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By Lauri Pajunen

DSA-anodes are widely used in metal electrowinning. In zinc electrowinning the electrolyte solution contains manganese ions, and the deposition of manganese dioxide happens on the anode. This manganese dioxide layer cannot be removed without losing the active coating of the DSA-anode. The same problem can be found with hybrid anodes. In hybrid anodes mixed metal oxide coated titanium mesh is attached to a lead base material. In this study, the effect of dissolved manganese on anode behaviour is studied with three different anodes. These anodes are lead anode with 0.6% silver, hybrid anode and DSA-mesh. Methods of study include polarization, galvanostatic and potential mapping experiments.

Jan 1, 2003

By Masayuki Kudoh, Tohru Maruyama, Yohichi. Ito

When hypo-peritectic carbon steel is quenched during unidirectional solidification, the region of fine columnar grain is observed. It is classified into two coexisting phases. One is coexisting phases of liquid, delta and gamma in the upper part of the region, and the other is coexisting phases of delta and gamma in the lower part of the region. To form the coexisting part of the three phases means that solidification in this experiment proceeds in non-equilibrium state. The size of the narrow side of one fine columnar grain coincides with the arm spacing of a primary dendrite and this result is the same as the hyper-peritectic carbon steel. However, the boundary of the fine grain in the hypo-peritectic carbon steel is formed in different location from that of the hyper-peritectic carbon steel. The former is formed in the skeleton of the dendrite, while the latter is formed in the interspacing of the dendrite. The region of the fine grain changes suddenly to that of the coarse grain when the delta phase in the coexisting part of two phases disappears completely. Therefore, the delta phase in the hypo-peritectic carbon steel might prevent the growth of gamma grain. In order to recognize it, ferrite formers such as Mo, V and Ni are added in the sample. Then, the longitudinal length of the fine columnar grain extends in the sequence of the no addition, Mo, V and Nb.

Jan 1, 2000

By Oleg I. Platonov

The process for desulfurizing coke oven gas in a regenerative system ?scrubber-stripper?, with sour gas being fed to Sulfur Recovery Unit (SRU) and tail gas being recycled to raw coke gas scrubber, has been developed. A key problem of this process is the presence of elemental sulfur in the SRU off-gas, which may deposit on gas-blowing equipment, thus disrupting its operation. A new treatment technology for SRU off-gas that has been worked out for a Claus unit operated by «Russian Metallurgical Company» (RMC) in Magnitogorsk (Russia) is presented. It incorporates a catalytic hydrolysis/hydrogenation stage, where all sulfur-bearing species such as sulfur dioxide, carbonyl sulfide and elemental sulfur are converted to hydrogen sulfide. The SRU in Magnitogorsk comprises three main units: gas re-heater; catalytic hydrolysis reactor and waste gas cooler. Re-heater is required to increase temperature of the process gas up to a level of catalytic conversion (beyond 330-3500C). Oxygen utilized as an oxidizing agent reduces the volume of waste gas to a minimal possible value. The operational data garnered since 16.07.2004 clearly shows that the new technology allows high-level purification of Claus tail gas from elemental sulfur. Unlike SCOT ? process, this technology does not require separate stages for H2S removal and enrichment that tangibly simplifies its implementation at lower capital and operation expenditures.

Jan 1, 2006

By Veronica Escobar

This paper presents results from a two month pilot evaluation of EMEW® technology at CODELCO Radomiro Tomic, in Chile. A prime focus in the test programme was to assess the technology?s capabilities to recover high quality copper from the Radomiro Tomic electrowinning tank house bleed stream. The EMEW® cell developed by Electrometals Technologies Ltd. tolerates substantially higher levels of contaminants than those found in conventional tankhouse, operating at high current densities while maintaining high cathode copper quality all the way down to low copper concentrations. To maintain high copper purity in a copper electrowinning (or electro-refining) tank house, a continuous bleed of solution must be taken from the tank house inventory to prevent build-up of contaminants, and resulting degradation in cathode quality. In an SX-EW operation, this bleed stream is normally recycled back to the solvent extraction circuit, but is occasionally sent to the raffinate pond to re-enter the leach circuit. Return of the bleed stream to the solvent extraction circuit creates a continually recycling load of copper in solution, which may reduce overall plant capacity and expansion potential. Return to the leach circuit has a similar effect, and methods to reduce its impact are always under consideration. The use of the EMEW® technology allows for direct and efficient recovery of near 100% of the contained copper instead of recycling. Tests were run at ambient temperature on bleed electrolyte using current densities which varied between 250 and 1100 amps per square meter, with copper concentrations between 38 and 1 g/l. A profile of maximum allowable current density with respect to concentration was developed, showing that high grade copper can be obtained at all levels of concentrations tested, by choosing an appropriate current density and electrolyte flow rate. The results of this programme show that the recirculating bleed electrolyte from an SX-EW operation can be converted into an expansion in copper production at a comparatively low investment cost.

Jan 1, 2003

By Anita E. Lam

The thiosulfate leaching of gold generally requires the presence of a catalyst such as cupric tetraammine, Cu(NH3)42+, to obtain reasonable leaching rates and gold extractions. Unfortunately, this same catalyst that accelerates gold leaching also tends to accelerate thiosulfate oxidation to tetrathionate and other species. It is therefore imperative that a detailed understanding of the role of this catalyst and the factors affecting it is obtained. It is equally important for plant application that a method of assessing the catalyst be developed. In this work the role of the cupric tetraammine catalyst was studied using geochemical modeling for speciation prediction, thiosulfate leaching of gold ores, and chemical analyses of resulting leach solutions. It was found that the variables of pH, temperature, and the concentrations of ammonia, thiosulfate, and total copper all work in concert to affect the concentration of the cupric tetraammine species. It was also found that the presence of sufficient thiosulfate and cupric tetraammine was critical to the success of the leach.

Jan 1, 2003

The high pressure acid leach process (HPAL) is being commercially used in four plants around the world to treat limonitic laterites. The two major operating costs of the HPAL process are the sulphuric acid and the energy required to heat the pulp to the desired temperature (>240°C). As an alternative to acid injection and steam heating, the in-situ generation of sulphuric acid and heat, produced during the high temperature pressure oxidation of sulphur-bearing materials blended with laterites, has been investigated at the laboratory scale. Various sources of sulphur have been examined, in particular, elemental sulphur, pyrrhotite and a Cu-Ni low-grade bulk concentrate. Under the proper blend ratios, all sulphur sources tested generated sufficient acid to result in equivalent nickel and cobalt dissolutions. A significant improvement to the process economics can result from the addition of sulphur sources containing valuable by-products, such as nickellcobalt andlor precious metals (gold and PGMs). This is especially true in the latter case, when the HPAL can be operated under Platsol conditions (i.e. with the addition of 5-10g/L of chloride), to dissolve the base metals and precious metals simultaneously in the autoclave. Various examples of the application of this concept are presented, together with a brief discussion of its implication on the autoclave design and the downstream processes to recover the values from the leach solutions. Keywords: limonite, co-treatment, acid consumption, sulphur, sulphur compounds, pressure acid leach (HPAL, PAL), Platsol process

Jan 1, 2004

By J. A. Sekhar

Solidification processing/casting is increasingly being adopted as the preferred manufacturing technique for the fabrication of net shaped complex geometry components. Modeling of solidification processes is important both for design purposes as well as for understanding the physics of morphological evolution of the solidification microstructure. A fundamental aspect of such modeling involves the precise understanding? of heat transfer through the two phase solid/liquid region. A scheme to do this will be presented where the nonlinearity of the fraction liquid with change in temperature can be incorporated into the numerical calculations. The importance of properly accounting for the non-linear mushy zone will be discussed. Typical processes like squeeze casting and electromagnetic stirring will be discussed to illustrate how precise modeling of the solid/liquid region can aid in the calculation of accurate heat transfer coefficients for these processes.

Jan 1, 1990

By Alexander I. Raitchenko

"An electroconductive viscous liquid may flow in laminar or turbulent regime under Lorentz-force generated by the intercrossed electric current and magnetic field. When there is a starting flat layer between hard and free boundaries with surface tension the spatial Lorentz-force can create a specific stationary regime of flow: the plane free surface will transform into the wavy one, and the movement in the depth will be not laminar and not turbulent, but this regime will be characterized by organized forms with indications of ""rolling of long cylindrical drops"". Wave-length is determined by the viscosity, the density, the surface tension, the average thickness of layer, and Lorentz-force. ·The limit of wavy regime is determined by most long of wave which is directly proportional to the critical value of specific flow and inversely proportional to the kinetic viscosity. The proper critical value of Reynolds number is determined by the dimensionless combination containing surface tension, density, viscosity, and Lorentz-force. The mentioned dimensio.nless combination in our case is some criterion substituting the known Kapitsa number for case of the thin viscous liquid layers under gravity. Spreading of admixture by mechanism of wavy regime is more rapid than by common diffusion or by laminar flow. The suggested conception can be a contribution into the theoretical basis for elaboration of some specific liquid metals technologies."

Jan 1, 1999

By S. Ozbilen, B. Erdogan, M. Erdogan

To study by thermal analyses the response of precipitation hardenable alloys of Al-Cu-Mg and Al-Li-Cu-Mg system to natural and artificial ageing, a series of ternary and quaternary Al-alloys with nominal compositions of Al-l.13wt%Cu-0:65wt%Mg (alloy-I), Al-1.15wt%Cu-0.57wt%Mg-0.07wt%Li (alloy-2), Al-l.19wt%Cu-0.56wt%Mg-0.75wt%Li (alloy-3), Al-2.0lwt%Cu-0.89wt%Mg (alloy-4), Al-2.14wt%Cu"0.56wt%Mg-0.07wt%Li (alloy-5) were used in the present investigation. Samples in the form of rolled sheets are subjected to water quenching at 25EC after solution treatment at 530EC for 20 min. Alloys were aged naturally at room temperature (25EC) up to 2 months and artificially at 190EC up to 2 days. By using differential scanning calorimetry (DSC) in the temperature range of25-300EC, differential thermal analysis (DTA) in the temperature range of25-600EC together with Vicker's hardness measurements, the response to natural and artificial ageing of the alloys used in the present study were investigated. It was observed that in these alloys, GPB(Cu, Mg) zones [Guinier-Preston zones with Cu and Mg] do form during water quenching at 20EC following solutionizing heat treatment. Natural ageing of the same alloys causes formation of more GPB(Cu, Mg) zones, which results in hardening in the alloys. Artificial ageing at 190EC up to l day results in GPB zone dissolution causing preliminary decrease in hardness values while two days of artificial ageing in the alloys cause S' (Al2CuMg) precipitation confirmed by DSC/DTA analyses resulting in an increase in hardness values. Li addition up to 0.75wt% helps T1 (Al2CuLi) and T 2 (Al6CuLi3) phase formation together with S' precipitation as DSC/DTA analyses show after the same heat treatment.

Jan 1, 1998

By Ana E. Bohé, Fabiola J. Alvarez

"The separation of nickel from the aluminum present in spent catalysts and different metallic industrial residues, is proposed in the following systems: alloy Al2Ni and the mixtures 50 wt% Ni + 50 wt% Al, 10 wt% Ni + 90 wt% Al2O3 and 12 wt% NiO + 88 wt% Al2O3. The experiments were carried out in a tubular reactor with a flow of 2 l/h of gaseous chlorine and from 200 ° to 800 °C. The final products of the reaction, extracted from the hottest zones of the reactor where characterized by XRD, SEM, EDS, AA and XRF, as NiCl2 y NiCl2.6H2O while in the coldest regions AlCl3 was deposited in the first two cases and in the other there was a residue of ?, a- Al2O3, sometimes mixed with some remainder of Ni and NiO. The procedure attained different separation factors which showed the optimun conditions for the recovery of both metals. Introduction Some studies of nickel corrosion were carried out in chlorine gas at temperatures above 950ºC, and suggested that nickel is not corroded below 538ºC. [1] However, in a previous work it was shown that the chlorination allows the separation of nickel from aluminum and the formation of NiCl2 was detected from 200ºC in binary mixtures Ni-Al 50 wt%, for isothermal conditions in chlorine flux. [2] Other researchers obtained selective chlorination above 650ºC of a fly ash containing 1.4 wt% of Ni and other metals (V, Mg, Al and Fe). The Ni was separated from the Mg and NiCl2 started to vaporize at 550ºC and was after condensed in a zone of the reactor above 380ºC with 90% of purity. [3]"

Jan 1, 2008

By Alva L. Kuestermeyer

This paper presents the results of an economic analysis in the production opportunities of various co-product and minor metals in the base metals smelting 'industry. Pro forma cash flow statements were prepared for each co-product and/or minor metal analyzed utilizing US tax laws for items such as depreciation and taxes. The generated cash flows are based on anticipated revenues, estimated capital and operating costs (where applicable), and nominal production data for the respective co-products and minor metals. The economic analysis includes consideration of items such as metal payfors and bonus metals ,payments per current smelting terms. Sensitivity analysis to market prices is also ,addressed.

Jan 1, 1995

By Jakub Kaczorowski

In the production of Mn-alloys, the Boudouard reaction significantly influences the mass and energy balance. The endothermic nature of this reaction requires more energy for the process, while the direct consumption of carbon is reflected in the greater demand for carbonaceous raw materials. Therefore, it is desirable to eliminate or suppress the reaction. The kinetics of the Boudouard reaction are a function of many factors, of which coke properties and the conditions around the particles (i.e. temperature, gas composition) seem to be the most important. In the present study properties of selected single source and commercial metallurgical cokes are compared with reactivity results. The single source cokes represent a single coal that has been carbonized in a laboratory scale furnace. The commercial cokes are products of carbonization of coal blends under industrial conditions. The coke properties include proximate, ultimate and ash analysis. Also, coke petrography with carbon forms is included. The reactivity tests were performed on different particle sizes at various temperatures, gas compositions and gas flow rates. The experimental parameters were chosen to simulate the conditions in an industrial furnace. The results show that highly graphitized structure of cokes, minimal surface area and a low concentration of ash retard the reactivity. Of the other factors, the temperature and the gas composition have the greatest impact on the reactivity.

Jan 1, 2006

By Liangying Wen, Feng Xia, Chenguang Bai

"The situation of the Ti-V-Magnetite samples reduced with microwave has been investigated in laboratory. Firstly, the paper focuses on the heating behaviors of vanadium-titanium magnetite and characteristics of carbothermic reduction of V-Ti-magnetite in the microwave field. The effect of concentrate's size, quality on heating behaviors and reduction processes were researched. Results show that microwave heating may be a new heating resource replace of carbonic combustion reaction in reducing reaction. When the allocation of carbon is (16.7-30)%, carbothermic reduction of V-Ti-magnetite in the microwave field can proceed; with the increasing of carbon mixed, the metallization rate increases; and Fe, V can be reduced from their oxides in the microwave field; Titanic low oxide can be reduced from TiO2.1. IntroductionThe resource of Ti-V-Magnetite is abundant in the western area of Panzhihua in China, so far a mineral deposit of 4.64 billion tons have been proved up, it contains 14.75 million tons of V2O S which accounted for 87% of the vanadium and 5.93 hundred million tons of TiO2 accounted for 94% of the titanium resource respectively in China. The previous study proved that the major composition of mineral of the Ti-V-magnetite are Ti-magnetite, limonite, iron spinel, magnesium spinel etc, and the main elements of the Ti-V-magnetite in this area are Fe, Ti, V, Cr, Co, Ni, Ga, Sc etc[1] Due to the restrict of the BF-BOF process technical, during the smelting of the iron, the level of extracting the vanadium, titanium as well as other metal elements is limited. This results serious wasting of resources. To develop a new reduction process of Ti-V-magnetite is on the agenda, the microwave assistant reduction could meets this need, based on its characteristic of easy controlling of heating rate. To make use of the microwave energy to substitute the released heat sources of carbon combustion with air, use the solid phase state reduction at a relative lower temperature, make the beneficial element in Ti-V-magnetite transferred into the metal phase, then separated from the impurity. It is well worth to point out that once the microwave based reduction method has its industrial scale, it will take an outstanding position by its less release of carbon dioxide. This new environment-friendly process will play a vital role in the development of social industry and economy."

Jan 1, 2008

The generation of acid mine water is? due to the oxidation and weathering of sulfide bearing tailings and overburdens. Ferrite precipitation prooess has been applied to treat acid mine water. The conventional ferrite preC1pitatlon requires air oxidation at high temperature, or long aging time or addition of magnetite powder ,as promoter. In this investigation, a modified ferrite, precipitation process is developed by which magnetic ferrite can be produced at an ambient temperature. Acid mine waters from Berkeley Pit (Montana, U. S. A.) and from Noranda Tailings (Quebec, Canada) were used. The co precipitation of heavy metals from these two acid mine waters is studied as a function of FeIM molar ratio, oxidation time and settling rate under applied magnetic field. The investigation indicates that the modified ferrite co precipitation can remove substantially all of the, dissolved metal ions from acid mine water. The ferrite product obtained after precipitation' is characterized by XRD, SEM, BET and saturation magnetization. The results show that spinel ferrite, precipitation can be achieved at room temperature and the saturation magnetization of ferrite product from,acid mine water is comparable to that of pure ferrites.

Jan 1, 1995

By Garg. D.

Premixed bronze powders are widely used to produce a wide variety of P/M components including bearings and bushings by the powder metal industry. The physical and mechanical properties of sintered bronze components such as dimensions, strength, microstructural characteristics, and sintered density are well known to change with sinlering furnace design, particle size distribution in powders, green density, preheating and sinlering time" and temperature, and protective atmosphere flow rate. " However, not much is known about the effect of protective atmosphere composition on physical and mechanical properties of sintered bronze components; This paper describes effects of protective atmosphere composition and sintering temperature on physical and mechanical properties of sintered bronze components

Jan 1, 1996

By David Ellis

The next generation of Reusable Launch Vehicle (RLV) will utilize regeneratively cooled combustion chamber liners in the engines. The current design calls for using a new Cu-8 at. % Cr-4 at. % Nb (Cu-8 Cr-4 Nb) alloy for the liners. Work is ongoing to characterize the thermophysical and mechanical properties of the alloy from - 253 to 800°C, the temperature range to which the alloy will be subjected during service. The alloy has been commercially produced in quantity for NASA. The powder size has been characterized and the microstructure examined. The powder was extruded into bar using a commercial extrusion press. In addition, samples have been hot isostatically pressed (HIPed) at NASA Glenn Research Center. Both processing methods produced fully consolidated material. Transmission electron microscopy (TEM) revealed highly faulted Cr2Nb and some elemental precipitates. Cryogenic tensile testing showed the extruded specimens had significantly higher strengths than NARloy-Z (Cu-3 wt % Ag-0.5 wt % Zr) even after being subjected to a simulated braze cycle. The Young's moduli (Cu-8 Cr-4 Nb) were lower than NARloy-Z. The lower moduli is highly beneficial for reducing thermally induced stresses in rocket engine combustion chamber liners and similar applications.

Jan 1, 1999

By Jinjing Dua, Jun Zhua, Kuiren Liub, Bin Wang, Xiaolei Wua

V-Ti-Fe as hydrogen storage alloy was prepared by reducing metal oxides with a metallothermic reduction method. The deoxidation process of the V-Ti-Fe alloy was performed by electro-deoxidation and vacuum induction melting method, respectively. The results showed that the content of oxygen impurity can be controlled at about 0.2wt% after electrolyzing for 240min. Both the maximum values of hydrogen absorption capacity and the effective hydrogen desorption capacity are 2.65wt% and 1.01wt%, respectively. The deoxidization effect of vacuum induction melting process is more remarkable, with Ce as the reducing agent. It is found that Ce addition is beneficial for reducing the componential segregation, promoting the hydrogen absorption activation of V-Ti-Fe alloy. When m(Ce)/m(alloy) is up to 5%, the oxygen content has been reduced to 0.05wt% and the maximum hydrogen absorption capacity and the effective hydrogen desorption capacity are up to 3.36wt% and 1.85wt%, respectively.

Jan 1, 2015

By S. J. Kohut

Until recently SX-EW technology has only been used to produce conventional cathode for the cyclical commodity marketplace. Unlike electrorefining, SX-EW lends itself to the integration with the downstream manufacturing technologies for direct mine site production of value added products. The integration of SX-EW and downstream manufacturing results in the elimination of redundant process steps, the cost savings, and the access to value added product markets which can buffer the producer from swings in the cathode market. SX-EW production of copper powder and powder-based products has been demonstrated at the pilot plant level. The SX-EW process has been successfully redesigned to meet the more specific demands of engineered products. Challenges include the solution purity, the cell ventilation, the high current density operation and the product handling. Successful demonstration of mine site production of value added SX- EW products opens up new non-commodity marketplaces to the mining industry.

Jan 1, 1999

By Charles I. Richman

Aquispirillum magnetotacticum (AM) is gram-negative hetrotrophic bacteria that belongs to a class ,of magnetotactic bacteria that have an ecological niche in marine marches and fresh water swamp sediments. Thiobacillus Ferrooxidans (TF) is a Gram-negative, acidophillic chemoliths that may have similar chemical conditions within the cytoplasmic membrane as Aquaspirillum M. to support growth of Magnetosomes. Magnetosomes are cellular bodies that accumulate under slightly aerobic conditions. Magnetotactic motion occurs in an external magnetic field and depends on the medium viscosity. The Atomic Force Microscope equipped with a magnetic tip shows the presence of Magnetosomes in these bacteria strains. The size, shape of magnetosomes in AM and TF strains are characterized.

Jan 1, 1998

By Andre Thess, Jurij Kolesnikov, Christian Karcher

"During the motion of molten metal under external non-homogeneous magnetic field the induced electric currents produce Lorentz body forces in the opposite direction to the flow, causing deformation of velocity profile, vortical structures, and adding a pressure drop across the magnetic field. The same Lorentz force acts on the magnet system. We analyse these phenomena in metallurgy, namely, at molten metal pumping, stirring, continuous casting, and in contactless Lorentz force flowmeter (LFF). Experiments with liquid metal alloy, including direct measurements of Lorentz forces, velocities, and flow structure visualization were conducted. Based on this study the industrial prototypes of LFF systems were designed, built, and tested in a secondary aluminium production. A molten metal flow at high temperature (700°C-850°C) can be effectively measured. The LFF technique method allows measuring precisely the volumetric and mass flow rates linked with Lorentz force, and the mass accumulated within production process.IntroductionThe present work demonstrates the development of a non-contact electromagnetic system for measurement of a liquid metal flow. Our approach embodies the Lorentz force velocimetry [1-6] technique which is physically based on a measurement of the force acting on an external magnet system the field of which interacts with the flow. This force is exactly equal to the braking Lorentz force induced in a flowing conducting fluid. In what follows a measurement system based on the Lorentz force velocimetry principle. For monitoring and controlling the production process it is desirable to measure continuously the mean velocity of the liquid metal in order to deduce the mass-flux and volume-flux from it. The form and dimensions of the magnet system are in agreement with geometry of the operating channel. We consider here a version of magnet systems in a composition of permanent magnets.The LFF possesses a number of advantages which make it attractive for the measurement of flows in hot and aggressive melts. The relation between the measured force and the desired volumetric flow rate is often linear (for closed channel or at a constant liquid metal level in open channel). For the converting of the measured force into volumetric and mass flow rate we should know the calibration factor. The calibration factor is independent of the viscosity and density of the liquid metal and depends only on the magnetic field magnitude, the electrical conductivity of the liquid metal and the geometry of the channel in which the liquid metal flows. In aluminium production, for instance, there exists a number of standard alloy compositions having welldefined conductivities for which the calibration factors can thus be tabulated. We consider below consistently effects in liquid metals arising under influencing magnetic field, construction principle of LFF and measurements of metal flows at industrial conditions."

Jan 1, 2011