Autor: |
Náfrádi M; Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary., Alapi T; Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary., Farkas L; Department of Inorganic and Analytical Chemistry, University of Szeged, Dóm tér 7, H-6720 Szeged, Hungary., Bencsik G; Department of Physical Chemistry and Materials Science, University of Szeged, Rerrich Béla tér 1, H-6720 Szeged, Hungary., Kozma G; Department of Applied and Environmental Chemistry, University of Szeged, Rerrich Béla tér 1, H-6720 Szeged, Hungary., Hernádi K; Institute of Physical Metallurgy, Metal Forming and Nanotechnology, University of Miskolc, C/2-5 Building 209, H-3515 Miskolc-Egyetemvaros, Hungary. |
Abstrakt: |
The comparison of the efficiency of the commercially available photocatalysts, TiO 2 and ZnO, irradiated with 365 nm and 398 nm light, is presented for the removal of two antibiotics, sulfamethazine (SMT) and sulfamethoxypyridazine (SMP). The • OH formation rate was compared using coumarin, and higher efficiency was proved for TiO 2 than ZnO, while for 1,4-benzoquinone in O 2 -free suspensions, the higher contribution of the photogenerated electrons to the conversion was observed for ZnO than TiO 2 , especially at 398 nm irradiation. An extremely fast transformation and high quantum yield of SMP in the TiO 2 /LED 398nm process were observed. The transformation was fast in both O 2 containing and O 2 -free suspensions and takes place via desulfonation, while in other cases, mainly hydroxylated products form. The effect of reaction parameters (methanol, dissolved O 2 content, HCO 3 - and Cl - ) confirmed that a quite rarely observed energy transfer between the excited state P25 and SMP might be responsible for this unique behavior. In our opinion, these results highlight that "non-conventional" mechanisms could occur even in the case of the well-known TiO 2 photocatalyst, and the effect of wavelength is also worth investigating. |