Photocatalytic Degradation Mechanism of Oxytetracyclines Using Fe2O3-TiO2 Nanopowders
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作者:
Li, Rong
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Shanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R ChinaShanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R China
Li, Rong
[1
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Liu, Jia
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Shanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R ChinaShanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R China
Liu, Jia
[1
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Jia, Yuefa
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Hankuk Univ Foreign Studies, Dept Phys, Yongin 449791, South Korea
Hankuk Univ Foreign Studies, Oxide Res Ctr, Yongin 449791, South KoreaShanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R China
Jia, Yuefa
[2
,3
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Zhen, Qiang
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Shanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R ChinaShanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R China
Zhen, Qiang
[1
]
机构:
[1] Shanghai Univ, Nanosci & Technol Res Ctr, Shanghai 200444, Peoples R China
[2] Hankuk Univ Foreign Studies, Dept Phys, Yongin 449791, South Korea
[3] Hankuk Univ Foreign Studies, Oxide Res Ctr, Yongin 449791, South Korea
Photocatalytic degradation performance of oxytetracycline (OTC) was investigated in aqueous solution using Fe2O3-TiO2 nanopowders under UV and visible light, respectively. Compare with pure TiO2, the Fe2O3-TiO2 nanopowder had improved photocatalytic activity under visible light, while had a bit decrease under UV light. Photoluminescence (PL) spectrum measurement, (OH)-O-center dot radical test and trapping experiments were carried out to investigate the photocatalytic mechanism. Under UV light, photogenerated electrons-holes can transfer from TiO2 to the conduction band and valence band of Fe2O3, respectively, and further participated in the degradation of OTC, thus both O-2(center dot-) and holes are the main active species in this case. Under visible light, Fe2O3 was activated and yield charge carriers, then the photogenerated electrons immigrated to the trapping site of TiO2, the photogenerated holes accumulate in the valence band (VB) of Fe2O3 was the major active species reacted with OTC.
机构:
State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing
School of Metallurgical Ecological Engineering, University of Science and Technology BeijingState Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing
Zhong-shan Ren
Xiao-jun Hu
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State Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing
School of Metallurgical Ecological Engineering, University of Science and Technology BeijingState Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing
Xiao-jun Hu
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机构:
Shen-yang Li
Xiang-xin Xue
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机构:
School of Materials and Metallurgy, Northeastern UniversityState Key Laboratory of Advanced Metallurgy, University of Science and Technology Beijing