Application of phosphate and surfactant-modified zeolite for remediation/attenuation of trace elements in soil and coal fly ash

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dc.contributor Zheng, Chunmiao
dc.contributor Andrus, C. Fred T.
dc.contributor Tick, Geoffrey R.
dc.contributor Arai, Yuji
dc.contributor.advisor Donahoe, Rona Jean
dc.contributor.author Neupane, Ghanashyam
dc.date.accessioned 2017-03-01T16:37:08Z
dc.date.available 2017-03-01T16:37:08Z
dc.date.issued 2012
dc.identifier.other u0015_0000001_0001133
dc.identifier.other Neupane_alatus_0004D_11265
dc.identifier.uri https://ir.ua.edu/handle/123456789/1611
dc.description Electronic Thesis or Dissertation
dc.description.abstract This dissertation presents results of a research work aimed at understanding and addressing trace element contamination sourced by coal fly ash and arsenic trioxide herbicide. Both alkaline and acidic fly ash samples were found to contain significant concentrations of environmentally available trace elements. The treatment of fly ash leachate with surfactant-modified zeolite (SMZ) decreased the mobility of several trace elements. In general, up to 30% of the As, Mo, and V; up to 80% of the Cr; and up to 20% of the Se and Sr were removed from the leachate after SMZ treatment. Batch experiments, surface complexation modeling, and X-ray spectroscopic tools were used to elucidate the kinetics and mechanisms of arsenate (As(V)) and phosphate (Pi) adsorption on ferric hydroxide. Both oxyanions showed similar adsorptions during single-ion adsorption experiments; however, As(V) was preferentially adsorbed during competitive adsorption experiments. Similarly, more As(V) was adsorbed when it was loaded in sequence in Pi-equilibrated system than vice versa. Both oxyanions competed for adsorption on ferric-hydroxide and each of them showed a limited capacity to desorb the other, and relatively, more pre-equilibrated Pi was desorbed by sequentially added As(V) than vice versa. The As K-edge EXAFS analysis indicated the presence mononuclear and binuclear bidentate As(V) surface complexes. The Fe coordination numbers (CN) of these complexes increased with increasing time and decreased with addition of Pi into the system. Finally, an arsenic-contaminated soil collected from an industrial site located in the southeastern United States was amended with Pi and Ca to precipitate the arsenic as As-bearing apatite-like minerals. Phosphoric acid amendment of the soil with simultaneous addition of Ca dramatically decreased the mobility of soil As to near zero at pH > 6. Characterization of precipitate separated from the Ca-Pi treated soil by X-ray diffraction indicated that a carbonate-apatite mineral was formed in the soil and likely incorporated As(V) into its structure. The low solubilities of many of the Ca-Pi-As(V) minerals suggest that Ca-Pi treatment has promise as an effective, long-term method for in situ chemical fixation of As in contaminated soils and wastewaters.
dc.format.extent 256 p.
dc.format.medium electronic
dc.format.mimetype application/pdf
dc.language English
dc.language.iso en_US
dc.publisher University of Alabama Libraries
dc.relation.ispartof The University of Alabama Electronic Theses and Dissertations
dc.relation.ispartof The University of Alabama Libraries Digital Collections
dc.relation.hasversion born digital
dc.rights All rights reserved by the author unless otherwise indicated.
dc.subject.other Geochemistry
dc.subject.other Geology
dc.subject.other Geological engineering
dc.title Application of phosphate and surfactant-modified zeolite for remediation/attenuation of trace elements in soil and coal fly ash
dc.type thesis
dc.type text
etdms.degree.department University of Alabama. Dept. of Geological Sciences
etdms.degree.discipline Geology
etdms.degree.grantor The University of Alabama
etdms.degree.level doctoral
etdms.degree.name Ph.D.


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