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    Inductively coupled plasma - mass spectrometry and - optical emission spectrometry determination of trace elements in water

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    ICP-MS and ICP-OES instrumental conditions were optimized for the determination of Li, Be, B, AI, V, Cr, Mn, Fe, CO, Ni, Cu, Zn, As, Se, Rb, Sr, Ag, Cd, Sb, CS, Ba, Hg, TI, Pb, and Bi to achieve low detection limits (DLs) and good precision. Routine ICP-MS and ICP-OES DLs were in the 0.01-2.0 ug/L and 0.7-25.0 ug/L range, respectively. Precision was evaluated at one sigma relative standard deviation (RSD) for three replicate sets of analyses. Accuracy was evaluated by analysis of certified reference materials for water (SRM 1643c and SLRS-3), using the standard additions method for natural waters having a different chemical composition and total dissolved solids up to 10 g/L. Precision and accuracy of most elements at concentrations above the ug/L level were <10%. ICP-MS precision of <19% was observed at concentrations of 0.03 ug/L, while sub-ug/L concentrations for the elements considered could not be determined by ICP-OES

    Evoluzione della qualità delle acque nelle miniere dell'Iglesiente

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    Intense dewatering from 1930 to 1996 at Monteponi caused the aquifer salinization, due to seawater contamination at depth. The cessation of pumping in 1997 caused flooding of the underground workings. The deep saline water mixed with the shallow groundwater, increasing salinity. At Campo Pisano the peak in salinity occurred in 1998. In 1999-2001, stratification caused the saline water at depth to settle in all mine sites. In 1997-1998, an increase in Zn, Cd, Fe and Mn concentrations occurred, especially at Campo Pisano. In 2004, after seven years of rebound, salinity and metal concentrations decreased significantly, but Pb concentrations are relatively high at many sites. Sampling at different depths in the Monteponi and Campo Pisano mines shows that the water quality deteriorates as depth increases, due to higher salinity and higher concentrations in Zn and Cd
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