How Photocatalyst Dosage and Ultrasound Application Influence the Photocatalytic Degradation Rate of Phenol in Water: Elucidating the Mechanisms Behind

被引:15
作者
Van de Moortel, Wim [1 ]
Kamali, Mohammadreza [1 ]
Sniegowski, Kristel [2 ]
Braeken, Leen [2 ]
Degreve, Jan [3 ]
Luyten, Jan [1 ]
Dewil, Raf [1 ]
机构
[1] Katholieke Univ Leuven, Proc & Environm Technol Lab, Dept Chem Engn, B-2860 St Katelijne Waver, Belgium
[2] Katholieke Univ Leuven, Dept Chem Engn, Ctr Ind Proc Technol, B-3590 Diepenbeek, Belgium
[3] Katholieke Univ Leuven, Reactor Engn & Safety Sect, Dept Chem Engn, Bio & Chem Syst Technol, B-3001 Leuven, Belgium
关键词
phenol; advanced oxidation processes; ultrasound; photocatalysis; deagglomeration; WET AIR OXIDATION; WASTE-WATER; SONOPHOTOCATALYSIS; DISINFECTION; PRETREATMENT; EFFICIENCY; REMOVAL;
D O I
10.3390/w12061672
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Photocatalysis is of high interest for the treatment of wastewater containing non-biodegradable organic components. In this work, the photocatalytic degradation of phenol by TiO(2)photocatalysis was assessed, the influence of ultrasound (US) treatment was evaluated, and the mechanisms behind it were elucidated. It was shown that the TiO(2)concentration (in suspension) has a large influence on the degradation kinetics. At high TiO(2)concentrations, a reduced efficiency was observed due to the shielding of the UV light by TiO(2)particles. US treatment effectively increased phenol degradation by improving the mass transfer while it was shown by the experimental data that particle deagglomeration did not play a significant role. The degradation mainly occurred through indirect phenol oxidation by hydroxyl (OH*) radicals, which were formed in situ at the surface of the photocatalyst. Finally, based on the partial least squares (PLS) methodology, a mathematical model was developed, representing phenol degradation as a function of the selected process conditions.
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页数:13
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