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By Pinai Mungsantisuk

Keywords: Pd-Ni alloys, Pd-Fe alloys, Pd-Co alloys, Magnetostriction, Magnetic Properties The presence of congruent melting minima, the occurrence of ferromagnetic transition over a large composition range, and FCC type crystal structure make Pd-Ni, Pd-Co, and Pd-Fe based systems attractive candidates in our search for materials with no rare-earths, large low-field magnetostriction, and good mechanical properties. The presence of paramagnetic-ferromagnetic transition over a broad range of composition also provides opportunity for fundamental studies. In this work, we have examined the magnetic and magnetostrictive behavior of Pd-Ni, Pd-Co, and Pd-Fe alloys over the entire composition range. Alloy sample rods were prepared by arc melting and casting. X-ray diffractometer was used to obtain lattice parameter data. Magnetostriction was measured along the rod axis using strain gages. Magnetic properties were measured using a vibrating sample magnetometer.

Jan 1, 2005

By Shadia J. Ikhmayies

Polycrystalline CdTe thin films were prepared by vacuum evaporation on glass substrates. The I-V plots which were linear were used to find the resistivity. A value of 2.10×106 .cm was obtained. The transmittance was measured in the wavelength range 400-1100 nm. The bandgap energy was found to be 1.48 eV. X-ray diffraction pattern shows that the material deposits in the zinc blend structure with one strong reflection from the C(111) plane. The scanning electron microscope image shows a uniform surface with a small density of large (mµ1£) grains scattered on the surface.

Jan 1, 2009

By A. Iván, Patiño C. Francisco, Flores B. Javier, Peréz L. Miguel, Hernandez A. Juan, Trapála P. Norma, Salinas R. Eleazar, Rivera L. Isauro, G. Flores, U. Mizraim

"Tills work is related with the production of tiles using wastes from mining and metallurgical industry of Hidalgo State, as raw material. These wastes present a majority particle size (60 %), minor than 53 m (mesh 270, in Tyler Series) with the following composition; 70.01 % wt. of Si02, 12.82 % wt. of Ah03, 3.80 % wt. of Fe, 0.70 % wt. of Mn, 3.98 % wt. ofK20, 3.34 % wt. of CaO, 2.50 % wt. ofNa20, 0.04 % wt. of Zn, 0.026 % wt. of Pb, 56 grams per ton of Ag and 0.6 grams per ton of Au. In this work, the partial results and experimental conditions for the preparation of some composites to produce tiles are shown. The composite that offers the best results in productions of tiles was that with 66.67 % wt. of mining waste, 26.67 % wt. of red mud and 6.67 % wt. of black mud.IntroductionTo now, mining activities carried out during more than 457 years in Hidalgo State, Mexico; has lead a great volume of wastes; which can be classified into different types, having among the more common; Acid mining water, solid transport water, elements in radical form, abandoned minerals without processing and processing minerals wastes known as burrows, being these the most abundant in the region counting with an approximated volume of 110 million of tons, presenting a fine particle size that can affect population health during windy epochs [1 -4].Form metallurgical point of view, is well known that a fundamental characterization study it is necessary to know the viability of reusing or recycling of these wastes. According this, these residues can also be considered as raw materials in other economical activities, due its Si, Fe, AI, Ca, Na and P oxides contents, its mineralogy and the distribution of chemical elements in the primary and secondary phases [1,2,5,6]."

Jan 1, 2012

By Antrekowitsch Jürgen

The recycling of residues from metal producing by-products has become a main field of interest in metallurgical investigations. Forced by a stricter environmental legislation and the resulting increase of landfilling costs, combined with the aim to recover as many valuable metals as possible, a lot of different processes have been developed in the last two decades. Because of the high yearly tonnage residues from the iron and steel industry like slags, dusts and sludges have moved in the center of interest. Dusts from the steel mill, containing heavy metal oxides and halides did not play a considerable role as secondary raw materials for a long time. They even contain a huge amount of leachable elements and compounds which cause noticeable problems in case of a dumping. Nevertheless, the implementation of a new landfilling regulation, including a prohibition of aboveground dumping without inertisation, caused a rising interest concerning recycling technologies for such residues. In addition, the zinc content of these dusts became higher and higher and began to play the most important role for the economy of dust recycling.

Jan 1, 2006

By S. R. Reddy

Thennodynamic properties of several quaternary systems are calculated using our recently modified Margules equations. The modified Margules equations are expressed up to infinite order in the vicinity of solvent. Quaternary system of one solvent and three,solute partials are derived. First order interaction coefficients of binary, ternary and cross -interaction parameters of quaternary system are used to'evaluate the partial functions. In the original fonn of Margules equations,derived partial functions are convergent and same 'as Unified ,Interaction Parameter Fonnalism. But considering up to infinite order of the Margules coefficients, the functions are divergent, in order to overcome this restriction, Margules equations are modified to get consistent equations. Derived partial functions are thennodynamica Hy consistent with Maxwell and Gibbs Duhem relations. The derived logarithmic activity coefficient of the solvent and solutes are consistent with the ternary systems. The calculated data, ie., activity coefficient values of nitrogen and interaction coefficients are in good agreement with the data of Fe-Cr-V -N. Fe-Ni-V -N, Fe-Cr-Ta-N and Fe-Ni-Ta-N systems.

Jan 1, 1999

By John Jiang, Yeonuk Choi, Olivia Wang, Gus Van Weert

"As part of a general review of processing double refractory ores through Barrick Gold's autoclaves/CIL facility at Goldstrike, Nevada, blanking the gold cyanide adsorbing native carbon in the ore with hard (m.p. >55°C) paraffin wax was proposed. To avoid interference from other ore constituents in the exploratory testwork, commercial activated carbon was substituted for native carbon in the ore to establish the best conditions for de-activation of carbon with molten wax.IntroductionDouble refractory gold ores present two barriers to gold extraction. The first is generally a physical barrier: the gold is encapsulated or dispersed in a matrix which is impervious to the gold lixiviant. In most cases, including the Goldstrike deposit, this involves a pyrite or arsenopyrite matrix, although minor gold may also be dispersed in competent silica (quartz) or iron oxides. Gold can be rendered accessible by oxidative destruction of such sulphide matrices. At Goldstrike this is practised by roasting and autoclave oxidation (POX). It is the latter route to which this paper refers.The second barrier refers more correctly to gold recovery. Gold may be extracted from the autoclave oxidized solids with cyanide, forming a gold cyanide complex. One characteristic of this complex is that it adsorbs on graphitic surfaces. This behaviour is used advantageously on a large scale by gold millers, who use man made activated carbon particles to remove the gold from solution during leaching: the Carbon-In-Leach, or CIL process. The gold bearing carbon particles are larger than the ore solids and can be separately recovered by screening. Goldstrike uses the CIL technology to recover gold after autoclave oxidation."

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 Xinghua He, Shujing Zhu

"In this paper, the chemical composition, the content and the leachability of heavy metals in dredged sludge are tested and analyzed. It is shown that the leachability of Pb and Cr exceeds the leaching toxicity standard, and so the dredged sludge is considered as hazardous waste and must be solidified. The effect of solidifying the dredged sludge by the hydraulic ash-slag cementitious composites is studied, and it indicates that the heavy metals can be well immobilized if the mass fraction of the dredged sludge is appropriate. The heavy metals are immobilized within the hydraulic ash-slag cementitious composites hydration products through either physical fixation, substitution, deposition or adsorption mechanisms.IntroductionDredged sludge is classified as a hazardous waste because it usually contains concentrated heavy metals and chlorinated organic compounds, as well as soluble salts, and is also composed of very fine particles. Moreover, inorganic pollutants are typically associated with soluble compounds, which are, therefore, highly leachable from dredged sludge when dredged sludge is contacted by a liquid medium[l1. Thus, dredged sludge must be stabilized in order to reduce its environmental impact on the final disposal site. The frequent means of dredged sludge disposal used include(!) Chemical stabilization (2) acidic extractionChemical stabilization is translating mobile heavy metals into low dissolution and low toxicity form through chemical reaction. The commonly chemical medicaments are sodium hydroxide, soldium sulfide, thiourea, EDTA. But Zhao et al [ZJ found sodium hydroxide is not fit for Pb stabilization, the other three are effective, but the chemical properties of sodium sulfide are not stable, thiourea and EDTA are very expensive, and so it is very difficult to apply them. Moreover, because of the complexity of heavy metal conformation and dredged sludge composition, it is very difficult to find a cheap and prevalent stabilization medicament in point[31 ."

Jan 1, 2013

By Xinghui Meng

The leaching behavior of platinum powder in .iodide solutions under oxygen pressure in an autoclave was investigated. Ammonium salts were added to the leaching solution at neutral pH as a key lixiviant for platinum. The effect of temperature, partial pressure of oxygen, concentration of iodide and of arttmonium salts on the dissolution rate of platinum was examined. Under experimental conditions, the leaching behavior of platinum powder exhibited a complex reaction mechanism. A precipitate was found during the leaching process and was identified to be platinum ammine iodide, Pt(NH3hI4. The dissolution rate was controlled by a series of chemical reactions, the equilibrium concentration of the platinum ammine iodide being responsible for the ultimate limit to the recovery.

Jan 1, 1996

By Emmanuel N. Zevgolis Ismene-Polyxeni Kostika

Keywords: reduction, kinetics, laterites, rotary kiln, dust In this work, the reduction kinetics of dust from nickeliferous Greek laterites is investigated. The dust is a by-product from laterite treatment in rotary kilns and it comes from washing towers, electrostatic filters and polycyclones. Laboratory made pellets from this dust were also examined. Reducibility was studied in the temperature range of 700°C to 850°C in a laboratory tube furnace. Kinetic analysis of the results showed that at lower temperature values the mixed kinetic model verifies the experimental results of dust and pellet samples. At higher temperatures (800° and 850°C) diffusion becomes the rate controlling mechanism. The calculated activation energy values verify also the above mentioned results.

Jan 1, 2005

Sm-Co alloy is a kind of magnetic material with high power and has been applied in modern industry widely. In this study, the wet chemical co-precipitation was developed for synthesis of the Sm-Co alloy oxide precursor. The thermodynamic analysis of the studied system was done to clarify the solution behavior theoretically based on the thermodynamic equilibrium and simultaneous equilibrium. Then, the experiments were done to address the various effects on the wet chemical process, including solution pH, reactant concentration, dispersant, reaction temperature and time, etc. It is found that by precise control of the process, the Sm-Co alloy oxide precursor was synthesized with fine crystallization and special size & size distribution.

Jan 1, 2005

By Michal Rzyman, Nakamura Takashi, Shibata Etsuro, Grabda Mariusz, Oleszek-Kudlak Sylwia

"Thermodynamic considerations indicate that heavy metal oxides should easily react with HBr, the main gaseous product from the thermal decomposition of tetrabromobisphenol A (TBBPA), forming low boiling point metallic bromides suitable for volatile separation. Mechanisms and kinetics of the bromination reactions must be well recognized prior to developing of a new treatment for the simultaneous recycling of plastic waste containing brominated flame retardants (BFRs) and metal oxides (printed circuit boards, automotive shredder residue, plating sludge, metallurgical dusts). In this work, a differential scanning calorimeter and laboratory-scale furnace were used to investigate the possibility and conditions of the bromination of ZnO by product of thermal decomposition of TBBPA. The formed solid, condensed and gaseous products were analyzed by X-ray diffraction analysis, electron probe microanalysis, inductively coupled plasma analysis, ion chromatography and gas chromatography coupled with mass spectrometry. Introduction Tetrabromobisphenol A (TBBPA) is the largest volume brominated flame retardant (BFR) in production today and is used in more than 70% of the world’s electronic and electric (E&E) appliances [1]. The growth in the production of E&E products and the fact they become obsolete so quickly cause significant problems in the safe disposal and recycling of the electrical and electric waste (E-waste) and other BFR-containing waste [2]. Among various treatment processes, thermal methods are most useful since they allow the recycling and recovery of both the organic and inorganic fractions of the waste. However, incineration of the BFR-containing wastes results in the emission of hazardous organobromine compounds, while the main portion of bromine released from decomposed BFRs is present in flue gas as hydrogen bromide (HBr) [3]. HBr, which is known to damage incineration systems, seems to be a very effective bromination agent for many metallic oxides present in waste. The concept of this study is to take advantage this of its property."

Jan 1, 2008

By Garth James

Bacterial consortia capable of degrading cyanide and metal-cyanide complexes were obtained from gold mine process waters using enrichment cultures. The cultures contained either cyanide, tetracyanonickelate, or ferrocyanide as a sole nitrogen source. Several bacteria were isolated from the consortia, but none of these organisms were capable of degrading cyanide or cyanide-metal complexes at rates equivalent to those of the intact consortia. The consortium from the cyanide enrichment was capable of completely degrading cyanide from an initial concentration of over 100 ppm in less than one day, when cultured using a fed-batch method. Tetracyanonickelate and ferrocyanide were degraded more slowly. Overall, these results demonstrate that bacteria capable of degrading cyanide and cyanide-metal complexes can be isolated from mine process solutions and are capable of significantly reducing cyanide concentrations under appropriate conditions.

Jan 1, 1998

By Jafar Safarian

A new kinetic modelling technique has been applied to study the rate of MnO reduction from slags by dissolved carbon in liquid iron. Based on a consideration of the fundamental reaction kinetics, a general differential equation for the slag reduction process has been formulated, which then is solved analytically for certain special cases. By re-writing the solutions in a dimensionless form the poorly known kinetic constants are eliminated, which makes the model both flexible and applicable to a wide range of experimental conditions. For example, changes in process parameters such as temperature, metal composition, slag composition, gas composition can readily be captured along with variations in the crucible geometry. Based on a comparison with a series of experimental reduction curves being reported in the literature, it is concluded that the predictive power of the model is surprisingly good, yielding outputs that are both reliable and physically reasonable. An attractive feature of the model is that it provides an alternative way of calculating the activation energies from experimental reductions curves. For example, it suggests that the activation energy for the reduction of MnO by dissolved carbon in liquid iron is about 90 kJ/mol, which is different from the previously reported activation energies. The model also suggests that the crucible geometry, which affects both slag the volume and the resulting slag/metal interfacial area, has a significant influence on the overall reduction kinetics. This design parameter is a key to further optimisation of the process on an industrial scale.

Jan 1, 2006

By J. R. Parga

A shortage of landfill space and growing environmental concerns in Mexico are renewing interest in the recyclability of scrap from automobiles. This work describes a pyroumetallurgical process for the recovery of metallic lead from waste lead paste. Argentopyrite concentrate is commingled with lead paste residue and smelted in a fuming process thereby transferring the precious metals into lead bullion. The process consists of smelting lead paste and argentopyrite, sodium carbonate, and metallic iron at smelting temperatures of about 1100 T. The reaction products are slag and molten lead bullion enriched with precious metals. A major feature of this process is the removal of precious metals from the bullion by means of zinc, whereby a silver-zinc intermetallic compound is formed and floats out of the lead. The recoveries of precious metals are about 98%.

Jan 1, 1996

By Cleusa Cristina Bueno Martha de Souza

Hydrometallurgical techniques for processing metals are becoming an efficient method for recovering metals. Although batteries' manufacturers have got rid of mercury content, some efforts have been made for recovering other metals enclosed in the battery formula. This paper discusses the bench scale experiments in the purification process of leached solutions from alkaline spent batteries. After leaching process using sulfuric acid as leachant, the solutions containing Fe, Cd, Pb, MIl, Zn and K were neutralized to precipitate iron hydroxide. In a second step, the purification experiments were carried out with excess of zinc dust to try to remove Cd while Mn and Zn still remain in the solution to be recovered in an electrolysis stage. The purification experiments procedures were conducted at different temperatures and times to find out properly conditions from the viewpoint of metals removal After filtration the solutions were submitted to chemical analysis to certify the metals content extracted.

Jan 1, 2001

By A. Bruynesteyn

It is well known that most North American gold deposits are of a hydrothermal origin and therefore they are often associated with sulphide minerals such as pyrite and arsenopyrite. When the precious metals in such ores are held captive inside sulphide crystals, the ores are called refractory because they do not respond to treatment by direct cyanidation. In these cases, it is necessary to recover the contained precious metals using high temperature treatments such as smelting or roasting, or high pressure leaching processes to break down the sulphide crystal matrices and thus liberate the precious metals for subsequent extraction by cyanidation. Sulphidic gold ores containing arsenic and/or antimony are considerably more difficult to treat because, in addition to their refractory nature, the arsenic and antimony content also prohibits treatment by direct cyanidation or amalgamation. These ores must be milled and their sulphidic gold values concentrated by flotation. The resultant concentrates must then be roasted to break down the sulphides before cyanide treatment can be applied.

Jan 1, 1985

By D. Maurice, W. D. Riley, J. A. Hawk

"The increased penetration of wrought aluminum into the automotive market is stimulating a need to separate wrought aluminum from cast aluminum because of: a) the additional value of scrap wrought alloys and b) the increase in the total amount of aluminum automotive scrap will outstrip the demands of secondary aluminum foundry industry. The availability of clean fractions of wrought and cast aluminum and incidentally, a clean cast magnesium fraction will allow increased recycling of aluminum used in the automotive industry.Hot crushing has been tested previously and proposed as a means to separate cast from wrought alunrinum product. The underlying concept is that when a mixture of cast and wrought aluminum is thermally processed and then subjected to crushing action, differences in toughness between wrought and cast aluminum alloys will become more pronounced. Hence, it should be possible for conditions can be established such that the cast material fragments, while the wrought material, having lost much less of its toughness, merely deforms. The two types of product could then be separated by simple sizing methods.In this paper we report on the testing of this concept. We were unable to replicate the results which originally demonstrated proof of concept. Possible reasons for this are discussed, as well as the possibility that the original results may not be as desirable as the current results for subsequent sorting."

Jan 1, 2000

By A. Tsubouchi, F. Noguchi, T. Takasu

"A high current density operation is desired to improve the productivity in copper electrorefining. However, a lot of problems still remain such as passivation at anode, dendritic deposition at cathode and impurity behavior during the electro refining.Effects of the current densitY on the morphology of copper deposition on the cathode, and passivation at the anode were investigated at various fluid velocity of electrolyte in the present study.Although a granular appearance of the copper deposition was obtained with increasing high current density, it was depressed by an increase of the fluid velocity of the electrolyte. A uniform deposition on the cathode was also observed when the fluid velocity of the electrolyte become higher. It was ascertained that passivation at the anode was suppressed by circulating electrolyte during electrolysis. INTRODUCTIONIt is desirable to operate at high current density in copper electrorefining in order to improve plant productivity without enlarging the size of electrodes(1). However, there are many problems in copper electrorefining at high current density with the usual commercial practice, for example, anode passivation, dendritic deposition and an increase of impurities in the cathode.In general, it is effective to agitate the electrolyte in order to suppress these problems(2). Smith et a1.(3) have performed electro refining experiments at various current densities in the range of 8 to 32 Aldm2 and at electrolyte fluid velocities in the range of 40 to 120 mlmin, and they obtained well consolidated, void free copper even at high current density in a high electrolyte velocity. However, they did not discuss the recovery ratio and the passivation behaviour at the anode. Walsh et a1.(4)(5)(6) experimented with the rotating cylinder electrode, and ascertained that electrolysis can be carried out at high current densities under the condition of pure electrolyte.With regards to anode passivation, there are several papers by previous workers(7)(8). Our group ascertained the process of producing anode slime during electrolysis(9). However, these experiments were carried out without forced circulation of electrolyte. Therefore, in the present study, to solve these problems, we electrolyzed at current densities in the range of 4 to 50 Aldm2 with circulating electrolyte in the range of 0 to 48 mlrnin. The effect of electrolyte fluid velocity on the surface morphology of deposited copper at cathode and passivation at anode were investigated when electrolysis were carried out with circulating electrolyte at high fluid velocity and at high current density."

Jan 1, 1997

By Jukka Tuominen

The history of making blister copper in an Outokumpu Flash Smelting Furnace dates back to the late 1960?s, when Outokumpu first piloted the Outokumpu Direct Blister (ODB) process. The first commercial scale applications have been in use at Glogow, Poland, since 1978 and at Olympic Dam, Australia, since 1988. These applications utilize special concentrates, which are low in iron, and thus the formation of slag is also low. In 1995 the same principle was applied to smelting copper matte into blister copper in industrial scale at Kennecott Utah Copper. This application, the Kennecott-Outokumpu Flash Converting process, will celebrate its 10th anniversary of commercial scale operation this year. This paper outlines the development in efficiency and flexibility of Blister Flash Smelting processes compared to other smelting and converting options. The focus is on the economical aspects i.e. on the total feasibility of both greenfield investment projects and revamping of existing smelters.

Jan 1, 2005