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By Wen-Ming Chien

Low temperature X-ray diffraction and thermal property studies of the solid-solid state phase transition for the polyalcohols (pentaerythritol (PE), pentaglycerine (PG) and neopentylglycol (NPG)) thermal energy storage solid solutions have been investigated by using X-ray diffractometry and differential scanning calorimetry (DSC) methods. X-ray diffraction studies on polyalcohols solid solutions, PE-NPG and PG-NPG, are from ?10oC to 50oC. XRD results shows the + mixed phase at the related low temperature (?10oC) for both PE-NPG and PG-NPG solid solutions. At high temperature range, XRD results show phase for PG-NPG solid solution and + mixed phase for PE-NPG solid solution. There are only two Bragg peaks, (111) and (200), shown in phase XRD patterns. The polyalcohols solid solutions have been cycled 5 times between -20oC to 100oC at different DSC scan rates to study the phase transition properties. DSC results of both PE-NPG and PG-NPG solid solutions show that the solid-solid state phase transition is near room temperature. Details of low temperature phase transition XRD and DSC results of PE-NPG and PG-NPG solid solutions will be presented

Jan 1, 2006

By Hector M. Henao

There is an increasing trend in the copper smelters to recycle electronic materials, which contain relatively high concentration of precious metals. As a consequence, the amount of precious metals lost in the slag phase is increasing. To determine the portion of the precious metals chemically dissolved and that associated with the mechanically trapped matte in the slag will be a key factor to improve the recovery of those metals. Thus, an experimental study was carried out to determine the distribution of precious metals (Au, Pt, Pd, Rh, Ru) between the equilibrated copper matte and iron-silicate slag phases. The experiments were made in a magnesia crucible at 1573 K and a fixed partial pressure of SO2 of 0.1 atm for the matte grades between 40 and 70 mass% of copper. It was found that the distribution ratios (defined as mass% X in slag/mass% X in matte, where X represents the precious metal) are around 10-2 for Ru, 10-3 for Au, Pt and Pd and 10-4 for Rh. The distribution ratios show a tendency to increase when the grade of matte is increased.

Jan 1, 2006

By Rodney T. Jones

Mintek has developed and piloted a novel process for the treatment of nickel-copper and PGM (platinum group metal) sulphide concentrates. The ConRoast process is based on the removal of sulphur by roasting, followed by smelting of the dead-roasted concentrate in a DC arc furnace using an iron-based alloy as a collector for nickel, copper, cobalt, and PGMs. The environmental benefits with respect to sulphur emissions are considerable, in that essentially all of the sulphur is removed from the enclosed roasting equipment in a continuous stream of SO2 of an appropriate strength for feeding to a sulphuric acid plant. This process allows great flexibility with respect to the selection of ore types, and does not impose limits on the minimum quantities of contained base metals or sulphur, and can tolerate very high contents of chromite in the concentrate. The furnace alloy is water-atomized prior to leaching. Iron may be rejected from the alloy hydrometallurgically, by precipitation as hematite for example. The ConRoast process achieves very high metal recoveries, and produces high-purity metals, and a clean high- grade PGM concentrate.

Jan 1, 2002

By R. Gordon Bloomquist

The economic benefits of the co-production of minerals from geothermal brines far exceeds the potential revenue stream from the sale of marketable by-products such as silica, zinc, manganese, lithium and a number of rare earths. Extraction of silica can avoid scaling problems often associated with many geothermal power projects and may allow for additional power production through the use of bottoming cycles or the use of the brine in direct use applications now impractical due to scaling problems. An additional benefit of silica removal is the opportunity to use the geothermal brine as a source of water for enhanced evaporative cooling ? a technique that can significantly improve the summer power output from binary power plants employing air cooling for condensing the working fluid.

Jan 1, 2006

By Takao Mori

Novel rare earth boron icosahedral compounds are investigated as potential high temperature thermoelectric materials. REB50-type compounds and REB22C2N compounds were synthesized and the thermoelectric properties measured. Seebeck coefficients in excess of 200 V/K are observed at temperatures above 1000 K for the REB50-type compounds. Strikingly, n-type behavior was observed for REB22C2N. Up to now, non-doped B12 icosahedral compounds have all been p-type. The discovery of an n-type compound is extremely important in terms of the potential development of this class of compounds as viable thermoelectric materials. Low thermal conductivities of < 0.03 W/cm/K at room temperature was observed for these rare earth boron cluster compounds.

Jan 1, 2006

By J. P. Constantinea

The use of fluidized beds for the roasting of zinc sulphide concentrates marked a milestone in the electrolytic production of zinc. Stable operation of a fluidized bed for zinc roasting requires a particle size distribution that minimizes the risk of defluidization and helps control carryover to manageable levels. However, the understanding of the roasting process is limited, and changes in operating conditions mainly rely on intuition, experience, and trial and error. A research program has been initiated at UBC to study the phenomena that influence the particle size distribution of fluidized bed zinc roasters. In preparation for the experimental phase, this paper reviews the current literature on the phenomena that affect the particle size distribution during fluidized bed roasting and other fluidized bed processes.

Jan 1, 2002

By Brian Cochran, C. Edward Eckert

"EXECUTIVE SUMMARYINTRODUCTIONThe commercial incentives for using molten aluminum in casting operations are numerous and substantial. Although these incentives apply broadly to both shape castings (foundry) operations and wrought alloy production, the merit of a particular motive is indeed downstream processing sensitive. Melting cost reduction is a universal incentive that impacts on essentially all aluminum products. At a natural gas burner cost of $4.50 per therm, for example, the reverberatory furnace energy cost is at least $0.01 per pound of aluminum melted, exclusive of melt loss, fixed costs, and other expenses. The Aluminum Statistical Review' cited 3.188 million metric tons of secondary aluminum that was recovered by the industry in 1995. This represents a re-melt energy cost of over $70 million. Other incentives to use molten secondary aluminum include throughput enhancement, metal chemistry assurances, environmental considerations, and the avoidance of an in-house scrap processing operation.A traditional disincentive to use molten secondary aluminum is metal quality. If a particular secondary processing operation was successful in achieving and preserving an acceptable metal quality level prior to shipment, the subsequent metal transfer and ladle delivery events would frequently obviate these efforts. For example, a metal superheat on the order of several hundred degrees is required for an unheated transfer ladle to travel 3 to 4 hours to a customer location. The rate of the y-alumina formation reaction approximately doubles for every 120°F increase in temperature, therefore, the effect of excess superheat on melt loss and metal quality is considerable. Linear oxidation reactions, such as magnesia formation in magnesium containing alloys, are influenced to an even greater extent by temperature.The typical quality detractor events are:"

Jan 1, 2000

By Fiseha Tesfaye, Pekka Taskinen

"A thermodynamic study of the equilibrium phase assemblage AgBi3S5-Bi2S3-S was made by an EMF-technique, using the RbAg4l5 solid electrolyte. The ternary phase was synthesized from the pure Ag2S and Bi2S3 in an evacuated silica ampoule and grinded into powder and mixed with appropriate compositions of B12S3 and S, in a series of experiments, for pressing in to pellets. The pellets were assembled to form the galvanic cells Pt (-) | Ag ] RbAg4ls | AgBi3S5+ Bi2S3 + S + (C) I Pt (+). The EMF-measurements were made in the temperature range 299 - 460 K.In this paper, thermodynamic functions of the ternary phase AgBi3S5 (pavonite) have been determined. The agreement between the obtained results and the literature values were established.IntroductionThe complex group of ore minerals constitutes from trace amounts to a major proportions of sulfosalts. Although the sulfosalts rarely form massive ore bodies, they are commonly associated with rich sulfide ore minerals for the base and precious metals and widely distributed in a metal poor sulfide minerals [1]. For instance, Ag-bearing sulfosalts are encountered in ore minerals for the production of the base metals and are common sources of silver. Nevertheless, thermodynamic properties of the sulfosalts are poorly known.Reliable thermochemical data are essential for quantitative modeling of the chemical behavior of the sulfosalts in equilibrium with sulfides, which in turn would promote the optimization of complex minerals treatment and extractive metallurgy of the valuable metals."

Jan 1, 2012

By J. M. Brupbacher, D. C. Nagle

"The XD TM * approach to producing metal matrix composites employs an in-situ precipitation technique for the formation of the reinforcement directly in the matrix of interest. Key features include: thermodynamically stable reinforcement; clean particle/matrix interfaces, single-crystal reinforcement; size, chemistry, and shape control; uniform distribution; compatibility with conventional ingot techniques; and grain refinement.Using XD~ technology it is possible to simultaneously introduce a number of different reinforcements in a given matrix, thus allowing for designing the microstructure to meet a specific material need. Thus, XD1l'1 technology is a very useful technique for achieving ""designer"" or ""engineered"" microstructures. XD TM technology has been applied to a number of systems including AI, NiAI, TiAI and Cu. Materials property and processing benefits will be discussed."

Jan 1, 1988

By Linda C. White

The use of red mud, a waste product of the ?Bayer? process for bauxite refining, was investigated for its arsenic removal effectiveness from aqueous solutions under various conditions. Red mud efficiently removed As(III) between a pH range of 7.6 and 9; and As(V) in the pH range between 5.5 and 6. Pre-washing of the red mud with salt water considerably improved its arsenic adsorption capabilities. With appropriate red mud dosage, the residual arsenic in solution was decreased below the regulated acceptable arsenic limit (0.1 mg/L) from aqueous industrial wastes. The arsenic adsorption followed first-order rate kinetics and fitted the Langmuir isotherm model. Results suggest that red mud is potentially a useful adsorbent for removal of arsenic from contaminated water or industrial waste solutions.

Jan 1, 2003

By Renato G. Bautista

The prospect for recovery of rare earths from red mud, the bauxite tailings from the production of alumina is examined. The Jamaican red mud by far has the higher trace concentrations of lanthanum, cerium, neodymium, and yttrium. Scandium is also present. The dissolution of the rare earths is a major extraction problem because of the large volume of other materials present. The recovery processes that have been proposed include the production of co-products such as iron, alumina, and titania concentrates, with the rare earths going with the titania A critical examination of the possible chemical processes for the complete utilization of the red mud are presented Recommendations for research projects considered to be important in the development of a chemical separation process where no pig iron product is contemplated are also discussed.

Jan 1, 1992

By A. N. Lasseigne

Hydrogenation behavior of the NaAlH4 intermetallics is investigated utilizing thermoelectric power and magnetic analyses. Using both thermoelectric power and magnetic susceptibility measurements on these intermetallics allows for confirmation and further insight into hydrogen&apos;s role in altering the material&apos;s electronic structure. The electronic and magnetic property correlations will indicate the direction for further alloy development to optimize hydrogen storage.

Jan 1, 2006

Silver has the highest electrical conductivity of all metals and consequently this property is an attractive feature which makes it a leading candidate for use in electronic devices. The research conducted was focused primarily on the development of a process for obtaining a deposited silver-coating onto alumina, for applications related to electrical-conducting devices and, ancillarily, catalysts. Alumina balls and plane substrates were utilized for the investigation. The coating process employed an aqueous arnmoniacal silver-nitrate electrolytes with a formaldehyde solution as the reductant. Modifying additives - an activator which would be expected to promote good deposition-characteristics onto the (dielectric) substrate and an inhibitor which would obviate homogeneous reduction (precipitation) of silver was observed when the activator-containing silver-electrolyte reductant constituents were combined. However, the silver-electrolyte/reductant system with inhibitor could be employed (at 80°C) to achieve a viable (subject to future research optimization) coating on alumina. The influence of the processing temperature on the deposition process was delineated during the course of the research. The morphology of the deposited-silver on the alumina balls was assessed by SEM imaging. A tape-peel test was employed, with the plane substrates, to semi-quantitatively characterize the adhesion to the alumina.

Jan 1, 1998

By W. L. Dalmijn, E. A. Schokker, N. Fraunholcz, P. C. Rem

Many processes developed for the mechanical processing of Automotive Shredder Residue (ASR) suffer from high processing costs. We offer a distinct concept for low-cost mechanical processing still allowing high value-added recycling of the recovered materials. The basic idea behind this approach is to produce saleable pre-concentrates at the lowest possible costs that can be further processed in existing separation facilities. Our process includes screening, size reduction and magnetic separation. Preliminary studies showed that fibers in ASR are magnetic due to adhering rust particles allowing separation into a fiber fraction and a non-magnetic rigid fraction by high-intensity magnetic separation. The fiber fraction is most suited for thermal processing. The rigid fraction mainly consists of plastics and rubbers with up to 10 wt.-% of non-ferrous metals, some inert material and copper wires. This fraction is very well suited for mechanical processing by, e.g., sink-float separation in existing metal separation plants. The non-metal fraction can be processed further to recover the plastics and rubbers. The process proposed in this study is expected to be substantially cheaper than full thermal processing. In addition, as it mainly relies on existing separation facilities, it can be applied in the short term.

Jan 1, 2000

By K. Osseo-Asare

Rate laws for the hydrogen reduction of metal ions are typically of the form: [r = -d[M(II)]/dt = k[M(II)]xPy2H] where k is an apparent rate constant, [M(II)] and PH2 represent dissolved metal concentration and hydrogen pressure respectively, while x = 0 - 1 and y = 0.5 - 2. Half-order dependences have been reported for some M(II)/H2 systems; however, no satisfactory explanations have been offered. In an effort to bridge this gap in our understanding, the published precipitation rate data (for M(II) = Cu(II), Ni(II), and Co(II)) are reviewed (with emphasis on the reported reaction orders) and compared with the corresponding but limited electrochemical polarization data. Based on the available literature on the electrochemical kinetics of the M/M(II) and H2/H+ systems it is demonstrated theoretically that, under certain conditions (e.g., in the presence of electron-conducting solids), the rate of the M(II)/H2 reaction can be expressed as: [-d[M2+]/dt = k[M2+]2/1P2/12H] It is concluded that electrochemical processes probably play an important role in the hydrogen reduction of metal ions, especially for systems that involve heterogeneous catalysis.

Jan 1, 2003

By N. Lohja

Metallurgical industries are generally big producers of solid residues of various kinds. In contrast with the past where environmental sensibilities were not so elevated and the accumulated mass of these residues were not considerable, these days the solid residues are everywhere scrutinized among others in term of their harmful environmental impact and as possible materials for valuable elements extraction or secondary utilisation. As a case study, the present paper gives an overview of the solid residues discharged by the metallurgical industry in Albania for the last tens of years. The results of two monitoring study on the solid residues of copper, iron and ferrochromium producing industries are also summarized. The first deals with the origin, quantities and chemical composition of these residues and the second one with the impact of harmful ingredients of these residues in the environment. Some methods for the processing of these solid residues are also proposed in order to ensure a clean environment and to make not just possible but also economically viable their secondary utilisation. This work is part of a bigger cooperation project among local institutions and foreign expert companies such as Flogen Technologies Inc and other in various countries that will not only monitor the situation but will also develop appropriate technologies for treatment of these specific residues.

Jan 1, 2006

By Michael S. Moats, Daniel Kim, Shijie Wang

"The behavior and deportment of lead, arsenic, antimony and bismuth are critical in producing high quality cathode by copper electrorefining. A critical review of research related to these elements is presented along with a comparison to industrial data, where appropriate. These elements exist predominantly in the anode as complex oxides along die grain boundaries. Upon dissolution, Group 15 elements report both to the electrolyte and slimes while lead essentially enters the slimes. The deportment of the Group 15 elements appears to be influenced by several chemical interactions which are discussed. The effect of these elements on floating slimes and anode passivation is reviewed. Under normal electrorefining conditions, lead, antimony and bismuth are thought to enter the cathode through the encapsulation of slime particles. The literature indicates that arsenic enters the cathode predominately by electrolyte entrainment. Finally, areas for future research regarding these elements are presented.IntroductionControlling lead, arsenic, antimony and bismuth is critically important for the production of high quality cathode in copper electrorefining. The reasons for this are twofold. First, ASTM Grade 1 Cathode specifications [1] for these elements are low, as listed in Table 1. Second, they can affect the efficiency of the electrorefining process (e.g., through passivation, current efficiency, slime processing)."

Jan 1, 2012

The reported values of the standard reduction potentials of the Au(NH3)2+/Au(0) and Au(S2O3)23-/Au(0) couples are reviewed to emphasise the experimental difficulties associated with the measurement of reliable values for these quantities. The standard reduction potential for Ag(I)/Ag(0) in ammonia and thiosulphate solutions measured at ionic strength 0.1 and 25oCis used to predict the following relevant stability constants () for gold complexes based on the linear free energy correlations: Au(NH3)2+2 = 1013, Au(S2O3)23-2 = 1024 and Au(NH3)43+4 = 1033. The equilibrium constant ( 10-11) for the reaction Au(S2O3)23- + 2NH3 = Au(NH3)2+ + 2S2O32- based on these stability constants is in reasonable agreement with the measured value (10-9) based on potentiometric and spectroscopic data when excess ammonia was added to a solution of Na3Au(S2O3)2. This also indicates that the stability constant of Au(NH3)2+ is 9 to11 orders of magnitude less than that of Au(S2O3)23-. Relevant species distribution and Eh-pH diagrams based on the revised data are presented.

Jan 1, 2003

By F. Leuzzi

Asbestos is a natural mineral fibre which has been known and utilized commercially for about a century. From the forties, it was employed on an ever-increasing scale throughout the mechanical engineering, building, paper-making and plastics sectors, to name but a few. There are essentially five minerals which provide fibres for industrial applications, namely, the chrysotile variety of serpentine and the amphiboles such as riebeckite, anthophyllite, cummingtonite-grunerite (amosite) and tremolite. About a fifth of the world&apos;s asbestos output was once taken by Europe for the manufacture of asbestos-cement products, reinforced plastics, paper and cardboard, panels, soft insulation and spray-on powders. However, in the sixties and seventies the hypothesis regarding the pathogenic nature of asbestos fibres started to gain ground. Moreover, between the sixties and eighties the EU issued a series of regulations designed to bring about a steady decrease in asbestos consumption. This line of action has culminated in recent years in a whole set of directives banning the use of asbestos in all products. This created a major problem, namely, how to clean-up the several million tons of various types of asbestos products in various states of conservation existing in Western Europe. CORDIAM (Pat. RM95 A 000269 and Pat. RM96 A 000782 in the name of ECOTEC S.r.1.) is one of the thermal inertization techniques recently proposed for this purpose. The process provides for the low-temperature ceramization of the toxic-harmful material. Of course, with such a great variety of waste materials and the volumes to be treated, as well as the need to ensure the correct dimensional design of the thermal sections of the treatment plant, it is necessary to know as much as possible about the thermal behaviour of the wastes concerned. This paper details the steps taken firstly to ascertain the thermal behaviour of such materials as may be encountered in day-to-day practice and secondly to examine the influence of the main process parameters on the preliminary design of gas- or fuel-oil-fired rotary kilns of the kind used for waste treatment.

Jan 1, 1999

By Dirce H. Jacomo, Jaciele G. Teixeira, Anibal Y. Abreu Castillo, EsperidianaA. B. Moura, Yalquiria A. Silva, Rene R. Oliveira, Michelle G. Gomes

"Composites consisting of poly(vinyl alcohol), starch and sugarcane bagasse ashes, using glycerol as plasticizer agent, were prepared by solution casting method. Composites prepared were subjected to electron-beam radiation treatments, at radiation dose of 50 and 80 kGy using a Dynamitron electron beam accelerator, at room temperature in the presence of air. The composite samples obtained were evaluated for their water absorption, mechanical and morphological properties.1. IntroductionThe potential of biodegradable polymers and more specifically of biocomposites obtained from agro-resources have long been well established [1-3]. Starch, derivate from variety of botanical sources (cereals, legumes, and tubers) is widely available raw material and one of the most studied and promising agro-resources for the production of biodegradable polymers as matrices for biocomposite applications. However, starch itself is very brittle, hydrophilic and its mechanical properties are very poor for many applications [3 - 5]. The blending of starch with conventional polymers is a promising approach to improve its drawbacks. Recently, many efforts have been made to blend starch with biodegradable synthetic polymers [5, 6]. Polyvinyl alcohol (PYA) is a particularly well-suited synthetic polymer for the formulation of blends with natural polymers, as it is highly polar and can also be manipulated in water solutions, and depending upon its grade, in functional organic solvents as well [3, 7]. PY A has been reported to be an option to blend with starch. Most of the starch/PY A composites have been prepared by casting. However, it is well known that starch/PY A composites has poor in water resistance and mechanical properties after absorbing water [3,8]. Attempts to improve the mechanical properties and to decrease the water absorption property of the starch/PY A composites are made by adding the cross-linkers and plasticizers. Park et al. prepared starch/PY A/citric acid films by the casting method. They also studied the effect of (spell out) citric acid on the mechanical properties and water resistance of composites [9]. Zhai et al. prepared the starch/PY A hydrogels using electron-beam radiation [10]. Different kinds of lignocellulosic fibers have been investigated in blends for formulation of biocomposites."

Jan 1, 2013