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By Thomas Brynjulfsen, Merete Tangstad, Eli Ringdalen

Manganese ore fines cannot be added to the submerged arc furnace directly as they will prevent even gas flow through the burden. Low gas permeability in the burden will lower the degree of pre-reduction of ore subsequently increase the carbon and energy consumption of the process. In order to utilize manganese ore fines in the furnace, they are typically agglomerated into sinter. In this work, the melting and reduction properties of Gabonese sinter and Gabonese ore have been investigated in pilot scale experiments. Two experiments were conducted, one with 100% sinter as manganese source and one with 50/50 sinter and ore. Lime was used to achieve a charge basicity of 0.72 in both experiments. The composition of slag samples from the excavation of the furnace was established using EPMA(WDS), and the composition of the tapped slag and metal was found using XRF. It was found that while the coke-bed size would determine the tapped slag composition, the melting behavior of the Mn source would determine the mixing with lime.

Jan 1, 2014

By D. C. Azubike

Wolframite (FeWO4) usually having cassiterite (SnO2) as a major impurity is a primary source of tungsten. Its direct reduction/carburisation with carbon in the temperature range 1000-1400°C, and with hydrogen at 600-900°C followed by carburisation with CO at 900°C are described. Depending on the conditions and reactants employed, Fe, Fe2W, B-Sn,WC, W2C, Fe3W3C and Fe6W6C are the products. Tin was found to inhibit the overall reduction and carburisation reactions significantly. The potential for either efficient separation of iron and tungsten or a one-stage production of an iron-based metal carbide composite is discussed.

Jan 1, 1992

By Micheal McCarter, Biswadeep Saha, Meenakshisundaram Ramanathan, Chai Ren, Sivaraman Guruswamy

"Three-point bend test was used to study the effect of electrochemically charged hydrogen and magnetic field on the embrittlement behavior of AISI 4340 steel in this work. Acoustic emission signals were collected during the test and analyzed to gain an understanding of the crack growth process. Cathodic hydrogen charging in AISI 4340 steel resulted in drastic reduction of ductility and strength. Hydrogen embrittlement was characterized by a change in fracture surface from dimpled ductile surface to quasi cleavage type fracture. No significant effect was observed in the presence of magnetic field. The acoustic emission signals collected during the test provided an indication of the extent of energy released during the crack growth process.*Support of this work by NSF through the award DMR-0854166 is gratefully acknowledgedIntroductionGrowing interest in hydrogen as a clean fuel and use of steel and other iron based alloys for storage and transport of hydrogen has led to extensive study of the influence of hydrogen on the mechanical properties of these alloys. Hydrogen interaction with materials may result in degradation of mechanical properties. Embrittlement, either ductile or brittle, can be described as a condition which decreases the toughness of the material or increases the ease of crack growth. Hydrogen present even in few parts per million is sufficient to embrittle steels at room temperature [1]. In most cases, hydrogen exposure is through an electrochemical process in aqueous corroding environments. In such cases, they are prone to be exposed simultaneously to electrically induced magnetic fields, which are also believed to affect the hydrogen embrittlement susceptibility of these alloys. So it is also important to study the effect of magnetic field on the hydrogen embrittlement susceptibility. Hydrogen solubility by electrochemical process in aqueous solution is proportional to square root of current density for iron. [2,3]"

Jan 1, 2012

By Marcela Morvová, Mário Janda, Morva Imrich

"The possibilities of greenhouse gas mitigation using various methods are brought out. The special case of utilization of mixture of CO2 with other greenhouse gases in a synergetic way inside non-thermal plasma based system is described in detail.Measurements on pilot system comprising pyrolysis chamber as alternative energy system (production of hydrogen and liquid tar) were made for various biomass and waste as the input material. The exhaust from this system was treated with non-thermal plasma gap suitable for up to 650Nm3/hour of exhaust gas flow. Condensable portion of exhaust is liquefied in distillation unit; produced hydrogen is stored on-line inside nano sized carbon of our own production.The CO2 removal efficiency varies depending on exhaust composition between 45 to 98%. Other oxides as CO, NOx, SOx and several hydrocarbons and VOC are also removed. The main product connected with CO2 removal is a solid powder of proteinoid nature. There exist strong probability, that precursor of the origin of life on the Earth from primary atmosphere were formed in the similar way as it is present in the electric discharge system used. Our system is equipped with on-line as well as ex-post analysis of all forms of products. We have also developed a system for recuperation of all forms of produced heat. It is stored inside as latent heat of waxes.IntroductionNatural greenhouse effect on the Earth is caused mainly by water vapour with the average absolute concentration about 4%. Other gases able to absorb long-wave radiation and thus this causing greenhouse effect are CO2, CH4, N2O, halocarbons and as precursors ozone and NOX. Some of them we produce and introduce into atmosphere in large quantities during production of energy and in transport. This factor leads to permanent increase of average temperature of air, sea and oceans, so called global warming.Nowadays large amount of data exists showing that the temperature of Earth in the last 150 years has been continually increasing. It represents about 03°C per ten years and the most of climatologist believe, that the increased concentration of greenhouse gases in the atmosphere is responsible for this effect.The most important greenhouse gas is carbon dioxide CO2. Majority of CO2 emissions comes from electric power stations working with fossil fuels, cars and industry. Burning of fossil fuels contribute up to 80% to world wide anthropogenetic emissions of CO2."

Jan 1, 2010

By Robert W. Bartlett

Biooxidation of an ore heap containing only a few percent of sulfide minerals requires insertion of a very large amount of oxygen either by natural air convection, forced air ventilation or gaseous diffusion. While shallow heaps, those with lateral distances much greater than their height, are of great interest for many heaped ore processing operations, natural convection is often ineffective for oxidizing them because of inadequate lateral flow into the heap's interior. Oxygen can diffuse into a shallow heap from its upper, horizontal surface in contact with air. Oxygen diffuses through the air-filled void space within the heap, driven by the oxygen concentration gradient resulting from internal oxygen depletion caused by mineral oxidation. Oxygen diffusion, coupled with the chemical reaction kinetics oxidizing the sulfide minerals, is analyzed for conditions of rapid mineral oxidation kinetics, requiring small mineral grain sizes, and for typical ore heap biooxidation parameters. Practical limits on heap heights are presented for effective biooxidation of the sulfide minerals within times of interest for heap biooxidation of refractory sulfide gold ores, one to three years.

Jan 1, 1995

By Arvind Thekdi, Cynthia Belt2

"Waste heat from industrial operations in metals industry represents 20% to 50% of the total energy used in most manufacturing plants. Reduction and recovery of waste heat offers the most attractive and cost effective method of reducing energy intensity for an industrial plant to meet corporate energy saving goals. It is possible to reduce or recover 30% to 60% of the available waste heat by using conventional and readily available technologies. Projects to reduce or recovery waste heat may offer less than 3 years payback to as short as a few months. This paper presents information on most commonly used methods for waste heat reduction and recovery in the metals industry operations. It describes the methods and use of analysis tools that would allow a user to estimate energy savings, CO2 or GHG reduction potential, and economic benefit and includes appropriate case histories.Waste Heat SourcesSources of waste heat abound with the metals industry. While the overall quantity of energy is high, the sources are distributed throughout a plant. The largest source within the metals industry is within furnace exhaust / flue gases. This includes the high temperature gases from burners in process heating such melting, calcining, and sintering operations. It also includes lower temperature gases from heat treat, dryers, and heaters. Lower temperatures are also found after post processed hot gases. This could include heat left after heat exchangers, regenerative systems, thermal oxidizers, and emission control systems. Other hot gases include air used in direct and indirect cooling.While waste heat in form of exhaust gases is readily recognized, waste heat can also be found within liquids and solids. Waste heat within liquids includes things such as cooling water, heated wash water, and blow down water. Solids can be hot product at discharge after processing or reactions are complete. Indeed, not only is energy wasted in the hot metal that slowly air-cools, but additional energy may be used in providing air or water-cooling to increase the speed of cooling. Other waste heat sources are not as apparent and include things like hot surfaces, steam leaks, boiler blow down water, etc. Table 1 and Figure 1 show several major sources along with the temperature range and characteristics of the source."

Jan 1, 2011

This symposium is dedicated to the lifetime achievements of Professor H.Y. Sohn. It covers the scientific fields, processing routes and investigation techniques in which Prof. Sohn has worked during his career and is based in the equally important three topical areas: Principles, Technologies, and Industrial practice. Professor Sohn was General Chair of the very first TMS Fall Extraction and Processing Symposium in 1983 in San Francisco which led to the Annual such symposia as this International symposium. Furthermore, the theme of that symposium was sulfide smelting, which is also included in this symposium. [ ] Professor Sohn was born in a beautiful dynastic capital Kaesung, Korea on August 21, 1941. He received his B.S. degree in 1962 from Seoul National University, M.Sc. in 1966 from the University of New Brunswick, Fredericton, N.B., Canada, and his Ph.D. degree in 1970 from theUniversity of California at Berkeley all in Chemical Engineering. After working as a Research Associate at the State University of New York at Buffalo and as a Research Engineer at Du Pont?s Engineering Technology Laboratory, Dr. Sohn joined the Department of Metallurgical Engineering at the University of Utah in 1974 and currently holds the ranks of Professor of Metallurgical Engineering and Adjunct Professor of Chemical Engineering.

Jan 1, 2006

This symposium is dedicated to the lifetime achievements of Professor H.Y. Sohn. It covers the scientific fields, processing routes and investigation techniques in which Prof. Sohn has worked during his career and is based in the equally important three topical areas: Principles, Technologies, and Industrial practice. Professor Sohn was General Chair of the very first TMS Fall Extraction and Processing Symposium in 1983 in San Francisco which led to the Annual such symposia as this International symposium. Furthermore, the theme of that symposium was sulfide smelting, which is also included in this symposium. [ ] Professor Sohn was born in a beautiful dynastic capital Kaesung, Korea on August 21, 1941. He received his B.S. degree in 1962 from Seoul National University, M.Sc. in 1966 from the University of New Brunswick, Fredericton, N.B., Canada, and his Ph.D. degree in 1970 from theUniversity of California at Berkeley all in Chemical Engineering. After working as a Research Associate at the State University of New York at Buffalo and as a Research Engineer at Du Pont?s Engineering Technology Laboratory, Dr. Sohn joined the Department of Metallurgical Engineering at the University of Utah in 1974 and currently holds the ranks of Professor of Metallurgical Engineering and Adjunct Professor of Chemical Engineering.

Jan 1, 2006

By Walter Curlook

An improved process of hydrometallurgical treatment of laterite ores of the limonitic type for the recovery of nickel and cobalt using sulphuric acid has been developed and patented [I]. The major improvement is brought about by recycling a significant portion of the "mother liquor" emanating from the pressure leaching reaction back to the feed preparation stage thereby substituting for all or at least a major proportion of the fresh water that must be added. The amount of process effluent waters is correspondingly reduced. Concomitantly with the major savings in fresh water requirements, a degree of reduction in new sulphuric acid requirements is effected, along with a savings in limestone and lime required for subsequent neutralizations. Keywords: Acid pressure leaching; Nickel laterites

Jan 1, 2004

By Moo Eob Choi

The reduction of iron oxide particles by hydrogen is one of the most widely investigated gas-solid reactions. The search for new methods for producing iron by the direct reduction of iron oxide has resulted in a large number of exhaustive studies of the various aspects of this reaction. However, previous studies have largely been done with either pellets or lump ores. Little has been published on the hydrogen reduction of very fine concentrate particles smaller than 37 µm (-400 mesh). The kinetics of hydrogen reduction of fine iron oxide concentrates were investigated in the temperature range of 900 - 1300°C.

Jan 1, 2006

By Qixing Yang, Björn Haase, Fredrik Engström, Anita Wedholm

"MiMeR, the Minerals and Metals Recycling Research Centre at Luleå University of Technology, Sweden, started industry-related research work to stabilize an EAF slag from Höganäs AB with of CaO/SiO2 values near to 3.2. The intention was to determine the suitability of the EAF slag as construction material after stabilization. Some of the stabilizers effective for preventing disintegration of AOD slag were examined in laboratory tests for stabilization of the EAF slag. The EAF slag samples were mixed together with stabilizers for melting at 1600ºC and then cooling in a crucible system. With a laboratory granulation system, the liquid EAF slag was cooled rapidly using air. Samples from the tests were characterized by different techniques, including XRD and SEM. Some of the results from the work may be useful for preventing slag disintegration and, thus, enhancing utilization of the EAF slag as construction material, thereby saving valuable natural resources.IntroductionAt steel plants of some MiMeR member companies, steel grades with low carbon contents were produced in Electric Arc Furnaces (EAF). EAF slag was tapped out of the furnace to slag pots for transport to slag yards, where the slag was poured on the ground. Very often, the EAF slag disintegrated during cooling on the ground. Fines from the slag disintegration were often difficult to handle and use as material for road construction [1, 2]. The EAF slag disintegration was rather similar to the disintegration occurring in the slag tapped from some AOD (Argon Oxygen Decarburization) converter heats.Literature studies show that formation of dicalcium silicate (C2S) is the main reason for the disintegration or dusting of AOD slag from production of stainless steel [1-4]. The C2S can form while the content ratio of CaO to SiO2 of the slag, CaO/SiO2, exceeds 1.4 [1]. Values of CaO/SiO2 for the AOD slag are often near to 2.0, making the C2S a predominant slag component. The ß phase of C2S, ß-C2S, transforms into its low temperature ? form in the temperature range of 400-500°C, inducing a volume expansion of nearly 12% [1-4]. The volume expansion disintegrates the AOD slag."

Jan 1, 2008

By Lan Li, Izaak Williamson

"The efficient separation and storage of CO2 from power plant flue gases can reduce the amount of CO2 released into the atmosphere and mitigate global warming. Potential candidates for industrial applications are solid sorbent materials. Crucial factors to control the efficiency of porous sorbent materials include the framework and pore structure, and the chemical and physical reactivity of CO2 within the pores. Computational modeling approaches, based on density functional theory (DFT) and van der Waals-DFT, have been applied to nanoporous solid – manganese dioxide a-MnO2. We found that the types and charges of cations as dopants in the a-MnO2 and the concentration of CO2 influence the structural features of a-MnO2, which control its CO2 selectivity performance within the flue gases.IntroductionCarbon capture and storage is a technique to separate large quantities of CO2 from power plant flue gases before being released into the atmosphere. Porous solids are a potential candidate as sorbents to “trap” CO2 through chemical or physical adsorption on their porous surfaces[1]. Such separation efficiency is determined by the size and shape of its pores and by the interaction between the porous surface and the gas adsorbates. The incorporation of cations into the pore can act as a means of structural support and alter the pore diameter to be comparable to the kinetic diameter of the gas adsorbate, such as CO2.A porous solid of particular interest for CCS is manganese dioxide a-MnO2, an octahedral molecular sieve (OMS) composed of edge-sharing MnO6 octahedra that are linked into a nanoporous framework[2]. The framework consists of (1×1) and (2×2) tunnels, referred to as OMS-2. Due to the larger tunnel size, cations and gas adsorbates prefer to reside along the (2×2) tunnel axis of the OMS-2. As seen in Figure 1, a potassium cation K+ is located in the (2×2) tunnel, known as cryptomelane-type MnO2. Its pore diameter of ~ 4.6 Å gives it a good CO2 selectivity performance, because the diameter is comparable to the kinetic diameter of 3.3 Å for CO2[3]. Alternatively, replacing potassium K+ with other cations, e.g. barium Ba2+, sodium Na+ or lithium Li+, in the OMS-2 tunnel is of great research interest, due to the effects of their concentrations, types and charges on the CO2 selectivity efficiency and sorption hysteresis phenomenon[2,4]."

Jan 1, 2014

By Chenhui Liu, Ka-ma Huang, Hong-ying Xia, Bingguo Liu, Hua Chen, Jinhui Peng, Libo Zhang

"The rising popularity of microwave heating in mineral processing has fuelled the need for knowledge concerning dielectric properties of minerals. Dielectric property and microwave absorption property of anthracite were measured over a temperature range of 20-100°C at 2.45GHz by using an open-ended coaxial sensor measurement system. The results show that the dielectric constant, loss factor and loss tangent increase with temperature rising at 2.45GHz. Microwave absorption properties of anthracite are highly dependent on temperature and frequency. At frequency of 2.45GHz frequency used in microwave metallurgy, anthracite is suitable for reducing agent to achieve fast elevation of temperature then returning to original state. The research will be helpful in explaining the thermal running of microwave dielectric heating the anthracite.IntroductionThe application of microwave heating in minerals processing and treatment has recently attracted great interest from the metallurgical industry. Compared with conventional heating methods, the advantages of microwave heating include rapid and selective heating, uniform distribution, high efficiency, fast on and off switching as well as flexible and modular design[l-3]. As a result of these advantages, microwave heating has been applied in a variety of mineral processing and extractive metallurgy, such as microwave-assisted ore grinding, microwave heating for carbothermic reduction and acid leaching of ilmenite ore, microwave drying, microwave-assisted roasting and smelting of sulfide concentrate, microwave-assisted spent carbon regeneration and microwave-assisted waste management [ 4-6]. Though the application of microwave heating in the metallurgical industry is promising, further studies on the interaction between microwave radiation and minerals and its effects are highly desired to develop innovative techniques for minerals processing and ore treatment using microwave heating [7]."

Jan 1, 2013

By S. Saptharishi

Selenium, which is a 6A group element of the periodic table, constitutes about 7x10-5 % of the earth?s crust. Even though selenium is a dispersed element with respect to its commercial exploitation, it is capable of forming number of minerals and nearly forty selenium minerals have been identified, out of which the copper ores are the richest sources of selenium. Electronics industries and glass industries are the major consumers of selenium, while pharma grade selenium used as micronutrient for humans and animals. Various methods have been developed to recover selenium as a by-product from copper anode slime during copper refining. Selenium being amphoteric in nature, it is soluble in both acid and alkali. While acid roast process is widely used, considerable work has been carried out in Russia for recovering selenium through alkali route. This paper enlightens the process developed at Central Research and Development Laboratory, for recovering selenium from decopperised slime through alkali pressure leaching. The decopperised slime is pressure leached with alkali under oxidizing conditions by which almost all the selenium present is converted to alkali selenate, which is easily separable from the rest of the decopperised slime. The solution so obtained is neutralized, during which, most of the impurities are precipitated out. Then selenium is precipitated in its elemental form upon purging sulphur-di-oxide under warm acidic medium. The purity of the selenium obtained by this process is higher than that of the selenium from acid roast process. Moreover selenium can be crystallized as sodium selenate and it can be marketed. The acidic content of the effluent is recovered and it is recycled back to the process. The sodium content of the effluent is converted into high purity sodium sulphate, which is marketable. The hazardous waste containing arsenic is precipitated as its sulphide and can be disposed off as landfill.

Jan 1, 2006

By P. A. Davidson, D. J. Short

"In this paper we describe a 'non-contact' electromagnetic nozzle suitable for sprayforming and gas atomization processes. In such processes there is a need to control the flow rate and diameter of the liquid metal jet whilst minimising contamination of the stream. This can be achieved using an electromagnetic valve, which partially levitates the jet in freespace, using a segmented cylinder surrounded by an induction coil. This valve will significantly enhance the quality of the titanium alloys and nickel-based superalloys used in sprayforming and gas atomization. This paper describes the design and test of a laboratory prototype valve based on experiments performed with liquid tin.1. Introduction In many industries there is an increasing need for clean, high quality metals and alloys based on titanium and nickel. Two important processes are: 1) Spray deposition which allows the liquid metal to be converted to a near-net shape, thus alleviating the need for subsequent forging and extensive machining and; 2) Powder production of titanium by gas atomisation.In centrifugal spray deposition of titanium (see figure 1) the metal is induction melted in a cold crucible. The crucible consists of a number of water-cooled segments, which allows the high frequency magnetic field of the coil to pass through the crucible, and into the melt. The charge is melted by the induced eddy currents. Locally at the crucible walls the liquid metal solidifies, and is contained within a. 'skull' of its own solid, thus reducing contamination from the crucible wall. Once melted the metal is poured through an electrically heated graphite nozzle and into the spray forming chamber. The principal limitation of the process to-date, however, is that it currently uses a graphite and /or ceramic nozzle to direct the flow of liquid metal to the atomizing disk and as such there is considerable risk of nozzle erosion with inevitable effects in terms of contamination of the melt stream and variability in flow conditions. In this research programme we develop a. non-contact electromagnetic nozzle, which will totally eliminate refractories and/or ceramic materials from the melting and casting process. This will greatly enhance the technological capabilities of sprayforming and gas atomization processes."

Jan 1, 1999

By P. A. Botha

The coal seams in the Waterberg basin occur in correlates of the Vryheid and Volksrust Formations as developed in the main Karoo basin. In the Vryheid Formation, five thick seams of predominantly dull coal are present, whereas a multitude of thin, lenticular seams (a few millimetres to 2 metres}, predominantly of bright coal, are developed in the overlying Grootegeluk Formation. During exploration, the coal seams were divided into 11 zones. Analytical data on float and middlings fractions (RD less than 1.40 and between 140 and 1.80, respectively} were used mainly for stratigraphic correlation of the zones in the Grootegeluk Formation. The affinities of the major and trace elements for different mineral phases and/or organic material are discussed on the basis of correlation matrices and vertical variation diagrams. Titanium and vanadium clearly show some degree of organic affinity. P 205' AI203 and alkaline-earth elements are also positively correlated by the presence of goyazite in the coal. This type of investigation gives an indication of the degree to which undesirable elements like P and S can be removed during coal beneficiation, of which coal zones are unsuitable for the production of metallurgical coal on account of a high content of these elements, and to what extent the blending of different coal zones is required to keep the concentration of these elements within acceptable limits.

Jan 1, 1991

By Carl W. Dalrymple

A wide variety of contaminants (heavy metals, suspended solids, colloids, oils, organics) have been successfully removed from wastewater using an electrocoagulation process. An innovative electrocoagulation system is described. This process involves a procedure which subjects dissolved and suspended wastewater contaminants to the simultaneous addition of metal ions in the presence of direct current. During the treatment process Ionic and other charged particles in the wastewater are neutralized with oppositely charged ions generating the coagulation of contaminants: The process Is called CURE, and' presented here with application to wastewaters containing mainly heavy metals.

Jan 1, 1995

By R. F. Hammen

Copper is one of the most widely used metals in industrial processes and is also present in most mining operations. Extraction of copper from solutions often proves difficult due to the presence of complexing agents. ChromatoChem, Inc. has developed a Solid Phase Extraction (SPE) support (HiPAC) for removal and recovery of metals from wastewater. The HiPAC SPE support employs chelating agents covalently coupled to a long linker molecule. Several solutions containing copper and complexing agents were tested including 1) copper and carbonate, pH 9.8, 2) mixed metals and anions with copper and cyanide, pH 11, and 3) copper and the chelating agent EDTA, pH 11. The copper was extracted from solutions one and two at high pH, but the EDTA containing solution needed the pH lowered to make the copper available for capture. In each example, the copper concentration was significantly reduced by HiPAC SPE treatment.

Jan 1, 1994

By O. M. G. Newman

Research into potential applications of spouted bed electrowinning (SBE) in the zinc industry was conducted, in a collaboration between our two organizations. The main system investigated was zinc from acidic sulfate electrolytes. However, SBE can be extended to other electrolytes, or recovery of other elements. Electrolytic tests were carried out at the 0.01 to 0.1 m2 scale. Spouting behaviour has been studied at a larger scale, approaching a size suitable for an industrial unit cell. Much of our work was carried out using a micro-porous separator (Daramic®). However, we have also shown that ion exchange properties can have a controlling effect on the process chemistry, electrochemical efficiency, and plant flowsheet. In initial 0.1 m2 scale electrolytic tests, design and engineering issues for scale-up were identified. We review the major achievements, promising areas for application in the zinc industry, current status, and remaining barriers to development of SBE technology.

Jan 1, 2003

By Ryosuke Matsuoka

Keywords: Tantalum capacitor, Scrap, Recovery, Titanium, Chlorination A recycling process for tantalum from capacitor scraps using an oxidation process followed by mechanical separation and chemical treatment was investigated. This study demonstrates that sintered tantalum electrodes inside the capacitor scraps can be mechanically collected after the oxidation of the scraps in air, and high-purity tantalum oxide powder (Ta2O5) was efficiently recovered after chemical treatment. By reducing the Ta2O5 obtained through magnesiothermic reduction, tantalum powder with 99 mass-% purity was obtained. Using the chlorination for tantalum recovery was also investigated, and the tantalum or tantalum compounds were reacted with chloride wastes such as FeClx. It was found that tantalum was effectively separated and purified when tantalum powder is reacted with FeClx at 1100 K under an argon atmosphere. This recycling process utilizing chloride scrap has now been extended to other reactive metals such as titanium.

Jan 1, 2004