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dc.contributor.authorRitchie, Vanessa J.
dc.date.accessioned2020-10-16T23:55:44Z
dc.date.available2020-10-16T23:55:44Z
dc.date.issued2011-05
dc.identifier.urihttp://hdl.handle.net/11122/11371
dc.descriptionThesis (M.S.) University of Alaska Fairbanks, 2011en_US
dc.description.abstractOxidative weathering processes of acid-forming sulfide minerals, such as pyrite (FeS₂), and associated arsenopyrite (FeAsS) and stibnite (Sb₂S₃), can have a significant impact on water quality associated with current and legacy mining operations. Concentrations of toxic metals and metalloids, such as antimony (Sb) and arsenic (As), in acid mine drainage can exceed drinking water quality standards by orders of magnitude. This study provides a detailed hydrogeochemical assessment of the mobility and chemical fate of antimony and arsenic in streams draining from historic antimony mines within Denali National Park and Preserve, Alaska. Antimony and arsenic concentrations in stream water reach up to 720 parts per billion (ppb) and 239 ppb, respectively. Aqueous phase antimony and arsenic speciation was determined using liquid chromatography coupled to an inductively coupled plasma mass spectrometer. Antimony in all water samples is predominantly found as Sb⁵ whereas arsenic was detected as mixtures of As³ /As⁵⁺ . Elevated antimony concentrations extend over 8 km downstream from the source, whereas arsenic quickly attenuates within 1.5 km. High correlation between antimony/arsenic and iron concentrations in fine-fraction streambed sediment indicates that sorption and (co)precipitation with iron (hydr)oxides is an important pathway for the attenuation of antimony and arsenic in natural waters.en_US
dc.description.tableofcontents1. Introduction and objectives -- 1.1. Sources and impacts of antimony and arsenic contamination -- 1.2. Geochemistry of acid mine drainage from sulfidic mine tailings -- 1.2.1. Acidic water formation -- 1.2.2. Controls on drainage chemical composition -- 1.3. Antimony and arsenic in natural waters -- 1.4. Antimony aqueous geochemistry -- 1.4.1. Thermodynamic equilibrium predictions for antimony -- 1.4.2. Kinetic influences on antimony speciation -- 1.4.3. Antimony mobility -- 1.5. Arsenic aqueous geochemistry -- 1.5.1. Thermodynamic equilibrium predictions for arsenic -- 1.5.2. Kinetic influences on arsenic speciation -- 1.5.3. Arsenic mobility -- 1.6. Research objectives -- 1.7. Outline of presented work -- References -- 2. Field study: site description, experimental methods, results and discussion -- Abstract -- 2.1. Introduction -- 2.2. Study area -- 2.3. Methods -- 2.3.1. Field sampling and in situ measurements -- 2.3.2. Analytical methods -- 2.4. Results and discussion -- 2.4.1. Major/minor element aqueous chemistry -- 2.4.2. Aqueous speciation and redox potentials -- 2.4.3. Mobility and attenuation of Sb and As -- 2.5. Summary -- Acknowledgements -- References -- 3. Conclusions and future work -- Appendix.en_US
dc.language.isoen_USen_US
dc.subjectgold mines and miningen_US
dc.subjectAlaskaen_US
dc.subjectKantishna Hillsen_US
dc.subjectantimonyen_US
dc.subjectarsenicen_US
dc.subjectacid mine drainageen_US
dc.titleMobility and chemical fate of antimony and arsenic in historic mining environments of Kantishna Hills, Denali National Park and Preserve, Alaskaen_US
dc.typeThesisen_US
dc.type.degreemsen_US
dc.identifier.departmentDepartment of Chemistry and Biochemistryen_US
refterms.dateFOA2020-10-16T23:55:45Z


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