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By Jose Antonio Silva Souza, Emanuel Negrao Macedo, Iara Ferreira Santos, Otacilio Dias, Luis C. A. Venancio

"The Bayer process alumina production generates 0.7 to 2.0 ton of bauxite residue (BR) and an average of 1.0 ton of C02 per ton of alumina produced. The direct reaction of exhaust gases to reduce the alkalinity of the BR may allow a triple gain: improve the storage conditions, open a range of new applications for BR and sequester from 16 to 102 kg of C02 per ton of alumina. This paper shows the measurement of C02 captured during a pilot scale reaction of a suspension of BR in water with flue gas, produced from direct oil burning. Three different types of reactors were used: one spray tower and two packed columns. The inlet and exhaust gases were analyzed using electrochemical and non dispersive infrared sensors. The pH of the suspension was monitored during and after the reaction to evaluate the buffer effect.IntroductionAlumina is mainly produced from refining bauxite using the Bayer process. This process consists of extracting the aluminum oxide through its dissolution in caustic soda and the separation of insoluble residues. The remaining bauxite residue (BR) although not particularly toxic, poses risks to the environment due to the large volume and its reactivity. According to the latest technology it is stacked on sealed deposits specially constructed. To date the vast majority of the bauxite residue that has been produced was stored and were not incorporated into any existing production processes to significant amount with exception to some extent of the sintering process residue at Russia and China [l]. On the other hand, a strategic goal was set in 2010 by the Bauxite and Alumina Committee of the International Aluminium Institute (formed by the majority of the industries) to reuse 20% of BR in 2025 [2]. China has established the same objective for 2015[1].This paper is a sequel of two others presented at TMS 2010/2012 [3-4] and describes:• A pilot plant assembled for testing the carbonation process of BR with gaseous effluents similar of the refining process.• The methodology used to measure the amount of C02 captured during the carbonation process.• The results of the carbonation process, the C02 capture and the buffering effect of the pH.This process is studied in order to consume minimal power and use the effluent as efficiently as possible in different reactors from low cost to ultra high performance. The process is designed for minimizing the power consumption and equipment investment."

Jan 1, 2013

By Zhou Aiping, Lv Guozhi, Niu Liping, Wang Wenbo, Zhang Ting’an, Jiang Xiaoli

The current method used to produce sponge titanium utilizes a process cycle of magnesium metal and chlorine gas via the electrolysis of magnesium chloride. The primary issues are the high capital cost of the electrolysis process and the environmental regulations limiting high chloride concentrations. Thus, the authors have developed a conceptual method involving theelectrolysis of magnesium chloride as well as a reduction process which allows for a cycle of magnesium and chloride. In the new method, MgCl2 which was distilled during the titanium extracting process as raw material was directly pyrolyzed at elevated temperatures yielding high purity magnesium oxide and chlorine. The resulting magnesium oxide can be used in the production of magnesium metal. This work examines and compares the energy consumption and economic benefits of the Kroll method as well as the new proposed method. The results from the study demonstrated that in comparison to the traditional Kroll method, the new method provided considerable economic and environmental benefits.

Jan 1, 2014

By Nobuaki Sato

For decontamination of SO2 containing waste gases from industries such as ferrous and non-ferrous metal companies, desulfurization with hydrogen production by the reaction of Br2 and SO2 was proposed as bromine-sulfur (BS) process. In this process, SO2 is fixed as H2SO4 in the presence of Br2 and H2O forming H2SO4 and HBr. Then hydrogen is produced by the decomposition of HBr and Br2 as byproduct is recycled. The reaction of Br2, SO2 and H2O was found not to occur in liquid phase but to occur in vapor one. The production ratios of H2SO4 and HBr showed a maximum at temperatures around 60 oC. The highest production ratio was obtained at 70 oC with a mixing ratio of Br2:SO2:H2O=1:1:10. The experimental results were discussed with thermodynamic consideration.

Jan 1, 2006

By N. Moelans

A method using an ex-situ electrochemical measurement device was developed to determine the oxygen potential of non-ferrous metallurgical slags. The electrochemical cell consists of the molten slag sample, an inert Ir electrode, a stabilized Zr02 solid electrolyte and a NiINiO reference electrode. Different slags from non-ferrous pyrometallurgical processes were analysed at 1100 and 1200°C and pO2 values between 10-3 and 10.12 bar were obtained. The measurements were evaluated with? thermodynamic calculations and using processing considerations. It was found that the reproducibility and stability of the measurement was significantly improved by shielding the molten slag from the atmosphere by a thin layer of carbon, especially for slags with a low oxygen potential.

Jan 1, 2003

By S. V. Ketov, V. P. Menushenkov, V. S. Shubakov

"The glass samples were obtained by melting of the oxides mixture SrO-Fe2O3-B2O3(Al2O3) at 1200-1250°C with subsequent quenching of the melt on quickly rotating steel roller. Submicronsized Sr(Fe,Al)12O19 particles were formed in glass-ceramic matrix during the crystallization aging of glass. The aging temperature Tag varied in the range 650-950°C. The submicron-sized hexaferrite powder was obtained by removing of the matrix phases using etching. The samples were characterized by X-ray diffraction, scamiing electron microscopy and magnetization measurements. The glass-ceramic material exhibits very high coercivity value up to 10 kOe. The samples of magnets were obtained by pressing of the hexaferrite powder at RT and subsequent aging in the range 900-1200°C. The aged samples exhibit coercivity value up to 8 kOe.IntroductionStrontium M-type hexaferrites have been widely used in technology and industry mainly for production of permanent magnets owing to their appropriate magnetic properties, chemical stability and low cost [1,2]. The SrFe12019-based compounds are characterized by high magnetocrystalline anisotropy and single easy magnetization axis. The highest coercivity is received for monodomain, defect-free single crystal particles with size D - 100 mn. Finely grained strontium hexaferrite prepared by chemical methods such as sol-gel pyrolysis and oxide glass crystallization exhibits high coercivity up to 6-8 kOe [3-5]. Owing to the partial substitution of Al for Fe in the strontium hexaferrite leading to the increase in the magnetic anisotropy field Ha=2Ki/M,, the increase in the coercivity may be received [6]. The notable results were achieved using the SrO-Fe2O3-AlzO3-B2O3 glass crystallization and formation of perfect submicron crystals of alumina-doped hexaferrite [ 6, 7]. The coercive force of glassceramics reached values of up to 10 kOe. Hexaferrite particles are well faceted and have the shape ofhexagonal bipyramids with truncated vertexes [7].In the present paper, we report results of our investigation into the SrO-Fe2O3-B2O3(Al2O3) glass crystallization, hexaferrite powders and permanent magnets, which were prepared by pressing submicron-sized hexaferrite powders at RT and subsequent sintering at 900-1200°C."

Jan 1, 2012

By Chi-Ming Chang

Alloy powders are commonly used in the purification of zinc sulfate solutions for use in standard electrowinning practice. The primary goal of this research was to study the use of zinc-lead alloys for similar reactions in the galvanic stripping of impurities from organic solutions. The effects of various parameters on the electrochemical behavior of commercially produced zinc-lead alloy powders were determined. A qualitative evaluation and summary of the influence of the more pertinent parameters on iron removal from di-(2-ethylhexyl) phosphoric acid (D2EHPA) by galvanic stripping is given. Water concentration, oxygen content and reaction temperature were the principal factors affecting the reaction rate and process efficiency. Activation energies were also calculated and indicated that the reaction changes from chemical to diffusion control .with increasing temperature in the range of 35" to 45°C. The results showed that zinc-lead alloy gave faster reaction rates with less sensitivity to process variables than SHG zinc as a reducing agent for galvanic stripping. The role of lead could be as cathodic sites for the reaction which enhances the zinc dissolution or anodic half reaction. The morphology of the zinc-lead alloy surfaces, before and after the reactions, supports this assumption.

Jan 1, 1998

By KNona C. Liddell

The time and spatial dependence of component and species concentrations during in situ uraninite leaching have been modeled using a reactive transport model based on partial equilibrium between reactive minerals and the solution. The flow field is represented by mixing cells in series. The effects of the H2O2, (NH4)2CO3, and NH4HCO3 component concentrations have been simulated, and results are presented for a one-dimensional flow field.

Jan 1, 1995

By P. M. Swash

This paper reviews the application of some mineralogical techniques in the evaluation of the Uitkomst Ni-Cu deposit, South Africa. The low grade of the ore necessitates detailed and representative characterisation in order to establish the prospects viability. The relevant mineralogical information is generated by using optical microscopy, magnetic and heavy liquid . separations, XRD. SEM and EMPA. Methods used are briefly reviewed. The cost savings and metallurgical understanding that is provided by the mineralogical work is described especially with regard to milling, flotation and the presence of by-products (PGMs and chromite).

Jan 1, 1991

By Keizo Uematsu, Satoshi Tanaka, Zenji Kato, Nozomu Uchida

"A novel technique is developed and applied to evaluate the binder segregated at the· surface of granule. Compressive strength of each granule was measured directly with a micro-compressive instrument. The relation between compressive characteristics and the amount of binder was discussed quantitatively.IntroductionCharacterization of granules is essential in the production of ceramics, since they govern the structure of green compact and thus the structures and properties of ceramics. However, there is no research to clarify the relation between the strength of granules and structure of granules, especially of binder segregation at granule surface. We develop a novel technique to determine the binder concentration in the granules by the iodine method. In this study, we measure yield strength of granules directly and discuss the relevance between compressive characteristics and the concentration of binder.ExperimentalGranules were prepared by spray-drying of aqueous slurry of commercial alumina (AL160-SG1. Showa Denko, Tokyo, Japan) and PVA (PVA 105 Kurare, Japan). PVA. concentration in granules was 1.1, 1.5 and 2.3 wt%. The inlet and outer air temperatures were 200 and 95 °C , respectively. Iodine-potassium iodide solution was prepared by dissolving iodine (0.15mol) and potassium iodide (0.15mol) in diluted water (50ml). A saturated boric acid solution was prepared by mixing boric acid powder with a diluted water."

Jan 1, 2000

By Jari Aromaa, Antti Kekki, Olof Forsén

"The deposition of copper on inert substrate depends on the number of active sites that will react at certain overpotential. The critical overpotential depends on surface morphology, surface film resistance and additives on cathode surface. The effects of surface properties on copper nucleation and growth rates were studied for used stainless steel blanks from several tankhouses. The surfaces of the blanks were characterized with electrochemical and mechanical methods. Electrochemical deposition tests were done at current density of 300 A/m2 for 10, 30 and 60 seconds. The nucleation density and copper coverage were estimated using image analysis. The surface film resistance did not correlate with copper growth. Increasing surface roughness correlated with lower copper growth.IntroductionStainless steel cathode blanks in copper electrorefming are usually made of AISI 3 I6L type steel. They have a typical lifetime over 10 years. During use the surface will collect deposits and become rough due to wear and corrosion. These factors can affect the nucleation and growth of copper. The nucleation and deposition of copper on inert substrate depends on the number of active sites that will react at certain overpotential. The critical overpotential can depend on surface film resistance, surface morphology, and additives adsorbed on cathode surface.The deposition potential of metallic ions on a foreign substrate is usually higher than the deposition potential on the electrode made of the same metal due to crystallographic substrate/metal misfit [I]. If the substrate has traces of the depositing metal they will be preferential growth sites. For a smooth deposit a large number of simultaneous nuclei is necessary. However, excessive nucleation density can lead to porous deposits [2]. Surface films of good conductivity are needed for dense nucleation and small nuclei. On cathode blanks the number of active sites increases with increasing surface film conductivity [3-5] and/or surface film porosity [6]. On AISI 3 I6 L stainless steel a more resistive oxide has been found to limit favourable sites for copper nucleation and more conductive film promoted high-density copper nucleation [7]. Also Urda-Kiel et al. have concluded that thicker oxide layers on AISI 304 stainless steel resulted in lower nucleation [8]. Increase in overpotential or current density activates more and more of the potential nucleation sites and this can be seen as higher number of nuclei [9] or smaller average distance between nuclei [10]."

Jan 1, 2012

By Philippe Henry

"Hydrometal provides an adequate technology to reintroduce otherwise lost metal units into the industrial cycle, thereby saving resources and energy, while keeping the environment cleaner. Two case studies at an integrated hydrometallurgical recycling facility (Hydrométal) in Belgium are discussed: (I) Residual low quality acid and caustic are used in the processing of zinc industry cements to produce copper, nickel, cobalt and zinc concentrates by several consecutive selective leach - precipitation processes.(II) Copper anode slimes are treated and their precious metal contents are recovered. Depending on the composition of the slimes, separate or combined concentrates of copper, bismuth, tellurium/selenium and silver/precious metals can be produced."

Jan 1, 2008

By Timothy W. Skszek, Adrian S. Sabau, Hebi Yin, Gerard M. Ludtka, Xiaoping Niu

"A constitutive model has been developed to predict the yield strength aging curves for aluminum casting alloys during non-isothermal age-hardening processes. The model provides the specific relationship between the process variables and yield strength. Several aging heat treatment scenarios have been investigated using the proposed model, including two-step aging recipes. Two-step aging heat treatments involve a low temperature regime to promote nucleation of secondary phases and a second step at higher temperature for the growth of the secondary phases. The predicted results show that a yield strength of approximately 300MPa might be obtained in a shorter aging time, of approximately 30 minutes. As a result, better mechanical properties can be obtained by optimizing the time-temperature schedules for the precipitation hardening process of heat treatable aluminum alloys.IntroductionA356 is one of the commercially heat treatable aluminum casting alloys, and T6 is one of the heat-treated conditions to improve mechanical properties. The first stage of a T6 temper is solution treatment at an elevated temperature, generally in the range of 480 - 540°C. After solution treatment, the cast part is typically quenched in water/air to retain the solute-rich homogeneous matrix chemistry at room temperature. Subsequent ageing treatment stages capitalize on this super-saturated solid solution to generate controlled dispersions of very small strengthening precipitates within the matrix of Al grains [l]."

Jan 1, 2013

By Antonio Luraschi

The constituents iron, oxygen, silica and cop- per are of principal interest in slags utilized in pyrornetallurgical processes for producing copper. Accordingly, phase relationships in the.Cu-Fe-0-SiO2 system are important when one considers the physico- chemical behavior of slags. These phase relation- ships for the quaternary and constituent ternary systems are developed from available information. Isothermal composition and composition-oxygen potential diagrams, and oxygen potential-temperature diagrams are utilized to describe the' important relationships.

Jan 1, 1976

By Yasuhiko Ito

"This talk is concentrated on the topics of compound film formation on the substrate electrode by interdiffusion of substrate element and electrochemically deposited species and/or by direct electrochemical implantation of the component element of the film into the substrate. As a typical example, electrochemical implantation of nitrogen atom into Ti metal to form TiN surface film is described. Another example is the formation of various kinds of intermetallic compound films including Ni2Y, Ni2Dy and Pd3 Y by the electrochemical implantation of lanthanoid elements into transition metal electrodes. By combining these two methods, Sm-Fe-N ternary material film also could be formed. The principle and application of the ""electrochemical implantation"" are discussed in detail.IntroductionGenerally speaking, surface film formation by molten salt electrochemical process can be divided into the following three categories:(i) single element film formation on the electrode by electrodeposition,(ii) compound film formation on the electrode by electrocodepostion of more than two elements, and(iii) compound film formation on the substrate electrode by interdiffusion of substrate element and electrochemically deposited species and/or by direct electrochemical implantation of the component element of the film into the substrate.This talk is .concentrated on the topics of category (iii), especially on the electrochemical implantation. Typical example can be seen in the electrochemical implantation of nitrogen atom into Ti metal to form TiN surface film. Another example is the formation of various kinds of intermetallic compound films including Ni2 Y, Ni2Dy and Pd3 Y by the electrochemical implantation of lanthanoid elements into transition metal electrodes. By combining these two methods, Sm-Fe-N ternary material film also could be formed. The principle and application of the ""electrochemical implantation"" are discussed in detail with examples above as well as other experimental results also obtained very recently in the author's laboratory."

Jan 1, 2000

By Andrzej Szymanski

Recent developments in medicine have stimulated activities that? involve mineralogy. They include inplantation of inorganic and organic parts into bones and soft tissues, and uses of elements as basic stimulators for the human body. In addition contamination of the environment has increased the concentration of sane elements in food. Consequently f both the environment and food structure vary with geographical regions and influence human health. These activities in medicine have created the new fields of biomineralogy and of biogeochemistry as activities for the future.

Jan 1, 1989

By David K. Melgaard

Electroslag Remelting (ESR) is a complex process used to produce high quality specialty alloy materials. The quality can be directly correlated to variances in melt rate and immersion depth. Conventional ESR furnaces control these quantities using two independent control loops using proportional changes in current for melt rate and driving the electrode up and down to match a voltage set point for immersion depth. However it is well known that the control loops are highly coupled, i.e. changing the current to account for melt rate deviations changes the voltage depth relationship and vice verse. In addition the noise in measurements of the ESR process can be considerable, forcing conventional controllers to use highly damped responses. A new model-based controller has been developed to embody the coupling and improve responsiveness by using estimates from a reduced-order linear ESR model and the typical process measurements to control melt rate and immersion depth simultaneously. Kalman filtering is used to optimally combine the model estimates of eight process states and the measurements of voltage, current, position and mass to estimate the instantaneous melt rate and immersion depth. Several ESR melts under steady state and transient conditions were conducted to evaluate the performance of the new controller. This paper will discuss the design of the new ESR model and controller and will present experimental results demonstrating its much improved control and responsiveness. While this controller was developed for the ESR process, the effectiveness of model-based control in managing such a complex process with relatively simple equations suggests the approach could be employed for many other processes as well.

Jan 1, 2006

By Kazuhiro Asai

Nippon Mining and Metals Company has an annual indium production capacity of 30 tons at its Saganoseki smelter and refinery. Lately, indium content in the. zinc smelting dust, one of the main sources, has been on the decrease while the amount of impurity in it on the increase. The present process at Saganoseki does not permit efficient elimination of a large. amount of impurity. Therefore, studies were conducted to improve its recovery process. As a result, a new indium recovery process consisting of leaching, solvent extraction and electrowinning has been developed. The new process was tested at a pilot plant and satisfactory results were obtained. This new process is discussed in this paper.

Jan 1, 1995

By Tadafumi Adschiri

"Supercritical water can provide an unique reaction atmosphere for synthesizing metal oxide nanoparticles. Due to the drastic change of properties of water around the critical point, including density, dielectric constant and ionic product, the reaction phase with O 2 or H2 gas and the reaction rate and equilibrium can be varied to synthesize new materials or define particle morphologies. In this work, hydrothermal crystallization experiments are performed with several types of flow apparatus that allow convenient manipulation of variables such as temperature, pressure, and residence time. Key features in the flow modes and material preparation are discussed. The proposed supercritical hydrothermal synthesis method has the following desirable features: i) nanoparticles can be produced, ii) morphology of the produced particles can be controlled with small changes in pressure or temperature, and iii) a reducing or oxidizing atmosphere can be applied by introducing oxygen or hydrogen or other gases. An overview of this method is given for functional material synthesis of significant industrial interest including barium hexaferrite magnetic particles, YAO/Tb phosphor fine particles and lithium cobalt fine crystals.IntroductionHydrothermal crystallization, a method of metal oxide formation from metal salt solutions, is typically used at temperatures ranging from 373 K to 473 K. We are developing a new process for hydrothermal crystallizations that uses temperatures in the range of 673 K to 723 K, which is just above the critical temperature of water1 • 8 • In this work, we refer to this process as supercritical hydrothermal synthesis. The supercritical state of water allows one to vary reaction rate and reaction equilibrium by shifting the dielectric constant and solvent density with pressure and temperature. From of our research on material production in supercritical water, we have identified the following specific features of the supercritical hydrothermal synthesis method: (i) ultrafine particles can be produced, (ii) morphology of the produced particles can be controlled to some extent with pressure and/or temperature, and (iii) a homogeneous reducing or oxidizing atmospheres can be provided by introducing gases, such as O 2, H2, H2O 2• and so on.1"

Jan 1, 2000

By Sergio Sanchez-Segado, Yuan Zhang, Animesh Jha, Ahmad Fahmi Ruzaidi

Niobium and tantalum are considered critical materials because the increasing demand in the energy sector which is reliant on limited abundance of these two metals in minerals. Traditionally, niobium and tantalum mineralsare digested using hydrofluoric acid at moderate temperatures, producing oxy-fluorides which are separated by solvent extraction, involving the use ofhazardous chemicals. The increasing environmental pressures are forcing the industry to search for alternative low carbon processing methods. In this paper alkali roasting based separation and beneficiation, which is not well understood in the literature, is proposed, for which the kinetics and thermodynamic equilibria for the formation of sodium tantalate and niobate with sodium hydroxide are analyzedat the temperature range of 400ºC to 700ºC. The apparent activation energy of formation,changes from 31.0±0.8 to 22.3±1.2 kJ mol-1 and from 23.8±1.2 to110.2±12.8 kJ mol-1, for tantalate and niobate, respectively. The reaction mechanism is examined on the basis of the analysis of reaction products using X-ray powder diffraction (XRPD) and X-ray fluorescence (XRF).

Jan 1, 2015

By H. Cepin

Production of non-ferrous metals is still principally performed in shaft and flame fired furnaces. Electric furnaces increase metal recovery, reduce environmental burdens and decrease energy consumption compared to conventional processes. Because non-ferrous metals have low melting and boiling points and aggressive slags design of the furnace, energy input, and slag conductivity and composition are very important. Secondary materials are easily handled in electric furnaces. Since additional amounts of lead, zinc and tin will become available from secondary sources in the future, electric furnaces are expected to replace conventional smelting furnaces. The paper describes technical, electrical, and process designs of electric furnaces peculiar to the reduction of non-ferrous metals. Electric and various thermic furnace processes are compared.

Jan 1, 1990