Search Documents

By Matthew Tunnicliffe, Akram Alfantazi, Paul Nesbitt, Farzad Mohammadi

"Lead and its alloys are proper candidates for anodes in electrowinning processes mainly because they are insoluble in the leach solutions and relatively cheap. However, the annual cost of corrosion problems associated with these anodes is millions of dollars. In this study lead-silver and lead-calcium anodes were tested under typical nickel electrowinning conditions and the effect of chloride on the corrosion performance of the anode materials was investigated. Corrosion rates of the anodes were calculated using the discharge plateau (reduction of lead dioxide to lead sulfate) after galvanostatic experiments. It was found that lead calcium anodes have the highest corrosion rate both in the presence and absence of chloride. Surface morphology of the electrodes was studied using SEM and the corrosion products were characterized using XRD.IntroductionLead (Pb) is usually the preferred material for commercial anodes since it is insoluble in the leach solution and the costs are manageable. One advantage of using an insoluble material as an anode is the higher purity of the cathodic deposits and better quality of the end product. During nickel electrowinning, metallic nickel is deposited on the cathode while oxygen evolution reaction (OER) takes place on the anode. In practice, relatively high potentials are necessary for the reaction to proceed at the desired rate because of the high overpotential of OER on lead. Lead anodes get oxidized in typical electrowinning conditions and usually have two to three years of lifetime. Although the price of each anode is insignificant, the overall cost of corrosion of these anodes is considerable, which is due to the large number of anodes used in a plant, typically two to three thousand. Therefore, corrosion is a significant problem associated with lead anodes in commercial nickel electrowinning plants and industries show interest in addressing this problem. Corrosion of lead electrodes in acidic environments has been previously the subject of many research studies [I-7]. It has been reported that, during the anodic polarization of lead, several phases may be present on the surface, depending on the potential range that is being studied [8]. Lander showed that lead is oxidized at potentials higher than 0.252 YsHE with tetragonal lead monoxide being the main reaction product [9]. At 0.666 YsHE lead can transform to lead dioxide; however, it is not stable and transforms to lead sulfate and lead oxide. At potentials higher than 1.684 YsHE, lead dioxide is eventually a stable phase and forms a protective layer on the surface [I 0, 11]. Under conditions of a typical nickel electrowinning plant, usually a 200 A/m2 current density is passed through the electrodes."

Jan 1, 2012

By Toshiyuki Hashida, Victor M. Lopez-Hirata

"Small-punch tests and determination of fracture toughness JIC were conducted at 4 and 77 K on new cryogenic JN1, JJ1 and JK2 austenitic stainless steels, after isothermal aging. Equivalent fracture strain ?qf determined by measuring the reduction of thickness in the small-punch test specimen. A linear dependence of JIC on ?qf was found in these new materials. Regression analysis of experimental data produced the following linear relation JIC = 1304.1 ?qf + 8.09 [kJm-2]. An analysis of present work relation was pursued on the basis of material properties and evaluation method of he. Results showed that the slope value has a strong dependence on material yield strength and JIC evaluation method. This linear relation is useful for the evaluation of fracture toughness JIC, measuring the equivalent fracture strain ?qf by means of small-punch test. Thus it can be useful for assessing the degradation of fracture toughness in small areas such as, the heat-affected zone in welded components.IntroductionCryogenic structural materials for superconducting magnets of fusion nuclear reactor are required to possess a good combination of strength and toughness. The mechanical properties are required beyond the capability of conventional austenitic stainless steels [1]. New cryogenic JN1, JJ1 and JK2 austenitic stainless steels were developed by the Japan Atomic Energy Research Institute (JAERI) [1]. The structure of superconducting magnets is constructed by welding of 200 = thick plates of these steels, which are solution treated at high temperatures and then water-quenched to avoid intergranular precipitation. However, the welding process involves heating and cooling [2], which cause microstructural changes in both base metal and weld. In this heterogeneous microstructure, it is important to estimate the fracture toughness of these materials at cryogenic temperatures. Therefore, it is necessary to evaluate the effect of aging process on the fracture toughness behavior of these new steels. To determine the cryogenic fracture toughness, the elastic-plastic JIC value has been co=only used [2]; however, the specimen size is much larger than heat-affected zones in welded components. Small-punch (SP) testing method, employing miniature specimens, has permitted to evaluate the fracture toughness behavior at different temperatures in different nuclear reactor materials [3,4]. Mao et al. [5,6] and Misawa et al. [7] found a linear relation between JIC value and equivalent fracture strain ?qf, determined by SP method in non-ferrous alloys and ferritic steels at room temperature and austenitic stainless steels at 4 and 77 K, respectively. So that, this kind of correlation would be very useful to assess the fracture toughness JICe values by means of SP test in small zones of welded components."

Jan 1, 2012

By Shadia J. Ikhmayies

"Cadmium telluride (CdTe) is a very interesting material that has many applications. Thin films of p-type CdTe can be used as the absorber layer in the heterojunction CdS/CdTe thin film solar cells in which n-type cadmium sulfide (CdS) works as the window layer. A review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques was performed. The presence of defects and impurities such as oxygen and chlorine influence the PL spectrum. Copper and other dopants change the PL spectra and enhance the defects band. Chemical-heat treatment especially with CdCh is known to improve the quality of CdTe thin films because it decreases the Cd vacancies and quenches deep traps, so it enhances the PL signal. A discussion of chemical-heat treatment especially with CdCh, the effect of the ambient atmosphere, and that of the measuring temperature is performed.IntroductionCadmium telluride (CdTe) is a II-VI compound semiconductor that has a cubic zincblende (sphalerite) structure with a lattice constant of 0 A4~11]. Other than all of II -VI semiconductors, CdTe can be made both n- and p-type. But due to self compensation it is not easy to get p-type CdTe films [2]. Polycrystalline CdTe thin films are interesting because they have a lot of applications. Most of the problems associated with the use of these films are attributed to inhomogeneity, self-compensation, and the difficulty of forming a stable and lowresistivity ohmic contact [3]. CdTe technology has been established for a large number of applications, including solar cells, optical and nuclear detectors, and thermal- and radiationimaging devices [3]. At present, the highest demonstrated conversion efficiency for a CdTe based heterojunction (ID), with CdS as a window layer, is 16.5% [4, 5]. CdTe thin films can be prepared by different experimental techniques, such as thermal evaporation [l], electrochemical deposition (ED) [3], close-spaced sublimation (CSS) [3, 4, 6], physical vapor deposition (PVD) [3], chemical molecular beam deposition (CMBD) [7], and close space vapor transport (CSVT) [8].The objective of this paper is to make a review of the photoluminescence (PL) spectra ofp-type CdTe thin films prepared by different techniques and discuss the factors that influence the PL spectra. The composition of the film is very interesting in determining its PL spectrum. Different kinds of defects, impurities and dopants have their finger prints in the PL spectrum. Deposition techniques and deposition parameters such as the deposition temperature and ambient atmosphere also have their influence. Heat and chemical treatments which are known to improve crystallization and reduce the defects change the PL spectrum."

Jan 1, 2013

By Norihiko Fukatsu, Takashi Iwamoto, Noriaki Kurita, Koji Katahira, Kunihiro Koide, Teruo Ohashi

"The galvanic cell-type hydrogen sensor employing CaZro.9Ino.t03-a. as the solid electrolyte was designed for the measurement of hydrogen activities in molten copper under industrial .conditions. The sensor probe consists of the cap-shaped solid electrolyte with porous platinum electrode on the inside and alumina refractory tube. The gas mixture of the composition 4%H2-0.5%02-Ar was made to flow on the inside electrode. The hydrogen sensor probe was inserted directly into molten copper and the melt was used as the outer electrode. The effect of oxygen activity gradient to EMF was eliminated theoretically by measuring the oxygen activity in the melt simultaneously with an oxygen sensor. The high stability of output and excellent response to the change of hydrogen activity were obtained over the wide range of industrial copper melting conditions.IntroductionIn the metal casting process, hydrogen easily dissolves in molten metals from water vapor in the surrounding atmosphere. Owing to the large difference in hydrogen solubility between liquid and solid metal, dissolved hydrogen becomes a cause of the defects of blowholes in castings or ingots. It is necessary to control the hydrogen content in the molten metals [l]. Using proton-conducting ceramics as a solid electrolyte, high temperature-type hydrogen sensor can be constructed [2]. SrCe03- and BaCe03-based perovskite-type oxides exhibit appreciable proton conduction under hydrogen containing atmosphere at high temperature [3-5]. A hydrogen sensor for molten aluminum using CaZro.91no.103-a. has been developed and widely used in the ·process control in the aluminum melting industry [6,7]. The same type of hydrogen sensor has also been expected in the copper melting industry. .. However, CaZro.91no.103-a shows ·not only proton but also oxide ion conduction in the high temperature and at low oxygen activies like the copper melting· conditions. Then we studied the oxide ion conduction in CaZro.91no.103-a. iit · detail [8]. From the consideration on the EMF of the galvanic cell employing this material as electrolyte, it was shown that the unknown hydrogen activity may be precisely determined from cell potential which is corrected for the effect of oxygen potential gradient And the hydrogen sensor based in this principle was constructed and tested in laboratory-scale [9,10]. We repeated the similar tests in factory-scale and developed the sensor system for practical uses [11, 12]. In this report, the structure and system of the hydrogen sensor for molten copper will be introduced first. The reliability of the sensor will then be demonstrated from the results of experiments for sensor probes carried out in TYK's laboratory."

Jan 1, 2000

By Xiaobing Yang, Animesh Jha, Greg Doughty

"Successful use of inert anodes should reduce the CO2 footprint in aluminum production. The search for a “holy grail” inert anode for metal electro-winning from constituent oxides using molten salt bath as an electrolytic medium is continuing. In this article we demonstrate the engineering approaches for the fabrication of intermetallic anodes, based on a quaternary Al-Ti-Cu-M (M:Ni, Fe) system for primary aluminium production. In particular, we examine the microstructural and electrochemical properties of alloys, based on the quaternary compositions. We explain the aspects of phase stability under anodic potential, which leads to the loss of anodic materials in the temperature range of 850-1050oC. The results are analysed in the context of oxidation reaction and formation of oxide layers which readily dissolve in the cryolite melt and prevent passivation. The paper also describes the conditions under which the reduction of aluminium at the graphite cathode occurs which also strongly depends on the molten salt chemistry for the nucleation of molten aluminium at the cathode.1. IntroductionOxygen-evolving inert anodes are an alternative to the conventional consumable carbon anodes for the production of primary aluminium. In this paper the materials selection criteria chosen for the engineering of anode is based on the understanding of the thermodynamic stabilities of aluminide intermetallic phases, some of which are formed and remained stable in fluoride melts. For example, the formation Al3Ti dispersed in aluminium metal via molten-fluoride flux reaction is well known in the context of aluminium casting and grain refining [1-3]. It is for this reason in our research we concentrated on the engineering of stable intermetallic phase mixture in the Al-Ti-Cu ternary system, shown in Figure 1 [4]. In this figure two compositions in the Al3-0.5zTi1-0.5zCuz family are shown with the substitution of 7 atomic % and 11 atomic % copper. However initial investigations showed that these two compositions were unsuitable due to the formation of low-temperature liquid (~540oC) and intermetallic phase, Al2Cu along the Al-Cu binary edge during solidification. The Al2Cu phase segregated along the boundaries of Al3Ti and Al5Ti2Cu, and dissolved away when electrolysis was carried out using these anodes above 800oC. The presence of consequential porosity in the anode material increased the corrosion of the alloy through local heating due to high current density at 0.8 A cm-2. The early tests were carried out with cryolite melts, shown in Figure 2, having 3 weight percent of Al2O3 in the bath at 850oC."

Jan 1, 2010

By L. L. Tavlarides, N. V. Deorkar

"Recovery/Recycling of metal ions from industrial process waste streams is a preferred alternative to disposal by conventional techniques. This paper presents methods for preparation of inorganic chemically active adsorbents to be used in fixed bed adsorbers. Methods for immobilization of chelating agents on the inorganic supports are discussed. The prepared adsorbents are characterized to determine coverage density of functional groups, effect of pH on metal ion removal efficiency, regeneration efficiency and uptake capacity. Results from the laboratory scale and bench scale experiments are presented here.IntroductionRemoval of heavy metal ions from processing wastes in various industries is an important problem. Waste streams in electroplating, electronic, catalyst preparation and hydrometallurgical industries contain metal ions such as copper, nickel, chromium, lead, tin, cadmium, silver, gold and platinum. One major concern for the non-ferrous metal industry is secondary recovery of precious metals and cyanide from cyanide leachate from smelter residue and hydrometallurgical waste streams.Recovery methods recently considered include evaporation, electrolyte metal recovery, reverse osmosis (1), adsorption, ion exchange (2,3), membrane separation (4,5) and Solvent extraction. These processes have met with various levels of limited success. The use of liquid ion exchange molecules to selectively extract metal ions for on-site treatment of these waste streams is currently receiving substantial interest (6,7). This interest seems from an awareness of the advances made in the development of commercial extractants for metal ion separation in hydrometallurgical industries (8). However, separation by solvent extraction processes is generally considered to be economical in the range of aqueous metal ion concentrations from 0.01 to 1.0 mol/lit (9). In order to exploit the selectivity of chelating agents, the idea of immobilizing chelating agent into a solid matrix has attracted growing attention in recent years. Many supports such as inorganic oxides, organic polymers, cellulose powder and polyurethane foam can be used for immobilization of chelating agents. Over the last decade, considerable efforts have been directed toward attachment/introduction of chelating agents into a polymer matrix (10,11). Inorganic supports as compared to polymer supports provide high mechanical strength, chemical and thermal stability, and high reaction rates due to open pore structure. On the contrary, organic resins shrink and swell, thus affecting mass transfer (12). Many of the disadvantages of polymer supports can be excluded by the use of inorganic supports. Innovative use of immobilization techniques can produce inorganic chemically active adsorbents with comparable capacity, stability and reaction rates. Consequently, the objective of our program is the development of inorganic chemically active adsorbents to be used in a fixed-bed unit operation as an alternative heavy metal ion recovery process. Methods of preparation of inorganic chemically active adsorbents, (ICAAs) characterization and applications are discussed in this paper. A brief summary of the results from laboratory scale studies and bench scale studies is presented."

Jan 1, 1996

By Qingbo Yu, Qin Qin, Junxiang Liu

"Dry-granulation is a new process of molten blast furnace slag treatment and air is used as heat exchange medium. There are some shortages: poor effectiveness of granulation, high air-slag ratio and high energy consumption, which are the obstacles to popularize dry-granulation. Based on rotary cup atomization, the technique of recovering waste heat of molten blast furnace slag through waste heat boiler producing high pressure steam is exploited. The molten blast furnace slag is granulated to uniform small slag granules with high temperature, and slag granules pour into the waste heat boiler. It could produce steam, obtained in first row and second row tubes, when descending velocity of slag granules equaled 1.1mm/s and the Reynolds number equaled 7100. The application of the system for recovering waste heat from high temperature molten blast furnace slag has a significant meaning.IntroductionBlast furnace slag is one kind of solid waste in iron making process, which is discharged at the temperature range from 1723 to 1923K. In China, there was 0.162 billion tons of slag discharged in 2009, and the energy contained in the slag is equivalent to the energy in 9.4 million tons of coal equivalent. The sensible heat of molten slag is a very valuable waste heat source, so it is worthwhile to recover the sensible heat. At present, the molten slag is treated by a water quenching method. But in this process, the sensible heat is not recovered, moreover, an amount of water is consumed and harmful waste gas is discharged into the environment. Due to the considerations of energy conversation and environmental protection, the iron making industry pays close attention to dry-granulation, which is useful to obtain more benefits [1-4]. The sensible heat is recovered and an amount of water is saved by the method of dry-granulation. The amorphous content of slag granules obtained from dry-granulation is over 95% [5, 6], so the slag granules can be used as a perfect raw material for cement [7, 8].In the late 1970s, the Sumitomo Metal Industries, Ltd. and the Ishikawajima-Harima Heavy Industries, Ltd. jointly undertook the research of rotary drum granulation. This method has several disadvantages: the processing capacity and efficiency are low, and it is not adoptive to operate continuously in production [9]. From 1980, Nippon Steel, NKK, Kawasaki Steel, Kobe Steel, Sumitomo Metal Industries and Nisshin Steel were engaged on air granulation, and the experiments were operated for 6 years on the blast furnace in Nippon Steel. In the process of air granulation, there was great power consumption. The complexity of structure and the great floor space of the air granulation device caused high cost of investment. In 1986, Ukraine exploited a new method of heat recovery referring to the technology of Continuous Casting and Rolling [10]."

Jan 1, 2011

By Min Chen, Zhen Tian, Hongxu Cui

"The effects of adjusting technology on the phosphorous enrichment in converter slag were investigated. The results showed that the grain size of 2CaO·SiO2 with high phosphorus containing content increased slightly with the decreasing of cooling rate, and the proper cooling rate was confirmed to be about l.0°C.min-1. Moreover, the morphology of the phosphorus-rich phase of 2CaO·SiO2-3CaO·P2O 5 was changed from granular for the higher basicity of converter slag to the coexistence of granular shape and rod-like for the lower basicity of adjusted slag. With the addition of adjusting agent such as SiO2 to lower the basicity of converter slag, the phosphorus in converter slag could be transferred into 2CaO·Si02 phase effectively, and P2O 5 content in high phosphorus containing phase reached to above 30%.IntroductionThe yield of converter slag is very large in China, but most of the slag is stacked usually after the separation of iron, which not only takes up a lot of land, but also affects the ecological environment seriously. Therefore, improving the comprehensive utilization and value-added products of converter slag is of great significance to recycle the steelmaking slag[l-3]. On the other hand, the refining of hot metal with high phosphorous content is an unavoidable problem with the decreasing of high grade iron ore, and as a result, more amounts of high phosphorus containing steelmaking slag are produced. However, the current recycle of converter slag is more focused on the emission reduction and reuse of steelmaking slag inside the iron and steelmaking process without considering the recycle of phosphorous resources[4-6]. At the same time, the development and utilization of phosphate ore as a strategic resource is drawing more and more attention, but the phosphate ore in China is mostly low grade and significant amounts of tailings are produced which is harmful to the environment. Therefore, it is important to separate phosphorous resources in steelmaking slag which can be used as phosphate ore for fertilizer material[7-9].Literature studies showed that most of the phosphorus in steelmaking slag existing as 2CaO·SiO2-3CaO·P2O 5 solid solution phase in 2CaO·SiO2 particle. The P2O 5 content in the phosphorus containing phase is very low due to the fact that the basicity of converter slag is usually high and the precipitated amounts of 2CaO·SiO2 particles during cooling are very large, resulting in the fact that the P2O 5 contents in 2CaO·SiO2-3CaO·P2O 5 solid solution phase are much lower which is impossible to be used as phosphorous resources instead of phosphate ore. Thus, the enrichment of phosphorus in steelmaking slag is need[ 10-14]."

Jan 1, 2011

By David G. Dixon, Ahmad Ghahremaninezhad, Edouard Asselin

"In this study pertaining to the electrochemistry of chalcopyrite, the active/passive behavior of a chalcopyrite electrode in 0.5M sulfuric acid solution was investigated. Potentiostatic and potentiodynamic polarization and multi-cyclic voltanunetry were conducted to analyze the electrodissolution parameters of the electrode.The potentiodynamic and potentiostatic polarizations of chalcopyrite revealed the formation of a passive film on the surface of chalcopyrite. From the potentiostatic study in the passive potential region, a decrease in the dissolution current density by increasing the potential was observed. From this, it was concluded that the passive film is an n-type semiconductor and cation interstitial defects or anion vacancies are the charge carriers. From multi-cyclic voltammetry studies, four cathodic peaks at - 0.37, 0.30, -0.10 and-0.20 YsHE were detected on the surface of a passivated chalcopyrite electrode. The cathodic peaks at 0.37 and 0.30 V were connected to ferric to ferrous reduction and copper sulfide formation, respectively. The peaks at -0.10 and - 0.20 were related to chalcopyrite reduction. The products of the chalcopyrite reduction reactions were suggested to be Cu2S, Cu9fesS16 and Cu5feS4 and evolution of hydrogen sulfide gas (H2S).IntroductionChalcopyrite is the most abundant copper bearing mineral in the world and its dissolution behavior represents the most important technological consideration in the hydrometallurgical extraction of copper [I]. Since the current pyrometallurgical methods for copper extraction from chalcopyrite have environmental issues, many studies have considered the leaching and dissolution of CuFeS2 in different aqueous media [2-5]. The main problem associated with leaching processes is the slow dissolution rate of the mineral [6]. During the dissolution process, increasing the potential of the chalcopyrite in the anodic direction will cause the formation of surface layers which hinder the dissolution rate of the mineral [7]. The precise composition of the layers is in dispute. Previous studies have concluded that these layers could be sulfur [8-9], precipitated iron compounds [8], a solid electrolyte interphase (SEI) - which slows the rate of electron transfer- [10], a metal deficient sulfide [ll], or polysulfidic in nature [12-13]. In order to increase the leaching kinetics of chalcopyrite, the characterization of the layers formed during dissolution is essential and electrochemical methods are important to this end. Studies by Biegler [14] show nucleation and growth of a thin two-dimensional sulfide phase on the surface of chalcopyrite during the exposure of a polished sample in HzS04 solution or air. More studies by Biegler and Swift [15] have shown evidence for nucleation and growth of a 3-dimensional phase at low anodic potentials (around 200 mV vs. OCP). The current-time behavior of the dissolution process in this potential area has the characteristics of expansion and overlap of localized dissolution centers."

Jan 1, 2012

By H. Kung, T. R. Jervis, M. Nastasi, T. E. Mitchell

"A systematic study of the structure-mechanical properties relationship is reported for nanolayered composites of MoSh-SiC, Mo-MoSh, Mo-MoShNx, MoSi2-MoSi2Nx, and Mo-MoShMoSi2Nx (x=3-4) synthesised by sputtering techniques. These composites have been studied by nano-indentation and cross-sectional TEM as a function of annealing temperature. As-deposited layers are amorphous except for Mo. With increasing annealing temperature, first MoSh and then SiC crystallize, while the hardness progressively increases until the layers start to spheroidize and grain growth sets in at 900ºC. For the case of Mo-MoSi2, the layers react and the composite deteriorates rapidly. However, MoSi2Nx remains amorphous up to 1000ºC, suggesting that it could act as a diffusion barrier between Mo and MoSi2. In fact the Mo. MoSi2Nx, MoSi2-MoSi2Nx and Mo-MoSi2-MoSi2Nx nanolayers are found to remain stable up to such temperatures. IntroductionMolybdenum dislicide, MoSh, is a potential matrix material for high temperature structural composites due to its high melting point and good oxidation resistance at elevated temperature [1]. The two major drawbacks for structural applications are inadequate high temperature strength and poor low temperature ductility. Silicon Carbide (SiC) being hard and thermally compatible with most ceramics and intermetallic compounds, has been found to be suitable for second phase reinforcement in various structural applications and, in particular, the addition of SiC whiskers improves the high temperature yield strength of MoSi2 [2]. While most of the research in MoSb-SiC composites has been on the particulate form of SiC, laminated composites may offer unique properties. It has been shown that synthetic multilayers with alternating layers of metal and/or compounds may exhibit interesting mechanical properties [3]. Enhancement in mechanical properties by decreasing the wavelength of multilayer spacing has been studied extensively. In general, two types of strengthening have been proposed: (1) Hall-Petch strengthening [4,5], where the strength increase is inversely proportional to the square root of the layer thickness; (2) Koehler modulus strengthening [6], which increases with modulus difference and decreasing layer thickness. In the present study, we have performed a systematic study of the relationship between strength and structure in a number of different nanolayered systems based on MoSh. Layer thicknesses have been varied and their nanostructures have been varied by heat treatment. Previous work on MoSi2-SiC is summarized [7]. In an attempt to improve fracture toughness, MoSh-Mo nanolayered materials have been prepared but are found to react and deteriorate. Previous work has shown that nitrided MoSi2 (MoSi2Nx with x=3-4) is highly stable [8] and so nanolayered composites of MoSi2-MoSi2Nx and Mo-MoSi2-MoSi2Nx have been prepared to assess the' stability and mechanical properties of these composites. Preliminary results are presented."

Jan 1, 1994

By K. S. Han, M. Yoshimuura, H. Fujita, Y. Sato, S. W. Song

"Film of LlCoO2 as cathode material for rechargeable lithium microbatteries has been fabricated on the platinum metal substrate by electrochemical-hydrothermal method in concentrated LiOH solution at 200 °C as Soft Solution-Processing. The film fabrication has been understood in terms of dissolution of cobalt metal powders and subsequent oxidative deposition on the substrate. The film structure was characterized using scanning electron microscope, X-ray diffraction analysis; X-ray photoelectron spectroscopy and micro-Raman spectroscopy.IntroductionRapid growth of wireless communications and emerging integrated optoelectronic circuits caused the miniaturization· cif electronic devices, thus the demand for high energy density microbatteries as a power source for the microelectronics increases. In this regard, all solid-state lithium microbatteries including LiCoO2 and LlMn2O 4 [l-4], the most promising intercalation cathode material, have been developed. However, major difficulty of .fabrication of a lithium microbattery arose from the preparation of cathode film, according to a· recent report on Rare Metal News [5]. Although many attempts have been made to deposit the cathode films, all those methods are mostly chemical vapor deposiiton (CVD), various evaporation, sputtering techniques and spray pyrolysis. These methods require preparation of bulk cathode materials cir its precursor, then deposition with complicated instruments including high· vacuum system, and even postsynthesis annealing to obtain desire electrochemical 'properties. It is clear that all of these techniques are neither economic nor environmentally friendly. Compared to those methods, film form.ation from an aqueous solution is thought to be simpler and more economical, and requires much· less energy consumption. Our .group has demonstrated the utility of Soft SolutionProcessing [6,7], which is defined as environmentally friendly processing using (aqueous) solutions, to produce films of a variety of functional solid materials. According to the Pourvaix's diagram [8], some metal can be dissolved in an alkaline solution and consequently combined with hydroxyl group or oxygen anion forming metalate or metalite. Cobalt also seemed to form cobaltite, HCoOi in strong alkaline solution in the Pourvaix's pH-potential diagram. Based on this information, it was expected that LiCoO2 could be prepared using the cobalt metal in Li OH solution by Soft Solution-Processing. Recently, we reported the successful single step fabrication of electrochemically active LlCoO2 films on the cobalt metal substrate by hydrothermal methods without any post-synthesis annealing as Soft SolutionProcessing [9,10]. Film formation mechanism could be elucidated by the following evidences. . As expected from Pourvaix's diagram, cobalt metal was dissolved in concentrated LiOH solution forming dissolved cobalt species which was detected by an observation of absorption band in UV-VIS absorption spectrum [10]. Thus the reaction was assumed to be started from dissolution. Time dependent potential of Co electrode exhibited only one-step evolution with 0.6 eV from Co metal to LiCoO2 [10]. Another strong evidence was the finding of LiCoO2 powder precipitates at the bottom of tetlon beaker after the reaction [11]. Based on those experimental findings, it was understood that film is formed by dissolution-precipitation mechanism [9-11]."

Jan 1, 2000

By Wei-ling Wang, Ryosuke O. Suzuki, Xiang-ning Meng, Miao-yong Zhu

"A finite-element thermal-stress model of continuous casting mold is conducted to predict deformation of copper plates and its change with different cooling structure. The results show that deformation behavior of copper plates is mainly governed by cooling structure and thermal- mechanical conditions, deformation amount is related to structure geometry, and a small deformation mutation occurs in cooper-nickel boundary due to different properties. The maximum deformation of hot surface centricities of wide face locate at 100 mm below meniscus and that of narrow face locate at meniscus and terminal of water slots and significant curvature fluctuations on both sides of copper-nickel boundary. The maximum deformation of centricities is increased up to 0.05 mm with thickness increment 5 mm of copper plates, and maximum deformations are only depressed 0.01 mm and 0.02 mm with increments of 1 mm nickel layer thickness and 2 mm water slot depth respectively.IntroductionIn conventional continuous casting of steel, a large amount of sensible and latent heat of molten steel dissipate in primary cooling zone and make continuous casting mold under enormous heating load giving rise to thermal stress, deformation, high-temperature fatigue and creep not only depress mold life-span, but reduce casting stability [1] Many studies focused more on heat transfer, solidification and shrinkage of solidifying shell to provide inverse proposals for optimizing cooling system and even designing new taper of mold [2,3], but it is generally useless to those of having been manufactured or being put into production. Therefore, mold-related forward problems show necessity to be discussed deeply, and stress and deformation distributions based on special thermal conditions in mold should be analyzed in order to explore suitable cooling structure of mold directly. Samarasekera et al. [4] examined heat flow and distortion of two-dimensional longitudinal sections and investigated effect of cooling water velocity, copper plates thickness and carbon content on formation of rhomboidity and longitudinal comer cracks. O'Connor et al. [5] developed a three-dimensional mathematical model to compute thermo-mechanical state in thin-slab mold and calculated temperature and deformation of mold wall to assess roles of various process parameters on impacting mold life. Thomas et al. [6] predicted temperature, distortion and residual stress in mold and indicated increased distortion requires increased remachining, which reduces mold life and increased residual stress increases the probability of a catastrophic crack failure. Park et al. [7l determined heat-flux profiles in funnel-shaped and parallel thin-slab molds based on an inverse heat conduction model and thermocouple temperature measured in-plant and put them into three- dimensional finite-element thermal-stress model to predict temperature, distortion and residual stress of mold wall. Korie et al. [SJ focused on prediction of temperature, distortion and residual stress in mold and in particular to clarify that mold life is significantly affected by temperature and its rigidity, but little effect by mechanical including clamping force, bolt prestress, friction and ferrostatic pressure. Meng et al. [9l predicted temperature and thermal stress in a slab mold and analyzed effect by cooling system geometry and casting speed quantitatively. In present study, a three-dimensional finite-element thermo-mechanical model with type-switched element is transformed from previous heat-transfer finite-element model [9l, and mold deformation is simulated in order to shed light on thermo-mechanical behavior with special thermal conditions and different mold geometry at high casting speed."

Jan 1, 2013

By Muhammad Abid, Kh. .. S. Karimov

"In this study, design and investigation of biogas digester consisting of methane tank with built-in solar collector to utilize solar energy for the heating of the slurry prepared from the dung and heat exchanger is designed, developed and tested. The digester was laboratory type and consists of cylindrical metallic tank of size of 0.5 m in diameter; 1 m in height and 200 liters in volume. The surface of the digester from outside was covered by thermo insulated material a glass wool, except of south side (in northern hemisphere). This side played the role of built-in collector and was blackened to increase absorption of solar irradiation and covered under 45o by glass. In the blackened side of the digester on the different heights it was installed metallic pipes for the inlet and outlet of the air, connected with heat exchanger installed inside of the digester. The heat exchanger was fixed in the level above of the inlet pipe. The horizontal plane reflector concentrates solar beams to blackened side of the digester. In the winter period, it was found that the retention time of this digester is shorter on 15% and produced biogas volume is larger on 20% with respect of ordinary biogas digester. This digester is used for the demonstrative purposes and as a teaching aid presently and base on the results it may be used for the construction of large volume digesters for use in the farms, especially located in the remote and mountain areas where the climate in the winter period is cold. Introduction At present many experts around the world have focused their efforts to energy crises because energy is one of the most important factors for the development of the society. It is known that consuming energy is proportional to quality or standard of life. There is a close relationship between energy consumption and the Gross National Product (GNP). It is obvious that for further development of the country additional sources of energy is required, which are cheap, safe and environmentally compatible with respect to the action on possible wastes. Utilization of renewable energy is one route to help in solving the above mentioned problems. In particular, biogas as a source of renewable energy is produced by biotechnology and used wide on residential scale [1]. The biogas was produced for the very first time in 1814 by Deivy from organic wastes. In 1900 production of biogas was started in Bombay (India) [2, 3]. Biogas consists of 55-70% methane (CH4) and around of 27-44% carbon dioxide (CO2) and less than 1% H2 and H2S. At present biogas is used widely in some countries for lighting, machines, and vehicles, generators, cooking and heating. Biogas generation is suitable for small to large scale operation and at present is realized in a number of developed and developing countries as USA, Hungary, China, India etc. Since 1990s biogas projects construction in China has developed steadily by the end of 1998, there were altogether 6.88 million household biogas digesters [4]. In Russia biogas digesters are used for processing of hard dung into biogas [5]. Over the last few years the very first biogas digesters were constructed in Tajikistan as well [6,7] and it was found that the digesters can work with sufficiently high efficiency in mountain areas as well ."

Jan 1, 2008

By Keiji Okumura, Hong Lan, Masamichi Sano

"Magnesium has been well known as one of the excellent agent of desulfurization, deoxidation, etc. in iron- and steelmaking because of its high reactivity. Since its production is energy nitensive, the price is very high. Thus magnesium has not widely been used as an agent in metal refining ·processes. In the present work, reduction of magnesia by carbon and aluminum is examined. Because the reaction is very sensitive to temperature, non-isothermal technique is applied to investigate the reaction kinetics. The effects of heating rate .and reaction interface area on the reaction kinetics .are studied. .A kinetic model is proposed based on the experimental results.IntroductionFor the metal refining processes, the production of high purity metal has been one of the most important research subject. In order to produce the high purity metal, the amount of the refining agent and the consumed energy is increasing. Therefore, if the future earth environment is taken into consideration, the further efficient and energy saving processes are required. Generally, Cao slag has mainly been used for desulfurization of molten iron as a desulfurization agent. However, environmental problems, such as recycling of disposal slags, are still unsolved. On the other hand, the deoxidation of molten steel is mainly performed by addition of aluminum. Therefore, the alumina inclusions· remain in. molten steel and the great efforts have been made to the removal of the inclusions. The affinity of magnesium with sulfur and oxygen is strong, and magnesium is well known as a powerful desulfurization and deoxidation agent. However, magnesium has been seldom used for the steel' refining process. The following reasons are considered. Generally, magnesium is expensive. And at iron- and steelmaking temperatures, the refining efficiency becomes low due to its abruptly .evaporation."

Jan 1, 2000

By M. Tamura, K. Fujita, K Shinozuka, H. Daimon, H. Esaka

"In-situ observation of unidirectional solidification using transparent substance has been performed to investigate the growth direction of solid phase. Cell or dendrite of which preferred growth direction is not parallel to the heat flow direction was observed with various solidification conditions. Dimensionless growth direction (p) changes from 0 to 1 with increasing growth velocity at a constant temperature gradient. Introducing the dimensionless growth velocity, the relation between p and growth condition could be correlated.IntroductionTransition in macroscopic solidified structure from chill to columnar zone which is found in normal castings takes place via grain selection1). Cast products such as turbine blades are unidirectionally solidified, grain selection plays an important role to choose suitable crystals which have reasonable orientation in the region called ""starter"", which is a very initial part of casting2). Therefore, grain selection is a very important process in the formation of casting structure. The present authors have been studying on the process of grain selection using succinonitrile, which is a transparent organic substance and have found that the growth distance necessary for grain selection depends upon the solidification condition3-5). When the solid/liquid interface is dendritic, the grain selection occurs quickly. On the other hand, when the solid/liquid interface is cellular, it occurs slowly. We supposed that the growth direction of dendrite is different from that of cell when the substance is unidirectionally solidified. Indeed, Kurz and Fisher wrote in their text book that dendrite grows along its preferred growth direction, <100>, regardless of heat flow direction and that cell grows along heat flow direction regardless of its preferred growth direction1). However, there is no quantitative description about the growth direction when the solid/liquid interfacial morphology is cellular. Furthermore, there have been little works6) to study the growth direction of cell and dendrite."

Jan 1, 2000

By U. Meyer, A. Alonso, P. Banios

The sampling of cathodes has changed with the introduction of the ISA-process in copper refineries. A Jernkontoret joint working group of refineries and rod plants from both primary and recycled copper plants has been investigating whether the actual sampling of cathodes is representative for this type of cathodes. As a first stage, samples were sent to the members of the working group with the objective to find an easy basis for a comparison of the results of the next stages. All samples show the same tendency for nearly all elements. In some cases, there may exist differences in calibration and for some elements the detection limits are too high, especially when Optical Spectrometry is used. In the second stage, discs were compared with melted samples to answer the question whether the punching of discs is sufficient for the quality control of the cathode. The analyses of the discs represent fairly well the cathode quality. There are differences between cathodes from different crops. Three punches are sufficient to determine the cathode quality. Finally, samples from various lots of cathodes were compared with samples from the rod produced from these cathodes. The impurity content of the rod corresponds to the impurity content of the cathode.

Jan 1, 2000

By Zhou Jiemin

In order to fully understand the behavior of the rectangular six- electrode electric smelting furnace and improve its design and operation, a three-dimensional mathematical model has been developed which incorporates the electrical and thermal flows into numerical solutions, assuming a steady state regime. The model has been used to simulate the performance of the 16500 kVA nickel matte smelter at Jinchuan in China, and various factors have been investigated. The results of computation are in agreement with the measured data obtained from this furnace and its physical model. Application of this model is described and the calculation on the Jinchuan smelter shows that the operation expenses can be reduced by optimizing the furnace geometry and some operating parameters.

Jan 1, 1991

By S. Sundarraj

The morphological transition between columnar and equiaxed structures is an important solidification phenomenon frequently observed in castings, especially complex parts with varying cross-section, The mechanical properties and the occurrence of defects such as hot tears are strongly dependent on the structure formed in the casting. Hence, it is important to understand the conditions leading to columnar or equiaxed structures. Although extensive work has been done in modeling solidification systems, almost all of the existing models are based on the assumption that the structure formed in the casting is either purely columnar or purely equiaxed. Prediction of the columnar-equiaxed transition (CET) requires a solidification model which accounts for the formation of both columnar and equiaxed structures, along with related microscopic and macroscopic solidification phenomena. In this paper a CET model is presented which: (i) takes account of both columnar and equiaxed structures, (ii) accounts for macroscopic heat transfer coupled with microscopic phenomena such as nucleation, growth and microsegregation, (iii) satisfies solute conservation, and (iv) is easy to implement in commercial finite element and finite difference software. The proposed model predictions of CET have been validated with available experimental results for a uni-directional solidification of an aluminum-copper alloy. A sensitivity analysis has also been carried out to determine the effects of various parameters on the CET model predictions. The model is being extended to other alloy systems and more complex geometries. This work will be published in due course.

Jan 1, 1996

By G. S. Hanumanth

Sedimentation of particles during the liquid metal processing of particulate metal-matrix composites can affect the homogeneity, and thereby the properties, of the cast product. A novel electrical probe has been developed to measure the in-situ volume fraction of ceramic particles in molten metal baths. Using this probe, sedimentation rates for 90 pm silicon carbide particles dispersed in molten aluminum A356 alloy were measured over a wide range of particle volume fraction, 0.05 to 0.3. The sedimentation rate was found to depend strongly on particle volume fraction; the time to clarify a 0.15 m depth increased from approximately 60 to 500 seconds as the volume fraction increased from 0.05 to 0.3. Measured sedimentation rates agree well with the predictions of a sedimentation model based on one-dimensional, two-phase flow theory in which the inter-phase drag function is derived from the momentum equation, utilizing the Richardson-Zaki Equation for sedimentation in aqueous systems. The implications for solidification are discussed.

Jan 1, 1993

By Caisa Samuelsson, Fredrik Engström, Bo Björkman, Margareta Lidström Larsson

"Large amounts of by-products are generated by the Swedish steel industry each year. The EAF-process generates about 400 000 ton of slag, from which 80% is deposit. An alternative to deposit is to use slag as road construction material. However, metal content in the slag can be a problem, due to the leaching. The aim of this work was to investigate how stable these materials are when ageing and kept outside. Five different EAF-slags from domestic steel plants were used in this study. The materials were characterised after 0, 6, 12, 18 and 24 month to evaluate the ageing process. Scanning electron microscope (SEM), x-ray diffraction pattern (XRD) and a standard test for leaching were used. The changes in behaviour differ between the five materials. The total leachability decreases with time for all samples. CaCO3 is formed on slag surfaces as CaO reacts with moister and CO2 in the air. Introduction The slag generation in the Swedish steel industry is about 1.5 million tonnes annually, of which more than 500 000 ton is generated in EAF (Electric Arc Furnace), AOD- (Argon Oxygen Decarburization) converters and during the refining of steel in the ladle metallurgy. Some of the slags are used in different applications, but most of the steelmaking slags produced in Sweden are landfilled today. The chemistry, mineralogy and physical characteristics of slags make it a suitable material in construction, replacing for example, gravel and rock [1]. In some respects, in road construction, it may even be technically superior to virgin material. Slag from scrapbased steelmaking is used for road construction in Europe. The reason for the low utilization in Sweden is mainly due to potential leaching of harmful elements, legislations and competition with easily available natural raw materials. Except the potential leaching, the technical obstacles for not using some slags in construction include:"

Jan 1, 2008