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By J. A. Voigt

In an effort to determine the optimum conditions for preparing high purity, fine particle size high temperature superconducting oxide powder, we have investigated how calcination conditions influence the conversion of a chemically prepared hydroxycarbonate precursor powder to YBa2Cu307. We find that the precursor can be converted to phase pure YBa2Cu307 in either oxygen or synthetic air (20% 02. 80% N2) at 850°C. This temperature is substantially lower than the temperature (>900°C) normally used for the calcination of mixed-oxide powders. The lower calcination temperature prevents particle sintering and maintains the desired fine particle size. Powder processed in synthetic air shows a low degree of crystallinity indicating it may be more sinterable than the highly crystalline powders produced when an oxygen atmosphere is used. Intimate contact between powder particle surfaces and a flowing gas atmosphere promotes the reaction between the BaCO3 component of the precursor powder and the Y and Cu constituents.

Jan 1, 1989

By Varadajan Seshadri

The increase in production of continuous casting machines requires long ladle sequences without interruption. Very often the production schedule has to accommodate a variety of steel grades. In such cases downgrading may be inevitable. Models must be made available to study the alternatives that would make possible mixing of steels in the tundish but minimizing the losses due to downgrading the slabs. Physical modeling was used to evaluate the influence of variables such as internal geometry of the tundish, presence of turbulence inhibitors, depth of ladle long nozzle, weight of steel in the tundish, steel throughput upon the tundish transition curve. Expressions for minimum residence time and transition period have been determined. Mixing-transition is allowed to continue inside the liquid pool in the mold and the final solute distribution in a given cross section is captured by a solidification model. The result is a map of the transition in the final product.

Jan 1, 2006

By F. Field, R. Kirchain, J. Gregory

Utilizing alternative materials is an important tactic to improve the environmental performanceof products. Currently a growing array of materials candidates confronts today’s product designer. While life-cycle assessment (LCA) methods provide quantitative input into this selection decision, their implementations are evolving and disparate. The goal of this paper is to explore several major analytical variations of LCA implementations and the implications of these variants across a range of application contexts. Specifically, this paper examines analytical variations in valuation method and treatment of recycling by exploring allocation methods that affect product end-of-life. Case studies across a range of materials are presented, including materials that exhibit a spectrum in variation of environmental performance and material degradation between primary and secondary applications. Preliminary results indicate that the choice of analytical method can have real impacts on individual metrics and there are sets of analytical variation over which strategic results are strongly affected.

Jan 1, 2008

By Andrew A. Fyfe

The start-up and operating results obtained at Zia Technology Inc.'s first commercial operating facility at Caldwell, Texas are described. The operation which stated in early 1991 is the first to employ the patented Inclined Rotary Reduction System (IRRS') with the associated 'all-metallic retort for the recovery of all metallics contained in EAF dust.

Jan 1, 1992

By Takeshi Yoshikawa

For the development of low-cost silicon refining process for solar cells, the present authors have been studying the low temperature refining technique, ?solidification refining of Si with Si-Al melts at 1173 ? 1273K?. In the present work, we have investigated the B removal in that refining, utilizing the segregation effect and also the effect of Ti addition to the melt. Segregation ratio of B between solid Si and Si-Al melt was measured by the temperature gradient zone melting technique and it indicated the B removal fraction would be as much as 90%. Titanium addition to the melt was found to produce the TiB2 precipitation with soluble B in that melt and bring the effective B removal of refined Si to its content of 1ppma.

Jan 1, 2006

By Henry Freiser

For the last several years, a systematic investigation of the equilibrium extraction behavior of selective tervalent lanthanides with representative chelating extractions of a variety of chelating agent families has been undertaken for the purpose of learning how to obtain chelating extractants of improved selectivity for separating individual lanthanide ions. The equilibrium extraction data (expressed as log Kex) for each reagent system are linearly related to the reciprocal ionic radius of the tervalent lanthanide ions. The role of adduct formation, steric hindrance, as well as the nature of the bonding atom in the chelate ring, represent some of the factors affecting selectivity arising out of our database of over 200 individual extraction systems, which will be discussed.

Jan 1, 1989

By Weyman Dunaway

This paper will present a description of the development and commissioning of the world?s most efficient process for manufacturing high purity aqueous zinc bromide. The method for making aqueous zinc bromide from metallic zinc and bromine comprises contacting zinc with bromine dissolved in a reaction solvent containing a metal halide salt. The reaction temperature is maintained at less than 60°C. The reaction solvent preferably comprises an alkali, alkaline earth, or transition metal halide; the halide salt preferably comprises a chloride or a bromide. One preferred method includes the step of recirculating the zinc bromide product stream back to the reaction vessel. The reaction vessel can be either a one stage or a multiple stage reactor. The resulting product stream is a high density aqueous zinc bromide solution. The process is so novel that Tetra Technologies, Inc. was awarded US Patent Number 6,036,937.

Jan 1, 2006

By P. G. West-Sells

Recovery of gold from thiosulfate leachates can be accomplished by adsorption of the gold thiosulfate complex by a strong base resin. Two of the most significant impurities that can decrease this gold adsorption are tetrathionate and trithionate, which are produced as oxidation products of thiosulfate during gold leaching. This paper investigates gold adsorption on a strong base resin (Purolite A500C) as a function of the concentration of these impurities. It is shown that concentrations of tetrathionate and trithionate as low as 150 mg/L can decrease gold loading by an order of magnitude, and that of the two ions, tetrathionate has a stronger detrimental effect. The resin and solution gold concentration profiles were successfully fit using a Freundlich isotherm, which further shows the strong effect of tetrathionate. To counteract the decrease in gold adsorption by tetrathionate, a novel process was proposed. Sulfite was added to the solution to oxidize tetrathionate to trithionate, and a nitrogen blanket was added to ensure that no further oxidation of thiosulfate could take place. It is shown that by incorporating this process, gold adsorption was doubled from both synthetic and real gold thiosulfate leachates.

Jan 1, 2003

By Barry T. Kilbourn

There is a continuous quest for better-performing materials, for example, to withstand higher temperatures, to resist more efficiently degradation or to be electrically conductive under extreme conditions. The oxides, and similar compounds, of the lanthanides and yttrium can, in some cases, help provide such behavior. Other advanced materials, such as hydrocarbon catalysts, optical ceramics or sensitive phosphors, may also require these oxides for some essential function. The role of the oxides in a wide variety of technologies, some novel and developing, will be reviewed and the underlying physico-chemical principles, the common threads, between several less well-known and apparently unrelated uses discussed.

Jan 1, 1989

By J. W. Matousek

Copper losses in smelter slags are :typically normalized with some form of the distribution coefficient, written as the ratio of the weight percent assays of metal in slag to the metal in matte or its inverse: L(s/m) = %(Cu)/%[Cu] or L(m/s) = %[Cu]/%(Cu) However, this simple approach ignores the dynamics of the smelting process. It overlooks the effect of the chemical work done in producing a given matte grade from concentrates of different grades -- or from a single concentrate blended with varying quantities of copper bearing precipitates or reverts. This paper examines the combined influences of matte grade and the work done in smelting on the copper content of smelting furnace slags. A simple model for the relationship is proposed.

Jan 1, 1999

By J. C. Riani

The release of heavy metals into the environment is increasing among others due to human activities such paint and pigment industries, tanneries, and metal finishing industries. Among metal releases, chromium is notable because this metal is carcinogenic. Thus, the aim of this work is to use an ion exchange system composed of one cationic resin column and one anionic resin column in order to adsorb the chromium (III, VI) from chromium electroplating effluents with the objective of recycling the water. The methodology consists of chromium adsorption tests using the ion exchange resins system with Purolite the 850 (polystyrene matrix, functional group quaternary amine) and Purolite C 150 (polystyrene matrix, functional group sulfonic acid). The contaminated solutions were passed through the columns with the assistance of peristaltic pump. Samples of the outgoing solution were taken in order to control the conductivity and pH and analyze the metals. The effects of the feeding outflow on the chromium adsorption were evaluated. The results show that the quality of the water collected at the end of the process is within the Brazilian standards about the discarding of toxic substances in the environment (CONAMA 357/05). This makes possible the recycling of water into the process and also its discharge in the rivers.

Jan 1, 2006

By Gerardo R. Alvear

The ability to efficiently remove impurities contained in concentrates is a key point to consider when selecting copper smelting technology for new plants or modernisation projects. Volatilisation of impurities such As and Sb should occur as early as possible in the process, and preferably in the smelting furnace, so that they do not impact on downstream unit operations. The ISASMELTTM process has been demonstrated to remove impurities efficiently, through high levels of volatilisation. This behaviour is promoted by attributes of the process such as the strong bath agitation, and the flexible nature of the process design, allowing the operator to choose the optimal matte grade for impurity partitioning, and the positive effect of the moisture content in the feed. This paper presents the distribution of minor elements in the copper ISASMELTTM furnace. Distribution impurities of As, Sb, Pb, Zn and Co observed in the ISASMELTTM furnace at Mount Isa Smelter are reported. Then, based on plant results and thermodynamic considerations, the potential application of ISASMELTTM technology for processing complex concentrates is discussed.

Jan 1, 2006

By Akira Yazawa

Oxidic dissolution loss of metal in slag is discussed thermodynamically in terms of oxygen potential, activity coefficient and equilibrium constant. To understand basic principle, regular solution model is applied for model calculation of the activity behaviour of metal oxide in FeO-SiO2-CaO slag, and effects of slag composition, temperature, and basicity of oxide on dissolution loss are demonstrated. As: a simplified but practical conclusion, the dissolved metal loss in slag is inversely proportional to activity coefficient of metal oxide, and also to FeO content in slag when amount of slag is taken account.

Jan 1, 1994

By C. R. Bennett

The first phase in the design, development and implementation of a comprehensive computational model of a copper stockpile leach process is presented. The model accounts for transport phenomena through the stockpile, reaction kinetics for the important mineral species, oxygen and bacterial effects on the leach reactions, plus heat, energy and acid balances for the overall leach process. The paper describes the formulation of the leach process model and its implementation in PHYSICA+, a computational fluid dynamic (CFD) software environment. The model draws on a number of phenomena to represent the competing physical and chemical features active in the process model. The phenomena are essentially represented by a three-phase (solid-liquid-gas) multi-component transport system; novel algorithms and procedures are required to solve the model equations, including a methodology for dealing with multiple chemical species with different reaction rates in ore represented by multiple particle size fractions. Some initial validation results and application simulations are shown to illustrate the potential of the model.

Jan 1, 2003

By Han Ilhan

This paper discusses and describes aspects of a cost effective and safe tailings impoundment selection. In light of the current low metal prices and recent tailings embankment failures around the world, it is becoming extremely more important to develop tailings impoundment design that balance cost efficiency with safety. The paper will present critical design components associated with a tailings impoundment which need to be addressed during the planning phase. Procedures for identifying various tailings impoundment alternatives, and evaluation and selection of alternatives are presented.

Jan 1, 1999

By María Cristina Ruiz

In the processing of copper concentrates by the conventional smelting-converting technology, complying with the increasingly severity of environmental legislation in some countries has become difficult, mainly due to severe fugitive emissions of gases produced during the batch PS (Peirce-Smith) converting step. In this work, the results of an investigation on the pressure leaching with sulfuric acid and oxygen of white metal (produced in a Teniente Converter reactor) are discussed. The study was carried out at laboratory scale and the main variables studied were temperature, concentration of sulfuric acid and partial pressure of oxygen. The experimental results indicated that most of the sulfur in the white metal was oxidized to sulfate in the whole range of temperature studied (105ºC to 150 ºC). The concentration of sulfuric acid over 0.05 M, and oxygen partial pressure over 6 atm had little effect on the dissolution of copper from the white metal. On the other hand, temperature had the most significant effect on copper dissolution; below 130 ºC copper dissolution was incomplete after 5 hours of leaching while at 150 ºC the dissolution was complete in 90 minutes and 10 atm of partial pressure of oxygen

Jan 1, 2006

By A. Robles

The main goal of the present work is to propose a viable alternative for selective arsenic elimination from copper smelter flue dust without the need of a global leaching scheme for all the individual components of the flue dust. Using this alternative, the inherent copper recovery problems are avoided. Arsenic precipitation is also considered for regenerating the solution and completing the process cycle. The experimental results for arsenic extraction and precipitation are satisfactory. Concentration of NaOH used was relatively low. The main reason for succeeding in high arsenic extraction and low NaOH consumption is due to the previous water washing of the flue dust. Water washing dissolves much of the iron and copper that are present in certain percentage as sulphate.

Jan 1, 1999

By Y. F. Jia

Arsenic constitutes a major contaminant for the hydrometallurgical industry. Its removal and immobilization from process effluents typically involves lime neutralization and co-precipitation with ferric iron (Fe (III)/As(V)>3). Alternatively, precipitation of scorodite (FeAsO4?2H2O (cr)) may be applied to arsenic fixation. The mechanism of arsenic fixation in the former process has been suggested to be surface adsorption. Unequivocal characterization of these products is difficult because of their amorphous nature hence a variety of methods need to be applied including the particularly powerful method, extended x-ray absorption fine structure (EXAFS) spectroscopy. In this study, we have investigated the preparation of arsenate-adsorbed ferrihydrite with the purpose to compare its structure to that of Fe(III)-As(V) co-precipitates and scorodite (both amorphous and crystalline). Furthermore the solubilities of these Fe(III)-As(V) solids are measured as a function of pH. Their structures are elucidated and correlated to their solubilities and thereby the application of these findings to the practice of arsenic removal and disposal is assessed.

Jan 1, 2003

By B. C. Tripathy

The effects of alkali metal ions Li+, Na+, K+and transition metal ions Cr3+ and Mo6+ on the cathodic current efficiency, deposit quality, crystallographic orientations, deposit morphology and polarisation behaviour of the cathode during nickel electrocrystallisation on stainless steel substrate from aqueous sulphate solutions containing boric acid were investigated. The alkali metal ions had virtually no effect on the cathodic current efficiency, deposit quality, crystallographic orientations, deposit morphology and cathodic polarisation. On the other hand, there were significant variations in the current efficiency and deposit characteristics when Cr3+or Mo6+ were present in the electrolyte. Current efficiency decreased by more than 10% even at lower concentrations (> 100 mg/L). Similarly purity of the deposits was affected by the presence of either of the metal ions. In the presence of Cr3+, there was progressive shifting of the nucleation potential of nickel towards more negative values, whereas, in the case of Mo6+the nucleation potential shifted initially towards positive values in the concentration range 2-40 mg/L, but then towards negative values when its concentration exceeded 40 mg/L.

Jan 1, 2003

By Daniel Gauthier, Patrick Sharrock, Cedric Verwilghen, Gilles Flamant, Ange Nzihou, Jocelyn Ramaroson

Clean processes are needed to dispose of many wastes. The incineration of 1 ton of municipal solid waste generates 6000 Nm3 of combustion gases contaminated with heavy metals and other pollutants. Gas scrubbing processes are required to clean incineration fumes in order not to transfer pollution to the atmosphere. We are investigating the use of Hydroxylapatite (Ca-HA) particles for use as sorbent for the removal of volatile heavy metals. We have carried out the synthesis of Ca-HA by two precipitation methods from solution and obtained solids with specific surface areas reaching more than 100 m2/g. Preliminary adsorption experiments were conducted in a horizontal furnace by mixing Ca-HA with 5% by weight of cadmium chloride in solid state. The mixture was heated to 600°C under air atmosphere during 6 hours. Chemical analysis of the solids confirmed that 85 % of the cadmium was retained in the solid phase. Such laboratory results showed that Ca-HA is capable of adsorbing cadmium chloride vapors, and pilot scale studies confirmed cadmium abatement in an industrial context.

Jan 1, 2008