Demand for high purity silica used in component manufacture is set to outstrip current supply in the near future. As such, alternative processing routes to feed-stock materials suitable for use in lighting and solar cell fabrication are required, without having to rely on reject material from semi-conductor manufacture. In this work, we report a facile, environmentally friendly method of producing quartz powder with a total residual impurity level of 30 ± 3 ppm from whole pebbles having an initial impurity level of 158 ± 22 ppm. This has been achieved using a metallurgical upgrading process incorporating microwave pre-treatment, crushing and milling, High Intensity Wet Magnetic Separation (HIWMS) and acid leaching. This process yielded a quartz powder having an 80% reduction in residual impurities compared to the untreated quartz pebbles. Pre-treatment of whole quartz pebbles in a multimode microwave cavity for 10 minutes yielded a reduction of the residual elemental impurity content associated with micro-fluidic inclusion sites containing calcium, potassium and sodium of 84, 78, and 50 % respectively. Statistically significant reduction in residual aluminium phases was also observed (83%) compared to the as received material to below the IOTA® specification for Ultra High Pure Quartz produced by Sibleco. Mechanistically, this has been achieved by selectively heating impurity containing microfluidic inclusion sites. Resulting in their explosive decrepitation and enabling removal of the impurities in subsequent processing steps. It has been concluded that natural quartz pebbles can be upgraded through a combination of microwave treatment, magnetic and chemical refinement to produce a viable feedstock for the subsequent production of solar grade silicon.

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This paper shows how feedstock densification gives rise to a step change in the time required to create a metallurgical grade coke using microwave energy. Five densified coking and noncoking coals were heated in a multi-mode microwave 2450 MHz cavity for varying treatment times (2-20 minutes) with a fixed power input (6 kW). Proximate analysis, intrinsic reactivity, coke reactivity, dielectric properties, and petrographic analysis of the coals and microwave produced lump cokes were compared to a commercial lump coke. Densifying the sample prior to microwave treatment enabled a dramatic acceleration of the coking process when combined with targeted high microwave energy densities. It was possible to form fused coke lump structures with only 2 minutes of microwave heating compared to 16-24 hours via conventional coking. Anisotropic coke morphologies (lenticular and circular) were formed from non-coking coal that are not possible with conventional coking and increasing treatment time improved overall coke reflectance. Three of the coals produced coke with equivalent coke reactivity index values of 20-30, which are in the acceptable range for blast furnaces. The study demonstrated that via this process, non-coking coals could potentially be used to produce high quality cokes, potentially expanding the raw material options for metallurgical coke production.

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