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在单质铁存在下超声增强五氯苯酚降解的机制

Mechanism of the enhanced degradation of pentachlorophenol by ultrasound in the presence of elemental iron.

作者信息

Dai Youzhi, Li Fenfang, Ge Fei, Zhu Fei, Wu Lanyan, Yang Xiangzheng

机构信息

Department of Environmental Engineering, Xiangtan University, Xiangtan, Hunan 411105, China.

出版信息

J Hazard Mater. 2006 Oct 11;137(3):1424-9. doi: 10.1016/j.jhazmat.2006.04.025. Epub 2006 Apr 25.

Abstract

Ultrasound combined with elemental iron (US/Fe(0)) is effective in oxidizing organic contaminants in water. The sonolysis degradation of pentachlorophenol (PCP) was significantly enhanced by a factor of 4.2 with the addition of elemental iron, mainly via reaction with hydroxyl radicals (OH radicals), and the synergistic mechanism of the enhancement in the combined system was investigated. Experiments were performed with (1) sole ultrasonic treatment; (2) ultrasound in presence of iron; (3) ultrasound combined with copper powder as the same particle size as iron powder; (4) ultrasound in presence of Fe(II). It was observed that PCP degradation and OH radicals production were both enhanced in these combined methods, and the pitting on the sonicated iron surface was apparent. These results indicated that the rate enhancements in US/Fe(0) system were attributed to (1) the iron solid effect and the catalysis of Fe(II) produced from corroded-iron with promoting the production of OH radicals; (2) the increased surface area of iron particles by acoustic cavitation with promoting the adsorption process.

摘要

超声与单质铁(US/Fe(0))联合使用可有效氧化水中的有机污染物。添加单质铁后,五氯苯酚(PCP)的声解降解显著增强,增强因子为4.2,主要通过与羟基自由基(OH自由基)反应实现,同时对联合体系中增强作用的协同机制进行了研究。实验采用以下方式进行:(1)单独超声处理;(2)铁存在下的超声处理;(3)超声与粒径相同的铜粉联合处理;(4)Fe(II)存在下的超声处理。观察发现,这些联合方法均增强了PCP降解和OH自由基的产生,且超声处理后的铁表面出现明显点蚀。这些结果表明,US/Fe(0)体系中的速率增强归因于:(1)铁固体效应以及腐蚀产生的Fe(II)的催化作用促进了OH自由基的产生;(2)声空化作用增加了铁颗粒的表面积,促进了吸附过程。

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