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By Ted H. Eyde

Natural Zeolites are a less expensive and in certain applications a superior alternative to organic ion exchange resins. Mining and metallurgical waste streams are difficult to treat because the effluents which contain potentially valuable heavy metals such as copper, lead, and silver are often highly acidic and contain significant quantities of suspended solids. Under rigorous operational conditions, certain natural zeolites can remove the metals, which if desired can be recovered by either elution or conventional smelting techniques. There are significant differences in cation exchange rate, selectivity and capacity as well as resistance to either high or low pH, blocking cations and tolerance to elevated or depressed temperature and pressure not only between different zeolite minerals but between the same mineral from different deposits. Applying natural zeolites to the treatment of mining and metallurgical waste streams depends on matching the specific zeolite to the effluent by characterization of the zeolite minerals.

Jan 1, 1993

By Jinqian Zhao, Jiarong Li, Shizhong Liu

"Creep cavitation of in single crystal (SX) superalloy was investigated. The constant load creep tests, in single crystal superalloys DD6, were conducted at the conditions of 800°C/700MPa, 850°C/550MPa and 900°C/450MPa, respectively. It was found that there were square facets on the stress fracture surface, and microscopic cavities in the ruptured specimens in the vicinity of the fracture surface. Both the square facets on the fracture surface and microscopic cavities in the section of the ruptured specimens show the morphology of the same thing at the different views, namely creep cavities, which are take the form of flatten cuboid. In fact, creep cavities are the longitudinally tensiled creep cracks slowly growing during the stress tensiling. The factors of creep cracks nucleation and growth conditions include: (a) enough high temperature to activate diffusion (b) casting pores as nucleation origination (c) high strains and strain rates. Eventually, the instantaneous fracture mechanism of creep specimen is cleavage fracture.IntroductionFor the materials used in elevated temperature service, creep behavior has to be accounted for. It is well recognized that creep rupture in polycrystalline materials at high temperature occurs principally by the nucleation and growth of microscopic cavities at grain boundaries, followed by microscopic cavities linkage to form micro- and eventually macro-intergranular cracks[l,2]. Without the usual grain boundaries, SX superalloys have superior capabilities at high temperatures to polycrystalline superalloys, and have become an established feature of gas turbine technology where they are commonly employed in the manufacture of high performance blades[3]. A considerable amount of work has been done over the past tens of years, and many models for nucleation and growth of creep cavities have been proposed, however, those are mainly for polycrystalline materials.In order to improve creep resistance that single crystal superalloys, in which grain boundaries are removed, have been developed. Because there don't exist grain boundaries in SX superalloy, the mechanism of nucleation and growth of creep cavities must be different from that in polycrystalline materials.Understanding the formation and characteristics of creep cavitation is crucial to model the lives of single crystal superalloys.M. Marchionni and L.G. Zhao et al. found that there were square facets on the stress fracture surface [4,5]. Roger C. Reed pointed out creep cavities lie in the necked region[6]. In this paper, the effects on the formation of creep cavities are discussed, as well as the morphology of creep cavities and fracture mechanism of SX superalloys."

Jan 1, 2013

The resist profile simulation is carried out using the combined data obtained. The nematic liquid crystal is clear only when a long range order exists, in the whole medium. using the Jones matrix method. Director can change from point to point and is, in general, a function of space. Details of the lens structure and of the devices fabrication and performance are described. Light from conventional light source or laser is passed through a polarizer and then incident on the specimen At the nematicisotropic, transition temperature, the medium becomes isotropic and looks clear and transparent. The transition can be approached by changing the impurity concentration or, indirectly, by tuning the temperature since the pinning strengths of the random and crystal potential have in general a different temperature dependence.

Jan 1, 2006

By Rush Kramer

A bulk compositional chemical analysis often provides incomplete information to help the mineral processor when faced with the problem of removing troublesome contaminants in low concentrations. Michigan Tech has developed a unique approach for addressing this problem. A combination of Scanning Electron Microscopy (SEM). Energy Dispersive Spectroscopy (EDS). and image analysis was successfully used to characterize the species responsible for phosphorus contamination of less than .05 weight percent in iron ore. An automated routine acquired the chemical signature of each particle on a backscattered electron image. The few particles containing phosphorus were identified from the hundreds of particles examined. and the phosphate phases present were easily characterized.

Jan 1, 1991

By William A. Fuchs

A study of carbonaceous ore at the Santa Fe mine (Corona Gold Inc.) shows that there is no quantitative relationship between organic carbon content and preg rob, although much of this material preg robs. However, there is a relation between K20 and preg rob. Preg rob generally occurs only in those samples with greater than 2% K20. X-ray diffraction and chemical . studies show that the critical factor is the illite content of mixed (possibly interstratified) illite-smectite. Apparently illite, at a certain threshold, "geo-activates" the carbon. The potential for easily monitoring preg rob using a gamma ray spectrometer is discussed.

Jan 1, 1990

By N. A. McKay, J. G. Davison

"Heap leachable ore deposits from many countries have been submitted for process mineralogical evaluation and laboratory testwork. Numerous factors must be addressed and integrated by the mineralogist, geologist, metallurgist and engineer. Projects encompass grass roots exploration, preliminary petrographic analysis, predictive and process mineralogy, dye penetration analysis of rocks and thin sections, metallurgical beneficiation testwork and plant optimization studies. The significance of mineralogical factors, such as geological controls, degree of oxidation, dye amenability, liberation, deleterious minerals, refractoriness, and the impact of mineralogy on gold recovery and process considerations, will be presented.ABSTRACT ONLY"

Jan 1, 1997

By Aliye Arabaci

In the present investigation, an attempt has been made to study the reduction behavior of composite pellets consisting two different types of iron oxide fines (high and low grade) and coke or lignite fines as reducing agents. The reduction experiments were carried out under isothermal conditions and constant flow of nitrogen gas in the temperature range of 900 ? 1100 oC. The variables investigated are the reduction temperature, Cfix/Fe3O4 ratio, reduction time and reductant type. In the experiments carried out with Sivas Divrigi A head magnetite ores (high grade) at a temperature of 1100 oC, for 40 minutes and on the condition that Cfix/Fe3O4 ratio is 0.2, in which lignite and coke fines were used as reductant, degree of reduction was obtained as 91 % and 86 %, respectively. Whereas, in the experiments realized with Malatya-Hekimhan-Hasançelebi magnetite ores (low grade) on the same conditions by using lignite as the reductant, around 60 % degree of reduction was found.

Jan 1, 2008

By Selvin Yesilay, Guray Kaya, Bekir Karasu, Asli Cakir

"In this investigation, the wastes of Eti Maden Kirka Boron Company of Turkiye were evaluated in the production of diopside and anorthite-based glass-ceramic glazes suitable for porcelain tiles fast and single-fired under industrial conditions. First of all, high wear resistant frits were produced with the use of concentrator and derivative borax wastes. Second of all, pre-engobed porcelain tile bodies were coated with the standard and newly produced frit-based glazes and industrial fast single-firing was employed. Final products were undergone to the certain standard tests to determine their Vickers hardness, wear resistance, thermal expansion coefficient values, gloss and coloring parameters. The micro-structures and phase formations of the fired glazes were also studied. Consequently, it was confirmed that the utilization of borax solid wastes in fast single-fired porcelain tile glass-ceramic glazes is possible. Introduction Porcelain tiles were introduced at the end of 1980s by Friandre, one of the leading Italian porcelain manufacturers. The American National Standard Specifications for Ceramic Tile defines porcelain tiles as: dense, smooth, impervious (with water absorption value less than 0.5 %) and stain resistant [1]. The excellent technical performances for ceramic tiles, such as mechanical, wear, frost and chemical resistance that make their use possible in indoor and outdoor building applications [2-3]. In the last decade, the growth rate of the global production of porcelain tiles increased more than those of other ceramic products; in fact, the technical properties of porcelain tile, coupled with even more improved aesthetic appearance, gave it a prominent role on the tile market [2]. Glass-ceramics are composed materials of one or more crystalline phases immersed in a residual glassy phase [4-5]. Glass-ceramic technology is based on controlled nucleation and crystallization of bulk glass [6]. The concepts of controlled crystallization of glass designate the separation of a crystalline phase from the parent glass in the form of tiny crystals. Their growth rate and final size are controlled by a suitable heat treatment [7]."

Jan 1, 2008

By Donna Post Guillen

"Cyclopentane, a flammable hydrocarbon, is being considered as a working fluid for waste heat recovery applications using Organic Rankine Cycles with Direct Evaporators. A postulated failure mode consisting of a pinhole leak in a heat exchanger tube raises safety concerns due to autoignition of the working fluid. Experiments were conducted to determine the ignition delay time (IDT) of cyclopentane using an Ignition Quality Test™ (IQT™) device. Two sets of experiments were conducted per ASTM D6890 (with exception to charge pressure and temperature) to determine ignition delay of the fuel at atmospheric pressure for standard air (-20.95% oxygen) and vitiated air (13.3% oxygen) at a temperature of 803 K. Operation of the IQT device at a much lower pressure (1 bar) than normal operation (21.4 bar) with a standard injector led to very rich conditions and wetting of the stainless steel chamber walls. Catalytic effects are postulated to produce the small IDTs observed. Experiments were repeated with a modified injector to prevent wall wetting, resulting in average IDTs that are substantially longer.IntroductionCyclopentane is being considered for use as a working fluid in a Direct Evaporator of an Organic Rankine Cycle (ORC). In this configuration, the heat exchanger is placed directly in the flow of the hot exhaust gas, rather than using a secondary heat transfer loop to isolate the flammable working fluid from the heat source. This configuration offers the advantages of approximately 15% lower cost and improved efficiency over a standard ORC. However, placing a heat exchanger operating with a flammable hydrocarbon in the hot exhaust gas stream presents potential safety risks. If a pinhole leak were to occur in the heat exchanger, working fluid could leak into the hot exhaust stream. Gas turbine exhaust is provided to the Direct Evaporator at a temperature of approximately 803 K, whereas the autoignition temperature of cyclopentane is 634 K (Gallant and Yaws, 1993). Autoignition of the working fluid has been identified as the key risk for this type of system.Autoignition occurs when sufficient self-heating by chemical reactions takes place to accelerate reaction rates to produce full-scale combustion. This is in contrast to forced ignition, in which an external source (e.g., spark) is employed to initiate the combustion process. For combustion to occur, the fuel to oxidizer concentration must be between the lower (lean) and upper (rich) flammable limits. The reaction rate depends on the species concentration of the fuel and oxidant, the local temperature and pressure. Ignition processes are comprised of steps that take a fmite amount of time. This latent period prior to the start of combustion is referred to as ignition delay time (IDT)."

Jan 1, 2012

By P. Chris Pistorius

"Use of coke in blast furnace ironmaking is the main origin of carbon dioxide emissions from integrated steelmaking. Use of pre-reduced iron feedstocks would reduce the coke rate and, if pre-reduction were carried out with natural gas, would decrease the overall carbon intensity of ironmaking. Blast furnace productivity would also increase, because the blast volume per unit of hot metal would decrease. This paper shows that these trends can be predicted quantitatively, by using a conceptually simple Rist-style blast furnace mass and energy balance, assuming furnace productivity to be limited by the tuyere gas flow rate. Such predictions would assist in optimizing the choice of the degree of reduction and relative amount of pre-reduced blast furnace feed.IntroductionSteelmaking is responsible for some 5% of world CO2 emissions, at a rate of approximately 1.9 tonnes of CO2 per tonne of cast steel [1]. In integrated steelmaking, the ultimate source of most of the CO2 emissions is coke, the indispensible (and expensive) fuel and reductant for blast furnaces. There are several research programs underway worldwide which seek to lower the carbon intensity of ironmaking; one of the largest is the European ULCOS program [2], in which the main proposed change to blast furnace ironmaking is to scrub CO2 from the furnace off-gas (for possible sequestration), recycling the remaining gas to the furnace. To limit the recycling nitrogen load, oxygen rather than air is used to combust coke.A conceptually simpler approach is to charge prereduced feed (direct-reduced iron) to the blast furnace. This approach has been used for some two decades at the AK Steel Middletown plant, where some 200 kg of direct-reduced iron (DRI) is charged per tonne of hot metal [3]. The Middletown blast furnace has exceptionally high productivity (rate of iron production relative to the furnace hearth area), simply because less coke is required per ton of hot metal if part of the feed is already metallic. Midrex [4] has provided some quantitative predictions of the implications of DRI use in the blast furnace, stating that for every 10% of Fe in the feedstock that is in metallic form, the fuel requirement decreases by 7% and the productivity increases by 8%."

Jan 1, 2012

By Kimio Itagaki

As a fundamental study for smelting the copper matte with high contents of arsenic and antimony in a strongly reducing condition, phase relations between the liquid matte and copper-rich alloy phases in the Cu-Fe-S-As or -Sb quaternary system and between the liquid matte and iron-rich alloy phases in the Cu-Fe-S-As or -Sb system saturated with carbon were determined at 1473 K by a quenching method. Activities of arsenic and antimony in these systems were also measured at 1473K by Knudsen cell-mass spectrometry. Furthermore, distribution ratios of silver, gold and platinum between the liquid matte and copper-rich or iron-rich alloy phases were determined in relation to the arsenic or antimony content in the systems. On the basis of these data, the elimination of arsenic and antimony from the matte to the iron-rich alloy (speiss) and the recovery of precious metals in reduction smelting of the copper matte were evaluated. It was suggested that the addition of pig iron to make a strongly reducing condition and form the iron-rich alloy, which is fluid at smelting temperatures, will be useful for fixing arsenic in the speiss.

Jan 1, 2006

By G Hope, C Young, R. N. Gow

"The presence of enargite (Cu3AsS4) is problematic in gold processing as it is refractory, increasing cyanide and oxygen consumption, and enviromnentally hazardous. Selective leaching and treatment of the arsenic would prove advantageous to conventional gold leaching methods. The reactivity of enargite samples from Montana, US and Quiruvilca, Peru were studied under alkaline conditions, pH range of 8-13, using a cyclic voltammetry corrosion cell setup. Raman spectra of the surface were taken during and after cycling to compare surface species against theoretical predominance diagrams. Under slightly oxidizing conditions, covellite (CuS) peaks were found on the surface in a short matter of time, above - 200m V vs SHE for pH 9-13, suggesting arsenic leaching, but for longer conditioning times, elemental sulfur peaks were also found, which created a passivating surface layer. By operating above pH 12, under reducing conditions, ~-500mV vs SHE, arsenic can be leached as a thioarsenate (AsS4-xOx3-), without sulfur formation.IntroductionEnviromnental limitations on pyrometallurgical processing of arsenic has pushed the desire to process enargite-, Cu3AsS4, bearing concentrates towards a hydrometallurgical solution. Attempts to process can be broken down into two categories - the co-dissolution of arsenic and copper under acidic conditions or the selective leaching of arsenic under basic conditions. The selective leaching of arsenic would preferably leave behind a chalcocite, Cu2S, or covellite, CuS, phase that would be more amenable to conventional processing methods of the copper and gold industries. These methods employ bi- or poly-sulfides to leach arsenic as Assl· [1-4], hypochlorite leaching [5-7], ammoniacal leaching [8] or fine grinding to mechanically activate the enargite surface and increase normally slow reaction kinetics[9]. This study looked into the surface formations of an enargite electrode under alkaline conditions, in a pH range from 8-13, as it cycled from -1000 mV to 1000 mV vs SHE. The understanding of the formations and under what conditions they form will be helpful in further development of any of the aforementioned processes."

Jan 1, 2012

By Afrodite Ntziouni, Vassilia Kasselouri – Rigopoulou, Athanasia Kyritsi, Konstantinos N. Pistiolas, Stamatia Gavela, Konstantinos Kordatos, Lazaros Iliadis

"The present study deals with the production and characterization of rice husk ash (RHA) and its use in the synthesis of zeolite of type ZSM-5. Rice husk was combusted in various temperatures with aim to find the suitable conditions for the production of amorphous silica. The resulted amorphous silica ash was then utilized as a starting material for the synthesis of ZSM-5 zeolite using the low temperature and atmospheric pressure process. The method led successfully to the synthesis of highly siliceous zeolite of type ZSM-5. The produced material was characterized using x-ray diffraction (XRD) and scanning electron microscopy (SEM).IntroductionRice husk is a major by-product of the rice-milling industries and it is usually used as a fuel for steam generation due to its high calorific power. During its combustion, rice husk ash (RHA) is produced. Knowing that the annual rice world production is over 615 million tons (2005), thus resulting in a potential production of more than 22 million tons of RHA [1], it can be understood that the RHA disposal is a crucial issue towards the environmental protection. However, due to the high silica content, RHA can be used as an alternative cheap source of silica for many uses, including as filler in polymers [2], concrete [3] and synthesis of zeolites [4-7].The burning of rice husk in air results in the formation of RHA with content in SiO2 that varies from 87 to 97% depending on the burning conditions, the rice variety, the climate and the geographic area [8]. Some small amounts of inorganic impurities are always present in the ash along with unburned carbon. The unburned carbon can be removed from the ash by further heating treatments in high temperatures, but this usually leads to the crystallization of the amorphous silica to cristobalite and/or tridymite [9]. The crystallization of the contained silica of the ash is also occurred when the burning conditions of husk are uncontrolled [10]. This crystallization is a disadvantage towards the preparation of silicon based materials, because the silica ash is rendered inactive in its crystalline form [11]."

Jan 1, 2008

By R. Boussaa, Y. Fautrelle, K. Zaidat, O. Budenkova, B. Saadi, X-D. Wang, L. Hachani, H. Ben Hadid

"Comparison of experimental data obtained in a benchmark experiment of solidification of a Sn-3%wt.Pb ingot and numerical results of two-dimensional and three-dimensional simulations of the process is presented. The benchmark experiment consisted in solidifying a rectangular ingot of Sn-3%wt.Pb alloy using two heat exchangers. Conditions of solidification were thoroughly controlled due to six thermocouples embedded into each heat exchanger. Due to another array of thermocouples the evolution of the temperature field at a lateral wall of the crucible was registered during the whole experiment. A treatment of the temperature data provided an estimation of the velocity field in the experiment. Post-mortem analyses of the sample provided the pattern of macrostructure of the sample and qualitative segregations pattern. 2D and 3D numerical solidification models are developed to give the distribution of the solute in a solidified sample.IntroductionConvection, either natural or forced, plays a very important role during the solidification. Its intensity and flow pattern affect heat and mass transfer and, consequently, macrostructure and segregation in a solidified ingot [1-4]. The effect of buoyancy convection during solidification has been studied in many laboratory-scale experiments [5-6]. Due to these experiments a general comprehension of formation of various defects in the ingot has been achieved. However, mentioned studies were not consistent since alloys, solidification conditions and configurations were every time chosen arbitrary. That is why the role of each parameter characterizing solidification process remains unclear. Moreover, the question of reproducibility of defects under the same solidification conditions still exists. In addition, most of the experiments suffer from the insufficient knowledge of control parameters that makes difficult their use for validation of models for solidification. These parameters serve as boundary conditions for numerical modeling and their incomplete description leads unavoidably to the errors in simulations. This situation motivated us to develop a setup for benchmark solidification experiments and to perform a set of the solidification experiments which we reported in [7]. Here we presented a comparison between results obtained in a benchmark experiment of solidification of Sn-3%wtPb ingot and its numerical modeling, which was performed in two-dimensional and three-dimensional configurations."

Jan 1, 2012

By Karl-Heinz Daum

Outokumpu Lurgi Metallurgie GmbH, Oberursel, Germany ? give saleable by-products, ? not interfere with smelter performance, ? treat all gas streams simultaneously, and ? comply with environmental regulations. The latest developments in sulphuric acid plant design are presented.

Jan 1, 2002

By Beatriz Ribeiro Nogueira, Vijaya Kumar Rangari, Esperidiana A. B. Moura, Anne Chinellat, Arifa Parveen, Angel Visentim Ortiz

"Composite consisting of ethylene vinyl alcohol (EVOH) with short piassava fibers were prepared by extrusion process and their thermal and morphological behavior were investigated. The EVOH reinforced with 5 and 10 % of pi as sa va (Attaleafunifera Mart) fiber particle, based on the percentage weight ratio (wt %), untreated and treated with a commercial silane coupling agent, were prepared and the influence of fiber loading and the effect of chemical treatment on their thermal and morphological behavior were evaluated by SEM, DSC and TG analyses. Melt flow index (MFI) of the composites have been determined to evaluate the effects of fiber reinforcement on dynamic viscoelastic melt of the EVOH. In addition, piassava fibers characterization by SEM, FTIR, and organic and inorganic composition have also been carried out. The SEM results of the composites showed surface micrographs without microvoids and a good distribution, dispersion and compatibility between the fillers and the EVOH matrix. Concerning the piassava fibers characterization, the results showed that piassava has higher lignin content than cellulose and hemicelluloses, and around 0.7 % of ash with 52 % of silica (Si02). This high concentration of silica is consistent with the SEM analysis of the fiber that showed a large amount of ""silica rings"" encrusted on their surface.IntroductionLately, great worldwide interest has arisen in developing new technologies that enable the use of products with less environmental impact. Effort has been put into seeking natural modifier applications, particularly regarding the use of natural fibers. Special attention has been given to the use of natural vegetable fibers, because of the huge variety of species available. Such vegetable fibers are usually referred to as lignocellulosic materials [1]. This work evaluated the effects of piassava (Attalea funifera Mart.) fiber incorporation in an ethylene and vinyl alcohol copolymer (EVOH). The EVOH belongs to a family of copolymers with excellent gas barrier properties and resistance to organic compounds, which allow its application in different segments, from food packaging to gas tanks. However, EVOH is very sensitive to moisture, and in conditions of high humidity its gas barrier properties, thermal and mechanical properties are affected."

Jan 1, 2012

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

By Jean Igor Margem, Lucas Barbosa de Souza Martins, Frederico Muylaert Margem, Noan Tonini SImonassi, Sérgio Neves Monteiro, Rômulo Leite Loiola

"Fibers of giant bamboo (Dendrocalmus Giganteus) are amongst the strongest lignocellulosic fibers. Although studies have been already performed, limited information exists on the mechanical properties of polymeric composites reinforced with continuous and aligned giant bamboo fibers. This work evaluates the tensile strength of this type of composite. Standard tensile specimens were fabricated with up to 30% of fibers aligned along the specimen's length. The fibers were press molded with a commercial epoxy resin mixed with a hardener and cured for 24 hours at room temperature. The specimens were tested in an Instron machine and the fracture surface analyzed by scanning electron microscopy. The tensile strength increased significantly with the amount of giant bamboo fiber reinforcing the composite. This performance can be associated with the difficult of rupture imposed by the fibers as well as with the type of cracks resulting from the bamboo fiber/epoxy matrix interaction, which prevents rupture to occur.IntroductionDue to growing concern about the ambient impacts from industrial activities, our society is ever more using environmentally friendly materials. In this regard, cellulose-based natural fibers, known as lignocellulosic fibers, become a promising solution. Nowadays, they are being considered as a substitute for synthetic fibers, such as glass fiber, used by the industry on a large scale [1-5]. The application of these natural fibers is also motivated by many advantages like good toughness and less wear of equipment used in the processing of composites. In addition, such composites are environmentally friendly because they are renewable, biodegradable and neutral with respect to C02 emissions, the main responsible for global warming and climate changes. [3,5,6].Lignocellulosic fibers also have some disadvantages in relation to synthetic fibers such as the difficulty of coupling with polymer matrices, due to the hydrophilic character of fiber and the hydrophobic nature of the matrix, as well as dimensional heterogeneity [ 4,5]. This last one is characteristic of the nature of this material and constitutes an obstacle to the use of these fibers in certain projects, especially those that aim high performance. The above mentioned disadvantages are worrisome reasons for the occurrence of reduction in the strengthening capacity, as indicated by the rule of mixtures for composites [7]."

Jan 1, 2013

By Viktor Mukhin

"Among the methods proposed for spent activated carbon regeneration, the most acceptable is, thermal reactivation, because in this case the existing equipment for manufacture of activated carbon can be adapted for this purpose.In order to conduct the process of thermal re-activation of spent activated carbon directly at gold mills, a fullscale drum-type furnace with external electric heating has been developed, i.e. EPV-300 model with a throughput rate of 50 to 120 kg/hour. Its use ensures restoration of the adsorption properties of carbon up to the level of fresh activated carbon with an insignificant (by 0.7%) decrease in strength and with a high (95% to 97%) yield of reactivated carbon.During the recent years, activated powder carbon has been extensively used in flotation processes for treating polymetallic ores at ore treating plants to improve recoveries of main metals (copper, lead, nickel, etc.).Especially large volumes of activated powder carbon are used at the Talnakh concentrator of the Norilsk Mining and Metallurgical Complex in Russia for absorption of residual flotation reagents from recycled water in order to ensure efficient selective separation of minerals with similar physical and chemical properties.IntroductionSorption technology based on active carbons use starts being applied in such an important in the widest sense of the word strategical branch of economics as non-ferrous metallurgy. Thus since the middle ninetieth Russian gold extraction industry began to apply widely the processes of sorption from pulps and solutions by means of high-resistant granulated active carbons. That provided the start of gold ore minefield exploration, increasing of gold extraction from the ore and reducing its loss with the ""tails"" of process. At present more than 40% of Russian gold is extracted with the help of sorption technologies [1].Another field of active carbons application in non-ferrous metallurgy is the processes of non-ferrous ores floatation at ore-mining and processing enterprise. For that purpose powdered (less than l00µm) active carbons are used for providing the effective selection of minerals with similar physicochemical properties. This method not only increases the metal extraction level but provides deeper division of them."

Jan 1, 2008

By Blas Melissari, Stavros A. Argyropoulos

"In this paper a computational approach was employed to estimate the melting of solid spheres immersed in different liquid metals and under different convective conditions. The spheres are made from the same material as the liquid metal. The SIMPLER algorithm was implemented using a three-dimensional system in Cartesian co-ordinates. Experimental validation of the dimensionless correlation was carried out in two fluids with vastly different Prandtl numbers. The dimensionless heat transfer coefficient (Nusselt number) is obtained as a function. of the Reynolds and Prandtl number.IntroductionThere is a paucity of dimensionless convective heat transfer correlations applicable to fluids like liquid metals. The existing correlations cover single Prandtl number metals [l] or at most two different Prandtl number metals [2]. A knowledge of heat transfer rates from particles at high flux levels has become increasingly important to the design of energy transfer systems. Melting of solid particles has been studied extensively as it relates to many engineering and environmental applications, such as materials processing, space applications, water resource and energy conversion. When objects are immersed in a fluid with a temperature higher than their melting point, they melt and produce molten material that then mixes with the surrounding fluid. These objects experience not only size variation but also changes in their shape. This observation is more pronounced when the melting occurs in a forced convective flow.Yuge performed pioneering experimental work on the heat transfer from a sphere to air under mixed convection [3]. He suggested procedures for predicting the Nusselt number. Hieber et al [4] studied the spherical system analytically, but their study was limited to flow with small Reynolds numbers. Many researchers studied the melting dynamics of ice spheres in water at different convective regimes. Aziz et al [5] and Hao et al [6] performed measurements of the heat transfer coefficient in the water system by measuring the melting time of ice spheres in forced convection. Hao et al [7] performed visualization studies of ice spheres melting in water under mixed convection regime. All of this groundbreaking work, however, did not involve the use of liquid metals"

Jan 1, 2004