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By Hector M. Henao

To provide thermodynamic data for converting nickel matte to liquid nickel at high temperature, an experimental study was conducted on the phase equilibrium between the Ni-S alloy and the FeOX-SiO2, FeOx-CaO, and CaO-A12O3 base slag in a magnesia crucible and the CaO-Al2O3-MgO slag in an alumina crucible. All experiments were carried out at 1773 K under controlled pso2 of 0.1 atm and po2 in a range between 5x10- and 10-5 atm by using CO-CO2-SO2 gas mixtures. The dissolution of nickel in the slag was found to be minimum for the CaO-Al203¬-MgO slag with a molar ratio of NCaO/NA1203=1.7. The solubility of nickel in this slag at p02 of 6x10 atm (just before the precipitation of solid NiO) was 4 mass%. This result suggests that a CaO-A12O3 base slag could be used in converting Ni-S melt to nickel while minimizing nickel losses to the slag.

Jan 1, 2002

By Jin Zuomei

The kinetics of dissolution of nickel matte in the presence of manganese dioxide with silver ions was investigated. The catalytic silver ions enchanced the leaching rate up to a factor of 17. The effects of stirring, temperature, particle size, concentrations of Mn02, silver and ferric ions, and the experimental procedures were studied. Solid residues at various levels of nickel extraction were examined by SEM, TEM, electron micoprobe and X-ray diffraction. These results indicated that the dissolution reaction was topochemical and fits a surface reaction control model. The activation energy was calculated to be 39.15 KJ/mol. The leaching rate of Ni3S2 was independent with stirring rate, but the reaction rate constant was inversely proportional to the initial particle diameter. The order of the reaction rate are 0.41, 0.69, 0.33 with respect to Ag+, Mn4+ and Fe'+ con-centration respectively. Thus a kinetic rate equation was developed. Moreover, we propose a mechanism of silver catalyzed leaching of Ni3S2'

Jan 1, 1990

By Paul Pajunen, Michael Sheedy

"Acid separation using short bed ion exchange is a now well established technology in copper refinery tankhouses. Refinery bleed streams from liberator cells are treated by short bed systems to produce an acid-free byproduct stream that contains the bleed metals and valuable nickel salts. Removing the acid eliminates the need for a black acid evaporator and reduces the amount of sodium carbonate required in nickel selective precipitation processes. The recovered sulfuric acid can be recycled to the tankhouse. This same technology is routinely used to treat other acids such as hydrochloric, nitric, and hydrofluoric. In the case of hydrochloric acid, the process can selectively separate chloro-anionic complexes such as Zn, Pb, and Cu, which are then eluted with water. The acid recovery technology can also be closely coupled with ion exchange processes in order to minimize regenerant acid consumption. In many hydrometallurgical applications resin regeneration often requires an acid dosage multiple times the stoichiometric minimum. Coupling an acid recovery bed with the IX column allows recovery and recycle of the free acid in the spent regenerant, thus reducing the overall acid consumption to just slightly more than stoichiometric.Short Bed Ion ExchangeThe short bed ion exchange process has been extensively used in the metal finishing industries since the early 1970s [1,2]. Short bed systems have also been sold to primary metals producers for the separation of sulfuric acid from copper refinery bleed streams [3] and for the recovery of nickel and cobalt from plant effluent streams. This unique technology optimizes the ion exchange process and offers a number of significant advantages over conventional ion exchange. The principal features and benefits of this technology are presented below."

Jan 1, 2012

By Veronica Escobar

This paper presents results from a two month pilot evaluation of EMEW® technology at CODELCO Radomiro Tomic, in Chile. A prime focus in the test programme was to assess the technology?s capabilities to recover high quality copper from the Radomiro Tomic electrowinning tank house bleed stream. The EMEW® cell developed by Electrometals Technologies Ltd. tolerates substantially higher levels of contaminants than those found in conventional tankhouse, operating at high current densities while maintaining high cathode copper quality all the way down to low copper concentrations. To maintain high copper purity in a copper electrowinning (or electro-refining) tank house, a continuous bleed of solution must be taken from the tank house inventory to prevent build-up of contaminants, and resulting degradation in cathode quality. In an SX-EW operation, this bleed stream is normally recycled back to the solvent extraction circuit, but is occasionally sent to the raffinate pond to re-enter the leach circuit. Return of the bleed stream to the solvent extraction circuit creates a continually recycling load of copper in solution, which may reduce overall plant capacity and expansion potential. Return to the leach circuit has a similar effect, and methods to reduce its impact are always under consideration. The use of the EMEW® technology allows for direct and efficient recovery of near 100% of the contained copper instead of recycling. Tests were run at ambient temperature on bleed electrolyte using current densities which varied between 250 and 1100 amps per square meter, with copper concentrations between 38 and 1 g/l. A profile of maximum allowable current density with respect to concentration was developed, showing that high grade copper can be obtained at all levels of concentrations tested, by choosing an appropriate current density and electrolyte flow rate. The results of this programme show that the recirculating bleed electrolyte from an SX-EW operation can be converted into an expansion in copper production at a comparatively low investment cost.

Jan 1, 2003

By M. J. Perpich

Electrochemical and chemical leaching tests were carried out on chalcocite, covellite and chalcopyrite in acidified iron sulfate solutions sparged with a mixture of O2 - SO2. The gas mixture catalyzed the ferrous to ferric oxidation reaction in situ and, therefore, increased the redox potential and oxidizing strength of the solution. Anodic polarization curves in dilute sulfuric acid on copper sulfide electrodes showed that chalcopyrite passivates and dissolves at current densities orders of magnitude less than chalcocite and covellite. The addition of a depassivating agent (Ag+) increased the passive current density of chalcopyrite and caused breakdown near 0.625 V (SCE). The depassivating effect was also observed during the leaching of chalcopyrite particulate samples as small amounts of Ag+ added to acidified iron sulfate solutions in the presence of O2 - SO2 mixtures greatly increased the leaching rate and the total amount of Cu oxidized (> 90%). Passivation was prevented in the absence of Ag+ by decreasing the initial oxidizing power of the solution and by pretreating the sample in a reductive leach. Both of these methods resulted in transformation of the chalcopyrite surface from its characteristic greenish-gold into deep black. Increased concentrations of Fe+++ due to 02 - S02 sparging were then able to oxidize the transformation product.

Jan 1, 1999

By Wei Liu

A new process for extracting cadmium from the electric precipitated dust produced by ISP process was studied. A leaching rate of 89.1% of cadmium was attained by leaching the dust with NH3?H2O-(NH4)2SO4 system under the best leaching conditions: ratio of liquid to solid(l:s)=2.5, c(NH3):c(NH4+)=3:5, total concentration of ammonium and ammonia=8 mol?L-1, leaching time= 1.5h, temperature=35. The most troublesome impurity of lead could be deposited from the leached out solution automatically after put it static more than 15h when the total concentration of zinc and cadmium was up to 45gL-1 , and the final concentration of lead was 0.0047 gL-1, which meant 99% of it was removed. Metallic cadmium which contained cadmium more than 99% was prepared by electrowinning under the conditions: current density=750Am-2, total concentration of Cd2+ and Zn2+>25gL-1. The current efficiency was about 87% and the energy consumption for every ton of cadmium was about 548KWht-1. Main impurities of the metallic cadmium were copper and zinc and all of they could be got rid of in the following pyrometallurgical refining step.

Jan 1, 2006

By Peter J. Koros

The current wave of interest in this topic is the result of increased use of titaniferous ores or ilmenite in blast furnace burdens for the purpose of repairing hearth damage. The titanium compounds that promote deposition of ?patching? materials in blast furnaces are the cause of downstream problems in the steelmaking shops. Steelmakers historically have objected to significant amounts of titanium in hot metal (>0.10 % Ti) for several reasons: 1) accretions caused by the TiC.TiN needles that float out of the iron as it cools in transit and in transfers make the accompanying slag sticky and crusty, causing problems in desulfurization and increasing time and Fe yield loss at the subsequent raking, 2) defensive measures have been taken in treatment, such as use of argon for carrier gas, but without technical rationale for this approach, 3) difficulty in removal of the ladle slag by the raker, with subsequent sulfur addition to the vessel charge, and 4) transfer into the BOF and/or formation of a very corrosive TiO2 containing acid slag during the early part of the BOF blow which, in addition to causing lining damage, results in loss of sulfur removal capability by the vessel slag. Based on a conceptual analysis of the metal-slag-atmosphere interactions during transfer ladle desulfurization treatment, a mechanism is postulated for the apparent effectiveness of the use of argon in reducing the deleterious effect of titanium and an alternate technique, possibly more effective, is proposed. As probably the use of argon causes increased exposure to atmospheric oxidation of the titanium carbonitrides contained in the ladle slag, the same benefit can be obtained by use of either oxygen or an air blast to oxidize the noxious reaction compounds. Validity of the concept has been demonstrated in a pilot plant setting. These issues, and related effects on testing the hot metal, are examined in detail with reference to the literature and plant and laboratory experience.

Jan 1, 2006

By P. R. Bruggink

"A quantitative tool has been developed to assess the impact of changes in recycling rates on the environmental impact of aluminum supply. It has been applied to the USA to forecast sources of aluminum scrap and to examine the impact of an increase in Old Scrap recovery on the USA supply system and the subsequent effect on the Life Cycle Impact of aluminum supply. The reported data for primary, secondary and import/export supply and product shipments for aluminum in the USA show a fairly good balance between supply and demand on average over the years. Therefore, it is reasonable to use the data, along with published estimates of average product lives, recycling rates and recoveries to draw conclusions about future aluminum scrap generation· and recovery. The Life Cycle Impacts of increasing post-consumer recovery rates to recover an additional 450,000 MT/yr (1 billion lb/yr) has been estimated using the model.The spreadsheet model upon which this work was based was developed in U.S. Customary units. Converting the figures to Metric units would have required converting the entire model and rebuilding the figures. I have chosen to leave the figures in U.S. Customary units. I apologize for any inconvenience this may cause."

Jan 1, 2000

By Purushottam Kumar

Keywords: Magnetostriction, magnetic properties, Pd(Fe,Co,Ni) single crystals Fe-Pd, Co-Pd and Ni-Pd alloy systems show appreciable magnetostrictive strains that are of interest for sensor applications. These systems exhibit congruent melting minima. In this work the magnetic and magnetostrictive behavior of congruent melting Fe-Pd, Co-Pd, and Ni-Pd compositions have been examined. The alloys examined include Fe-54.9 at.-% Pd, Ni-45.4 at.-% Pd, and Co-45 at.-% Pd. The paper describes the growth of bulk single crystals of these alloys using Czochralski technique. X-ray diffractometer was used to obtain rocking curves that were used to determine the [001] crystal direction. Magnetostriction in [001] direction was measured using strain gages. Magnetic properties were measured using a vibrating sample magnetometer. Ni-Pd showed the highest magnetostriction values among the congruent melting compositions. Magnetic and magnetostrictive behaviors of these alloy single crystals are presented.

Jan 1, 2005

By Shinya Hodoshima

A catalysis pair of tetralin dehydrogenation / naphthalene hydrogenation has been proposed in the present paper as a liquid organic hydride for operating stationary fuel cells. Catalytic naphthalene hydrogenation, having been commercialized since the 1940s, proceeds to generate decalin via tetralin as an intermediate. The storage capacities of tetralin (3.0 wt%, 28.2 kg-H2 / m3) are lower than decalin (7.3 wt%, 64.8 kg-H2 / m3) but both tetralin dehydrogenation and naphthalene hydrogenation are much faster than the decalin / naphthalene pair. Moreover, existing infrastructures such as gas stations, chemical tankers and tank lorries are available for storage, transportation and supply of hydrogen. With respect to the stationary fuel cells with large space for hydrogen storage, tetralin as a hydrogen carrier is superior to decalin in terms of fast hydrogen supply or power density. Rapid hydrogen supply from tetralin under mild conditions was only accomplished with the carbon-supported metal catalysts in the ?superheated liquid-film states? under reactive distillation conditions. In contrast to the ordinary suspended states, the catalyst layers superheated in the liquid-film state gave high catalytic performances at around 250OC. As a consequence, both serious coke formation over the catalyst surface and excessive consumption of exergy were prevented simultaneously.

Jan 1, 2006

By Andrew A. Fyfe

The start-up and operating results obtained at Zia Technology Inc.'s first commercial operating facility at Caldwell, Texas are described. The operation which stated in early 1991 is the first to employ the patented Inclined Rotary Reduction System (IRRS') with the associated 'all-metallic retort for the recovery of all metallics contained in EAF dust.

Jan 1, 1992

By Luciano B. Oliveira, Angela O. Costa, Sergio N. Monteiro, Luis Guilherme C. Marques

"Biofuels are gaining a relevant role in today’s world not only as a solution for the decreasing petroleum reserves but mainly as a positive contribution to the efforts in global warming mitigation. In Brazil, since 1975, the replacement of gasoline by ethanol started a so-called PROALCHOOOL program, which is now being complemented with the replacement of petroleum diesel by biodiesel. This biodiesel program was officially created in 2005 with mandatory goals, supported by legislation, of 2% addition in 2008 and 5% addition in 2013 into all commercialized regular diesel. In this work, a critical analysis of the Brazilian biodiesel program is presented. The technical aspects related to the different raw materials, including wastes, available for biodiesel conversion as well as the economical conditions associated with production costs and market logistic are discussed. The environmental benefits associated with the retention of greenhouse gases are also discussed.IntroductionToday the commonly accepted fact that the petroleum world reserves are probably passing through a maximum and start declining in terms of the total amount that can be extracted by existing technologies is motivating significant changes in our society. The continuous increase in the price of gasoline and other liquid fuels is an immediate worrisome and visible consequence. However, more than an economical problem, our civilization is already facing the effects of global warming, due to CO2 emission from burning fossil fuels, mainly from coal and petroleum. It is now realized that a large scale solution for these problems demands the prompt substitution of non-renewable fossil fuels by others that, in addition of being renewable, have a relatively lower contribution to the greenhouse gases."

Jan 1, 2008

By Fatbardha Osmani, Skender Osmani

"A system analysis of the resource and environment management (water, energy etc) starts from its definition. Unfortunately, there is not a unique semantics of the mentioned concept. On these circumstances, in this paper the following issues are presented: 1.A short view on the existing concepts of management. 2.A new definition on the concept of management. It is considered as a complex and rational activity on human and natural resources ,environment etc, which starts from a analysis of infrastructure ,technology , etc, mission , alternatives , project etc. and ends to an optimal output. Basing on this definition, the management has two principal components: strategy and policy. The strategy is referred as a blue print program (the same definition as in Game Theory), which contains all the contingency alternatives. , while the policy is referred as a strategy applied into practice. The strategy is the first , while the policy is the second one. The best alternative of a policy is the project, Each strategy has one and only one project. The mentioned definition erases the differences between concept of policy and politics. Each strategy has its alternatives ,the next has its sub strategy and so on, i.e. whatever are going to be the strategy, there are a hierarchy composed by sub strategies up to the simplest strategies applied by a single individual (human beings or robots). The strategy objectives are necessary and sufficient conditions for its realization i.e . the strategy is an optimal activity, in which all resources are integrated and processed . Several strategies could be joined into one( for example the surface water strategies of the Balkan countries) . In this view, the strategy could be globalized into optimal way basing on different criteria’s as social, economic, environmental, their risks and effectiveness etc. etc An example from the water management illustrates the mentioned concepts."

Jan 1, 2008

By Toshiaki Nakai, Kunihiko Takeda, Kimio Imaizumi, Hiroaki Shirasaka

"The new type of nano-porous silica particle was considered to be constructed by the spinodal decomposition-type process which was found to have narrower pores than those of conventional porous silica prepared from boron silicate or ""Shirasu"" balloon. Nano-porous silica particles were fabricated by the calcination of silica gel mixed with well-dispersed complex salts composed of phosphorous and molybdenum compounds. Both silica and inorganic salts were not perfectly dissolved in the suspension solution. After removing of the water, the silica-inorganic salts complex was volatized and successively calcinated at a temperature ranging from 650 °C to 800 °C. Then, the inorganic salts were removed by dissolving in hot water. Other inorganic salts such as potassium halides were also found to be effective as a pore-size controller.IntroductionControl of structure has an important role in the field of industry as well as in the separation and purification technology for metals and organic syntheses. Many studies on the control of material structures have been reported regarding porous materials with pores ranging from nanometer to micrometer scale. 1 ) One example is zeolite as a naturally yielded porous inorganic material. Various types of synthetic zeolites have been studied as ""molecular sieve"" materials with ordinary pore-size of less than one nanometer. In 1992, crystalline meso-porous material with a large surface area named MCM-41 was synthesized through the use of template synthesis. 2) In direct relation to our study, amorphous borate glass having 4 to 100 nm of fine pores known as Corning glass 3l or SiO2-Al2OrB2O 3-CaO porous glass having large pore dispersity ranging from 4 to 10,000 nm have been reported. 4 ) S) 6 ) Some examples of several reported studies are as follows: phase-separated porous glass consisting of B2OrAl2O3-ZrO2-RO-R2O complex oxide 7 ) glass with finer pore induced from hydrolysis of silane alkoxide, porous material attained by condensation polymerization through the use of sol-gel process 8), alumina meso-porous material 9 ) 10), silica-zirconia material 11), carbon porous material 12), etc.."

Jan 1, 2000

By Gary Kordosky

Equilibrium modifiers, first introduced into copper solvent extraction reagents in the late 1960?s, are widely used. The properties of various equilibrium modifiers with respect to copper extraction, selectivity, reagent stability and entrainment are discussed and some conclusions are drawn relating the structure of the modifier to the properties of the modifier. A new highly selective, low viscosity modifier is also introduced.

Jan 1, 2003

By Moo Eob Choi

A new process for converting sulfur dioxide to elemental sulfur by a cyclic process involving calcium sulfide and calcium sulfate without generating secondary pollutants was developed at the University of Utah. In this process, sulfur dioxide is reacted with calcium sulfide to produce elemental sulfur and calcium sulfate. The latter is reduced by hydrogen to regenerate calcium sulfide. In the present work, the effects of different pelletization conditions for the initial reactant calcium sulfate on the strength and reactivity of the pellets were determined. These conditions include the type, amount, and impregnation method of catalyst, binder amount, and sintering. Experiments were also performed to determine the effects of temperature in the range of 973-1173 K, pellet size, cycle repetition, and water vapor or carbon dioxide content in sulfur dioxide stream on the reaction rates of the cyclic process. Nickel-catalyzed fired pellets produced by the use of molasses or cement as a binder showed good reactivity as well as high compressive strength during the cyclic tests. The binder amount did not significantly affect the reaction rate.

Jan 1, 2006

By lchiro Aoi, Hideo Nakae, Makoto Yoshida, Makoto Ishino

"The influence 6f gravity on the microstructure of unidirectionally solidified Cu-Pb monotectic, Ag-Si and Fe-C eutectic alloys is studied. In order to examine the influence of gravity in a lg environment, both the upward (opposite to direction of gravity) and downward (direction of gravity) unidirectional solidifications are carried out. The results are as follows: (1) For the upward solidified Ag-Si eutectic alloy, the eutectic Si continuously grows. On the other hand, in the downward solidified Ag-Si alloy, the Si grows discontinuously and disperses into the ex-Ag matrix. (2) No morphological difference in the eutectic growth is observed between the upward and downward solidified Fe-C eutectic alloys. (3) In the case of the upward solidified Cu-Pb monotectic alloy, a banded structure, which consists of Pb-rich layers and Cu-rich layers, is observed. However, such a banded structure -is not observed in the downward specimen. (4) The banded structure is not found in the upward solidified Cu-Pb-0.05 mass % Al and Cu-Pb-0.1 mass % Al alloys. In the Cu-Pb-0.05 mass% Al alloy, a fibrous -L 2 phase grows continuously parallel to the growth direction at low growth rate. Only 500 mass ppm addition of aluminum induces the morphological change of the monotectic L2 phase.IntroductionThe influence of gravity on the solidification of eutectic and monotectic alloys has been investigated in microgravity environments [l-9]. The purpose of these studies was to obtain a homogeneous microstructure of eutectic or monotectic alloys, most of which alloys tend to solidify with macro-segregation under gravity. However, in most of the previous experiments, e.g., in free fall systems, in aircraft or in space laboratories, the growth rate was too high to realize a planar solid/liquid interface. This would be due to the limited time for solidification. Thus, it was difficult to examine the influence of gravity on the planar coupled growth of the eutectic or monotectic alloy. In this study, both the downward U.D.S. (unidirectional solidification by gravity) and upward U.D.S. (opposite direction to gravity) are carried out in order to examine the influence of gravity on the coupled growth in a lg environment [l0, 11]. In the case of the downward U.D.S. using the current Bridgman method, the molten alloy must be confined between the crucible and the solid."

Jan 1, 2000

By Biao Zhou, Qian Li, Kuo-Chih Chou, Yi-Long Liang, Jie-Yu Zhang, Qun Luo

"In this work, the phase transformational behaviors and microstructural characteristics of 60Si2CrVAT spring steel were systematically investigated as a function of applied cooling rates in the range of 0.l-10°C/s. A quenching deformation dilatometer was used to austenize and quench. The dilatometric curves between length changes and temperature of samples suggest three characteristic stages could be identified as different ranges of cooling rates, which meets well with metallographic examination and the measured hardness results. As the cooling rate increases, the structure transformed from pearlite, granular bainite to finally martensite. The F + P and B zones are completely overlapping in continuous cooling transformation (CCI) curve, which indicates that this steel is difficult to become single bainite and shows good hardenability.IntroductionThe 60Si2CrVAT, a high-carbon low ally super-high strength steel developed from the ?OCT 60C2XFA and 60Si2MnA, is often used for coil spring of heavy vehicles and high-speed railway by hot deformation or cold deformation [1-3]. The addition of Si improves relaxation resistance significantly, through the refinement of tempered carbides as the result of the retardation of E -carbide conversion to cementite during tempering. Due to its deleterious effects on decarburization and toughness, the maxinJum content of Si has limited to 1.5 or 2.0% [4-5]. Additionally, V and Cr can improve sag resistance due to the precipitation of fine carbonitrides during hot rolling [6-7]. To best of our knowledge, the strengthening by precipitation of alloy carbides of Cr and V often referred to secondary hardening [8]."

Jan 1, 2013

By V. Kamavaram

Keywords: Recycling, Aluminum Metal Matrix Composite, Ionic Liquids, BMIC Recycling of aluminum metal matrix composites (MMC) via electrolysis in ionic liquids at near room temperature was investigated. The electrolytic melt comprised of 1-butyl-3-methylimidazolium chloride (BMIC) and anhydrous AlCl3. Impure aluminum composite (Duralcan MMC Al-380, 20 vol % SiC) was electrochemically dissolved at the anode and pure aluminum (>98%) was deposited on a copper cathode. The deposits were characterized by scanning electron microscope, X-ray diffractrometer, and mass spectrometer. The influence of various process parameters such as concentration of electrolyte, and applied cell voltage on the recycling process was studied. The recycling process yielded current densities in the range of 200-500 A/m2, and cathode current efficiency of about 85%. The results indicated that impurities such as Cu, Si, Ni, Fe, Mg, Mn, and SiC particles were removed as anode residue. Energy consumption of about 3.7-6.3 kWh/kg-Al was obtained at a cell voltage of 1.0-2.0 V and cell temperature of 100 ± 5°C. Low energy consumption and no emission of pollutants are the two main advantages of this process compared to present recycling processes.

Jan 1, 2005

By W. M. Cross

Bubble attachment time measurements for the rare-earth phosphate minerals monazite and xenotime were made as a function of oleate concentration, sodium fluoride addition, and temperature. Results indicate that the rare-earth phosphates behave similarly to other phosphate minerals, notably collophanlte and fluorapatite, which have been studied previously. The addition of sodium fluoride yielded a modest decrease in bubble attachment time with fluoride additions below the apparent fluoride surface precipitation point, while at fluoride additions greater than the apparent precipitation point a significant decrease in attachment time occurs. Increasing the temperature or the system gave a slight decrease in bubble attachment time in the absence or sodium fluoride. With sodium fluoride addition and below the apparent fluoride surface precipitation point, an increase in temperature actually increased the attachment time. For sodium fluoride additions above the apparent fluoride surface precipitation point, a temperature increase significantly decreased the attachment time.

Jan 1, 1989