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By Guohui Zheng

The ever increasing quantities of solid wastes generated by various industries are at the source of the growing need for proper waste disposal methods. Thermal treatment of combustible wastes is a proven technology which permits the reduction of hazardous material having to be landfilled. However, this method is not universally applicable to waste disposal. For example, the transferal of heavy toxic metals into the thermal remediation products is a major issue of public concern. This paper focuses on the analysis of morphology changes from solid sludge to ash which is a product of the sludge combustion. The morphological parameters analyzed were particle size and external surface. They were determined using Jeol 840 Super Probe. The experiments were conducted in a computer-controlled high-temperature combustion system consisting of the thermogravimetric furnace coupled with Fourier transform infrared spectrometer (TGA-FTIR). Sludge particles were made of complex fibers trapped in the aluminosilicate matrix. At low temperatures, up to 680 K, the solid residue looked similar to the initial sludge. Between 680 K and 1180 K the sludge underwent intensive burning and steadily changed into powdered ash. At the temperature of 1050 K the ash was composed of separate, flat flakes with sizes ranging from 5 to 20 um. At 1470 K the flakes aggregated into large particles. The surface observed at 1670 K was a mixture of mullite crystals. Such structure could result from the solidification of the ash material after its melting. Morphological changes influenced the distribution of metals in the solid residue. For example, Cr was concentrated in small aggregates. Such distribution should allow for recovery of valuable metals from the solid waste residue.

Jan 1, 1996

By Zhao wen Wang, Ramana G. Reddy, Min Li

"The electroreduction of Co(II) in l-butyl-3-methylimidazolium tetrafluoroborate (BMlMBF4) ionic liquid was investigated by cyclic volatrnmetry at 353 K. The results show that the reaction of Co(II) to Co is irreversible in one step with two electrons transferred. The diffusion coefficient of Co(II) was estimated to be 7.6 x 10-8 cm2 s·1 at 353 K. Then the electrodeposition of cobalt was studied at different cathodic potentials (-0.80 to -0.95 V) and different temperatures (333 to 363 K) in BMIMBF 4 containing 0.20 mol L-1 Co(BF4)z. The deposits were characterized using scanning electron microscope (SEM), energy-dispersive spectroscopy (EDS), and X-ray diffraction (XRD). SEM images show that a uniform, dense, and compact deposit was obtained at -0.80 V and 333 K. The deposits were identified as high-purity metallic Co for all experiments by EDS and XRD.IntroductionCobalt is known as a hard magnetic material and cobalt alloys have been shown to have excellent magnetic properties with adequate mechanical durability and corrosion resistance, which are needed for high performance magnetic recording applications [1-4]. The electrodeposition of Co alloy in the aqueous solution is generally difficult because of the narrow electrochemical potential window of water, which leads to the low current efficiency and worse quality of deposits due to the hydrogen embrittlement. Thus, aprotic ionic liquids (ILs) are expected to be the ideal alternative media for electrodeposition of cobalt or its alloy since ILs usually provide a wide working potential windows, negligible vapor pressure, and acceptable conductivity for electrolysis without the occurring of hydrogen evolution [5, 6]."

Jan 1, 2014

By Padmavathy Mahadevan, Samir Chefai, Eduard Guerra

"Electrocoagulation is a technique for treating wastewater streams from metallurgical plants whereby electrodes are corroded to generate gases (most notably oxygen at the anode and hydrogen at the cathode) and solid particulates which acts as substrates for coprecipitation of impurities. The performance of electrocoagulation reactors, in terms of their efficiency for removing a particular impurity, is highly dependent on several factors, most notably: the nature of the electrodes, the spacing between electrodes, the current density, the height of the electrodes, the solution flow rate, and application of periodic current reversal. Because these variables have complex interactions, in order to ensure reliable scale-up of laboratory results, experiments should be conducted under conditions that closely match those that would be employed at an industrial scale. To that end, this article describes the design and commissioning of a versatile laboratory scale electrocoagulation reactor that allows for the control of all the aforementioned variables along with the ability to measure the instantaneous spatial distribution of current within the reactor.IntroductionArsenic is often removed from metallurgical waste streams in stirred tank reactors by coprecipitating it with ferric ions as an arsenical ferrihydrite [ 1]. Electrocoagulation is an electrolytic technology that can accomplish the same task, but has not yet been widely adopted to treat metallurgical waste streams [2]. The electrocoagulation process involves the use of an external DC power supply to drive the dissolution of a relatively non-toxic metal into the wastewater stream, usually either iron or aluminum, which then largely precipitates as oxyhydroxide phases that adsorb undesired impurities [l]. At the anode, the metal is dissolved and oxygen is often evolved, lowering the local pH and enhancing metal ion solubility."

Jan 1, 2012

By José Sancho, Julia Ayala, Purificación García, Begoña Fernández

"Electrofilter dust, a residue generated in the last stage of the Bayer process in the hydroxide aluminum calcination, was characterized to evaluate the alumina that was potentially extractable with sulfuric acid. The process studied aims to produce aluminum sulfate for water coagulant uses, taking advantage of the residues that accumulate in large quantities in the proximity of plants with difficult recycling for storage. Acid leaching is carried out at different concentrations of sulfuric acid, at different temperatures, pulp densities, and times, to dissolve gibbsite and transition aluminas. The result is an aluminum sulfate solution without iron and with commercial specifications.IntroductionElectrofilter dust is a residue generated in the last stage of the Bayer Process [1] in the hydroxide aluminium calcination. The residue is a mixture of alumina and hydrates which have not completed their calcination process.Electrofilter dust, composed by alpha alumina, gibbsite and transition aluminas [2] can be leached in an acid medium by putting most of the aluminium in solution; the remaining residue should be mainly andisolved alpha alumina. In many hydrometallurgical processes, sulphuric acid has been selected as the cheapest and the most effective leachant [3,4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15]The aim of this study is to determine the effect of temperature, acid concentration and pulp density on the sulphuric acid leaching of electrofilter fines for aluminium dissolution, in order to produce aluminium sulphate for water coagulant uses. This will provide a commercial product and at the same time eliminate the environmental problem created as a result of the storage of large quantities of electrofilter fines in the vicinity of the Bayer plant."

Jan 1, 2008

By Carlos Schvezov, Eliana Agaliotis, Alicia E. Ares, Mario Rosenberger

"The interaction between a solidification front and a spherical particle was modeled and simulated in order to study the phenomenon of ""pushing"". Finite element methods were employed in axisymetric domains. The drag force is calculated from the calculated fluid flow field and the repulsion force is the Lifshitz-Van der Waal force. The thermal field is decoupled from the force field. The model is applied to a metallic matrix containing particles with similar, lower or higher thermal conductivities than the matrix, resulting in planar, convex and concave interface shapes, respectively.The results show that the critical velocities for pushing for concave and convex interfaces are about one order of magnitude larger and one order of magnitude lower than the critical velocity for flat interfaces, respectively. The simulated results were in very good agreement with reported experimental results.IntroductionThe solidification interface of materials containing spherical particles in some cases can push the particle ahead the interface. This phenomenon generally occurs during the solidification of different materials such as, metallic alloys containing native particles, metal matrix composites containing particles or fibers as reinforcements and crystallization of semiconductor, optical, optoelectronic or biological materials. In all cases the interaction strongly determines the distribution of particles and the resulting physical and physic-chemical properties of the resulting material. The phenomenon has been investigated for many years both experimentally and by mathematical modeling [1-21]. The process is complex due to the variety of phenomena involved during pushing. In all cases, the physical problem depends on the properties, nature, and morphology of the interacting media; the particle, melt and solid; and external fields such as gravity, thermal and electromagnetic fields."

Jan 1, 2012

By Georgina De Micco

The National Commission of Atomic Energy is investigating a suitable physicochemical process for the conditioning of spent nuclear fuel and treatment of the scrap of research reactors of the Al-UxSiy type. A possible way of processing is through dry chlorination of the cladding with the purpose of selective separation of the aluminium from the remaining elements such as Fe, Ni, Zn, Cu, etc. transforming them into volatile chlorides. Some important advantages of this method are the thermal stability of the chlorides that allow the easy separation of the halides by physical methods and the low volume of radioactive waste generated. The interactions in the following systems were studied in the range of temperature between 150º-500°C: Al-Fe, Al-Ni, Al-Cu, Al-Zn, Cu-Zn and the pure metals. We found that the reactivity was different depending on if the elements were alloyed or separated. The separation factors of the systems under study were determined. Nickel is perfectly separated from aluminium for all temperatures, whereas good conditions for copper separation were achieved below 400ºC. In the case of iron, complete isolation was never attained. However, by decreasing temperature to 150ºC it is possible to obtain aluminium chloride with less iron content. The separation of zinc from the product was also difficult. It was detected that zinc chloride volatilization decreases when other chlorides were present, for example cooper chlorides. In the Cu-Zn alloy, zinc chlorides remained in the condensed product due to interactions with copper. The samples were characterized by scanning- electron microscopy (SEM), X ray diffraction (XRD) and atomic absorption.

Jan 1, 2006

By C. Wieckert

Concentrated solar energy can be used as heat source for the production of metals. One of the most promising respective processes, the solar carbothermic production of Zn from ZnO, is investigated within the European research project SOLZINC, a cooperation of institutes and industries from France, Germany, Israel, Sweden and Switzerland. The solar produced Zn can be used as commodity or as an energy carrier for further processing on demand to electricity in Zn-air fuel cells/batteries or to generate hydrogen by reaction with steam. In both cases the Zn is oxidized to form ZnO, which can be recycled back to the solar plant. In these cyclic processes Zn acts as a means to store and eventually transport solar energy. Second product of the solar process step is a CO-rich offgas, which may e.g. drive a gas engine or may be shifted to hydrogen in a conventional reaction with steam. A pilot plant using 300kW concentrated solar power input has been constructed and operated successfully. 86mass-% of ZnO mixed with 14mass-% of charcoal are reacted to produce Zn and CO at a temperature of about 1200°C, yielding about 50 kg gaseous Zn per hour. Zn-dust with 95% purity is recovered from the offgas system that was designed to produce Zn for Zn-air fuel cells. Based on the results and findings from the pilot plant, a two tons Zn/h solar demonstration plant has been designed conceptually. Cost studies have been performed and scenarios for producing electricity or H2 via these ZnO/Zn-cyclic processes are evaluated.

Jan 1, 2006

By Donald P. Ziegler, James F. Klausner, Srinivas S. Garimella

"By 2015, nearly half the world's population will live in ""water stressed"" areas. Production of fresh water utilizing waste heat from industrial processes has been identified globally as a research priority.About 15% of the electricity required to produce aluminum is lost as waste heat in the off-gas. However, the low temperature (low grade) of the heat limits reuse. The off-gases contain 50-150 ppm SO2 ; tightening regulations coupled with increasing coke sulfur levels are motivating SO2 control, for which seawater scrubbing is attractive for smelters with suitable access.We describe a process that produces fresh water, utilizing the waste heat while scrubbing SO2 . It uses direct contact between seawater and off-gas to humidify the off-gas. The vapor is subsequently condensed. In smelter trials, a unit treating a slip stream produced high quality water in the anticipated quantity, attaining over 95% SO2 scrubbing. Future work involves scaling the process to be economically attractive.BackgroundPopulation growth, coupled with industrialization and urbanization, are increasing demand for water. Water scarcity already affects every continent. Around 1.2 billion people, or almost one-fifth of the world's population, live in areas of water scarcity, and 500 million people are approaching this situation. By 2025, 1.8 billion people will be living in countries or regions with absolute water scarcity, and two-thirds of the world's population could be living under water stressed conditions (< 1,700 m3 per person annually) [1]. An assessment by the U.S. General Accounting Office revealed that under normal conditions, by 2013, water managers in 36 states in the USA anticipate water shortages, and that the number might grow to 46 states under drought conditions [2].The obvious choice to alleviate water scarcity is the 97% of available water in the oceans, which is saline and requires desalination for use in biological, agricultural and industrial applications. Technologies developed for desalination include Thermal Distillation, Reverse Osmosis (RO), Electro-Dialysis, and Vacuum Freezing. Distillation and RO are the most commercially prominent. Thermal distillation technologies include Multiple Effect Distillation (MED) and Multi-Stage Flashing (MSF). The report commissioned by the World Bank [3] is one of the many excellent references on desalination technologies. According to the International Desalination Association working paper [4], there were more than 17,348 industrial scale desalination plants installed or contracted by 2004. The total production from these plants is on the order of 8.3 billion imperial gallons per day. RO provides 47.2% of the total capacity. The leading thermal process, MSF, provides 36.5% of the total capacity. Although MSF and RO technologies currently provide the most cost effective means for desalination, their drawback is that they are very energy intensive, and whether or not they remain cost effective strongly depends on energy prices and energy supply."

Jan 1, 2012

By Duck Jae Lee, Kwan Ho Kim, Ji Whan Ahn

"In Korea, reutilization of constructions waste is gaining an increasing attention as generation of construction waste is projected to increase continuously. In current practices, the concrete waste is simply crushed and used as a low application such as paving, back filling, etc. In this study, a new process was developed comprising of heat pretreatment, autogenous milling, and density separation for complete reutilization of concrete waste. Firstly, the concrete waste was crushed using autogenous milling. The coarse size fractions from autogenous milling have a density of 2.5g/cm3 and a water absorption ration 3.0%, which meet the specification of the first class of KS F 2573. The fine size fractions were further separated using a hindered-settling column into two products 1) underflow, 2) overflow. The underflow sample was a high quality fine recycled aggregate which can be used for concrete making, and the overflow sample was an enriched cement material can be also used for CO2 sequestration by mineral carbonation. Introduction Kwan Ho Kim1, Ji Whan Ahn2, Duck Jae Lee1, Hee Chan Cho1 Recently, the importance of resource recycling is gaining a greater attention due to the increasing price of natural resource. Recycling is beneficial for not only the management of waste, but also the reducing of consumption of natural resources and huge energy consumption to treat of natural resource. The construction and demolition waste comprises the major industrial waste generated in Korea. It increased to 54 million tons in 2004, and is projected to increase to over 300 million tons in 2020, as many buildings reach the end of their 30 years life. Among total waste, the proportion of concrete waste was about 30% in Korea. Due to its large volume, recycling of concrete waste is the most important aspect of the waste management. In the current practices, the concrete waste is simply crushed and used as a recycled aggregate. The recycled aggregate has a low quality and most of them are down cycled for usage as paving material, back-filling material, concrete bricks, etc. It cannot be reused for replacement of natural aggregates because cement mortar is not separated perfectly from aggregates. These kinds of recycled aggregates tent to be weaker, more porous and have a higher value of water absorption. When these aggregates are used in concrete making, there are problems of higher total water demand, low compressive strength and durability [1-5]. And recycled fine aggregate is not almost recycled due to its low quality. In this study, a new processing circuit is developed to produce not only highquality recycled coarse aggregates but also fine aggregates and cement material from concrete waste."

Jan 1, 2008

By H. H. Law

Large amounts of waste material in the form of flue dust are generated in the operation of copper smelter furnaces. As a result of increasingly stringent disposal, it has become important to develop methods for treating such metallurgical wastes to extract metals and convert them into salable products. A two-step closed-loop hydrometallurgical process, has been developed: (1) extraction with sulfuric acid removes about 90% of zinc and decreases the dust volume by 50%; (2) extraction with hydrochloric acid dissolves the lead and further decrease the dust volume by 75%. A process scheme for generating salable products is proposed.

Jan 1, 1992

By Yuzhe Zhang, Xiaodi Huang, Xinli Wang, Bowen Li, Matthew Andriese, Jiann-Yang Hwang, Zhiwei Peng

The recycling of waste tires has been a big environmental problem. About 280 million waste tires are produced annually in the United States and more than 2 billion tires are stockpiled, which cause fire hazards and health issues. Tire rubbers are insoluble elastic high polymer materials. They are not biodegradable and may take hundreds of years to decompose in the natural environment. Microwave irradiation can be a thermal processing method for the decomposition of tire rubbers. In this study, the microwave absorption properties of waste tire at various temperatures are characterized to determine the conditions favorable for the microwave heating of waste tires.

Jan 1, 2015

By E. Anelli

Based on experimental continuous cooling transformation (CCT) diagrams, an artificial neural network has been trained to predict the amount of microsturctural constituents and hardness resulting from and controlled cooling at rates from 150 to 0.015 K/s. It can be applied to quenching and normalizing processes of low-alloy steels with 0.05-0.30 C% and 0.4-2.0% Mn -with possible microalloying additions. Examples of the good predictive capabilities about 15 Vickers standard deviation for hardness and a few percent for volume fraction of phases) are reported&apos; Keywords: Austenite decomposition, low. And medium-carbon steels, artificial neural networks

Jan 1, 2003

By Y. Z. Zhang

Electrochemical oxidation of arsenopyrite in ferric sulphate media in the absence and presence of bacteria T jerrooxidans has been investigated for the purpose of understanding the dissolution chemistry of arsenopyrite and the bacteria attack mechanism. Mixed potential, polarization resistance measurements, polarization curve, cyclic voltammetry experiments were conducted in a ferric sulphate medium of 10g/L FeH, temp.25-35°C, pH 1.5-2.5 in the absence and presence of bacteria Tjerrooxidans, respectively. For the anodic process, a two-step reaction sequence is suggested by the electrochemical measurements. The initial step at a low potential is described by:

Jan 1, 1996

By Petrus Christiaan Pistorius, Farzin Fatollahi-Fard

The production of synthetic rutile—a common starting material for most titanium production processes—from iron-rich titanium minerals such as pseudorutile and ilmenite is described. The process for “upgrading” the mineral to synthetic rutile is by carbothermal reduction of the mineral while immersed in a molten salt at high temperature, followed by magnetic separation of the reduced iron. A variety of factors are also investigated, such as particle size of the mineral, the type of mineral, and the molten salt used. The solubility of iron(III) oxide in different molten salts is also experimentally determined.

Jan 1, 2016

By W. L. Cornell

Bulk sulfide concentrate produced from Missouri Pb ore concentrator tailings must be reground to liberate sulfide values for subsequent sepa-ration. Studies to determine grinding parameters for optimum liberation were carried out using optical microscopy coupled with image analysis. The major sulfide phases present in the ground mineral particulates are marca-site, pyrite, sphalerite, galena, chalcopyrite, siegenite. and bravoite. Results showed that the base metal minerals were liberated by grinding to 74 micrometers (200 mesh), but the siegenite and bravoite required grinding to 20 micrometers or less to achieve liberation. Both the experimental method and results are presented.

Jan 1, 1987

By M. I. Novgorodova

Most of the gold in the earth&apos;s crust occurs as finely-dispersed gold and accounts for much of the gold lost in extraction processes and during exploration for gold. The Compositions, sizes, and morphology of fine gold particles (0.01 to 10 ~m in diameter) were studied with high resolution electron microscopy coupled with electron microprobe and microdiffraction devices, using colloidal carbon replicas. Correlations were made between fine gold, mineral associations and ore genesis. The results provide qualitative information on the proportions of finely dispersed, invisible and visible gold distribution in ores. Such knowledge is fundamental when planning an optimum technological recovery process.

Jan 1, 1991

By Alessandro Blasi, Massimo Morgana, Corradino Sposato, Pietro Garzone, Giuseppe Devincenzis

A comparison among (2-ethylhexyl)-mono (2-ethylhexyl) ester Phosphonic acid (P507), Secondary-octyl phenoxy acetic acid (CA-12) and Bis(2,4,4-trimethylpentyl) phosphinic acid (Cyanex272), in heavy rare earths separation via hydrometallurgical processes has been investigated. The separation coefficients, , were obtained and the extraction selectivity has been evaluated using a mixture of heavy rare earths from Samarium to Ytterbium. The experimental results indicated that P507 and Cyanex 272 display a greater affinity for heavier rare earths while CA12 proved to be more effective for the lighter rare earth metals.

Jan 1, 2014

By Yoichi Takeda

The CaO-FeO,-Cu20 slag has been practically applied to continuous converting of copper, and also has potential for refining of copper. Liquidus lines of the slag system and phase stability diagram for the liquid slag and the existing solid compounds under copper saturation are presented. Liquidus composition was determined by chemical analysis of slag sample saturated primary solid. The temperatures of invariant equilibria were investigated by thermal analyses. Oxygen potentials on the liquidus lines, the univariant and invariant equilibria were estimated from the relation slag composition and oxygen potential that relation was confirmed in separate experiments.

Jan 1, 2003

By Yoichi Takeda

The CaO-FeOx-Cu20 slag has been practically applied to continuous converting of copper, and also has potential for refining of copper. Liquidus lines of the slag system and phase stability diagram for the liquid slag and the existing solid compounds under copper saturation are presented. Liquidus composition was determined by chemical analysis of slag sample saturated primary solid. The temperatures of invariant equilibria were investigated by thermal analyses. Oxygen potentials on the liquidus lines, the univariant and invariant equilibria were estimated from the relation slag composition and oxygen potential that relation was confirmed in separate experiments.

Jan 1, 2003

By R. H. Rubisov

Sulphuric acid pressure leaching of nickeliferous laterites has attracted considerable attention from the nickel industry during the past five years. The process is especially advantageous for limonitic laterites that mostly contain goethite, because iron precipitates releasing acid and thus rendering low acid consumption. It is also applicable to mixtures of limonites and saprolites, although at higher acid consumption due to magnesium. Effective process design requires the solubility of metals that precipitate during the process to be known. In the present work, determination of metal solubilities is based on a simple speciation program that assumes the presence of only one dominant complex for each metal. The thermodynamic data for the precipitation reactions are extracted from high-temperature experiments with monometallic systems published previously. The validity of the approach is then tested against mixed bimetallic systems, and finally applied to calculate the solubility of aluminium, iron and magnesium in laterite leaching effluents "at temperature". In both cases of limonitic feed and limoniticfsaprolitic blends, the prediction closely follows metal solubilities measured experimentally at temperatures from 230 to 270°C and at terminal he acidities ranging from 10 to 75 g/L.

Jan 1, 1999