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By Hyun Soo Kim, Joon Soo Kim, Myong Jun Kim, Jyothi Rajesh Kumar, Jin-Young Lee

Rare earth materials have an ever growing variety of applications in the modern and hitech technology. They apply to many an industry with crucial materials and they provide numerous a customers with benefits. Rare earth materials utilization increasing day-by-day in the worldwide, at the same time the resources is very limited in many countries like Korea. The present general article divided four sorts such as 1) mineral processing of Korean ore deals the gravity, magnetic separation and froth flotation, 2) decomposition and leaching of concentrates included sodium hydroxide fritting, sodium hydroxide hot digestion, hydrochloric acid leaching, 3) separation and purification of rare earth elements in mixed rare earth chloride solution consists reduction and oxidation method, solvent extraction, 4) preparation of rare earth oxide compound from purified elemental rare earth chloride solution having oxalate salt precipitation by reaction crystallization. The last part consists of a summary of the present study.

Jan 1, 2015

By Stella Agatzini

Column leach tests were conducted to evaluate the amenability of poor Greece nickel laterites to heap leaching with dilute sulfuric acid at ambient temperature. The ore tested was a limonitic laterite with less than 1 % nickel and it was subjected to a suitable pretreatment with water prior to it being loaded into the columns, following findings of preliminary research work. The acid solution was recycled after suitable pH adjustment. Factorial designs were used to determine the effects and interactions of the following factors: sulfuric acid concentration, ore column height, ore grain size and ratio of leach solution volume to the ore quantity. The response which were investigated included nickel and cobalt recoveries, codissolution of iron, calcium, magnesium, aluminum, chromium and silica and also sulfuric acid consumption. Experimental error was also detennined. The tests showed that a nickel recovery of 88% could be achieved in 60 days.

Jan 1, 1993

By Mark L. Dietz

The unique physicochemical properties of room-temperature ionic liquids (RTILs) have led to intense interest in these materials as alternatives to conventional organic solvents in a range of synthetic, catalytic, and electrochemical applications. Recently, there has been growing interest in their potential use in various separation processes, among them the liquid-liquid extraction of metal ions. Although certain RTIL-extractant combinations (e.g., crown ethers in 1-alkyl-3-methylimidazolium bis[(trifluoromethylsulfonyl] imides) have been shown to provide extraction efficiencies far exceeding those observed with conventional solvents, recent work suggests that the utility of RTILs may be limited by solubilization losses and difficulties in recovering extracted metal ions. In this work, we demonstrate that these limitations arise, in part, from differences in the mechanism of metal ion partitioning in RTIL systems versus conventional organic diluents and consider approaches by which they might be overcome.

Jan 1, 2003

By R. S. Tahautdinov, A. N. Posazhennikov, V. V. Bastrygin

"The Bakal (South Ural, Russia) deposit of iron ore bearing iron carbonate (siderite) with the capacity of more than 1 billion tones belongs to the MMK. This ore cannot be fully processed via blast furnace technology because of high content of MgO. According to the investigations carried out in the USA and Japan in 1999-2004 the ITmk3 (Ironmaking Technology mark three) RHF technology is a breakthrough in Ironmaking. Four iron ore types (hematite, magnetite, high and low Al2O3/SiO2) were tested. Reduction, melting and slag removal can be achieved in just 10 min. The main objective of the investigation is to establish optimum operation conditions for the production of iron nuggets from iron carbonate bearing ore via the ITmk3 by means of the lab scale testing. Samples of iron ore and carbon reductant were chemically and physically analyzed. Green pellets were processed via a lab tube furnace to simulate RHF conditions. The nuggets and slag were chemically analyzed. This preliminary test work provides valuable information which may be used for large-scale testing in a commercially sized RHF.IntroductionThe ITmk3 process upon which this paper focuses was developed by Kobe Steel in its research facilities in 1996 [1]. After pilot testing at Kobe Steel’s Kakogava Works in 1999-2004 the pilot demonstration plant was built and operations were successfully carried out by Mesabi Nugget joint venture in 2002-2004. Steel Dynamics has committed to building the commercial plant at the Mesabi Nugget site in Hoyt Lakes (Minnesota). Only 4 iron ore types (hematite, magnetite, high Al2O3/SiO2 and low Al2O3/SiO2), as well as 4 coal types with range of volatility, ash and fixed carbon were tested. Results were consistent with nugget characteristics confirming ITmk3’s flexibility with respect to raw material inputs. At the same time, no research in the field of nugget from iron carbonate bearing ore with high content of MgO has been done. Such kind of iron ore is restricted for charging into the blast furnace due to contamination of MgO. The reason for restriction is the limitation of load of MgO in the blast furnace. If a lot of MgO enters the blast furnace, slag becomes viscous. The viscous slag is obstacle for stable operation of the blast furnace."

Jan 1, 2011

By E. V. Redin

"The Bakal (South Ural, Russia) deposit of iron ore bearing iron carbonate (siderite) with the capacity of more than 1 billion tones belongs to the MMK. This ore cannot be fully processed via blast furnace technology because of high content of MgO. According to the investigations carried out in the USA and Japan in 1999-2004 the ITmk3 (Ironmaking Technology mark three) RHF technology is a breakthrough in Ironmaking. Four iron ore types (hematite, magnetite, high and low Al2O3/SiO2) were tested. Reduction, melting and slag removal can be achieved in just 10 min. The main objective of the investigation is to establish optimum operation conditions for the production of iron nuggets from iron carbonate bearing ore via the ITmk3 by means of the lab scale testing. Green pellets were processed via a lab tube (chamber) furnace to simulate RHF conditions. This preliminary test work provides valuable information which may be used for large-scale testing in a commercially sized RHF.IntroductionThe ITmk3 process upon which this paper focuses was developed by Kobe Steel in its research facilities in 1996 [1]. After pilot testing at Kobe Steel’s Kakogava Works in 1999-2004 the pilot demonstration plant was built and operations were successfully carried out by Mesabi Nugget joint venture in 2002-2004. Steel Dynamics has committed to building the commercial plant at the Mesabi Nugget site in Hoyt Lakes (Minnesota). Only 4 iron ore types (hematite, magnetite, high Al2O3/SiO2 and low Al2O3/SiO2), as well as 4 coal types with range of volatility, ash and fixed carbon were tested. Results were consistent with nugget characteristics confirming ITmk3’s flexibility with respect to raw material inputs. At the same time, no research in the field of nugget from iron carbonate bearing ore with high content of MgO has been done. Such kind of iron ore is restricted for charging into the blast furnace due to contamination of MgO. The reason for restriction is the limitation of load of MgO in the blast furnace. If a lot of MgO enters the blast furnace, slag becomes viscous. The viscous slag is obstacle for stable operation of the blast furnace."

Jan 1, 2012

By Feng Ningchuan, Guo Xueyi, Tian qinghua, Liang Sha

"In this study, copper adsorption by orange peel which was chemically treated with sodium hydroxide was investigated. The morphological and chemical characteristics of the adsorbent were evaluated by spectroscopy and N2-adsorption techniques. Equilibrium isotherms and kinetics were obtained and the effects of solutions pH, adsorbent concentrations and temperature were studied in batch experiments. Equilibrium was well described by Langmuir and Freundlich isotherms and kinetics was found to fit pseudo-second order type adsorptions kinetics. According to the Langmuir equation, the maximum adsorption capacities (qm) for Cu(II) was 50.25 mg·g-1 at pH 5.3. With the temperature increased from 16 to 60°C, copper removal decreased. The loaded adsorbent was regenerated using HCl solution and could be used repeatedly at five cycles with little loss of adsorption capacity. The results show additional chemical treatment of the adsorbent by NaOH, is favor of improving the adsorption capacity. Introduction Increased use of metals and chemicals in manufacture industries has resulted in generation of large quantities of effluent that contains high level of toxic heavy metals and it poses environmental-disposal problems due to its non-degradable, persistence nature and accumulation throughout the food chain [1, 2]. Copper is known to be a commonly used heavy metal. This metal, which found many useful applications in our life, is very harmful if charged into natural water resources and may pose finally a serious health hazard. Many methods, such as chemical precipitation, ion exchange, reverse osmosis and adsorption, etc., have been used for heavy metal ions removal from various aqueous solutions. In recent years, there has been considerable interests in use of biological materials including algae, bacteria, fungi, agricultural by-products and residues as adsorbents to remove toxic metals from aqueous solutions by adsorption [3-8]. Adsorption process has been extensively used to remove copper from aquatic medium using low cost adsorbents such as peanut husks [9], plant materials [10] and cellulose materials [11]. Among them, agricultural by-products and biomass are relatively cheap and show very high adsorption capacities. However, to apply untreated agricultural by-products as adsorbents has the disadvantages such as low adsorption capacity, high chemical oxygen demand (COD) and biological chemical demand (BOD) as well as total organic carbon (TOC), due to the release of soluble organic compounds contained in the plant materials such as lignin, tannin, pectin and cellulose, into the solutions [12-14]."

Jan 1, 2008

By Kazusuke Sato, Takahiro Uno, Koji Hoshino

"A novel Ni coating technique of Ni(OH)2 powders was developed to improve the positive-electrode performance· of the Ni-MH batteries. It was found out that Ni(OH)2 powder was reduced by N2H4 without any catalysts in an alkaline - solution at high temperatures. In result of observation of pH and potential changes in the solution during the reaction, it was found that the reduced species was HNio2- ion dissociated from Ni(OH)2 in the alkaline solution. The molar fraction of reduced Ni of the Ni(OH)2 was increased in proportion to the amount of added N2H4. At the small Ni fraction, a porous Ni layer was formed on the surface of Ni(OH)2 powder. Open cell tests were carried out with the paste type electrodes made of either the Ni coated Ni(OH)2 powder or non-coat powder, and cell performances were compared. In result, it was found that the Ni coating technique is effective on improvement in the utilization of Ni(OH); as a positive-electrode active material under high current densities.IntroductionNi-MH rechargeable battery is generally used for the power source of portable machines and electric vehicles because of its good performance at high energy density and. long term cyclical life as well as cleanness and good safety. Cell component materials have been improved respectively, and as concerns ·the positive-electrode reducing 'the internal resistance is a principal problem to improve the discharging performance at higher current densities.In recent years, improved Ni(OH)2 powders coated with conductive materials as NI. or CoOOH have been developed for the· positive-electrode active materials in order to· reduce the internal resistance of the electrode1)· 2) The Ni coated Ni(OH)2, however, is costly because it is fabricated by .the -non-electrode plate technique which needs a expensive precious ·metal catalyst as PdC12We found that Ni(OH)2 powder was reduced by N2H4 without any cryatalysts in an alkaline solution at high temperatures. After the treatment, Ni(OH)2 powder become gray color like Ni powder from light-green color; and. turned into a magnetic. In this study, the mechanism of the -reducing reaction was investigated to apply the reactions .to a novel Ni coating technique of Ni(OH)2 powders, · and the performance of the Ni coated Ni(OH)2 powder obtained by the reducing process was evaluated as an -positive-electrode active material of Ni-MH batteries."

Jan 1, 2000

By F. Raupp-Pereira, G. G. Cunto, J. A. Junkes, D. Hotza, V. P. Della

"The present work investigated the valorization of wastes as alternative raw materials for ceramic industries. Different industrial wastes based on the SiO2-Al2O3-CaO system and classified as non-hazardous were selected: sludge from varvite cutting process, sludge from gneiss breaks processes, sludge from filtration/clarification of potable water and a clay classified also as waste. All as-received residues were characterized by X-ray fluorescence, differential thermal analysis, thermogravimetry and particle size distribution. The applicability of these materials in ceramic formulations was then evaluated. The formulated mixtures were subjected to forming by pressing and extrusion followed by thermal treatment. After optimization of the processing conditions, the properties of the samples sintered at different temperatures were also evaluated. The waste materials studied proved to be alternative raw materials to natural mineral resources for the ceramic industry.IntroductionOne of the most important problems that have accompanied the humanity in recent decades is the environment’s degradation. In the same context, the natural resources exploration and technological development are phenomena which, if aren’t controlled, can cause ecological disequilibrium with unpredictable consequences [1]. It is in this perspective that recycling of various wastes assumes relevant importance.The recycling, understood here as the waste process reuse, is a common practice in the First World countries, where the raw materials have strategic aspects and the disposal techniques of solid wastes have considerable economic costs. In Brazil, the ecological conscience begins to be aroused due to, in the last ten years, the implementation of stricter laws for environmental control, in general, and licensing of waste generating from industrial activities, in special. The terms “residue” or “waste” are normally used to describe what remains of a production process; when an application for this material is not found. When wastes or residues are susceptible to be incorporated as raw materials or energy sources in a new material production, they can be understood as by-products [2].The valorization of industrial wastes is important, due to the need to pollute less and give an ecologically correct destination for wastes. The waste recycling, independent of its kind, presents several advantages in relation to using primary natural resources, such as reduction in the volume of raw materials extraction, lower energy consumption, lower levels of pollutant emissions and improvement of the health and safety of the population. The most visible advantage of recycling is the preservation of natural resources, extending its life and reducing the destruction of landscape and ecosystems [3]."

Jan 1, 2008

By Carlos Maurício Fontes Vieira, Sergio Neves Monteiro

"A ceramic body traditionally used to produce bricks and roofing tiles with kaolinitic clays was reformulated by the addition of sand and illitic clay. The objective was to obtain a ceramic product with better technological properties. Specimens were made by uniaxial press-molding at 20 MPa and then fired at 850, 900 and 950°C. The determined technological properties were: linear shrinkage, water absorption and flexural rupture strength. The results showed that both sand and illitic clay contribute to reduce the water absorption of the industrial clayey body. With respect to the flexural behavior, it was observed that the incorporation of sand decreased the mechanical strength. On the other hand, the illitic, incorporated in an amounts of 30 wt.% contributed to increase the mechanical strength of the clayey ceramic.IntroductionCeramic bodies industrially fabricated in the county of Campos, north of the State of Rio de Janeiro, in Brazil, are still empirically elaborated using a mixture of local clays. These clays are predominantly kaolinitic mineral in nature, associated with high plasticity and elevated weight loss during the firing stage. Due to the excessive plasticity of the ceramic bodies, dimensional defects, which occur after drying and firing are usually obtained. Moreover, the kaolinitic nature and the presence of aluminum hydroxide (gibbsite) confer a refractory behavior to the local clays, which impairs sintering during the firing operation. In the case of clay ceramic products for civil construction, this results in greater porosity associated with elevated values of water absorption and low mechanical strength [1,2]. To avoid these problems, it is necessary to reformulate the ceramic body composition. The addition of both non-plastic materials to reduce plasticity and fluxes to condition the refractoriness is a possible alternative.As an alternative to reduce the plasticity of clayey ceramics sand, which is predominantly constituted of silica, can be used. The incorporation of sand in amounts of up to 25 wt.% to a clayey ceramic body used for roofing tiles fabrication was studied by Vieira et al. [3]. In that work specimens were prepared by extrusion and fired at 850°C. The results indicated that in the pre-firing stages the sand improved the workability of the investigated clayey ceramic body and facilitates the drying stage. It was also observed that the incorporated sand significantly improved the physical and mechanical properties of the clayey ceramic after firing. On the other hand, the apport of flux oxides could be done by the use of illitic clays that have a higher amount of alkaline oxides in comparison with the kaolinitics clays."

Jan 1, 2013

By O. P. Pandey, Rama Arora, Gurmel Singh, Suresh Kumar

The tribological behavior of Dual Particles Size (DPS) rutile reinforced LM13 alloy composite was investigated under varying applied pressure from 125 kPa to 625 kPa at a constant sliding speed of 1.6 m/s. In the present studies, 15 wt.% of rutile particles of different sizes (50-75 μm and 106-125 μm) are reinforced in the Al-12Si alloy (LM13) by liquid metallurgy route. Microhardness of the prepared samples was measured in different phases. Microstructure, wear mechanism and surface morphology of the wear surfaces and debris was observed under optical and scanning electron microscope. The change in wear behavior has been explained with reference to the observed EDS analysis of the wear track and debris. However, an interesting change in wear feature, mild to severe wear transition at critical pressure was noticed in wear behavior of the composite. The Al-DPS composite has immense potential to be used as a component material for tribological applications.

Jan 1, 2015

By Zhi-biao Yin

Copper smelter flue dusts often cannot be directly recycled to the smelting process and accumulate as hazardous wastes requiring environmentally acceptable disposal. Because of the limited amount of flue dust, a separate copper extraction process must be simple and require-a small plant investment. A flue dust process has been developed, consisting of the following steps: (1) roasting a pelletized mixture of hydrated lime and flue dust to fix arsenic and sulfur as insoluble calcium salts, (2) heap leaching the roasted pellets with a buffered ammonia/ammonium salt solution to extract copper as an ammine complex in a lined cell that is the final repository of the leached pellets, and (3) boiling ammonia from the lixiviant to precipitate copper. Condensed ammonia and the filtered solution are returned to leaching. Heap leaching in the final repository cell lowers the capital investment significantly compared with competing extraction processes. Chemistry with respect to arsenic, sulfur and copper is discussed.

Jan 1, 1992

By Tsisana Gagnidze

A processing of technogenous wastes, which involve a gold-containing sulphide minerals, is a potential source to supplement the gold reserves. Hence, searching of ecologically safe and economically reasonable methods for processing of gold-containing technogenous wastes is a topical problem. To increase a parameters of gold extraction and to simplify a technology of the processing of above-mentioned wastes of sulphide minerals, an investigations have been carried out in the direction of the use of the method of electrochemical leaching without any preliminary processing of the mineral. It was established experimentally that an introduction of nitrogen containing organic additive into chloride solution favours to reduce a Red/Ox potential of the solution from 0,8÷1,2 V to 0,35÷0,5V, which permits to conduct the process of direct electrochemical leaching at ?soft? oxidation regimes at temperatures 20-300C C without an environmental contamination by molecular chlorine and with a high degree of a gold extraction up to 80-90%.

Jan 1, 2008

By Wang Dawan

During the process of arsenic bearing gold concentration biooxidation, the content of chloride ion in water is a very important factor to the activity of bacteria and the oxidation of sulfide minerals. In this paper, the influence of underground mine water with different chloride ion content to the biooxidation of arsenic bearing gold concentration and the limit of chloride ion content to bacteria were summarized. These results indicated if the content of chloride ion was less than 1.2g/L, the bacteria?s ability to oxidize sulfide minerals was little affected, and if the content of chloride ion were increased to 2g/L or more, the activity of bacteria was seriously restrained, and if the content of chloride ion were increased to 4g/L, the activity of bacteria was absolutely restrained. So, as the content of chloride ion in water was cumulated to 2g/L or more in biooxidation plant, the water must be refreshed to maintain normal production.

Jan 1, 2008

By F. Sakurai

The enlarged Mitsubishi process in Naoshima has been in steady operation since. May 1991. However, the sulfuric acid plants have been in operation for more than 30 years. The acid plants were modernized between 1999 and 2001 by renewing some of main equipment such as the drying tower and gas heat exchangers, and introducing new technology. At the same time, as an electric energy saving measure, the electric power consumption in the sulfuric acid plant was vastly improved by decreasing the volume of gas treated the installation of low temperature activity catalyst in the 1st pass of the converter and optimization of main gas blower runner. Furthermore, last year, the oxygen plant was replaced and enlarged, and anode production increased from 240,000 to 280,000 tonnes per year with an associated increase of sulfuric acid from 550,000 to 660,000 tonnes per year. This paper describes these recent improvements in the acid plant at Naoshima smelter.

Jan 1, 2002

By Rodney L. LeRoy, Michel G. Drouet, Peter G. Tsantrizos

"DROSRITE is a unique process that makes possible economic in-plant recovery of metal from hot aluminum dross. It is environmentally friendly, requiring no salt and producing no C02 or NOx gases. The salt-free residues of the process are suitable for production of calcium aluminate or for other value-added use. The process is highly energy efficient, extracting process heat from energy in the residue and, thus, it does not require an external plasma torch, electric arc or fuel heat source.A DROSRITE pilot unit built by PyroGenesis has been tested with both black and white dross types. The unit was installed at two different aluminum plant locations, and tests were conducted for a total of six weeks ""online"" with hot metal holding furnaces where the dross was skimmed.Results of both of these industrial trials are presented, together with an economic analysis indicating cost savings in excess of $1 70 per ton of dross treated."

Jan 1, 2000

By Min Chen, Zhen Tian, Hongxu Cui

"The effects of adjusting technology on the phosphorous enrichment in converter slag were investigated. The results showed that the grain size of 2CaO·SiO2 with high phosphorus containing content increased slightly with the decreasing of cooling rate, and the proper cooling rate was confirmed to be about l.0°C.min-1. Moreover, the morphology of the phosphorus-rich phase of 2CaO·SiO2-3CaO·P2O 5 was changed from granular for the higher basicity of converter slag to the coexistence of granular shape and rod-like for the lower basicity of adjusted slag. With the addition of adjusting agent such as SiO2 to lower the basicity of converter slag, the phosphorus in converter slag could be transferred into 2CaO·Si02 phase effectively, and P2O 5 content in high phosphorus containing phase reached to above 30%.IntroductionThe yield of converter slag is very large in China, but most of the slag is stacked usually after the separation of iron, which not only takes up a lot of land, but also affects the ecological environment seriously. Therefore, improving the comprehensive utilization and value-added products of converter slag is of great significance to recycle the steelmaking slag[l-3]. On the other hand, the refining of hot metal with high phosphorous content is an unavoidable problem with the decreasing of high grade iron ore, and as a result, more amounts of high phosphorus containing steelmaking slag are produced. However, the current recycle of converter slag is more focused on the emission reduction and reuse of steelmaking slag inside the iron and steelmaking process without considering the recycle of phosphorous resources[4-6]. At the same time, the development and utilization of phosphate ore as a strategic resource is drawing more and more attention, but the phosphate ore in China is mostly low grade and significant amounts of tailings are produced which is harmful to the environment. Therefore, it is important to separate phosphorous resources in steelmaking slag which can be used as phosphate ore for fertilizer material[7-9].Literature studies showed that most of the phosphorus in steelmaking slag existing as 2CaO·SiO2-3CaO·P2O 5 solid solution phase in 2CaO·SiO2 particle. The P2O 5 content in the phosphorus containing phase is very low due to the fact that the basicity of converter slag is usually high and the precipitated amounts of 2CaO·SiO2 particles during cooling are very large, resulting in the fact that the P2O 5 contents in 2CaO·SiO2-3CaO·P2O 5 solid solution phase are much lower which is impossible to be used as phosphorous resources instead of phosphate ore. Thus, the enrichment of phosphorus in steelmaking slag is need[ 10-14]."

Jan 1, 2011

By H. Y. Sohn, Haitao Wang, Moo Eob Choi

"A novel ironmaking technology is under development at the University of Utah. This technology produces iron directly from iron ore concentrate by gas-solid suspension reduction. Hydrogen is the main reducing agent for high reactivity and for the elimination of carbon dioxide release in this ironmaking process. The direct use of concentrates allows bypassing the problematic pelletization/sintering and cokemaking steps in the steel industry.Intrinsic kinetics of the suspension reduction of magnetite concentrate particles by hydrogen has been measured. Experiments were carried out in the temperature range of 1423-1673 K, other experimental variable being hydrogen partial pressure, the amount of excess hydrogen and particle size. Under most experimental conditions, 95% reduction was attained within several seconds, which presents sufficiently rapid kinetics for a suspension reduction process. The reaction kinetics followed the nucleation-and-growth equation, and a rate equation that contains all the effects of the experimental parameters has been obtained.IntroductionWith the rapid increase in steel production, it is critical to control CO2 emissions which is the main greenhouse gas. It is inevitable to release a huge amount of CO2 when coke and/or coal are used as the main reducing agent in producing iron. As one of the methods to reduce the CO2 emission from ironmaking, the utilization of the gaseous reducing agents and fuels, including hydrogen, has been investigated [1-6]. The use of such gases forms the basis for a new ironmaking technology under development for producing iron directly from fine concentrates by a gas-solid suspension technology. This technology would reduce energy consumption by about 40% of the amount required by the blast furnace and drastically lower environmental pollution, especially CO2 emission, from the steel industry [4]. This is accomplished by adopting H2-based reductant and bypassing pelletization/sintering and cokemaking steps. Unlike other gas-based alternative ironmaking processes using shaft furnaces or fluidized-bed reactors, the suspension reduction technology is a high-intensity process because it will not suffer from the problems that other processes do when operated at high temperatures mainly from the sticking and fusion of particles."

Jan 1, 2011

By Ruixiang Wang, Jinhui Li, Youjun Xiao, Daoling Xiong, Hao Chen

"Leaching solution prepared from spent battery materials contains large quantities of valuable metals, such as Cu, Ni, Co, Mn and Fe. Therefore, recovery of valuable metals from acidic polymetallic aqueous solutions is of great importance for every plant. In this work, a method is introduced of recovery of Ni, Co and Mn from polymetallic solution prepared by leaching spent battery material. The basic concept includes copper was removed through replacement by iron powder followed by iron precipitation in goethite method. The experimental results show that Cu can be removed 99% at least through replacement by Fe powder, and the removal of Fe can achieve 99% by goethite method. At the same time, the loss of Ni, Co and Mn are about 2%, 3 % and 2%, respectively. The process of differential removal of metals can be selected as the treatment alternative that combines simplicity, efficiency and reliability with low capital and maintenance costs. The purified solution which only contains Ni, Co and Mn can be used to prepare NixCoyMnz ternary system precursor.1 IntroductionNickel and Cobalt are very important metals which are applied in many fields, such as energy material and support material for some new material field. The world demands for such metals is progressively increasing, while raw resources are being depleted and with the constraints raised by the Law and related legislation assigned to protect the environment from hazardous wastes in the world. Nowadays study on reutilization of waste materials has great significance for achieving secondary resources recycling and preventing environmental pollution. There are many hydrometallurgy methods applied for dealing with these wastes, while they usually contain large quantities of valuable metals, such as Cu, Co, Mn and Ni, as well as impurities, such as Fe, Zn, and etc. Therefore, proper treatment of these leaching solutions prior to their discharge is of great importance, so that the contained valuable metals can be recovered.Separation and extraction of metals from leaching solution can use some methods through solvent extraction[l,2], ion exchange[3,4], precipitation with sulfide[ 5] or alkali[ 6] and electrolytic recovery[?]. Among the appropriate treatment alternatives, replacement and differential precipitation is the most attractive treatment that combines simplicity, efficiency and reliability with low capital and maintenance costs."

Jan 1, 2011

By Luis Velazquez, Andrea Zavala, Nora Munguia

"This paper is aimed at describing the evolutive strategy in which the University of Sonora is following for optimizing the organic and inorganic material life cycle in the products used on campus. The institutional strategy has be oriented towards new patterns of behaviors in order to integrate the principles of sustainability as a guideline for preventing, eliminating, and/or reducing the negative environmental and occupational impacts generated when performing university substantive functions of teaching, research, and outreaching and partnership as well as its management operation tasks.IntroductionThe University of Sonora is the largest and most important university among several other universities in both the city and the state. It is a public university with a 29,792 students in three campuses in the state. The main campus of the University of Sonora is located in the capital city of Hermosillo, which has a population of more than 609,829, in the state of Sonora in the northwestern region of Mexico [1].Despite the fact that in the University of Sonora there were, in the eighties, some projects dealing with environmental issues, there was not until 1992 that the sustainability efforts were really initiated. It happened when the Sustainable Development Group was created in the Department of Industrial and Systems Engineering as a response to the need for adapting the industrial engineering curricula to the challenge of sustainable development [2]. In order to promote sustainability, it has been necessary to cope and break with several university paradigms. For this reason, the strategy for becoming a sustainable university has continuously evolved throughout the years from a simple structure composed by individual and isolated projects to a systematic and integrative Sustainability Management System. Thanks to this evolution, the University of Sonora has won a respectable reputation in the greater community and it is seen in the region as an icon of sustainability promoter. In this sense, the substantives functions of education, research, and outreach and partnership, which are considered supportive and integrative, have also evolved to play a key role for the success of sustainability initiatives.The institution has followed four avenues for becoming a sustainable university; education, research, outreaching and partnership and greening the campus [3]."

Jan 1, 2008

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

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

Jan 1, 2008