TY - JOUR
T1 - Adsorption mechanisms of PFOA onto activated carbon anchored with quaternary ammonium/epoxide-forming compounds
T2 - A combination of experiment and model studies
AU - Yuan, Chen
AU - Huang, Yang
AU - Cannon, Fred S.
AU - Zhao, Zhiwei
N1 - Funding Information:
The authors gratefully acknowledge funding from Evoqua Company and the National Natural Science Foundation of China (Nos. 51878090 and 51808066); and thank the Chinese Scholarship Council for financial support that made this research possible. We are grateful for the electron microscopy and EDS analyses conducted by Julie Marie Anderson at Penn State, the sample preparation and polishing conducted by Manuel R. Villalpando at Penn State, the guidance by Zhijie Liang and Cong Geng.
Funding Information:
The authors gratefully acknowledge funding from Evoqua Company and the National Natural Science Foundation of China (Nos. 51878090 and 51808066 ); and thank the Chinese Scholarship Council for financial support that made this research possible. We are grateful for the electron microscopy and EDS analyses conducted by Julie Marie Anderson at Penn State, the sample preparation and polishing conducted by Manuel R. Villalpando at Penn State, the guidance by Zhijie Liang and Cong Geng.
Publisher Copyright:
© 2020
PY - 2020/12
Y1 - 2020/12
N2 - When wood-based activated carbon was tailored with quaternary ammonium/epoxide (QAE) forming compounds (QAE-AC), this tailoring dramatically improved the carbon's effectiveness for removing perfluorooctanoic acid (PFOA) from groundwater. With favorable tailoring, QAE-AC removed PFOA from groundwater for 118,000 bed volumes before half-breakthrough in rapid small scale column tests, while the influent PFOA concentration was 200 ng/L. The tailoring involved pre-dosing QAE at an array of proportions onto this carbon, and then monitoring bed life for PFOA removal. When pre-dosing with 1 mL QAE, this PFOA bed life reached an interim peak, whereas bed life was less following 3 mL QAE pre-dosing, then PFOA bed life exhibited a steady rise for yet subsequently higher QAE pre-dosing levels. Large-scale atomistic modelling was used herein to provide new insight into the mechanism of PFOA removal by QAE-AC. Based on experimental results and modelling, the authors perceived that the QAE's epoxide functionalities cross-linked with phenolics that were present along the activated carbon's graphene edge sites, in a manner that created mesopores within macroporous regions or created micropores within mesopores regions. Also, the QAE could react with hydroxyls outside of these pore, including the hydroxyls of both graphene edge sites and other QAE molecules. This latter reaction formed new pore-like structures that were external to the activated carbon grains. Adsorption of PFOA could occur via either charge balance between negatively charged PFOA with positively charged QAE, or by van der Waals forces between PFOA's fluoro-carbon tail and the graphene or QAE carbon surfaces.
AB - When wood-based activated carbon was tailored with quaternary ammonium/epoxide (QAE) forming compounds (QAE-AC), this tailoring dramatically improved the carbon's effectiveness for removing perfluorooctanoic acid (PFOA) from groundwater. With favorable tailoring, QAE-AC removed PFOA from groundwater for 118,000 bed volumes before half-breakthrough in rapid small scale column tests, while the influent PFOA concentration was 200 ng/L. The tailoring involved pre-dosing QAE at an array of proportions onto this carbon, and then monitoring bed life for PFOA removal. When pre-dosing with 1 mL QAE, this PFOA bed life reached an interim peak, whereas bed life was less following 3 mL QAE pre-dosing, then PFOA bed life exhibited a steady rise for yet subsequently higher QAE pre-dosing levels. Large-scale atomistic modelling was used herein to provide new insight into the mechanism of PFOA removal by QAE-AC. Based on experimental results and modelling, the authors perceived that the QAE's epoxide functionalities cross-linked with phenolics that were present along the activated carbon's graphene edge sites, in a manner that created mesopores within macroporous regions or created micropores within mesopores regions. Also, the QAE could react with hydroxyls outside of these pore, including the hydroxyls of both graphene edge sites and other QAE molecules. This latter reaction formed new pore-like structures that were external to the activated carbon grains. Adsorption of PFOA could occur via either charge balance between negatively charged PFOA with positively charged QAE, or by van der Waals forces between PFOA's fluoro-carbon tail and the graphene or QAE carbon surfaces.
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U2 - 10.1016/j.jes.2020.05.019
DO - 10.1016/j.jes.2020.05.019
M3 - Article
C2 - 33097163
AN - SCOPUS:85086468498
SN - 1001-0742
VL - 98
SP - 94
EP - 102
JO - Journal of Environmental Sciences
JF - Journal of Environmental Sciences
ER -