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Sodium is added to aluminum-silicon eutectic alloys to modify the structure. The ideal amount is about 100 ppm but due to the fact that sodium is lighter than aluminum and can float to the surface where it bums, oxidizes ad volatilizes, a far greater amount is usually added. Furthermore, as the sodium is continually lost from the alloy the optimum amount is only present for a limited time. The net result is a process which is hard to control, produces fumes and a considerable amount of dross. It is shown that by electrochemically titrating sodium through a tube of sodium beta alumina electrolyte that the sodium can be added continuously in a controlled way. As the sodium is added to the bulk of the aluminum, there is no sodium on the surface of the alloy so that little surface oxidation occurs, and no fumes and dross are produced. This leads to an improved product and working conditions.

Jan 1, 1995

By K. H. Ho

This paper describes a simplified numerical model which is used to study the skull formation of liquid metal on a rapidly rotating disc in centrifugal atomisation. The skull formation is one of the problems limiting the wide use of centrifugal atomisation. The enlarging skull on the atomising disc reduces the yield of metal powder produced and produces a resistance to the centrifugal force which worsens the quality of the powder. It is costly and often difficult to study the flow behaviour by experiments due to the complex heat transfer and phase transformation during the processing. Computer modelling is therefore a powerful tool for mechanistic understanding of centrifugal atomisation. This paper investigates the flow pattern of the melt on the rotating disc as a function of initial temperature, melt flow rate and disc rotation speed as well as the physical properties of the melt, such as density, surface tension and viscosity using the commercial package Flow-3D. Keywords: Solidification, Rotating disk, Centrifugal Atomization

Jan 1, 2003

By Mituo Tougo, Mitsuo Tokunoh, Takayasu Kisaragi, Fuminori Chiba

We have about 200,000 tons/year of dross residue produced after the collection of aluminum from the dross generated during the aluminum remelting process. 130,000 tons of the dross residue is used as a steel deoxidant or a cement material, and the remaining 70,000 tons is abolished and buried in the ground at authorized places. The dross residue is increasing along with the increase in the aluminum production. This situation will grow more serious with a large amount of aluminum window sashes which have been mass-produced since 60's and will return before long as scraps. Our effort is being directed to the development of technologies which enable the dross residue to be recycled and reused for some purposes such as road aggregates, refractories and others, in such a way as to comply with the social requirement which gives prfority to the recycling industry, as well as to the environmental preservation.

Jan 1, 2000

By J. W. Whitney

Itronics Inc., through its wholly owned subsidiary Itronics Metallurgical, Inc. (IMI), has successfully developed technology that allows it to be fully integrated as a photochemical recycler. IMI is now using this technology to expand its regional operation, which collects used photographic chemicals, chemically removes 99.997% of the silver and uses the residual to make a line of high quality liquid multinutrient liquid fertilizer products. Elevated silver discharges from the Reno-Sparks sewage treatment facility, that were traced back to incoming waste photographic chemicals and which were seriously impacting the sensitive fishery, provided the impetus for this project. This paper is updated from a paper presented at the Twenty-Second International Precious Metals Conference Toronto, Ontario, Canada in June 1998. It presents an overview of the scope of the problem solved by the technology, some of the permitting and development issues, and some of the specific fertilization formulations that are now being marketed.

Jan 1, 2000

By Hazoor Singh Sidhu

Materials degradation due to corrosion is the major problem in power generation equipment, gas turbine, fluidized bed combustion, industrial waste incinerators etc. Some super alloys have been developed, but they are unable to have different properties to meet the demand of today?s industry. Therefore, a composite system of a base material providing the necessary mechanical strength with a protective surface layer different in structure and/or chemical composition can be an optimum choice in combining material properties. Thermal spray coating of the components before they put into service by suitable surfacing alloy and with suitable coating method can increase the life of these components several fold. Choice of right coating method and alloy for a particular application is extremely important to get the desired service life. The corrosion of some materials and the role of HVOF thermal spray coatings to counteract the same have been reviewed, with an aim to understand the phenomena along with various applications.

Jan 1, 2006

A full-scale test of chalcocite heap bioleaching was undertaken at Straits? Nifty Copper Operation. Straits worked closely with the CSIRO to investigate the chemical and biological changes over the life cycle of this chalcocite heap bioleach system. Results indicated nearly 80% copper recovery was achieved in just over 300 days. Significant changes in iron chemistry and microbiological activity were detected. Temperatures in the heap reached as high as 70 ºC during the time of maximal copper recovery rate. The dominant cultivatable bacterial strains were typical mesophilic bacteria, however, naturally occurring moderately thermophilic bacteria were detected by culture and culture independent molecular (PCR followed by denaturing gradient electrophoresis [DGGE]) and signature lipid methods. Signatures for the iron and sulfur-oxidising species Acidithiobacillus ferrooxidans and Sulfobacillus spp., as well as the moderately thermophilic heterotroph Alicyclobacillus sp. were detected. Biomass was greatest in ?warm? but not ?hot? parts of the heap, and Hyperthermophilic Archaea were not detected.

Jan 1, 2003

By William Ewing

Copper is rapidly being adopted by the semiconductor industry as the interconnect material of choice. The aqueous processing techniques used generate wastes such as spent electrolyte from electroplating, electroplating rinse water, copper solutions from removing copper from the back of the wafer and CMP waste streams. We are examining the use of chelating resins as a means of recovering copper from these streams within the processing plant, thereby allowing recycling of process water and minimizing hazardous waste disposal costs. We have examined the effect of model plating additives (and other organic complexing agents) on the efficacy of Dowex M4195. Although these might have had a significant effect, commonly used electroplating additives polyethylene glycol (PEG), benzotriazole (BTA), thiourea, glycine, and 3-mercapto-1-propanesulfonate (MPSA) each had little or no effect on the ability of the resin to chelate copper and remove it from solution. This suggests that Dowex M4195 could be useful for treating waste solutions of rather variable compositions.

Jan 1, 2003

By Xu Weihong

After being pre-treated, composite electro-deposits of semi-bright nickel/nano-SiO2 with bright nickel or with amorphous Ni-P alloy, and Composite electro-deposits of Zinc were prepared on Nd-Fe-B magnetic material. The effect of cathodic current density, nano-SiO2 concentration, stirring strength and surfactants on the corrosion resistance of electro-deposits were studied. In addition surface appearance and structure of the composite coatings were analyzed by SEM. The present investigation shows that the corrosion resistance of composite electro-deposits of semi-bright nickel/nano-SiO2 with amorphous Ni-P alloy was the best, the solution system of semi-bright nickel/nano-SiO2 with bright nickel was stable and its electro-deposits also had an excellent corrosion resistance, composite electro-deposits of Zinc not only had good corrosion resistance, but also low cost, thus making it an excellent electro-deposit for medium or low-class Nd-Fe-B magnetic material.

Jan 1, 2006

By Carlos Maurício Fontes Vieira, Sergio Neves Monteiro

"A ceramic body traditionally used to produce bricks and roofing tiles with kaolinitic clays was reformulated by the addition of sand and illitic clay. The objective was to obtain a ceramic product with better technological properties. Specimens were made by uniaxial press-molding at 20 MPa and then fired at 850, 900 and 950°C. The determined technological properties were: linear shrinkage, water absorption and flexural rupture strength. The results showed that both sand and illitic clay contribute to reduce the water absorption of the industrial clayey body. With respect to the flexural behavior, it was observed that the incorporation of sand decreased the mechanical strength. On the other hand, the illitic, incorporated in an amounts of 30 wt.% contributed to increase the mechanical strength of the clayey ceramic.IntroductionCeramic bodies industrially fabricated in the county of Campos, north of the State of Rio de Janeiro, in Brazil, are still empirically elaborated using a mixture of local clays. These clays are predominantly kaolinitic mineral in nature, associated with high plasticity and elevated weight loss during the firing stage. Due to the excessive plasticity of the ceramic bodies, dimensional defects, which occur after drying and firing are usually obtained. Moreover, the kaolinitic nature and the presence of aluminum hydroxide (gibbsite) confer a refractory behavior to the local clays, which impairs sintering during the firing operation. In the case of clay ceramic products for civil construction, this results in greater porosity associated with elevated values of water absorption and low mechanical strength [1,2]. To avoid these problems, it is necessary to reformulate the ceramic body composition. The addition of both non-plastic materials to reduce plasticity and fluxes to condition the refractoriness is a possible alternative.As an alternative to reduce the plasticity of clayey ceramics sand, which is predominantly constituted of silica, can be used. The incorporation of sand in amounts of up to 25 wt.% to a clayey ceramic body used for roofing tiles fabrication was studied by Vieira et al. [3]. In that work specimens were prepared by extrusion and fired at 850°C. The results indicated that in the pre-firing stages the sand improved the workability of the investigated clayey ceramic body and facilitates the drying stage. It was also observed that the incorporated sand significantly improved the physical and mechanical properties of the clayey ceramic after firing. On the other hand, the apport of flux oxides could be done by the use of illitic clays that have a higher amount of alkaline oxides in comparison with the kaolinitics clays."

Jan 1, 2013

By Jeffrey Shepherd, Scott R. Smith, Eduard Guerra

"Electrochemical and spectroscopic evidence for the dissolution of a Au electrode by meso-2,3- dimercaptosuccinic acid (DMSA) from an acidic LiCl04 electrolyte is presented. Near the potential of zero charge, DMSA was determined to form a stable layer on the metal surface but at more anodic polarizations, DMSA was displaced from the metal through an oxidative process. The anodic displacement of the layer from the electrode resulted in a small amount of Au that was detected in the electrolyte using atomic absorption analysis. The extent of Au dissolution, was monitored while holding the potential of the electrode for 24 hours at the thermodynamic Eo/H,O in LiCl04 electrolytes containing 10 mM DMSA. This routine resulted in detectable quantities of a soluble Au-DMSA complex in the electrolyte and the greatest leaching was observed at a pH = 2.0. At room temperature, the leaching rate was stable at 10.9 µg cm·2 hr·' however, upon increasing the temperature to 50.0°C, the rate of Au dissolution increased yielding an average rate of extraction of 40.1 µg cm·2 hr- 1. Interestingly, after the first 12 hours of leaching at 50.0°C, the leaching current decreased dramatically suggesting surface passivation which prevented further Au extraction. The implications of this process in the industrial leaching of Au will be discussed.IntroductionThe use of cyanide in the industrial process of leaching Au from ores has raised concerns regarding both operational safety and environmental issues surrounding the disposal of spent leaching eftluents in tailings ponds. Depending on the chemical nature of the processed ore, the spent solutions that are released into the tailings ponds can contain toxic cyanide, either dissolved or complexed with different metals and may pose serious risk to wildlife as well as freshwater contamination to nearby water systems. Because of these issues, some recent studies have focused on the exploration of more environmentally-friendly molecules to selectively leach Au with appropriate kinetics. However, to effectively leach Au into an aqueous solution, a suitable ligand that reacts to form a stable chemical bond with Au is needed to form soluble Au complexes that can be later recovered [I]. Recently several sulfur bearing alternatives have been shown to leach significant quantities of Au in aqueous solutions. These include thiourea [2], thiocyanate [3], and thiosulphate [4]. However, alkylthiols are also known to quickly form a stable covalent Au-S bond [5], but have been relatively understudied in term of their ability to leach Au in solution, even though some short chain thiols are water soluble and relatively nontoxic."

Jan 1, 2012

By Hongmin Zhu, Qiuyu Wang, Shuqiang Jiao, Guojing Hu

"The equilibrium between titanium ions and metal titanium was investigated in fluoride-chloride molten salt. The electrochemical properties of titanium ions in fluoride-chloride were studied on a molybdenum electrode by cyclic voltammetry (CV) and square wave voltammetry (SWV). The equilibrium constant of the equilibrium between titanium ions and metal Ti was calculated in KCI-NaCl- 2.5wt %K2 Tif 6 at the temperature of 1073K.IntroductionTitanium, the ninth most abundant element in the earth's crust, is endowed with high strength, low density, excellent flexibility, strong spring back characteristics, high-temperature performance, corrosion resistance and biocompatibility. These characteristics make titanium eminently suitable to be used in aerospace, marine industries, and harsh chemical environments. Although it has many excellent properties, the application of titanium in industry was limited by its high-cost. Therefore, many methods have been investigated for producing high-purity titanium at low cost. Electrolysis, involving the extraction and preparation of pure metal from ore using an electrolytic process, is considered a promising method for titanium metallurgy. Many studies have focused on the electrochemical behaviour and electrodeposition of titanium in molten chloride, fluoride, and chloride-fluoride electrolytes (1-IOJ. The electroreduction mechanism of Ti3+ ions in molten alkali chlorides has previously been studied by several workers. Two reduction steps, Ti3+ -Ti2+ -Ti, have been observed in various molten alkali chlorides [IJ. One reduction step, Ti3+ -Ti, has been observed in alkali fluoride molten salts l21. The behaviour of Ti4+ in fluoride or chloride-fluoride molten salts has also been investigated in the literature; it was proposed that the reduction of Ti4+ ions in the molten salts proceeded in a two step process: Ti4+-Ti3+-Ti l3l or a three step process: Ti4+ -Ti3+ -Ti2+-Ti ri. 4l Indeed, the stability of the titanium oxidation states depends on the bath composition l5l. The valence state was Ti2+ in alkali chloride melts, which was a lower oxidation state and correspondingly, in alkali fluoride melts, the higher oxidation states ofTi4+ and Til+ were more stable.The aim of the present work is to explore the effect of F/Cl atomic ratio on the equilibrium between titanium ions and metal titanium in fluoride-chloride at the temperature of 1073K. The electrochemical properties of titanium ions in fluoride-chloride were studied on a molybdenum electrode by cyclic voltammetry (CV) and square wave voltammetry (SWV). The solubility product of the equilibrium between titanium ions and metal Ti was calculated."

Jan 1, 2012

By John Frederick Colloghon, O&apos

Bulong remains the only hydrometallurgical process plant in the world that recovers nickel and cobalt directly from high pressure acid leach (HPAL) laterite leach liquors without need for precipitation of an intermediate product (e.g. sulphide, hydroxide or carbonate). Direct solvent extraction (DSX) of both nickel and cobalt in combination with electrowinning of nickel has been operation at Bulong since early 1999. Focus in the first years has been on ramp-up and resolution of commissioning problems. More recently the focus has been on de-bottlenecking and process optimisation. A number of significant process problems have been resolved, the most difficult being the formation of gypsum in the nickel solvent extraction circuit. Sound control of process chemistry is essential to ensure the production of high quality nickel and cobalt products at the lowest possible cost. This paper describes the numerous changes and enhancements to the process chemistry and plant equipment at Bulong and discusses the importance of ore leach chemistry on downstream impurity metal removal. Potential additional enhancements to further reduce unit costs are also presented.

Jan 1, 2004

By G. Riverin, C. Simard, W. D. Stevens

"An on-line technique to measure the efficiency of decoating I delacquering processes is being developed by Alcan' s Arvida R & D Centre. Decoating processes are used to remove moisture and coatings from shredded coated material such as Used Beverage Containers (UBC) before melting. Complete removal has been demonstrated to maximize metal recovery. Quantifying the weight of carbon and organic residue adhering to the shred surfaces is very difficult to measure directly, as the material can be highly folded. The technique developed indirectly measures the residue remaining by analysing the concentration of CO evolved in the decoater end zone exhaust gas.A commercial CEMS (Continuous Emission Monitoring System) incorporating an infrared type CO gas analyser was modified for on-line process exhaust gas analysis. Both pilot and plant trials had demonstrated that the CO concentration measured was inversely proportional to the efficiency of the organic removal achieved. As the quality of coated purchased scrap can be highly variable in moisture and organic content, continuous measurement should permit adjusting the feed rate and other decoater process parameters to the quality of decoating required."

Jan 1, 2000

By Larry Southwick

In the early 1940's, the Caron ammonia ? ammonia carbonate leach process was used to produce nickel from Mayari ores at the Nicaro plant in Oriente Province, Cuba. While plant operation was generally successful, it was not broadly economical and was shut down. The plant was later restarted in the 1950's and a number of investigations initiated to resolve the more serious operational and performance issues. Processing steps studied included iron reduction (chemistry ? nickel and iron, reductant, equipment), ore variability (homogeneity and consistency of mineral concentrations, serpentine vs. laterite), leach solution strength, nickel recovery (temperature ? reduction and leaching, reoxidation) and a variety of other topics. These studies and their findings will be discussed. Caron himself obtained good results on these ores in the laboratory. They could not be duplicated in the field, the reasons for which will be reviewed. (Note: the ore looked like garden dirt; charcoal made from palm trees was one of the reductants attempted; and ammonia was the leach solution. Mixing the three, so to speak, was to yield nickel.)

Jan 1, 2006

By Takayuki Ichikawa

Hydrogen storage properties of ballmilled mixtures composed of the hydrogenated nano-structured carbon (CnanoHx) and lithium hydride (LiH) were examined by thermal and optical spectroscopic analyses. LiH needs higher temperature than 600°C for hydrogen desorption even under vacuum condition, while CnanoHx, which was mechanochemically synthesized from graphite powder by ballmilling under hydrogen atmosphere, reveals hydrogen and hydrocarbons desorption in wide temperature range from 300 to 800°C. Nevertheless, the composite of CnanoHxand LiH prepared by ballmilling desorbs hydrogen in relatively lower temperature range from 150 to 450°C. These phenomena indicate that the thermally liberated hydrocarbon radicals immediately react with LiH and release hydrogen instead of hydrocarbons emission, because CnanoHx contains hydrocarbon groups at the edge of nano-meter sized graphenes, which are recognized as IR active C-H stretching mode, and LiH is well-known as an ionic crystal. Furthermore, it is of interest that a nanostructural feature persists in this composite even after annealing at 350°C, which shows excellent cycle properties as hydrogen storage media.

Jan 1, 2006

By Rainer Köster, Tobias Wagner, Markus Delay, Fritz Hartmann Frimmel, Wolfgang Ferstl, Wolfgang Höll

"The mobilization of contaminants from industrial residues like ashes from municipal solid waste incinerators in case of leaching is investigated world wide. In classical leach tests only soluble species are considered. In addition the geochemical behaviour of residues has to be completed by assessing the mobilization via colloidal particles. This transport is well known from natural aquatic systems. Quantification of aquatic colloids is associated with considerable difficulties, because they are often found in low concentrations and in a size distribution where small particles with diameters below 0.1 µm predominate. In the past years, the Laser-induced Breakdown Detection (LIBD) has been developed as a novel sensitive method for quantifying colloids. Column leaching experiments with directly coupled LIBD were used to quantify the release of heavy metals and colloids out of bottom ashes. Some typical colloid bound heavy metal concentrations in the leachate are in some cases exceeding the limits defined by German authorities. The LIBD with a flow-through cell allowed to assign absolute values to colloid size and concentration."

Jan 1, 2008

By Jeaneth S. Benedetto

The physical and chemical processes developed for recovery of uranium and phosphor from phosphoro-uraniferous ore bodies consists of three basic steps: concentration of the phosphate bearing uranium by flotation, chemical dissolution of the concentrate by wet phosphoric acid and extraction of uranium by solvent. In this process two products are obtained: 1) uranium and 2) phosphoric acid. The purpose of this work was to develop technological know-how of phosphoric acid purification though an extraction of P2O5 by solvents. It was investigated by two lines of research. In the first one the uranium was extracted before the phosphoric acid purification. In the second, the phosphoric acid was extracted before uranium recovery. The comparison of the two processes is shown in this paper. Experimental work was developed on a laboratory scale to select and optimize the process variables. After the laboratory study, the research of extraction and stripping was continued on a pilot scale in pulsed perforated-plate columns in order to investigate the main operational and process conditions. The first phosphoric acid extraction experiments showed good results using a raffinate sample obtained from the uranium extraction process. It was possible to obtain a high purity phosphoric acid.

Jan 1, 2003

By R. D. MacDonald

The papers presented in this chapter cover a wide range of hydrometallurgical topics and might be considered to be unrelated to each other. All of the authors, however, utilized the basic methods of process mineralogy to characterize the reactants in their experiments and the products produced. The wide range of research topics which can be pursued successfully by the use of the methods of process mineralogy is a matter of interest in itself. One might speculate that the methods could be even more widely applied if only their utility were better recognized. These methods for characterizing reactants and products include principally x-ray diffraction, optical micros-copy, wet chemical analyses, instrumental chemical analyses, high intensity magnetic separation, micro-scale gravity separation, differential thermal analysis, micro-hardness testing, and judicious use of the sledgehammer and cold chisel. It is perhaps not by coincidence that most of the papers in this chapter were prepared not by mineralogists, but by hydrometallurgists, who are recognizing the importance of thinking in terms of mineral phases, and not just assays! It appears that the gap between process mineralogy and the mineral industry is closing, and that future AIME sessions promise to become established forums where mutual discussion of such topics as metallurgical "troubleshooting" and process design may become commonplace between plant engineer and process mineralogist.

Jan 1, 1981

By Peng Fan

Nitride capacity is usually employed as the measure of slag?s ability to remove nitrogen from liquid metal, since nitrogen distribution ratio between slag and metal can be calculated from nitride capacity provided that the value of oxygen activity in liquid metal is available. However, during liquid metal refining processes, oxygen activity in liquid metal is usually unknown and thus it is impossible to get nitrogen distribution ratio from nitride capacity under this usual condition. In this paper, thermodynamic analysis indicates that the activity coefficient of nitride in slag can be used to measure slag?s ability to remove nitrogen from liquid metal, because nitrogen distribution ratio between slag and metal can be calculated from the activity coefficient of nitride in slag provided that the content of oxygen potential controlling element like Al in liquid metal is available. Review of reported nitrogen removal studies and our recent study has verified that for a given Al content in metal, the lower the AlN activity coefficient in slag is, the higher the nitrogen distribution ratio. Titanium monoxide based slag has been found to be much more effective to remove nitrogen than other slags. Since Al content in liquid metal is usually available during liquid metal refining processes, AlN seems to be a better measure of slag?s ability to remove nitrogen from liquid metal.

Jan 1, 2006

By I. A. Ibrahim

Ilmenite, in its natural form, is an inactive mineral from which the selective removal of iron is rather difficult. The reactivity of ilmenite. so that it can be leached with dilute hydrochloric acid, can be enhanced by chemical reduction in solution using a suitable metal as a reducing agent. The present paper aims at the evaluation of an Egyptian ilmenite ore for the production of synthetic rutile by direct leaching with hydrochloric acid in presence of iron powder. In this process, the titanium and iron contents are dissolved; meanwhile, the dissolved titanium is hydrolyzed and re-precipitated leaving mainly iron in solution. Leaching conditions were optimized to obtain less iron in the final solid product. Addition of sufficient amount of iron powder during leaching reduces the dissolved Fe3+ to Fe2+ and reduces the dissolved Ti4+ to Ti3+. The creation of Ti3+ in solution is assumed to have a role in dissolving the ferric iron and hence increasing the reactivity of the ilmenite ore. Synthetic rutile of about 90% TiO2 and 0.77% Fe2O3 was obtained from ore with a grain size 100% passing 200 mesh and a 5-hour leach time with 20% HCl at boiling temperature (110°C) and 0.11 g iron powder / g ore.

Jan 1, 2003