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By Junji Shibata

Waste solution from the Ni non-electric plating process contains 4.0 kg/m3 Ni, 0.1 kglm3 Fe, 0.0 I kg/m3 Zn, 48 kg/m3 S042-, 98 kg/m3 HP032-and 31 kg/m3 laetic acid as a typical composition. Solvent extraction, cementation, ion exchange resin and precipitation methods are possible to use for the treatment of this kind of solution. In this study, solvent extraction of Ni was investigated using two kinds of extractants to clarify the relation between extraction percent and pH for various extractant mixtures. As Ni ion has an octahedral structure with ligands, the synergistic effect for Ni extraction is considered to take place in solvent extraction using two types of extractants. The investigation of the synergistic effect for Ni extraction was carried out in case of various extractant systems.

Jan 1, 2003

By Hyun Soo Kim, Joon Soo Kim, Myong Jun Kim, Jyothi Rajesh Kumar, Jin-Young Lee

Rare earth materials have an ever growing variety of applications in the modern and hitech technology. They apply to many an industry with crucial materials and they provide numerous a customers with benefits. Rare earth materials utilization increasing day-by-day in the worldwide, at the same time the resources is very limited in many countries like Korea. The present general article divided four sorts such as 1) mineral processing of Korean ore deals the gravity, magnetic separation and froth flotation, 2) decomposition and leaching of concentrates included sodium hydroxide fritting, sodium hydroxide hot digestion, hydrochloric acid leaching, 3) separation and purification of rare earth elements in mixed rare earth chloride solution consists reduction and oxidation method, solvent extraction, 4) preparation of rare earth oxide compound from purified elemental rare earth chloride solution having oxalate salt precipitation by reaction crystallization. The last part consists of a summary of the present study.

Jan 1, 2015

By R. Escalera-Lozano, M. Herrera-Trejo, M. A. Pech-Canul, J. López-Cuevas, A. L. Leal-Cruz, M. I. Pech-Canul

"The use fly-ash (FA) and rice-hull-ash (RHA) offers the potential for the manufacture of hybrid Al/SiCp/spinel composites via reactive infiltration, both with recycled aluminum. The main reason behind this statement is the beneficial role that both waste materials play in preventing the degradation of SiCp reinforcements when the composites are processed with aluminum in molten state. Experimentally, MgAl2O4 is formed in situ during the infiltration of SiCp-preforms in the temperature range 1050-1150 oC for 50-70 min in argon atmosphere at a pressure slightly above to that of the atmospheric pressure. Results reveal that both FA and RHA help in preventing SiCp dissolution and the subsequent formation of the unwanted Al4C3; and although FA-composites still might be susceptible to corrosion via Al4C3 -by the interaction of native carbon in FA with liquid aluminum- a proper FA treatment significantly mitigates its deleterious effect. Primary corrosion mechanisms and strategies to overcome the potential degradation effects are outlined.IntroductionOwing to inherent materials characteristics and post-processing complications –such as corrosion damage- development of metal matrix composites (MMCs) from recycling/waste sources might be a challenging task. Fly-ash (FA) and rice-hull-ash (RHA) are two primary waste materials that offer excellent opportunities for the development of Al matrix composites. Due to its singular hollow-spherical shape and low density, FA has attracted the attention of many researchers. For this reason, most of the efforts to develop Al-based composites from waste materials have been centered on the use of fly ash. Extensive research efforts in the use of FA for Al-based composites have been undertaken by Rohatgi and coworkers [1-4]. In addition to lowering costs, incorporation of fly ash into aluminum has been proved to decrease the materials’ density, increase their hardness, abrasion resistance and stiffness [1]. One of the major outcomes from the mechanical evaluation of aluminum composites prepared with fly ash is that related to their compression characteristics. Typical compressive stress-strain curves form A356/hollow fly ash composites show a linear elastic region followed by a plateau (associated to the collapse of the hollow particles), and then an increase in stress, representing densification of the foam. The crushing of the cenospheres in the composites has been related to an enhancement in the energy absorption capabilities of the material and to a better damage tolerance [4]."

Jan 1, 2008

By Mitsuhiro Ohtaki, Tetsuzo Arakawa, Fujio Murata

Refining of Zn from aluminum scrap melt by some vacuum distillation processes was studied to promote aluminum scrap recycling. Effects of distillation conditions, such as melt temperature, vacuum pressure and holding time, on Zn distillation behavior were investigated theoretically and experimentally by 0.3kg/ch scale vacuum resistance furnace. Three methods to increase the surface-area/volume ratio of liquid metal, such as gas atomizing, mechanical atomizing and mechanical stirring, were tested to increase the Zn distillation rate in 5kg/ch scale vacuum resistance-furnace. It was easy to lower the remaining Zn content to less than 0.1 wt% within one minute by mechanical stirring method. A water-model simulation experiment indicated that a significant agitation of the melt by stirring would be effective to increase the distillation rate. Continuous agitation vacuum distillation process (CA VP) has been designed and the pilot plant is now in construction.

Jan 1, 2000

By M. C. Ruiz

The conventional pyrometallurgical methods to treat copper sulfide concentrates include generally, one or more oxidizing steps where the formation of SO2 gas can not be prevented. From the economical point of view and the nature of some of the processes in which SO2 is produced, its complete capture is not feasible; therefore an important fraction is released to the atmosphere as fugitive emissions. In this research, the reduction of chalcocite was studied in the presence of lime as an alternative method, which overcomes the pollution problems related to SO2 emissions. The effect of temperature, time, concentration of carbon and CaO on the reduction rate were studied. Among these variables, temperature affects most the reduction rate. Conversions over 95 % can be obtained in less that 20 minutes at temperatures over 1000 ° C. The measured partial pressures of the gaseous components indicated that the chalcocite reduction proceeded through the gaseous intermediate species CO, C02, and the overall kinetics was controlled by the Boudouard reaction. The kinetic model In(1-X)= kt fits well the experimental data. Apparent activation energy of 3 14 kJ/mol was calculated for the temperature range of 900 0C-1050 °C.

Jan 1, 1999

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 Nan Wang

Based on the commercial computational fluid dynamics software, Fluent, a three dimensional finite-volume model has been established, and the fluid flow and heat transfer in the super-wide slab mold (cross section 3250mm×150mm) of Nanjing Iron and Steel Company has been simulated. The basic feature of flow and temperature field in a super-wide mold has been analyzed, and the effects of mold width, the submergence depth of SEN, outlet angle of SEN, casting speed, superheat and cooling rate on the flow and temperature field have been investigated. The results by comparing several simulated calculations for 3250mm×150mm slab show that a more proper fluid flow and temperature field in the super-wide mold can be obtained with 15°outlet angle, 120~150mm submergence depth of SEN and 1.2~1.4m/min casting speed. The results through numerical simulation provide a theoretical basis for optimizing the configuration design of SEN and choosing reasonable processing parameters for the continuous casting mold of super-wide slab.

Jan 1, 2009

By Nobuhiro Kuriyama

Electrochemical activation behavior of an AB2-Laves-phase type hydrogen storage alloy, Zr0,9Ti0.lNi1.lCo0.1Mn0.6V0.2 was studied to make clear activation process of pellet-type metal hydride electrodes. An alkaline treatment of the electrodes with heated alkaline solution gave alloy surface enriched with nickel, and the treated electrode was more easily activated. The treated electrode desorbed more hydrogen during the first charge-discharge cycle, and was activated without induction period. A cross sectional view of the activated electrode showed finer pulverization of alloy particles than the annealed alloy, and impedance spectroscopy indicated larger surface area of the electrode using the as-cast alloy. Since the as-cast alloy contains inhomogeneities, multi-phase microstructure and stress in the particle, the finer pulverization of alloy particles with hydrogenation are considered to increase surface area in an earlier cycle in the case of the as-cast alloy, which leads larger reaction area and faster activation of the as-cast alloy electrode.

Jan 1, 2002

By R. N. Reddy

The Pseudo capacitance of layered type Mn02 electrode material for electrochemical capacitors (EC's) was investigated. MnO2 was synthesized in our laboratory. Mn02 was prepared from heating of KMn04 at 300°C in air. Cyclic Voltammetry (CV) experiments were carried out using three electrode system, Saturated calomel electrode as reference electrode, platinum mesh as a counter electrode, and MnOz composite material mounted in a platinum mesh used as a working electrode. Two kinds of composite working electrode materials were used, one was mixture of MnOz and 25 wt% acetylene black, while the other was MnOz, 25 wt% acetylene black and 25 wt% carbon. All the experiments were carried out at 25OC. A maximum specific capacitance of 130 Fig and 118 Fig were observed at the scan rate of 2 mV/s and 20 mV/s respectively in 1M KC1 for composite electrode made with carbon. Results obtained in this study are compared with that of other electrode materials.

Jan 1, 2002

By Toshiyuki Nohira, Eiichi Takeuchi, Tetsuo Oishi, Hideki Ono, Hirokazu Konishi

The Dy-Nd-Pr-Ni alloy sample was prepared by cathodic potentiostatic electrolysis at 0.65 V (vs. Li+/Li) for 1 h using a Ni plate in a molten LiCl-KCl-DyCl3-NdCl3-PrCl3 system at 723 K. The highest mass ratio (Dy/Nd+Pr) in the alloy sample was observed to be 50 at 0.65 V. Anodic potentiostatic electrolysis at 2.20 V for 12 h was conducted using the Nd-Fe-B magnet electrode in a molten LiCl-KCl system. All elements were almost dissolved from the magnet, and the original form of the magnet disintegrated. After anodic potentiostatic electrolysis at 2.20 V, cathodic potentiostatic electrolysis was conducted at 1.00 V for 5 h using a Mo plate in order to remove the dissolved Fe from the bath. Finally, cathodic potentiostatic electrolysis was conducted at 0.65 V for 12 h using a Ni plate. The mass ratio of Dy/Nd in the alloy sample was determined to be about 18.

Jan 1, 2015

By Dhanesh Chandra

Long term stability studies were conducted on four variants of LaNi5; 10,000 hydriding/dehydriding cycles were used to evaluate their suitability for a metal hydride cooling system. Thermodynamic and structural studies were conducted to determine changes in these materials during cycling test period. The hydrogen sorption properties of LaNi5.2, and Lao 9Gd0.1Ni5 and LaNi4.75In0.27 were seriously degraded during the tests but the LaNi4.8Sn0.22 hydride was virtually unaffected. Hydride isotherms were measured at the beginning and at intervals through out the test period to observe the nature and extent of damage degradation in the sorption properties. X-ray diffraction studies of the alloys (LaNi5.2, LaO.9Gd0.1Ni5 LaNi4 8Sn0.22) and their respective hydride, before and after test, provided insight with regards to the observed changes in the hydride properties. Electron microscopic studies were also conducted to evaluate the changes in particle sizes.

Jan 1, 1989

By G. Johnston, J. Greenly, R. G. Buchheit, D. C. McIntyre, R. Muenchausen, D. J. Rej, R W. Stinnett

"Rapid thermal treatment of materials using high energy, high flux, pulsed ion beams can produce modified surface layers with unique microstrutures and properties. High energy ions loose their energy during the slowing down process in the workpiece and thus deposit their energy continuously over a depth of a few microns. The deposition of energy can lead to melting and in some causes ablation of the heated layer. Because the pulse duration of the ion beams is typically only 50-200 ns, steep thermal gradients generated during heating facilitate rapid cooling (107K/sec-108K/sec) of the treated layer by thermal diffusion into the underlying material. Rapid heating and cooling of materials can generate surface layers with non-equilibrium amorphous or nano-crystalline microstructures that exhibit increased hardness, wear resistance, and corrosion resistance. Pulsed ion beam treatment can also lead to surface smoothening or can be used to mix thin « 1 11m thick) coatings into underlying substrates. Pulsed ion beams can be generated using existing ""flashover"" ion source technology which is capable of producing single shot, mixed C, H, and O ion beams with beam cross sections of approximately 100 cm2 and energy fluxes up to 100 J/ cm2. Recent advances in repetitive high energy pulsed power technology and development of magnetically confined anode plasma ion sources have facilitated the development of ion beam systems that generate single species beams that pulse continuously at 120 shots/second. These capabilities will allow rapid treatment of large surface area workpieces at low cost.IntroductionThe rapid solidification of liquid materials can create unique materials and material microstructures that often have properties that can lead to enhanced performance. Rapid solidification processing of the surfaces of materials using continuous and pulsed laser beams (laser glazing) has been explored for over 20 years (1-5). Advances in high energy, pulsed electron and ion beam technologies over the past decade have provided rapid thermal treatment techniques that may be less expensive to impliment than laser surface treatment for many surface modification applications (6). High energy pulsed ion beams have recently been used to harden aluminum(7), copper(8) and tool steel surfaces (6,9), increase corrosion resistance of Al alloys (6), mix coatings into underlying substrates (10), and create amorphous films (11,12)."

Jan 1, 1994

By A. J. Duncan, S. Viswanathan, Q. Han

"Measurements of liquid permeability in the mushy zones of Al-15.42% Cu and Al-8.68% Cu alloy samples have been performed isothermally just above the eutectic temperature, using eutectic liquid as the fluid. A modified method has been developed to determine the specific permeability, Ks, as a function of time during the test from the data collected on these alloys. Factors affecting permeability measurements are discussed. Permeabilties are observed to vary throughout the experiment. This is attributed to rnicrostructural coarsening and channeling that occurs in the sample during the experiment. The permeability is related to the rnicrostructure of the sample using the Kozeny-Carman equation. The correlation between the measured Ks, liquid fraction, gL and the specific solid surface area, Sv, improves markedly when compared to previous studies in which rnicrostructural coarsening was ignored.IntroductionThe permeability of interdendritic liquids flowing through dendritic structures ·is an important parameter needed to predict the level of porosity in castings. The permeability is a component of Darcy's Law, used to estimate the pressure drop due to the resistance to the flow of interdendritic fluid to feed shrinkage. Therefore, much research has focused on measuring the permeability of alloys in the mushy zone (1-10). The Kozeny-Carman equation for liquid permeability in the mushy zones of alloys may be written as"

Jan 1, 1999

By Jie Li, Shu Yang, Zhongliang Tian, Xun Hu, Yanqing Lai, Shaolong Ye

The electrolyte with high solubility for Sc2O3 is very important to realize the preparation of Al-Sc master alloy by the molten salt electrolysis. The solubility of Sc2O3 in K3AlF6- Na3AlF6-AlF3 melts is determined with an isothermal saturation method. The effects of KR (ratio of K3AlF6 to K3AlF6+Na3AlF6), the concentration of Al2O3 and the temperature on the solubility of Sc2O3 are also investigated. The results indicate that the solubility of Sc2O3 in K3AlF6-Na3AlF6-AlF3 melts increases and then decreases with KR increasing. The solubility of Sc2O3 is 8.698 wt.% in (K3AlF6-Na3AlF6)(KR25%)-18 wt.%AlF3 melts at 940℃. The effect of temperature on the solubility is little, and the values are 8.575 wt.% and 8.762 wt.% respectively when the temperatures are 930℃ and 960℃. The solubility decreases from 8.809 wt.% to 7.058 wt.% as the concentration of Al2O3 increases from 1.5 wt.% to 5.0 wt.% at 950℃.

Jan 1, 2015

By F. Mucciardi

With the increasing trend to continuous smelting and converting, granulation of copper matte is gaining prominence as a means of decoupling the smelting and converting operations. Moreover, granulation is also being seen as a possible avenue to using higher grade oxygen in converters. By feeding cold solid matte, the oxygen concentration can be increased to compensate for the lower enthalpy feed. This leads to a higher grade of SO2 in the off gas and a lower total flow rate. Current granulation technology relies on the cooling of a falling matte film by water jets. This technology while effective has several drawbacks including those related to safety. Noranda and McGill University have developed a new process (patent pending) for solidifying copper matte (or slag). It overcomes many of the negatives of current technology. The system is based on an air cooled twin roll caster. This: new system uses no water and instead incorporates heat pipe technology to transfer the heat from the solidifying matte to the cooling air to produce a thin strip of 1 to 2 mm in thickness. Testing of a prototype unit demonstrated its viability. This paper describes this newly developed, twin roll casting system that is completely waterless. The advantages of this process as well as the findings from several tests are also detailed.

Jan 1, 1999

By Laurentiu Nastac

"The importance of investigating solute redistribution during the unidirectional solidification of multi-component alloys is broadly discussed in the literature. A previously developed analytical model that was experimentally validated for Al-Cu, Sn- Bi and Fe-Si dilute binary alloy systems is used in this article to study in detail the solute redistribution, the liquid/solid interface stability based on an extended transient constitutional undercooling criterion and the size of the initial transient region during the unidirectional solidification of Ti-6-4 and Ti-17 alloys. A comparison between Ti-6-4 and Ti-17 alloy systems with respect to interface stability and the size of the initial transient region is also provided. The effective partition coefficients of the alloying elements in these alloys were determined based on specially designed experimental measurements.IntroductionThe importance of investigating solute redistribution during alloy solidification is broadly discussed in the literature [1-5]. One of the relevant applications of this study would be the mathematical modeling of equiaxed and columnar solidification of multicomponent alloys. This includes the instability of the solid/liquid interface. There are several mass and heat transfer processes that involve the calculation of solute redistribution during directional solidification such as industrial directional solidification processes, continuous casting, remelting processes, Czochralski crystal growth technique, floating zone techniques, etc."

Jan 1, 2012

By Junji Shibata

Heavier rare earth, which is contained in a small amount in ores such as bastnesite and monazite, has been accumulated as a heavier rare earth residue without doing separation and purification due to the lack of suitable methods. The heavier rare earth residue includes seven rare earth elements such as Tb, Dy, Ho, Y, Er, Tm and Yb. Separation and recovery process of Dy, Y, Tm and Yb from leached solution of the heavier rare earth residue was investigated by using a column method with solvent impregnated resin. The solvent impregnated resin was prepared by impregnation of organophosphorous extractant whose trade name is PC-88A into a macro porous resin, Amberlite XAD-7. It was almost impossible to separate them in simple adosorption and elution steps. However, we attained to individually separate Dy, Y, Tm and Yb from the leached solution first by changing eluent concentration gradually from pH2 to 0.02kmol/m3 HC1 in the elution step, and secondly by using a development column and changing eluerit concentration in the elution step. The separation process flow was proposed for a heavier rare earth residue by using the solvent impregnated resin method.

Jan 1, 1998

By Daniel Kim, Michael Free, Justin McAllister, Urian Marshall, Shijie Wang

"Cathode impurity levels of electrorefined copper were evaluated based on 1/10* scale laboratory electrorefining tests. Cathodes were evaluated near the top, mid-section, and bottom sections of cathodes on both the set and mold sides and strip and scrap cycles. Slime weights were measured, and slime and electrolyte samples were also evaluated for impurities. Results from these tests have been compiled and compared to evaluate the effects of changes in operating conditions and electrode location on cathode impurities.IntroductionMany types of impurities are commonly found in commercial copper electrorefining anodes. The smelter operations that produce the anodes process concentrates that contain a wide variety of impurities that vary based on the mineralogy of the ore. Most anode impurities are removed during electrorefining. However, a portion of the anode impurities is incorporated into the copper cathode product. The mechanisms by which impurities are transported from the anode to the cathode are not well understood. Some impurities can be transported as anode slime particles to the cathode where they are incorporated into the cathode. Other impurities can be transported as dissolved species that are electrochemically reduced with the copper to become part of the cathode. Although research has been performed on anode slimes and impurities [1-4], there is a need for additional information regarding the relationships associated with electrorefining cycles, electrode faces, local electrode positions, anode impurities and specific cathode impurities. The objective of this study was to evaluate lead, arsenic, and antimony cathode impurity trends associated with electrorefining cycles, electrode faces, local electrode positions, and anode impurities. A variety of techniques including electrolyte filtering, anode heat treatment, high electrolyte arsenic concentration, high arsenic and/or lead in anodes, flocculation of slime particles, and appropriate current density control were used to vary cathode impurity levels. Each test was performed only once for a strip cycle and once for a scrap cycle. Consequently, the results for the individual conditions are preliminary and are not the focus of this study. However, the collective set of data with varying impurity modifying techniques provides a broad range of impurity levels, and the associated trends with respect to lead, arsenic, and antimony are discussed in this paper. Approximately 180 analyses of copper cathode were used to track the antimony, arsenic, and lead impurities. Eighteen anode slime samples were also analyzed for antimony, arsenic, and lead."

Jan 1, 2012

By Y. Takasaki

For zinc hydrometallurgical extraction, reducing the electric power consumption of the electrowinning process is an important issue for energy savings. At the Zinc & Lead 2000 symposium, the authors suggested that by using the Pb-0.5%Ag-0.6%Ca alloy, the electrolysis energy can be decreased compared to the conventional Pb-0.9%Ag alloy. In this study, the corrosion behaviors of the Pb-Ag-Ca electrode in a sulfuric-acid electrolyte were investigated. Based on the results Or me Pb-0.5%Ag-0.6%Ca anode after 20 days of electrolysis, the bath voltage and the quantity of anode slime decreased compared to the Pb-I%Ag anode. Subsequently, beta-PbO2 on the electrode surface was detected by XRD and its peaks were sharper than the Pb-1 %Ag anode. Moreover, a dense beta-PbO2 layer on the 0.6%Ca a anode surface was observed. Therefore, it was suggested that the dense beta-PbO2 layer on the anode surface is one of the factors that leads to a lower bath voltage and decreasing quantity of anode slime.

Jan 1, 2003

By Stephan Mulch, Christian His, Patrick M. Stephan, Thibault Champion

"When fuel costs increase dramatically, waste to energy (WTE) conversion technologies become a good alternative to produce energy. The potential energy available in domestic wastes, in developed countries, could be upwards of 4% of their total energy needs. Due to low energy recovery and low level of treated domestic wastes in many countries, the energy coming from waste is generally less than 0.5% of the country needs.Domestic waste incineration can convert heat to electricity for industry and housing and allow waste volume reduction in countries where land fills are a scarce resource.There is a request to improve existing combustion technology by increasing energy recovery with better heat transfer in the boiler and also by increasing lining durability with more resistant materials and technologies.The knowledge of corrosion phenomena and material performance allows Saint-Gobain Group to develop and propose high performance refractory lining solutions.IntroductionThe interest in alternative energy has been growing dramatically in the two last decades due to several combined factors, such as global energy demand, fuels prices evolution (e.g. crude oil, Figure 1) or environmental and geopolitics factors"

Jan 1, 2008