Mineralization of bisphenol A by catalytic ozonation over alumina

被引:37
作者
Keykavoos, R. [1 ]
Mankidy, R. [2 ,3 ]
Ma, H. [2 ,3 ]
Jones, P. [2 ,3 ]
Soltan, J. [1 ]
机构
[1] Univ Saskatchewan, Dept Chem & Biol Engn, Saskatoon, SK S7N 5A9, Canada
[2] Univ Saskatchewan, Dept Vet Sci, Saskatoon, SK S7N 5A9, Canada
[3] Univ Saskatchewan, Toxicol Ctr, Saskatoon, SK S7N 5A9, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Bisphenol A; Ozonation; Heterogeneous catalytic ozonation; Mineralization; ADVANCED OXIDATION PROCESSES; WASTE-WATER; ENDOCRINE DISRUPTORS; ACTIVATED CARBON; AQUEOUS-SOLUTION; OZONE; DEGRADATION; KINETICS; REMOVAL; CARE;
D O I
10.1016/j.seppur.2013.01.050
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Total mineralization of bisphenol A (BPA) has been investigated through non-catalytic and catalytic ozonation treatments in a semi-batch reactor. Non-catalytic ozonation led to complete degradation of BPA in less than 4 min, but did not convert the by-products of BPA ozonation completely. In sole ozonation systems only 35% conversion of the total organic carbon (TOC) was achieved in 60 min. Using 1 g/L alumina catalyst increased the TOC removal to 90%. Study of the effect of catalyst particles showed that by reducing the particle size from pellets to powder, TOC removal increased significantly from 44% to 90% under particular reaction conditions. However, increasing the amount of alumina catalyst from 0.5 g/L to 4 g/L did not show a strong effect on the TOC removal. Catalyst reusability and deactivation studies indicated that catalyst showed stable activity after three consecutive cycles of catalytic ozonation. A two-stage kinetic regime was used to express rate of TOC removal for both non-catalytic and catalytic ozonation of BPA. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:310 / 317
页数:8
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