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By Carlos Maurício Fontes Vieira, Sergio Neves Monteiro

"A ceramic body traditionally used to produce bricks and roofing tiles with kaolinitic clays was reformulated by the addition of sand and illitic clay. The objective was to obtain a ceramic product with better technological properties. Specimens were made by uniaxial press-molding at 20 MPa and then fired at 850, 900 and 950°C. The determined technological properties were: linear shrinkage, water absorption and flexural rupture strength. The results showed that both sand and illitic clay contribute to reduce the water absorption of the industrial clayey body. With respect to the flexural behavior, it was observed that the incorporation of sand decreased the mechanical strength. On the other hand, the illitic, incorporated in an amounts of 30 wt.% contributed to increase the mechanical strength of the clayey ceramic.IntroductionCeramic bodies industrially fabricated in the county of Campos, north of the State of Rio de Janeiro, in Brazil, are still empirically elaborated using a mixture of local clays. These clays are predominantly kaolinitic mineral in nature, associated with high plasticity and elevated weight loss during the firing stage. Due to the excessive plasticity of the ceramic bodies, dimensional defects, which occur after drying and firing are usually obtained. Moreover, the kaolinitic nature and the presence of aluminum hydroxide (gibbsite) confer a refractory behavior to the local clays, which impairs sintering during the firing operation. In the case of clay ceramic products for civil construction, this results in greater porosity associated with elevated values of water absorption and low mechanical strength [1,2]. To avoid these problems, it is necessary to reformulate the ceramic body composition. The addition of both non-plastic materials to reduce plasticity and fluxes to condition the refractoriness is a possible alternative.As an alternative to reduce the plasticity of clayey ceramics sand, which is predominantly constituted of silica, can be used. The incorporation of sand in amounts of up to 25 wt.% to a clayey ceramic body used for roofing tiles fabrication was studied by Vieira et al. [3]. In that work specimens were prepared by extrusion and fired at 850°C. The results indicated that in the pre-firing stages the sand improved the workability of the investigated clayey ceramic body and facilitates the drying stage. It was also observed that the incorporated sand significantly improved the physical and mechanical properties of the clayey ceramic after firing. On the other hand, the apport of flux oxides could be done by the use of illitic clays that have a higher amount of alkaline oxides in comparison with the kaolinitics clays."

Jan 1, 2013

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Ramana G. Reddy

In the past, many lead-containing slags and wastes were stored in piles or landfills. However, shortages of landfill space as well as increased public, concern about the toxic nature of disposing lead containing industrial wastes in landfills have led to review of disposal methods. Several lead wastes are processed to provide commercial products. They are used on-site in land reclamation projects. or are processed and sold as a by-product. These by-products contain nutrient elements needed for plants or animals and also may contain heavy? metal contaminants such as As, Cr. Cu, Zn and Ph. Use of such by-products containing unacceptable levels of these contaminants could cause plant and animal toxicity. In this paper. role of viscosity in conversion of lead slag wastes into commercial products containing ,low content of lead and other, heavy metals is presented. Effects of slag viscosity on the velocity of movement of metal' and matte prills through themolten slag layer in the melting furnace is discussed. Current and emerging slag cleaning technology, foamed, granulated and pelletized slag technologies are reviewed.

Jan 1, 1995

By John Frederick Colloghon, O&apos

Bulong remains the only hydrometallurgical process plant in the world that recovers nickel and cobalt directly from high pressure acid leach (HPAL) laterite leach liquors without need for precipitation of an intermediate product (e.g. sulphide, hydroxide or carbonate). Direct solvent extraction (DSX) of both nickel and cobalt in combination with electrowinning of nickel has been operation at Bulong since early 1999. Focus in the first years has been on ramp-up and resolution of commissioning problems. More recently the focus has been on de-bottlenecking and process optimisation. A number of significant process problems have been resolved, the most difficult being the formation of gypsum in the nickel solvent extraction circuit. Sound control of process chemistry is essential to ensure the production of high quality nickel and cobalt products at the lowest possible cost. This paper describes the numerous changes and enhancements to the process chemistry and plant equipment at Bulong and discusses the importance of ore leach chemistry on downstream impurity metal removal. Potential additional enhancements to further reduce unit costs are also presented.

Jan 1, 2004

By G. Riverin, C. Simard, W. D. Stevens

"An on-line technique to measure the efficiency of decoating I delacquering processes is being developed by Alcan' s Arvida R & D Centre. Decoating processes are used to remove moisture and coatings from shredded coated material such as Used Beverage Containers (UBC) before melting. Complete removal has been demonstrated to maximize metal recovery. Quantifying the weight of carbon and organic residue adhering to the shred surfaces is very difficult to measure directly, as the material can be highly folded. The technique developed indirectly measures the residue remaining by analysing the concentration of CO evolved in the decoater end zone exhaust gas.A commercial CEMS (Continuous Emission Monitoring System) incorporating an infrared type CO gas analyser was modified for on-line process exhaust gas analysis. Both pilot and plant trials had demonstrated that the CO concentration measured was inversely proportional to the efficiency of the organic removal achieved. As the quality of coated purchased scrap can be highly variable in moisture and organic content, continuous measurement should permit adjusting the feed rate and other decoater process parameters to the quality of decoating required."

Jan 1, 2000

By Larry Southwick

In the early 1940's, the Caron ammonia ? ammonia carbonate leach process was used to produce nickel from Mayari ores at the Nicaro plant in Oriente Province, Cuba. While plant operation was generally successful, it was not broadly economical and was shut down. The plant was later restarted in the 1950's and a number of investigations initiated to resolve the more serious operational and performance issues. Processing steps studied included iron reduction (chemistry ? nickel and iron, reductant, equipment), ore variability (homogeneity and consistency of mineral concentrations, serpentine vs. laterite), leach solution strength, nickel recovery (temperature ? reduction and leaching, reoxidation) and a variety of other topics. These studies and their findings will be discussed. Caron himself obtained good results on these ores in the laboratory. They could not be duplicated in the field, the reasons for which will be reviewed. (Note: the ore looked like garden dirt; charcoal made from palm trees was one of the reductants attempted; and ammonia was the leach solution. Mixing the three, so to speak, was to yield nickel.)

Jan 1, 2006

By S. C. Grand, T. J. Auping, K. Born

Process control, environmental monitoring, budgeting and accounting are based on process data. Without appropriate tools for data analysis, the process data could remain unused and wasted. This paper demonstrates how data reconciliation can be used as a tool to develop closed mass balances. Mass balances are the initial step in plant optimisation (technical, economical or environmental). From mass balances, fundamental process models can be developed. These balances link process parameters (e.g., feed materials) to process performance (e.g., recovery of valuable elements). Some of these models could find their way into simulators useful to plant operators. Classical regression methods regularly fail when they are applied to complex non-linear problems involving a large number of variables. Alternatively, multiparametrical regression analysis can be successfully applied with the aid of neural networks based on reconciled data. Both methods have been applied to plant data originating from the hydrometallurgical zinc plant at Ruhr-Zink, which in this paper serves as a case study. Very promising and useful results were obtained from this study.

Jan 1, 2000

By Roberto Parra

The wear and corrosion phenomena in the furnace lining of the ferrous and non ferrous pyrometallurgical processes are complex problems where chemical, interfacial and mechanical phenomena are presents. The characteristics of the processes determine the conditions to which these materials are submitted, where the thermal conditions reached during the operation is one of the most important parameter. Assuming that all the degradation phenomena are thermal activated, the rate of the different steps of the wear mechanism will depend on the thermal field in the lining. In view to apply the independent physicochemical knowledge of degradation mechanisms to the analysis and design of furnace lining the methodology of the Nodal Wear Model (NWM) was done. It combines the mathematical modelling of the heat transfer in the lining with the physicochemical control equation for the wear-corrosion phenomena. The NWM has been applied to different examples: theoretical analysis, laboratory scale test and industrial applications. We present in this paper the theoretical background of the model and two examples of applications: the sole of an electric furnace and the earth of a blast furnace.

Jan 1, 2006

By Vladimir Lobanov, Vladimir Skorohodov, Andrew Evdokimov, Ural State Technical University 19, Boris Radionov

"The bulk of raw materials in metallurgy of secondary platinum metals are the wastes such as multilayered ceramic-metal systems, e.g. the spent catalysts of the chemical and petrochemical industry, automobile catalysts, etc. Due high chemical resistance of a ceramic basis the extraction of platinum metals by leaching even at very fine crushing is poor. The study of sorption leaching of platinum and a palladium from the spent automobile catalysts are carried out. The average content of PGM is 0.5%. A few methods of raw materials sampling were compared: 1) direct hydrometallurgical leaching of platinum metals from the fine-grained catalyst and atomic absorption analysis of the obtained solutions; 2) fusion to a metal or sulphidic collector of precious metals with the alloy analysis by direct spectrometry; 3) fusion with dissolution of a precious metals collector and atomic absorption analysis of PGM in solutions. Leaching allows detecting out no more than 90% of a palladium and 80% of platinum. Fusion to a collector gives the best results at the chemical ending. Researches on sorption leaching are executed. Under optimum conditions the extraction of platinum metals to concentrates is comparable with similar indicators of collector fusion.The large part of raw materials in metallurgy of secondary platinum metals are the multilayered or tridimensional ceramic-metal systems, in particular the spent catalysts of the chemical and petrochemical industry, automobile catalysts, ceramic-metal condensers, etc. The content of the sum of PGMs can be from hundreds grams per ton to several percent. For processing of such materials the hydrometallurgical methods of platinum metals leaching by various reagents are used commonly. High chemical resistance of the ceramic basis covering the metal particles causes low recovery even at very fine grinding. Other fundamentally different method of catalysts opening includes dissolution of the ceramic basis in the solutions of hydrofluoric acid and the subsequent recovery of platinum metals from insoluble residue. Application of this method is associated to use of corrosive medias and appropriate equipment. Fusion of the specified materials with collecting of PGM by copper, nickel or lead at the specialized enterprises provides higher extraction in semiproduct. At the same time, complexity and duration of the subsequent extraction of platinum metals concentrates causes high total cost per unit. Thereby this method is economically acceptable only for rather poor raw materials (no more than 0,1%). Undoubtedly, that the raw materials with the high content of PGM are reasonable to process by individual technology. In the present work the processing of some kinds of ceramic-metal raw materials, particularly automobile catalysts (neutralizers) with various collectors at the conditions of a target fusion are investigated."

Jan 1, 2008

By Shadia J. Ikhmayies

"Cadmium telluride (CdTe) is a very interesting material that has many applications. Thin films of p-type CdTe can be used as the absorber layer in the heterojunction CdS/CdTe thin film solar cells in which n-type cadmium sulfide (CdS) works as the window layer. A review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques was performed. The presence of defects and impurities such as oxygen and chlorine influence the PL spectrum. Copper and other dopants change the PL spectra and enhance the defects band. Chemical-heat treatment especially with CdCh is known to improve the quality of CdTe thin films because it decreases the Cd vacancies and quenches deep traps, so it enhances the PL signal. A discussion of chemical-heat treatment especially with CdCh, the effect of the ambient atmosphere, and that of the measuring temperature is performed.IntroductionCadmium telluride (CdTe) is a II-VI compound semiconductor that has a cubic zincblende (sphalerite) structure with a lattice constant of 0 A4~11]. Other than all of II -VI semiconductors, CdTe can be made both n- and p-type. But due to self compensation it is not easy to get p-type CdTe films [2]. Polycrystalline CdTe thin films are interesting because they have a lot of applications. Most of the problems associated with the use of these films are attributed to inhomogeneity, self-compensation, and the difficulty of forming a stable and lowresistivity ohmic contact [3]. CdTe technology has been established for a large number of applications, including solar cells, optical and nuclear detectors, and thermal- and radiationimaging devices [3]. At present, the highest demonstrated conversion efficiency for a CdTe based heterojunction (ID), with CdS as a window layer, is 16.5% [4, 5]. CdTe thin films can be prepared by different experimental techniques, such as thermal evaporation [l], electrochemical deposition (ED) [3], close-spaced sublimation (CSS) [3, 4, 6], physical vapor deposition (PVD) [3], chemical molecular beam deposition (CMBD) [7], and close space vapor transport (CSVT) [8].The objective of this paper is to make a review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques and discuss the factors that influence the PL spectra. The composition of the film is very interesting in determining its PL spectrum. Different kinds of defects, impurities and dopants have their finger prints in the PL spectrum. Deposition techniques and deposition parameters such as the deposition temperature and ambient atmosphere also have their influence. Heat and chemical treatments which are known to improve crystallization and reduce the defects change the PL spectrum."

Jan 1, 2013

By Roger Agnew

Sulphide ores mined by Inco Limited in the Sudbury District contain small quantities of cobalt. During beneficiation, cobalt distribution to various streams is similar to nickel. After smelting, nickel is selectively extracted by carbonyl refining and the cobalt remains in the carbonylation residue. This residue is processed in a specialized hydrometallurgical plant to produce precious metal residues, copper cathodes, and a nickel- cobalt carbonate intermediate product. The nickel-cobalt is shipped to Port Colborne where the cobalt is separated as cobaltic hydroxide and refined to metallic cobalt. This paper deals specifically with the recently constructed Electro Cobalt Refinery. The cobaltic hydroxide is dissolved and residual zinc, copper and nickel are removed by ion exchange and organics by a carbon column. The purified cobalt solution is fed to the electrowinning circuit where cobalt rounds are produced on stainless steel mandrels. In the design and construction of the refinery, special attention was directed to materials of construction both for the process equipment and the physical plant, operating control and flexibility, and the quality of the working environment. The end result is an efficient and clean operation which yields a product of excellent quality.

Jan 1, 1988

By Peter G. Smith

Tri-calcium aluminate (TCA) is a dominant alkaline component of the red mud residue from the Bayer process. A method being considered for industrial implementation partially neutralizes the residue by contacting it with gaseous CO2. This paper outlines the chemistry of CO2neutralisation of TCA under conditions relevant to the treatment of Bayer residue. CO2 neutralisation of the liquor is fast. It results in the formation of amorphous aluminium hydroxide and dawsonite that agglomerate together. Neutralisation of solid TCA is slower and leads to the formation of calcite, dawsonite and amorphous aluminium hydroxide. The dissolution of TCA in partially neutralised slurries causes pH reversion. However the carbonated solutions contain a store of bicarbonate that can supply aqueous carbon dioxide to complete the transformation. The pH at which the carbonation is carried out will affect the degree of TCA transformation during the carbonation process. In particular, if the pH of the carbonation is too low (near 7.0), calcite precipitation is inhibited and the degree of transformation is low. Controlling the carbonation pH helps to optimise the neutralisation process.

Jan 1, 2003

By J. H. Meza

La Caridad copper smelter is located in the magnificent but rugged Sierra Madre Mountains. This project presents unusual challenges that require the utmost in detailed analysis and planning. The smelter, owned by Mexicana de Cobre, S.A. de C.V., has an annual production capacity of 225,000 metric tons of copper and 600,000 metric tons of sulfuric acid. It utilizes only the Flash Smelting process. This project will expand the annual production capacity to 270,000 metric tons of copper and 1,000,000 metric tons of sulfuric acid. Offgases from the Flash Furnace and the Teniente Converter will be sent to a mixing chamber, from which it will be led to two sulfuric acid plants. This project will then produce a high quality sulfuric acid.

Jan 1, 1995

By Lee Fergusson

"The primary features of ViroMine™ Technology are introduced and applications of ViroMine™ Technology to mine site remediation and the treatment of a variety of intractable waste-streams, including a technical discussion of acid neutralizing capacity, metals binding capacity and longterm stability of results. Outcomes from four applications at high-profile international mine sites are presented: 1) the superfund site at the Gilt Edge Mine, South Dakota, USA (four years of data on the treatment of acidity, TDS and metals such as Al, Co, Fe, Mn and Zn); 2) one of Australia’s most polluted sites at King River Delta in Tasmania (treatment of TAA and TPA, and metal and metalloid contaminants such as As, Cr and Hg); 3) The Aljustrel “Aqua Forte” mine site in Portugal (high acidity, metal and metalloid contaminants such as Al, As, Cu and Zn) and 4) the Ulsan Iron Ore Mine at Ulsan, South Korea (treatment of metal and metalloid contaminants such as As, Cd and Ni).IntroductionThe commercialisation of ViroMine™ Technology has resolved some of the most intractable pollution issues associated with historic mining ventures on a global scale and has facilitated the neutralisation of Acid Rock Drainage (ARD), remediation of acidic and metal contaminated impoundments (including tailings dams) and promoted revegetation on tailings deposits and waste rock dumps. ViroMine™ Technology also enables current mining ventures to manage effluent simply and efficiently to meet increasingly stringent environmental standards and is enabling the mining sector to reconceptualise the management of mine spoil. The abilities of ViroMine™ reagents to neutralise the actual and potential acidity of sulphidic mine spoil coupled with the ability to bind metal and metalloid contaminants into non-bio-available forms are the key features delivering environmental and economic benefits to the mining sector and the broader community. Results from four projects utilising ViroMine™ Technology are presented to highlight the suitability of ViroMine™ Technology to treat all forms sulphidic mining wastes. 37"

Jan 1, 2008

By David G. Dixon, Ahmad Ghahremaninezhad, Edouard Asselin

"In this study pertaining to the electrochemistry of chalcopyrite, the active/passive behavior of a chalcopyrite electrode in 0.5M sulfuric acid solution was investigated. Potentiostatic and potentiodynamic polarization and multi-cyclic voltanunetry were conducted to analyze the electrodissolution parameters of the electrode.The potentiodynamic and potentiostatic polarizations of chalcopyrite revealed the formation of a passive film on the surface of chalcopyrite. From the potentiostatic study in the passive potential region, a decrease in the dissolution current density by increasing the potential was observed. From this, it was concluded that the passive film is an n-type semiconductor and cation interstitial defects or anion vacancies are the charge carriers. From multi-cyclic voltammetry studies, four cathodic peaks at - 0.37, 0.30, -0.10 and-0.20 YsHE were detected on the surface of a passivated chalcopyrite electrode. The cathodic peaks at 0.37 and 0.30 V were connected to ferric to ferrous reduction and copper sulfide formation, respectively. The peaks at -0.10 and - 0.20 were related to chalcopyrite reduction. The products of the chalcopyrite reduction reactions were suggested to be Cu2S, Cu9fesS16 and Cu5feS4 and evolution of hydrogen sulfide gas (H2S).IntroductionChalcopyrite is the most abundant copper bearing mineral in the world and its dissolution behavior represents the most important technological consideration in the hydrometallurgical extraction of copper [I]. Since the current pyrometallurgical methods for copper extraction from chalcopyrite have environmental issues, many studies have considered the leaching and dissolution of CuFeS2 in different aqueous media [2-5]. The main problem associated with leaching processes is the slow dissolution rate of the mineral [6]. During the dissolution process, increasing the potential of the chalcopyrite in the anodic direction will cause the formation of surface layers which hinder the dissolution rate of the mineral [7]. The precise composition of the layers is in dispute. Previous studies have concluded that these layers could be sulfur [8-9], precipitated iron compounds [8], a solid electrolyte interphase (SEI) - which slows the rate of electron transfer- [10], a metal deficient sulfide [ll], or polysulfidic in nature [12-13]. In order to increase the leaching kinetics of chalcopyrite, the characterization of the layers formed during dissolution is essential and electrochemical methods are important to this end. Studies by Biegler [14] show nucleation and growth of a thin two-dimensional sulfide phase on the surface of chalcopyrite during the exposure of a polished sample in HzS04 solution or air. More studies by Biegler and Swift [15] have shown evidence for nucleation and growth of a 3-dimensional phase at low anodic potentials (around 200 mV vs. OCP). The current-time behavior of the dissolution process in this potential area has the characteristics of expansion and overlap of localized dissolution centers."

Jan 1, 2012

By John E. Dutrizac, Tzong T. Chen

"Laboratory experiments were undertaken to ascertain the behaviour of various ""impurity"" species during the precipitation of hematite directly from ferric sulphate solutions at 225°C and in the presence of 40 or 50 g/L of hematite seed. Copper, nickel and zinc are not significantly incorporated in hematite precipitates. Although the nickel contents increase to 0.22% as the Ni concentration increases to 60 g/L, the solid solution Ni contents are low relative to the bulk Ni contents. Thus, part of the Ni may be present as tiny particles of poorly soluble NiS04.H20. Increasing germanium concentrations to 2,000 mg/L result in products containing up to 0.59% Ge. The Ge occurs either in solid solution in the hematite or is adsorbed on the nanometer-size hematite crystallites. Increasing As(V) concentrations to 10 g/L increase the AsO4 contents of the products up to 16%. However, the products consist of hematite together with As04-containing Fe(SO4)(OH) and an unknown Fe-AsO4 species. All the hematite products contain - 1% SO4 which appears to be adsorbed on the nanometer-size hematite crystallites.IntroductionDissolved iron is a common impurity in most hydrometallurgical processing circuits and, generally, the iron must be eliminated prior to the subsequent recovery of the sought after metals. Simple neutralization of iron-rich solutions yields slurries which are difficult to thicken and filter. To address these concerns, the jarosite, goethite and hematite processes have been developed, and these technologies are able to reject the dissolved iron in a readily filterable form [1]. Despite its higher cost, the hematite process offers several potential advantages. Because hematite is an iron-rich, high-density compound, its formation would reduce the mass of residue and the size of a residue storage pond. Hematite is the thermodynamically stable form of iron under ambient conditions, and this stability would facilitate the impoundment of hematite precipitates. Furthermore, hematite has some market potential for cement manufacture and even for iron making [2]. In all the commercial hematite processes, the dissolved ferric ions are first reduced to the ferrous state. Subsequently, the pH of the solution is adjusted and the solution is then oxidized. The ferric ions gradually generated during solution oxidation hydrolyze and precipitate mostly as hematite, although commercial hematite products also contain trace or minor amounts of jarosite-type compounds. However, there are potential advantages in precipitating hematite directly from ferric ion solutions, as the reduction and subsequent oxidation of the iron are not required. Although the precipitation of hematite directly from relatively concentrated ferric sulphate solutions (up to 0.5 M Fe(SO4)is) was recently demonstrated [3], the behaviour of impurity species during hematite precipitation is largely unknown. To address this issue, systematic laboratory experiments were undertaken to ascertain the behaviour of a number of ""impurity"" species during the precipitation of hematite directly from ferric sulphate solutions at 225°C, and the results are presented in this paper."

Jan 1, 2012

By Jeaneth S. Benedetto

The physical and chemical processes developed for recovery of uranium and phosphor from phosphoro-uraniferous ore bodies consists of three basic steps: concentration of the phosphate bearing uranium by flotation, chemical dissolution of the concentrate by wet phosphoric acid and extraction of uranium by solvent. In this process two products are obtained: 1) uranium and 2) phosphoric acid. The purpose of this work was to develop technological know-how of phosphoric acid purification though an extraction of P2O5 by solvents. It was investigated by two lines of research. In the first one the uranium was extracted before the phosphoric acid purification. In the second, the phosphoric acid was extracted before uranium recovery. The comparison of the two processes is shown in this paper. Experimental work was developed on a laboratory scale to select and optimize the process variables. After the laboratory study, the research of extraction and stripping was continued on a pilot scale in pulsed perforated-plate columns in order to investigate the main operational and process conditions. The first phosphoric acid extraction experiments showed good results using a raffinate sample obtained from the uranium extraction process. It was possible to obtain a high purity phosphoric acid.

Jan 1, 2003

By M. I. Zinigrad

A model of an ideal associated solution is presented. This model takes into account the existence of complexes of various compositions, sizes and geometries and allows calculating thermodynamic properties and phase diagrams of binary alloys. The model has been used formerly to calculate thermodynamic parameters and the position of the liquidus line for binary eutectic systems and also those having a stable compound in the solid phase. In all the cases the model parameters were not adjusted rather estimated from melting temperatures of the components. The recent studies dealt with the influence of arbitrary-stoichiometry associates on the equilibrium thermodynamic properties of liquid alloys. The application of the model to eutectic systems and systems having an unlimited solubility in solid and liquid states close to liquidus has been considered. It was shown that if the difference in melting temperatures of the components was small, different types of fusibility diagrams were possible: eutectic diagrams, cigar-shaped diagrams or diagrams with upper or lower azeotropic points. Peritectic transformations could take place when the difference in melting temperatures of the components was large. The present work is devoted to calculation of phase diagrams and thermodynamic properties of binary systems on the basis of chrome.

Jan 1, 2006

By R. D. MacDonald

The papers presented in this chapter cover a wide range of hydrometallurgical topics and might be considered to be unrelated to each other. All of the authors, however, utilized the basic methods of process mineralogy to characterize the reactants in their experiments and the products produced. The wide range of research topics which can be pursued successfully by the use of the methods of process mineralogy is a matter of interest in itself. One might speculate that the methods could be even more widely applied if only their utility were better recognized. These methods for characterizing reactants and products include principally x-ray diffraction, optical micros-copy, wet chemical analyses, instrumental chemical analyses, high intensity magnetic separation, micro-scale gravity separation, differential thermal analysis, micro-hardness testing, and judicious use of the sledgehammer and cold chisel. It is perhaps not by coincidence that most of the papers in this chapter were prepared not by mineralogists, but by hydrometallurgists, who are recognizing the importance of thinking in terms of mineral phases, and not just assays! It appears that the gap between process mineralogy and the mineral industry is closing, and that future AIME sessions promise to become established forums where mutual discussion of such topics as metallurgical "troubleshooting" and process design may become commonplace between plant engineer and process mineralogist.

Jan 1, 1981

By Guo Jun

In this study, BaTiO3 ultrafine particles surface-modified with stearic acid were synthesized by the hydrothermal method in a system of BaCl2-TiCl4-NaOH. The effects of NaOH/TiCl4 molar ratio, Ba/Ti ratio and time on structure and morphology of BaTiO3 ultrafine particles were investigated experimentally. The formation mechanism of different crystalline BaTiO3 particles was discussed, and it is considered that in a hydrothermal system, the main factors determining BaTiO3 crystalline are H+ replacement of Ba2+ causing H+ deficiency and anatase growth units involving in crystal growth, which clogs the axial channel for Ba2+ transference. By means of increasing the alkalinity of system and barium content, H+ deficiency and involvement of anatase growth units in crystal growth could be effectively controlled. The results show that when molar ratio of NaOH to TiCl4 is 9 and ratio of Ba to Ti 1.5, and time 8 hours, high purity tetragonal BaTiO3 ultrafine particles with a narrow grain-size distribution and nonpolar surface are obtained at 240oC. The particles have excellent flowability, which is ascribed that the surface polarity of barium titanium powder modified with stearic acid is changed and the interaction between the particles is weakened.

Jan 1, 2006