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By Enrique Posada

"The Valle de Aburrá area, corresponds to the city of Medellín and neighboring municipalities, with more than 3 million people. The area generates a sizable amount of solid waste, which has been taken to landfills for the last 20 years. This paper proposes a model for public policy making which considers the cost and benefit of different alternatives to handle the wastes in the coming 20 years. Combinations of several alternatives: Recycling, waste reduction, waste separation, incineration, land filling with lixiviate treating and gas energy recovery, and organic waste composting are considered and modeled and the results presented as a contribution for a more rational approach to policy making than the one currently being employed.IntroductionThe author, working for INDISA S.A., acted as a consultant for the direction of planning of the Empresas Varias de Medellín in 2004. This entity has the responsibility for the handling of the solid wastes of the city of Medellín and some of the neighboring municipalities. At the present time more the 700.000 annual tons of waste are taken to the site of La Pradera, located in very rainy location (3.000 mm of precipitation per year), with complex in topography and very far away from the sources of the waste. During the work the author detected important problems that should be addressed, as follows:Lack of adequate technical administration and resources. The entity did not count with sufficient human resources to focus on the appropriate technical handling of the solid waste. The organization worked mostly with independent contractors, lacking enough coherence and integration. The internal workload was too large for the few people who had technical responsibility and this gave rise to attention problems. It is important to have clear technical procedures, technical know how and human resources, continuity in the activities. It is important to have a clear capacity to plan, to study, to make tests and monitoring, to pursuit and develop ideas, to optimize the processes and to introduce changes, to respond to environmental authorities, to the communities and to mass media and to handle the contractors. All this was basically lacking. In the case of the handling of the sanitary filling of La Pradera, for example, although the people in charge were very able and dedicated, the magnitude of the task was too large and the resources they had were insufficient. As a result, the site had at the time of the study, problems with thousands of vultures, lack of immediate cover up for the waste, uncontrolled leaching, the area being dirty and little attractive, despite being called a park."

Jan 1, 2008

By Manfred Schmidt

Realizing an invention of Professors Queneau and Schuhmann, Lurgi GmbH has developed a radically new lead smelting technology, which was demonstrated on a ?30,000 tpy scale at Berzelius Metallhiltten GmbH between 1981 and 1986. Designed to treat all grades? of lead concentrates as well as complex secondaries, the novel QSL-Process applied one bottom-blown, refractory-lined long reactor and comprises two basic steps: Continuous oxygen smelting of the green charge is followed by continuous carbothermic slag reduction. Four firm orders and a number of serious inquiries from major lead producers confirm that the QSL-technology has convinced the industry of inherent process advantages. These include low investment and operating costs, flexibility and environmental acceptance. In the fall of 1986 Cominco Ltd. decided to erect a 120,000 tpy QSL plant at the site of the Trail lead smelter. Feed materials will consist of lead concentrates and zinc leach residues. The designed QSL reactor has a total length of approx. 41 m, and working diameters of 3.74 m for the oxidation section and 3. 24 m for the reduction section .. Separate gas offtakes on both sections will enable to? reduce the sulfur dioxide gas volume, and to recover a mixed zinc-lead oxide fume. Operation of the QSL reactor will start end of September 1989. First results will be presented.

Jan 1, 1990

By Congcong Yang, Jian Pan, Deqing Zhu, Yang Zhong

A study of pelletization of one imported chromite concentrate with coarse site, poor ballability and refractory roasting performance was conducted in small scale tests, and high pressure grinding rollers (HPGR) was used to improve the pelletization. The mechanism of HPGR was revealed by means of SEM images and optical microscopy. Compared with the ball milling pretreatment, HPGR pretreatment can not only enhance the ballability of pellet feed but also drop the roasting temperature. Fired pellets, containing proper chemical compositions with high compressive strength of 2917N/pellet and good metallurgical performances, have been manufactured. The mechanism of HPGR reveals that chromite particle surface turns to more irregular after HPGR treatment and more new surface being formed because of more cracks, sharp corners and edges appearing, resulting in higher surface chemical activity, all of which improve the ballability of the chromite concentrate and contribute to the consolidation of fired pellets.

Jan 1, 2015

By J. Michael Canty

Over 25 years of US research in Mineral Recovery from Geothermal Solutions have lead to few commercial applications. With the World Bank program in Kamchatka, Russia in September 2005 a step was taken to vitalize and coordinate the many efforts to advance economic mineral recovery systems worldwide. The US Department of Energy is helping to spur on the interest and research needed to realize the many benefits of extracting minerals from geothermal solutions. The excitement of recovery of minerals from geothermal brines has many positive angles. The economics of certain geothermal site is improved if a revenue is arrived from a sellable commodity with the geothermal power. The use of cleaner geothermal brines also improves the capable use of the brine before reinjection. We will review the history of Geothermal in the USA and the opportunities for recovery of different minerals and the markets for them.

Jan 1, 2006

By W. H. Jay

Sulphide-containing minerals, particularly iron, lead to acid formation. In turn, the acid generates effluents such as copper acid drainage (AMD). The Berkeley Pit in Butte, Montana, USA and Mt Lyell in Tasmania, Australia, represent just two of many sites throughout the world for which acceptable treatment methods are required. In the gold cyanidation process, the presence of copper creates both a significant cost impediment and a potential environmental hazard. The tailings dam failure at Baia Mare in Romania which led to the release of copper and zinc cyanides created a major environmental disaster. The application of non-toxic water soluble polymers and ion exchange resins to selectively recover copper from AMD solutions, and the in-plant treatment of copper cyanide solutions and slurries to recover copper and recycle cyanide to prevent cyanide entering the tailings impoundment will be discussed. The economics of the various processes will be highlighted.

Jan 1, 2003

By Lætitia H. Delmau

SXFIT is the latest in a series of programs developed in our group to model solvent extraction systems of increasing complexity. SXFIT permits the user complete freedom to define the constituents from which the composition of each phase is to be specified in the data and from which all species of a model for a system are assumed to be formed. Activity coefficients in the nonaqueous and aqueous phases, water activity, apparent molar volumes of aqueous species, and solution density needed for the conversion of concentration from the molarity to the molarity scale are all taken into account by the program. Several extraction systems relevant to nuclear-waste treatment were modeled successfully using this program. As an example, the cesium extraction efficiency of the CSSX process chosen by the USDOE for cesium removal from high-level waste stored at the Savannah River Site can be predicted correctly for varying feed composition.

Jan 1, 2003

By E. V. Redin, B. A. Dubrovsky, E. V. Knyazev, A. I. Starikov

"Ti-V magnetite is one of the most abundant composite ore resources in the world. This ore cannot be fully processed via blast furnace technology because of high content of Ti02. According to the investigations carried out in the USA and Japan ITmk3 RHF (Rotary Hearth Furnace) technology is a breakthrough in Ironmaking. 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 Ti-V magnetite ore via the ITmk3 by means of the lab scale testing. Samples of ore from the Maly Kuybas deposit (Southern Ural), carbon reductant and fluxes were chemically analyzed. Green pellets were processed via a lab chamber 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 [l]. 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 put into operation the commercial plant at the Mesabi Nugget site in Hoyt Lakes (Minnesota) in 2010. 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 the Ti-V magnetite bearing ore with high content of Ti02 and Alz03 has been done. It is well known, if a lot of Ti02 and Alz03 enter the blast furnace, slag becomes viscous. The viscous slag is obstacle for stable operation of the blast furnace. Besides, high content of Alz03 raises the melting temperature of gangue minerals disturbing the coalescence of reduced iron to the nuggets."

Jan 1, 2013

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 Andrzej Szymanski

Recent developments in medicine have stimulated activities that? involve mineralogy. They include inplantation of inorganic and organic parts into bones and soft tissues, and uses of elements as basic stimulators for the human body. In addition contamination of the environment has increased the concentration of sane elements in food. Consequently f both the environment and food structure vary with geographical regions and influence human health. These activities in medicine have created the new fields of biomineralogy and of biogeochemistry as activities for the future.

Jan 1, 1989

By Arpad E. Torma

The identification and characterization of lithographic iron and sulfur oxidizing bacteria in the 1940' s. opened up new possibilities and challenges for the mining and metallurgical industries. These were exploited during the 1950's and' 1960's, when it was demonstrated' that mining wastes and complex unused mineral resources could be economically treated by bacterially assisted heap and dump leaching processes?. During the 1970's this technology grew into a more structured discipline called "biohydrometallurgy". In the l980's efforts were devoted to the identification of a variety of organisms involved in naturally occurring leaching processes. Further efforts dealt with the elucidation, of leaching mechanisms; the leach ability of nickel, coban, zinc, and precious metals; the desulfurization of coal; and diverse biosorpion phenomena. The application of genetic engineering techniques for the improvement of microbial performance was also initiated?. Current trends in biohydrometallurgy include improvement of many of the techniques noted above, as well as application of leaching. technolog.ies to. environmental remediation scenarios. These activities afford considerable opportunities for research in the 1990's. For example, bioremectiation of abandoned mining and processing sites requires development of new and economically viable technologies capable of removing low concentrations of toxic metals from high volumes of solid and/or liquid wastes.

Jan 1, 1991

By J. N. Kondo, M. Hara, T. Smida, N. Ooto, K. Domen

"A porous material composed of two-dimensional anionic sheets of a layered perovskite, KSrNb30 10, was studied as photocatalyst for the production of Hz in the presence of alcohol sacrificial donors. Colloidal single and multi-layered HSr2Nb30 10 sheets were formed by intercalating ietra(n-buthylammonium) cations into the interlayeres of H+-exchanged KSr2Nb30 10 (HSr2Nb30 10), and addition of HN03 solution to the colloidal suspension precipitated the porous materials in which HSrNb30 10 sh~ets rand~mly stuck together. Original HSr2Nb30 10 before exfoliation had a BET surface area of 1 m2 g-1, whereas the surface area of a porous material prepared under optimal conditions exceeded 100 m2 g-1. The porous HSr2Nb30 10 had considerably higher photocatalytic'activitie8 for oxidation of 1-propanol and 1-buthanol than HSr2Nb39io, indicating that in the porous materials many niobate sheets are available for decomposition of these large alcohols.IntroductionQuite a research effort has gone into the design and study of porous materials. Such materials with large surface areas would have applications in highly efficient adsorbents or catalytic reactions.We have been studying photocatalytic reaction by cation-exchangeable layered metal oxides, where alkali metal cations are intercalated into the interlayers of inorganic sheets.[1,2] There are several advantages to using layered compounds rather than bulk powders for photocatalysis. Layered compound is rich in variety, in addition, modifications of them are easily performed by exchanging alkali metal cations in the inter layers for H + or other metal cations. The most important advantage is that some layered compounds have considerably high photocatalytic activities than bulk catalysts because the electrons and holes generated in each thin inorganic sheet readily reach interlayer spaces as reaction sites at the illterlayer spaces. It should be very important for further improvements· of layered photocatalysts to utilize two-dimensional inorganic sheets effectively."

Jan 1, 2000

By Bowen Li, Matthew D. Andriese, Jiann-Yang Hwang, Zhiwei Peng

"Magnetic iron sulfide ore particles heat rapidly by microwave (MW) irradiation generating plasma during oxidation of surfaces. The high temperatures produced by the exothermic event decompose local portions of samples forming a differentiated flux of partially melted silicate (si-mt) with entrained metal-sulfide (sul-mt) droplets. The si-mt forms crystals of olivine (01) in Ca-rich pyroxene (Cpx) melt that resorbs a portion of iron sulfide (Po). The immiscible sul-mt droplets of (Fe,Ni,Cu)1-xS contain magnetic subsolidus Ni-pyrrhotite (Ni-Po) with Cr-bearing ferrospinel (Mag). Sub-micron sized flecks of Au are found on the surface of a sul-mt droplet with scanning electron microscope (SEM).IntroductionSulfide ore deposits supply the world's mineral resource in the production of non-ferrous metals. Particularly, Cu-Ni deposits are chemically enriched in metals from high sulfur saturation during magmatic formation that creates the proper geochemical environment for metals enrichment [1, 2]. The sulfur and oxygen fugacity control redox conditions of a differentiated silicate/sulfur magmatic melt with the concentration of iron playing a dominate role in the chemical partitioning of metals in sulfide liquid [3, 4]. The initial magnetic crystallization of (Fe,Ni)i-xS monosulfide solution (mss) from metal-sulfide liquid has an exclusive effect on the fractionation of mineral assemblages (zoning) [5].Phase equilibria of sulfide melt (sul-mt) components are related by a miscibility gap with mss forming Ni-rich pyrrhotite (Ni-Po) followed by the crystallization of (Fe,Cu)1-xS intermediate sulfide solution (iss) [6]. Precious metals form stable chacogenides and are retained in solution until the final liquid solidifies. The redistribution of metals now occurs by subsolidus cooling of mss and iss that exsolve low-temperature Fe-Cu-Ni bearing mineral assemblages [7]. The proper interpretation of ore genesis increases processing capabilities by isolating chemically enriched zones during extraction and should be used to aid in sustainable mine site development [8-11]."

Jan 1, 2013

By Felipe Costa Hashimoto Bertin, Jorge Alberto Soares Tenório, Rodrigo de Souza Dalti Pereira, Denise Crocce Romano Espinosa

"The increasing amount of portable devices and their fast obsolescence generates an increasing quantity of discarded batteries. The recycling process of discarded batteries allows the recovery of metals for further use and avoids the contamination of soil and water. Even though there are several researches on the topic, few papers focus on mixed batteries. The purpose of this work is to characterize a mass of collected mixed batteries and study the hydrometallurgical process of recycling. The specific leaching parameters studied were pH, temperature and reduction potential. The specific goal was testing the selectivity of pH for leaching each metal. The results show that the optimal leaching occurs in acid solutions with negative pH at IM of sulfuric acid and at room temperature (25°C).IntroductionThe increasing portability of electronic devices in the past century along with their fast obsolescence produce tons of discarded materials yearly that could be recycled generating new materials for the industry. For example, metals such as cobalt and nickel, that are worth respectively US$ 30.00 and US$ 16.10 per kilogram[l,2] are disposed in urban trash yearly, which means that millions of dollars are thrown away instead of being recovered and reused[3].Besides the obvious fact that the society is throwing money away, most of these metals are toxic for the environment and all mammals, so when badly stored after use they can be found contaminating ground water which will contaminate the entire lifecycle. Some of these metals can cause cancer, serious lung problems and have bioaccumulative properties [4] resulting in lower productions of natural products and maybe death for consumers.So in compliance to new regulations such as the National Solid Residue Politic (PNRS) and the CONAMA-Resolution N°401 from November of 2008[5]- (that follows similar restrictions and regulations as the European directives) all those urban and electronic wastes need to be correctly disposed and treated before being thrown away on local dump sites.In Brazil the national rate of garbage recovery is around 70%, which only 5% is properly recycled, accordingly to the research of the UFSC, also electronic waste grows at 5% per year [6]The present study was motivated by the fact that recycling processes for batteries are not spread through the country and by the fact that most papers do not try to recycle a mixed mass of batteries, but a specific mixture which does not represent the composition of traditional household wastes."

Jan 1, 2014

By Xiyun Yang, Hui Xu, Xichang Shi, Xiang Xiao

"Rod-like magnetite particles were prepared by precipitation of iron salts with urea under the induction of magnetic field. Temperature and initial Fe3+/Fe2+ ratio have a significant effect on the composition of the product. Magnetite particles change from spherical into rod shape in the presence of a 0.35 T magnetic field, The addition of a small amount of spherical seeds increases the rod-like magnetite particles yield. The seeds are prepared by aging ferrous and ferric solution with sodium hydroxide as precipitator. The aspect ratio of the rod is controlled by varying the volume ratio of seed to iron salt.IntroductionMagnetite, an important member of magnetic materials, has attracted a lot of attentions for its super magnetic properties. The rod-like magnetite particles have high anisotropy and coercive force as well as super magnetic properties compared to other shapes, and are widely used as high magnetic density media, magnetic devices and microwave materials [1-4]. Recent studies have found that magnetic field can direct magnetite growing along easy magnetization axis to get one-dimension particles [5-6]. Chen et al. [7] synthesized single crystalline nanorod magnetite under magnetic field. Wang et al. [8] discovered that magnetite grew along easy-magnetization directions under 0.35T magnetic field. Vereda et al. [9-1 O] found that magnetic field had a dramatic effect on the morphology, inducing the aggregates to line along one direction to form rodlike particles.At present, most of the synthesis methods reported in the literature result in a low yield of rod particles and the aspect ratio are difficult to control. Recently, we developed a seed-mediated growth approach to making rod-like particles in an aqueous solution. The spherical magnetite generated by oxidation serves as a seed. These seeds are then added to a solution containing iron salt and urea, and provide nucleation sites for magnetite rod growth."

Jan 1, 2011

By G. Kyle Green

Zirconium chlorinator residues contain an array of rare earths, scandium, unreacted coke, and radioactive thorium and radium. Because of the radioactivity, the residues must be disposed in special waste containment facilities. As these sites become more congested, and with stricter environmental regulations, disposal of large volumes of wastes may become more difficult. To reduce the mass of disposed material, the U.S. Bureau of Mines (USBM) developed technology to recover rare earths, thorium and radium, and unreacted coke from these residues. This technology employs an HCl leach to solubilize over 99% of the scandium and thorium, and over 90% of the rare earths. The leach liquor is processed through several solvent extraction stages to selectively recover scandium, thorium, and rare earths. The leach residue is further leached with an organic acid to solubilize radium, thus allowing unreacted coke to be recycled to the chlorinator. The thorium and radium waste products, which comprise only 2.1% of the original residue mass, can then be sent to the radioactive waste facility.

Jan 1, 1995

By Corby G. Anderson

For over a century, the Sunshine Mine in Idaho has been a major producer of silver. An estimated 335,000,000 troy ounces of silver has been mined. This has established the Sunshine Mine as the largest single source of silver in the world. Because the dominant silver containing mineral is tetrahedrite, a copper and antimony sulfide, normal metallurgical treatments to recover the precious metal are not practical. Thus, over the course of the company's history, novel, hydrometallurgical technologies have been developed on-site to handle complex, precious metal containing materials. Recently, the use of Sunshine technology has been extended to the recycle of secondary materials. As well, the use of Sunshine technology by other organizations for treatment of both primary and secondary feedstocks containing precious and base metals is an area of growing interest. This paper will provide an overview of Sunshine hydrometallurgical technologies including the applicability of Sunshine technology to the recycling of precious and base metals.

Jan 1, 1995

By Olga A. Gomon, Alexey N. Lozhko

The technology of heat treatment for metal frequently includes multiple fast heating and cooling of the products surface. If the product is heavy-weight or long-size, its moving from a zone of cooling to a zone of heating and return require a long time. Other important condition of ensuring qualitative surface at heat treatment is intensification of cooling phase. It is known that turbulization of a flow activates heat exchange and increases efficacy of cooling without increasing volume flow rate of water. Additional difficulty is to ensure the regularity of heating and cooling on length of a product. The technology of cyclic heat treatment of rolling products, at which mobile zone of turbulent heat exchange is formed on the surface of a product, was developed and realized. The submission of water occurs through to face spray systems. Each of the systems has six long-range atomizers, which are located circularly. Two flows of water move towards one another along a surface of a product. When they collide, the right zone of turbulent heat exchange creates heat transfer in this zone of 10-15 time more intensive than on other surface of a product. The effect of moving turbulent zone on length of a product is reached by changing the proportion of volume flow rate of water, which is created by face sprays. The speed of movement for turbulent zone along a surface of a product is chosen so, that the cooling takes place on a small depth only. Then after passing the turbulent zone over a determined site of a surface, its temperature recovers fast owing to hot internal layers. The parameters of process were determined by mathematical simulation of cooling in an installation. The equations for dynamics of movement of collision point of flows, which were received this way, are interesting supplementary products of research. The experiments show that frequency of movement of turbulent zone is an important technological parameter. It defines mechanical properties of a surface and should be chosen depending on a profile of product and metal grade. The results of comparison of mechanical properties of a surface of various rolling products, which were received by developed and conventional technologies, are described in this report. Dependence of regularity of mechanical properties on frequency of movement of turbulent zone is adduced.

Jan 1, 1998

By Shigehito Deki

"A new wet process has been developed for the synthesis of various kinds of oxide thin films on various kinds of substrates, even which have complex surface morphology, from aqueous solution. The process was named as the LPD, Liquid Phase Deposition, method, which has some advantages over the conventional dry processes. This process can be applied to an on-site synthesis of advanced materials in the thin film technology. In this paper, some current topics on the synthesis of the composite thin oxide films by the LPD method, are presented.IntroductionGenerally, metal oxide thin films have been made by different preparative processes such as r.f. sputtering, chemical vapor depositon, CVD, laser ablation and sol-gel method, etc [1-3]. Each method has it own advantages and disadvantage. In some cases, the process is not suitable for the preparation of thin film on substrate with large surface area or complex surface morphology, and makes the deposition apparatus complicated and expenisve. By using Liquid Phase Deposition, LPD, method which overcomes some of those problems, metal oxide or hydroxide thin film can be formed on the substrate with large surface area and complex surface morphology, which are immersed into the aqueous solution only at ambient temperature and under atmosphere without any special equipments and high energy. And also, multicomponent oxide thin films can be formed readily by mixing solutions containing the objective metal ions, because it is performed in the aqueous solution which is typically a homogeneous mixing system. This process utilizes ligand-exchange, hydrolysis, equlibrium reaction of metal-fluoro complex species, MF x (x-2n>-, and F consumptive reaction. In the aqueous solution, MFx<x-2n>-is hydrolyzed with water to release F ions by a ligand exchange equilibrium reaction as following;"

Jan 1, 2000

By W. Zhao

Several years ago, Reddy and Blander presented upriori model for calculating the sulfide capacity of binary silicate melts. It is modified now to apply to CaO-AlO 1.5 melts at different temperatures and compositions. Our predictions are in very good agreement with the available experimental data. From a comparison of binary calcium aluminate and calcium silicate systems, higher sulfide capacities are obtained in aluminate systems. The sulfur can be removed from hot metal more effectively by adding aluminate melts.

Jan 1, 1995