Search Documents

By Ligang Zhang, Wen Chen, Xinghua Liu, Jialin Li, Xiaoyin Liu, Zhenhong Liao

A research-scale fluidization and magnetization roasting device was developed to evaluate a processing option that might offset the complexity and high cost of the conventional magnetization roasting process on siderite. In this study, the operating parameters of the fluidization and magnetization roasting device for siderite were evaluated through cold-flow tests and magnetization roasting tests. The reaction mechanism functions of the fluidized roasting process are revealed with kinetic studies.

Jan 1, 2015

By Liping Gu, Gordon A. Irons

"A 1/3 scale ""thin-slice"" model of an electric arc furnace was developed so that gas could be injected to simulate foaming gas evolution. The influence of arc jets, oxygen lancing and bottom bubbling was also simulated. Liquid velocities were measured by a white light particle image velocimetry system. Numerical simulations of some of these effects were made using commercial CFD packages. Comparisons with measured results show that considerable care is required to select the appropriate model and to interpret the computational results.INTRODUCTIONDuring recent years electric arc furnaces (EAF) have captured a significant share of steel production, partially due to increased productivity through the introduction of advanced technology such as oxygen injection, slag foaming and long-arc operation, process automation and post-combustion. However, systematic analysis of the process and these effects on heat transfer and fluid flow in the furnace is still in its infancy. Most investigationsl1 6l have been restricted to a specific application such as oxygen lancing or bottom stirring. In addition, it is very difficult to make comparisons between these computed results and experimental/industrial results. In this work a 1/3-scale ""thin-slice"" model of Dofasco's 190 ton EAF was built. The fluid flow in the bath due to the arc jets, bottom stirring, oxygen lancing and CO evolution was simulated. The velocity distributions in the bath were measured using Particle Image Velocimetry (PIV) System. In addition, numerical simulations of bottom stirring and CO evolution were carried out using two commercial CFD packages (Fluent and Phoenics). The objective of this work is to validate the mathematical models so that they can be applied to the full-scale furnaces."

Jan 1, 1999

By J. C. Huyhua

The effect or various oxidants on gold and silver dissolution in thiourea solutions (0.05 M in H2SO4) was studied using the rotating disc technique, a.t 2s c and 600 rpm. These studies were carried out at constant (4:1) initial molar ratio or thiourea to oxidant concentrations, to produce 50 % thiourea. oxidation. The initial dissolution rate of gold was approximately four times higher in the presence. of ferric sulfate (5.37 x 10-3mg cm-2 s-1) than in the presence of hydrogen peroxide (H2O2), potassium persultate (K2S2O3), or monopersulfa.te (KHS06). The dissolution rates for silver were considerably lower than gold for the same oxidants. Oxidation of thiourea in the presence of peroxygen and persulta.te compounds is a. fast reaction and it is completed in less than ten minutes. On the other hand, the oxidation or thiourea with? ferric.sulfate is slow, yielding a second-order reaction rate constant k = 6.09 I mol-1 h-1. Sulfur formation in the ferric thiourea system begins when ferric ion reduction approaches to completion. With hydrogen peroxide, sulfur is observed at lower thiourea concentration than ferric. Suifate. The presence of a large excess or free thiourea i.e., s to 20 % thiourea oxidation) retards sulfur formation and maintains favorable dissolution rates. Finally, carbon-in-leach experiments indicate that thiourea solutions a.re stable for several days, with ferric sulfate or hydrogen peroxide. The dissolution rates of gold and silver doubles in the presence or activated carbon when hydrogen peroxide is used as oxidant.

Jan 1, 1989

By Phillip B. Messersmith, Emmanuel P. Giannelis

"A versatile in-situ polymerization approach is described for the synthesis of polymerceramic nanocomposites consisting of two-dimensional layers of mica-type silicate (MTS) within polymer matrices. Functionalized, organically modified mica-type silicates (OMTS) were used to promote delamination/dispersion of the host layers and initiate polymerization of organic rrionomer. Epoxy nanocomposites prepared in this manner exhibit substantial modulus reinforcement at low silicate loadings. The water vapor permeability of the poly(?-caprolactone) nanocomposite containing 4.8% silicate by volume was reduced by nearly an order of magnitude compared to pure poly (?-caprolactone).IntroductionPolymer matrix nanocomposites are a relatively new class of materials with dimensions typically in the range of 1-100 nm.1 In general, because of the ultrafine phase dimensions involved, nanocomposites exhibit new and improved properties when compared to their micro- or macrocomposite counterparts. We as well as others are currently investigating the design, synthesis and characterization of polymer-ceramic nanocomposites. Our effort, in particular, has focused on the use of mica-type silicates (MTS) with various thermoplastic and thermosetting matrices.2-5MTS's belong to the general family of 2: 1 layered silicates. Their crystal structure consists of layers of two silica tetrahedral sheets fused to an edge-shared octahedral sheet of either aluminum or magnesium hydroxide. Stacking of the layers leads to a regular van der Waals gap or interlayer.6 Isomorphic substitution within the layers generates negative charges that are counterbalanced by cations residing in the interlayers. Although the natural forms of MTS's usually contain hydrated Na+ or K+ ions, ion exchange reactions with organic cations (e.g. alkylammonium ions) can render the normally hydrophilic MTS's organophilic."

Jan 1, 1994

By T. Kozuka, K. Sassa, S. Asai

"A new atomization process is developed. The principle of this process is completely different from that of conventional processes. This process uses electromagnetic energy induced by direct electric current and direct magnetic field instead of kinetic energy produced by fluid impingement or disk rotation.Experimental work of this process was carried out using pure tin, and it was found that the crucial factor for a stable operation is the contact state of molten metal with the electrode. In order to control the condition, a delay time controlling unit was developed and combined with this process. It is noticed that this controller works well to produce uniformly sized particles.A linear relation between the impulse and the momentum of atomized particles is found by use of experimental data and is explained by theoretical analysis.IntroductionIn atomization processes prevailing in metal powder technology, kinetic energy is currently employed for atomizing molten metal. That is, molten metal is broken into small particles by other fluid (e.g. water, argon gas, etc) or by impinged upon a rotating solid disk. This splashing process is always accompanied with uncertain factors for shape and size of the particles. The diameter distribution of products, therefore, comparatively spreads over a wide range. From another standpoint, the restriction of atmosphere is inevitable in some of these processes. As a pulverizing technology, the process which can produce uniformly sized particles and permits the choice of atmosphere is strongly desired.On the other hand, a great attention has been paid to the spray casting process as a new near net shape casting. In this process, a small size spraying device is favorable."

Jan 1, 1988

By G. O. Onyedika, M. U. Obidiegwu, G. C. Onuegbu

The effect of kolanut (KN) filler and compatibilizer (maleic anhydride) contents on the transport of toluene through low density polyethylene (LDPE) and low density polyethylene composite were studied at the temperatures 40, 60 and 80 °C.The kolanut powder used was ground to 25 μm particle size. In preparation of composite 0–5 wt% of kolanut powder and 0–2.5 wt% of the compatibilizer were mixed with 200 g of low density polyethylene in an injection moulding machine. The injected polyethylene and polyethylene/kolanut composites (LDPE/KN) were taken for sorption test. The sorption data obtained for low density polyethylene and kolanut powder filled low density polyethylene at the different temperature investigated were expressed as the molar percentage uptake (% Qt) of toluene per gram of the kola nut composites. Results show that the uptake of toluene at the five filler content (0–5 wt%) generally increased with increase in sorption temperature but decreased with increase in compatibilizer and filler contents. This can be seen at 80 °C and 0, 1, 1.5 and 2.5 wt% of compatibilizer respectively. The molar percentage uptake of toluene at 1 wt% of filler yielded the following values; 8.6789, 8.4768, 8.3476 and 8.2679 respectively. At 2 wt% it yielded 8.6224, 8.1333, 7.9525 and 7.9042 respectively, at 3 wt% it gave 8.4336, 7.9450,7.8900 and 7.7823 respectively, at 4 wt% it yielded 8.0263,7.9614,7.8218 and 7.6800 respectively and at 5 wt% it gave 7.9635, 7.8630, 7.6256 and 7.5013 respectively.

Mar 1, 2017

By Zhao wen Wang, Ramana G. Reddy, Min Li

"The electroreduction of Co(II) in l-butyl-3-methylimidazolium tetrafluoroborate (BMlMBF4) ionic liquid was investigated by cyclic volatrnmetry at 353 K. The results show that the reaction of Co(II) to Co is irreversible in one step with two electrons transferred. The diffusion coefficient of Co(II) was estimated to be 7.6 x 10-8 cm2 s·1 at 353 K. Then the electrodeposition of cobalt was studied at different cathodic potentials (-0.80 to -0.95 V) and different temperatures (333 to 363 K) in BMIMBF 4 containing 0.20 mol L-1 Co(BF4)z. The deposits were characterized using scanning electron microscope (SEM), energy-dispersive spectroscopy (EDS), and X-ray diffraction (XRD). SEM images show that a uniform, dense, and compact deposit was obtained at -0.80 V and 333 K. The deposits were identified as high-purity metallic Co for all experiments by EDS and XRD.IntroductionCobalt is known as a hard magnetic material and cobalt alloys have been shown to have excellent magnetic properties with adequate mechanical durability and corrosion resistance, which are needed for high performance magnetic recording applications [1-4]. The electrodeposition of Co alloy in the aqueous solution is generally difficult because of the narrow electrochemical potential window of water, which leads to the low current efficiency and worse quality of deposits due to the hydrogen embrittlement. Thus, aprotic ionic liquids (ILs) are expected to be the ideal alternative media for electrodeposition of cobalt or its alloy since ILs usually provide a wide working potential windows, negligible vapor pressure, and acceptable conductivity for electrolysis without the occurring of hydrogen evolution [5, 6]."

Jan 1, 2014

By D. Pradhan, R. G. Reddy

"Electrorefining of aluminum scrap was investigated from AlCl3 –1-Ethyl-3-methyl-imidazolium chloride (EMIC) (Molar ratio 1.65) chloroaluminate electrolyte using copper cathodes at temperature of 90±3°C and cell voltage of 1.5 V. The deposits were characterized using scanning electron microscope (SEM), energy dispersive spectroscopy (EDS) and X-ray diffraction (XRD). The study was focused to determine the effect of electrode surface modification as well as deposition time on dendritic depositions of aluminum. Their effect on current density was investigated also. It was shown that the surface modification of electrodes reduced the dendritic depositions of aluminum. Pure aluminum (>99%) was deposited for all experiments with the current efficiency of 94-97%. The use of ionic liquids not only reduced the energy consumption but also minimized pollutant emissions (CO, CO2 etc.) compared to the commercial high temperature aluminum production.1. IntroductionAluminum electrorefining/recycling from aluminum scrap using ionic liquid electrolyte is an attractive process today because of the unique chemical and physical properties such as wide temperature range for the liquid phase, high thermal stability, negligible vapor pressure, low melting point and wide electrochemical window. But in conventional practice, melting of aluminum scrap and high temperature molten salt electrolysis makes this process more expensive and less energy intensive (average 13 kWh/ kilogram of aluminum) [1] . Although recycling scrap aluminum requires only 5% of the energy used to make new aluminum [1-2], but the green house emissions like CO2, CO and HF have to be counted for environmental reason. Approximately, 5.31 kilogram of CO2 emitted per kilogram of aluminum production in most of the US industries."

Jan 1, 2009

By Kinya Atsumi, Kanjana Khunathai, Hisaya Kato, Hidetka Kawakita, Keisuke Ohto, Katsutoshi Inoue

"Crosslinked microalgae were prepared from the residue generated in the production of biofuel, by crosslinking-condensation in concentrated sulfuric acid. These microalgae were tested for adsorption of various metal ions in hydrochloric acid medium. The crosslinked microalgae exhibited high selectivity for Au(III) over other precious and base metal ions. From an isotherm experiment, the maximum adsorption capacity was evaluated to be 3.25 mol/kg of dry gel for Au(III) which was many times higher than that of the original microalgae residue. SEM and X-ray diffraction confirmed the formation of metallic gold particles, suggesting the occurrence of a redox reaction between surface functional groups on the gel surface and trivalent gold ion.IntroductionSubstantial quantities of precious metals are being used by the electronic industry because of their excellent electrical conductivity and resistance to corrosion. In recent years, recovery of precious metals from secondary sources such as electronic scrap [1,2 ], and leach liquors is being favored because of environmental concerns. Of course, recovery is only practical, if its cost is lower than the value of the metals (gold, platinum and palladium) recovered.Traditional methods of separation and refining do not fulfill this requirement. In order to overcome this problem, attempts have been made in recent years to develop new processes including total leaching in hydrochloric acid containing chlorine gas or hypochlorite, followed by solvent extraction and ion exchange [3]. In the new processes, new solvent extraction reagents or ion exchange resins with high selectivity and high loading capacity are used to simplify the process and to reduce the operating costs."

Jan 1, 2011

By Ann M. Hagni

"Ceramic matrix composites are inorganic materials that are particularly resistant to heat and abrasion. A magnesia (MgO) and aluminum nitride (AlN) based composite is formed by exposing a magnesia preform to a metallic alloy block in a nitrogen atmosphere at 950°C. The metallic alloy, which is composed primarily of aluminum, is wicked into the preform. Aluminum nitride matrix is grown between MgO particles as the wicked metallic aluminum reacts with nitrogen. Unused metallic alloy, remnant metallic alloy (carcass), and composite produced after 8 hours, 50 hours, and 225 hours of processing are characterized mineralogically. Reflected light microscopy, transmitted light microscopy, scanning electron microscopy, energy dispersive spectroscopy, and X-ray diffraction techniques reveal that in addition to anhedral to euhedral AhNi, AbSbSr, and Al crystallizing in the metallic alloy carcass, AIN and (Al,Si)N have formed as well. Nitride rings and nodules in the carcass may hinder AIN growth in the composite. Fine-grained residual AhNi and AhShSr are dispersed throughout the composite matrix. The nitride matrix is composed of AIN and (Al,Si)N. Rim replacement of MgO by spine! occurs in the composite. Aluminum nitrides in the metallic carcass cathodoluminesce deep violet-blue, unlike non-luminescent AIN in the composite matrix. This distinction in cathodoluminescence suggests a different mode of formation for composite AIN than for carcass AIN. Phase interpretations and textural characterizations deduced from the implementation of sophisticated mineralogical techniques have contributed to the understanding, and will aid in the improvement, of MgO/ AlN-based ceramic matrix compositeprocessing."

Jan 1, 1999

By Jorge A. S. Tenorio, Girley F. Rodrigues, Joner O. Alves, Denise C. R. Espinosa

"Rock wools are mineral fibers composed of amorphous silicates, due to their thermo-acoustic characteristics this material has a broad consumer market in the construction, automotive, and electric-electronics industries. This work studied the recovery of wastes from ornamental rocks (granite and marble) as partial raw materials in the production of rock wools. Residues from granite and marble cuttings are industrial wastes with considerable production and limited applications. These wastes should be appropriately managed because when discharged in rivers or lakes can cause siltation, and also they can cause serious human health problems, such as silicosis. Samples of produced materials with thickness smaller than 500µm were characterized by chemical analyses, XRD, and DTA. Results showed that the rock wools produced using granite or marble wastes have important properties, especially the melting point. This process decreases the extraction of mineral resources and provides a profitable destination for the ornamental rock wastes.IntroductionThe ornamental rocks industry is a sector with large production of wastes. During the granite and marble extraction processes and specifically during the rocks cutting (see Figure 1), approximately 35 tons of powdered rock per month can be produced. These residues should be appropriately managed, because when discharged in rivers, lakes or watersheds, they can cause siltation. Also, these wastes can cause serious human health problems, such as silicosis [1].Currently, the granite and marble wastes are mainly used in civil construction to produce materials in the form of mortar, bricks and tiles. However, due the current produced volumes and the average growth of world production estimated at 6% per year, new applications for these wastes are necessary [2]."

Jan 1, 2011

By Nozomu Uchida, Uematsu Keizo, Daisuke Shouji

"Grain orientated microstructure was developed for the improvement of ceramic characteristics. Novel polarized light microscopy was developed to examine the grain orientation quantitatively. The degree of grain orientation was estimated from the retardation determined with a Berek compensator. The method was essential to determine a minor grain orientation, which could not be analyzed by means of conventional X-ray measurements. The data were favorably related to ceramics characteristics. The comparis of the ceramics with various degree of orientation was very important to explain the change of ceramic characteristics with processing.IntroductionMicrostructure with grain orientation has a high potential for greatly improving characteristics of ceramic. However, there has been strong restriction on processing and material for developing this structure. It has been crucial to apply forming methods involving high shear such as injection molding1). Grains must have an elongated shape.In recent years, much attention has been paid on the effect of high magnetic field on diamagnetic materials2)3)4), Many ceramic materials are known to be diamagnetic. High magnetic field has a high potential to orient grains. The principal driving force for grain orientation is the magnetic anisotropy of material, which is generated by non-cubic crystal symmetr5). This method of grain orientation is not restricted by grain shape, and can be applied to all materials having non-cubic crystal structure.This study uses alumina as raw materials, and produces alumina ceramics with orientated grain in high magnetic field (10T). Alumina has a magnetic anisotropy due to hexagonal crystal structure. The degree of grain orientation in the green and sintered bodies will be examined and their relevance to magnetic field will be discussed."

Jan 1, 2000

By Milance Mitovski, Milorad Cirkovic, Vlastimir Trujic, Dragana Živkovic

"In this article, it is analysed the possibilitis and the effects utility waste energy of process sulfuric acid production in the existing technical-technological conditions. The utility second process energy, reduction the fuels consumption, reduction environment pollution and its effects are shown, too. High heat quantity is produced as the result of exothermal reactions in the production process of sulfuric acid in Bor. A part of this heat is sufficient for the process development, and significant part of this heat presents low-temperature heat energy that is irretrievable lost. Investigations were carried out based on production of 485 t of monohydrate/day of sulfuric acid. By recovery of this heat quantity for heating purposes, about 20.000 – 25.000 t of coal/year would be saved, what would significantly improve the power efficiency of the smelter copper production. IntroductionTechnological process of copper production in RTB BOR (Serbia) produces a significant quantities of high temperature secondary (waste) heat energy that is uncontrolled “lost” in the vicinity. Secondary heat energy is produced in pyrometallurgical copper production in quantity of 1,621 kWth/kg of dry concentrate or existing heat (that presents a difference of heat at furnace outlet and heat at temperature over temperature of dew point of sulphuric acid gases) in quantity of 1,315 kWth/kg of dry concentrate. For designed capacity of Copper Smelter in Bor, the existing heat power of secondary energy is 92,111 MWt, what is an equivalent to the power of steam-turbo plant where the Rankine-Clausius heating cycle is done, and that is 28,334 MWe."

Jan 1, 2008

By Eiki Ono, Atsushi Yamatodani, Shigeru Sunagawa, Yasushi Takasaki, Atsushi Shibayama, Yasunori Higuchi

"During metallurgical processing of non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product.In this research, some experimental feasibilities were investigated to recover/remove Cu and As from the residue. Primarily, the removal of As and volatilized materials from the residue was examined by pyrometallurgical treatment (dry-process). In the second stage after treating the residue with a dry-process, leaching and solvent extraction as hydrometallurgical treatments (wet-process) were also investigated by using H2SO4 solution as a two stage leaching treatment, to dissolve various metals from the leach residue. Then, solvent extraction was examined by using LIX-84I as an extractant to recover and separate Cu from impurities from the final (2nd) leached solution. For the leaching stages, the removal of 90 % As and the leaching rate of 85 % Cu could be achieved by 0.25 mol/l and 1.0 mol/l H2SO4 solution, respectively. On the other hand, the extraction of over 90 % Cu and stripping was carried out by solvent extraction. 1. IntroductionIn metallurgical process for non-ferrous metals, smelting residue (inc. smelter slag, flue gas and so on) is inevitably generated as secondary product, i.e., flue dust, slug and so on. The smelting residue includes some useful metals and undesired toxic materials; Cu, Pb, Ca and As, etc.In Japan there is one undisclosed place stockpiled with 10,000 ton of smelting residue from abandoned smelters about 25 years ago. Therefore it is necessary to reduce the residual amount for space and environmental protection including water treatment by separating and removing toxic materials."

Jan 1, 2008

By Geir Wedde, Anders Sorhuus

"Vast quantities of energy are released as heat to the environment from industrial operations. Many countries target waste heat recovery to mitigate CO2 emission. Exhaust gases from industries such as primary aluminium smelting, carry a substantial portion of the waste heat generated. For a cost efficient capture of more valuable heat (higher exergy), heat exchangers should operate on the exhaust gases upstream of the gas treatment plants. Heat exchange surface would be exposed to dust laden gases with risk of fouling. Heat exchangers of innovated design and operation have overcome the potential of excessive fouling rates. Heat exchangers of the ""shell and tube"" design have been demonstrated for exhaust gases from ferroalloy as well as primary aluminium smelters. In addition to the heat recovery, gas cooling results in smaller gas treatment plants with lower costs and reduced emission. The aluminium experience is exampled in the paper.IntroductionIndustrial usage of energy continues to grow as a result of increasing volumes of production, a trend that is likely to continue in the coming decades as living standards keep rising globally. World energy consumption (Figure la) is to grow 49 % by 2035 (ref. 2010) as reported by EIA [1]. The industrial sector consumes somewhat more than 50% of the total world energy consumption predominantly the energy increased demand comes from non-OECD countries in Asia. The industrial consumption by production of metals iron and steel accounts for 14 % and for non-ferrous metals 3 % mostly for aluminium production (Figure lb). Aluminium production will be discussed in this paper as an example of an industry with large quantities of waste heat to recover"

Jan 1, 2012

By J. E. Klein

Bench scale tests using a stack of ten whole SAES St909 pellets, 6 grams, to crack methane have been completed with pure methane feed. Test conditions ranged from 600 to 800°C at 101 kPa (760 ton) with a methane feed rate of ten sccm. Methane reformation tests, test where hydrogen was passed through a St909 bed after cracking methane, were performed to determine if and how much methane can be generated under "reformation" conditions. Phase structure determinations of St909, composed of a ZrMnFe alloy with aluminum used as a pellet binder, after methane cracking were complicated by the number of materials that can be formed by the elements in the St909 and the carbon from methane cracking. It was determined that the aluminum not only alloys with the Zr, Mn, and Fe in the St909 alloy, but also forms aluminum transition metal carbides in addition to ZrC as the carbon content and the temperature of the St909 increases. Some A14C3 was also found in some pellets. Passing hydrogen over St909 pellets after methane cracking formed methane at various rates in the temperature range of 600 to 800°C. Temperatures of 800°C gave the best methane cracking performance and efficiencies decreased rapidly with temperature.

Jan 1, 2002

By A. H. Castillejos E., F. A. Acosta G.

Filtration is widely used as a terminal refining step for metals, particularly for the casting of aluminum alloys, but still more knowledge is required to understand how several factors affect the efficiency of removal of inclusions. In this study, both, initial and long term filtration efficiencies of a ceramic foam filter have been obtained from the computed trajectories of solid particles suspended in molten aluminum. The complex structure of the foam filters is represented by a unit cell which is formed by a pair of pores with average dimensions. The fluid flow field was determined from the numerical solution of the Navier-Stokes equation, and periodic fully developed flow was assumed at the inlet of the calculation domain, as a boundary condition. This flow field corresponds to laminar flow as that found in ceramic filters operating under normal conditions. Computed initial filtration efficiencies showed that filtration efficiency decreases sharply with fluid velocity for particles larger than 30 µm, but smaller particles are better trapped at higher fluid velocities. Finally, it was found that long term filtration efficiency for particles of 8 µm decreased with time, in spite that perfect particle-wall attachment was assumed. Filter aging was considered in this study, and it was found that the distorted flow field, around the already trapped small inclusions prevented further collection.

Jan 1, 1999

By Ole Rud Bendixen

Topsoe has developed a Wet gas Sulphuric Acid (WSA) process which effectively recovers SO2 in off-gases from non-ferrous smelters and roosters. The product is concentrated sulphuric acid of typically more than 96 wt% irrespective of SO, concentration in off-gas. The process does not generate any waste products or waste water and does not use any absorbents or other chemicals. In the process, up to 99.3% of the SO2 is converted catalytically into SO3, which reacts with water in the gas, hereby forming gaseous sulphuric acid. The acid is condensed in a WSA condenser of proprietary design. Excellent heat economy and practically no sensitivity to the water balance mean that no extra sulphur burning is required at any S02 concentration, The process is especially well suited for treating off-gases where the SO2 content is lower than approx. 5-6%, and it is a good alternative to a complete renovation of a smelter. However, also off-gas from flash smelter may be treated. The process has found good use in both molybdenum and lead roosters. An example from a molybdenum roaster in Chile shows that 97-98wt% acid is produced from a 2.3 % S02 gas. This plant is situated in the outskirts of Santiago and represented a major local source of SO2. The plan was started in May 1993.

Jan 1, 1996

By Martín Reyes

Iron concentration by ion flotation techniques, from sulfate solutions in presence of zinc was studied in a laboratory flotation column by continuous mode using a synthesized sand shell plate sparger, an anionic collector, promoters, and surfactant propylenglicol 400. Effects of experimental parameters, such as the concentration of reagent: potassium amyl xanthate and dithiophosphate, superficial gas velocity, and superficial liquid velocity were studied in terms of the recovery and enrichment of Fe (III). The results show that the iron elimination from the solution in the presence and absence of zinc (II) are of 59 % and 72 % respectively. The flotation efficiencies decrease with an increase of the concentration of xanthate and air flow rate. The best recovery was achieved, at Jg 0.1 cm/s, Jl 0.72 cm/s and a mixture of xanthate and dithiophosphate as promoter. It was also demonstrated that it is possible to selectively separate and concentrate iron (III) from solutions containing zinc. The behavior of iron ion flotation in a flotation column is reported in this research as a gas hold up, superficial gas velocity, bubble size and superficial bubbles area flux function. The results show that the extraction of aqueous ions of metal iron by ion flotation is strongly affected by: [C], Jg (cm/s), eg (%), Db (mm), Jl (cm/s), y Sb (s-1).

Jan 1, 2009

By Feng Chen, Lirong Chen, Yufeng Guo, Wenjie Weng, Tao Jiang

"In this paper, the carbonthermal reduction behavior and the influencing factors of Panzhihua ilmenite under the condition of carbon-burdened were systematically investigated. The results show that the ilmenite forms into titanium nitride during the reduction process at 1200 °C under the condition of carbon-burdened. Carbon-burdened is beneficial to the reduction of iron oxide, but less favorable for the growth of iron grain.IntroductionThe titanium ferrous resources are very rich in Panzhihua-xichang area, accounting for about 38.85% of the world's proved reserves [1]. However, TiO2 grade of this kind of ilmenite is low and calcium magnesium content is high, it generally requires preconcentration to titanium-rich material—titanium slag or synthetic rutile.Chlorination process is an advanced method for production of titanium dioxide, which should takes high quality titanium-rich material with low content of calcium and magnesium as raw materials (the content of MgO and CaO are less than 1.0%). Ilmenite in Panxi area, however, contains high calcium and magnesium; it is not suitable as a raw material for chloride process. Methods of producing titanium-rich materials which have been applied in industry are electric smelting, various acid leaching and reduction rust [2-5]. There still exist some problems such as CaO and MgO removed not thoroughly, low resource utilization, high energy consumption and environmental pollution."

Jan 1, 2012