Search Documents

By Luiz A. Teixeira

This paper reports the results of kinetic studies involving the precipitation of arsenic from aqueous solutions as FeAs041 Fe(OH)3' using FeS04 as source of Fe ions, and Air or H202 as oxidizing agents. Both systems lead to an efficient removal of arsenic. The differences in oxidants performances are in the precipitation reaction rate -much faster using hydrogen peroxide. Mechanisms of reactions were suggested based on the following main steps:

Jan 1, 1996

By Nathanael Hudson, Ruel A. Overfelt, Sushil H. Bhavnani

"In the aerospace and automotive industries, complex shapes exist which require casting. The problem with these cast parts is the empiricism required to develop the casting process and the accompanying time and expense to develop that process.There has been an interest in using fluidized beds to allow molding sand to better encapsulate the complicated surface geometries of lost foam patterns. Fluidization coupled with a mixing jet helps to homogenize the sand through stirring and may improve the integrity of the casting.At issue is the hydrodynamics of the sand and air around the foam pattern. The commercial package PHOENlCSTM is used to simulate the flow around the pre-casting foam geometry. Employing a two fluid approach, each component is considered a fluid that interpenetrates the other phase. To this end, the kinetic theory of granular 'flow for the sand phase was incorporated into the re-compilable PHOENlCSTM code.The results of this study consist of time-averaged void fraction patterns, with voidage being defined as the fraction of air in the mixture, around the foam pattern submerged in a two-dimensional fluidized bed. The model was benchmarked against past fluidized bed experiments. In order to better understand the dependence of the void fraction pattern around the lost foam pattern, certain physical parameters are varied and the resultant void fraction maps are predicted with the model. Physical parameters such as the aspect ratio of length to width, the placement of the mixing jet, and different mixing jet velocities are varied to illustrate the dependence of the time-averaged void fraction on those variables.Results consistently indicate the presence of channeling around the lost foam pattern, with the extent of the channeling and void formation reliant to a greater degree upon the placement of the mixing jet, and to a lesser degree on mixing jet velocity and aspect ratio.The increase in radial position of the mixing jet from the bed centerline had the desirable effect of granting the churning benefits of a penetrating jet, while at the same time minimizing the formation of excess void fraction at the top of the pattern."

Jan 1, 2001

By Shubin Wang

Copper(II) and nickel(II) are often recovered from ammoniacal alkaline solutions by solvent extraction using hydroxyoxime extractants: both copper(II) and nickel(II) are extracted from ammoniacal alkaline solutions and, from the loaded organic phase, nickel(II) is selectively stripped with a dilute acid followed by copper(II) stripping with an acid of higher concentration. Since a small portion of ammonia is co-extracted with copper and nickel, the extracted ammonia should be scrubbed using a dilute acid before metal stripping. In the present study, a mechanistic model has been developed in order to support design and control of this process. The equilibrium distribution ratios of copper(II), nickel(II), and ammonia at 298 K using LIX® 84-I (active component, 2-hydroxy-5-nonylacetophenone oxime) as the extractant are successfully correlated by considering the relevant equilibria. Based on these results, quantitative prediction of equilibrium distribution ratios in the process has been made possible, and suitable conditions for the efficient separation of copper(II) and nickel(II) are discussed.

By Yang Hong-ying, Yu Juan

Electrochemical behavior of natural chalcopyrite in electrolyte solution at pH value of 6.97 was studied by cyclic voltammetry, X-ray photoelectron spectroscopy and electrochemical impedance spectroscopy. The results showed that the electrochemical processes occurred on electrode surface were controlled mainly by the growth of sulfur species at lower applied potentials (<0.35Vvs.SHE), and the oxidative dissolution of sulfur species and the hydroxylation of iron at higher applied potential (>0.45V). The EIS spectra of oxide product layers could be illustrated by the equivalent circuit of Re(QdlRct(QfRf)), and the degree of hydrophilicity for chalcopyrite was higher when the value of charge transfer resistance Rct. was greater. The optimum potential range for the floatation of chalcopyrite in collectorless solution at pH value of 6.97 was between OCP (0.165V) and 0.35V.`

Jan 1, 2015

By Moo Eob Choi

A new process for converting sulfur dioxide to elemental sulfur by a cyclic process involving calcium sulfide and calcium sulfate without generating secondary pollutants was developed at the University of Utah. In this process, sulfur dioxide is reacted with calcium sulfide to produce elemental sulfur and calcium sulfate. The latter is reduced by hydrogen to regenerate calcium sulfide. In the present work, the effects of different pelletization conditions for the initial reactant calcium sulfate on the strength and reactivity of the pellets were determined. These conditions include the type, amount, and impregnation method of catalyst, binder amount, and sintering. Experiments were also performed to determine the effects of temperature in the range of 973-1173 K, pellet size, cycle repetition, and water vapor or carbon dioxide content in sulfur dioxide stream on the reaction rates of the cyclic process. Nickel-catalyzed fired pellets produced by the use of molasses or cement as a binder showed good reactivity as well as high compressive strength during the cyclic tests. The binder amount did not significantly affect the reaction rate.

Jan 1, 2006

By Guilian Gao

TbFeCo is a common choice for many rare-earth transition metal films currently used as the magneto-optic layer for magneto-optical: recording devices. Since the environmental stability of RE-TM alloys is typically poor compared with traditional metal oxide particle media, such devices rely on multiple functional overlayers (metallic and/or dielectric) and organic coatings for durability. This paper presents an electrochemical evaluation of the degree of protection of several candidates for the reflective layer, Al, AlCr and AIPt and for the dielectric layer, SiN, AISIN and AIN. Cyclic voltammetry In 0.2M K2SO4 solutions at room temperature revealed that AIPt film offers superior corrosion protection compared to Al and AICr films. Of the three dielectric layers examined, SIN seems to be the most corrosion resistant. Examination by optical and scanning electron microscope confirm the findings of electrochemical experiments. The corrosion resistance of single layers of Al, AICr and AIPt has also been examined and factors affecting their performance are discussed.

Jan 1, 1992

By Mahmood Alemrajabi

When LKAB processes their iron ores in northern Sweden, they generate apatite as a by-product. The apatite has been recovered by flotation and the concentrate contains about 0.4 wt% rare earth elements (REE). Both phosphate rock and REE are listed as critical raw materials for the European union. In the present study, the recovery of REE within the nitrophosphate process of fertilizer production has been studied. In the first stage, the REE are precipitated and isolated as a phosphate concentrate. For further purification and individual separation of REE by solvent extraction, removal of phosphorous from the concentrate to enhance the dissolution of REE in mild acidic solutions is essential. In this study, thermal treatment of the concentrate with sodium hydroxide at elevated temperatures followed by water leaching has been studied in order to separate the phosphorous and thereby facilitate dissolution of the REE. The results show that 95% of total phosphorous initially present in the REE phosphate concentrate is removed after thermal treatment with NaOH 1:1 mass ratio, at 400 °C.

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 R. M. Cunningham

Asarco operates one of the largest individual copper electrolytic refineries in the world at Amarillo, Texas. The feed for this refinery is a mixture of anodes produced at Asarco smelters and copper purchased t?om a number of primary and secondary sources. The variation in feed makes it imperative that the refinery practices state-of-the-art quality control to minimize the effects&apos;of unwanted impurities in the electrolytic refining process. In late 1993, a plant designed to sigru6cantly reduce the antimony and bismuth levels in the electrolyte was commissioned. The purification plant uses ion exchange technology in conjunction with a novel strippiing system developed by Zeneca Specialties (U.K.). The strippiing system permits the recycling of the eluant and thus avoids the extremely high costs of stripping with conventional reagents. In addition, the environmental impact of treating the eluant for recovery of antimony and bismuth is minimized. This paper outlines the development of the technology and, in particular, describes the operational practices and improvements at Amarillo since the commissioning of the plant.

Jan 1, 1997

By June-Yong Eom, Jong-Jin Pak, Jung-Mock Jang, Min-Kyu Paek

The nitrogen solubility in liquid Mn-Si, Mn-Si-Fe, Mn-Si-C and Mn-Si-Fe-C alloys has been measured by the gas-liquid metal equilibration technique in the temperature range of 1673-1773 K. The additions of silicon, iron and carbon significantly decreased the nitrogen solubility in liquid manganese alloys. The experimental results were thermodynamically analyzed by the Wagner’s formalism to determine the first- and second-order interaction parameters of silicon, iron and carbon on nitrogen in liquid manganese. The thermodynamic parameters can be used to predict the nitrogen solubility in ferromanganese and silicomanganese alloy melts as functions of the melt composition and temperature at given nitrogen partial pressures.

Jan 1, 2014

By Gerardo Muñoz

All along this century CODELCO&apos;s smelters have been operating on conventional technology, which Codelco has streamlined by using oxygen, developing oxy-fuel burners for reverberatory furnaces and introducing oxygen smelting of concentrates in converters (Teniente Converters). Chuquicamata began capturing sulfur from its first Teniente Converter in 1985. Since then, it has implemented a program allowing to gradually increase such capture. In 1994 a Frame Law on the Environment was enacted in Chile. By virtue thereof and of CODELCO&apos;s corporate environmental policy, an investment program aimed at capturing more than 95% of gaseous pollutants in all its smelters in a term not exceeding twelve years was established. The above entails a substantial improvement of the operational management as regards fugitive gases capture and treatment. This paper describes the way CODELCO is to deal with this challenge with a view to fully complying with environmental regulations and obtaining the required environmental certifications of its operations.

Jan 1, 1996

By Ejike Emmanuel, Nwoye Chukwuka, Ogwuegbu Martin, Asuwaji Ayuk, Onyedika Gerald

"Microwave pre-treatment of cassiterite ore prior to leaching was carried out in an attempt to obtain high grade of Sn02 and to conserve the total energy expended during processing. Microwave treatment was selected due to the presence of associated minerals which behaves differently to microwave energy. Studies in this work showed that microwave pretreatment of cassiterite ore can be applied to increase the recovery of tin oxide within 5 minutes of leaching. Microwave treatment of the ore resulted in mineral liberation at all particle sizes. Tin oxide was separated from the major impurities via leaching in potassium hydroxide solution and precipitation, resulting in 98% Sn02 at pH 7.IntroductionIn the nineties, the available techniques used for ore processing and analysis in Nigeria was the solution methods of either alkaline fusion or acid digestion [1,2]. A process in which cassiterite is made acid soluble by reduction to SnO2 , which stabilizes by glass formation and the tin was extracted by leaching the glass with sulphuric acid, followed by electrowinning was reported [3,4]. In another study, Baba et al [5] studied the dissolution kinetics of a Nigerian casiterite ore in hydrochloric acid solution. The effects of acid concentration,temperature, particle size and stirring speed were examined. It was found that the dissolution rates of cassiterite depends on hydrogen ion concentration, H+, stirring speed and ore particle dimensions. These were believed to report low data due to incomplete solubilization of the ore minerals in aqeous medium [6]. Analytical chemists have used microwave heating devices routinely for the dissolution of metals, minerals and various chemical products in chemical analysis [7,8]. It offers faster heating rate and consequently faster dissolution rate than conventional heating. The principle of the dissolution of analytical samples has been applied to the leaching of various minerals contained in an ore or concentrate sample. Some researchers [9, 10] conducted microwave assisted leaching of laterite ores containing oxides of nickel, cobalt, and iron. The metals of these mineral components were converted into their chlorides by microwave heating (1200 W, 2450 MHz, Nz atmosphere) a mixture of the ore and ammonium chloride between l 77°C and 312° C for 4-5 min, followed by water leaching at 80° C for 30 min. Nickel and cobalt extractions were 70% and 85%, and respectively, and are comparable with roasting at 300°C in a conventional rotary kiln for 2 hours."

Jan 1, 2013

By Tong Deng

Clean processing of copper converter slags for reclaiming cobalt and copper could be a challenge. An innovative and environmentally benign approach for recovering metal values from such a slag was developed in the present work. Curing the slag with sulfuric acid, without re-smelting or roasting as currently practiced in the industry, made it amenable to leaching, and more than 95% of the cobalt and up to 90% of the copper was extracted, together with iron, by water leaching, leaving silica behind in a residue. Copper in the leach liquor was recovered by cementation with iron, and the dissolved iron crystallized as ferrous sulfate monohydrate. Cobalt in the pregnant solution rich in iron was recovered by either cementation or sulfide precipitation. Chemical and mineralogical characterization of the slag and its products were examined and compared to determine the nature of the changes occurring during curing and leaching. Operating variables were also investigated and optimized.

Jan 1, 2003

By W. H. Jay

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

Jan 1, 2003

By G. Achurra

The products of the smelting of copper concentrates in an El Teniente Converter (CT) are a high grade matte, analyzing 74-76% Cu; and a highly oxidized slag, typically containing 15-20% Fe3O4 and 4-10% Cu. The El Teniente Division of CODELCO¬CHILE has developed a slag reduction-cleaning process, that is practised in a tilting, horizontal furnace, to recover copper from these slags. The El Teniente slag cleaning process has been successfully implemented at the El Teniente Caletones smelter and various other smelters in Chile: Today, eight such slag cleaning furnaces, each with a capacity of 800-1000 tonnes/day, are in operation in Chile. This paper discusses basic laboratory research and industrial tests that led to substantial reductions in the slag cleaning cycle time and the specific consumption of fuel and reductants. Simultaneously, the slag cleaning off-gas quality was improved. Based on the experimental results, recommendations were made to improve the practice of the El Teniente slag cleaning process. The recommended modifications have been fully implemented at the Caletones smelter.

Jan 1, 1999

By Marco Olper

The CX-EW technology, developed by B.U.S Engitec, is improved introducing besides the battery paste electrowinning, the direct electrorefining of metallic lead (grids and poles) obtained from CX breakers. This new concept of electrorefming the antimonial lead scrap is aimed to the production of 99.99 lead and of slimes with high antimony content, avoiding gaseous emissions in melting lead scrap, and expensive and pollutant thermic refining operations. In this way, practically all lead content in the battery is available as 99.99 lead, hence with a wider market for the lead recyclers. This paper will describe the tests performed on a pilot plant scale with special reference to the relatively low energy consumption of the process.

Jan 1, 1993

By Ibrahim Yusufoglu, Cem Kahruman, Mert Zoraga

In this study, a strontium sulfate mineral (celestite) was converted to strontium oxalate in solutions containing ammonium oxalate as a reactant. The experiments were carried out under isothermal conditions. The effects of stirring speed, ammonium oxalate concentration, particle size and temperature on the conversion rate were investigated. During the conversion process, definite volumes of solutions were taken from the reactor after different reaction times for the determination of sulfate ions using ICPOES. Fractional conversions of strontium sulfate were determined at different times and fractional conversion vs time diagrams were generated. It was found that the conversion of strontium sulfate was increased by increasing the ammonium oxalate concentration and temperature in addition to decreasing the particle size. The effect of stirring speed was negligible on the reaction rate. It was observed that above 328 K, a protective layer of strontium oxalate was formed on the strontium sulfate particles. X-ray Powder Diffraction technique was used for characterization of solid substances.

Jan 1, 2014

By Seiji Yokoyama

As a series of fundamental study on the gas evaporation method, a levitation-melted aluminum was evaporated in the gas mixture of argon and ammonia to synthesize ultrafine particles of aluminum nitride. When the ammonia partial pressure were more than 2kPa, the formation ratio of aluminum nitride was about 95%. The particles of aluminum nitride were mainly hexagonal. The mean size of the particles of aluminum nitride was about 57 nm, and it was constant without depending on the temperature of the levitated aluminum and the partial pressure pf ammonia. The aluminum nitride was formed by the reaction between ammonia and condensed liquid aluminum particle whose size was relatively small.

Jan 1, 2006

By G. Roy Chaudhury

Adsorption techniques are comparatively low cost and effective for treatment of arsenic contaminated drinking water. Various adsorbents such as alumina, ferrihydrite and manganese ores have been used, but there has been little investigation of modifying the structure of ferrihydrite to improve its adsorptive efficiency of As(III) and As(V). In the present study the incorporation of manganese oxide into the ferrihydrite structure was carried out and the prepared materials used in arsenic adsorption experiments. The compounds were X-ray amorphous, but TGA/DTA and FTIR analysis showed some structural characteristics. Sorption studies reported in this paper indicate the excellent arsenic removal properties of the manganese/iron compounds with a loading capacity of 0.3 mmol/g. Adsorption follows first order kinetics and the results fitted to adsorption and mass transfer models. Arsenic levels in water containing 1 mg/L As(V) were reduced by 50% in 20 minutes and 90% in 60 minutes using 1 g/L manganic ferric oxyhydroxide.

Jan 1, 2003

By Richard Elliott

Current methods for producing low-carbon manganese alloying materials for the steel industry are energy intensive and costly. To enable wider implementation of high Mn steel alloys, a novel solid-state Mn ore reduction strategy is therefore being investigated. This solid-state process, modelled on existing Direct Reduced Iron technology, employs a methane-containing atmosphere to reduce Mn ore pellets to a metal carbide. These pellets may then be smelted, yielding a Mn-rich master alloy. It is well established that CH4 is a suitable reductant for Mn ore powders; however, the reduction behaviour of industrially relevant Mn ore pellets by CH4 is poorly understood. The present work reports the results of an investigation undertaken to address this knowledge gap. The results of this study highlight the significantly different reduction behaviour exhibited by the Mn ore pellets relative to the ore powder under similar conditions and suggest that the diffusion of CH4 into the pellet interior is the limiting factor in achieving complete reduction.