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By C. A. Morais

The present work describes the development of an efficient and relatively simple process to obtain high grade CeO2 from a mixed rare earth chloride solution. The process involves cerium oxidation and precipitation by addition of a KMnO4-NaCO3 solution. The experiments were carried out at room temperature (25 1° C). The results indicated that the major parameters affecting cerium recovery are the molar ratio of KMnO4/Ce, the initial acidity of the chloride feed solution and final pH of Ce(OH)4 precipitation. In strong acid solutions (pH < 1), the oxidation of Cl to Clo took place in addition to the oxidation of Ce(III) to Ce(IV), so increasing the permanganate consumption. Conversely, low acidity (pH >3) led to coprecipitation of the other rare earth elements. Under the selected conditions, cerium was selectively precipitated as ceric hydroxide, together with some manganese dioxide. Further purification was carried out by the dissolution of Ce(OH)4 in HCl, followed by precipitation as cerium carbonate. The filtrate was neutralised with a Na2CO3 solution in order to recover the associated rare earth elements for further separation. The final product, assaying 99.7 % CeO2, was obtained with a recovery of nearly 100%.

Jan 1, 2003

By R. M. Westcott

A two-electrode, direct current, slag resistance furnace (SRF) has been constructed and operated to selectively reduce the zinc and lead contents of non-ferrous slags. The experimental SRF is equipped with multiple methods of gas/solids injection for both mixing and reaction. A computer is used to position the electrodes and for data acquisition. A geometric factor correlation was previously developed at Columbia University for calculating the electrical resistance on the basis of furnace geometry and slag conductivity. The experimental SRF was used to test this correlation.

Jan 1, 1994

By Lan Li, Izaak Williamson

"The efficient separation and storage of CO2 from power plant flue gases can reduce the amount of CO2 released into the atmosphere and mitigate global warming. Potential candidates for industrial applications are solid sorbent materials. Crucial factors to control the efficiency of porous sorbent materials include the framework and pore structure, and the chemical and physical reactivity of CO2 within the pores. Computational modeling approaches, based on density functional theory (DFT) and van der Waals-DFT, have been applied to nanoporous solid – manganese dioxide a-MnO2. We found that the types and charges of cations as dopants in the a-MnO2 and the concentration of CO2 influence the structural features of a-MnO2, which control its CO2 selectivity performance within the flue gases.IntroductionCarbon capture and storage is a technique to separate large quantities of CO2 from power plant flue gases before being released into the atmosphere. Porous solids are a potential candidate as sorbents to “trap” CO2 through chemical or physical adsorption on their porous surfaces[1]. Such separation efficiency is determined by the size and shape of its pores and by the interaction between the porous surface and the gas adsorbates. The incorporation of cations into the pore can act as a means of structural support and alter the pore diameter to be comparable to the kinetic diameter of the gas adsorbate, such as CO2.A porous solid of particular interest for CCS is manganese dioxide a-MnO2, an octahedral molecular sieve (OMS) composed of edge-sharing MnO6 octahedra that are linked into a nanoporous framework[2]. The framework consists of (1×1) and (2×2) tunnels, referred to as OMS-2. Due to the larger tunnel size, cations and gas adsorbates prefer to reside along the (2×2) tunnel axis of the OMS-2. As seen in Figure 1, a potassium cation K+ is located in the (2×2) tunnel, known as cryptomelane-type MnO2. Its pore diameter of ~ 4.6 Å gives it a good CO2 selectivity performance, because the diameter is comparable to the kinetic diameter of 3.3 Å for CO2[3]. Alternatively, replacing potassium K+ with other cations, e.g. barium Ba2+, sodium Na+ or lithium Li+, in the OMS-2 tunnel is of great research interest, due to the effects of their concentrations, types and charges on the CO2 selectivity efficiency and sorption hysteresis phenomenon[2,4]."

Jan 1, 2014

By K. A. Elbarawy

Processing of Egyptian barite ore with a composition of 85.5% BaSO4; 2.75%SiO2;1.56%Fe2O3 and 5.1% Al2O3 was performed with the aim to prepare pure barium salts. The process took place through pelletization-solid state reduction and leaching steps. Each of these steps was optimized. Pure barium sulphate (99% < 0.82µm) and carbonate (99%<0.75µm )were the final products. This article deals with the reduction process that occur whn coal was added to the ore during pelletization in the ratio of 5:1 stoichiometry. Optimum reduction of pellets of 8-12mm in diameter was achieved after 60 minutes at 1050oC and under a rate of 5 lmin-1 of nitrogen atmosphere, where 87.79% of the ore was reduced. The kinetic studies showed that the reduction process could be modeled according to the core mechanism of diffusion control in which the effective diffusivity is based on the surface area of unreacted ore. The activation energy calculated was 92.7 kJmol-1.

Jan 1, 2006

By José Roberto de Oliveira

Based on literature review one can see that the main objectives of MnO reduction is the comprehension of slag interactions and reactions with other elements beyond carbon. That&apos;s because it is worthwhile to study pure MnO reduction, where there will be not oxides interaction and just carbon will be the reduction agent. By a thermodynamic analysis we know that Si can react with MnO, then it&apos;s important to study this influence, so as Mn content. Our work aims to develop kinetics parameters for the MnO reduction, varying Mn and Si contents in bath. This has been given by pressure measure of CO in a Fe-C bath. The CO is generated by the oxide reduction with carbon. It has been proved that: - Mn content decreases the MnO reduction; - the MnO reduction is mainly influenced by Si content in a bath containing Iron, Carbon and Manganese so as Silicium

Jan 1, 1997

By Tabbetha A. Dobbins

We report studies concerning the time frame for catalytic reactions between NaAlH4 (sodium alanate) and TiCl3 during high energy milling. Spectral features in x-ray absorption spectra were analyzed for samples milled for various times (0 minutes, 1 minute, 5 minutes, 25 minutes, and 125 minutes). A structural transition from Ti3+ to Ti0 is observed within the first 5 minutes of milling. The Ti0 structure persists for samples milled for times longer than 5 minutes?even after those samples underwent a subsequent single hydrogen desorption/absorption cycle. Samples milled for less than 5 minutes retain Ti3+. For samples milled for 1 minute, the Ti-K edge position shifts from Ti3+ to Ti0 after a single desorption/absorption cycle. However, the first coordination sphere around the Ti0 absorber occurs at longer distances for 1 minute milled sample. These results hint at the formation of Ti0 pure metallic clusters upon desorption/adsorption cycling of 1 minute milled sample. Previously reported x-ray absorption spectroscopy studies have demonstrated the structural transition from Ti3+ (in TiCl3) to Ti0(determined to be TiAl3 found at the surface of the alanate powder). Aluminum deficiency on the NaAlH4 lattice is responsible for controlling hydrogen absorption capacity. These time-resolved spectroscopy studies suggest the possibility for controlling aluminum deficiency, while still maintaining titanium activation of the alanate powder, by manipulating the coordination environment of the titanium dopant during the first five minutes of high energy milling. Specifically, a possible approach to mitigating aluminum deficiency during doping would be to introduce an alternative species to which the to Ti3+ catalyst would form a metallic bond after the TiCl3 has attached at the surface of the sodium alanate powder and before the Ti3+ forms the TiAl3 intermetallic species.

Jan 1, 2006

By Carl W. Dalrymple

A wide variety of contaminants (heavy metals, suspended solids, colloids, oils, organics) have been successfully removed from wastewater using an electrocoagulation process. An innovative electrocoagulation system is described. This process involves a procedure which subjects dissolved and suspended wastewater contaminants to the simultaneous addition of metal ions in the presence of direct current. During the treatment process Ionic and other charged particles in the wastewater are neutralized with oppositely charged ions generating the coagulation of contaminants: The process Is called CURE, and&apos; presented here with application to wastewaters containing mainly heavy metals.

Jan 1, 1995

By K. H. Bech, S. T. Johansen

"The mass transfer at fluid-fluid interfaces due to turbulent agitation is investigated theoretically. In particular a theory is derived for interface stresses due to interface energy and surface renewal. This theory indicates that surface renewal may take place if the geometry is sufficiently large and if surface tension is sufficiently low.By using a model for a typical turbulent structure we compute the interface mass transfer for a stressless interface and a fully interface. Results for the general situation is not presently available. The computed results are used to derive analytical expressions for the mass transfer based on turbulent kinetic energy and free stream turbulent length scales.One important application of the theory is the mass transfer at the electrolyte side of the bath-metal interface in the Hall-Heroult process. For this process we show that mass transfer should be expected to be of the rigid surface type."

Jan 1, 1999

By B. Thompson

"1. AbstractMagnesium alloys have been successfully recycled for decades and have won acceptance for use by die casters and most of the automotive industry. As the supply chain for magnesium and magnesium alloys continues to change, due to the consolidation of producers, it is essential that quality control methods be closely examined with each new supplier added. An examination of the various process steps that are needed to assure quality in the final product will be discussed thus giving a basis for the auditing of new magnesium suppliers.2. IntroductionMagnesium recycling in the past has been somewhat limited due to its use more as an alloying agent for aluminum based alloys and as a desulfurization agent in iron and steel than in more readily recycled structural products. Recycling efforts continue to improve as more production is finding its way into automotive structural components, hand tools, and a variety of computer and cellular telephone applications.With the closure of several large North American primary magnesium production facilities over the past decade we have only recently witnessed a tightness in supply that is driving magnesium prices significantly higher, nearly doubling the price in the last year alone. The rapid escalation in pricing will provide additional economic incentives to fully utilize recycling for the recovery of an even greater percentage of both old and new sources of magnesium scrap. Political pressure continues to intensify towards the secondary recovery of any and all recoverable resources of which magnesium recycling readily applies.Economics will also likely drive the development of new sources of magnesium production, both from primary and secondary production. As new sources of magnesium are offered to the marketplace the potential for product quality issues may increase. When considering any new raw material supplier a decision must be made as to the impact of defective material on the intermediate or finished product. Quality defects in magnesium ingot can result in a variety of appearance, corrosion, and even adverse structural effects in the finished product. The potential severity of the impact of defective raw materials on the finished product will determine and often justify a close look at any new supplier. An on-site audit of a new supplier of a critical raw material is often justified to ensure that an adequate quality assurance system is in place. We will now look at a number of key production points that should be examined during an on-site audit that have can have an impact on the overall quality of the finished product."

Jan 1, 2008

By Akira Kaneda

Mitsubishi continuous process employs an electric furnace for settling matte from slag. Electrodes are immersed into the slag layer in the slag-cleaning furnace and the temperature of the melt is maintained at a predetermined level by Joule&apos;s heat. Electrodes are immersed to the depth where the current of each electrode is kept at a set value, and they are raised or lowered automatically to compensate for the deviation from it. Because electric resistance of the bath is varied with the matte level in the furnace and the composition and temperature of the slag, the immersion depth of the electrodes is affected by them. Therefore by monitoring the immersion depth and its change with time, abnormal situations in the furnace, such a~ rise of matte level or local abnormal state of melt, can be detected. In this paper, relations between state of the furnace and electrode behavior are discussed based on the plant data, and then a new and simple monitoring method of the condition of the furnace is proposed.

Jan 1, 2001

By Michael L. Sorokin

The metallic nickel production by converting of nickel matte is analysed from the thermodynamic point of view using earlier developed thermodynamic models for sulphide, metal and slag phase. Three-suffix Margules equations are used to calculate thermodynamic properties of melts. Potential diagrams of Ni-FeS-OSiO2 system are calculated for various temperatures and Fe to Ni ratios. The diagrams used for consideration about possibilities of the direct one-stage metallic nickel production.

Jan 1, 1995

By A. V. Tarasov

In the course of research aimed at improving the performance of the Vanyukov smelting process (VP) for treating sulfur raw materials in a pilot-scale furnace it has been found that an increase in the calcium oxide content up to 12% to 14% in case of smelting to produce high-grade matte results in a decrease in the copper content of slag by 0.05% to 0.3%. The residual copper content of slag can be computed by a formula taking into account an increase in the calcium oxide content of the feed material and that in the slag. In the course of research for improving the performance of the zinc-containing slag fuming process with blowing of the slag bath with combustion products of natural gas it has been found that the silica and calcium oxide contents have an effect on the degree of zinc sublimation. In case of slag containing 24.4% SiO₂ and 6.95% CaO by weight (SiO₂:CaO = 3.51), the residual zinc content of slag was 3.25%. The minimum residual zinc content of 1.95% was obtained in case of slag containing 22.5% SiO₂ and 14.5% CaO by weight (SiO₂:CaO = 1.55). An increase in the CaO content of slag up to 16% by weight with a ratio of SiO₂:CaO = 1.25 to 1.35 permits minimization of zinc losses in slag by achieving a residual zinc content of final slag in the order of 1%.

Jan 1, 2006

By M Kolbe

Co-Cu exhibits a metastable miscibility gap in the region of the undercooled melt. Specimens have been undercooled and solidified containerlessly into the metastable miscibility gap in an electromagnetic levitation facility (EML) and in drop tube (DT) experiments. Due to the high undercooling the velocity of the solidification front is very high and the microstructure is frozen in instantaneously. The microstructure of samples processed in the EML is influenced by the electromagnetic stirring due to the induction of electrical currents into the melt. A variety of microstructures has been observed. After undercooling below the binodal the liquid melt separates into the Co-rich L1-phase and the Cu-rich L2-phase. Two basic morphologies of the L1-phase can be observed, they can be attributed to the transition in dendrite growth from diffusionally and thermally controlled to only thermally controlled growth. Transient microstructures are observed after solidification in the vicinity of the binodal. Drop tube experiments, which lead to a rapid solidification of a distribution of droplets under reduced gravity conditions, in contrary allow for the observation of the early stages of demixing: the microstructure shows a homogeneous distribution of spherical particles of the minority phase in the droplets. The cooling rate of the droplets and its dependence on the droplet radius has been calculated. The solidification velocity as a function of undercooling has been measured in the EML for the composition Co-lB.Bat%Cu. The data are analysed in the framework of the LKTlBCT model with a velocity-dependent distribution coefficient as well as within a model of Galenko and Danilov using a kinetic growth coefficient of u=0.22 m/Ks.

Jan 1, 2002

By James A. Warren

The phase field method has been successfully employed as both a tool to model heterogeneous materials and as numerical method for calculating the motion of interfaces and phase boundaries without explicitly tracking those interfaces. The method has been used to model a diverse suite of problems describing the microstructural evolution in materials. These models are derived from thermodynamic arguments and symmetry principles, and usually guarantee positive local entropy production for systems out of equilibrium. Descriptions of how phase field methods can be applied to the problems of solidification, grain growth, and electroplating will be presented.

Jan 1, 2001

By Robert G. Robins

Precipitation of ferric arsenate is an effective method for removing arsenic(v) from hydrometallurgical process solutions. The solubility and stability of this compound. FeAs04.2H20, has received some attention in recent years and the reported solubilities of amorphous and crystalline material have varied considerably. This paper reviews previous studies and reports some recent work with a consistent model to explain the variable results. Free energy data for ferric arsenate and its associated dissolved complexes are presented.

Jan 1, 1990

By Alex I. Kociubczyk, Wilky Desrosin, Lucía Mabel Boycho, Alicia E. Ares, Carlos E. Schvezov

In the present research, commercially pure Sn and Zn, and Sn-Zn alloys (Sn-1wt.%Zn, Sn- 2wt.%Zn, Sn-4wt.%Zn, Sn-8wt.%Zn and Sn-8.9wt.%Zn, weight percent) were obtained by a horizontal directional solidification process with two opposite senses and heat extraction. The solidification process was realized using a horizontal furnace with two heat extraction systems at both ends. The temperature was measured using eight K-type thermocouples and an electronic recorder of temperature data. The resulting structures were analyzed using optical microscopy. From the solidification process the thermal and metallographic parameters were determined in all samples. The presence of defects in the solidified pieces was observed. Internal defects pretended to be dependent not only on the composition of the alloys under consideration but also on the size of the structures formed, also, on the velocities and accelerations of interphases, and on the variation of thermal gradients. A model of the phenomenon from the first principles is presented.

Jan 1, 2015

By Saskia Duyvesteyn

Ion flotation is a technique applicable to the removal of metal ions from dilute solutions, using ionic surfactants.- While there are a number of physical and chemical parameters that influence the ion flotation process, this paper focuses on two of the important chemical ones, namely frother concentration and ionic strength. The effect of several frothers, including ethanol, iso-propanol and MIBC at concentrations ranging from 0% to 0.4%, was studied for the model Cd-dodecylsulfate and Cu-dodecylsulfate systems. The ionic strength, as well as the effect of monovalent and multivalent counter ions, was also studied in the range of 1@3 - 1 M, at constant pH. The results are discussed in terms of applicability to a range of effluents from minerals and materials processing operations.

Jan 1, 1994

By Jafar Safarian

Bauxite is the main raw material used for the production of alumina (Al2O3) through the well-known commercial Bayer process. This process has significant challenges such as limitation in using low-grade bauxites as they contain significant amounts of impurities such as Fe, Si, Ti. The Bayer process residue, which is known as red mud, is also a global environmental challenge due to huge amount of this low value residue production. An alternative sustainable process with high potential to solve these problems and produce valuable and consumable by-products is a pyrometallurgical-hydrometallurgical process in which the low-grade bauxite ore is treated through a smelting-reduction process, yielding iron alloys and a calcium-aluminate slag. Alumina is then produced from the slag by hydrometallurgical treatment. In the present work, the reduction of pellets produced from different bauxite ores by hydrogen is studied and it is shown that complete iron oxides reduction is possible. Further smelting and smelting-aluminothermic reduction of the reduced pellets show that iron and silicon ferroalloys can be produced, in addition to a proper slag for alumina extraction.

By D. W. Collins

Several organic and inorganic substances are widely used to control deposit structure and morphology during the electroprocessing of copper. Methods for monitoring the levels of thiourea, glue and guar gum during electrorefining and electrowinning have been successfully developed under the trade names of Reatrol and CollaMat. Other instrumental methods have been developed for additives and decomposition products associated with the electroplating of copper and other metals. Generally, these methods have been found to be either insufficiently sensitive or lacking in the desired selectivity for some or all of the additives. These procedures have mostly employed DC techniques; i.e., cyclic voltammetry, Tafel analysis, etc. In this work, chronopotentiometry (CP) and AC voltammetry were used to examine the interaction of glue, guar gum, thiourea and chloride during the electroplating of copper onto a platinum electrode. In addition, the interactions between the additives have been explored. It was found that glue in pure electrolyte (H2S04 and CuS04 only) had no effect on the chronopotentiogram. Glue was only active if chloride ions were present. The addition of thiourea resulted in several different chronopotentiograms depending on the presence of either chloride or chloride and glue. Thiourea used in conjunction with glue and chloride showed a significant increase in the polarization during copper deposition when compared to the electrolyte containing only glue and chloride. The use of a modified channel electrode further increased the sensitivity of CP. The use of AC voltammetry was explored as a technique to monitor some of the additives. AC voltammograms have more spectral detail then their DC counterparts and it is possible to monitor some of the additives at very low concentrations with AC techniques.

Jan 1, 1999

By Jie Ma, Bo Wang, Jieyu Zhang, Jian Zhao, Zheng Chen

"In this paper, solidification process of steel ingot was simulated by ProCAST software, based on cellular automaton-finite element (CAFE) model. A 22 t steel ingot was divided into continuous small zones (100x150x180 mm) in radial direction, then the temperature field, shrinkage cavity and porosity, particularly, the microstructure were simulated. The results show that: there was a columnar-to-equiaxed transition in microstructure on radial direction. Zones, closing to the center of the ingot, had a more developed and fined equiaxed zone, while zones closing to the periphery of the ingot had a more developed columnar zone. It indicated that temperature gradient has a great influence on microstructural morphology. Thus, the simulation results were highly agree with the experimental results, verifying the feasibility of this simulation method. It significantly reduces the time of simulation, and has important significance for predicting the microstructure of large steel ingot.IntroductionSolidification microstructure of steel ingot have a significant effect on the quality of the final steel products. Although many experimental works have been carried out in order to obtain the optimum condition for solidification process of continuous casting, it is also very desirable to establish mathematical models to simulate the evolution of solidification structure. The simulation methods can be divided into deterministic models and stochastic models, which have been developed rapidly over the last couple of decades. Cellular automaton method is one of the stochastic models. Rappaz and Gandin [1, 2], Nasatac and Stefanescu [3, 4] are the earliest researchers engaged in the this field. Moreover, Rappaz and Gandin simulated the solidification structure and CET (columnar grain to equiaxed grain transition) of metals using the CAFE method (cellular automaton-finite element method) for the first time [1, 2]. Recently, the CA (cellular automaton) model also considered the effects of fluid flow on the solidification process. Zhu, et al. [5-11] improved method of CA , they used the KGT model to describe the undercooling needed during the growth of the dendrite tip."

Jan 1, 2014