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Impact of iron and redox chemistry on the environmental fate and transport of metalloids and radionuclides

dc.contributor.authorTroyer, Lyndsay D., author
dc.contributor.authorBorch, Thomas, advisor
dc.contributor.authorLadanyi, Branka M., committee member
dc.contributor.authorLevinger, Nancy E., committee member
dc.contributor.authorHenry, Charles S., committee member
dc.contributor.authorKelly, Eugene F., committee member
dc.date.accessioned2007-01-03T06:48:44Z
dc.date.available2015-06-30T05:57:00Z
dc.date.issued2014
dc.description.abstractMillions of cubic meters of uranium (U) mine tailings worldwide and millions of gallons of contaminated groundwater are the result of U mining and milling activity. Arsenic can occur at up to 10 weight percent in U ore, so both U and As can be released during U mining. Although these elements commonly occur together, little research into their redox behavior when present in the same environmental system has been performed. The goal of this research is to gain an improved understanding of how redox chemistry affects U and As speciation and complexation when the two elements are present together as co-contaminants. The North Cave Hills in Harding County, South Dakota is an abandoned U mine where overburden has been left open to weathering and transport since mining began in 1955. The exposed overburden has resulted in above-background level concentrations of U and As in sediments and groundwater in the surrounding wetlands. We conducted a field-scale study to investigate U and As redox chemistry at the North Cave Hills by taking sediment samples from the tailings pile and the down gradient watershed in order to assess U and As fate and transport. As sediments pass through anoxic zones at the field site, U is immobilized as reduction takes place but As can simultaneously be released into surface waters as reductive dissolution of Fe minerals also occurs. A laboratory-based study was conducted in order to examine the redox chemistry of U and As in North Cave Hills sediments under controlled conditions. Upon microbial reduction of sulfate and formation of mackinawite in batch systems, U(VI) and As(V) were reduced to nano- UO2 and a reduced As-sulfide mineral phase respectively during biostimulation by three different electron donors. When these systems were exposed to air for 24 hours, mackinawite protected U and As from oxidation and little change in their solid-phase speciation was observed. While mackinawite was shown to play a role in reduction, we could not determine if direct microbial reduction of U and As was also taking place in the systems. In order to further explore the reduction of U(VI) and As(V) by mackinawite, an experiment was set up to determine if As(V) prevented U(VI) reduction, especially following the formation of uranyl arsenate precipitates. As(V) only had an impact on the extent of U reduction at concentrations higher than would occur in most environmental systems. When As(V) concentrations were high, U(VI) was shown to be resistant to reduction because of the precipitation of a uranyl arsenate mineral phase. The findings in this dissertation contribute important information that will improve our current understanding of U and As redox behavior that will lead to improved remediation strategies to effectively prevent the mobilization of both elements in environmental systems.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.identifierTroyer_colostate_0053A_12364.pdf
dc.identifier.urihttp://hdl.handle.net/10217/82665
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectredox
dc.subjectmining
dc.subjectarsenic
dc.subjecttailings
dc.subjecturanium
dc.titleImpact of iron and redox chemistry on the environmental fate and transport of metalloids and radionuclides
dc.typeText
dcterms.embargo.expires2015-06-30
dcterms.embargo.terms2015-06-30
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemistry
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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