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By F. Leclerc, V. Rebeyrolle, M. Revil-Baudard, A. Jardy, M. Založnik, H. Combeau

"Since the quality of Vacuum Arc Remelted ingots is linked to their chemical homogeneity and metallurgical structure, a modeling study of the solidification during VAR has been undertaken. It is based on the solution of the coupled transient heat, momentum and solute transport equations during the remelting of a cylindrical ingot. Solidification mechanisms implemented in the model include a full coupling between energy and solute transport in the mushy zone, and accounting for nucleation and finite diffusion of solutes at the microscopic scale, in both solid and liquid phases. This modeling can be applied to actual multi-component alloys. In this paper, the macrosegregation in Zircaloy 4 ingots is investigated. To validate the model, one single melt of a homogeneous electrode has been specifically performed. The comparison between the predicted macrosegregation and the experimental results shows the importance of accounting for solutal convection to forecast properly the macrosegregation in remelted ingots.IntroductionVacuum Arc Remelting of zirconium alloy ingots is a key step in the manufacturing process of fuel assembly components in nuclear reactors. The control of the chemical homogeneity is indeed fundamental to ensure the quality and the in-reactor performance of the final products. Despite the use of electromagnetic stirring to homogenize the liquid melt composition, chemical heterogeneities develop in the mushy zone during the solidification stage. One of the main challenges for zirconium producers, as well as titanium producers, is to master the VAR process in order to control the macrosegregation in remelted ingots. Macrosegregation results from the association of microsegregation and transport phenomena. The latter are primarily due to the flow in the liquid and mushy parts. It is now well established [1-4] that the hydrodynamics of the melt pool in a VAR ingot depends on the combined action of the followings: thermal and solutal buoyancy, self-induced electromagnetic force and the periodic centrifugal force caused by the angular movement generated by the stirring. However, for zirconium alloy ingots, the effects of thermal and solutal buoyancy forces on macrosegregation through their influence on the flow in the mushy zone have not been clearly identified."

Jan 1, 2012

By J. E. Dutrizac

A mineralogical study of a weak acid leach residue from the Clarksville zinc plant of Savage Zinc Inc. was carried out. The study focused on Pb and Cd as these elements most significantly impact on the environmentally acceptable disposal of the residue. The residue consists of major amounts of bassanite, zinc ferrite and various Zn-Pb-Fe-Cd silicate species. Also present are lesser quantities of PbSO4, sphalerite, Fe2O3 quartz, Mn-Pb-Fe oxides, SrS04, (Pb,Sr)SO4 iron gel-silica gel, jarosite and Ti oxide. The principal Cd carriers are the zinc ferrite, which contains up to 9.00% Cd and likely accounts for -45% of the total Cd content of the residue, and the various silicate species which contain up to 6.97% Cd and account for about 45 % of the total Cd. The sphalerite is a minor Cd carrier containing an average of 0.35 % Cd and accounting for -5 % of the total Cd; the other carriers contribute only trace amounts to the total Cd content. The major Pb carriers are PbS04, Pb-bearing silicates and Mn-Pb-Fe oxides. Minor proportions of the total 1.09% Pb content of the residue are carried by SrS04 and (pb,Sr)S04' Trace Ph carriers include the iron gel-silica gel, Fe-Zn-AI oxide and bassanite. The residue after the toxicity characteristic leaching procedure (TCLP) is mineralogically very similar to the initial weak acid leach residue; the amounts of calcium sulphate are approximately the same in the two products. The principal Cd and Pb carriers are also the same as those noted in the initial residue, except that some dissolution and reprecipitation of Pb-Sr sulphate takes place. That the residue fails the TCLP test is likely a consequence of the superficial dissolution of Pb and Cd from species such as PbS04 or Zn-Pb-Fe-Cd silicate.

Jan 1, 1995

By Pragna Bhakta

Newmont has investigated potential treatment options for low-grade refractory gold ores since 1988. After extensive R&D at Newmont?s laboratories, biooxidation pretreatment followed by ammonium thiosulfate leaching was selected for application to sulfidic preg robbing ores. A heap biooxidation and ammonium thiosulfate leaching demonstration facility was constructed in 1995 to conduct large-scale pilot tests at Newmont?s Carlin Operations. This paper presents Newmont?s experience with the recovery of gold from preg robbing ores using ammonium thiosulfate.

Jan 1, 2003

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010

By Scott A. Howard

MgO is routinely used as the basis for refractory materials, however, its susceptibility to hydration may result in dimensional instability and subsequent failure. The addition of boron has been shown to reduce th,e hydration susceptibility of MgO yet its dissolution into certain grades of steel may degrade their performance. In order to predict the efficacy of reducing hydration susceptibility by the incorporation of mono-, di-and tri-and quadravalent cations, the lattices of various cation-substituted systems were modeled. To more accurately simulate the substituted lattices, either cation or anion vacancies were incorporated to maintain electrical neutrality and all possible arrangements of defects in a 2x2x2 MgO supercell were investigated. Correlations were then made between the lattice energies of these systems and their susceptibility to hydration as reported in the literature. The results indicate the presence of higher charged cations tended to increase lattice stability while the cations with lower valency tended to have lower lattice energies. The relatively small body of experimental results available in the literature are consistent' with this study's results.

Jan 1, 1989

By Arpad E. Torma

The identification and characterization of lithographic iron and sulfur oxidizing bacteria in the 1940' s. opened up new possibilities and challenges for the mining and metallurgical industries. These were exploited during the 1950's and' 1960's, when it was demonstrated' that mining wastes and complex unused mineral resources could be economically treated by bacterially assisted heap and dump leaching processes?. During the 1970's this technology grew into a more structured discipline called "biohydrometallurgy". In the l980's efforts were devoted to the identification of a variety of organisms involved in naturally occurring leaching processes. Further efforts dealt with the elucidation, of leaching mechanisms; the leach ability of nickel, coban, zinc, and precious metals; the desulfurization of coal; and diverse biosorpion phenomena. The application of genetic engineering techniques for the improvement of microbial performance was also initiated?. Current trends in biohydrometallurgy include improvement of many of the techniques noted above, as well as application of leaching. technolog.ies to. environmental remediation scenarios. These activities afford considerable opportunities for research in the 1990's. For example, bioremectiation of abandoned mining and processing sites requires development of new and economically viable technologies capable of removing low concentrations of toxic metals from high volumes of solid and/or liquid wastes.

Jan 1, 1991

By Federica Paglietti

In this work is presented SEX (Structural & Elemental X-Ray Instrument), the first spectrometer completely portable which make non-destructive X-ray fluorescence and diffraction analysis, in contemporary and in real time. This instrument has been realized using miniaturized detectors, the same model installed on the mission Pathfinder NASA, and X-ray microtubes. SEX allows the chemical and mineplogical characterization of all kind of solid materials and allows to make chemical stratigraphy and liquids analysis.

Jan 1, 1998

By Mahin Rameshni

WorleyParsons innovative SO2 reduction process efficiently recovers sulfur from SO2 streams. Effluent gases from ore roasters and smelters and coal-fired power plants can be treated to reduce sulfur emissions. This exciting new process is an innovative combination of well-established processes of reaction of CH4 and sulfur vapor to produce CS2, followed by catalytic hydrolysis of CS2 to H2S, and Claus reaction of H2S and SO2 to sulfur. Key advantages are lower fuel consumption, reduced emissions, better product sulfur quality and better operational stability. The Production of elemental sulfur from SO2 is being called Rameshni SO2 Reduction (RSR) and it is patent pending.

Jan 1, 2006

Many studies have been conducted over the past 3 decades on the leaching of gold in solutions containing thiosulfate, ammonia and copper. However, most of these studies have been carried out using ore samples, with very few fundamental studies of this system being attempted. The majority of the published studies have failed to acknowledge the undesirable side reaction between copper(H) and thiosulfate, let alone account for its effect. The fact that the solution chemistry is constantly changing makes it very difficult to perform a fundamental study of gold leaching. With the advent of the rotating electrochemical quartz crystal microbalance (REQCM), such fundamental studies are possible as this instrument measures mass in real time. This has allowed leach kinetics to be measured in a matter of minutes and hence at essentially constant solution conditions; The present paper highlights that a sufficient concentration of copper(II) and ammonia are required in order to achieve appreciable gold leach rates. However, the use of air (oxygen) to maintain the copper(Il) concentration catalyses the undesirable copper(II) reaction with thiosulfate. The presence of ammonium ions is shown to have an effect on this undesirable reaction as well as on the gold leaching ?reaction. Preliminary electrochemical studies into .gold electrowinning using the REQCM show that gold(I) thiosulfate cannot be readily reduced to metallic gold in the potential region at which cementation usually occurs. However, it is well known that gold cementation onto copper occurs rapidly. The current study addresses this discrepancy by studying the effect that copper and silver have on the reduction of gold thiosulfate. It has been found that the presence of both silver and copper enhance gold deposition, particularly at low over potentials. While this is beneficial in cementation, the presence of copper and silver in solution has been found to cause passivation of the cathode surface during electrowinning at 'higher overpotentials.

Jan 1, 1998

By D. M. Hausen

A refractory siliceous low-grade silver ore (265 g/t Ag) from a prospect in Sonora, Mexico was investigated mineralogically and metallurgically to evaluate extraction of the silver by conventional methods. Approximately half of the silver was recoverable, occurring as coarsely crystalline acanthite (70-300 Am) that was liberated in material crushed to minus 10 mesh. The remaining silver is refractory and occurs mostly as finely locked (-2 to 0.2 Am) acanthite in cherty quartz, and as minor amounts of finely disseminated stylotypite or freibergite in fluorite. The mineralogic data have thus served to explain the 50-60% recovery of silver by flotation and cyanidation.

Jan 1, 1991

By Alejandro R. Alonso, Lizet Alvarado, Gretchen T. Lapidus

"Cobalt and lithium recovery from spent Li-ion secondary batteries has been increasingly studied in recent years due to the high value of both metals and the low proven reserves for lithium. The standard method employed until now has been the deactivation and crushing of the batteries, followed by leaching of the L1C0O2 spinel from the battery cathode using acid solutions, such as 1.5 to 2.0 M HC1 or H2SO4, in a temperature range from 120°C to 250°C. Once leached, the cobalt is separated by electrodeposition and the lithium by precipitation, using large amounts of carbonate to bring the solution to alkaline pH values. In the present work, citric-thiosulfate solutions are used for the spinel leach at room temperature, favoring a reductive environment at room temperature, which stabilizes the cobalt(II) as cobalt citrate and lithium(I) at pH 5, and recovers approximately 99% of both metals.IntroductionThe Li-ion batteries industry has become an important economic sector in recent years. This type of battery is the most promising system for energy storage, because of its high efficiency in charge-discharge cycles, and its adaptability to many configurations. The demand will probably increase because of the need for mobile energy sources in many types of devices ranging from cell phones, tablets, and laptops to medical, navigation and sophisticated communication equipment and even in automobiles.One major problem related to the use of these batteries is the method employed for recycling the components, mostly cobalt and lithium. Currently, there are two processes employed on an industrial scale: the Sony/Sumimoto process, used since 1990 [1] and the Toxco Process [2]. In the first case, incineration is used to open the batteries and at same time volatilize the organic solvents. After that, the metals (copper, iron and aluminum) are physically separated. The cobalt and lithium are recovered as oxides and then thermally treated in order to recycle them for new batteries manufacture."

Jan 1, 2012

By M. Z. Quadir, M. A. Islam, P. J. Hazell, G. J. Appleby-Thomas, J. P. Escobedo

The mechanical response of closed-cell aluminium metallic foams subjected to low and high strain-rate loading has been investigated. A set of quasi-static and dynamic (shock) compressive tests have been conducted on closed-cell aluminium foams (CYMAT) with densities of 0.50 and 0.30 g/cc. Post-mortem characterization via optical microscopy and electron backscatter diffraction (EBSD) was performed on pristine and deformed specimens to elucidate the dominant deformation mechanisms in these materials. The combination of these techniques allowed for the assessment of critical deformation parameters such as changes in cell geometry and morphology, as well as microstructural evolution and deformation of the aluminium cellular network. These findings aim to aid in the design and development of optimized material structures for impact and blast protection.

Jan 1, 2015

By R. H. Hanewald

INMETCO, a subsidiary of Inco Limited, is the only facility in North America that provides High Temperature Metals Recovery for nickel-, chromium-, and iron-bearing wastes. Since 1978, this process has prevented more than 775,000 tons of materials from becoming part of the nation's waste stream. The paper describes Inco's experience in metals recovery, traces the development and explains the operation of the High Temperature Metals Recovery Process, and examines the procedures and criteria used to determine whether spent catalysts meet process feed specifications. An overview of the current requirements for transporting spent catalysts is provided. The paper concludes with brief case histories of catalysts users employing High Temperature Recovery to manage spent catalyst.

Jan 1, 1995

By A. D. Zunkel

Increasing amounts of electric arc furnace dust (EAFD) are being generated worldwide as more steel is produced from electric furnace melting of galvanized steel scrap. In most countries, the management of this material is a costly technical, economic, and legal problem for minimill steelmakers. Many technologies and processes are being developed and implemented worldwide to manage this material to recover contained zinc, lead, and iron values and render it nonhazardous. These processes are pyrometallurgical, hydrometallurgical, or hybrid in nature. Some produce zinc oxide, some zinc metal, some lead metal, and some lead cement. Some are successful, some have failed, many are dormant. or abandoned, and others continue to be developed and emerge. This paper updates the current status of 20-30 processes in various stages of commercial application and development used worldwide to manage EAFD and recover its nonferrous, particularly zinc and lead, and ferrous values.

Jan 1, 2000

By Hyun Kyu Shin, Byeong Deok Lee, Young Eun Lee

The reduction of Mn oxides at pre-smelting steps is an integral part of smelting processes for Mn alloys, and an understanding of its reaction mechanism is expected to contribute to the improvement of processing efficiency for Mn alloys smelting. The phase diagram shows that five Mn carbides are operative in the Mn-C system. Although they are expected to participate in the reduction of Mn oxides, no specific information is available yet to clarify their roles in presmelting carbothermic reaction of Mn oxides. Experiments with composite pellets prepared with Mn oxides and graphite powders show that Mn3O4 is reduced initially to MnO at about 1130oC and, subsequently, to Mn7C3 carbide as temperature increases further. At 1331oC, Mn7C3 carbide dissociates to Mn alloy and carbon. The degree of reducing reaction increases with increasing carbon balance in composite pellets and increasing temperatures.

Jan 1, 2014

By Freddy Syvertsen

"During the past two years the Association of Norwegian Foundries in Norway has been running a project in evaluation of CAD/CAM systems for foundries.In this work we have had a closer look to the various steps from drawings to the finished castings. On this background we have made a specification of the special needs in the foundry process. The main content of this paper is a presentation of this specification.Some CAD/CAM sytems have been compared with the specification and a summary of the result is presented.In the project we have also had a closer look at some systems where we actually have tried the user interface and some of the possibilities in the systems. In this way we have gained a more detailed knowledge of the systems and we have also got some experience in NC-machining from the systems.IntroductionThe development of CAD/CAM systems has taken place with almost no interaction with the foundry business. This becomes clear when you are having a closer look at the systems. Most of them have not the possibility to describe the complex sculptured surfaces that is often found on castings. The people developing the software, have paid little or no attention to the problems arising when a geometry is going to be transformed for the casting process. Among the problems are the decision of where to place the parting line and to adjust the draft angle. These problems must be solved properly to be able to withdraw the model from the sandmould. In die casting the problems must be solved to be able to get the casting out of the die.In Norway some companies have been developing CAD/CAM systems for several years, with limited interest in foundry problems till 1983. To present the special foundry problems to them a specification of the needs was made that year. Another reason for making this specification, was to compare it with the CAD/CAM systems on the market (1).Design of castingsGeometry transferThe foundries in Norway are small units with almost no design of their own casting products. They are subcontractors receiving paper drawings and limited informations about the product from the mechanical industry both in Norway and in other European countries. This is going to change, and in the future the geometry will be transferred by magnetic tape or by a network of computers."

Jan 1, 1986

By S. Vellinga, G. H. R. Janssen, C. J. N. Buisman, C. F. M. Copini

Non-ferrous metallurgical plants are often confronted with the need to neutralize bleed streams or effluents containing sulfates. The treatment of these streams could produce large amounts of gypsum. With a biological sulfate-reduction process, the production of gypsum is avoided and the metals can be recovered as sulfides. In this paper, the biological treatment of an industrial stream is presented. The bleed solution from a roaster gas scrubber was treated by means of a two-step process. First, the acid was neutralized with calcine. The resulting zinc sulfate solution was converted to ZnS with bacteria using PAQUES-THIOPAQ® technology. The precipitated ZnS was de-watered to 70 wt% solids, and was returned to the roasters. The quality of the effluent stream complied with the environmental regulations.

Jan 1, 2000

By Baohua Li, Yanhui Liu, Shengping Li, Xuewei Lv, Yun Chen

There are almost ten billion tons of vanadium-bearing titanomagnetite in Panzhihua-Xichang area. However, iron ores in Hongge, which has the most abundant reserves in the four mine areas in Panzhihua, have not been utilized sufficiently so far. The reason behind this is the relatively high Cr2O3 in the ores (0.49 %~0.82 %), that due to its high melting temperature will negatively influence the blast furnace reduction and slagging process. Therefore, in the blast furnace process, Cr is hope to be reduced into molten iron, which can reduce slag viscosity problems. Slag iron reduction experiments were conducted to quantify the Cr reduction. Experimental results shows that with the increase of TiO2, the content of Cr in the hot metal is decreased when balanced. And during the initial stage of the reduction reaction, the reaction kinetic model is a first-order reaction.

Jan 1, 2016

By Ramasamy Santhanam

"India’s present annual marine fish catch is 2.9 million tonnes and its low value fishes such as sardines, sciaenids, goat fishes and leiognathids amount to 60%. The fish meal obtained from these resources is mainly used presently as an ingredient in live stock and aquaculture feeds. These fishes offer vast scope in the production of pet foods. Pet foods prepared with leiognathid fish meal (60%), maize flour (10%), wheat flour (5%), vitamin and mineral mixture (5%) and water (20%) and experimented with 50 cats and 50 dogs were found to be ideal. Depending on protein level, feeds are being formulated for experimenting with more number of pet animals. Training programmes are also planned for unemployed people to popularize pet foods for commercial purposes.IntroductionIndia’s present annual marine fish catch is 2.9 million tonnes and low-value fishes sucha s sardines (Sardinella albella, s. gibbosa, S. fimbriata and S. melanura); sciaenids (Otolithus spp. and Jhonius dussumieri); engraulids (Stolephorus indicus); and leiognathids Leiognathus bindus, L. equilus and Gazza achlamys) constitute 60% (Figure 1)[1]. The fish meal obtained from these resources is now mainly used as an ingredient in livestock, poultry and aquaculture feeds. Considering the rich nutritional status of these low-value fishes, it is felt that these resources could be converted into value-added products viz. pet foods."

Jan 1, 2008

By Balladares V. Eduardo

Most of the arsenic contained in copper concentrates is removed in the gas phase during the smelting and converting processes and, according to recent environmental regulations, it is required to fix it in a solid stable form. In this regards, ferric arsenate has been reported as thermal and aqueous stable compound. Therefore, various alternatives for treating gas containing arsenic were considered in this work. From data obtained at laboratory scale on fixation of arsenic using iron oxide, a new process to treat copper concentrates containing arsenic was evaluated. The effect of temperature, oxygen potential and the sample porosity on the fixation of arsenic contained in a gaseous stream was studied, and the iron oxide converted into ferric arsenate was up to 10%. The obtained results suggest a new alternative for gas treatment with an interesting and attractive technical development. The arsenic was retained as ferric arsenate with thermal and aqueous stability, and it allows a safe disposal keeping the environmental restrictions. The kinetics parameters are used to scale up laboratory results to higher processing rates.

Jan 1, 2005