Search Documents

By T. C. -M. Cheng

Iron removal and disposal in zinc plants has imposed a major environmental challenge to the industry. Among the existing options of precipitating iron as jarosite, goethite, and hematite, the Hematite Process seems to be the best candidate for the future development of a waste-free technology, because of its potential of producing saleable iron oxide residues for feed in iron-steel making industry. Unfortunately, under the current practice of the Hematite Process, it is not possible to produce iron residues clean enough to meet the specifications of the said industry. In this paper, the practice of industrial hematite precipitation and the relevant technical literature are reviewed with the objective to identify the critical processing parameters which are responsible for the contamination of hematite, particularly with sulfur and zinc. The analysis is conducted from a crystallization theory standpoint with emphasis given to the role of supersaturation with respect to the cleanliness of hematite precipitates.

Jan 1, 1997

By Xiang-dong XING, Zhen-yang wang, Jian-Liang Zhang

Distribution behavior of titanium between CaO-SiO2-MgO-Al2O3-TiO2 and hot metal was studied between 1350 °C to 1600 °C. Experimental results indicate that the reaction temperature influenced the activity coefficients of titanium and resulted in the variation of equilibrium constant. Finally, the Gibbs free energy formula of titanium carbothermic reduction was fit out using the thermodynamic model of Wagner and congregated electron phase models.

Jan 1, 2015

By Mark Cross, Diane McBride, Nick Croft

Extractive metallurgical processes rate amongst the most complex from the perspective of computational modeling. They typically involve multi-phase and multi-component fluid flow in very complex geometries, heat transfer driven by a number of interacting phenomena, solidliquid- gaseous phase change and mass transfer together with complex thermodynamics and associated chemical reactions. Beyond the model building itself, key challenges have always involved being able to identify the phenomena present together with interactions to characterize processes and experimental laboratory and plant data to parameterize the arising models – it is in this milieu, which require considerable process understanding and subtlety of thought, that David Robertson has made his contributions. We will review the achievements, over the last couple of decades, in computational modeling of extractive metallurgical processes and address some of the remaining challenges to enable simulation based process design, as we move through the 21st century.

Jan 1, 2014

By Kumar P. Dharmasena, Haydn N. G. Wadley, Bill W. Choi

"Non-contact eddy current sensing methods have been developed and applied to Cd0.955Zn0.045Te crystal growth to obtain a better understanding of the melt, solid nucleation, and the growth process. The application of this sensor approach relies on a large difference in liquid and solid electrical conductivities near the melting point and requires knowledge of the relationships between the electrical conductivity, melt composition, and temperature. Using a multifrequency encircling eddy current sensor, the electrical conductivities of three different Cd1-xZnxTe (x=0.00, 0.045, and 0.08) alloys were measured as a function of temperature in a laboratory-scale vertical Bridgman furnace. The measured solid and liquid electrical conductivities were then used in electromagnetic finite element models to analyze the multifrequency responses of eddy current sensor designs during the simulated growth of a crystal. These eddy current sensors were fabricated and installed in a vertical Bridgman furnace and used to monitor many Cd0.955Zn0.045 Te growth runs. One sensor was placed in the vicinity of the ampoule tip to detect undercooling/spontaneous nucleation and two other sensors (""absolute"" and ""differential"" designs) placed to monitor the movement/curvature of the liquid-solid interface during crystal growth. The sensor data was used to characterize the initial melt state, detect the onset of nucle-ation, determine the growth velocity, and identify the shape of the interface.IntroductionSingle crystal CdTe and its solid solution Cd1-xZnxTe alloys (0.03<x<0.05) are used as infrared transparent substrates for infrared focal plane array (IRFPA) detectors [1-6] and as solid state y- ray detectors [7-9j. Cd1-xZnxTe substrates are normally ""mined"" from large polycrystalline boules grown by the unseeded directional solidification of Cd1-xZnxTe melts using either a vertical or horizontal Bridgman process [10-14]. The vertical Bridgman method is particularly popular for growing CdTe and its related compounds. In this process, a Cd1-xZnxTe ingot is produced by first melting a charge in the hot zone of the furnace and then vertically translating the furnace (with its associated axial temperature profile) relative to the stationary crucible to cause directional solidification. In spite of many experimental efforts to investigate the relationships between material purity, stoichiometry, the controllable growth parameters (furnace temperature profiles, ampoule geometries/materials, furnace translation rates and starting position) and the resulting material characteristics (grain structure, dislocation densities, IR transmission, macro-segregation etc.), the yield of Cd1-xZnxTe of a quality suitable for large area (e.g. 4 cm x 6 cm) substrates remains low (<10%). Since much of this poor yield is directly associated with the crystal growth process (e.g. melt stoichiometry, solidification velocity, interface shape, temperature gradients, cooling rate, etc.) intensive efforts are under way to improve this technology."

Jan 1, 1997

By Donald L. Stewart, Ken Overfield, Edward M. Williams

"Recent increases in energy cost have lead to a renewed focus on energy efficiency during aluminum melting operations to reduce fuel usage. The goals of a batch melting operation are to melt the charge using the minimum required energy, to melt the metal to the required temperature within the required timeframe, and to avoid generating unwanted contaminants by overheating the charge.The heat transfer efficiency of a conventional hydrocarbon fired aluminum melting furnace varies over the course of the melt cycle, depending on the conditions in the furnace. The purpose of this work was to develop a method of determining the transient heat transfer efficiency throughout the furnace cycle and to take advantage of this knowledge to optimize the melting process through furnace controls and proper production operations. This furnace survey methodology has been developed and used to evaluate a number of furnaces.Description of a Typical Batch Melting Furnace CycleA typical batch melting furnace cycle will consist of three stages:1. Charging – Solid metal charged through an open roof, solid or molten charged through an open door, and/or molten poured through a furnace blister2. Melting – From the time the door or roof is closed and the burners are turned to high fire until the charge is all liquid and has reached a temperature suitable for alloying (typically ~1350 °F / 730 °C)3. Holding – From the end of the melting stage until transfer or casting is completeIn some cases, further charging can take place after the melting cycle has started. This can happen when the entire solid charge will not fit in the furnace in one load, or if additional molten metal is added while the charge is melting. The bulk of the energy used in the melter is consumed during the melting cycle. The thermodynamic minimum energy requirements for melting pure aluminum are:• Energy required to heat pure aluminum from room temperature to the melting point at 1220°F (660°C) is 288 BTU/lb (670 kJ/kg)• Energy required to change state of pure aluminum from solid to liquid (heat of fusion) is 171 BTU/lb (397 kJ/kg)• Energy required to heat molten from melting point at 1220°F (660°C) to 1350°F (730°C) is 36 BTU/lb (83 kJ/kg)• Total energy required to melt a solid charge from room temperature to 1350°F (730°C ) is 495 BTU/lb (1151 kJ/kg)"

Jan 1, 2009

By Wing Ka Ng

Substitution of pulverized coal injection by solid biocarbon fuel has the potential to achieve substantial reduction in GHG emissions associated with blast furnace ironmaking. A systematic evaluation was conducted on the performance of solid bio-carbons produced from a single raw biomass source using different pyrolysis technologies. The potential of solid biocarbon in reducing GHG emission of the blast furnace ironmaking process is strongly influenced by its O/C mass ratio. In order to achieve substantial GHG reduction, it is necessary to replace coal injection by solid biocarbon having a low O/C mass ratio. The pyrolysis technology and conditions employed are key parameters influencing O/C mass ratio of the resultant solid biocarbon. Close collaboration between steelmakers and solid biocarbon producers is critical for producing suitable solid biocarbon fuel to replace pulverized coal injection. A successful partnership should pave the way in achieving substantial reduction in GHG emissions of the blast furnace ironmaking process.

By Liang Sha

In this study, adsorption of copper by chemically modified orange peel was investigated. A conspicuous change occurs in the surface morphology of the biomass due to modification, which is depicted by SEM images. Equilibrium isotherms and kinetics were obtained and the effects of various factors, including solution pH, contact time, initial metal ions concentration and temperature, were studied by batch experiments. Kinetics was found to be best-fit pseudosecond- order equations. Equilibrium was better described by Langermuir isotherms rather than Freudlich isotherms. At 25?, pH5.30, the maximum adsorption capacity was 70.67mg?g-1 . With increase of temperature, adsorption efficiency decreased. The biosorbent was suitable for repeated use for more than five cycles.

Jan 1, 2009

By G. G. Krishna Murthy

Several experiments were conducted to determine the rates of heat transfer coefficients of CaO-SiO2-A1203-FeO slags at temperatures in the range 1623-1823 K The experimental technique involved measuring heating rates of a solid specimen, sub¬merged in slag phase, using a temperature probe made of Pt\ 10%Rh-Pt. Effect of %FeO (3-10%), %FeS (0.1-0.68%), %P205 (0.2-3.0%), %MgO(5-6%), and %MnO (0.96-3.84%) present in the slag on overall heat transfer coefficient, U, of slags was investigated. Simple first order heat balance equation in combination with experimental plots rising temperature of solid specimen versus time were employed to determine the values of U. The values of U determined in the present investigation were present in the range of 70-260 cal/Ks.m2. The value of U increased with increasing the slag temperature. The values of U were not effected by increased amounts of sulfur in the slag phase. The increased concentrations of MgO, FeO, MnO, and P205 in the slag phase decreased the values of U. On the other hand, the increased amounts of Fe2O3 in the slag phase increased the value of U. Comparison of the results, obtained using the slag bath stirred by argon injection, with those determined without any stirring indicated that both radiative and conductive heat transfer mechanisms are important even at high temperatures.

Jan 1, 1993

By Deventer Johanna van

Ore bodies around the world are declining in grade, whilst increasing in complexity. The level of impurities relative to the valuable metal is steadily increasing, posing new challenges to existing operations. Ion exchange is widely used in the hydrometallurgical industry for both primary recovery of metals and the removal of impurities. The superior selectivity of ion exchange resins makes them exceptionally suitable for the removal of target impurities to very low levels, thereby saving operating costs, increasing the value of the final product and significantly improving revenue. The ion exchange process in these applications is very simple, using standard ion exchange equipment and acid regeneration. The process can be fully automated, requiring minimal operator interference and supervision Examples of impurities that are successfully removed via ion exchange include iron, antimony and bismuth from copper electrolyte. In the copper electrolysis process, antimony, bismuth and arsenic tend to form slimes which are dispersed in the electrolyte. These slimes contaminate the cathode and/or decrease the quality of the copper deposition. A special chelating resin was developed to remove antimony and bismuth, while at the same time ensuring minimal chloride leakage to the sulphate matrix. The work is described in more detail in this paper. Ion exchange is also used to remove copper, zinc and nickel from cobalt electrolyte. This paper addresses a few of these examples in more detail.

By John Snowberger III, J. Brent Hiskey

The electrochemical dissolution of super alloys containing different amounts of rhenium was investigated. The initial part of the investigation focused on the anodic dissolution of rhenium from second-generation (3% Re) and third-generation (6% Re) nickel based alloys. Exploratory electrochemical tests were conducted to evaluate solution chemistries and to establish fundamental dissolution behavior of the alloys. These included rotating disc electrode (RDE) cyclic voltammetry, linear sweep voltammetry, and chronoamperometry tests. Electrolytes comprising sulfuric acid, hydrochloric acid, and ammonium sulfate were examined. Of these, a 0.1 M HCl solution proved to be extremely effective for electrochemical dissolution of samples of CMSX-4, CMSX-10, and SC-180 alloys. This paper discusses in detail the electrochemical behavior of these alloys.

Jan 1, 2014

By Robert Vidal

The performance of a laboratory-scale cell for the electrolysis of an aqueous chrome alum solution was studied. Electrode potentials, pH, and Eh were recorded. An optimum catholyte pH of about 2.5, consistent with information from the literature was observed. Values exceeding this range resulted in a precipitate formation and are detected by wavering cathode potentials. The role of anodically produced dichromate ions was investigated by chemical analysis. It was found that the steady state concentration of dichromate ions varies inversely with fluid flow from catholyte to anolyte. This concentration was also reduced with the use of precious metal coated titanium anodes.

Jan 1, 1994

By J. L. Liow

Studies have been carried out on the causes and effects of slopping in an annular cylindrical geometry such as the top submerged combustion reactor. Properties of standing waves formed such as the wave profile, period, pressure distribution and velocity have been derived analytically. The wear profile due to wave erosion was calculated based on the assumption of linear motion and that the wear is a dissolution process. The use of the j, factor showed that the wear was proportional to the square root of the wave velocity at any point. Using the dimensions of the lsasmelt reactor given by Errington et al. (1987)[11, the wear profile due to wave erosion was calculated using the analytical solution. The wear profile calculated was shown to have a maximum just below the initial bath surface. The wear was found to be concentrated in the region where the first asymmetric standing wave was most active. The results showed that the refractory near the bath surface will be affected by wave erosion, more so than any other parts of the reactor. The contribution of wave erosion on wear must be accounted for in assessing the total refractory wear of a vessel in which slopping exists.

Jan 1, 1991

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

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

Jan 1, 2014

By Sylvain Gouttebroze, Mohammed M'Hamdi

In a previous work, a small scale Bridgman furnace has been used to study silicon bi-grain crystallization at different cooling rate. This work expands the analysis by studying the mechanical interaction between the crucible and ingot during the solidification and cooling. The thermal model is based on a 2D-axisymetric heat-transfer model. The flux histories are then transferred to the ingot-crucible 3D-model. Anisotropic Elastic and Crystal Plasticity model are used to model the silicon deformation. Four different assumptions are applied to model the mechanical contact crucible-ingot and three grain misorientations are considered. The results show the strong impact of the alumina crucible contraction on the stresses and deformations in the silicon ingot.

Jan 1, 2015

By C. M. F. Vieira

Crushed fired brick waste, known as grog, screened at two different particle size, 840 (20 mesh) and 180 µm (80 mesh), was used in mixtures with clayey body to make typical red ceramics for bricks. The effect of the grog addition up to 20 wt.% on the properties of bricks fired at 700oC was evaluated. The results indicated that both the particle size and the amount of grog addition changed the fired properties of the clayey body. Additions above 5 wt.% of grog, with a coarser particle size, decreased the mechanical strength of both the dry body and the fired ceramic pieces. By contrast, grog with a finer particle size may be used up to 10% wt. without deteriorate the properties and corresponding microstructure of the clayey body.

Jan 1, 2009

By F. M. Nakla

Various methods of Applied Mineralogy were used for determining the nature and composition of products yielded by flotation tests for Maghara coal beneficiation. Coal samples obtained from the Sa fa mine in Northern Sinai, Egypt, were crushed, sieved, &apos;and <32 mesh size fraction was cleaned by froth flotation. Experiments were conducted to determine the effect of certain parameters on beneficiation of Maghara coal by flotation. The investigated factors included nature of frothing and/or collecting reagents, pH value of the medium, particle size distribution in the head sample, and pulp density of the coal slurry. The quality of head samples, coal concentrates, and tailing products were determined by chemical analysis, microscopic study, x-ray diffraction analysis, and occasionally by infrared (IR) absorption spectroscopy.

Jan 1, 1989

By John T. Berry, Robert D. Pehlke, Michael J. Beffel

"Pattern making and metal casting organizations are currently adopting CAD/CAM systems and implementing this technology in design and production. Al though significant progress has been reported, these systems generally are based on two or two and one half dimensional analyses. Very few are based on solid geometric modelers.The present paper emphasizes the need for solid geometric modeling of the casting and rigging system and linkage with a solidification simulator. The nature of some of the technological challenges which have slowed this development are discussed, including accurate description of complex surfaces and their intersections and the bridging of computer encoded information with NC technologies and with FEM-based simulators for stress and thermal analyses. A recently prepared modular-structured FEM simulation code implemented on a micro computer is described.Construction of a solid geometric model of the casting and rigging and validation of the combination for optimum characteristics of soundness, quality and yield by solidification simulation are I inked as key elements in the foundry of the future. Data base support for this CAD/CAM system is rapidly being developed throughout the world.INTRODUCTIONThe simulation of shaped casting solidification using the digital computer, goes back to at least the early nineteen-sixties when Forsund (1) in Denmark applied the technique to the problems of casting surface quality.Prior to that time, the work of Paschkis and co-workers using the analog computer ranges back to the nineteen-forties, when work sponsored by the AFS Heat Transfer Committee at Columbia University revealed many hitherto unknown or only partly anticipated aspects of casting solidification (2).Three reviews of the various historical aspects of simulation should be referenced. Firstly, the AFS monograph by one of the present writers (RDP) and his colleagues - describing background and later work, again sponsored by the AFS Heat Transfer Committee at the University of Michigan (3). Secondly, a review prepared by Durham and Berry (4) which discusses broad aspects of casting solidification simulation. Thirdly, a review by Erickson (5) which contains an excellent bibliography to 1980. In addition to these papers, the publications lists of the CADCAST project* and the proceedings of the two Engineering Foundation Conferences of Casting and Welding Modeling, published by ASME, are also most notable (6) •"

Jan 1, 1986

By John L. H. Patterson

Handheld XRF has become the favorite way of measuring the content and identity of alloys in the field. This is because of the very portable nature of the instrumentation and its simple operation. However, these analyzers have been unable to determine the concentration of the light elements like Mg and Si due to the very low energy of the x-rays produced by these elements. In the past accessories such as vacuum and He flush have given some analyzers the ability to determine these light elements with modest detection limits. The introduction of the Silicon Drift Detector (SDD) into this class of instrumentation has added a new level of analysis capability to portable XRF instrumentation. X-ray fluorescence is achieved by exciting a sample with a beam of x-rays, which in recent portable equipment are generated by a small tube. This results in the emission of characteristic x-rays from the sample under test. By measuring the energy of each x-ray it is possible to determine what element generated it. By counting the number of x-rays at each energy it is possible to determine the concentration of each element. The detection limit for each element is dependent upon the number of x-rays which reach the detector. As the number of x-rays increases the detection limit will improve. One of the major factors in an x-ray reaching the detector is the energy of the x-ray. As the energy of an x-ray increases the probability of that x-ray reaching the detector increases. The energy of an x-ray is inversely proportional to the atomic number (AN) of the element generating the x-ray. For example, an iron x-ray (AN=26) is 6.40 keV while an aluminum x-ray (AN=13) is 1.49 keV. As the energy decreases, the detection of the x-ray becomes less and less probable because the x-ray may be absorbed by the windows which are part of the instrument and detector or the air in the path between the sample and detector. In SiPIN based portable XRF analyzers, the lowest element which is detected with acceptable detection limits is normally considered to be Ti (AN=22). The detection limits for 60 second measurements on typical SiPIN XRF analyzer are given in Table I. Thus, portable analyzers have not been useful for measurement of aluminum and titanium alloys as major components of these alloys are Mg (AN=12), Al (AN=13) and Si (AN=14).

Jan 1, 2009

By C. E. Hunt

Since the turn of the century, copper-nickel sulphide ores have been processed at the Sudbury, Ontario operations of INCO Limited, currently the largest integrated mining, milling, smelting and refining complex in the free world. Through the years operational, ecomomic, social and legislative changes have dictated the need for research and development directed at mitigating the impact of existing operations on the surrounding natural environment and also the reclamation of areas affected by earlier mining activities. Approximately one hundred years of mining history and the current annual processing of some 12 million tons of ore presents significant challenges with respect to waste disposal, liquid effluent treatment and land reclamation, particularly in light of rapidly evolving environmental regulations&apos; and controls within the Province of Ontario.

Jan 1, 1992

By Yuanbo Zhang, FENG ZHOU, Guanghui Li, Zhengwei Yu, RuijunWang, Tao Jiang

Composite agglomeration process (CAP) of iron ore fines has been proved an effective route for ironmaking burden production, and is characterized by low the fuel consumption and high the productivity compared with the traditional sintering process. Sintering behavior of pelletizing feed in CAP has not been studied fully yet. In this study, individual pellet and simulated CAP cells were roasted under the simulated sintering conditions. The compressive strength, FeO content and microstructures of roasted samples were investigated. The results show that pelletizing feed either from magnetite ore hematite concentrate can be indurated under the conditions of conventional iron ore sintering. Hematite pelletizing feed has better sintering property than magnetite pelletizing feed. Pelletizing feed consolidation in CAP cells is identical to the individual pelletizing feed, but the strength of CAP cells is much higher than the individual pelletizing feed. Higher basicity in both pelletizing feed and matrix feed is beneficial to the strength of CAP cells. Individual strength of pelletizing feed is not the decisive factor in CAP as the pelletizing feed has been embedded into the matrix with high basicity and formed an organic whole. The main chemical compositions and basicity of pelletizing feed and basicity matching with matrix feed is important.

Jan 1, 2015