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By John Norton

"This presentation will cover the physical properties of waste heat recovery. It is a two part presentation. The first deals with actually recovering the heat with new state of the art heat exchangers and applying that heat to the furnace combustion and the second part will cover what other processes you can enhance with this ""free"" heat. It will also talk about converting it to steam, hot air or electricity to be used or sold back to the utility company. The economics of various schemes will be reviewed. A brief discussion on State and Federal grants and subsidies will be presented.IntroductionThere are large quantities of wasted heat in the usual aluminum melting process. And, there are several techniques for reducing and/or using some of that wasted heat as you have seen. Any technique that can make use of wasted heat is a form of recovery. This can range from simply preheating aluminum billets prior to melting, to more complicated processes like air-to-air heat exchangers using the boiling and condensing characteristics of special fluids in “heat pipes.” The objective of this type energy recovery process is to move the wasted heat from the hot and dirty exhaust gas stream into some useful process.Waste Heat Recovery in the Aluminum Melting Furnace.There are considerations, of course:1) What might the value be of the recovered energy?2) Can the recovered energy be used within the process? Within the plant? Or by theneighbors?3) What is the capital cost?4) Is the recovery process complicated?5) Will it take additional staff?6) Will it cause additional downtime on the melting line?7) Will the operations staff need to be licensed?Ideally, the process will be simple and inexpensive, the recovered energy will be very valuable, and the whole effort will cause little distraction to the aluminum melting process itself. These would be ideal."

Jan 1, 2011

By Hector Henao

To provide thermodynamic data for converting the nickel matte to liquid nickel, an experimental study was conducted in the phase equilibrium between the Ni-S alloy and the CaO-Al2O3 based slag melted in a MgO crucible at 1873 K under controlled Pso2 of 10.1 kPa and Po2 in a range between 2.5x 10-and 10.1 Pa by using CO-CO2-SO2 gas mixtures. The content of nickel in the slag at Po, of 10.1 Pa, above which solid NiO is expected to precipitate in the equilibrium state, was found to be 4, I mass% and the contents of sulfur and oxygen in the nickel melt were 0.4 and 02 mass%, respectively. ft was clarified that increase in the temperature reduces the solubility of nickel in the slag and the contents of sulfur and oxygen in the alloy, The distribution of minor elements such as gold, silver, copper, cobalt, iron, arsenic and antimony between the Ni-S alloy and the CaO-Al2O3 based slag was also studied. The distribution ratios of iron and cobalt, defined by (%X in slag)/[%X in alloy] where X is the minor element, are larger values than that of nickel, while those of copper, silver and antimony are similar to that of nickel. The distribution ratios of arsenic and gold are lower than that of nickel in the higher range of oxygen partial pressure.

Jan 1, 2003

By A. Treverrow, G. A. Brooks, H. K. Worner

"The work by H.K Worner and co-workers at CRA in the 1960s, and early 1970s, established that molten metals could be refined continuously utilising counter current flow of metal and slag. Womer also demonstrated that counter current refining could produce highly refined metal products. These developments coincided with the advent of high intensity metallurgical reactors in both the ferrous and non-ferrous industries (e.g. BOS, Q-BOP and later Sirosmelt) that utilised high levels of gas injection to produce rapid stirring and very fast reaction. These new generation of high intensity metallurgical reactors allowed high tonnage rates through relatively small volume vessels.Whilst, it is well known that the counter current flow of reacting phases offers the potential of efficient mass transfer and high purity products, the application of counter current reactors to molten metal/slag systems has been criticized on the basis that they suffer from either low intensity or, alternately, from poor refining due to excessive dispersion. These criticisms relate to the balance between intensity and the refining capacity of a reactor. That is, whilst high levels of mixing transversely to the direction of flow promotes high mass transfer, longitudinal mixing (dispersion) is detrimental to refining. Of course, mixing in one direction invariably leads to mixing in other directions, thus creating a playoff between high mass transfer and excessive dispersion.This balance between intensity and refining has been the subject of recent studies overseas, and at"" the University of Wollongong, using cold modelling techniques to evaluate the effect of mixing on dispersion in a counter current refining launder. These studies have shown that for a given geometry and mixing regime, dispersion decreases with increasing flow of liquid phases. This means that whilst high mass transfer cannot be achieved in a refining launder without sacrificing the degree of refinement, there is no impediment to achieving high productivity through such a system, in fact, high through puts may favour good refining. Thus, it may be possible to match a high productivity smelting operation with a equally productive counter current refining stage."

Jan 1, 1996

By Melvin H. Miles

"Considerable research has been conducted on the anodic oxidation of methanol in fuel cells. The electrochemical reduction of carbon dioxide in aqueous solutions to form methanol is the same reaction in reverse, i.e. CO2 + 6 H+ + 6 e- ? CH3OH + H2O. The same catalysts and conditions may operate for both reaction directions. This carbon dioxide reduction reaction, however, must be able to compete with the electrochemical reduction of water to form hydrogen gas. Thermodynamically, the reduction of CO2 to form CH3OH is slightly more favorable than the reduction of water. The use of nearly neutral electrolytes rather than acidic electrolytes makes the reduction of CO2 kinetically more favorable. The thermodynamics of various reaction steps are presented. Similarities exist with the electrochemical reduction of CO2 and the green-plant photosynthesis process that converts CO2 to carbohydrates.IntroductionVirtually all of the oxygen in the earth’s atmosphere is of biological origin having been generated by green-plant photosynthesis from water and carbon dioxide [1]. The net reaction can be represented byCO2 + H2O ? O2 + [CH2O] (carbohydrates, etc.) (1)Chlorophyll and enzymes promote this reaction, and the energy required comes from sunlight. The actual photosynthesis process is a complex multistage reaction and requires 469 kJ mol-1 of energy supplied by the sun. Isotope tracer experiments using 18O have shown that both the oxygen atoms in the O2 molecule originate from H2O, whereas oxygen atoms in the carbohydrates come from CO2 [1]. The total amount of water on the earth is split by photosynthesis and reconstituted by respiration and combustion once every 2 million years or so. The photosynthetically generated oxygen gas temporarily enters the atmosphere and is recycled about once every 2000 years [1]. The carbon dioxide is partly recycled in the atmosphere and oceans after an average residence time of 300 years and is partly fixed by precipitation of CaCO3 and other carbonate minerals [1]."

Jan 1, 2008

By I. C. Howard, E. J. Palmiere

"Heat transfer and friction in hot flat rolling have traditionally been characterised by an average heat transfer coefficient (h) and an average friction coefficient (p.). However, the presence of oxide scales and asperities at the interface question the use of such averages. The apparent irregularity and lack of pattern of interactions at the interface has prompted this present investigation to move away from averaged h and 11 values, and to study their local evolution based on probabilistic rules. The approach is based on the probability of finding the workpiece surface in a specific configuration at a particular instance of time in the roll gap. These rules are based on observations of surface phenomena such as scale behaviour during hot rolling. The model is implemented using user-subroutines integrated with the commercially available finite element program ABAQUS™. The results show the strong dependence of h and u on the local scale interactions. In particular, the effect of scale thickness, material behaviour and processing conditions on the evolution of hand 11 are discussed. Finally, the development of a Cellular Automata based Finite Element (CAFE) model is proposed to model the combined interfacial phenomenon of friction and heat transfer at the tool-work piece interface.IntroductionIntricate interactions between process variables in hot rolling of steels make it a challenge to the modelling community. For a given material and geometry combination, reducing interfacial power losses can increase the efficiency of the rolling process. The roll-strip interface, therefore, forms the critical zone and is currently the domain of intense investigation, especially to characterize interfacial frictionl • 2 and heat transfer3 • 4 . These interfacial phenomena are inter-related and cannot be studied in isolation. However, very few mathematical models4 • 5 combine an analysis of friction and heat transfer and deformation of the strip-roll interface taking into account the role of asperities and oxide scales."

Jan 1, 2001

By James Cornwell, John A. Elton

"Thermionic induced reactions and radiation resonance catalysis of aluminum and aluminum oxide materials exposed to microwaves and triboemissions will be described and explained from both a fundamental and practical level. Magnetron operation at distinct operating conditions that generates both plasmon and triboemissive radiation will be explained and the resulting tribochemical and radiation resonance catalytic reactions between aluminum, aluminum oxide, water and graphite will be delineated. The generation of hydrogen from these materials using triboemissive radiation and microwaves will be described, and the application of this methodology for hydrogen based technologies will be discussed.IntroductionProtective Systems Directed Energy RadiationProtective Systems, Inc, has developed a new radiation device called the EMR (Electromagnetic Resonator) that has unique characteristics that separates it from traditional microwave and rf radiation devices. The radiation from the EMR device is generated using a modified electronresonance magnetron with proprietary filters and operating characteristics.Electronic Device Shutoff. When electronic devices such as cell phones, computers, and other IC based electronics are placed within the EMR radiation, these devices become non-functional as long as the EMR beam is active. Upon removal of the EMR radiation the devices either become operational again or become operational after a cold start. The devices are not damaged by the irradiation.Faraday Cage Interaction Effect. When any of the above electronic devices are placed in a Faraday cage and activated within the Faraday cage without EMR radiation, they operate normally. However, these devices will still be rendered inoperative when an EMR beam generated outside the Faraday cage is directed at the electronic."

Jan 1, 2010

By H. Conrad, K. Jung

"The effect of an external electric field E=5(+) kV/cm applied during the solution heat treatment at 500°-550°C of three commercial Al-Mg-Si alloys (AA6061, AA6022 and AA61l1) on the asquenched resistivity Pw and hardness H.,NULL, w was investigated. It was found that the field gave a significant increase in Pw and in Hv,w, for AA6022 and AA6111, but had no clear effect on AA6061. Thermodynamic analysis gave that the effect of the field on AA6022 and AA6111 was to reduce both the enthalpy ?H, and entropy ?H, of solution. Considering the chemical composition of the three alloys it appears that the influence of the field may depend on the amount of Cu plus excess Si present in the alloy.IntroductionKlypin and Soloviev [1, 2] were the first to report that the application of an external electric field during solution heat treatment (SHT) of Al alloys gave an increase in the as-quenched resistivity and hardness. They attributed these effects of the field to an increase in solubility of the alloying constituents during the SHT. More recently Liu and coworkers [3, 4] also reported an increase in the as-quenched resistivity of Al-Li alloys with application of an electric field during SHT. Further, the present authors [5] found that the application of an electric field during the SHT of the commercial Al-Mg-Si alloys AA6022 and AA61i1 increased their as-quenched resistivity and hardness. Their thermodynamic analysis of the results indicated that the field decreased both the enthalpy ?H, and entropy ?S, of solution."

Jan 1, 2004

By J. R. Donald

Electric arc furnace (EAF) dust, which can be considered as a by-product of the steel recycling process, contains significant quantities of recoverable zinc and iron, as well as hazardous elements such as cadmium, lead and chromium, which can be leached by ground water. The zinc in the EAF dust is found almost entirely in the form of either zinc oxide or zinc ferrite, the latter accounting for 20 to 50 percent of the total zinc. It is important that an efficient process be developed which renders the dust inert, while reclaiming the valuable metals to off-set processing costs. During the conventional carbothermic reduction processes, iron is formed, and this iron can participate in the reduction of the zinc oxide in zinc ferrite. In the present work, the reduction of the zinc oxide in zinc ferrite by iron according to the following reaction: ZnO-Fe2O3(s,s) + 2 Fe(s) = Zn(g) + 4 FeO(s) was studied in an argon atmosphere using a thennogravimetric technique. First, a thermodynamic analysis was performed using the F*A*C*T computational system. Then, the effects of briquette aspect ratio (lid), temperature, zinc ferrite particle size, amount of iron added, as well as additions such as lime, sodium chloride, and calcium fluoride were investigated. It was found that, initially, the reaction was chemically controlled with an activation energy of 178.1 kJ/mol. Then, after a product layer had formed on the outer surface of the briquette, the reaction was restricted by the diffusion of zinc gas away from the reaction interface. The parabolic rate law was fitted to the experimental data, and the parabolic rate constant was found to be: = -6.2275 + 0.0054 T (K)

Jan 1, 1995

By F. J. Arriagada

Where gold is present in a finely disseminated form within sulfide particles, the porosity and surface area of the calcined material strongly influence leaching since they control the penetration of solution inside the gold-bearing grains. On the basis of a stability diagram for the Fe-O-S in the temperature range of 400 to 750aC, the expected sequence chemical transformations associated with the oxidation of pyrite is discus-sed. By using analytical techniques which include scanning electron microscopy, X-ray diffraction and BET gas adsorption, the chemical and structural changes experienced by auriferous pyrite-arsenopyrite concentrates and pure pyrite samples are studied under an oxidizing roasting atmosphere of com-position 80% N + 20% O2 in the temperature range of 450 to 750°C. The results indicate that as the roasting temperature increases, the surface area of the calcines decreases sharply after a maximum value attained at about 450-500°C. SEM micrographs show that the needle-shaped tips which characterize the surface of the oxide product become wider and the size of the pores between them is decreased when the roasting temperature is in-creased from 550 to 750°C. This effect suggests that the formation of a more "closed" hematite product at higher temperatures is due to sintering associated with a faster growth and crystallization of the oxide. A strong correlation is shown between increasing roasting temperature and increase in gold lost in cyanidation tailings, an effect which may be partly attributed to the loss in surface area of the calcines.

Jan 1, 1982

By Michael S. Moats, Scott C. Campin, J. Brent Hiskey

"Electrochemical techniques are a valuable means of analyzing the passivation of commercial copper anodes. Electrochemical impedance spectroscopy (EIS) provides information concerning transport and reaction phenomena occurring at an electrode surface. Commercial. copper anodes of varying compositions have been examined using EIS. Experiments were conducted in a flat cell with an electrolyte of 40 gil Cu2 + and 160 gil H2S04 maintained at 65 DC. Impedance spectra were obtained at the potentials characteristic of the open circuit voltage and passive region for each anode. The spectra of the passivating films exhibited a flattened resistive/capacitive loop at middle to high frequencies and an inductive loop at low frequencies. An equivalent· circuit utilizing an inductor-resistor series in parallel with the double layer capacitance and charge transfer resistance was adequate in modeling the impedance data. The influence of anodes impurities on the components of the equivalent circuit is discussed and correlated with a hi-layer passivation model.IntroductionPassivation of copper anodes during industrial electrorefining has received considerable attention in the past few decades. Great strides have been made in understanding the roles of anode impurities [1-25], electrolysis parameters [20,26], and electrolyte chemistries [20,26]. Even so, passivation still occurs even in the most modem of refineries. The exact cause of passivation is not fully understood. It is known that the anode surface becomes covered by a passivating film. This film has been proposed to be CuS04'&5H20, Cu20, or mixed oxides. The localized concentrations of Ft, Cu+, and Cu2+ ions determines which phase is more favorable. The presence of these ions is controlled by the reaction kinetics and diffusion of species through the slimes layer.Reaction kinetics between Cu, Cu +, and Cu2+ are based on the dissolution mechanism of copper. There exists four different models to describe the dissolution of pure copper. The classical model of Mattsson and Bockris [27] involves two single electron transfers with the cuprous-cupric reaction being the rate detennining step. More recently, Wong, Collier, and MacFarlane [28] used ac impedance to elucidate a more complex mechanism involving the affect of pH and anions. Their findings indicate that the formation of cuprous ions in solution, Cu(I)so~ is favored over Cu(1I) ions adsorbed to the electrode surface in the presence of sulfate and as pH increases from pH 1 to pH 5."

Jan 1, 1997

By Caisa Samuelsson, Taishi Matsushita, Hannes Holmgren, Sina Mostaghel

"Rönnskär Smelter of Boliden Mineral AB, Sweden, is a large end-processor of secondary raw materials and waste, including electronic scrap. Electronic scrap may introduce various impurities to the smelter's flow-sheet, among which alumina is a common and significant one. This article summarizes the results of an ongoing research at Luleä University of Technology, Sweden, to study the influences of alumina on different properties of slag from the zinc fuming process at Rönnskär smelter. A combination of different experimental techniques and thermodynamic calculations have been used to investigate properties such as density, surface tension, effective thermal diffusivity, viscosity, and melting/leaching behaviors. Results show that the addition of alumina to this slag increases the degree of polymerization of the melt, and physical properties vary correspondingly. Mineralogy of the semi-rapidly solidified samples is also changed due to alumina addition. A correlation between mineralogy and leaching behavior can be observed.IntroductionBoliden's Rönnskär Smelter is a base- and precious-metals producer located in north of Sweden. Its main products are copper, zinc clinker, lead, gold, and silver. Sulphuric acid, liquid sulphuric dioxide and iron sand (granulated slag) are some of its main by-products. In order to optimize the overall outcome of the process, different refining units are integrated in the smelter's flow-sheet (Figure 1). Copper concentrates and fluxing materials (mainly silica sand) are charged to the process. The produced matte is sent to the converter and the generated slag is charged to the fuming furnace, where it is treated by reducing gases to produce zinc clinker. The converter's slag is charged to the electric furnace, while the fumed slag is tapped into the settling furnace for further cleaning, where matte, slag and speiss (residual metals) are separated. The matte from the settling furnace is also sent to the converters; its speiss is sold to external customers; and its slag is water granulated and sold as construction material, which is known as iron sand."

Jan 1, 2012

By Tetsuya Uda, Sakae Shirayama

"With the aim of producing nickel (Ni) metal directly from acidic aqueous solution containing cobalt (Co) and other impurities, selective reduction of Ni was examined. As a preliminary experiment, sodium hypophosphite monohydrate (NaH2PO2·H2O) was selected as a reductant, and reacted with aqueous solution containing 0.1 mol L-1 nickel sulfate (NiSO4·6H2O) and 0 ~ 0.05 mol L-1 cobalt sulfate (CoSO4·7H2O) for 3 hours at 90 °C. As a result, it was revealed that Ni was selectively reduced and separated from Co in the acidic region (pH= 4.8). In this study, differences of reduction behavior between Ni and Co were investigated, and the feasibility of Ni I Co separation by the selective reduction of Ni was discussed.IntroductionEfficient Ni condensation and separation from Co are essential in nickel hydrometallurgical processes. Currently, the hydrometallurgical production of Ni from oxide ore is mainly carried out by acid leaching at elevated temperature, followed by the removal of impurities using neutralization, and condensation of Ni and Co into intermediate products such as hydroxides and sulfides. Then, the intermediate product is dissolved in acid aqueous solutions, and Ni I Co separation is conducted by solvent extraction. Finally, Ni and Co are recovered by electro-winning. This complicated process consumes large amounts of alkali, hydrogen sulfide (H2S), and organic solution in a multiple-staged process'. To reduce the consumption of these chemicals, it is important to recover Ni more efficiently from acidic aqueous solution containing impurities."

Jan 1, 2014

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 Matthew John M. Krane

"The macrosegregation patterns and convective behavior of a Pb-5wt%Sb-35wt%Sn alloy are studied using new numerical treatments of solid particle motion and of transport phenomena occurring during the solidification of ternary metal systems. At this composition, the solidification which occurs while the local liquid composition is in the (Pb)-(SbSn) binary eutectic trough has a significant effect on these phenomena. The effects of this solidification path on fluid flow and macrosegregation are compared to the more familiar binary alloy patterns and the effect of solid particle transport is evaluated. The final predictions of macrosegregation are compared to measured composition profiles. IntroductionThe macroscopic maldistribution of alloy constituents during solidification, commonly called macrosegregation, is a defect which occurs in real metal processing systems. This nonuniformity of species distribution, especially when it forms a high composition gradient or a poor distribution of secondary phases, can lead to areas of high stress concentration, which contribute to cracking during extrusion or forging of wrought alloys or when an as-cast piece is severely loaded in service [1, 2]. Macrosegregation studies in binary systems have become quite common since the introduction of single-domain numerical models which feature one set of conservation equations and boundary conditions for an entire, fixed computational domain containing solid, liquid and multiphase regions. A complete review up to 1995 has been presented by Prescott and Incropera [3]. However, most commercial alloys generally have more than two species in amounts significant enough to affect the convective flows which lead to macrosegregation and other defects. The formation of secondary solid phases, including eutectic and peritectic reactions, also may occur in commercial metal alloys and should be treated using appropriate thermodynamic models."

Jan 1, 1999

By Tao Zeng, Jianchao Li, Chang Jie, Jieyu Zhang, Jifang Xu, Kuochih Chou

"The densities of the selected quaternary Ca0-5%Mg0-Alz03-Si02 slag with low silica were measured by the Archimedean method in a wide temperature range from l 723K to 1823K. Slag compositions were chosen based on five different levels of Si02 content between 0.00 pct and 11.40 pct. The MgO content was equaled to 5.00 pct. The mass ratio of CaO/Alz03 was varied from 0.67 to 2.14. The effects of temperature, Ca0/Alz03 ratio and optical basicity were studied. It is shown that density decrease approximately linearly with an increase in temperature. With the same Si02 content, the density decreases with increasing of CaO/Alz03 ratio and optical basicity. Based on the experimental data as the boundary of the homogenous phase region predicated by F ACTSAGE software, the mass triangle model is used to calculate the density of selected limited homogenous phase region. The results showed that the mass triangle model is working well.IntroductionIt is of great importance to measure density of slag melt not only to the theory research for melt, which that is directly amenable to the structure correlations of molten slags, but also to the industrial application. Many metallurgy phenomena such as inclusion formation in molten melt and its removing, slag foaming, slag-metal reaction are closely related to the density of slag. Density is also required to estimate other fundamental properties, like surface tension, viscosity, and thermal conductivity from thermal diffusivity so that a relatively complete picture in regard to the behavior of high-temperature molten oxides could be made."

Jan 1, 2013

By J. Priede, G. Gerbeth

"Two different instability mechanisms of electromagnetically levitated bodies are analyzed. The first is due to the virtual coupling between the electric current passing through the magnetic system and the variation of position of the body. This mechanism can result in unstable mass center oscillations of a levitated solid body. Another type of instabilities may occur because of the coupling between the motion and the electric currents induced in the body. This effect can cause a spontaneous rotation of the body setting in as the frequency of the alternating magnetic field exceeds certain critical threshold depending on the configuration of the field. This instability can be suppressed by an axial steady magnetic field of strength comparable to that of the levitating field. 1 IntroductionAn alternating magnetic field interacting with eddy currents induced in a conducting body causes repulsion between the body and the coil generating the field. Besides, the eddy currents provide a contactless heating of the body. In such a way metallic samples can be levitated and melted without a contacting crucible. This technique allows to avoid contamination of the melt with container material and so to achieve a considerable super-cooling of the melt before it solidifies. Nowadays electromagnetic levitation is widely used in material research for measuring of the thermophysical properties of molten metals (2) .It has been observed since early fifties when the first experiments on the electromagnetic levitation were done that under certain circumstances solid levitated samples start to rotate or oscillate [l]. Surface oscillations can appear in addition when the sample is melted. Such phenomena are undesirable because they often result in failure of the levitation. Recently we showed that rotational as well as oscillatory instabilities can have electrodynamic origin related to additional eddy currents induced by motion of the body in an alternating magnetic field [3] , [4].In the first part of the present paper we analyze another possible cause of oscillatory instability due to the coupling between the electric current passing trough the magnetic system with variation of the position of the levitated body. The second part of the paper deals with the origin and suppression of rotational instability in a uniform alternating magnetic field."

Jan 1, 1999

By Luis W. Pommier

The wastes of the plating industry are generated in the process of rinsing the plated objects and during the cleaning of the plating shops. High volumes of hazardous waters are neutralized on site producing recyclable water, generating a metal rich, hazardous, filter cake. Occasionally, a complete plating bath has to be discarded which increases the metal content of the filter cakes. These filter cakes are discarded as hazardous at a cost of over $ 250 per ton. The metals found in the cakes are generally copper, nickel and chromium or zinc, lead and cadmium, assaying from 2% to 15% or even higher content of each metal The metals and their contents are highly variable. Some plating shops discard their products directly to hazardous waste sites, others, have them collected by companies which consolidate wastes from several producers prior to discarding. These wastes, richer in metal content than mine ores, need neither mining nor crushing and grinding for concentration. The commonly found impurities in the mine ores, i.e.: pyrites, arsenic, and valuable metals which are present in minute quantities, are absent in the filter cakes. The processes available to selectively recover the metals from the filter cakes, are discussed based on their technical and economic merits. The flow-sheets include leaching, solvent extraction when required, and electrolytic refining. Examples, showing the separation of copper, nickel and chromium and also of zinc and lead in pilot plants, show the technical and economic viability of the processes.

Jan 1, 1996

By Andre Thess, Oleg Zikanov

"Direct numerical simulation methods are applied to study the influence of a constant magnetic field on turbulent flows of liquid metals. The flow is assumed to be homogeneous and the problem is reduced to the classical case of the turbulent flow in a 3D box with periodic boundary conditions. The main subject of the study is the anisotropy developing in a liquid metal flow affected by constant magnetic field.To investigate the long-time evolution of initially isotropic flow the large-scale forcing is applied to maintain the flow energy at a statistically steady level. It is found that the flow evolution depend strongly on the magnetic interaction parameter (Stuart number). In the case of small Stuart number, the flow remains three-dimensional, turbulent, an approximately isotropic. At large Stuart number (strong magnetic field) the turbulence is suppressed rapidly and the flow becomes two-dimensional and laminar. Very interesting is the intermittent flow evolution at moderate Stuart number. Long periods of almost two-dimensional, laminar behavior are interrupted by strong turbulent three-dimensional bursts.The influence of a constant magnetic field on scalar transport properties of liquid metal turbulence is investigated using the simplified formulation of homogeneous flow driven by an imposed mean temperature gradient. Such a flow consists primarily of two turbulent antiparallel jets providing an effective mechanism for heat transfer. It is shown that the magnetic field parallel to the mean temperature gradient stabilizes the jets and, thus, enhances heat transfer considerably."

Jan 1, 1999

By Thomas W. Chapman, Shi-Chern Yen, I-Min Lu

"An electric field was applied to a metal-bearing kaolinite specimen to investigate the efficiency of electro-osmosis in removing heavy metals from contaminated soils. The electric field induces a flow of water through the porous medium, called electro-osmosis, which is superimposed on the hydraulic flow. Because the electro-osmotic flow is relatively stronger in smaller pores, it can enhance the displacement of contaminated solution by fluid convection. Furthermore, local changes in pH caused by the electrode reactions can affect adsorption equilibria and the distribution of solutes between the solution and the solid surfaces.The electro-osmosis experiments were conducted by applying either a constant current or a constant voltage across 8-cm inside diameter, 25 to 30-cm long specimens of kaolinite clay with graphite electrodes. Samples of the pore fluid and of the clay were analyzed to determine metal content, pH, and conductivity as functions of time and position. Results show that removal of heavy metals from soil can be accomplished effectively by electrokinetic treatment of sufficient duration. Approximately 95% of the lead was removed after 189 days.IntroductionRemediation of soils contaminated with toxic chemicals is a difficult and expensive task. Washing or leaching are not particularly effective if the contaminate is sequestered in small pores; hydraulic flows of water pass through larger pores leaving the smaller pores relatively untouched. Electro-osmosis appears to be the most promising new technology for removing heavy metals and organic substances from contaminated soils (Segal, 1980; Hamed et al., 1991, Masliyah, 1994).Electro-osmosis is one of several electrokinetic phenomena that occur through the interactions among an electric field, fluid motion, solute adsorption, and the existence of a net charge on a solid-fluid interface (Newman, 1991, Masliyah, 1994). Electro-osmosis refers to the fluid flow in a porous medium that results when an electric field acts on the mobile region of the electrical double layer, the solution-side region of charge separation that exists at the pore walls."

Jan 1, 1996

By R. Schaller, Ch. Karcher, A. Thess

"Electron beam evaporation of liquid metals is an innovative technology increasingly used in industry to produce very thin coatings of high purity. In this process the surface of a metal ingot, placed in a water-cooled copper crucible, is heated by bombarding it with a high-energy electron beam gun. The material melts, forming a free surface and eventually starting to evaporate. The rising vapor cloud condensates as a thin film on a moving substrate. The strong energy input at the free surface gives rise to vigorous thermos capillary and buoyancy driven convective motion within the melt, leading to unwelcome heat losses. This paper aims to show how these losses can be reduced by optimizing the geometry of the crucible and by using external magnetic fields. We present both experimental and numerical results.IntroductionElectron beam evaporation of liquid metals [l] is an innovative PVD-technology which is excellently suited for the industrial production of high-quality coatings. In this vacuum process a high-energy electron beam heats up the surface of a metal ingot. The ingot melts and forms a free surface. A schematic view of the arrangement is shown in Figure 1. When the temperature of the free surface exceeds the actual (pressure-dependent) saturation temperature of the ambient gas, the liquid starts to vaporize. The rising vapor cloud finally condensates on a moving substrate located at some distance above. To guarantee a superior quality of the coating the melt is typically confined in a water-cooled copper crucible. The intensive cooling is necessary to avoid chemical reactions between the melt and the crucible walls, that is, crucible materials and their reaction products are practically excluded from evaporation."

Jan 1, 1999