TY - JOUR
T1 - Highly Defective UiO-66 Materials for the Adsorptive Removal of Perfluorooctanesulfonate
AU - Clark, Chelsea A.
AU - Heck, Kimberly N.
AU - Powell, Camilah D.
AU - Wong, Michael S.
N1 - Funding Information:
We thank Mr. S. Yuan (Texas A&M University) for generously providing the CIF file for the hcp UiO-66 structure. We thank Dr. D. Zhao (National University of Singapore) for the helpful discussions. We also thank P. Dias da Silva for the assistance in TGA characterization. This work is partially supported by the National Science Foundation (NSF) Graduate Research Fellowship Program under Grant No. DGE-1450681, and the NSF Nanosystems Engineering Research Center on Nanotechnology-Enabled Water Research (EEC-1449500). Any opinions, findings, and conclusions or recommendations expressed in this material are those of the author(s) and do not necessarily reflect the views of the National Science Foundation.
Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Perfluorooctanesulfonate (PFOS) is a persistent organic pollutant that is bioaccumulative and toxic. While its use in most countries has been restricted to certain industrial applications due to environmental and health concerns, chrome plating and semiconductor manufacturing facilities are industrial point sources of PFOS-containing wastewater. Current remediation technologies are ineffective at treating these highly concentrated industrial effluents. In this work, UiO-66 metal-organic frameworks (MOFs) of several defect concentrations were studied as sorbents for the removal of PFOS from concentrated aqueous solutions. PFOS sorption isotherms indicated that defective UiO-66, prepared with HCl as a modulator, had a maximum Langmuir sorption capacity of 1.24 mmol/g, which was ∼2× greater than powdered activated carbon (PAC), but ∼2× less than that of a commercial ion-exchange resin. Defective UiO-66 adsorbed PFOS 2 orders of magnitude faster than the ion-exchange resin. Large pore defects (∼16 and ∼20 Å) within the framework were critical to the increased adsorption capacity due to higher internal surface area and an increased number of coordinatively unsaturated Zr sites to bind the PFOS head groups. Of the common co-contaminants in chrome plating wastewaters, chloride ions have a negligible effect on PFOS sorption, while sulfate and hexavalent chromium anions compete for cationically charged adsorption sites. These materials were also effective adsorbents for the shorter-chain homologue, perfluorobutanesulfonate (PFBS). The enhanced PFOS and PFBS adsorptive properties of UiO-66 highlight the advantage of structurally defective MOFs as a water treatment approach toward environmental sustainability.
AB - Perfluorooctanesulfonate (PFOS) is a persistent organic pollutant that is bioaccumulative and toxic. While its use in most countries has been restricted to certain industrial applications due to environmental and health concerns, chrome plating and semiconductor manufacturing facilities are industrial point sources of PFOS-containing wastewater. Current remediation technologies are ineffective at treating these highly concentrated industrial effluents. In this work, UiO-66 metal-organic frameworks (MOFs) of several defect concentrations were studied as sorbents for the removal of PFOS from concentrated aqueous solutions. PFOS sorption isotherms indicated that defective UiO-66, prepared with HCl as a modulator, had a maximum Langmuir sorption capacity of 1.24 mmol/g, which was ∼2× greater than powdered activated carbon (PAC), but ∼2× less than that of a commercial ion-exchange resin. Defective UiO-66 adsorbed PFOS 2 orders of magnitude faster than the ion-exchange resin. Large pore defects (∼16 and ∼20 Å) within the framework were critical to the increased adsorption capacity due to higher internal surface area and an increased number of coordinatively unsaturated Zr sites to bind the PFOS head groups. Of the common co-contaminants in chrome plating wastewaters, chloride ions have a negligible effect on PFOS sorption, while sulfate and hexavalent chromium anions compete for cationically charged adsorption sites. These materials were also effective adsorbents for the shorter-chain homologue, perfluorobutanesulfonate (PFBS). The enhanced PFOS and PFBS adsorptive properties of UiO-66 highlight the advantage of structurally defective MOFs as a water treatment approach toward environmental sustainability.
KW - Adsorption
KW - Defect
KW - Metal-organic frameworks
KW - Perfluoroalkyl substance
KW - Perfluorobutanesulfonate
KW - Perfluorooctanesulfonate
KW - UiO-66
UR - http://www.scopus.com/inward/record.url?scp=85063165846&partnerID=8YFLogxK
U2 - 10.1021/acssuschemeng.8b05572
DO - 10.1021/acssuschemeng.8b05572
M3 - Article
AN - SCOPUS:85063165846
SN - 2168-0485
VL - 7
SP - 6619
EP - 6628
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 7
ER -