Phase partitioning during fragmentation revealed by QEMSCAN Particle Mineralogical Analysis of volcanic ash.

Volcanic ash particle properties depend upon their genetic fragmentation processes. Here, we introduce QEMSCAN Particle Mineralogical Analysis (PMA) to quantify the phase distribution in ash samples collected during activity at Santiaguito, Guatemala and assess the fragmentation mechanisms. Volcanic ash from a vulcanian explosion and from a pyroclastic density current resulting from a dome collapse were selected. The ash particles resulting from both fragmentation modes are dense and blocky, typical of open-vent dome volcanoes and have a componentry consistent with their andesitic composition. We use image analysis to compare the fraction of each phase at particle boundaries compared to the total particle fraction. Our results show that the explosion-derived ash has an even distribution of plagioclase and glass, but boundaries enriched in pyroxene and amphibole. In contrast, the ash generated during dome collapse has an increased fraction of glass and decreased fraction of plagioclase at particle boundaries, suggesting that fractures preferentially propagate through glass during abrasion and milling in pyroclastic flows. This study presents QEMSCAN PMA as a new resource to identify generation mechanisms of volcanic ash, which is pertinent to volcanology, aviation, respiratory health and environmental hazards, and highlights the need for further experimental constraints on the fragmentation mechanism fingerprint.

Geotechnical and mineralogical characterisations of marine-dredged sediments before and after stabilisation to optimise their use as a road material.

Dredging activities to extend, deepen and maintain access to harbours generate significant volumes of waste dredged material. Some ways are investigated to add value to these sediments. One solution described here is their use in road construction following treatment with hydraulic binders. This paper presents the characterisation of four sediments, in their raw state and after 90 days of curing following stabilisation treatment with lime and cement, using a combination of novel and established analytical techniques to investigate subsequent changes in mineralogy. These sediments are classified as fine, moderately to highly organic and highly plastic and their behaviour is linked to the presence of smectite clays. The main minerals found in the sediments using X-ray diffraction (XRD) and automated mineralogy are quartz, calcite, feldspars, aluminium silicates, pyrite and halite. Stabilisation was found to improve the mechanical performances of all the sediments. The formation of cementitious hydrates was not specifically detected using automated mineralogy or XRD. However, a decrease in the percentage volume of aluminium silicates and aluminium-iron silicates and an increase of the percentage volume of feldspars and carbonates was observed.

Geochemistry and mineralogy of arsenic in mine wastes and stream sediments in a historic metal mining area in the UK.

Mining generates large amounts of waste which may contain potentially toxic elements (PTE), which, if released into the wider environment, can cause air, water and soil pollution long after mining operations have ceased. The fate and toxicological impact of PTEs are determined by their partitioning and speciation and in this study, the concentrations and mineralogy of arsenic in mine wastes and stream sediments in a former metal mining area of the UK are investigated. Pseudo-total (aqua-regia extractable) arsenic concentrations in all samples from the mining area exceeded background and guideline values by 1-5 orders of magnitude, with a maximum concentration in mine wastes of 1.8×10(5)mgkg(-1) As and concentrations in stream sediments of up to 2.5×10(4)mgkg(-1) As, raising concerns over potential environmental impacts. Mineralogical analysis of the wastes and sediments was undertaken by scanning electron microscopy (SEM) and automated SEM-EDS based quantitative evaluation (QEMSCAN®). The main arsenic mineral in the mine waste was scorodite and this was significantly correlated with pseudo-total As concentrations and significantly inversely correlated with potentially mobile arsenic, as estimated from the sum of exchangeable, reducible and oxidisable arsenic fractions obtained from a sequential extraction procedure; these findings correspond with the low solubility of scorodite in acidic mine wastes. The work presented shows that the study area remains grossly polluted by historical mining and processing and illustrates the value of combining mineralogical data with acid and sequential extractions to increase our understanding of potential environmental threats.