| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4482603 | Water Research | 2012 | 8 Pages |
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 cm2 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 cm2 mJ−1), the degradation was completely inhibited for the UV/TiO2 process (k′ = 0.00007 cm2 mJ−1) due to the blockage of active sites on TiO2 surface by the background organic material.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (88 K)Download as PowerPoint slideHighlights► The same kOH is achieved for both processes under optimum conditions. ► The optimum molar ratio between oxidant and metaldehyde is significantly higher for H2O2 than for TiO2. ► Background organic matter has a greater influence on UV/TiO2 than UV/H2O2.
