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By Kunihiko Takeda, Kimio Imaizumi, Tsuyoshi Arai

"The study on the preparation of mono-dispersed liquid droplet was performed using ultrasonic as one of the steps of producing the perfectly mono-dispersed particle. The ultrasonic system was a 33.6kHz ultrasonic generator, an amplifier, an electric distortion element, and a bolted Langevin type horn installed in .a cell. For the first time, a liquid pillar under a nozzle of the cell ·was stably formed. Then, dense and coarse parts were alternatively constructed by oscillating the wavelength of the ultrasonic.· The diameter of those liquid droplets were found to be· perfectly uniform, therefore, it was measured by ""multiplex photography"" using a synchronized stroboscope with the ultrasonic.- From the results, more than 30,000 of perfectly uniform liquid droplets in 1 second were observed by this method.IntroductionRecently, research on the control of physical form is done in various fields of industry. Some examples are the processing technology of the minute compound material of micro-machines and integrated circuits, and the form control of molecule size like catalysts. There is a need for such material to take on various forms in correspondence to its use. ""Form control"" as used in this study will indicate ""research on physical chemistry factors which determine the size of the material"" and will refer to the contour uniformity of comparatively little particles. A well-known method of preparing particles is to spout a mist of liquid and slurry from a nozzle l) 2). Particles for metals, catalysts and food have been prepared by this method. In this case, although an approximate particle diameter can be decided by controlling the nozzle diameter and the violent outflow velocity, it is not easy to completely control ·the contour and to prepare a particle with uniform diameter. ·However, the preparation of perfectly uniform particles is necessary for solders for the adhesion of electronic wiring 3), ion exchange resins4), catalysts and so on. Large quantities of fine particles and super-fine particles are generated when manufactured in the usual way. Large quantities of these fine· particles and super-fine particles have polluted the internal and external' environments of factories. The products yield' ·decreases, also. From such a background, this study examines the preparation of perfectly uniform particles that could be· collected -100% as products. Recently, NASA has succeeded in the preparation of perfectly uniform particles in zero gravity 5). But the preparation of 'perfectly uniform particles by this method is difficult, and it can not be used in general industry"

Jan 1, 2000

By Dong Liu, Zejian Yang, Yong Li, Tao Jiang, Xiangxin Xue, He Yang

"The structure, composition, morphology, and adsorption property of UV-vis light of as-prepared samples were characterized using XRD, SEM, FTIR-EDS, and UV-vis DRS. UV-visible light induced photocatalytic degradation of methylene blue ~) over Ti02-doped diopside was investigated. Experimental results show that doping Fe + induced the formation of Ti-0 or Ti-0-Si in diopside, and promoted the light adsorption property of diopside. Photocatalytic reactivity of Ti02-doped diopside obviously depended on content of doping Ti02. The diopside with 3% Ti02 exhibited the superior photocatalytic activity with 76% degradation of methylene blue under light irradiation for 3 h.IntroductionPhotocatalytic technology has been extensively studied in the process of dealing with inorganic and organic pollutants. Ti02, with its own non-toxic, stable, low-cost and other advantages, has become the most widely studied photocatalytic materials[l-SJ_ The low utilization quantum made it restricted in the practical application. SrTi03 as the representative of the perovskite[9·121, Bi2W06 for the composite oxide[13,141, also attracted wide interest in the photocatalytic studies. However, these photocatalytic material has been mostly prepared in relatively strict experimental conditions with chemical reagents, they had small production, high cost, which made them difficult for practical applications.In our country, there has 400 million tonnes of ti-bearing blast furnace slag (TBBFS) each year in the process of smelting pig iron, which has lead to waste of titanium resources and pollution of the surrounding environment. In recent years, studies have shown that TBBFS instead of pure Ti02 to be photocatalytic materials is feasible[ 151. TBBFS has not only been higher photocatalytic degradation activity for the o-nitrophenol, methyl orange, nitrobenzene and other organic matter[16-191,but also exhibited excellent in the process of dealing with inorganic heavy metals in waste water (containing Cr6+i201. If TBBFS can be successfully applied to photocatalytic technology, the will make large accumulation of titanium-bearing slag reasonable used, so as promote the re-use of energy. At present, our understanding of the photocatalytic activity of TBBFS is steadily deepening. Photocatalytic activity ofCaTi03 has been reported as one of the main minerals ofTBBFS [21'21J, However, there were few studies for Another major mineral of TBBFS - diopside which had the content of9-15%. diopside would doped with Ti02 In the process of smelting pig iron, therefore, Ti02-doped diopside's photocatalytic activity in the UV-Vis was mainly studied in this paper."

Jan 1, 2013

By R. Escalera-Lozano, M. Herrera-Trejo, M. A. Pech-Canul, J. López-Cuevas, A. L. Leal-Cruz, M. I. Pech-Canul

"The use fly-ash (FA) and rice-hull-ash (RHA) offers the potential for the manufacture of hybrid Al/SiCp/spinel composites via reactive infiltration, both with recycled aluminum. The main reason behind this statement is the beneficial role that both waste materials play in preventing the degradation of SiCp reinforcements when the composites are processed with aluminum in molten state. Experimentally, MgAl2O4 is formed in situ during the infiltration of SiCp-preforms in the temperature range 1050-1150 oC for 50-70 min in argon atmosphere at a pressure slightly above to that of the atmospheric pressure. Results reveal that both FA and RHA help in preventing SiCp dissolution and the subsequent formation of the unwanted Al4C3; and although FA-composites still might be susceptible to corrosion via Al4C3 -by the interaction of native carbon in FA with liquid aluminum- a proper FA treatment significantly mitigates its deleterious effect. Primary corrosion mechanisms and strategies to overcome the potential degradation effects are outlined.IntroductionOwing to inherent materials characteristics and post-processing complications –such as corrosion damage- development of metal matrix composites (MMCs) from recycling/waste sources might be a challenging task. Fly-ash (FA) and rice-hull-ash (RHA) are two primary waste materials that offer excellent opportunities for the development of Al matrix composites. Due to its singular hollow-spherical shape and low density, FA has attracted the attention of many researchers. For this reason, most of the efforts to develop Al-based composites from waste materials have been centered on the use of fly ash. Extensive research efforts in the use of FA for Al-based composites have been undertaken by Rohatgi and coworkers [1-4]. In addition to lowering costs, incorporation of fly ash into aluminum has been proved to decrease the materials’ density, increase their hardness, abrasion resistance and stiffness [1]. One of the major outcomes from the mechanical evaluation of aluminum composites prepared with fly ash is that related to their compression characteristics. Typical compressive stress-strain curves form A356/hollow fly ash composites show a linear elastic region followed by a plateau (associated to the collapse of the hollow particles), and then an increase in stress, representing densification of the foam. The crushing of the cenospheres in the composites has been related to an enhancement in the energy absorption capabilities of the material and to a better damage tolerance [4]."

Jan 1, 2008

By Jean P. Murray

The extractive metallurgical industry is a major consumer of high-temperature process heat. It is, consequently, a major contributor of C02 emissions and other greenhouse gases derived from the combustion of fossil fuels for heat and electricity generation, or from the process itself. These emissions can be substantially reduced by replacing fossil fuels with solar energy as the source of process heat. Concentrated solar radiation can supply a large amount of thermal energy to endothermic reactions at temperatures exceeding 2000 K. Another potential for C02 emission reduction exists as well. Thermodynamically, the total amount of energy required for metal production at any given temperature is the enthalpy change of the reaction, AH. Of this total, an amount equal to the Gibbs free energy AG must be supplied as high quality energy in the form of electrical work or by using a reducing agent. Many conventional metallurgical electrolytic processes and reducing furnaces are unable to add only the thermodynamically required electricaVchemical energy due to process inefficiencies. Electrical work in excess of AG for the reaction may be used to supply process heat, or excess chemical reducing agent burned to supply process heat. Besides the thermodynamic and economic drawback, this inefficiency results in excess C02 emissions derived from the combustion of fossil fuels. With these practices, energy becomes an important cost element of the metal produced. Highly-concentrated solar energy has the demonstrated potential to separate these two forms of process energies, allowing the addition of only the thermodynamically required high-quality energy while high-temperature solar process heat is provided to the reactor. Examples of metal oxide reduction processes that have been studied experimentally in solar furnaces include the production of Fe, Al, AI/Si alloy, Mg, Zn, Tic, Sic, CaC2, TIN, Si3N4, and AIN by carbothermic reduction of their oxides, and the high-temperature solar- electrothermal reduction of ZnO.

Jan 1, 1999

By L. Yin, R. B. Haber, N. Sobh, D. A. Tortorelli, R. W. Hyland Jr.

"We optimize continuous quench process parameters to produce a desired precipitate distribution in aluminum alloy extrudates. To perform this task, an optimization problem is defined and solved using a standard nonlinear programming algorithm. Ingredients of this algorithm include a cost function, constraint functions and their sensitivities with respect to the process parameters. These functions are dependent on the temperature and precipitate size which are obtained by balancing energy to determine the temperature distribution and by using a reaction-rate theory to determine a discrete precipitate particle size distribution. Both the temperature and the precipitate models are solved via the finite element method. Since we use a discrete particle size model, there are as many as 105 degrees-of-freedom per finite element node. After we compute the temperature and precipitate size distributions, we must also compute their sensitivities. This seemingly intractable computational task is resolved by using an element-by-element discontinuous Galerkin finite element formulation and a direct differentiation sensitivity analysis which allows us to perform all of the computations on a PC.1 IntroductionThis work addresses the need for an integrated design capability that links microstructure evolution to the process parameters. It is motivated by the manufacture of lightweight aluminum-alloy extrusions for use in automotive structures. Aluminum alloys offer obvious benefits, however, care must be taken to manufacture favorable microstructures that ensure acceptable structural performance. For example, the manufacturing process for 6000-series components involves hot extrusion of cast aluminum billets followed by either an air or water quench process. The bill~t's initial grain structure is dramatically altered during extrusion by massive mechanical deformations and recrystallization processes. The microstructure continues to evolve during the quench, as complex chemical processes determine the formation of precipitates. The control of the precipit'ate size distribution is vital. Indeed, large precipitates located on grain boundaries serve as crack initiation sites which adversely effect structural crash· worthiness."

Jan 1, 2000

By Lijuan Li, Zheng Lu, Xin Xia, Qijie Zhai, Qingchun Li

"Pulsed current and pulsed magnetic field have been applied to the bainite transformation of Cr5 steel. Three groups of experiments were conducted. In the first group, ordinary resistance furnace was used for heat treatment. The Cr5 specimens were rapidly heated up to austenitization temperature 940 °C, held for 20 min, air cooled to bainite transformation temperature 350 °C, held for 10, 20, or 40 min and then air cooled to room temperature. The second and the third group shared the same temperature-time curve with that of the first group, but their heat resources came from the Joule heat produced by pulsed current. 1.5 T pulsed magnetic field was exerted on the third group specimens when they were held at 350 °C, but the second group specimens did not undergo the treatment of magnetic field. It was found that both pulsed current and pulsed magnetic field obviously retarded the bainite transformation. The phenomena were discussed in terms ofliterature results.IntroductionApplying pulsed current and pulsed magnetic field technology are very pronnsmg ways to change the microstructure of materials by affecting the phase transformation process. People had found that pulsed current dramatically influences the behaviors of materials, for example, electromigration effect [l], the solidification of metals and alloys [2, 3], electroplasticity [4, 5], crystallization of amorphous alloys [6], healing of metal materials [7] and so on. As to pulsed magnetic field technology, a lot of effort had been spent on grain refinement in solidification of metals [8, 9], recrystallization of cold-worked metals and alloys [10] and Fe-based alloys solid-state phase transformation [11, 12]. Though application of pulsed current and pulsed magnetic field technology have proliferated in recent years, investigation on their effects on solid/solid phase transformation, especially bainite transformation, is lacking. The aim of this paper is to show the effects of pulsed current treatment (C-T) and the combined treatment of pulsed current and pulsed magnetic field (CM-T) on bainite transformation of commercial Cr5 steel"

Jan 1, 2014

By Christopher Gammons

In developing countries throughout the world, gold ores are being processed by mercury amal-gamation, a technique long banned in the U.S. - unless a retort operation is used for mercury recovery - due to mercury toxicity and its effects on the environment. Amalgamation is a simple process that involves contacting a ground, slurried concentrate or ore with mercury in a slightly agitated vessel, usually for several hours, The amalgamated mercury is separated by gravity and then filtered through a fine cloth to collect the gold amalgam as a sponge, which is then fired to remove the final remnants of mercury and produce high quality gold. However, in Peru and other developing countries in South America and throughout the world, tailings are simply discarded into uncontrolled drainages and ponds and the sponge is fired in the open air. Clearly, in this case, environmental friendly and, to make matters worse, is typically conducted by family members of all ages without proper protection. Furthermore, the technique is inefficient, yielding approximately 50% gold recovery. For the past two years, faculty members from Montana Tech in Butte, MT, USA and the Universidad Nactonal del Altiplano in Puno, Peru have teamed to study the La Rinconada Mine Complex located in southern Peru approximately 100 kilometers north of Lake Titicaca and 25 kilometers west of Bolivia. The mining complex is over 5,000 meters above sea level and exists at the foot of a receding glacier in the Andes Mountains. A suite of soil and water samples collected in 2001 documented extensive Hg contamination in the Rinconada area [1]. The present paper summa¬rizes a follow-up investigation in July-2002, in which water samples were collected at numerous locations along the 200 km length of the Rio Ramis, from the Rinconada mine com¬plex to Lake Titicaca, In addition, we report new results of Hg analyses of fish from Lake Titi¬caca, The results of this study have relevance to safety and health concerns for the miners as well as people in downstream communities.

Jan 1, 2003

By Kerri-Ann Hue, Kerry Hasapidis, Ken Babcock, Patrick O'Hagan

"Metallic nanoparticles exhibit properties that are significantly different from individual atoms or bulk materials. Their applications are diverse and have varying uses in areas such as cancer treatment, biochemical sensors, nanoelectronics, and drug delivery. For each application extensive characterization must be performed in order to probe the unique properties of these nanoparticles. In this study, ultra-high resolution mass sensors consisting of MEMs-fabricated, suspended microchannel resonators (SMRs) were used to determine the size and concentration of metallic nanoparticles. With femtogram (10- 15 g) mass resolution, ultra-high resolution mass sensors can weigh individual particles suspended in fluid, and so measure their mass, density, and size. Particle size analysis with these sensors provides excellent accuracy and resolution compared to mature technologies such as light scattering. This technique also provides quantitative information via the ability count particles.IntroductionThe unique electronic, chemical, and optical properties associated with nanoparticles vary with their size, shape, and composition[ 1-4]. These properties are attributed to increased surface area and nanosized mean free path of electrons to the particle surface. Nanoparticle colloidal solutions have been prepared and are commercially available. In recent years, noble metals such as gold, copper, and silver have been extensively researched[5-7]. In order to tailor the optical, electronic, and electrical properties of nanoparticles, size and shape must be controlled. For many applications a monodisperse colloidal solution is ideal. Methods of size characterization include Transmission Electron Microscopy (TEM), Dynamic Light Scattering (DLS), and Electrophoretic Mobility Measurements to name a few[6, 8]. Although TEM can provide shape and size distributions, sample preparation requires that samples be dried on a metal grid and cannot be analyzed in solution. DLS uses curve fitting algorithms that while useful for determining mean particle diameters are not ideal for polydisperse colloidal solutions. New technologies are therefore needed to accurately determine the particle size distributions of metallic nanoparticles."

Jan 1, 2011

By Marcelo A. Martorano, Moyses L. Lima, João B. F. Neto

"Directional solidification is an essential refining step to obtain solar grade silicon from metallurgical silicon. This step can be carried out in a Bridgman furnace, where nearly constant temperature gradients and solidification velocities are imposed on the solid-liquid interface. In the present work, this directional solidification was conducted in a static furnace, in which large temperature gradients and low solidification velocities were enforced to increase macrosegregation. The resulting ingots were analyzed regarding their macrostructures, microstructures and chemical composition. Using measured cooling curves in the ingot as boundary conditions, a mathematical model based on the concept of a stagnant liquid layer at the solid-liquid interface was implemented to predict the macrosegregation profiles. The chemical analyses of the ingots show macrosegregation of several impurities to the ingots top. The mathematical model indicates that liquid convection plays an important role in stabilizing the planar solid-liquid interface, increasing the macrosegregation of impurities.IntroductionMost of silicon used for photovoltaic (PV) energy production is obtained by chemical processes, such as, Siemens and its derivations [1]. However, these chemical processes have drawbacks related to relatively high energy consumption and investment costs, and to safety and environmental problems. In order to overcome these difficulties and to fulfill the silicon demand for PV applications, several metallurgical routes are under development [2] to produce silicon of enough purity to PV applications (SoG-Si) from metallurgical grade silicon (MG-Si).Metallurgical routes involve different steps among which the directional solidification is pointed out as a fundamental one [1]. Directional solidification can cause macrosegregation of impurities to the last part of the ingot to solidify. The impurity segregation during solidification is related to the low solute partition coefficient (k0) between liquid and solid silicon. Most of the impurities in MG-Si have k0 << 1, except for boron, phosphorus and oxygen, which require specific steps of the metallurgical routes to be eliminated. The equilibrium partition coefficient and the solubility limits for the most important impurities in MG-Si are shown in table 1"

Jan 1, 2014

By Orion Ciftja, Arjan Ciftja

"The directional solidification method is routinely used to produce polycrystalline silicon, an important material for the photovoltaic (PV) industry. The form of the solid-liquid interface during solidification has considerable influence on the material quality. The dissolved impurities and the solid inclusions above the solidification front affect the interface and may cause interface breakdown. We investigate the effects of pushing and engulfment of silicon carbide (SiC) particles by the solidification front during directional solidification of silicon. We employ a 12kg directional-crystallization furnace to cast the molten silicon. We use upgraded metallurgical grade silicon with low concentrations of metallic impurities (< 5ppm) and a high content of carbon (700 ppm) present as SiC particles. Samples from the cast polycrystalline silicon ingots are investigated by light microscope. The expected interaction of impurities with the solidification front is investigated theoretically using empirical models. The data obtained from the models are in good agreement with the experimental results.IntroductionDirectional solidification is a well-known method for producing multi-crystalline silicon for the PV industry. In this method a planar front, achieved during solidification, results in a clearly defined interface between the solid and the liquid phase. The solubility of major impurities is higher in the liquid than in the solid phase. Therefore, directional solidification will work as a purification process where the impurities are retained in the liquid phase [1]. Apart from the process of removing the dissolved elements in molten silicon, the directional solidification plays also another role. It will interact with the solid particles that may be present in the melt. When a liquid containing an insoluble particle is solidified, three distinct interaction phenomena are observed: engulfment of particles, continuous pushing, and entrapment [2]. The term “engulfment” is used to describe incorporation of a particle by a planar interface, and the term “entrapment” is used for particle incorporation by a cellular or dendritic interface (see Figure 1) [3]."

Jan 1, 2014

By Marco Zurco, Claudia M. Mendez, Alicia E. Ares, Carlos E. Schvezov, Carlos M. Rodriguez

"Zinc-Tin alloys were solidified in horizontal form and the obtained results were analyzed. During solidification the distribution of temperatures were measured by using thermocouples located strategically along the length of the samples. From the measured temperatures the following parameters were derived; the local temperature gradient, the cooling rate and the velocities of the liquid and solids fronts. Comparing the structure of the samples and the values of these parameters it was found that the temperature gradient reaches minimum values of as low as - 0.6 °C/cm, and velocities of the fronts of around 0.1 cm/s. In addition, the grain size was measured along the samples. The results are presented and discussed in the frame of the results previously obtained for other alloys.IntroductionGenerally solidification leads to two types of grain morphologies: columnar and equiaxed. The origin of each one has been the subject of numerous theoretical and experimental researches in the field of metallurgy for many years [1-7]. The columnar-to-equiaxed transition, CET, is considered as an object of high technological relevance with respect to the directional solidification of metallic alloys. This structure transition may be sharp or gradual and it has been reported to be dependent on thermal conditions associated with the casting process, including melt convection, heat transfer coefficients at the metal-mold interface, growth rates, thermal gradients, cooling rates, transport of solute, alloy composition, melt superheat, mold temperature, mold design, casting size, casting geometry, and the concentration of nucleating particles. As a consequence, it is critical for industrial applications to understand the physical mechanisms which control this transition during solidification. Many studies highlight the importance of the relative growth of the equiaxed and columnar grains and develop expressions or numerical procedures to describe a criterion for the CET. A number of experimental investigations reported in the literature suggest that the CET occurs when GL in the melt reaches a minimum critical value [5-7]."

Jan 1, 2012

By Shenghui Guo, Ying Lei, Hao Niu, Huilong Luo, Jinhui Peng, Libo Zhang, Yu Li

"In this work, the combination of microwave drying (MWD) and heat pump drying (HPD) drying experiments were designed by response surface methodology (RSM) based on central composite design (CCD) using design expert software (Version 7.15), and the process parameters were optimized. The conditions given by software are: the MWD time is 4.6 or 4.4 min; the HPD time is 9.0 or 8.6 min; and the sample mass is 620 or 600 g. Under those conditions the moisture content is 1.0 10-2kg water/kg wet basis, and the effectiveness ratio is 0.70 kg water/kwh. The results of confirmatory experiments conducted under the optimized conditions show the combined drying have superiority of decrease of energy consumption and increase of handling capacity over the single MWD or HPD.1 IntroductionSilica sand is one of a silicate mineral with properties as hard, anti-friction and less reactive, commonly used as raw material for foundry and construction. The silica sand obtained from mineral dressing processes such as scrubbing, magnetic separation and flotation. Its moisture content is approximately 0.08~0.12 kg water/kg wet basis. The most common methods used for drying are solar drying and hot air drying. But these methods have some shortcomings: for example, the solar drying has longer process time due to low energy yield, [1] hot air drying has low-energy efficiency and a lengthy drying time. [2]Microwave is electromagnetic waves with frequency are 300MHz to 300GHz. The outstanding features of microwave heating are rapidity and selectivity. The water specific inductive capacity of 60~78 is much bigger than common materials, the moisture always quickly absorb electromagnetic wave and rapidly transfer to vapors. So, it can significant reduce the drying time. [3] Heat pumps (HPs) are devices for raising the temperature of low grade heat energy to a more useful level using a relatively small amount of high grade energy."

Jan 1, 2011

By LeoJ. Miller

Exploration for an ore deposit commences with an outline of the regional ore controlling environment and is followed by the application of tools to focus the target area. One of the most essential focusing is the mapping of the mineral assemblages within the area of the ore. Key elements of mineralizing fluids, either epigenetic or syngenetic, enter into mineral assemblages that extend far beyond ore deposits. Portions of these assemblages may consist of new matrix minerals or alteration of previously existing minerals. Today, ore deposits are divided into genetic classes and each class is d8fined by a specific geological environment. Ore deposits within a given class are associated with a mineralogy, that is characteristic of the ore deposit class. So faithful is the mineral assemblage surrounding, or within an ore deposit, that recognition of the assemblage may be sufficient to define the class. Porphyry copper deposits have long been noted for their halos of alter-ation minerals. The outermost ring of chlorite, epidote and calcite extend thousands of feet away from the main ore zone. The mineral associated with porphyry copper deposits have been well documented by our distinguished speaker Paul Kerr, at Santa Rita (1), and Silver Bell&apos; (2), and by excellent papers from S. C. Creasey, 1959 (3), Sales, 1948 (4), T. S. Lovering, 1949 (5), our Co-Chairman John Guilbert, 1970 (6), and many others. Several recent porphyry copper mines have been discovered in recent years by utilizing the mineral assemblage model described by Lowell and Guilbert, 1970 (6). Dave Lowell applied his own model of mineral halos for the discovery of Kalamazoo at San Manuel (7), Arizona, and Casa Grande West, Arizona. The purpose of this paper is to outline the application of mineralogy for discoveries of deposits other than porphyry copper mines and in particular, to ore discoveries in which mineralogy has played a key roll.

Jan 1, 1981

By Ann M. Hagni

Flash reduction of zinc oxides is an alternative, environmentally safe method to leaching and electrowinning for zinc recovery. Zinc and lead are volatilized in a flash reactor, a non-hazardous residue is generated, and the fuel source is inexpensive coal in the flash reduction process. Results from experimental laboratory tests yielded low zinc recovery for this process. Mineralogical and textural characterization of the residues from the flash reduction tests for different feed materials and temperatures were conducted to determine the cause for the low zinc recovery. Reflected light microscopy, cathodoluminescence microscopy, scanning electron microscopy-energy dispersive spectroscopy, and X-ray diffraction were utilized in this applied mineralogical research. The original zinc calcine is composed primarily of fine-grained, iron-bearing zincite particles, 25-40 um in diameter, in a porous texture. Pellets processed at 1150°C were found to produce reaction rims of franklinite-magnetite-jacobsite solid solution that are 125-200 um thick and surround cores of unreacted iron-bearing zincite in a Zn-Fe-Si-Ca glass matrix. The reaction rims have subsequently oxidized to form an outer 10 ~m thick rim of hematite. Slags from calcines processed at 1275°C are primarily triangular particles with porous centers, cenospheres, and spheres of iron-bearing zincite, in addition to rectangular particles composed of non-porous franklinite-magnetite solid solution cores with iron-bearing zincite rims. Slag particles from calcine processed at 1200°C are predominantly 100-250 ~m triangular-shaped, spheres, and cenospheres containing fine-grained franklinite and franklinite-magnetite solid solution in an iron-bearing zincite matrix. Slag from calcine processed at 1300°C are also predominantly 1 00-250 um triangular-shaped, spheres, and cenospheres but contain coarser-grained iron-bearing zincite. The zincite in the penets and the slags typically contain 10-20% iron. Based upon these mineralogical observations, it is concluded that the significant amounts of iron in the zincite prevent volatilization of the zinc in the flash reduction process.

Jan 1, 1995

By Atsuhiro Nabei, Ken-ichi Yamaguchi

"Wet chlorination process of de-copperized anode slime is followed by de-chlorination stage in which lead-sulfate and metallic silver form silver residue. The silver residue is subsequently reduced to Ag2Se matte and PbO-SiO2 slag to remove lead to the slag in a short rotary furnace. Although this smelting process is proven well in actual operations, few papers have investigated its metallurgical aspects. This paper will describe the effectiveness of controlling parameters adopted at the Naoshima Smelter & Refinery and discuss the decisive factors influencing silver loss to PbO-SiO2 slag.IntroductionThe precious metals plant at Naoshima smelter & refinery was established in 1989, and has produced electrolytic silver, refined gold and platinum-group metals (PGM) from de-copperized anode slime as by-products of electrolytic copper. The process for gold production has been innovated from conventional smelting process to hydrometallurgical process since 2004 [1], while the process for silver production has still remained the same.The process for silver production at the Naoshima smelter & refinery is illustrated schematically in Figure 1. De-copperized anode slime is, at first, concentrated in the froth flotation process, then leached in the wet-chlorination process, and converted to silver residue in the de-chlorination process. The silver residue, which is a mixture of lead-sulfate and metallic silver, is charged to a short rotary furnace for the oxidation roasting to volatilize selenium dioxide and subsequent reduction smelting. In the smelting stage, silver residue and reverts containing selenium are smelted with flux and carbonaceous materials to form PbO-SiO2 slag and Ag2Se matte. Furthermore, Ag2Se matte is transferred to a rotary cupell and oxidized by air with the addition of sodium carbonate and sodium nitrate to produce silver anodes while removing impurities into litharge. Silver anodes are electrolytically refined by the Moebius process. Electrolytic silver is washed, dried and, finally, cast into 30kg-bars."

Jan 1, 2011

By Leonardo Mota, Lucas L. da Costa, Milton B. Filho, Sergio N. Monteiro, Helion Vargas, Tammy G. R. Portela da Silva

"A natural biofoam extracted from the buriti palm tree has shown characteristics for potential substitution of synthetic foams. In the present work, a photoacoustic thermal characterization was performed on buriti biofoam samples. An open photoacoustic cell technique and a photothermal rise method performed under continuous laser illumination were employed in order to determine the thermal diffusivity and the specific heat capacity of such material. In addition to their intrinsic values (finger print), these physical parameters represent the light-into-heat conversion efficiency and the amount of heat stored per unit volume, respectively. The results showed that the buriti biofoam presents thermal properties that permit its use as an effective insulation material.IntroductionSolid foams are very light materials with increasing engineering applications [1]. A natural biofoam obtained from the petiole of the buriti palm tree (Mauritia flexuosa) has been recently investigated [2-4]. The evaluation of the buriti biofoam properties and the characterization of its microstructural aspects have shown that this biofoam has a potential as a new engineering material with very low density. Additionally, its reduced open porosity and low absorbed humidity revealed a promising material for packing and floating applications. In fact, this buriti biofoam, extracted from the palm tree natural of the north region of Brazil, is being used by the low income population as a modest substitute for Styrofoam® [1].As a potential insulating material, the buriti foam needs to be characterized in terms of its thermal and acoustic properties. A preliminary investigation [3] on the thermal behavior of this natural biofoam by thermogravimetric analysis, TGA, and its derivative, DTG, as well as differential scanning calorimetry, DSC, revealed parametric conditions associated with water loss and structural decomposition. Both the surface humidity and the release of hydration water were determined. Different decomposition events were attributed to both, more rigid as well as to more flexible molecular segments. Table 1 depicts technical data obtained so far for the buriti biofoam. These data are compared to those corresponding to Styrofoam®."

Jan 1, 2011

By Dan Wang, Qian Li, Yong-bin Yang, Tao Jiang

"Thiosulfate is one of the most promising non-cyanide lixiviants for gold leaching. However, the undesirable reaction between thiosulfate and copper (II) gives rise to increased reagent consumption, which results in high cost and huge limit to its development. This paper presents study on the effect of ammonia, copper (II) and Cu(NH3)l+ ions on the oxidative decomposition of thioulfate. It shows that the presence of copper (II) and Cu(NH3)l+ can significantly increase the thiosulfate oxidation, while ammonia is relatively unaffected. The oxidation of thiosulfate by copper(II) in the absence of ammonia is fast at first and then decreases as time increased within a certain time, which can postulate that an intermediate product is responsible for the decreased consumption. The effect of ammonia is depended on the interaction with copper (II), which was found to significantly affect the consumption of thiosulfate.IntroductionFor over one century cyanidation is widely used in industrial production of gold, due to its simplity of process and low cost of production. However, cyanide is a highly toxic chemical reagent used dangerously and brings serious environmental pollution. What's more, cyanidation has slow speed of leaching gold and poorly leaching effective for refractory ores. With the exhausting of free-milling gold ores and promoted environmental protection requests, the disadvantage of cyanidation becomes a growing problem. In recent years, more and more research activities have been focused on alternative processes using non-cyanide lixiviants. Among the non-cyanide lixiviants, thiosulfate is considered as the most promising one[l-5].Compared to cyanide, thiosulfate is an inexpensive, nontoxic and less-pollution reagent, which can form complexes with many metal ions. Thiosulfate leaching of gold has an acceptable leaching rate and is insensitivity to impurities. Moreover it presents advantage on the treatment of refractory gold ores such as carbonaceous gold ores, copper gold ores, complex arsenic and sulfur gold ores, and so on[6]."

Jan 1, 2013

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

By Monteirom Sergio N., Romulo L. Loiola, Giulio R. Altoe, Noan Simonassi, Frederico M. Margem

"The environmental concern is creating pressure for the substitution of high energy consumption materials for natural and sustainable ones. Compared to synthetic fibers, natural fibers have shown advantages in technical aspects such as flexibility and toughness. So there is a growing worldwide interest in the use of these fibers. Buriti fiber extracted from buriti palm tree (Mauritia flexuosa), presents some significant characteristic, but until now only few studies on buriti fiber were performed. This work aims to make the analysis of the tensile strength of epoxy composites reinforced with buriti fibers. This analysis was performed in fibers with diameters between 0.1 and 0.4 mm. Those fibers were incorporated into the epoxy matrix with volume fraction from 0 to 30%. The fiber diameters were measured by a profile projector. After fracture the specimens were analyzed by a SEM (scanning electron microscope).IntroductionNatural fibers with high amount of cellulose, also known as lignocellulosic fibers, have been used from primeval times of our civilization. In the last century, synthetic fibers such as nylon, carbon, aramid and glass fibers gained interest owing to superior strength and precise dimensional control. Natural fibers were then replaced by synthetics in many fields such as textiles, sports goods and appliances. In the past decades, however, environmental issues drawn, once again, the attention to lignocellulosic fibers as possible substitute for intensive energy-consuming and long term polluting synthetics, specially the glass fiber(1). In particular, research works have disclosed the potential advantages associated with the use of lignocellulosic fibers as the reinforcing phase in polymer composites(2-3). Among the advantages it is worth mentioning the renewability, recyclability, biodegradability and the fact that natural fibers are neutral with respect to CO2 emissions responsible for global warming. In addition to environmental benefits(l,10) the lignocellulosic fibers present economical advantages, such as worldwide abundance and comparatively low costs as well as some technical properties associated with flexibility and toughness( 4), which contribute to the performance of automobile components fabricated with natural fibers composites(l 1-13)."

Jan 1, 2013

By Thomas Gliick, Jianming Lu, David Dreisinger

"The Boleo project of Baja Mining (Vancouver) will process a mixed oxide-sulfide ore using an acid oxidation and reduction process in seawater to extract copper, zinc, cobalt and manganese. Copper will be extracted via SX-EW as copper cathode, zinc will be recovered as a zinc sulphate monohydrate crystal and cobalt will be produced as a cobalt cathode product after phosphinic acid extraction. Manganese may be recovered from the final solvent extraction raffinate by precipitation as manganese carbonate.The development of the cobalt recovery process (solvent extraction and electrowinning) will be discussed. The pilot plant solvent extraction circuit and subsequent bench and small pilot testing of cobalt electrowinning will be discussed. The Boleo project will produce approximately 1708 tonnes per armum of cobalt metal when fully commissioned.INTRODUCTIONThe Boleo property is held by the Mexican company, Minera y Metalllrgica del Boleo S.A. de C.V. (MMB). MMB is owned 70% by Baja Mining Corp. and 30% by a consortium of Korean companies consisting of KORES - Korea Resources Corporation, LS Nikko Copper, Hyundai Hysco, SK Networks and Iljin Copper. The project is fully financed and is now under construction with an expected startup in early 2013 .Average annual production, for the first six years for each of the metals is forecast as: 56,697 tonnes of copper cathode, 1,708 tonnes of cobalt cathode and 25,364 tonnes of zinc sulphate monohydrate. The project has an average life-of-mine cash cost (based on the three year trailing average metal prices, as of December 31, 2009, in accordance with SEC guidelines) of -$0.29/lb Cu, net of by-product credits for cobalt and zinc and with no credit for manganese production. There is the potential to produce up to 220,000 tonnes per armum of manganese carbonate (- 100,000 tpa contained Mn) via the relatively simple addition of a small number of unit operations to the proposed plant. The recovery of manganese metals from the manganese carbonate intermediate material is discussed in a separate paper in this proceeding."

Jan 1, 2012