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By Y. W. Chung, W. I. Chia

"The interaction of water vapor with single crystal Ni3(Al,Ti) and polycrystalline Ni3Fe, with and without the presence of oxygen, has been studied with Auger electron spectroscopy, photoemission spectroscopy, thermal desorption and isotope exchange. Water dissociates to produce atomic hydrogen above 200 K on both Ni3(Al,Ti) and Ni3Fe surfaces. For Ni3(Al, Ti), the reaction is structure-sensitive. Pre-adsorbed or co-adsorbed oxygen on Ni3(Al,Ti) and Ni3Fe significantly suppresses hydrogen production due to water dissociation. This suppression process occurs more efficiently on Ni3Fe than Ni3(Al, Ti).IntroductionOrdered intermetallic compounds such as aluminides, silicides and titanides are very attractive for structural applications at high temperatures. This is because these intermetallics tend to form adherent oxides in oxidizing environments which protect the base materials from excessive oxidation and corrosion. In addition, they have low density, relatively high melting points and good high-temperature strength. However, the moisture in air severely embrittles many ordered intermetallics such as FeAl [1-3], Fe3A1 [4,5], C03Ti [6,7], (Co,Fe)) V [8], Ni3Si [9], Ni3(Si,Ti) [10], Ni3(AI,Mn) [Ill, and Ni3A1 [12-14], resulting in low 'ductility and brittle fracture at room temperature. Recent studies by Liu and coworkers (see review by George and Liu [15]) provide a qualitative description of the mechanism for this moisture-induced embrittlement. During elongation testing, cracks are formed, thus exposing fresh alloy surfaces. One or more active components of the alloy react with water vapor in the environment to produce atomic hydrogen which penetrates into crack tips and causes hydrogen embrittlement. This is similar to that proposed for moisture-induced embrittlement of aluminum alloys [16]."

Jan 1, 1996

By Paul O. Malan

"The Tusc gold deposit is located along the Carlin Trend approximately 13 kilometers north of Carlin, Nevada and 2.5 kilometers northwest of the Gold Quarry mine. Tusc is one of several structurally controlled oxide gold deposits located along the Good Hope fault within the Maggie Creek subdistrict. Mining commenced in 1994 with an oxide reserve of780,000 troy ounces of gold at an average grade of 1.34 g/t Au. The Good Hope fault forms the southwestern edge of the Schroeder Mountain uplift (also known as the Carlin Window) and juxtaposes carbonate rocks of the Siluro-Devonian Roberts Mountains Formation against siliceous mudstone, siltstone, and silty limestone of the Devonian Rodeo Creek unit. Submicroscopic gold mineralization is disseminated in the Good Hope fault system and in fractured hanging wall carbonate rocks. Wallrock alteration includes silicification, deca!cification, sericitization, and late alunite replacement and veins. All Tusc ore is transported 2.5 kilometers to Gold Quarry for processing. Leach-grade ore (0.2 - 1.7 g/t gold) is placed on the oxide leach pads, and mill-grade ore(> 1.7 g/t gold) is processed through the CIL oxide mill. IntroductionThe Tusc gold deposit is located in Eureka County, Nevada, U.S. A, approximately 13 kilometers north of the town of Carlin and 2.5 kilometers northwest of the Gold Quarry mine (Fig. 1 ). Tusc is one of several open-pit, oxide, gold deposits within the Maggie Creek subdistrict of the Carlin Trend. Tusc is a structurally controlled gold deposit located along the Good Hope fault. Submicroscopic gold mineralization is disseminated in the brecciated and silicified Good Hope fault zone and along intersecting northeast and northwest striking structures."

Jan 1, 1997

By Bohumir Jelinek, Sergio Felicelli, Mohsen Eshraghi

"We present a parallel lattice Boltzmann - cellular automaton model of the two-dimensional dendritic growth during solidification of binary alloys. The model incorporates effects of solute and energy transport under melt convection. The parallel performance of the algorithm is assessed. A loss in the parallel efficiency is observed when multiple computational cores per processor are utilized. Excellent strong scaling up to thousands of computing cores is obtained across the nodes of a computer cluster, along with the near-perfect weak scaling up to forty thousand cores. The presented solidification model shows a good scalability up to centimeter size domains, including millions of dendrites.IntroductionLattice Boltzmann method (LBM) is an attractive numerical technique for solving fluid dynamics problems. Its advantages are simple formulation and locality, with locality facilitating parallel implementation. In the present model, interface kinetic is driven by the difference between local actual and local equilibrium liquid composition [1]. The cellular automaton (CA) technique is deployed to track the solid-liquid interface [2]. A serial version of the present LBM-CA model with a small number of dendrites was validated against theoretical and experimental results in the previous publications [3, 4]. In this work, it is the first time that simulations with millions of dendrites were performed, something not possible with the computationally much more costly phasefield method [5].This research effort examines a technique for simulations of millions of dendrites in centimeter size domains, including thermal, convection, and solute redistribution effects. Nearly ideal scaling properties of the model are demonstrated. This extensively large landmark was achieved because of• the CA technique being two orders of magnitude faster than alternative, phase-field methods [5]• highly parallelizable LBM method, convenient for simulations of flow within complex and time dependent boundaries• availability of the powerful NSF Extreme Science and Engineering Discovery Environment (XSEDE) supercomputing resources"

Jan 1, 2013

By Scott Samson, Weidong Wang, Shekhar Bhansali, Vandana Upadhyay

"We present an improved design for the two-arm polysilicon thermal actuator. The classic thermal actuator design produces a localized hot spot at approximately the center of the thin actuator arm. This phenomenon limits the actuator efficiency, lifetime, and reliability. Since the actuator deflection is based on thermal expansion of the material, advantage may be gained by making the temperature profile more uniform along the hot-arm length. In our design, the geometry of the thin arm is modified by forming a nonlinear structure near the approximate location of the original hot spot. Electromechanical simulations of this design show an increase in deflection, due to a flattening of the temperature profile along the hot arm. The solid model generation, finite element analysis and simulations are carried out using PEA software. Experimental devices are in the process of being fabricated by using a polysilicon rnicromachining process.1. IntroductionMost active MEMS devices employ some kind of actuating mechanism to increase functionality. Various actuating mechanisms like magnetic, electrostatic, thermal, magnetostatic and piezoelectric have been investigated and incorporated for actuating microstructures. The primary features required from many on-chip actuating mechanisms are large deflection (>10 µm), low actuation voltage, low power.consumption, reliability, fast response, ease of design and fabrication, and small size. Thermal actuation is an attractive mechanism for rnicromechanical devices requiring high actuation forces, large deflections, good linearity and low actuation voltage. Thermal actuators, also known as ""electrothermal actuators"", ""heatuators"" or ""U-shaped thermal actuators"", have been largely used in MEMS based devices to provide both in-plane and out-of-plane actuation [l] .Thermal actuators are also easily compatible with standard CMOS circuitry due to their low driving voltage. However, high power consumption remains a major drawback of the thermal actuation mechanism."

Jan 1, 2004

By Ting Lei, Mingjun Rao, Guanghui Li, Tao Jiang

"With the rapid development of iron and steel industry, the supply of iron ores can not meet the present demand for iron and steel industry in China. Large reserves of oolitic hematite have been discovered with low iron grade (30% ~ 45%) and high phosphorus content (0.4% ~ 1.8%). Traditional processes for utilization of this ore are characterized as either high cost or low dephosphorization. In this study, sodium salts-modified paigeite (SSMP) was added to enhance on the dephosphorization of high-phosphorus oolitic hematite by using reduction roasting followed by magnetic separation. Various parameters, including the amount of SSMP, reduction time,reduction temperature, grinding fineness and the magnetic field intensity were investigated. As a consequence, a magnetic concentrate of metallic iron powder with total iron grade of 93.2% and phosphorus content of 0.08% was obtained under the optimal conditions. The results also provide a potential avenue for the comprehensive utilization of paigeite ore.IntroductionOolitic hematite is currently recognized as one of the most refractory iron ore resources in the world. Over 4.0 billion tons of reserves of such resources have been found in China, and more than 10 billion tons in the long-term. This kind of ore is characterized as low iron grade (30%~45% TFe) and high phosphorus content (0.4%~1.8% P), as well as fine particle size distribution of ferrous minerals (the size distribution varies from 5~30 µm, even less than 2 µm) and the complex association between iron and other gangue elements [1~5]. The unique structural characteristics of the high phosphorus oolitic hematite make it difficult to obtain high iron recovery and good dephosphorization efficiency by using the conventional processes [1,2]. Traditional processes are characterized as high cost and low dephosphorization for oolitic hematite beneficiation [9~15]."

Jan 1, 2012

By S. Suda

Hydrogen storage materials have been investigated for more than 30 years, particularly on metal hydrides. These materials are, however, considered today impractical because of their poor hydrogen capacity measured by mass density and their poor surface properties and characteristics against impurities. Recent R&D activities have been located in new categories of materials such as complex hydrides and chemical hydrides. Among these materials, NaAlH4 (one of alanates), Li-based complex hydride, and NaBH4 (SBH: sodium borohydride) are 3 major candidates as hydrogen storage materials. In the presentation, SBH as a non-reversible on-site but recyclable off-site is described in view of its practical availability as the source of H- (protide) applied for a new type of fuel cell named Direct Borohydride Fuel Cell (DBFC) and H2 (hydrogen) for Proton Exchange Membrane Fuel Cell (PEMFC).

Jan 1, 2006

By Gerson de Araújo Filho

This paper shows the use of tires as fuel to be employed into blast furnaces. The tires can substitute coal or even charcoal in the blast furnaces tuyeres. The injection into tuyeres, besides the contribution for energy generation, can also produce gas for iron oxide reduction. The tires, as powder to be injected into blast furnaces, contributes for an environmental use of this waste, which helps to obtain a high value product as well. So, the advantage of using such material is that it is waste and has lower cost for preparation. The obtained results showed that the tires have good combustibility. This one was obtained in a model that simulates the same conditions occurring in the blast furnaces tuyeres; these used raw materiais include tires and mixtures of tires with coal or even with charcoal.

Jan 1, 2006

By N. L. Piret, E. N. Mounsey

Ausmelt technology is successfully used to process primary and secondary materials to produce lead in large-scale commercial operations and to meet stringent environmental standards. The development and commercial data covering these applications and the results with respect to metallurgical, cost and environmental performance are reviewed in commercial operations. A new smelter is scheduled for commissioning in 2000 at Korea Zinc's Onsan site to process lead fume and other secondary materials to produce 50,000 tonnes per annum of lead bullion. The unique features of Ausmelt technology also allow for the efficient processing of polymetallic concentrates and secondary materials, particularly copper and lead, through the effective separation of these elements into metal, slag and fume species. This capability has been successfully demonstrated at a commercial scale and the results and implications for the industry are discussed.

Jan 1, 2000

By F. E. Katrak

Rare earths markets by definition usually include not only the rare earth elements, but also yttrium. They can be subdivided into a very large light rare earth fraction (about 95 percent by weight of all rare earths consumed) consisting mainly of cerium and lanthanum and a smaller fraction (with much higher unit value) consisting of selected high-purity oxides or elements such as yttrium, europium, samarium, or neodymium. CRA estimates that the noncomnunist world market for all rare earths and yttrim was on the order of US$750 million in 1986. The main focus of this paper is on the principal uses for rare earths, some CRA-developed proprietary data on their consumption by region, and the selective nature of business opportunities in the rare earth markets. We also provide forecasts on the future trends in these markets.

Jan 1, 1989

By G. G. Barbante

Copper anode slimes are a valuable source of the precious metals, and selenium and tellurium. They are mineralogically complex and this has led to a great variety of process flowsheets for treating them. The traditional pyrometallurgical method utilises oxidation in a reverberatory furnace, but has numerous shortcomings. Recently deep-bath intensive smelting methods have been developed for use in the larger refineries. Despite these process advances, the thermodynamics of the reactions involved remains poorly understood. An initial description of the thermodynamics of slimes smelting is presented, but is severely limited by a lack of basic data. It is shown that slimes smelting is superficially similar to copper converting, but has many unique features. More basic thermodynamic data on selenium-based systems are needed before the process model presented can be further refined, and work in this direction has already commenced.

Jan 1, 1994

By Meyer Steinberg

"Some early experiences of a Cooper Union Chemical Engineer on the Manhattan project and his latest studies on CO2 Greenhouse Gas Mitigation Technologies are presented. Mitigating Global Greenhouse effect while maintaining a fossil fuel economy, requires improving the efficiency of conversion and utilization of fossil fuels, use of high hydrogen content fossil fuels, decarbonization of fossil fuels and sequestration of carbon and CO2 applied to all energy consuming sectors of the economy including electric power generation, materials production, transportation and industrial domestic heating. Decarbonization means removal of carbon as C or CO2 either before or after fossil fuel utilization and sequestration means long term disposal of C or CO2. The review will cover the principles of removal and recovery from power plant, stacks, the oceanographic and geological disposal of CO2 and the conversion of CO2 to gaseous and liquid transportation fuels. The global economic aspects of CO2 mitigation technologies are touched upon.IntroductionThis is an odyssey of a chemical engineer. My career started with the production of U235 at the Gaseous Diffusion Plant in Oak Ridge, Tennessee and the production of PU-239 metal at Los Alamos on the Manhattan Project. After 40 years at Brookhaven National Laboratory, I wound up performing studies on CO2 mitigation technologies. The following is a power point presentation on the subject of global warmingThe DOE is proposing to increase its sequestration development program in order to maintain the utilization of our vast resources in coal both for power and for transportation fuel production. Congress is considering steps to promote energy efficiency in attempts to solve not only the CO2 problem, but also the prime problem of energy supply. We will be promoting increases in energy efficiency as time goes on."

Jan 1, 2008

By Justin Karl, Ali Gordon, James DeMarco, Yongho Sohn

"Aluminum metal-matrix composites are lightweight materials that have the potential to supplant steel in many applications. The current work helps to identify the parameters that confer maximal strength and ductility. Torsion tests were performed on the as-cast aluminum metal-matrix composite A359-SiCp-30% at a variety of temperatures and twist rates. Dependence of material properties on temperature and strain rate were identified from equivalent stress-strain curves constructed from the reduced data. Examination of the microstructure was performed on the as-cast material and on fracture surfaces. A temperature-and strain rate-dependent constitutive model was applied to simulation of the mechanical response of the torsion specimen. Trends in material properties corroborate and extend trends identified previously under tensile loading with regard to temperature and strain rate dependence. Shear properties of simulated specimens agree with properties obtained through experimentation.IntroductionAluminum metal-matrix composites (A1-MMCs) have become increasingly popu1ar in recent years. While unreinforced aluminum alloys have low densities and high ductilities, they are not suitable for many applications due to their lack of strength and stiffness. To provide added strength and stiffness while maintaining favorable densities, it has become common to reinforce aluminum alloys with silicon carbide in various forms, although usually the inclusions are in the form of whiskers or particles. The result is a composite material with superior specific strength and stiffness. While whisker-reinforced composites are expensive due to the necessity of processing by nonstandard techniques and have low transverse properties when rolled, particle reinforced Al-MMCs have transverse material property values almost as high as the longitudinal properties and are not as expensive to process as whisker-reinforced Al-MMCs [1]."

Jan 1, 2012

By Donghai Li, Cheng Pan, Xuyang Liu, Xuewei Lv, Chenguang Bai

"Fine chromite ore is the common raw material to produce ferrochrome alloy through the submerged electric furnace process. The electric resistivity of fine chromite ore plays an important role in the operation efficiency because it determines the current distribution. The effect of particle size and the contact area of the particles on electric resistivity for several of chromite were investigated at room temperature, and the relationship between the electric resistivity of mixed particles and the volume fraction of lump ore to fine ore was also studied. The results shown that the electric resistivity increases with the increase of particle size, and the electric resistivity of mixture decreases with the increase of volume ratio of fine ore.IntroductionChromium is one of the most important alloying elements in manufacturing of stainless steel that used at high temperature and corrosive environment applications [I, 2]. As the raw materials to be charged into the steel, ferrochromium alloys and charge chromium are produced directly by smelting of chromite ore with the reducing agent in submerged electric arc furnace (SAF). During the process, the oxides of chromium and iron were reduced by carbon and meanwhile the electrical energy were consumed [3,4]. The ideal industrial process is to achieve high recovery level of Cr and Fe with minimal power consumption. In SAF process, the electric resistivity of charge stock has significant effect on the current distribution, which determines the heat distribution, molten bath structure and chemical reactions in the furnace. High resistance of the charge is desired to reduce the current distribution through the charge stock, thus the electrodes may insert into the charge stock with proper depth to form a high temperature arc heat source, and proper smelting can be realized[5]."

Jan 1, 2012

By Thomas Schemmel, Bertram Kesseiheim, Helge Jansen, Uwe Kreme

"During the last decades the refractory life time of the different aggregates of the secondary aluminium production was improved significantly. However, each repair and installation of refractory material affects the operating schedule and can cause costs in the million range. The downtime of just one melting furnace generate costs of 100.000 to 400.000 $ per day. Besides cooling down of the furnace and its repair, the heating-up procedure accounts for the longest time of the shutdown. Usually, heating-up of low cement or ultra low cement castables takes 120 to 150 hours. In order to reduce such expensive downtimes Refratechnik developed a unique and novel product series: Nanobond. These materials can be heated-up in only a third of the usual time. This paper talks about the theoretical aspects, as well as the mechanical and physical properties and especially practical experience of using Nanobond.Theoretical Aspects and Laboratory ResultsCement containing castables such as RCC, MCC, LCC or ULCC are considered standard in many refractory applications. Over the years a wide range of possible raw materials and practical installation methods were developed. However, all of these cement bonded refractory mixes possess one main important drawback. Such materials are characterized by the hydration of the cement bonding. As a result the physical bonded and the hydraulic water has to be removed in a relatively complicated drying procedure. The hydraulic water specifically demands a very careful and cautious heating up procedure. Most of the dreaded steam explosions can occur at a furnace temperature of approx. 250 oC. [1] To avoid such destructions, the heating-up of a new lined or repaired furnace can be very complex and slow. Depending on the furnace or the casted part a drying time of several days with long curing times are common."

Jan 1, 2012

By N. R. Green, N. J. Humphreys, D. McBride, T. N. Croft, M. Cross, D. M. Shevchenko

"Centrifugal casting offers a route to high quality products in difficult to cast high temperature low superheat alloys and thin section molds. Under centrifugal forces metal is forced into thin sections and can fill thicknesses of less than a millimeter. However, due to the high liquid metal velocities there is a high risk of surface turbulent flow and air entrainment within the liquid metal. The combination of interacting flow-thermal-solidification phenomena and associated defects is a challenging modeling task which the authors have previously described and validated. Capturing the metal-air interface, on what are inevitably complex three dimensional geometries, results in highly computationally expensive simulations and simulating a single cast can take weeks on a single processor. This contribution reports on modeling a complex centrifugal cast, gas entrainment, bubble transport and solidification, employing meshes of up to a million elements and investigates the scalability of the model on high performance clusters.Introduction The ultimate goal of any casting procedure is to produce a defect-free product. For difficult to cast alloys, such as Titanium, centrifugal casting has a number of advantage over conventional gravity methods [1]. In the casting of thin sections, such as turbine blades, the metal is forced into the thin sections under centrifugal forces. The centrifugal force can overcome the backpressure due to surface tension and the metal can fill mould sections with thicknesses substantially less than a millimeter. However, the materials used in these castings [2] tend to be highly reactive and requires low superheat. High liquid metal velocity gives rise to a high risk of free surface turbulent flow and of associated entrainment through free surface turbulence [3] and trapping of gas present in the flow [1]."

Jan 1, 2012

By Nan Zhang, Lei Zhang, Gai-feng Xue, Lina Wang, Pu Liu

"A novel ß-diketone modified silica gel was synthesized by a simple reaction. The prepared material was characterized by diffuse reflectance FTIR spectroscopy and it was used for the adsorption of heave metal ions in the industrial waste water. The main parameters affecting the sorption of heavy metal ions, including pH, water flow rate, and elution, have been investigated in detail. Under the optimized operating conditions, most of the targeted heavy metal ions could be removed. The material could be simply regenerated by hydrochloric acid solution. The method is rapid, selective, economic and applicable to the removal of heavy metal ions from industrial waste water.IntroductionToxic organic pollutants and heavy metals ions mainly from industrial activities such as plating, metallurgy and dyeing industries, are a threat to human health and the surrounding environment, because of their toxicity and persistence after being released into the natural environment [1]. These pollutants must be removed or degraded to an acceptable level, before being discharged to the receiving waters. Therefore, detection and determination of heavy metal ions in industrial waste water is very important.Inductively coupled plasma optical emission spectrometry (ICP-OES) is the most used technique for the determination of heavy metal ions because of its capability for rapid multi-element detection over a wide concentration range and with relatively low detection limits. Compared to other techniques such as neutron activation analysis (NAA), X-ray fluorescence spectrometry (XRF) and inductively coupled plasma mass spectrometry (ICP-MS), ICP-OES has the above advantages. Some constituents in industrial waters, such as organic compounds and inorganic salts, may cause matrix effects. In order to achieve accurate and reliable results, an efficient preconcentration of heavy metal ions and their separation from the matrix are usually required."

Jan 1, 2012

By M. A. Halim, V. I. Lakshmanan, T. Sheikhzeinoddin, R. Roy

"Chloride metallurgy is emerging as an alternative process for the production of base metals. Process Research ORTECH Inc. (PRO) has been at the forefront of technological development of chloride metallurgy. PRO has developed an innovative technology for the production of high purity titanium dioxide, iron oxide and vanadium pentoxide from ilmenite ores and concentrates. PRO is also developing its proprietary mixed chloride technology for the extraction of vanadium from other sources such as oil shales. In this paper, results from the test work conducted at PRO for the extraction of Ti and V using a mixed chloride lixiviant are presented.IntroductionTitanium and vanadium alloys and compounds have numerous industrial applications. Titanium dioxide is used in paints, plastics, rubber, paper, inks, textiles and a number of other miscellaneous applications. Currently nanosize T1O2 is being investigated for application in the cosmetics industry. Inorganic sunscreens mainly use T1O2 or ZnO particles, which reflect and scatter ultra-violet light. T1O2 nanomaterial is also finding application in smart construction materials and coatings, as a photo-catalytic converter. Nano TiO2 can catalyze the dissociation of NOX gases and other automotive emissions, thereby reducing the smog in urban centers. After the construction material is exposed to sunlight or ultra-violet light, the T1O2 is photo-activated and degrades the pollutants.Titanium metal and titanium dioxide are produced from ilmenite (FeTiOs) or rutile (naturally occurring T1O2) ore. Only about 6% of the titanium resources are used to produce titanium metal and the rest is used to produce T1O2. Many of the titanium ore deposits currently have unacceptable levels of transition metals which limits their processing by conventional routes."

Jan 1, 2012

By K. Verbeken, E. Wettinck, M. Verhaege

Iron (III) can easily and selectively be removed from acidic sulphate solutions with organo-phosphoric acids like Di-2-Ethyl-Hexyl-Phosphoric Acid [D2EHPA]. Stripping of the iron (III) loaded organic, however, is difficult unless highly concentrated inorganic acid solutions are used. In this paper results are shown for the enhanced stripping of iron from loaded D2EHPA by electro-reduction. The loaded solvent is contacted with a 2 M H2SO4 solution, which is continuously recycled in an electrochemical reactor where iron (III) is reduced to iron(II). As iron (II) is not extracted by D2EHPA, the equilibrium for iron (III)- D2EHPA is shifted towards the aqueous iron (Il)-sulphuric acid solution. The electro-reduction unit is a vessel with separated catholyte and anolyte chambers. The catholyte is the actual stripping solution where iron (III) is reduced to iron (II) on a stainless steel electrode. The anolyte is a 2 M H2SO4 solution where oxygen is evolved on a lead alloy electrode. A sintered glass plug separates the compartments. With this unit, enhanced stripping of iron from the solvent is possible under mild acid conditions [2 M H2SO4], and a concentrated ferrous sulphate solution can be obtained. The results shown have mainly been obtained by studying the parameters affecting the electro-reductive stripping of a D2EHPA loaded organic phase in a batch reactor. From an iron (IH)-saturated 20 vol. % D2EHPA solvent containing ~ 12.5 g/1 Fe (III) over 90% of the iron can be stripped in one stage with a 2 M H2SO4 solution at 50°C. It is shown that in this way it should be possible to obtain a concentrated ferrous sulphate solution which can be processed downstream to recover a pure iron product.

Jan 1, 2000

By Carlos Eduardo Gomes de Souza, Luis G. S. Sobral, Paulo A. Medeiros da Silva, Selma G. F. Leite, Renata de B. Lima

"The use of mixed cultures of acidophilus microorganisms that act in different temperature ranges, aims at speeding up the digestion of chalcopyrite, highly refractory sulphide mineral, the major mineral in the flotation concentrate of Caraíba Mining Co., with an attractive processing cost. The concentrate under consideration contains mainly chalcopyrite (CuFeS2) and bornite (Cu5FeS4) with contents of, approximately, 70 and 30%, respectively. It was observed in this study, the performance of consortium of mesophiles, moderate and extreme thermophile microorganisms, in the oxidation of the aforementioned sulphides minerals, evaluating operational parameters such as pH of the leaching solution, the reaction temperature and redox potential, with consequent extraction of 80% of the concentrate copper content within 60 days of bioleaching. Such high copper extraction was achieved in column bioleaching tests.INTRODUCTIONThe solubilization of metals by the application of microorganisms from the mineral ores and the subsequent recovery of metals from solution are referred to as bioleaching (Rohwerder, T et al, 2003). This is an economical method for the recovery of metals from minerals; especially lowgrade ores, overburden, and waste from current mining operations which requires moderate capital investment with operating cost (Watling, 2006).Furthermore, bioleaching is generally more environmentally friendly than conventional metal recovery processes such as concentration and smelting. Those physicochemical metal extraction processes generate sulphur dioxide, a toxic emission that is increasingly the target of regulatory legislation (Stott et al., 2000; Olson et al., 2003). Bioleaching of chalcopyrite is the key industry target. The main problem hindering commercial application of chalcopyrite bioleaching is the slow dissolution rate (Fu et al, 2008).Dissolution of acid-soluble sulphide minerals such as sphalerite, and to a lesser extent chalcopyrite, occurs by a combination of ferric iron and proton attack via the polysulphide pathway (Rohwerder et al., 2003)."

Jan 1, 2008

By M. Vijayalakshmi, S. Saroja, C. Sudha, T. N. Prasanthi

"Ti-5Ta-2Nb alloy and 304L austenitic stainless steel were joined by explosive cladding process. Investigations on 'as received' explosive clad revealed high hardness very near the interface due to martensitic transformation of 304L steel base plate. To improve ductility, explosive clads were heat treated in the temperature range of 823 to 1073 K for 1 to 20 h. Consequent change in the microstructure and microchemistry of the clad interface was studied. No change in the interface microstructure was observed for heat treatment at 823 K. Increase in temperature lead to the formation of various reaction zones at the interface, their number and width increase with temperature and time of thermal exposure. Growth kinetics of the reaction zones was monitored and activation energy required for formation was calculated. From elemental redistribution profiles, effective inter-diffusivities of alloying elements were calculated as a function of concentration and activation energy required for inter-diffusion was evaluated.IntroductionFor engineering components exposed to highly oxidizing and corrosive environments, a titanium based alloy i.e Ti-5Ta-2Nb (Ti-Ta-Nb) is often chosen as a structural material [1,2]. For economic consideration, vessels and piping exposed to non-oxidizing conditions are fabricated from 304L austenitic stainless steel (304L SS). Hence, dissimilar joint of Ti-5Ta-2Nb alloy and austenitic stainless steel becomes unavoidable. Fusion welding processes are not suitable for joining Ti and Fe based alloys due to the propensity for the formation of intermetallic phases and subsequent reduction in the bond strength [3,4]. Hence, explosive cladding, a solid state welding technique, was used to achieve high integrity, corrosion resistant joints between the two alloys."

Jan 1, 2012