期刊
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
卷 169, 期 3, 页码 271-278出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2004.07.009
关键词
photocatalysis of lignin model compounds; TiO(2) suspensions; radical intermediates; diffusion controlled processes; mass transfer controlled processes
Semiconductor slurries of TiO(2) were used during the photodegradation of the lignin model compound 3-methoxy-4-hydroxyphenylmethylcarbinol (from now on 3M-4HC). The TiO(2) P25 Degussa suspensions (1 mg/ml) of 3M-4HC were irradiated with a medium pressure mercury lamp in the pH range 3-8. The 3M-4HC (0.85 mM) disappeared within 40 min when using TiO(2) P25 Aeroxide Degussa and within 60 min with TiO(2) P25 Degussa as monitored by high pressure liquid chromatography (HPLC). The mineralization of 3M-4HC was observed to proceed within 120 and 180 min, respectively, indicating the existence of long-lived intermediates under light irradiation in solution. The addition of H(2)O(2) accelerated the decomposition of 3M-4HC to almost completion within 30 min while the mineralization was observed to be complete only after 90 min. TiO(2) Suspensions could be used repetitively as photocatalysts in the decomposition of 3M-4HC. The decomposition of 3M-4HC followed diffusion controlled pseudo first-order kinetics but the TOC seems to follow a mass transfer controlled process. No 3M-4HC decomposition was observed in the dark in the presence of TiO(2). The abatement of 3M-4HC was observed to be sensitive to the crystallographic structure, the crystal radius and the surface area (BET) of the TiO(2) used. The role of the oxygen singlet ((1)O(2)), of the superoxide anion radical HO(2)(.-) and of the OH-radical during the photocatalyzed degradation of 3M-4HC was elucidated by using sodium azide (NaN(3)) benzoquinone (BQ) and OH-radical scavengers (methanol and tert-butanol), respectively. Evidence is presented for the intervention of these radical species produced on the TiO(2) surface under light irradiation during the 3M-4HC degradation. (C) 2004 Elsevier B.V. All rights reserved.
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