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By Yong Hack Lee

Electric Arc Furnace (EAF) dust is generated when scraps are treated in the electric arc furnace and usually classified as hazardous industrial waste in most countries. EAF dust usually contains 15 to 25% of zinc and 3% of lead. It is usually treated in rotary kiln (Waelz process) or landfilled after a solidification and stabilization treatment. Numerous methods have been proposed as the EAF dust treatment technology, but few of them are in operation as a commercial scale except the Waelz process. Korea Zinc performed a plant test in which 600 tons of EAF dust was treated using TSL (Top Submerged Lance) technology. The TSL technology is a low cost, proven technology for processing zinc-bearing residues. The EAF dust was first de-chlorinated and fed to the TSL furnace. Finally, clean slag satisfying toxicity criteria was generated and valuable metals such as zinc and lead were recovered as fume oxide. The fume oxide was de-halogenated by sodium carbonate and sent to zinc refinery to recover zinc and lead. The recovery of zinc and lead was 90% and 93%, respectively. Most of the dioxin in the EAF dust was discomposed so dioxin less than the Korean regulation limit was detected in the offgas, which proves that the TSL technology is the best solution to treat EAF dust.

Jan 1, 2006

By W. G. Davenport

Chapter 4 examined Inco (oxygen) flash smelting of pure chalcopyrite concentrate. It showed that the oxygen and flux requirements for auto thermal smelting are readily determined by a matrix calculation. This chapter extends this matrix approach by applying it to a multi-mineral concentrate.

Jan 1, 2001

By Kyle S. Brinkman, Kenneth L. Reifsnider, Fazle Rabbi

"Mixed ionic and electronic conducting (MIEC) ceramic membranes are HeteroFoaM's which play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC), oxygen separation and permeation membranes, partial oxidization membrane reactors for natural gas processing, and high temperature electrolysis cells. Dual phase oxygen membranes consisting of an ionic conducting phase Ceo.sGdo.z02 (CGO) and an electronic conductive phase C0Fe204 (CFO) were fabricated and characterized by structural (XRD), microstructural (SEM-EDS) and broadband dielectric measurement techniques. In-situ measurements of the dielectric properties of working oxygen separation membranes are presented which indicate that the material's dielectric behavior can be an indicator for MIECperformance.IntroductionCeramic membranes which transport oxygen ions play an essential role in a number of energy conversion related systems including the solid oxide fuel cell (SOFC) [l ], oxygen separation and permeation membranes in the commercial and nuclear arena [2, 3], partial oxidization membrane reactors for natural gas processing [4], and high temperature electrolysis cells [5]. For the electrolyte functions, the membranes must transport oxygen ions only. On the other hand, permeation membranes, typically used in combustion devices to support oxy-fuel combustion or for partial oxidation reactions involving the production of synthesis gases, require mixed oxygen ion and electronic conduction (MIEC). Traditionally the tailoring of the ratio of ionic conductivity to the materials electronic conductivity, measured as the transference number, has been accomplished by the introduction of aliovalent doping elements creating point defects in the material facilitating the diffusion of charged species. However, several decades of research have not yet produced single phase materials which possess the concomitant ionic and electronic conductivity required for use in membrane separation applications. It is clear that novel ""dual phase"" heterogeneous materials will be required and that the surface reactions of these materials will be of particular importance as the industry moves toward thin films membranes [6]."

Jan 1, 2013

By Daniel Chen, Jewel Andrew Gomes, Venkata Palla, Sadia Afrin Jame, David Cocke, Paul Bemazzani

"Textile industries use various kinds of chemicals including dyestuffs and pigments during dyeing and finishing processes. The effluent from these processes includes suspended particles, strong color, high pH and high chemical oxygen demand (COD) that are extremely toxic and make environmental hazard. Although physical, chemical, photochemical, and biological methods are available for treating such wastewater, the electrochemical technique, electrocoagulation (EC), has emerged as an efficient, simple, and cost-effective technology in the last few decades. In this study we present the applicability of EC technique for removing dye, such as direct red dye using iron electrodes, and the optimized conditions such as dye concentration, current density and pH. The degradation of dye molecules was investigated using UV-visible spectroscopy. The EC-floe was also characterized using SEM/EDS, XRD and FTIR.IntroductionWastewaters generated by textile industries contain large amounts of toxic aromatic compounds, especially azo dyes. Azo dyes and their degradation products, such as aromatic amines, are highly carcinogenic. These effluents are also responsible for causing high levels of color. The colored wastewater released into the environment is also a source for disruption of aquatic life and aesthetic pollution as well [1].In most textile industries, dyeing and finishing are the two important processes which are generally applied. These two common processes generate significant amount of wastewater, which may contain, suspended particles, high pH, strong color and high chemical oxygen demand (COD) concentration [2]. Low pH and high temperature are other polluting factors from the waste water. Textile industries make use of about 10,000 dyes and pigments [3]. Disposal of these colored wastewaters poses a major problem for the industries as well as a threat to the environment. In textile industries, because of the low efficiency (60-90%) of dye fixing on textile fibers, substantial amounts of unfixed dyes are released in waste waters. The conventional method for treatment of textile wastewater was a combination of biological, physical and chemical methods [2]."

Jan 1, 2011

By Toshiyuki Hiranami, Keizou Uematsu

"AbstractionSpray freeze drying method was proposed to fabricate ·ceramic: powder granules for high performance ceramics. Obtained granules and their green compact were characterized by SEM and immersion liquid technique. Granules have a spherical shape of about l 00 µ m in diameter, ·and no binder segregation was found with the immersion liquid technique. The granule had sufficient strength for usual handling, while the strength was much lower than that of granules prepared by conventional spray-drying. Unlike the conventional green compacts, granule interfaces were not observed in the green body made with the spray-freeze dried granules.IntroductionIt was well kn9wn that spray-dried granules have binder segregation layer on their surfaces. The trace of this segregation layer survives in the later processes i.e. compaction and firing, and behaves as fracture origins in the sintered bodies. The origin of this problem is solvent drying process from slurry droplet surface in spray drying system. As alternative method we propose a freeze drying process for granule preparation, in which solvent is remove by sublimation though the process, binder segregation can be prevent.In this study, we applied spray freeze drying method to fabricate alumina powder granule, and characterized the obtained granules, and their green compacts and sintered bodies.Experimental procedure.Alumina powders and additives aqueous solution were mixed for 24 hours using a ball mill to· prepare the slurry for spray freeze drying. .The solid loading of the slurry was 30vo1%. Deflocculant (PAA-NH4 type) was added 0.5mass%, and the binder (PVA). 1.0, 2.0 or 3.0mass% of alumina. Obtained slurries were sprayed into liquid nitrogen to make frozen granules. The granules were freeze dried.For the characterization of the granules, immersion, liquid technique observation and single granule strength test were carried out. Strength of individual granule wa5 measured using micro compression testing machine (MCTM, SHIMADZU). Granule strength was calculated from following equation."

Jan 1, 2000

By Xingye Guo, Yeon-Gil Jung, James Knapp, Zhe Lu, Jing Zhang, Li Li

La2Zr2O7 is a promising thermal barrier coating material due to its low thermal conductivity and superior high temperature stability. In this work, Bilayer La2Zr2O7 and conventional 8 wt% yttria stabilized zirconia (8YSZ) coatings were deposited using plasma spray technique. Both singlelayer La2Zr2O7 and double-layer 8YSZ/La2Zr2O7 coating architectures were designed. Thermal cycling and thermal shock tests were used to evaluate coatings’ thermomechanical properties. All La2Zr2O7 coats were delaminated in the furnace cycle test in less than 20 cycles. This is because residual thermal stresses accumulated during thermal cycling. In the jet engine thermal shock (JETS) tests, the SCL La2Zr2O7 and DCL dense 8YSZ/La2Zr2O7 coatings were fully delaminated. In contrast, the DCL porous 8YSZ/La2Zr2O7 coating sample only partially delaminated on the edge. This is because of the porous 8YSZ layer provides strain compliance. The findings will help to propose efficient thermal barrier coating systems.

Jan 1, 2016

By W. G. Davenport

Chapter 6 examined autotherrnal smelting of pure chalcopyrite concentrate with 50 mass% O2-50 mass% N2 blast. It showed that production of 1500 K products with this blast requires: 181 kg of pure oxygen 337 kg of air per tonne, of concentrate. It also showed that the grade of matte produced with this blast is 58% Cu. This chapter re-examines autotherrnal smelting by asking: (A) WHAT COMPOSITION BLAST (MASS% 02 -MASS% N2), 298 K, WILL AUTOTHERMALL Y PRODUCE 65% Cu MATTE 1500 K FROM PURE CHALCOPYRITE CONCENTRATE? (B) HOW MUCH PURE OXYGEN AND AIR WILL BE NEEDED? These are important questions for flash? smelting because furnace operators usually want to send specific composition matte to converting. This chapter shows how a specified matte can be produced autotherrnally with 298 K oxygen-air blast. Later chapters show how it can be done with hot blast, hydrocarbon combustion, different concentrates etc.

Jan 1, 2001

By Xinghui Meng

The recovery of platinum and palladium from automotive catalysts has been investigated by leaching in iodide solutions with oxidants including oxygen and iodine in an autoclave. An ammonium salt was presented in a neutral leaching solution as a key leaching reagent to achieve high recoveries of the platinum group metals (PGM). The effect of temperature, and concentrations of oxidants and of ammonium salt on the recovery of PGM was examined. Under the experimental conditions studied, the recovery of platinum and palladium was found to be greater than 95%. An economical assessment of this process has also been examined and discussed.

Jan 1, 1995

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 J. E. Dutrizac

The behaviour of the lanthanide elements during the precipitation of sodium and potassium jarosites at 98oC from sulphate media was systematically investigated. The lower atomic weight lanthanide elements (La to Gd) are characterized by the limited solubility of their alkali-lanthanide sulphates, such as NaNd(SO4)2?H2O, which commonly contaminate the jarosite precipitates. Hence, single phase jarosite-type compounds were precipitated only from solutions containing <0.4 g/L of the La to Sm lanthanides. The sulphates of the heavier atomic weight lanthanide elements (Tb to Lu) have significantly higher solubilities such that solutions containing up to 10 g/L of the individual lanthanides could be investigated without the precipitation of alkali-lanthanide sulphate species. Even at the highest lanthanide concentrations, however, none of the jarosite precipitates incorporated more than 0.3 wt% of any of the lanthanide elements. Comparable levels of lanthanide incorporation were noted in both Na-jarosite and K-jarosite. Although the mass of the jarosite precipitate increased with increasing ferric sulphate concentration or with increasing pH, the extent of lanthanide incorporation was not significantly affected. Clearly, the trivalent lanthanide elements do not substitute extensively for trivalent iron in the jarosite structure. This behaviour likely reflects the significantly lower hydrolyzability and larger size of the trivalent lanthanide ions relative to ferric ions.

Jan 1, 2003

By S. N. Ashrafizadeh

Nowadays, hard carbides have found various industrial application in the manufacture of cutting and drilling tools as well as metal forming devices. About 60% of the world tungsten production is consumed in the manufacture of hard carbide pieces. Regarding the high economic value of hard carbide components, i.e., Ni, Co, TaC, TiC, and WC, their recovery from scrap species is attracting much interest. In the current research, the cobalt and tungsten content were recovered from scrap cemented carbide pieces through the application of high voltage electrolysis in nitric acid media. By this method, cobalt and tungsten were initially recovered as cobalt nitrate and tungstic acid, respectively. The precipitate of tungstic acid was calcined at 800ºC after being washed twice with distilled water. A pure tungstic oxide was obtained. The effects of current density, electrolyte concentration, speed of agitation, and the surface area of the anode on the efficiency of the electrolysis process were investigated. The optimum conditions of current density of 1500 A/m2, an acid concentration of 1.5 M, and a cell temperature in the vicinity of 60 to 80ºC were obtained. At the optimum conditions, an acceptable rate of collapse for the anodic carbide pieces of about 3.1 g/h was achieved, which remained constant up to the completion of the recovery process without any passivation .

Jan 1, 2003

By Fathi Habashi

Solid gas reactions of metallurgical importance can be classified into three groups: Physical processes, e.g., drying and sublimation Chemical processes which may be an addition or a thermal decomposition reaction Electrochemical processes which may be addition, oxidation-reduction, or displacement reactions. Examples are given and the role of the boundary layer is emphasized.

Jan 1, 1996

Pyrometallurgical reactors constitute a key processing component in the total primary and secondary resource cycle, being involved both in primary smelting, converting and extraction, as well as the reprocessing of scrap, from aluminum cans to end-of-life automobiles. To effectively control the overall resource cycle, one needs to take a systems modeling approach of the whole cycle, seeking to also understand the dynamic process behavior of the individual components of the cycle, and then especially the part that contributes most to the chemical conversion, namely the pyrometallurgical reactor. This paper highlights the role of pyrometallurgical thermodynamics, in the whole resource cycle and specifically places equilibrium thermochemistry in the context of process dynamics where large variable inventories are recycled or maintained within the system. This paper will therefore review the semi-empirical dynamic modeling tools, which are used to model complex systems with the specific goal of developing dynamic predictive models, which also include slag-alloy chemistry, towards controlling the recycling in a feed forward manner. To illustrate the primary processing side, high carbon ferrochrome will be presented as a brief case study. It also will show how the distributed nature of the chemistry of melts in the case of primary extraction, and secondary materials such as recycled end-of-Iife vehicles, have a significant impact on the process outcomes and model predictions. It is therefore argued that the fundamental thermodynamics and kinetics in metallurgical reactors playa final crucial role in modeling the closed material cycle, but only when it is used in conjunction with process systems theory based on reconciled data for parameter estimation and model calibration.

Jan 1, 2003

By Marcelo Jimenez Bustos

The Chagres Smelter was the first in Chile to follow environmental regulations to control sulfur dioxide emissions. Because of this, the operation and development plans have had to incorporate environmental planning as part of its policies for almost three decades. The present article shows the development of the environmental standards applied to its operations, investments and operational improvements carried out to meet the regulations and improve competitiveness. Results to-date and future plans are outlined, as well as their impact on operations and the environment.

Jan 1, 1993

By Eduard Ouerra, Nuo Jin

"The use of polytetrafluoroethylene, PTFE, as a solid sorbent for elemental sulfur during pressure oxidation of chalcopyrite was investigated. The effects of agitation, PTFE particle size and lingin sulfonate addition were evaluated using leaching conditions that were otherwise similar to those employed in the CESL process. The effects of these factors and their interactions on chalcopyrite oxidation are explained in terms of interfacial forces and solid-solid interactions. Using relatively fine PTFE powder with vigorous agitation resulted in about 100% copper extraction in less than 90 minutes without the need for grinding of the flotation concentrate.IntroductionThe extraction of copper from sulfide ores has always been dominated by the conventional pyrometallurgical smelting process. Though much effort has been made to develop various hydrometallurgical processing routes, smelting remains as the dominant process, treating approximately 80% of the chalcopyrite concentrates worldwide [1]. However, some of recently emerged techniques for treating chalcopyrite through hydrometallurgical routes are showing results that are competitive with smelting in terms of economical feasibility. Representative methods include: Activox Process, CESL Process, Anglo/UBC Process, High Temperature Pressure Oxidation, and Bio-Oxidation. Among these, the CESL processes operate at a medium temperature range (typically 140-150GC) and oxygen pressure of 100 psi, with chloride as a catalyst, and reportedly achieve copper extractions of about 95% with a light regrinding of flotation concentrate to a p95 of 45 ìðé [2]. In spite of this satisfactory extraction result, the leach residues contain significant amounts of conglomerates which contain a small amount of unreacted concentrate [2], The conglomerations are formed because the elemental sulfur generated is liquid and sticky (melting point of sulfur being 119°C), and has a tendency to wet the sulfide mineral surface, a fact which inhibits the oxidation of the minerals. The overall process chemistry of the CESL process may be summarized as follows [3]:"

Jan 1, 2012

By W. Marnette

Norddeutsche Affinerie is the largest West European copper producer with an annual output of more than 350,000 tonnes of refined copper, about half of which is produced from copper concentrates. However, in addition to concentrates, Norddeutsche Affinerie processes secondary raw materials and recycling materials which contain a combination of copper and lead. These materials were previously treated in blast furnaces, a technology which has meanwhile been superseded at NA by the electric furnace process, primarily owing to the necessity of complying with the increasingly stringent requirements for environmental protection.

Jan 1, 1994

By Majid Sarkari, Hossein Atashi, Farhad Fazlollahi

"The aim of this research work was to prepare the efficient catalyst to purify pollutant output gases such as SO2 , NO2 and CO. This catalyst, lanthanum cobaltat (LaCo03) was prepared by the proper method in the analysis laboratory of Tabriz Oil .The first materials were chosen through calcination operation and temperatures of operation related to the Tamman temperature, therefore the basis for the first material of catalyst was nitrate and aqueous and since we had no availability to lanthanum nitrate, lanthanum oxide was used to prepare the nitrate one. Before all else, the first materials of catalyst were mixed together with the equal mole proportions and then, at the lower and upper temperatures of Tanunan temperature, calcination operation was carried out. To determine the molecular structure, the XRD analysis was utilized and specified that prepared lanthanum cobaltat was sixth aqueous and had the crystal structure type Triclinic.IntroductionLaCo03 has presented a vast interest because of its special electrical, magnetic and catalytic properties [1-4]. The catalyst LaCo03 can be prepared by means of several methods such as spray drying, freeze drying and also co-precipitation [5-12]. Some methods including hydrothermal, sol gel and citrate [13] This material usually has been synthesized by ceramic method and certainly the high temperature for the calcination operation. [14]. Lanthanum catalysts have been researched because of having such an active state [15]. One of the unique properties of this catalyst is the simultaneous conversion of pollutant elements. Nowadays CO oxidation has important applications in environment protection, such as indoor air cleaning and automotive exhaust treatment. LaCoO3 is one of the most important catalysts for CO oxidation."

Jan 1, 2013

By Ying-Chu Hoh

The extraction of cerium(IV) by valence change with two-phase electrolysis was studied experimentally. The results show that the electro-oxidation extraction depends mainly on the distribution of the solute between the two phases, the reaction on the electrode surface and the diffusion of the reactant and product between the electrode and aqueous interphases. The effects of various parameters on cerium extraction were also studied. The selected parameters were background current, catholyte acidity, agitation speed, operation current and voltage and surfactant addition. The electro-oxidation extraction mechanism can be divided into eight steps. In addition, Wee the rate of extraction is quite fast, the percentage extraction Ce+4 can be taken as an index to show the conversion rate of Ce+3 J to Ce+4.

Jan 1, 1989

By Zenjiro Asaki

The copper concentrate particles dissolve quickly into the molten matte in the smelting furnace of Mitsubishi Process, which indicates that the sulfide smelting is essentially a gas/liquid reaction. In this paper, theoretical calculation has been made on the rate of oxidation of FeS component in the matte to form FeO by rising gas bubbles using the penetration theory. The results showed that all the oxygen in the bubble of 1.2 cm in diameter, which is the maximum stable diameter, is consumed in 3 ms. This time required is sufficiently short, and it results in the actual operation of smelting furnace of 1100% oxygen-efficiency. These calculations indicate that most smelting reactions are completed just under the lance, except slag formation.

Jan 1, 2002

By Dai Xi

In the present work, the viscosities of molten FenO-MgO-Si02 and FenO-MgO-CaO-Si02 semi-synthetic slags for nickel flash smelting were measured in the temperature range from 1473 to 1723K by a rotational viscometer. The ratio of Fe to Si02 was fixed at 1.2, calcium and magnesium oxide contents varied in the range from 2 to 8 mass% and 9 to 12 mass%, respectively. The results showed that silicate anions became smaller by increasing CaO content, which results in a decrease of the viscosity of the slag. In the case of MgO addition the viscosity behavior was complicated. At MgO content below 11 mass%, the viscosity increased with the increase of MgO at all temperatures tested. However, when the MgO content was above II mass%, the viscosity decreased slightly for FenO-MgO-CaO-Si02 system. At higher MgO contents, low-viscosity slags can be obtained by adding CaO. At a given composition, the viscosity decreased with increasing temperature. The higher the temperature, the more MgO can be added before saturation. The effect of Fe304 on the viscosity was quite significant. The viscosity of slag increased by 300mPa&apos;s at l573K when Fe304 content varied from 3 to 9 mass%. The viscosity values are presented as the functions of temperature and composition. A comparison between FenO-MgO-Si02 and FenO-MgO-CaO-Si02 systems is given in this study.

Jan 1, 2003