Heterogeneous photocatalytic degradation of methyl orange in schwertmannite/oxalate suspension under UV irradiation

被引:41
作者
Wu, Yong [1 ]
Guo, Jing [1 ]
Jiang, Danjun [1 ]
Zhou, Pei [1 ]
Lan, Yeqing [1 ]
Zhou, Lixiang [2 ]
机构
[1] Nanjing Agr Univ, Coll Sci, Nanjing 210095, Jiangsu, Peoples R China
[2] Nanjing Agr Univ, Coll Resources & Environm, Nanjing 210095, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Methyl orange; Schwertmannite; Oxalate; Photocatalytic degradation; LOW-COST ADSORBENTS; AZO-DYE; AQUEOUS SUSPENSIONS; CARBON SLURRY; IRON-OXIDES; PHOTODEGRADATION; REMOVAL; OXALATE; ACID; WATER;
D O I
10.1007/s11356-012-0740-4
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Schwertmannite was synthesized through an oxidation of FeSO4 by Acidithiobacillus ferrooxidans LX5 cell suspension at an initial pH 2.5 and 28A degrees C for 3 days and characterized using X-ray diffraction spectroscopy and scanning electron microscope. The schwertmannite photocatalytic degradation of methyl orange (MO) by oxalate was investigated at different initial pH values, concentrations of schwertmannite, oxalate, and MO. The results demonstrated that photodegradation of MO in the presence of schwertmannite or oxalate alone was very weak. However, the removal of MO was significantly enhanced when schwertmannite and oxalate coexisted in the reaction system. Low pH (4 or less) was beneficial to the degradation of MO. The optimal doses of schwertmannite and oxalate were 0.2 g L-1 and 2 mM, respectively. Hydroxyl radicals (center dot OH) and Fe(II), the intermediate products, were also examined during the reaction to explore their correlation with the degradation of MO. A possible mechanism for the photocatalytic decomposition of MO in the study was proposed. The formation of Fe(III)-oxalate complexes on the surface of schwertmannite was a precursor of H2O2 and Fe(II) production, further leading to the yield of center dot OH responsible for the decomposition of MO.
引用
收藏
页码:2313 / 2320
页数:8
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