Thermodynamics of arsenates, selenites, and sulfates in the oxidation zone of sulfide ores: IV. Eh-pH diagrams of the Me-Se-H2O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) at 25°C

Abstract

The behavior of arsenic at the Earth’s surface and nearby at low temperatures and pressures depends mainly on the redox potential and the acidity-alkalinity of the crystallization media. These parameters determine the migration of arsenic compounds and their precipitation as various solid phases. Understanding the mechanism of arsenic’s behavior under surface conditions, which is important for solving environmental problems, is an urgent task of contemporary mineralogy and geochemistry. The activities of the components in natural waters beyond the zones of natural (oxidation zones) and man-made contamination with arsenic (aΣAs = 3 × 10−8, aΣFe = 10−5, aΣCu = 10−7, aΣZn = 5 × 10−7, aΣCo = 10−8, aΣNi = 6 × 10−8, aΣPb = 10−8) and in waters formed in the oxidation zone (aΣSe = 10−3, aΣFe = 10−2, aΣCu = 10−2, aΣZn = 5 × 10−2, aΣCo = 10−3, aΣNi = 10−2, aΣPb = 10−4) have been estimated. Eh-pH diagrams were calculated and plotted using the Geochemist’s Workbench (GMB 7.0) software package. The database comprises the thermodynamic parameters of 46 elements, 47 main particles, 48 redox pairs, 551 particles in solution, 624 solid phases, and 10 gases. The Eh-pH diagrams of the Me-As-H2O systems (Me = Co, Ni, Fe, Cu, Zn, Pb) were plotted for the average contents of these elements in the underground water and for their higher contents in the oxidation zones of sulfide deposits. The formation of Co, Ni, Fe, Cu, Zn, and Pb arsenates at the surface is discussed.