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dc.rights.licenseUsers may download and share copies with attribution in accordance with a Creative Commons Attribution-Noncommercial-No Derivative Works 3.0 license. No commercial use or derivatives are permitted without the explicit approval of the author.
dc.contributorHedden, Ronald
dc.contributorWoodcock, Corey
dc.contributor.advisorChakrapani, Vidhya
dc.contributor.authorCantone, David, M.
dc.date.accessioned2023-06-01T19:13:56Z
dc.date.available2023-06-01T19:13:56Z
dc.date.issued2023-05
dc.identifier.urihttps://hdl.handle.net/20.500.13015/6643
dc.descriptionMay2023
dc.descriptionSchool of Engineering
dc.description.abstractCertain transition metal oxides are known to readily reduce chromium ion from its highly toxic +VI oxidation state to its +III state, which is an important nutrient for human biological functions. Herein, the factors which govern the reduction of Cr (VI) to Cr (III) by five selected Fe and Mn based metal oxides were investigated in order to better understand the mechanism driving the reduction. Results show that of the five metal oxides (hematite, hollandite, magnetite, manganite, and Romanechite), only Romanechite displayed the capability of reducing the concentration of Cr (VI) in isolation. This distinctive capability is likely related to their differences in their electronic properties, namely the differing band alignment with respect to Cr (VI) / Cr (III) redox couple in the aqueous environment.
dc.languageENG
dc.language.isoen_US
dc.publisherRensselaer Polytechnic Institute, Troy, NY
dc.relation.ispartofRensselaer Theses and Dissertations Online Collection
dc.subjectChemical engineering
dc.titleLinking mineral reactivity to its semiconducting band structure
dc.typeElectronic thesis
dc.typeThesis
dc.date.updated2023-06-01T19:13:59Z
dc.rights.holderThis electronic version is a licensed copy owned by Rensselaer Polytechnic Institute (RPI), Troy, NY. Copyright of original work retained by author.
dc.creator.identifierhttps://orcid.org/0009-0008-8753-7009
dc.description.degreeMS
dc.relation.departmentDept. of Chemical and Biological Engineering


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