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By W. G. Davenport

Chapter 10 showed that any given smelting task, e.g. production of 65% Cu matte, 1500 K, from CuFeS2, can be done with many different combinations of: blast%02 hydrocarbon fuel blast temperature. This chapter repeats the Chapter 10 calculations but reports the results in terms of the mass industrial oxygen mass hydrocarbon fuel blast preheat energy combinations that will produce 65% Cu matte, 1500 K, from CuFeS2 concentrate. It also determines the energy inputs equivalent to these combinations.

Jan 1, 2001

By Takafumi Kondo, Satoshi Yamashita, Noboru Masuko

"Aqueous oxidation of phosphite ions to phosphate ions with dissolved oxygen was examined at 80° C and pH 4.5 mainly from the stichiometric point of view. Dissolved oxygen alone can not oxidize sodilim phosphite in aqueous solution, but when sulfur dioxide is coexistent, cooperative oxidation for both sulfite and phosphite can occur in aqueous solution. Sulfur dioxide itself is well known as a reducing agent, but it also reacts as an oxidation-promoting agent for other species under a certain condition. So sulfur dioxide is· a promising cheap reagent for waste phosphite processing.IntroductionIn a liquid-phase oxidation reaction using the dissolved oxygen gas, the eoexistence of a copper salt is required generally. Recently, it was reported that the oxidation reaction progressed by using mixed gas of sulfur dioxide and oxygen without the copper catalysis, and the attention has been collected1·3). The present authors also noticed the phenomenon since the early time and have been studying on the reaction mechanism of sulfur dioxide in liquid phase oxidation 4l. It was found that; by using the SO2-O2 mixed gas, the oxidation of phosphite ions to phosphate ions proceeded efficiently in sulfuric acid solutions. In the present report, the applicability of SO2-O2 mixed gas as a cheap oxidizing agent to the industrial processing of the waste solution of electroless nickel· plating is investigated. It is well known that the sulfur oxide dissolved in aqueous solution is oxidized ·by the oxygen in the air to sulfuric acid according to the following equation"

Jan 1, 2000

By F. Begazo

The most common approach to increase production in copper refineries is to increase current densities. However, if these increases are not well thought out beforehand and are not properly and effectively controlled, the end results could be reduced plant performance and a deterioration in cathode quality. Both of these factors result in lower efficiencies and increased costs. At the Ilo Refinery of Southern Peru Copper Corporation, a modernization and expansion program was implemented shortly after the Refinery was purchased from Minero Peru, in 1994. This program was intended to increase production from 195,200 mtpy of cathode to 227,000 mtpy over a 3-year period. Part of this production increase would come from increasing current density. During the period from 1994 to 1997, current density at the Ilo Refinery was increased from 218 A/m2 to 230 A/m2, while plant efficiencies were maintained at consistently high levels. The current efficiencies were maintained at >97.5% and time efficiencies were maintained at >98%. During 1998, additional increases in current density were implemented while the high plant performance was maintained at the same levels. By the end of 1998, the current density was 241 A/m2, while current efficiency and time efficiency of 98% were maintained. This paper describes the control processes used at the Ilo Refinery to maintain high plant performance levels while increasing the current density. Additionally, expected plant performances from extended test programs at current densities up to 280 A/m2, for future production increases, are reviewed and discussed.

Jan 1, 1999

By Jorge Alberto Soares Tenório, Romano Espinosa, Felipe Fardin Grillo, José Roberto de Oliveira, Denise Crocce

"The aim of this work was evaluation of the recovery of Zn and Fe of the EAFD added to the hot metal in the form of briquette at temperature of 1500°C. The EAFD was agglomerated by cold briquetting and introduced in the hot metal. This study utilized a bench-scale equipment to melt, during this process to kept a flow rate of inert gas above the bath. Were collected periodically metal samples and the samples were analyzed for determination of the content of total silicon and carbon by chemical analysis. Zinc oxide, zinc ferrite and other oxides were reduced and were volatized and collected by a cleaning system of dust (baghouse) located on top of the oven. More than 98% of iron were recovered from EAFD during the test. It was possible to produce a dust containing about 68% zinc by means of adding of EAFD.IntroductionIn the first semester of 2010, steel production was about 706 million tons, 27.9 % more than in the first half of 2009. Not a significantly increase if 2010 data is compared with the first semester of 2007 (only 7.2 % higher), before the world’s economic crises. Steel production is divided into two main routes. The first one, and most used, is the Basic Oxygen Furnace Process (BOF process), which in 2008 accounted for approximately 67.1 % of steel production. The second route is carried out in the Electric Arc Furnace (EAF) that in 2008 represented 30.6 % [1 ].Electric arc furnace dust (EAFD) is a solid waste generated during the steel making process. It is classi?ed according to NBR 10004 as dangerous solid waste-class I, because the elements Pb e Cd leach in water exceeding the maximum limits permitted by the NBR 10004 [2 ]."

Jan 1, 2012

By Naixiang Feng, Shaohu Tao, Zhihui Wang, Yuezhong Di

"A novel vacuum aluminothermic reduction lithium process was developed in present work which used lithium carbonate, alumina and calcium oxide as raw material. The process mainly contained three steps. The first step is that LiA102 clinker is prepared in ambient environment, then metal lithium is vacuum extracted from LiAl02 clinker with aluminum power as reducing agent, and the last step is that alumina is leached from the reduction residue with a mixture of sodium hydroxide and sodium carbonate. The results show that the lithium reduction ratio can be over 95% under the conditions of reduction temperature 1423K, reduction time 3h, and aluminum excess 20%. The main components of reduction residue are CaO· Al203 and 12Ca0·7Alz03. The alumina leaching rate of calcium aluminate in residue is over 80%. High-whiteness aluminum hydroxide can be obtained by carbonation precipitation of the reduction slag leaching solution.IntroductionWith a density about half of water, lithium is with the lowest density of all solids, mere 0.5 g/cm3 at 20 °C [l]. Lithium is widely used in aerospace, aviation, nuclear-generated power and electric battery industry. Nowadays, over 90 % of the world's primary lithium is produced by molten salt electrolysis [2-4]. But the development of molten salt electrolysis will be effected by some factors: cost, environment, and so on. Vacuum thermal reduction may be used extensively in future because of its low-energy consumption, high-purity and short-cycle."

Jan 1, 2013

By S. Mondon

Hibi Smelter which is a Copper Smelter lining a blast furnace, produces 2,700 metric tons of anode copper per month. Generally, in a copper refinery, arsenic and antimony are considerably troublesome impurities. With regard to the elimination of antimony, Hibi Smelter has two handicaps described as follows. (1) Smelting under the slightly oxidizing atmosphere in the blast furnace. (2) Recycling the converter slag to the blast furnace after cooling. Therefore antimony and arsenic, mainly antimony, elimination tests, in which the alkaline flux was injected through the two tuyeres in the blowing stage, were carried out in the rotary anode furnace. Antimony and arsenic were respectively removed more than 90 96 from the molten copper, and their high eliminations are discussed by application of the transitory and permanent reaction model with the flux injection, which was presented by T. Lehner.

Jan 1, 1983

By Mingming Zhang, Mallikharjuna R. Bogala, Ramana G. Reddy

Steelmaking desulfurization slag samples were characterized using chemical, X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) methods. The objective of this work is to investigate the occurrence of sulfur and phosphorus components in the slag samples and to identify their origin and associations with the iron phases. Thermodynamic calculations results confirm the presence of phosphorus and sulfur components in the slag sample at high temperatures (1400 to 1800oC). The main constituents of slag include Ca3SiO5 (28.1%), MgO (9.31%), Ca3(PO4)2 (9.18%), CaS (8.39%) and CaO (5.68%). The major phosphorus and sulfur components of the slag are Ca3PO4 (99.2%) and CaS (79.3%) respectively. Characterization studies indicate the presence of microparticles of different sizes and shapes in the slag sample. Elemental analysis of these particles confirm the presence of major elements (O, Mg, Al, Si, S, Ca and Fe) in the slag sample.

Jan 1, 2015

By C. Dresen

This paper discussed the reaction kinetics of the reduction of industrial phosphate pellets for P4 production. In the reduction process of various phosphate ores, the following parameters were investigated: Diffusion of the phosphorus oxide and other gaseous products from the reaction mixture after having been reduced on the reductant (coke) surface. Influence of silica on reaction kinetics. Temperature influence. Influence of mineralogy and morphology (different ores). Particle size influence of silica and coke. Experiments were carried out in a vertical tube furnace with 2 ores, 2 types of silica and one type of coke. Selected experimental conditions simulated furnace conditions. The following conclusions could be made: Reaction rate increases with the addition of SiO2 into the pellet. The reaction rate increases above 1350°C (melting temperature of the slag). Mixing different ore types in the pellets leads to differences in reduction kinetics. Particle size of the coke particles influence reduction kinetics. The amount of slag formation is influenced by silica addition, coke size and temperature.

Jan 1, 2002

By John O. Burckle

For years, the measurement of fugitive emissions from the primary copper converter has defied all attempts based on inferential measurements, It has been concluded by virtually all investigators that the only dependable tech¬nique to measure these emissions would be to completely enclose an operating converter to permit the capture and measurement of all emissions. However, complete enclosure with a metal hood is difficult; many of the most serious fugitive emissions result during periods when the converter must be attended with crane-operated equipment. This approach would require either opening of the enclosure to permit the entry of large items of equipment or completely new methods for charging and tapping converters' The installation of the air curtain hooding system at ASARCO's Tacoma smelter has permitted a quantitative approach to the direct measurement of the fugitive for the first time. In this program, the fugitives captured by the air curtain were measured at a downstream sampling point in the exhaust side of the air curtain system during the various portions of the converter cycle. Emission factors were established for sulfur dioxide, filterable particulate (method 5), inhalable particulate, and selected trace elements.

Jan 1, 1983

By Jinxia Nie, Yunnen Chen, Dachao Zhang

"Rare earth resources are strategic and non-renewable resources. But disordered exploitation on rare earth metals leads to resources waste, environmental pollution and ecosystem destroyed. In this paper, soil collected from garden was cultured in thermostated incubator. Adding exogenous rare earth to the soil and the effects of recombination action of rare earth lanthanum, cerium and yttrium on soil enzymatic activities were studied. The results showed that single metal La and Ce can increase urease activity, but Y inhibits its. Coexist La/Y or La/Ce in soil inhibit the urease activity, coexist Y /Ce or coexist three metals promote its. Single metal La, Y and Ce can promote catalase activity, and that of coexist three metals. Pairwise coexist La, Y, Ce in soil inhibit catalase activity. With certain concentration of rare earth recombination action, urease activity in soil has been very significant direct proportion to ionic impulse, but catalase activity been insignificant inverse proportion to its.1. IntroductionThe increase of rare earth element content due to anthropogenic inputs frequently takes place in agro-industrial areas, leading to soil pollution episodes that may cause serious environmental problems because of their potential toxicity to microorganisms, plants, animals and human beings [ 1]. China is abundant in lanthanides resources. Rare earth metals are used in many frontier technologies such as photic devices, magnetic materials, and fine ceramics, and the amount of the rare earth metals used in these industries has been increasing. In addition to their use in industry, rare earth metals are more widely applied to cropland as microelement fertilizers due to their ability to promote growth and productivity of some crops [2]. As a result, more and more rare earth metals are moving into the ecosystems. While a permanent contamination of soils results in populations of micro-organisms with high resistance to rare earth metals, a short-term burden of contaminants at high concentrations could exert inhibitory effects on microbial carbon [3]. They accumulate in soils, bioaccumulate in crops, and enter the food chain, causing a potential problem of rare earth metals environmental pollution in China [4]. This contamination may also severely influence organisms and soil activities [5]."

Jan 1, 2011

By Johan Sundström

Anhydrous DyC13 was prepared by dehydration of DyCl3?6H20 in a fluidized bed using both batch- wise and continuous feeding. A gas mixture with varied composition of argon and HCl was used. The productivity was high, reaching values of 0.25 mol H20/m2-st during the reaction step 6- 1 and 0.062 mol H2O/m2.s during the reaction step 1-0. The product was free from hydrolytic compounds, such as DyOCI, if control of inlet gas composition versus temperature was achieved. From the results of various experiments, some relations between HCI-concentration and temperature in order to avoid hydrolysis have been deduced. The fluidization process efficiency decreases drastically after the dehydration has proceeded down to about 10 mol% of remaining water. Therefore, in a final treatment the last traces of water were removed by slowly purging gas through a packed bed. The water content could thereby be reduced to less than 1 mol%.

Jan 1, 1997

By N. S. Narayanan

Monazite, one of the major sources of rare earths, is normally opened by digestion with hot concentrated caustic soda solution. Caustic digestion dissolves phosphate and leaves a hydrated mixed metal oxides cake containing thorium, uranium and rare earths. By leaching this cake with hydrochloric acid at pH 3.0 to 3.2 bulk of the rare earths are preferentially removed and separated. The slurry left after removal of major portion of rare earths contains all the thorium and uranium present In the feed monazite. In addition this slurry also contains substantial quantities of rare earths. Solvent extraction tests were carried out to develop a process to separate rare earths, thorium and uranium present in the mixed chloride solution obtained by dissolving the above slurry in hydrochloric acid. Based on these tests a solvent extraction flow sheet was developed with di-2-ethyl hexyl phosphonic acid mono 2-ethyl hexyl ester as the extractant. The details of experimental work and results obtained are discussed and a flow sheet for processing monazite Incorporating the new process is suggested.

Jan 1, 1997

By W. D. Cho

Fast dissolution of nonmetallic inclusions such as alumina particles in molten slags has been required in secondary steelmaking -ladle and tundish - to minimize the amount and the size of nonmetallic inclusions in steel products. In the present work, the dissolution behavior of alumina particles in molten CaO-A12O3 and CaO-A12O3-SiO2 slags at the temperatures between 1450 and 1550°C have been investigated in terms of kinetics and mechanism. Alumina particles were added directly into the slags and the variation of the particle size with time was determined using optical and electron microscopies. The conventional types of slag for ladle and tundish were included in the dissolution study. The effects of Al2O3, Siq, CaF2 and MgO contents on the dissolution rate of alumina particles have also been determined. The diffusion boundary layer between alumina particle and bulk slag phase has been observed and analyzed using SEM and EDS. Based on the analysis of kinetic data and the boundary layer, the dissolution mechanism has been discussed.

Jan 1, 2002

By Kwan Soo Han

A thermodynamic model for predicting the distribution coefficients has been developed by taking into account the extraction mech-.ism and the chloride complexation when Sm, Eu, Gd, Tb, Dy and Ho for single component systems are extracted from acidic chloride solutions by di-2-ethylhexyl phosphoric acid and 2-ethylhexyl phosphonic acid mono-2-ethylhexyl ester in kerosene, respectively. The model equation includes two constants, of which one corresponds to the apparent extraction equilibrium constant and the other is due to the variation of the activity coefficients of organic species. These values are determined from a few experimental data by the curve fitting method Then, the distribution coefficients under untried conditions have been predicted from only the initial data by iterative calculations. Bromley's formulation is used to estimate the activity coefficients of aqueous species and the interaction parameters for some rare earth chlorides are reported in terms of molality and molarity using data from Spedding et al. The validity of this method has been confirmed by excellent agreement between the experimental and the predicted distribution coefficients.

Jan 1, 1989

By Hongbo Zhu, Jinhui Peng, Linqing Dai

"To optimize the process variables for making direct reduced iron (DRI) by microwave heating, the reduction temperature, reduction time and the ratio of coal to material were studied with the central composite design (CCD) and their interactions on the Metallization rate were also investigated. The predictive polynomial quadratic equations model was analyzed by ANOVA. Optimal conditions of making DRI can be concluded as follows: 28 min at 1139?, the ratio of coal to material is 20.95%. Under these conditions, the metallization rate is up to 97.06%.1. IntroductionThere are some technical problems in making direct reduced iron (DRI) or sponge iron using iron ore concentrates containing coal and lime. In reduction of the iron ore concentrates containing coal with microwave heating, the strength of pellets needn’t to be considered. It reduces the costs and improve quality of materials, but also eliminates the need for pellet preparation process, simplifying the process and achieving a cleaner production.Microwave energy is a clean energy, and has characteristic of selective heating. The speed of heating is also fast. It researched by Chen Jin that when the mole mass of C: O is 0.627 and the microwave power is 15KW, it only spends 15min from 15? to 1021.6? with 1 kg iron ore containing coal with microwave heating [1]. There are many factors affecting metallization rate. In order to find a suitable condition for reduction process, it is necessary to design a series of suitable experiments.Response surface methodology (RSM) is one of the relevant multivariate techniques which can deal with multivariant experimental design strategy, statistical modeling and process optimization [2–5]. It is used to examine the relationship between one or more response variables and a set of quantitative experimental variables or factors. This method is often employed after the identification of the vital controllable factors to find the factor settings that optimize the response. Designs of this type are usually chosen when a curvature in the response surface is suspected. The process optimization of the microwave reduced iron ore was seldom reported in literature. Hence the present work intends to assess the effects of variables such as reduction time, reduction temperature and the ratio of coal to identify the optimum conditions using a central composite design (CCD). The characteristic of product was assessed using scanning electron microscope (SEM)."

Jan 1, 2011

By Haotian Xue

A new process to extracted antimony directly from stibnite concentrate by reductive sulfur-fixation smelting in sodium molten salt has been presented. The influences of sodium salt content and composition, ferric oxide addition, temperature and time was investigated, respectively. The optimum conditions was determined as follows: W????: ??concentrate=40%, W??alt: ????concentrate =88.75%, WFe2O3 :Wconcentrate =55.13%, W??aCl: ????alt=40%, 1123K, 1h. Under above-mentioned optimum conditions, the average direct recovery ratio of antimony can reach 91.48%, and the main chemical composition of obtained crude antimony is Sb 94.31%, Fe 4.436%, Pb 0.502%, Au 0.0236%. In comparison to traditional antimony pyrometallurgical process, the smelting temperature of present process is reduced from 1423~1473K to 1123~1173K. During the smelting operation, SO2 emision can be avoided completely due to sulfur-fixation as FeS. Furthermore , S0 can be obtained when the molten slag is handled by water leaching with conditions of 323K, L/S=5/1, 2h.

Jan 1, 2014

By Jin Liu

In the early 1990?s, Inco successfully installed two new flash furnaces as part of their SO2abatement project to reduce SO2 emissions from the Copper Cliff Smelter by 60%. The flash furnace off-gas is cooled and cleaned through two new Monsanto Dynawave gas cleaning systems that replaced the traditional venturi scrubbing system. It was discovered that the flash furnace production capacity is often limited by the capacity of the gas cleaning system. The key task is to eliminate pressure drop from the system. The froth column is responsible for by far the largest pressure drop in the gas cleaning system. Initially, the column was fitted with 22 plates. In 1994, both #1 and #2 froth columns were modified by reducing the number of plates in each column from 22 to 18 and increasing the interplate spacing on lower plates. With increasing demand for more throughput in the flash furnaces, further modifications on the froth columns were made in 2005. This paper describes these modifications and results together with some fundamental analysis of the froth column characteristics.

Jan 1, 2006

By V. M. Lsoitko

Statistical methods of technological mineralogy are used to model processing flowsheets in order to improve ore dressing efficiencies. The procedure involves determining geological and mineralogical characteristics of ores, classifying ore types and metallurgical procedures, and developing computer programs to interpret essential mineralogical parameters from on-stream analysis data. The on-stream analysis data include magnetism, radioactivity, luminescence and assays. The data are interpreted by computer and appropriate adjustments are made automatically in the plant.

Jan 1, 1989

By Denise Corrêa de Oliveira

Common dry batteries use zinc as the negative electrode. Producers commonly use additives such as mercury to prevent corrosion and to increase the mechanical resistance of the zinc anode. Alkaline batteries also contain it, as an anti-corrosive agent. When mixed with the common municipal solid waste, heavy metals as zinc and mercury pollute soil and ground water supplies, moving to the food-chain and affecting human health. Due to these possible damages, this kind of waste must be properly disposed, or recycled. Thus, even in low amounts (ppm) in batteries, mercury has to be eliminated or, at least, its content should be reduced. This work presents the use of pyromettalurgical processes, to reduce mercury content and recover zinc. The tests involved batteries treatment at temperatures from 300° to 1000°C. Mercury is eliminated up to 650°C, and zinc is evaporated at higher temperature treatment. C

Jan 1, 2001

By Hoda Emami

In this study, a combined pyrometallurgical and hydrometallurgical technique has been designed and used to recover rare earth mixture elements (REE) and cobalt from a NdFeB magnetic waste. while addressing the cost of reagent and process facility. This process can be adjusted to different magnetic wastes regardless of their compositions. Prior to the leaching, the magnet scrap was pretreated by two rounds of roasting (750°C in air) and a mechanical grinding in between, to convert iron metal to ferric oxide. Subsequent leaching was performed using optimized conditions (pH, temperature and retention time) where the extraction ratio of REE to Fe III is the highest. After removing iron content from the leachate (pH ≈ 3), REE was precipitated selectively and purified further. The produced REE concentrate reaches 99% purity with 85% recovery in a single run. The cobalt oxide was isolated from the PLS as a by-product with 99.8% purity.