硝基苯
化学
降级(电信)
激进的
光化学
金属
矿化(土壤科学)
催化作用
紫外线
辐照
无机化学
核化学
氮气
材料科学
有机化学
核物理学
物理
电信
光电子学
计算机科学
作者
Ahmed E. ElMetwally,Gh. Eshaq,A.M. Al-Sabagh,F.Z. Yehia,Christine A. Philip,Nabawaya A. Moussa,Gamal M.S. ElShafei
标识
DOI:10.1016/j.seppur.2018.08.029
摘要
Heterogeneous Fenton degradation of nitrobenzene (NB, 20 ppm) was investigated at room temperature and pH = 7 using 0.1 g L−1 of FeOCl (I), CuOCl (II), ZnOCl (III) and BiOCl (IV) metal oxychlorides catalysts in presence of ultrasonic (US, 20 kHz), ultraviolet (UV, 6 W, λ = 254 nm) and UV/US double irradiation with H2O2 (5 mM) as an oxidant. The results showed that the order of the investigated systems with regard to their degradation performance was US/UV > UV > US, with I > II > IV > III but with mineralization extents of 46%, 41%, 35% and 33%, respectively under dual irradiation for 60 min. The synergistic effect correlates with the values of band gap of used oxychlorides and plays a vital role in enhancing the degradation performance of the dual system through generated reactive radicals (OH & O2−) besides photo-born holes (h+) and electrons (e−). Experiments conducted in presence of different scavengers indicated that (OH) and (h+) play a major and more important role than that of (O2−) in the degradation process. Scavenging the generated electrons indicated that they act as degradation inhibitors. Band gap values dictated the variable activities shown by different metal oxychlorides.
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