Search Documents

By K. A. Lewandowski

Agglomeration of ore can be used to immobilize fine particles during heap leaching by agglomerating them into granules. Without agglomeration, the fine ore particles can migrate within the heap, clogging flow channels and producing large areas where access of solution to the ore is very poor. The benefits of agglomeration are well-known in gold heap leaching operations, which can be effectively agglomerated using binders such as Portland cement due to the alkaline leaching solutions used. However, agglomeration has not been very effective in the heap leaching of copper ores, because these ores require an acidic leaching solution. Acid destroys the effectiveness of most binders, causing the agglomerates to disintegrate as soon as the leaching solution is applied. In order to gain the benefits of agglomeration in copper heap leaching, an economical, acid-resistant binder is needed. The two issues that needed to be addressed were: 1) Lack of effective methods for evaluating binder acid resistance before performing expensive, time-consuming, full-scale heap leaching tests, and 2) The vast majority of known binders react poorly to acid conditions, and so a basis was needed for determining which binders are most likely to be acid-resistant. In this paper, the development of two new tests for evaluating binder acid resistance in the laboratory are described. The ?soak test? determines the degree to which agglomerates disintegrate and release fines on contact with acidic solution, measuring the relative quantities of fines released by agglomerates made with different binders under controlled conditions, and serves as a rapid means for comparing large numbers of binders. The ?percolation test? measures several different parameters to determine how a binder is likely to perform in heap leaching: 1) the degree of ?slump? and compaction of agglomerates as they are wetted by acidic solutions; 2) the hydraulic conductivity of the agglomerate bed; 3) the migration of fines through the bed as the solution flows through it; and 4) the quantity of liquid retained in the agglomerates after they are drained. Using these tests, a broad spectrum of binders were examined. Soak testing determined that the most acid-resistant binders were nonionic polymers. Five of these binders were further evaluated using percolation testing.

Jan 1, 2006

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 Dmitri Goljandin, Jaan Kers, Xiangjun Zuo, Lifeng Zhang, Priidu Peetsalu

"In this paper, the mechanical milling of the electronic wastes was carried out. The metal parts and plastic parts were roughly separated. The final plastic powder size could be as small as ~100 µm. Then the pyrometallurgical recycling Printed Circuit Boards (PCB) was executed. The mechanisms of thermal degradation and combustion are investigated using TG/DTA and MS. Some chemical powders, such as Na2CO3, NaHCO3, NaOH and CaCO3 are used to control the exhausted toxic gas such as Br2. Introduction Waste electric and electronic equipment (WEEE), or electronic wastes (E-wastes), has been taken into consideration not only by the government but also by the public due to their hazardous material components [1-3]. From the point of material composition, electronic wastes can be defined as a mixture of various metals, particularly copper, aluminum, and steel, attached to, covered with, or mixed with various types of plastics and ceramics [4]. Precious metals have a wide application in the manufacture of electronic appliances, serving as contact materials due to their high chemical stability and their good conducting properties. Platinum group metals are used among other things in switching contacts (relays, switches) or as sensors to ascertain the electrical measurand as a function of the temperature [5]. Table 1 [6] gives examples of the metal composition of different electronic scraps from literatures. Additionally, non-ferrous metals and precious metals content have gradually decreased in concentration in scraps. The value distributions for different electronic scrap samples are shown in Table 2 [6], where the metal price data are from London Metal Exchange (LME) (Octoebr 2007). It can be seen that for cell phones, calculators, and printed circuit board scraps, the precious metals make up more than 70% of the value, for TV boards and the DVD player they still contribute to about 40%. This indicates that the major economic driver for recycling of electronic waste in industry is from the recovery of precious metals. Behind the precious metals come copper and zinc, while Al, Pb, and Fe are less value. Recycling of electronic waste is an important subject not only from the point of waste treatment but also from the recovery aspect of valuable materials."

Jan 1, 2008

By Huanyu Zhang, Zhancheng Guo, Liqiang Fan, Huiqing Tang

"In this study, a simple process has been developed for zinc oxide recovery from RHF (rotary hearth furnace) secondary dust. The results have shown that a high dissolution efficiency of soluble zinc was achieved with water leach at ambient temperature with a liquid/solid ratio of 10/1 in 30min while 20% of the dust was left as solid residue. The rate of dissolution increased slowly after the dissolution efficiency reached 90%. The leaching process was found to be controlled by external diffusion. After separation, zinc was precipitated in leached liquor by introducing a precipitation agent of potassium hydroxide. The resulting solid was purified and dried at 393K. Zinc powder in the form of ZnO with purity of 98.5 mass% was obtained with an average size of 12.4µm.IntroductionThe RHF (rotary hearth furnace) direct reduction process is widely used in many iron and steel enterprises to deal with various metallurgical dusts [l]. The basic principle of this process is that first various metallurgical dusts (BF dust, EAF dust and so on) are pelletized with a coal reductant, and they are then subjected to a fast reduction using RHF after being dried. Highly metallic pellets are produced and at the same time, nonferrous elements such as Zn, Pb, K and Na are evaporated into the RHF flu gas as secondary dust. Zinc is listed by the Enviromnental Protection Agency as one of the 129 priority pollutants. Therefore, recovering zinc from the industrial wastes is important in terms of enviromnental protection [2-3]. On the other hand, nowadays China is in shortage of zinc resource and the annual output from metal recycle only accounts for some 13% of the total zinc resource. There are many ways proposed to recover zinc from various wastes [ 4-7]. The aim of this paper is to recover zinc oxide from RHF secondary dust by a method with water leach followed by caustic precipitation. This work investigated the influence of the leaching temperature and leaching liquid/solid ratio on the zinc recovery efficiency. The process consisted of three stages: (1) leaching with water; (2) liquor/residue separation; and (3) zinc precipitation in caustic milieu."

Jan 1, 2014

By Laurentiu Nastac

"An advanced casting simulation-based optimization approach was applied in this study to assist in the improvement of the mold design of aerospace components made of A3 56 alloy. By using this approach, mold filling and solidification related defects (including macro-shrinkage and shrinkage porosity) were significantly minimized and hence it helped in cost reduction, performance enhancement and quality assurance of complex A3 56 cast parts.An experimental validation and detailed calibration procedures of the models for prediction of macro-shrinkage and shrinkage porosities were performed using A3 5 6 plates cast in fiiran-silica sand molds using the Prometal's Rapid Casting Technology (RCT) - mold printing technology. Correlations between Niyama values and the pore percentage were also developed. Thus, the severity level of shrinkage porosity can be determined via the Niyama criterion. Predictions were then compared with the macro-shrinkage and porosity measurements in plates of various plate thicknesses and in other commercial A3 56 casting components.IntroductionThis paper describes the process modeling approach used in the development of the mold design technology used to produce assist in the improvement of the mold design of aerospace components made of A356 alloy. Nova Flow&Solid™ software [3] was applied in this study. This casting simulation software was previously validated for several alloys including Ti, steel and superalloys [1-4]. The objective of this paper is to calibrate and validate the simulation software for A356 alloy sand mold castings. For this purpose, an experimental validation and detailed calibration procedures of the models for prediction of macro-shrinkage and microshrinkage (e.g., shrinkage porosities) were performed using A356 plates cast in fiiran-silica sand molds using the Prometal Rapid Casting Technology (RCT) mold printing technology. The details of the RCT technology are shown in Fig. 1 [5]. Prometal's RCT technology is used for rapid production of sand molds and cores directly from CAD files. The RCT technology relies upon ink jet printer technology to selectively bind the grains of sand to create three-dimensional sand molds and cores. Mold filling and solidification modeling as well as stress analysis are typically performed to properly design the casting and the rig system of each prototype component."

Jan 1, 2012

By L. Katgerman, E. N. Straatsma, Suyitno

"Single-roll strip casting process is studied using computational fluid dynamics which takes into account fluid flow, heat transfer and solidification. The computational model is based on the conservation Jaws of momentum, energy and continuity. Correlation of strip thickness, solidification zone length, and puddle shape on single-roll strip casting of Al-1 %Mn is explored. Feeding pressure and roll speed are investigated. The results show that the··strip thickness slightly increases with pressure, similarly the length of solidification zone. The variations of strip thickness and solidification zone length with roll speed show a sharp decline for strip thickness and slight decline for the length of solidification zone with increasing roll speed. The constraint and free-jet flow have different feature in term of flow field. Severe turbulence is observed on the free-jet flow.IntroductionThe near-net shape casting of strip metals is a demand nowadays. The demand is particularly stimulated by the challenge to become more competitive through enhanced performance. The improvement in the existing processes and new innovative technologies are introduced by the metal industry to gain better product quality, more efficiency in energy consumption, low throughput, yield and operating costs [1-3].There are many advantages that can be obtained by the direct casting of strip. The most prominence is the elimination of hot rolling. Beside that the high rate of heat extraction associated with strip casting offers the possibility of a finer, Jess segregated cast structure. The microstructure will result in the improvement of mechanical properties compared to conventional material, or alternatively the opportunity of using grades of metal outside the normal range for continuous casting.The concept of single-roll strip casting has been difficult to commercialize, because of the complex interactions between fluid flow, solidification, shrinkage, and stress, which lead to serious quality problems. Besides that, the quality and the thickness of the strip are affected by the thermal properties of the strip, roll cooling conditions, roll geometry, and other process parameters. To understand how these parameters affect the strip formation, some researchers have modeled the process [4]."

Jan 1, 2004

By R. Winand, M. Degrez, C. Temmerman

"The influence of the copper electro crystallization inhibitors (mainly thiourea, gelatin and chloride ions) is studied in a new fully automatic pilot plan. This paper describes the conception and the building of this plan. The new approach is to reproduce the experimental conditions observed in the industry with the three additives present simultaneously in the electrolyte and secondly to study the influence of a slight modification of the concentration of one inhibitor, the others being present in the electrolyte with their industrial nominalconcentrations.1. INTRODUCTIONDespite the fact that gelatine, thiourea and chloride ions have been used in copper electrorefining for a long time, precise knowledge concerning their influence on the cathode deposit, metallographic structure and associated properties is still lacking.Many authors studied the influence of each additive separately, or of two added at a time. Only a few authors studied the combined influence of the three additives added simultaneously. The general conclusion that can be drawn is that the combined influence is far from that forseen from the influence of each additive separately, or even from two additives used at a time. Moreover most of the experiments described in the literature were performed by adding all additives at once initially. It is however, well known that gelatine looses a great part of its activity during the first half hour due to degradation by sulfuric acid (as shown by the cathode overpotential drop). Thiourea is rapidly replaced by a number of degradation mole,cules and complex ions including cations from the solution, changing even the equilibrium between Cu, Cu(I) and Cu(II).Chloride ions are consumed by precipitation.A number of successive research projects [1-9] led pregressively to the concept that, in order to obtain reproducible results representative of industrial cathodes, it was necessary to simulate as far as possible industrial conditions. It was essential that all additives were added continuously during the electrolysis, with, as consequence, a continuous bleed.The purpose of this paper is to describe the concept of a new fully automatic pilot plan for copper electrorefining and to present the first results."

Jan 1, 1997

By Hye-Sung Kim, Dong-Wha Kum, Gyeungho Kim

"Mechanical alloying is an effective way to finely distribute inert dispersoids in AI-TM (TM is a transition metal element) systems. It is considered that high melting point aluminides are formed by precipitation from the supersaturated aluminum matrix. The analysis is based on the fact that much higher content of TM than the solubility limit can be dissolved in alpha aluminum during the high energy ball milling. Nonetheless, the role of undissolved TM particles affecting the formation of aluminides is not suitably considered. In this paper, authors present experimental observation on the formation of Ab3Ti particles from mechanically alloyed AI-Ti alloys in the hyper-peritectic region. This study showed that, in the mechanically alloyed AI-20wt%Ti specimen, intermediate phase of cubic Ab3Ti and tetragonal AIz4Tis formed at 300 - 400°C and 400 - 500°C, respectively, before the MA-state reaches to the global equilibrium at higher temperatures. The formation behavior of Lh- Ab3Ti is interpreted by interdiffusion of Al and Ti in solid state based on the fact that large amount of nano-sized Ti particles exist in the milled powder. Present analysis indicated undissolved Ti particles of nanosize should have played an important role initiating the formation of Ab3Ti phase during annealing.IntroductionInterest in the hyper-peritectic AI-Ti alloys is based on industrial demand for high-modulus and high-temperature aluminum alloys. Earlier works on hyper-peritectic AI-Ti alloys with 4 to 12wt%Ti show that these alloys are strong at ambient temperature and maintain high strength above 300°C when titanium-trialuminide (e.g., Ab3Ti) is finely distributed in the aluminum matrix [1,2]. High melting point and high stiffness with low density of AbTi make the AI-Ti alloys strong with greater thermal stability while keeping weight savings as much as possible. Titanium in aluminum shares other merits of transition metal additions because Ti solubility in Al is low (i.e., 1.l5wt%Ti at 665°C and virtually zero below 400°C), and fine dispersion of Ab3Ti particles is readily accomplished and resists grain coarsening effectively."

Jan 1, 1996

By Yingtao Zhang, Shaofeng Du, Yiming Rong, Wenjun Zhao, Gang Wang

"20Cr2Ni4A steel is a kind of high quality steel mainly used for manufacturing high-duty gears in the world. The high-duty gear with good performance must have wear and fatigue resistance properties. In order to get the good properties, the high-duty gear needs a high hardness gear surface and a good hardness gradient along the depth direction. In this paper, the samples were designed and a vacuum carbonitriding process was put forward to improve the surface hardness of parts for 20Cr2Ni4A. The process contained carbonitriding, quenching, cryogenics, and tempering process. The surface hardness and hardness gradient of carbonitrided samples were measured and the good microstructure was gained. The surface hardness is 67.SHRC and the case depth is 1.2mm.IntroductionSteels are widely used in industry, but the fatigue strength and the wear resistance of steel is much low. So the heat treatment process is put forward to improve the mechanical properties of steel. It can be improved by high-energy heat treatment methods for medium-carbon and highcarbon steel. Those methods will not alter the chemistry of the base metal [ 1].For low-carbon steels, carburizing and quenching should be used to improve the steels' mechanical properties, especially the surface properties. Compared with the carburizing, carbonitriding has more advantages, such as a short production cycle, low temperature and small deformation of parts. Carbonitriding is a modified form of gas carburizing, rather than a form of nitriding. The modification consists of introducing ammonia into the gas carburizing atmosphere to add nitrogen to the carburized case as it is being produced. Nascent nitrogen forms at the work surface by the dissociation of ammonia in the furnace atmosphere; the nitrogen diffuses into the steel simultaneously with carbon. Typically, carbonitriding is carried out at a lower temperature and for a shorter time than is gas carburizing, producing a shallower case than is usual in production carburizing [2]. As a material surface strengthening technology, carbonitriding has been widely used in the production [3]. And vacuum carbonitriding process is better than carbonitriding, because the vacuum carbonitriding temperature can be higher than carbonitriding without surface oxidation."

Jan 1, 2014

By Michal Rehor, Vladimir Cablik, Peter Fecko, Tomas Lang

"1. Introduction The North-Bohemian Basin area is known for its largest Czech brown coal deposit. About 50% brown coal reserves have been exploited in the North-Bohemian Basin by the mining company of Severoceske doly, a.s. (North Bohemian Mines, j.s.c.) today. The opencast mining of brown coal naturally led to vast landscape damages. Therefore reclamation work has acquired great significance. The specific feature of Severoceske doly, a.s. mining is the fact that the mining has been realized in two geologically absolutely different localities. This fact demands even rather different methods of reclamations. The main problem at Doly Bilina localities is the occurrence of overburden rocks from the series of rocks of coal seams. These rocks are texturally light but large amounts of coal (cca 5 %) and sulphur (cca below 3 %) which makes the soil reaction extremely acid. If they appear on the surface of the dump, they create a phytotoxic area, reclamation of which requires special methods. Rocks from Doly Nastup Tusimice localities are more suitable to reclamation use, but texturally extremely heavy rocks with large fraction of physical clays appear there that can generate a sterile soil area. Their reclamation requirements are completely different from those on Doly Bilina phytotoxic areas. That is the reason of the application of some non – traditional restoration methods. This report briefly summarises the experience in application of fertilizable soils, power plant stabilizer, power plant ash and aerial sowing of charlock. The results are documented by the monitoring of the physical, mineralogical and pedological parameters of rocks in testing areas.2. Properties of Overburden Rocks in Opencast Mines Bilina and Libous The reclamation work methodology in the North Bohemian Basin is above all determined by the properties of overburden rocks which occur in the top horizon of the reclaimed sites. The research of the rocks reclamation properties dealt with four current mining localities in the central part of the basin. It concerned the Bilina and Libous mines. This chapter states the stratigraphic status properties of these sites with respect to reclamation availability. The total status of the area of interest is shown in the figure No. 1."

Jan 1, 2008

By Vladimir Lobanov, Pritchinm Alexander, Nikifor Ageev

"Sulfuric anhydride is one of the most voluminous technological emissions. The possibility of high-temperature SO2 oxidations without catalyst in presence of calcium-bearing filling materials (CaO, Ca(OH)2 and CaCO3) with obtaining of binding material on the basis of waterless calcium sulfate is studied. Due to application package HSC-4 the thermodynamic analysis of the specified interactions is made and following conclusions are drawn: 1) Reactions are feasible in the all range of investigated temperatures (400 – 1000 °?); 2) The best results should be expected at use of ???; 3) The heat of reaction does possible autogenous behavior of process. The researches have shown: 1) Practical possibility of the process; 2) SO2 oxidation without the catalyst is feasible in presence of ???, Ca(OH)2 and CaCO3; 3) The optimum temperature range is 600-800 °?; 4) The content of waterless calcium sulfate in a product reaches 48% that makes it possible to use as the binding material; 5) At excess of ??? the degree of SO2 collection is nearer to 100%. Introduction At processing of sulfide raw materials in metallurgical furnaces the significant amount of sulfur, mainly in the form of sulfuric anhydride is escaped. Rich gases (SO2>3 %) are used for the sulfuric acid or element sulfur production. Chemism of sulfuric acid manufacturing is based on catalytic high-temperature oxidation of anhydride. Poor gases of metal works (SO2 =2,5 %) and power combustion units (SO2 =0,5 %) after clearing discharge into the atmosphere. Commonly, to recovery of weak sulfuric anhydride the chemical and physicochemical methods are applied. A few chemical ways of recycling sulfur dioxide are applied practically. In a number of methods for SO2 recovery a pulp of metals oxides (magnesium, zinc, etc.) with formation of sulfites is used. In other case sulfuric anhydride is catch by weak sulfuric acid in the presence of an oxidizer (pyrolusite ore). Methods of absorption SO2 by solid sorbents, (carbon fibers, silica gels, zeolites) are known and put into practice. Regeneration of the saturated sorbents is realized by thermal decomposition or extraction. Obtained as a result high-concentrated solutions are a commercial product."

Jan 1, 2008

By Nobuyuki Masuda

In Japan, the municipal solid waste, which amounts to 50 million tons, is generated every year and most of it is incinerated. The fly ash from the municipal waste incineration (the primary fly ash) contains heavy metals, such as lead and zinc, etc., and dioxins. In case of melting, the fly ash from the process (the secondary fly ash) contains high concentration of heavy metals (e.g., Zn; 1-20%, Pb, 1-10%). Metal Mining Agency of Japan launched a four-year project in 1999 to establish the integrated technologies to recover the valuable metals from, and to decontaminate, the primary and secondary fly-ashes in the practical scale by utilizing the existing metallurgical processes and facilities, along with the energy saving. The segregation, flotation and chemical treatment are applied to the treatment of the primary fly ash. The secondary fly ash is treated with MY (Mitsui-type blast furnace) Process after the chlorine removal to recover the heavy metals in the ash, In this paper, the segregation and flotation process for primary fly ash and MF process for secondary fly ash are explained. The main results of experiments done from 1999 to the mid of 2001 to design the pilot plants and to optimize the operating conditions are described. The main results of the experiments are as follows: - The segregation reaction of Cu was confirmed by the experiment on the treatment condition of 800 and 900`C with adding oil cokes and water to the primary fly ash, and 99.98% (toxicity equivalent) of the dioxins were decomposed by the treatment. - Washing tests of secondary fly ash to feed MF resulted that more than 70% of chloride were removed, but still lower than expected, and agglomeration tests were successful by the results of the sufficient strength of briquettes produced though a little more binder for the agglomeration is required than usual operation. - Smelting experiment by downsized MF showed that valuable metals, such as zinc and lead, are recoverable in the furnace dust. Recovery ratios, Zn: 58% and 67%, Pb: 74% and 83%, are accomplished.

Jan 1, 2002

By Rzyman Michal, Nakamura Takashi, Shibata Etsuro, Grabda Mariusz, Oleszek-Kudlak Sylwia

"Tetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in many materials such as plastics and textiles. Thermal degradation of BFR containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3. Our thermodynamic considerations indicate that these gases can act as bromination agents for metallic oxides such as ZnO, Cu2O, CuO, PbO and FeO. Moreover, these metallic oxides have the thermodynamic tendency to brominate easier than does Sb2O3. The aim of this study was to investigate experimentally the reactivity of ZnO with 1) HBr originating from the thermal decomposition of TBBPA and 2) SbBr3, which is formed during thermal degradation of brominated flame retardant plastics. The thermal treatments of the mixture of compounds of interest were investigated by thermogravimetry coupled with mass spectrometry.IntroductionTetrabromobisphenol A (TBBPA) and many systems based on the synergistic effect of brominated organic compounds with Sb2O3 are extensively used as effective brominated flame retardants (BFRs) in materials such as plastics and textiles. For instance, 4.5 million tons of flame retardant plastics containing BFRs are produced in Japan each year. Thus, in thermal treatments such as the incineration and melting of solid wastes, BFR containing plastics are intentionally or unintentionally included in the wastes. Thermal degradation of BFR-containing plastics leads to the formation of hydrocarbons and gaseous compounds such as HBr and SbBr3 [1-5]. Our thermodynamic considerations [6] indicate that heavy metal oxides such as ZnO, Cu2O, CuO, PbO and FeO should easily react with HBr prior to Sb2O3 and also with SbBr3, the main gaseous product in the thermal decomposition of TBBPA, forming low boiling point metallic bromides suitable for the volatile separation of heavy metals. The metal oxides are also expected to qualitatively and quantitatively affect debromination and decomposition of the flame retardant."

Jan 1, 2008

By Anurag Tripathi, J. K. Saha, S. K. Ajmani, J. B. Singh

"The quality of steel is a major concern in the metallurgical industry. The control of liquid steel temperature can enhance the level of cleanliness in steel. Ladle is one of the major vessels used to transfer liquid steel between different stations. The heat transfer phenomenon taking place in this vessel needs to be monitored for controlling the liquid steel temperature. A CFD model was developed for prediction of liquid steel temperature during complete process cycle of ladles in direct heats. The model was validated with liquid steel temperature measured at on-line purging station and tundish during teeming from one of the actual steel plant. The accuracy of model was 96 %. The results obtained show insignificant effect of slag thickness, tapping temperature and ladle life on liquid steel temperature in the ladle. However, the importance of initial refractory temperature was noticed. The CFD model developed in present work can generate the thermal history of liquid steel and refractory walls of any ladle at any stage.1. IntroductionThe control of liquid steel temperature is desired to achieve required steel quality. The low casting temperature is detrimental and may result in nozzle blockages due to premature solidification in the tundish. The phenomenon of heat losses taking place in ladles needs to be understood for prediction of liquid steel temperature. The assessment of thermal profile of liquid steel from BOF converter to caster can be done through consideration of heat losses at all points. Hlinka and Miller [1] showed that the ladle pouring temperature varies due to heat losses from molten steel into surrounding refractory layers. The phenomenon of thermal stratification was numerically simulated by Ilegbusi and Szekeley [2]. The effects of slag cover on heat loss and liquid steel flow in ladle before and during teeming to a continuous casting tundish was numerically simulated by Chakraborty and Sahai [3]. Investigators also developed some simple models to predict the steel temperature for some of the processes taking place in ladles [4-9].The present work is an effort to generate the full information about the temperature drop taking place in any ladle throughout its process cycle. This information can be used to predict liquid steel temperature and to take decisions to minimize heat losses."

Jan 1, 2012

By Tadafumi Adschiri

"Supercritical water can provide an unique reaction atmosphere for synthesizing metal oxide nanoparticles. Due to the drastic change of properties of water around the critical point, including density, dielectric constant and ionic product, the reaction phase with O 2 or H2 gas and the reaction rate and equilibrium can be varied to synthesize new materials or define particle morphologies. In this work, hydrothermal crystallization experiments are performed with several types of flow apparatus that allow convenient manipulation of variables such as temperature, pressure, and residence time. Key features in the flow modes and material preparation are discussed. The proposed supercritical hydrothermal synthesis method has the following desirable features: i) nanoparticles can be produced, ii) morphology of the produced particles can be controlled with small changes in pressure or temperature, and iii) a reducing or oxidizing atmosphere can be applied by introducing oxygen or hydrogen or other gases. An overview of this method is given for functional material synthesis of significant industrial interest including barium hexaferrite magnetic particles, YAO/Tb phosphor fine particles and lithium cobalt fine crystals.IntroductionHydrothermal crystallization, a method of metal oxide formation from metal salt solutions, is typically used at temperatures ranging from 373 K to 473 K. We are developing a new process for hydrothermal crystallizations that uses temperatures in the range of 673 K to 723 K, which is just above the critical temperature of water1 • 8 • In this work, we refer to this process as supercritical hydrothermal synthesis. The supercritical state of water allows one to vary reaction rate and reaction equilibrium by shifting the dielectric constant and solvent density with pressure and temperature. From of our research on material production in supercritical water, we have identified the following specific features of the supercritical hydrothermal synthesis method: (i) ultrafine particles can be produced, (ii) morphology of the produced particles can be controlled to some extent with pressure and/or temperature, and (iii) a homogeneous reducing or oxidizing atmospheres can be provided by introducing gases, such as O 2, H2, H2O 2• and so on.1"

Jan 1, 2000

By Noboru Masuko, Sachiko Ono

"The structure and composition of anodic films formed on aluminum in a borate solution have been investigated by using TEM and SIMS with respect to the effect of current density and electrolyte temperature. The film is composed of a boron-containing outer layer and a boron-free inner layer with disc-like crystals present at the interface. The thickness of the film formed at constant current density up to an identical voltage, decreases with increasing current density. The thickness increases remarkably with elevated temperature. The transport number of Al3+ estimated from the thickness ratio .of the cuter to the inner layers is 0.4 when the film is formed at the current density of 20 Am-2 at 60°C. It increases slightly with increasing current density and decreases significantly with increasing temperature. Content of boron in the outer layer increases 1.5 times when current density .increases 10 times. These changes in film structure and composition with electrolysis conditions must have a significant role in the determination of electric properties of anodic alumina films as a capacitor material.IntroductionThe growth of anodic alumina film in ·a neutral electrolyte proceeds at both film/electrolyte and film/substrate interfaces giving a duplex structure. The oxide layer formed at the former interface includes electrolyte anions while a-pure alumina layer is formed at the latter interface. The thickness ratios of each layer respectively represent transport numbers of Al3+ and 0 2 - (1). The film thickness and the incorporated anion content as well as transport numbers of both ions must affect the dielectric properties of the film as a capacitor material. However, the correlation between film structure and electrolytic conditions is not fully understood (2). For the further clarification of anodic film growth mechanism, more detailed characterization of anodic films in relation to electrolytic conditions is advantageous. In the present paper, therefore, the effect of current density and electrolyte temperature on the microstructure and composition of anodic barrier films formed in a neutral borate solution was studied. The films were characterized by direct observation using transmission electron microscopy (TEM) and depth profiles of constituent elements obtained by secondary ion mass spectroscopy (SIMS)."

Jan 1, 2000

By P. C. A. Maia, J Alexandre, F. A. J. Saboya, A. R. G. Azevedo, G. C. Xavier

"This work shows the characterization of clay and the granite waste by-product from the sawing process of the granitic blocks, used as raw material for brick ceramic. Besides, shows the degradation of the ceramic material obtained with different by-product contents in the waste after lab test degradation, is investigated. The clay is obtained from mine use areas of ceramic industry in Campos-RI and the waste is originating from of the area of Cachoeiro-ES, an important center of decorative stone in Brazil. The mixes were made by the addition of 0% up to 10% of the waste in the raw material. After drying and firing up to 900°C, obtained prismatic pieces were considered intact. Physico-mechanical properties were obtained from wet and drying tests in laboratory considering 50 and 150 cycles. The results showed that the use of powder byproduct has a considerably influence on the weathering and strength of the material.IntroductionThe ornamental rocks and coating defines the most promising areas of business in the mineral sector [l]. In this context, the Espirito Santo appears as the main Brazilian state in production and export of ornamental rocks, representing 47% of national production [2] which in tum is one of the economic sectors most representative of this State, due of its transport logistics and port vocation that facilitates the export of such products.It is estimated that the state of Espirito Santo there are approximately 1,200 companies dedicated to the activities of ornamental rock by providing 20,000 direct jobs [ 1]. These mobilize support activities, such as companies that provide machinery, equipment and supplies for industries, including service providers for maintenance.However, the production of rocks produces about 15,000 tons of granite waste/month [3] only in the municipality of Cachoeiro ltapemirim-ES. This is justified by the presence of more than 500 extraction industries, cutting and processing of stone, with about 900 looms, waste generators.According to [4], there is great potential for the use of granite waste in red ceramics introduced for the manufacture of bricks, blocks structural ceramics. and other ceramic products, especially when evaluated on exposure to weathering."

Jan 1, 2014

By Carla Lupi, Alessandro Pescetelli

"Spent lead battery recycling still shows few weak points in the achievement of a 100% recycling of different waste matters and by- products arising from the recycling process. Some of said problems are dealing with aqueous streams outgoing the recycling plant, and more particularly, a) the waste waters discarded from the breaking and separation unit, b) purification of the spent electrolyte drained from waste batteries and upgrade to a quality compatible with full re-use by the batteries’ manufacturers, c) purification of the mother liquors discarded in the sodium sulfate crystallization process so to produce a salt of commercial grade. All of the above listed problems have been satisfactorily overcome applying an electrochemical process that, through different process conditions and parameters, is able to remove the harmful impurities that hinder the successful commercialization of such by products, or, at least, that can avoid heavy and expensive treatment plant and operation.IntroductionAlmost 100% of commercial lead and lead alloys produced by secondary lead plants is recycled to the new lead accumulators manufacture. The other by-products and residues produced through the lead recycling process may be classified into two groups:a) matters reusable in the new accumulators production processb) matters produced as a result of various reagents and additives used in the recycling process, to be sold to different market sectorsQuality and saleability of by-products are significant points for the economics of the secondary lead plant operation, because, if said by-products are not saleable, they are just wastes, so offsetting potential revenues, and, at the same time, adding a heavy burden to operating cost, like disposal cost [1]. When looking at a typical, modern lead scrap batteries recovery cycle, it is quite evident that we are still rather far from dealing with a waste-less technology (fig.1).The group a) includes 3 by-products produced through the breaking process: among those matters the polypropylene only usually reaches a standard quality suitable for sale to lead manufacturing sector or to other sectors as well. The other two by-products, electrolyte and separators, do not still reach, through a viable and effective regeneration process, a quality standard sufficient for their re-use in the lead batteries sector ."

Jan 1, 2008

By Arvind Thekdi, Cynthia Belt2

"Waste heat from industrial operations in metals industry represents 20% to 50% of the total energy used in most manufacturing plants. Reduction and recovery of waste heat offers the most attractive and cost effective method of reducing energy intensity for an industrial plant to meet corporate energy saving goals. It is possible to reduce or recover 30% to 60% of the available waste heat by using conventional and readily available technologies. Projects to reduce or recovery waste heat may offer less than 3 years payback to as short as a few months. This paper presents information on most commonly used methods for waste heat reduction and recovery in the metals industry operations. It describes the methods and use of analysis tools that would allow a user to estimate energy savings, CO2 or GHG reduction potential, and economic benefit and includes appropriate case histories.Waste Heat SourcesSources of waste heat abound with the metals industry. While the overall quantity of energy is high, the sources are distributed throughout a plant. The largest source within the metals industry is within furnace exhaust / flue gases. This includes the high temperature gases from burners in process heating such melting, calcining, and sintering operations. It also includes lower temperature gases from heat treat, dryers, and heaters. Lower temperatures are also found after post processed hot gases. This could include heat left after heat exchangers, regenerative systems, thermal oxidizers, and emission control systems. Other hot gases include air used in direct and indirect cooling.While waste heat in form of exhaust gases is readily recognized, waste heat can also be found within liquids and solids. Waste heat within liquids includes things such as cooling water, heated wash water, and blow down water. Solids can be hot product at discharge after processing or reactions are complete. Indeed, not only is energy wasted in the hot metal that slowly air-cools, but additional energy may be used in providing air or water-cooling to increase the speed of cooling. Other waste heat sources are not as apparent and include things like hot surfaces, steam leaks, boiler blow down water, etc. Table 1 and Figure 1 show several major sources along with the temperature range and characteristics of the source."

Jan 1, 2011

By M. Rockandel

"Universal Dynamics Ltd. of Vancouver, Canada has developed, patented and commercialized the ""REMERC"" process for the treatment of mercury contaminated sludges and soils. Mercury is extracted into an acidified and oxidizing, sodium chloride brine solution. REMERC was initially developed to treat mercury contaminated EPA listed wastes (K106) generated by the chlor-alkali industry. More recent work has expanded the capability;' of REMERC to include remediation of mercury contaminated sites, equipment and building materials.In the process mercury is currently recovered from solution by cementation on iron powder in an agitated reactor. The process recovers high purity elemental mercury (99.9% purity). Cementation typically recovers about 90-95% of the mercury in 30 minutes. Higher recovery is not necessary because of the recirculation of the leach solution. When treating highly contaminated chloralkali wastes (5-13% mercury content), REMERC will reduce the mercury laden solutions from 400-1,000 mg/L mercury to 50-100 mg/L. In the treatment of less concentrated wastes «1,000 mg/kg mercury) such as those encountered in site remediation, the treated solutions will generally contain 10-20 mg/L mercury. Cementation while being simple and able to achieve the required recovery has the. undesirable properties of; requiring a solid-liquid separation and adding iron to solution which must be precipitated, ultimately increasing the weight of residue to landfill. .The potential advantages of electrolysis were recognized early in the development of REMERC. Mercury electrolysis is well known in gold and chloralkali processing. Initial testwork utilized a liquid mercury cathode and a coated titanium anode both common to chloralkali producers. The mercury cathode appeared susceptible to polarization and solution impurities significantly affected performance. Agitation of the mercury pool improved performance but it was still not possible to achieve the reduction objectives. Current efficiencies were low, near 10%, and it was apparent that a relatively large cathode pool would be required to limit the current density. A number of electrode combinations with and without a membrane were then tested in a vertical electrode' configuration but the desired performance was not obtained."

Jan 1, 1997