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By Seshadri Seetharuman

The present paper summarises a series of measurements of the interaction parameter of oxygen in liquid copper with respect to a third element, e(M)o, where M is Mn, Zn, As, Se or Te which are common impurities in the liquid metal. The technique employed was the solid electrolyte galvanic cell method. The cell used may be represented as Pt, W or cermet / Cu-O-M // ZrO2 - CaO // AO, A /PT where AO/A represents a suitable oxide/metal reference. The measurements indicate that Mn and Zn interact very strongly with oxygen in liquid copper while, in the case of arsenic the interaction parameter is nearly zero. The behaviour of the elements Se and Te is unique with respect to oxygen interactions in copper bath. At oxygen levels, xo= 10-4 ? 10-5, the apparent interaction parameters are negative, comparable to that for sulphur. On the other hand, at lower oxygen levels, the results indicate that the interaction parameter values are positive. The results are discussed in the light of some of the theoretical models for solute interactions in liquid metals.

Jan 1, 1993

By Ann M. Hagni

The mineralogical, chemical, microtextural, and particle size character of electric arc furnace (EAF) dusts are being studied by reflected light microscopy, scanning electron microscope-energy dispersive spectroscopic analysis (SEM-EDS) and electron probe microanalysis (EPMA). The dusts consist predominantly of metallic iron, iron oxide, and calcium-iron-manganese silicate phases, together with smaller amounts of iron-manganese-zinc-calcium, iron-calcium-zinc-manganese, and calcium-iron-manganese silicates. The samples vary in their zinc contents. Chlorine occurs in phases containing iron, lead, zinc, manganese, and calcium. The dust particles range greatly in size from 1 to more than 300 ~m, but most particles are about 1 to 6 ~m. Larger particles. about 20-50 um across. also are present. They are predominantly spherical in shape, but some are cenospheres, and others are more angular particles, some of which are broken spheres and cenospheres. Their internal microtextures exhibit evidence of liquid immiscibility, exsolution, skeletal crystal growth, and oxidation react i on rims. Because EAF dusts have been classified by EPA as hazardous wastes, there is heightened interest in the treatment of these dusts to render them non-hazardous. The mineralogy of products of pyrometallurgical treatment of EAF dusts by flash furnace and pyrohydrolysis are currently under study.

Jan 1, 1991

By Mingsheng He, Yunhui Tang

The structure and granularity of biological origin aragonite from abalone shell during wet grinding in a ball mill were studied with X-ray diffractometer, with morphology studied by scanning electron microscope (SEM). It is shown from the results that the particle sizes of aragonite decreased with grinding time, so did the X-ray diffraction (XRD) peak intensities, while the full widths at half maximum increased. A calcite XRD peak with low intensity and great width was observed in nearly all the samples with various grinding time, whereas the intensity of the peak increased obviously after grinding time 300 min. It is shown from the SEM results that the size of aragonite dropped with grinding time until it reached 20 nm and then kept constant, while that of calcite dropped first and then rose at the minimum about 10 nm until to the constant size as in aragonite. It was observed that the mineral content obtained from XRD show an obviously change that the calcite increases while aragonite decreases, which indicated the occurring of a polymorphic transformation of aragonite into calcite.

Mar 1, 2017

By D. C. Cupertino

Oxime based solvent extraction provides the user with a selective concentration process for copper prior to electrowinning. The selectivity required is largely for copper(II) over iron(III) and this is achieved by the preferential formation of the square planar copper-oxime complex in the organic phase. The copper/iron selectivity of oximes can however, be altered by modifiers or other types of oximes and may be enhanced in the presence of certain esters. Whilst the oxime based SX processes is important for operations leaching copper from laterite ores, the high selectivity will also be significant in processing streams arising from other leaching regimes which are currently under development, for example leaching of sulfide mineral ores. This paper presents some initial results using Molecular Modelling techniques to further our understanding of the nature of the copper/iron-oxime complexation processes together with some plant studies undertaken at a number of different mine sites investigating selectivity, and other properties, for some modified reagents. Some studies of the interfacial properties of the these systems are reported to explain in part the practical observations.

Jan 1, 1999

By Y. Takasaki

For zinc hydrometallurgical extraction, reducing the electric power consumption of the electrowinning process is an important issue for energy savings. At the Zinc & Lead 2000 symposium, the authors suggested that by using the Pb-0.5%Ag-0.6%Ca alloy, the electrolysis energy can be decreased compared to the conventional Pb-0.9%Ag alloy. In this study, the corrosion behaviors of the Pb-Ag-Ca electrode in a sulfuric-acid electrolyte were investigated. Based on the results Or me Pb-0.5%Ag-0.6%Ca anode after 20 days of electrolysis, the bath voltage and the quantity of anode slime decreased compared to the Pb-I%Ag anode. Subsequently, beta-PbO2 on the electrode surface was detected by XRD and its peaks were sharper than the Pb-1 %Ag anode. Moreover, a dense beta-PbO2 layer on the 0.6%Ca a anode surface was observed. Therefore, it was suggested that the dense beta-PbO2 layer on the anode surface is one of the factors that leads to a lower bath voltage and decreasing quantity of anode slime.

Jan 1, 2003

By F. G. Caballero, J. L. Gonzalez-Carrasco, S. Barrius, H. Carreon, M. Lieblich

"The grit blasting is a low-cost technique successfully used to enhance mechanical fixation of the implants through increasing their roughness. As a result of the severe plastic surface deformation, it produces subsurface effects such as grain refinement, hardening and compressive residual stresses which are generally evaluated with destructive techniques. In this research work, non-contacting and contacting thermoelectric power measurements are performed in blasted 316L VM and Ti-6AI-4V specimens using Ah03 and Zr02 particles which yield a coarse and a fine rough surface, respectively. This study correlates the microstructural changes induced by the grit blasting treatment and the limitations and advantages of each of the nondestructive thermoelectric techniques based on the Seebeck effect used to evaluate these biomaterials.IntroductionIt is well known that surface properties play an important role in metallic materials used in bio-medical applications. Since the biological response is correlated directly with surface properties it is comprehensible the intense activity in superficial modification by physics or chemistry methods in this field. Grit blasting, one of the most popular surface modification of metallic biomaterials, enhances the mechanical fixation of the implant through the increase in roughness [1-3]. Roughening is developed by bombarding the surface with a high-velocity jet of ceramic particles, being the final roughness a function of the processing parameters (pressure, distance, time, ... ) and blasting particles (nature, shape, size). As the plastically deformed surface layer tries to expand relatively to the intact interior of the specimen, residual compressive stress gradients develops perpendicular to the surface at shallow depths with a maximum value at a depth in the range of 5 to 60 µm. This surface treatment also may cause subtle variations in the subsurface material properties, such as increased hardness and grain size refinement, which are consequences of the significant plastic deformation through cold work. Blasted affected zones may extend to a depth of up to about 200 µm. The subsurface hardening and the near-surface compressive stress gradient playa beneficial role by retarding fatigue crack nucleation and further growth, ultimately extending the fatigue life of the metallic part [4]. In this work, two non-destructive thermoelectric techniques (NDTT), the non-contacting and contacting thermoelectric power measurements were used to analyze the subsurface induced changes on blasted Ti-6AI-4V and 316L VM specimens using Al2O3 and Zr02 particles. Detailed information on the microstructural induced effects and subsurface mechanical properties were published elsewhere [5-8]. Here the nondestructive evaluation of the involved microstructural changes is used to assess the global subsurface damage. Advantages of using nondestructive techniques during manufacturing are envisaged."

Jan 1, 2012

By Luciano B. Oliveira, Alexandre M. Stumbo, Luis G. C. Marques, Valdo S. Marques, Sergio N. Monteiro

"Similar to the ethanol program, initiated more than 30 years ago, the recently created biodiesel program in Brazil is expected to rely on private initiative based on agribusiness for vegetable oil production. Campos dos Goytacazes is a large county in the northern of the state of Rio de Janeiro with land still available for oily vegetables plantation in addition to the land traditionally occupied by sugar cane plantation, which is used to produce ethanol. In order to extend the biodiesel program to Campos dos Goytacazes, the State University of Northern Rio de Janeiro (UENF) is conducting a technical project for the development of the infrastructure for biodiesel production. In this work, the infrastructure based on versatile equipment for biodiesel esterification built in the Center for Alternative Energy of the UENF is presented.IntroductionBiofuels are gaining worldwide attention as a possible economical solution for the prediction of declining reserves of petroleum and related increase in price of barrel. However, nowadays, a more relevant question is the climate changes caused by burning fossil fuels. This is especially the case of coal and petroleum based fuels, mainly gasoline and diesel that propel the majority of vehicles and generate a large amount of CO2 emissions responsible for global warming. This combination of economical an environmental problems is already providing a strong motivation to substitute conventional fossil fuels by renewable biofuels. More than just the interest of the market financial forces, government legislation is imposing a new order that obliges the use of biofuel. Many countries including the USA, the European Community, Japan and Brazil are committed to gradually substitute biofuels into their fleet of vehicles."

Jan 1, 2008

By Omid Marzoughi

Chromium has a wide range of applications, including as an alloy addition in various steels and also as a corrosion resistance coating. Carbothermal reduction of chromite ore (FeCr2O4) in a submerged arc furnace is an important industrial process for extracting chromium, but the energy consumption is excessive. It is suggested that one area for future research is the low temperature carbothermic solid state reduction of chromite to produce an intermediate product, which can subsequently be upgraded to ferrochromium. In this regard, a thermodynamic model has been developed to investigate this process and the effects of temperature, carbon additions and ore composition on the recovery of chromium and the grade of the ferrochromium, have been studied. Further development of the model may allow it to be applied to the simulation of other processes for the recovery of chromium from chromite ores.

By Takashi Nagai, Hideaki Sasaki, Masafumi Maeda

"The production of solar cells is increasing dramatically and the shortage of polycrystalline silicon for these cells has become a serious problem, making development of a low-cost production process for solar grade silicon essential. An electron beam melting technique is known to be effective for the removal of phosphorus from molten silicon. Although the phosphorus is removed by preferential evaporation in this process, the rate of removal is not sufficient, and its improvement requires thermodynamic information on phosphorus in the molten silicon. In this research, the vapor pressure of phosphorus in equilibrium with a siliconphosphorus alloy was measured by double Knudsen cell mass spectrometry with a system blowing gas into the Knudsen cell. The activity of phosphorus in silicon, the Gibbs energy change of the dissolution of phosphorus in silicon, and other factors were estimated from the results. Using these data, we provided guidelines on how this process can be improved.IntroductionSolar energy is in great demand since it is inexhaustible and cleaner than that from conventional energy resources. Silicon is the material most widely used to convert solar energy into electricity. Figure 1 shows the recent production of solar cells. High purity silicon for solar cells, namely solar grade silicon (SOG-Si), has been commercially supplied mainly from off-grade high purity silicon in the semiconductor industry. However, production of solar cells has increased rapidly in recent years, and the shortage of SOG-Si has become a serious problem, so that a new processes which can produce SOG-Si economically are required.Directional solidification was applied to remove transition metal elements such as Fe or Ti by segregating them from the remaining melt. However, such solidification is useless for phosphorus because the segregation coefficient of phosphorus is nearly unity. Numerous approaches have been made in an attempt to produce a resource of low cost SOG-Si from metallurgical-grade silicon (MG-Si). [1,2]"

Jan 1, 2012

By Edgar Blanco

A thermodynamic and experimental investigation to develop a new process for converting molybdenite concentrate to molybdenum dioxide by a water-vapor oxidation process was carried out. In addition, the behavior of rhenium and selenium in molybdenum concentrate during the process was investigated. The kinetics of the reaction were determined by measuring the weight change of a sample with time in water vapor at temperatures between 700-1000°C. The results were analyzed by a Shrinking Unreacted Core model under chemical reaction control, which showed an activation energy value of 102 kJ/mol. To determine the behavior of rhenium and selenium, their concentrations in the molybdenum sulfide and the product molybdenum dioxide were measured by the use of ICP. While most rhenium remained with the molybdenum dioxide after the water vapor oxidation, almost all selenium volatilized. These results agree with thermodynamic analysis.

Jan 1, 2006

Bath smelting options for recovering valuable metals from jarositic residues containing 22-28% lead and 16-30% sulphur obtained from pressure leaching zinc-lead-copper bulk concentrates were investigated using thermochemical computations and crucible-scale experiments. Direct fuming of lead and zinc from a slaglmatte bath at 1250-300°C was demonstrated successfully. Up to 93% of the lead was recovered in the fume and steady-state recoveries of zinc were predicted in the range 82-95% under these conditions. The energy required for the fuming reactions was supplied by partial combustion of the fuel, added as char, with air. An important feature of the process is that the recoveries to the fume are not significantly affected by changing: the fuel:air ratio over a wide range. Thermodynamic computations, confirmed by experimental results also showed that the presence of a matte phase is not essential for high recovery of lead and zinc to the fume. Operating conditions which produced a matte ensured that about 70% of the silver and 80-90% of the copper were recovered into that phase. Approximately 98% of the arsenic in the residue was fumed. In the absence of matte the slags contained high arsenic levels (260-330 ppm) but low arsenic (20-60 ppm) levels were achieved when matte was produced.

Jan 1, 1994

By Victoria Vaccarezza, Corby Anderson

Due to the demand for rare earth elements for everyday technology and applications, there has been much research initiation into the extraction and recovery of rare earth elements. An otherwise unknown mineral, eudialyte is a zircon silicate consisting of rare earth oxides, specifically the heavy REO yttrium (III), with only trace amounts of thorium and uranium. The first part of this project aimed at finding an efficient way to liberate and upgrade eudialyte to concentrate the REO content. A combination of gravity and magnetic separation techniques were employed, resulting in limited success. The second part looked at the hydrometallurgical processing of eudialyte through various leaching experiments with sulfuric acid. In all, this project will discuss why certain processes were utilized over others, as well as the difficulties that arose during processing.

Mar 1, 2018

By Ramana G. Reddy

In the past, many lead-containing slags and wastes were stored in piles or landfills. However, shortages of landfill space as well as increased public, concern about the toxic nature of disposing lead containing industrial wastes in landfills have led to review of disposal methods. Several lead wastes are processed to provide commercial products. They are used on-site in land reclamation projects. or are processed and sold as a by-product. These by-products contain nutrient elements needed for plants or animals and also may contain heavy? metal contaminants such as As, Cr. Cu, Zn and Ph. Use of such by-products containing unacceptable levels of these contaminants could cause plant and animal toxicity. In this paper. role of viscosity in conversion of lead slag wastes into commercial products containing ,low content of lead and other, heavy metals is presented. Effects of slag viscosity on the velocity of movement of metal' and matte prills through themolten slag layer in the melting furnace is discussed. Current and emerging slag cleaning technology, foamed, granulated and pelletized slag technologies are reviewed.

Jan 1, 1995

By Michael Stelter

Lead alloys are a typical material for anodes in technical electrowinning processes. The life time of those anodes differs from 2 years to more than 5 years in tankhouse practice depending on the type of alloy, the mechanical damaging and last but not least the chemical corrosion in the electrolyte. Different types of alloys, such as PbSb, PbCa, PbAg, PbSnCa or PbAgCa have been developed and used in the past, their rate of corrosion being more or less a philosophic discussion. Comparable investigations on the corrosion behavior in dependence of the concentrations of alloying metals, the grain structure and the mechanical and thermal treatment during production have not been conducted before. In the last years the Institute for Nonferrous Metallurgy and Purest Materials of the TU Bergakademie Freiberg investigated the corrosion behavior of the typical lead alloys for metal electrowinning under comparable conditions. Correlations between different alloys, mechanical treatments like rolling or thermal treatment like annealing to the rate of corrosion were made, leading to the conclusion that grain structure and grain size are of eminent importance for the rate of corrosion in technical electrolytes. From these results new and optimized lead alloy anodes can be produced with an increase in life time of the factor 3 ? 5. The optimized lifetime in terms of corrosion stability can not protect from mechanical damaging in tankhouse practice, but with a careful practice the increase in lifetime can save a lot of money and problems.

Jan 1, 2006

By T. T. Chen

The manganese oxide scales, consisting mainly of MnO2, characteristically occur in banded colloform structures which adhere to porous layers of PbSO4 and PbO2 that oxidized from the rolled Pb-0.7% Ag anodes. Hydrous Mn oxides, Mn3O4 and amorphous Mn oxides are believed to be also present. Tiny particles of gypsum, PbSO4, SrSO4 and AgCl are entrapped in the colloform masses. The gypsum originated from the Zn electrolyte; strontium carbonate was added to the ZnSO4 solution to control Pb, and silver originated from the anodes. Some of the colloform bands contain minor amounts of Pb, implying a limited degree of dissolution of the Pb during electrolysis. Other colloform bands incorporate trace amounts of Zn. Colloform structures permeated with silica gel are presumably caused by the high silica content of the electrolyte.

Jan 1, 2009

By Yahui Feng, Zhiwen Wu, Chen Chen, Xin Hong

Large amounts of copper slag containing about 40 wt% iron is generated during the process of producing copper. Recovery of iron from the copper slag is very essential not only for recycling the valuable metals and mineral resources but also for protecting the environment. The purpose of this study was to investigate the possibility of separating fayalite by oxidation-reduction process into Magnetite and silicate phases in intermediate temperature condition. Experimental results show that when the oxidation reaction at 1000℃ for 120min and the oxygen flow is 0.1L/min, most fayalite decompose to hematite, less part of magnetite and silica. And then, the mixture of carbon and oxidation product is pressed into blocks and reduced to magnetite and silica at 900℃ for 90min. A magnetic product containing about 57.9wt% iron was obtained from the magnetic separation under a magnetic field strength of 100 mT.

Jan 1, 2015

By Jewel Gomes

Green rust is an important intermediate in oxidative transformation of Fe(II) phase. This unstable compound contains a mixture of ferrous and ferric hydroxides that belong to a family of minerals known as layered double hydroxides (LDH). Its general formula is [FeII(6-x) FeIIIx (OH)12]x+[Ax/n-*yH2O] x-, where A is an n-valent anion mainly Cl-, CO3-2 and SO4-2, and in which either the bivalent or the trivalent iron can be replaced for other trivalent or bivalent metal ions. It was first identified as corrosion product, later in soils as a product of interactions between microbes and metals in soils. Due to its high reactivity, it is used in the reduction of organic and inorganic compounds, As removal, and the treatment of acid mine drainage. In this paper, we described the method of electrochemical generation of green rust, its characterization by XRD, SEM and FT-IR, and its implications to electrocoagulation.

Jan 1, 2009

By W. Persson

The first installation at a copper smelter of a Semtech OPC System for continuous, on-line production control of copper converting in PS converters took place in 1994. At present OPC systems are installed at 19 PS converters. The technology presents to the operator real-time information on the progress of the process he is controlling in the form of optical process parameters, thus facilitating dynamic process control. The optical process parameters are based on time- and wavelength resolved registrations of the light emitted by the off-gas flames and identification of correlation between these parameters and characteristic metallurgical process data. The present paper provides a description of the technology as seen by the furnace operators and a summary of operating experiences made during five years of full-scale, operation at various smelters, reviews influences from the technology on smelter operational practises and comments on recent developments as regards new applications of the technology.

Jan 1, 1999

By John Petersen

Heap bioleaching technology has become well established for the exploitation of copper sulfide ores. Still, in many operations the rate of copper extraction is rather slow, often taking two years or more to recover 80% of the copper. Chalcocite, the most common secondary copper sulfide, leaches by a two-stage mechanism. The first stage is rapid, whereas the second stage has a high activation energy and proceeds slowly at ambient temperatures. Nonetheless, this rate is still considerably faster than what is typically realized in a full-scale heap. A comprehensive column bioleaching study of a chalcocite ore has shown that the chalcocite columns are leached in a zone-wise fashion. The first zone corresponds to the first stage of chalcocite leaching, where all ferric produced by the bacteria is immediately consumed and all acid entering with the feed solution is consumed within a relatively narrow band. The second stage of chalcocite leaching proceeds much more slowly in the wake of the first stage, within a zone that grows gradually over the entire length of the column. The overall rate of leaching is thus determined by the rate of acid supply into the column rather than by mineral or bacterial kinetics, at least until the entire column is engaged in second-stage chalcocite leaching. In full scale heaps, there is evidence to suggest that solution distribution favours channelling between relatively large clusters of material which are exposed only to stagnant solution. Reagents have to migrate into such clusters by diffusion, which retards the delivery of acid dramatically. Thus, we believe that the rate of chalcocite oxidation in heaps is governed by sideways diffusion rather than downward migration. Column experimental results have been reproduced with a comprehensive heap-modelling tool. The model predicts that by simply changing the length of the average diffusion channel from column conditions (a few cm) to heap conditions (tens of cm), extraction times can change from weeks to years under otherwise identical conditions.

Jan 1, 2003

By Katsutoshi Inoue, Shafiq Alam

Several novel types of chemically modified chitosan were prepared by immobilizing functional groups of EDTA and DTPA onto polymer matrices of chitosan in order to investigate their potential for mutual adsorptive separation among rare earths. Following the batch wise adsorption tests to elucidate their basic adsorption characteristics for rare earths, mutual separation was carried out using a column packed with the chemically modified chitosan. The separation between Sm(III) and Y(III) was tested using a column packed with EDTA-type chitosan while mutual separation among 4 light rare earths, La(III), Ce(III), Pr(III) and Nd(III) was tested using a column packed with DTPA-type chitosan. In both cases, satisfactory mutual separation was achieved by the chromatographic operation using these chemically modified chitosan.

Jan 1, 2014