Enhanced Adsorption of PFOA and PFOS on Multiwalled Carbon Nanotubes under Electrochemical Assistance

Removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) from aqueous solution has attracted wide attention in light of their environmental persistence, bioaccumulation, and potential toxicity. Although various destructive technologies were developed, removal of PFOX (X = A and...

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Bibliographic Details
Published inEnvironmental science & technology Vol. 45; no. 19; pp. 8498 - 8505
Main Authors Li, Xiaona, Chen, Shuo, Quan, Xie, Zhang, Yaobin
Format Journal Article
LanguageEnglish
Published Washington, DC American Chemical Society 01.10.2011
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Summary:Removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS) from aqueous solution has attracted wide attention in light of their environmental persistence, bioaccumulation, and potential toxicity. Although various destructive technologies were developed, removal of PFOX (X = A and S) under mild conditions are still desirable. In this work, multiwalled carbon nanotubes (MWNTs) were applied to remove PFOX in electrochemically assistant adsorption. Electrosorption kinetics and isotherms were investigated relative to open circuit (OC) adsorption and adsorption on powder MWNTs. Compared with powder MWNTs adsorption, the initial adsorption rate (υ0) of 100 μg/L PFOX at 0.6 V increased 60-fold (PFOA) and 41-fold (PFOS) according to pseudosecond-order kinetics model and the maximum electrosorption capacity (q m) of PFOX (50 μg/L to 10 mg/L) increased 150-fold (PFOA) and 94-fold (PFOS) simulated with Langmuir model. These significant improvements were assumed to benefit from enhanced electrostatic attraction under electrochemical assistance. Furthermore, the used MWNTs were found to be regenerative and reusable. This work provides not only a new approach to effective removal of perfluorochemicals from aqueous solution but also a low energy-consumption and environmentally-friendly strategy for application of carbon nanotubes in water treatment.
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ISSN:0013-936X
1520-5851
1520-5851
DOI:10.1021/es202026v