Comparison of UV/H2O2 and UV/TiO2 for the degradation of metaldehyde: Kinetics and the impact of background organics

被引:48
作者
Autin, Olivier [1 ]
Hart, Julie [2 ]
Jarvis, Peter [1 ]
MacAdam, Jitka [1 ]
Parsons, Simon A. [1 ]
Jefferson, Bruce [1 ]
机构
[1] Cranfield Univ, Dept Environm Sci & Technol, Cranfield Water Sci Inst, Cranfield MK43 0AL, Beds, England
[2] Severn Trent Water LTD, Severn Trent Ctr, Coventry CV3 9FH, W Midlands, England
关键词
Metaldehyde; Advanced oxidation processes; Hydrogen peroxide; Titanium dioxide; Kinetics; Natural organic matter; ADVANCED OXIDATION PROCESSES; RADICAL RATE CONSTANTS; PHOTOCATALYTIC DEGRADATION; HYDROGEN-PEROXIDE; LOW-PRESSURE; WASTE-WATER; HYDROXYL RADICALS; PULSE-RADIOLYSIS; PHOTODEGRADATION; PHOTOLYSIS;
D O I
10.1016/j.watres.2012.07.057
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The kinetics of photodegradation of the pesticide metaldehyde by UV/H2O2 and UV/TiO2 in laboratory grade water and a natural surface water were studied. Experiments were carried out in a bench scale collimated beam device using UVC radiation. Metaldehyde was efficiently degraded by both processes in laboratory grade water at identical rates of degradation (0.0070 and 0.0067 cm(2) mJ(-1) for UV/TiO2 and UV/H2O2 respectively) when optimised doses were used. The ratio between oxidant and metaldehyde was significantly higher for H2O2 due to its low photon absorption efficiency at 254 nm. However, the presence of background organic compounds in natural water severely affected the rate of degradation, and whilst the pseudo first-order rate constant of degradation by UV/H2O2 was slowed down (0.0020 cm(2) mJ(-1)), the degradation was completely inhibited for the UV/TiO2 process (k' = 0.00007 cm(2) mJ(-1)) due to the blockage of active sites on TiO2 surface by the background organic material. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5655 / 5662
页数:8
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