Spelling suggestions: "subject:"bickel asulphide"" "subject:"bickel disulphide""
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The influence of particle aggregation and pulp chemistry on the flotation of pentlandite fines in the slimes stream at Mt Keith /McQuie, James D. Unknown Date (has links)
Thesis (MAppSc)--University of South Australia, [1999?]
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The influence of pH and dispersants on pentlandite-lizardite interactions and flotation selectivity /Jowett, Leanne Katrina Unknown Date (has links)
Thesis (MAppSc)--University of South Australia, 1999
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Chemical aspects in the flotation of pentlandite in Western Australian nickel oresPietrobon, Michael C January 1996 (has links)
Thesis (MAppSc)--University of South Australia, 1996
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Chemical aspects in the flotation of pentlandite in Western Australian nickel oresPietrobon, Michael C January 1996 (has links)
Thesis (MAppSc)--University of South Australia, 1996
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Chemical aspects in the flotation of pentlandite in Western Australian nickel oresPietrobon, Michael C January 1996 (has links)
Thesis (MAppSc)--University of South Australia, 1996
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Application of electrochemical kinetics to elucidate the leaching mechanism in the bio-oxidation of a synthetic nickel sulphideHuberts, Robert 06 February 2015 (has links)
The importance of the direct and indirect mechanisms in
the bacterial leaching of a synthetic nickel sulphide is
investigated using an electrochemical leaching model.
Sterile controls runs, in which only ferric leaching
took place, are compared with runs in the presence of an
active, adapted bacterial culture.
The direct mechanism occurs when bacteria attach to the
sulphide mineral and catalyze the oxidation of the
mineral, presumably with enzymes (biological catalysts).
No evidence was found of the direct mechanism, in fact
ferric leaching appeared to be inhibited as the bacterial
presence increased due to growth. Considering
evidence obtained by the fitting of the electrochemical
model, it is tentatively suggested that leaching of the
mineral is largely due to chemical ferric leaching, with
the leaching role of bacteria restricted to re-oxidizing
the resulting ferrous ions. Whether this is the case
for other minerals remains to be established.
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Cosmos greenstone terrane : insights into an Archaean volcanic arc, associated with komatiite-hosted nickel sulphide mineralisation, from U-Pb dating, volcanic stratigraphy and geochemistryDe Joux, Alexandra January 2014 (has links)
The Neoarchaean Agnew-Wiluna greenstone belt (AWB) of the Kalgoorlie Terrane, within the Eastern Goldfields Superterrane (EGS) of the Yilgarn Craton, Western Australia, contains several world-class, komatiite-hosted, nickel-sulphide ore bodies. These are commonly associated with felsic volcanic successions, many of which are considered to have a tonalite-trondhjemite-dacite (TTD) affinity. The Cosmos greenstone sequence lies on the western edge of the AWB and this previously unstudied mineralised volcanic succession contrasts markedly in age, geochemistry, emplacement mechanisms and probable tectonic setting to that of the majority of the AWB and wider EGS. Detailed subsurface mapping has shown that the footwall to the Cosmos mineralised ultramafic sequence consists of an intricate succession of both fragmental and coherent extrusive lithologies, ranging from basaltic andesites through to rhyolites, plus later-formed felsic and basaltic intrusions. The occurrence of thick sequences of amygdaloidal intermediate lavas intercalated with extensive sequences of dacite lapilli tuff, coupled with the absence of marine sediments or hydrovolcanic products, indicates the succession was formed in a subaerial environment. Chemical composition of the non-ultramafic lithologies is typified by a high-K calc-alkaline to shoshonite signature, indicative of formation in a volcanic arc setting. Assimilation-fractional crystallisation modelling has shown that at least two compositionally distinct sources must be invoked to explain the observed basaltic andesite to rhyolite magma suite. High resolution U-Pb dating of several units within the succession underpins stratigraphic relationships established in the field and indicates that the emplacement of the Cosmos succession took place between ~2736 Ma and ~2653 Ma, making it significantly older and longer-lived than most other greenstone successions within the Kalgoorlie Terrane. Extrusive periodic volcanism spanned ~50 Myrs with three cycles of bimodal intermediate/felsic and ultramafic volcanism occurring between ~2736 Ma and ~2685 Ma. Periodic intrusive activity, related to the local granite plutonism, lasted for a further ~32 Myrs or until ~2653 Ma. The Cosmos succession either represents a separate, older terrane in its own right or it has an autochthonous relationship with the AWB but volcanism initiated much earlier in this region than currently considered. Dating of the Cosmos succession has demonstrated that high-resolution geochronology within individual greenstone successions can be achieved and provides more robust platforms for interpreting the evolution of ancient mineralised volcanic successions. The geochemical affinity of the Cosmos succession indicates a subduction zone was operating in the Kalgoorlie Terrane by ~2736 Ma, much earlier than considered in current regional geodynamic models. The Cosmos volcanic succession provides further evidence that plate tectonics was in operation during the Neoarchaean, contrary to some recently proposed tectonic models.
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Bioleaching of low-grade nickel sulphide ore at elevated pHCameron, Rory 18 February 2011 (has links)
This thesis examines the bioleaching of six different Canadian nickel sulphide ores at pH levels above what is generally considered optimum (~ 2). The majority of work discussed in this thesis was conducted with a low-grade metamorphosed ultramafic nickel sulphide ore from Manitoba, Canada (Ore 3), which is not currently exploitable with conventional technologies. The ore contains 21% magnesium and 0.3% nickel. Nickel is the only significant metal value, and is present primarily as pentlandite. A substantial fraction of the magnesium is present as the serpentine mineral lizardite, making processing difficult with conventional pyro- and biohydrometallurgical techniques. The work with this ore has two equally important objectives: to minimize magnesium mobilization and to obtain an acceptable level of nickel extraction. Batch stirred-tank bioleaching experiments were conducted with finely ground ore ( 147 µm) with temperature and pH control. The first phase of experimentation examined the effect of pH (2 to 6) at 30 °C, and the second phase examined all combinations of three pH levels (3, 4 and 5) and five temperatures (5, 15, 22.5, 30, and 45 °C).
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Bioleaching of low-grade nickel sulphide ore at elevated pHCameron, Rory 18 February 2011 (has links)
This thesis examines the bioleaching of six different Canadian nickel sulphide ores at pH levels above what is generally considered optimum (~ 2). The majority of work discussed in this thesis was conducted with a low-grade metamorphosed ultramafic nickel sulphide ore from Manitoba, Canada (Ore 3), which is not currently exploitable with conventional technologies. The ore contains 21% magnesium and 0.3% nickel. Nickel is the only significant metal value, and is present primarily as pentlandite. A substantial fraction of the magnesium is present as the serpentine mineral lizardite, making processing difficult with conventional pyro- and biohydrometallurgical techniques. The work with this ore has two equally important objectives: to minimize magnesium mobilization and to obtain an acceptable level of nickel extraction. Batch stirred-tank bioleaching experiments were conducted with finely ground ore ( 147 µm) with temperature and pH control. The first phase of experimentation examined the effect of pH (2 to 6) at 30 °C, and the second phase examined all combinations of three pH levels (3, 4 and 5) and five temperatures (5, 15, 22.5, 30, and 45 °C).
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Bioleaching of low-grade nickel sulphide ore at elevated pHCameron, Rory 18 February 2011 (has links)
This thesis examines the bioleaching of six different Canadian nickel sulphide ores at pH levels above what is generally considered optimum (~ 2). The majority of work discussed in this thesis was conducted with a low-grade metamorphosed ultramafic nickel sulphide ore from Manitoba, Canada (Ore 3), which is not currently exploitable with conventional technologies. The ore contains 21% magnesium and 0.3% nickel. Nickel is the only significant metal value, and is present primarily as pentlandite. A substantial fraction of the magnesium is present as the serpentine mineral lizardite, making processing difficult with conventional pyro- and biohydrometallurgical techniques. The work with this ore has two equally important objectives: to minimize magnesium mobilization and to obtain an acceptable level of nickel extraction. Batch stirred-tank bioleaching experiments were conducted with finely ground ore ( 147 µm) with temperature and pH control. The first phase of experimentation examined the effect of pH (2 to 6) at 30 °C, and the second phase examined all combinations of three pH levels (3, 4 and 5) and five temperatures (5, 15, 22.5, 30, and 45 °C).
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