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Tracing on-axis diffuse fluids by chalcophile elements distribution in upper oceanic crust at Pito Deep, East Pacific RiseTian, Zhu 29 November 2016 (has links)
Mid-ocean ridge hydrothermal systems play an important role in the cycling of energy and mass between the solid earth and oceans. The on-axis low-temperature diffuse fluids (temperature lower than ~100 °C) carry ~90% of the on-axis heat fluxes, but diffuse fluids generation is poorly constrained. This study uses the abundance of the chalcophile elements, which form metal-sulphides in the rock record, to test models for diffuse fluids generation. These include mixing between seawater and high-temperature hydrothermal fluids and conductive cooling of high- temperature hydrothermal fluids.
This thesis determined the concentrations of the elements of interest (As, Mo, Ag, Cd, Sn, and Tl) in geological reference materials using standard addition method in ICP-MS. These values were used to calibrate the analysis of samples from Pito Deep to trace the abundance of these elements within the upper oceanic crust. The results show that the Zn, Cu, As, Ag, Cd, Tl, and Pb are generally depleted in sheeted dikes and enriched in the lava unit and/or the transition zone, which is consistent with previous studies on fast-spreading EPR crust at Hole 504B, Hess Deep and Hole 1256D. The enrichment of these elements in the lava unit and/or the transition zone suggests that cooling high-temperature hydrothermal fluids to form diffuse fluids occurred in this
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iv area of the oceanic crust. Molybdenum and Sb are added into all units of the crust by
recharging seawater. The concentrations of chalcophile elements in diffuse fluids were calculated by a mass balance. The results of this study favored a diffuse fluids generation model that involves mixing of seawater and high-temperature hydrothermal fluids. Results also show that the observed concentrations of Mo and Sb requires extra input source besides recharging seawater and oceanic crust, possibly particulates in seawater. / Graduate / juliatian2013@gmail.com
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In-situ Removal of Hydrogen Sulphide from Landfill Gas : Arising from the Interaction between Municipal Solid Waste and Sulphide Mine Environments within Bioreactor ConditionsLazarevic, David Andrew January 2007 (has links)
This project was compiled in co-operation with the Royal Institute of Technology, Stockholm and Veolia Environmental Services (Australia) at the Woodlawn Bioreactor in NSW, Australia. Hydrogen sulphide is an unwanted component of landfill gas, raising occupational health and safety concerns, whilst leading to acid gas corrosion of power generation equipment and increased emissions of SOx, a primary constituent of acidification. Australian governmental requirements to place a periodic cover over the unused proportion of the tipping surface of landfills and bioreactors create an interesting opportunity for the removal of the hydrogen sulphide component of landfill gas. Using waste materials containing a high concentration of metals as waste cover can enhance the precipitation of sulphur in the form of metal sulphides. The reduction of sulphate via sulphate reducing bacteria is prevalent in sites that have a sizeable inflow of sulphate. The Woodlawn Bioreactor is located in an area where the influence of sulphate has a critical influence of bioreactor performance and production of hydrogen sulphide. Through a series of experimental bioreactors it was established that from the use of metalliferous periodic waste covers, the hydrogen sulphide component of landfill gas was maintained at an extremely low level when compared to the levels of hydrogen sulphide produced in waste under the influence of high sulphate loads with no waste cover. / www.ima.kth.se
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