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By Hongxu Li, Pu Liu, Hao Bai, Daqiang Cang, Lihua Zhao

"Coal, as the main energy in ferrous metallurgy, is consumed on a large scale and great amount of CO2 is emitted likewise. In this paper, a model, based on carbon balance, was developed for CO2 emission analysis, with data obtained from a typical integrated steelworks in China. The result shows that, CO2 emissions increase almost constantly with the growth of steel production. However, coals of different classes and product variety in the steelworks exerted an influence on CO2 emissions. Furthermore, three scenarios, including natural gas instead of coal for power generation, EAF process partly replacing integrated steelmaking, and feasible techniques applied to achieve lowest process energy consumption (FLPEC), were assumed to seek possible ways of carbon emission reduction. The result proves that the second scenario is most effective. If 40% of the steel product could be from EAF process, CO2 emissions would be reduced by 45.07%.IntroductionGlobal warming has become a global environmental problem, which is generally caused by excessive emission of greenhouse gases, such as CO2, generated from human activities and industrial processes. It is estimated that about 7% of global CO2 emissions was from iron and steel industry. Further, if the ore and coal’s mining and transportation are included, the CO2 emissions would reach 10%[1]. In general, the relationship between energy saving and CO2 emission reduction is positive correlation. However, in iron and steel enterprises, due to different types of energy resources like coal, heavy oil, natural gas, the consumption of which will generate different amount of CO2, are used, different energy consumption structure in iron and steel enterprises will lead to difference of CO2 emissions.In order to assess the CO2 emission reduction potential of China’s steel industry, Ke Wang etc.[2] developed a model using LEAP software to generate 3 different CO2 emission scenarios for the industry from 2000 to 2030. LEAP is a scenario-based software tool for integrated energy-environment and greenhouse gas mitigation analysis. The amount of CO2 emissions was obtained by the following equation:"

Jan 1, 2011

By Reza Rahimi, M. Nili Ahmadabadi

"Because of high cost and shortage of primary resources of Ni-base superalloys, revert alloys can be used as a part of charging materials for production of superalloys ingots. The current study is based on recycling of IN738LC, a Ni-base superalloy, using 30% and 50% reverted alloy and balanced amount of virgin raw materials. Therefore, it has been attempted to cast an alloy with references to standard chemical composition and mechanical properties. After charging and casting in vacuum melting furnaces, chemical composition verification and non-destructive tests (i.e. Penetration and Radiography Tests), quality of samples were evaluated at elevated temperature by stress-rupture test. Results acquired from chemical composition and mechanical test indicate that cast ingots using 30% and 50% reverted alloy is reliable and consistent with the quality control requirements.IntroductionIn recent years, there have been many fluctuations in cost and availability of raw materials which are extremely determining in Ni-base superalloys production. Accessibility to the high purity metals such as Cobalt, Molybdenum, Tantalum, Niobium and etc. have been problematical during the past decades. Therefore, shortages of critical raw materials beside the economical considerations motivated the alloy suppliers and investigators to study and find alternate sources such as reclamation and recycling of scraps [1].There are a lot of reasons for the necessity of recycling; perhaps the most justifiable one is that consumers themselves produce scraps. For example, the weight of a finished superalloy product could be less than one-third of the cast alloy weight and in the case of complicated machined parts; this portion may reach to one-tenth [2]. High values of constituents, reduction of energy consumption and environmental concerns have all strengthened the obligation of recycling in Ni-base superalloys.Because of the high degree of risk in usage of improper materials for production of turbine blades, a delicately controlled program for recycling is needed. Depending on the type of scraps, this program can define the recycling procedure, required instruments, allowable percentage of scrap for usage and finally confidence level of the process."

Jan 1, 2012

By Y. Iguchi, T. Narushima, T. Shiozawa, M. Maruyama, R. Arashi

"In situ observation system for thermal oxidation using Raman spectroscopy' was constructed, and oxide films formed on liquid pure Al and Al-Mg alloys (Mg contents = 1 and 4 mass%) were analyzed at room temperature to 1273 K in dry oxygen. In situ Raman spectra of the surface of a liquid Al-:-4mass%Mg indicated the formation of MgO • AlP3 (spinel) as oxidation products, while a -AlP3 and MgO • Alz03 (spinel) were observed on a liquid Al-1mass%Mg alloy. It was suggested that the formation of MgO film affected oxidation behavior of these alloys.IntroductionLiquid aluminum alloys are cast to ingots mainly by the continuous casting process. It is well-.known that surface cracks could be caused by oxide films formed on the surface of melt during continuous casting and defects due to the film. With regard to oxidation behavior of liquid aluminum alloys, many investigations l -s have been carried out from the view point of formation of ceramic metal composites(CMC) which are expected as cutting tools and structural materials 1.2. It is very important for reasonable continuous casting and CMC formation processes to elucidate oxidation behavior of melts.Oxidation behavior of materials generally depends on compositions and properties of oxide films formed on the surface. If in situ observations of oxide films are available during oxidation, evaluation of oxide films and interpretation of oxidation mechanism could be expected. Laser Raman spectroscopy is one of the most appropriate techniques for in situ observation of oxide films under various atmosphere at high temperatures. The authors have discussed the effects of atmospheres and sample compositions on oxide film formation mechanism on Fe-Si alloy6 and SiC-B4C composite7 on basis of an in situ observation by Raman spectroscopy. In spite of many previous studies, systematic and clear explanations have never been gotten on oxidation behavior of liquid aluminum alloys. And no in situ observation has been made except for transmission electron microscopy(TEM) and X-ray diffraction(XRD)."

Jan 1, 1996

By Takeshi Yoshikawa, Kazuki Morita, Kunitoshi Matsunaga

"In metallurgical grade silicon (MG-Si), most impurities mainly exist at the grain boundaries and distribute in silicon grains at extremely small contents. Grain boundary phases in MG-Si transform into liquid above the eutectic temperature, and migrate towards high temperature regions when heated under a temperature gradient. With the migration of all liquid phases in MG-Si to the surface, the impurity contents will be decreased less than their solubilities in principle.In the present work, the fundamental research was conducted to discuss the possibility for purification using the liquid phase migration technique. The purification limit was estimated by thermodynamic calculations, and metallic impurities were estimated to be effectively removed except for Fe and Al. The migration behavior of the liquid phase in the synthesized silicon substrate was investigated by unidirectional heating under infrared radiation at 1523-1548 K, and the proceeding of migration was confirmed. The migration velocity was 1.4--2.0xl0-7 mis, and found to be controlled by the liquid phase diffusion.IntroductionPhotovoltaic energy is one of promising energy resources in a sustainable society because of its inexhaustibility and cleanliness. Although the production and installation of solar cells have increased significantly during the last decade, the cost of solar cell installation is still high. To enable the widespread use of photovoltaics and for the photovoltaic electricity price to reach grid parity, a low-cost and abundant feedstock of solar grade silicon (SOG-Si) is essential. Recently, a modified Siemens process and a fluidized bed reactor process were developed to address the cost and energy issues associated with the conventional Siemens process. However, their cost reduction potential is limited because of the large energy consumption needed to convert silicon into gaseous compounds. Purification of silicon through metallurgical routes offers a promising way for producing SOG-Si from metallurgical grade silicon (MG-Si), because it enhances productivity and can also lower the process costs. Although several metallurgical processes such as directional solidification [l ], vacuum refining [2-4] and plasma oxidation [5-7], have been developed, processing times and refining efficiencies still have to be optimized."

Jan 1, 2013

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 J. D. Zhu, T. Ohmichi, H. Yasuda, S. Kashiwai, I. Ohnaka

"Since the casting process affects the properties of castings, its computer simulation has been greatly developed in the last decades. This paper presents our recent works, especially on mold filling simulation, because most casting defects such as porosities and inclusions that greatly affect the properties originate during mold filling. The first topic is the mold filling simulation with consideration of cavity pressure change during mold filling, including direct observation of flow phenomena with X-ray and pressure measurement. The second .one is the mold filling simulation in the lost foam process, in which gasification of polystyrene pattern and gas outflow through the coating and mold have been considered. The simulation can predict not only the mold filling sequences but also periodical vibration of the gas layer between the melt and pattern. The third one is the comparison of simulation of Al melt flow in a metallic runner and direct observation through a transparent mold, showing that the entrapped gas or inclusions is expelled ahead through the melt and its simulation needs very fine meshes. These examples show that the comparison of simulation and observation is very important to develop the numerical simulation further.IntroductionThe mechanical properties of castings are greatly affected by casting defects such as porosities and inclusions, and solidification structure. Although recently the structure simulation has greatly progressed [1-4 ], the application in plants is very limited, because the structure is mostly determined by chemical compositions and cooling rate, enabling us to estimate it from the structure of past similar castings without simulation.On the other hand, the casting defects often vary with each casting or time. Among the defects, porosities and inclusions are main causes to deteriorate the properties and mostly originate during mold filling. Therefore, a lot of efforts to simulate the mold filling and estimate those defects have been made in the last decades [l,5,6]. These efforts have been mostly to develop numerical techniques to solve the Navier-Stokes equation. However, the flow phenomena in molds have not been well understood, because the direct observation of the flow phenomena in mold is not easy. This means the accuracy of the simulation is still not clear."

Jan 1, 2000

By Isabela Leao Amaral da Silva, Felipe Perisse Duarte Lopes, Alice Barreto Bevitori, Sergio Neves Monteiro, Ruben Sanchez Rodriguez

"The fibers extracted from the stem of the ramie plant are among the strongest natural lignocellulosic fibers with a potential to be used as reinforcement of polymer matrix composites. Characterization of the ramie fiber has recently been conducted for its physical and mechanical properties. However, the effect of increasing temperature on the ramie fiber behavior has not yet been fully investigated. Therefore, the objective of this work was to perform a thermal analysis on ramie fibers with different diameters within the naturally found range of practical interest. The analysis was conducted by thermo-gravimetric, TGA and DTG, as well as differential scanning calorimetric, DSC, techniques. It was found that the ramie fibers present thermal stability up to 200°C and then suffer a sharp deterioration between 300 and 500°C, resulting in characteristic peaks.IntroductionSince the middle of last century, polymer composites have substituted many conventional monolithic materials in applications ranging from aerospace to sport [l]. The main advantages of these composites are the low density and flexible properties specially using fiber as reinforcement to suit the mechanical performance requirements [2]. These are usually high strength and stiffness requirements that could be reached with synthetic fibers such as glass, carbon and aramid fibers. In recent years, however, the use of synthetic fibers is being questioned in terms of problems caused to the environment. In fact, as non degradable material, synthetic fibers are associated with long term pollution when discarded. Moreover, the expended energy for fabrication and processing can be related to relatively large amounts of C02 emissions and represents a contribution to global warming [3]. Glass fiber, in addition, is toxic and cannot be incinerated as a waste in thermal power plants [ 4]. Possible substitutes for glass fiber are the natural fibers. Many natural fibers are today being considered as viable alternatives to replace glass fiber as reinforcement of polymer composites. In particular, some natural lignocellulosic fiber extracted from plants present a real potential for this replacement [2-8]. Their comparative advantages are lower density and reduced cost as well as renewability, biodegradability, recyclability and neutrality with respect to C02 emission [3]."

Jan 1, 2011

By W. F. Drinkard

Many in the environmental movement have focused on this element. But, nothing they or anyone does will change the amount of arsenic in the world. This report is on actual commercial plants that we developed and operated to recover or stabilize arsenic values from metallurgical dusts from gold and copper pyro operations and arsenical gold bearing ores. When they were available gold and copper values were recovered. Our experience in arsenic extends over thirty years. My first corporation, Mineral Research & Development Corporation was the first in North America to manufacture the then new CCA (copper-chrome-arsenic) wood preservatives. This class of wood preservatives proved to be so effective that it made wood into an entirely new material of construction. It is not uncommon for wood properly treated with arsenical CCA preservatives to last for thirty; forty, and sixty years. Over a hundred years have been projected in some field tests. Hundreds of thousands of trees have been saved. Millions more trees would have been saved had environmentalists not decided that their arsenic phobia was more important than trees. There are several variations of CCA. The most popular is CCA-C. Its formula is: CrO3 . . . . . . . . . . . . . . . . . . . 47.5% CuO . . . . . . . . . . . . . . . . . . . 18.5% As2O5 . . . . . . . . . . . . . . . . . 34.0% Until recent restrictions were placed on the consumption of arsenical wood preservatives, annual consumption in North America was about 150,000,000 lbs./yr. About 64,500,000 of arsenic as the pentoxide was safely consumed this way. World CCA consumption has been about double the above figures or 300,000,000 lbs. as 100% CCA and 129,000,000 lbs/yr as As2O5. Close to 100% of all the arsenic used in wood preservatives is derived from gold or copper processing. The valence of arsenic required for CCA wood preservatives and many other markets is the same valence that is required for stabilization. The economic challenge is how to get there. We have built and operated eleven plants to oxidize arsenic trioxide to its pentavalent form. Most of these have been classic in that they used a common oxidants such as hydrogen peroxide or nitric acid to achieve this.

Jan 1, 2005

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 Yuan-bo Zhang, Gui-hong Han, Yan-fang Huang, Tao Jiang, Guang-hui Li

"Under isothermal conditions, the reduction behavior of oxidized pellets balled with bentonite was investigated with CO-CO2gas mixers in the temperature range from 900°C to 1100°C. The whole reduction of oxidized pellets was followed up by means of weight-loss technique. And the swelling index of pellets was examined by visualizing physical changes of pellet in a horizontal tube furnace. The results present that the reduction rate of oxidized pellets is increased with the increase of reduction temperature. While the swelling index is firstly increased and then decreased with the increase of reduction time and reduction extent, which can be ascribed to the disruptive stresses induced during the transformation of hematite to magnetite. The maximum swelling index is gradually increased with the increase of reduction temperature and CO content.IntroductionWith the rapidly development of iron and steel industry, direct reduction iron has been considered as one kind of high quality burdens in electric furnace steelmaking [1]. At present, ""Two-step"" coal-based direct reduction process, which employs oxidized pellets as raw materials, has been used in industrial production [2]. The reduction behavior of iron ore oxidized pellets has been becoming one of the most frequently studied topics in extractive metallurgy[3]. The heat and mass transfer in direct reduction processes results in a series of stepwise reduction reaction (hematite--magnetite--wustite--iron), accompany with the volumetric swelling of pellets[4]. A lot of literatures have been reported on the reduction model of ferrous oxides and swelling behavior of pellets. A. A. El-Geassy K, et.al [5-7] revealed that the reduction process was controlled by chemical reaction at early stage by employing pure Fe203 as raw materials and CO as reduction gas. Chen Y [8] made research on the reduction kinetics of porous oxidized pellets and obtained the rate constant and activation energy of at different reduction stage. In addition, the swelling and disintegration of iron ore pellets was affected by chemical composition of pellet and reducing parameters, which have been studied by numerous investigators [3,9, 1O]."

Jan 1, 2013

By Zhongming Ren

"A new process of near net shape continuous casting of metal pipe has been put out. The specialty of the process is that no inner core is used. The principle of the process has been presented, and the effect of several factors on the thickness of the pipe has been investigated experimentally and numerically. It is shown that the temperature and the level of the molten metal, cooling intensity of the mold, and the velocity of casting influenced the thickness of the pipe apparently. In order to improve evenness of the thickness of the pipe, the mold was dedicatedly designed, and special methods were taken. By this process, a metallic material like ""bamboo"" was fabricated.IntroductionMetal pipe is a widely used material. Up to now, many processes have been put out to produce the pipe. However, the processes are usually expensive and inefficient. For instance, the welding pipe, which is most widely used, is produced through continuous casting of slab, rolling of the slab into sheet, and welding, with several times of heating and processing. Continuous casting of pipe can not produce small diameter of pipe, which is mostly needed, due to the inner core. Even though. OCC process is novel in fabricating the pipe with small diameter, it is inefficient. In this paper, the no-inner core continuous casting of pipe was proposed. With this process, pipe with small diameter can be produced efficiently. The influence of several parameters on the thickness and evenness of piper wall. With this process, a ""bamboolike"" pipe was fabricated.ExperimentThe experimental apparatus is shown in Fig. I. It is composed of mold, furnace, melt level adjuster, and dummy pipe. In the process, the level of the melt was adjusted at a proper position, then the mold along with the dummy pipe was inserted into the melt in a certain depth. The melt in the mold began solidifying, forming a solid shell. After that, the dummy pipe was pulled upward in a certain speed, drawing the solid shell out of the mold. Thus, a pipe was continuously cast."

Jan 1, 2000

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

By Tobias Pröll, Bernhard Kronberger, Joachim Rohovec, Werner Hölt, Hermann Hofbauer

"As this is only a first draft, more precise explanations as well as detailed schemes, figures and plots will be included in the final draft. The description og the 100 kW test rig will also be mor detailed as construction is ongoing and will be finished during the summer. Furthermore simulations are to be finished shortly; so details on combustibles and gas concentrations will also be included in the final draft.AbstractOxyFuel combustion is a key technology for the efficient separation of CO2 from fuel combus¬tion (especially coal). Since coal plays a minor role in the Austrian energy mix the application of OxyFuel towards other fuels (biomass, waste fuels) is interesting to reduce greenhouse gas emissions from Austrian energy sector. The investigation of OxyFuel technology for alter¬native fuels is also interesting from a strategic point of view in order to generate knowledge for operation of capture ready cofiring and waste/sludge-incineration plants. OxyFuel uses a synthetic mixture of 02 and recycled exhaust gas where the 02 content may vary. This supplementary degree of freedom allows improved operation especially for low calorific fuels. Heavy fuel oil addition for low calorific combustibles can be omitted when using OxyFuel combustion. Application of alternative fuels (wood, waste wood, municipal waste, sewage sludge) in a 100-kW CFB plant is investigated in combination with process simulation.IntroductionOxyFuel combustion is discussed as one of the key technologies for the efficient separation of CO2 from combustion of fossil fuels (especially coal). Since coal plays only a minor role as primary energy source in Austria, the broadening of the scope towards OxyFuel of other fuels like biomass or waste fuels is necessary to reduce greenhouse gas emissions from Austrian energy sector. The investigation of OxyFuel technology for alternative fuels besides the large coal-oriented projects is interesting also from the strategic point of view. The presented project aims at the generation of knowledge in order to design and operate capture ready cofiring and waste/sludge incineration plants."

Jan 1, 2008

By L. S. Montagna, R. M. C. Santana

"Since the industrial revolution, plastic products sector has growing bigly, however this fact presents as consequence the increase of municipal plastic waste (MPW).The aim of this work is to developmet polymer mixture from MPW with the adittion of rubber tire (TR) post use and to study the mechanical and morphologycal properties. The polymer mixtures Polypropylene/High impact polystyrene/TR (PP/HIPS/TR), where rate weight TR used was 10, 20 and 30 % and with three size particles (500, 710 e 1000 µm). The specimen tests were obtained by injection molding. Preliminary results of mechanical properties showed that the increase of TR influence in a reduction of the flexural and tensile resistance. Results by scanning electronic microscopy on the fracture surface of mixtures PP/HIPS/TR showed a better interaction of TR particle with HIPS than with PP. Also, the presence of microcavoids was observed, characteristic in PP/HIPS blends, favouring in the increase of its opacity.IntroductionOne great part of the municipal solid waste (MSW) is composed of polymer mixed since commodity plastics, blend to polymer composite. The processing of plastics mixtures for recycling has been attempted with some success, but poor mechanical properties and uncertain economic value limit their more versatile reuse. Polyethylene (PE), polypropylene (PP), polyethylene terephthalate (PET), poly(vinyl chloride) (PVC) and polystyrene (PS) are among the most common plastic waste, predominantly used in packaging food industry [1].One other problem that preoccupy to the society is the increase of rubber tire waste in the proportion of MSW. In Brazil, from 1999 to 2004, 39 % from 386 mil ton of tire post-use were destined to ciment Industry as source of energy [2]. However this destiny produces one other problem, environment pollution, due to gas mixture emitted.Recycling represents a valid alternative to the disposal of post-consumer plastics in common landfills if it is possible to obtain new materials with good final properties compatible with practical and, above all, by cheap methods [3]The reutilization of group tire rubber (TR) powder as a dispersed elastomeric phase in a thermoplastic matrix offers an opportunity to design second generation materials which would be recyclable due to the thermoplastic matrix and which potentially could present thermoplastic elastomer (TPE)-like mechanical behavior. [4]."

Jan 1, 2008

By Mingming Zhang

"Three samples received from the EAF shop have been characterized by chemical, X-ray diffraction (XRD), optical microscopy (OM) and scanning electron microscopy (SEM) methods. The objective of this characterization work is to investigate the occurrence of nickel, copper, zinc, sulfur and phosphorus in these samples and identity their origin and associations with iron minerals in the concentrate samples that are from mines.The samples were identified as Mineral, Pellet, and HRD. The latter is the DR! product. All three samples were received as fine powders. The results indicate that, in the mineral sample, magnetite is the major iron oxide mineral with hematite as a second phase based on the OM and XRD studies. Pyrite [FeS2], chalcopyrite [CuFeS2] and bravoite [(Fe,Ni)S2] are major sulfide minerals. Trace amounts of apatite [Ca5(P04)3(F,Cl,OH)], wardite [Na4CaA112(P04)8(OH)8 6H20], giniite [Fe5(P04)4(OH)3 2H20] and vivianite [Fe3(p04)2 8H20] were identified by SEM and XRD. Microscopic studies also indicated that most of the sulfide grains in the mineral sample are present either as liberated fine particles (about 10 microns) or as inclusions within the magnetite and hematite grains. XRD studies revealed magnetite as the major mineral with subordinate amounts of hematite and pyrite confirming the microscopic findings. Copper, nickel, and zinc are mainly present as chalcopyrite, bravoite, and franklinite [(Zn,Mn,Fe)(Fe,Mn)204] in trace amount in the mineral samples, respectively. Impurities carry over to the Pellet and HRD samples.Chemical analyses of the three iron-bearing samples indicate that sulfur and phosphorus in the Pellet sample exceeded the specification. Since liberated pyrite and chalcopyrite particles were observed both in mineral and pellet samples, magnetic and flotation processing routes for this ore should be effective for sulfide removal but at the cost of iron losses. The high phosphorus content of all three samples indicates that there are phosphates which are difficult to remove by the current concentrating process (magnetic separation and flotation)"

Jan 1, 2012

By Laurence G. Dyer, David G. Dixon, John Rumball, Maziar Eghbalnia, Edouard Asselin

"Linear scan voltarnmetry was used to determine the reactions that occur during the cyanidation of petzite (Ag3AuTe2). Gold oxidation in petzite requires more oxidising conditions than are required for pure gold, it also does not achieve the same current (related to reaction rate). Tellurium oxidation occurs at a similar potential in water and cyanide, but as a component of petzite is impeded somewhat in water, likely due to the stability of the precious metals. Pre-treatment of petzite to oxidise tellurium in the absence of cyanide prior to gold recovery appears to be at least moderately successful.IntroductionWhile gold occurs most prevalently in its native form, many other gold bearing phases appear throughout natural systems [I]. Tellurides are a common group of such minerals, many of which also contain silver, often existing in association with native gold deposits. The six major gold-bearing tellurides are calaverite (AuTe2), sylvanite [(Au, Ag)2Te4], montbrayite [(AuSb)zTe3], krennerite [(Au1-x, Ag,)Te2], petzite (Ag3AuTe2) and muthmannite (AuAgTe2) [2]. While several other phases exist they are much more complex (i .e. buckhornite), which dilutes and confuses the influence of each specific component. Studies of gold tellurides have predominantly focussed on calaverite as it is the simplest and most common phase, however petzite, commonly found in Australia and North America, is the focus of this investigation.Gold processing via cyanidation has been operated for more than a century and is a highly effective hydrometallurgical treatment of native gold deposits. However, some gold alloys such as tellurides have proven to be somewhat less responsive under the same conditions. Several groups have shown that gold/silver tellurides are amenable to cyanidation, but are significantly more refractory than native gold [3]. Pre-oxidation steps have been tested to remove constituents that would consume cyanide such as sulfides. Such species are also linked to the precipitation of oxidised telluriwn, forming a passive layer, further inhibiting gold recovery [2]. It is uncertain to the definite reasons underpinning the refractory nature of precious metal tellurides in conventional cyanidation."

Jan 1, 2012

By M. Frades, C. Frías, G. Díaz, A. B. Mejías

"In recent years, zinc recovery from flue dusts and other industrial wastes has been increased, offering to the market a large tonnage of secondary zinc oxides, which can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content.The ZINCEXTM Technology has been commercially applied for more than thirty years and represents the most suitable solution to deal with secondary or crude zinc oxides due to its flexibility, simplicity, and cost-efficiency, allowing production of SHG electrolytic zinc and pure zinc sulfate salts thanks to the flexibility and selectivity of the zinc solvent extraction unit regarding to get rid of impurities.A dual plant able to produce electrolytic zinc and crystallized zinc sulfate has been engineered to provide a flexible and profitable solution to zinc market. A description of the study and the relevant achievements is presented in this paper.IntroductionZinc is a valuable commodity in the marketplace and can be recycled again and again and still maintain its physical and chemical properties. Zinc recycling offers both environmental and economic benefits such as reducing volumes of material that end up in landfills, saving energy by reducing the need for mining and smelting, and relieving environmental impact on the land and water, and conserving zinc ore [1].The supply of zinc able to be re-processed will be increasing from year to year according to secondary materials enter the recycling stream, and as a result, more recycled zinc will become available in the market. Thus, some existing zinc refineries are implementing an annexed treatment line to process secondary oxides in conjunction with primary zinc concentrates [2].The galvanized steel scrap is normally recycled in electric arc furnaces or in basic oxygen furnaces, which generates a large tonnage of zinc-bearing flue dusts (EAFD). Around one million ton EAFD is yearly produced at the USA and the EU, respectively. The flue dusts are treated commercially by pyrometallurgical ways such as waelz kilns, electrothermic furnaces, etc, to yield secondary zinc oxides that can not be processed directly to render high quality zinc because of the hazardous impurities and halogens content [3]."

Jan 1, 2008

By Elsa Olivetti, Randolph Kirchain, Gabrielle Gaustad

"As scrap usage increases, it is often necessary to “dilute” the melt with primary aluminum to ensure the finished product meets compositional specifications. Secondary raw materials, particularly postconsumer scraps, often include high levels of unwanted or “tramp” elements, such as iron and silicon in the case of aluminum. Recent literature on this issue cites several causes including inherent contamination during processing as well as ineffective segmentation at end-of-life. To address this accumulation problem, “upgrading” solutions have been developed including: dismantling of end-of-life products, spectrographic or magnetic sorting of shredded scrap, and “filtration” technologies that remove tramp elements in the melt. Although it is clear that upgrading strategies enable increased usage of scrap, it is not clear that they would be economic or efficient. This work presents a set of analytical methods, based on chance constrained optimization, to quantify the potential environmental and economic value of several scrap upgrading technologies.IntroductionAluminum recycling has a number of key environmental and economic benefits. Compared to other materials, aluminum production has one of the largest energy differences between primary and secondary production: 175 MJ/kg for primary compared to 10-20 MJ/kg for secondary[1]. With energy and cost savings in mind, many producers now have targets of increasing their usage of secondary materials[2, 3]. However, the accumulation of impurities in these recycled material streams provides a significant compositional barrier to these goals[4].A growing number of studies and literature would suggest that accumulation of unwanted elements is a growing problem, in all recycled material streams. In the case of aluminum, the list of problematic impurities is quite large, including but not limited to: Si[5, 6], Mg, Ni, Zn, Pb, Cr[7], Fe[5-7], Cu[6, 7], V, and Mn[6]. Metals recycling is a metallurgical process and is therefore governed by the laws of thermodynamics. The removal of unwanted elements in the scrap stream is dictated by the energy considerations of the melt process. Compared to many metals, aluminum has a high degree of difficulty in the removal of tramp elements, due to thermodynamic barriers. Therefore, with no simple thermodynamic solution, producers must identify strategies through-out the production process to mitigate this elemental accumulation."

Jan 1, 2008

By Bradford C. Wesstrom, Omar Araujo

"Impurities from an electrolytic refinery are typically extracted from the electrolyte utilizing conventional electrowinning cells. These cells are arranged in series with cascading solution flow and are commonly referred to as liberator cells. The Freeport McMoRan Copper & Gold El Paso Refinery has optimized the removal of arsenic in cascading liberator cells by utilizing two separate feed solutions. The primary feed solution is recycled liberator electrolyte and the secondary feed solution is ""neat"" tank house electrolyte. The secondary feed solution is added based on the voltage response across the individual cells utilizing independent variable frequency drive (VFD) pumps. When the voltage across a cell changes, a signal is sent to the VFD pump to maintain a cell voltage of 1.98 volts. By maintaining this voltage the copper content in each cell exits at 2-4 grams per liter. This safely optimizes the arsenic removal as copper arsenides on the liberator cathodes.IntroductionDuring the electrolytic refining of copper, impurities from the copper anode report both to the bottom of the electrolytic refining cell as slimes and to the electrolyte. The impurities which enter the electrolyte are arsenic, antimony, bismuth and nickel. The impurities that report to the electrolyte during the electrolysis process gradually increase. As these impurities increase, they are incorporated into the refined copper cathode. There are many processes that have been used to remove these impurities from refinery electrolytes. Some of them are listed as follows: solvent extraction, ion exchange, hydrogen sulfide reduction, bioreactor, adsorption onto a low - solubility metal-oxide hydrate, adsorption onto activated carbon and EMEW cells. The conventional process used by the copper refining industry for controlling the level of impurities in electrolyte involves multistage electrolytic cascading liberator cells. In these cascading liberator cells copper, arsenic, antimony and bismuth are removed as various mixed deposits from the electrolyte. Removal of these impurities is achieved through an increase in voltage resulting from the depletion of copper in the electrolyte through electrowinning. With this higher voltage, the Group Vb elements, arsenic, antimony and bismuth are deposited on the copper cathode and report as slimes to the bottom of the cells. Nickel is removed in a subsequent process."

Jan 1, 2012

By Alberto Oalvez, Lucya Yunus, Pengfii Tan

"Laboratory flotation tests of slow cooled converter slag have showed that 92.5% copper recovery at the copper cut-off grade of 24 - 25 % can be achieved by using a 50:50 ratio of DSP330 and SIBX (sodium isobutyl xanthate) at the natural pH of 7 and with a grinding time of 18.5 minutes. 70ìéç is the P80 achieved at this grinding time. MIBC is the frother and the solid content of the flotation feed was 46%. In the plant trials, two types of collectors at two different feed particle sizes for both the normal and slow cooled slag were operated. The particle size was controlled by the feed rate. The P80 of 75 ìçé at a feed rate between 32 - 36 t/h were tested. The plant trials have demonstrated that the copper recovery in the milling and flotation process of the slow cooled slags was improved by 3%. IntroductionIt is proposed to float the slow cooled converter slag, in the auxiliary circuit of the copper concentrator at Mount Isa, by using the processing conditions identified from several laboratory flotation tests. Among these laboratory tests, one produced a copper recovery of 4 % higher than those achieved from a normal cooled slag with the same slag feed grade and the same copper content (24 - 26 %) in the concentrate. These test conditions were selected for further studies.Laboratory Test Work and Plant TrialsThere has been a lot of work conducted under laboratory and plant conditions [1]. However, the achieved results did not justify their total implementation in the Mount Isa Copper Concentrator. Initially, the lab trials were carried out with slag cooled 100% in air; then it was changed to combined cooling for 12 h with air and 2.5 days with water sprays. The reason for this change was the shortage of space when the slag was cooled 100% in air, as it takes several days to achieve safe temperatures for its removal. The San Manuel Copper Smelter has reported that their slag was left for air cooling in pits for 8 h and then was followed by water cooling for 2-3 days [2]"

Jan 1, 2012