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By Pengfu Tan

A thermodynamic model has been developed to model the desilverising process of lead by the addition of zinc during lead refining, whereby silver-zinc solid solutions are formed, and floats out of the dissolved zinc/silver in the lead bath. The solubility of silver-zinc solid solutions in lead decreases with falling temperature. A number of variations and modifications of the desilverising process are modeled, and applied to a wide range of silver contents in lead bullions in the industry.

Jan 1, 2005

By David C. Lynch

The molecular form of trace elements in matte has been shown to depend on the chemical potential of sulfur and the propensity of the trace element to form a sulfide. Of the four trace elements (As, Sb, Bi and Pb) arsenic and lead behave nearly as opposites, with lead readily forming a sulfide while arsenic forms complexes with free copper and ion in the matte. Antimony and bismuth both display the dissolution characteristics as As and Pb, suggesting that these elements dissolve in matte in multiple forms of significant concentration. While in the present investigation the dissolution characteristics of all four trace elements are examined, the primary focus is on the multiple dissolution behavior of Sb and Bi.

Jan 1, 1995

By C. Camurri

Results from the Metallurgical Department of Universidad de Conception showed that fire-refined copper could be rolled without previous remelting for deoxidation. The goal of this work is to determine the rheology of fire-refined copper from tensile tests at different temperatures and strain rates, and Ford plane compression tests. All that in order to simulate and calculate rolling process variables. For rheology hardness coefficients, n variables between 0.28 at 600°C and 0.46 at ambient temperature are obtained. The sensibility coefficient for strain rate m varies between 0.056 at 600°C and 0.006 at ambient temperature. The activation energy for plastic flow Q in the considered temperature range is 1436 cal/mol.

Jan 1, 1999

By Kezhuan Gu

Data on the kinetics and thermodynamics of dephosphorization are analyzed in terms of the dynamic partition ratio, determined by a combination of slag thermodynamic properties and the balance of oxygen supply and consumption. A recently developed phosphate capacity correlation is combined with data on kinetics to quantify the most significant parameters in controlling the interfacial oxygen potential. The role of slag composition, entrained gas fraction and temperature are discussed in addition to metal carbon and sulfur content. It is demonstrated that the mass transport of oxygen in the slag is enhanced by factors increasing conductivity and inhibited by entrained gas. The mass transfer of phosphorus in the metal is described considering surface renewal induced by CO bubbles.

By J. M. Khodadadi

"A computational study of the effect of thermocapillary convection on melting of a droplet under the influence of an incident uniform heat flux is presented. The computations are based on an iterative, finite-volume numerical procedure using primitive dependent variables, whereby the time-dependent continuity, momentum and energy equations in the spherical coordinate system are solved. During the early periods of the melting process, conduction mode of heat transfer is dominant. As the thermocapillary convection is strengthened due to the growth of the melt zone, melting on the side of the droplet is observed to be much faster in comparison to the conduction-only case. Due to the skewedness of the temperature field, a new recirculating vortex is created which promotes melting within the droplet. The effects of the change in the sign of the surface-tension temperature coefficient on the melting pattern are also investigated.1. IntroductionMelting and solidification of materials are important processes which are encountered in nature and numerous industrial applications. Due to the recent upsurge of interest in such processes as spray casting, space radiators, rapid solidification, purification of materials, containerless processing, etc., there is a need to analyze the transport phenomena of melting and solidification in spherical configurations. Specifically, the effect of thermocapillary convection on the melting of metallic droplets has not been addressed at all. Only a few authors have studied the transport phenomena without phase change in spherical droplets. Oliver and DeWitt [l] worked out a series solution for the thermal and surface-tension-driven flow fields for a droplet experiencing an irradiant energy flux in the microgravity environment. Kudo et al. [2] solved the coupled momentum and energy equations numerically for the same problem without dropping the convective terms. Due to the nonexistence of any previous work on transport phenomena during the thermocapillary-assisted melting of metal droplets, this study was initiated to elucidate the features of the phenomenon."

Jan 1, 1999

By Andrew Shabalin, Vladimir Skorohodov, Svetlana Babaeva, ?lga Makovskaya

"At processing of some kinds of wastes (electronic scrap, secondary materials, spent nuclear fuel) in nitric acid solutions, and also in technology of silver refining, the significant amounts of palladium and platinum passes into a solution. The ion-exchange concentration of palladium and platinum in nitric acid solutions (5-500/dm3) are investigated. More than 30 various classes of ionites are tested. The most chemically resistance resins at the given conditions are identified. It is shown, that the maximum sorptive capacity to studied metals at high acidity the complexing, synthetic and inorganic sorbents possess. To definition of platinum metals sorption optimum conditions the kinetics is studied, isotherms of a sorption at various parameters from nitrate solutions are obtained. The conditions of the platinum and a palladium desorption from the pregnant sorbents and its regeneration with the subsequent reuse of materials were defined. The raw materials containing precious metals have very diverse composition and physical properties. Commonly the materials are processed by hydrometallurgical way. If gold or PGMs there are in raw materials to its opening hydrochloric acid solutions are applied. As an oxidizer nitric acid, hydrogen peroxide, gaseous chlorine, etc are used. Nevertheless, at processing of argentiferous materials and preliminary treatment of a waste including the spent nuclear fuel, nitric acid solutions are often used and the specified metals in some extent pass into solution [1]. Therefore selective extraction of PGMs from nitrate solutions is an actual problem. In the present work the ion-exchange concentrations of palladium and platinum in nitric acid solutions (5-500 g/dm3) are investigated. At the testing more than 30 various classes of ionites the most chemically resistance resins at the given conditions are identified. These resins are synthesized on the base of polyacrylate, styrene-divinylbenzene and vinylpyridine. For a selection of the most effective resin among what are made in Russia and overseas, a number of ionites with various functional groups were studied. Influence of functional groups type on a PGM sorption is shown for extraction of a palladium as an example (table 1). The presented data shows, that palladium concentration in a phase of ionites depends on sorbent type. If the increasing of solution acidity essentially reduces palladium sorption by sulfonic cation-exchange resins (KU-2×8) than its sorption by strongly basic anionites is approximately equal. Intermediate position is occupied by complexing sorbents. The latter (AN-31, SN-3, ANKB-35, Lewatit TP 207, Purolite S 930) are the most effective for extraction of PGMs from nitrate solutions from the point of view of capacity value. According to [2], solution behavior of Pt (II) and Pd (II) are similar. As is known from coordination chemistry, ligand environment of the metal ions substantially impacts to character of electronic spectra. The figure 1 shows the results of measurements of optical density of platinum bearing solutions with various concentration of nitric acid at ?=400 nanometers"

Jan 1, 2008

By Pradip

The selective adsorption of chemisorbing fatty acids at high temperatures together with the addition of soda ash and lignin sulfonate as depressants is the key to the industrial processing of bastnaesite ores. This paper presents the results of a fundamental investigation that indicate that alkyl hydroxamates can be an alternative collector for the beneficiation of bastnaesite ores that contain barite and calcite as the principal gangue minerals. The primary mechanism for providing sites for the chemisorption of hydroxamate on bastnaesite appears to be through dissolution of cations, formation of the respective hydroxo complexes and readsorption at the interface.

Jan 1, 1989

By Christophe Thiébaut

Keywords: Pyrochemistry, Salts Treatment, Distillation The pyrochemical purification of metal generates spent salts. When this metal is an actinide such as plutonium, the slags cannot be discarded and are thus disposed in nuclear facility. In order to handle with these slags, the decision has been taken to reduce stored quantities. The development of a pyrochemical treatment is in progress in the CEA Valduc centre. The feed salt, typically composed of various Pu and Am species contained into monovalent or divalent chloride matrix, is first oxidized to convert the actinides into oxides. Then the chlorides are separated from the actinide oxides by vacuum distillation. Temperatures higher than 750°C for monochloride salts mixture NaCl/KCl and higher than 1100°C for divalent CaCl2 base salts, are required to produce an industrial flow of vaporization. Inactive qualification of the process for NaCl/KCl base salt has been carried out with lanthanide surrogates. Then, a pilot equipment, called distillator has been designed and built for production-scale distillation of NaCl/KCl and CaCl2 oxidized plutonium salts. Industrial flows of vaporization have been obtained with this pilot equipment : about 4 g/cm²/h for NaCl/KCl at 800?900°C and 1 Pa, and more than 1,5 g/cm²/h for CaCl2 base salts between 1000?1200°C at 0.1 Pa. The last step, now in progress, is the integration of the distillator into a glove box.

Jan 1, 2005

By Md Sazzadur Rahman

Electrochemical Impedance Spectroscopy studies were conducted on two organic thermal energy storage materials; Neopentylglycol (NPG) and 2-Amino-2-Methyl-1,3-Propanediol (AMPL). The ionic conductivities and dielectric relaxation times in the low temperature ordered a-phase (monoclinic for both NPG and AMPL) as well as high temperature orientationally disordered cubic y-phase are reported.

Jan 1, 2006

By Minh H. Pham

This paper presents a technique for imaging the extent of solidification of molten metal flowing in a cooled pipe based on the concept of eddy currents. A 3D mathematical model, which relates the geometry of solidification to the scattered field induced in a solenoid external to the pipe, is derived. The model is described by a set of integral equations which are solved numerically using the moments method. An iterative algorithm is developed to reconstruct the solidification distribution image. Experimental measurements have shown that the eddy current technique is sufficiently sensitive for practical purposes.

Jan 1, 2001

By F. Raupp-Pereira, G. G. Cunto, J. A. Junkes, D. Hotza, V. P. Della

"The present work investigated the valorization of wastes as alternative raw materials for ceramic industries. Different industrial wastes based on the SiO2-Al2O3-CaO system and classified as non-hazardous were selected: sludge from varvite cutting process, sludge from gneiss breaks processes, sludge from filtration/clarification of potable water and a clay classified also as waste. All as-received residues were characterized by X-ray fluorescence, differential thermal analysis, thermogravimetry and particle size distribution. The applicability of these materials in ceramic formulations was then evaluated. The formulated mixtures were subjected to forming by pressing and extrusion followed by thermal treatment. After optimization of the processing conditions, the properties of the samples sintered at different temperatures were also evaluated. The waste materials studied proved to be alternative raw materials to natural mineral resources for the ceramic industry.IntroductionOne of the most important problems that have accompanied the humanity in recent decades is the environment’s degradation. In the same context, the natural resources exploration and technological development are phenomena which, if aren’t controlled, can cause ecological disequilibrium with unpredictable consequences [1]. It is in this perspective that recycling of various wastes assumes relevant importance.The recycling, understood here as the waste process reuse, is a common practice in the First World countries, where the raw materials have strategic aspects and the disposal techniques of solid wastes have considerable economic costs. In Brazil, the ecological conscience begins to be aroused due to, in the last ten years, the implementation of stricter laws for environmental control, in general, and licensing of waste generating from industrial activities, in special. The terms “residue” or “waste” are normally used to describe what remains of a production process; when an application for this material is not found. When wastes or residues are susceptible to be incorporated as raw materials or energy sources in a new material production, they can be understood as by-products [2].The valorization of industrial wastes is important, due to the need to pollute less and give an ecologically correct destination for wastes. The waste recycling, independent of its kind, presents several advantages in relation to using primary natural resources, such as reduction in the volume of raw materials extraction, lower energy consumption, lower levels of pollutant emissions and improvement of the health and safety of the population. The most visible advantage of recycling is the preservation of natural resources, extending its life and reducing the destruction of landscape and ecosystems [3]."

Jan 1, 2008

By Luciano R. G. Santos

Keywords: biosorption, cadmium, copper, biomass, spent zeolite. The majority of the industrial activities produce some kind of solid wastes. In this work two industrial residues (spent zeolite and wood sawdust) were chemically modified to increase their heavy metals sorption capacities. Manilkara longifolia (a Brazilian plant known as parajú) sawdust was first treated with NaOH and modified with different citric acid concentrations (0.6-1.2 mol/L) at 120°C, for 90 min. Infrared spectroscopy confirmed the presence of carboxylate groups in the wood structure as result of their mixing. Similarly, spent zeolites were also submitted to a chemical treatment (NaOH) to remove carbon deposited during oil cracking and to recover its sorption capacity. Batch experiments carried out at ambient temperature showed that both materials present sorption capacity for copper and cadmium comparable to weak acid ion exchange resins. A maximum of 78 mg-Cd/g and 59.7 mg-Cu/g as well as 29.9 mg-Cd/g and 14.6 mg-Cu/g were observed for the sawdust and the zeolite, respectively. The results were modeled according to the Freundlich and Langmuir equilibrium isotherms and compared with results of other studies.

Jan 1, 2005

By R. L. Miller

Oil -bearing metal sulfide sludges produced in treatment of an industrial wastewater, which includes plating wastes, have yielded to treatment by electrooxidation and hydrogen peroxide processes. The oxidation can be controlled to be mild enough to avoid decomposition of the organic phase while oxidizing the sulfides to sulfates. The pH is controlled to near neutral conditions where iron, aluminum and chromium(II1) precipitate as hydrous oxides. Other metals, such as lead and barium, may be present as sulfate precipitates with limited solubility, while metals such as nickel and cadmium would be present as complexed ions in a sulfate solution. The oxidations were found to proceed smoothly, without vigorous reaction; heat liberation was minimal.

Jan 1, 1992

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 Scott A. Shuey

Keywords: E-Waste, Pyrometallurgy Many might think addressing the issue of e-waste is a new area of study. Electronics disposal has been discussed in some circles for at least the past 25 years. The recycling of electronic waste (e-waste) tends to be a rather complex undertaking when considering the intimate bonding of materials in the average printed circuit board. The development of a recycling process is further complicated when considering the wide variety of products being generated under the heading of ?electronics.? Focusing only on the primary constituents (polymers, Cu, Al, Fe, etc.) tends to lead one to fairly simple flowsheets. Ignoring trace elements, and the various halide species generated, will lead process engineers down a development path that is sure to cause material handling issues. Researchers at Colorado School of Mines are modeling the complex chemistry that exists within the body of e-waste?comprising 39 of the known elements. An understanding of the systems thermodynamic behavior will result in the development of a more robust, long-term process for the recovery of valuable materials from the e-waste stream.

Jan 1, 2005

Testing is in progress to address compatibility issues with regard to long term storage of plutonium in contact with two different intermetallic systems. The two intermetallic systems are: 1. dental amalgam, i.e., mercury plus silver alloy powder, and 2. liquid gallium alloy plus copper powder. Both of these are plasto-metallic materials that undergo a solidification reaction at room temperature. Each system is allowed to react in contact with both high-purity alpha plutonium and a delta stabilized plutonium alloy at varying temperatures in an argon atmosphere. Wetting characteristics and possible interaction will be studied metallographically in the post-mortem condition. Complete results including metallographic examinations will be presented.

Jan 1, 1995

By Mitsuru Tanahashi

Oxidation removal of boron from molten silicon by injecting oxygen and highly basic CaO-CaF2flux powder has been investigated with special attention to the dynamic behavior of the injected flux particles and gas bubbles. Since oxygen gas is injected into the melt, high oxygen partial pressure is maintained at the flux-O2-Si interface and the removal of boron proceeds under nonequilibrium conditions. By applying this process, boron concentration in metallurgical-grade silicon can be reduced to a single-ppm level. In this paper, the effects of the dynamic behavior of the flux particles injected into the silicon melt and the area of the reaction field (the flux-O2-Siinterface) formed in the vicinity of the flux-gas exit of the injection nozzle on the rate of the boron removal are discussed from the viewpoint of process dynamics. The experimental results clarified that the boron removal rate is affected by the kinetic energy of the flux particles which is determined by the injection conditions, such as the gas-flow rate of oxygen and the size of the flux particles. At higher oxygen gas-flow rates, the injected flux particles are expected to possess a significantly high kinetic energy such that they penetrate the O2-Si interface formed at the nozzle exit, which results in the formation of a new reaction field for boron removal. On the other hand, at lower gas-flow rates, the injected flux particles possess too low kinetic energy to penetrate the interface. In this case where the formation of the reaction field is limited, it is shown experimentally that the rate of the boron removal is constant, independently of the flux injection rate.

Jan 1, 2006

By Carlos Eduardo Gomes de Souza, Luis G. S. Sobral, Paulo A. Medeiros da Silva, Selma G. F. Leite, Renata de B. Lima

"The use of mixed cultures of acidophilus microorganisms that act in different temperature ranges, aims at speeding up the digestion of chalcopyrite, highly refractory sulphide mineral, the major mineral in the flotation concentrate of Caraíba Mining Co., with an attractive processing cost. The concentrate under consideration contains mainly chalcopyrite (CuFeS2) and bornite (Cu5FeS4) with contents of, approximately, 70 and 30%, respectively. It was observed in this study, the performance of consortium of mesophiles, moderate and extreme thermophile microorganisms, in the oxidation of the aforementioned sulphides minerals, evaluating operational parameters such as pH of the leaching solution, the reaction temperature and redox potential, with consequent extraction of 80% of the concentrate copper content within 60 days of bioleaching. Such high copper extraction was achieved in column bioleaching tests.INTRODUCTIONThe solubilization of metals by the application of microorganisms from the mineral ores and the subsequent recovery of metals from solution are referred to as bioleaching (Rohwerder, T et al, 2003). This is an economical method for the recovery of metals from minerals; especially lowgrade ores, overburden, and waste from current mining operations which requires moderate capital investment with operating cost (Watling, 2006).Furthermore, bioleaching is generally more environmentally friendly than conventional metal recovery processes such as concentration and smelting. Those physicochemical metal extraction processes generate sulphur dioxide, a toxic emission that is increasingly the target of regulatory legislation (Stott et al., 2000; Olson et al., 2003). Bioleaching of chalcopyrite is the key industry target. The main problem hindering commercial application of chalcopyrite bioleaching is the slow dissolution rate (Fu et al, 2008).Dissolution of acid-soluble sulphide minerals such as sphalerite, and to a lesser extent chalcopyrite, occurs by a combination of ferric iron and proton attack via the polysulphide pathway (Rohwerder et al., 2003)."

Jan 1, 2008

By Alexander A. Knminskii

Polymorphism of BaR2F8 compounds is analyzed, and some peculiarities of obtaining monoclinic low-temperature (3-BaR2F8 crystals (R=Y, Ho-Yb) and orthorhombic high¬temperature a-ßaR2F8 crystals (R=Yb, Lu) by the Bridgman-Stockbarger growth technique are discussed. We pay a special attention to BaYb2F8:Er3+ crystals, which are able to generate both 2:µm SE using the new four-level operating scheme (4F9/2?4I11/2 laser channel) and 2- and 3-µm SE by means of the cascade scheme (4F92?+4I11/2?+4I31/2). This 2-µm generation of Er3+ ions has an advantage over similar SE of Ho3+ and Tm3+ ions (especially under diode laser pumping), that is important in designing the medicine and ecology laser. We report on orthorhombic BaR2F8 crystals with the ordered structure, a new crystalline materials for generating Ln3+ ions. The growth conditions are determined and orthorhombic BaLu2F8 crystals of several cm3 in volume doped with Ce3+, Nd3+, Ho3+, Er3+, and Tm3+ ions are obtained for the first time. Spectroscopic and laser characteristics of these crystals are discussed for Nd3+-and Era+-doped samples serving as representative examples. In particular, low-threshold stimulated emission was excited in 4F3/2?+4I11/2 channel of Nd3+ ions in the BaLu2F8. Room-temperature generation was obtained also at -1.317 µm wavelength for Nd3+ and at ~2.8 µm (several lines) for Era+ ions in this new laser crystalline host with a threshold of about 20 J.

Jan 1, 1997

By Peter J. Hancock

The pyrometallurgical .processing of non-ferrous, complex materials and wastes will be surveyed. Pyrometallurgy offers the most versatile way of processing a large variety of such materials because of its high temperatures, closely-controlled oxidation potential and the availability of commercially-proven reactor configurations. Some current industrial applications will be reviewed and possible new applications as well as future trends will be outlined.

Jan 1, 1994