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1	Liquidus surface for the high cryolite/low alumina portion of the Na₃AlF₆-AlF₃-CaF₂-Al₂O₃ system Xu, Ming-Wei Paul January 1983 (has links) The purpose of this work was to determine the liquidus surface of the cryolite-rich portion of the ternary system Na₃AlF₆-CaF₂-AlF₃ and to establish the effect of Al₂O₃ on the operation of the Hall cell electrolysis. A series of isotherm of the cryolite-rich portion were graphed. It was shown that pseudo-binary phase diagrams of Al₂O₃ and bulk composition in the cryolite-rich portion of the Na₃AlF₆-CaF₂-AlF₃ system were found to be simple eutectic. The temperatures and the alumina contents of the double solubility limit, two important parameters for the Hall cell, of the joins 95 Na₃AlF₆/5 AlF₃-Na₃AlF₆, 90 Na₃AlF₆/ 10 NaCaAlF₆ and 85 Na₃AlF₃/15 AlF₃-NaCaAlF₆ were determined. The cryolite liquidus temperature of the quaternary system Na₃AlF₆-CaF₂-AlF₃-Al₂O₃ was found to be expressed by: T<sub>Liq.</sub>. (C) = 1009.4 + 4.059(CaF₂) - 1.167(CaF₂)² + 0.968 x (CaF₂)(AlF₃) - 0.105(CaF₂)(AlF₃)² + 0.073 x (CaF₂)²(AlF₃) + 0.002(CaF₂)² (AlF₃)² - 4.165 x (AlF₃) - 0.054(AlF₃)² - 5.33(Al₂O₃) for CaF₂ 3.8~11.25%, AlF₃ 5~20%. / M.S. LD5655.V855 1983.X85 Aluminum -- Electrometallurgy Cryolite Hall Héroult process
2	Phase equilibria in the system Na₃AlF₆-Al₂0₃- NaCaAlF₆ Parks, William P. January 1982 (has links) The NaCaAlF₆-Al₂O₃ and Na₃AlF₆-Al₂O₃-NaCaAlF₆ phase diagrams were determined using DTA, x-ray diffraction, quench analysis, and optical microscopy. The NaCaAlF₆-Al₂O₃ system was a simple eutectic system with the eutectic located below 0.5 weight percent NaCaAlF₆. The ternary system was a eutectic system showing solid solution of NaCaAlF₆ in both polymorphs of Na₃AlF₆. Alumina exhibited no appreciable solubility in Na₃AlF₆ and, in the ternary system, less than 2% solubility above 15% NaCaAlF₆. / Master of Science LD5655.V855 1982.P375 Aluminum -- Electrometallurgy Phase rule and equilibrium Hall Héroult process
3	The Effect of Aluminium Industry Effluents on Sediment Bacterial Communities Gill, Hardeep 19 October 2012 (has links) The goal of this project was to develop novel bacterial biomarkers for use in an industrial context. These biomarkers would be used to determine aluminium industry activity impact on a local ecosystem. Sediment bacterial communities of the Saguenay River are subjected to industrial effluent produced by industry in Jonquière, QC. In-situ responses of these communities to effluent exposure were measured and evaluated as potential biomarker candidates for exposure to past and present effluent discharge. Bacterial community structure and composition between control and affected sites were investigated. Differences observed between the communities were used as indicators of a response to industrial activity through exposure to effluent by-products. Diversity indices were not significantly different between sites with increased effluent exposure. However, differences were observed with the inclusion of algae and cyanobacteria. UniFrac analyses indicated that a control (NNB) and an affected site (Site 2) were more similar to one another with regard to community structure than either was to a medially affected site (Site 5) (Figure 2.4). We did not observe a signature of the microbial community structure that could be predicted with effluent exposure. Microbial community function in relation to bacterial mercury resistance (HgR) was also evaluated as a specific response to the mercury component present in sediments. Novel PCR primers and amplification conditions were developed to amplify merP, merT and merA genes belonging to the mer-operon which confers HgR (Table 5.6). To our knowledge, the roles of merP and merT have not been explored as possible tools to confirm the presence of the operon. HgR gene abundance in sediment microbial communities was significantly correlated (p < 0.05) to total mercury levels (Figure 3.4) but gene expression was not measurable. We could not solely attribute the release of Hg0 from sediments in bioreactor experiments to a biogenic origin. However, there was a 1000 fold difference in measured Hg0 release between control and affected sites suggesting that processes of natural remediation may be taking place at contaminated sites (Figure 3.7). Abundance measurements of HgR related genes represent a strong response target to the mercury immobilized in sediments. Biomarkers built on this response can be used by industry to measure long term effects of industrially derived mercury on local ecosystems. The abundance of mer-operon genes in affected sites indicates the presence of a thriving bacterial community harbouring HgR potential. These communities have the capacity to naturally remediate the sites they occupy. This remediation could be further investigated. Additional studies will be required to develop biomarkers that are more responsive to contemporary industrial activity such as those based on the integrative oxidative stress response. bacteria heavy metal resistance mercury mer operon sediment biomarker community diversity mercuric reductase sediment metagenome environmental microbiology industry bauxite alumina red mud Saguenay River, QC PCR qPCR bioreactor gene merT merP merA rpoB katG glnA river system environmental DNA aluminum industry Bayer Process Hall–Héroult Process 16S rRNA UniFrac sediment wash buffer community richness mothur ribosomal database project DNA sequencing aluminum aluminium RNA metatranscriptome ecotoxicology environmental contaminants industrial effluent
4	The Effect of Aluminium Industry Effluents on Sediment Bacterial Communities Gill, Hardeep 19 October 2012 (has links) The goal of this project was to develop novel bacterial biomarkers for use in an industrial context. These biomarkers would be used to determine aluminium industry activity impact on a local ecosystem. Sediment bacterial communities of the Saguenay River are subjected to industrial effluent produced by industry in Jonquière, QC. In-situ responses of these communities to effluent exposure were measured and evaluated as potential biomarker candidates for exposure to past and present effluent discharge. Bacterial community structure and composition between control and affected sites were investigated. Differences observed between the communities were used as indicators of a response to industrial activity through exposure to effluent by-products. Diversity indices were not significantly different between sites with increased effluent exposure. However, differences were observed with the inclusion of algae and cyanobacteria. UniFrac analyses indicated that a control (NNB) and an affected site (Site 2) were more similar to one another with regard to community structure than either was to a medially affected site (Site 5) (Figure 2.4). We did not observe a signature of the microbial community structure that could be predicted with effluent exposure. Microbial community function in relation to bacterial mercury resistance (HgR) was also evaluated as a specific response to the mercury component present in sediments. Novel PCR primers and amplification conditions were developed to amplify merP, merT and merA genes belonging to the mer-operon which confers HgR (Table 5.6). To our knowledge, the roles of merP and merT have not been explored as possible tools to confirm the presence of the operon. HgR gene abundance in sediment microbial communities was significantly correlated (p < 0.05) to total mercury levels (Figure 3.4) but gene expression was not measurable. We could not solely attribute the release of Hg0 from sediments in bioreactor experiments to a biogenic origin. However, there was a 1000 fold difference in measured Hg0 release between control and affected sites suggesting that processes of natural remediation may be taking place at contaminated sites (Figure 3.7). Abundance measurements of HgR related genes represent a strong response target to the mercury immobilized in sediments. Biomarkers built on this response can be used by industry to measure long term effects of industrially derived mercury on local ecosystems. The abundance of mer-operon genes in affected sites indicates the presence of a thriving bacterial community harbouring HgR potential. These communities have the capacity to naturally remediate the sites they occupy. This remediation could be further investigated. Additional studies will be required to develop biomarkers that are more responsive to contemporary industrial activity such as those based on the integrative oxidative stress response. bacteria heavy metal resistance mercury mer operon sediment biomarker community diversity mercuric reductase sediment metagenome environmental microbiology industry bauxite alumina red mud Saguenay River, QC PCR qPCR bioreactor gene merT merP merA rpoB katG glnA river system environmental DNA aluminum industry Bayer Process Hall–Héroult Process 16S rRNA UniFrac sediment wash buffer community richness mothur ribosomal database project DNA sequencing aluminum aluminium RNA metatranscriptome ecotoxicology environmental contaminants industrial effluent
5	The Effect of Aluminium Industry Effluents on Sediment Bacterial Communities Gill, Hardeep January 2012 (has links) The goal of this project was to develop novel bacterial biomarkers for use in an industrial context. These biomarkers would be used to determine aluminium industry activity impact on a local ecosystem. Sediment bacterial communities of the Saguenay River are subjected to industrial effluent produced by industry in Jonquière, QC. In-situ responses of these communities to effluent exposure were measured and evaluated as potential biomarker candidates for exposure to past and present effluent discharge. Bacterial community structure and composition between control and affected sites were investigated. Differences observed between the communities were used as indicators of a response to industrial activity through exposure to effluent by-products. Diversity indices were not significantly different between sites with increased effluent exposure. However, differences were observed with the inclusion of algae and cyanobacteria. UniFrac analyses indicated that a control (NNB) and an affected site (Site 2) were more similar to one another with regard to community structure than either was to a medially affected site (Site 5) (Figure 2.4). We did not observe a signature of the microbial community structure that could be predicted with effluent exposure. Microbial community function in relation to bacterial mercury resistance (HgR) was also evaluated as a specific response to the mercury component present in sediments. Novel PCR primers and amplification conditions were developed to amplify merP, merT and merA genes belonging to the mer-operon which confers HgR (Table 5.6). To our knowledge, the roles of merP and merT have not been explored as possible tools to confirm the presence of the operon. HgR gene abundance in sediment microbial communities was significantly correlated (p < 0.05) to total mercury levels (Figure 3.4) but gene expression was not measurable. We could not solely attribute the release of Hg0 from sediments in bioreactor experiments to a biogenic origin. However, there was a 1000 fold difference in measured Hg0 release between control and affected sites suggesting that processes of natural remediation may be taking place at contaminated sites (Figure 3.7). Abundance measurements of HgR related genes represent a strong response target to the mercury immobilized in sediments. Biomarkers built on this response can be used by industry to measure long term effects of industrially derived mercury on local ecosystems. The abundance of mer-operon genes in affected sites indicates the presence of a thriving bacterial community harbouring HgR potential. These communities have the capacity to naturally remediate the sites they occupy. This remediation could be further investigated. Additional studies will be required to develop biomarkers that are more responsive to contemporary industrial activity such as those based on the integrative oxidative stress response. bacteria heavy metal resistance mercury mer operon sediment biomarker community diversity mercuric reductase sediment metagenome environmental microbiology industry bauxite alumina red mud Saguenay River, QC PCR qPCR bioreactor gene merT merP merA rpoB katG glnA river system environmental DNA aluminum industry Bayer Process Hall–Héroult Process 16S rRNA UniFrac sediment wash buffer community richness mothur ribosomal database project DNA sequencing aluminum aluminium RNA metatranscriptome ecotoxicology environmental contaminants industrial effluent

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