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By Milton Manrique, Edgar E. Vidal, Patrick R. Taylor

"Ultrafine zirconium carbide powder has been synthesized using zircon concentrate and methane in a thermal plasma reactor. The effect of several experimental variables, such as power used and zircon particle size, on the conversion has been studied. A thermodynamic analysis of the possible reactions and stable compounds was performed. A mathematical model that describes the in-flight decomposition of zircon particles was developed based on a description of the temperature and velocity profiles calculated in the reactor. It was shown that the formation of zirconium carbide from zircon and methane is thermodynamically possible. Complete 'vaporization of zircon in the reactor is predicted when the particle size is below 45flm and the effective power entering the reactor is 15 kW. The powders were collected and characterized by XRD, SEM, TEM and chemical analysis using ICP. Results of the product analysis indicated the presence of zirconium carbide, zirconium oxide, silicon carbide and silicon oxide.IntroductionIn recent years there has been an increased interest in the production of nanometric sized powders of ceramic materials for use in advanced materials applications. One possible method to produce these powders is with a thermal plasma reactor, which offers high temperatures and fast quenching rates. This technology has been called - Thermal Plasma Synthesis - [1].Zirconium Carbide (ZrCx) has typical properties of transition metal carbides: elevated hardness - between alumina and diamond - a high melting temperature of 3420°C and high chemical stability at room temperature [2]. ZrCx has a Bl crystal structure with deficiencies in the number of carbon atoms in the cell with x between 0.6 and 1 [3]. Different methods have been used to produce ZrC, one method is by direct reaction of zirconium hydride or halide with carbon. Other methods used are direct reduction and carburization of zirconium oxide (Zr02) and reaction of metallic zirconium with a caburizing gas such as acetylene [3]. Recently small films of ZrC have been obtained using a sputtering device [4,5]. ZrC has been used in nuclear plants as a low neutron absorbing and high mechanical resistant refractory material and also as a constituent in cathodes made of UC-ZrC [6]. It is also used in the form of tubes, boats and crucibles to handle molten metals and as part of electronic devices used for thermoionic transducers. Recently ZrC has been used along with zirconium diboride (ZrB2) to produce composite materials [7,8]."

Jan 1, 1996

By Maria D. Salazar-Villalpando, Anthony Cugini, Bryan Reyes

"The electrochemical reduction of CO2 was performed in a laboratory-made, divided Htype cell. A copper electrode was used as the cathode. An Aldrich Nafion 117-type ion exchange membrane (0.18mm thickness) was used as the diaphragm. NaHCO3 and KHCO3 were studied as the catholytes. Hydrogen evolution from water reduction and products from CO2 electrochemical conversion were recorded. Higher CO2 reduction enhancement was observed by KHCO3 as compared to NaHCO3. The main conclusion of this work is that in fact CO2 can be electrochemically reduced with copper electrodes.1.-INTRODUCTIONThe direct electrochemical reduction of CO2 may allow for a simple process and, by avoiding high temperature reactors, would enable the process production rate to be quickly varied to follow the time of day availability of surplus electricity [1]. Temperature has a major effect on the electrochemical conversion of CO2 since its solubility increases when temperature decreases [2]. The electrical potential applied to the electrochemical reacting system will have an influence on the product distribution, as well. For example, a narrow potential range during cyclo-voltagraphic studies will determine the detection of a lower number of products. A recommended potential range to study the electrochemical reduction of CO2 is -2V to 2V. Moreover, the reaction rate on the electrode is governed by various processes, such as the kinetics of electron transfer, adsorption/desorption at the electrode surface, and diffusion of CO2 to the Cu electrode. The availability of active species, CO2 for electro-reduction, is extremely low at the vicinity of the electrode surface and it seriously interferes with the rate of mass transfer. In batch type electrolytic reactors, depletion of CO2 at the surface takes place first. CO2 from the bulk then has to diffuse to the electrode surface, resulting in mass transfer controlled kinetic phenomena. During the above process, several other competitive side reactions could suppress the primary reaction even though the cathode has good electro catalytic properties for reduction of carbon dioxide. When the dynamic supply of specific active species is ensured to electrode surface, the mass transfer effects are minimized to certain extent. Hence it is envisaged that a continuous flow reactor is more efficient for the electro-reduction of CO2 in CO2 saturated aqueous electrolytes. The primary reactions that occur at the copper electrode during the reduction of CO2 are listed below (with the standard potentials calculated using formation energies [1] :"

Jan 1, 2010

By Kouji Mimura, Manabu Kishida, Minoru Isshiki

"Purification of metallurgical grade silicon (MG-Si) by the plasma-arc zone melting method (PZM) has been examined. The process consisted in the horizontal displacement of a molten zone heated by Ar- and 10%H2+Ar- plasma-arc under atmospheric pressure. This technique, especially using hydrogen plasma-arc, promoted the segregation of impurities from the head to the tail of the bar and the vaporization of impurities of higher vapor pressures. Metallic impurities such as Fe, Ti, Cr, Mn,. Cu, Al and Ca were reduced to less than 1 mass ppm at the head side of the Si bar. Non-metallic impurities such as boron, phosphorous, carbon and oxygen were also reduced by the zoning effect and, furthermore, by activated hydrogen atoms dissociated in the high temperature plasma-arc according to the following reaction: Q (in liq.Si) + 2H = H20. Plasma-arc zone melting with hydrogen plasma has been recognized to become an effective purification technique of MG-Si for the production of a low cost solar grade Si (SOG-Si).IntroductionDemand of high-purity Si for solar grade silicon (SOG-Si) is supposed to be further growing in the near future. The purity of SOG-Si required for the photovoltaic cell is more than six nines. An expensive semiconductor grade silicon (SEG-Si) with the purity of around eleven nines has been used to satisfy the demand. Development of techniques and processes for the production of a low cost SOG-Si is therefore necessary [l]. Although many purification techniques, such as directional solidification, plasmaarc melting and electron beam melting [1-6], and processes, such as carbothermic reduction of high purity silica [7], have been examined and proposed for this purpose, a more efficient and practical purification technique is still required.In the present work, the purification of MG-Si has been investigated using a plasma-arc zone melting (PZM) technique developed by the authors. Plasma-arc melting, which is well· known as a useful melting method for various metals and alloys, has been recognized to be efficient for refining and degassing several metals if hydrogen is added to the plasma generating gas, resulting in the so-called hydrogen plasma-arc. For example, deoxidation of Fe, Co and Ta [8,9], decarburization of Fe [9] and removal of metallic impurities from Zr, Ta and Fe [10-12] have been reported. This excellent refining effect is considered to be caused by dissociated and activated hydrogen atoms formed in the high temperature plasma-arc."

Jan 1, 2000

By John A. Mavrogenes

The Texaco gasification system developed at the Monte Bello pilot plant efficiently bums petroleum-coke thereby producing syn-gas and electricity. This system produces more electricity than conventional burners, yet the only by-products are pharmaceutical grade sulfur and V -rich slag. Vanadium is known to exist in multiple valence states in compounds which possess a wide range of melting points and physical properties. Consequently, it becomes important to carefully regulate oxygen fugacity throughout the system in order to control vanadium valence state. Vanadium phase equilibria is presently poorly understood, in large part because of the multiple oxidation states of vanadium (-I, 0, +2, +3, +4, and +5) and the difficulty of unequivocally identifying the valence state(s) in many compounds. The operation of these gasifiers at approximately 1400°C is well above the melting point of V20S but considerably below the melting temperature of V02 and V 203. If J02 can be regulated to keep the burner within the V 205 field, slag material would more likely remain molten and more easily flow out of the bottom of the burner. In pure V oxides. the oxidation state is readily determined by microprobe analysis. where V20S (V+5) is 56% V, V02 (V+4) is 61.4% V, and V203 (V+3) is 68% V. However, V valence in multi-element phases (especially phases containing other elements of variable valence) cannot be resolved by microprobe analysis alone. Petroleum-coke gasification slags collected from within the gasifier under different oxidation conditions were studied by electron microprobe analysis (EMPA). X-ray diffraction (XRD). X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy. Raman spectrometry in conjunction with microprobe analysis was found to resolve the valence of vanadium in the phases of these slags. Raman spectra collected from homogeneous single phase V-oxide standards in vacuum at low temperatures (-150°C) yielded peaks characteristic to each valence state. Gasifier slag samples are, however, much more complicated. Oxidized samples contain: fine grained (Ca. Mg, Fe. V) oxide matrix of variable composition, (Fe. V, Ni) spinel. (Fe, AI, V, Ni, Mg) spinel, V205laths, AI-Si glass blebs and Ni sulfides. Reduced samples contain: crystalline Ca-siIicate matrix, subhedral to euhedral (V, Fe, Mg, AI) spinel, subhedral V02, Fe and Fe-Ni sulfides, Fe-Ni alloys, and complex Ca-oxide matrix. The different spinel assemblages, the characteristic V-oxides and the distinctly different character of the matrices makes the oxidized and reduced slags readily discernible.

Jan 1, 1995

By M. M. Sadawy

"The increased rate of exploitation of iron ores has resulted in a rapid depletion of high-grade iron ore deposits in Egypt. New iron reserves have to be discovered to secure the iron ore for steel production. This paper aims to study the characterization and magnetic separation of low grade Aswan iron ore. The results showed that Aswan iron ore is composed of oolitic hematite, goethite, quartz and kaolinite. The screen analysis indicated that Aswan iron ore had a uniform distribution of iron and silica in the different particle size fractions and there is no any particle size has high amount of iron or low content of silica. On the other hand the results of dry high intensity magnetic separation illustrated that this technique is not suitable for upgrading this ore.IntroductionIron is one of the common metals used in industry, as well as being the fundamental raw material used in iron-steel industry; products are wide spread even in daily uses. The total iron ore reserves of the world have been estimated as 3 70 billion tones; 160 billion tones is classified as economical, while 210 billion tones as potentially economical [1]. An estimated 98% of the iron ore exploited in the world is used in the manufacture of pig iron and steel, which are non-substitutable backbones of modem society. The rapid increase of world steel production over the last few years have required an equal increase in iron ore production, from 876.8 Mt in 2006 to 948.1 Mt in 2007 [2]. The increased rate of exploitation of iron ores has resulted in a rapid depletion of known high-grade iron ore deposits. This, in turn, has led to a dramatic increase of prices. In the absence of any major new discoveries of high-grade iron ore deposits, mining companies have turned to lower-grade materials to assess their beneficiation potential to expand their production base and beneficiation capacity, in order to satisfy future demand. Egypt is going to face shortage in iron production, consequently new iron reserves have to be discovered to secure the iron needed for the country [3]. Exploitation of low grade ores requires special equipments and techniques for recovery of minerals values. High gradient magnetic separators offer promise and great potential of application both technologically and economically in the processing of fine particles containing weakly or feebly paramagnetic components [4-6]. Within this existing framework, this research was initiated to assess the beneficiation potential of low-grade Aswan iron ore by high intensity magnetic separation."

Jan 1, 2013

By Ehsan Vahidi, Fereshteh Rashchi, Amirhossein Shahnazi

"The pig iron from steel manufacturing plants contains a high concentration of vanadium-bearing materials smelted with iron ore. During the oxidation process of the molten pig iron with oxygen lances, vanadium transfers to the slag. In this research, recovery of vanadium from LD (Linz-Donawitz) converter slag of steelmaking plant was investigated. The leaching residue was characterized by XRD and XRF techniques. The maximum vanadium recovery was achieved at optimum leaching conditions of 70 °C, S/L: 1/15, sodium hydroxide concentration: 3 M and leaching time: 150 minutes. The dissolution rate increased with rising sodium hydroxide concentration and temperature and decreasing particle size. The experimental data are treated graphically to explain the kinetics of the vanadium recovery process using shrinking core model (SCM). As a result, the controlling regimes in the SCM were analyzed separately using liquid film diffusion control, solid product diffusion control, and reaction control mechanisms.IntroductionVanadium is commercially important as a constituent of several alloys and catalysts. Nowadays, vanadium is mostly recovered as a by-product from secondary sources or from industrial waste streams such as titaniferrous magnetite, fly ash, spent catalysts, and petroleum coke. Steelmaking operations are specifically concerned by this problem due to the production of a huge quantity of by-products [1]. These by-products, including LD converter slag, sludge, fly ash, spent catalyst, ash, and alloyed scrap, contain a notable amount of heavy metals which may cause environmental problems. Solvent extraction is one of the techniques being increasingly used for the recovery of vanadium [2]. Apart from vanadium ore, secondary resources such as titanmagnetite, ilmenite and slag from the ferrous industry are a major source of supply. The pig iron from steel manufacturing contains a majority of vanadium-bearing materials smelted with iron ore. In a heat resistant shaking ladle the molten pig iron is oxidized with oxygen lances, causing the vanadium to be transferred to the slag. Normally, the vanadium in LD converter steel slag (coming from Linz-Donawitz steelmaking process) is ca. 5% as vanadium pentoxide (V2O5). This slag is the world's principal raw material for vanadium production [3, 4]. Moskalyk and Alfantazi [4] reported that a roast-leach process is used in South Africa for the production of vanadium oxides from magnetite ores while some of the slag was converted to ferrovanadium. A portion of the slag was exported to Europe for the production of vanadium oxide. The researchers mentioned that alkaline roasting was the main process at that time employed to extract vanadium pentoxide from vanadium slags."

Jan 1, 2012

By M. Zamalloa

Slag foaming is an important phenomenon in many metallurgical processes. It creates large surface areas for multi-phase reactions to take place. In other applications, it protects electrodes and improves the energy efficiency by reducing radiation from hot surfaces. However, it may also be a source of serious disturbances. To control and optimize the use of slag foams, an extensive knowledge of the factors controlling the foam formation and stability is required. Slag foaming experiments were carried out using synthetic FeO-CaO-Si02 slags at temperatures ranging from 1200 to 1350 "C. A data acquisition system was used to continuously measure the foam height, gas flow rate, bubble frequency and temperature. The experimental results show that the gas injection rate has a strong effect on the behaviour of slag foams. At high flow rates and rapid bubbling, unstable foams with short decay times were created. The addition of P20, favours the foam formation and stability by lowering the surface tension of the slag. The average foam life increases with decreasing basicity (CaO/Si02). It is proposed that this is attributed to the increase of the surface viscosity due to surface adsorption of a thin film of silica, retarding the drainage of the liquid films.

Jan 1, 1992

By O. Chemezov, Yu Zaikov, A. Apisarov, A. Isakov

"Silicon deposits containing 99,9 wt.% of main component were obtained by SiO2 electrolysis from chloride-fluoride melts. The operating temperature was varied from 973 up to 1073 K. The conditions for obtaining crystalline fibrous micro- or nanodeposits were determined. The deposits were investigated by ESM methodIntroductionThere are large reserves of natural quartz of high purity in Russia. Processing of this raw material by electrolysis in molten salts produces silicon containing 99.9 weight percent of basic substance.[1]This method is less energy-consuming in comparison to existing methods for producing high purity silicon from gas phase.Another advantage of the electrolytic method for producing silicon from its oxide in molten salts is the possibility of production of high-purity silicon under air atmosphere. It dramatically reduces costs of the electrolytic cell construction, and the operating costs at electrolysis.On our opinion, the main advantage of the electrolytic production from SiO2 in molten salts is a unique opportunity to obtain micro-and nanostructures of silicon deposits. In particular, it is possible to obtain fibrous structures of silicon. The electrolytic method allows smoothly adjusting the thickness and length of silicon micro- and nano-wires by varying the cathode current density and temperature of the process."

Jan 1, 2012

By A. S. Mustafinova, A. A. Zharmenov

"Production of electrolytic copper is characterized by large volumes of acidic spent solutions the utilization of which requires considerable expenditures of neutralizing agents. At present, an economically substantiated technology does not exist for treatment of sulfuric acid rinse solutions and spent copper electrolyte which will allow for repeated use of the acid and the metal salts. Therefore, for this aim the most advantageous is the use of electromembrane methods. In the paper there is stated the essence of developed technologies which are distinguished by low waste and provide the extraction from the solutions of metallic copper, nickel and sulphuric acid. There are also considered methods of copper electrolyte processing allowing to regulate its composition by that or another component (H2S04, Cu, Ni, As).On the base of the detailed study of the behaviour of various types of ion- exchanger membranes in copper-, nickel-, zinc-, arsenic- bearing sulphate solutions there is realized the selection of the most suitable membranes (MK -401, MA-411, MB-2 and MKL-l/MAL-2).Some variants of electro membrane processing of spent solutions of the hydrometallurgy process have passed productions tests on a number of copper-electrolyte enterprises of the countries of CIS (cooperation of Independent States). These tests showed high efficiency of developed methods."

Jan 1, 1997

By Tracy Morris, Weldon Read, Luis Navarro

"Bismuth is a recognized contaminant in the electrolytic refining of copper that can render many cathodes to be outside ASTM standards and unsuitable for copper rod and other downstream products if not carefully controlled. This paper portrays the performance of Molecular Recognition Technology (MRT) for bismuth removal at the Amarillo Copper Refinery (ACR) and describes how the highly selectivity gel has been successfully used to achieve good bismuth removal and how many pit falls and draw backs have been overcome.IntroductionASARCO operates one of the largest copper refineries in the world at Amarillo, Texas. The main feed for this refinery is produced at the Hayden smelter in Arizona. During the operation of this smelter a variety of metals are carried as impurities in the copper anodes because of the diversity of concentrates and residue products used as raw materials in the smelter feed mix. Even though the impurities are concentrated enough to be detected at the smelter, it is difficult to remove them completely. A simple way to control impurities at the smelter is to minimize the addition of material with a high concentration of impurities to the charge in order to reduce the output of this metal species. All this leads us to have a ""refinery problem"" [1,2,3]."

Jan 1, 2012

By W. L. Dalmijn, E. A. Schokker, N. Fraunholcz, P. C. Rem

Many processes developed for the mechanical processing of Automotive Shredder Residue (ASR) suffer from high processing costs. We offer a distinct concept for low-cost mechanical processing still allowing high value-added recycling of the recovered materials. The basic idea behind this approach is to produce saleable pre-concentrates at the lowest possible costs that can be further processed in existing separation facilities. Our process includes screening, size reduction and magnetic separation. Preliminary studies showed that fibers in ASR are magnetic due to adhering rust particles allowing separation into a fiber fraction and a non-magnetic rigid fraction by high-intensity magnetic separation. The fiber fraction is most suited for thermal processing. The rigid fraction mainly consists of plastics and rubbers with up to 10 wt.-% of non-ferrous metals, some inert material and copper wires. This fraction is very well suited for mechanical processing by, e.g., sink-float separation in existing metal separation plants. The non-metal fraction can be processed further to recover the plastics and rubbers. The process proposed in this study is expected to be substantially cheaper than full thermal processing. In addition, as it mainly relies on existing separation facilities, it can be applied in the short term.

Jan 1, 2000

By Matthias Frommer, Carl-Peter Reipl, Reinhard Flende

"Today there is a growing demand for strip of superior steels with specifically tailored technological properties. Especially strips of high-strength, micro-alloyed steel grades applied to manufacture longitudinally and spiral-welded pipes are a growth market. Tubes are generally required to have high strength and sufficient toughness values and thus favour specific hot strip microstructures. The correlation of chemical analysis, process parameters and mechanical properties with microstructural features is still a challenging task. During the last decades, scanning electron microscopy (SEM) and electron backscatter diffraction (EBSD) have become useful tools for the characterization of complex microstructures. The EBSD data provides an immense variety of post-processing possibilities, e.g. related to grains, grain boundaries, misorientations or texture. This paper highlights the results of an advanced analysis of microstructures representing industrial produced hot-rolled strips and presents an approach to define and quantify some essential microstructural parameters.IntroductionHigh-strength microalloyed steels have been used for the production of welded pipes for more than 30 years. However, the alloy design of pipeline grades is being continuously modified and the process technology optimized because of the increasing high strength-toughness combination requirement for pipeline steels. Compact strip production (CSP®) technology is an upcoming promising route for the production of high-quality pipeline steel grades [1]."

Jan 1, 2012

By He De-wen

The increasing population and living standard in urban areas, have been accompanied with the growing quantity and composition complexity of rubbish, which are causing well-known social effects of pollution, while rubbish (solid waste) is a recyclable resource. To convert rubbish into useful materials, the essential measure is to carry out sorted collection of rubbish. The preconditions of implementing sorted collection are presented in the paper. 1 Characteristics of rubbish composition and amounts of recyclable contents are basic condition to implement sorted collection. 2 The existing available technologies of recycling, economic benefit from recycling, and disposal scheme of residual rubbish are restrained condition for sorted collection. 3 Public understanding and support to sorted collection are the key to success. 4 The government policies to be favorable for sorted collection is the pledge of success. 5 The establishment of a steady solid waste recycling market is also a guarantee to implement sorted collection continuously. 6 To establish management system of rubbish recycling as soon as possible. Further, the methods and procedure of sorted collection are discussed in detail and beneficial comments and theoretical basis to promote sorted collection of rubbish in urban area are presented; it will contribute reference value to municipal solid waste management.

Jan 1, 2006

By Maria Cristina Ruiz

The removal of iron from the leaching circuits is a common problem in the hydrometallurgical processing of non ferrous metals. Among the currently available processes, hematite precipitation is the most recommendable from an environmental point of view. This paper is concerned with the batch precipitation of hematite from ferrous sulfate solutions. One of the main objectives of the study was to determine the effect of the experimental conditions on the extent of iron precipitation as well as the purity and the particle size distribution of the precipitates. The main variables studied were temperature (180 to 220 ºC), concentration of sulfuric acid (1 to 10 gpl), initial iron concentration (1 to 15 gpl) and partial pressure of oxygen (3 to 7 atm). The results showed that increasing the oxygen partial pressure from 3 to 7 atm produced a very small increase on the rate of hematite precipitation indicating that a large partial pressure of oxygen is not needed for an effective ferrous to ferric oxidation. An increase in the temperature produced finer precipitates with lower sulfur contents. On the other hand, an increase in sulfuric acid concentration and initial iron concentration produced precipitates with larger particle sizes and higher sulfur contents.

Jan 1, 2006

By Norbert L. Piret

During smelting of copper, arsenic in the feed reports to a large extent to the gas phase and some enters the anode copper. From the gas phase it is transferred during wet gas cleaning directly, or indirectly after dust processing, to aqueous solution. During the electrorefining and anode slimes processing, the anode arsenic content is also transferred to aqueous solution. Technology for the efficient removal of arsenic from process streams and cleaning of aqueous effluents is well established. However, the arsenic-bearing products, which thereby are generated, can vary widely in consistency, quality and quantity, from large amounts of gypsum contaminated with water-soluble arsenic compounds to residues with high arsenic content ' or arsenic products. Arsenic management in a copper smelter not only is involved with the duty of compliance to the gaseous and aqueous emissions standards but also should have as objective the minimization of the generation of arsenic-bearing and, in general, heavy metal-bearing solid waste. The present paper outlines options and the associated economic aspects for minimization of arsenic-bearing solid waste generation, for improvement of the environmental compatibility of the residues to be deposited and for the .production of commerciable arsenic compounds under appropriate market conditions.

Jan 1, 1999

Lance based copper-nickel matte converters have become an established technology in the field of base metal sulphide smelting and converting. An Ausmmelt® converter is currently being constructed at Anglo Platinum in South Africa to convert a nickel-copper rich matte containing platinum group metals (PGM's). The accurate prediction of the matte chemistry is required to control the composition at the endpoint which influences segregation of PGM's during the subsequent slow cooling and magnetic separation processes. A hybrid modelling approach is introduced in this paper that incorporates both the effect of thermochemistry and system dynamics. It will be shown how the model relates to fundamental conservation laws, while still providing enough flexibility to adapt to changing operating conditions. It will also show how off-line modelling can be incorporated into a robust on-line model. Based on the data from many pilot plant trials, the model prediction performance is shown to be within the accuracy requirement set by industry and therefore constitutes a reliable basis for model based control. The final generic model structure takes on the form of an thermodynamically integrated ARMAX hybrid model. The final model has the advantages of being dynamic, adaptive, robust and it can be related to thermochemical fundamentals.

Jan 1, 2002

By J. E. Dutrizac

Mineralogical studies were carried out on nodulated copper cathodes from three primary refineries to characterize the nodular growths and to elucidate the causes of the nodulation. Nodulation is often initiated at the surface of the starter sheet or the stainless steel plating blank, although a layer of smooth copper sometimes is deposited before nodulation commences. In some instances, the "roots" of the nodules exhibit a pronounced dendritic texture that is associated with an abundance of cavities. Slimes particles are not usually associated with these growth features which lead to a globular surface deposit. The globules sometimes develop into larger nodules, and this type of nodulation is likely caused by improper addition agent concentrations. The nodules on most cathodes, however, exhibit "roots" at the contact with the substrate that are associated with microcavities and large clusters (>40 µm) of slimes particles. The slimes constituents are commonly Ag powder, PbSO4 and Cu2(Se,Te) but not AgCu(Se,Te) or Ag,(Se,Te). The size of the slimes clusters, rather than their composition, appears to be the important factor causing the copper to grow into nodules. Tiny individual slimes particles themselves do not appear to cause cathode nodulation.

Jan 1, 1999

By Norihiro Murayama

The hydrothermal syntheses of zeolites from coal fly ash were carried out using NaOH and KOH as an alkali source. The cation exchange capacity (CEC) and the ion exchange selectivity were investigated for the zeolites synthesized by a hydrothermal treatment. The effective usage of the zeolite as a cation exchanger was considered from the viewpoint of engineering. Zeolite P, HS (hydroxysodalite) and K-CHA (potassium-chabazite) are mainly formed as zeolite species in NaOH or KOH solution at 393K. The zeolite P and K-CHA have a large exchange capacity as a cation exchanger. The cation exchange isotherms of various monovalent and divalent cations with various zeolites are investigated. The order of selectivity of the zeolites is as follows, NH4+> K+> Li+.For the divalent cation, the largest removal amount is obtained for Pb2+ in the low equilibrium concentrations below 0.2mmol/dm3, and almost perfect removal can be achieved for Pd2+. The order of selectivity of zeolites in low concentration is expressed in the following order; Pb2+> Co2+> Cd2+> Ca2+> Mg2+> Ni2+. Ii is considered the zeolites obtained from coal fly ash can be used as an excellent cation exchanger.

Jan 1, 2006

By Jari Aromaa, Olof Forsen

"Oxygen evolution by decomposition of water is the main anodic· reaction in sulphuric acid solution. Traditional anode materials have been relatively low-cost lead alloys, though the active lead dioxide layer has a high oxygen evolution overpotential. This causes a significant increase of cell voltage. To lower total energy use in metal production, electrocatalytical properties or corrosion resistance to decrease replacement costs must be improved. Addition of an catalyzing ion will decrease oxygen evolution potential. The effective area of an anode increases by calcium additions and by producing anodes with fine microstructure. Remelting and rapid quenching is possibly a method that is economically feasible and technically simple enough to be adopted.IntroductionPermanent anodes are widely used in several electrochemical processes and cathodic protection applications. The permanent or ""inert"" anodes can be either massive or coated anodes. The massive anodes are metals, like lead alloys, or non-metals, like magnetite, graphite or ferrite. The coated anodes are made of a valve metal base (titanium, niobium or tantalum) coated with an electrochemically active coating. The purpose of anodes is to supply current to the electrochemical cell. A vast number of materials and their combinations are electrical conductors and may hence be used as anode materials. However, good anode materials must survive in aggressive environments and also be able to pass high current densities. These opposite requirements restrict the amount of possible materials. Generally, an useful anode material must meet three requirements, electrical conductivity, electro catalysis and stability. Good electrical conductivity is essential for energy efficiency. Good electrocatalytical properties are essential to improve product yield. Long term stability is also an important property, because electrode wear and corrosion may cause product contamination, increasing energy consumption and material and labor costs due to need of periodical maintenance. Electrical conductivity and electrocatalytical properties are more widely studied subjects than long term stability of anodes, and a good amount of information about these two subjects can be found in the open literature. Wear and corrosion mechanisms of the anodes vary depending on the operational conditions, i.e. concentration of different species, temperature and operating current density."

Jan 1, 1997

By Mark Khinkis, Huajun Yuan, Mark Zak, Yaroslav Chudnovsky, Aleksandr Kozlov

"An afterburner for green petroleum coke calcination in electrothermal fluidized bed was designed, fabricated, installed, and tested on a pilot fluidized bed calcination furnace. The experimental set-up comprised a combustion chamber, in which fine particles and volatiles of the furnace off-gas were fully combusted, and a cooler equipped to calculate the related heat recovery and losses. Off-gas composition was analyzed to evaluate the combustion process. The energy balance confirmed the potential to recover a large part of the heat value of volatiles and fme particles from the GPC. Potential future applications of the results are discussed.IntroductionGreen petroleum coke (GPC) is an oil refining byproduct that can be used directly as solid fuel or as feedstock for the production of calcined petroleum coke [1-2]. GPC contains a high amount of volatiles and sulfur. With coke calcination, the GPC is heated to remove the volatiles and sulfur in the calciner off-gas to produce purified calcined coke, which is used in the production of graphite, electrodes, metal carburizers, and other carbon products. Currently, more than 80% of calcined coke is produced in rotary kilns or rotary hearth furnaces. These technologies provide partial heat utilization of the calcined coke to increase efficiency of the calcination process, but they also share some operating disadvantages [3]. On the other hand, coke calcination in an electrothermal fluidized bed opens up a number of potential benefits for the production enhancement while reducing the capital and operating costs.The increased usage of heavy crude oil in recent years has resulted higher sulfur content in green coke produced from oil refinery process, which requires a significant increase in the calcinations temperature and residence time [ 4]. The calorific value of the process off-gas is quite substantial and can be effectively utilized for combined heat and power (CHP) production to complement the energy demand. Waste heat recovered from the product cooling could also contribute to the overall economics of the calcination process. Preliminary estimates indicated the decrease in energy consumption by 35-50% as well as a proportional decrease in greenhouse gas emissions. So, efficiency improvement of the coke calcinations systems is attracting close attention of the researchers and engineers throughout the world."

Jan 1, 2014