Cationic surfactant-assisted foam fractionation enhances the removal of short-chain perfluoroalkyl substances from impacted water
Several studies have demonstrated that air-bubbling and foam fractionation techniques can efficiently remove long-chain PFAS from contaminated water. However, removing short-chain PFAS is challenging due to its lower surface activity and inability to form self-assembly structures at the air-water in...
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description | Several studies have demonstrated that air-bubbling and foam fractionation techniques can efficiently remove long-chain PFAS from contaminated water. However, removing short-chain PFAS is challenging due to its lower surface activity and inability to form self-assembly structures at the air-water interface. In this study, we tested various additives, including salts, surfactants, and polymers, to improve short-chain PFAS (e.g., perfluorobutanesulfonic acid (PFBS) and perfluorobutanoic acid (PFBA)) removal in non-foaming solutions using a bench-scale system. We found that in the presence of cetyltrimethylammonium chloride (CTAC) and salt, air-bubbling can significantly remove 0.5 μg L−1 of PFBS and PFBA in deionized water by >99% (15 min) and 81% (60 min), respectively. The decline of surface tension and the formation of thin foam-like layers during bubbling, controlled by the concentration of CTAC, significantly improved the removal of short-chain PFAS. Adding anionic and neutral surfactants showed no removal of short-chain PFAS during bubbling, suggesting the importance of the electrostatic interactions between short-chain PFAS and the cationic CTAC. We observed a 1:1 M ratio between CTAC and PFBS removed from the solution, suggesting the formation of ion pairs in the solution and enhancing the surface activity of the overall neutral (PFAS-CTAC) complex. A mass balance of the system revealed that the primary mechanism by which PFAS was removed from non-foaming waters was through aerosol generation (70−100%). Using the optimized condition, PFAS mixtures (short- and long-chain PFAS, including five recently regulated PFAS by USPEA, 2 nM each) in deionized water and natural groundwater were successfully removed to below detection (>99% removal; |
doi_str_mv | 10.1016/j.chemosphere.2024.142614 |
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[Display omitted]
•Cationic surfactant enhanced short-chain PFAS removal during foam-fractionation.•Ion-pair formation between PFAS and CTAC increased surface activity of short-chains.•Aerosolization was the primary pathway for PFAS removal in non-foaming waters.•Mass balance of PFAS in the system can achieve 70–100% when aerosols were measured.</description><identifier>ISSN: 0045-6535</identifier><identifier>ISSN: 1879-1298</identifier><identifier>EISSN: 1879-1298</identifier><identifier>DOI: 10.1016/j.chemosphere.2024.142614</identifier><identifier>PMID: 38878978</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Aerosols ; Bubbling ; CTAC ; Foam fractionation ; Ion pair ; PFAS</subject><ispartof>Chemosphere (Oxford), 2024-08, Vol.362, p.142614, Article 142614</ispartof><rights>2024 Elsevier Ltd</rights><rights>Copyright © 2024. Published by Elsevier Ltd.</rights><rights>Copyright © 2024 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1668-abb3fc57cab7742dbedb056c4a7b6b68b92e42aeaf36467d1ef9f0c5182813e33</cites><orcidid>0000-0001-9760-9004</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S004565352401508X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38878978$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Cheng-Shiuan</creatorcontrib><creatorcontrib>Venkatesan, Arjun K.</creatorcontrib><title>Cationic surfactant-assisted foam fractionation enhances the removal of short-chain perfluoroalkyl substances from impacted water</title><title>Chemosphere (Oxford)</title><addtitle>Chemosphere</addtitle><description>Several studies have demonstrated that air-bubbling and foam fractionation techniques can efficiently remove long-chain PFAS from contaminated water. However, removing short-chain PFAS is challenging due to its lower surface activity and inability to form self-assembly structures at the air-water interface. In this study, we tested various additives, including salts, surfactants, and polymers, to improve short-chain PFAS (e.g., perfluorobutanesulfonic acid (PFBS) and perfluorobutanoic acid (PFBA)) removal in non-foaming solutions using a bench-scale system. We found that in the presence of cetyltrimethylammonium chloride (CTAC) and salt, air-bubbling can significantly remove 0.5 μg L−1 of PFBS and PFBA in deionized water by >99% (15 min) and 81% (60 min), respectively. The decline of surface tension and the formation of thin foam-like layers during bubbling, controlled by the concentration of CTAC, significantly improved the removal of short-chain PFAS. Adding anionic and neutral surfactants showed no removal of short-chain PFAS during bubbling, suggesting the importance of the electrostatic interactions between short-chain PFAS and the cationic CTAC. We observed a 1:1 M ratio between CTAC and PFBS removed from the solution, suggesting the formation of ion pairs in the solution and enhancing the surface activity of the overall neutral (PFAS-CTAC) complex. A mass balance of the system revealed that the primary mechanism by which PFAS was removed from non-foaming waters was through aerosol generation (70−100%). Using the optimized condition, PFAS mixtures (short- and long-chain PFAS, including five recently regulated PFAS by USPEA, 2 nM each) in deionized water and natural groundwater were successfully removed to below detection (>99% removal; <2 ng L−1), except for PFBA (25−73% removal). These results provide an improved understanding of the mechanism by which PFAS is removed during foam fractionation and highlight the need for capturing aerosols enriched with PFAS to prevent secondary contamination.
[Display omitted]
•Cationic surfactant enhanced short-chain PFAS removal during foam-fractionation.•Ion-pair formation between PFAS and CTAC increased surface activity of short-chains.•Aerosolization was the primary pathway for PFAS removal in non-foaming waters.•Mass balance of PFAS in the system can achieve 70–100% when aerosols were measured.</description><subject>Aerosols</subject><subject>Bubbling</subject><subject>CTAC</subject><subject>Foam fractionation</subject><subject>Ion pair</subject><subject>PFAS</subject><issn>0045-6535</issn><issn>1879-1298</issn><issn>1879-1298</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqNkUtv1TAQhS1ERS-Fv4DMjk0uduJXluiKl1SJTbu2bGes-JLEwXaKuuSf1yUFsWQ10ug7Zx4HobeUHCmh4v356EaYY15HSHBsScuOlLWCsmfoQJXsG9r26jk6EMJ4I3jHL9HLnM-EVDHvX6DLTimpeqkO6NfJlBCX4HDekjeumKU0JueQCwzYRzNjn2q7Mr9BDMtoFgcZlxFwqlvcmQlHj_MYU2ncaMKCV0h-2mKKZvp-P1Vnm8su8inOOMxrdaz2P02B9ApdeDNleP1Ur9Dtp483py_N9bfPX08frhtHhVCNsbbzjktnrJSsHSwMlnDhmJFWWKFs3wJrDRjfCSbkQMH3njhOVatoB113hd7tvmuKPzbIRc8hO5gms0Dcsu6IUJIrrlhF-x11KeacwOs1hdmke02JfkxAn_U_CejHBPSeQNW-eRqz2RmGv8o_L6_AaQegHnsXIOnsAtTvDCGBK3qI4T_GPAAn1aIO</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Lee, Cheng-Shiuan</creator><creator>Venkatesan, Arjun K.</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-9760-9004</orcidid></search><sort><creationdate>20240801</creationdate><title>Cationic surfactant-assisted foam fractionation enhances the removal of short-chain perfluoroalkyl substances from impacted water</title><author>Lee, Cheng-Shiuan ; Venkatesan, Arjun K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1668-abb3fc57cab7742dbedb056c4a7b6b68b92e42aeaf36467d1ef9f0c5182813e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aerosols</topic><topic>Bubbling</topic><topic>CTAC</topic><topic>Foam fractionation</topic><topic>Ion pair</topic><topic>PFAS</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Cheng-Shiuan</creatorcontrib><creatorcontrib>Venkatesan, Arjun K.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Chemosphere (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Cheng-Shiuan</au><au>Venkatesan, Arjun K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cationic surfactant-assisted foam fractionation enhances the removal of short-chain perfluoroalkyl substances from impacted water</atitle><jtitle>Chemosphere (Oxford)</jtitle><addtitle>Chemosphere</addtitle><date>2024-08-01</date><risdate>2024</risdate><volume>362</volume><spage>142614</spage><pages>142614-</pages><artnum>142614</artnum><issn>0045-6535</issn><issn>1879-1298</issn><eissn>1879-1298</eissn><abstract>Several studies have demonstrated that air-bubbling and foam fractionation techniques can efficiently remove long-chain PFAS from contaminated water. However, removing short-chain PFAS is challenging due to its lower surface activity and inability to form self-assembly structures at the air-water interface. In this study, we tested various additives, including salts, surfactants, and polymers, to improve short-chain PFAS (e.g., perfluorobutanesulfonic acid (PFBS) and perfluorobutanoic acid (PFBA)) removal in non-foaming solutions using a bench-scale system. We found that in the presence of cetyltrimethylammonium chloride (CTAC) and salt, air-bubbling can significantly remove 0.5 μg L−1 of PFBS and PFBA in deionized water by >99% (15 min) and 81% (60 min), respectively. The decline of surface tension and the formation of thin foam-like layers during bubbling, controlled by the concentration of CTAC, significantly improved the removal of short-chain PFAS. Adding anionic and neutral surfactants showed no removal of short-chain PFAS during bubbling, suggesting the importance of the electrostatic interactions between short-chain PFAS and the cationic CTAC. We observed a 1:1 M ratio between CTAC and PFBS removed from the solution, suggesting the formation of ion pairs in the solution and enhancing the surface activity of the overall neutral (PFAS-CTAC) complex. A mass balance of the system revealed that the primary mechanism by which PFAS was removed from non-foaming waters was through aerosol generation (70−100%). Using the optimized condition, PFAS mixtures (short- and long-chain PFAS, including five recently regulated PFAS by USPEA, 2 nM each) in deionized water and natural groundwater were successfully removed to below detection (>99% removal; <2 ng L−1), except for PFBA (25−73% removal). These results provide an improved understanding of the mechanism by which PFAS is removed during foam fractionation and highlight the need for capturing aerosols enriched with PFAS to prevent secondary contamination.
[Display omitted]
•Cationic surfactant enhanced short-chain PFAS removal during foam-fractionation.•Ion-pair formation between PFAS and CTAC increased surface activity of short-chains.•Aerosolization was the primary pathway for PFAS removal in non-foaming waters.•Mass balance of PFAS in the system can achieve 70–100% when aerosols were measured.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>38878978</pmid><doi>10.1016/j.chemosphere.2024.142614</doi><orcidid>https://orcid.org/0000-0001-9760-9004</orcidid></addata></record> |
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subjects | Aerosols Bubbling CTAC Foam fractionation Ion pair PFAS |
title | Cationic surfactant-assisted foam fractionation enhances the removal of short-chain perfluoroalkyl substances from impacted water |
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