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By F. K. Letowski

Leaching in froth is a particular case of a three phase (liquid-solid-gaseous) process which combines flotation with leaching by using a reactive gaseous reagent as a flotation carrier and a leaching solution as the reactive liquid medium to fonn the foam (froth) in' which the solid particles are suspended. Some physico-chemical and engineering aspects of leaching in froth are discussed and illustrated by its application for cleaning the mineral graphite. Leaching of the graphite concentrate containing 4L4% of the elemental carbon and 3.16% of the sulphidic 'sulphur was canied out in the froth fonned by: (a) a concentrated chloride solution, with a small addition of nitric acid, in the foam state; (b) a mixture of gaseous O2, NO., and H20 encapsulated in the foam; and (c) notable particles of graphite suspended in the foam. The laboratory experiments werecanied out in a "flotation column"-type reactor ala temperature from 80 to !08°C and under total pressure of 100 to 200kPa. In the 3-stage leaching-flotation process, the non-flotable fraction of particles was separated three times from the notable fraction. The concentration of carbon and elemental sulphur in the final flotable fraction was 96% C and 0.38% S respectively. The expected advantages and possible application in hydrometallurgy are suggested.

Jan 1, 1995

By M. M. Coleman

An investigation of the behaviour of sphalerite, chalcopyrite, galena and pyrite during flotation was conducted on selected circuits in the Brunswick Mining and Smelting Corporation Ltd. concentrator in Bathurst, NB. Samples were collected from 59 locations and analyzed for Zn, Pb, Cu, Ag, Fe, As, Sb, Sn, Bi and S. Metal balances were computed using the CAMP Material Balance Program (MATBAL 5) and the metal recoveries for each cell and circuit were calculated. An automated image analyzer interfaced with an electron microprobe was programmed to measure the size of sphalerite, chalcopyrite, galena and pyrite grains in each sample. The percentage of each mineral occurring as free grains and the relative amount of each mineral present in binary and ternary particles was calculated. The recoveries and losses of Pb, Zn and Cu are compared with the amount of liberated and unliberated galena, sphalerite and chalcopyrite present in the concentrates and tailings.

Jan 1, 1989

By P. S. Dunn, A. D. Rollett, H. D. Lewis

"The results of preliminary work on the modeling and measurement of the heat transfer coefficients of metal/mold interfaces is reported. The system investigated is the casting of uranium in graphite molds. The motivation for the work is primarily to improve the accuracy of process modeling of prototype mold designs at the Los Alamos Foundry. The evolution in design of a suitable mold for unidirectional solidification is described, illustrating the value of simulating mold designs prior to use. Experiment indicated a heat transfer coefficient of 2 kW/m /K both with and without superheat. It was possible to distinguish between solidification due to the mold and that due to radiative heat loss. This permitted an experimental estimate of the emissivity, ~ = 0.2, of the solidified metal.IntroductionA feature that distinguishes casting processes from welding processes is the presence of an interface with a low heat transfer coefficient between the mold and the casting. Especially when chill casting, the interface delays the start of solidification and increases freezing times significantly. By comparison welds can be assumed to have a very high heat transfer coefficient. The heat transfer coefficient controls such phenomena as folds and laps on the surface of castings which can be crucial to the acceptability of a casting. The time delay for the start of solidification influences the occurrence of cold shut defects. The standard mold material for uranium casting is high quality graphite which is an excellent refractory when used in vacuum and coated with a refractory wash. Graphite is an effective chill material and has a thermal diffusivity approximately twice that of uranium. Experience has shown that practicable superheat without mold pre-heat is not sufficient for avoiding cold shut defects when casting in graphite molds.TheoryIt is possible to calculate the position of the freeze front s, as a function of time, t, the superheat and interface heat transfer coefficient, h, [1]. However, the value of h cannot be obtained explicitly. The Virtual Adjunct Method (VAM) [2] offers a method for extending the standard equation for an insulating mold where s is proportional to the square root of time. By considering the effect of the interface to be equivalent to finite thicknesses of mold and metal, the following quadratic equation is obtained,"

Jan 1, 1986

By J. E. Klein

Bench scale tests using a stack of ten whole SAES St909 pellets, 6 grams, to crack methane have been completed with pure methane feed. Test conditions ranged from 600 to 800°C at 101 kPa (760 ton) with a methane feed rate of ten sccm. Methane reformation tests, test where hydrogen was passed through a St909 bed after cracking methane, were performed to determine if and how much methane can be generated under "reformation" conditions. Phase structure determinations of St909, composed of a ZrMnFe alloy with aluminum used as a pellet binder, after methane cracking were complicated by the number of materials that can be formed by the elements in the St909 and the carbon from methane cracking. It was determined that the aluminum not only alloys with the Zr, Mn, and Fe in the St909 alloy, but also forms aluminum transition metal carbides in addition to ZrC as the carbon content and the temperature of the St909 increases. Some A14C3 was also found in some pellets. Passing hydrogen over St909 pellets after methane cracking formed methane at various rates in the temperature range of 600 to 800°C. Temperatures of 800°C gave the best methane cracking performance and efficiencies decreased rapidly with temperature.

Jan 1, 2002

By Qin Hua, Xiangru Chen, Qijie Zhai, Yongsheng Yan, Liang Chang

"In this paper, pure bainite ductile iron and their alloying form of 0.2wt% niobium were prepared by a controlled cooling heat-treatment. The effect of niobium alloying on the microstructure, hardness and impact toughness of bainite ductile iron was studied. The results show that adding niobium effectively improves the hardness and toughness of bainite ductile iron. The hardness and the impact toughness of niobium-alloyed bainite ductile iron were investigated by varying the temperature at which samples were fed to the incubator.IntroductionThere are two essential methods to prepare the bainite ductile iron: isothermal quenching [I-31, and alloying [4• 51• Isothermal quenching process is very time and energy consumable, concerned as a high cost technique for mass production. Besides, there are certain limitations on the size and shape of castings in this process. In addition, it potentially harms the environment. As for the alloying, Ni, Mo, and Cu have to be utilized to obtain bainite. However, the large demand and high cost of Ni makes it not feasible in practice.It is well known that niobium can promote the formation of carbon compound, and improves the stability ofundercooled austenite, which is preferred to the increase of the hardenability. Previous studies showed that niobium could refine the grain and improve the mechanical properties of gray cast iron [6-81 • Therefore, in the present work, the effects of niobium and the temperature at which samples were fed to the incubator on the microstructures and properties of niobium alloyed bainite ductile iron were investigated."

Jan 1, 2014

By Joseph Sofra

It has become increasingly evident that sustainable metals production in the 21st century requires producers to balance the needs of cost effective, high value production with that of responsible plant operation. This is becoming more difficult as lower grade and more complex feed materials, including recycled scrap and residues, are being processed to reduce production costs and decrease exposure to primary metal market fluctuations. One particular facet of the metals industry facing these challenges in the 21st century are copper producers, The recent steady decline in the copper price has seen the industry cut expenditure, tighten control on income streams and focus on high returns on capital investment. For these reasons copper producers are looking towards flexible technologies that can deliver high value products, with minimal environmental impact at low capital and low sustainable operating costs. Ausmelt's Top Submerged Lancing (TSL) technology for copper production is a low cost, proven technology for the processing of both primary and secondary copper materials. Both the smelting and converting operations introduce significant advantages in environmental performance, improved process efficiencies and high rates of metal recovery, Ausmelt has made significant gains in the past 4 years in establishing a strong market position for its copper technology, New installations in China, South Africa and India as well as existing operations in Zimbabwe and China have demonstrated its effectiveness. This paper reviews the application of Ausmelt Technology for both smelting and converting of primary and secondary sources, It discusses Ausmelt's design and implementation philosophy, and how this philosophy meshes with the needs of the end user.

Jan 1, 2003

By Nathaniel R. Quick

"Nd: YAG, KrF excimer, and Cu-vapor lasers are used in air to synthesize conductors and semiconductors as a second phase in silicon carbide and aluminum nitride. Conductor resistivities as low as 104 O-cm are formed in these substrates; the resistivities for the untreated substrates range from 10 11to 1014 O-cm. The silicon carbide conversion is relatively independent of wavelength while the aluminum nitride conversion shows a dependence on wavelength over the range 248 nm to 1064 nm. Silicon carbide conductors, evaluated over the range 15 K to greater than 300 K, exhibit metal like conductivity; resistivity increases with temperature. Silicon, carbon, and oxygen are identified as the principal chemical species associated with the conductor in SiC substrates while aluminum, nitrogen, and oxygen are identified as the principal chemical species associated with the conductor in aluminum nitride substrates. The silicon carbide system, which has the less complex phase diagram, is evaluated in more depth to explain the synthesis mechanism. Oxygen was principally on the surface and increasing SiC conductivity is associated with decreasing spacing between 5 µm, or less, diameter carbon globules. This technology is proposed as a replacement for metallization in electronic packages, sensors and devices. INTRODUCTIONCeramics are commonly used for multichip module, hybrid and multilayer electronic packaging; semiconductor device and sensor applications because of the insulating, conducting, semiconducting, or superconducting properties that these materials possess (1,2) The majority of ceramics, however, have not been known to exhibit conductive or semi conductive properties when exposed to rapid thermal heat processing. A ceramic and process which through selective conversion can combine two or more of these electrical properties to eliminate the need for metallization is of interest to both the commercial and military sectors."

Jan 1, 1994

By Timothy W. Skszek, Adrian S. Sabau, Hebi Yin, Xiaoping Niu

The microstructure evolution during solution treatment plays an important role in mechanical properties of heat-treated aluminum alloys. In this paper, models were reviewed that can predict the microstructure evolution during the solutionizing process of the aging heat treatment of aluminum alloys. The dissolution ofMg2Si particles has been modeled as a diffusion process of Mg in the a-Al matrix. The evolution of volumetric fraction of fragmented silicon as a function of time and temperature was also considered. The growth and coarsening of silicon particles during the heat treatment was considered. It was found that constitutive equations and required property data for most of the phenomena that need to be considered are available. Several model parameters that need to be obtained from material characterization were identified. Pending the availability of these model parameters, this comprehensive model can be used to describe the microstructure evolution of aluminum alloys in order to optimize the solutionizing heat treatment for energy savings.

Jan 1, 2013

By Paykan Safe

Computational Fluid Dynamic (CFD) modeling provides a powerful tool to assist with the design of ventilation and fume control systems in smelters and other high temperature metallurgical facilities. For this paper, this tool has been used to analyze the off-gas flow patterns exiting the mouth of a Peirce-Smith converter into a water-cooled hood and drop out box. The effects of various process and physical plant design parameters on process gas and fume capture and potential build up on the converter hoods was examined, and the optimum design and operating parameters were determined.

Jan 1, 2000

By Toshiaki Nakai, Kunihiko Takeda, Kimio Imaizumi, Hiroaki Shirasaka

"The new type of nano-porous silica particle was considered to be constructed by the spinodal decomposition-type process which was found to have narrower pores than those of conventional porous silica prepared from boron silicate or ""Shirasu"" balloon. Nano-porous silica particles were fabricated by the calcination of silica gel mixed with well-dispersed complex salts composed of phosphorous and molybdenum compounds. Both silica and inorganic salts were not perfectly dissolved in the suspension solution. After removing of the water, the silica-inorganic salts complex was volatized and successively calcinated at a temperature ranging from 650 °C to 800 °C. Then, the inorganic salts were removed by dissolving in hot water. Other inorganic salts such as potassium halides were also found to be effective as a pore-size controller.IntroductionControl of structure has an important role in the field of industry as well as in the separation and purification technology for metals and organic syntheses. Many studies on the control of material structures have been reported regarding porous materials with pores ranging from nanometer to micrometer scale. 1 ) One example is zeolite as a naturally yielded porous inorganic material. Various types of synthetic zeolites have been studied as ""molecular sieve"" materials with ordinary pore-size of less than one nanometer. In 1992, crystalline meso-porous material with a large surface area named MCM-41 was synthesized through the use of template synthesis. 2) In direct relation to our study, amorphous borate glass having 4 to 100 nm of fine pores known as Corning glass 3l or SiO2-Al2OrB2O 3-CaO porous glass having large pore dispersity ranging from 4 to 10,000 nm have been reported. 4 ) S) 6 ) Some examples of several reported studies are as follows: phase-separated porous glass consisting of B2OrAl2O3-ZrO2-RO-R2O complex oxide 7 ) glass with finer pore induced from hydrolysis of silane alkoxide, porous material attained by condensation polymerization through the use of sol-gel process 8), alumina meso-porous material 9 ) 10), silica-zirconia material 11), carbon porous material 12), etc.."

Jan 1, 2000

By W. F. Ranson, R. C. Progelhof

"I. THE PROBLEM: MANUFACTURING PRODUCTIVITYThe 1985 President's Commission [I] on Industrial Competitiveness found compelling evidence of the declining economic position of the United States in world markets. The annual rate of increase in the United States productivity is approximately one-seventh that of our major trading partners over the last decade: profit levels in manufacturing investments are below those of the mid-1960's; an increasingly negative trade balance since 1971; and a sharp decline in the United States share of world trade in manufactured goods for more than two decades. A particularly dramatic example of the shifting economic balance is the fact that Japanese productivity growth has been five times greater than that of this country since 1960. In face, Japan's productivity now exceeds that of the United States in such critical industries as steel, transportation equipment, electronics and electrical machinery.American employees have experienced the competitive consequences of this nation's lagging industrial performance. Between 1980 and 1984 alone, the population of non-farm employees engaged in manufacturing dropped from 22.4% to 20.6%. This reduction in manufacturing must be arrested.Commissions RecommendationsThe comprehensive set of recommendations offered by the President's Commission recognized the nation's ""key competitive advantages"", technology and human resources, and calls for their strengthening. Particular emphasis is placed on manufacturing technology and the fact that this country does not translate research into new technologies rapidly and fully.""Perhaps the most glaring deficiency in America's technological capabilities has been our failure to devote enough attention to manufacturing or 'process' technology. It does us little good to design state-of-the-art products if within a short time our foreign competitors can manufacture them more cheaply. The United States has failed to apply its own technologies to manufacturing. Robotics automation and statistical quality control were all first developed in the United States but in recent years they have been more effectively applied elsewhere""."

Jan 1, 1988

By D. M. Hausen

A refractory siliceous low-grade silver ore (265 g/t Ag) from a prospect in Sonora, Mexico was investigated mineralogically and metallurgically to evaluate extraction of the silver by conventional methods. Approximately half of the silver was recoverable, occurring as coarsely crystalline acanthite (70-300 Am) that was liberated in material crushed to minus 10 mesh. The remaining silver is refractory and occurs mostly as finely locked (-2 to 0.2 Am) acanthite in cherty quartz, and as minor amounts of finely disseminated stylotypite or freibergite in fluorite. The mineralogic data have thus served to explain the 50-60% recovery of silver by flotation and cyanidation.

Jan 1, 1991

By C. Gasparrini

Mineralogy may be applied to the selection of appropriate separation techniques, as well as to assist in the evaluation of problems causing loss of metals and other economically important elements during plant processing. Mineralogic studies may thus help develop techniques to optimize metal recoveries. The present paper describes how such factors as the minerals in which the elements of interest are concentrated, their chemistry, the chemistry of the associated minerals, grain size and textural associations with other minerals in the ore, may affect decisions on separation techniques for the recovery of economic elements. A number of case studies are described in which the mineralogical observation of ore samples has revealed the cause of problems experienced in the extraction of select precious and base metals, or has been decisive in the choice of appropriate techniques for recovery.

Jan 1, 1981

By A. F. Saavedra, N. E. Richards, C. J. McMinn

"The aluminum industry in general and Reynolds Metals Company in particular have continued to support development work for improvement of the Hall cell design and for alternative processes for the reduction of alumina. The evolution of the Hall cell design will continue into the next century as a result of further development of mathematical models, sophisticated control systems and new materials for cell components. This paper discusses the areas in which the new generation cell advances will differ from the present day design. Additionally, Reynolds Metal s has supported work for the development of a carbo thermic process to reduce alumina. Theoretical work has indicated that this process could possibly have economic advantage over the Hall process. Several complicated furnace configurations have been proposed to provide the conditions for successfully reducing alumina. The results of small pilot scale operation and most promising furnace design are discussed. For comparison, projected capital investment costs and operation costs are discussed. IntroductionThe evolution of the Hall-Heroult process will continue into the next century. This evolution will be influenced by economics, more .restrictive environment and worker protection requirements, and technological development. These factors will also cause changes in the competitive position of alternate processes for aluminum production.Several aluminum producers have made major investments in alternate processes for aluminum production in the past three decades and there is continued support in some companies for improvements in the Hall-Heroult process and for alternate processes. The more visible development work in reduction technology, not aimed at significant process changes, is in the areas of higher amperage cells with bus bar designs to reduce harmful magnetic effects, more advanced and automated feed, voltage and electrolyte composition control, improved energy efficiency and sol id waste disposal . Efforts to bring significant change to the reduction process are being made in development of materials that can function as inert anodes and cathodes. These materials could lead to the development of reduction cells with multiple bipolar electrodes operating on oxide feed and fluoride electrolytes. Development work on new processes was reduced in the last decade by several companies because of economic and technological realities. Reynolds Metals supported work on a carbothermic process to reduce alumina and produce commercial pure aluminum. This work progressed through small pilot plant operation, and resulted in development of furnace designs and operation regimes. This paper reviews how this and other technologies could influence the reduction of alumina beyond the year 2000."

Jan 1, 1988

By Leijun Li, M. M. Mahapatra

"A three-dimensional finite element model with moving heat source was developed for pulsed-laser powder deposition (PLPD) process. Experiments were conducted to study the repair of superalloy components using the PLPD process. During the experiments, IN 625 powder was deposited on a superalloy substrate similar to IN 738. The process was modeled using three-dimensional finite element analysis. Element birth and death technique was used in the finite element model for simulating the deposition of powder layer on the substrate. A moving distributed heat source was used in the thermal model for realistic simulation of the process. Temperature dependent thermal material properties including enthalpy were used for the powder and the substrate in the transient thermal analyses. The fusion zones and peak temperature distributions of the deposits were predicted from the transient thermal analyses.IntroductionPoor weldability is a critical issue of superalloy repairing. The microstructural directionality of the superalloy components are disrupted when repaired by the fusion welding processes. Currently there is no widely accepted method to economically and reliably repair directionally solidified superalloys components. Pulsed laser powder deposition process (PLPD) is a promising repairing technique as the substrate is not severely affected by the heat source.In this study PLPD technology is used as the tool for superalloy repairing. In most of the land based turbine engines the directionally solidified nickel based superalloy similar to IN 738 [1] is used as the bucket material. The turbine engine blade tips are subjected to a combination of extreme operating conditions and corrosive environment. The tip of the nickel based turbine engine blades can be repaired using IN 625 material as suggested in the literature [1-2]. IN 625 is considered to be ductile and strong enough for the purpose of Ni based turbine engine blade tip repair[1-2]. During the present PLPD investigation, IN 625 powder was used as the deposit material on an experimental super alloy substrate similar to IN 738 superalloy used as the cast superalloy for the turbine engine blades."

Jan 1, 2012

By Carla Lupi, Alessandro Pescetelli

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

Jan 1, 2008

By Edita Vircikova

The best demonstrated available technology (BOAT) for the removal of dissolved arsenic and some heavy metals as reported by USEPA (Contaminants and Remedial Options at Metal Sites, Draft Report, August 1993) (1) is still the chemical precipitation. Coprecipitation with the excess of iron is usually practised because of the availability of iron at low/no cost and also in order to meet the stringent regulatory discharge limits. The arsenic is usually removed with iron because of its common occurence in the mined orebodies and the excellent adsorptive property of the precipitated hydrous ferric oxide compounds. There has been controversy, however, over the long-term stability of the arsenic-bearing ferrihydrite which is produced.

Jan 1, 1995

By Seung-Chul Lee

Transparent conducting tin(1V) oxide thin films have been studies and developed for the electrode materials of solar cell substrate. Fabrication of tin oxide thin films by sol-gel method is process development of lower cost photovoltaic solar cell system. The research is focused on the establishment of process condition and development of precursor. The precursor solution was made of tin isopropoxide dissolved in isopropyl alcohol. The hydrolysis rate was controlled by addition of triethanolamine. Dip and spin coating technique were applied to coat tin oxide on borosilicate glass. The resistivity of the thin film was lower than 0.18-cm and the transmittance is higher than 90% in a visible range.

Jan 1, 1999

By Yong Xian, Zhaohui Sun, Honggang Zhong, Qijie Zhai, Jie Sun

Vacuum refining is admitted as an effective means to remove impurities in the process of alloy smelting. In this paper, Orthogonal and single factor experiments were carried out to investigate effects of multiple factors, such as superheat degree of the melt, degassing time and vacuum degree, on the vacuum refining process. The results showed that the best removal rate of oxygen and nitrogen is up to 82.71% and 61.3%, respectively, due to high vacuum degassing efficiency. It is found that the superheat degree is minimal impact on the deoxidization rate, in addition, nitrogen removal is controlled by the degassing time. The inclusions exist in the AlV55 alloy are mainly composed of oxides and vanadium-nitrogen compounds.

Jan 1, 2015

By Bruce W. Wessels

"Metal-organic chemical vapor deposition has been shown to be a highly versatile technique for the synthesis of complex oxides. High dielectric constant oxide thin films of SrTiO3, BaTiO3, Ba1-xSrxTiO3 and SrxBa1-xNb2O6 can be be be deposited at 800 ºC with this technique. The fluorine substituted B-diketonate precursors have been shown to be well-suited for the deposition of high quality, epitaxial thin films of these materials.IntroductionThere has been a resurgence of interest in thin film ferroelectric oxides as a result of the development of techniques to deposit high quality material. Both physical and chemical vapor deposition techniques have been realized. Of the chemical vapor deposition techniques, metal-organic chemical vapor deposition (MOCVD) has received the most interest for the deposition of ferroelectric oxide thin films. This results, in part, from the availability of a number of volatile metal-organic precursors.(l) Moreover, MOCVD offers the advantages of high growth rates, uniform coverage over large areas, conformability, abrupt interfaces and excellent epitaxial crystallinity. Of the metalorganic precursors, the B-diketonate complexes have played an important role especially in the deposition of ferroelectric oxides containing alkaline-earth metals such as BaTi03 and Ba1•XSrxTi03. For example, barium tetramethylheptanedionate Ba(thd)2 has been used in the preparation of BaTi03 by MOCVD.(2) These compounds, however, are not without their problems. Ba(dpm)2 has a relatively low volatility; and as a consequence, temperatures in excess of 180·C are required for volatilization. This leads to the necessity of a complex precursor delivery system to insure that the precursor does not condense before the reaction zone. Moreover, the Ba precursor tends to oligomerize leading to a decrease in vapor pressure as well as a problem with reproducibility. To counter these problems, novel liquid source and solid source precursor delivery systems have been developed. (3)(4)"

Jan 1, 1994