Search Documents

By Vinod K. Namilakonda

In situ synthesis of discontinuously reinforced aluminum alloy metal matrix composites was investigated. Aluminum alloy (A356: Al-7 wt% Si) was reinforced with dispersed AlN particles. Thermodynamic calculations were made for the composition determination of various phases formed during bubbling of NH3 gas into the Al alloy melts in the temperature range 1173-1473 K. Experiments were carried out for in situ production of AlN particles with the reaction between Al melt and NH3 gas in high temperature resistance furnace at 1473 K. The products were characterized using SEM, EDS and XRD. Effect of bubbling time of NH3 gas on the AlN formed in the composites was studied. The amount of AlN reinforcement in the Al alloy composites was observed to be in the range of 5 to 35 wt%. Good agreement was observed between the experimental and thermodynamic calculated data on the composition of AlN in Al alloy composites.

Jan 1, 2006

By Jason Graetz

Aluminum hydride is a covalent, binary hydride that has been known for more than 60 years and is an attractive medium for on-board automotive hydrogen storage, since it contains 10.1 % by wt. hydrogen with a density of 1.48 g/ml. There are at least 7 non-solvated AlH3 phases, namely a, a', a, ?, d, e and ?. The properties of a-AlH3, obtained from the Dow Chemical Co. in 1980, have been previously reported. Here we present a description of the thermodynamic and kinetic properties of freshly prepared a, 0 and y phases of AlH3. In all cases the decomposition kinetics are appreciable below 100" C and all will meet the DOE 2010 gravimetric and volumetric vehicular system targets (6 wt% H2 and 0.045 kg/L). However, further research will be required to develop an efficient and economical process to regenerate AlH3 from the spent A1 powder.

Jan 1, 2006

By Ian M. Ritchie

Cementation or metal displacement reactions such as Cu2+ + Fe Cu + Fe2+ are among the oldest known hydrometallurgical reactions. They are still used in the recovery of some metals and in the purification of process liquors and waste water streams. However, they are often more complex than the stoichiometric reaction would suggest because they involve the simultaneous deposition of one metal onto a second which is dissolving. For example, sometimes a cementation will not take place, even though it is thermodynamically favoured. On other occasions, a cementation reaction will start but come to a halt as the depositing metal blankets the reacting surface. On yet other occasions, side reactions, catalyzed by the deposit, can be important. In this paper, the electrochemical basis of cementation reactions is described. The conditions for each of the complications encountered in these reactions are described and illustrated by examples drawn from a number of hydrometallurgical processes. The cementation reaction between activated carbon and gold thiosulfate is also briefly described, this reaction being unusual in that no dissolution of the carbon occurs.

Jan 1, 2003

By Heikki Jalkanen

Oxygen converting of hot metal (LD/BOF) is contemplated as an object of simulation. Oxygen converting is a highly complex thermo-chemical process comprising a series of matter and energy transformation and transportation steps that makes the simulation very challenging. The basic principles of CONSIM 5 oxygen converter simulator are presented. Simulator is a comprehensive combination of a physical model with several empirical submodels describing all properties and processes that affect the final result of a converter blow, final mass and composition of steel, slag, dust and converter gas as well as the end temperature of steel. CONSIM simulator is used for simulation of series of high and low carbon steel blows. Simulated steel temperatures, oxygen consumption, blow time and iron oxide content of slag are compared with measured values. Problems of simulation and requirements for quantitative simulation of oxygen converter process are discussed.

Jan 1, 2006

By Anita E. Lam

The thiosulfate leaching of gold generally requires the presence of a catalyst such as cupric tetraammine, Cu(NH3)42+, to obtain reasonable leaching rates and gold extractions. Unfortunately, this same catalyst that accelerates gold leaching also tends to accelerate thiosulfate oxidation to tetrathionate and other species. It is therefore imperative that a detailed understanding of the role of this catalyst and the factors affecting it is obtained. It is equally important for plant application that a method of assessing the catalyst be developed. In this work the role of the cupric tetraammine catalyst was studied using geochemical modeling for speciation prediction, thiosulfate leaching of gold ores, and chemical analyses of resulting leach solutions. It was found that the variables of pH, temperature, and the concentrations of ammonia, thiosulfate, and total copper all work in concert to affect the concentration of the cupric tetraammine species. It was also found that the presence of sufficient thiosulfate and cupric tetraammine was critical to the success of the leach.

Jan 1, 2003

By L. B. Tsymbulov

At present data on thermodynamic properties of metallic melts, containing copper and ?iron family? metals, is rather limited. Determination of the activity of metallic melts components under high temperature by experimental methods requires high level of labour inputs. With this it is not always possible to obtain the results with high level of accuracy. Due to that in a number of cases it is more appropriate to apply different methods of analysis, with the help of which there can be calculated thermodynamic properties of ternary and even more complicated systems, prominent thermodynamic properties of binary systems being used as a basis for these calculations. This work presents the results of calculations of different components activity and activity ratio in such ternary system melts as Ni-Cu-Fe, Ni-Cu-Co, Fe-Cu-Co and Fe-Co-Ni. Good compliance of calculations results with those obtained in the course of reliable experimental investigations fulfilment is demonstrated. There are presented the results of activity and activity ration analysis for some compositions of Cu-Ni-Co-Fe system.

Jan 1, 2006

By G. S. Nus

Technology for treating man-made metal-containing raw materials in DC electric furnaces with polarization of the bottom phase (PDF furnaces) has been developed and proven on a semi-commercial scale. PDF furnaces permit processing of man-made raw materials, i.e. current and accumulated intermediate products with rather high contents of valuable metals (i.e. slags, sludge, residues, Waelz slag, etc.), as well as secondary raw materials and virtually any type of waste using an environmentally safe technique based on sublimation of volatile metals and transfer of non-volatile metals and sulfur into the bottom phase in the furnace. Processes developed on the basis of the use of PDF furnaces make it possible to take advantage on a full commercial scale of electrolysis of molten materials, including electrochemical reduction of metals, intensification of their settling into the bottom phase and sublimation of volatile components, as well as to significantly improve recoveries of nonferrous metals, resolve the problem of excessive accretion formation in slagging processes and substantially improve the environmental situation. The low-grade discard slag obtained can be utilized in the construction industry; in particular, slag can be added to the limestone feed for cement manufacture.

Jan 1, 2006

By Helena Byrdziak

KGHM Polska Miedz S.A. is a significant European copper producer with production of 447,000 mtpy, operating three underground mines and three smelters. The company has been involved for years in environmental activity, which was stimulated not only by the company itself, but by the development of environmental regulations as well. The first set of regulations, concerning water protection, was' established in Poland' in 1974, while a comprehensive environmental law was passed in 1980. This law in general requires industry to submit all data of environmental significance to the local authorities. Based on this data, they establish limits concerning emissions into the air, water and ground, the amount of wastes produced and the means of their disposal. A company has to pay fees for each tonne of emitted substances and stored wastes. When the emission of a substance exceeds the limit, the company has to pay a penalty which is about ten times higher than the fees. This approach in general is effective because it forces companies toward: reduction of their emissions. The problem is that the law is constantly subject to change and is becoming not only more restrictive but is involving more and more bureaucracy.

Jan 1, 1999

By Varadajan Seshadri

Torpedo cars have been extensively used for pig iron desulfurization although its geometry is not considered to be ideal as far as mixing and mass transfer are concerned. Complications arise from scaffolds formed through aggregation of flux, slag and pig iron during operation. Following industry demand a 1:6 torpedo car physical model was operated to assess the optimum refining conditions for pig iron desulfurization. Similarity between the model and prototype were established through Froude and turbulent Reynolds criteria. Mixing times were evaluated by pulse tracer addition and the kinetics of metal/slag interactions were assessed from experiments investigating iodine transfer from kerosene to water. The influence of parameters such as level of metal, gas flow rate, lance penetration, lance orientation, presence of scaffold were evaluated. Mixing times were found to be shorter than regular desulfurization time and also not very sensitive to scaffold presence. Scaffold contributes to the reduction of the useful volume only. Mass transfer at the permanent reactor is more effective when the torpedo is operated at its full capacity. The experiments also highlight the dominance of the transitory reactor as compared with the permanent reactor.

Jan 1, 2006

By H. Y. Cheng

A pulse column solvent extraction system was evaluated as an alternative to mixer-settlers for the separation and purification of rare earths. The column tested had an inside diameter of 44.5 mm and had 36 sieve plates with a free area of 25%. Pulsing was provided pneumatically using a solenoid valve controlled by a timer so that both pulse amplitude and frequency could be varied. Feed to the column was a mixed rare earth chloride solution containing 10 g RE L-1. The extractant was 5% Ionquest® 801 in Shellsol 2037 diluent. Hydraulic performance of the pulse column was excellent with no propensity towards stable emulsions or crud formation under normal operating conditions. The column was operated in organic-continuous mode with flow rates chosen so that yttrium and the heavy rare earths were extracted with high efficiency while the light rare earths were rejected. Yttrium extraction varied from 83 to 99.2%. Concentration profiles were measured in both the aqueous and organic phases, and, from this data, the height of a transfer unit (HTU), the mass transfer coefficient (Kxa) and the continuous-phase axial dispersion coefficient (Ey) were computed. The HTU ranged from 17-92 an which is within the range of values reported for other (non rare earth) pulse column systems.

Jan 1, 1992

"Silver is traditionally recovered in base metal smelters (lead and copper), or as a by-product of other precious metals (gold and/or PGM's). This paper presents the results of non-conventional techniques to recover silver from complex materials. The PLATSOL® process has been developed to recover, in one step and without the use of cyanide, base metals (copper, cobalt, nickel) and precious metals (gold, PGM's) from sulphide concentrates too low in grade to enter the mainstream extraction processes. Silver is only partially recovered in solution with gold and the PGM's during the PLATSOL® process. However, the silver minerals are transformed into silver chloride, which can then be recovered from the PLATSOL® residue using conventional techniques. Some South American silver concentrates contain levels of impurity (mostly arsenic) so elevated that the penalties incurred significantly affect the process economics. The present results have shown that a low temperature calcination process transforms the concentrate into a product well suited for traditional recovery treatments. Metallurgical details will be provided, as well as the results of mineralogical studies that helped clarify the process mechanisms.IntroductionSilver occurrences in nature are very diversified, and, therefore, primary silver is produced as a by-product of many base metal and precious metal operations [1], as well as a co-product of most gold ores. However, difficulties can arise when high temperature processes are used for refractory gold ores or copper concentrates, or when the silver concentrate contains impurity elements such as arsenic that trigger high penalties."

Jan 1, 2012

By P. Chris Pistorius

Calcium treatment of alumina inclusions, to convert the alumina to molten or partially molten calcium aluminates, is a well-established treatment for steel, to improve the castability of aluminium-killed steel. However, the role of magnesium in calcium-treated steel is not fully clear, nor is the origin of the several percent of magnesium oxide that is often present in calcium-treated inclusions. To study this, steel was sampled after calcium treatment at an industrial steel plant, and the inclusions identified by energy-dispersive X-ray microanalysis (EDX) on polished sections of the samples (analysing the samples in a scanning electron microscope). The predicted fraction liquid in the inclusion was estimated from the ternary alumina-magnesia-lime phase diagram. Inclusions with higher CaO contents generally had lower MgO contents, indicating that the calcium wire is not the origin of the magnesium in the inclusions; this was also confirmed by wet chemical analysis of the calcium wire. Instead, it appears that magnesium-alumina spinel inclusions form during extended ladle contact after aluminium killing and before calcium treatment. While such spinels have been stated to cause poor castability (clogging the submerged-entry nozzle), it is clear that calcium treatment successfully modifies the spinel inclusions to mixed alumina-lime-magnesia inclusions, where the magnesia content contributes substantially to liquefaction of the inclusions: for typical MgO contents of around 10%, the range of Ca:O ratios which yield liquid (or partially liquid) inclusions is extended substantially to lower Ca:O ratios.

Jan 1, 2006

By C. O. Bounds

The magnetic properties of (NdDy)15Fe78B6 sintered magnets have been evaluated using powder prepared by Inert gas atomization. The atomized powder had a particle size distribution from 1 to approximate 1000 microns. The as atomized powders have been sieved into, coarse, intermediate, and fine fractions; magnetic properties were evaluated for the as produced powder and each fraction. A B, of 11.7 kG, a Hci of 11.0 kOe and a BHmax of 32.5 MGOe was -obtained on a sintered magnet made from the as-atomized powder. The magnet made from coarse powder exhibited a slightly higher B, of 12.1 kG, while that from fine powder showed a decrease in B, to 11.2 kG. Hydrogen decrepitation has been utilized to study its effect on the magnetic properties. Finally, cast ingots with a definite columnar structure have also been used to compare the magnetic properties of magnets of the same nominal, composition but of different alloy preparation process. Hydrogen decrepitation does not appear to improve the magnetic properties of magnets made from thin cast ingots. However, it does show a significant improvement in the Hci of magnets made from the atomized powders. Possible causes for the differences in the magnetic properties on magnets made from each process have been discussed in the paper.

Jan 1, 1992

By Ibrahim Yusufoglu, Cem Kahruman, Sedat Ilhan, Ahmet Orkun Kalpakhi

"Scheelite is the main raw material in tungsten production. In hydrometallurgical processes, extraction of tungstate ions into solution is very important. During the leaching of scheelite in oxalic acid solutions, tungsten dissolves as a chelate complex. Scheelite includes impurities along with calcium tungstate. Determination of the dissolution of these impurities is important in the subsequent tungsten production stages. In this study, scheelite was dissolved in oxalic acid solutions and the dissolution of impurities was investigated. The quantities of dissolved impurities were determined by ICP - OES and characterization of the undissolved impurities in the leach residues was carried out by SEM - EDS analysisIntroductionScheelite and wolframite ores are used for the industrial production of tungsten. Both ores are dissolved in acidic or basic solutions, and ammonium paratungstate is obtained as an intermediate product. Prior to crystallisation of ammonium paratungstate, all the impurities must be removed. Among these, Fe, Si, P, Mn, Mg and Mo are classified as ""harmful"" elements and different methods are used for their removal [1]. During purification, solvent extraction, ion exchange, etc. methods are used.Potashnikov et al. [2] studied the dissolution of scheelite in acidic solutions and the effects of stirring speed, temperature and oxalic acid concentration on the dissolution kinetics.There are no works in the literature about the removal of impurities from scheelite ores in oxalic acid solutions. Therefore, the aim of this work was to investigate the dissolution mechanisms of impurities during the leaching of scheelite in oxalic acid solutions. The effects of temperature and oxalic acid concentration on the dissolution were also investigated. In addition, the characterization of the impurities which were not dissolved was studied."

Jan 1, 2012

By Junji Shibata

As one of the effective usages of various wastes discharged in non-ferrous metal industry, the synthesis of hydrotalcite was carried out using aluminum dross as a raw material. Hydrotalcite is one of the inorganic anion exchangers and has layered structure of complex hydroxide. The removal of toxic metal ions such as As(III), As(V), Cr(VI) and Se(IV) with the hydrotalcite was investigated, and the removal properties were compared from the viewpoint of the anion exchange amount and exchange rate. Hydrotalcite can be obtained by a co-precipitation method from the aluminum dross and the waste MgCl2 solution discharged in an aluminum regeneration process. Slight amounts of SiO2, Al2O3, Fe2O3 and so on remain in the reaction product as an impurity component. Interlayer distance of the obtained hydrotalcite is about 0.3nm. Hydrotalcite changes to Mg-Al oxide by the calcination at 773K for 3h, and then hydrotalcite is formed again by a rehydration operation after calcination. The toxic metal ions are removed from aqueous solution by the anion exchange reaction in the pH region where toxic metal ions exist as the anionic species like AsO2-, HAsO42-,CrO42-, and SeO32-. The exchange amount is considerably concerned with the valence of anionic species and the size of anionic species. The removal of toxic metal ions were investigated from the engineering aspects such as the low concentration limit to be removed, the amount of hydrotalcite to be used for the perfect removal of toxic metal ions and so on.

Jan 1, 2006

By Henrique Ventura Oliveira

Continuous casting is the most important process for solidification of steels. In this process, the fluid flow pattern in the tundish and in the mould have significant effect on the product quality. Problems associated to fluid flow in the tundish include surface turbulence, ?short-circuits?, formation of dead zones and vortexing. During grade changes, mixing in the tundish plays a significant role in determining the length of the intermixed slab. All these flow aspects can be studied by means of mathematical and physical models. In the last years, numerical simulation of fluid flow has become a very popular tool in the analysis of the performance of continuous casting tundishes. In setting-up these numerical simulations, special care should be taken in choosing the appropriate mesh distribution, the interpolation scheme, the adequate location of the inlet boundary and the turbulence model. In the present paper, turbulent fluid flow in different configurations of tundishes was simulated. Different turbulence models were used in the simulations. Residence time distribution (RTD) and mixing curves during grade changes were predicted and compared to results obtained in physical models. The performances of the different turbulence models were evaluated. For the tundishes that have been studied, the performances of the different turbulence models tested in the present work were similar. There is no evidence that any of the models provided sustained improvement when compared to the well-established standard k- model. All turbulence models tested presented limitations in simulating flows under low turbulent Reynolds numbers.

Jan 1, 2006

By Feng Ningchuan, Guo Xueyi, Tian qinghua, Liang Sha

"In this study, copper adsorption by orange peel which was chemically treated with sodium hydroxide was investigated. The morphological and chemical characteristics of the adsorbent were evaluated by spectroscopy and N2-adsorption techniques. Equilibrium isotherms and kinetics were obtained and the effects of solutions pH, adsorbent concentrations and temperature were studied in batch experiments. Equilibrium was well described by Langmuir and Freundlich isotherms and kinetics was found to fit pseudo-second order type adsorptions kinetics. According to the Langmuir equation, the maximum adsorption capacities (qm) for Cu(II) was 50.25 mg·g-1 at pH 5.3. With the temperature increased from 16 to 60°C, copper removal decreased. The loaded adsorbent was regenerated using HCl solution and could be used repeatedly at five cycles with little loss of adsorption capacity. The results show additional chemical treatment of the adsorbent by NaOH, is favor of improving the adsorption capacity. Introduction Increased use of metals and chemicals in manufacture industries has resulted in generation of large quantities of effluent that contains high level of toxic heavy metals and it poses environmental-disposal problems due to its non-degradable, persistence nature and accumulation throughout the food chain [1, 2]. Copper is known to be a commonly used heavy metal. This metal, which found many useful applications in our life, is very harmful if charged into natural water resources and may pose finally a serious health hazard. Many methods, such as chemical precipitation, ion exchange, reverse osmosis and adsorption, etc., have been used for heavy metal ions removal from various aqueous solutions. In recent years, there has been considerable interests in use of biological materials including algae, bacteria, fungi, agricultural by-products and residues as adsorbents to remove toxic metals from aqueous solutions by adsorption [3-8]. Adsorption process has been extensively used to remove copper from aquatic medium using low cost adsorbents such as peanut husks [9], plant materials [10] and cellulose materials [11]. Among them, agricultural by-products and biomass are relatively cheap and show very high adsorption capacities. However, to apply untreated agricultural by-products as adsorbents has the disadvantages such as low adsorption capacity, high chemical oxygen demand (COD) and biological chemical demand (BOD) as well as total organic carbon (TOC), due to the release of soluble organic compounds contained in the plant materials such as lignin, tannin, pectin and cellulose, into the solutions [12-14]."

Jan 1, 2008

By Iris Filzwieser

The secondary copper producer, Montanwerke Brixlegg AG (Austria), produces 73 000 tonnes of cathodic copper per year using ISA tankhouse technology. METTOP GmbH (Austria) evaluated the different anode qualities from the plant with relation to the current efficiency and specific energy consumption. Parameters including the chemical and physical anode quality, current and current density distribution at each cathode, voltage, and distance between each cathode and anode were examined. In addition, the temperature, chemical analysis, and conductivity of the electrolyte was determined for each investigated cell, as well as the anode weight, anode scrap, cathode sheet, and short circuits. Metallographic analysis was also performed on selected dendrites. The investigations resulted in specific improvements in the tankhouse process including the level of anode impurities, and future projects are planned for further tankhouse optimization.

Jan 1, 2006

By M. J. Collins, L. C. Trytten, K. R. Buban, I. M. Masters

Both pressure leaching of zinc concentrate, in an autoclave, and atmospheric leaching, in stirred tanks, have been employed in the expansion of zinc production at plants employing roast-leach-electrowin technology. These direct leaching methods result in the conversion of the sulphur in the feed to the elemental form, rather than to sulphur dioxide, decoupling zinc production from acid production. Atmospheric and pressure leaching methods are also readily implemented over a wide range of production rates. In choosing the best technology for expansion, capital and operating costs, zinc recovery, byproduct quality and the compatibility of recycle streams with the existing refinery must be compared. Leach testwork with several zinc concentrates using both methods has been performed by Dynatec. Recent results are presented, along with a discussion of their implications for process selection.

Jan 1, 2000

By Robert T. Oxnard

"EXECUTIVE SUMMARYThe history of Refractory Recycling indicates there was little recycling until the 1950s. Energy incentives were the primary reason for the beginnings of a recycling effort by the refractory brick manufacturers. Quality benefits quickly became evident and fewer rejects were the result. Today, economic factors including higher valued raw materials and increased competition are the driving forces of refractory recycling.There are some success stories in refractory recycling but we have a long way to go. Few incentives, quality concerns, relatively cheap energy, comparatively lax government regulations, inexpensive landfills and inexpensive substitutes make recycling a difficult choice for many companies. Marketing advantages such as ISO 14000, eliminating multiple audits and reduced liability exposure can tip the scales toward recycling viability. Increasingly, the ideological philosophy of a company, a desire to minimize environmental impact and develop favorable public and other interested party perceptions can drive recycling and waste minimization efforts.Recycled materials can be more trouble ""up front"" and harder to ""manage"" due to their suspect quality. However, due to their nearly inexhaustible supply and the fact that once developed, they constantly contribute to the bottom line, they are certain to be the materials of the future. Waste refractory materials will likely see the same bright future as the steel scrap yards and slag piles of yesterday. In hindsight, we will realize that now was the perfect time to prepare and plan for the bright future of refractory recycling."

Jan 1, 2000