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By M. Patel, A. W. Piper, R. A. Forsdick

"Lead bullion is refined in kettles to remove the contained impurities such as copper, antimony, silver and bismuth. These impurities are removed sequentially by the addition of one, or more, reagents to the bath. Impurity elements react selectively with the reagents to form a dross layer on the surface that is subsequently removed for further processing. Mixing the lead bath using specific impeller designs, which form a vortex to ensure that good contact takes place, carries out the reactions. It is important that the mixing is controlled to achieve the optimum bath conditions and hence good dross grades.This paper presents initial modelling work on the kettle refining process using both physical modelling (Water Models) and mathematical modelling (Computational Fluid Dynamics - CFD). Comparisons between measured plant data and simulation results are given.IntroductionThe refining of lead bullion takes place in hemispherical kettles of varying sizes. It is normal practice to remove the impurity elements sequentially, by the addition of reagents, which selectively react with the impurity element. The impurity element forms a dross layer on the surface, which can be removed for subsequent processing at the end of the reaction period.All the refining stages in the production of lead and lead alloys involve mixing the lead bath, although different conditions are required for each stage. At Britannia Refined Metals mixing is achieved using either 3 or 4 angled or flat blade impellers, which generate a vortex in the central region of the kettle. However, throughout the industry a wide range of mixer types are used which are all trying to achieve the same result."

Jan 1, 1999

By Takafumi Kondo, Satoshi Yamashita, Noboru Masuko

"Aqueous oxidation of phosphite ions to phosphate ions with dissolved oxygen was examined at 80° C and pH 4.5 mainly from the stichiometric point of view. Dissolved oxygen alone can not oxidize sodilim phosphite in aqueous solution, but when sulfur dioxide is coexistent, cooperative oxidation for both sulfite and phosphite can occur in aqueous solution. Sulfur dioxide itself is well known as a reducing agent, but it also reacts as an oxidation-promoting agent for other species under a certain condition. So sulfur dioxide is· a promising cheap reagent for waste phosphite processing.IntroductionIn a liquid-phase oxidation reaction using the dissolved oxygen gas, the eoexistence of a copper salt is required generally. Recently, it was reported that the oxidation reaction progressed by using mixed gas of sulfur dioxide and oxygen without the copper catalysis, and the attention has been collected1·3). The present authors also noticed the phenomenon since the early time and have been studying on the reaction mechanism of sulfur dioxide in liquid phase oxidation 4l. It was found that; by using the SO2-O2 mixed gas, the oxidation of phosphite ions to phosphate ions proceeded efficiently in sulfuric acid solutions. In the present report, the applicability of SO2-O2 mixed gas as a cheap oxidizing agent to the industrial processing of the waste solution of electroless nickel· plating is investigated. It is well known that the sulfur oxide dissolved in aqueous solution is oxidized ·by the oxygen in the air to sulfuric acid according to the following equation"

Jan 1, 2000

Aluminum has experienced significant growth in automotive applications over the last decade as a result of its properties and performance attributes. Looking to the future, the opportunities for continued growth in powertrain and suspension applications plus light weighting of body structures offer the potential for considerable further growth. This represents a growing "energy bank" of aluminum that will become available for recycling at the end of these vehicles' lives. Today, around 90% of the aluminum is recovered and recycled from scrapped vehicles because of its high value relative to other materials. The future growth offers opportunity for new technology and practices, to maximize scrap quality and recycling application. This paper will review the demand for these new technologies and practices and will discuss industry activities being pursued in this area.

Jan 1, 2000

By S. S. Bogomolov

The relationship between the magnetic properties and micro- structures of Pr-Fe alloys rapidly quenched by melt-spinning and highly undercooled by containerless processing in the Cambridge drop-tube was studied. The maximum measured coercivity, Hc, of as-cast samples was 4450 Oe for Pr-2 wt.%Fe. However, rapid quenching or melt undercooling decreases coercivity for hypo- eutectic alloys (<10 wt.%Fe) and increases Hc for hyper-eutectic systems.

Jan 1, 1992

By H. Fukushima, T. Ohgai, N. Baba

The electrodeposition behavior of Zn and the morphology of the deposited Zn were studied in electrowinning solutions containing polymer additives such as gelatin and polyethylene glycol (PEG). The cathode potential was shifted in a less noble direction and the polarization resistance for Zn deposition increased with increasing concentrations and molecular weights of both gelatin and PEG added to the electrolytic solutions. However, when the molecular weights of these additives exceeded about lxlO4, the cathode was depolarized and the polarization resistance for Zn deposition decreased with increasing molecular weight. The crystal grain size and the (002) orientation of the deposited Zn became smaller when the concentration and molecular weight of the additives increased, and the cathode was polarized.

Jan 1, 2000

By Tejs Vegge

The lack of suitable means of storing hydrogen for use in the transport sector is generally viewed as a primary showstopper for a hydrogen economy. Recent developments within solid state hydrogen storage in complex hydrides and metal ammines have sparked new hope of a long term solution, but as of now, no materials fulfill all the DoE targets for onboard storage [1]. A detailed physical understanding of the ab-/desorption processes and the role of the essential catalytic additives is an essential prerequisite for the development of new optimized hydrogen storage systems. Here, we illustrate the potential of utilizing the synergy of combining state-of-the-art in theoretical methods and experimental techniques in the analysis and design of materials for hydrogen storage. Recent advances in computer hard- and software has made it possible to treat many of the essential problems in such materials, i.e. structural stability, hydrogen dissociation and diffusion, with high accuracy methods like density functional theory. We rely on such results to guide our synthesis of new materials, and to interpret our experimental results from, e.g. time dependant in situ x-ray diffraction, synchrotron/neutron experiments, and advanced materials testing. Through a continuous feed-back optimization loop between theory and experiments, the obtained nano-scale insight is used to expedite the design and development of novel materials for hydrogen storage.

Jan 1, 2006

By Dong Hoon Han

The simultaneous sulfation by sulhr dioxide and oxygen of CaO and MgO in calcined CMA (calcium magnesium acetate) were investigated. he experiments were carried out in the temperature range from 700 to 830 "C and at the SO2 concentrations of 0.3 to 1 mol %. The oxygen concentration was kept at 5 %. Each sample was calcined completely before the temperature was lowered to the sulfation temperature. According to the ranges of partial pressure of sulhr dioxide and temperature, there exist three regions for the sulfation reaction: region I in which neither oxide is sulfated, region I1 in which only CaO is sulfated, and region 111 in which both oxides are sulfated. It was shown that the MgO in calcined CMA is sulfated at a rate comparable to that of CaO by forming a mixed sulfate phase. Thus, unlike MgO contained in other desulhrization materials, the MgO content in calcined CMA can be fully utilized for flue gas desulhrization.

Jan 1, 1999

By K. Abe

Onahama Smelter has two green-charge reverberatory furnaces and the annual smelting capacity is 600 thousand tons copper concentrate. In addition to the concentrate, various kind of industrial wastes has been processed and utilized. First, the brick waste from converter is ground and used as raw material of castable for repairing the copper melt launders. Second, the slag containing calcium-sulfide from other foundry is fed to the reverberatory furnaces. Calcium sulfide is oxidized to CaO. The melting rate of concentrate is accelenlled and the slag loss is decreased. Third, the tip tire made of waste car tire is charged into the reverberatory furnaces as fuel. The steam of waste heat boiler for turbine generators has been increased so as to decrease the electricity cost. Fourth, the sulfur accretion from other chemical plant is blended into the copper concentrate and the sulfur is recovered as the gypsum for sale. Fifth, the processed waste oil has been utilized in the copper concentrate dryer by which the smelting capacity was increased effectively. Consequently, Onahama smelter contributes to the society by processing the wastes to the harmless slag and utilizing them as fuel through the copper smelting.

Jan 1, 1996

By Jeong-Hwan Kim

The liquid-liquid reactive process (solution process) is often adopted as a synthetic method for precipitated calcium carbonate (PCC) in laboratory studies for its simplicity in operation or ease in controlling process variables. Still, PCC are produced commercially by passing carbon dioxide through a milk of lime, i.e., by a gas-liquid reacting method (carbonation process). Few studies on the carbonation process have been conducted, since the process variables are interrelated and difficult to control compared to the solution process. In this study, both carbonation and solution processes were employed to study the polymorphs of calcium carbonate and growth rate of PCC crystals. The effects of the characteristics of limestone ores as a raw material in the synthetic system of PCC on the synthetic characteristics of PCC were also investigated. To control the nucleation rate in the synthetic systems, the shape factor was considered most important. Single-phase aragonite PCC could be synthesized under a variety of controlled experimental conditions such as ionic strength, solution composition, concentrations of additive ions, and temperature.

Jan 1, 2006

By David G. C. Robertson

A new approach is described for the calculation of the kinetics of metal/slag, metal/slag/gas, and metal/matte/slag/gas reactions. The algorithm assumes that equilibrium is achieved at the interface between phases, and uses an equilibrium solver (such as SOLGASMIX) to compute the equilibrium state at the interface at each time step during the reaction. For multiple phase systems a number of unit operations, representing the different phases and interfaces, must be connected together in a reasonalbly complex manner, and the METSIM software package has been utilized for this purpose. The new approach is superior to the SMAK software developed by the author and his co-workers over the past decade, for the reasons discussed in this paper.

Jan 1, 1995

By J. E. Sallee

An experimental study has been conducted on the level of arsenic contamination in samples of zinc oxide when the zinc oxide is contacted with gas mixtures containing As4O6(g). This contamination has been determined as a function of A4O6 saturation pressure, temperature, zinc oxide sample surface area, impurities, and oxygen level in the gas mixture. The results indicated a rather clean separation can be achieved between condensed zinc oxide and gaseous arsenic oxide as long as attention is given to temperature control, and the final zinc oxide surface area. For a 300°C operation temperature and an AqOg saturation pressure of 0.38 TORR (or 0.05% As406 by volume), the contamination level is expected to be approximately 100 ppm. This suggests that arsenical dusts can be treated in the HRD flame reactor process and a reasonable purity zinc oxideproduct produced. The results also show no evidence of zinc arsenite or zinc arsenate formation.

Jan 1, 1994

By K. Pagalthivarthi, P. V. Desai

"During solidification of alloys, many inter-related physical processes, such as melt convection, mass diffusion, heat transport, macrosegregation and melt-undercooling occur. Several research workers have studied one or more of these effects separately. To answer important questions on solidification behavior, an overall approach interrelating the processes is necessaryAs a first step toward accomplishing the overall modeling, the freezing of a binary liquid metal is examined. The various stages during freezing of the alloy are critically described to build a continuum model for the entire process. Diffusive mixture theory is used to write the conservation equations for the liquid and the mushy zones. The concept of local thermodynamic equilibrium in the presence of curvature effects is used to restrict the number of degrees of freedom within the mushy zone. Constitutive equations relating flux quantities and affinities, the governing differential equations and boundary conditions are discussed briefly for the freezing process.IntroductionA solidification study encompasses such facets as solifidication time, microstructure, macrosegregation of the solute, shrinkage effects and soundness of the casting. Influence of one or more of the coupled heat and mass transfer phenomena such as local solute redistribution, thermosolutal convection, melt undercooling at dendrite tips and heat dissipation to the ambient have all been previously examined [1-3J. Several studies have examined the individual facets of alloy solidification as isolated processses. In fact, the transport processes occur simultaneously and a comprehensive model should include their inter-relationships. In particular, some of the existing studies of the mushy zone [4-6J do not emphasize thermodynamic completeness. This work represents an attempt to develop a thermodynamically consistent model of the entire solidification process on physical grounds."

Jan 1, 1986

By Don Ibana

The use of solvent extraction (SX) in process metallurgy is particularly attractive as it is applicable to a wide range of solute concentration and pH, and it allows complete separation of chemically similar metals such as nickel and cobalt and the rare earths among others. It is therefore applicable to the processing of low grade and complex ores, which is increasing and expanding owing to the diminishing reserves of quality ores, and this has driven the increasing and expanding use of SX.The current SX technology, however, has inherent limitations owing to the use of mechanical agitation as it induces high shear mixing. Excessive shear produces very fine droplets, and while this favours mass transfer, it also leads to sluggish phase separation. High shear mixing is also known to favour crud formation. All these factors as well as high power and reagents consumptions contribute to poor process efficiency. Electrostatic solvent extraction (ESX) is similar to conventional SX except that mechanical agitation is replaced with electrostatic agitation. In direct contrast to mechanical agitation, it allows the production of very small droplets that can be made to maintain intense motion, which favours mass transfer, without affecting the phase separation. In addition, as it uses an electrostatic field, the power consumption is minimal. Hence, it promises to be a superior alternative to conventional SX mixing although an application of the technique is yet to be achieved.Our work to develop an application of the technique in process metallurgy has now established that electrostatic field has no effect on either the stability of the reagents or the chemistry of the process. A volumetric flowrate that is comparable to that of a conventional sieve plate pulse column is achievable. We have also established that electrostatic fields can be made to yield much narrower droplet size distributions than those of mechanically agitated contactors, and they allow better control of droplet motions, which include oscillation and linear motion and hence, mass transfer. These are significant advancements toward our goal and shall be discussed in this presentation.

By P. Ruz

A melt transfer ladle was 3D modeled by means of a mathematical fluid dynamics and heat transfer program. Internal temperature profiles were calculated as a time function for a normal ladle and for a pre-heated refractory lined ladle. It was shown that in a normal ladle the molten metal cools down quickly forming accretions. By using an inner lining there are practically no accretions build up within a typical time of operation. Therefore, by applying a refractory lining to a melt transfer ladle and keeping it at a moderate to high temperature it is possible to reduce cold dope circulation in the smelter.

Jan 1, 1999

By Per Anders Eidem, Merete Tangstad, Jens Davidsen

"During excavations of submerged arc furnaces producing silicomanganese, silicon carbide (SiC) has been found. Contributing to the size of the inactive area of the furnace, the active area of the furnace where reactions occur will decrease, thus reducing the potential for pre-reduction in the furnace.This work studied the formation of SiC from the liquid-solid reaction between slag, metal, and metallurgical coke. Slags and metals with different levels of silica (S1O2) and silicon (Si) have been studied. The slag and metal has been heated together with coke, and the samples investigated by microprobe. The results show that SiC was formed on the coke particle through reactions with both slag and metal. For the metal, the carbon most likely diffused through the SiC to react with Si in the alloy. SiC formation with slag is likely to go through the reduction of Si02 to Si.IntroductionToday, Silicomanganese (SiMn) is produced in submerged arc furnaces (SAF) by reduction of S1O2 and manganese oxides, mainly with metallurgical cokes. Typically, the tapped metal has a silicon content of 17 - 20 wt.%. To achieve higher levels of Si, the metal can be refined by adding off-grade silicon metal, yielding low carbon SiMn. [1]. What is believed to be SiC that has been found during dig-outs of SiMn furnaces producing high silicon alloy. It is possible that excess amounts of SiC in the furnace cause operational problems, since SiC will occupy furnace volume. As SiC accumulates, the active volume of the furnace will decrease, increasing the flow of material and gas in the active areas of the furnace. Formation of SiC is inevitable, so it is desired to keep the formation as low as possible. To be able to control the formation of SiC, one has to understand the basic mechanisms."

Jan 1, 2012

By Ron Bernard

HW Process Technologies has successfully developed and commercialized various applications utilizing Engineered Membrane Separation (EMS?) systems for the processing of acidic copper hydrometallurgical solutions and wastewaters. Copper hydrometallurgical EMS? applications include water balance control and increased copper concentration in heap and dump copper leach operations, tankhouse bleed stream treatment to separate/recover copper and cobalt from iron, and removal of PLS/Electrolyte suspended solids/colloids to eliminate "crud" formation during copper SX/EW. Similar applications are underdevelopment to provide ionic separations in copper refinery bleed streams, copper smelter acid plant streams, as well as organic/LIX removal from aqueous electrolyte and raffinate streams. Copper mine wastewater EMS? applications include treatment of copper leach solution contaminated groundwaters for copper recovery and treatment of unwanted heap/dump drainage to provide enhanced precipitation, a smaller precipitation plant, improved operating costs and better quality discharge water, particularly in terms of TDS and sulfates. A discussion of the EMS? technology and general separation results on typical process solutions and wastewaters will be presented. HW Process Technologies, Inc. commercial installations treating copper pregnant solutions and leach solution contaminated groundwaters are in-place at an old Asarco smelter/refining operation, Mexicana de Cananea copper mine, and a major U.S. copper mine, with several additional installations pending. Several case studies, including results from a selection of these installations, will be included with detailed capital, operating cost, and system payback data.

Jan 1, 1999

By Karin Soldenhoff

Recovery of uranium in conventional ion exchange circuits, using strong base or weak base resins containing quaternary or tertiary amine functional groups, is based on an anion exchange mechanism. In saline liquors, chloride competes with uranium for the active resin sites and reduces resin loading. This results in significant negative impacts on the IX process in terms of plant throughput and operating costs. In this paper we present the results of a study on the recovery of uranium from an acidic in situ leach liquor containing approximately 9 g/L chloride. A range of resins was tested, and a high capacity strong base resin was identified with significantly enhanced loading compared to conventional resins. Other process-relevant criteria such as loading kinetics and elution efficacy are also discussed. The process developed was successfully tested during a recent ion exchange pilot plant operated in conjunction with a field-leach trial.

By Lincoln McCrabb

Correct measurement and interpretation of viscosity data is critical for design of any thickening and pumping process that involves a non Newtonian slurry. The nickel laterite pressure acid leach (PAL) process relies on producing a slurry of maximum achievable solids concentration. Small variations of 1-2% solids concentration can alter economics significantly. For the Ravensthorpe Nickel Project, a rheology protocol has been developed which optimizes the solids concentration across a range of ore types. The vane yield stress technique has been utilized to accurately quantify the flow of thickened slurry in the lower shear range. A yield stress of 100Pa has been used as a benchmark to determine the optimum solids concentration achievable utilizing deep cone thickening. Statistical analysis of the data shows critical rheology distinctions between ore type, particle size, lithology and geochemistry. Linear and power law models have been applied to rheology flow curves to reconcile the material transport properties with the anticipated thickener underflow solids concentration. Keywords: Vane Yield Stress, Thickening, Rheograms

Jan 1, 2004

By Leonard J. Friedman

The contact process for the production of sulfuric acid has been used commercially since before the turn of the century (1880?s), and rapidly replaced the chamber process after the development of vanadium catalysts in the early 1900&apos;s (1910&apos;s - 1920&apos;s). Plant size has increased from a few tons per week to single train units in excess of 4,000 tons per day. Much of the history of the contact process is in the minds of the few remaining early process pioneers that started in the industry in the 1920&apos;s and 1930?s, and in sulfuric acid industry books published in 1921, 1925, 1936, and the last Deucker and West in 1959. Since those not familiar with history are doomed to repeat the failures and mistakes of the past, this paper includes a brief history of the contact process along with the history and development of equipment and materials in each equipment area of the process. The main focus of the paper is to present the development and analysis of equipment and materials in the contact section of the sulfuric acid plant - from the dry tower to stack.

Jan 1, 1999

By Kunio Nakahara, Kashiwagim Junichi, Takao Hayashi

"There are many problems for electronic devices and parts which were caused electrostatic damage by static electricity. It is necessary for prevention of electrostatic charge to decrease surface resistivity of material using electroconductive coating. Mitsui Mining & Smelting Co., Ltd. developed metal oxide type electroconductive pigment PASSTRAN (trade mark) Type-IV which is barium sulfate coated with SnOz(Sb) thin electroconductive layer. This paper shows about pigment characteristics and film condition of antistatic transparency paint which contained PASS TRAN.L.IntroductionRecently rapid development of electronics technology diffused electronic devices and products to Office, Factory, Laboratory and our life. But the other side, there are many problems for electronics parts which were caused electrostatic damage under static electricity. Demand of antistatic materials were become lager by this situation.There is close relationship between surface resistivity of material and static electricity. If the surface resistivity of object is enough low (under 109 Q /Sq), static electricity is dissipated quickly. So it is necessary for prevention of electrostatic charge to decrease surface resistivity of material using electroconductive coating.1) There are many type of electroconductive materials, for example, carbon black, metal powder, electroconductive polymer and so on. Especially, carbon black is used for general purpose by reason of its low cost, but it has big problem of black color. It can not get any color without black, and it caused contamination of carbon.In recent years, metal oxide electroconductive pigment (ECP) was developed and used for special purpose which demands transparent coating or easy dispersion to make ECP paint or endurance under hard environment and so on. Mitsui Mining & Smelting Co., Ltd. developed electroconductive pigment PASSTRAN Type-IV which is BaS04 coated with electro-conductive Tin oxide layer."

Jan 1, 1998