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D'Agostino, Fabio
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D'Agostino, Fabio
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- PublicationRestrictedHg and CO2 emissions from soil diffuse degassing and fumaroles at Furnas Volcano (São Miguel Island, Azores): Gas flux and thermal energy output(2018)
; ; ; ; ; ; ; ; ; ; ;Gaseous elemental mercury (Hg0 g or GEM) and CO2 are emitted from active hydrothermal systems in volcanic areas mostly through diffuse degassing. Here, data from about 400 simultaneous measurements of soil GEM and CO2 flux performed within the caldera of Furnas Volcano, São Miguel Island (Azores) are discussed for the first time. This survey aimed at providing a new insight into the origin and magnitude of GEM in the investigated hydrothermal/volcanic environment and its relation with CO2 release. The distribution of GEM and CO2 emissions over an area of about 0.04km2 are correlated with soil temperature, and measurements have provided total CO2 and GEM output of 39td−1 and 1.8×10−6td−1, respectively. These results are similar to the emission from currently active volcanic/hydrothermal areas elsewhere, as well as from important non-volcanic areas, such as Sulphur Bank Mercury Mine (California, USA) and Idrija Mercury Mine (Slovenia, EU), pointing out the relevance of diffuse degassing processes at Furnas Volcano. Atmospheric spot measurements in the most vigorous fumarole vents of the geothermal field have shown that the fumarolic GEM contribution (9.2 ×10−7td−1) represents a minor fraction of the total (fumarolic+diffusive) GEM output (2.7 ×10−6td−1) for the study area of this volcano. Basing upon the integration of the hydrothermal CO2 released and the H2O/CO2 ratio in the fumarolic gas, we have also estimated the thermal energy release associated with diffuse degassing at Furnas Volcano. Our estimates are ∼7.8MW and 9.8MW, respectively for Furnas Lake and Furnas Village fumaroles.42 1 - PublicationRestrictedGroundwater of Sicily (Italy) Close to Landfill Sites: Quality and Human Health Risk Assessment(2021-05-30)
; ; ; ; ; ; ; ; ; ; ; ; ; ;; ; ;Groundwater close to three municipal solid waste landfll sites in Sicily (southern Italy) was sampled to determine the presence of contaminants and the risk associated with its possible use as drinking and sanitary water. Polycyclic aromatic hydrocarbons, polychlorinated biphenyls, polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans, and metals were investigated. These target compounds are the most common pollutants present in leachates. Risk Assessment Guidance for Superfund (RAGS, US EPA) was used to assess human health risk. Ingestion, dermal, and total exposure to these xenobiotic contaminants in groundwater were evaluated, and the cancer and non-cancer risk indexes were calculated. The results revealed that, while the groundwater complied with Italian Drinking Water Directive 30/2001, it did not comply with the "good environmental state" criteria of Directive 30/2009 at two of the three sites investigated. Worrying results were revealed by the risk assessment at the investigated sites. Cancer and non-cancer risk indexes indicated a probable risk, mainly due to dermal exposure to groundwater. These results underline the importance of assessing the risk for all possible routes, evaluating not only ingestion but also dermal exposure, especially when organic pollutants are present. The results of this study show that human health risk has probably been underestimated in the past, as dermal exposure to organic pollutants has only rarely been evaluated in the literature.149 196 - PublicationRestrictedFirst simultaneous mercury and major volatiles characterization of atmospheric hydrothermal emissions at the Pisciarelli's fumarolic system (Campi Flegrei, Italy)(2020-10-12)
; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; Hydrothermal systems with active surface expressions are important natural source of atmospheric mercury. Here we report on the first simultaneous assessment of gaseous elemental mercury (GEM) and major volatiles (H2S and CO2) fluxes from the fumarolic system of Pisciarelli, currently the most active at the Campi Flegrei caldera (CFc), Naples (Italy). Thiswas achieved via a GPS-synchronized Lumex and MultiGAS surveywhich extends similar investigations reported elsewhere. GEM concentrations measured in the fumarolic emissions were consistently above background air level close to the degassing area (mean ~ 8 ± 3 ng m−3 on average) and ranged up to 12,000 ng m−3. Our data evidenced pulsed sequences of GEM increases in the fumarole plume, closely matched by temporally consistent increases in CO2 and H2S (r2 =0.9), supporting the idea that major volatiles, such as CO2 acts as potential carrier in transporting GEM within the magmatic/hydrothermal systems. The slope of the best fit calculated for the dispersion of our data provides a GEM/CO2 molar ratio of 1.1 × 10−8 and a GEM/H2S of5×10−6, respectively. These ratios are comparable to those reported for both low(~ 100 °C) and high-T (~250 °C) fumaroles from non-explosive volcanic/hydrothermal degassing systems elsewhere. We adopted an adhoc method that combines video footages and gas measurements to obtain high precision concentration maps of gas emissions used to estimate the total atmospheric GEM, CO2 and H2S flux of about 0.0113, 225059 and 511 t y−1, respectively. The human health risk assessment related to the GEM emissions at Pisciarelli, confirms that, except for the degassing fumarolic area, all the main sites affected by the plume dispersion, always remain well below the safe threshold recommended by the health authorities.797 3 - PublicationRestrictedDirect determination of total mercury in phosphate rock using alkaline fusion digestion(2014-12-10)
; ; ; ; ; ; ; ; ; ; ;The aim of this work was to develop a new method to determine the mercury (Hg) concentrations in phosphate rock using a dedicated analytical instrument (the DMA80 Tricell by Milestone) that employs an integrated sequence of thermal decomposition followed by catalyst conversion, amalgamation and atomic absorption spectrophotometry. However, this instrument underestimates Hg concentrations when phosphorite and apatite rocks are investigated with a classic thermal decomposition treatment that complies with US EPA method 7473. Therefore, to improve the recovery of total Hg, we performed alkaline fusion digestion (AFD) directly inside the furnace of the instrument, using BCR(32) as a certified reference material (Moroccan phosphate rock--phosphorite). The salts used for the AFD were a mixture of Na2CO3, K2CO3 and Li2CO3, which melt at about 400°C, due to their ability to form a ternary eutectic and to decompose the phosphorite matrices at 700°C. By adopting this analytical approach, the Hg recovery in BCR(32) was about 100%, compared to 40% when the reference material was analysed without using the alkaline fusion salt. We suggest that the AFD allowed the decomposition of the sample matrix and that some Hg compounds linked with other functional groups may be transformed in carbonates that sublimate at lower temperatures than other Hg compounds. This original method was tested on a number of different geological samples to compare the differences between the AFD method and the thermal treatment in order to verify the working range and to check the robustness of the new approach.25 1