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By Rajesh K. Mishra

In secondary precious metals refining, the feed to the plant itself is a waste generated in manufacturing processes. Constant changes in manufacturing processes produce ever changing feed materials to the secondary PGM (platinum Group Metals) refineries. After extracting the precious metals, secondary wastes are generated. The discharge of effluent is dictated by both the PGM losses in wastes and the regulatory mandates. This paper will discuss some. of the conventional as well as some newer approaches to face both the challenges.

Jan 1, 1995

By Michael J. Virnig

The formation of crud is a normal part of operating a solvent extraction circuit for the recovery of copper. It periodically must be removed from the circuit. This results in significant costs in terms of manpower, downtime, and loss of circuit organic. Field studies have been carried out that show that the presence of a thermodynamic modifier in the organic phase contributes to crud formation. In an effort to better understand what factors contribute to crud formation, laboratory studies involving competitive adsorption studies with model solids have been carried out. The results of these laboratory studies will be integrated with the results of the field studies to present a better understanding of crud formation.

Jan 1, 1999

By Animesh Jha

Univariant diagrams are constructed for the reduction of nickel and cobalt oxide and sulphide minerals. The results from the carbothermic and hydrogen reduction of sulphide minerals are compared. The importance role of lime and calcium sulphate in controlling the emission of sulphurous- gases during reduction reaction is also explained. The mechanism of carbothermic reduction of nickel sulphide is explained by examining the sulphur exchange and reduction reactions. The phase equilibrium relationships that determine the formation of multicomponent liquid are characterised. Also the governing equilibria for inert atmosphere calcination- roasting of nickel and cobalt sulphide minerals are also described for the metallization of nickel and cobalt.

Jan 1, 1993

By Shize Jin

Effect of four polyols, namely ethylene glycol (EGL), glycerol (GCL), propanediol (PDL), butanediol (BDL) and three organic acids, namely oxalic acid (OA), malonic acid (MA) and succinic acid (SA) on the current efficiency (CE) and the cell voltage during zinc electrowinning was studied. Galvanostatic polarization was conducted in a supporting electrolyte (SE) containing 180 g dm-³ H2SO4, 60 g dm-³ Zn2+ and 8 g dm-³ Mn2+ at 38°C with magnetic stirring. The imposed current density was 50 mA cm-². The anodes were made of a Pb-Ag alloy and the cathodes were made of an aluminum alloy. The results showed that all the polyols tested in this study decreased the current efficiency and the cell voltage, but the decrease of the cell voltage was not important. Oxalic and succinic acids decreased the current efficiency to a less extent than the polyols, but did not decrease the cell voltage much. The only compound that increased the current efficiency was malonic acid, and its capacity of decreasing the cell voltage was the highest within the seven tested organic compounds.

Jan 1, 2003

Acid generation from reactive sulphide mineral tailings has become a major environmental problem in the mining industry. Initiation of chemical and biochemical oxidation reactions of the sulphide mineral leads to acid generation. A novel concept of safe disposal and utilization of reactive fine mill tailings is presented in this paper. The paper also presents the results of a preliminary laboratory experimental .study of the concept. The tailings are agglomerated using portland cement as a binder. The cold bonded agglomerates are encapsulated with other chemical additives to act as acid neutralizers, oxygen and ironoxidizing bactericides., The primary. factors influencing the choice of bacterfoides to inhibit the acid generating bacteria are their costs, toxicity and environmental friendliness. The paper discusses the utilization of agglomerated' products as aggregates for underground backfill, or as gravel for surface land cover.

Jan 1, 1991

By C. M. Acuña

Copper losses in slags are of great concern, specially in smelting and slag cleaning processes. It is widely accepted that the suspension of metallic copper and matte droplets is strongly affected by the viscosity of the slag. The Chuquicamata Division of Codelco- Chile produces concentrates high in zinc, an element which reports mainly to the slag phase. The ZnO may affect the viscosity and therefore the copper losses. This work aimed to investigate the effect of lime to control the viscosity of slags, and in turn to control the copper losses. By using the experimental viscosity data and the Stoke's law, the settling rate of matte prills in various slags was estimated. The results indicate the possibility of increasing the recovery of copper and/or decrease the process time.

Jan 1, 1999

By Mala Nath, Atjit Mallick, Asheesh Kumar

"The present research work is aimed to focus on the development of chemically stable light weight microporous carbonaceous material, such as activated charcoal incorporated either with titanium n-butoxide, titanium diisopropoxide bis(2,4-pentanedionate), vanadium 2,4-pentane-dionate or zinc 2,4-pentanedionate having varying wt% of the metal (2-8%) using ethanol as solvent at 40--50 oC followed by calcinations at 100, 150 and 200 cC, except the samples with titanium diisopropoxide bis(2,4-pentanedionate) which are calcinated at 80 oC. Atomic absorption studies along with FESEM revealed that the maximum incorporation of metals (Zn, V and Ti) in activated charcoal was observed with 4 wt% of zinc 2,4-pentanedionate calcinated at 150 oC , 4 wt% of vanadium 2,4-pentanedionate at 100 oC, 2 wt% of titanium n-butoxide at 100 oC and 2 wt% of titanium diisopropoxide bis(2,4-pentanedionate) at 80 oC, and equilibration time of 20-24 h was used in each case. Hydrogen sorption behavior in these carbonaceous materials has also been studied at 77.4 K and low pressure up to I bar. The highest hydrogen uptake obtained was 1.45 wt% (164.5 cm3 (STP)/g at P/Po = 1.0) for activated charcoal incorporated with 4 wt% of zinc 2,4-pentanedionate calcinated at 150 oC.IntroductionTwo of the major challenges for humanity in the next twenty years are the shrinking availability of fossil fuels, the global warming and potential climate changes that result from their ever-increasing use. So it is necessary to fmd an energy source that is convenient, flexible and controllable. One possible solution to these problems is to use an energy carrier such as hydrogen, and ways to produce and store hydrogen in electric power plants and vehicles. Hydrogen storage is the bottleneck for the breakthrough of hydrogen as energy carrier in automotive applications [1]."

Jan 1, 2012

By J. -C. Tedenac, C. Colinet, X. Tao, P. Jund, R. Viennois

"We report an ab-initio study of the stability and electronic properties of transition metal silicides in order to study their potential for high temperature thermoelectric applications. We focus on the family M5Si3 (M = Ta, W) which is stable up to about 2000 °C. We first investigate the structural stability of the two compounds and then determine the thermopower of the equilibrium structure using the electronic density of states and Mott’s law. We find that W5Si3 has a relatively large thermopower but probably not sufficient enough for thermoelectric applications.IntroductionIn the search of new sustainable energies, thermogeneration of electricity is one of the promising ways, notably because it is able to produce electricity from different kinds of heat wastes and to its portability. However, despite recent progress in the field, the state-of-the art materials have specificities making their mass-production difficult or even impossible: toxicity (thallium, chalcogen or/and pnictogen based alloys), weak abundance (tellurium based alloys) or cost (germanium or rare-earth based alloys). For all these reasons, finding thermoelectric materials without these drawbacks is vital if we wish to use high temperature thermoelectricity for generating electricity in the near future. Due to their abundance, low cost and low toxicity, transition metal silicides are candidate materials of primary interest and the slightest advance in this field would immediately find an application for the thermogeneration of electricity."

Jan 1, 2011

Today’s world relies upon advanced green technologies that are made of critical elements with unique properties. Examples include rare earth elements (REEs) that are critical in the manufacturing of wind turbines and electric/hybrid vehicle batteries, key components of a greener future that face supply uncertainty and near zero recycling. To tackle their supply challenges, activities have begun for urban mining from waste electrical and electronic equipment (WEEE) that contain considerable amount of REEs, but their current level of recycling is less than 1%. Current recycling practices use either pyrometallurgy, which is energy intensive, or hydrometallurgy that utilizes large volumes of acids and solvents and generates large volumes of hazardous waste. In this study, we developed a novel and sustainable process to recycle REEs from WEEE, NiMH batteries in particular. The developed process relies on supercritical fluid extraction (SCFE) utilizing CO2 as the solvent, which is abundant, safe, cost effective, and inert. The effect of seven operating parameters, namely temperature, pressure, residence time, sample to chelating agent ratio, agitation rate, complex formulation, and methanol addition on REE extraction efficiency was investigated, and optimum operating conditions were determined. This work is the first to utilize a very efficient and safe process that runs at low temperature to extract metals from postconsumer products with minimum hazardous waste generation, while offering about 90% leaching efficiency for REEs. We expect our process to find widespread applicability in urban mining of REEs using green chemistry.

By Brent W. Madsen

The acid-ferric sulfate leaching of low-grade sulfide copper mine waste provides more than 10 percent of the U.S. supply of new copper, but recoveries and leaching rates are very low. In Federal Bureau of Mines research to improve the leaching process, experiments on 5- to 10-ton lots of mine-run ore were more revealing than bench-scale tests on fine ore. This report discusses the results obtained by leaching run-of-mine and minus 6-inch plus 112-inch samples of low-grade chalcocite-bearing mine waste. The samples were leached for 461 days and 61.6 and 37.7 percent of the copper was extracted from the minus 6-inch plus -112-inch and run-of- mine samples, respectively. A mixed kinetics model was applied successfully to the leaching of the sample with the fines removed where bulk solution transport was not rate controlling. The model, when applied to the run-of- mine ore, gave somewhat higher predicted copper extractions than experimentally determined. Subsequently, oxygen was introduced into the run-of- mine ore, leaching continued for an additional 312 days, and an additional 53.0 percent of the copper was extracted. Before the leaching experiment was dismantled and the residue sampled, the ore was treated with sulfur dioxide and its permeability was improved markedly. The results of each of these procedures are interpreted in relation to the attendant condition of the test.

Jan 1, 1976

By Dale T. Peters

In the United States, the United Kingdom and numerous other countries, copper has long been the plumbing material of choice. This has been the case since the late 1920s in the United States and since World War II in the United Kingdom. However, in recent years the plumbing tube market has caught the eye of the chemical industry, and several plastic resins have been introduced to the marketplace as substitutes for copper in household plumbing systems. One of these, polybutylene tube, had so many failures in the United States that a class action law suit was filed, and the manufactures of this product were forced to create a trust fund of nearly one billion dollars to repair damages caused by their product. Chlorinated polyvinylchloride (CPVC), in rigid pipe form, on the other hand, has been mechanically acceptable albeit its recent introduction precludes the test of time enjoyed by copper tube in this application. This paper reviews the State of California's portrayal of copper's environmental effects and will be largely based on the data and information assembled by the Copper Development Association Inc. in its presentation to the State of California in August, 1998 in response to the State's Draft Environmental Impact Report for Chlorinated Polyvinyl Chloride (CVPC) Pipe for Use for Potable Water Piping in Residential Buildings. The paper is intended for use as a model for the use of other copper organizations and individuals in responding to similar situations.

Jan 1, 1999

By Peter Koh

The velocity solid charge attains when dropping down concentrate chutes is an important boundary condition when developing mathematical models of flash furnace burners and reaction shafts. In this work an experimental rig was developed to measure the velocity attained when nickel concentrate and sand were dropped down a vertical pipe 3m long. The velocity measurements showed that the nickel concentrate did not fall as individual particles. The measured values of the velocity approached, but did not attain, those calculated for solid bodies, the disparity being attributed to friction at the pipe wall and fluid drag losses. After falling 2 m velocities between 5-6 m/s were attained. The analysis was extended and applied to understanding the intermittent problem of puffing which sometimes occurs from the top of the concentrate chute. The pressure at the bottom of the chute is the net result of two opposing pressures, namely that developed by (a)the process air entering through the velocity control device, and (b) the solids falling down the concentrate chute. Flow back up the chute occurs when the former exceeds the latter. The process air pressures in the burner were obtained from CFD simulations of a full burner. Variables considered included air speed through the velocity control device, drop height and furnace draft. The analysis was useful in highlighting the operating conditions which were conducive to puffing and in establishing procedures to minimise its occurrence.

Jan 1, 2006

By S. H. Castro

The El Teniente molybdenite plant (Chile), with a nominal capacity of 3,200 tpd of bulk Cu-Mo concentrate, produced approximately 3,385 metric tonnes of Mo during 1998 by using the phosphate Nokes process (LR-744 reagent). This is the only Chilean moly plant which traditionally has depressed copper and iron sulfides with LR 744 reagent, which is a hydrolysis product of P2S5 and NaOH. El Teniente's ore Mo grade is 0.02%Mo and is concentrated to 0.45%-0.50% Mo in bulk Cu-Mo flotation. Subsequently, molybdenite is floated by selective flotation to depress Cu and Fe sulfides, such as chalcopyrite, bornite, digenite and pyrite, to produce typically a 49%-50%Mo molybdenite concentrate. An optimisation program during the last two years was undertaken to improve molybdenite recoveries. Current molybdenite plant technology at El Teniente and use of phosphate Nokes in the process process is reported. Use of phosphate Nokes reagent has increased average Mo recovery from 70.5% in 1977 to a mean 74.7% for the first 4 months of 1999. The global Mo recovery, including bulk flotation, incresed from 42.3% in 1997 to 46.8% in 1998, with a projection of 55.5% for 1999. Mo production per year has increased from 3,181 tons in 1997 to 3,385 tons in 1998 and a projected 4,000 tons for 1999.

Jan 1, 1999

By Alpagut Kara

Turkey is the fifth biggest ceramic tile exporter in the world. Considering the expectation that the Turkish tile sector continues to expand, further studies both on the improvement and the development of tile formulations are necessary in order to make the producers advantaged in the world market while maintaining the capital and running costs at reasonably competitive levels as well. In addition to such studies, waste management in tile manufacturing has also recently become an important issue. Accordingly, the industrial use of wastes in the traditional ceramic industry has been intensively investigated in the recent years. This work describes part of a detailed research project carried out jointly on the possible re-use of muds (raw production waste) from glazing and pressing lines of a local tile company in the development of new wall and floor tile formulations. In order to achieve this, the waste material was firstly investigated in function of chemical and mineralogical compositions. Then, the particular focus was given to the presence of the waste material in increasing amounts on the thermal behaviour and physico-mechanical properties of the re-formulated tile bodies. During the studies, SEM in combination with EDS, and thermal analysis techniques such as non-contact dilatometry were widely employed. The results indicated that it was possible to use the waste materials in the commercial tile production without deteriorating the relevant technological properties.

Jan 1, 2006

By D. I. Chalmers

The Brockman rare-metals and rare earth resource is located within volcanic and volcanogenic sediments of the later Proterozoic Halls Creek Group in the East Kimberley region of Western Australia. Exploration including surface trenching, percussion and diamond drilling has defined a major resource of rare-metals and heavy rare earth elements. The host&apos; is a steeply dipping ash-flow tuff, described informally as the Niobium Tuff, enriched in zirconium, hafnium, yttrium, niobium, tantalum, rare earth elements, gallium and beryllium. The mineralization is fine- grained (<20 micrometres) and is the result of alteration and re- mobilization of comparatively simple precursor minerals such as columbite and zircon by fluorine-rich deuteric solutions that were retained in the tuff following eruption. The ultra fine-grained structure of the tuff precludes mineral liberation and separation by physical methods. However, values can be converted to water soluble sulphates by reacting with concentrated sulphuric acid at 250°C. The solution containing aluminium, niobium, tantalum, zirconium, hafnium, yttrium, rare earths and gallium can then be processed to pure products in a sequence of solvent extraction and ion-exchange steps. As a result of these processing techniques, the commercial products obtainable from the resource include mixed rare earth and yttrium concentrates, zirconium-hafnium concentrate, niobium-tantalum concentrate and ceramic grade alumina. Further separation could result in high purity products suitable for ceramic and electronic applications.

Jan 1, 1992

By Ehsan Vahidi, Fereshteh Rashchi, Ataollah Babakhani, Alireza Zakeri

"The synergistic effect of Cyanex 302 on solvent extraction of nickel and cadmium from sulfate solution with D2EHPA diluted in kerosene was investigated with the aim of increasing separation efficiency. Experiments were carried out within a pH range of 0.1-5.0 using sole D2EHPA and D2EHPA-Cyanex 302 mixtures in different ratios. Increasing Cyanex 302 to D2EHPA ratios in the organic phase caused a left shifting of the extraction isotherm of cadmium and a right shifting of the extraction isotherm of nickel. As a result, optimum separation was found with a Cyanex 302 to D2EHPA ratio of 0.1M:0.5M. In the present system, effect of a modifying reagent such as TBP was studied. The influence of various diluents including kerosene and carbon tetrachloride was also investigated.IntroductionBatteries are popular sources of portable energy. Ni-Cd batteries are manufactured in two main groups of small domestic cells and large industrial batteries with 80% being in domestic use. Ni-Cd cells have various uses, for example in cordless electric utensils, cordless telephones, airplane engine starters, and communicational distribution systems [1].Depleted Ni-Cd batteries are classified as hazardous waste since nickel and cadmium are heavy metals and suspected carcinogens. Given the risk associated with uncontrolled disposal, directions for issuing legislation on disposal and recycling of used batteries have been made in industrialized countries [2]. Recycling of Ni-Cd batteries is important from both economic and environmental points of view. Different methods have been used for recycling these wastes through pyrometallurgy [3], biotechnology [4,5], and hydrometallurgy [1,2].Due to the advantages of hydrometallurgical processes, several studies have been implemented on leaching and solvent extraction (SX) of the used Ni-Cd batteries. Leaching of batteries is usually done in sulfate or chloride media; while solvent extraction has been used in different extractants: two-stage solvent extraction by D2EHPA and Cyanex 272 [6]. Solvent extraction of Cd from leach solutions has been studied using various extractants; Cyanex 301 [1], D2EHPA [7], Cyanex 302 [8], Cyanex 923 [9], Cyanex 272, Tops 99, PC88A [10]. Application of phosphorus based extractants for the solvent extraction studies of Ni such as TOPS 99 [11], D2EHPA [12], Cyanex 272 [2], has been investigated. Separation of Cd(ll), Ni(II), and Co(ll) from chloride leach liquor of spent batteries [13], were explored in the earlier studies. Cd extraction with D2EHPA involves co-extraction of both Ni and Co [14], which causes issues in the separation process efficiency."

Jan 1, 2012

By P. L. Sibrell

The U.S. Bureau of Mines has tested cyanide leaching for recovery of palladium (Pd) from spent petroleum processing catalysts. Three different catalyst samples were supplied by a spent-catalyst processor. These catalysts consisted of a zeolite base and contained 0.4 to 0.7 pct Pd. During alkaline cyanide leaching, the catalysts exhibited ion-exchange properties due to their zeolite matrices. Hydrogen ions were released from the zeolite in exchange for sodium ions in solution, resulting in a significant decrease in solution pH. This could present a safety hazard because of the potential for release of toxic hydrogen cyanide gas. A pretreatment .step where the catalysts were contacted with a 1.0M sodium hydroxide solution was found to prevent the pH shift from occurring. Following the sodium hydroxide pretreatment, two stages of leaching at 160 °C with solution containing 1 pct sodium cyanide and 0.1M sodium hydroxide gave at least 75 and up to 95 pct Pd recovery. The Pd was quantitatively recovered from the leach solution by thermal decomposition in an autoclave at 250 °C for 1 h. The Pd content of the precipitate was over 50 pct. Thermal decomposition also decreased the total cyanide content of the barren solution to less than 0.2 mg/L. The catalyst leach residues passed the Federal Toxicity Characteristic Leaching Procedure and the California Waste Extraction Test, indicating that landfill disposal of the leach residues would be acceptable.

Jan 1, 1995

By Rong Yang, Qijie Zhai, Wenbin Xia, Changjiang Song

"Tills paper focus on the influence of carbon content and cooling rate on the microstructure and phase formation of Fe-Mn-C alloys under near-rapid solidification. When manganese content is about 11wt.%, more s-martensite can be obtained with cooling rate increasing when carbon content is 0.14wt.%, the formed phase changed from a phase to y phase when 0.74wt.% carbon is added to the samples, and when carbon content up to 2.1wt.%, carbide can be obtained in the sample. A host of stacking fault, which attributes to the strain-induced martensite, can be observed in the sample. The microhardness increased with cooling rate increasing, and under the same cooling rate, the microhardness of samples with 0.14wt.% carbon is highest.IntroductionTo obtain high performance materials is eternal pursuit of material science research. Material scientists have explored many new ways to obtain high performance materials from long time ago. Rapid solidification is one of most popular ways to produce advanced materials by obtaining metastable phases, because it is widely known that the solidification of metals in metastable phases gives access to a whole range of materials with novel properties [1]. Furthermore, nowadays metastable materials have been extensively used in many fields, for example, many of our modem high performance materials such as steel products or aluminum alloys for aeronautical applications are in the form of metastable rather than stable phases [1]."

Jan 1, 2012

By Brad Wahlquist

An ex-situ biological treatment system was implemented at a gold mine site in South Dakota. The system removes selenium and nitrate from a mixture of groundwater and surface water runoff at ambient water temperatures. The Applied Biosciences? system replaced a denitrification system that did not perform consistently, did not treat for selenium and required heating of the influent water. Installation was completed in phases starting with the selenium circuit being brought into operation in February, 2002 and the nitrate circuit in March, 2002. System design can accommodate average flows of 380 L/min (100 gallons/minute) and a maximum flow of 1,136 L/min (300 gallons/min). Four cells were designed to remove nitrate from approximately 30 mg/L to below 10 mg/L and two cells were designed to remove selenium from 0.01 mg/L and higher, to below 0.005 mg/L. No pretreatment is required to operate the system at ambient temperatures, which can fall as low as -12C in the winter, and treat water at temperatures ranging between 8C to 16C. Nutrient requirements are met using a sugar based nutrient mixture that includes a balanced C:N:P:S ratio, trace elements and vitamins. Since start up, the system has consistently been in compliance for nitrate and selenium, treating water to below detection limits for both contaminants. This paper discusses laboratory biotreatability testing of a system designed to remove selenium, arsenic, and nitrate and full-scale implementation and optimization of a system to remove nitrate and selenium.

Jan 1, 2003

By Lifeng Zhang

The transport of fluid, heat and particles (bubbles and solid inclusions) in flowing molten steel is investigated in steel refining ladles, the continuous casting tundish, continuous casting mold and strand, and steel ingot casting processes. Inclusion removal from the molten steel by flow transport and bubble flotation, and inclusion growth by collision and diffusion are discussed. Removal of impurity elements such as [C] and [O] during steel refining are reported.

Jan 1, 2006