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By Guozhu Ye, Mikael Lindvall

"Swedish iron ore contains about 0.1 %V. The vanadium is reduced to the hot metal in a blast furnace and oxidised to the slag in a converter. The high V-content, up to 5 % V, leads to a very limited external application of the steel slag in Sweden. Since 2004, MISTRA - the Swedish Foundation for Strategic Environmental Research has together with the steel and mining industry in Sweden and Finland initiated and supported a long term project aiming at efficient recovery of vanadium in the slag, and at the same time a useful slag product with low V-content. The proposed concept consists of a reduction step and a phosphorus removal step. This paper will highlight some of the results with focus on the various metallurgical reactors used for slag reduction, including results from recently performed pilot trials using a DC furnace for cotreatment of metallurgical slags and other wastes.IntroductionToday, less than half of the produced LD-slag in Sweden is recycled to the blast furnace as a lime source and the rest is temporarily stored inside the steel plant. The steel slags cannot be used externally due to its content of vanadium and free lime. As the slag storage area is limited, this has become a problem for Swedish steel producers. The disposition of the slag is also a great waste of a valuable vanadium resource. The current potential value of vanadium in the discharged steel slag annually amounts to roughly US$ 100 million. Currently, Swerea MEFOS is conducting an 8-year vanadium recovery project called VILD (Vanadium in LD-slag) aiming at efficient recovery of vanadium and at the same time producing a useful slag product with low V-content. The project is financed by MISTRA - the Swedish Foundation for Strategic Environmental Research and the steel and mining industry in Sweden and Finland. Various reactors and process options have been tested in the past 7 years, from 3 kg laboratory scale, 150 kg induction furnace, 3 MVA pilot DC furnace, 5 MVA pilot AC furnace, 5 tons Kaldo furnace, to full scale direct hot slag reduction in the industrial site (12 tons of slag). This paper will introduce the VILD-concept and review the experiences gained from these trials. The advantages and disadvantages of the different options will be discussed and concluded."

Jan 1, 2012

By LeoJ. Miller

Exploration for an ore deposit commences with an outline of the regional ore controlling environment and is followed by the application of tools to focus the target area. One of the most essential focusing is the mapping of the mineral assemblages within the area of the ore. Key elements of mineralizing fluids, either epigenetic or syngenetic, enter into mineral assemblages that extend far beyond ore deposits. Portions of these assemblages may consist of new matrix minerals or alteration of previously existing minerals. Today, ore deposits are divided into genetic classes and each class is d8fined by a specific geological environment. Ore deposits within a given class are associated with a mineralogy, that is characteristic of the ore deposit class. So faithful is the mineral assemblage surrounding, or within an ore deposit, that recognition of the assemblage may be sufficient to define the class. Porphyry copper deposits have long been noted for their halos of alter-ation minerals. The outermost ring of chlorite, epidote and calcite extend thousands of feet away from the main ore zone. The mineral associated with porphyry copper deposits have been well documented by our distinguished speaker Paul Kerr, at Santa Rita (1), and Silver Bell' (2), and by excellent papers from S. C. Creasey, 1959 (3), Sales, 1948 (4), T. S. Lovering, 1949 (5), our Co-Chairman John Guilbert, 1970 (6), and many others. Several recent porphyry copper mines have been discovered in recent years by utilizing the mineral assemblage model described by Lowell and Guilbert, 1970 (6). Dave Lowell applied his own model of mineral halos for the discovery of Kalamazoo at San Manuel (7), Arizona, and Casa Grande West, Arizona. The purpose of this paper is to outline the application of mineralogy for discoveries of deposits other than porphyry copper mines and in particular, to ore discoveries in which mineralogy has played a key roll.

Jan 1, 1981

By Thomas Gliick, Jianming Lu, David Dreisinger

"The recovery of manganese from the Boleo project of Baja Mining is via an acid oxidation and acid reduction process in seawater. Manganese as manganese dioxide is leached into solution as manganese sulphate with the addition of sulphur dioxide gas as a reductant and then precipitated as a manganese carbonate. The use of the manganese carbonate intermediate to produce electrolytic manganese metal (EMM) has been extensively studied. The manganese carbonate can be used in place of natural (MnC03) or reduced ores (MnO) of manganese as a feed to the EMM plant. Manganese carbonate can be dissolved in spent electrolyte from manganese plating, followed by purification using ammonium sulphide precipitation of minor elements and then electrowinning in a selenium free process. The results of small cell testing of manganese electrowinning are reported.IntroductionThe Boleo Project of Baja Mining is a greenfields development currently under construction approximately 5 km north of the town of Santa Rosalia, Baja California Sur, Mexico. The Boleo property is held by the Mexican company, Minera y Metalurgica del Boleo S.A. de C. V. (MMB). MMB is owned 70% by Baja Mining Corp. and 30% by a consortium of Korean companies consisting of KORES - Korea Resources Corporation, LS Nikko Copper, Hyundai Hysco, SK Networks and lljin Copper.The Boleo deposit has Measured and Indicated resources of264.7 million tonnes grading 1.50% copper equivalent (CuEq) & Inferred resources of 159.9 million tonnes grading 1.15% CuEq. The calculation of copper equivalent is based on a combination of metal prices and predicted metallurgical recoveries (Table I). The metallurgical recoveries have been confined by extensive bench and pilot plant testing. Proven and probable reserves are available at Boleo to provide for more than a 30 year mine life. Initially, 25 years of mine life and 23 years of process plant operation have been scheduled in the February 2010 Technical Report Update (www.sedar.com)"

Jan 1, 2012

By Felipe P. D. Lopes, Ailton Silva Ferreira, Sergio N. Monteiro

"Environmental issues such as global warming and water pollution are motivating fast changes in scientific and technological paradigms. Special importance is now being given to the so called environmentally friendly materials, which are renewable, recyclable and biodegradable. An example is the natural fibers with increasing industrial applications beyond the conventional uses as baskets, fabrics, ropes and carpets. In addition to traditional natural fibers, others like curaua (Ananas erectifolius) are being investigated for possible use as reinforcement of industrial composites. Since epoxy matrix is not yet incorporated with curaua fibers, the objective of this paper was to study the basic properties of epoxy composites reinforced with different amounts of curaua waste fibers. A comparative analysis aiming at the use of these composites as substitute for conventional building materials was carried out.IntroductionThis new millennium, which initiates with the 21th century, is experiencing a fast degradation of the environment by pollution and climate changes. Most of the problems are related to our methods of development associated with the use of fossil fuels and the energy intensive processing and production of synthetic materials. As a consequence, environmental issues such as global warming and ocean pollution are motivating rapid changes in technological paradigms. One relevant example is the current importance given to natural materials like the lignocellulosic fibers extracted from cultivated plants or found as industrial wastes [1]. These fibers are considered environmentally correct alternatives to substitute energy intensive conventional synthetic fibers such as carbon, glass, nylon and aramid. In addition to the renewable recyclable and biodegradable nature of the lignocellulosic fibers, the low cost and abundance in developing regions are major advantages that justify their increasing application as reinforcement of composites [2,3].In fact, nowadays, the use of natural fibers is no longer restricted to baskets, ropes, clothes and carpets. Industrial composites are introducing these fibers in large technological segments associated with car making, building construction and furniture [4,5]."

Jan 1, 2008

By Kouji Mimura, Masahito Uchikoshi, Minoru Isshiki

"HfO2 is expected to be a gate dielectric used in ULSI alternatives to S1O2. Although the materials used in ULSI are required to be significantly pure, commercial Hf contains > 2 mass% Zr. It is important to establish a process for removing Zr from Hf. In the present study, anion-exchange separation using a multi-column method was employed. The separation tests were carried out at variety of temperatures and flow rates. The decrease in the flow rate of the mobile phase made the elution curves of both Hf(IV) and Zr(IV) broaden contrary to the case of Co(II), Cu(II), or Fe(III). This is caused by the difference in adsorption rate on the anion exchange resin. In addition, more than one column was connected in series in order to enhance the separation. As a result, the content of Zr(IV) was successfully reduced to 1/100 of that relative to the raw material.IntroductionHafnium is one of the most important materials in modem society. The main applications of Hf metal are as a control rod in a nuclear reactors because of its large neutron-capture cross-section and as an additive to various alloys because of its corrosion resistance [1]. In addition to those applications, attention has been recently paid to HfCh as a high-x"" dielectric used in ultra large scale integration, ULSI, as well as ZrCh, AI2O3 and La2C>3, which are expected to be alternatives to conventional S1O2 thin films [2].The materials used in ULSI are required to have a high purity in order to avoid unexpected errors due to impurities. Furthermore, high purity Hf is indispensable for investigating the intrinsic properties of Hf metal. Thus, it is significant to establish the purification process for Hf from both the industrial and academic perspectives."

Jan 1, 2012

By Per Anders Eidem, Merete Tangstad, Jens Davidsen

"During excavations of submerged arc furnaces producing silicomanganese, silicon carbide (SiC) has been found. Contributing to the size of the inactive area of the furnace, the active area of the furnace where reactions occur will decrease, thus reducing the potential for pre-reduction in the furnace.This work studied the formation of SiC from the liquid-solid reaction between slag, metal, and metallurgical coke. Slags and metals with different levels of silica (S1O2) and silicon (Si) have been studied. The slag and metal has been heated together with coke, and the samples investigated by microprobe. The results show that SiC was formed on the coke particle through reactions with both slag and metal. For the metal, the carbon most likely diffused through the SiC to react with Si in the alloy. SiC formation with slag is likely to go through the reduction of Si02 to Si.IntroductionToday, Silicomanganese (SiMn) is produced in submerged arc furnaces (SAF) by reduction of S1O2 and manganese oxides, mainly with metallurgical cokes. Typically, the tapped metal has a silicon content of 17 - 20 wt.%. To achieve higher levels of Si, the metal can be refined by adding off-grade silicon metal, yielding low carbon SiMn. [1]. What is believed to be SiC that has been found during dig-outs of SiMn furnaces producing high silicon alloy. It is possible that excess amounts of SiC in the furnace cause operational problems, since SiC will occupy furnace volume. As SiC accumulates, the active volume of the furnace will decrease, increasing the flow of material and gas in the active areas of the furnace. Formation of SiC is inevitable, so it is desired to keep the formation as low as possible. To be able to control the formation of SiC, one has to understand the basic mechanisms."

Jan 1, 2012

By Hiroshi Maeta, Takao Kino, Hirota Osono, Kikuo Matsusaka, Azusa Shida

"Prior to refine an ultra-high purity material, it is necessary to estimate the surface cleanness of a base material. In this report, the cleaning method of a surface for refining of an ultra-high purity aluminum has been studied. Aluminum sample of 99.999% purity was p9lished mechanically and electrically and washed with various solvents. Surface composition and a depth profile near the surface were examined. Based on the experimental results, surface structure of an ultra-high purity aluminum was discussed.IntroductionRecently, studies on high purity metals have become of interest, and we have reported .various properties of an ultra- high purity aluminum1- 2)In order to purify a metal, it is necessary to clean a work area and to make vacuous as possible. So, we are studying the purification of aluminum by an ultra-high vacuum refining system and a zone refining system set up in a clean room with cleanliness class of 1000.Now, in order to avoid a mixing of impurities into the refining metal, a surface cleanness of a base metal is very important factor. The purity of the base aluminum used our work is 99.999%, but the surface state of the base aluminum is not clear. Aims in this work .are to investigate the surface state and to obtain the cleaning method of the base aluminum.Experimental procedureSamples used in this work were 99.9% (3N), 99.99%(4N) and 99.999% (SN) aluminum produced industrially and 99.9999% (6N) aluminum purified by us."

Jan 1, 2000

By Rachel De Lucas

Current methods of hydrogen storage are an impediment to the transition of our energy infrastructure from a hydrocarbon to a hydrogen base. The transportation, handling, and storage costs of hydrogen gas account for a majority of its selling price. Magnesium hydride slurry is a safe, environmentally friendly alternative for hydrogen storage. If this form of storage is to be adopted on a large scale, a cost-effective method for recycling the enormous amounts of magnesium hydroxide byproduct must be identified. The solid oxide membrane (SOM) process can be used to recycle the magnesium hydroxide byproduct into magnesium metal, which can be reformed into magnesium hydride and reused for fuel storage. Conventional magnesium extraction/recycling technologies require a great deal of energy and create byproducts that are harmful to the environment and human health. The SOM process poses none of these detrimental effects and requires less energy and feed preparation. The economic viability of a facility that utilizes the solid oxide membrane process for the direct reduction of magnesium must be examined in more detail if industry is to consider it. Cost analysis data related to the commercial viability of a scale-up will be compared to two standard industrial processes: current magnesium production techniques including electrolytic and metallo-thermic processes. We have shown in our cost comparison that the SOM process is cheaper than these traditional techniques and that it is also comparable to aluminum's Hall-Héroult process in cost but with none of the environmentally harmful byproducts.

Jan 1, 2006

By Pradeep kumar Jha, Manas Mohan Mahapatra, Sabin Kumar Mishra, Satish Kumar Ajmani, Satish C. Sharma

"Due to mechanical/ electrical failure in the C.C. line or inadequate availability of molten steel from coming ladle, sometimes one/two outlets of a multi-strand tundish in continuous casting unit is closed. Closing any of the outlets affects the flow distribution inside the tundish which in turn governs the quality of steel coming out. Hence it is important to study which of the outlets should be closed to have proper results in terms of flow behavior and inclusion removal inside the tundish. Present study aims at finding the effect of closing one or two outlets on flow behavior and inclusion removal in a multi strand tundish. It was found that closing the near outlet (outlet near to the inlet) increases the inclusion removal tendency than closing the other two outlets in a six-strand billet caster tundish (only three outlets are considered because of symmetry).IntroductionContinuous casting process transforms molten metal into solid on a continuous basis. This process is the most efficient way to solidify large volumes of metal into simple shapes for subsequent processing [1]. Molten metal is tapped into the ladle from furnaces. From the ladle, the hot metal is transferred via a refractory shroud (pipe) to a holding bath called a tundish. The tundish allows a reservoir of metal to feed the casting machine while ladles are switched, thus acting as a buffer of hot metal as well as smoothing out flow, regulating metal feed to the moulds and cleaning the metal [2]."

Jan 1, 2012

By Aly M. Abdel-Rehim

The present work deals with a study of the mechanical activation of processing of Egyptian monazite by its simultaneous ball-milling and pressure leaching in order to improve the recovery of thorium and lanthanides from monazite. Experiments of simultaneous ball-milling and alkaline leaching of monazite contrary to autoclave leaching were carried out in stainless steel ball-mills of cylindrical shape under different conditions of temperature, pressure, time and alkali amount and strength. The ball-mills were heated and mechanically rotated in an electric furnace by means of roll mechanism. The effective rotation speed was fixed at 130 rpm in all tests. The charge of steel balls of different diameters was equivalent to 45% of the total mill volume. Monazite was charged in ball-mill without preliminary grinding. It is found that high rate of monazite leaching by ball-milling leaching method is achieved at lower temperature, shorter time and lower expense of alkali than in autoclaves. The results obtained show that complete recovery of thorium and lanthanides from monazite (99.8%) by simultaneous ball milling and alkaline leaching is attained at 140°C within 2 h. It is concluded that processing of monazite by its simultaneous ball-milling and leaching is mechanically activated and accelerated as a result of grinding action of steel balls that caused the continuous removal of the hydroxide product from reacting particle surfaces. This leads to the exposing of fresh and activated monazite particles surfaces to alkali leach solution and consequently the acceleration of the reaction of monazite processing.

Jan 1, 2006

By Tomas Astorga

APEC, the Asia Pacific Economic Cooperation is the forum of 18 economies, having a combined GDP of approximately 56% of the total world income, and over 45% of global trade. Its mining sector produces a large portion of the main minerals and metals in the world. In 1997, APEC economies produced 67% of world copper output, 55% of gold, and over 45% of other base metals. Mining in APEC captures more than 60% of the total mining investment in the world. Against this background, the Expert Group on Minerals and Energy Exploration and Development, in short GEMEED, was created in 1996, under the auspices of the APEC Energy Working Group. The sustainable development of mining activities is a main concern in APEC and GEMEED. Several programs related to the subject are actively being pursued by the Expert Group. Among them, it should be noticed the creation of an Environmental Cooperation Sub Group coordinated by Japan, whose main aim is to encourage proposals related to the environmental soundness of mining projects in the region. Also, it should be noted the existence of a Database Steering Committee whose focus is the development of an information network related to mining opportunities in the region GEMEED is a gathering of experts from all the APEC economies. As such, it represents a privileged forum to discuss policy issues related to mining. On this regard, the paper focuses on concrete actions taken by GEMEED to enhance the sustainability of the copper activity in the region.

Jan 1, 1999

By Gavin K. W. Freeman

The efficient separation of cobalt from nickel is a fundamental objective in the refining of cobalt. Based on recent experience at the Corefco refinery in Fort Saskatchewan, the identification of a novel process for the selective precipitation of cobalt from aqueous ammonia leach liquors is described. The addition of calcium sulphate, CaSO4.2H2O (gypsum), to an aqueous solution containing cobalt(III) hexammine sulphate, [Co(NH3)6]2(SO4)3, will result in the precipitation of a sparingly soluble double salt having the stoichiometry, [Co(NH3)6]2(SO4)3.2CaSO4.xH2O, where x = 4 or 6. Leach residues, which may contain a significant quantity of cobalt associated with the cobalt calcium double salt, can be washed with process solutions that contain ammonium carbonate. After contact with ammonium carbonate, the cobalt is recovered into solution, while the calcium is re-precipitated as the insoluble carbonate. The simplicity of this elemental separation and its high selectivity for cobalt, as well as the demonstrated usefulness in improving cobalt recoveries, are the basis for the potential applications of this process.

Jan 1, 2003

By M. Kawakami

In the blast furnace, the reduction of iron oxide and gasification of coke occur simultaneously. It is well accepted that the gasification reaction controls the simultaneous reaction. Therefore, it is important to develop highly reactive carbonaceous materials. It is also known that the reaction is accelerated catalytically with the addition of some materials. In the present work, the catalytic effect of iron, nickel and CaO on the gasification of graphite and coke was examined. The catalytic effect of iron, nickel and CaO on the reaction rate of graphite was noticed The effect was larger at lower temperature. At 1373 K, the effect almost vanished. The effect was larger in the order of CaO, iron and nickel. The reaction rate of de-ashed coke increased by the addition of iron and nickel. The effect of iron was larger than that of nickel. The effect was larger at higher temperature, which was contrary to the case of graphite. The reactive surface area increased also by the addition. Therefore, the catalytic effect on reaction rate might be attributable to the increase in the reactive surface area.

Jan 1, 2006

By Donald O. Voit

A BASIC language program has been written that simulates the performance of an integrated solvent extraction circuit consisting of an extractor, a reflux fed scrubber, and a stripper. The program is designed to simulate the performance of a circuit having an aqueous feed containing each of the lanthanides as well as yttrium. The Kremser equation is used to determine the separation occuring in each section of the circuit. The required input variables are the feed composition, the separation factors, the light key extraction factors and extractor feed zone distribution coefficient, the number of stages, and the reflux ratios. The program calculates the composition of the streams at each node in the circuit, the total loading, and the remaining distribution coefficients. User interaction with the program is essential. The program has no capability to determine if the calculated values are consistent with various real restraints. Knowledge of the physical, chemical, and equilibrium behavior is essential to successfully utilize the program. The number of iterations required to achieve steady-state provides insight to the circuit response times. With suitable supervision the program can be used as a simulator for operator training.

Jan 1, 1989

By F. W. Warnaars

Chanarcillo is a historically well-known silver deposit which produced over 100 million ounces. High grade vein-type mineralization is confined to a prominent set of nearly vertical, NNW to NE fractures that intersected limestones, andesites and tuffs of Early Cretaceous age. A significant amount of disseminated silver mineralization extends laterally outward from the fractures for considerable distances in pyritic carbonaceous limestones, whereas more competent volcanic beds rarely contain lateral mineralization. Local exposures of skarns are mostly barren. Silver and minor base metal mineralization was probably formed peripheral to a granodioritic intrusion inferred to exist at shallow depth. Part of this intrusion is exposed nearby where it contains significant hydrothermal mineralization and alteration. This intrusion was dated at 83.8 m.y.

Jan 1, 1987

By Shengli Wu, Yuandong Pei, Shaoguo Chen, Zhixing Zhao, Haijun Kang, Jiangshan Shi, Wen Pan, Zhengming Cheng, Yaosheng Luo

Grate bar is the key component of the sinter machine used for loading sinter and raw materials. Bar channels are sometimes bonded into blocks, which affects the service life of bar, and more importantly reduces the effective ventilation area of the sintering, affecting the normal production of sintering, resulting in unstable negative pressure, higher electricity consumption, and lower production and quality of sinter. In order to solve this problem, the systematic study was done on bonding materials of bars, based on which bonding mechanism of sinter grate bars was obtained. The KCl is an important characterization of bonding. Control standard of blending ore that prevents bonding is K2O content below 0.06% and Cl content below 0.05%.

Mar 1, 2018

By R. L. Miller

An industrial wastewater, including plating wastes, is treated with sodium sulfide and ferrous sulfate to form a sulfide-oxide precipitate containing chromium and other toxic metals. Hydrocarbons, in the water, coat the sulfide-oxide particles, impeding metal recovery. Froth flotation, without reagent addition, was found to recover 93.9% of the solids from the sludge with simultaneous rejection of 89% of the water. Methyl isobutyl carbinol (MIBC) improved recovery and potassium amyl xanthate improved both recovery and grade. The process design has wastewater feed (without MIBC) to the rougher circuit. The rougher concentrate is conditioned with MIBC and fed to a cleaner circuit to achieve a high grade concentrate. About 95% of the water is recirculated to the waste treatment plant.

Jan 1, 1992

By R. J. Wesely

Non-ferrous smelters traditionally have a hot gas handling system. In these systems, the dust is captured as a dry material which is often recycled to the process. Some smelters use wet gas cleaning methods with the recovery of the dust as a wet sludge. Although this sludge can be recycled to the process, in some cases it is preferable to dispose of the sludge. This paper will discuss the disposal methods available and specifically will deal with one type of sludge which has a high arsenic and high lead content. Problems with this sludge were investigated and methods were tested with the aim of stabilizing the sludge so that it passes the EPA TCLP test. Results of the laboratory tests are given.

Jan 1, 2000

By M. Olper, M. Maccagni, C. J. N. Buisman, C. E. Schultz

The key point of the CX-EWS process is the conversion of lead compounds, contained in the active mass of spent batteries, into lead sulphide. The obtained lead sulphide is leached with ferric fluoborate electrolyte to dissolve lead and oxidize the sulphur from sulphide to the elemental form. The lead-rich solution is fed into a diaphragm electrolytic cell depositing lead and regenerating ferric fluoborate. The introduction of sulphate reducing bacteria technology in the sulphidization step of the battery paste improves dramatically the economics of the CXEWS process, reducing the costs of chemicals, avoiding gypsum disposal and minimising the unit operations of the process. This paper describes in detail this technology change with reference to the economics of the process.

Jan 1, 2000

By P. T. Velu

Light weight aluminum alloys are the major construction materials for a number of structures in automobile and aerospace industries. Higher cost of production is the key impediment which restricts the usage of these alloys. A new electrochemical process route for the low cost production of aluminum alloys is being investigated, in which alloying elements are obtained from the dissolved compound. In the present investigation, solubility of lithium compound has been determined by measuring the EMF, when it is dissolved in the electrolyte. The solubility of Li2CO3 increased with temperature from 2.95 wt pct at 1063 K to 7.57 wt pct at 1093 K. Activities of the compound in the electrolyte were deduced using Temkin's ideal solution approach.

Jan 1, 1995