Evaluation of sorbent amendments for in situ remediation of metal-contaminated sediments

dc.contributor.authorKwon, Seokjoon
dc.contributor.authorThomas, Jeff
dc.contributor.authorReed, Brian
dc.contributor.authorLevine, Laura
dc.contributor.authorMagar, Victor S.
dc.contributor.authorFarrar, Daniel
dc.contributor.authorBridges, Todd S.
dc.contributor.authorGhosh, Upal
dc.date.accessioned2025-07-09T17:54:39Z
dc.date.issued2010-09-01
dc.description.abstractThe present study evaluated sorbent amendments for in situ remediation of sediments contaminated with two divalent metals. A literature review screening was performed to identify low-cost natural mineral-based metal sorbents and high-performance commercial sorbents that were carried forward into laboratory experiments. Aqueous phase metal sorptivity of the selected sorbents was evaluated because dissolved metals in sediment porewater constitute an important route of exposure to benthic organisms. Based on pH-edge sorption test results, natural sorbents were eliminated due to inferior performance. The potential as in situ sediment amendment was explored by comparing the sorption properties of the engineered amendments in freshwater and saltwater (10 PPT salinity estuarine water) matrices. Self-assembled monolayers on mesoporous supports with thiols (Thiol-SAMMS™) and a titanosilicate mineral (ATS™) demonstrated the highest sorption capacity for cadmium (Cd) and lead (Pb), respectively. Sequential extraction tests conducted after mixing engineered sorbents with contaminated sediment demonstrated transfer of metal contaminants from a weakly bound state to a more strongly bound state. Biouptake of Cd in a freshwater oligochaete was reduced by 98% after 5-d contact of sediment with 4% Thiol-SAMMS and sorbed Cd was not bioavailable. While treatment with ATS reduced the small easily extractable portion of Pb in the sediment, the change in biouptake of Pb was not significant because most of the native lead was strongly bound. The selected sorbents added to sediments at a dose of 5% were mostly nontoxic to a range of sensitive freshwater and estuarine benthic organisms. Metal sorbent amendments in conjunction with activated carbon have the potential to simultaneously reduce metal and hydrophobic contaminant bioavailability in sediments. Environ. Toxicol. Chem. 2010;29:1883–1892. © 2010 SETAC
dc.description.sponsorshipThis work was supported by the Department of Defense Strategic Environmental Research and Development Program through project ER-1491. The authors thank John Higley from Steward Environmental for providing Thiol-SAMMS for the present study and Derek Arnold for laboratory assistance in this project.
dc.description.urihttps://academic.oup.com/etc/article/29/9/1883/7763256
dc.format.extent10 pages
dc.genrejournal articles
dc.identifierdoi:10.13016/m2wvj2-eklc
dc.identifier.citationKwon, Seokjoon, Jeff Thomas, Brian E. Reed, Laura Levine, Victor S. Magar, Daniel Farrar, Todd S. Bridges, and Upal Ghosh. “Evaluation of Sorbent Amendments for in Situ Remediation of Metal-contaminated Sediments.” Environmental Toxicology and Chemistry 29, no. 9 (September 1, 2010): 1883–92. https://doi.org/10.1002/etc.249.
dc.identifier.urihttps://doi.org/10.1002/etc.249
dc.identifier.urihttp://hdl.handle.net/11603/39187
dc.language.isoen_US
dc.publisherOxford University Press
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Chemical, Biochemical & Environmental Engineering Department
dc.relation.ispartofUMBC Student Collection
dc.rightsThis work was written as part of one of the author's official duties as an Employee of the United States Government and is therefore a work of the United States Government. In accordance with 17 U.S.C. 105, no copyright protection is available for such works under U.S. Law.
dc.rightsPublic Domain
dc.rights.urihttps://creativecommons.org/publicdomain/mark/1.0/
dc.titleEvaluation of sorbent amendments for in situ remediation of metal-contaminated sediments
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0001-7155-3671

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