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By Fumiatsu Sato

In recent years, an increasing number of urban soil contamination cases have been found during redevelopment of former factory sites. Hydroclassification technique, separating heavily contaminated fine soil particles from contaminated sites, is one of the economical remediation techniques for contaminated soil by heavy metals, but the separated fine soil particles are generally landfilled because of the difficulty in removing strongly adsorbed heavy metals on them. In the previous study, the authors have investigated the mechanism and the optimum condition of chlorination-volatilization technique to eliminate heavy metals from inorganic waste and found it was needed to heat up around 1273K. In this paper, a new remediation technique for lead contaminated fine soil particles is proposed. This technique is composed of chlorination and subsequent warm water extraction. In the chlorination step, water-insoluble lead complex is chlorinated to be water-soluble lead chloride without volatilization, by heating the soils with MgCl2-CaCl2-KCl salt mixture at relatively low temperature. By subsequent warm water extraction, lead chloride is leached out. Effects of chlorination conditions, such as time, temperature, composition of the salt and added salt ratio, on lead behavior were investigated. It was proved that lead concentration could be reduced below Japanese environmental standard.

Jan 1, 2006

By Ronald L. Pariani

To date, significant advances have been made regarding the development and commercial implementation of full deposit stripping in the copper industry such as practiced at Copper Refineries, LTD in Townsville, Australia. The paper describes the history and current practice of Electrowinning (EW) plants which may be coupled with solvent extraction. The modular nature and degree of automation are described in relation to the various sizes of operations. Reference is made to the expansion capability of commercial equipment plus associated economics of the mechanical processes for producing full cathode deposits. It is recognized that the technology described may be adaptable to other nonferrous refining areas where feasible. The paper highlights the state of the art in mechanized stripping equipment as applied to current and planned SX-EW plants.

Jan 1, 1987

By Mao Chen, Baojun Zhao, Zhixiang Cui

Bottom blown oxygen copper smelting process, operated at high grade matte (up to 75 wt% Cu) with relatively low (2-3 wt%) Cu in slag, has been commercialized for more than five years at Dongying Fangyuan Nonferrous Metals CO., Ltd. Quenched slag and matte samples have been collected at different operating conditions while the slag temperature was measured by thermocouple. The samples were analysed by X-ray Fluorescence and Electron Probe X-ray Microanalysis. FactSage computational software was used to explain the observations of the industrial samples. The analyses show that the copper loss was closely related to the operation parameters. The Fe/SiO2 in slag and temperature determine the solid proportion, which significantly affects the physical entrained and also chemically dissolved copper in the slag. The present study will be useful in understanding the slag chemistry of bottom blown copper smelting furnace and in optimization of the operating conditions to lower Cu loss in the slag.

Jan 1, 2015

By Ryokichi Shimpo, Akio Fuwa

"In order to elucidate the present status of process-control technology, survey study has been made on the present process control schemes of representative copper smelting and converting processes in Japan. Conceptual control flow diagrams have been deduced and shown on respective functional reactors, i.e. drying, smelting, converting and fire-refining units, where the objective OUTPUT items are correlated to the INPUT variables through respective CAUSE-AND-EFFECT RELATIONSHIPSFuture view has been also discussed on several feasible and desirable improvement and refinement ~n measurements and control system for better copper smelting and converting operations.INTRODUCTIONIn other to seek for the better and efficient operation in copper smelting and converting process, survey study has been first conducted on the present process-control schemes of respective functional unit processes, i.e. drying, smelting, converting and refining unit processes, of representative copper production processes in Japan. Conceptual process flow chart of control scheme has been then deduced where output items are correlated to input items through the respective cause-and-effect relationships.After this survey study, future view has been discussed on the feasible and desirable improvement and refinement in the measurement and control system in these processes. Emphasis has been placed on the better and precise measurements of temperature, oxygen partial pressures in respective furnaces and end-point in converting and refining unit operations."

Jan 1, 1989

By Chikabumi Yamauchi, Mitsuru Tanahashi, Tsuyoshi Taniguchi, Nobuo Furuta, Toshiharu Fujisawa

"It is essential to clarify the equilibrium relations among nonmetallic inclusions of the Mn0-SiO2-CrOx system and molten stainless steel in order to control non-metallic inclusions formed by the deoxidation of stainless steel with silicon. In the present study, the phase equilibria of the MnO-SiO2-CrOx system were measured by conducting the following experiments under controlled oxygen partial pressure, Po2, at 1873 K:1) Phase equilibria of the MnO-Cr20 3 binary system were measured for Po2 = 2 x 10-6 ~2 x 102 Pa.2) Phase equilibria of the MnO-SiO2-CrOx ternary system were measured for Po2 = 2 X 10-6 Pa.Based on the results, the phase diagram of this ternary system was established under the condition of the Si-deoxidation process of stainless steel (Po2 = 2 x 10-6 Pa and T = 1873 K).IntroductionAt the deoxidation stage in steelmaking process, generally multiple deoxidizers participate in deoxidation reactions, and the composition of deoxidation products ""non-metallic inclusions"" greatly varies depending on deoxidizing efoments and their contents. In order to control non-metallic inclusions formed by the refining process of steel, it is essential to clarify the equilibrium relations among non-metallic inclusions and molten steel.Especially, during the refining process of stainless steel, nonmetallic inclusions in molten steel seem to- change as follows. After the oxidation refining, Mn-chromite is formed in molten steel as non-metallic inclusion. By the deoxidation with silicon addition (mainly less than 1 mass%), Mn-chromite inclusions are changed their compositions to Mn-silicate. Segawa et al.[l] have reported the effect of amount of silicon addition on composition and mass ratio· of non-metallic inclusions during the Sideoxidation process of 18Cr-8Ni stainless steel at 1873 K, as shown in Figuri; L At higher silicon content than 0.5 mass%, only Mn-silicate was identified as non-metallic inclusion. On the other hand, at lower silicon content, both of Mn-chromite (MnO Cr2O 3) and Mn-silicate were identified. However, the thermodynamic and the kinetic analyses of the above-mentioned Sicdeoxidation process have not been made due to lack in the thermodynamic data for the non-metallic inclusions· of the MnO-SiO2-CrOx system, such as the phase diagrams, the activities of the components, and the free energy of intermediate compounds. In relation to the phase diagram of this system, those of the MnO-SiO2 [2] and the SiO2-Cr2O 3 [3] binary systems have been only reported"

Jan 1, 2000

By Robert J. Stevenson

The chemical variation of central North American lignite fly ash can be compared using the major and minor oxide analyses and the distribution pattern of the inter-grain chemistries of the individual fly ash have been used to illustrate the variations in bulk ,sample and individual grain chemistry. This information documents the chemical variability of the lignite fly ashes by geographic region. There is a direct relationship between grains rich in SiOa and AlaO, and in the NazO content of the grains in lignite derived fly ashes. There is also a direct relationship between grains rich in Ca0 and the MgO and SO, content of the grains in lignite derived fly ashes,. These variations are shown using CaO-SiO2-Al2O3 and CaO-Na2O-MgO ternary diagrams.

Jan 1, 1992

By Shuichiro Okada

Various efforts to reduce energy consumption and smelting cost are made at Tamano Smelter. Production of anode copper has been increased by about 30 % and energy requirement has been decreased about 50 % respectively. Challenges toward more higher goal are being continued. Details about the following are described in this paper. 1 Waste heat recovery Steam recovery at up-take of FSFE Heat recovery from waste gas of anode furnaces 2 Application of tonnage oxygen 3 Application of pulverized carbonaceous fuels to the flash smelting furnace with furnace electrodes ( FSFE ) 4 Application of computer control system to copper smelting 5 Improvement of the fugitive gas collecting system 6 Improvement of the mechanical tuyere puncher for the converter furnace

Jan 1, 1983

By Z. Zhang, Cuihuan Huang, Zongshu Zou, Nan Wang, Xueqian Xin

"Vitrification is considered as an attractive procedure for municipal solid waste incineration ash, which can realize the volume reduction and innocent treatment of incineration ash, as well as reuse of bottom ash. The main oxide components of molten ash slag are CaO, Al2O3, SiO2, Fe2O3, MgO, and Na2O, accounting for more than 90% of the total mass. The phase relations and thermodynamic properties of the CaO-Al2O3-SiO2-FeOx-MgO-Na2O oxide system is highly required, and is of great scientific significance for optimization of vitrification processing and sustainable resource utilization of melting slag. A study on the equilibria phase relations of CaO-SiO2-MgO-FeOx system was done by using CALPHAD method based on FactSage in this paper. The modeling parameters for the thermodynamic properties of liquid phase in CaO-SiO2-MgO-FeOx system were established and the equilibrium phase relations of MgO-SiO2-FeOx and CaO-SiO2-FeOx-MgO systems were calculated for different temperatures and oxygen partial pressures.IntroductionThe main oxide components of vitrified bottom ash slag are CaO, Al2O3, SiO2, Fe2O3, MgO, and Na2O, accounting for more than 90% of the bottom ash by weight [1]. During slag processing and modification, the knowledge of thermodynamic properties and liquidus temperature in the related slag system is highly required [2-5], which is not yet available. Through literature survey [6-9], it is clear that the systematic information on the concerned complex slag system is scarce. Most binary subsystems except FeOx-Na2O have been investigated well. Among ternary subsystems, few phase relations of the Na2O-MgO-SiO2 ternary system are available. For the phase relations of the system Na2O-MgO-Al2O3, all the studies are focused on the Al2O3-rich region. Investigation on the CaO-Al2O3-FeOx system is limited to Fe2O3-containing system with relatively higher oxygen potential. Most quaternary systems are not studied well except the CaO-MgO-Al2O3-SiO2 system, mainly due to their metallurgical importance. Figure 1 demonstrates the research status of the vitrified bottom ash slag with almost zero effort [10]. The effort here is defined based on the published literature by considering the number of publications, the investigated composition ranges, and the research details. So far the engineers in the field have to make assumptions of the thermodynamic properties of the simplified oxide system, without taking into consideration the interactions of the different oxide components, which hinders the development of the slag valorization and utilization. In order to provide thermodynamic properties for the application of the vitrified bottom ash, the six-component oxide system (CaO-MgO-Al2O3-SiO2-FeOx-Na2O) will be investigated through both experimental approach and computer modeling."

Jan 1, 2011

By Gökhan Demirci, Ishak Karakaya

"Energy consumption in electrolytic magnesium cells is well above the theoretical values. However, the mechanism of the back reaction, the main cause of the current losses, has not been fully understood yet. Magnesium dissolution into the melt is generally regarded as the limiting step for the back reaction. Accordingly, present cell designs are made with priority given to fast magnesium removal from the cell. However, experimental data and modeling results in this study indicate that the limiting step for the back reaction between magnesium and chlorine is the chlorine dissolution into the electrolyte when physical contact between electrolysis products was eliminated. Effects of chlorine bubbles on the current efficiency and the cell potential were investigated. Results show that the extent of back reaction is proportional to the chlorine surface area in contact with the electrolyte per unit time, and the cell potential increases with the amount of chlorine bubbles inside the electrolyte.1. IntroductionMagnesium is less dense than the electrolyte in electrolytic magnesium production. Therefore, both electrode products, magnesium and the chlorine gas, move upwards inside the molten salt electrolyte during electrolysis. The upward motion of electrode products promotes the most important current loss mechanism, the ""back reaction"". Separation of the highly reactive species; liquid magnesium and the chlorine gas in the cell, to prevent their recombination is one of the main concerns in cell designs. The employment of large inter-electrode distance or a separation wall in early cell designs; decreased the extent of recombination, but increased the cell voltage and energy consumption. Recent cell designs, on the other hand, make use of lifting action of chlorine gas [1,2] by utilizing smaller inter electrode distances to separate the magnesium and chlorine gas faster. Although energy consumption was reduced, but more physical interactions between electrode products make electrolytic magnesium cells still highly inefficient when energy consumptions are compared with the theoretical values. Today, the most efficient industrial cells utilizing high purity feed operate at 10.5-11.5 kWh kg-1 Mg [3-5] and it is considerably higher than the theoretically attainable value of about 6.0 kWh kg-1 [6]. This large gap demonstrates the necessity of more research on physics and chemistry of magnesium cell electrolysis."

Jan 1, 2011

By Guo Xian Jian

In this paper, an alternative process to recover the value metals from polymetallic gold ore by FeCh leaching was proposed. In the process, gold was recovered by direct cyanidation from the leaching residue, the isolative electrolyte in chloride solution was selected to recover lead, the cementation with copper powder was used to recover silver and the solvent extracting was applied to recover copper and zinc. The total recovery of gold, lead, copper, silver and zinc in the process is 90.8%,96.05%,84.3%,81.98% and 54% to the bullion of gold, lead and silver and sulfate of copper and zinc, respectively. The process conditions selected for FeCh leaching are the temperature of 104°C, leaching time of 6 hours, Fe3+ content of 140 g/l and stoichiometry of FeCl3.

Jan 1, 1996

By Lei Wang, Xiancong Zhao, Hongxu Li, Lifeng Zhang

Recovery of Fe from red mud has been studied using statistically designed experiments. The effects of three factors, namely: reduction temperature, reduction time and proportion of additive on recovery of Fe have been investigated. Experiments have been carried out using orthogonal central composite design and factorial design methods. A model has been obtained through variance analysis at 92.5% confidence level.

Jan 1, 2015

By Jie Li, Shu Yang, Zhongliang Tian, Xun Hu, Yanqing Lai, Shaolong Ye

The electrolyte with high solubility for Sc2O3 is very important to realize the preparation of Al-Sc master alloy by the molten salt electrolysis. The solubility of Sc2O3 in K3AlF6- Na3AlF6-AlF3 melts is determined with an isothermal saturation method. The effects of KR (ratio of K3AlF6 to K3AlF6+Na3AlF6), the concentration of Al2O3 and the temperature on the solubility of Sc2O3 are also investigated. The results indicate that the solubility of Sc2O3 in K3AlF6-Na3AlF6-AlF3 melts increases and then decreases with KR increasing. The solubility of Sc2O3 is 8.698 wt.% in (K3AlF6-Na3AlF6)(KR25%)-18 wt.%AlF3 melts at 940℃. The effect of temperature on the solubility is little, and the values are 8.575 wt.% and 8.762 wt.% respectively when the temperatures are 930℃ and 960℃. The solubility decreases from 8.809 wt.% to 7.058 wt.% as the concentration of Al2O3 increases from 1.5 wt.% to 5.0 wt.% at 950℃.

Jan 1, 2015

By Terry C. Cheng

The Akita Hematite Process is currently the only hydrometallurgical iron removal process producing saleable iron by-products in the zinc industry. In this study, McGill University and Akita Zinc Co. have worked together into elucidating the basic precipitation chemistry of the process from the standpoints of hematite product quality and prevailing precipitation kinetics. This work determined that hematite is produced under the applied conditions (T = 195?200oC,PO2 = 103?414 kPa) directly without prior formation of basic ferric sulphate and transformation of the latter to hematite as thought originally. The rate-limiting step responsible for the long retention time (~180 min) was found to be either the re-dissolution of ferrous sulphate according to the batch reactor studies, or the slow hydrolysis of the remaining ferric sulphate according to the continuous reactor studies. Another interesting contrast between the batch and continuous reactor data was the degree of sulphur contamination (1.5 vs. 3.8%, respectively) and the specific surface area of the product (10 vs. 30 m2/g, respectively). These differences in addition to the co-precipitation of SO4-containing phases such as jarosites, alunite, and anhydrite were attributed to the significantly higher supersaturation level prevailing in the industrial continuous autoclaves that yields highly aggregated sub-micron hematite crystallites contaminated with chemisorbed sulphate ions.

Jan 1, 2003

By Ruth Marlene Campomanes Santana, Michel Tieccher, Marcondes Mafacioli Pacheco, Juliano Urach

"IntroductionThe gaseous emissions of fuel burning by mobile sources are responsible for incidence and increase of many lung and cardiovascular diseases (Braga et al., 2007). These implications can watch in morbity as much as mortality, even when the levels of pollution are considerate restrained or lower. (Leite et al., 2002).Sample of mobile sources exhausts contain not only particles directly shaped by burning, but also secondary particles that results of reaction between other compounds (Burtscher, 2004).One of the principal pollutants produced by combustion process with major toxicity and raiser of adverse effects to health is the particulate material. In its constitution there are fine and ultrafine particles that can to extend deep portion of breath system, break epithelial barrier and reach the interstitial of lungs and then, to unleash inflammatory process (Arbex, 2004).The Particulate Material is employed to define a mixture of solid particles and liquid drops suspense in atmosphere. Queiroz et al. (2007) declare that this material can be divided in two types separated by size interval that together, represent the major class of disperse particles: the fine particles type of 2,5 µm de (breath particulate) and the type of earthliness particles, major than 2,5 µm to 10 µm (inhale particle). The difference of size between the particles influences on the physics and chemistry properties. They affirm that exist correlation between size of particle and heavy metals; how many lower was the dimension of particulate materials, major is the concentration of heavy metals.The inhale particulate (MP10) that is object of present study can exhibit in your composition sulfates, nitrates, amoniacal, marine salt (NaCl), soil elements (Al, Ca, Fe, Si, Ti), metals (Cd, Cr, Cu, Ni, Pb, V, Zn) and water (Queiroz et al., 2007).Recent studies have exhibit strong relation between daily levels of particulate material inhale (MP10) with diameter until 10 µm and others pollutants and one infinity of effects to health that go since total mortality of population, sicken for specific causes until congenital bad formation or even difficult win weight by the fern during gestation (Gouveia et al., 2006)."

Jan 1, 2008

By Rod Samuels, Rupert Allen, Thomas Harper

"Viceroy Resource Corporation of Vancouver, B.C., has recently developed and brought into production the Brewery Creek Mine, an open-pit heap leach gold mine, located 55km east of Dawson City in Yukon, Canada. Mineable reserves are 15.2 million tonnes of ore grading 1.45 grams/tonne, containing 22 tonnes (707,315 oz) of gold. Ore processing employs the heap leach technology using run-of-mine ore. Highlights of 1996 activity included construction of a 158,000 m2 of leach pad, placing 1.9 million tonnes of ore at a grade of 1. 46 gpt to the leach pad, construction and successful commissioning of the ADR plant, and pouring of the first gold bar on November 15th.Permitting of this mine has drawn significant attention because of the innovated heap leach technology; although this technology has been proven in other jurisdictions, it has not been used at such extreme northern sites where winter temperatures routinely reach -45°C for extended periods.ABSTRACT ONLY"

Jan 1, 1997

By Musa Karakus

Zirconia-based refractorics arc finding increasing use for specialized applications in steelmaking technology, making optimization of their resistance to corrosion by steelmaking slags more important. Samples of calcia- and magnesia-stabilized zirconia refractories have been exposed to slags in the CaO - FeO - SiO, system at 155WC for the purposes of measuring corrosion rates. Examination by SEM/EDX and cathodoluminescence of the mineralogy of the attacked specimens reveals important clues about the mechanism of attack.

Jan 1, 1992

By He Zhi-jun, Ning Zhe, Pang Qing-hai, Zhang Jun-hong, Zhan Wen-long

In this study, Raman spectroscopy was utilized to investigate the evolution of char structure in pulverized coal (PC) during microwave irradiation. The results indicated that though microwave treatment was carried out at low powers of 132W or 264W, significant variation in char structure was still observed. Char structure turned out to be more irregular firstly under microwave irradiation. However, char structure of superior regularity was obtained with the extension of irradiation time. It can be conclude that short time microwave treatment may facilitate the chemical activity of coal, while long time microwave irradiation on PC may deteriorate its combustion or pyrolysis property.

Jan 1, 2016

By M. D. Bishop

Loss of organic solvent extraction circuits occurs through several accepted methods. Losses are commonly attributed to entrainment of the plant organic and evaporative loss of diluent. Evaporative losses of diluent have been estimated using various models or by considering all losses over and above entrainment to be due to evaporation. Other possible loss mechanisms are discussed and data on losses during weather conditions are presented. Accurate estimation of evaporative loss is vitally important to the industry due to both cost factors and environmental concerns. Data for and description of the Diffusive Flux Model are presented as an improved-method of estimating evaporative losses:

Jan 1, 1999

By M. C. Ruiz

The conventional pyrometallurgical methods to treat copper sulfide concentrates include generally, one or more oxidizing steps where the formation of SO2 gas can not be prevented. From the economical point of view and the nature of some of the processes in which SO2 is produced, its complete capture is not feasible; therefore an important fraction is released to the atmosphere as fugitive emissions. In this research, the reduction of chalcocite was studied in the presence of lime as an alternative method, which overcomes the pollution problems related to SO2 emissions. The effect of temperature, time, concentration of carbon and CaO on the reduction rate were studied. Among these variables, temperature affects most the reduction rate. Conversions over 95 % can be obtained in less that 20 minutes at temperatures over 1000 ° C. The measured partial pressures of the gaseous components indicated that the chalcocite reduction proceeded through the gaseous intermediate species CO, C02, and the overall kinetics was controlled by the Boudouard reaction. The kinetic model In(1-X)= kt fits well the experimental data. Apparent activation energy of 3 14 kJ/mol was calculated for the temperature range of 900 0C-1050 °C.

Jan 1, 1999

By M. Benavides

An experimental study is carried out With sulphide ore obtained from Bailadores-Venezuela as well as artificial concentrates. Concentrates of the minerals from froth flotation are fused to study equilibrium between the matte and slag phases. The first part of the work deals with obtaining a concentrate by flotation experiments with collective and selective reagents, with acceptable metallurgical recovery, studying the influence of different parameters in the process. The second part gives the results of the experimental investigation. on thermodynamic equilibrium in smelting which facilitates knowledge of the elemental processes, giving bases for the possibilities of reducing the loss of metal in slag.

Jan 1, 1983