Search Documents

By Jilai Xue, Jun Zhu, Liang Liu

"Separation removal of fluorite and calcite from scheelite is a difficult technical operation in current industrial practice with a heating process causing large energy consumption and high production costs. In this work, the floatation separation at room temperature were carried out using two types of skarn scheelite ores. The results showed that CaO and Na203 are better than NaOH as a regulator in pH value. In the rough floatation and first cleaning floatation, CaO (500g/t), Na203 (3000g/t) were used as a pH regulator, waterglass (4000g/t) was as a gangue depressant, oleic acid or sodium oleate were used as a collector. The degree of the obtained W03 concentrate was more than 65% (commercial product).IntroductionThe mainly gangue in scheelite are quartz, calcite, barite and some rare metal ores. There are three main types of scheelite for floatation: scheelite--quartz (silicate minerals) type, scheelite-calcite/ fluorite type, scheelite--calcite/fluorite/barite type. Generally speaking, scheelite--quartz type is separated easily, and others are difficult, on the contrary. The last two kinds of scheelite are always called scheelite--calcite/fluorite (barite) type, because there are similar floatation ability and floatation process between them. Scheelite, calcite and fluorite have same cation - Ca2+, it makes them have close floatation property [1]. Separation removal of fluorite and calcite from scheelite is a difficult technical operation in current industrial practice.The traditional separation method is a heating floatation process (Petrov's process) [2]. It can deal with many kinds of scheelite, and can be obtained stable quality ofW03 concentrate. On the other hand Petrov's process causes large energy consumption, high production costs and bad operational environments. Since 1980s, scheelite ambient temperature floatation has become the mainstream of study [3]. Nowadays more and more studies on scheelite floatation focus on complex reagent system [4, 5], rigid operating rules and at the same time development new regulator [1, 5]. Some research show there are new regulators can concentrate scheelite efficiently, but it may cause high costs, potential pollution and difficulty to spread. Oleic acid and sodium oleate used as collector have high adsorption capacity to scheelite, but same to calcite and fluorite[6]. So, it would not get ideal effect for separation of scheelite. In this work, the floatation separation at room temperature were carried out using two kinds of skarn scheelite ores. Calcium oxide and sodium carbonate was used as a pH value regulator, waterglass was used as a depressant and Oleic acid/sodium oleate was used as a collector. The result of experiment showed that the degree of the obtained W03 concentrate was more than 65% by one time ambient temperature roughing floatation, several times ambient temperature cleaning process."

Jan 1, 2014

By Xiang-ning Meng, Miao-yong Zhu

"A three-dimensional finite-element heat-transfer model is conducted to predict temperature of hot copper plate in a slab continuous casting mold and the effect of casting speed on temperature difference between copper plate and solidifying shell is simulated in combination with process data. The results show that centre temperature of hot copper surface at casting speed 1.8 m·min-1 and 2.0 m·min-1 are higher than that of 1.6 m·min-1 casting speed 4.7-5.2 °C and 11.2-12.2 °C respectively and temperature is not increased linearly with casting speed. Temperature difference in meniscus between mold and shell is influenced obviously by casting speed and increased 4.0- 6.0 °C with increment of casting speed 0.2 m·min-1• Fluctuation of temperature difference in meniscus is a main reason to deteriorate casting quality as increasing casting speed.IntroductionIn conventional continuous casting of steel, a large amount of sensible and latent heat of molten steel dissipates in primary cooling zone and mold becomes a critical component of caster to govern steel quality, meanwhile, thermal load on mold is increased constantly and environment is also more abominable since high productivity and quality are required and high-effective technologies are applied. So, an in-depth understanding of thermal behavior of mold at high casting speed is essential to design cooling structure and maintain casting stability. Many studies have been carried out to shed light on thermal behavior in mold. Chow et al. [l] applied a mathematical model to heat transfer in billet mold at a high casting speed to give a new taper in order to minimize mold-strand interaction. Thomas et al. [2] researched relation between mold geometry and temperature distribution based on a finite-element heat-transfer model. Lu et al. [3] indicated that slab mold temperature are mainly affected by thickness of copper plate and nickel layer by a heat transfer model. Samarasekera et al. [4, 5] researched temperature of copper plates for both billet and slab molds and effect of a large number of factors ranging from water quality to casting speed. Park and Thomas et al. [6, 7] developed a finite-element thermal-stress model to determine temperature and thermal distortion and stress in both thin and slab molds and O'Connor et al. [8] applied an elastic-plastic-creep finite-element model in a funnel shaped mold to achieve same goals. Cicutti et al. [9] evaluated heat transfer and temperature fluctuation in a slab mold and proposed an expression to predict global heat flux as a function of process parameters and an index to quantify thermal instability. All mentioned above shown that thermal behavior is not only important to casting stability, it is also premise to further understand mechanical behavior in mold."

Jan 1, 2011

By Yuanyuan Wang, Hong Li, Xueting Liu, Hao Bai, Kang Zhou

"Phase change materials are widely used in efficient utilization of energy and new energy technology. Especially, more attention has been paid to composite phase material, which is applied on architectural energy-saving and efficient working fluid. In this paper, stearic acid-silicon dioxide composite material was prepared by sol-gel process from tetraethyl orthosilicate (TEOS) and stearic acid (SA). The material was investigated by Field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR) and Differential scanning calorimeter (DSC). The FE-SEM results show that 3D-grids of silicon dioxide were formed clearly and SA was encapsulated in the silicon dioxide shell. The FT-IR results show that there were no chemical reactions between silicon dioxide and SA, which is the chemical property of the composite material, is stable. The DSC results show that the composite phase change material has favorable heat capacity. This material is expected to be used to make a cooling working fluid.1. IntroductionEnergy thermal storage becomes increasingly prominent issue in recent years, because thermal storage has been used in many aspects, for example, it can be added into building materials to improve heat conditioning. Another potential application of thermal storage materials is that the intermittent waste heat can be collected and recycled effectively by using the thermal storage facility. Thus, energy thermal storage plays a significant role in conserving available energy and improving its utilization [1]. Energy thermal storage includes sensible heat storage and latent heat storage. The latent heat storage has great heat density with a constant temperature during the phase change process [2-5]. Large quantities of latent heat storage will be absorbed and released when phase change takes place. Based on the former researches, some phase change material (PCM), such as fatty acid and paraffin waxes, has been proved to have high latent heat storage capacity and appropriate thermal properties [5-6]. However, using the PCM in energy storage systems directly is restricted, e.g. some properties of organic PCM, like form-stability and thermal conductivity, are not good enough to use. Meanwhile, almost all the inorganic PCMs are corrosive and most materials may cause sub cooling and segregation [7-9].The other problem is that the leakage when the temperature reaches the phase change point. Therefore, encapsulated composite phase change material (CPCM) emerged in order to solve the problem of leaking out, minimize the sub cooling and prevent phase segregation. [10-13] However, the easy flammability of fatty acid also has hindered the development of PCM. Accordingly, it has been found out that silicon compounds are environmentally friendly promising substitutes for halogen-containing flame retardants. Especially, silsesquioxanes are excellent in the flame retardancy. So CPCM can be encapsulated with SiO2 acting supporting material."

Jan 1, 2014

By Clemens Schmetterer, Patrick J. Masset

"The surface tension represents an important property for the modelling of high temperature processes. In this study the surface tension of two Al2O3 – CaO – SiO2 model slags and the influence of the admixture of 5 up to 30 wt.% FeO were studied. The surface tension measurements were carried out using the sessile drop technique on BN substrates under Ar atmosphere (10-6 atm O2) up to 1500 °C.IntroductionThe aim of VIRTUHCON1 is the virtualization of high temperature conversion processes, a task that requires thorough understanding of these processes. In many of these conversion processes slag plays an important role to control the properties of the product, to protect the reactor lining or simply as waste. Slag surface tension is one of the materials properties that is needed for the description of such processes, since it influences the interactions between the components in the reactor, e.g. at the slag – Fe interface in the blast furnace.Surface and interfacial tensions have thus received considerable attention in research, but the number of investigations in this particular pseudo-quaternary system is surprisingly low. Furthermore, the literature data are subject to different measurement conditions and techniques which complicates the data analysis and comparison.The slag atlas [1] offers a compilation of the available literature until 1986 (shown in Table I), but literature search has not revealed more recent studies of this system until now. For example, Elliott and Mounier [2] determined the surface tension of ACSF slags using the double tube maximum bubble pressure technique at 1200 °C. They kept their slags in contact with Cu-S-F mattes, and the slag therefore contained a certain amount of sulphur which acts as a surfactant and lowers the surface tension. The compositions of their slags were scattered over a wide composition range and they did not use a common ACS base mixture for their tests, either. The surface tension values vary between 417 and 446 mN/m, but due to the reasons just mentioned no trend in the measurements can be observed and the influence of FeO admixture on the surface tension cannot be deduced. Further information including the temperature dependence is available from Pavlov et al. [3], Ishchanov and Shushkov [4] and Murav’eva and Kaplun [5]; the diagram on page 446 in Ref. [1] has been drawn from these sources. Both positive and negative temperature coefficients are reported in these works. SiO2 is the only pure constituent that has a positive temperature coefficient [6], but a correlation of the temperature coefficient with the SiO2 content was not found to be conclusive."

Jan 1, 2011

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 R. Colás, A. Salas, M. P. Guerrero Mata, R. Garza

"The use of the finite element method (FEM) for studying the plastic behavior of metals has become a common practice over the past few years, because it has been proved to be a good means of evaluating processes parameters, and predicting and improving processes, avoiding the traditional trail and error technique. FEM was used via a commercial package (Abaqus) to create two dimensional models to simulate uniaxial tensile tests for a galvanized low carbon steel. The aim of the work was to analyse the plastic behaviour of a distribution of grains on the zinc cover of a set of galvanized low carbon steel samples. A mesh with lines 2 mm apart was drawn on one of the faces of the samples that were deformed at room temperature, at constant crosshead speed, stopping the deformation at different times. Before and during the stops the deformation measurements were recorded for further calculations in an image analyser in order to compare these with computational predictions, as well as validate the numerical model. The results of this study can be extended to other testing conditions, besides the model can be used for obtaining constitutive equations of the materials.INTRODUCTIONThe use of the finite element method has been widely spread during the last two decades in most engineering areas, it is a good means of obtaining approach values at a first try [1-4]. Thanks to the software and hardware developments it is now possible to run huge problems within hours or minutes, making the technique more accessible and useful for the industry.The aim of this work is to create a finite element model for the uniaxial simple tension test, and compare the results with some experimental results, and asses the validity of the model.The plastic behaviour of the materials with FEM has been studied for a long time [5] and there is always something new to learn about this behaviour of the metals in particular, as well as to characterized new materials and alloys [6,7]. The tension test has been used since XIX century to get knowledge of the materials [5,8], it is the test that has been used the most and the only that is fully standardized, although it has the limiting of low strains, it is still the most widely used, especially in the industry.Two different finite element models in two dimensions (2D) have been developed, one called the mesh model and the other one the grain model, attention was focused on the geometry and strain prediction. The model is validated with experimental test, by using the data and directly comparing it with the numerical predictions. All the tests were carried out at the same constant crosshead speed at room temperature. An analysis of the grid distortion using FEM and analytical methods has been carried out."

Jan 1, 2001

By Dong Liang, Honggang Zhong, Zhenxing Yin, Qijie Zhai

"2507 super duplex stainless steel (SDSS) has been widely applied in a marine environment, attributing to its excellent pitting corrosion resistance and mechanical properties which are particularly determined by the nitrogen precipitation behaviors and volume fraction of ferrite. In this paper, various cooling rates were obtained by applying four different moulds with the common gating system. By which the influence of cooling rates on nitrogen precipitation behaviors and the ferrite fraction in cast 2507 SDSS was comparatively investigated. The results showed that nitrogen porosity could easily precipitate in cast 2507 SDSS under standard atmospheric pressure. The number of nitrogen holes increased with decreasing the cooling rates, and the holes mainly distributed in three zones, i.e. the interface between the horizontal and vertical columnar grains, top vertical columnar grains and the final solidification region. Additionally, higher ferrite fraction was obtained with lower cooling rates.IntroductionDuplex stainless steels (DSS) have a dual-phase microstructure consisting of ferrite (d) and aus-tenite (?). Due to the combined advantageous properties of d and ? phase, their application rapid-ly increased in industry [1, 2]. Super duplex Stainless Steel (SDSS) is the third generation of du-plex stainless steels, of which the alloy elements Cr, Ni and N content are higher than the stand-ard 2205 DSS. Because it has high contents of alloy elements, the SDSS has better mechanical properties, and its pitting resistance equivalent number (PREN) reached a point 43. Hence SDSS has been used in petroleum chemical industry, the marine equipment and harsh corrosion environments [3]. SDSS contains ferrite stabilizing elements, such as Cr, Mo and Si, and austenite stabilizing elements like Ni, Mn and N [4]. Many researchers have studied the effects of these elements on the stabilization of d and ? phase and the ratio of the two phases. High nitrogen con-tent is another prominent feature of SDSS. Nitrogen addition to SDSS is very effective for improving its mechanical properties [5] and corrosion resistance [6], such as pitting resistance in NOx environment. To increase the nitrogen content in steels, a lot of work had been done. N. Nakamura and S. Takaki [7] examined the behavior of nitrogen absorption in Fe-23Cr alloy powder by sintering in nitrogen gas atmosphere, they found nitrogen content easily up to 1.0 wt. %. Using devised NH3 gas injection system, W. Park et al. [8] successfully produced austenitic Fe–23.5Cr alloys containing over 3 wt. % of nitrogen. Further-more, W.P. Tong et al. [9] stated that nitrogen percent was extraordinary high (about 10 wt. %) in pure iron plate. However, the above methods are difficult to be applied to large-scale industrial production."

Jan 1, 2012

By Yuanyuan Zhang, Patrick J. Masset

"The reduction of FexO in slag is one of the fundamental reactions in iron and steelmaking technology, including the blast furnace process (BF). Experiments on the reduction reaction of iron oxide using CaO-SiO2-Al2O3-FexO-C mixtures were carried out using thermogravimetric analysis (TGA) under reducing conditions at temperatures up to 1100°C. The composition of the primary slag was chosen so that the FexO concentration varied between 0 and 75 wt % and the CaO/SiO2 ratio being kept constant to 0.90. From the TGA curves recorded isothermally at different temperatures the kinetic parameters of the iron oxide reduction were determined.IntroductionIn blast furnace the iron ores and coke are charged in layers from the top. The reduction of iron oxide by coke is one of the fundamental reactions in the blast furnace process. Although a great amount of work has been done on the topic of reduction of composites [1, 2, 3], gasification of carbon [4, 5] and reduction of iron oxides by CO [4, 5, 6], the mechanism of reduction in iron oxide - carbon powder mixtures is not fully understood. Fruehan [1] and Rao [2] studied the reaction rate of the reduction of iron oxide by different types of carbon and concluded that the reaction mechanism is controlled by the oxidation of carbon at temperatures up to 1200°C. Rao [2] studied the reaction of hematite with graphite as carbon source up to 1080°C. An activation energy close to 300 kJ/mol was calculated within the temperature range of 950°C to 1087°C. In his study, Fruehan [1] determined the rate of reduction of Fe2O3 and FeO by coal, coke and coconut charcoal as carbon sources within the 900°C to 1200°C temperature range. He found that the reduction of Fe2O3 by carbon occurs in two stages and that the reduction of Fe2O3 to FeO is faster than that of FeO to Fe. This is due to the fact that the CO2/CO equilibrium ratio is higher, and hence, the rate of oxidation of carbon is faster. Fortini and Fruehan [3] have studied the reduction reaction of wustite by graphite and wood charcoal. They found that the wustite reduction can have a significant effect on the overall rate of reduction in composites at high temperatures or in the presence of a large excess of carbon. The calculated activation energy of the reduction reaction by wood charcoal was close to 368 kJ/mol, while the activation energy of the reduction reaction by graphite was 444 kJ/mol."

Jan 1, 2011

By Jordan Mayorga, Joseph Kopp, Robert Boehm, Daniel P. Cook

"Solar generated power has long been considered a useful energy source only for low-energy density and non-mission critical use, such as providing electricity for residential applications. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar- 1 near Las Vegas, have demonstrated that solar does have application to high energy density industries such as materials and chemical production. This paper will discuss the current operating con_guration of the Solar-1 facility and show how proposed modi_cations, such as addition of thermal storage and use of liquid salts as the working uid, can further improve the e_ciency and energy production of the plant.IntroductionThe United States as a nation is the largest consumer of energy in the world at an estimated 29 trillion kWh per year[1], which is roughly 15% of total global energy consumption[2]. On a per capita basis, the United States also leads most of the world, using an average of 96,000 kWh per person[3]. Roughly 40% of the energy consumed in the United States was produced from petroleum, 23% from coal, 23% from natural gas, 9% from nuclear and the remaining 5% from renewable sources such as solar, geothermal, wind, and hydroelectric[1].Energy demands associated with the industrial-scale production of chemicals and materials is a signicant portion of the United States total energy consumption. Roughly 33% of the energy consumed in the United States is used by the industrial sector, with 22% of this amount used in chemical production, 16% used in petroleum rening, and 14% used in the smelting and rening of metals[1]. Energy costs are also a signicant, if not the most signicant, portion of the total production costs for many materials. For example, roughly 30% of the cost of producing aluminum is the electricity used in the Hall-Heroult process [4], while the cost of energy is roughly 15% of the total cost of producing steel products [5].The primary sources of power for the industrial sector have been coal, petroleum, hydro- electric and nuclear. The use of alternative energy sources, e.g. solar, wind, geothermal, for industrial materials production has been slow in coming because they are intermittent and low-energy density sources, i.e. no solar power at night, no wind power when the air is still, etc. The success of Concentrating Solar Power (CSP) facilities, such as the 64 MW Nevada Solar-1 (NS-1) near Las Vegas, have demonstrated that solar can have application to high energy density industries such as materials and chemical production.This paper will discuss the current conguration of the NS-1 facility, and potential modications to the facility that will increase both its power e_ciency and power density."

Jan 1, 2010

By Duck Jae Lee, Kwan Ho Kim, Ji Whan Ahn

"In Korea, reutilization of constructions waste is gaining an increasing attention as generation of construction waste is projected to increase continuously. In current practices, the concrete waste is simply crushed and used as a low application such as paving, back filling, etc. In this study, a new process was developed comprising of heat pretreatment, autogenous milling, and density separation for complete reutilization of concrete waste. Firstly, the concrete waste was crushed using autogenous milling. The coarse size fractions from autogenous milling have a density of 2.5g/cm3 and a water absorption ration 3.0%, which meet the specification of the first class of KS F 2573. The fine size fractions were further separated using a hindered-settling column into two products 1) underflow, 2) overflow. The underflow sample was a high quality fine recycled aggregate which can be used for concrete making, and the overflow sample was an enriched cement material can be also used for CO2 sequestration by mineral carbonation. Introduction Kwan Ho Kim1, Ji Whan Ahn2, Duck Jae Lee1, Hee Chan Cho1 Recently, the importance of resource recycling is gaining a greater attention due to the increasing price of natural resource. Recycling is beneficial for not only the management of waste, but also the reducing of consumption of natural resources and huge energy consumption to treat of natural resource. The construction and demolition waste comprises the major industrial waste generated in Korea. It increased to 54 million tons in 2004, and is projected to increase to over 300 million tons in 2020, as many buildings reach the end of their 30 years life. Among total waste, the proportion of concrete waste was about 30% in Korea. Due to its large volume, recycling of concrete waste is the most important aspect of the waste management. In the current practices, the concrete waste is simply crushed and used as a recycled aggregate. The recycled aggregate has a low quality and most of them are down cycled for usage as paving material, back-filling material, concrete bricks, etc. It cannot be reused for replacement of natural aggregates because cement mortar is not separated perfectly from aggregates. These kinds of recycled aggregates tent to be weaker, more porous and have a higher value of water absorption. When these aggregates are used in concrete making, there are problems of higher total water demand, low compressive strength and durability [1-5]. And recycled fine aggregate is not almost recycled due to its low quality. In this study, a new processing circuit is developed to produce not only highquality recycled coarse aggregates but also fine aggregates and cement material from concrete waste."

Jan 1, 2008

By Olga K. Karakasi, Angeliki Moutsatsou, Ioanna Kavallari

"The present study focuses on the amelioration of the behaviour of high calcium fly ash (HCFA), investigating its application in a new environmental field: oil spill clean up. High calcium fly ash is a by-product of electric power plants, produced annually in large quantities, whose greater amount is landfilled. Some of its properties, such as its chemical and mineralogical composition, its fine particle size, its porosity, floating ability and hydrophobic character make it an attractive material for this purpose. Researches showed that when added to an oil spill, it forms a semi-solid phase, which allows the quite total removal of the oil, but it is not stably retained on the surface. In order to ameliorate its floating ability, the decrease in its specific gravity by mixing with a lighter material is investigated. In the present study the mixing with two materials, already used in oil spill clean up, sawdust and a polymer, has been examined. Addition of 15-25% w/w sawdust to HCFA results in a material with better performance than HCFA or sawdust alone: it has a satisfactory floating ability and allows total removal of oil. Addition of the polymer, however, has resulted in no significant amelioration of the oil sorption behaviour of HCFA, probably because no affinity between HCFA and polymer has been achieved.IntroductionCoal fly ash is a by-product of coal combustion in electric power plants, produced worldwide in huge quantities, approximately 500 million tones annually. High calcium fly ash (HCFA) is classified to class C presenting a (Al2O3 + SiO2 + Fe2O3) > 50%. The production of lignite fly ash in Greece comes up to 13 million tones annually, of which only 12% is used in construction applications, the other being landfilled [5, 6].Besides its limited application worldwide as a construction material, research is focusing on the development of new environmental applications, such as waste stabilisation and solidification, soil and water environmental improvement [9, 12]. For the application of fly ash in further environmental fields several chemical modifications have been applied, in order to improve its properties. Extensive research has been focused on the conversion of both coal and lignite fly ash to zeolite and its further application in environmental field, such as the uptake of inorganic (heavy metals and ammonium [8, 11]) or even organic compounds (methylene blue [15]) from waste water streams, or the use as molecular sieves, to adsorb water molecules, SO2 and NH3 from gas streams, due to the high cation exchange capacity and porosity of the produced zeolithic material. Furthermore, lignite fly ash has been combined with sodium silicate solution, prepared by treatment of rice husk ash, and tetrapropylammonium bromide, to synthesise hydrophobic zeolite ZSM-5 [4]."

Jan 1, 2008

By Jamil M. Khalifeh, Shadia J. Ikhmayies, Bothina A. Hamad

"The structural and electronic properties of cubic d -NbN are investigated using density functional theory (DFT) and all-electron full potential linearized augmented plane wave method (FPLAPW). The equilibrium structural parameters are determined by fitting the total energy as a function of volume to the Murnaghan's equation of state. We calculated the total and partial densities of states (DOS) and compared them with those computed by different authors. Our DOS at Fermi level is found to be very close to the experimental value. The band structure is computed, discussed and used to find the characteristic energy separations. Valence electron density contours are recorded and discussed. We deduced the partial charge densities of different bands and binding energies of valence core levels and compared them with experimental and theoretical results obtained by different authors.IntroductionNiobium nitride has been intensively investigated over the last decades because of its interesting physical properties and technological applications (superconducting microdevices, microelectronic, catalytic probes, and hard coatings) [l]. While the group IV transition metal nitrides (TMN) mainly crystallize in the cubic NaCl structure (Bl type), those of group V and VI nitrides occur as different phases. Thus for niobium nitride, many phases have been reported in the literature: cubic fcc d -NbN, tetragonal ? -Nb4N3, hexagonal d -NbN, hexagonal e -NbN, and low nitrogen content hexagonal ß -Nb2N [l, 2].Structural and electronic properties of niobium nitride were investigated theoretically and experimentally by many authors. For example, in 1975 Schwarz [3] obtained the partial density of states for NbC and NbN from APW band structure calculations. In 1975 Kallne and Pessa [4] studied the electronic structure of Nb, NbC and NbN by using X-ray emission. In 2003 Amriou et al. [5] studied the electronic structure and bonding mechanism of NbC and NbN compounds using first principle total energy calculations using the full-potential linearized augmented plane wave method. Also in 2006 Sanjines et. al [l] studied the electronic structure of the hexagonal~Nb2N, hexagonal' d -NbN, and cubic d -NbN thin fihns by using X-ray photoemission spectroscopy. They [l] also calculated the densities of states for these phases and used them in the interpretation of the experimental valance band spectra. Most of these studies are old and there is a need for more recent studies. According to our knowledge, there are little comprehensive theoretical studies on this subject by using FP-LAPW method [5], which proved its ability to give accurate results. In this work we used the FP-LAPW method to study the structural and electronic properties of the cubic (fee) o-NbN (space group Fm-3m, prototype NaCl) crystal."

Jan 1, 2013

By F. G. Caballero, J. L. Gonzalez-Carrasco, S. Barrius, H. Carreon, M. Lieblich

"The grit blasting is a low-cost technique successfully used to enhance mechanical fixation of the implants through increasing their roughness. As a result of the severe plastic surface deformation, it produces subsurface effects such as grain refinement, hardening and compressive residual stresses which are generally evaluated with destructive techniques. In this research work, non-contacting and contacting thermoelectric power measurements are performed in blasted 316L VM and Ti-6AI-4V specimens using Ah03 and Zr02 particles which yield a coarse and a fine rough surface, respectively. This study correlates the microstructural changes induced by the grit blasting treatment and the limitations and advantages of each of the nondestructive thermoelectric techniques based on the Seebeck effect used to evaluate these biomaterials.IntroductionIt is well known that surface properties play an important role in metallic materials used in bio-medical applications. Since the biological response is correlated directly with surface properties it is comprehensible the intense activity in superficial modification by physics or chemistry methods in this field. Grit blasting, one of the most popular surface modification of metallic biomaterials, enhances the mechanical fixation of the implant through the increase in roughness [1-3]. Roughening is developed by bombarding the surface with a high-velocity jet of ceramic particles, being the final roughness a function of the processing parameters (pressure, distance, time, ... ) and blasting particles (nature, shape, size). As the plastically deformed surface layer tries to expand relatively to the intact interior of the specimen, residual compressive stress gradients develops perpendicular to the surface at shallow depths with a maximum value at a depth in the range of 5 to 60 µm. This surface treatment also may cause subtle variations in the subsurface material properties, such as increased hardness and grain size refinement, which are consequences of the significant plastic deformation through cold work. Blasted affected zones may extend to a depth of up to about 200 µm. The subsurface hardening and the near-surface compressive stress gradient playa beneficial role by retarding fatigue crack nucleation and further growth, ultimately extending the fatigue life of the metallic part [4]. In this work, two non-destructive thermoelectric techniques (NDTT), the non-contacting and contacting thermoelectric power measurements were used to analyze the subsurface induced changes on blasted Ti-6AI-4V and 316L VM specimens using Al2O3 and Zr02 particles. Detailed information on the microstructural induced effects and subsurface mechanical properties were published elsewhere [5-8]. Here the nondestructive evaluation of the involved microstructural changes is used to assess the global subsurface damage. Advantages of using nondestructive techniques during manufacturing are envisaged."

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 Xinghua He, Shujing Zhu

"Cycled fluidized bed ash (CFBA), a significant portion of fly ash produced from coal-fired power plants and rejected from the ash classifying process, has remained unused due to its high free CaO and S03 content. It is necessary to extend research on the method to reduce the expansion and improve the compressive strength by some effective chemical activator. This paper presents experimental results on the expansion by Le chaterlier tester and the compressive strength. Hydraulic ash-zeolite (HAZ) cementitious material was blended as the chemical activator to study the effects of the activator on the expansion and the compressive strength. The results show that HAZ can not only reduce the expansion, but also increase the prisms compressive strength. Scanning electron microscope observation and X-ray diffraction analysis indicate that the main hydrated products of the sample are calcium hydroxide, ettringite, zeolite and calcite, which can explain the results of the expansion and the strength tests.IntroductionNearly 80% of the electricity in China is produced by coal-fired plants, which results in the production of a large quantity of coal combustion residues, among which coal fly ash is the major component. Because of that the air-pollution becomes heavier as time going on. Cycle-fluidized-bed-combustion systems are retrofitted to meet air-emission standards mandated by China Clean Air Act. Cycle fluidized bed ash (CFBA) will present new challenges for coal-combustion byproduct management. The use of cycle-fluidized-bed ash as a cement replacement in concrete is the most attractive one because of its high volume utilization and widespread construction. However, the replacement of cement with cycle fluidized bed ash in Portland cement concrete usually increases the expansion and decreases the early strength of concrete. In many research of this field, most of them were focus on the activation of pozzolanic activity of CFBA and to make all kinds of blend cement. A number of studies had been carried out on the activation of CFBA using chemical activators. These studies involved using different activating methods including alkali activation and sulfate activation 11, 2]. The former involved the breaking down of the glass phases in an elevated alkaline environment to accelerate the reaction [3, 4]. The later is based on the ability of sulfates to react with aluminum oxide in the glass phase of CFBA to produce ettringite that contributes to the strength at early ages [5-7]. With respect to sulfate activation, the use of gypsum and sodium sulfate had been well studied [5-8]. HAZ is one of HAS sub-products which is a patentd chemical activator made by Wuhan University (ZL98113594.3). It had been used to activate CFBA to produce blend cement in many Chinese engineering projects and time has told us that it is a good activator."

Jan 1, 2012

By Guozhu Ye, Mikael Larsson, Eric Burström, Sten Ångström

"Increased use of scrap in steelmaking including scrap use in BOF has a high economic and environmental potential in terms of increased productivity, energy saving and reduced emission of CO2. Preheating and surface cleaning of steel scrap is a concept developed by MEFOS in a four year research program funded by MISTRA, Swedish Foundation of Strategic Environmental Research. The process concept consists of four major steps: 1) Combustion of ASR or other waste fuel and composing of the gas composition. 2) Scrap heating and cleaning in a shaft where the coated zinc is removed as ZnCl2 and scrap is heated to about 600 ºC. 3) Dust separation for recovery of metal zinc. 4) Gas cleaning. This paper will describe the process concept and highlight the major results from preliminary trials around the scrap heating and cleaning shaft.IntroductionSteel is often coated to increase the corrosion resistance. Share of coated and galvanized steel in the world marked is steadily increasing. This results in increased amounts of scrap with different types of coatings. Use of galvanized scrap in EAF plant results in an EAF dust with high content of zinc ferrite and many other impurities like Pb, Hg, Cd and halide. EAF dust is classified as hazardous waste in most of the developed countries and the steel plant has to pay for external treatment for zinc recovery. For use in BOF plant this will result in a BOF dust containing typically 1-5%Zn making it impossible for recycling to the blast furnace.Different approaches for surface cleaning have been investigated in past. Dapper et al. [1] examined the possibility to evaporate Zn, Ni, Cr, Sn from coated materials using chlorine. Chlorinated rinsing of non iron oxides and metals using HCl from combustion of PVC was discussed by Fray [2]. Further studies by Tee and Fray [3-5] have been concentrated on the possibility to vaporize coatings with an air and chlorine gas mixture. The O2:Cl2 ratio in the gas mixture was found to have great importance for control of the process. To avoid the chlorination of iron, this ratio should be kept at a level of 10:1.Scrap pre-heating up to about 600 ºC is a well known method and this alone could save up to 100 kWh per ton steel. The technology has been established since many years and efficient processes were developed in the 90’s. However, no process has fully gained the expected energy savings as the large quantity of the exhaust gas has to be reheated to over 1000 ºC again to destroy the hazardous components like dioxins."

Jan 1, 2008

By M. A. Rabah, F. E. Farghaly, M. A. Motaleb

"Wastewater from industrial galvanization industry was reclaimed under current flow stream conditions. Results showed that the raw water contains 0.7 % by weight total suspended solids (TSS) causing turbidity amounting to 30. Measurements of Zeta potential as a function of pH revealed that solid separation takes place at pH 9. Addition of H2O2 to the polmer solution helps to oxdize ions of iron and zinc metals toinsoluble ferric oxide and zinc hydroxide to a higher state of oxidation. Addition of 5 mg/L of cationic magna flocculants polymeric solution helps the rapid separation of the turbidity. Separation of floccules so formed takes place by filtration. Addition of peroxide ions to the turbid wastewater confirms the physical stability of the flocs so formed. Impurity flocculation takes place in few seconds. Maximum temperature for safe solid removal was <30°C. The treated water was pure and safe for recycling or use in domestic purposes.IntroductionStocks and et. al. [1] show that the galvanizing process introduces spent pickling acid waste production, but its major constituent, could be used. Survey of the operational procedures adopted and the acid wastes produced by UK Galvanizers are reported. Various methods to recovery spent acid of suitable composition and to eliminate zinc contamination was considered. Application of the Kleingarn acid management system reduces waste volume, saves hydrochloric acid (HCl) and increases component throughput whilst, in conjunction with zinc elimination, could allow recycling of the majority of galvanizer’s acid wastes.Dahab [2]; Kerney [3] reported recycling of galvanizing products, including pickleliquor. Kerney suggested a mobile treatment plant for recycling pickling acids. Dahab found that pollution reduction could be achieved by relatively simple operational changes to the process that gave fairly short payback times.Rozenblat and et. al.[4] studied the extraction of zinc (II), iron(III) and iron(II) with Tributyl phosphate (TBP) from hydrochloric acid solutions containing high zinc(II) concentration. Two technological approaches for the separation are considered. Firstly, the selective extraction of iron(III) (iron(II) is oxidized to iron(III)) over zinc(II) with TBP deficiency. Secondly, iron(III) reduction to iron(II) followed by zinc(II) selective extraction with an excess of TBP. Prior stripping, the organic phase was washed with small amounts of water. Scrubbing of TBP solutions containing iron(III) contaminated with zinc(II) gives always a mixture of zinc(II) and iron(III) which must be recycled to the extraction step in continuous process. The following technological concept is proposed: reduction of iron(III) to iron(II), extraction of zinc(II) with 5-10 volume excess of TBP, washing of TBP phase contaminated with iron(II) with small volumes of water and recycling of the scrubbings and stripping of zinc with water."

Jan 1, 2008

By Batric Pesic

Calcium silicate slag (Di-Cal) and magnesium oxide condensate (MgO) are the by-products of magnesium smelting operations, As these oxides have acid neutralizing and metal precipitating properties, it was decided to examine their reactions with (a) individual heavy metals and (b) with a mixture of metals in solution, The resulting solid reaction products were further tested with respect to the stability of the contained metals, The stability of the solid precipitates were examined as a function of the method of precipitation and as function of the solution pH With respect to the method of precipitation, the performance of Di-Cal and MgO was compared to the performance of lime, an industry standard for heavy metal precipitation, Four different pH solutions (4,0, 5,0, 7,0 and 1 LO) were used to study the effect of pH on the stability of the precipitates. It was found that Di-Cal, in most cases, produced the most stable precipitates and thus, outperformed lime, Metal precipitates prepared by the addition of MgO were the most soluble for each metal studied, except for Se,

Jan 1, 2001

By J. Y. Foley

Platinum-group elements (PGE) are preferentially associated with chromian spinels, including high-iron chromite, magnesian-chromian hercynite, and chromian magnetite in clinopyroxene-rich upper stratigraphic portions of the Tonsina ultramafic complex in southern Alaska. Ratios of Pt:Pt+Pd are proportional to chromium content in the associated chromian spinels. The maximum PGE content of geochemical rock samples from Dust Mountain is greater than 20.000 ppb (>0.6 oz/ton) with minor gold values. The maximum PGE content of tabled chromite concentrates is 3.430 ppb (0.1 oz/ton) at Dust Mountain. 1.029 ppb (0.03 oz/ton) at Sheep Hill, and 1,749 ppb (0.051 oz/ton) at Bernard Mountain. High-iron chromite at Dust Mountain yields tabled chromite concentrates with Cr:Fe ratios between 0.5 and 1.2. Lower PGE contents are found in more chromium-rich chromitites from Sheep Hill and Bernard Mountain that yield concentrates with Cr:Fe ratios between 1.0 and 2.8. Platinum-group minerals include amalgams. arsenides. PGE alloys, and sulfides. These minerals are between 3 and 40 microns in size and are concentrated along grain boundaries and fractures of metasomatically and hydrothermally altered chromian spinel grains.

Jan 1, 1987

By Aichun Dou

Au-Sb alloy sample in which the total amount of Cu and Ni is below 25% (wt. %). In practice, Cu and Ni were difficult to be dissolved in sulphuric acid solution by oxidative leaching under the atmospheric pressure conditions, because of the lower concentration of Cu and Ni in the sample. In this paper, pressure oxidation leaching in sulphuric acid system (POLS) followed by hydrochloric acid leaching (HAL) was employed to remove impurities in the Au-Sb alloy. The effects of variables in POLS on leaching ratios of different metals were investigated in detail. Under the optimal conditions: the concentration of H2SO4 is 1.5 mol/L, liquid-solid ratio is 7:1, the amount of oxidizer is 1.2 times of the theoretical amount, leaching time is 4h and leaching temperature is 427K, the leaching ratios of copper and nickel reached up to 99%, antimony, lead and silver were not dissolved in dilute sulphuric acid solution. The residue from POLS was then treated with hydrochloric acid solution in fixed conditions, the leaching ratio of antimony reached over 92%, the grade of gold in the ultima residue was enriched up to 66%.

Jan 1, 2016