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By Huang Chao

The thermodynamics analysis on reducing-matting smelting of sulfide ore of lead, antimony and bismuth which use ferric oxide as sulfur fixed agent is first analyzed. Due to the analysis of reaction mechanism, ferric oxide is first reduced to ferrous oxide, then ferrous oxide produce reducing-matting reaction with sulfide ore and reducing agent as reaction equation: MeS+FeO+CO=Me+FeS+CO2. The reaction thermodynamic calculation shows that the reducing-matting reactions of lead sulfide, antimony sulfide, Jamesonite, and bismuth sulfide are feasible, but is infeasible for zinc sulfide. These conclusion provide a feasible method for solve the pollution which produced in the smelting of sulfide ore of lead, antimony and bismuth.

Jan 1, 2006

By Rudolf Keller

In the electrolysis of neodymium oxide from a molten fluoride electrolyte, anode effects may occur at the carbon anodes, interfering with smooth cell operation. In laboratory experiments, we attempted to circumvent this problem by selecting electrolytes with a high oxide concentration, possibly at relatively low rare earth content, but cathodic deposition was not satisfactory. A regime at higher cell voltage was discovered to yield good cell performance, but evolution of considerable amounts of fluorocarbon compounds suggested that a reactive treatment of the off-gases would be necessary for environmental acceptability. Subsequent experimentation at low cell voltage revealed conditions for satisfactory operation without occurrence of anode effects and without formation of any CF4 or C2F8.

Jan 1, 1997

By H. J. Garcia

Biodegradation of cyanide by microorganisms isolated from solids previously exposed to cyanide has been investigated. Initial sodium cyanide concentration was 300 ppm at pH 10.5. The kinetics of biodegradation were found to be first order with respect to cyanide concentration, and the overall reaction rate constant is k = 0.102 day-1. The activation energy and the frequency factor were determined to be { A }Ea = 5.45 Kcal/mol and A = 1.28 x 10-2 sec-1, respectively. Based on these values, thermodynamic properties of an intermediate activated complex were assessed. All tests resulted in cyanide concentrations less than 0.1 ppm in about 35 days at 250C, whereas at 350C the time of biodegradation to reach this cyanide level was 30 days. Kinetic data were also established to relate biodegradation to amount of inoculum. The maximum theoretically-attainable rate, Vm , and the optimum amount of inoculum, K , were determined to be 4.8 x 10-4 M NaCN/day and 7.5 % of amount of inoculum. With respect to the mechanism of biodegradation, cyanide was shown to decompose to carbonate, bicarbonate and ammonia. Titrimetric analyses revealed concentrations of 5.6 x 10-3, 4.8 x 10-3 M, and 70.2 ppm for carbonate, bicarbonate and ammonia, respectively. The average cell population was determined to be 3.75 x 108 cells/mL.

Jan 1, 1994

By M. A. Barakat

Large amounts of zinc ash and flue dust containing more than 80 % zinc are accumulated during galvanization processes at the surface of molten zinc bath and in the chimney respectively. Pyrometallurgical recovery of zinc from both of the ash and dust samples has been carried out. The ash was sieved with the help of an industrial sieve shaker provided with mesh sieve having a pore size 0.9 mm. The oversize fraction cut (+ 0.9 mm) was melted at 550 °C under ambient conditions. The produced ingot (1) was analyzed whereas the coarse fraction of the produced slag (+ 0.9 mm) was treated as the coarse ash or added to it. The dust was enriched with suitable fluxing salt prior to heat treatment at 600 °C for 1 h. The produced ingot (2) was analyzed whereas the resulting slag was mixed with the fines of the ash and treated by hydrometallurgical processing to prepare valuable salts of zinc. Parameters affecting recovery processes such as time, temperature and flux percentage were studied. Results obtained revealed that the two prepared ingots (1&2) were successfully recovered with recovery efficiency amounts to =85 %. The obtained samples meet the standard specifications with relatively low price. Also in the light of the strict environmental regulations of pollution control, reuse of these wastes materials will help in keeping the environment clean.

Jan 1, 2000

By E. Kuzeci, R. Kammel

"Lately various voltametric methods have gained increased attention as an analytic tool in hydrometallurgy. Voltammograms with mercury drop electrodes or glassy carbon electrodes provide information about the electrocrystallization of cathodic deposits and allow calculation of kinetic data by means of characteristic parameters like the peak potential and peak current and their variation with the voltage scanning rate.Cyclic voltammograms are also suitable for identification of reaction sequences. Voltammograms with carbon paste electroactive electrodes containing metal sulphide additions reveal information about the dissolution behavior. The stripping voltammetry can be applied to analyze metal ions and organic additives (e. g., thiourea) in extreme low concentration. Typical application of the various methods studied with microcomputer controlled measurement system are explained by examples selected from copper hydrometallurgy.IntroductionThe use of electroanalytical methods in metallurgical process control can be dated back to the starting period of industrial copper refining, when the deposition of the metal ions was followed electro-gravimetrically by weighing the electrode with deposits (1). The principles of metal deposition and dissolution have not changed but the methods to follow these phenomena were subjected to noticeable developments and especially the introduction of polarographic investigations by Heyrowsky (2) has greatly contributed to the progress in electro-analysis. A review about the fundamental work on the electrochemical kinetics in earlier time is compiled in a monograph of Vetter (2). With the steady improvements in the instrumental techniques, it is nowadays possible to apply several current and potential modulations for measurements with improved selectivity and sensibility. There is however, still a lack in theoretical interpretation of the data obtained. More theoretical information are already available for linear voltametric methods for systems where reduced as well as oxidized species are dissolved in the electrolyte (4, 5). Some recent investigations have also shown the reliability of these techniques to study electro-crystallization (6, 7). Main fields of the application in the hydro - and electro-metallurgy are:"

Jan 1, 1989

By Dai Xi

In the present work, the viscosities of molten FenO-MgO-Si02 and FenO-MgO-CaO-Si02 semi-synthetic slags for nickel flash smelting were measured in the temperature range from 1473 to 1723K by a rotational viscometer. The ratio of Fe to Si02 was fixed at 1.2, calcium and magnesium oxide contents varied in the range from 2 to 8 mass% and 9 to 12 mass%, respectively. The results showed that silicate anions became smaller by increasing CaO content, which results in a decrease of the viscosity of the slag. In the case of MgO addition the viscosity behavior was complicated. At MgO content below 11 mass%, the viscosity increased with the increase of MgO at all temperatures tested. However, when the MgO content was above II mass%, the viscosity decreased slightly for FenO-MgO-CaO-Si02 system. At higher MgO contents, low-viscosity slags can be obtained by adding CaO. At a given composition, the viscosity decreased with increasing temperature. The higher the temperature, the more MgO can be added before saturation. The effect of Fe304 on the viscosity was quite significant. The viscosity of slag increased by 300mPa's at l573K when Fe304 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-Si02 and FenO-MgO-CaO-Si02 systems is given in this study.

Jan 1, 2003

By KNona C. Liddell

"Many metal recovery processes involve heterogeneous reactions in porous media accompanied by fluid flow and mass transfer. Modeling such systems is difficult because of the number of rate processes involved and is complicated even further by effects due to the structure of the porous medium. Data on even bulk properties of the medium are often severely limited or unavailable. For many such systems, a cell model may provide an attractive alternative to models based on transport mechanisms in a differential volume. A cell model requires less input data and is computationally efficient. Identical residence time distributions can be obtained with models of both types, and both allow conversion and concentration profiles and histories to be calculated. The formulation and properties of cell models for metals recovery are described in detail.INTRODUCTIONSubsurface mineral leaching, metal ion recovery and environmental remediation are significant modeling challenges. They involve one-, two-, or three-dimensional reactive flow in multi reaction open systems. Dissolution, adsorption, and ion exchange occur at reactive mineral surfaces, and these heterogeneous reactions are accompanied by acid-base, complexation, and redox reactions in the solution phase.Two approaches have been taken to reactive flow problems in geologic media: mixing cell and transport models. Mixing cell models, the subject of this review, are based on a network of connected cells, each with a specified number of input and output streams. Mixing cells are assumed to have no internal solute concentration gradients, that is, each cell behaves like a well-stirred tank. Gradients are represented by step changes between connected cells; this results in a model that is spatially discretized at the outset. Different methods of discretizing the model equations are considered more fully below. Although this is not strictly necessary, it has usually been assumed in subsurface flow applications that all cells in the network have the same volume and identical initial properties."

Jan 1, 1996

By Shubin Wang

Copper(II) and nickel(II) are often recovered from ammoniacal alkaline solutions by solvent extraction using hydroxyoxime extractants: both copper(II) and nickel(II) are extracted from ammoniacal alkaline solutions and, from the loaded organic phase, nickel(II) is selectively stripped with a dilute acid followed by copper(II) stripping with an acid of higher concentration. Since a small portion of ammonia is co-extracted with copper and nickel, the extracted ammonia should be scrubbed using a dilute acid before metal stripping. In the present study, a mechanistic model has been developed in order to support design and control of this process. The equilibrium distribution ratios of copper(II), nickel(II), and ammonia at 298 K using LIX® 84-I (active component, 2-hydroxy-5-nonylacetophenone oxime) as the extractant are successfully correlated by considering the relevant equilibria. Based on these results, quantitative prediction of equilibrium distribution ratios in the process has been made possible, and suitable conditions for the efficient separation of copper(II) and nickel(II) are discussed.

By Jong-Oh Jo1

Thermodynamics of Ti, N and O in liquid iron was studied in order to establish a data base for the prediction of TiN and TiOx formation in liquid stainless steels containing various alloying elements including Cr, Ni and Si as a function of temperature. The interaction parameters of these elements on Ti and N were determined using the metal-nitride-gas equilibration technique. The TiN stability diagram for a commercial stainless steel grade was constructed from the measured thermodynamic parameters, and its validity was confirmed experimentally. The interaction parameters between Ti and O, and the equilibrium constants for Ti deoxidation reactions for the formation of Ti2O3 and Ti3O5 were also determined by the equilibration of the melts with those oxides identified by the XRD and the EPMA analyses.

Jan 1, 2006

By A. V. Tarasov

A flow-sheet for waste-less processing of spent lead batteries comprises mechanized separation of batteries, smelting of the metallic fraction in a kettle, electrothermal smelting of oxysulfate fraction, refining of crude lead and processing of reverts to produce commercial products. Smelting of lead-containing fraction is performed in an electrothermal furnace using a processing technology developed in the Gintsvetmet Institute and differing from conventional processes by the fact that it does not require any fluxing agent (soda); no matte is formed in the process and the amount of slag produced is minimal, because its formation depends only on the ash content of coke and the quality of battery scrap separation. The process has been patented. It has been introduced on a commercial scale in 1.8 MVA furnaces at the plant of A0 "RyazTsvetmet" (Ryazan, Russia). The process has the following main advantages as compared with conventional shaft-furnace smelting and smelting in a short-drum furnace: the process does not require technical-grade oxygen, the amount of process gas generated is minimized ensuring a decrease in lead-containing dust and sulfur dioxide emissions by 3 to 5 times per unit of lead recovered; a decrease in dust entrainment resulting in lower amounts of recycled dust; lower slag yield (a decrease from 20-25% to 3-5%); lower coke requirement (a decrease from 10-14% to 3-4%). Refining of crude lead is performed using conventional technology but there are several unique features for which know-how is available. Processing of by-products of electrothermal smelting and secondary lead refining (slag, drosses, skimmings) and ebonite fraction (crushed battery casings) is performed in a slag-fuming furnace.

Jan 1, 2002

By W. E. Wallace

Rare earth elements combine with most, of the metallic elements. As early as 1971 over a thousand intermetallics had been identified and described(1) From a magnetics viewpoint, systems involving. the d-transition metals Fe, Co and Ni are particularly interesting. In these systems there are at least four significant interactions: R-R exchange (R - a rare earth), R-T exchange (T = a transition metal), R-R exchange and the crystal field interaction acting upon the. rare earth ion. There is complex interplay between these interactions leading to bewildering variety in their magnetic behavior., Because of this and in view of the commercial significance of some rare earth intermetallics, studies of these systems has been an unusually active area of inquiry for the past two or three decades. The large magnetic moment of many of the rare earths, viz., 10 µB per atom for Dy and Ho, 9 1B for Tb and Er, etc., attracted, attention many years ago to the rare earths as potential ingredients for alloys to be used in permanent magnet fabrication. The utility of a permanent magnet in high perform¬ance devices (travelling wave tubes, voice coil motors, brushless motors, etc.) is in large measure determined by its maximum energy product, (BH)max. [(BH)max is the maximum value of B (magnetic induction) and H in the 2nd quadrant of the hysteresis loop.] Enhanced atomic moment in princple can lead to increased B and a large maximum energy product. Until about 1970 the largest (BH)max value known was about 5 MGOe(mega-gauss Oersted). This was for A1NiCo - an alloy involving Al, Ni and Co. It was recognized that the rare-earths had the potential for much higher energy product; in the case of Dy the theoretical energy product is about 35.0 MGOe., 70 times that of Alnico. (Needless to say, this theoretical value has never been achieved.) Large-scale efforts began about 30 years ago to synthesize magnetic materials containing rare earths and which would be suitable for permanent magnet fabrication. It was recognized by Strnat(2) et al. that a material to, be useful in high energy magnet fabrication would have to satisfy three. criteria:

Jan 1, 1992

By E. Saez, M. Bellet, T. Coupez, O. Jaouen

"The paper presents a 3D finite element solver for non-steady state fluid flow. The thermomechanical simulation package REM3D® has been initially developed to model Stokes' flow for polymer injection. The mechanical module is based on a Eulerian velocitypressure formulation. The spatial discretization uses P 1+IP1 tetrahedral elements. The front tracking module consists of the resolution of a transport equation, thanks to a space-time discontinuous Galerkin formulation. It includes mesh adaptation, which permits a dynamic refinement at the front, thus controling the numerical diffusion. The same approach is used to solve heat transfer. In this paper, we focus on the specific adaptations done to treat Navier Stokes flow. The treatment of inertia is detailed, as well as the implementation of sliding conditions at mould surface, using conservative normals. Industrial applications are presented.IntroductionThe study of the mould filling stage in casting processes requires the ability to simulate complex non steady-state three-dimensional flows. Most commercial software use the volume of fluid (VOF) method, associated with a Eulerian formulation, see for instance the series of conferences ""Modelling of Casting, Welding and Advanced Solidification Processes"" [1-3]. The VOF method [4] consists in solving the conservation equation dF / dt = 0 for a variable F - the volumic fraction of fluid - whose value is 1 in filled regions and 0 elsewhere. Two fluids are actually considered: the molten alloy and a gas in the empty regions. This method suffers generally from numerical diffusion in the resolution of the free surface tracking equation, which is of pure advective type. The precision of the computation is then strongly dependent on the mesh density. Since the mesh is fixed (Eulerian formulation) this implies that in case of complex flow the user must have a priori a fairly good idea of the flow characteristics in order to capture properly the critical features of the flow. In addition, the method can hardly handle the discontinuity of the material viscosity at the interface. To prevent this difficulty, the viscosity value is smoothed around the interfuce, adding once again some inaccuracy. Since the value F = ½ is supposed to represent the free surface, it results in a smeared fluid surface. An alternative to the fixed mesh methods are the methods in which the mesh covers the fluid domain only, as proposed by Navti and Lewis [5-6], or Gaston and Bellet [7]. Based on updated Lagrangian schemes, they must be associated with an ALE formulation (arbitrary LagrangianEulerian) in order to reduce the number of full remeshing operations."

Jan 1, 2004

By Patricio Barrios

This paper discusses the revamp and expansion of Atlantic Copper's (formerly Rio Tinto Metal) copper smelter located at Huelva, Spain. The plant was expanded from 150,000 to 270,000 tpy new copper in anodes, and from 133,000 to 215,000 tpy cathodes. Lurgi successfully executed this contract on a lump-sum, turnkey basis in just 19 months. The Lurgi on-site task force performed this work in close cooperation with Atlantic Copper's personnel, with a minimum of disruption in the plant's ongoing operation. The contractual performance parameters were achieved to the client's satisfaction shortly after the mechanical completion of the respective plant sections.

Jan 1, 1998

By Johan Sundström

Anhydrous DyC13 was prepared by dehydration of DyCl3?6H20 in a fluidized bed using both batch- wise and continuous feeding. A gas mixture with varied composition of argon and HCl was used. The productivity was high, reaching values of 0.25 mol H20/m2-st during the reaction step 6- 1 and 0.062 mol H2O/m2.s during the reaction step 1-0. The product was free from hydrolytic compounds, such as DyOCI, if control of inlet gas composition versus temperature was achieved. From the results of various experiments, some relations between HCI-concentration and temperature in order to avoid hydrolysis have been deduced. The fluidization process efficiency decreases drastically after the dehydration has proceeded down to about 10 mol% of remaining water. Therefore, in a final treatment the last traces of water were removed by slowly purging gas through a packed bed. The water content could thereby be reduced to less than 1 mol%.

Jan 1, 1997

By Vladimir Mindin

Simulation of complex equilibria is usually done in the P-T-X coordinates, where "Xu is the amount of individual chemical components in the system. This approach is not productive in some very important cases: (i) investigation of "open" systems, (ii) determination of coordinates (trajectories) of mono-variant points, among others. To solve these and some other problems, we use the idea of chemical potentials of elements (CPE) of the system. A system of different coordinates axes (CPE-axes ) leads to a new strategy of simulation, observing the results of the simulation, and to efficient technology of compressing and storage the data of the simulation.

Jan 1, 1994

By Terry C. Cheng

The Akita Hematite Process is currently the only hydrometallurgical iron removal process producing saleable iron by-products in the zinc industry. In this study, McGill University and Akita Zinc Co. have worked together into elucidating the basic precipitation chemistry of the process from the standpoints of hematite product quality and prevailing precipitation kinetics. This work determined that hematite is produced under the applied conditions (T = 195?200oC,PO2 = 103?414 kPa) directly without prior formation of basic ferric sulphate and transformation of the latter to hematite as thought originally. The rate-limiting step responsible for the long retention time (~180 min) was found to be either the re-dissolution of ferrous sulphate according to the batch reactor studies, or the slow hydrolysis of the remaining ferric sulphate according to the continuous reactor studies. Another interesting contrast between the batch and continuous reactor data was the degree of sulphur contamination (1.5 vs. 3.8%, respectively) and the specific surface area of the product (10 vs. 30 m2/g, respectively). These differences in addition to the co-precipitation of SO4-containing phases such as jarosites, alunite, and anhydrite were attributed to the significantly higher supersaturation level prevailing in the industrial continuous autoclaves that yields highly aggregated sub-micron hematite crystallites contaminated with chemisorbed sulphate ions.

Jan 1, 2003

By J. E. Dutrizac

The behaviour of the lanthanide elements during the precipitation of sodium and potassium jarosites at 98oC from sulphate media was systematically investigated. The lower atomic weight lanthanide elements (La to Gd) are characterized by the limited solubility of their alkali-lanthanide sulphates, such as NaNd(SO4)2?H2O, which commonly contaminate the jarosite precipitates. Hence, single phase jarosite-type compounds were precipitated only from solutions containing <0.4 g/L of the La to Sm lanthanides. The sulphates of the heavier atomic weight lanthanide elements (Tb to Lu) have significantly higher solubilities such that solutions containing up to 10 g/L of the individual lanthanides could be investigated without the precipitation of alkali-lanthanide sulphate species. Even at the highest lanthanide concentrations, however, none of the jarosite precipitates incorporated more than 0.3 wt% of any of the lanthanide elements. Comparable levels of lanthanide incorporation were noted in both Na-jarosite and K-jarosite. Although the mass of the jarosite precipitate increased with increasing ferric sulphate concentration or with increasing pH, the extent of lanthanide incorporation was not significantly affected. Clearly, the trivalent lanthanide elements do not substitute extensively for trivalent iron in the jarosite structure. This behaviour likely reflects the significantly lower hydrolyzability and larger size of the trivalent lanthanide ions relative to ferric ions.

Jan 1, 2003

By Jun Iwai, Osamu Takai, Yasushi Inoue, Hiroyuki Sugimura

"Infrared reflection absorption measurement was performed during plasma-enhanced chemical vapor deposition of silicon dioxide films at room temperature. Hydrocarbon contaminants adsorbed onto growing film surface are oxidized by oxygen radicals in plasma resulting functional groups which include C=O and C-O bondings. These groups exist only near the surface and are hydrolyzed rapidly after exposure to air.IntroductionRecently low-temperature silicon dioxide (SiO2) deposition has been in a growing industrial demand in pa1ticular, polymelic substrates such as polycarbonate and polyethylene telephthalate, which have poor heat resistance, need low process temperature (near room temperature) in coating of SiO2 which is a suitable material to improve optical and mechanical properties of polymenc products. Plasma enhanced chemical vapor deposition (PECVD) using organosilicon reactants is one of the most promising technique for lowering process temperature, so that it has been extensively studied1-12. In the present; however, hydrocarbon contaminants and a plenty of Si-OH termination in Si-O-Si networks tend to exist in the films, which degrade mechanical, optical and electrical properties of the films. It is necessary to understand the deposition mechanism at, low temperature in order to solve the problems. We have studied the low-temperature PECVD of Si02 by spectroscopic diagnosing techniques such as optical emission and mass analysis6-7, 11- 12Infrared reflection absorption spectroscopy (IR-RAS) has been a well-established technique for characterization of thin films on metals as· well as on semiconductors and insulators13-17. In this paper, we report on' the surface reaction of room-temperature PECVD of Si02by using in situ IR-RAS."

Jan 1, 2000

By Ludy C. Motta, Denise C. O. Nascimento, Sergio N. Monteiro

"Natural cellulose-based fibers are nowadays of growing interest for modern industrial composites. Relatively unknown fibers like piassava, curaua and gourde have shown promising behavior as reinforcement of polymeric composites. However, the hydrophilic characteristics of the natural fibers impair its adhesion to the normally hydrophobic polymeric matrix. Surface treatments can, in principle, improve this adhesion and the fiber/matrix interfacial strength. In this paper, the effect of alkali treatment of the surface of piassava (Atallea funifera) waste fibers was investigated in terms of the change in strength of epoxy composites reinforced with these waste fibers.IntroductionThe consequences of global warming and the increase in the price of petroleum are motivating the use of natural materials as substitute for energy intensive synthetic materials [1]. In particular, natural fibers obtained both, from cultivated plants such as jute, sisal, hemp and flax as well as from industrial waste such as sugar come bagasse and coir, are being considered to replace synthetic glass fibers [2,3]. These natural fibers, also known as lignocellulosic fibers, present the comparative advantages of being renewable, recyclable and biodegradable. Moreover, lignocellulosic fibers require less amount of processing energy and are neutral with respect to CO2 emission, which causes the atmospheric greenhouse effect responsible for the global warming [4]. Low cost is another important economical advantage of the natural fibers over the synthetic ones and the application of lignocellulosic is also associated with a lower wear of processing equipment and better finishing of molded components [5]. Moreover, for some fibers, properties such as the mechanical strength and impact resistance can be superiors to the corresponding properties of synthetic glass fiber [6]. The characteristics and properties of several lignocellulosic fibers are, nowadays being extensively discussed in the literature. It is beyond the scope of this work to comment on the hundreds of papers dealing with this subject. However, there are still less known fibers with great potential as engineering material that deserves investigation."

Jan 1, 2008

By Xinli Wang, Matthew Andriese, Jiann-Yang Hwang, Zhiwei Peng, Byoung-Gon Kim

"The microwave dielectric properties of silicon dioxide at frequencies of 915 and 2450 MHz were characterized in the temperature range of 24 to approximately 1000 °C using the cavity perturbation technique. It is shown that the relative dielectric constant of silicon dioxide at both frequencies remains almost unchanged below 500 °C, above which there is a slight increase of 2%. The relative dielectric loss factor of silicon dioxide exhibits a strong temperature dependence above 500 °C and increases by approximately 7 and 5 times at 915 and 2450 MHz, respectively. The substantial increase in the relative dielectric loss factor is mainly attributed to the enhanced dielectric polarization and accelerated electrical transport in silicon dioxide at elevated temperatures.IntroductionSilicon dioxide (Si02) is usually considered a microwave transparent material due to its poor absorption capability at room temperature [1]. This characteristic has led to various applications of silicon dioxide in microwave processing of materials and communication. For instance, Si02 has been used to produce sample holders for microwave heating and substrates for electronic devices [2,3]. These applications generally require the material to withstand high temperatures under microwave irradiation. This indicates that microwave absorption capabilities of silicon dioxide at elevated temperatures are also important for its utilization.The microwave absorption capability of Si02 can be determined based on dielectric characterization (permittivity measurement) of the material at commonly used microwave frequencies, 915 and 2450 MHz, in a broad temperature range. To date, however, no detailed work on the dielectric properties (permittivity) of silicon dioxide at high temperatures has been reported. The present work is aimed to study the dielectric properties of silicon dioxide from room temperature to approximately 1000 °C at 915 and 2450 MHz. The results show that the permittivity of silicon dioxide has a strong temperature dependence above 500 °C, suggesting a substantial increase in its microwave absorption capability."

Jan 1, 2013