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By Francis Vanbellen

Umicore Precious Metals Refining operates an integrated precious metals smelting and refining plant in Hoboken, Belgium. Once a smelter and refiner of complex concentrates, the plant today?s feed consists exclusively of industrial and consumer recycled products, making it the world?s largest recycling facility for precious metals. Unlike the fairy tale of the Frog Prince, it took much more than a princess? kiss to successfully realize this makeover. A completely renewed plant has been built over the past decade. The most visible technological innovation was the commissioning of the Pb-Cu smelter. Its flexibility towards very different types of feed makes it perfectly suited as main entry to the Hoboken flow sheet. A new Cu-leaching & electro winning plant and precious metals refinery make up the Precious Metals Operations (PMO) whose targets are fast throughput and maximized yields for gold, silver and the platinum group metals. The Base Metals Operations (BMO), flexibly process the by-products from the PMO, valorizing ?impurities? like indium, tellurium, selenium and others. Off gas and waste water treatments ensure compliance with strict environmental standards. Precious metals recycling is an art that goes beyond mastering a unique flow sheet. Umicore Precious Metals Refining offers a complete recycling service, taking care of sampling and assaying, metals management and logistics. The quality of this integral service is recognized through the attribution of ISO certifications for our operational activities, sampling and the environmental care. And it?s an art that follows Michelangelo?s experience: ?Art is 5% of inspiration and 95% of transpiration.?

Jan 1, 2006

By Kunihiko Takeda, Kimio Imaizumi, Tsuyoshi Arai

"The study on the preparation of mono-dispersed liquid droplet was performed using ultrasonic as one of the steps of producing the perfectly mono-dispersed particle. The ultrasonic system was a 33.6kHz ultrasonic generator, an amplifier, an electric distortion element, and a bolted Langevin type horn installed in .a cell. For the first time, a liquid pillar under a nozzle of the cell ·was stably formed. Then, dense and coarse parts were alternatively constructed by oscillating the wavelength of the ultrasonic.· The diameter of those liquid droplets were found to be· perfectly uniform, therefore, it was measured by ""multiplex photography"" using a synchronized stroboscope with the ultrasonic.- From the results, more than 30,000 of perfectly uniform liquid droplets in 1 second were observed by this method.IntroductionRecently, research on the control of physical form is done in various fields of industry. Some examples are the processing technology of the minute compound material of micro-machines and integrated circuits, and the form control of molecule size like catalysts. There is a need for such material to take on various forms in correspondence to its use. ""Form control"" as used in this study will indicate ""research on physical chemistry factors which determine the size of the material"" and will refer to the contour uniformity of comparatively little particles. A well-known method of preparing particles is to spout a mist of liquid and slurry from a nozzle l) 2). Particles for metals, catalysts and food have been prepared by this method. In this case, although an approximate particle diameter can be decided by controlling the nozzle diameter and the violent outflow velocity, it is not easy to completely control ·the contour and to prepare a particle with uniform diameter. ·However, the preparation of perfectly uniform particles is necessary for solders for the adhesion of electronic wiring 3), ion exchange resins4), catalysts and so on. Large quantities of fine particles and super-fine particles are generated when manufactured in the usual way. Large quantities of these fine· particles and super-fine particles have polluted the internal and external' environments of factories. The products yield' ·decreases, also. From such a background, this study examines the preparation of perfectly uniform particles that could be· collected -100% as products. Recently, NASA has succeeded in the preparation of perfectly uniform particles in zero gravity 5). But the preparation of 'perfectly uniform particles by this method is difficult, and it can not be used in general industry"

Jan 1, 2000

By Fjeldstad Karin Jusnes

Two quartz types used in the silicon and ferrosilicon industry were heated to temperatures of 1600 and 1700 °C. The parameters varied were the temperature and the holding time at maximum temperature. The amount of quartz, cristobalite and intermediate amorphous phase were measured using XRD and the internal standard method. Type P showed a much larger ability to transform to cristobalite at lower temperatures than type A. Type P had a larger amount of alkali and alkaline earth impurities. This could have enhanced the transformation to cristobalite. For quartz type A the amount of cristobalite was larger at 1600 °C than 1700 °C. This can also be seen for some of the samples of type P at shorter holding times.

By F. Guevara

The paper presents results of physical and turbulent three-dimensional numerical simulation of the gas flow in the wind box and reaction shaft of the concentrate burner of a flash furnace. Physical simulation work was carried out in a 1:5 linear scale model, where the velocity field was measured using a Pitot tube. The mathematical model consists of the three-dimensional averaged Navier-Stokes equations, turbulent kinetic energy and dissipation of turbulent kinetic energy using the Renormalization Group (RNG) theory for the k-e turbulence model. Computations were performed using FLUENT, based in a finite- volume code. The geometry of the concentrate burner was separated in two sections: wind box and reaction tower. Results obtained at the exit of the wind box were used as boundary conditions for the reaction shaft. The effect of boundary conditions on the numerical results was also studied. Results of physical and numerical simulations show an asymmetry of the velocity field at the exit of wind box. This asymmetry is possibly due to existence of a separated flow in the back of the exit ring. The agreement of physical and numerical results assess the capacity of the turbulence RNG k-e model to reproduce correctly the behaviour of the velocity field at the exit of the concentrate burner.

Jan 1, 1999

By W. G. Davenport

The Cu content of industrial flash furnace concentrates varies considerably. It is usually around 30% Cu (Tables 2.1, 3.1) but it may be as high as 55% Cu and as low as 20% Cu. The mineralogy of flash furnace concentrates also varies. The most common Cu mineral is chalcopyrite (CuFeSz), but many concentrates contain bornite (CuSFeS4), chalcocite (CU2S), covellite (CuS) and even native copper (CUO). Pyrite (FeSz) :is also present in many concentrates. This chapter examines how concentrate composition affects flash smelting -with specific reference to 'low-Cu-grade' FeS2-CuFeSz concentrates. Chapter 14 does the same with 'high-Cu-grade' CuzS-CuFeSz?concentrates.

Jan 1, 2001

By Martin Reyes, Juan Hernández, Julio Cesar Juárez, Isauro Rivera, Ma. de los Ángeles Hernández, Francisco Patiño

The dissolution of Ag contained in metallurgical tailings was studied by adding ions Cu2+ and Zn2+ in S2O3 2- medium. Chemical analysis of mine tailings by cupellation revealed a Ag concentration of 71 g/ton. The XRF and XRD analysis confirmed the preponderance of SiO2 in the mineral matrix. The experimental dissolution process was conducted in alkaline solution using six concentrations of NaOH and five of S2O3 2-, at different temperatures, also using five concentrations of Cu2+ and Zn2+ as a catalyst. The results showed similar values for both systems (96.8% and 97.13%). The ion Cu2+ and Zn2+ increases the dissolution of Ag, and decrease the reaction time of dissolution. Under the conditions used, pH and stirring rate did not affect the dissolution of Ag.

Jan 1, 2015

By Carlos A. Nogueira

Spent Ni-Cd batteries contain in the electrode materials heavy metals like Ni, Cd and Co, which must be recycled due to environmental problems. Pyrometallurgy is normally used for recycling these end-of-life products, but alternative processes by hydrometallurgy, integrating also physical operations, can be used. Hydrometallurgy seems to be useful, because metals can be efficiently recuperated in chemical forms with commercial value. The economical viability of this recycling process can be improved increasing the treatment capacity, through the application to different types of residues with similar characteristics like Ni-MH and domestic batteries, or other residues containing Ni/Co, like sludges, dusts or spent catalysts. Spent Ni-Cd batteries were first physically processed using shredding and wet sieving operations. Best results were achieved using an output of 6 mm in the shredder and 1.4-2 mm in the physical separation by wet sieving, resulting a fine fraction containing 70% of the initial electrode material and only 6% of the initial scrap. The acid leaching of the obtained material in the previous operation was studied, being the parameters like: temperature, H2SO4 concentration and the liquid/solid ratio (L/S) optimized. The values attributed to the factors which concerned the best results obtained on the leaching process were mainly influenced by Ni recovery. In opposition, Co and Cd were easily leached in a wide range of conditions. To attain an overall recovery, with minimum costs, of the three metals, the values of T~100ºC, [H2SO4]=2.3-2.7 M and L/S=8-10 L/kg were considered the most appropriate.

Jan 1, 2006

By Lu Lin, Yanping Bao, Xiang Li, Linzhu Wang, Xiaobai Yan

The results showed the microinclusions were mainly Al2O3 and sulfide inclusions from tapping to the beginning of LF refining. Al2O3 inclusions were modificated into calcium aluminates after calcium treatment. Lots of spherical calcium aluminates composite inclusions containing MgO, TiO2 and MnS were found after soft blowing and during tundish metallurgy and left in the slab which caused the defects of beam plates. Pure Al2O3 inclusions were observed again after soft blowing 8min. Average sulfur content in inclusions decreased because of the high desulfurization ability of refining slag. Average Ca/Al ratio value in inclusions increased during LF refinging because of the reduction of CaO in slag by carbon and it increased obviously during the process of soft blowing 8min because of the dissolusion of calcium wire.

Jan 1, 2015

By Shengli Wu, Laixin Wang, Minyin Kou, Xinliang Liu, Weidong Zhuang, Yujue Wang

COREX process has obvious advantages in environment protection but still has some disadvantages, for example, it has a higher sulfur content of hot metal than blast furnace. In this paper, the thermodynamics and dynamics of desulfurization have been investigated to obtain the main operation parameters related to the mass fraction of sulfur in the hot metal. In addition, statistical analyses have been carried out to study the relationship between operating parameters and sulfur content of COREX hot metal based on actual plant data. It has been found that the mass fraction of sulfur in hot metal is significantly influenced by the C content in hot metal, MgO/Al2O3 in slag, the concentration of MgO in slag, the temperature of hot metal and binary basicity (R2).A linear model has been developed and subsequently used for reducing the mass fraction of sulfur in hot metal, improve the quality of hot metal and contribute to low carbon ironmaking.

Jan 1, 2016

By Pandey H. D.

The paper describes a fluidised bed ion exchange method for simultaneous removal of phenols and cyanide from the effluent. Use of an eluant enables regeneration of the resin in the continuous operation mode. The breakthrough experiments conducted both on the laboratory scale and on a pilot plant scale have shown that while the level of phenol can be brought down from 462 ppm to about 6 ppm, the free cyanide is almost totally removed. An examination of data indicates that the method can serve the twin objectives of pollution control and phenolic compounds recovery.

Jan 1, 1992

By C. Lupi

"The energy consumption of copper production by electrowinning, generally represents more than 1/4 of the total energy requirement in hydrometallurgical traditional process (roasting, leaching, purification and electrowinning). The considerable saving can be achieved just in this step that requires about 2.2 kWhlkg of the produced copper. To save energy the cell voltage, or more appropriately its anodic component, can be reduced: that is because the anodic voltage represents the main component of cell voltage and so it is largely responsible for the excessive energy consumption in copper sulphate electrowinning.In this work some ways are studied to lower the anodic voltage. First the cobalt ions were added to the sulphate solution in order to study the catalytic effect on oxygen discharge. Then lead alloys anodes (Pb-Ag, Pb-Sb-Ag and Pb-Ca) were used to promote a better oxygen evolution as a result of a different anodic surface. Their behaviour was compared with the PbSb traditional ones. Finally, as already pointed out by several authors for zinc electrowinning, ethylene glycol was employed as anodic depolariser in order to verify its effectiveness in the case of copper electrowinning. By combining all the above-mentioned ways, energy saving ranging from 20% to 27% is achieved.All the tests were carried out on a laboratory pilot-plant for long time to simulate the industrial conditions. The obtained copper deposits were observed by SEM to highlight their morphology."

Jan 1, 1997

By Mark C. Bronson

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

Jan 1, 1995

By A. V. Tarasov

Investigations of thermodynamic properties of Cu-Ni and Cu-Ni-S systems and mattes have been conducted with the aid of a MC-130 I mass-spectrometer designed for studies of processes of vapor formation of hardly volatile substances. The instrument comprised a combination of an evaporator of Knudsen chamber type with a mass-spectrometer for analysis of the vapor phase. In the process of studies of molten Cu-Ni-S systems and commercial-grade mattes within a temperature interval of 1400-1800 K the partial pressure of sulfur was measured by means of complete isothermal evaporation and the partial pressure of copper and nickel by comparison of ionic currents. The partial pressure values of the components above the molten Cu-Ni-S were used for calculation of activities of the respective components in the melt. The copper and nickel activity data obtained was used for assessing the amount of dissolved losses of these metals in autogenous smelting slags.

Jan 1, 2003

By John J. Mortvedt

Application of some by-products of the metals industry which contain plant nutrients to agricultural lands could constitute resource recovery instead of costly disposal. Some industrial by-products contain appreciable concentrations of heavy metal contaminants, such as Cd, Cr, Ni, and Pb. After land application, these metals may be absorbed by plants and enter the human food chain or be leached to groundwaters. Plant uptake of these heavy metals varies with plant species:, soil pH, soil texture, and the particular metal. Certain leafy vegetables can absorb significant amounts of heavy metals, while absorbed metals are usually poorly translocated to cereal grains. Allowable heavy metal concentrations in fertilizers now are not regulated, but EPA is considering such regulations. Heavy metal impurities in animal feed supplements are regulated by the states; so some by-products may not be permitted for this use.

Jan 1, 1992

By José Antonio, Silva Souza, Luis Alves Venancio, Emanuel Negrão Macedo, Antonio Ernandes M. Paiva

"The production of alumina from bauxite using the Bayer process generate 1.25 ton of the residue known by red mud and 460 kg of CO2 per ton of alumina.The direct use of exhaust gases from the alumina refineries to react and neutralize the bauxite residue may allow a double gain: open a wide range of new applications for bauxite residue reducing the reactivity of red mud and sequester approximately 15% or 67 kg of CO2 per ton of alumina.This paper shows the reaction of a suspension of bauxite residue-water with a simulation of the calcinator exhaust gases of the refinery. The influence of the temperature and the ratio water red mud is also analyzed.2 IntroductionThe production of millions of tons per year of alumina around the world generates around 1.25 tones of the residue known as red mud and 0.4 ton of CO2 per ton of alumina . The vast majority of the red mud is stored in large sealed lakes. Due to the high reactivity is considered dangerous and currently there is no operating process capable of reuse all the material at any refinery. These lakes after filled of solid material eventually have the surface revegetated. Otherwise will need monitoring for decades and remain as an environmental passive. The search of a industrial process that combine the reduction of the CO2 emission and the reduction the pH of the red mud opening the possibility of use in large scale in a economically viable way is the main objective of this work.The use of the exhaust gases of the refineries to neutralize the bauxite residue may allow a double gain: Open a large array of new applications for the residue with the reduction of its reactivity and sequester million of tones of CO2 plus other gases like SO2 [7] and NOx.This project main objective is to study the reaction of the CO2 with the Bayer process residue in order to obtain the basic parameters to design an equipment capable of process this reaction on a pilot scale. With this objective compositions of red mud on spray were processed with flow of gas containing CO2 at different temperatures and with concentration similar to the exhaust gases of the calcination process of the refineries. With the results, basic concepts of a pilot scale equipment were evaluated.A revision of the work already done on this type of residue were done [3, 9, 10]. Alternatives and potential barriers on chemistry and environmental fields were discussed. With the objective of industrial application the potential use of these materials were evaluated through the pH control, mass balance and x-ray diffraction."

Jan 1, 2010

By Richard W. Lawrence

Leaching of copper from sulfide minerals using biooxidation offers a potential route for copper recovery. Oxidation of . sulfide sulfur can proceed either; to sulfate or to elemental sulfur depending on mineralogy and process conditions. The advances in commercial application of biooxidation for sulfidic gold ores has made available operating and cost data which allow the derivation of conceptual costs for copper ore processing for comparison with conventional processing routes. Although costs for copper biooxidation generally remain high relative to conventional smelting, application might be competitive in specific cases. Biooxidation becomes more competitive in the general case if the cost ofS02 emissions in pyrometallurgical processing were to be internalized to a greater degree than currently required. This paper describes the technical aspects of biological processing of copper sulfide ores and concentrates, specifically with respect to the fate of sulfur. The environmental and economic implications of the biooxidation route are discussed in relation to conventional processing.

Jan 1, 1996

By Demaerel. J. P.

Arsenic plays a major role during electroreflning of copper. Both the arsenic content in the anode and the arsenic concentration of the electrolyte have, in conjunction with other impurities such as lead, antimony, bismuth and oxygen, a direct influence on the quality of the cathode. The mechanisms are currently slime. inclusion and precipitation of insoluble compounds in the bulk of the electrolyte. Arsenic has also been reported to have a depassivating effect on the anode. An influence on the anode slime adhesion has also been found. A literature survey is given and these data are compared with and completed by our own results based on lab and pilot scale experiments as well as on Olen tank.house practice.

Jan 1, 1987

By Cong Wang, Siyang Long, Pengcheng Zhang, Haibin Zuo

The present study describes central segregation of the High-carbon steel billets of 150mm square and its heredity to the following hot-rolled wire rods, whose sizes are 10mm and 6.5mm in diameter separately. The relationship between center segregation of the billets and solute element distribution of rods, the mechanical properties and microstructure of rods were studied experimentally. The results show that segregation index of C is higher than that of Mn. With the increase of central segregation, the stability of the mechanical property of the rods becomes worse. The formation of carbide network and central martensite in the rolled products can be attributed to the heredity of the as-cast central segregation. The 6.5mm-diameter-rod has higher tensile strength than that of 10mm diameter which might be due to bigger reduction ratio. Thermo Mechanical Control Process (TMCP) should be used together with Billet Centersegregation- controlling (BCSC) to improve the overall properties of rolled products effectively.

Jan 1, 2016

By Ying Mao, Zhancheng Guo, Long Ma, Huiqing Tang

"A new 2D computational fluid dynamic (CFD) model was developed for the gaseous reduction of iron ore fines in an innovative reactor-multilayer moving-fluidized bed. The solution of the proposed model was performed by integration of FLUENT and PHOENICS. Numerical results of cold state were compared with the experimental data and the agreement between them was good. A hot case-gaseous reduction of iron ore fines using syngas with this reactor was simulated using the present CFD mode. Results indicate that under the given simulation conditions, total pressure drop is 90 Pa less than that under cold state though the gas supply rate is increased about 4m3 under hot state. Gas temperature decreases from 1073 K at the bottom to 500 K at the top, Utilization efficiency of the gas reduction potential is about 27 %. For ore fines reduction, the final reduction fraction could reach 0. 70 and solid temperature 900 K.IntroductionWith the development of coal gasification technology, various coals could be converted to Syngas with air or steam. Therefore gaseous reduction of iron ore fmes becomes an acceptable alternative process for iron making besides blast furnace route[!] and moreover it still has some advantages in processing low grade iron ore fines[2]. Gaseous reduction using fluidized bed technologies is the most competitive in all direct reduction iron-making processes up to now. It has the advantage that ore fines can be directly charged to the process without prior treatment while its disadvantages are particle agglomeration and high gas/solid ratio[3]. To avoid these advantages, a new reactor, multilayer moving-fluidized bed reactor has been developed for carrying out the gaseous reduction. Hydrodynamic behaviors of gas and fines in the reactor were studied and the results were satisfying[4]. However, due to its unique structure of the multilayer moving-fluidized bed and unique gas-solid flow pattern, models of multiphase flow as IPSA, DPM and Eulerian Model could not give a satisfying solution. The current paper is developed a new CFD model and a new solution approach for simulation of the reactive gas-solid flow in the multilayer moving-fluidized bed for its optimization, design improvement and future scale-up."

Jan 1, 2013

By E. Salinas-Rodriguez, J. Hernández-Ávila, E. O. Ávila-Dávila, A. Romero-Serrano, M. Perez-Labra, G. Juárez-López

"Single phase rubidium jarosite was synthesized by precipitation from aqueous solution. X-ray diffraction and SEM-EDS analyses showed that the synthetic rubidium jarosite formed in subspherical particles with an average particle size of about 35 µm. The chemical analysis showed an approximate composition of Rbo9432Fe3(SO4)2 1245(OH)6. The decomposition behaviour of the jarosite in terms of solution pH was thermodynamically modeled using FACTSage by constructing the potential-pH diagram at 298.15 K. The E-pH diagram showed that the decomposition of jarosite leads to goethite (FeOOH) together with Rb+ and SO42- ions. The experimental decomposition of the Rb-jarosite was carried out in alkaline solutions with five different Ca(OH)2 concentrations. The decomposition process showed an ""induction period"" followed y a progressive conversion period where the Rb+ and SO42- ions formed in the aqueous solution. In contrast, calcium was incorporated in the solid residue and iron was transformed into amorphous ferrihydrite. The kinetic analysis showed that this process can be represented by the unreacted-core chemically controlled model. The reaction order with respect to Ca(OH)2 is 0.4342 and the calculated activation energy is 98.70 kJ mol-1. IntroductionJarosite type compounds are hydrous sulfate minerals containing alkalis and ferric ions, MFe3(SO4)2(OH)6, where M can be H3O+· Na+, K+, Rb+, Ag+, NH4 +, Tl+, ½ Pb2+ or ½ Hg2+. Jarosite-type compounds were formed by the natural ""in situ"" oxidation of pyritic ores leading to the replacement of the original iron sulfides and iron oxides (Dutrizac and Kaiman) [1]. The great interest in jarosites is due to its ability to eliminate or diminish the iron concentration of the acid leach solutions produced in the hydrometallurgical zinc process, with relatively low losses of divalent metals such as Zn2+, Cd2+, Cu2+ or Co . However, the losses of the metal values demand a careful study of the conditions under which the jarosite compounds are formed together with their chemical properties."

Jan 1, 2012