Search Documents

By Ajit Kumar Jaiswal

"Electric Arc Furnace (EAF) being a power-intensive equipment, EAF based industries are highly dependent on scarce electric energy. This is the reason Government of India is highly concerned about this and laid emphasis on the conservation of electric energy.This paper highlights factors contributing to reduction in specific electric energy consumption in EAF and suggests measures not only for power saving, but also for productivity improvement. To name a few, these are proper sealing of furnace, introduction of oxy-fuel burners, foamy slag practice, increased usage of hot metal/DRI, post-combustion of CO gas for preheating of scrap, improved selection & design criteria of electrics, power demand management, and process automation. Few cases also have been cited, where the above measures have helped in reaping significant benefits.IntroductionFor a long time, Government of India had focused on increase in energy supply, in particular, through electricity generation. Now the emphasis of Government of India has shifted from electricity generation to its conservation for following two reasons:??Power plants have become very cost-intensive??By saving energy, more of it can be delivered at lower cost to the consumersPower generating units, transmission & distribution agencies as well as consumers all have roles to play in the area of energy conservation. By energy conservation, we mean curtailing energy requirement by reducing energy wastages and taking up measures to improve energy efficiency of electric equipment/appliances. In almost all cases, this would be economically beneficial.India’s cost-effective energy conservation potential has been estimated by the Planning Commission at 23 per cent of total commercial energy generated ?1?. A national movement for energy conservation can significantly reduce the need for fresh investment in energy supply systems in coming years. It is imperative that we make all-out effort to realize this potential. Whether a household or a factory, a small shop or a large commercial building, a farmer or an office worker, every user can and must make this effort for his own benefit and for the nation’s benefit as well."

Jan 1, 2009

By Camila Martini Matos, Maria das Graças da Silva Valenzuela, Francisco Rolando Valenzuela Diaz, Lucy Gomes de Sant' Anna, Orley de Oliveira Magalhães, Flavio M. S. Carvalho, Isaac Jamil Sayeg

"Kaolin clays are widely used in various industry segments. Its main properties are fine granulometry, chemical inertness and whiteness. In general, kaolins are not easily organophiilized as a result of its 1: 1 structure. The aim of this paper is to describe the modification of a Brazilian kaolin sample, in order to obtain an organophilic kaolin of high performance. The clay as received was identified by X-ray diffraction and characterized by optical microscopy, cation exchange capacity and swelling tests for observation of their performance in water and organic solvents. Then, the sample was treated with a 10% sodium carbonate solution and with ammonium quaternary, washed several times with distilled water, dried at 60°C, and characterized by XRD and swelling assays. Our results show that the clay was organophiilized and its ability to swell in organic solvents has increased.IntroductionThe kaolin clay, also known as ""china clay"" is chemically a hydrated aluminum silicate characterized as a very fine powder and lamellar structure (1:1), being constituted mainly by kaolinite [l]. Kaolin is a mineral extremely used as raw material. Its properties such as color, softness, small particle size and chemical inertness make it a suitable material for several industrial applications. The desired properties of kaolin varies widely for each application, beginning with its largest use in the paper industry until minor uses in the sectors of cosmetics and pharmaceutics. These two last applications require purified kaolin with defined functionality [2]. To find improvements in the functionality of kaolin for specific applications is important for many industrial uses. Sometimes the way to find these improvements might be modification of the kaolin clay by treatment with a chemical substance as ammonium quaternary, causing surface modifications [3,4]. In this work is described the modification of a Brazilian kaolin sample by treatment with cetyl trimethylammonium chloride (CTAC). The properties of the modified kaolin are being assessed by characterization and essays to understand its functionality and industrial application."

Jan 1, 2013

By H. Ipek

In this study the effects of interstitial ratios on k-feldspar samples were investigated. The k-feldspar samples were taken from Egypt using dry batch grinding conditions and a kinetic model. Three different mono size fractions (-3350+2360, -850+600 and -300+212 µm) were ground separately for 0.5, 1, 4, and 8 minutes and at four different interstitial ratios (125%, 100%, 75% and 50%) using a Bond mill with a mixture of five ball sizes. The mill used was at a size of 30.5 cm diameters, with 30.5 cm length, providing a total mill volume of 22272 cm3. The mill has a total mass consisting of 22648 g. steel ball mixtures of 38.10, 31.75, 25.40, 19.05 and 12.70mm diameters, occupying 22% of mill volume. The mill rotates at a speed of 70 rpm. The weights of the feed charges were 3000, 2000, 1000, and 500 g for 125%, 100%, 75% and 50% filling of the interstices of the balls respectively. The specific rate of breakage (Si) was determined from the top size fractions at different grinding times that were mentioned above and the model parameters were compared for the four different powder filling ratios (U). In many investigations, it has been found that an interstitial filling ratio of U = 0.6-1.1 is a good powder ball loading ratio to give an efficient breakage in a ball mill. In this study, it was found that U=1.25 is a good ratio for K-Feldspar.

Jan 1, 2006

By M. J. Soria-Aguilar, F. R. Carrillo-Pedroza, S. Preciado-Nuñez

"Dust originated from the Iron Blast Furnace (BF) and the Basic Oxygen Furnace (BOF) containing alkalis and zinc are not completely recycled because due affects the process efficiency. These types of dust represents an economical lost as a consequence of values contents of iron and carbon. Several processes in aqueous media have been developed to treat the steelmaking dust. This work presents a laboratory study for reduce zinc and alkali containing in BF and BOF dust, using different acid and alkaline solutions and oxidants as ozone. The results obtained show that the elimination of zinc and alkalis can vary from 5 % to 80 % depending on the treatment conditions (the solution, the oxidant and the temperature). The dust obtained from this treatment can to be recycling to the steelmaking processes to recovery iron and carbon values.IntroductionEach one of the steel making industry processes generate several sub-products and residues containing useful units of iron, carbon and other elements that are or could be recycled to the productive process. Some of those sub products are the dust from the gas cleaning system of the blast furnace and the dust from BOF reductive process; such dusts are sent to the sedimentary lagoons. The dust represent a lost of 2 % of the total iron and coal mineral’s content feed to the process.The typical iron, carbon and zinc content of the blast furnace dust is approximately 40, 24 and 0.3 % and the content of the BOF dust are 50, 15 and 0.9 % weight respectively, with physics - chemical characteristics that became them susceptible to be agglomerated and feed to the blast furnace. But the high content of zinc does not allow recycling it into the process. At the blast furnace the presence of zinc propitiate the formation of film in the furnace wall; these elements are vaporized in the low section of the cube of the furnace and they are dragged by the gases to the top and condensed again at the cube. Part of these condensed materials strongly adheres to the furnace cover harming it and reducing the empty space of that section, causing eventually a severe perturbation of the ascendant gas flux [1]."

Jan 1, 2008

By K. S. Kawatra

In recent years, there have been several efforts to develop binder mixtures for iron ore pelletization. Some efforts have been fruitful, while others have encountered failure. For example, adding corn starch to bentonite is effective, while adding fly ash to bentonite is not. When binders are made with fly ash, a pozzolanic reaction occurs, but no such reaction occurs when bentonite and corn starch are used together. The authors analyzed which binders can be mixed, and which binders will succeed. The authors confirmed this analysis with several laboratory and plant studies. This paper presents this critical analysis, along with various combinations of binders for making Iron Ore Pellets.

By Takeo Fujino, Nobuaki Sato, Yarong Wang, Kohta Yamada

"Ternary mixed sulfides of some transition metals MTS3 (M=Ba, ·Pb, T=Ti, Zr) were synthesized by a relatively low temperature process using sulfur melt. The mixture of starting materials, such as, metals and/or binary sulfides and a large excess of sulfur was reacted in a vacuum-sealed Pyrex or quartz ampoule at 350- 600 °C for one to three weeks. After the reaction, the remaining sulfur was completely removed by a process composed of filtration of sulfur melt and followed dissolution in CS2• The binary sulfides impurities coexisted in the products were removed by rinsing the products in water and acetone. By using the above method, BaTiS3, PbTiS3 and BaZrS3 'Were obtained in pure form. The effect of addition of halides on the yields of these ternary sulfides were also discussed.IntroductionThere have been a vast number of studies on the preparation and physical and /or chemical properties of mixed metal oxides. As is well known, some of such compounds exhibit excellent materials properties, causing them for use in mechanical, electronic, magnetic and chemical devices. Not a few mixed metal sulfides show similar physico-chemical properties to those of the corresponding mixed metal oxides. However, the study of the mixed sulfide crystals is rather sparse mainly due to difficulties in preparing these compounds. In various methods which have been adopted for preparing mixed sulfides, the simplest method would be the solid-solid reaction of the component binary sulfides or elements. However, there are always diffusional constraints with regard to the reactions in solid phases causing it necessary to heat the reactants at sufficiently high temperatures, viz. 800-1200°C. On the other hand, some mixed sulfides are unstable at high temperatures or to change their materials properties due to sulfur nonstoichiometry and structural modification depending on temperature, i.e., synthesis of such compounds needs to be made at lower temperatures. Processing in alkali halide melts is hopeful to overcome the above problems but to obtain the halide melts the temperatures above ~ 600 °C is needed. Low temperature reaction has been carried out for the preparation of Hg1.24TiS4, which was formed by the ·combination of TiS2 and molten Hg metal at 320°C[l]. Reaction of WS2 with LiBH4 melt at 350°C yielded LixWS2[2]. These sophisticated methods, however, can be applied only to the vary special cases."

Jan 1, 2000

By Mark C. Bronson

The feasibility of several pyrochemical approaches-for separating non-radioactive constituents from ICPP HLW calcine were examined. The removal of aluminum as AICI3 from aluminia calcine was successfully demonstrated. The examination of pyrochemical processes to remove non-radioactive constituents, primarily aluminium, zirconium, calcium and fluorine, from zirconia calcine showed that fluorine removal was required in order to chlorinate the calcine. A molten calcium chloride wash, a calcium reduction, and. a sulfuric acid treatment were examined as possible zirconia calcine pretreatment options for fluorine removal. Fluorine removal from simulated ICPP zirconia calcine was demonstrated by both a CaCl2 wash method and a sulfuric acid treatment method. X-ray fluorescence analysis indicated that greater than 97% of the fluorine can be removed by either method. Fluorine removal by a calcium reduction using an alloying agent, zinc, or a calcium reduction using, a filtration separation were also demonstrated, but the efficiencies of fluorine removal were considerably less ranging from 50 to 90%. Regeneration of CaCl2 from the salt and oxide residues of the CaCl2 wash experiments was also demonstrated 'by an aqueous dissolution method. From the salt residue, 85% or more of the CaCl2 was recovered and contained little if any CaF2 or CaO. From the oxide residue close to 100% of the CaC12 was recovered. Because of the overall success of the CaCI2 wash, it was determined to be the preferred fluorine removal process. The sulfuric acid treatment to remove fluorine is effective, but the proposed overall flowsheet has not' been adequately demonstrated.

Jan 1, 1995

By Kampe. S. L., Baker. Andrew H., Tony Zahrah

"Experimental heats of reaction for the formation of several Al3Ti + TiB2 intermetallic composite formulations have been determined utilizing bomb calorimetry. To overcome the kinetic constraints and achieve ignition in these formulations, a boron (B)/potassium nitrate (KNO3) initiation aid was incorporated within the blended reactant compact. The heat contribution from the initiation aid was regressed to provide estimates of the heat of reaction of the nominal formulations. Powder x-ray diffraction was utilized to identify the products of the reaction and discern any differences between the predicted equilibrium products of the formulation and the actual products.IntroductionReaction synthesis is a technique for the creation of ceramics, intermetallics, and in-situ composite materials [1]. Reaction synthesis is defined by its self, propagating mechanism, where the energy liberated from a localized reaction within a green powder compact is enough to carry the bulk reaction to completion. Achieving a self, propagating state can be achieved in variations of two primary methods of initiation: uniform volumetric heating and directional propagation [2].Uniform volumetric heating involves subjecting a green compact of the unreacted formulation to uniform heating in a furnace to encourage diffusion to initiate the reaction (Figure 1a) throughout the bulk material. Directional propagation utilizes a point heat source at one section of a green compact of unreacted formulation (Figure 1b). The localized exothermic reaction at one point in the compact then initiates the reaction in the section of the compact adjacent to it and fully propagates throughout the entire compact until completion. Initiation of the localized reaction is generally associated with the melting of the constituent with the lowest melting point, with instantaneous initiation of the reaction usually occurring close to that melting point [1]. This melting point can be high in some systems of interest, such as the titanium (Ti) and boron (B) system in equation 1:"

Jan 1, 2011

By Jordan Mayorga, Joseph Kopp, Robert Boehm, Daniel P. Cook

"Solar generated power has long been considered a useful energy source only for low-energy density and non-mission critical use, such as providing electricity for residential applications. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar- 1 near Las Vegas, have demonstrated that solar does have application to high energy density industries such as materials and chemical production. This paper will discuss the current operating con_guration of the Solar-1 facility and show how proposed modi_cations, such as addition of thermal storage and use of liquid salts as the working uid, can further improve the e_ciency and energy production of the plant.IntroductionThe United States as a nation is the largest consumer of energy in the world at an estimated 29 trillion kWh per year[1], which is roughly 15% of total global energy consumption[2]. On a per capita basis, the United States also leads most of the world, using an average of 96,000 kWh per person[3]. Roughly 40% of the energy consumed in the United States was produced from petroleum, 23% from coal, 23% from natural gas, 9% from nuclear and the remaining 5% from renewable sources such as solar, geothermal, wind, and hydroelectric[1].Energy demands associated with the industrial-scale production of chemicals and materials is a signicant portion of the United States total energy consumption. Roughly 33% of the energy consumed in the United States is used by the industrial sector, with 22% of this amount used in chemical production, 16% used in petroleum rening, and 14% used in the smelting and rening of metals[1]. Energy costs are also a signicant, if not the most signicant, portion of the total production costs for many materials. For example, roughly 30% of the cost of producing aluminum is the electricity used in the Hall-Heroult process [4], while the cost of energy is roughly 15% of the total cost of producing steel products [5].The primary sources of power for the industrial sector have been coal, petroleum, hydro- electric and nuclear. The use of alternative energy sources, e.g. solar, wind, geothermal, for industrial materials production has been slow in coming because they are intermittent and low-energy density sources, i.e. no solar power at night, no wind power when the air is still, etc. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar-1 (NS-1) near Las Vegas, have demonstrated that solar can have application to high energy density industries such as materials and chemical production.This paper will discuss the current conguration of the NS-1 facility, and potential modications to the facility that will increase both its power e_ciency and power density."

Jan 1, 2010

By Jerome Feinman, Sven O. Santen

"The principles involved in the generation and application of plasma energy are reviewed briefly and the major developments in commercial and semi-commercial primary metal and alloy production are described and discussed in broad outline, with emphasis on present performance and future potential. New concepts in the application of plasma energy in primary operations are described with emphasis on the expected advantages over conventional technology and the problems that have to be solved to enable effective implementation.IntroductionThe use of plasma energy in industrial processes is generally considered to have started in 1905 with the operation of the Birkeland process for nitrogen fixation for fertilizer production. Although it seems logical to apply plasma energy to metallurgical processes, which also usually require considerable energy at high temperature levels, serious development work along these lines did not begin until the early 1970's. The reasons for this hiatus are associated in part with recognized difficulties in applying plasma energy in processes involving tonnage quantities of solids in severe industrial environments and the delicate nature of the earlier plasma generators. Another, and perhaps overriding factor, is the fairly steady improvement in efficiency and economy of most primary metal producing processes by conventional developments and modifications through the 1950's and 60's. Examples of these evolutionary changes include burden preparation and fuel injection in blast furnace applications and prereduction treatments in ferroalloy operations. By the end of the 1970's most primary metal producing processes had been optimized close to the limit, at least in terms of those operations that were able and willing to implement the developed improvements. In this context, plasma energy offered the possibility to achieve further significant improvements in primary operations where conventional means were exhausted."

Jan 1, 1988

By Zheng Wei, Jian Cheni, Zhenliang Weng, Wei Liang, Hongbo Zhu, Jinhui Peng, Linqing Dai, Qianxu Ye

"By testing the dielectric constant and the dielectric loss factor of concentrated Dahongshan, mill scale, anthracite and light-burned dolomite in different frequency and temperature, and by studying the temperature-rising characteristics of the materials in the microwave field of 2.45GHz in frequency, the research in the paper shows that to reach at 1250°C under the same condition -2KW the microwave power and 30g the mass --the time concentrated Dahongshan takes is 330s, whereas the millscale is 855s and the anthracite is 820s. About the last one, the higher the temperature is, the stronger the absorptivity is. After the temperature has rose to 400°C, the anthracite's absorptivity increases dramatically. The result of the research would serve as the foundation of the further study on making direct reduced iron by microwave heating.1. IntroductionUnder the microwave fields, materials' dissipation of dielectric bodies would generate thermal effect. Therefore, the dielectric constant and the dielectric loss factor are closely related to materials' ability of absorbing microwave energy-the larger the dielectric constant and the dielectric loss factor are, the stronger the material's ability of absorbing microwave energy is, and the better the thermal effect would be[1-2]. In order to research how to make reduced iron from iron ore fines by microwave heating deeply and systematically, the test of raw materials' dielectric constants and dielectric loss factors are of the essence. What's more, because a mineral' conductivity is influenced by its components and crystal structure[3], it is necessary to study different materials' different temperature-rising characteristics; hence such studies would provide theoretical foundation of further research."

Jan 1, 2012

By Karl A. Gschneidner

Magnetic refrigeration was first used in the mid-1920's and new developments seem to have taken place about every 20 years, and this is especially true for the mid-1990's. The active magnetic regenerator magnetic refrigerator has the promise to become the first practical machine utilizing the magnetocaloric effect for cooling (and also heating). The basic principles are briefly discussed. Since the temperature lift for the magnetocaloric effect spans about 50 K, one will need to utilize several ferromagnets with different magnetic ordering temperatures in order to reach temperatures below ~250 K. The basic properties, behaviors, limitations, and new phenomena and knowledge are discussed.

Jan 1, 1997

By Vladimir Lobanov, Pritchinm Alexander, Nikifor Ageev

"Sulfuric anhydride is one of the most voluminous technological emissions. The possibility of high-temperature SO2 oxidations without catalyst in presence of calcium-bearing filling materials (CaO, Ca(OH)2 and CaCO3) with obtaining of binding material on the basis of waterless calcium sulfate is studied. Due to application package HSC-4 the thermodynamic analysis of the specified interactions is made and following conclusions are drawn: 1) Reactions are feasible in the all range of investigated temperatures (400 – 1000 °?); 2) The best results should be expected at use of ???; 3) The heat of reaction does possible autogenous behavior of process. The researches have shown: 1) Practical possibility of the process; 2) SO2 oxidation without the catalyst is feasible in presence of ???, Ca(OH)2 and CaCO3; 3) The optimum temperature range is 600-800 °?; 4) The content of waterless calcium sulfate in a product reaches 48% that makes it possible to use as the binding material; 5) At excess of ??? the degree of SO2 collection is nearer to 100%. Introduction At processing of sulfide raw materials in metallurgical furnaces the significant amount of sulfur, mainly in the form of sulfuric anhydride is escaped. Rich gases (SO2>3 %) are used for the sulfuric acid or element sulfur production. Chemism of sulfuric acid manufacturing is based on catalytic high-temperature oxidation of anhydride. Poor gases of metal works (SO2 =2,5 %) and power combustion units (SO2 =0,5 %) after clearing discharge into the atmosphere. Commonly, to recovery of weak sulfuric anhydride the chemical and physicochemical methods are applied. A few chemical ways of recycling sulfur dioxide are applied practically. In a number of methods for SO2 recovery a pulp of metals oxides (magnesium, zinc, etc.) with formation of sulfites is used. In other case sulfuric anhydride is catch by weak sulfuric acid in the presence of an oxidizer (pyrolusite ore). Methods of absorption SO2 by solid sorbents, (carbon fibers, silica gels, zeolites) are known and put into practice. Regeneration of the saturated sorbents is realized by thermal decomposition or extraction. Obtained as a result high-concentrated solutions are a commercial product."

Jan 1, 2008

By Jeong-Soo, Joon Soo Kim, Rajesh Kumar, Sohn, Jin-Young Lee

"Liquid-liquid extraction (LLE) studies of tetravalent platinum from acidic chloride solutions have been carried out with Alamine 336 as an extractant diluted in kerosene. The title metal shows the inverse behavior at higher acid concentrations. Plot of log D vs. log [Acid], mol.L-1 gave a straight line with a negative slope of 0.8±0.03 indicating the exchange of one mole of hydrogen ions for every mole of platinum(IV) extracted into the organic phase. Extraction of platinum(IV) increases with increase of extractant concentration. The plot of log D vs. log [Extractant], mol.L-1 is linear with slope 1±0.3, indicating the association of one mole of extractant with the extracted metal species. The plot between metal distributions to aqueous to organic phases is 1.3±0.01; it indicates monomeric species was formed in organic phase. Stripping of metal from the loaded organic (LO) with mineral acids such as hydrochloric, sulphuric, nitric acids and bases like ammonia, hydrogen peroxide and sodium hydroxide are studied. The results indicated that hydrochloric acid and sodium hydroxide are the better stripping agents when compared with other acids and bases. Increase of temperature decreases the percentage extraction of metal indicating the process is endothermic. Regeneration and recycling capacity of Alamine 336 and extraction behavior of associated elements such as aluminium(III), magnesium(II), cobalt(II), iron(III) and nickel(II) were studied.IntroductionThe demand for platinum group metals (PGM’s) has risen in the last five years expected to keep in rising. Right now, the demand is already beyond the supply. The primary use of PGM’s today is in the automotive industry. Catalytic converters used in the PGM’s process to reduce greenhouse gases. Because of the current demand to reduce the green house effect the expected need for platinum is here stay. Country’s now advancing in the use of car production also are phasing increasing the needs for this metal. Chemical processing also use it, too. These industries account for more than 50% of all platinum production. Jewelry is other primary use of this precious metal whose value is much greater than gold. Other uses include computer data storage, scientific developments, fuel cell technology and in the glass manufacturing processes."

Jan 1, 2008

By Luis M. González, Guzmánm Guillermo D., Davis Juan C.

"The Teniente converter (CT) of the Ventanas Smelter and Refinery of Codelco-Chile has two tuyeres for dry concentrate injection directly into the melt.The diluted phase injection system can feed 15 to 20 kg of concentrate for 1 kg of air, which creates a very abrasive solid/gas phase. The tuyeres commonly used lasted for about 3.5 days due to the accelerated decay of the shell, and 1.5 hours were necessary for the replacement of new ones in the reactor.Tests were carried out with common shell tuyeres with a tungsten based welding cover, and a life span of 28 days was reached, increasing the Teniente converter operational continuity between 1.5 to 2 %."

Jan 1, 2009

By S. Vellinga, G. H. R. Janssen, C. J. N. Buisman, C. F. M. Copini

Non-ferrous metallurgical plants are often confronted with the need to neutralize bleed streams or effluents containing sulfates. The treatment of these streams could produce large amounts of gypsum. With a biological sulfate-reduction process, the production of gypsum is avoided and the metals can be recovered as sulfides. In this paper, the biological treatment of an industrial stream is presented. The bleed solution from a roaster gas scrubber was treated by means of a two-step process. First, the acid was neutralized with calcine. The resulting zinc sulfate solution was converted to ZnS with bacteria using PAQUES-THIOPAQ® technology. The precipitated ZnS was de-watered to 70 wt% solids, and was returned to the roasters. The quality of the effluent stream complied with the environmental regulations.

Jan 1, 2000

By Chang Wei, Fan Zhang, Zhigan Deng, Minting Li, Cunxiong Li, Gang Fan, Xingbin Li

Marmatite is an important resource of zinc, which exist in forms of high iron and high indium. In order to recycle the valuable metal from these ores, the testwork of simultaneous leaching on neutral residue mixed with zinc concentrate of high iron and high indium has been conducted. The primary objectives are to leach the zinc and indium remaining in the neutral leach residue as ferrite using acid, and to reduce the ferric iron in solution to the ferrous by zinc concentrate, thereby extracting the zinc and indium in the zinc concentrate. The results indicated that in the following conditions, mass ratio of neutral residue to zinc concentrate of 1:0.25, particle size of 74-58 μm, initial sulfuric acid concentration of 150 g/L, liquid to solid ratio of 8 L/kg, temperature of 90°C, reaction time of 4h, the leaching efficiency of zinc and indium were over 95%, nearly 90% Fe was Ferrous in the leaching solution. This process effectively extracted zinc and indium and converted Fe3+ into Fe2+ in solution, and simplified the traditional process of reduction after leaching.

Jan 1, 2016

By Michael J. Marinigh

"Increased safety requirements, higher operational costs, greater environmental restrictions, and new competitive processing techniques are the challenges smelter operators must confront in order to remain economically viable.In converting furnaces which have tuyères such as the Noranda Reactor and the Teniente, Peirce- Smith and Hoboken converters, efficient tuyère line management is critical to optimizing blowing rates, increasing refractory life, and improving safety.This paper will describe recent improvements made to equipment used for tuyère punching, tuyère silencing, tuyère pyrometry and refractory drilling of tuyères and how the proper application of the equipment can lead to operational and safety improvements."

Jan 1, 2009

By R. C. Hubli

Copper (II) chloride has proven to be an efficient lixiviant for copper sulphide ores and secondary sources of copper such as scrap. Nickel sulphides are generally associated with copper ores and copper-nickel matte is an intermediate product of processing mixed sulphides. While the copper species in aqueous chloride media are present as chlorocomplexes, the presence of nickel as Ni++ offers effective separation between the two by solvent extraction techniques. Oxidation of millerite by cupric chloride in sodium chloride solutions has been studied as a function of rate of agitation, leaching time, temperature, acid concentration and total initial cupric concentration. The reaction has a 1/2 order of dependence on initial cupric concentration in the range of 0.0 to 0.5M. The activation energy for the temperature range 333 -363 K has been found to be 59.2 kJ/mol with chemical reaction at the unreacted mineral surface as the rate controlling step. The rate expression, according to the shrinking-core model, for initial cupric concentrations between 0.0 to O.5M, is evaluated as

Jan 1, 1996

By S. Mattlgod

Self-assembled monolayers on mesoporous supports (SAMMS) have been developed for the removal of heavy metals and some transition metals. The thiol functional groups were assembled on the internal and external surfaces of mesoporous silica with a uniform pore size of about 55 A. The mesoporous supports provide high surface area (>900 m2/g) needed for high metal loading in chemical separation. Self-assembled monolayers of organic molecules bond to the ceramic substrate with prescribed densities, and with terminal functional groups for excellent molecular selectivity. The unique characteristics include: (1) High metal absorption capacity, up to 3.2 mmol/g of SAMMS. (2) Fast Hg-binding kinetics (reducing mercury concentration from 0.5 ppm to 0.5 ppb in less than 5 minutes). (3) High selectivity in the presence of a range of cations, anions, and organic species. (4) Applicability in both aqueous and non-aqueous solvents. (5) Flexibility in surface chemistry. The materials can be designed to adsorb heavy metals, transitional metals, and radionuclides. (6) Chemical stability, and potential for regeneration or waste storage. This paper discusses the results on mercury adsorption.

Jan 1, 1999