18 research outputs found

    Chalcopyrite leaching in acid media: a review

    Get PDF
    In the modern practice of copper production, more and more attention is paid to the possibility of treating low-percentage sulfide ores that cannot be treated with conventional procedures (crushing, grinding, flotation). In addition to this, the processes of obtaining copper from complex sulfide concentrates, which cannot undergo pyrometallurgical processing, are increasingly being investigated. Extraction of copper from such raw materials is in most cases achieved by applying leaching procedures. Since chalcopyrite (CuFeS2) is by far the most abundant copper sulfide mineral, a large portion of the research is focused on studying the behavior of chalcopyrite in the leaching process, because processes of copper extraction from increasingly poor raw materials may be created using results of these studies. In addition, the main objective of this research is examining the kinetics and mechanism of chalcopyrite oxidation under the influence of various oxidants (O2, Fe3 +, H2O2, chlorate ions, etc.) and at the same time obtaining data necessary for the development of copper production process that could satisfy increasingly stringent technological, economic and environmental criteria. The paper presents the existing knowledge of the chalcopyrite leaching procedure and phenomena that accompany chalcopyrite oxidation in acidic sulfate and chloride solutions

    Space-Time High-Resolution Data of The Potential Insolation and Solar Duration for Montenegro

    Get PDF
    The assessment of the potential use of renewable energy resources requires reliable and precise data inputs for sustainable energy planning on a regional, national and local scale. In this study, we examine high spatial resolution grids of potential insolation and solar duration in order to determine the location of potential solar power plants in Montenegro. Grids with a 25-m spatial resolution of potential solar radiation and duration were produced based on observational records and publicly available high-resolution digital elevation model provided by the European Environment Agency. These results could be further used for the estimation and selection of a specific location for solar panels. With an average annual potential insolation of 1800 kWh/mĀ² and solar duration of over 2000 h per year for most of its territory, Montenegro is one of the European countries with the highest potential for the development, production, and consumption of solar energy

    Molecular mobility of hydroxyethyl cellulose (HEC) films characterised by thermally stimulated currents (TSC) spectroscopy

    Get PDF
    Molecular mobility has long been established to relate to textural properties and stability of polymer films and is therefore an important property to characterise to better understand pharmaceutical film formulations. The molecular mobility of solvent cast hydroxyethyl cellulose (HEC) films has been investigated by means of thermally stimulated current (TSC) below the temperature at which the film was formed. Preliminary physical characterisation of the films was performed using XRPD, TGA, DSC and texture analysis (tensile properties). XRPD results showed the films to be completely amorphous with Tg determined by DSC to be 127 Ā± 1 Ā°C. TGA analysis showed the films to contain 8 Ā± 1% water and film was dried to only 0.06 Ā± 0.01% water content when heated to 160 Ā°C. Application of TSC detected molecular mobility in HEC films at sub-zero temperatures. Two motional transitions with average relaxation time of 50 Ā± 3 s were identified; a Ī²-relaxation at āˆ’57 Ā± 2 Ā°C, attributed to localised non-cooperative orientation of HEC polymer chain ends and the hydroxyethyl side groups and an Ī±-relaxation, originating from cooperative segmental mobility, at āˆ’20 Ā± 2 Ā°C. The tensile properties i.e., elongation, tensile strength and elastic modulus of the HEC film have been related to the molecular relaxation processes detected by TSC

    Phase behaviour of dehydrated phosphatidylcholines

    Get PDF
    Dehydrated DLPC, DMPC, DPPC and DSPC have been characterised at temperatures below the diacyl carbon chain-melting transition (Tm), using DSC. For the first time, the existence of pre-Tm transition processes, which are, usually, only observed in the colloidal/liposomal state of saturated phospholipids have been detected for the dehydrated phosphatidylcholines. Temperature modulated differential scanning calorimetry (TMDSC) was used to characterize the several complex, overlapping pre-Tm transition processes. Kinetic studies of the chain-melting (Tm) transition show the activation energy dependence on Ī± (conversion rate) i.e. activation energy decreases as the transition progresses, pointing to the importance of initial cooperative (intra- and inter-molecular) mobility. Furthermore the activation energy increases with increase in diacyl chain length of the phosphatidylcholines which supports the finding that greater molecular interactions of the polymer chain and its head groups in the dehydrated solid state lead to enhanced stability of dehydrated phosphatidylcholines

    Actual contamination of the Danube and Sava Rivers at Belgrade (2013)

    Get PDF
    This study was focussed on a comprehensive investigation on the state of pollution of the Danube and Sava Rivers in the region of Belgrade. Different complementary analytical approaches were employed covering both i) organic contaminants in the river water by target analyses of hormones and neonicotinoids as well as non-target screening analyses and ii) heavy metals in the sediments. Finally, some common water quality parameters were analysed. The overall state of pollution is on a moderate level. Bulk parameters did not reveal any unusual observations. Moreover, quantification of preselected organic contaminants did not indicate to elevated pollution. More significant contaminations were registered for chromium, nickel, zinc and partially copper in sediments with values above the target values according to Serbian regulations. Lastly, non-target screening analysis revealed a wider spectrum of organic contaminants comprising pharmaceuticals, technical additives, personal care products and pesticides. The study presented a comprehensive view on the state of pollution of the Sava and Danube Rivers and is the base for setting up further monitoring programs. As a superior outcome, it was illustrated how different chemical analyses can result in different assessments of the river quality. A comparison of target and non-target analyses pointed to potential misinterpretation of the real state of pollution

    Synthesis and characterization of new Tiā€“Bi2O3 anode and its use for reactive dye degradation

    Get PDF
    This paper reports the synthesis, characterization and application of a Tiā€“Bi2O3 anode for the electrochemical decolorization of the textile dye Reactive Red 2. The anode was synthesized by electrodeposition on a Ti substrate immersed in an acidic bismuth (III) solution at constant potential, followed by calcination in air at 600 Ā°C. Thermogravimetric Analysis (TGA), Energy-dispersive X-ray spectroscopy (EDX) and X-ray diffraction (XRD) analysis revealed that the electrodeposited material was predominantly metallic bismuth, which was oxidized to pure Ī±-Bi2O3 during the calcination in air. SEM micrographs revealed that the Bi2O3 coat at the anode surface was inhomogeneous and porous. Reactive Red 2 was completely electrochemically decolorized at the synthesized anode in the presence of H2O2. The applied current density, H2O2 and Na2SO4 concentration, medium pH and initial dye concentration affected the dye decolorization rate. The optimal process parameters were found to be as follows: an applied current density of 40 mA cmāˆ’2 using a mixture of 10 mmol dmāˆ’3 H2O2 and 10 mmol dmāˆ’3 Na2SO4 at pH 7. The dye decolorization rate was shown to decrease as its initial concentration increased. The decolorization reactions were found to follow pseudo-first order kinetics

    Oxidation of pyrite: Consequences and significance

    No full text
    This paper presents the most important studies on the oxidation of pyrite particularly in aqueous solutions. The consequences of pyrite oxidation was examined, as well as its importance, from both the technical-technological and environmental points of view. The oxidation of pyrite was considered in two parts. The spontaneous oxidation of pyrite in nature was described in the first part, with this part comprising pyrite oxidation in deposits depots and mines. It is explained how way natural electrochemical processes lead to the decomposition of pyrite and other minerals associated with pyrite. The oxidation of pyrite occurring during technological processes such as grinding, flotation and leaching, was shown in the second part. Particular emphasis was placed on the oxidation of pyrite during leaching. This part includes the leaching of sulphide and oxide ores, the leaching of pyrite coal and the leaching of refractory gold-bearing ores (pressure oxidation, bacterial oxidation, oxidation by means of strong oxidants and the electrolysis of pyrite suspensions). Various mechanisms of pyrite oxidation and of the galvanic interaction of pyrite with other sulphide minerals are shown
    corecore