying . Catalytic Wet Peroxide Oxidation of Phenol on CeO2 -ZSM-5 Fixed Bed Reactor[J]. Journal of South China University of Technology(Natural Science), 2017 , 45(6) : 117 -123,130 . DOI: 10.3969/j.issn.1000-565X.2017.06.018

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