Search Documents

By Chengxian Lui

Detailed mineralogical and metallurgical investigations were carried out on a phosphorous-bearing manganese carbonate ore from the Huayuan manganese mine, Hunan, China. Microprobe analyses indicate that the Manganese occurs mainly in calc-rhodochrosite and in rhodochrosite. The cOll'pOsitional range of these manganese carbonate minerals is 50 -80 % MnOJ3, 0 -35 % CaOJ3, 5-35 % MgC03 and 0 -15 F~. The manganese carbonate minerals are very fine grained, IOOSt are between 4.6 and 9.4 1m in diameter. The small grains are clustered into aggregates that form bands 0.5 to 10 rnn wide. The phosphorous-bearing mineral in the ore is fluorapatite and is in grains that are generally smaller than 6 1m in diameter. Metallurgical tests show that it is possible to concentrate the aggregates of manganese carbonate minerals by high intensity magnetic separation, and to reduce the phosphorous content by rpasting the concentrate to convert the manganese carl::x>nates to insoluble hausmannite, and then leaching the roast product with HCI to dissolve the fluorapatite.

Jan 1, 1989

By Tapio Ahokainen

Commercial modeling software and increasingly efficient computers enable today computational fluid dynamics (CFD) to be used as a tool for a more comprehensive understanding of the flash smelting and flash converting processes. CFD modeling can be used for design purposes in many technological areas, but some relevant physical and chemical phenomena are still missing in the commercial CFD solver packages. Therefore, Outokumpu has developed several subroutines for solvers to describe analytically the phenomena in the flash smelting environment. CFD sub-models of the copper concentrate and matte combustion, the particle-particle-wall interactions and for more accurate radiation properties of the gas-particle suspension are needed to ensure reliability of numerical simulations on the flash smelting and converting vessels. Several basic combustion phenomena can be modeled with a number of commercial solver packages, but own models for combustion must be included in the case of sulfides as the feed. Mathematical models for copper concentrate and solid matte combustion have been developed during the last decade. They calculate compositions of the particles and temperature, based on extensive experimental research work in laboratory scale furnaces with validated kinetic parameters and temperature measurements of reacting particles. Inside and near the concentrate burner, the standard particle tracking methods do not include the particle-particle interactions and the particle-wall interaction is too much simplified to describe properly the particle collisions with the distribution cone. Therefore, additional models for the particle-particle as well as particle-wall interactions have been written and implemented. For thermal radiation, models for the emissivity of a gas mixture and for calculating the particle absorption and scattering coefficients have been developed and tested. In addition, the advanced radiation model can be used i.e. in the enhanced simulation of off-gas cooling in the heat recovery boiler area of the flash smelter.

Jan 1, 2006

By Andreas Siegmund

Cast or rolled lead anodes employed in zinc electrowinning typically contain between 0.5?1.0% silver to decrease the overall corrosion rate. The production of cast lead-silver or lead-silver-calcium anodes often results in the formation of numerous holes, voids or laps in the anode surface that can initiate internal corrosion in localized areas. In rolled anodes the presence of internal porosity is significantly reduced, thus resulting in extended service life. The obtained grain structure of cast or rolled Pb-Ag anodes, however, requires a relatively long period of time to form a stable protective PbO2/MnO2 layer that can evolve oxygen without excessive lead contamination of the cathode. Therefore, these anodes are often mechanically, chemically or electrochemically conditioned prior to being placed in the electrowinning process. RSR Technologies has developed an improved anode for zinc electrowinning. The anode consists of a rolled Pb-Ag-Ca-alloy with controlled surface grain structure. The preferred calcium and silver content of the alloy is 0.05?0.08 % and 0.3?0.4%, respectively. Since May 2001, industrial-scale tests have been carried out at two zinc refineries in North America in industrial electrowinning cells. The controlled grain structure of these anodes allows forming an adherent protective oxide coating within a short period of several days when placed in an electrowinning cell without the necessity of being preconditioned. Anode sludge growth is evenly distributed. The anodes stay dimensionally stable and no short-circuits have been observed. Consequently, low corrosion rates and improved current efficiencies have been achieved.

Jan 1, 2003

By Luciano B. Oliveira, Luis G. C. Marques, Sergio N. Monteiro, Marcos V. M. Fagundes

"Biodiesel production is normally associated with large plantations of oily vegetables such as soybean and colza, in large rural areas. However, in the municipal limits of the city of Rio de Janeiro, southeast of Brazil, biodiesel is being produced from wastes commonly generated by typical urban activities such as sewage sludge, discarded fat from meat markets and post-used cooking oils. In the present work, the experience of producing biodiesel from urban wastes in Rio de Janeiro is assessed. The type of precursor materials, equipments and logistics are presented. The environmental and economical advantages as well as the drawbacks are discussed.IntroductionThe interest for a liquid fuel that could substitute those obtained from petroleum started more than one hundred years ago when Rudolph Diesel tested his no-spark internal combustion engine, impelled by compression, with peanut oil. By that time, petroleum was beginning to be extracted in large scale and no one was concerned with the future environmental problems and its eventual depletion. In the last century, the successful association of petroleum based fuels with the automotive industry was an almost insurmountable obstacle to any attempt to use nonmineral oils [1]. In addition to the greater efficiency and, by then, lower price of the diesel from petroleum, the use of plain vegetable oils introduced undesirable carbon deposits and reduced the engine lifetime. Today, the situation is reverse. The continuous increase in the price of petroleum and, above all, its contribution to climate changes are strongly motivating the use of biofuels to replace those obtained from fossil fuels such as petroleum, natural gas and coal [2].In the case of the common petroleum derived diesel, many countries are now engaged in large scale substitution programs. The USA should produce more than 700 million litters of biodiesel, while the European Community is expected too produce around 6.5 billion litters in 2008. In Brazil, the federal biodiesel program imposed a minimum of 2% addition to the common diesel. This would demand a production of 800 million litters in 2008 [3]. The Brazilian biodiesel is made from a diversified source of vegetables mainly castor bean, African palm and soybean. The main producers are agrobusiness firms located in large rural areas of the Brazilian hinterland [4]."

Jan 1, 2008

By Robert Corson

Zinc has a large solubility in Fe and a completely filled ?d? shell. With the discovery of dramatic increase of the magnetostriction in Fe by Ga addition, an examination of element Zinc that is adjacent to Ga in the periodic table is of significant interest. In this work, the effect of binary alloying of Zn with Fe on the magnetic and magnetostrictive properties is examined. The FeZn alloys were processed using powder metallurgy and vapor phase synthesis, and Zn contents were varied from 5% to 30%. An examination of the influence of different processing parameters and the Zn content on the resulting alloy properties is presented. The alloys were characterized using X-ray diffraction and SEM. Magnetostriction measurements were carried out at different pre-stress levels. Magnetic properties were measured using a vibrating sample magnetometer.

Jan 1, 2006

By Ali Akbar Mottahedi

Chromate conversion coating is a process for making a complex layer at the surface of zinc galvanized steel which makes the metal more resistant to corrosion, especially at marine atmosphere, and increases the adhesiveness of color. In this work the influences of various compositions on commercial zinc galvanized steel sheet to the color of chromate conversion coating has been investigated at normal temperature and the factors that affect the control and optimization of the process have been determined. A bath composition of 20 g/liter Cr203 and 10 g/liter NaOH and a dipping time of 50 seconds at room temperature (25-30°C) make a desirable color of chromate coating. A slow agitation at a constant pH of I (with additions of NaOH or H2SO4) assures a constant bath condition and develops the color. This kind of coating has more corrosion resistance and this bath condition and composition are also more economical.

Jan 1, 2003

By P. A. Olubambi

The effect of ore mineralogy on the bioleaching of metals from complex sulphides was studied by investigating the bioleaching of zinc and copper from a bulk complex sulphide ore from Ishiagu, Nigeria, using mixed cultures of Thiobacillus ferrooxidans, Thiobacillus thiooxidans and Leptospirillum in mechanically stirred reactors at varying particle sizes. Mineral phases within the varied particle sizes of -53, 53, 75 and 106µm were identified using X-Ray Diffraction (XRD), while the elemental distribution within the varied particles sizes was determined by X-Ray Fluorescence (XRF) and Optical Emission Spectrometry using Inductively Coupled Plasma- Optical Emission Spectrometer (ICP-OES). Bulk ore and the leached residues were examined by X-Ray Diffraction. The highest bioleaching recoveries were obtained at particle size of 75µm, while particle size of 106µm gave the least recoveries. Lower recoveries at particle sizes of 53 and -53µm were as a result of their higher silica and siderite content which affects pH, iron mobility and oxidation.

Jan 1, 2006

By Juan H. Rojas C.

The Chuquicamata mining and metallurgical complex is the main Division belonging to Corporation Nacional del Cobre de Chile (CODELCO-CHILE) and it accounts for 50% of the 1.4 Mt of fine copper output of the Corporation. It has been producing copper since 1915. The paper refers to the challenges that Chuquicamata has to solve in the near future. These challenges are: the increasing operation costs associated to a 800 m depth pit with low prices in an overstocked copper market; the increasing people's sensitivity to environmental preservation; and, the transformation needed for achieving high levels of organizational effectiveness. According to Corporate policy, Chuquicamata is making efforts to switch from a management style focused on supply to a management style focused on demand side of the industry. In this direction is tempting to establish strategic alliances to develop both new copper products and uses, to rise the metal demand. In more than 80 years of operation, Chuquicamata had exploited just one third of its geological resources. The exploitation of the remaining two third is a huge engineering challenge, taking into account the depth of the deposit, the impurities content, the decreasing ore grades and the transportation distances for waste dumping. All those factors are relevant in the economical process of transforming geological resources into ore reserves. Chuquicamata has other limitations. First, a 20,000 people town just aside the pit that limits the mining rates because of dust generation; second the scarceness of water in the desert area where Chuquicamata deposit is located; and, finally, the new tailing pond is a problem which solution will demand huge engineering efforts and investments. People are the principal factor associated to a company success. In this field, Chuquicamata have been progressing, but much more efforts from people will be necessary to reduce production costs for being successful as any other price-taker within the copper industry. Chuquicamata must develop the skills of its Supervisors to transform them into leaders and entrepreneurs, who additionally have the challenge of passing on their knowledge to non-professional workers. It is an ethic commitment to assure personal and professional growth of workers, as the only sustainable way to get real and integral success.

Jan 1, 1999

By Corby Anderson

The efficient separation of palladium from the transition metals copper, nickel and iron can be effected by passing a leach solution of these metals through a column of the silica polyamine composite material, WP-1, patented by Purity Systems Inc (PSI), Assignee, University of Montana with exclusive license to PSI. The separation can be done at the intrinsic pH of a nitrogen species catalyzed (NSC) oxidative pressure leach solution (~0) and stripping of the palladium from the composite can be effected with hydrochloric acid/ammonium chloride solutions at 50oC. Batch capacities of the composite for palladium are ~ 1.8 mmol/g resin. The possibilities for isolating the metal from the strip are discussed. Given the proven longevity and rapid capture kinetics of the polyamine composites, this new approach should prove to be an economically viable alternative to the multi-step concentration processes practiced in the PGM industry to date.

Jan 1, 2003

This symposium is dedicated to the lifetime achievements of Professor H.Y. Sohn. It covers the scientific fields, processing routes and investigation techniques in which Prof. Sohn has worked during his career and is based in the equally important three topical areas: Principles, Technologies, and Industrial practice. Professor Sohn was General Chair of the very first TMS Fall Extraction and Processing Symposium in 1983 in San Francisco which led to the Annual such symposia as this International symposium. Furthermore, the theme of that symposium was sulfide smelting, which is also included in this symposium. [ ] Professor Sohn was born in a beautiful dynastic capital Kaesung, Korea on August 21, 1941. He received his B.S. degree in 1962 from Seoul National University, M.Sc. in 1966 from the University of New Brunswick, Fredericton, N.B., Canada, and his Ph.D. degree in 1970 from theUniversity of California at Berkeley all in Chemical Engineering. After working as a Research Associate at the State University of New York at Buffalo and as a Research Engineer at Du Pont?s Engineering Technology Laboratory, Dr. Sohn joined the Department of Metallurgical Engineering at the University of Utah in 1974 and currently holds the ranks of Professor of Metallurgical Engineering and Adjunct Professor of Chemical Engineering.

Jan 1, 2006

By G. G. Barbante

Copper anode slimes are a valuable source of the precious metals, and selenium and tellurium. They are mineralogically complex and this has led to a great variety of process flowsheets for treating them. The traditional pyrometallurgical method utilises oxidation in a reverberatory furnace, but has numerous shortcomings. Recently deep-bath intensive smelting methods have been developed for use in the larger refineries. Despite these process advances, the thermodynamics of the reactions involved remains poorly understood. An initial description of the thermodynamics of slimes smelting is presented, but is severely limited by a lack of basic data. It is shown that slimes smelting is superficially similar to copper converting, but has many unique features. More basic thermodynamic data on selenium-based systems are needed before the process model presented can be further refined, and work in this direction has already commenced.

Jan 1, 1994

By Bryn Harris

Much has been written over the past twenty years on the removal and chemical stabilization of arsenic from metallurgical process solutions. This paper reviews again the latest developments in this field, and concludes as before that the high-iron arsenical ferrihydrites, together with the high temperature arsenic minerals, scorodite and Type II, remain as the best and most viable vehicles for industrial control and disposal. However, a cautionary note is introduced, in that chemical environments cannot be considered in isolation, and that cogniscence has to be taken of microbiological activity in determining the disposal method. Data are also presented on a survey of industrial practice, which shows that arsenical ferrihydrite is by far the most widely-practiced and accepted method used worldwide. Finally, the disaster in Bangladesh is briefly discussed with reference to lessons that the metallurgical community might learn from this.

Jan 1, 2003

By Derek Fray

Molten salts have been used for the extraction of metals since the 19th century but, recently, many interesting processes have been investigated using mixtures of molten salts and different cathodic materials. In several existing processes, the cation is simply discharged from melt but, in some cases, complications arise when the electrode potentials of the cations are relatively close. For example, the co-deposition of sodium with aluminium in the Hall-Heroult process is discussed in terms of electrode potentials of the components in the molten electrolyte. Similar considerations will also be given to the anodic reactions with respect to chlorine, oxygen, carbon dioxide or monoxide evolution from chloride-oxide melts. In some cases, the cathodic product interacts with the cathode to produce new and exciting products such as nanotubes from carbon or titanates and reduced titanium oxides from titanium dioxide. Depending on the electrode potentials, it is also possible to completely change the cathodic reaction from discharge of the cation in the salt to ionisation of the anions in the cathode. Examples are given of the reduction of metal oxides to produce metals, high technology alloys and nanomaterials and the cathodic refining of liquid metals.

Jan 1, 2006

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 Kazuki Morita

Dissolution mechanism and solubility of chlorine in the oxide melts, such as CaO-SiO2-Al2O3 (-Na2O), Na2O-SiO2-Al2O3 and CaO-SiO2-FeO systems, have been equilibrium technique was employed with controlled Po2 and PCl2, (Po2 = 10-6 -10 19 atm, PCl2 10-6 -10-13 atm at 1673-1748 K). The solubility of chlorine in the 40mass%CaO-40mass%SiO2- 20mass%Al2O3, slag was found to vary in proportion to Pb2/ w and pc/z/p' which proved that chlorine dissolved in the melts as C1 anion. Hence, the chloride capacity (CCI-), indicating the ability of molten oxide to absorb chlorine, has been defined as; The Ccl value was observed to increase with increasing slag basicity and temperature, and showed a reasonable relationship with that Of CS2-. Based on the result obtained in the present study, chlorine distribution during incineration with slags was predicted quantitatively.

Jan 1, 2003

By Bryn Harris

Chesbar Resources Inc.1 is developing a nickel-cobalt laterite project in Guatemala, Central America, by applying existing atmospheric chloride technology to a known resource. The tropical laterite project has an inferred resource of 133 million tonnes grading 1.51% nickel, which represents ~20% of Chesbar?s land holdings in Guatemala. Within its boundaries, the Sechol area has a measured resource of 14 million tonnes grading 1.46 % nickel and 0.08% cobalt, and an indicated resource of 23 million tonnes grading 1.34% nickel and 0.08% cobalt. Notwithstanding the impressive overall resource, the company has taken an innovative approach to a laterite project and is concentrating on El Inicio, a high-grade starter pit with five million tonnes grading 2.1% nickel and 0.08 % cobalt. The process flowsheet is based on atmospheric chloride leaching in a slightly acidic magnesium chloride brine, solution purification by recycled magnesia, precipitation of a mixed nickel/cobalt hydroxide intermediate product, and lixiviant regeneration by modified pyrohydrolysis technology. Initial results suggest that >90% of the contained nickel and cobalt in the non-magnetic fraction of the feed can be recovered, with <5% of the iron leaching. A metallurgical scoping study has established preliminary capital and operating costs for a production facility at a proposed rate of 20,000 tonnes per year of nickel as the intermediate mixed hydroxide. A preliminary assessment of producing a magnesium oxide by-product has also been carried out. This paper reports on the current development of the project and highlights the advantages of working in a chloride medium at atmospheric pressure and slightly elevated temperatures.

Jan 1, 2003

By Peter Kong

This paper provides a general discussion of atmospheric-pressure plasma generation, processes, and applications. There are two distinct categories of atmospheric-pressure plasmas: thermal and nonthermal. Thermal atmospheric-pressure plasmas include those produced in high intensity arcs, plasma torches, or in high intensity, high frequency discharges. Although nonthermal plasmas are at room temperatures, they are extremely effective in producing activated species, e.g., free radicals and excited state atoms. Thus, both thermal and nonthermal atmospheric-pressure plasmas are finding applications in a wide variety of industrial processes, e.g. waste destruction, material recovery, extractive metallurgy, powder synthesis, and energy conversion. A brief discussion of recent plasma technology research and development activities at the Idaho National Laboratory is included.

Jan 1, 2006

By Hiroyuki Sano, Chikabumi Yamauchi, Mitsuru Tanahashi, Toshiharu Fujisawa, Shin-ya Iwahori

"Pyrometallurgical process using Cu2O-based slag was proposed as a recycling process for copper scrap. However, it is difficult to remove nickel from copper by oxidative refining. Therefore, it is necessary to reduce the concentration of nickel in copper before the oxidative refining. In the present work, the copper enrichment stage in this recycling process, where copper scrap melt is separated into the Fe-C-Cu melt and the molten copper, was taken up and the compositions of both melts were measured. Based on the above results, the distribution ratios of nickel between the Fe-C-Cu melt and the molten copper were calculated. Furthermore, the optimum condition of copper enrichment stage was discussed from the viewpoint of nickel removal and copper recovery. The possibility of recovering 4N-purity copper by using this recycling process was confirmed.IntroductionRecycling is well known as a method for saving resources and reducing environmental damage. More than 99% of copper is used in metallic form - as metal or copper alloys[l]. High-grade copper scrap is directly re-melted and reused, while low-grade copper scrap is transported to copper smelters to be pyrorefined and electrorefined. Nevertheless, a great amount of copper is being stockpiled in the cities and should be recycled in the near future. At that time, the current recycling process will face new problems due to the increases in the recycling rate to the smelters. This includes insufficient combustion heat to melt copper scrap and ·almost no benefit in electrorefining because the scrap does not contain gold and silver. Thus, an alternative pyrometallurgical method for copper scrap refining will be required."

Jan 1, 2000

By Sheng-hai Yang

The ultrafine, monodispersed, spherical cobalt powder has been fabricated by reducing cobalt hydroxide with glycol. It were investigated that the effect of NaOH concentration on the reaction rate and the effects of the concentration of cobalt hydroxide and surfactant on the morphology and particle size. The particles were characterized by the X-ray diffraction(XRD), scanning electron microscope(SEM), laser diffraction particle size analyzer and BET specific surface analyzer respectively. The XRD shows that the cobalt powders exist mostly in face centered cubic (fcc) structure, a little in simple hexagonal. The cobalt powders prepared at Co(OH)2150g/L, NaOH 40 g/L and surfactant 30g/L, its average particle size, specific surface area and cobalt content, were 0.88µm, 2.705m2/g. and more than 99.5% respectively.

Jan 1, 2006

By Bo Jiang, Lianyun Liu, Hongmin Zhu, Kai Huang

"Watermelon peel is selected as a novel adsorbent to remove Pb(II) from aqueous solution. A simple saponification process is proposed to modify the peel and the adsorbent is characterized by SEM and FTIR. The effects of pH, contact time, initial concentration of Pb(ll), biosorbent dosage and temperature on adsorption of Pb(II) are investigated. Different models are used to fit experimental data. These models indicate that the adsorption process follows the Langmuir model and pseudo-second-order model. The maximum adsorption capacity obtained from Langmuir model is 1.05mol kg-1 for the prepared sorbent. Equilibrium time is attained in 5-10 min for the studied concentrations. The watermelon peel can be used as an effective and low-cost biosorbent for removal of Pb(ll) from aqueous solution.IntroductionRecently, removal of heavy metal ions from industrial effluents by biosorption has become a very attractive topic, since the more serious pollution issues caused by heavy metals emerge frequently, and more strict requirements for its control are called upon by society [1,2]. In this case, most conventional purification technologies are not suitable due to poor cost-effectiveness [3]. For example, chemical precipitation by alkaline reagents usually can not decrease the metal ion concentration below the permissive levels, and also it will produce a large amount of sludge containing toxic metals. Membrane separation techniques can realize deep purification of wastewater easily, although its operating cost is usually high. Thus, considering the high effectiveness, low cost and free-sludge operation, bisorption has become a promising technique in water treatment [4]. The most important thing for this technology is the synthesis of a suitable biosorbent, whose adsorption properties will determine the removal efficiency and economic cost for the whole process. Watermelon is one of the most popular fruits for mankind for its delicious flavor. Usually, the watermelon is consumed mainly for its edible pulp, and its peel is discarded or only used as feed for livestock. Considering the pectin contained in the watermelon peel, just like that in orange wastes in the reported literatures [3], the idea of using it as the raw material to prepare the biosorbents for heavy metal ions removal from the aqueous solution was evaluated in this study."

Jan 1, 2012