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Comparative study of catalytic activity of different Fe-pillared bentonites in the presence of UV light and H2O2
被引:49
作者:
Chen, Jianxin
[1
,2
]
Zhu, Lizhong
[1
]
机构:
[1] Zhejiang Univ, Dept Environm Sci, Hangzhou 310028, Zhejiang, Peoples R China
[2] Nanchang Univ, Sch Environm Sci & Engn, Nanchang 330031, Peoples R China
基金:
中国国家自然科学基金;
关键词:
UV-Fenton;
Fe-pillared bentonite;
Catalyst activity;
Orange II;
Degradation;
PHOTO-FENTON DEGRADATION;
ORANGE-II;
AZO-DYE;
MINERALIZATION;
DISCOLORATION;
SURFACES;
D O I:
10.1016/j.seppur.2009.03.036
中图分类号:
TQ [化学工业];
学科分类号:
0817 ;
摘要:
To study the relationship of catalytic activity with Fe configuration over bentonite, three kinds of Fe-pillared bentonites were prepared by pillaring the bentonite with different Fe configurations (Fe-polycation, alpha-Fe2O3 and alpha-FeOOH). The characteristics of Fe-pillared bentonites were detected by N-2 adsorption/desorption, XRF, XRD, FTIR, AFM and UV-vis. Their catalytic activities were compared by discoloration and mineralization of Orange II in the presence of UV light and H2O2. The order of catalytic activity of Fe-pillared bentonites for dye discoloration was alpha-Fe2O3-pillared bentonite (alpha-Fe2O3-PB)>hydroxyl-Fe-pillared bentonite (H-Fe-P-B) >alpha-FeOOH-pillared bentonite (alpha-FeOOH-P-B). And that for dye mineralization was alpha-Fe2O3-P-B=H-Fe-P-B >>alpha-FeOOH-P-B. A possible catalytic mechanism was proposed for surface and solution reactions to discuss the difference in their catalytic activities. The rate constants of UV-Fenton reaction decreased but the catalytic activities of Fe-pillared bentonites for H2O2 became more obvious when the UV light wavelength increased. Furthermore, the reaction activation energy of UV-Fenton reaction was 18.6 kJ mol(-1), 20.1 kJ mol(-1) and 23.9 kJ mol(-1) with catalyst of H-Fe-P-B, alpha-Fe2O3-P-B and alpha-FeOOH-P-B, respectively. The results showed that both alpha-Fe2O3-P-B and H-Fe-P-B were promising catalysts for UV-Fenton system because of its physical and chemical stability and highly catalytic activity. (C) 2009 Published by Elsevier B.V.
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页码:282 / 288
页数:7
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