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By N. Kanarin

A thermodynamic study is reported on the chlorination of Fe(1-x.)O, Fe2O3, Cr2O3, MgO, Mg2SiO4 with chlorine in the presence or the absence of reducing atmospheres. The reactivities of these compounds as well as that of Mg3Si2O5(OH)4 using Cl2+N2, Cl2+air, and Cl2+CO gas mixtures were studied by non isothermal thermogravimetric analysis between 20 and 1000 °C. The same solids were chlorinated in a horizontal experimental set, during two hours between 350 and 1000 °C, in reducing and oxidizing atmospheres: The chlorination products were examined by XRD and SEM, and possible reaction paths were examined. Results indicate that the carbochlorination of these solids was better than their chlorination; Furthermore, the carbochlorination was performed at lower temperatures than those of the chlorination. Finally, the reaction extent was higher in the case of carbo-chlorination of these compounds. Based on these results, a process was suggested for the selective recovery of chromium compounds from the chromite concentrate.

Jan 1, 1995

By L. -C. Lai

A series of LaNi5-based alloys, with partial substitution of Ni by Al, Co, or V, were prepared The gas-phase hydrogen absorption kinetics and pressure-composition-temperature curves were measured The activation became easier and the plateau pressure was reduced as Ni was partially substituted by Al Substitution with Co reduced the hysteresis as well as the hydrogenation capacity, but enhanced the absorption kinetics Vanadium is often considered as a hydride former, but when it was added to LaNi5, it was found that V occupied the B site. A small amount of substitution of Ni with V led to a higher hydrogenation capacity and faster activation rate Based on these properties, an alloys LaNia 25CO0.5V0.1Al0. 15 was fabricated as an electrode. Compared with LaNi4.85Al0.15, it was found to exhibit faster activation, higher discharge capacity, and longer cycle life. The variation of the hydrogenation characteristics is discussed based on the physical and chemical properties of the alloying elements.

Jan 1, 1997

By Jin Liu

In the early 1990?s, Inco successfully installed two new flash furnaces as part of their SO2abatement project to reduce SO2 emissions from the Copper Cliff Smelter by 60%. The flash furnace off-gas is cooled and cleaned through two new Monsanto Dynawave gas cleaning systems that replaced the traditional venturi scrubbing system. It was discovered that the flash furnace production capacity is often limited by the capacity of the gas cleaning system. The key task is to eliminate pressure drop from the system. The froth column is responsible for by far the largest pressure drop in the gas cleaning system. Initially, the column was fitted with 22 plates. In 1994, both #1 and #2 froth columns were modified by reducing the number of plates in each column from 22 to 18 and increasing the interplate spacing on lower plates. With increasing demand for more throughput in the flash furnaces, further modifications on the froth columns were made in 2005. This paper describes these modifications and results together with some fundamental analysis of the froth column characteristics.

Jan 1, 2006

By Yu. A. Grinin, Yu. A. Sannikov, M. A. Lyamina, V. A. Shumskij, L. V. Slobodkin, N. N. Ushakov

This manuscript describes the Kivcet treatment of lead-bearing materials having high contents of copper and zinc. The tests were carried out on bulk concentrates from the Zyrianovsk Mining and Concentrating complex, "Kazzinc" JSC (Kazakhstan) with the following composition: Pb 37.6%, Cu 10.4% and Zn 6.8%. Two properties of the concentrate were under investigation: their calorific value and their desulphurization rate. By adding flux, the charge properties were brought close to the properties of high-grade lead sulphide concentrate. The charge was melted with high productivity. To ensure high copper recovery, Waelz residue was added to the charge. The residue contained more than 20% carbon and about 30% iron metal. The residue was partially replaced by coke that facilitates high copper recovery into the matte. The smelting achieved a production rate of 20 t/h with one burner. Lead recovery into the lead bullion was 88.8%; copper recovery into matte was 92.3%; zinc recovery into slag was 75.5%; and zinc recovery into the fume was 5.1%.

Jan 1, 2000

By Alan M. Peel

"Over the past years there has been an increasing demand by aluminium cast -house operations to obtain a greater return from their existing installed plant. This has included increasing existing furnace production capacity to match new and higher downstream production requirements, reducing melt losses and more efficient alloying.The paper discusses how Electromagnetic Pumping, which was developed for the combined purpose of;1. Melting light gauge aluminium scrap with a reduced melt loss and; 2. Effective circulation of the aluminium melt,has established its self in recent years, as an effective means of satisfying many of these industry requirements, but how it has also provided many other additional operational benefits to the aluminium cast house.The paper will discuss operational performance of the system with a particular emphasis on its effect on the metal bath quality (alloying, chemical and temperature homogeneity), metal recovery and increased production due to the high circulation.The technology having now been adopted by a variety of industry leaders has a number of prominent references and the paper will discuss the operational benefits and experiences from some of these."

Jan 1, 2000

By Habib Saridikmen

In this experimental study the effects of slag composition on the phosphide capacities of the slag as well as on the phosphorus distribution ratios between the slag and metal phases encountered in ferromanganese smelting have been determined at 1500°C under carbon monoxide atmosphere. The distribution results were employed to calculate the phosphide capacities of the SiO2-Al2O3-CaO-MgO-MnO slags in equilibrium with the Mn-Fe-Si-Csatd.metal phase. The classical gas-slag-metal equilibrium-quenching technique was employed using CO gas atmosphere and graphite crucibles to saturate the metal phase with respect to carbon. The phosphorus distribution ratio increased from 0.045 to 0.375 when the slag basicity increased from 0.72 to 1.39. As expected, the distribution ratio decreased from 0.375 to 0.105 when silica increased from 37 % to 45.8% in the slag phase. The phosphide capacity values were calculated by using the results of experiments. Empirical relationships were developed to express the phosphorus distribution ratios and phosphide capacities of the above slags.

Jan 1, 2006

By R. Winand, M. Degrez, C. Temmerman

"The influence of the copper electro crystallization inhibitors (mainly thiourea, gelatin and chloride ions) is studied in a new fully automatic pilot plan. This paper describes the conception and the building of this plan. The new approach is to reproduce the experimental conditions observed in the industry with the three additives present simultaneously in the electrolyte and secondly to study the influence of a slight modification of the concentration of one inhibitor, the others being present in the electrolyte with their industrial nominalconcentrations.1. INTRODUCTIONDespite the fact that gelatine, thiourea and chloride ions have been used in copper electrorefining for a long time, precise knowledge concerning their influence on the cathode deposit, metallographic structure and associated properties is still lacking.Many authors studied the influence of each additive separately, or of two added at a time. Only a few authors studied the combined influence of the three additives added simultaneously. The general conclusion that can be drawn is that the combined influence is far from that forseen from the influence of each additive separately, or even from two additives used at a time. Moreover most of the experiments described in the literature were performed by adding all additives at once initially. It is however, well known that gelatine looses a great part of its activity during the first half hour due to degradation by sulfuric acid (as shown by the cathode overpotential drop). Thiourea is rapidly replaced by a number of degradation mole,cules and complex ions including cations from the solution, changing even the equilibrium between Cu, Cu(I) and Cu(II).Chloride ions are consumed by precipitation.A number of successive research projects [1-9] led pregressively to the concept that, in order to obtain reproducible results representative of industrial cathodes, it was necessary to simulate as far as possible industrial conditions. It was essential that all additives were added continuously during the electrolysis, with, as consequence, a continuous bleed.The purpose of this paper is to describe the concept of a new fully automatic pilot plan for copper electrorefining and to present the first results."

Jan 1, 1997

By Noboru Masuko, Sachiko Ono

"The structure and composition of anodic films formed on aluminum in a borate solution have been investigated by using TEM and SIMS with respect to the effect of current density and electrolyte temperature. The film is composed of a boron-containing outer layer and a boron-free inner layer with disc-like crystals present at the interface. The thickness of the film formed at constant current density up to an identical voltage, decreases with increasing current density. The thickness increases remarkably with elevated temperature. The transport number of Al3+ estimated from the thickness ratio .of the cuter to the inner layers is 0.4 when the film is formed at the current density of 20 Am-2 at 60°C. It increases slightly with increasing current density and decreases significantly with increasing temperature. Content of boron in the outer layer increases 1.5 times when current density .increases 10 times. These changes in film structure and composition with electrolysis conditions must have a significant role in the determination of electric properties of anodic alumina films as a capacitor material.IntroductionThe growth of anodic alumina film in ·a neutral electrolyte proceeds at both film/electrolyte and film/substrate interfaces giving a duplex structure. The oxide layer formed at the former interface includes electrolyte anions while a-pure alumina layer is formed at the latter interface. The thickness ratios of each layer respectively represent transport numbers of Al3+ and 0 2 - (1). The film thickness and the incorporated anion content as well as transport numbers of both ions must affect the dielectric properties of the film as a capacitor material. However, the correlation between film structure and electrolytic conditions is not fully understood (2). For the further clarification of anodic film growth mechanism, more detailed characterization of anodic films in relation to electrolytic conditions is advantageous. In the present paper, therefore, the effect of current density and electrolyte temperature on the microstructure and composition of anodic barrier films formed in a neutral borate solution was studied. The films were characterized by direct observation using transmission electron microscopy (TEM) and depth profiles of constituent elements obtained by secondary ion mass spectroscopy (SIMS)."

Jan 1, 2000

By Xingming Zhang, Huawei Zhang, Yanxiang Li

"A hybrid porous metal with nano-micro double scale pore size and regular-random bimodal porous structure has been fabricated by unidirectional solidification of a lotus-type alloy followed by dealloying treatment to the base alloy. The base alloy selected is a Cu-Mn binary alloy. The lotus-type porous Cu-Mn alloy with straight pores of several hundred micrometers in diameter was manufactured by unidirectional solidification with a mould casting process. Dealloying treatment was then done to the lotus-type porous structure of Cu-Mn alloy. The solid Cu-Mn alloy wall of the lotus-type porous structure was transformed to random porous structure of dozens to hundreds nanometers. The influence of corrosion parameters, such as the current and time in electrochemical corrosion, temperature and corrosion agent in chemical corrosion, on the nano-porous structure formed has been studied systematically.1. IntroductionA hybrid porous metal is a kind of cellular structure with different porous or cellular forms inside, which possesses special properties and can be applied in many fields as fuel cells, catalysis, sensors, etc. Several means have been developed to fabricate this kind of porous material [1-2]. In this paper, a novel process of Gasar plus dealloying is introduced to fabricate a new form of hybrid porous metal with nano-micro double size and regular-random bimodal structure.The Gasar process, also called the metal-gas eutectic directional solidification, that invented by Shapovalov [3] in Ukraine and now in USA some twenty years ago, is used to fabricate porous metals with regularly aligned pores basing on the solubility difference of a gaseous element in solid and liquid metal. Nakajima and his colleagues [4] in Japan studied this process further and called this kind of structure a lotus-type porous metal. They put more attention to various fabrication techniques and properties of lotus-type porous metals. Li heading a group [5-6] in P.R. China studied the mechanism of Gasar process and process controlling techniques. The Gasar pore structure and porosity can be controlled by processing parameters, and a regular Gasar structure with oriented pores distributing uniformly in the solid matrix can be obtained under optimized processing parameters."

Jan 1, 2014

By Okechukwu Anopuo, Gerhard Tober, Petra Maier

"In this study, an investigation on the microstructure of hot rolled steel S355J2+N was conducted to optimize process parameters of complex forming, which combines rolling and bending. The best sets of parameters are worked out based on homogeneous mechanical properties and microstructure within the varied deformation degree with maximum at <p = 1.14 on a 25 mm thick plates. Mechanical properties, especially of heavy plates, are strongly influenced by the local deformation degree, strain rate and temperature. Detailed microstructural analyses showed that the ferrite-pearlite band structure changes near the surface, while maintaining homogeneous microstructure within the deformed work piece. Surface decarburization was also observed and this leads to decrease in hardness. To minimize iron oxide formation which could lead to side cracking, reduction in exposure time to temperature was suggested. On the other hand, temperature reduction below a critical value would risk the accurate forming process.IntroductionThis work presents the preliminary results of research to develop a new complex deformation process of thick steel plates. Complexity is given because the forming process combines rolling to reduce thickness and profiling by bending. The work piece will experience a thickness reduction from 25mm to 8 mm and is double curved. To explain and understand forming of thick plates basics of sheet forming as well as massive forming need to be used. At the moment there is no forming process established to produce double curved plates including reducing thickness in one process step. Technologies nowadays consist of two process steps: flat rolling and pressing in shape. Due to good weldability and formability the final product will be made of steel S355J2+N. This low-carbon steel is well understood and has a low strengthening exponent, which is expected to keep the forming forces down. Reduction of thickness from 25 mm to 8 mm gives furthermore a high deformation degree. Thus, hot forming has to be applied. The determination of process parameters is the main aim of overall research project; temperatures above lOOO°C are expected. Flow curves in literature are given at various temperatures and strain rates [1]. However, experiments with data close to the industrial application are rarely found, especially at low strain rates and high deformation degrees. Pre-test were done by flat rolling, being aware that the influence of bending is eliminated. The microstructure evolution were characterised in relationship to material formability with special attention to grain size change and recrystallization. Representative samples should be selected from specific locations in the deformation zone according to the knowledge about the metal forming process [2]. Due to no further alloying elements in S355, no precipitation hardening is expected to take place during hot forming, which keeps the mechanisms simple and the concentration on the feasibility of the complex forming process is given."

Jan 1, 2012

By Dirce H. Jacomo, Jaciele G. Teixeira, Anibal Y. Abreu Castillo, EsperidianaA. B. Moura, Yalquiria A. Silva, Rene R. Oliveira, Michelle G. Gomes

"Composites consisting of poly(vinyl alcohol), starch and sugarcane bagasse ashes, using glycerol as plasticizer agent, were prepared by solution casting method. Composites prepared were subjected to electron-beam radiation treatments, at radiation dose of 50 and 80 kGy using a Dynamitron electron beam accelerator, at room temperature in the presence of air. The composite samples obtained were evaluated for their water absorption, mechanical and morphological properties.1. IntroductionThe potential of biodegradable polymers and more specifically of biocomposites obtained from agro-resources have long been well established [1-3]. Starch, derivate from variety of botanical sources (cereals, legumes, and tubers) is widely available raw material and one of the most studied and promising agro-resources for the production of biodegradable polymers as matrices for biocomposite applications. However, starch itself is very brittle, hydrophilic and its mechanical properties are very poor for many applications [3 - 5]. The blending of starch with conventional polymers is a promising approach to improve its drawbacks. Recently, many efforts have been made to blend starch with biodegradable synthetic polymers [5, 6]. Polyvinyl alcohol (PYA) is a particularly well-suited synthetic polymer for the formulation of blends with natural polymers, as it is highly polar and can also be manipulated in water solutions, and depending upon its grade, in functional organic solvents as well [3, 7]. PY A has been reported to be an option to blend with starch. Most of the starch/PY A composites have been prepared by casting. However, it is well known that starch/PY A composites has poor in water resistance and mechanical properties after absorbing water [3,8]. Attempts to improve the mechanical properties and to decrease the water absorption property of the starch/PY A composites are made by adding the cross-linkers and plasticizers. Park et al. prepared starch/PY A/citric acid films by the casting method. They also studied the effect of (spell out) citric acid on the mechanical properties and water resistance of composites [9]. Zhai et al. prepared the starch/PY A hydrogels using electron-beam radiation [10]. Different kinds of lignocellulosic fibers have been investigated in blends for formulation of biocomposites."

Jan 1, 2013

By Raj P. Singh

Two design-of-experiments studies were carried out to investigate the leaching of technical grade molybdenum tri-oxide (TGM) in the presence of hydrochloric acid and the mother liquor of ammonium di-molybdate crystallization used as an ammonia source. Results indicated that leaching of TGM in HCl is possible only when used at about 1N concentration. In high concentrations of HCl, technical grade MoO3 had very high solubility (7.5 to 40 g/L Mo). The most suitable conditions for HCl leaching of TGM were obtained at a slightly elevated temperature of 80°C. Using about 1N HCl at 80°C, potassium in the leached solids (TGM) decreased to about 110 ppm, a value typically obtained in TGM leached in HNO3 - NH4NO3media (3.5 - 4.0 moles /L HNO3 + 0.5 ? 1.0 moles/L NH4NO3). Mo losses under these conditions were 0.8-0.9 g/L Mo. The HCl-leach method, presented here-in, has a significant advantage in chemical cost and environmental benefits over HNO3 ? NH4NO3 purification method.

Jan 1, 2006

By Shaohua Ju, Huang Chang-yuan, Lu Shuaidan, Peng Jin-hui, Wu Guoqin, Yaqian Wei, Zhang Li-bo

"The contrastive studies of microwave and conventional roasting copper residue from zinc hydrometallurgical was carried. The experimental results showed that the microwave roasting has the higher dechlorination rate in the same condition such as temperature, heat preservation time and atmosphere. When the samples with 100 mesh grain size, the Cl content turned from 14.27% to 1.33% and the dechlorination rate achieved over 90% at 400°C with 2h microwave roasting. And in the same conditions, the materials' dechlorination rate after conventional roasting just reached around 78%. The phase changes of the roasting process was investigated with X-ray diffraction analysis.IntroductionCl element can be accumulated gradually in the solution of Zinc hydrometallurgical system. When Cl content in electrolysis solution comes up to 100 mg/L, the stability of electrodeposits process would be severely affected [ 1]. It would not only accelerate the consumption of cathode and anode plate, elevate the power consumption, but also cause serious corrosion of device, increase production costs and lower the quality of electrolytic zinc [2]. Thus, C1- contained in the solution should be removed before electrodeposits."

Jan 1, 2013

By Supachai Surapunl

The distribution behavior of VA minor elements (As, Sb and Bi) in the smelting stage of the Mitsubishi process were evaluated thermodynamically based on thermodynamic data and operating data. The fractional distributions between the gas, slag and matte phases considered as the degree of vapor saturation of l.0 are as follows: 53.8, 27.2 and 19% for As, 23.6, 56.6 and 19.8% for Sb, and 91.3, l.1 and 7.6% for Bi, respectively. Arsenic is mostly distributed to the gas and slag phases. It is effectively eliminated by volatilizing and slagging. Antimony is mainly in the slag phase, which is suitably removed by slagging. Bismuth is easily vaporized to gas phase. The degree of vapor saturation has a large effect on the distribution behaviors of the three elements between the three phases. The amount of a minor element in the charge has an effect on the distribution of As but no effect on the distributions of Sb and Bi. Increasing matte grade and temperature results in the change of distributions for As and Sb, significantly. The change in the distribution ratio between slag and matte phases also considerably affects the distributions of As and Sb. The distribution behavior of Bi is not significantly changed by the change in matte grade, temperature and distribution ratio.

Jan 1, 2003

By Rikiya Kamezawa, Rudiono, Manabu Takeuchi

"Schottky type solar cells based on phthalocyanine (Pc) thin films were fabricated, and their photovoltaic performance was investigated in various ambient atmospheres. Most of cells prepared in this study showed a good rectification and photovoltaic effects in the visible wavelength region. The introduction ofN02 gas into the measuring chamber was confirmed to increase the current both in dark and under light illumination. However, chemical reaction between the Al electrode and N02 formed some oxide and deteriorated the Schottky barrier, resulting in an increase in cell resistivity. SF 6 gas also showed similar effects on the cell performance.IntroductionPhthalocyanine is one of the typical organic semiconductors, which shows high photoconductive sensitivity in the visible to infrared region. Today, several kinds of metal phthalocyanines are used in electrophotographic photoreceptors. In addition, application of phthalocyanines to solar cells have also been trying by many workers [1, 2]. Many efforts have been made for improving performance of phthalocyanine solar cells by modification of device structure [3, 4], doping by dye or pigment [5, 6] and incorporation of metal clusters [7]. It is known that electrical conductivity in phthalocyanine is increased by adsorption ofNO2 [8, 9]. We tried to improve photovoltaic performance ofphthalocyanine solar cell by adsorption ofNO2. This paper describes the influence of N02 adsorption on the photovoltaic behavior of phthalocyanine solar cells."

Jan 1, 2000

By Steven Wright

BHP Billiton?s Olympic Dam copper flash smelter employs the direct to blister process for smelting high grade copper concentrates. SO2 evolution during tapping gives rise to safety concerns. A thermodynamic model for the blister copper (Cu-Fe-S-O) was used to predict the volumes of SO2 evolved. The Multiple Phase Equilibria Model (MPE) was used to evaluate the slag chemistry inside the furnace. The blister copper model was used to explore the relationship between %S and %O in the copper and the amount of SO2 evolved on cooling. The volume of SO2 evolved was sensitive to the O content with reduction to levels below 0.2 ? 0.15% likely to suppress SO2evolution on cooling. Concentrations of S and O in copper samples from trials generally lay above the equilibrium line calculated for an average temperature of 1275C and a partial pressure of SO2 of 1 atm. Consequently there is a thermodynamic driving force for SO2evolution when cooling to this temperature during tapping. A number of potential process options to suppress SO2 evolution on tapping were investigated thermodynamically. Some of the options require treatment of the blister in a forehearth or separate furnace, while others impact on current practises in the flash furnace with slag present. The opportunities that these options present are discussed.

Jan 1, 2006

By Rafael Padilla

The recovery of copper from chalcopyrite concentrates by leaching is difficult due to the slow dissolution kinetics of this mineral in most leaching media. However, recovery of copper from sulfidized chalcopyrite (a mixture of CuS and FeS2) by leaching is faster and could be selective depending on the leaching media. In this paper, the result of an investigation on the H2SO4-O2 pressure leaching of sulfidized chalcopyrite is presented. The variables considered in the study were stirring speed, concentration of sulfuric acid, temperature, and partial pressure of oxygen. The experimental data indicated that stirring speed over 500 rpm and sulfuric acid concentration over 0.1 M had very little effect on the leaching rate. An increase in temperature from 90 to 100 ºC increased both copper and iron dissolution; however, further increase to 120 ºC affected negatively the copper dissolution. Oxygen partial pressure was found to be the main variable that controls the copper/iron selectivity of the leaching. An increase in oxygen partial pressure increased significantly the rate of copper dissolution but deteriorated the copper/iron selectivity. The analysis for sulfur of the leaching solid residues indicated that most of the copper sulfide sulfur in the sulfidized concentrate oxidized to elemental sulfur.

Jan 1, 2006

By C. G. Anderson, L. G. Twidwell

"Throughout the world, there are many orebodies or materials which have significant value but also contain arsenic, antimony, and mercury. As regulations on the transport, exposure, disposition and emission of these elements have become more stringent; it has become increasingly more difficult to derive the values from the resources. This paper outlines the fundamentals of alkaline sulfide hydrometallurgy and its successful application to arsenic, antimony and mercury bearing ores, concentrates, by-products, and other materials.Fundamental Alkaline Sulfide HydrometallurgyHydrometallurgical methods can be employed for treatment of gold, arsenic, antimony, tin and mercury containing materials, concentrates and ores as well as complex ones containing any number of metals. The alkaline sulfide system is one of these and is essentially a mixture of sodium sulfide and sodium hydroxide. This is a unique hydrometallurgical system as it is a very selective lixiviant for the distinct leaching of tin, gold, antimony, arsenic and mercury [1-7]. Worldwide, it is employed industrially in the CIS, China and the United States for the production of antimony [8-15].As an example, when the system is applied to an arsenic containing material like orpiment, As2S3, a solution of sodium thioarsenite is formed. This is illustrated as:"

Jan 1, 2008

By Steven Wright

The extent and the rate of reduction of slags produced from the smelting of recycled lead batteries were investigated under laboratory conditions using graphite as reductant. Simultaneous reduction of PbO, Fe2O3, Sb2O3 and As2O3 occurred at temperatures of 1180 and 1200°C, with Sb and As reporting to the metal phase while the PbO content of the slag was above 2 wt%. Fuming of As from the metal occurred at lower concentrations of lead in the slag. Discard slags with low levels of As, Pb and Sb were produced. Arsenic levels were reduced to less than accurately measurable by ICP analysis, and Sb levels in the final slags were in the range of 0.1 to 0.2 wt%. The kinetic data obtained were analysed and compared with other measurements on lead oxide containing slags. The results showing a dependence of the reduction rate on the oxidation state and the basicity are consistent with other studies on well characterised industrial and. synthetic lead slags. These results indicate that when carbonaceous reductants are used, the rate of interfacial reactions play an important role in enabling the production of environmentally acceptable discard slags.

Jan 1, 1994

By Jeaneth S. Benedetto

The physical and chemical processes developed for recovery of uranium and phosphor from phosphoro-uraniferous ore bodies consists of three basic steps: concentration of the phosphate bearing uranium by flotation, chemical dissolution of the concentrate by wet phosphoric acid and extraction of uranium by solvent. In this process two products are obtained: 1) uranium and 2) phosphoric acid. The purpose of this work was to develop technological know-how of phosphoric acid purification though an extraction of P2O5 by solvents. It was investigated by two lines of research. In the first one the uranium was extracted before the phosphoric acid purification. In the second, the phosphoric acid was extracted before uranium recovery. The comparison of the two processes is shown in this paper. Experimental work was developed on a laboratory scale to select and optimize the process variables. After the laboratory study, the research of extraction and stripping was continued on a pilot scale in pulsed perforated-plate columns in order to investigate the main operational and process conditions. The first phosphoric acid extraction experiments showed good results using a raffinate sample obtained from the uranium extraction process. It was possible to obtain a high purity phosphoric acid.

Jan 1, 2003