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By Ana Bohé

Nowadays, Gas-solid processes are widely used in the industry. The chloration and carbochlorination of metallic compounds are some of this kind of non catalitic heterogeneous reactions. In particular those related with extractive metallurgy of refractory elements (Zr, Ti, Nb, Ta, RE, etc). The development of materials to be used in reactors at elevated temperatures and with high corrosion performance, enhance the application of this kind of processes. Although they are currently carried out in the production of many comodities, the mechanism of most of them are yet not well understood. The present work is a deep discussion on the most important aspects to take into account for determining the mechanism of gas- solid reaction, and those criteria fulfil in this analysis were applied to chlorination and carbochlorination examples. The microstructural characteristic of solids, the mass and heat transfer phenomenon, the adsorption and desorption of gaseous species on active surface, surface diffusion processes and chemical elementary steps, which are the mainly contributions to the mechanism of these reactions were analysed. Furthermore, the effect of them on the reactivity of solids and the control step of the reactions were determined. The application of catalitic mathematical models to this kind of reaction and the modification for the better interpretation of experimental results is also undertaken. The most appropriate experimental procedures for following these reactions and the microstructural characterization techniques needed to be use in each case, there limits and applicability are also indicated.

Jan 1, 2006

By V. Tsukerman, Ivanovam L.

"The potential of hydrocarbon resources in the Arctic oil and gas provinces is enormous. Oil, gas and condensate constitute the basis of mineral resource base of the shelf zone of the Russian Arctic; summary volume of hydrocarbons exceeds 100 billion tons of conventional fuel. Only in the Shtockman gas condensate field in the Barents Sea explored balance reserves equal to 3.2 trillion m3 of gas. It is necessary to establish a special regime of nature management in the Arctic. Environmentally oriented economic activities should be more actively stimulated. The Energy Strategy plans that starting from 2010 in the Barents and Pechora Seas up to 10 million tons of oil and 50 billion m3 of gas will be extracted, reaching the level of 30 million tons of oil and 130 billion m3 of gas in 2020. This task cannot be solved without intensification of geological exploration on the continental shelf. IntroductionThe elaborated strategy of mining enterprises should correspond to the modern paradigm of mining industry development which is not only for extraction of minerals but also for multi-profile structure having comprehensive use of the resources on the rational basis intended for rational complex utilization of mineral resources of the Arctic zone of Russia which by the definition includes maximally full use of the whole aggregate of resources on the economically rational basis with obligatory environmental with resource reproductive and socio-economic functions and deterrents"

Jan 1, 2008

By V. Kamavaram

Ionic liquids are novel salts used as potential non-aqueous electrolytes for aluminum electrolysis at low temperatures. In the current research di-alkylimidazolium chloride ionic liquids such as 1-butyl-3-methylimidazolium chloride ([BMIM]Cl) and 1-hexyl-3-methylimidazolium chloride ([HMIM]Cl) were investigated for aluminum electrolysis. Melt formed by mixing ionic liquid with AlCl3 is termed as chloroaluminate and is composed of several polymeric chloroaluminate anions. Ionic liquids are studied as electrolytes for aluminum electrowinning and electrorefining of aluminum based materials (A356, A360, & Al-MMC) at low temperatures. Mechanism of aluminum electrodeposition in these chloroaluminate ionic liquid electrolytes was investigated using electroanalytical techniques such as cyclic-voltammetry and chronoamperometry. Aluminum electrodeposition on pure copper substrate in AlCl3-[BMIM]Cl (1.5:1.0) electrolyte at 30°C melts was found to be quasi-reversible process with a charge transfer coefficient ( of 0.40. Chronoamperograms obtained at different voltages in the range (-0.1 to -1.0 V) revealed that the initial stages of aluminum deposition in AlCl3-[BMIM]Cl melts was instantaneous nucleation followed by diffusion controlled growth of three-dimensional aluminum nuclei. The diffusion coefficient of electroactive species Al2Cl7¯ in AlCl3-[BMIM]Cl melts was found to be 6.5×10-7 cm2 s-1 from Cottrell?s equation and 3.9×10-7 cm2 s-1 from the dimensionless current-time transients.

Jan 1, 2006

By S. H. Castro

The El Teniente molybdenite plant (Chile), with a nominal capacity of 3,200 tpd of bulk Cu-Mo concentrate, produced approximately 3,385 metric tonnes of Mo during 1998 by using the phosphate Nokes process (LR-744 reagent). This is the only Chilean moly plant which traditionally has depressed copper and iron sulfides with LR 744 reagent, which is a hydrolysis product of P2S5 and NaOH. El Teniente's ore Mo grade is 0.02%Mo and is concentrated to 0.45%-0.50% Mo in bulk Cu-Mo flotation. Subsequently, molybdenite is floated by selective flotation to depress Cu and Fe sulfides, such as chalcopyrite, bornite, digenite and pyrite, to produce typically a 49%-50%Mo molybdenite concentrate. An optimisation program during the last two years was undertaken to improve molybdenite recoveries. Current molybdenite plant technology at El Teniente and use of phosphate Nokes in the process process is reported. Use of phosphate Nokes reagent has increased average Mo recovery from 70.5% in 1977 to a mean 74.7% for the first 4 months of 1999. The global Mo recovery, including bulk flotation, incresed from 42.3% in 1997 to 46.8% in 1998, with a projection of 55.5% for 1999. Mo production per year has increased from 3,181 tons in 1997 to 3,385 tons in 1998 and a projected 4,000 tons for 1999.

Jan 1, 1999

By Eliezer Martinez-Jimenez, Gretchen T. Lapidus

"Electro-assisted reduction is an effective pretreatment to render chalcopyrite less refractory towards oxidative leaching. In this process, chalcopyrite is selectively converted to chalcocite or copper metal in an electrolytic cell under ambient conditions, while ferrous ion is leached into solution. However, the reaction velocity is hampered by the formation of a ferrous sulfide passivating layer on the solid surface, especially at elevated solid to liquid ratios. In the present work, several strategies for overcoming this problem were evaluated. On one hand, specific ligands for ferrous ion were added in order to increase its solubility and, on the other, an anode material which promotes the oxidation of the sulfide ion was chosen. Leaching tests showed citric acid to be an effective ligand for both ferrous and ferric ions and, in combination with a lead-silver anode, significantly increased the kinetics of chalcopyrite reduction and subsequent copper leaching.IntroductionAttempts to oxidize chalcopyrite at a rapid rate in aqueous solutions, below their normal boiling point, have met with difficulties because of passivation by some of its own components. An alternative line of research explores reductive pretreatment, transforming the chalcopyrite into less refractory copper phases, which can later be oxidized. A recompilation of these efforts up until 2000 was published by Dreisinger and Abed [1]. However, this practice usually requires large excesses of reducing agents, such as copper, lead, aluminum or iron, and in this last case at near-boiling temperatures, in highly"

Jan 1, 2012

By Laurentiu Nastac

"Two advanced control solidification technologies were studied in this article to improve the quality of the cast ingots as well as to control the solidification structure evolution during the plasma arc melting (PAM) processing of Ti-6-4 ingots: (i) electromagnetic stirring (EMS), and (ii) ultrasonic treatment (UST). The developed EMS modeling approach is based on the numerical solution of Maxwell's equations, fluid flow, and heat transfer equations, and mesoscopic modeling of the grain structure. The UST analysis tool is capable to model acoustic streaming and cavitation. It is used in this work to study ingot solidification under the presence of ultrasound. Predictions of the macrostructure, GET formation and primary dendrite arm spacing for PAM Ti-6-4 ingots processed with and without EMS or UST were discussed.1. IntroductionTitanium (Ti) alloys are melted, refined and cast into ingots through plasma arc cold hearth melting (PAM), electron beam cold hearth melting (EBM) and vacuum arc remelting (VAR) for jet engine applications. Process modeling has become a viable tool to optimize the PAM, EBM, and VAR processes. A comprehensive modeling approach to simulate ingot solidification phenomena in primary melting and secondary remelting processes of Ti alloys would include models for macroscopic mass transfer, heat transfer, fluid flow, acoustic, electromagnetic and species transport. The approach should also include microscopic models to predict the evolution of grain structure in solidifying ingots in conjunction with electromagnetic stirring (EMS) and ultrasonic stirring (UST)."

Jan 1, 2012

By A. Filzwieser

The highest current density suitable for the electrowinning process is between 50 to 60 % of its limiting current density. One of the most important influences on the limiting current density is the thickness of the hydrodynamic boundary layer near the electrode surface. Therefore, the fluid flow in a copper electrowinning cell is calculated. The numerical simulation - using the CFD-software package FIRE® - considers all three different types of the fluid flow, namely, the natural convection, the forced convection by electrolyte circulation and the forced convection by electrochemically induced gas stirring. The simulation of natural convection is based on the different density values in the boundary layer at the electrode surface given by a density/concentration correlation. The copper concentration - linked with the current density by Faraday law - is solved by an additional transport equation. The simulation of the forced convection by the electrochemically-induced gas stirring is done by using a real two-phase calculation. That means that all differential equations are solved again for the second phase. The numerical solution of the fluid flow field is compared with the results of LDA- measurements, which were done in a special cell. The software for the LDA enabled a calculation of the void fraction possible and therefore a rough estimate of the mass transfer coefficient through the prevailing gas bubble induced convection can be made by assuming the influence of relative bubble volume.

Jan 1, 1999

By Pertti Pekkala

Outokumpu has 25 years of experience in the SX area. The development of the solvent extraction plants responds to an ever increasing demand for lower operational costs wd for adaptability to process disturbances with minimized risks. In this paper the features of the VSF ("Vertical Smooth Flow") SX technology are described, such as the separated pumping and mixing, the homogenous gentle mixing, the droplet coalescence and the ultra pure settling. A major advantage of the mixing technology is the high stage efficiency of above 99 per cent. The connection between this and some features of the settler front section is clarified. The present design of VSF plants is based on experience of existing operations at, for example, Zaldivar, Radomiro, Morenci, Kokkola and Harjavalta. These production plants cover a unit capacity range of 60 to 3,600 m3/h expressed as a total flow. It is evident that there are no restrictive factors to increase the total flow up to 5,000-6,000 m3/h by introducing the VSF technology. The copper SX technology has a long history reflecting many individual features of the separate copper SX plants. Still it is necessary to verify all actual running parameters by pilot tests taking into account impurities, chemicals used etc. The design of SX plants is not only about the delivery of equipment but also a process concept, and it is best tailor-made and adapted to specific local requirements.

Jan 1, 1999

By Kongfang Feng, Fei Ruan, Zhiyu Liu, Jieyu Zhang, Xin Hong, Shaobo Zheng, Jixu Wang, Jinyin Xie

"Mixing phenomena in smelting reduction furnaces with asymmetric side blowing were studied in this paper. Mixing phenomena in a smelting reduction furnace was represented as the mixing time by electrical conductivity measurements. Experiments were performed in a water model under various operating conditions to determine the effects of horizontal angle, radial angle, inserting depth, flow rate of the upper and the lower side nozzle, the included angle between the upper side nozzle, and the lower side nozzle on mixing phenomena in smelting reduction furnace. Comparing mixing time and mixing phenomena, the optimal conditions were obtained for an asymmetric side blowing process.IntroductionIn recent years, many countries have put forward development strategies for saving resources and environment-friendly, the development of various industries had to face its influence for resources and the environment .As we all know, the steel industry is a pillar industry of the global economy, in which ironmaking is an important part of it. In the modern ironmaking process, the blast furnace is regarded as the most important equipment and tool. But with the increasing scarcity of metallurgical coke resources and considering the environmental impact of such processes, metallurgists proposed the concept of smelting reduction. Smelting reduction processes to produce hot metal from iron ore and coal were being developed as a possible alternative to the traditional blast furnace. At present, a number of smelting reduction processes had been developed all over the world, they were mainly included COREX, HISMELT, FINEX, DIOS, etc."

Jan 1, 2012

By Jamil M. Khalifeh, Shadia J. Ikhmayies, Bothina A. Hamad

"The structural and electronic properties of cubic d -NbN are investigated using density functional theory (DFT) and all-electron full potential linearized augmented plane wave method (FPLAPW). The equilibrium structural parameters are determined by fitting the total energy as a function of volume to the Murnaghan's equation of state. We calculated the total and partial densities of states (DOS) and compared them with those computed by different authors. Our DOS at Fermi level is found to be very close to the experimental value. The band structure is computed, discussed and used to find the characteristic energy separations. Valence electron density contours are recorded and discussed. We deduced the partial charge densities of different bands and binding energies of valence core levels and compared them with experimental and theoretical results obtained by different authors.IntroductionNiobium nitride has been intensively investigated over the last decades because of its interesting physical properties and technological applications (superconducting microdevices, microelectronic, catalytic probes, and hard coatings) [l]. While the group IV transition metal nitrides (TMN) mainly crystallize in the cubic NaCl structure (Bl type), those of group V and VI nitrides occur as different phases. Thus for niobium nitride, many phases have been reported in the literature: cubic fcc d -NbN, tetragonal ? -Nb4N3, hexagonal d -NbN, hexagonal e -NbN, and low nitrogen content hexagonal ß -Nb2N [l, 2].Structural and electronic properties of niobium nitride were investigated theoretically and experimentally by many authors. For example, in 1975 Schwarz [3] obtained the partial density of states for NbC and NbN from APW band structure calculations. In 1975 Kallne and Pessa [4] studied the electronic structure of Nb, NbC and NbN by using X-ray emission. In 2003 Amriou et al. [5] studied the electronic structure and bonding mechanism of NbC and NbN compounds using first principle total energy calculations using the full-potential linearized augmented plane wave method. Also in 2006 Sanjines et. al [l] studied the electronic structure of the hexagonal~Nb2N, hexagonal' d -NbN, and cubic d -NbN thin fihns by using X-ray photoemission spectroscopy. They [l] also calculated the densities of states for these phases and used them in the interpretation of the experimental valance band spectra. Most of these studies are old and there is a need for more recent studies. According to our knowledge, there are little comprehensive theoretical studies on this subject by using FP-LAPW method [5], which proved its ability to give accurate results. In this work we used the FP-LAPW method to study the structural and electronic properties of the cubic (fee) o-NbN (space group Fm-3m, prototype NaCl) crystal."

Jan 1, 2013

By Yotamu Stephen Rainford Hara

"The study focuses on the reduction mechanisms of copper, cobalt and iron during carbothermic reduction of copper-cobalt mineral sulphide concentrates in the presence of lime, in the temperature range of 1073K and 1273K. We have used three types of mineral concentrates which were derived from froth flotation from the Copperbelt region in Zambia. The reduction mechanisms were studied using thermogravimetric analysis in which selected reactions were stopped at different times for characterising the reaction mechanism using optical microscopy, XRD and SEM-EDX analyses. Using SEM-EDX analysis, we have analysed in details the stages of metallic phase formation during reduction process. Metallic cobalt and iron were embedded into copper, thereby permitting magnetic separation of the reduced metals even though copper is diamagnetic. Methods of preferential reduction of metal values were investigated by analysing the metallic phase formation.IntroductionIn conventional smelting or converting of copper sulphide minerals, metallic copper forms by giving off S02 gas on. Although in terms of overall energy balance the selective oxidation for metal production has major advantages, the process suffers from drawbacks in smelting complex concentrates containing copper, cobalt and iron sulphides minerals and these are: (i) cobalt and iron are oxidised, and consequently cobalt is lost into the slag phase. (ii) The volume of S02 gas produced is in low concentrations, which is insufficient for extracting sulphur or manufacturing sulphuric acid. The release of dilute S02 causes serious environmental pollution. The major cause for the loss of cobalt and iron into the slag, is due to that fact that the oxides of these metals are more stable than their sulphides. Since cobalt and copper are more valuable than iron, reducing conditions are required in a separate slag treatment reactor using electric arc melting for recovering the lost metal oxides from slag. This energy-intensive step makes metal making expensive.During chemical beneficiation of mineral sulphides (Cu2S, CoS, FeS) in the presence oflime (CaO), two types of equilibrium conditions may be set up either by forming CaS under reducing conditions, or by stabilizing CaS04 under oxidising conditions [l]. By comparison in the presence of carbon, CaS and metallic phases form, enabling the recovery of metals from sulphide minerals, which have been investigated by a number of authors [2-9]. During reduction of metal sulphide in the presence of lime and with carbon, it has been proven that the overall reaction le proceeds via two main steps: [5, 8, 9] (i) the anion exchange reaction between metal sulphides (MS) and CaO as shown in equation la, followed by (ii) the reduction of metal oxide (MO) via reaction lb."

Jan 1, 2013

By Mark Khinkis, Huajun Yuan, Mark Zak, Yaroslav Chudnovsky, Aleksandr Kozlov

"An afterburner for green petroleum coke calcination in electrothermal fluidized bed was designed, fabricated, installed, and tested on a pilot fluidized bed calcination furnace. The experimental set-up comprised a combustion chamber, in which fine particles and volatiles of the furnace off-gas were fully combusted, and a cooler equipped to calculate the related heat recovery and losses. Off-gas composition was analyzed to evaluate the combustion process. The energy balance confirmed the potential to recover a large part of the heat value of volatiles and fme particles from the GPC. Potential future applications of the results are discussed.IntroductionGreen petroleum coke (GPC) is an oil refining byproduct that can be used directly as solid fuel or as feedstock for the production of calcined petroleum coke [1-2]. GPC contains a high amount of volatiles and sulfur. With coke calcination, the GPC is heated to remove the volatiles and sulfur in the calciner off-gas to produce purified calcined coke, which is used in the production of graphite, electrodes, metal carburizers, and other carbon products. Currently, more than 80% of calcined coke is produced in rotary kilns or rotary hearth furnaces. These technologies provide partial heat utilization of the calcined coke to increase efficiency of the calcination process, but they also share some operating disadvantages [3]. On the other hand, coke calcination in an electrothermal fluidized bed opens up a number of potential benefits for the production enhancement while reducing the capital and operating costs.The increased usage of heavy crude oil in recent years has resulted higher sulfur content in green coke produced from oil refinery process, which requires a significant increase in the calcinations temperature and residence time [ 4]. The calorific value of the process off-gas is quite substantial and can be effectively utilized for combined heat and power (CHP) production to complement the energy demand. Waste heat recovered from the product cooling could also contribute to the overall economics of the calcination process. Preliminary estimates indicated the decrease in energy consumption by 35-50% as well as a proportional decrease in greenhouse gas emissions. So, efficiency improvement of the coke calcinations systems is attracting close attention of the researchers and engineers throughout the world."

Jan 1, 2014

By E. A. Werner, A. Pichler, A. Spalek, G. Reisner, P. Stiaszny

"Interstitial free (IF) sheet steels are used for complex shaped parts because of their excellent formability. If a deep drawn part is subjected· to a impact deformation at low temperature brittle fracture of the part may occur. This phenomenon\ is called secondary work embrittlement (SWE). One possibility to characterize this material/structural behavior is the drop-weight test. The result of .this .test is a temperature at and below which a crack can initiated in a deep drawn part under the investigated set of parameters. This paper addresses the influence of the preforming process on the sus- . . ceptibili.ty of IF steels to SWE.IntroductionInterstiiial:free (IF-) steels are frequently used in the automotive industry for complex· shaped p·arts because of their excellent deep drawability. The microstructure of the steel consists of a highly ductile ferritic matrix with embedded precipitates of nitrides and/or carbides. Brittle fracture can occur in deep drawn parts, if they are subjected to a high speed deformation at lo""w temperature. This phenomenon is called ~econdary Work gmbrittlement (SWE) [1-11]. Up to now there are no standardized testing procedures available to quantify the sensibility of IF-sheet steel to SWE. Neveitheless, a reasonable testing procedure which allows to quantify the tendency of a predeformed part to SWE is necessary for further material development. A commonly used test method is the drop-weight test performed at low temperatures. In such ·tests a cone-like drop weight expands a deep drawn cylindrical cup [l-3, 6, 8, 9, 11]. From this expansion experiment the temperature is determined at and below which a brittle crack can be initiated in the deep drawn cup under the investigated impact test parameters. The highest measured temperature at which a deep drawn cup fails by brittle fracture is called frack appearances !emperature (CAPT). The lower the value of the CAPT the lower is the sensibility of a deep drawn part of IF-sheet steel to SWE. This paper aims to clarify the role of the preforming process on the impact behavior of an IF steel. For this purpose a numerical analysis of the deep drawing process and cup expansion tests are conducted."

Jan 1, 2000

By S. K. Varma, Miriam Regalado, Daniel Salas, Erica Corral, Erika Esquivel

"Age hardenable 2014 aluminum alloys and composites containing 0.10 and 0.15 volume fractions of alumina particles (VFAP) have been solutionized at 540 and 550°C for up to 20 hours. The solutionized samples, heat treated for 5 and 20 hours, have been subjected to room temperature rolling until cracking develops. The work hardening curves have been compared to determine the effect of solutionizing time on the rolling characteristics from both hardness and the microstructural evolution points of view. Solutionizing at two different temperatures results in differences in the extent to which the composites can be rolled until fracture. The microstructural characterization by TEM has been performed to understand the room temperature rolling behavior.IntroductionThe effect of solutionizing on the age hardening response of 6061 and 2014 aluminum alloys and composites reinforced with 0.10, 0.15 and 0.20 volume fractions of alumina particles (VFAP) have been reported in the literature [1-4]. A comparison of the monolith and composites indicates that particles promote the aging process through differences in the microstructures in solutionized condition. The first effect of solutionizing is to produce a grain growth process which follows a grain growth law (square of grain diameter as a function of solutionizing time). It appears that it is possible for vacancies to be emitted during grain growth period as they try to minimize the total grain boundary surface area by increasing their diameter. This may be common to both the monolith and the composites. However, the second effect must be exclusively considered for the composites. The particles generate dislocations during the solutionizing process due to the differences in the values of the coefficient of thermal expansion (CTE) between the particles and aluminum base metal. It has been determined [1] that the dislocation density increases with increase in solutionizing time in the composites of 6061 aluminum alloys reinforced with 0.10, 0.15 and 0.20 VFAP. The improved bonding between particles and matrix can give rise to additional generation of dislocations due to curvature effects [1] with the result that the dislocation density continues to increase with increase in solutionizing time even after the CTE effect is considered to have been stabilized."

Jan 1, 1998

By K. Itagaki, H. Henao

"The experimental study on the phase equilibrium and distribution of minor elements such as chromium and copper between magnesia saturated FeOx-MgO-SiO2 slag and Fe-Ni alloy were carried out under controlled oxygen partial pressure between 10-6-5 and 10-10 using CO and CO2 mixed gas at 1773 and 1873 K.The effect of slag additives such as lime (CaO/SiO2 molar ratio: 1) and alumina (AlO1.5/SiO2 molar ratio: 0.1) on the distribution behavior of the minor elements was also investigated.The value of distribution ratio for chromium, defined by (%Cr in slag)/[%Cr in alloy], is larger than 70 at the pO2 region conducted in the present study for the MgO saturated FeOx-MgO-SiO2 slag at 1773K. These value are almost 4-order higher then that of nickel though the distribution ratio of copper shows similar values with nickel. Analysis of the data indicates that addition of lime in the slag and the increase of temperature reduce the dissolution of chromium into the slag and the addition of aluminum increases the dissolution of chromium into the slag while reduces the dissolution of copper and nickel.IntroductionChromium. is a minor element in a nickel oxide ore but a Japan major component in the secondary material of stainless steel and is also introduced in the Fe-Ni production process due to dissolving bricks of a furnace. Chromium is a concerned matter for the beneficial utilization and disposition of ·slag because Cr6+ is a harmful element. Considering Fe-Ni as an alloy component in steel making, and the demand of high purity nickel, chromium is an -undesirable element that has to be eliminated into slag prior to the steel making, or the production of high temperature refractory alloys. On · the other ·hand chromium is an element of steel alloy for many applications, thus Fe-Ni containing chromium in minor element is desirable in some stainless steel making."

Jan 1, 2000

By R. Boussaa, Y. Fautrelle, K. Zaidat, O. Budenkova, B. Saadi, X-D. Wang, L. Hachani, H. Ben Hadid

"Comparison of experimental data obtained in a benchmark experiment of solidification of a Sn-3%wt.Pb ingot and numerical results of two-dimensional and three-dimensional simulations of the process is presented. The benchmark experiment consisted in solidifying a rectangular ingot of Sn-3%wt.Pb alloy using two heat exchangers. Conditions of solidification were thoroughly controlled due to six thermocouples embedded into each heat exchanger. Due to another array of thermocouples the evolution of the temperature field at a lateral wall of the crucible was registered during the whole experiment. A treatment of the temperature data provided an estimation of the velocity field in the experiment. Post-mortem analyses of the sample provided the pattern of macrostructure of the sample and qualitative segregations pattern. 2D and 3D numerical solidification models are developed to give the distribution of the solute in a solidified sample.IntroductionConvection, either natural or forced, plays a very important role during the solidification. Its intensity and flow pattern affect heat and mass transfer and, consequently, macrostructure and segregation in a solidified ingot [1-4]. The effect of buoyancy convection during solidification has been studied in many laboratory-scale experiments [5-6]. Due to these experiments a general comprehension of formation of various defects in the ingot has been achieved. However, mentioned studies were not consistent since alloys, solidification conditions and configurations were every time chosen arbitrary. That is why the role of each parameter characterizing solidification process remains unclear. Moreover, the question of reproducibility of defects under the same solidification conditions still exists. In addition, most of the experiments suffer from the insufficient knowledge of control parameters that makes difficult their use for validation of models for solidification. These parameters serve as boundary conditions for numerical modeling and their incomplete description leads unavoidably to the errors in simulations. This situation motivated us to develop a setup for benchmark solidification experiments and to perform a set of the solidification experiments which we reported in [7]. Here we presented a comparison between results obtained in a benchmark experiment of solidification of Sn-3%wtPb ingot and its numerical modeling, which was performed in two-dimensional and three-dimensional configurations."

Jan 1, 2012

By Y. Iguchi, T. Narushima, T. Shiozawa, M. Maruyama, R. Arashi

"In situ observation system for thermal oxidation using Raman spectroscopy' was constructed, and oxide films formed on liquid pure Al and Al-Mg alloys (Mg contents = 1 and 4 mass%) were analyzed at room temperature to 1273 K in dry oxygen. In situ Raman spectra of the surface of a liquid Al-:-4mass%Mg indicated the formation of MgO • AlP3 (spinel) as oxidation products, while a -AlP3 and MgO • Alz03 (spinel) were observed on a liquid Al-1mass%Mg alloy. It was suggested that the formation of MgO film affected oxidation behavior of these alloys.IntroductionLiquid aluminum alloys are cast to ingots mainly by the continuous casting process. It is well-.known that surface cracks could be caused by oxide films formed on the surface of melt during continuous casting and defects due to the film. With regard to oxidation behavior of liquid aluminum alloys, many investigations l -s have been carried out from the view point of formation of ceramic metal composites(CMC) which are expected as cutting tools and structural materials 1.2. It is very important for reasonable continuous casting and CMC formation processes to elucidate oxidation behavior of melts.Oxidation behavior of materials generally depends on compositions and properties of oxide films formed on the surface. If in situ observations of oxide films are available during oxidation, evaluation of oxide films and interpretation of oxidation mechanism could be expected. Laser Raman spectroscopy is one of the most appropriate techniques for in situ observation of oxide films under various atmosphere at high temperatures. The authors have discussed the effects of atmospheres and sample compositions on oxide film formation mechanism on Fe-Si alloy6 and SiC-B4C composite7 on basis of an in situ observation by Raman spectroscopy. In spite of many previous studies, systematic and clear explanations have never been gotten on oxidation behavior of liquid aluminum alloys. And no in situ observation has been made except for transmission electron microscopy(TEM) and X-ray diffraction(XRD)."

Jan 1, 1996

By W. C. Hellyer

The papers in this section provide several examples of the application of Process Mineralogy to metallurgical problems. Any experienced metallurgist could cite numerous other examples when process mineralogy has, or could have, provided data of value in his understanding of metallurgical processes. The data developed by mineralogic techniques may supplement conventional chemical analyses, but cannot be replaced by assays. Mineralogic and chemical analyses each provide different types of information. In order for the process mineralogist to interpret his results in the most useful manner, it is desirable that he should have some knowledge of metallurgical processes. Conversely, the metallurgist should have some knowledge of mineralogic techniques to understand the scope and limitations. Mineralogic examinations are time-consuming and expensive. To ensure the effort is not wasted, and indeed does not generate misleading information, the utmost care must be taken at every stage of sampling and sample preparation. The mineralogist may examine microscopically or by x-ray diffraction a one-gram sample representing a flow of possibly thousands of tons per day through a concentrator. Conditions in a concentrator change continually in response to changes in feed rate, feed characteristics, grind, reagent additions, temperature, circulating loads, etc. Lengthy sampling periods are required to ensure the samples examined are representative of average conditions. The sampling program should be drawn up jointly by the metallurgist and mineralogist. Sampling points should be selected with a view to ease of sample cutting. The sampler should be instructed in the method of cutting the samples, the weight or volume of sample to be taken at each cut, the sampling frequency, and sampling period. The sampling period required depends on the scope of the investigation. For example, if a complete survey is to be made of all final and intermediate products of a flotation concentrator, samples should be cut at not more than two-hour intervals, twenty-four hours per day, for not less than one week. For a more limited investigation of one circuit or one section of a concentrator, 'the sampling frequency could be increased to every hour and the sampling period reduced to one or two days.

Jan 1, 1981

By Adam Powell, David Dussault

"Electric Field-Enhanced Smelting and Refining is a process for driving the reaction between carbon in hot metal and iron oxide in slag, for example, in a steelmaking reactor. This process involves inserting electrodes into the slag and metal phases, such that the overall reaction FeO + C -> Fe + CO is separated into two half-cell reactions: Fe2+ + 2e· -> Fe at the cathode in the slag, and C + O 2 • -> CO + 2e· at the anodic slag-metal interface. Without the electrodes, the reaction is very slow, but with electrodes, the additional surface area available to the ferrous ions for reduction accelerates the reaction even without any applied bias. When a bias is applied to the electrodes, the electric field across the slag further accelerates the overall reaction.With or without applied bias, the process is first-order in the ferrous ion concentration, and limited by ferrous ion transport to the cathode. To complicate matters, as the liquid iron is reduced at the cathode, the Mullins-Sekerka instability leads to formation of dendrite-like liquid iron fingers which grow into the slag. Because of this, the design of the cathode can have a significant effect on the overall process kinetics, and understanding of the dynamics of these fingers and of their effect on mass transfer is necessary for the intelligent design of the overall process and the cathode in particular.Toward this end, a detailed mesoscopic two-phase slag-metal model is presented here which describes multi component diffusion in the slag and fluid flow in both phases in the vicinity of the cathode. Diffusion in the slag is driven by chemical and electrical potentials. The phase boundary is modeled as a diffuse interface using a phase field approach. Because this electrochemical reaction occurs at high-temperature, the kinetics of charge transfer and adsorption through the double layer are fast relative to transport, permitting the use of simple linear reaction kinetics. This also eliminates the need to discretize the double layer, with the result that charge neutrality may be assumed everywhere in the domain. Introducing electric field dependence of the gradient potential and well height coefficients in the free energy function allows the model to capture electrocapillarity at the interface."

Jan 1, 2001

By Norberto Benitez, Christian Ludwig, Simona Regenspurg, Fabian Mendez

"Navarro is the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it collects about 1.600 tons of waste daily. The environment surrounding Navarro is highly contaminated and the pollutants released by the dump threaten human health in the adjoining neighborhoods. The goal of our project is to identify major pollutants released from the dump and their distribution in the surrounding ecosystem. In a first phase of the sampling and analysis program landfill leachate was collected and screened for heavy metals and for the most common persistent organic pollutants. This allowed us to identify the most relevant compounds on which we focused in a more detailed second phase investigation. These compounds were quantified in the vicinity of the landfill (groundwater, surface water, drinking water and soil) to get information on their mobility and possible pathways into the human body.IntroductionThe usual technique of waste disposal in most developing countries is by landfilling on not -, or not well controlled sites, where people live close by or even on the waste itself. A typical example for this practice is Navarro, the main garbage dump in the city of Cali (Colombia). Operated since the late 1960s it now consists of about 23 million tons of household and industrial waste. The dump is located on a wetland in the riverbed of the Cauca River, the main drinking water source for Cali. Two ponds of unknown permeability located next to the landfill collect a fraction of the waste leachate. During the rainy season, the ponds frequently overflow and drain into the soil (alluvial, loamy sediments) of surrounding sugar cane fields. The environment of Navarro is assumed to be highly polluted and there is evidence that it affects the health of nearby inhabitants. Specifically, the incidence of respiratory diseases was higher among vulnerable individuals (<3 and >50 years old) living in a <3 km perimeter of Navarro as compared with a control group (Solano et al., 2006). Further, a clustering of extremely rare congenital malformations (sirenomelias and cyclops) was observed in a small area during a short time period (<6 months) (Filigrana et al., 2008)."

Jan 1, 2008