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By John Hollow

The Fort Knox Mine is an open-pit operation, located in Alaska, which started commercial production in March 1997. A conventional Mill processes 38,000 tpd of a low grade (1.0 g/t Au) free milling gold ore with a low sulphide component (below 1%). Gold production (11% from gravity and 89% from cyanidation) exceeds 400,000 ounces per year. Short retention time (20h), low temperature (7oC) and low grade make high leaching kinetics critical for the performance of the process. In April 2001, the treatment of True North ore, which represented 14.4% of the mill throughput and contained more sulphide in the form of pyrite, arsenopyrite and stibnite, resulted in a substantial drop in the average gold extraction from 87% to 72.6%. Laboratory investigations indicated that the addition of lead nitrate increased gold extraction to 91.7%. Further investigations were initiated to determine the leaching parameters and the nature of the problem. Subsequently, a lead nitrate addition scheme was implemented at the Fort Knox Mill that resulted in 2002 gold production being in excess of 31,000 ounces higher than that estimated for the non-lead nitrate reagent scheme. This paper presents the results of laboratory investigations and modifications in plant operating practices.

Jan 1, 2003

By Shigehito Isobe

The Li-N-H system composed of LiH and LiNH2 catalyzed by titanium compound desorbs ~6 mass% hydrogen and a quite small amount of ammonia in temperature range from 150 to 250 °C under He flow atmosphere. In this work, hydrogen desorption (H-desorption) mechanism in the reaction from LiH+LiNH2 to Li2NH+H2 in a non-equilibrium condition was clarified by TDMS, TG and FT-IR analyses for the products replaced by LiD or LiND2 for LiH or LiNH2,respectively. The results suggested that H-desorption reaction progresses through two-step elementary reactions mediated by ammonia. As a next step, we carefully determined the amount of the ammonia containing in desorbed hydrogen for the Li-N-H system in a closed system from the practical point of view. The results indicated that a quite small of ammonia thermodynamically coexisted in the desorbed hydrogen in closed system, although ammonia could not be almost detected in emitted hydrogen gas by TDMS under some non-equilibrium conditions. Moreover, for understanding the role of titanium, the chemical bonding state of the titanium compounds doped as catalyst in the mixture was examined by XAFS measurement. The results indicate that the Ti atoms, which can induce catalytic effect, are in a particular chemical bonding state.

Jan 1, 2006

By Jae-Chun Lee

Di-2-ethylhexyl phosphoric acid (D2EHPA) is widely used for separating rare-earth elements. In commercial plants, rare-earths are usually stripped from loaded extractant streams using mineral acid, then precipitated as oxalates. Many rare-earth uses demand specific powder characteristics, which are obtained by secondary processing. This paper demonstrates the feasibility of combining the stripping, precipitation and powder processing stages, thereby achieving considerable savings. MEHPA solutions were loaded with yttrium, then emulsified with oxalic acid-HC1 solutions to precipitate yttrium oxalate, which was readily calcined to yttrium oxide. The precipitation kinetics and yield were sensitive to process conditions. The morphology and size of the yttrium oxalate powders varied with the concentrations of D2EHPA and oxalic acid, and the presence of SPAN 60, which affected nucleation, growth, and the emulsion characteristics.

Jan 1, 1992

By E. Almendras de Siegel

Pyrometallurgical processes have the thermodynamic capability of treating complex and dirty ores and concentrates to produce high purity metals and inert slags. Modem pyrometallurgical processes are environmentally sound and competitive with other processes. However, there is still a need for sensors and other practical tools that permit a rapid evaluation of the performance of these processes. In order to contribute to satisfying this fundamental requirement, the authors developed the IDENT.LA software that permits the automatic mineralogical analyses of inorganic materials, including the final and intermediate products of pyrometallurgical processes. The technique allows determining the grain size distribution of mineralized inclusions, the surface relations between metallic phases, and conducting modal analyses of the essential phases that are present in the samples. Three basic automatic operations are performed: creating a representative image of the sample; identifying the metallic and non-metallic phases; and measuring the features of the resulting image. The results are used to evaluate the performance of pyrometallurgical and other processes. In this paper, the authors discuss the application of the technique to a sample of slag from a slag cleaning process that uses a carbonaceous reductant. In this case, process performance impacts not only on the efficient reduction of the slag magnetite and on copper recovery but also on the quality of the process off-gas. The mineralogical analysis of the slag is a valuable tool in assessing process performance and in recommending changes of operating conditions.

Jan 1, 1999

By Marcelo R. Esquivel

A MmNi5 alloy is synthesized by a combination of mechanical milling and low temperature heating processes. Synthesis time is 40 h for powders milled in a low energy ball mill at room temperature. A reduction in milling time is obtained if massive sample is mechanically milled at shorter times (2 h to 10 h) and heated at temperatures lower (600 ºC) than the usual temperatures used in equilibrium methods (>800 ºC). The alloy formation is detected even at a combination of temperatures as low as 200 ºC and milling times as short as 5 h. The temporal evolution of mechanical milling process was followed by both X-ray diffraction (XRD) and scanning electron microscopy (SEM) to detect the main stages of milling. Four stages were detected: Initial, Intermediate, Final and Completion. These stages were correlated to an enhancement of the synthesis method by combination of times of milling shorter than 10 h and temperatures of heating lower than 600 ºC.

Jan 1, 2006

By J. A. Jensen

In-situ composites were produced in both Ti matrix (Ti-20Y) and Mg matrix (Mg-20Ti, Mg- 20Nb, Mg-20Fe, and Mg-8Li) alloys. In Ti-20Y, a < 1010 > fiber texture formed in both the Ti and Y phases, and UTS increased from 240 MPa, (as-cast) to 950 MPa after deformation processing to a true strain of 7.3. Deformation processing produced smaller UTS increases in the Mg-matrix composites, but they showed exceptional resistance to weakening from exposure to elevated temperatures. The Mg-20Fe, Mg-20Nb. and Mg-20Ti composites tolerated 6-hour exposure to 400°C with no reduction in their 250 to 300 MPa room temperature UTS. All composites studied had excellent ductility and machinability.

Jan 1, 1995

By P. K. Narasimhargahavan

This paper discusses briefly the major reasons associated with the growth and its impact on the energy requirement and Environmental imbalance. A projection based on the present global Alumina and Al requirement indicate a substantial further growth of at least 30% over the next 10 years. It is indicated that the main factors which are likely to influence investments are the environmental factors such as the Climate Change and global response to the growing energy prices and sustainable development. Each of the developed / developing nations must find response to the GHG emissions which will encourage the Al Industry to make an effective contribution to global warming while preserving the international competitiveness of the industry - a challenging task. The efforts shall concentrate on improving energy efficiency in the industry possibly of the order of 25% over the next 10 to 20 years. The developments in this line are discussed.

Jan 1, 2010

By Akira Yazawa

The composition of ferrous calcium silicate slag is located on the tie line between FeOx and calcium silicates in ternary FeOx-SiO2-CaO system. This slag has never been used as copper smelting slag because of high sulfidic copper solubility. However, when the dissolved copper in slag is just oxidic, as in direct white metal production or in converting process, this slag is quite attractive and can be regarded as the third copper smelting slag after fayalite and calcium ferrite slags. Based on the authors&apos; studies on phase separation thermodynamics and laboratory experiments, it was clarified that the oxidic copper loss in this ferrous calcium silicate slag become the minimum not only %Cu in slag but also the total copper loss when the amount of slag is taken into account. It has been proven that calcium ferrite slag is suitable for continuous converting where the dissolved copper is oxidic, but there exist some drawbacks such as limited solubility of silica, low lead removability and too high fluidity. To overcome these difficulties accompanying traditional slags, ferrous calcium silicate slag is the hopeful alternative. In view of the general trends of modem copper smelting processes, the interesting features of this new slag system are discussed.

Jan 1, 1999

By Ron H. Schonewille

Experiments were conducted by injecting air-oxygen gas mixtures through a ceramic lance into molten copper matte and measuring the sulphur dioxide content of the offgas. The injection conditions were characterized by measuring pressure fluctuations immediately upstream of the lance and capturing the information on an oscilloscope screen. The parameters investigated were gas flowrate, lance geometry, lance immersion, orifice diameter and melt composition. An overhead nitrogen lance was used in specific tests to create an inert gas blanket directly above the bath surface to inhibit reaction in this region. The extent of oxidation was modeled by separating the gas-liquid contact into three stages; bubble growth, bubble rise and bubble rupture. The contribution of each stage to oxygen utilization was determined by varying the lance immersion and by performing tests both with and without an inert gas blanket. Bubble rise was found to be relatively unimportant, accounting for less than 5% of the total oxygen utilization. Bubble rupture and bubble growth were found to contribute approximately equally, with bubble rupture becoming more important with increasing gas flow rate. This study highlights the importance of reactions taking place above the bath surface in a copper converter.

Jan 1, 1999

By Aly M. Abdel-Rehim

The present work deals with a study of the mechanical activation of processing of Egyptian monazite by its simultaneous ball-milling and pressure leaching in order to improve the recovery of thorium and lanthanides from monazite. Experiments of simultaneous ball-milling and alkaline leaching of monazite contrary to autoclave leaching were carried out in stainless steel ball-mills of cylindrical shape under different conditions of temperature, pressure, time and alkali amount and strength. The ball-mills were heated and mechanically rotated in an electric furnace by means of roll mechanism. The effective rotation speed was fixed at 130 rpm in all tests. The charge of steel balls of different diameters was equivalent to 45% of the total mill volume. Monazite was charged in ball-mill without preliminary grinding. It is found that high rate of monazite leaching by ball-milling leaching method is achieved at lower temperature, shorter time and lower expense of alkali than in autoclaves. The results obtained show that complete recovery of thorium and lanthanides from monazite (99.8%) by simultaneous ball milling and alkaline leaching is attained at 140°C within 2 h. It is concluded that processing of monazite by its simultaneous ball-milling and leaching is mechanically activated and accelerated as a result of grinding action of steel balls that caused the continuous removal of the hydroxide product from reacting particle surfaces. This leads to the exposing of fresh and activated monazite particles surfaces to alkali leach solution and consequently the acceleration of the reaction of monazite processing.

Jan 1, 2006

By James Wang

In July 2003, The Office of Hydrogen, Fuel Cells and Infrastructure Technologies of the Department of Energy (DOE) Office of Energy Efficiency and Renewable Energy solicited Grand Challenge Proposals to establish three Centers of Excellence in hydrogen storage developments for reversible metal hydrides, non-reversible chemical hydrides and carbon storage materials, respectively. The program mission is to research and develop cost-effective, on-board hydrogen storage systems that enable a minimum range of 300 miles within the weight and volume constraints of the vehicle. Currently, no hydrogen storage technology available can meet the DOE cost and performance targets. In April 2004, Sandia National Laboratories was selected by DOE to lead the Metal Hydride Center of Excellence with partners from 5 other national laboratories. We will present the organization and recent accomplishments of the Metal Hydride Center which is confident to accomplish DOE/FreedomCAR and Fuels Partnership objectives for 2010 in hydrogen storage for vehicular transportation applications.

Jan 1, 2006

By J. M. Casas

This work presents the development of an ionic equilibrium model and its use to simulate the distribution and concentration of chemical species (speciation) in sulfuric acid - cupric sulfate solutions in the 0-2 pH range, 0.1-10 gpl copper concentration range and 15-45°C temperature range. The model consists of a set of equations which represent the equilibrium relationships for the ionic reactions and the mass balances for the components present in the system. The effect of ionic strength was taken into account by correcting the equilibrium constant in concentrated solutions. Several species can be formed at different pH and temperature values, the principal being: HSO-4, SO42-, CuSO4(aq), Cu2+, and H+ in order of increasing solution acidity. Simulations show that concentrations are highly dependent on pH. The sulfuric acid speciates mainly as bisulfate ion (HS0-4) and hydrogen ion (H+) at pH values lower than 1. The model presented in this work can be applied to predict and analyze the solution composition in electrolytic copper processes such as electrowinning, electrorefining and electrodialysis, as well as the purification of various industrial solutions.

Jan 1, 1999

By Li Zhang

A novel green technology to recovery Titanium compounds from Ti-bearing blast furnace slag under the dynamic oxidation condition was developed and tested. Air was blown into the molten slag as oxygen resource through a lance during the dynamic oxidation process, in which six important results were found: (1) The TiC, (Ti2O3), Fe and (FeO) in the slag were oxidized; (2) The temperature of slag temperature rapidly increased; (3) The viscosity of slag decreased; (4) The coalescence, growth and drop of the metallic Fe droplets in the molten slag were carried out under an air agitation condition; (5) The dispersed Ti components were selectively enriched into the perovslite phase, and the perovskite phase could be selectively precipitate and grow. And also, the perovskite phase can be separated by the dressing method. The oxidation of molten slag gives off a large amount of heat, which helps chemical reactions proceed, improve the rate of chemical reactions, and promote the precipitation and growth of the perovskite phase. The features of the technique are clean, low cost and a great capacity to deal with a large quantity of slag. It was confirmed by experiments that the precipitation of the perovskite (CaTiO3) in molten slag is obviously affected by operation factors such as temperature, chemical composition, heat-treatment, additives and so on. The precipitating kinetics and mechanism of the perovskite phase from molten slag during the dynamic oxidation processes were also investigated.

Jan 1, 2006

By Norbert L. Piret

During smelting of copper, arsenic in the feed reports to a large extent to the gas phase and some enters the anode copper. From the gas phase it is transferred during wet gas cleaning directly, or indirectly after dust processing, to aqueous solution. During the electrorefining and anode slimes processing, the anode arsenic content is also transferred to aqueous solution. Technology for the efficient removal of arsenic from process streams and cleaning of aqueous effluents is well established. However, the arsenic-bearing products, which thereby are generated, can vary widely in consistency, quality and quantity, from large amounts of gypsum contaminated with water-soluble arsenic compounds to residues with high arsenic content &apos; or arsenic products. Arsenic management in a copper smelter not only is involved with the duty of compliance to the gaseous and aqueous emissions standards but also should have as objective the minimization of the generation of arsenic-bearing and, in general, heavy metal-bearing solid waste. The present paper outlines options and the associated economic aspects for minimization of arsenic-bearing solid waste generation, for improvement of the environmental compatibility of the residues to be deposited and for the .production of commerciable arsenic compounds under appropriate market conditions.

Jan 1, 1999

The reported values of the standard reduction potentials of the Au(NH3)2+/Au(0) and Au(S2O3)23-/Au(0) couples are reviewed to emphasise the experimental difficulties associated with the measurement of reliable values for these quantities. The standard reduction potential for Ag(I)/Ag(0) in ammonia and thiosulphate solutions measured at ionic strength 0.1 and 25oCis used to predict the following relevant stability constants () for gold complexes based on the linear free energy correlations: Au(NH3)2+2 = 1013, Au(S2O3)23-2 = 1024 and Au(NH3)43+4 = 1033. The equilibrium constant ( 10-11) for the reaction Au(S2O3)23- + 2NH3 = Au(NH3)2+ + 2S2O32- based on these stability constants is in reasonable agreement with the measured value (10-9) based on potentiometric and spectroscopic data when excess ammonia was added to a solution of Na3Au(S2O3)2. This also indicates that the stability constant of Au(NH3)2+ is 9 to11 orders of magnitude less than that of Au(S2O3)23-. Relevant species distribution and Eh-pH diagrams based on the revised data are presented.

Jan 1, 2003

By Khosrow Nikkhah

Increasingly ion exchange systems are being included in design of hydrometallurgical plants for metal extraction or impurity removal. Because such systems operate sequentially and are based on resins that exchange one ion for another, store it temporarily and release it to a regenerating solution, the usual steady state heat and mass balancing tools and spreadsheets cannot be used to design them successfully. This paper outlines the role of dynamic simulation in design of ion exchange systems. Examples are given for use of dynamic simulation in design and investigation of equipment based on consideration of the effect of input criteria such as expected ion loading and elution profiles. The methodology for dynamic modeling using IDEAS in design of multi column ion exchange trains operating in parallel is presented. Results shown include the non-steady state distribution of extracted metal and limitations imposed on operating conditions. These conditions include proposed sequencing of columns for loading and elution cycles, loading, elution and recycle flow rates as well as size and choice of related ion exchange plant equipment.

Jan 1, 2003

By Alex Probst

With low metal prices and increasing value placed on plant water and tailings disposal areas, it is becoming essential to maximize the efficiency of solid-liquid separation processes. Since its inception over 25 years ago, the use of flocculants has grown exponentially. While flocculants play a crucial role in the sedimentation process, they are also a major operating cost. Recent innovations are revolutionizing the industry once again. New thickener designs are doubling thickener-loading rates while reducing flocculant consumption. The feedwell, as the heart of the thickener, is undergoing many significant metamorphoses. With CFD and other advanced computational analysis, feedwell technology is being examined more thoroughly than ever before, The result is that the thickener previously thought of, as a "Black Box" is now being mapped and controlled with state-of-the-art technology. This paper will examine recent design improvements in all aspects of thickeners in order to project the look of the thickener of tomorrow.

Jan 1, 1999

By Sun-Hee Cheong

This study sought to produce L(+)-calcium lactate using precipitated calcium carbonate as a starter culture composite of lactic acid bacteria in lactic acid fermentation. Specifically, precipitated calcium carbonate was synthesized by reacting calcium hydroxide with sodium carbonate in the previous study by the authors. Synthetic precipitated calcium carbonate was then used as the calcium source of lactic acid bacteria during the fermentation process. In general, precipitated calcium carbonate has low absorption rate in the human body. On the other hand, calcium lactate has high absorption rate; it is commonly used in food and drug industries as calcium additives in various foods such as cookies, beverages, bread, sauces, powdered milk, and fruit juice. Calcium lactate has two racemates, e.g., L(+)-lactate and D(-)-lactate. In particular, L(+)-lactate is known to be more soluble than D(-)-lactate and generally produced from lactose by homo-fermentative lactic acid bacteria such as Lactococcus spp., Lactobacillus plantarum, Lactobacillus casei, Lactobacillus curvatus, and Pediococcus spp. Thus, the characteristics of the pertinent lactic acid bacteria and optimal condition such as temperature, pH, precipitated calcium carbonate addition rate, and content of fermentation for increasing formation yield and purity were investigated. The findings suggested the possibility of manufacturing L(+)-calcium lactate using precipitated calcium carbonate as a calcium source with high value-added instead of commercial calcium lactate.

Jan 1, 2006

By M. A. Aziz

The electrochemical performance of a series of carbon materials produced from coconut shells, which are very cheap and readily available in Bangladesh was investigated for their viability as anode materials in rechargeable lithium-ion batteries. X-ray diffraction technique was used to measure the interlayer spacing (d002) of the produced carbon materials. A number of half-cells were prepared with the produced carbon materials from coconut shell as working electrode and metallic lithium as counter electrode with 1MLiPF6 electrolyte in a mixture of ethylene carbonate and dimethyl carbonate. The discharge-charge profiles were measured for the different half-cells by using Arbin 24-channel Cyler. The value of interlayer spacing of the coconut-based carbon material was found to be 0.397 nm at 900°C, which is most suitable for lithium-ion insertion into the carbon structure without any expansion. The specific discharge capacity of carbon material from coconut shell heat treated to 900°C was found to be 1015.65 mAh/g. The coconut carbon material heat treated to 900°C delivered 335.22 mAh/g reversible capacity, which is comparable to the commercial carbon/graphite presently used in lithium-ion battery systems. The irreversible capacity loss and coulombic efficiency in 25th cycle of half-cell made with coconut carbon material were found to be 0.16% and 99.83% respectively. The carbon material produced from coconut shell can, therefore, be used as a potential anode for rechargeable lithium-ion batteries.

Jan 1, 2006

By Lucas Lopes da Costa

Bamboo fibers were characterized in terms of diameter distribution and tensile properties. Polyester matrix composites reinforced with these fibers were investigated for their flexural mechanical behavior. Specimens with up to 30% in volume of continuous and aligned bamboo fiber composites were bend-tested until fracture. The results showed an improvement in the composite strength and stiffness with the amount of bamboo fiber. A microstructure analysis by scanning electron microscopy revealed a reasonable adhesion between the fiber and the polyester matrix which justifies the improved mechanical properties of the composites.

Jan 1, 2010