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By Zhi-biao Yin

Copper smelter flue dusts often cannot be directly recycled to the smelting process and accumulate as hazardous wastes requiring environmentally acceptable disposal. Because of the limited amount of flue dust, a separate copper extraction process must be simple and require-a small plant investment. A flue dust process has been developed, consisting of the following steps: (1) roasting a pelletized mixture of hydrated lime and flue dust to fix arsenic and sulfur as insoluble calcium salts, (2) heap leaching the roasted pellets with a buffered ammonia/ammonium salt solution to extract copper as an ammine complex in a lined cell that is the final repository of the leached pellets, and (3) boiling ammonia from the lixiviant to precipitate copper. Condensed ammonia and the filtered solution are returned to leaching. Heap leaching in the final repository cell lowers the capital investment significantly compared with competing extraction processes. Chemistry with respect to arsenic, sulfur and copper is discussed.

Jan 1, 1992

By Xi-Shan Li, Qian Li, Yong-bin Yang, Tao Jiang, Jie Ge

Compared with other pretreatments of sulfur & arsenic-bearing gold, double-layered pellet roasting has an advantage that sulfur dioxide and arsenic trioxide volatilizing from this refractory gold ores can be solidified into the coating without emission during the roasting. However, the separation of coating from roasted double-layered pellet should be focused on in the novel pretreatment. Based on the difference of physicochemical characteristics between roasted solidified coating and pellet core, several separation methods including grinding, drop impact and water quenching method had been systematically studied in this paper. The results showed that magnetic and gravity concentration could not obtain a satisfactory separation effect. The optimum separation rate of grinding was only 38.94% at grind time 12min, but it increased to 85.05% by drop impact under drop height 0.75m, drop times 20 and impact angle 45°, and that of water quenching taking advantage of slaking reaction of lime could approach 75.32%.

Jan 1, 2015

By K. Gao, R. Dry

"Carbon boil, which results in excessive spitting and even complete destruction of a metal drop, could significantly influence the efficiency of direct smelting processes. Carbon boil has been studied as a function of some key parameters such as melt sulfur content, oxygen partial pressure, and melt area/volume ratio. The time of carbon boil was determined using a CCO camera coupled with a time/date generator connected in parallel to a video recorder and a computer. The time of carbon boil was in the range ~5 - 15 seconds under the conditions in this study. A mechanism for carbon boil has been proposed.IntroductionThe occurrence of carbon boil in molten iron drops can result in excessive spitting and sometimes even complete destruction of a metal drop. In direct iron smelting processes, this could significantly influence the decarburisation of liquid metal and the post combustion and hence may influence the efficiency of smelting processes. The generation and consequent ejection of metal droplets into the gas phase occurs due to the intense turbulence in the bath which results from the injection of gases and coal. The aim of this investigation is to understand the fundamentals governing the carbon boil phenomenon under direct iron smelting conditions to assist control of process efficiency.Carbon boil phenomenon has been studied as a function of some key parameters such as melt sulfur content, oxygen partial pressure and melt area/volume ratio. The time for the occurrence of carbon boil has been determined in this study at 1440 °C using a novel approach which includes utilisation of a CCD camera coupled with a time/date generator connected in parallel to a video recorder and a computer. This arrangement permits the capture of the entire sequence of events leading up to carbon boil and therefore the determination of time of boil which is in the range -5 - 15 seconds under the conditions in this study."

Jan 1, 1996

By Janene Barter

Telfer Gold Mine treats both gold/copper oxide and sulfide ores in a remote location in the Great Sandy Desert, Western Australia. Currently, the oxide gold ore is treated in a conventional CIL circuit by blending the low and high grade copper ores to minimise cyanide consumption and allow smooth operation. The sulfide ore is treated through a flotation circuit to produce pyrite and copper concentrates. The pyrite concentrate is treated in the CIL. Copper concentrate is stockpiled and sold to a smelter for further processing. In recent times, as the depth of the pit has increased the copper head grade has also increased, to the point where the ore was becoming uneconomical to treat. In addition, it was desirable to reduce the amount of cyanide reporting to the tails dam both from an environmental and economical viewpoint. Newcrest Mining Limited engaged GRD Minproc Limited to evaluated a process to reduce the amount of cyanide entering the tail dam with consideration given to copper recovery. From this investigation, the Sulfidisation, Acidification, Recycle and Thickening (SART) process was selected. A detailed testwork program for SART was undertaken with the objective to design and construct a SART plant at Telfer. This paper outlines how the SART process was chosen and summarises the testwork that led to the design of the SART plant. It also touches on some of the important issues for designing this type of process.

Jan 1, 1998

By Thomas J. Keefe, O&apos

The effects of cobalt, B-naphthol, glue and antimony on the polarization behavior of zinc sulfate electrolyte were investigated. It was found that B-naphthol was beneficial in reducing the detrimental effects of cobalt while antimony and excess glue were each harmful. Since the nu cl eat ion over potential was insensiti1ve to coba1t, other regions of the polarization curve were used to indicate electrolyte balance. The low? current density area occurring in the reverse or anodic sweep direction was? often an indicator when an ?unstable condition existed. The two parameters evaluated were the degree of inflection in the polarization curve in the low current density region during scanning and the rate of current rise observed when the sample was potentiostated at -0.781 Volts (SHE). Using this technique, a two-additive system was shown to be desirable to control cobalt and antimony containing electrolytes. The structure of the deposits was examined using scanning electron microscope techniques.

Jan 1, 1985

By František Molnar, Zsolt Szentirmai, Juraj Schmiedl, Felix Sekula

"Hydrometallurgical nickel production in Sered Nickel Plant (Slovakia) that treated roasted Albanian ore left behind a considerable amount of the solid leaching residue. About 6 million tons of this fine-powder residue containing approximately 52 wt.% of iron in the form of oxides is to the present day stored in a stockpile. However, its iron content makes it a potentially interesting secondary raw material for iron production. This secondary raw material is not, unfortunately, suitable for direct treatment in iron and steelmaking processes.This paper presents results of the laboratory tests of pyrometallurgical method of processing of the leaching residue by its roasting and subsequent refining melting. The objective of the selective reducing agglomeration roasting was to reduce iron oxides and to simultaneously avoid reduction of chromium oxides and silica. Refining melting is carried out in an inert atmosphere. The products of melting are technically pure iron and slag.IntroductionThe leaching residue stockpiled on waste dump near already non-existing Nickel Plant Sered, Slovakia, is considered to be one of the most important environmental burdens in this country. The 40-years of an on-going effort focused on finding the methods for extracting metals and thus remove the waste dump have not been successful [1,4,5,6]. From the literature survey it is evident that past investigations have been following three main routes:1.Removal of chromium by mineral processing methods prior to its metallurgical treatment to achieve final chromium concentrations below 0.3 wt.%.2.Pelletization of solid leaching residue and its subsequent reduction in blast furnace and steelmaking plant and simultaneous removal of chromium.3.Pelletization of solid leaching residue followed by metallurgical processing of preliminary reduced semi-product in electric arc furnace (EAF) accompanied by partial reduction of chromium."

Jan 1, 2008

By A. A. Hejja

"Liquidus temperature and electrical conductivity data measured on synthetic slags were modelled by the use of neural nets (NN). In this work the applied multilayer feedforward NNs were trained by a conjugate-gradient optimisation for which a three layer formulation was used. Very good fits were obtained for both the liquidus temperature and the conductivity data. The synthetic slags were prepared from pure oxides to represent a wide range of compositions likely to be encountered in ferromanganese and silicomanganese smelting. The slag constituents were in the following range: Mn0;5-30%, Ca0;20-35%, Mg0;5-15%, Si02;27-58%, Al20 3;5%. Liquidus temperatures varied from 1300° to 1380° and increased with increasing basicity ratio. The electrical resistivity of slags decreased with the increase of basicity ratio from 0.55 to 1.1 but above 1.1 basicity ratio the resistivity tended to increase depending upon the MnO content.Neural NetsVarious neural net (NN) topologies such as Hopfied nets, Hamming nets, Carpenter/Grossberg classifiers have been discussed in some detail by Lipmann (1). In this work, the applied multilayer feedforward NNs are not trained by backpropagation (BP) using the generalized delta rule (2) (GDR), but by a conjugate-gradient optimisation [3,4] - a procedure similar to that proposed by Barnard and Cole [5]. A neural net is capable ·of learning the non-linear functional relationship existing between a set of inputs and outputs [ 6]. In this capacity a neural net is used to determine the functional relationship that exists . between N dependent and independent variables, which characterize the system under consideration For a three layer neural net [1] the following function may be formulated, which relates X; inputs to the output Y 0 from node o:"

Jan 1, 1997

By Kyle S. Brinkman, Kenneth L. Reifsnider, Fazle Rabbi

"Mixed ionic and electronic conducting (MIEC) ceramic membranes are HeteroFoaM's which play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC), oxygen separation and permeation membranes, partial oxidization membrane reactors for natural gas processing, and high temperature electrolysis cells. Dual phase oxygen membranes consisting of an ionic conducting phase Ceo.sGdo.z02 (CGO) and an electronic conductive phase C0Fe204 (CFO) were fabricated and characterized by structural (XRD), microstructural (SEM-EDS) and broadband dielectric measurement techniques. In-situ measurements of the dielectric properties of working oxygen separation membranes are presented which indicate that the material's dielectric behavior can be an indicator for MIECperformance.IntroductionCeramic membranes which transport oxygen ions play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC) [l ], oxygen separation and permeation membranes in the commercial and nuclear arena [2, 3], partial oxidization membrane reactors for natural gas processing [4], and high temperature electrolysis cells [5]. For the electrolyte functions, the membranes must transport oxygen ions only. On the other hand, permeation membranes, typically used in combustion devices to support oxy-fuel combustion or for partial oxidation reactions involving the production of synthesis gases, require mixed oxygen ion and electronic conduction (MIEC). Traditionally the tailoring of the ratio of ionic conductivity to the materials electronic conductivity, measured as the transference number, has been accomplished by the introduction of aliovalent doping elements creating point defects in the material facilitating the diffusion of charged species. However, several decades of research have not yet produced single phase materials which possess the concomitant ionic and electronic conductivity required for use in membrane separation applications. It is clear that novel ""dual phase"" heterogeneous materials will be required and that the surface reactions of these materials will be of particular importance as the industry moves toward thin films membranes [6]."

Jan 1, 2013

By Hyun Soo Kim, Joon Soo Kim, Myong Jun Kim, Jyothi Rajesh Kumar, Jin-Young Lee

Rare earth materials have an ever growing variety of applications in the modern and hitech technology. They apply to many an industry with crucial materials and they provide numerous a customers with benefits. Rare earth materials utilization increasing day-by-day in the worldwide, at the same time the resources is very limited in many countries like Korea. The present general article divided four sorts such as 1) mineral processing of Korean ore deals the gravity, magnetic separation and froth flotation, 2) decomposition and leaching of concentrates included sodium hydroxide fritting, sodium hydroxide hot digestion, hydrochloric acid leaching, 3) separation and purification of rare earth elements in mixed rare earth chloride solution consists reduction and oxidation method, solvent extraction, 4) preparation of rare earth oxide compound from purified elemental rare earth chloride solution having oxalate salt precipitation by reaction crystallization. The last part consists of a summary of the present study.

Jan 1, 2015

By Majid Sarkari, Hossein Atashi, Farhad Fazlollahi

"The aim of this research work was to prepare the efficient catalyst to purify pollutant output gases such as SO2 , NO2 and CO. This catalyst, lanthanum cobaltat (LaCo03) was prepared by the proper method in the analysis laboratory of Tabriz Oil .The first materials were chosen through calcination operation and temperatures of operation related to the Tamman temperature, therefore the basis for the first material of catalyst was nitrate and aqueous and since we had no availability to lanthanum nitrate, lanthanum oxide was used to prepare the nitrate one. Before all else, the first materials of catalyst were mixed together with the equal mole proportions and then, at the lower and upper temperatures of Tanunan temperature, calcination operation was carried out. To determine the molecular structure, the XRD analysis was utilized and specified that prepared lanthanum cobaltat was sixth aqueous and had the crystal structure type Triclinic.IntroductionLaCo03 has presented a vast interest because of its special electrical, magnetic and catalytic properties [1-4]. The catalyst LaCo03 can be prepared by means of several methods such as spray drying, freeze drying and also co-precipitation [5-12]. Some methods including hydrothermal, sol gel and citrate [13] This material usually has been synthesized by ceramic method and certainly the high temperature for the calcination operation. [14]. Lanthanum catalysts have been researched because of having such an active state [15]. One of the unique properties of this catalyst is the simultaneous conversion of pollutant elements. Nowadays CO oxidation has important applications in environment protection, such as indoor air cleaning and automotive exhaust treatment. LaCoO3 is one of the most important catalysts for CO oxidation."

Jan 1, 2013

By Anne C. Chinellato, Alejandra T. Soria, Nelida L. del Mastro, Amanda C. S. Pereiral, Esperidiana A. B. Moura, Anibal V. Abreu

"This work presents a comparative study of the thermo-mechanical and morphological properties of sugarcane bagasse fiber/HDPE composite treated with electron-beam and gamma radiation. The composite samples obtained by extrusion and injection molding processes were irradiated at 50 and 90 kGy using either a 1.5 MeV electron beam accelerator or gamma irradiator EMI-9, at room temperature in presence of air. The irradiated and non-irradiated samples were submitted to mechanical and MPI tests, differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), sol-gel analysis and X-Rays Diffraction (XRD) and the correlation between their properties was discussed. Improvement of the bagasse fiber/HDPE composite properties, using electron-beam or gamma radiation, was found.IntroductionResidues of sugarcane bagasse fiber are widely produced in Latin America and other countries: in Southern Africa, Egypt, South-Eastern Asia, India, China, Australia, Cuba, among other producers, as by-products of the sugar and bioethanol industry. The sugarcane industry in Brazil and Uruguay is well established and expanding with large potential to increase the production of sugarcane bagasse in the next years [1-3]. Although the major portion of the bagasse is currently burnt for energy supply in the sugarcane industry, the disposal of this byproduct is still inefficient and, consequently, it is critical for agricu1ture profitability and environmental protection. Sugarcane bagasse is a lignocellu1ose fiber mainly constituted by around 46 % cellu1ose, containing hemicellu1ose, lignin, fat and waxes, silica and other elements [3, 4]. Studies have reported that sugarcane bagasse can be used to produce thermoplastic polymeric composites with excellent properties for many applications. [5-8]. Based on this survey, the transformation of bagasse into high quality industrial products, such as bagasse-polymer composites, can provide its more effective utilization."

Jan 1, 2012

By B. Boryczko, J. Norwisz, Jose Escobedo Bocardo, Z. Kolenda, A. Holda

"Classical thermodynamic analysis of any thermal and chemical process is usually based on the first law of thermodynamics. Such an approach is not sufficient when deeper understanding of the nature of each elementary process is required. The use of the first and second law of thermodynamics together is necessary to solve practical process more effectively. Enthalpy and exergy balances allow to enhance our understanding of thermal processes especially when cumulative consumption of energy and exergy is calculated. To ensure reliability of such an analysis the least squares method for adjustment of mass balances of principal chemical elements has been applied and described in detail. Numerical analysis has been carried out to compare two different processes of copper production – shaft furnace and flash smelting.IntroductionClassical thermodynamic analysis of any technological process is usually based on the First Law of Thermodynamics in the form of energy (enthalpy) balances. Such an approach is useful in engineering practice as it makes analysis easier in the global scale neglecting modeling of the elementary processes, allows calculation of the thermal efficiency and makes possible to control quality of the measurement results. Additionally, graphical presentation of the energy balance is simple in the form of Sankey diagram.In the case of aluminum electrolysis process, design of the new electrolyzer or its modernization is always based on the enthalpy balance.However, deeper thermodynamic analysis leads to the conclusion that such an approach is not sufficient. The First Law of Thermodynamics guarantees the exact equivalence of the various forms of energy (allowing all forms to be measured in the common unit such as joules) but it does not guarantee interconversibility. Thermal energy (heat) is in a peculiar and unique position, for whereas all other forms can be completely converted into thermal energy, the reverse process id impossible, only a portion of the heat can be converted into mechanical energy. Explanation comes from application of exergy balances. As we know exergy expresses the amount of mechanical work necessary to produce a material in its specified state from components common in the natural environment, in a reversible way, heat being exchanged only with environment [1]. Consumption of exergy connected with the fabrication of some considered product appears not only in the plant manufacturing the product, but also in all plants delivering raw materials for the final production process"

Jan 1, 2008

By Lichao Ding, Chunhua Liu, Yunnen Chen

"In this paper the simulated acid magenta dye discoloring the reaction process was researched. The results showed that it attained highest decolorization efficiency for acidic magenta simulation dye wastewater when pH 9 and reaction time 10 min. With the initial dye wastewater concentration increased, the decolored rate decreased. The decolored rate in general kept a tendency to increase with the temperature increased. Kinetics researches showed that when pH 9, reaction temperature 20 and 35 ?, the decoloring reaction process for the dyes accorded with the First-order dynamic equation. The decoloring reaction rate constant was influenced by initial concentration of dye wastewater and temperature.1. IntroductionIn China, textile printing and dyeing industry is one of industrial departments which using more water and discharging more wastewater. There is about 7 billion tons of waste water discharge each year, of which 80% from the process of printing and dyeing. Being complex ingredients, high chroma, more toxic substances and severe environment pollution, the treatment of printing and dyeing wastewater becomes problem urgent to be resolved. The traditional treatment methods such as adsorption [1], coagulation [2], biochemical method [3,4], which has advantages of simple equipment, simple operation and mature process, but they can cause waste accumulation and secondary pollution [5,6].Magenta is a kind of organic compounds, which classified into acid and alkaline magenta. Considering the advantages of simple operation, low cost, simple experiment equipment and friendly to environment, acid magenta dyes wastewater was chose as object in this paper. Some parameters such as pH, contact time, temperature and the initial concentration on of simulative acid magenta dyes wastewater were studied."

Jan 1, 2012

By Toshiyuki Hiranami, Keizou Uematsu

"AbstractionSpray freeze drying method was proposed to fabricate ·ceramic: powder granules for high performance ceramics. Obtained granules and their green compact were characterized by SEM and immersion liquid technique. Granules have a spherical shape of about l 00 µ m in diameter, ·and no binder segregation was found with the immersion liquid technique. The granule had sufficient strength for usual handling, while the strength was much lower than that of granules prepared by conventional spray-drying. Unlike the conventional green compacts, granule interfaces were not observed in the green body made with the spray-freeze dried granules.IntroductionIt was well kn9wn that spray-dried granules have binder segregation layer on their surfaces. The trace of this segregation layer survives in the later processes i.e. compaction and firing, and behaves as fracture origins in the sintered bodies. The origin of this problem is solvent drying process from slurry droplet surface in spray drying system. As alternative method we propose a freeze drying process for granule preparation, in which solvent is remove by sublimation though the process, binder segregation can be prevent.In this study, we applied spray freeze drying method to fabricate alumina powder granule, and characterized the obtained granules, and their green compacts and sintered bodies.Experimental procedure.Alumina powders and additives aqueous solution were mixed for 24 hours using a ball mill to· prepare the slurry for spray freeze drying. .The solid loading of the slurry was 30vo1%. Deflocculant (PAA-NH4 type) was added 0.5mass%, and the binder (PVA). 1.0, 2.0 or 3.0mass% of alumina. Obtained slurries were sprayed into liquid nitrogen to make frozen granules. The granules were freeze dried.For the characterization of the granules, immersion, liquid technique observation and single granule strength test were carried out. Strength of individual granule wa5 measured using micro compression testing machine (MCTM, SHIMADZU). Granule strength was calculated from following equation."

Jan 1, 2000

By Bernd Kopacek

"Nowadays more and more consumers substitute their conventional TV-sets and computer monitors by LCD panels. In the near future huge amounts of LCDs will start coming back to recycling. As LCDs with hazardous mercury backlight lamps are used an appropriate recycling technology has to be implemented.IntroductionLiquid Crystal Displays (LCDs) are widely used in notebooks, organizers, mobile phones, pocket calculators, measuring and control instruments, electronic games, hand-held miniature TVs, audio-video equipment, large signboards, automotive displays and more and more also for PC monitors and TVs.According to a study from Stanford Resources (San Jose, California) the annual value of LCDproducts reached 35 billion EUR in 2002, about 30% of this within the European Union, representing a total area of 2,1 million m2 Liquid Crystal Displays. An annual increase rate of about 15% is estimated for the next years (up to 4,1 million m2 in 2005).As LCDs are already on the market for several years, larger quantities of the more than 2,5 billion LCDs are coming into their End-of-Life stage for treatment. In 2005 this figure will become even more dramatic - 40.000 tons of LCD-modules contained in 2 million tons of waste electrical and electronic equipment (WEEE) or about 30% of total WEEE within EU. An amount which is representing 400 million EUR costs for incineration.Currently the only method used to deal with redundant LCD units is incineration or landfill. Both are expensive and causes emissions into the atmosphere (global warming) respectively water contamination (Class II) and difficulties in biodegradation. Up to now there is no recycling solution for LC-Displays available.As a consequence European Commission requests the disassembly of LCDs with an area bigger than 100 cm2 in the Directive 2002/96/EC of the European Parliament and of the Council on Waste Electrical and Electronic Equipment (WEEE Directive) of February 13, 2003."

Jan 1, 2008

By Wander. L. Vasconcelos, Virgínia. S. T. Ciminelli, Angela. M. F. Guimarães

"The present work was aimed at synthesizing nanostructured hybrid materials derived from the functionalization of smectite clays with ligands containing thiol (-SH) groups for application in cadmium adsorption processes. An in nature Brazilian bentonite was investigated. The modification route was based on the grafting reaction between hydroxyl groups present on clay surface and the hydrolyzable alkoxy group of the (3-mercaptopropyl)trimethoxysilane in dry toluene under reflux. The present work showed that the proposed modification route was effective for the grafting of the thiol groups in the clay structure. The thiol-functionalized bentonite samples showed average binding capacities 160% higher with respect to Cd2+ to those obtained with the ungrafted material. These results support a mechanism of adsorption involving primarily ion complexation by the thiol groups (specific) instead of cation exchange (unspecific). The proposed modification processes are suggested for the preparation of novel adsorbent materials with controlled selectivity and specificity and therefore with good potential for separation and pre-concentration purposes.IntroductionMany efforts have recently been devoted to the design and preparation of inorganic-organic nanomaterials because of their potential application in novel functional materials. The intercalation of organic species within the spaces between interlayers of inorganic layered crystals provides nanostructures consisting of alternating layers of inorganic and organic compound. The intercalation reactions occur by insertion of mobile guest species (neutral, molecules, or ions) into the accessible crystallographic-defined vacant sites located between the layers (interlayer spacing) of the layered host structure [1}.Silane coupling agents, used widely for the modification of silica surfaces, have also been employed more recently for modification of layered silicates [2,3,4,5]. Modification with organosilane involves grafting reactions by establishing covalent bonds between the reactive groups of the layer, normally hydroxyl groups, and silane molecules. These reactions can be restricted to the external surface (the basal spacing remains unchanged) or to the interlayer surface, in which case an interlayer expansion occurs. The resulting material can be defined as a hybrid material or, more specifically, functionalized inorganic layered material [1]."

Jan 1, 2008

By M. Yoshida, S. Hanada, T. Takasugi

"A study has been conducted to examine the effect of ternary alloying elements on high temperature deformation of the C15 NbCr2 based intermetallics in Nb-Cr-X (X=V, Mo and W) alloy systems, which have attractive properties as high temperature structural materials. The high temperature deformation of the C15 NbCr2 intermetallics can be improved by two alloying methods. One method is based on geometrical consideration for site occupation and atomic size factor of component elements and additive elements in the single phase C15 lattice; addition of Mo and V can promote dislocation movement without introducing significant hardening. The other method is based on microstructural modification through ternary alloying; moderate addition of these elements results in a variety of duplex microstructure consisting of the C15 phase and bee solid solution without forming any intermediate phases, and can enhance the high temperature deformability. Particularly, alloys with duplex microstructure equilibrating with Cr-rich bee solid solution is shown to exhibit superior deform ability. Also, lattice property of the additive atoms in the C15 structure and phase relation between the C15 structure and the bee solid solution are investigated by OM, XRD, TEM and ALCHEMI observations and then discussed in association with observed mechanical behavior.IntroductionLaves intermetallics with AB2 stoichiometry belong to the largest group in a large number of intermetallics with various kind of crystal structures, and have a variation of the cubic CIS, the hexagonal C14 and the dihexagonal C36 structures, depending on stacking sequence of XYZ type, each of which consists of four interpenetrating atomic layers (1-3). Some of the Laves intermetallics have good functional properties and therefore are considered to be used as, for instance, magnetic materials, magneto-optical materials, hydrogen storage materials and superconducting materials (2). Also, the Laves intermetallics are considered to be good candidate as high temperature structural materials operating at high temperatures and in severe environment because they have high melting point, low density, and potential resistance to corrosion and oxidation. However, the Laves intermetallics are very brittle at low temperatures because they consist of complex crystal structures similar to many other intermetallics."

Jan 1, 1996

By P. Meyers, F. DeSilva, L. Gottlieb

A number of tests looking at lead removal using ion exchange resins of various types from various aqueous streams have been undertaken. The tests focused on strong acid cation (SAC) and weak acid cation 0N AC) resins. It was found that the mechanism of lead removal is partly by lead filtration rather than solely by ion exchange in a large portion of the applications studied. This is not surprising since lead carbonate is essentially insoluble and almost all water supplies contain at least some carbonate alkalinity. Regeneration of lead from exhausted resins containing significant amounts of lead may not be practical in some cases because of the large chemical and waste volumes involved. Since lead, .·along with many other very insoluble metals, is often present as a suspended solid rather than in ionic form, ion exchange is probably not always the best technology for bulk lead removal.

Jan 1, 2000

By Z. Y. Xie

The visualization techniques were employed for the analysis of computer simulation studies of dislocation core structure in ordered alloys. Atomistic computer simulation was used for the study of the local configuration of the material in the vicinity of the dislocation. Stresses were applied in the simulation in order to study the necessary stress level for the dislocation to move and onset plastic deformation of the material. The results were analyzed in terms of the strain tensor as a function of the position (x, y) in the material with the dislocation located at (0, 0). Various visualization packages are used to plot the invariants of this strain tensor and to visualize the changes that the dislocation core undergoes under stresses until it finally moves.

Jan 1, 1993

By Leah Penner, Thomas J. Ruth, Paul Schaffer, François Benard, Edouard Asselin, Stefan K. Zeisler, Thomas J. Morley

"This paper details the electrodeposition of metallic molybdenum from an aqueous, acetateelectrolyte containing molybdate ions. The deposition is carried out in a highly concentrated (up to I 0 M) acetate bath in the presence of a very low concentration of bone glue (60 µg/L). The molybdenum metal deposits are up to 20 µm thick and adherent. The deposits were characterized by XRD and XPS analysis. The deposition process is very inefficient, as up to 99% of the current is used to generate hydrogen during electrolysis. The effect of acetate concentration, pH, additives and current on the deposition efficiency and physical properties of the molybdenum deposit were investigated and optimized to obtain smooth, adherent coatings.IntroductionMolybdenum has increased thermal and wear resistance properties that are often utilized in material coatings [I]. These coatings are most often manufactured by sintering, pressing or spraying molybdenum powder at elevated temperatures, as a substitute method for standard metallurgical practices, such as electroplating [2, 3]. The lack of reports describing molybdenum deposition is most likely due to the highly oxophilic nature of molybdenum and the stability of its oxides, especially in water. Previous attempts to electrochemically reduce molybdenum from molybdate (Mool·) ions to molybdenum metal have reported the production of either a poorly adherent mixed oxide [4-6], or a thin(< 0.1 µm) metallic film [7-9]. Thick metallic molybdenum is capable of being co-deposited with one of the iron-group metals (Ni [10], Co [11] and Fe [12]) to produce an alloy [13, 14]. These alloys, however, may not be suitable for applications requiring pure molybdenum as they usually contain less than 50% molybdenum (often less than 30%)."

Jan 1, 2012