过硫酸盐
全氟辛酸
化学
活性炭
矿化(土壤科学)
分解
催化作用
吸附
激进的
降级(电信)
反应机理
无机化学
核化学
环境化学
有机化学
氮气
电信
计算机科学
作者
Yu‐Chi Lee,Shang‐Lien Lo,Jeff Kuo,Chin‐Pao Huang
标识
DOI:10.1016/j.jhazmat.2013.07.054
摘要
Treatment of persistent perfluorooctanoic acid (PFOA) in water using persulfate (PS) oxidation typically requires an elevated temperature or UV irradiation, which is energy-consuming. Under relatively low temperatures of 25–45 °C, activated carbon (AC) activated PS oxidation of PFOA was evaluated for its potential of practical applications. With presence of AC in PS oxidation, PFOA removal efficiency at 25 °C reached 682% with a high defluorination efficiency of 549% after 12 h and few intermediates of short-chain perfluorinated carboxylic acids (PFCAs) were found. The removal and defluorination rates with the combined AC/PS system were approximately 12 and 19 times higher than those of the PS-only system, respectively. Activated carbon not only removes PFOA through adsorption, but also activates PS to form sulfate radicals that accelerate the decomposition and mineralization of PFOA. The activation energy for PS oxidation of PFOA was reduced from 668 to 261 kJ/mol by the catalytic effect of AC, which implies a lower reaction temperature and a shorter reaction time would suffice. A 2-cycle schematic reaction mechanism was used to describe PS oxidation of PFOA with the generation of various intermediates and end-products.
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