An electrochemical study of pyrite oxidation in the presence of carbon coatings in cyanide medium

The anodic and cathodic behaviour of pyrite with clay and different carbon coatings of activated carbon, graphite and carbonaceous matter in cyanide medium was investigated using the potentiodynamic method. The presence of clay coating did not change the polarisation curve appearance for either the anodic oxidation of pyrite or the cathodic reduction of oxygen or the potential of the current plateau, but only decreased the plateau current especially at a higher coating thickness. The presence of the carbon coatings marginally shifted the rest potential for pyrite to a more anodic position and slightly changed the polarisation curve appearance for pyrite oxidation. The current density for pyrite oxidation largely increased in the presence of the carbon coatings, the potential at the plateau shifted to more cathodic positions, and the plateau width became smaller. These effects became more noticeable at a higher coating thickness. The activated carbon, graphite and carbonaceous matter coatings performed similarly in affecting pyrite oxidation at a similar thickness. The carbon coatings significantly increased the limiting current densities for oxygen reduction on pyrite, and the limiting current plateau became steeper at a higher coating thickness. The carbon coatings increased the limiting current density for oxygen reduction to a similar extent at a low coating thickness, but increased to varied extents at a higher coating thickness. The carbon coatings also greatly increased the cathodic current density for gold reduction on pyrite. The enhancement of pyrite oxidation and oxygen or gold reduction on pyrite by the carbon coatings was likely attributed to the electrochemical interaction between pyrite and the carbon materials with electron-rich surfaces and high conductivity. The presence of the carbon coatings significantly increased the oxidation of pyrite in aerated cyanide solutions and the preg-robbing of pyrite especially at a higher coating thickness.     

A surface complexation model for cadmium and lead adsorption onto diatom surface

This work is devoted to the physico-chemical study of cadmium and lead interaction with diatom–water interfaces for two marine planktonic (Thalassiosira weissflogii = TW, Skeletonema costatum = SC) and two freshwater periphytic species (Achnanthidium minutissimum = AMIN, Navicula minima = NMIN) by combining adsorption measurements with surface complexation modeling. Reversible adsorption experiments were performed at 20 °C after 3 h of exposure as a function of pH, metal concentration in solution, and ionic strength. While the shape of pH-dependent adsorption edge is similar among all four diatom species, the constant-pH adsorption isotherm and maximal binding capacities differ. These observations allowed us to construct a surface complexation model for cadmium and lead binding by diatom surfaces that postulates the constant capacitance of the electric double layer and considers Cd and Pb complexation with mainly carboxylic and, partially, silanol groups. Parameters of this model are in agreement with previous acid–base titration results and allow quantitative reproduction of all adsorption experiments.     

Hydrochemical and isotopical tracers in the lacustrine aquifer of the Cerro Prieto area, Baja California, México

A series of patterns in the chemical and isotopic composition of the groundwater of the Cerro Prieto area have been recognized. These patterns were used to define four hydrochemical and isotopical zones in the area. One of these areas located at the east side was found to be the source of recharge, while another in the central part is where an older aquifer exist in lacustrine deposits. The low permeability of the area causes the aquifer to act as an aquitard, which at least is partly surrounded by an interface zone where mixing of waters occurs. Tritium and radiocarbon method revealed that the aquitard is an isolate system whose residence time is of 32 ka.     

Holocene record of productivity in the NW Iberian continental shelf

A multiproxy approach (textural characteristics, heavy metal concentrations and benthic foraminifera data) was adopted to study the OMEX core KSGX 40, collected at the Galicia Mud Deposit (NW Iberian outer continental shelf) and recording the last ca. 4.8 ka cal BP. Geochemical profiles of Fe, Mn, Zn, Co, Cr, Cu, Ni, Pb, Al and Ca show significant temporal variations. Benthic foraminifera productivity proxy suggests that the recorded muddy events were contemporaneous of a higher C_org flux to the marine benthic environment. The higher flux of organic matter, following a long-term intensification of the upwelling and coinciding with a finer sedimentation, led to depressed levels of oxygen beneath the water-sediments interface and to early diagenetic processes of several redox-sensitive elements.     

Geochemistry and petrogenesis of the post-orogenic bimodal dyke swarms in NW Sinai, Egypt: constraints on the magmatic–tectonic processes during the late Precambrian

The study area in the northwest Sinai represents one of the most significant regions in the Egyptian basement intensely invaded by post-orogenic calc-alkaline dyke swarms. Two post-orogenic dyke swarms have been recognized in NW Sinai namely: (1) mafic dykes of basalt, basaltic andesite and andesite composition and (2) felsic dykes of dacite, rhyodacite and rhyolite composition. These basaltic to rhyolitic dykes intruded contemporaneously and shortly after the intrusion of the post-orogenic leucogranite. The mafic and felsic dykes are enriched in incompatible elements, especially in the large ion lithophile elements (e.g. K, Rb, Ba) and depleted in high field strength elements with negative P, Ti and Nb anomalies. Major and trace element geochemistry indicates that investigated mafic and felsic magma types are not related via fractional crystallization. The protoliths of the mafic and felsic dykes appear to have evolved from different parental magmas. The incompatible trace element patterns favour a derivation of the mafic dykes from melting of a garnet peridotite source followed by fractional crystallization of olivine, clinopyroxene amphibole and zircon. The felsic dykes, on the other hand, could be generated by melting of garnet-free source modified subsequently by fractional crystallization of plagioclase, apatite and titanomagnetite. This implies variable source characteristics at the end of the Pan-African in the NW Sinai.The mafic and felsic dykes can be related to an intracontinental setting and that this was accompanied by a chemical evolution of the subcontinental lithosphere. Magma generation and ascent in the area was favoured by extensional movements, which is already known from other areas in NE Africa.     

The Cauvery Shear Zone, Southern Granulite Terrain, India: A crustal-scale flower structure

The Cauvery Shear Zone (CSZ) is a crustal-scale shear system within the Southern Granulite Terrain along the southern margin of the Archaean Dharwar craton. Structural interpretation of satellite data and field observations reveal four major shear zones within the CSZ system. They show dextral shear kinematics synchronous with a major Neoproterozoic tectono-metamorphic event (D2) associated with intracrustal melting and migmatisation. The disposition, geometry and contemporaneity of shear fabrics of the CSZ system are modelled in terms of a crustal-scale flower structure akin to transpressional and collisional orogens. In the light of recent seismic evidence for a displaced Moho structure and a mid- to lower-crustal low velocity zone, the flower structure across the CSZ may extend to mantle depths.