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Degradation of Sulfamethoxazole Using Iron-Doped Titania and Simulated Solar Radiation
被引:35
作者:
Tsiampalis, Athanasios
[1
]
Frontistis, Zacharias
[2
]
Binas, Vassilios
[3
,4
]
Kiriakidis, George
[3
,4
]
Mantzavinos, Dionissios
[1
]
机构:
[1] Univ Patras, Dept Chem Engn, Caratheodory 1,Univ Campus, GR-26504 Patras, Greece
[2] Univ Western Macedonia, Dept Chem Engn, GR-50100 Kozani, Greece
[3] FORTH, IESL, POB 1527, GR-71110 Iraklion, Greece
[4] Univ Crete, Quantum Complex & Nanotechnol Ctr QCN, Dept Phys, POB 2208, GR-71110 Iraklion, Greece
来源:
关键词:
emerging micro-contaminants;
kinetics;
operating conditions;
photocatalysis;
water matrices;
WATER TREATMENT PLANTS;
WASTE-WATER;
PHOTOCATALYTIC DEGRADATION;
ANTIBIOTIC SULFAMETHOXAZOLE;
ADVANCED OXIDATION;
PHARMACEUTICALS;
MINERALIZATION;
ABATEMENT;
PRODUCTS;
INACTIVATION;
D O I:
10.3390/catal9070612
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
This work examined the photocatalytic destruction of sulfamethoxazole (SMX), a widely used antibiotic, under simulated solar radiation using iron-doped titanium dioxide as the photocatalyst. Amongst the various iron/titania ratios examined (in the range 0%-2%), the catalyst at 0.04% Fe/TiO2 molar ratio exhibited the highest photocatalytic efficiency. The reaction rate followed pseudo-first-order kinetics, where the apparent kinetic constant was reduced as the initial concentration of SMX or humic acid increased. The photodecomposition of SMX was favored in natural pH but retarded at alkaline conditions. Unexpectedly, the presence of bicarbonates (in the range of 0.125-2 g/L) improved the removal of SMX, however, experiments conducted in real environmental matrices showed that process efficiency decreased as the complexity of the water matrix increased. The presence of sodium persulfate as an electron acceptor enhanced the reaction rate. However, only a small synergy was observed between the two individual processes. On the contrary, the addition of tert-butanol, a well-known hydroxyl radical scavenger, hindered the reaction, indicating the significant contribution of these radicals to the photocatalytic degradation of SMX. The photocatalyst retained half of its initial activity after five successive experiments.
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页数:16
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