File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1016/j.watres.2011.03.007
- Scopus: eid_2-s2.0-79954628893
- PMID: 21453951
- WOS: WOS:000290821700020
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Adsorption of perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) on alumina: Influence of solution pH and cations
Title | Adsorption of perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) on alumina: Influence of solution pH and cations | ||||
---|---|---|---|---|---|
Authors | |||||
Keywords | Adsorption Alumina Electrostatic interaction PFOA PFOS | ||||
Issue Date | 2011 | ||||
Publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/watres | ||||
Citation | Water Research, 2011, v. 45 n. 9, p. 2925-2930 How to Cite? | ||||
Abstract | The persistent nature of perfluorochemicals (PFCs) has attracted global concern in recent years. Perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) are the most commonly found PFC compounds, and thus their fate and transport play key roles in PFC distribution in the natural environment. As most solid phases in natural water contain alumina, an investigation of PFOS and PFOA adsorption behavior on alumina should prove useful in evaluating the environmental impact of this type of persistent pollutant. Systematic experiments were carried out in this study to investigate the adsorption behavior of PFOS and PFOA onto alumina. The results of adsorption kinetics on alumina show that it takes 48 h to reach equilibrium. The adsorption isotherms reveal maximum adsorption capacities of 0.252 μg/m2 for PFOS and 0.157 μg/m2 for PFOA at pH = 4.3, with the difference primarily due to their different functional groups. An increase in pH leads to a decrease in PFOS and PFOA adsorption on alumina, which may be attributed to the reduction in electrostatic interaction. The adsorption of both PFOS and PFOA decreases with an increase in ionic strength for all four types of cations (Na+, K+, Mg2+, and Ca2+), due to the compression of the electrical double layer. Furthermore, the results also indicate that both Ca2+ and Mg2+ can form bridges with PFOA anions in solution, whereas only PFOS can be bridged by Ca2+ due to the higher covalent nature of magnesium. © 2011 Elsevier Ltd. | ||||
Persistent Identifier | http://hdl.handle.net/10722/139048 | ||||
ISSN | 2023 Impact Factor: 11.4 2023 SCImago Journal Rankings: 3.596 | ||||
ISI Accession Number ID |
Funding Information: We gratefully acknowledge the funding for this research provided by the General Research Fund Scheme of the Research Grants Council of Hong Kong (HKU 716809E). The authors are also grateful to Mr. Bing Li, Mr. Ke Yu, Dr. Tong Zhang, and Ms. Vicky Fung for assisting us with the LC/MS/MS analysis. We thank Professor Xiaoyan Li for providing the zeta-potential and surface area analyzers. | ||||
References | |||||
Grants |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Wang, F | en_HK |
dc.contributor.author | Shih, K | en_HK |
dc.date.accessioned | 2011-09-23T05:44:35Z | - |
dc.date.available | 2011-09-23T05:44:35Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Water Research, 2011, v. 45 n. 9, p. 2925-2930 | en_HK |
dc.identifier.issn | 0043-1354 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/139048 | - |
dc.description.abstract | The persistent nature of perfluorochemicals (PFCs) has attracted global concern in recent years. Perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) are the most commonly found PFC compounds, and thus their fate and transport play key roles in PFC distribution in the natural environment. As most solid phases in natural water contain alumina, an investigation of PFOS and PFOA adsorption behavior on alumina should prove useful in evaluating the environmental impact of this type of persistent pollutant. Systematic experiments were carried out in this study to investigate the adsorption behavior of PFOS and PFOA onto alumina. The results of adsorption kinetics on alumina show that it takes 48 h to reach equilibrium. The adsorption isotherms reveal maximum adsorption capacities of 0.252 μg/m2 for PFOS and 0.157 μg/m2 for PFOA at pH = 4.3, with the difference primarily due to their different functional groups. An increase in pH leads to a decrease in PFOS and PFOA adsorption on alumina, which may be attributed to the reduction in electrostatic interaction. The adsorption of both PFOS and PFOA decreases with an increase in ionic strength for all four types of cations (Na+, K+, Mg2+, and Ca2+), due to the compression of the electrical double layer. Furthermore, the results also indicate that both Ca2+ and Mg2+ can form bridges with PFOA anions in solution, whereas only PFOS can be bridged by Ca2+ due to the higher covalent nature of magnesium. © 2011 Elsevier Ltd. | en_HK |
dc.language | eng | en_US |
dc.publisher | Pergamon. The Journal's web site is located at http://www.elsevier.com/locate/watres | en_HK |
dc.relation.ispartof | Water Research | en_HK |
dc.subject | Adsorption | en_HK |
dc.subject | Alumina | en_HK |
dc.subject | Electrostatic interaction | en_HK |
dc.subject | PFOA | en_HK |
dc.subject | PFOS | en_HK |
dc.subject.mesh | Alkanesulfonic Acids - analysis - chemistry | - |
dc.subject.mesh | Aluminum Oxide - chemistry | - |
dc.subject.mesh | Fluorocarbons - analysis - chemistry | - |
dc.subject.mesh | Octanoic Acids - analysis - chemistry | - |
dc.subject.mesh | Water Pollutants, Chemical - analysis - chemistry | - |
dc.title | Adsorption of perfluorooctanesulfonate (PFOS) and perfluorooctanoate (PFOA) on alumina: Influence of solution pH and cations | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0043-1354&volume=45&issue=9&spage=2925&epage=2930&date=2011&atitle=Adsorption+of+perfluorooctanesulfonate+(PFOS)+and+perfluorooctanoate+(PFOA)+on+alumina:+Influence+of+solution+pH+and+cations | - |
dc.identifier.email | Shih, K:kshih@hkucc.hku.hk | en_HK |
dc.identifier.authority | Shih, K=rp00167 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.watres.2011.03.007 | en_HK |
dc.identifier.pmid | 21453951 | - |
dc.identifier.scopus | eid_2-s2.0-79954628893 | en_HK |
dc.identifier.hkuros | 193065 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79954628893&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 45 | en_HK |
dc.identifier.issue | 9 | en_HK |
dc.identifier.spage | 2925 | en_HK |
dc.identifier.epage | 2930 | en_HK |
dc.identifier.eissn | 1879-2448 | - |
dc.identifier.isi | WOS:000290821700020 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.relation.project | Sorption of Perfluorochemicals on Sediments and Sludge of Hong Kong | - |
dc.identifier.scopusauthorid | Wang, F=37123009300 | en_HK |
dc.identifier.scopusauthorid | Shih, K=14072108900 | en_HK |
dc.identifier.citeulike | 9008014 | - |
dc.identifier.issnl | 0043-1354 | - |