4.7 Article

Catalytic ozonation of dimethyl phthalate over cerium supported on activated carbon

期刊

JOURNAL OF HAZARDOUS MATERIALS
卷 170, 期 1, 页码 411-416

出版社

ELSEVIER
DOI: 10.1016/j.jhazmat.2009.04.081

关键词

Catalytic ozonation; Cerium supported on activated carbon; Dimethyl phthalate; TOC; Kinetics

资金

  1. Science & Technology Office of Guangdong Province [2006B36801005, 2007B031700006]
  2. National Natural Science Foundation of China [20773042]

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Cerium supported on activated carbon (Ce/AC), which was prepared by dipping method, was employed to degrade dimethyl phthalate (DMP) in water. The mineral matter present in the activated carbon positively contributes to its activity to enhance DMP ozonation process. A higher dipping Ce(NO3)(3) concentration and calcination process increase its microporous volume and surface area, and decreases its exterior surface area. The catalytic activity reaches optimal when 0.2% (w/w) cerium is deposited on activated carbon. Ce/AC catalyst was characterized by XRD, SEM and BET. The presence of either activated carbon or Ce/AC catalyst considerably improves their degradation and mineralization in the ozonation of DMP. During the ozonation (50 mg/h ozone flow rate) of a 30 mg/L DMP (initial pH 5.0) with the presence of Ce/AC catalyst, TOC removal rate reaches 68% at 60 min oxidation time, 48% using activated carbon as catalyst, only 22% with ozonation alone. The presence of tert-butanol (a well known (OH)-O-center dot radical scavenger) strongly inhibits DMP degradation by activated carbon or Ce/AC catalytic ozonation. TOC removal rate follows the second-order kinetics model well. In the ozonation of DMP with 50 mg/h ozone flow rate, its mineralization rate constant with the presence of Ce/AC catalyst is 2.5 times higher than that of activated carbon, 7.5 times higher than that Of 03 alone. Ce/AC catalyst shows the better catalytic activity and stability based on 780 min sequential reaction in the ozonation of DMP Ce/AC was a promising catalyst for ozonizing organic pollutants in the aqueous solution. (C) 2009 Elsevier B.V. All rights reserved.

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