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By Johannes Boonstra

High rate bacterial catalyzed processes can serve to improve hydrometallurgical operations. These solutions are not only economical but also environmental sustainable. With references around the globe, the value of this new approach is recognized by industry worldwide. For instance, metals can safely and economically be separated from process and waste streams using biotechnologically produced sulfide, recovering a valuable metal sulfide product instead of a waste gypsum stream for disposal. Both the natural biological sulfur and nitrogen cycles offer bioconversions that are applied on industrial scale. The shared advantage of these processes is that waste compounds are converted in either a reusable raw material or in a harmless product. This way, natural product cycles can be closed. Applications based upon bioconversions are for example: Sulfur based: Bioleaching, reduction of oxidized sulfur compounds to elemental sulfur, metal recovery with biogenic produced H2S, SO2removal from gas streams, etc. Nitrogen based: Ammonia removal using the anammox-process, biological removal of NOxfrom gas streams, nitrate removal from water streams, etc. Metals: Bacterial processes for the reduction of metals such as uranium, selenium and manganese have proven to offer great potential for clean-up of groundwater streams. This paper contains a description of the above applications. Further, a short introduction on engineered high rate bioreactor systems and a description of industrial biotechnological applications will be provided.

Jan 1, 2003

By P. Umadevi

In the light of the discovery of the new super-conducting YBa2Cu3O7-x (YBCO), reactions in the Y2O3¬CuO-BaO system at 1300°C was investigated. The search was for any new phase that may be formed in the system at 1300°C (only 950°C reactions are known so far). 35 mixtures of different compositions were prepared and heated at 1300°C. No new phase was obtained. It was found that YBCO is decomposed at this temperature and Y2O3 and BaCO3 are the major components in the solid obtained after firing in air. However, on cooling the melt slowly and annealing at 950°C YBCO reforms. Such reactions on cooling might have implications on processing of the superconductor YBCO for practical applications as well as on its crystal growth by flux method.

Jan 1, 1989

By J. Van Boven

The Hoboken plant has continued the program, started in 1973, for monitoring the impact of processes on the environment. Progressive improve¬ments including new installations and equipment have been commissioned resulting in reduced emissions of lead in air. The Hoboken Smelter now fully complies with regulation and observes a yearly mean value of less than 2 micrograms Pb per cubic meter of air in the vicinity of the plant. In addition a new central water-treatment installation permits the discharge of waste water to the River Schelde in accordance with present day regulations. Mention is made of methods used to measure the emissions and immissions at the plant. Results of modifications and new installations recently commissioned are discussed.

Jan 1, 1983

By Mitsuhiro Ohtaki, Tetsuzo Arakawa, Fujio Murata

Refining of Zn from aluminum scrap melt by some vacuum distillation processes was studied to promote aluminum scrap recycling. Effects of distillation conditions, such as melt temperature, vacuum pressure and holding time, on Zn distillation behavior were investigated theoretically and experimentally by 0.3kg/ch scale vacuum resistance furnace. Three methods to increase the surface-area/volume ratio of liquid metal, such as gas atomizing, mechanical atomizing and mechanical stirring, were tested to increase the Zn distillation rate in 5kg/ch scale vacuum resistance-furnace. It was easy to lower the remaining Zn content to less than 0.1 wt% within one minute by mechanical stirring method. A water-model simulation experiment indicated that a significant agitation of the melt by stirring would be effective to increase the distillation rate. Continuous agitation vacuum distillation process (CA VP) has been designed and the pilot plant is now in construction.

Jan 1, 2000

By Dean G. Heitt

"The Rain and SMZ mines from 1987 to 1994 produced a total of22.0 t of gold from a pre-mine reserve of 14.24 Mt of ore grading 2.13 g/t Au.Gold at Rain is hosted within the basal portion of the Mississippian Webb Formation. ·Mineralization is closely tied to the Rain Fault which is interpreted to be the main feeder for the deposit. Multiple collapse and hydrothermal breccia events provided permeability for the mineralizing fluids in the otherwise unreactive siltstones. Major alteration events include: decalcification and dolomitization of the Devils Gate Limestone; and silicification, baritization, argillization and oxidation of the Webb Fm. Six ore types based on XRD and visual rock chip Jogging have been identified: siliceous ore containing >40% quartz and <30% barite; siliceous-baritic ore containing mostly silica but >30% barite; baritic ore containing >40% barite; argillaceous ore containing >40% total clays (including alunite); calcareous ore containing mostly calcite and dolomite; and carbonaceous ore which has significant pyrite and organic carbon. Metallurgical testing of the oxide leach grade ores found that recoveries, on -1.3 cm crushed material, were greater than 70%. Results also found that Rain ore has strong grind dependency due to silica encapsulation.The Rain leach pad was commissioned in 1988, and to date 9.3·Mt at an average grade of0.65 g/t Au have been placed. Life to date recovery, through December 1995, is approximately 51 %, for a total of3.87 t of gold produced. Two major factors have contributed to the low leach recoveries at Rain when compared with the metallurgical testing: 1) More argillaceous ore than expected was placed on the pad especially late in the mine life and 2) approximately 50% of the tons placed were run-of-mine with no agglomeration."

Jan 1, 1997

By Toru H. Okabe

As part of a systematic study on the thermodynamic properties of complex nitrides, phase equilibria of the system Li-M-N (M Mg, AI, Ga) at 900 K were investigated. An attempt to determine the thermodynamic properties of complex nitrides was made by using the galvanic cell method, which utilizes LiMgN as an electrolyte under nitrogen atmosphere. The electromotive force (Emf) of the cell at temperatures between 800 and 1100 K was measured. While the Emf of the cell at 900 K was measured to be 0.137 V, data discrepancies of ±0.03 V were found. It was difficult to determine temperature dependence of the Emf. The Gibbs energy change for the reaction, 113 Li3N (s) + 1/3 Mg3N2 (s) = LiMgN (s), at 900 K was determined to be !&apos;J.Go, (LiMgN) = -13.2 (±2.9) kJ/mol. Using thermodynamic information on the binary nitride from literature, the standard Gibbs energy of LiMgN was derived to be !&apos;J.Go f (LiMgN)= - 121 kJ at 900 K. The thermodynamic stability range of nitride was discussed by constructing isothermal chemical potential diagrams that provide a better understanding of the stability region of the LiMgN phase. The diagram was found to be in good agreement with the isothermal phase diagram determined by the alloy equilibration method. Although the obtained data includes large uncertainties, the results provide a better understanding of the thermodynamic stability of nitrides. The potential application of this complex nitride to nitrogen chemical sensors or a medium for controlling nitrogen potential is also shown.

Jan 1, 2003

By Toru H. Okabe

As part of a systematic study on the thermodynamic properties of complex nitrides, phase equilibria of the system Li-M-N (M Mg, AI, Ga) at 900 K were investigated. An attempt to determine the thermodynamic properties of complex nitrides was made by using the galvanic cell method, which utilizes LiMgN as an electrolyte under nitrogen atmosphere. The electromotive force (Emf) of ilie cell at temperatures between 800 and 1100 K was measured. Whilc the Emf of the cell at 900 K was measured to be 0.137 V, data discrepancies of ±0.03V were found. It was difficult to determine temperature dependence of ilie Emf. The Gibbs energy change for the reaction, 113 LbN (s) + 1/3 Mg3N2 (s) = LiMgN (s), at 900 K was determined to be tJ.Gor (LiMgN) -13.2 (±2.9) kJ/mol. Using thermodynamic information on ilie binary nitride from literature, the standard Gibbs energy of LiMgN was derived to be AGO f (LiMgN)= - 121 kJ at 900 K. The thermodynamic stability range of nitride was discussed by constructing isothermal chemical potential diagrams that provide a better understanding of ilie stability region of the LiMgN phase. The diagram was found to be in good agreement with the isoiliermal phase diagram determined by ilie alloy equilibration meiliod. Although the obtained data includes large uncertainties, the results provide a better understanding of the iliermodynamic stability of nitrides. The potential application of this complex nitride to nitrogen chemical sensors or a medium for controlling nitrogen potential is also shown.

Jan 1, 2003

By H. Roberts, C. Hassall

The opening years of the new millennium will be characterised by the closure of many lead and zinc mines because of reserve depletion. However, weak commodity prices through the second half of the 1990s have slowed project evaluation and have made it difficult to raise finances for the development of new mines required to replace lost output and to meet increasing demand for metal in the future. Growth of lead and zinc demand will be determined by the pace of global economic activity, especially in the emerging economies. How rapidly demand grows will have a key bearing on the possible shortfall in mine output and the response of prices to the implied tightening of metal supplies early in the new millennium. These issues are the focus of a discussion of the critical lead and zinc supply developments which will unfold post 2000, taking into account project lead times and the role that recycled metal plays in meeting market demand.

Jan 1, 2000

By Stuart M. Jones

This paper describes the state of the art of grinding in the Copper Industry today including descriptions of the largest equipment and design features which allow processing of as much as 100,000 mtpd in a single mill line. We include a typical flowsheet, control philosophies, and maintenance techniques which result in low cost production which is essential in today&apos;s market.

Jan 1, 1999

By Mark Cross, Hadi Abou-Chakra, Nicholas Christakis, Mayur K. Patel, John Baxter, Ugur Tiizful

"In recent years significant effort has been put into using continuum mechanics for the description of granular flows. Although these models are partially successful in capturing some flow characteristics, they lack essential information on material properties, which are needed to account for the interactions between different particles. Thus, they are incomplete and can not be used to describe processes such as hopper filling/emptying and pneumatic conveying, where particle-particle interactions can lead to phenomena such as segregation, degradation and agglomeration. In this paper, a 3-D unstructured finite-volume framework is presented, which employs interface tracking techniques to solve for the individual material components of the granular mixture in the bulk and thus, determine the material-air interface. Various transport processes, arising from the micro-mechanical properties of the different particle species in the granular mixture, can be obtained through kinetic theory. The transport coefficients of each of the individual species can be determined and analysed in a micro-mechanical framework and the transport process parametrised in the form of constitutive models. These models provide the continuum theory with information on the micro-mechanics.This work describes the continuum framework and the micro-mechanical parametrisations, which are used to describe the processes and interactions at the microscopic level. Numerical simulations and comparisons with experimental data are then presented for the case of binary granular mixtures and conclusions are drawn on the capability of the model to realistically predict and quantify the main characteristics of granular flows."

Jan 1, 2001

By Andreas H. Vassiliou

Organic materials are major constituents of the ore in several uranium deposits. Some of these deposits have been described as "urano-organic" because, the organic materials are believed to have provided the dominant control for the accumulation and deposition of uranium and are directly and intimately intermingled with the uranium. The nature of these urano-organic deposits has been problematic in terms of (a) the origin of the associated organic materials and (b) the specific form of&apos; occurrence of uranium. The organic materials in urano-organic deposits have been genetically related to both coal and petroleum or their progenitors or deriva-tives. Analytical data presented here (infrared, chemical. D.T.A.) suggest that coaliferous materials or related plant derivatives represent the main source of the organic fractions in practically all major urano-organic ores analyzed from the Colorado Plateau and other areas. Recognition of the specific form of occurrence of uranium in urano-organic deposits has been problematic mainly because the uranium is usually in an extremely fine-grained and disseminated state in the organic matrix. Electron microprobe and X-ray diffraction analyses presented here show that fine-grained uranium minerals, specifically uraninite or coffinite. are disseminated in the organic matrix as the predominant form of uranium in most major deposits; however. the presence of true organo-uranium compounds is also suggested for some deposits.

Jan 1, 1981

By Emilia Visileanu, Eftalea Carpus

"Due to the demographic explosion and development without precedent of the consumer society, the capacity to destroy the ecological balance the entire planet life depends on, acquire new dimensions. In this context new approaches on society development are imposing as well as special responsibilities for stopping and preventing Earth destruction and repairing the damage already done. The zero waste is a call to action that has as an aim the changing of current mentality of human society. ”take, use, throw away”. The zero waste is a policy, a way, an aim and represents a new approach planned for the XXI century that include the resources preservation principles, pollution reducing, increasing of the opportunities to create new work places and providing the highest degree of the.1. INTRODUCTIONThe zero waste is a call to action that has as an aim the changing of current mentality of human society. ”take, use, throw away”. The zero waste is a policy, a way, an aim and represents a new approach planned for the XXI century that include the resources preservation principles, pollution reducing, increasing of the opportunities to create new work places and providing the highest degree of the economy stability.2. ECOLOGICAL CONCEPTSA long-living Romania means:The closing of the production cycles, by waste reusing and recycling; the reducing of the use of fossil fuel; the improving of the material qualities, for extending the economical life of the products made by these materials; the reducing of the transport traffic.In this context, ecology, the star science with the ability to conserving and renewal of the environment is making its way, having the following principles:•,everything is bind by everything – is referring to the importance which the environment has for a great number of allied fields;•,everything leads to somewhere – the principle of the indestructible property of material (in nature, there must not exist wastes);•,nature does it the best – ecology becomes the responsible science with the governing of the strategic laws between man and nature, man takes advantage of the natural resources which he cannot create by himself and nature must feel guarded and not destroyed by this alliance;•,nothing is for free – the polluter pays.The protection of the natural environment means:•, its strong knowledge and that of the interactions between the social economic system and the natural system, the foreseen of the most close and most distant consequences of these interactions;•,the rational usage with maximum economical character of the natural resources not depending on their origin;•,preventing and direct fighting against as well on the degradation of the environment caused by man, as on those produced by natural causes;•,the ability to harmonize immediate interest of the human society on long and permanent term, using the natural factors of the environment."

Jan 1, 2008

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

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

Jan 1, 2012

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012

By Ruiling DU, Xiao YUAN, Keng Wu, Daan XU, Changyao CHAO

To utilize low grade coals to produce high quality semi-coke which can be used in blast furnaces, the pyrolysis of low grade coals was studied in this paper. According to the characteristics of coal pyrolysis process, the temperature range was divided into three parts. The interfacial chemical reaction model, random pore model and the internal diffusion model with the shrinking volume of resultant were established to describe the different ranges of pyrolysis process respectively. The results showed that the experimental data was fitted well, and all the correlation coefficients (r2) exceeded 0.97. Finally, the kinetic parameters for each temperature range have been calculated, which laid a necessary foundation for the simulation and expanded production.

Jan 1, 2016

By Bora Derin, Sertac Yazici, M. Seref Sonmez

"In this study, the recycling conditions of waste liquor obtained after the production of tungsten boride powder from calcium tungstate by self-propagating high temperature synthesis (SHS) and the following hydrochloric acid leaching were investigated in detail. Environmentally unfriendly and extremely acidic (pH~ -0.3) liquor consisting of calcium, magnesium, and boron ions was treated with 1 M sodium carbonate solution to precipitate magnesium carbonate and calcium carbonate phases. The obtained amorphous precipitates were heated up to the temperature of 400°C for re-crystallization. As a result, MgO, CaC03 and CaMg(C03)z phases were obtained, while sodium, boron, chlorine ions were remain in the solution. The present study is still in progress.IntroductionSelf-propagating high temperature synthesis (SHS) is one of the techniques used in the production of a variety of advanced ceramics, inter-metallic, organic and inorganic compounds, oxygen free single crystals, and polymers [ 1, 2]. The reaction becomes selfsustaining and propagates in the reactant mixture, after initiation in SHS process. SHS products may contain the mixture of several unwanted compounds and elements. Therefore following acidic leaching process may be needed to purify the target product. In the previous study, calcium tungstate (Ca W04), magnesium (Mg) and boric acid (B20 3) mixture were reacted to produce tungsten boride powder by SHS process according to the Reaction 1. Then, magnesium and calcium containing byproducts (i.e. MgO, Mg3B206 and Ca3B206) found in the SHS product were leached out by using concentrated hydrochloric acid (HCl) solution to obtain pure tungsten boride powder [3].Ca W04 + 0.5B203 + 4.5Mg = WB + 4.5Mg0 + Cao (1)After the leaching, filtrate solution consisting of different amounts of magnesium, calcium, and boron requires additional treatment for the environmentally acceptable disposal.Several works were carried out about magnesium precipitation conditions and kinetics from brines. Rabadzhieva et al. investigated the precipitation of Mg(OH)z from brines by using NaOH as well as caustic soda [ 4]. Turek ve Gnot investigated the precipitation efficiency of Mg(OH)z for the temperature range between 10-40°C, while the reaction was kinetically experimented by Alamdiri et al [5, 6]. Homogeneous precipitation of nesquehonite (MgC03.3H20) by the reaction of MgCli with (NH4)2C03 in supersaturated solutions and factors that influence the precipitation of MgC03.3H20, such as reaction temperature, initial concentration, stirring speed, titration speed, equilibration time, have been studied by Wang et al [7]. The precipitation of Mg(OH)z by calcium hydroxide from aqueous solutions was studied by Baird et al. [8]. Stratful et al. focused on conditions influencing the precipitation of magnesium ammonium phosphate from wastewaters [9]. 1031"

Jan 1, 2011

By Harold R. Kokal

Lisakovsky is a 3-billion ton oolitic iron ore deposit in north-central Kazakhstan operated by Orken LLP, a subsidiary of Ispat Karmet and the LNM Group. The iron oxide minerals are goethite and limonite. The gangue occurs as discrete quartz grains and an unidentified form of colloidal silica-alumina. The concentrate produced contains about 49.5 percent iron (Fe) and 0.6-0.8 percent phosphorus (P) or 10-20 times the acceptable phosphorus level. The phosphorus is intimately associated with the iron oxide and colloidal gangue, no discrete phosphorus minerals are found, and beneficiation is not possible. Therefore, to reduce the phosphorus, a hydrometallurgical process that includes roasting followed by leaching in dilute sulfuric acid has been developed. Phosphorus extraction is 70-90 percent, with only a minor loss of iron. The process has been tested in the laboratory and in a pilot plant at 50-300 kg/h. Construction of a 900,000 t/y demonstration plant is underway.

Jan 1, 2003

By C. Sui

A common objective in many Cu/Zn concentrators is to reduce the loss of Zn to the Cu-concentrate. One suspected source of the problem is accidental activation of sphalerite by heavy metal ions such as lead. One method of quantifying surface metal ion concentration is extraction with ethylene-diamine-tetra-acetate (EDTA). This was used to survey Cu-rougher flotation at three Cu/Zn concentrators: Les Mines Selbaie, Falconbridge&apos;s Kidd Creek division, and Hudson Bay Mining and Smelting Although all have less than 0.2% galena in the ore, Pb ions proved an abundant extractable metal. From a laboratory study a model of surface coverage of lead species generated by an ore was combined with an estimate of surface concentration of lead required to activate sphalerite to explore the possibility of accidental activation. Ores with Pb-grade as low as 0.1% can produce sufficient Pb to be a potential problem.

Jan 1, 1999

By Matthew Tunnicliffe, Akram Alfantazi, Paul Nesbitt, Farzad Mohammadi

"Lead and its alloys are proper candidates for anodes in electrowinning processes mainly because they are insoluble in the leach solutions and relatively cheap. However, the annual cost of corrosion problems associated with these anodes is millions of dollars. In this study lead-silver and lead-calcium anodes were tested under typical nickel electrowinning conditions and the effect of chloride on the corrosion performance of the anode materials was investigated. Corrosion rates of the anodes were calculated using the discharge plateau (reduction of lead dioxide to lead sulfate) after galvanostatic experiments. It was found that lead calcium anodes have the highest corrosion rate both in the presence and absence of chloride. Surface morphology of the electrodes was studied using SEM and the corrosion products were characterized using XRD.IntroductionLead (Pb) is usually the preferred material for commercial anodes since it is insoluble in the leach solution and the costs are manageable. One advantage of using an insoluble material as an anode is the higher purity of the cathodic deposits and better quality of the end product. During nickel electrowinning, metallic nickel is deposited on the cathode while oxygen evolution reaction (OER) takes place on the anode. In practice, relatively high potentials are necessary for the reaction to proceed at the desired rate because of the high overpotential of OER on lead. Lead anodes get oxidized in typical electrowinning conditions and usually have two to three years of lifetime. Although the price of each anode is insignificant, the overall cost of corrosion of these anodes is considerable, which is due to the large number of anodes used in a plant, typically two to three thousand. Therefore, corrosion is a significant problem associated with lead anodes in commercial nickel electrowinning plants and industries show interest in addressing this problem. Corrosion of lead electrodes in acidic environments has been previously the subject of many research studies [I-7]. It has been reported that, during the anodic polarization of lead, several phases may be present on the surface, depending on the potential range that is being studied [8]. Lander showed that lead is oxidized at potentials higher than 0.252 YsHE with tetragonal lead monoxide being the main reaction product [9]. At 0.666 YsHE lead can transform to lead dioxide; however, it is not stable and transforms to lead sulfate and lead oxide. At potentials higher than 1.684 YsHE, lead dioxide is eventually a stable phase and forms a protective layer on the surface [I 0, 11]. Under conditions of a typical nickel electrowinning plant, usually a 200 A/m2 current density is passed through the electrodes."

Jan 1, 2012

By B. Ozturk, K. Ito, R. J. Fruehan

"A simulation model for bath smelting processes for the production of iron was developed which predicts the coal, flux, ore, and oxygen consumptions and the off gas volume, temperature and composition. The model is comprehensive in that it takes into account all of the important variables including coal composition, metal composition, ore composition, slag basicity, post combustion ratio, (PCR), prereduction degree (PRO), heat transfer coefficient (HTC) , flux, scrap charge, and heat losses. Four basic cases were considered: I. 30% PRO-50% PCR; II. 90% PRO-O% PCR; III. 60% PRO-30% PCR; and IV. 0% PRO-50% PCR. Several different coals were considered and a sensitivity analysis of the critical variables was performed. The model also estimates the sulfur content of the metal. The major conclusions included:1. Post combustion significantly reduces coal consumption but above 20% PCR little reduction of FeO to Fe can be performed with the off gas.2. Prereducing to FeO (Case I) and having as much post combustion as consistent with good heat transfer is an attractive process. This process only requires a simple pre reducer, uses less coal, and is relatively insensitive to the type of coal used.3. High off gas temperatures may pose a potential problem. The off gas temperature can be reduced by using an 02-Air mixture for post combustion, limiting post combustion or adding water to the gas.4. The use of CaC03 in place of CaO or of supplemental electricity does not appear attractive.5. The melting unit is theoretically an energy efficient scrap melter. For Case I using 200 kg of scrap as part of the charge the coal consumption decreases by about 80 kg.6. With PCR > 30% the FeO content of the slag is expected to be 2-5%, and the metal will not be saturated with carbon. These factors and the increased sulfur load since coal is the fuel indicate the sulfur content of the metal may exceed 0.25%"

Jan 1, 1988