INFLUENCE OF MICROBIAL SULFATE REDUCTION ON PORE-WATER CHEMISTRY IN OIL SANDS FROTH TREATMENT TAILINGS
| dc.contributor.advisor | Lindsay, Matthew BJ | |
| dc.contributor.committeeMember | Mcbeth, Joyce | |
| dc.contributor.committeeMember | Chang, Wonjae | |
| dc.contributor.committeeMember | Sproat, Colin | |
| dc.creator | Marchi, Jake Anthony Allen | |
| dc.creator.orcid | 0009-0007-5951-8284 | |
| dc.date.accessioned | 2024-01-17T19:46:19Z | |
| dc.date.available | 2024-01-17T19:46:19Z | |
| dc.date.copyright | 2023 | |
| dc.date.created | 2023-12 | |
| dc.date.issued | 2024-01-17 | |
| dc.date.submitted | December 2023 | |
| dc.date.updated | 2024-01-17T19:46:19Z | |
| dc.description.abstract | Oxidative weathering of froth treatment tailings (FTT) at oil sands mines in Northern Alberta has the potential to generate acidic and metalliferous porewater. Residual bitumen and light hydrocarbons in FTT support growth of a diverse range of microbes, including those capable of dissimilatory sulfate reduction (DSR). This biogeochemical process can be effective in removing sulfide-mineral oxidation products such as Fe, SO4, and trace elements including As, Co, Cu, Ni, Se, and Zn through sulfate reduction and sulfide mineral precipitation under anoxic conditions. While previous experiments that have stimulated sulfidogenesis through organic carbon amendments effectively decreased the mass flux of sulfide-mineral oxidation products in mining environments, the extent of this process and its ability to attenuate sulfide-mineral oxidation products in FTT supported by residual hydrocarbons is unknown. The objective of this thesis is to assess the impact of microbial sulfate reduction on FTT pore-water geochemistry and to determine the potential extent to which this process may be supported by residual hydrocarbons within the tailings deposit. Laboratory experiments were designed to examine the influence of sulfidogenesis on pore-water chemistry and to constrain rates of sulfate reduction, while assessing the capacity for metal(loid) removal due to this process. Through batch and column experiments sulfate reduction was found to contribute to metal(loid) and sulfate removal, as well as pH buffering and H2S generation. Removal of As, Co, Ni, and Se exceeded 90% in simulated porewater over a pH range of 5 – 8. Removal of Fe was minimal below pH 7, but exceeded 95% in solutions above pH 7 with long residence times. Zn removal was influenced by ∑S(-II)(aq) concentrations, with increased Zn removal seen at lower ∑S(-II)(aq) concentrations. Sulfur isotope samples taken during the batch experiment show an increase in 34S-SO4 with decreasing SO4(aq) concentrations over time, showing ongoing microbial sulfate reduction during the experiment. A mass-based approach to determine sulfate removal found sulfur removal rates remained constant around 1.5 μmol d-1 g-1 when solutions were not saturated with respect to gypsum. Residence time and pH were major influences on the effectiveness of sulfate reduction, with enhanced metal(loid) removal occurring with longer residence times at circumneutral pH. These results show the pool of organic carbon in FTT deposits is capable of supporting dissimilatory sulfate reduction and this process can decrease mass fluxes of sulfide-mineral oxidation products in FTT porewater. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.uri | https://hdl.handle.net/10388/15440 | |
| dc.language.iso | en | |
| dc.subject | Sulfate reduction | |
| dc.subject | oil sands mining | |
| dc.subject | froth treatment tailings | |
| dc.subject | AMD | |
| dc.subject | mine closure geochemistry | |
| dc.subject | microbial | |
| dc.title | INFLUENCE OF MICROBIAL SULFATE REDUCTION ON PORE-WATER CHEMISTRY IN OIL SANDS FROTH TREATMENT TAILINGS | |
| dc.type | Thesis | |
| dc.type.material | text | |
| thesis.degree.department | Geological Sciences | |
| thesis.degree.discipline | Geology | |
| thesis.degree.grantor | University of Saskatchewan | |
| thesis.degree.level | Masters | |
| thesis.degree.name | Master of Science (M.Sc.) |