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By James C. Sever

The mode of operation of dolomite kilns at a magnesium reduction plant using the Magnatherm process was designed to minimize operation cost and maximize kiln refractory life. Analysis of downstream operation issues shows the quality metric for dolime changed from loss on ignition to specific surface area. This produced a complete change in kiln operation; the net results being major plant productivity increases decrease in operating cost, and increases in both kiln operating costs and reline frequency.

Jan 1, 2015

By M. I. Kalashnikova

Gipronickel Institute has developed the technology of treatment of difficult to concentrate sulphide Pb-Zn concentrates (Zn-19,9%, Pb-8,4%, Cu-0,34%, Fe-8,8%, Ba-6,8%, S-18,7%, Ag-106 g/tonne). The technology consists of pressure leaching, impurity removal from leaching solution, electrowinning and Pb-Ag containing cake treatment. Despite low zinc content in initial concen-trate the technology allows production of solution which is suitable, after standard procedure of impurity removal, for electrowinning with production of zinc grade SHG. Comparing to the standard technologies the flowsheet developed provides the lesser expenses per zinc unit because of decreasing of liquid to solid ratio at pressure leaching stage. The initial concentrate is characterized along with low content of principal metals by high con-tent of barite, which makes flotation of pressure leaching residue more difficult. That is why in this case the hydrometallurgical treatment was chosen. At optimal parameters of chloride leach-ing found during laboratory experiments the principal components extraction was 99.5% for Pb and up to 92% for Ag.

Jan 1, 2006

By S. P. Marsh, M. E. Glicksman

"The effect of capillarity-driven diffusion on the recalescence of mushy zones is studied in pure materials. The solid-liquid mixture is formed by rapid partial solidification of an initially undercooled melt, and the ratio of the two phases is subsequently maintained constant by an externally imposed adiabatic constraint. A novel technique has been developed that permits tracking of the kinetics of the diffusion-controlled evolution process in situ using precision temperature measurements averaged on a length scale larger than that of the microstructure.The mean ""temperature of a mushy zone is slightly below the bulk equilibrium melting point, and is related to a characteristic length scale of the microstructure through an appropriate statistical average of the GibbsThomson equation. Theoretical considerations indicate that the diffusion controlled recalescence will progress as t- l / 3, where t is time. This behavior is experimentally verified for both succinonitrile (SCN) and ethylene carbonate (ETC), which have markedly different morphologies. The kinetic rate constant is observed to increase monotonically with increasing volume fraction of solid in the two-phase mixtures, although a firm theoretical foundation for this result has not been developed.INTRODUCTIONA dispersed multiphase system seeking equilibrium will generally contain variations in the local .free energy density. These density variations arise from such factors as variations in the bulk free energies of the phases and the distribution of interfacial energies. In this study, we examine the kinetics of diffusion-controlled recalescence in 1 solid-liquid mixture of a pure substance at its melting point. This type of two-phase system is particularly convenient to analyze because of the well-characterized physical properties of pure phases (crystals and their melts) and their interfacial energies, and the absence of any solutal effects."

Jan 1, 1986

By G. Cifuentes

It is known that the cathode purity and the electrolyte treatment are affected by the solids present in the electrolyte. Anodic slimes properties (e.g., chemical composition, crystalline composition, sedimentation) were studied in copper electrorefining. These properties were modified through anodic composition and current density. In this investigation, we have worked with anode material from the Ventana Smelting, Hernan Videla Lira Smelting (ex - Paipote) of ENAMI (National Mining Company) and El Teniente Smelting of CODELCO-Chile (National Corporation of Copper of Chile). The characterization of the anodic slimes was done as a function of current density and anodic composition.

Jan 1, 1999

By Zviad Kovziridze

It is stated that the specific character of SPHTS specimens of TiCx consists in crystal lattice strength reflecting the condition of synthesis in ?burning wave?. The use of roentgenographic and other methods of analysis allow to estimate the effect of the conditions of synthesis causing the carbon sablattice defect on the grinding intensity of TiCx -phases. The study of the kinetics of vibratory grinding of TiCx -phases in ethanol and benzene medium allows to establish high grinding intensity of the phases close to stoichiometry and the possibility of producing high dispersion powders (Ssp 4.5-6 m2/g).

Jan 1, 2006

By S. M. McDeavitt

Waste form alloys are being developed at Argonne National Laboratory for the disposal of remnant metallic wastes from an electrometallurgical process developed to treat spent nuclear fuel. This metal waste form consists of the fuel cladding (stainless steel or Zircaloy), noble metal fission products (e.g., Ru, Pd, Mo and Tc), and other metallic wastes. The main constituents of the metal waste stream are the cladding hulls (85 to 90 wt%); using the hulls as the dominant alloying component minimizes the overall waste volume as compared to vitrification or metal encapsulation. Two nominal compositions for the waste form are being developed: (1) stainless steel-IS wt% zirconium for stainless steel-clad fuels and (2) zirconium-8 wt% stainless steel for Zircaloy-clad fuels. The noble metal fission products are the primary source of radiation in the metal waste form. However, inclusion of actinides in the metal waste form is being investigated as an option for interim or ultimate storage. Simulated waste form alloys were prepared and analyzed to determine the baseline alloy microstructures and the microstructural distribution of noble metals and actinides. Corrosion tests of the metal waste form alloys indicate that they are highly resistant to corrosion.

Jan 1, 1996

By J. E. Sallee

An experimental study has been conducted on the level of arsenic contamination in samples of zinc oxide when the zinc oxide is contacted with gas mixtures containing As4O6(g). This contamination has been determined as a function of A4O6 saturation pressure, temperature, zinc oxide sample surface area, impurities, and oxygen level in the gas mixture. The results indicated a rather clean separation can be achieved between condensed zinc oxide and gaseous arsenic oxide as long as attention is given to temperature control, and the final zinc oxide surface area. For a 300°C operation temperature and an AqOg saturation pressure of 0.38 TORR (or 0.05% As406 by volume), the contamination level is expected to be approximately 100 ppm. This suggests that arsenical dusts can be treated in the HRD flame reactor process and a reasonable purity zinc oxideproduct produced. The results also show no evidence of zinc arsenite or zinc arsenate formation.

Jan 1, 1994

By Neal Schwartz, Robert De Saro, Richard Rosenthal, Ed Kear

"A Stack Melter has been installed and is currently operating at Lexington Die Casting. The Stack Melter consists of a 1 meter (3 foot) diameter refractory tube, 2 meters (7 feet) high. Specification ingots are continuously fed to the top of the melter and piled to nearly the top. A burner fires through the scrap which melts the lower portion and preheats the upper portion. As the lower portion is melted, it is drawn out and the upper preheated scrap falls to a lower level where it in tum melts. The molten metal is fed to one of two holding furnaces for eventual delivery to a casting machine.The Stack Melter's energy use is approximately 2900 joules/g (1,250 Btu/lbm), resulting in an overall energy savings of about 58%. This energy savings is brought about primarily because the flue gases preheat the scrap and the flue gas temperature is dropped to well under 528°C (1000°F)."

Jan 1, 2000

By Daniel Gauthier, Patrick Sharrock, Cedric Verwilghen, Gilles Flamant, Ange Nzihou, Jocelyn Ramaroson

Clean processes are needed to dispose of many wastes. The incineration of 1 ton of municipal solid waste generates 6000 Nm3 of combustion gases contaminated with heavy metals and other pollutants. Gas scrubbing processes are required to clean incineration fumes in order not to transfer pollution to the atmosphere. We are investigating the use of Hydroxylapatite (Ca-HA) particles for use as sorbent for the removal of volatile heavy metals. We have carried out the synthesis of Ca-HA by two precipitation methods from solution and obtained solids with specific surface areas reaching more than 100 m2/g. Preliminary adsorption experiments were conducted in a horizontal furnace by mixing Ca-HA with 5% by weight of cadmium chloride in solid state. The mixture was heated to 600°C under air atmosphere during 6 hours. Chemical analysis of the solids confirmed that 85 % of the cadmium was retained in the solid phase. Such laboratory results showed that Ca-HA is capable of adsorbing cadmium chloride vapors, and pilot scale studies confirmed cadmium abatement in an industrial context.

Jan 1, 2008

By R. Rajiv Srivastava

Brine leaching of a TSL processed zinc-plant residue (ZPR), containing 83.3% anglesite, has been investigated for lead recovery. A prior treatment of ZPR in acid solution did not show any significant effect of acid concentration in zinc dissolution. The study reveals that the solubility limits of PbCl2 is as an important factor with respect to the brine concentration and pulp density in lixiviant. The dissociated sulfate ions hinder the formation of PbCl2 on prolong leaching (above 60 min), while exhibiting the reverse solubility of lead as PbSO4. A 3-step leaching process could yield >92% leaching efficiency when the parameters were maintained as: 10% pulp density in a 250 g/L NaCl solution, 80 °C temperature, and 60 min time. This leaves the insoluble ferrite, sulfides and oxy-sulfates of zinc and lead in the final residue as revealed by the XRD characterization.

By Shengli Wu, Mingyin Kou, Feng Chang, Laixin Wang, Hua Lu, Jianliang Zhang

Sintering dust has been regarded as an important secondary resource in a modern steel plant. Sintering dust was mechanically treated using different milling machines and experimental conditions in air atmosphere. The changes in phase constitution, particle size, specific surface area, particle morphology, and lattice parameters of activated sintering dust were determined. It was found that the agglomeration of the particles take place during extended dry milling with accessible pores for Nitrogen gas. The maximum specific BET surface area in the stirring wet grinding and planetary wet grinding increases to 43.06 and 46.45 m2/g after activated 360 min respectively. With the increasing of energy input, the intensity of diffraction peaks of dolomite and hematite gradually decreased. Furthermore, the previous phase almost disappeared eventually under any experimental conditions. In addition, Fourier transform infrared spectroscopy indicates that organic matter and carbonate decompose easier than other phases, especially under stirring wet milling.

Jan 1, 2016

By T. A. Larssen

The efficiency in production of manganese ferroalloys is dependent on the gaseous reduction of the higher manganese oxides in the ores used as raw materials. The materials, descending in the furnace, will meet the furnace gas that contains significant amounts of CO(g) and reduce in subsequent steps, the last step being reduction of Mn3O4 to MnO. This step may to varying extent occur at temperatures exceeding 800 °C, i.e. in the active region of the Boudouard reaction. The gas reduction of Assmang and Comilog manganese ores were investigated in CO-CO2-atmosphere at temperatures up to 1000 °C. It was seen that decreasing ore size correlates to a lower reduction temperature and increasing reduction rate. Similar effect was observed with increasing CO-content in the gas atmosphere. Further, it was found that Comilog ore obtained a complete prereduction at 600 °C, whereas reduction of Assmang ore was not complete at 800 °C for the majority of the experiments.

By S. F. Cheng

Among the many extraordinary features of the rare earths are their magnetic and magnetoelastic properties. The rare earths, e.g. Tb, Dy, Nd, Sm, are known worldwide for their large magnetocrystalline anisotropy and magnetization, which has led to the importance of magnetic rare earths as vital ingredients of modem permanent magnets. In this paper, we focus on the strain dependence of these giant effects which gives rise to huge magnetostrictions, magnetomechanical couplings, and ?E effects. Magnetostrictions greater than 10-3 have been measured at temperatures as high as 500 K. At low temperatures magnetostrictions reaches -1%. ?E effects - 10. No other solid state material has matched these values. A proper balance of magnetic anisotropy and magnetostriction, plus a proper choice of crystal axes lead to alloys which can switch large quantities of energy between the internal (magnetic) and external (mechanical) states with the application of small triggering magnetic fields. In addition to the traditional use of these materials in transduction, they are particularly valuable for smart systems where reliability and robustness are needed such as active structure stiffening and active vibration control.

Jan 1, 1997

By D. M. Hausen

A refractory siliceous low-grade silver ore (265 g/t Ag) from a prospect in Sonora, Mexico was investigated mineralogically and metallurgically to evaluate extraction of the silver by conventional methods. Approximately half of the silver was recoverable, occurring as coarsely crystalline acanthite (70-300 Am) that was liberated in material crushed to minus 10 mesh. The remaining silver is refractory and occurs mostly as finely locked (-2 to 0.2 Am) acanthite in cherty quartz, and as minor amounts of finely disseminated stylotypite or freibergite in fluorite. The mineralogic data have thus served to explain the 50-60% recovery of silver by flotation and cyanidation.

Jan 1, 1991

By Xi Yun Yang

Ultrafine (0.1µm) spherical magnetite powder was prepared successfully by hydrothermal reaction of ferrous sulfate and sodium hydroxide with activated pyrite as reducing agent in the temperature range 120-140?. XRD and XPS analyses indicate that pH value and pyrite amount have a direct influence on the composition of the product. Stoichiometric Fe3O4 can be obtained only when pH value is 12 and the molar ratio of pyrite/ferrous sulfate is 1:1.8. The hysteresis loop of Fe3O4 shows a ferromagnetic behavior with a saturation magnetization of 75.2 emu/g and a coercivity of 152Oe.

Jan 1, 2006

By Victor Bredykhin

The reasons of formation low quality cathode deposits and conditions of the anode passivation in electrorefining of copper silver alloys with increased (more then 5%) silver content in electrolyte, g/l: Cu - 40; H2SO4-50; 150 and 250; T= 401C have been investigated. As it is shown, increased acidity, anodic current density and silver content in anodes favor passivation. The assumption is made that the ingress of silver on cathodeis the most probable reason of growing dendrites on cathode. We have determined that addition of ethylene carbonic acid to electrolyte in the amount of 3,5 ÷ 10 ml/l suppresses the dendrite formation.

Jan 1, 2006

By Yuanyuan Wang, Hong Li, Xueting Liu, Hao Bai, Kang Zhou

"Phase change materials are widely used in efficient utilization of energy and new energy technology. Especially, more attention has been paid to composite phase material, which is applied on architectural energy-saving and efficient working fluid. In this paper, stearic acid-silicon dioxide composite material was prepared by sol-gel process from tetraethyl orthosilicate (TEOS) and stearic acid (SA). The material was investigated by Field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR) and Differential scanning calorimeter (DSC). The FE-SEM results show that 3D-grids of silicon dioxide were formed clearly and SA was encapsulated in the silicon dioxide shell. The FT-IR results show that there were no chemical reactions between silicon dioxide and SA, which is the chemical property of the composite material, is stable. The DSC results show that the composite phase change material has favorable heat capacity. This material is expected to be used to make a cooling working fluid.1. IntroductionEnergy thermal storage becomes increasingly prominent issue in recent years, because thermal storage has been used in many aspects, for example, it can be added into building materials to improve heat conditioning. Another potential application of thermal storage materials is that the intermittent waste heat can be collected and recycled effectively by using the thermal storage facility. Thus, energy thermal storage plays a significant role in conserving available energy and improving its utilization [1]. Energy thermal storage includes sensible heat storage and latent heat storage. The latent heat storage has great heat density with a constant temperature during the phase change process [2-5]. Large quantities of latent heat storage will be absorbed and released when phase change takes place. Based on the former researches, some phase change material (PCM), such as fatty acid and paraffin waxes, has been proved to have high latent heat storage capacity and appropriate thermal properties [5-6]. However, using the PCM in energy storage systems directly is restricted, e.g. some properties of organic PCM, like form-stability and thermal conductivity, are not good enough to use. Meanwhile, almost all the inorganic PCMs are corrosive and most materials may cause sub cooling and segregation [7-9].The other problem is that the leakage when the temperature reaches the phase change point. Therefore, encapsulated composite phase change material (CPCM) emerged in order to solve the problem of leaking out, minimize the sub cooling and prevent phase segregation. [10-13] However, the easy flammability of fatty acid also has hindered the development of PCM. Accordingly, it has been found out that silicon compounds are environmentally friendly promising substitutes for halogen-containing flame retardants. Especially, silsesquioxanes are excellent in the flame retardancy. So CPCM can be encapsulated with SiO2 acting supporting material."

Jan 1, 2014

By A. Pagliero

The coulombimetric reduction method has been used as an evaluation technique for Pb-Ca-Sn anode corrosion in the LIX-SX-EW process. The proposed methodology involves three consecutive steps, i.e., cleaning, oxidation and reduction. They are carried out in the same experimental unit, in solutions containing 180 g/L H2S04 with and without the addition of cobalt. The authors have worked in a wide range of oxidation current densities, from 150 to 500 A/m2 for in a period from 0.5 to 120 hours. It can be concluded from the results that there would be a linear relationship between the applied electrical charge I*T (Coulomb) and the anode corrosion expressed as transformed Pb mass (mg), for solutions with or without the addition of cobalt. The exception is that for the last one the corrosion rate is 5 times faster, which was observed for every layer. From the evaluation of different corrosion layers, one can point out that its composition is mainly in the form of sulphate. In the presence of cobalt, about 67% of Pb would be as sulphate (PbSO4), about 27% as a basic oxide (PbO) and only 6% as oxide PbO2 on the surface. From this result, it appears that great transformations occurred in the metal/sulphate interface. Without the addition of cobalt, the proportion of oxide Pb02 on the surface increased up to 11.5%. According to the previous statement and considering that Pb was found mainly as sulphate, the authors recommend its determination be used as quality selection criterion. Its evaluation should be performed in the acid solutions with 200 ppm cobalt addition at an oxidation current density of 300 A/m2 for a period of 24 hours.

Jan 1, 1999

By Farouk Tedjar

The growth of miniaturization in one hand and energy density need lead to rapid development of new chemistry for batteries as observed during last decade particularly in secondary systems. However dark side of the progress is always in environment impact and scarcity of resources. In the lithium segment a jump from six electrochemical series (all non rechargeable systems) before 1990 to more than 15 systems including new rechargeable systems has been observe during last decade. Lithium battery chemistry was enriched with new electrolytes, conductive salts and new oxide composition. In the same time, lithium ion battery safety was strongly improved during last period. The progress of these technologies was strongly boosted by the substantial growth of the mobile telephone market in the mid 1990's (+ 1% a month in 2000, and a 71% penetration rate in Europe in 2005 compared to just a few percent in 1996). This market is constantly in search of higher electrochemical performance (mainly energy density in front of increasing miniaturization. Recycling of end of life product could be managed not only in environment aspect, but also under resource conservation and economic aspect of arising technology (mainly on the effect of re-injection recovered materials) The Li-ion segment is a new branch in the cobalt market and impact of LiCoOx will be fitted with the actual increase of the demand for this battery. For this reason all the processes aim to valorize active and packaging material. RECUPYL process project was conducted in this direction to offer a new solution for recycling those lithium systems. The process has been developed at pilot industrial scales using synergy between new equipment (for mechanical pre-treatment step) and existing line at RECUPYL facility (for chemical treatment) and should lead to high valorization rate with a minimum hazardous co-products. The process was also developed in order to be able to recover news cathode materials introduced in electrode like LiFEPO4, LiMxCoyO2 and new anode composition in substitution with former carbon anode.

Jan 1, 2006

By E. M. Timoshenko

Autoclave technology can be effectively used for liberation of complex mineral raw materials to transfer valuable constituents into solution for their subsequent recovery or to refine feed material in order to remove deleterious impurities, e.g. arsenic. The high efficiency of autoclave processes is attributed to the fact that they are suitable for processing of refractory raw materials, have low capital costs, high productivity, ensure integrated utilization of the feed materials, produce innovative saleable products, completely eliminate any air emissions, provide low-waste or waste-less technology, mechanization and automation of production processes. In the immediate future, it might be expected that autoclave processes will find use on commercial scale for production of heavy non-ferrous metals in combination with other processes (hydrometallurgical, upgrading, sorption and solvent extraction, electrolytic, etc.) to ensure: - Integrated processing of refractory ores and concentrates (pyrrhotite, zinc, copper-zinc, lead-zinc, nickel-cobalt, copper, pyrite); - Production of metallic powders of base metals as commercial products (copper, cobalt, nickel, etc.), composites on their bases, final products and saleable salts. Processing technologies incorporating autoclave processes, especially at the stage of liberation (chemical upgrading) of raw materials are characterized generally by high overall recoveries of valuable constituents significantly exceeding recoveries common for conventional pyrometallurgical processes (for some elements by several tens of percent).

Jan 1, 2006