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By Junji Shibata

Some fundamental studies were carried out in order to produce composite powders comprising of two or three metal salts by using liquid-liquid extraction and to develop the control technology of the particle size. The combination of samarium and cobalt was selected as the two component composite powders. Both stripping and crystallization occurred at the same time by emulsifying the organic phase loading the two metals extracted with Versa tic Acid 10 and the aqueous solution containing oxalic acid. The effect of aqueous pH, oxalic acid concentration and agitation speed was examined on some properties such as crystallization percent, particle size and shape of each metal oxalate powders obtained in this process. The analysis by using EDX showed that the two metal oxalates were distributed uniformly at the same ratio as the organic phase composition.

Jan 1, 2001

By Pinakin Chaubal

An analysis of the blast furnace and the low-pressure shaft DR furnace is carried out by redefining the reaction zones. The concept of a characteristic reaction gas temperature (CRGT) is introduced and the two reactors are compared and contrasted using some recent process developments with an aim to develop a platform for further synergistic innovations.

Jan 1, 2006

By Seyed Mohammad Taghavi

In this report, the efficacy of different factors such as temperature of reaction, time of reaction and depth of bed are investigated in a process of recovery of zinc oxide from zinc ore concentration residues in a fluidized bed furnace. Under optimum conditions, there was more than 93.5% zinc oxide in products.

Jan 1, 2006

By C. Alexandru Sonoc

Donnan Dialysis uses ion exchange membranes to extract and separate cations. The driving force is provided by differences in chemical potential, rather than by electric fields or pressure. A Donnan Dialysis based process to recover lithium, nickel, cobalt, manganese, and organic acid lixiviant from recycled lithium ion battery cathodes is under development. In this paper we present a model of Donnan Dialysis and results of simulations of the aforementioned process. The simulations show that 170 m2 of membranes can process 1000 L of leachate ([Li+] = 0.285 M, [Co2+] = [Ni2+] = [Mn2+] = 0.095 M, pH 2) in two days and recover 94.1% of the lithium (as lithium carbonate), 99.4% of the transition metals (as mixed sulphates ready for solvent extraction), and all of the organic acid using 423 mol of H2SO4 and 268 mol of KHCO3.

By David Norval

Ni, Co, Cu and Pt, mattes are common materials that require granulating and milling of the resultant granules for further processing. This route is acceptable if the material is brittle (friable) which is a property associated with the higher sulphur mattes. For lower sulphur levels, where the matte is less amenable to milling, the costs of the milling increases. This paper will compare water granulation with certain dry granulation processes and the downstream processes required for Hydrometallurgy. It will further introduce and expand on atomisation which offers a further safety benefit in the control of the metal flow into the 'wet zone' with the use of a tundish flow control also reducing the conversion from the matte to powder in one fairly straightforward operation.

Jan 1, 2006

By E. Burgos Cruz

The behaviour of S, N and P during refining of Fe-18 wt%Cr-10 wt%Ni with calcium carbide was investigated. The effects of the initial contents of C and N in the metal phase, as well as the supply method of calcium carbide to the melt on the removal degrees of S and P were evaluated. Heats were carried out at 1873K, in MgO crucibles, using a laboratory induction furnace. It was observed that simultaneously with S and P, N and O have also participated in the reactions. It seems that, in fact, O governs the behaviour of the other elements dissolved in the melt and that N is had to the removal of P with calcium carbide. It was also noticed that high C content in the metal phase have not altered the dephosphorization and desuffirization degrees, but that the supply of calcium carbide done by injection led to a lower dephosphorization degree than the one obtained by dumping it.

Jan 1, 1995

By E. R. Vance, D. R. M. Brew

"Historically, Ordinary Portland cement has been the preferred medium to immobilise arsenic. However, arsenic in cement gives rise to calcium-arsenic phases and their known decomposition to calcium carbonate and arsenic trioxide via atmospheric carbonation raises serious questions about the long-term suitability of cement for arsenic immobilisation. Alternative matrices such as low-temperature ceramics (LTCs) potentially offer superior resistance towards carbonation owing to the absence of calcium. Consequently, the potential for arsenic immobilisation using LTCs has been investigated. Both AsIII and AsV have been incorporated and samples assessed according to a standard leaching protocol. AsIII persists in the porewater of alkali-bonded LTCs as sodium arsenite rendering them unsuitable for immobilisation. Thermal treatment of these LTCs to consolidate the microstructure and reduce open porosity resulted in sodium-rich cryptocrystalline matrices that leached arsenic and sodium readily. The omission of sodium in acid-bonded LTC formulations resulted in leach data that were close to the target value of 5 µg/ml in Toxicity Characterisation Leaching Protocol tests.IntroductionArsenic is a carcinogenic substance and its adverse effects of on humans, flora and fauna have been well documented [1-5]. As a consequence, many papers have been written on the prospective handling of arsenic-bearing waste. These can largely be divided into: (a) cleanup of arsenic-contaminated water using bacteria, precipitation, and/or UV irradiation to generate arsenic-rich sludges for subsequent immobilisation; (b) cleanup of arsenic-contaminated soil via chemical extraction for immobilisation of the As concentrate; and (c) immobilisation of industrial waste contaminated with As."

Jan 1, 2008

By C. G. Anderson, L. G. Twidwell

"Throughout the world, there are many orebodies or materials which have significant value but also contain arsenic, antimony, and mercury. As regulations on the transport, exposure, disposition and emission of these elements have become more stringent; it has become increasingly more difficult to derive the values from the resources. This paper outlines the fundamentals of alkaline sulfide hydrometallurgy and its successful application to arsenic, antimony and mercury bearing ores, concentrates, by-products, and other materials.Fundamental Alkaline Sulfide HydrometallurgyHydrometallurgical methods can be employed for treatment of gold, arsenic, antimony, tin and mercury containing materials, concentrates and ores as well as complex ones containing any number of metals. The alkaline sulfide system is one of these and is essentially a mixture of sodium sulfide and sodium hydroxide. This is a unique hydrometallurgical system as it is a very selective lixiviant for the distinct leaching of tin, gold, antimony, arsenic and mercury [1-7]. Worldwide, it is employed industrially in the CIS, China and the United States for the production of antimony [8-15].As an example, when the system is applied to an arsenic containing material like orpiment, As2S3, a solution of sodium thioarsenite is formed. This is illustrated as:"

Jan 1, 2008

Electrocrystallization studies were conducted in a concentrated acid-copper electrolyte to determine the influence of chloride ions and glue on copper nucleation and on the structure of thin copper layers. Electrochemical experiments allied to SEM and XRD examination were performed to characterize the mechanism of nucleation in the presence of additives at 65°C. Results indicated that most of the copper nucleation from a 83 g dm-3 Cu2+ solution, with 140 g dm-3 of H2SO4 is achieved in a matter of milliseconds, Although the presence of chloride and glue, at the concentration levels tested, does not seem to substantially modify the nucleation mechanism, the morphology, nuclei density and the copper film structure and orientation are changed by the presence of additives and by electrolyte stirring.

Jan 1, 1999

By Jean Frenay

Bacterial leaching tests have been carried out on Portugese pyritic ores containing zinc, copper, lead and silver as valuable elements. Both indigenous and isolated strains of Thiobacillus ferrooxidans were used. During the tests the factors pH, Eh and dissolved oxygen were measured and related to the leaching activity of the bacteria. Different means to estimate or determine the real bacteria concentration were examined. The influence of nutrient media and particle size has been evaluated. The role of galvanic couples was studied by electrical linking of mineralogical samples of pyrite, sphalerite and chalcopyrite. Leach residues were examined by optical microscopy to follow the mineralogical alterations during the leaching. The results show a rather good leaching of the sphalerite. However, the dissolution of copper from chalcopyrite is much more difficult, 50 % recovery never being obtained.

Jan 1, 1985

By W. L. Cornell

Bulk sulfide concentrate produced from Missouri Pb ore concentrator tailings must be reground to liberate sulfide values for subsequent sepa-ration. Studies to determine grinding parameters for optimum liberation were carried out using optical microscopy coupled with image analysis. The major sulfide phases present in the ground mineral particulates are marca-site, pyrite, sphalerite, galena, chalcopyrite, siegenite. and bravoite. Results showed that the base metal minerals were liberated by grinding to 74 micrometers (200 mesh), but the siegenite and bravoite required grinding to 20 micrometers or less to achieve liberation. Both the experimental method and results are presented.

Jan 1, 1987

By Young-Sool Jin, Heung Nam Han, Hong Joon Kim, Jae Kon Lee

A mathematical model was developed considering non-symmetric cooling' and stress distribution in both thickness and width direction of strip on a run-out table of hot strip mill. In order to solve a transient heat transfer equation including the heat evolved from phase transformation, a finite element method coupled with thermodynamic and kinetic analyses was applied. The heat capacity of each phase and heat evolution due to phase transformation were obtained from the thermodynamic analysis of the Fe-C-Mn-Si system based on a sub lattice model. The phase transformation kinetics of the steels was derived by using an inverse additivity technique with continuous cooling experiments. Heat transfer coefficients of strips on the run-out table were, by applying an inverse method, determined from the actual mill data under various cooling conditions. As for the stress analysis, the density change of strip due to cooling and phase transformation, and the transformation superplasticity were considered. A 90nstitutive equation for the transformation superplasticity, which is related to the phase transformation kinetics and the internal stress due to the density change of strip, was applied. A finite element method was adopted to calculate the deformation behaviour of strip on a run-out table of hot strip mill. Using the models, the temperature-phase-deformation history and distribution of a strip on the run-outtable was calculated.

Jan 1, 2001

By J. Méndez-Nonell

The thermodynamic and chemical properties of SrSO4 and SrS in a gaseous flow of CO and CO2 at high temperature are discussed. The thermodynamic analysis of the system was made using data from the literature. The results obtained from the thermodynamic analysis were experimentally verified using the thermogravimetric technique. The experimental results suggest the formation of a complex compound between SrO and SrSO4. It was also found a change in the chemical mechanism of the process between SrSO4 and CO-CO2 and in the chemical mechanism of the process between SrS and pure CO2.

Jan 1, 1995

By M. Frades, C. Frías, G. Díaz, A. B. Mejías

"In recent years, zinc recovery from flue dusts and other industrial wastes has been increased, offering to the market a large tonnage of secondary zinc oxides, which can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content.The ZINCEXTM Technology has been commercially applied for more than thirty years and represents the most suitable solution to deal with secondary or crude zinc oxides due to its flexibility, simplicity, and cost-efficiency, allowing production of SHG electrolytic zinc and pure zinc sulfate salts thanks to the flexibility and selectivity of the zinc solvent extraction unit regarding to get rid of impurities.A dual plant able to produce electrolytic zinc and crystallized zinc sulfate has been engineered to provide a flexible and profitable solution to zinc market. A description of the study and the relevant achievements is presented in this paper.IntroductionZinc is a valuable commodity in the marketplace and can be recycled again and again and still maintain its physical and chemical properties. Zinc recycling offers both environmental and economic benefits such as reducing volumes of material that end up in landfills, saving energy by reducing the need for mining and smelting, and relieving environmental impact on the land and water, and conserving zinc ore [1].The supply of zinc able to be re-processed will be increasing from year to year according to secondary materials enter the recycling stream, and as a result, more recycled zinc will become available in the market. Thus, some existing zinc refineries are implementing an annexed treatment line to process secondary oxides in conjunction with primary zinc concentrates [2].The galvanized steel scrap is normally recycled in electric arc furnaces or in basic oxygen furnaces, which generates a large tonnage of zinc-bearing flue dusts (EAFD). Around one million ton EAFD is yearly produced at the USA and the EU, respectively. The flue dusts are treated commercially by pyrometallurgical ways such as waelz kilns, electrothermic furnaces, etc, to yield secondary zinc oxides that can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content [3]."

Jan 1, 2008

By Gustavo A. Munoz

Activated carbons owe their adsorption capacities to their extensively developed pore network structure. As a result, these adsorbents generally exhibit high specific surface areas. Currently, granular activated carbons produced from coconut shells are traditionally used for gold recovery by adsorption from cyanide leaching solutions. Magnetic activated carbons (MACs) for gold recovery from cyanide solutions produced from sources other than coconut shells have been developed at the University of Utah by mixing a magnetic precursor with a carbon source, and treating the mixture under controlled conditions of temperature and gas phase composition. The pore size distribution of the activated carbons is dependent on the degree of activation, among other factors. The significance of the MAC pore size distribution on gold adsorption kinetics and gold adsorption capacity is presented.

Jan 1, 2003

By Qian Fu

Although chlorine fluxing to remove magnesium has been widely practiced in the aluminum industry for many years, there appear to have been few fundamental studies of the kinetics and transport phenomena involved. The paper describes such a study in which the rates of reaction of individual argon/chlorine bubbles with aluminum/magnesium melts were measured. The detachment of bubbles from a submerged nozzle, at variable depth in the melt, was detected by a microphone and the arrival of the bubble at the top surface by conductivity probes. Analysis of exit gases and mass balances yielded the overall progress of reaction. Experimental results are interpreted in terms of heterogeneous reaction kinetics and mass transport to the bubble-melt interface,

Jan 1, 1996

By Nexhmedin Lohja

The production of high-carbon ferrochromium in a submerged electric furnace based on double-level technology has some advantages compared to close-type furnaces with one tap hole. These advantages include the reduction of the specific energy consumption for the overall process, good separation of ferrochromium from slag, an effective treatment of raw materials including lean chrome ores (low percentage of Cr2O3) etc. An outline of the operation of this furnace along with the production line of briquettes from fines of chrome ore by using organic and inorganic binders, will be followed by a description of the recent work carried out to improve the energy consumption in this furnace through a pre reduction process of Cr2O3 ores by the off-gas energy recuperated from the furnace and the use of SiC in the feed. A short theoretical analysis of the new work will also be given.

Jan 1, 2006

By Jong-Oh Jo1

Thermodynamics of Ti, N and O in liquid iron was studied in order to establish a data base for the prediction of TiN and TiOx formation in liquid stainless steels containing various alloying elements including Cr, Ni and Si as a function of temperature. The interaction parameters of these elements on Ti and N were determined using the metal-nitride-gas equilibration technique. The TiN stability diagram for a commercial stainless steel grade was constructed from the measured thermodynamic parameters, and its validity was confirmed experimentally. The interaction parameters between Ti and O, and the equilibrium constants for Ti deoxidation reactions for the formation of Ti2O3 and Ti3O5 were also determined by the equilibration of the melts with those oxides identified by the XRD and the EPMA analyses.

Jan 1, 2006

By Elizabeth M. Ho

Oxidants are added in uranium leaching in acid media to convert iron(II) in solution to iron(III). Iron(III) has an important role in the leaching of uranium by acting as an electron transfer agent for the oxidation of uranium(IV) to uranium(VI). The oxidation of iron(II) to iron(III) in sulfate solutions using sulfur dioxide/oxygen (SO2/O2) was carried out under typical uranium leaching conditions (pH 1-2, 20-50°C) to confirm literature trends and this work was then extended to the use of SO2/O2 in the leaching of uranium ore. The oxidation rate was found to be dependent on the initial SO2/O2 volumetric ratio and the oxygen mass transfer rate, but was independent of the initial iron(III) concentration above about 200 ppm at pH 2. The presence of 55 ppm organic extractant (Alamine 336) decreased the reaction rate. The oxygen mass transfer coefficient (kLa) for the mixing tank system was measured and was found to decrease with increasing solids density in a 1 g L-1 MgSO4.7H2O solution.

Jan 1, 2003

By G. Upadhya

Considerable success has been achieved recently in modeling microstructural evolution during solidification of castings bthrough the coupling of macroscopic heat transfer with microscopic solidification kinetics models. However, a complete model for simulation of solidification in complex shaped castings involves: (i) the description of fluid flow, during and after mold filling, coupled with (ii) heat transfer to the mold and surroundings by use of a macro model, followed by (iii) a description of subsequent solidification of liquid metal by use of a micro model for solidification of the alloy under consideration. This paper describes the coupling of solidification kinetics model to a 3D, transient, fully coupled fluid flow and heat transfer model. Coupling between the macremicro models is achieved by using the latent heat method. Micro models for the eutectics of gray, white and ductile iron are discussed. This coupled code has been used for predicting the thermal history and microstructural data for shaped castings. Various applications of the model, including prediction of shrinkage defects, grain density contours, and graylwhite transition region in the casting, are presented for a relatively complex casting geometry.

Jan 1, 1992