Activation of persulfates by carbon nanotubes: Oxidation of organic compounds by nonradical mechanism

被引:599
作者
Lee, Hongshin [1 ,2 ]
Lee, Hye-Jin [1 ,2 ]
Jeong, Joonseon [3 ]
Lee, Jaesang [4 ]
Park, Noh-Back [5 ]
Lee, Changha [1 ,2 ]
机构
[1] UNIST, Sch Urban & Environm Engn, Ulsan 689798, South Korea
[2] UNIST, KIST UNIST Ulsan Ctr Convergent Mat KUUC, Ulsan 689798, South Korea
[3] Samsung Elect Co Ltd, Energy Lab, Samsung Adv Inst Technol, Yongin 446712, Gyeonggi Do, South Korea
[4] Korea Univ, Sch Civil Environm & Architectural Engn, Seoul 136701, South Korea
[5] NFRDI, Pusan 619705, South Korea
基金
新加坡国家研究基金会;
关键词
Carbon nanotube; Persulfate; Oxidation; Nonradical mechanism; Organic compounds; ELECTRON-SPIN-RESONANCE; ZERO-VALENT IRON; CATALYTIC-OXIDATION; RADICAL GENERATION; AQUEOUS-SOLUTIONS; KINETICS; SULFATE; TRICHLOROETHYLENE; PEROXYMONOSULFATE; DEGRADATION;
D O I
10.1016/j.cej.2014.12.065
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Carbon nanotubes (CNTs) have been found to activate persulfates (i.e., peroxymonosulfate and peroxydisulfate) into reactive species that are capable of oxidizing organic compounds in water. In the presence of single- or multi-walled CNTs, persulfates effectively degraded phenolic compounds and certain pharmaceuticals. Phenyl derivatives substituted with electron-withdrawing groups, such as benzoic acid and nitrobenzene, were resistant to degradation by the CNT/persulfate system. Based on observations regarding persulfate decomposition and linear sweep voltammetry using a CNT electrode, it has been suggested that persulfates bind onto the surface of CNTs, forming reactive complexes that are immediately decomposed upon reaction with organic compounds. Electron paramagnetic resonance spectroscopy with spin-trapping indicates that these reactive species are distinct from sulfate radical anions or hydroxyl radicals. The CNT-activated persulfate system shows promise as a novel treatment technology for the selective oxidation of organic contaminants in water. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:28 / 33
页数:6
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