Chemisorption of Perfluorooctanoic Acid on Powdered Activated Carbon Initiated by Persulfate in Aqueous Solution

全氟辛酸 过硫酸盐 水溶液 化学吸附 活性炭 化学 核化学 无机化学 碳纤维 环境化学 吸附 有机化学 催化作用 材料科学 复合数 复合材料
作者
Bo Sun,Jun Ma,David L. Sedlak
出处
期刊:Environmental Science & Technology [American Chemical Society]
卷期号:50 (14): 7618-7624 被引量:78
标识
DOI:10.1021/acs.est.6b00411
摘要

Perfluorooctanoic acid (PFOA) is a perfluorocarboxylic acid that is difficult to treat by most conventional methods. As a result, it is often removed from solution by adsorption on powdered activated carbon (PAC), followed by incineration of the spent carbon. To provide a new approach for treatment, PFOA was exposed to sulfate radicals (SO4–•) produced by thermolysis of persulfate (S2O82–) in the presence of PAC. Under acidic conditions, thermal activation of persulfate resulted in transformation of PFOA to shorter-chain-length perfluorinated compounds, as previously reported. However, when thermolysis of persulfate occurred under circumneutral pH conditions in the presence of PAC, a new removal pathway for PFOA was observed. Under these conditions, the removal of PFOA was attributable to chemisorption, a process in which PAC catalyzed persulfate decomposition and reacted with the transformation products to produce covalently bound PFOA. At PAC concentrations between 200 and 1000 mg/L and an initial PFOA concentration of 0.5 μM, covalent bonding resulted in removal of 10–40% of the PFOA. Under these conditions, the process resulted in removal of more than half of a more hydrophilic perfluoroalkyl acid (i.e., perfluorobutanoic acid, PFBA), which was greater than the amount of PFBA removed by physical adsorption on PAC. Although the high reaction temperatures (i.e., 80 °C) and relatively high doses of PAC used in this study may be impractical for drinking water treatment, this process may be applied to the treatment of these recalcitrant compounds in industrial wastewater, reverse osmosis concentrate, and other waters that contain high concentrations of PFOA and other perfluorocarboxylic acids.
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