Effect of temperature on oxidative transformation of perfluorooctanoic acid (PFOA) by persulfate activation in water
被引:104
作者:
Liu, C. S.
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Univ Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
Guangdong Inst Eco Environmental & Soil Sci, Guangzhou 510650, Guangdong, Peoples R ChinaUniv Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
Liu, C. S.
[1
,2
]
Higgins, C. P.
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Colorado Sch Mines, Environm Sci & Engn Div, Golden, CO 80401 USAUniv Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
Higgins, C. P.
[3
]
Wang, F.
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Univ Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
Wang, F.
[1
]
Shih, K.
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Univ Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R ChinaUniv Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
Shih, K.
[1
]
机构:
[1] Univ Hong Kong, Dept Civil Engn, Hong Kong, Hong Kong, Peoples R China
[2] Guangdong Inst Eco Environmental & Soil Sci, Guangzhou 510650, Guangdong, Peoples R China
[3] Colorado Sch Mines, Environm Sci & Engn Div, Golden, CO 80401 USA
Perfluorooctanoic acid (PFOA) is an emerging environmental pollutant attracting significant attention due to its global distribution, high persistence, and bioaccumulation properties. In this study, the degradation of aqueous PFOA at different temperatures was examined using heat-activated persulfate. Using this approach, 93.5% of PFOA was degraded after 30 h at 85 degrees C with 43.6% of F- yield, and the shorter chain length compounds (PFHpA (C6F13COOH), PFHxA (C5F11COOH), PFPeA (C4F9COOH), and PFBA (C3F2COOH)) were observed as degradation intermediates. The sequential degradation mechanism of losing one CF2 unit from PFOA and its intermediates on a step-by-step basis were observed. Controlled temperature kinetics studies yielded an activation energy of approximately 60 kJ/mol for the degradation of PFOA by heat-activated persulfate. However, at elevated temperatures, excess persulfate is needed for efficient PFOA degradation, presumably due to more intensive SO4 center dot- scavenging. Lower reaction pH was generally found to inhibit PFOA degradation, presumably due to the more prevalent radical-to-radical interactions. (C) 2011 Elsevier B.V. All rights reserved.