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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 Fatbardha Osmani, Skender Osmani

"A system analysis of the resource and environment management (water, energy etc) starts from its definition. Unfortunately, there is not a unique semantics of the mentioned concept. On these circumstances, in this paper the following issues are presented: 1.A short view on the existing concepts of management. 2.A new definition on the concept of management. It is considered as a complex and rational activity on human and natural resources ,environment etc, which starts from a analysis of infrastructure ,technology , etc, mission , alternatives , project etc. and ends to an optimal output. Basing on this definition, the management has two principal components: strategy and policy. The strategy is referred as a blue print program (the same definition as in Game Theory), which contains all the contingency alternatives. , while the policy is referred as a strategy applied into practice. The strategy is the first , while the policy is the second one. The best alternative of a policy is the project, Each strategy has one and only one project. The mentioned definition erases the differences between concept of policy and politics. Each strategy has its alternatives ,the next has its sub strategy and so on, i.e. whatever are going to be the strategy, there are a hierarchy composed by sub strategies up to the simplest strategies applied by a single individual (human beings or robots). The strategy objectives are necessary and sufficient conditions for its realization i.e . the strategy is an optimal activity, in which all resources are integrated and processed . Several strategies could be joined into one( for example the surface water strategies of the Balkan countries) . In this view, the strategy could be globalized into optimal way basing on different criteria’s as social, economic, environmental, their risks and effectiveness etc. etc An example from the water management illustrates the mentioned concepts."

Jan 1, 2008

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 B. Boryczko, J. Norwisz, Jose Escobedo Bocardo, Z. Kolenda, A. Holda

"Classical thermodynamic analysis of any thermal and chemical process is usually based on the first law of thermodynamics. Such an approach is not sufficient when deeper understanding of the nature of each elementary process is required. The use of the first and second law of thermodynamics together is necessary to solve practical process more effectively. Enthalpy and exergy balances allow to enhance our understanding of thermal processes especially when cumulative consumption of energy and exergy is calculated. To ensure reliability of such an analysis the least squares method for adjustment of mass balances of principal chemical elements has been applied and described in detail. Numerical analysis has been carried out to compare two different processes of copper production – shaft furnace and flash smelting.IntroductionClassical thermodynamic analysis of any technological process is usually based on the First Law of Thermodynamics in the form of energy (enthalpy) balances. Such an approach is useful in engineering practice as it makes analysis easier in the global scale neglecting modeling of the elementary processes, allows calculation of the thermal efficiency and makes possible to control quality of the measurement results. Additionally, graphical presentation of the energy balance is simple in the form of Sankey diagram.In the case of aluminum electrolysis process, design of the new electrolyzer or its modernization is always based on the enthalpy balance.However, deeper thermodynamic analysis leads to the conclusion that such an approach is not sufficient. The First Law of Thermodynamics guarantees the exact equivalence of the various forms of energy (allowing all forms to be measured in the common unit such as joules) but it does not guarantee interconversibility. Thermal energy (heat) is in a peculiar and unique position, for whereas all other forms can be completely converted into thermal energy, the reverse process id impossible, only a portion of the heat can be converted into mechanical energy. Explanation comes from application of exergy balances. As we know exergy expresses the amount of mechanical work necessary to produce a material in its specified state from components common in the natural environment, in a reversible way, heat being exchanged only with environment [1]. Consumption of exergy connected with the fabrication of some considered product appears not only in the plant manufacturing the product, but also in all plants delivering raw materials for the final production process"

Jan 1, 2008

By Peng Bing

Stainless steelmaking dust is classified as a hazardous waste due to higher than acceptable heavy metal leachabilities such as zinc, lead, cadmium and chromium. In addition to being an environmental hazard, the flue dust is also an economical concern to stainless steelmakers as it contains large amounts of valuable alloying elements, especially for iron, chromium and nickel. A new technology of direct recycling of stainless steelmaking dust has been developed to recover the metals from the dust. But it was found that zinc was accumulated in the dust collection system in practical run of direct recycling. This study focuses on the effect of the operating parameters such as temperature, dust feed rate and the ratio of CO to dust on the reduction of zinc oxides present in the dust. The mathematical model for the reduction process was setup based on the experimental research. According to the mathematical model, the temperature has obvious effect on the reduction of zinc. It is benefit to the process of zinc reduction to increase the temperature. But the temperature will not be the main factor for the reduction process after 1228C. It will promote zinc reduction to decrease the dust feed rate and control the ratio of dust to CO. It was also found from the experiments that ZnFe2O4 in the dust could be decomposed at high temperature. Decomposing ZnFe2O4 in the dust increases the recovery of zinc from the dust distinctly.

Jan 1, 2006

By Antonio de Ita, Isaias Hilerio, Miguel Barron

"The influence of an unconventional lance with a central nozzle on the multiphase fluid flow in a steelmaking converter is studied in this work by means of computer simulations. The lance has four peripheral supersonic nozzles and a vertical central nozzle. Besides, the oxygen flow in the central nozzle is considered independent from the main oxygen supply. Transient two-dimensional numerical simulations were carried out considering just molten steel and gaseous oxygen as the existing phases. Numerical results show that bath agitation and droplet generation are enhanced as a result of the central nozzle. However, the performance of this lance strongly depends on the distance of the lance tip to the molten steel surface and the velocity of the oxygen jet.IntroductionCurrently, two thirds of the world crude steel is produced through the steelmaking oxygen converter [1]. Given the unquestionable economic importance of this technology, any improvement or optimization proposal is welcome. In the majority of current oxygen converters a top oxygen supersonic jet is blown onto the molten steel through a water-cooled lance to eliminate by oxidation some impurities such as carbon and phosphorus. Conventional lances have inclined peripheral nozzles whose number depends on the converter capacity. During the process, a large amount of gases evolves, forming metal droplets and a metal-slag-gas emulsion [2]. The droplets and the resultant emulsion increase the reaction interfacial area, promoting in this way carbon removal and dephosphorization of the molten steel bath [3]. However, during the blowing stage, the emulsion rises towards the lance and converter mouth and frequently forms layers which accumulate in the lance, reducing the life of the lance tip [4, 5]. It is possible that some freezing of the molten metal occurs due to the low oxygen injection temperature, however there are no reports on this. Besides, frequently undesirable operating phenomena such as spitting and slopping may arise as a result of inappropriate blowing practices or bad lance design. In the oxygen steelmaking industry, novel lances design are needed in order to enhance the decaburization rate and the slag formation and, at the same time, preventing operating practices that decrease productivity and move away the shop from safety standards."

Jan 1, 2012

By Katsuyoshi Kondoh

The synthesis processing of Mg2Si or Mg2Si/MgO at lower temperature from the elemental magnesium alloy powder/chips and Si or SiO2 powder mixture was established via the repeated plastic working (RPW) based on Powder Metallurgy (P/M) process. RPW is much effective on the mechanical breakage of MgO surface films, which prevent from the solid-state reaction between Mg and Si powder. The solid-state synthesized Mg2Si particle of 200nm-2JIm is extremely fine, compared to that via the conventional casting process, causing the coarse one of 50-100um. This is because of not coarsening during the solid-state synthesis of Mg2Si. By using in-situ forming process of Mg2Si via RPW and pre-heating before hot working such as extrusion and forging, the magnesium composite material with Mg2Si or Mg2Si/MgO dispersions was developed in employing Si or SiO2 particles, respectively. For example, when employing AZ31 chips as raw materials of the matrix, it has low density of 1.85g/cm) and extremely superior mechanical properties, such as tensile strength over 350MPa with 5-10% elongation and Young's modulus of 47-50GPa, to the conventional Mg-Al-Zn alloys. The Mg composite alloy wires and pipes were produced via the hot extrusion process in the manufacturing plant, and also showed excellent mechanical properties.

Jan 1, 2003

By W. F. Ranson, R. C. Progelhof

"I. THE PROBLEM: MANUFACTURING PRODUCTIVITYThe 1985 President's Commission [I] on Industrial Competitiveness found compelling evidence of the declining economic position of the United States in world markets. The annual rate of increase in the United States productivity is approximately one-seventh that of our major trading partners over the last decade: profit levels in manufacturing investments are below those of the mid-1960's; an increasingly negative trade balance since 1971; and a sharp decline in the United States share of world trade in manufactured goods for more than two decades. A particularly dramatic example of the shifting economic balance is the fact that Japanese productivity growth has been five times greater than that of this country since 1960. In face, Japan's productivity now exceeds that of the United States in such critical industries as steel, transportation equipment, electronics and electrical machinery.American employees have experienced the competitive consequences of this nation's lagging industrial performance. Between 1980 and 1984 alone, the population of non-farm employees engaged in manufacturing dropped from 22.4% to 20.6%. This reduction in manufacturing must be arrested.Commissions RecommendationsThe comprehensive set of recommendations offered by the President's Commission recognized the nation's ""key competitive advantages"", technology and human resources, and calls for their strengthening. Particular emphasis is placed on manufacturing technology and the fact that this country does not translate research into new technologies rapidly and fully.""Perhaps the most glaring deficiency in America's technological capabilities has been our failure to devote enough attention to manufacturing or 'process' technology. It does us little good to design state-of-the-art products if within a short time our foreign competitors can manufacture them more cheaply. The United States has failed to apply its own technologies to manufacturing. Robotics automation and statistical quality control were all first developed in the United States but in recent years they have been more effectively applied elsewhere""."

Jan 1, 1988

By E. S. Geskin, W. L. Chen, A. Vora

"This paper is concerned with the application of an abrasive waterjet for metal shaping. The waterjet cutting technology uses water compressed to the pressure up to 55,000 psia which is accelerated in a cylindric nozzle. Abrasive particles are then supplied into the water stream and accelerated by the water. Cutting occurs via the interaction between the water-particles stream and a workpiece that causes material erosion at the impingement zone. The mechanism of this interaction enables shaping of practically any material with a minimal effect on the metallurgy of subsurface. The motion of the jet penetrating through a material body is guided by a robotic arm. A waterjet cutter is becoming one of the principal tools for shaping titanium, super-alloys and other hard-to-machine metals and composites. The shaping, resulting from the waterjet cutter, is very similar to laser beam cutting. However, unlike laser processing, there is no damage to the subsurface structure.The presented work discusses the experimental study of cutting of titanium plates. The results of these experiments demonstrate the potential of the abrasive waterjet as a shaping tool. IntroductionOne of the main avenues in the development of metal shaping is the use of high energy beams as cutting tools (1,2). There are a number of advanced beam oriented material removal technologies, such as laser, electron beam, plasma and abrasive waterjet (AWJ) cutting. The advantages of AWJ cutting are well understood and documented (3-14). This technology has the potential of becoming the principal tool for netshaping and netsurfacing of parts. However, the use of AWJ is currently limited to cutting of hard-to-machine materials such as titanium, superalloys, glass, composites, etc. The cost of A W J cutting is much higher and the productivity is much lower than those of the thermal cutting. At the same time abrasive waterjet can be used for shaping any existing technological material from fabrics, plastics, aluminum to glass, composites, and diamonds. The material losses during AWJ shaping are minimal. The roughness and waveness of the surfaces generated during AWJ cutting are substantially less than those of the thermal cutting. Due to the size of the jet cross-section total force exerted by the jet on a workpiece does not exceed 30-50 newtons. This terminates the need in the use of complex fixture for material holding. Low applied forces and low surface temperature prevent the damage of metal subsurface in the course of cutting. The small size of the impingement area will determine the limited width of the kerf. Due to the size of kerf and unidirectional character of the water jet the formation of practically any metal contour is possible."

Jan 1, 1988

By Chikabumi Yamauchi, Mitsuru Tanahashi, Jutaro Miura, Takaharu Iwadachi, Toshiharu Fujisawa

"Tue oxidation behavior of molten Cu-Be alloys was investigated by exposing· the molten Cu-Be alloys to various Ar-O2 atmospheres to control the oxygen partial pressure, PO2 = 10 ~105 Pa at 1423 K. The following results were obtained:• The oxygen · partial pressure in gas phase affects the morphology of the oxide formed on the surface of the alloy and · the oxidation rate of beryllium.• At lower oxygen partial pressure, a molten Cu-Be alloy is covered with a homogeneous and compact internal layer of BeO. Thus, the beryllium oxidation rate can be minimized.• By adding a small amount of calcium or zirconium into the molten Cu-0.5 mass% Be alloy, a protective BeO layer is formed even at higher oxygen partial pressure. Thus, the beryllium oxidation rate can be reduced.IntroductionCopper-beryllium (Cu-Be) alloys are well recognized for their unique properties, such as high electrical conductivity, high strength, high fatigue strength, excellent properties at elevated temperatures, good formability and good corrosion resistance. .This extraordinary collection of properties are the reasons why Cu-Be alloys are expected to be ""Key-materials"", which are necessary to further advance science and technology and to be applied in.various fields such as electronic devices, machine parts, repeater housings of undersea optical fiber communication cables, etc.However, a large amount of beryllium is oxidized to BeO in melting stage of the current Cu-Be alloy production process, because beryllium is a highly reactive element. This is one of the ·main factors that negatively affect the production yield and th_e product quality."

Jan 1, 2000

By Yasuhiro Konishi, Yoshiyuki Noda

"This paper describes a new processing of rare-earth oxide precursor, in which rare-earth carbonate powders are precipitated directly from emulsions of rare-earth loaded carboxylate solutions, using CO2 gas and water. This synthetic route of rare earth carbonate is a combined process of the stripping and precipitation stages in a conventional solvent extraction. Using this technique, lanthanum carbonate and yttrium carbonate were prepared at temperatures of 10 to 80°C and CO2 pressures of 0.1 to 3.0 MPa for 120 min. The rates of carbonate precipitation in a batch autoclave were sensitive to processing parameters such as CO2 pressure, temperature, and organic-phase composition. The particle size distributions of the carbonate powders were markedly dependent on temperature and C02 pressure.IntroductionSolvent extraction is the most appropriate commercial technology for separation and purification of rare earths. In typical commercial processes, the rare earths are stripped from loaded solvent extractants using aqueous solutions of mineral acid. After adjusting the pH of the aqueous strip solution, the rare earths are precipitated as insoluble powders of oxalates or carbonates, from which oxides can be produced by calcination. Such conventional processing can be simplified when the stripping and precipitation stages are combined by emulsifying rare-earth loaded solvent extractant with aqueous oxalic acid solution. It is likely that the single-stage precipitation stripping results in a marked decline in the consumed amounts of precipitating and neutralizing agents, thereby saving on both running and capital costs.Yoon and Doyle1) first demonstrated that oxalate powders of lanthanum and yttrium are directly precipitated from rare-earth loaded carboxylic acid solvent extractant when contacted with aqueous oxalic acid solution at ambient temperature and atmospheric pressure. Yttrium oxalate pow4ers were also prepared by precipitation stripping of di-(2 ethylhexyl) phosphoric acid. (D2EHPA) extractant using oxalic acid-hydrochloric acid solutions. 2) Moreover, neodymium oxalates were directly precipitated from organic solutions of tertiary aliphatic monocarboxylic acid and 2-ethylhexyl phosphonic acid mono-2- ethylhexyl ester using aqueous oxalic acid solutions, and powder characteristics of the resulting oxalates were compared with those of powders by the conventional solvent extraction routes. 3 • 4) Recently, attention has been directed towards the influence of processing parameters on the particle size distributions of yttrium oxalate precipitates. 5)"

Jan 1, 2000

By E. Salinas-Rodriguez, J. Hernández-Ávila, E. O. Ávila-Dávila, A. Romero-Serrano, M. Perez-Labra, G. Juárez-López

"Single phase rubidium jarosite was synthesized by precipitation from aqueous solution. X-ray diffraction and SEM-EDS analyses showed that the synthetic rubidium jarosite formed in subspherical particles with an average particle size of about 35 µm. The chemical analysis showed an approximate composition of Rbo9432Fe3(SO4)2 1245(OH)6. The decomposition behaviour of the jarosite in terms of solution pH was thermodynamically modeled using FACTSage by constructing the potential-pH diagram at 298.15 K. The E-pH diagram showed that the decomposition of jarosite leads to goethite (FeOOH) together with Rb+ and SO42- ions. The experimental decomposition of the Rb-jarosite was carried out in alkaline solutions with five different Ca(OH)2 concentrations. The decomposition process showed an ""induction period"" followed y a progressive conversion period where the Rb+ and SO42- ions formed in the aqueous solution. In contrast, calcium was incorporated in the solid residue and iron was transformed into amorphous ferrihydrite. The kinetic analysis showed that this process can be represented by the unreacted-core chemically controlled model. The reaction order with respect to Ca(OH)2 is 0.4342 and the calculated activation energy is 98.70 kJ mol-1. IntroductionJarosite type compounds are hydrous sulfate minerals containing alkalis and ferric ions, MFe3(SO4)2(OH)6, where M can be H3O+· Na+, K+, Rb+, Ag+, NH4 +, Tl+, ½ Pb2+ or ½ Hg2+. Jarosite-type compounds were formed by the natural ""in situ"" oxidation of pyritic ores leading to the replacement of the original iron sulfides and iron oxides (Dutrizac and Kaiman) [1]. The great interest in jarosites is due to its ability to eliminate or diminish the iron concentration of the acid leach solutions produced in the hydrometallurgical zinc process, with relatively low losses of divalent metals such as Zn2+, Cd2+, Cu2+ or Co . However, the losses of the metal values demand a careful study of the conditions under which the jarosite compounds are formed together with their chemical properties."

Jan 1, 2012

By Maria G. Alves, Alexandre M. Stumbo, Francisca M. A. Pinheiro, Jonas Alexandre, Sergio N. Monteiro, Valdo da S. Marques, Paulo R. N. da Silva

"Brazil is among the few countries with potential for developing all sources of renewable forms of energy. In particular, the country is leading the world efforts of substituting petroleum based fuels for biofuels, such as ethanol and biodiesel. Most of the Brazilian petroleum, which has now achieved self sufficiency, is extracted from offshore wells located at the north region of the state of Rio de Janeiro. In view of the future depletion of petroleum, the State University of the Northern Rio de Janeiro (UENF) has created a Center for Alternative Energies (NEAL) to carry out R&D programs on renewable forms of energy. Today, the main project of the NEAL/UENF is a model park for generation of renewable forms of energy. The objective of this work is to present the structural concept of the park and discuss its contribution in terms of scientific, technological, economical and environmental benefitsIntroductionEnergy is presently a key issue in the world agenda for sustained development and environmental protection. It is of common agreement that the existing status of increasing use of fossil fuels, mainly petroleum, natural gas and coal will not only cause depletion of these resources with a consequent elevation in price but also climate changes, especially global warming. In fact, the humankind may be already facing an irreversible situation of climate alterations as well as reduction of conventional sources of energy. The worse predictions foreseen by specialists, still for this coming century, are dramatic disasters due to catastrophic weather in association with a profound energetic crisis. This scenario may, however, be avoided by actions that could effectively tackle the core of the problem. These actions have been suggested and discussed by scientists and leading authorities, especially in international symposia [1-3]. In particular, the Kyoto Protocol proposed goals for reduction of greenhouse gas emissions as well as a mechanism of carbon credits to allow for decreasing CO2 content in the atmosphere without affecting industrial production [3]."

Jan 1, 2008

By B. J. Scheiner

The presence of organic materials in gold ores interferes with gold extraction by cyanidation. The carbon contained in the ore has been shown to adsorb gold cyanide complex from solution. Removal of the carbon content by roasting or chemical oxidation prior to cyanidation results in gold extractions of 85 to 95%. This paper discusses how the mineralogy of the carbonaceous gold ores affects gold recovery by cyanidation. It also discusses the advantages and disadvantages of roasting and chemical treatment to render the ore amenable to cyanidation.

Jan 1, 1987

By R. K. F. Lam

Unacceptable levels of impurity were noted in high purity chromium melting. Analysis of recent melting data determined that oxygen content in chromium is the critical parameter. Thermodynamics studies identify zirconia to be the most stable oxide in the presence of liquid chromium, followed by alumina and silica. Iron oxide reacts readily with liquid Cr. A certain degree of chemical reaction between liquid chromium and oxides does occur, contamination by the crucible is therefore unavoidable. Equilibrium constants indicate that a chromium oxide addition decreases 'ceramic dissolution and reduces impurity contamination. Safe operating conditions with oxygen content between 1190 ppm and 2500 ppm were identified. Additions of chromium oxide (Cr2O3) of 161 grams and 264 grams to liquid chromium yielded acceptable levels of impurity, and oxygen content was respectively increased to 1624 ppm and 2 179 ppm. A new process of melting high purity chromium with chromium oxide addition for controlling the activity of Cr2O3 is recommended.

Jan 1, 1997

By Nico Steenekamp

At Lonrho Platinum in South Africa, ores from both the Merensky and UG2 reefs of the Bushveld Igneous complex are treated by flotation and smelting to produce a nickel-copper matte which serves as a collector for the platinum group metals (PGM' s). The nickel-copper matte was originally shipped to Norway for treatment and recovery of the contained base metals, with the return of the PGM rich concentrate to South Africa. The Lonrho Platinum Base Metal Refinery was commissioned in 1985. The original process employed a Shenitt Gordon design. The converter matte is treated in a refinery which utilises both atmospheric and pressure leaches for the dissolution of base metals to produce nickel sulphate crystals, copper cathode and a PGM concentrate. This paper refers to flowsheet and operating changes as well as improvements within the Base Metal Refinery.

Jan 1, 1999

By William Brinkman, Mark Jolly, Nasim Soleimanian, Karl Dearn, Oliver Brinkman

"Glass manufacturing is a heat intensive process. There is a direct correlation between the batch distribution techniques and the furnace energy consumption, productivity, and quality of the glass manufactured. All four major segments (float, container, fibre, and specialty glasses) would benefit from using an optimised batch distribution technique where possible. Oscillating batch chargers (OBC) have been in use since the early 70s, despite their superior batch shape, coverage, and in turn positive effects on the energy consumption and productivity of the furnace they are almost exclusively used in container glass manufacturing. The OBC’s main difference compared with other charging methods is its ability to directly influence the batch initial velocity. This paper reports on results achieved in CFD models (GFM) used to study effect of the machine on the overall energy consumption in the doghouse and the melt space.IntroductionGlass manufacturing can be divided to four major segments float glass, container glass, fiberglass, and specialty glasses. The financial cost of manufacture, its impact on the environment, lack of standardisation and mounting pressure imposed by the authorities for reduction in emissions means that the industry and its suppliers are utilising CFD modelling in order to tackle these challenges. The need for high temperature to create and maintain the viscous flow, homogenisation of the glass melt, and maintenance of the process to allow continuous output of glass of the right quality are the contributors to the energy intensive activities that are involved in continuous glass manufacturing. This in turn has resulted in design of large container glass furnaces which have high energy consumption, low specific performance, and high CO2 emissions where the most efficient furnaces in the container glass sector have a specific primary energy consumption of 3.8 GJ /tonne of glass at a level of 50% cullet in the batch making even very small improvements in efficiency by operation optimisation a value adding activity [1-14].The theoretical calculated energy required to melt glass is 2 to 3 times less than the energy actually used to melt glass as a result of glass melt passing a zone 5 to 8 times before leaving the tank.[8]. This causes contamination as the result of mixing between the completely molten glass free from bubbles returning to the batch area where there is freshly molten non-homogeneous glass, still containing very large numbers of bubbles and un-molten batch. At high temperature some components are dissolved rather than melted. Given that an un-molten batch is a good thermal insulator, it can be transported a long way into the furnace, increasing the need for homogenization which also increases the glass residence time of glass melt. This is why large unbroken strings of batch should be avoided, as should an overall blanket without gaps."

Jan 1, 2014

By M. Jahazi, P. P. Bhattacharjee, K. Chadha

The present work investigated the effect of strain reversal during high pressure torsion on the evolution of microstructure, texture and hardness properties of two different materials with different dynamic recovery behavior, namely, high purity (99%) Aluminum (2N-Al) and Aluminum-Magnesium (Al-2.5%Mg) alloy. In the two aluminum alloys subjected to different routes, the evolution of the ultrafine structure followed same trend. At lower strain level, sub grains with prominent LAGBs network were observed and at higher strains, ultrafine equiaxed grains separated by HAGBs were observed throughout the disk. The texture evolution in monotonically and strain reversal processed 2N-Al and Al-2.5%Mg showed presence of typical torsion texture components at different strain levels. The strength of the components was observed to follow different trends depending on the processing routes.

Jan 1, 2015

By J. Brent Hiskey, Rebecca Grace Copp

The solvent extraction of yttrium and neodymium from copper pregnant leach solutions (PLS) using Primene JM-T, a primary aliphatic amine, has been studied. Effect of contact time, pH, sulfate concentration, and extractant concentration were investigated using synthetic and actual PLS systems. Standard experimental conditions were 5 minute contact time, pH ~2.5, and 10 % v/v Primene JM-T concentration. Distribution isotherms were constructed for the pure systems and for actual copper leach solutions. Synthetic solutions contained 100 ppm Y and ~75 ppm Nd. Samples of PLS contained 2 - 10 ppm Nd and 14 - 30 ppm Y. Results showed that complete extraction of both yttrium and neodymium occurred within five minutes and at pH values greater than 1. It was also found that sulfate concentration does not inhibit extraction at any concentration. Additionally, the distribution isotherms created show that extraction for these metals can operationally take place in one stage.

Jan 1, 2016

By Ross R. Bhappu

Anticipating a major power cost increase in 1990, Cyprus Copper Company decided to modernize the Miami Smelter at a cost of $92.5 million. The modernization project included the addition of an Isasmelt vessel for use as the primary copper smelter and the modification of the existing electric furnace to a slaglmatte separating vessel. The project was completed in June of 1992 and is currently operating at close to its design capacity. This paper provides a summary of the decision making process, a description of the project, a summary of start-up problems and solutions and the current status of the smelter operation.

Jan 1, 1994