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By Milton Syamujulu

In 2004, KCM Nkana Smelter commissioned a 1200 tonne per day flash dryer and associated dry concentrate transport and injection system on the existing Teniente Modified converter (CT) unit. The aim was to upgrade the existing smelting unit, increase copper output and improve energy efficiency. This paper reviews the design, installation and commissioning phases of the introduction of this new technology and also discusses the initial two years of operating results for both the flash dryer and injection system at Nkana.

Jan 1, 2006

By Ivan Van Herpe

"ABSTRACT NOT AVAILABLEPresentation"

Jan 1, 2000

By F. Patisson

One of the major issues with multiparticle reactors is to handle their multiscale aspect. For modeling, it usually comes to coupling a reactor model (describing the phenomena at the macroscopic scale) with a so-called grain model (simulating the behavior of a single grain or a particle). An interesting approach proposed by H.Y. Sohn (1978) is to use the law of additive reaction times in order to calculate, approximately but analytically, the reaction rate of a particle in the reactor model. Its great advantage, compared to a numerical grain model, is to drastically reduce the computation time, particularly in the case of complex reactor models. This is the approach we retained for modeling the moving bed furnace, a counter-current gas-solid reactor used in the nuclear fuel-making route for producing uranium tetrafluoride from uranium trioxide. The numerical model we developed is 2-dimensional, steady-state and based on the finite volume method. It describes solid and gas flow, convective, conductive and radiative heat transfers, and six chemical reactions involved in the process. The law of additive reaction times is used to calculate analytically the rate of the three principal gas-solid reactions at every discrete point in the reactor. We have demonstrated the validity of this approach by comparing its results with those calculated from a numerical grain model. Also detailed in the paper are the main results of the moving bed furnace model itself and the possibilities of optimizing the process revealed by the calculations.

Jan 1, 2006

By Y. Houbaert, L. Kestens, R. Decocker

"A magneto-elastic model is presented to calculate the orientation dependence of the magnetostrictive strain, observed at saturated magnetisation in ferromagnetic materials with a cubic crystal structure and an arbitrary crystallographic texture. The formula of Becker and Doring is used to express the anisotropy of magnetostriction for a single crystal. In order to simulate the macroscopic average magnetostriction of a polycrystalline aggregate (with an arbitrary texture) the Reuss assumption of the elasticity theory was applied. According to this assumption the various orientations of the polycrystal can defonn without constraints, producing local strain incompatibilities in the microstructure but observing total stress equilibrium. The macroscopic strain is calculated as the weighted average of the individual strains of all orientations composing the polycrystal. The weight factors are determined by the volume fractions of the corresponding orientations of the given texture, which can be measured by standard X-ray diffraction techniques. The model is applied to simulate the variation of magnetostriction (at saturation) with respect to the rolling direction for a standard grade of Goss-oriented electrical steel. A brief comparison with experimental data allows validating the basic model assumptions. IntroductionBecause of tougher environmental constraints, the noise reduction in transformer cores has become increasingly important. It is generally accepted that the main source of noise is magnetostriction, which is known to be caused during the magnetisation process by the movement of 90° magnetic domain walls and the rotation of the magnetisation vector out of the easy directions. Therefore, it is obvious that when a ferromagnetic body is magnetised to saturation, the resulting magnetostriction will be dependent on the distribution of magnetic domains in the initial state.In the literature two coefficients are used to describe the resulting magnetostriction at a saturating magnetic field. The total strain, measured from an arbitrary demagnetised state to technical saturation, is called the saturation magnetostriction, and is denoted by (~)s. The tenn magnetostriction coefficient will be employed to designate the strain measured from the ideal demagnetised state (i.e. one in which no preferred orientation of domains exists) to technical saturation. Failure to recognise the difference between these two quantities has led to considerable confusion in the literature.The magnetostriction coefficient for a single crystal is a well-known property for ferromagnetic cubic materials. In 1939 Becker and Doring [1] have derived the following relation, describing the magnetostriction coefficient for single crystals with a cubic symmetry:"

Jan 1, 2001

By Jan G. H. du Preez, C. Viviers, B. J. A. M. van Brecht, H. E. Rohwer, Nicole M. Sumter

"At the basis of metal ion separation lies some particularly metal ion specific chemical property which lends itself towards exploitation. This could be in the form of an anionic complex or a neutral chelate complex. In the former a cationic centre with a particularly high affinity for the complex will have to be designed. In the latter case a stereospecific chelate ligand containing the correct symmetry and type of donor atoms will have to be designed. In both above cases the ""active centre"" can be entered in a from that it can function in different media of hydrophobicity, eg a precipitant, a resin or a solvent extractant. Recent results obtained in this laboratory will be used to illustrate how the above variables can be exploited to develop improved processes for the separation of base metal and platinum group metals.IntroductionThe separation of metal ions in hydrometallurgy can be performed broadly speaking with two major aims. Firstly the separation/removal of a certain group of metal ions, either as a means of preconcentration or as a removal from effluent as part of a purification process and, secondly the removal of a specific metal ion from an industrial stream in order to produce a specific metal in a pure form. This latter operation is by far the most difficult of the two and is becoming more so in the light of the fact that the world is moving in the direction of lower grade ores and increasing pollution. Such a process can be divided into three essential parts, firstly the molecular one in which an active centre is required to obtain specificity, secondly a matrix within which this active centre must function, i.e. as part of a resin or solvent extractant and thirdly the design of the total system to optimize the realization of the operation."

Jan 1, 1996

By Don Ibana

The use of solvent extraction (SX) in process metallurgy is particularly attractive as it is applicable to a wide range of solute concentration and pH, and it allows complete separation of chemically similar metals such as nickel and cobalt and the rare earths among others. It is therefore applicable to the processing of low grade and complex ores, which is increasing and expanding owing to the diminishing reserves of quality ores, and this has driven the increasing and expanding use of SX.The current SX technology, however, has inherent limitations owing to the use of mechanical agitation as it induces high shear mixing. Excessive shear produces very fine droplets, and while this favours mass transfer, it also leads to sluggish phase separation. High shear mixing is also known to favour crud formation. All these factors as well as high power and reagents consumptions contribute to poor process efficiency. Electrostatic solvent extraction (ESX) is similar to conventional SX except that mechanical agitation is replaced with electrostatic agitation. In direct contrast to mechanical agitation, it allows the production of very small droplets that can be made to maintain intense motion, which favours mass transfer, without affecting the phase separation. In addition, as it uses an electrostatic field, the power consumption is minimal. Hence, it promises to be a superior alternative to conventional SX mixing although an application of the technique is yet to be achieved.Our work to develop an application of the technique in process metallurgy has now established that electrostatic field has no effect on either the stability of the reagents or the chemistry of the process. A volumetric flowrate that is comparable to that of a conventional sieve plate pulse column is achievable. We have also established that electrostatic fields can be made to yield much narrower droplet size distributions than those of mechanically agitated contactors, and they allow better control of droplet motions, which include oscillation and linear motion and hence, mass transfer. These are significant advancements toward our goal and shall be discussed in this presentation.

By D. G. C. Robertson

The thermodynamics and kinetics of the reactions involved in fuming zinc from oxide slags using coal or coke were first studied in 1955 and have been the subject of many investigations since that time. The key reaction is ZnO(in slag) + CO Zn(g) + COl. This paper will review the some of the recent work, and will add new insights obtained in experiments carried out by the authors. In the first series of experiments it was shown that the reaction 2Fe2+ + ZnO = 2Fe3+ + Zn(g) or 2FeO + ZnO = Fe2O3 + Zn(g) does not occur at an appreciable rate, as is expected from thermodynamic considerations. In the second series of experiments it was shown that zinc does not fume from the slag at a significant rate unless a reductant has been added. This again is in accord with thermodynamic considerations, but is in contradiction to some of the experimental results reported in the literature. A third series of experiments was carried out with excess coke being present, so that the rate of supply of reductant was not in any way controlling the rate. The kinetics of zinc oxide reaction were then found to be independent of the zinc oxide concentration, but increased with increasing basicity, and temperature. The presence of high concentrations of FeO in the slag also improves the kinetics. At low zinc oxide concentrations iron oxide reduction occurred in parallel with zinc oxide reduction. We propose that (under the conditions of this work) the kinetics were controlled by a chemical step, namely the rate of desorption of an adsorbed CO2 species. This is the same mechanism as reported by Belton and co-workers for the kinetics of the reduction of FeO. This explains why the reduction of metal oxides in slags by hydrogen is often faster than by CO.

Jan 1, 2003

By Sang-Joon Kim, Hae-Geon Lee, Hyun-Jin Cho

"Decarburization phenomena on the surface of liquid iron have been simulated by numerical method and the results were compared to the experimental data. During the DeC process in a converter, a large amount of splashed droplets are generated from the top surface of the bath and consequently the reaction surface area is increasing tremendously. Since the decarburization mainly occurs at the interface, it is important to understand the reactions on the liquid iron droplets. The flow and species concentration fields around liquid droplets taking into account the reaction of carbon with oxygen at the interface were calculated by a commercial CFD code FLUENT which solving multiphase Navier-Stokes equation with Volume Of Fluid method, species transport equations and energy transport equation. The initial carbon concentration was fixed to 4 wt% and the concentrations of oxygen in the atmosphere were varied from 5 to 50 wt%. As comparing the numerical calculation with experimental data written in the reference, the results have a good agreement for decarburization rate.IntroductionIn a primary steelmaking process, one of the main functions is to decarburize from hot metal and the 4% of carbon is decreased to about 0.5% of carbon. Even though there are some possible reactions leading to the removal of carbon from hot metal, the main reaction occurs on the free surface by direct oxidation of carbon at the gas-liquid interface with producing the carbon monoxide gas. In many metallurgical processes involving a jet impinging onto a steel bath surface, especially in a Basic Oxygen Furnace (BOF) converter, it is important to understand the behavior of molten iron droplets splashing out of the steel. The iron droplets are generated by an oxygen or air jet blowing and it increases the total surface area of liquid iron tremendously. Since the decarburization reaction is mainly affected by the surface area, it is necessary to verify the decarburization phenomena around the splashed droplets from liquid iron in order to allow an analysis ofBOF process possible."

Jan 1, 2011

By E. Ilgar

"Deposition studies were conducted in acid copper electrolyte to determine the influence of chloride ions on cathode morphology. A statistically designed screening test was carried out in the absence and presence of 20 ppm CI- using a three factor, two level factorial design, in an electrolyte containing 36 gl'! Cu2+ and 150 gl-! H2S04, The independent variables evaluated were agitation; current density and temperature and their influence on surface roughness was determined. The copper deposited at current densities where activation was the primary control mechanism appeared similar in morphology whether stirring was used or not. The addition of 20 ppm CI- to the electrolyte gave rougher deposits under the same conditions. In the mixed control regions, considerably rougher, dendritic deposits were obtained when CI- was present. Agitation was effective in reducing the copper surface roughness both in the apparent activation and mixed control regions in the presence ofCI-. The results of this study showed that 20 ppm Cl- polarized the copper deposition at low overpotentials but caused depolarization at higher overpotentials.IntroductionChloride ion is inherently present in copper electrolyte, either as an additive or from other sources such as make up water. The behavior of the chloride ion is well documented in electrorefining operations, but its role in copper winning is less obvious. However in both cases there is evidence that cathode growth and solution chemistry are strongly influenced by its presence. The mechanism and electrochemical action of the Cl"" have been shown to be very complex, therefore a better understanding of its influence on electrocrystallization is essential for improved cathode deposit growth control. It was proposed that Cl"" polarizes the copper deposition reaction at low concentrations due to CuCI formation but depolarization occurs at higher concentrations due to the formation of a soluble CuCI2"" complex [1,2]. Franklin [3] reviewed the mechanism of additives in the electrodeposition process and proposed that the Cl"" complexed with copper, adsorbed on the cathode as an induced anion leading to an increase in the reduction rate. At cathodic overpotentials less than 100 mY, lppm NaCl had a polarizing effect, i.e. an increase in impedance of the charge transfer step. At higher Cl"" concentrations up to 100 ppm, depolarization occurred as evidenced by a decrease in impedance, which was attributed to soluble cuprous complexes [4]."

Jan 1, 1997

By Angus Hellawell

The application of the common tangent principle to free energy - composition surfaces is considered. It is shown that the construction requires that single phase surfaces on either side of a two phase volume must always exhibit the same sign of curvature - contrary to that shown in many published phase diagrams. In general, these curvatures will be such that the surfaces are mutually concave towards the more stable phase. A number of examples are discussed.

Jan 1, 1991

By Micheal McCarter, Biswadeep Saha, Meenakshisundaram Ramanathan, Chai Ren, Sivaraman Guruswamy

"Three-point bend test was used to study the effect of electrochemically charged hydrogen and magnetic field on the embrittlement behavior of AISI 4340 steel in this work. Acoustic emission signals were collected during the test and analyzed to gain an understanding of the crack growth process. Cathodic hydrogen charging in AISI 4340 steel resulted in drastic reduction of ductility and strength. Hydrogen embrittlement was characterized by a change in fracture surface from dimpled ductile surface to quasi cleavage type fracture. No significant effect was observed in the presence of magnetic field. The acoustic emission signals collected during the test provided an indication of the extent of energy released during the crack growth process.*Support of this work by NSF through the award DMR-0854166 is gratefully acknowledgedIntroductionGrowing interest in hydrogen as a clean fuel and use of steel and other iron based alloys for storage and transport of hydrogen has led to extensive study of the influence of hydrogen on the mechanical properties of these alloys. Hydrogen interaction with materials may result in degradation of mechanical properties. Embrittlement, either ductile or brittle, can be described as a condition which decreases the toughness of the material or increases the ease of crack growth. Hydrogen present even in few parts per million is sufficient to embrittle steels at room temperature [1]. In most cases, hydrogen exposure is through an electrochemical process in aqueous corroding environments. In such cases, they are prone to be exposed simultaneously to electrically induced magnetic fields, which are also believed to affect the hydrogen embrittlement susceptibility of these alloys. So it is also important to study the effect of magnetic field on the hydrogen embrittlement susceptibility. Hydrogen solubility by electrochemical process in aqueous solution is proportional to square root of current density for iron. [2,3]"

Jan 1, 2012

By P. M. Swash

The determination of the heavy minerals in beach sand samples is highly dependent on the preparation technique used. In this paper a simple reproducible method for the quantification of "recoverable" ilmenite, zircon, rutile and leucoxene by magnetic separation, is described. The procedure recommended yields information relevant to the metallurgical processing of the ore rather than to the total heavy minerals present in the samples. Finally the determination of mineral reserve estimations and grade assessments is greatly facilitated when this "mineral assay" method is employed. An assortment of other mineralogical methods are described including SEM, EMPA, XRD, XRF, Image analysis, Mossbauer. clerici and perm roll separations. The methods are briefly examined and the practical information that can be gained by using such techniques are reviewed. Experience has shown that an understanding of the relationship between the physical and chemical properties of the heavy minerals can contribute to the prediction of mineral particle behaviour. Such information may ultimately help reduce the prospect evaluation period and minimise expenditure on metallurgical testwork.

Jan 1, 1991

By G. Diáz

The PLACID process applied to the recycling of spent lead-acid batteries is being developed by an European Consortium within the Brite-Euram II programme. The status of the project entitled "Lead Recovery from Lead Oxide Secondaries" is described in this paper. The main laboratory and batch experimental results and the preliminary feasibility study are summarised. The description of the demonstration pilot plant and continuous campaigns programme for 1995 are also included. An interesting global approach is proposed, integrating the Placid process in the existing spent battery recycling pyrometallurgical facilities. This yields important improvements in the overall process. Grids would be easily treated by the conventional pyrometallurgical route, obtaining lead alloys,, while battery pastes, slags and fumes would be fed to the Placid process, obtaining pure electrolytic lead (>99.99 %), ideal for battery paste manufacturing. The implementation of the Placid process into the existing battery recycling pyrometallurgical facilities is analyzed from technical, environmental and economical viewpoints. Greater overall lead recovery, lower operating costs, reduced waste production, environmentally safer residues and much better lead product quality are the key advantages. The authors draw the following final conclusion : Integration of the Placid process with conventional pyrometallurgical treatment is a feasible and very attractive alternative route for spent lead-acid battery recycling.

Jan 1, 1995

By M. A. Vera

This paper proposes a simple two-parameter model for the typical inverse relationship between recovery and flotation concentrate grade. The model is based on the mineralogical limitations imposed by the material properties. One parameter (R*) describes the proportion of metal content which is floatable, and the other (b) is the rate at which the fastest floating particles are being contaminated by the other less valuable particles present in the mineral system. One significant feature of the recovery-grade curve is that initial recovery (i. e. R ? 0) is at the purest attainable mineral grade, (but as recovery rises the cumulative grade of the concentrate tends to the feed grade. The ideal recovery-grade curve for a particular mineralogical system can be obtained by release analysis: the release analysis curve determines the maximum or limiting separation efficiency. The model proposed in this work is similar to the linear recovery - cut-off grade model of Dell (1), but has the advantage of describing the whole curve.

Jan 1, 1999

By Germán Richter a

To comply with the chilean air quality regulation requirements, the Hernan Videla Lira Smelter which is a custom smelter having to cope with a wide variety of concentrates, has developed a two-step modernization plan. The main steps are: - A second acid plant of 80,000 Nm3/hr to be operating at the end of 1996. This will increase the sulphur capture from 43% to 701/o in association with the replacement of the Hoboken converter by a second PS-converter to reduce the operation problems resulting from the treating of high garde matte. - Oxygen enrichment, is going to be incorporated in 1998 in the Teniente Converter and PS-converters in association with tuyere injection of dry concentrates, increasing the sulphur capture to 90 - 93% of sulphur inputs. By this program, sulphur emissions will be decreased from 40,000 tpy today to less than 8,000 tpy and in this way to carry out the environmental regulations.

Jan 1, 1996

By Kosei Morita, Osamu Nakano, Katsuhiko Nagai, Kazuhiro Mori

"The Sumitomo Toyo Smelter and Refinery commenced its operation in 1971 with three Peirce- Smith (PS) converters. “2 hot – 1 blowing” operation was practiced, that is one of two available converters was blowing and the other was standby in a hot state while the third converter was under repair. After several improvements, the stack time ratio reached around 90%; and processing 5 batches a day became possible.As a result of the expansion program of the Toyo smelter and refinery that started in 2001, the converter operation pattern was shifted from “2 hot – 1 blowing” to “2 hot – 2 blowing” with the installation of second converter blowers and an additional ladle crane.In 2005 a, the fourth converter was installed and “3 hot – 2 blowing” operation began. Also, with improvements experienced in the anode furnaces and the anode-casting wheel operation, today, the number of cycles has been increased up to more than 8.5 a day.The treatment techniques of fugitive gas containing sulfur dioxide from converter furnaces have been gradually reinforced, and the fixation rate of treated sulfur is currently being maintained at more than 99.9%. This paper introduces the operations described above, and the improvements in environmental management techniques for the Toyo PS converter operation."

Jan 1, 2009

By M. Tomita

One of the most essential factors for a custom smelter to strengthen its competitive power is to Improve its comparative standing in purchase of concentrates from the world market. It is especially critical for Japanese smelters who depend almost 90% of their raw materials on import. In order to accomplish this breakthrough, the development of the new technology which enables us to treat concentrates containing higher Impurities is inevitable. Nippon Mining Company Ltd. made an intensive research on processing complex ore for three years from 1979, and successfully developed an original hydrometallurgical process to treat converter dust for eliminating impurities from the copper smelting circuit. The commercial plant was constructed at the Saganoseki Smelter & Refinery in 1982, and its nine years operation has been satisfactorily proven the advantages of the technology. The concept of this process and its operational performance are discussed.

Jan 1, 1992

By Damien Wagner

To reduce the emission of greenhouse gases by the steel industry, particularly for ironmaking, the production of DRI (Direct Reduced Iron) using hydrogen as the reducing gas instead of carbon monoxide is being considered. In this context, the reduction of pure hematite by hydrogen was studied at the laboratory scale, varying the experimental conditions and observing the rate and the course of the reaction. All the reduction experiments were performed in a thermobalance and supplementary characterization methods were used like scanning and transmission electron microscopy, X-ray diffraction, and Mössbauer spectrometry. The influence of rising temperature in the range 550-900°C is to accelerate the reaction; no slowing down was observed, contrary to some literature conclusions. A series of experiments consisted in interrupting the runs before complete conversion, thus enabling the characterization of partially reduced samples. Interpretation confirms the occurrence of three successive and rather separate reduction steps, through magnetite and wustite to iron, and illustrates a clear structural evolution of the samples. Finally, the influence of the sample type was revealed comparing a regular powder, a nanopowder and a sintered sample. The regular powder proved to be the most reactive despite its larger grain size, due to a more porous final structure.

Jan 1, 2006

By Gunther Klamp

Disposal of arsenic compounds from washing acid in metallurgical plants is becoming a severe problem when using lime neutralization. A further problem is the disposal of relatively large quantities of gypsum which is produced during this neutralization step and which Is also conta-minated with other toxic metal compounds. The Sachtleben-Lurgi process removes arsenic and other metals from washing acid in the form of insoluble sulphides. The purified acid contains less than 0.5 ppm of arsenic and can be used for standard sulphuric acid applications. The process Is demonstrated commercially at Sachtleben's acid plant since more than five years.

Jan 1, 1992

By M. A. Gerdel

In carboxylate collector flotation of bastnasite from other semisoluble salt type minerals such as barite various modifiers must be added in order to achieve selective flotation. One such modifier is a lignin sulfonate. It may function in part by acting as a sequestrant for metal ions present, preventing autoactivation in the system by metal ions derived from the minerals themselves. It also functions as a depressant for both bastnasite and barite, chemisorbing on both. However, it is shown that the lignin sulfonate functions as a much stronger depressant for barite than for bastnasite. It is suggested that the; strong depressing action on barite is related to a good fit of the sulfonate into the barite structure.

Jan 1, 1989