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By Chenhui Liu, Ka-ma Huang, Hong-ying Xia, Bingguo Liu, Hua Chen, Jinhui Peng, Libo Zhang

"The rising popularity of microwave heating in mineral processing has fuelled the need for knowledge concerning dielectric properties of minerals. Dielectric property and microwave absorption property of anthracite were measured over a temperature range of 20-100°C at 2.45GHz by using an open-ended coaxial sensor measurement system. The results show that the dielectric constant, loss factor and loss tangent increase with temperature rising at 2.45GHz. Microwave absorption properties of anthracite are highly dependent on temperature and frequency. At frequency of 2.45GHz frequency used in microwave metallurgy, anthracite is suitable for reducing agent to achieve fast elevation of temperature then returning to original state. The research will be helpful in explaining the thermal running of microwave dielectric heating the anthracite.IntroductionThe application of microwave heating in minerals processing and treatment has recently attracted great interest from the metallurgical industry. Compared with conventional heating methods, the advantages of microwave heating include rapid and selective heating, uniform distribution, high efficiency, fast on and off switching as well as flexible and modular design[l-3]. As a result of these advantages, microwave heating has been applied in a variety of mineral processing and extractive metallurgy, such as microwave-assisted ore grinding, microwave heating for carbothermic reduction and acid leaching of ilmenite ore, microwave drying, microwave-assisted roasting and smelting of sulfide concentrate, microwave-assisted spent carbon regeneration and microwave-assisted waste management [ 4-6]. Though the application of microwave heating in the metallurgical industry is promising, further studies on the interaction between microwave radiation and minerals and its effects are highly desired to develop innovative techniques for minerals processing and ore treatment using microwave heating [7]."

Jan 1, 2013

By M. A. Halim, V. I. Lakshmanan, T. Sheikhzeinoddin, R. Roy

"Chloride metallurgy is emerging as an alternative process for the production of base metals. Process Research ORTECH Inc. (PRO) has been at the forefront of technological development of chloride metallurgy. PRO has developed an innovative technology for the production of high purity titanium dioxide, iron oxide and vanadium pentoxide from ilmenite ores and concentrates. PRO is also developing its proprietary mixed chloride technology for the extraction of vanadium from other sources such as oil shales. In this paper, results from the test work conducted at PRO for the extraction of Ti and V using a mixed chloride lixiviant are presented.IntroductionTitanium and vanadium alloys and compounds have numerous industrial applications. Titanium dioxide is used in paints, plastics, rubber, paper, inks, textiles and a number of other miscellaneous applications. Currently nanosize T1O2 is being investigated for application in the cosmetics industry. Inorganic sunscreens mainly use T1O2 or ZnO particles, which reflect and scatter ultra-violet light. T1O2 nanomaterial is also finding application in smart construction materials and coatings, as a photo-catalytic converter. Nano TiO2 can catalyze the dissociation of NOX gases and other automotive emissions, thereby reducing the smog in urban centers. After the construction material is exposed to sunlight or ultra-violet light, the T1O2 is photo-activated and degrades the pollutants.Titanium metal and titanium dioxide are produced from ilmenite (FeTiOs) or rutile (naturally occurring T1O2) ore. Only about 6% of the titanium resources are used to produce titanium metal and the rest is used to produce T1O2. Many of the titanium ore deposits currently have unacceptable levels of transition metals which limits their processing by conventional routes."

Jan 1, 2012

By Honggang Zhong, Xin Cao, Qijie Zhai, Hongmei Song, Congsen Wu, Cheng Zhang, Jingzheng Ye

"The influence of superheat on the solidification structure and ferrite/austenite phase transformation of a novel lean duplex stainless steel (DSS) was investigated on a setup, which designed to thermally simulate the continuous casting process. The results showed that the macrostructure of the samples all exhibited chill zone, columnar zone and equiaxed zone. The distance from chill zone to position of columnar to equiaxed transition (CET) moved from 51.0 mm to 39.8 mm with an decrease of superheat from 70 °C to 10 °C, and that the grains in the chill zone tended to be finer. In equiaxed zone, the fme and uniform grains were observed when superheat higher than 40 °C; while, coarse grains were found in samples poured at low superheat. Generally, the volume fraction of ferrite increased along the dendritic growth direction, and stabilized in equiaxed zone. The high superheat decreased the volume fraction of ferrite in equiaxed zone, while it had indistinctive influence on chill zone and columnar zone.IntroductionDuplex stainless steel with approximately equal volume of ferrite and austenite, offering an attractive combination of corrosion resistance and mechanical properties. [ l]. The production of DSS, worldwide application in structural engineering[2] and petrochemical industry[3], have increase by more than 100% in the latest decade[4]. But due to the sharp prices increase of nickel and chromium, lean duplex stainless steels which have lower contents of alloy elements were developed. They perform well in both mechanical and corrosion resistance[S, 6] and even have TRlP(Transformation Induced Plasticity) effect[?]. Nonetheless , the mechanical properties of DSS was affected greatly by the solidification structure, such as columnar to equiaxed transition (CET), grain size and phase content[8]. So, the solidification behavior of stainless steel was investigated widely"

Jan 1, 2014

By Alexander V. Derevyanko, Victor P. Popov, Alexander I. Raitchenko

"If an electric current flows along some electroconductive suspension in columnar form the solid particles are 'experienced thermal, mechanical, and electromagnetic influences.The objects were suspension Sn (liquid) - Ni-Cr-Mo-W alloy (solid particles). This is refractory alloy on the Ni base. The direct constant current (with density -106 A/m2 ) flowed through the named suspension during 180+300 sec. At the beginning of experiments samples were ones containing particles suspended uniformly in volume. Although density of solid particles was ~9x103 kg/m3 , i. e. higher than density of liquid Sn (-6.8x103 kg/m3 ), after end of this processing, the non-uniform distribution of particles in volume of samples was observed: concentration of Ni-alloy particles in lower part was smaller than their concentration in upper part of samples, and simultaneously their concentration is increased near outer surface. There was probably the natural convection of Benard-Rayleigh type which had carried, so lid particles upwards, and, in same time, there was the action of spatial Lorentz-forces directed to center forcing the radial movement.The knowledge of named phenomena can be useful for elaboration of technology of gradient dispersed materials and development of some materials science fields.IntroductionThe liquid metal with the electric current or under the alternating magnetic field is experienced compression. This action causes the pressure within metal and the change of the surface of the metal column (see, for example, [1-4]). One of results of such an electromagnetic compression is extraction of the foreign solid particles from a cylindrical liquid sample to surface in the radial directions. However, more complicated paths of the inclusions are observed under some conditions of electric treatment."

Jan 1, 1999

By Fu-Shen Zhang, Mengjun Chen, Jianxin Zhu

"In the present study, different types of cathode ray tube (CRT) glasses were examined by sequential extraction combined with TCLP to provide possible explanations for how Pb and Ba leach out from the waste CRT glasses and to give possible reasons for why they leach out. Sequential extraction results showed that Pb and Ba in the CRT glasses dominanfly presented as the residual fraction. The exchangeable fractions of Pb and Ba were extremely low, less than 0.01 % of the total content, but they were higher than those required by the regulation limits, 5 and 100 mg/L for Pb and Ba, respectively. TCLP tests of the original CRT glasses and CRT glasses residues after each step of sequential extraction demonstrated that the extremely high leaching toxicity of CRT glasses mainly caused by its exchangeable and carbonate fractions of Pb and Ba.IntroductionIn recent years, the amount of cathode ray tube (CRT) contained monitors or TV sets in the market were sharply reduced, since they were substituted by novel and better electronic and electric equipments such as LCD and PDP, leaving huge amount of end-of-life CRTs. 50-85% of the total weight of this kind of computer monitor or a TV set is glass[1,2], which was classified to three categories according to their chemical compositions: black & white glass (BW), color panel glass (CP) and color funnel glass (CF)[3]. In order to provide shielding from X-rays generated during the picture projection process, lead, barium and strontium oxides were used in the glass. In general, a color CRT contains 1.6-3.2 kg of lead . Therefore, these glasses have attracted wide and tense attention due to the potential risk to the environment and human health."

Jan 1, 2011

By Jian Li, S. Penttila, W. Zheng

"Materials selection for Gen IV supercritical water reactor in-core components faces major challenges due to severe operating condition. Beside high-temperature mechanical properties, SCC and general corrosion resistance of commercially available materials are also major focuses in recent research. Recent reports suggest that certain types of surface modifications are beneficial to SCW corrosion resistance. In this study, the effects of surface modifications are investigated, and possible mechanisms for improved corrosion performance are discussed.IntroductionThe current Canadian pressure-tube supercritical water reactor (SCW) design specifies a core outlet temperature of 625°C under 25 MPa of pressure, with peak cladding temperature as high as 850°C. Challenges in materials selection include high-temperature mechanical properties, corrosion resistance, SCC resistance and radiation damage. Most of the SCW corrosion test results available are below 730°C. Early work by Allen [1] summarized the corrosion resistance of alloy groups including Ni-based super alloys, stainless and ferritic/matensitic (F/M) steels that can potentially be used for SCW reactors. F/M steels can only be used at low temperature sites (e.g. down stream piping). At 500°C and 25 MPa, F/M steels develop a thick but mechanically stable oxide layer. However, the long term stability of the surface oxide layer is largely unknown. Ni-based alloys appear to form very thin surface oxide, however pitting was observed in the vicinity of some intermetallic precipitates [2-5], and dissolution of major alloying components could pose significant problems for down stream piping [6]. In addition, concerns of Helium formation due to Ni transmutation prevented this alloy group to be used as fuel cladding. The corrosion resistant austenitic stainless steels (e.g. 316L) are found to be susceptible to localized corrosion such as pitting, intergranular attack and stress corrosion cracking (SCC) [7]."

Jan 1, 2012

By C. Carreno, A. D. Gonzalez Escarcega, M. A. Neri, A. Martinez –Villafane, O. Cobarrubias-Alvarado

"Waspaloy is a superalloy used to manufacture some aeronautical parts subjected to high temperatures and stresses. During thermo-mechanical processing cracks are generated, causing some parts to be rejected. In order to determine the causes of these cracks, this alloy was characterized using techniques such as chemical analysis, optical microscopy, scanning electron microscopy, and EDX analysis. Heterogeneous grain sizes in the microstructure cause a non-uniform strain distribution in these parts, creating cracks in zones with different grain sizes.IntroductionNickel-base superalloys are important materials for high-temperature service applications. The manufacture of components from these materials is typically based on solidification or powder-metallurgy processes [1]. Solidification techniques comprise either the direct casting of parts or the casting of ingots which subsequently undergo a series of thermo-mechanical-processing steps to refine the microstructure. During solidification, microsegregation is usually unavoidable. The primary solidification product is a disordered nickel solid solution with an fee crystal structure (?). In many alloys, the material which solidifies last is a mixture of ã and an ordered fee phase (? '). In prototypical nickel-base superalloys, the ?'-phase is Ni3(Al,Ti) [2-3].Waspaloy is a superalloy that is used in demanding high-temperature environments in which good creep and fatigue resistance are required. One of the most common applications of Waspaloy is for turbine engine rings. To ensure the required mechanical properties, the rings are usually forged and heat treated (Figure 1). Two distinct types of microstructures are usually found to be attractive for such applications: a) A microstructure with a grain size of ASTM 10 to 14 for tensile strength, ductility, and resistance to crack nucleation in low-cycle fatigue; or b) A microstructure with a grain size of ASTM 4 to 8 required for creep strength and resistance to crack propagation [4]. Because it is impossible to refine the grain size through heat treatment, a skillfully designed forging process is crucial for the control of the grain size and, hence the properties of the forged ring [5-6]."

Jan 1, 2012

By Hongmin Zhu, Guihua Wang, Xiangsheng Wang

"The anode process of carbon electrode in fluoride melt was studied by voltammetry and chronoamperometry. Anode gases were analyzed by gas chromatography on-line during controlled-potential electrolysis. Two peaks were observed on the cyclic voltammograms. According to the results of gas chromatography, the first peak was corresponded to the discharge of residual oxide ions, with the formation of CO and CO2. Discharge of fluoride ions occurred at 4.1 V vs. Li+/Li, and leading to the anode effect. With the occurrence of anode effect, small amount of CF4 was detected. As the potential reached 4.5 V, CF4 and C2F6 gas evolution occurred, and the current increased to form the second peak.1.IntroductionIn the primary production of Aluminum and some rare earth metals like neodymium, a departure from normal cell operation known as anode effect results in the generation of perfluorocarbons (PFCs), which have high global warming potentials [1]. Owing to the pressure of environmental protection, considerable research has been carried out to clarify the mechanism of anode effect and PFC generation of industry and laboratory cells in the aluminum electrolysis system [2-9]. The common result on PFC generation is that the PFCs are emitted from Hall-Heroult cells only when they are on anode effect. In this article, we selected LiF, the main electrolyte for the neodymium electrolysis [10-11], to perform further investigation on the underlying kinetics of PFC generation and the nature of the reactions at the electrode.2. ExperimentalAll experiments were carried out in an alumina tube reactor, which was filled with high purity helium atmosphere. Spectrographic graphite crucibles were used, which played the dual role of molten fluoride container and the counter electrode. Lithium fluoride was analytical grade. The experiments were carried out at 900 °C."

Jan 1, 2011

By R. Togashi, T. Aichi, T. Yamada

"A new automatic material- handling system for cathode transportation has been developed. The first system went into service in August 1994 and the remains will be operational subsequently.Because of the complex cell-layout and the number of cells in each row, the critical part of this work was achieving a planned cycle time. This cycle time is determined by the power costs.The central monitoring system for machine operation was started in June 1996, using original application software based on MICROSOFT EXCEL ® on WINDOWS 95® .As a result, only one person is now required to operate both a crane and a stripping machine for one row of about 50 cells.INTRODUCTIONMainly due to the strong yen and the relatively low price of metal, the zinc refineries in Japan are being forced to reduce production costs again and again.The trend of lijima's production costs is shown in Figure 1.[1] The ratio of labor costs becomes gradually higher. Therefore it is effective to reduce the labor costs in order to reduce the production costs. In Japan, electricity cost during day time is too high to produce zinc at a reasonable cost, that is why the actual production is far from the capacity of production at a cell house. That means a plant in Japan has the disadvantage of relatively low productivity for cell house operation.Saving labor costsSome automatic cranes have been applied to save labor costs for cell house operation in the world. In consideration of the mentioned low productivity, the installation of an Automatic Cathode Transfer (ACn system for transportation of cathodes was planned without changing the present cell house and stripping machines to lower the investment costs. The ACT system must keep up with the stripping machine which is able to strip deposit zinc from a cathode sheet at the rate of 6 seconds.The fifth ACT system of seven was installed in August 1996 and the last one will be operational subsequently."

Jan 1, 1997

By Yongyong Gong, Qijie Zhai, Zhichen Zhang, Qixin Li, Zhishuai Xu

"Microstructure of semisolid slurry of Al-4.5wt.%Cu alloy was investigated with pulse magnetooscillation (PMO) treatment, the results showed that the PMO treatment can refine the crystal structures of Al-4.5wt.%Cu alloy significantly. The discharging frequency of PMO had a great effect on the solidified structure transformation of semisolid slurry of Al-4.5wt. %Cu alloy, and the primary a-Al particles become much finer and rounder with an increase of discharging frequency. However, over a certain discharging frequency, the grains of primary a-Al become coarse.IntroductionOver the last decade, a lot of attentions have been paid on metal rheoforming process [1-4], since it has higher mechanical properties of formed components, strength to weight ratio and age hardenablity. Nevertheless, semi-solid forming is always performed at high solid fractions (40%-60%), so it has the limitation of viscosity, a tends to be difficult to pour semisolid slurry into the hole of the shot sleeve. Therefore, a series of novel semi-solid slurry preparation methods and rheoforming techniques have been invented, such as, semisolid vibration treatment [5], rheocasting [6], pulsed magnetic field process [7], annulus electromagnetic stirring [8], via ultrasonic vibration process [9], equal channel angular extrusion (ECAE) process [l0] and straininduced melt activation (SIMA) process [11].The electromagnetic field is characterized by its effective grain refinement, green, convenient manipulation and without contamination of melt. The mechanisms of dendrite was fragmentation by electromagnetic field have also been largely proposed [12-14]. The broken dendrite arms then undergo a coarsening process to provide the globular structures and obtain much finer and rounder a-Al particles. When compared with other external electromagnetic techniques, Pulse Magneto-Oscillation (PMO) has obtained more fuvors, owing to narrower pulse width and much lower energy consumption. Furthermore, the PMO treatment can reach finer grains with shorter time treatment [16, 17]. This work aims to study the effects of different discharging frequency ofPMO treatment on the microstructure transition of the semisolid slurry of Al-4.5 wt.%Cu alloy."

Jan 1, 2014

By Bruce W. Wessels

"Metal-organic chemical vapor deposition has been shown to be a highly versatile technique for the synthesis of complex oxides. High dielectric constant oxide thin films of SrTiO3, BaTiO3, Ba1-xSrxTiO3 and SrxBa1-xNb2O6 can be be be deposited at 800 ºC with this technique. The fluorine substituted B-diketonate precursors have been shown to be well-suited for the deposition of high quality, epitaxial thin films of these materials.IntroductionThere has been a resurgence of interest in thin film ferroelectric oxides as a result of the development of techniques to deposit high quality material. Both physical and chemical vapor deposition techniques have been realized. Of the chemical vapor deposition techniques, metal-organic chemical vapor deposition (MOCVD) has received the most interest for the deposition of ferroelectric oxide thin films. This results, in part, from the availability of a number of volatile metal-organic precursors.(l) Moreover, MOCVD offers the advantages of high growth rates, uniform coverage over large areas, conformability, abrupt interfaces and excellent epitaxial crystallinity. Of the metalorganic precursors, the B-diketonate complexes have played an important role especially in the deposition of ferroelectric oxides containing alkaline-earth metals such as BaTi03 and Ba1•XSrxTi03. For example, barium tetramethylheptanedionate Ba(thd)2 has been used in the preparation of BaTi03 by MOCVD.(2) These compounds, however, are not without their problems. Ba(dpm)2 has a relatively low volatility; and as a consequence, temperatures in excess of 180·C are required for volatilization. This leads to the necessity of a complex precursor delivery system to insure that the precursor does not condense before the reaction zone. Moreover, the Ba precursor tends to oligomerize leading to a decrease in vapor pressure as well as a problem with reproducibility. To counter these problems, novel liquid source and solid source precursor delivery systems have been developed. (3)(4)"

Jan 1, 1994

By C. M. Egert, S. Rajic

"We have developed a monolithic micro-spectrometer suitable for a variety of sensing applications including industrial process monitoring. The device consists of a solid structure with a volume less than 6 cubic centimeters. All optical components of the spectrometer including two aspheric mirrors, a diffraction grating, and entrance and exit surfaces are fabricated onto the surface of the structure. All light paths are internally contained within the structure. The result is a small, rugged spectroscopic sensor ideally suited for use as a process monitor. Due to its monolithic nature the device requires no post-fabrication alignment; nor can it be knocked out of alignment during use. Although many materials and thus wavelength regions were possible, the prototype device discussed here was produced in PMMA by precision diamond turning. However, lower cost manufacturing approaches involving injection molding are under development to produce an affordable sensor.Due to its rugged monolithic design, small footprint, and low cost the monolithic micro-spectrometer is ideally suited for distributed monitoring applications often required for industrial processes. It is expected that modified versions of this sensor designs will be required for specific applications so as to maximize the performance and resolution over the operating range. For example, the prototype device described here operates over a wavelength range of 500 nm to 1000 nm. The performance of this device as a real-time surface monitoring sensor will be discussed in detail. Our approach of using wavelength dependant scattering resulted in the reduction to practice of a miniature, monolithic, rugged, low-cost, micro-instrument in a sensor sized package. The process sensor applications community has been faced by the cost versus performance issue. Simple go/no-go sensors are typically inexpensive but they provide very limited and sometimes dubious data. Scaled down traditional instruments offer very good measurand information but are typically cost prohibitive, fragile, and still relatively large. This work will bridge the gap between these two extreme sensing alternatives."

Jan 1, 1997

By Yeliz Demiraya, Onuralp Yucelb

"Production of strontium metal from its oxide was studied under the pressure of 1-5 mbar by methalothermic process. SrO with 99 % purity was used in the experiments. Effects of Al powder addition (100, 200, 300 % of stoichiometric ratio) and time were investigated on recovering of metallic strontium. Effects of BaO addition (100 %, 200 %, 300 %) was also investigated. The final residues were examined for their chemical composition. XRD, AAS and Flame Photometer were used for chemical analysis. More than 96 % of strontium metal recovery can be obtained.IntroductionStrontium is an element which is used in many advanced technology applications. Barium strontium titanat, strontium bismuth titanat, and strontium bismuth tantalat thin films are promising materials in ferroelectric and Schottky-based microelectronics technologies, especially for memory applications. Physical vapor deposition (PVD) techniques as magnetron sputtering, thermal evaporation and molecular beam epitaxy (MBE) are the most widely used methods for growth of these thin films [1-3]. In these techniques high-purity of Sr metal is used as evaporation sources and sputtering targets. Furthermore, metallic strontium is used as a ""getter"" in electron tubes, and as an alloying elements in aluminum alloys [4].The most used Sr compound is SrCO3 and widespread process used in production of SrCO3 is the hydrometallurgical carbonation of celestite. Although there are considerable amount of Selestite reserves, SrCO3 and strontinum metal are not being produced in Turkey, yet [5].Concentrated celestite (SrSO4) is conversed to SrCO3 in carbonate media. Black ash and direct conversion processes are currently used methods. There are many satisfactory studies about hydrometallurgical carbonation of celestite and decomposition of SrCO3 [6, 7]. Since strontium metal is produced from it’s oxide (SrO), SrCO3 needs to be decomposed to SrO."

Jan 1, 2011

By Zhang Libo, Wang Xin, Peng Jin-hui, Ju Shaohua, Guo Sheng-hui, Xu Lei, Huang Meng-yang

"China is lacking high grade titanium ores. This work intends to leach impurities such as Fe, Ca and Mg from a low grade titanium ore, to increase the grade. The original material contained 65% TiO2 , 16.12% Fe, 9.4% CaO + MgO, 4.2% SiO2, 1.25% A12O3, and the particle size is between 0.053-0.045mm. Microwave energy was used to enhance the leaching effect. The results showed that when normal heating was used to leach the mineral, the extraction of impurities Fe, Ca and Mg was very low. However, when microwave energy is introduced, the extraction of Fe, Ca and Mg increased dramatically. The optimized conditions are: relative power 5W/g, the ratio of concentrate to HC1 isl5%, leaching at 160°C for 20 min with a ratio of liquid to solid 12:1 mL/g. The material obtained under these conditions contains 92.73% TiO2, 0.207% Ca + Mg, 0.8% Fe, with 94.6% Ti recovery. The poduct meets with the quality for boiling chlorine.IntroductionThe resources of titanium are very abundant, and are distributed all over the world. There are almost 140 minerals containing TiO2 with a content of more than 1%. However, there are only several minerals which can be used for producing sponge titanium. They are mainly rutile and ilmenite. The grade of nature rutile concentrates is higher than 95% TiO2, and it is a high quality raw material. But the resources of nature rutile are relatively low; after mining for many years, its resources are exhausting gradually. Although ilmenite reserves are great, ilmenite cannot be used as a raw material because of its low content of TiO2, only 45-70%; also it has a high impurity content of Ca, Mg and Fe. In these years, there is a tendency for titanium industry to use high grade concentrate."

Jan 1, 2012

By Baicheng Liu, Houfa Shen, Wensheng Li

"In order to understand the formation of macrosegregation in steel ingots, a mixture model has been developed which accounts for coupled mass, momentum, species, and energy transport to describe the sedimentation of free equiaxed grains during solidification. In this model, the mushy zone is divided into the slurry and porous regimes according to a solid packing fraction. Settling velocity of equiaxed grains in the slurry regime is given by an explicit expression. The solidification of a binary steel ingot (Fe-0.36wt.%C) with a two-dimensional geometry is numerically simulated. It is demonstrated that the predicted macrosegregation patterns agree to some extent with classical experimental results. Further refinement of this model is still necessary for realistically simulating steel ingot solidification.IntroductionModeling macrosegregation in steel ingots is still a challenging study, mainly due to the length scale of the products and the complexity of global multiphase transport phenomena coupled with microscopic solidification kinetics [l]. The thermal-solutal convection and the motion of equiaxed grains are the two main mechanisms responsible for macrosegregation. But there are few models that deal with the motion of equiaxed grains, which is confirmed as the main phenomenon that explains the negative macrosegregation along the centerline of large steel ingots [2]. A model which takes into account melt convection and grain sedimentation was first proposed by Beckermann and co-workers ([3], and references therein). More recently, similar multiphase solidification models with advanced nature have been presented by Wu and Ludwig [1,4] and Combeau and co-workers [5,6]. It is known that the application of these sophisticated models to steel ingot casting is at its beginning.In this paper, a solidification model based on continuum mixture approach, using much less sophisticated relations to obtain the settling velocity of free equiaxed grains, has been proposed in order to predict the macrosegregation in steel ingots. The model is applied to simulate the solidification of a binary steel ingot with a two-dimensional geometry, and preliminary modeling results are presented."

Jan 1, 2011

By Muhlis Nezihi Saridede, Burak Birol

"Plastic wastes become a huge problem day after day due to the growth of plastic industry. Hence, plastic wastes are used as a raw material for other industries to eliminate this problem. Polyethylene Terephthalate (PET), which is a commonly used for plastic bottles, may be used as a reductant for iron production because of its C and H content. In this study, composite pellets containing iron ore concentrate, flux and reductant were prepared. Crystallized PET bottles and coke were used as reductant after ground. The prepared pellets were reduced at 1400°C for 30 min. and iron nuggets were produced successfully. Usage of waste PET purely as reductant in composite pellets gives a higher metallization degree and proper carbon content than coke or PET and coke mixture.IntroductionPlastics can be seen everywhere, especially at packaging industry in our common life. The increase of plastic usage ends up with an important problem, the increase of plastic wastes. Many studies have been carried out about usage of plastics as reductant in blast furnace such as Ogaki et al.[1], Heo and Baek [2], Saridede [3], Minoru et al.[4], etc. Besides, Kato et al. [5], Nomura and Kato [ 6] and Rongfang et al. [7] have pointed out the use of plastics in coke ovens regarding to its calorific content. In EAF steelmaking, a mixture of coal/coke and plastics can be used as an energy resource instead of only coal or coke. [8] Also, the usage of PET and PC in self-reducing composite pellets increased the reduction rate. [12]PET (Polyethylene terephthalate ), which is commonly used for soft drink plastic bottles, is an important municipal waste due to its C and H content. Its molecular formula is (C10H8O 4)n. Demir and Dincer showed that PET can be crystallized at 250°C to have the ability to be ground to a size of -100 µm. [11]"

Jan 1, 2011

By Felipe P. D. Lopes, Jr. dos Santos, Sergio N. Monteiro, Frederico M. Margem

"Natural fibers are gaining attention as a class of low cost, biodegradable and renewable materials that also exhibit some interesting properties for specific applications. In particular, the incorporation of some natural fibers in polymeric matrix composites is nowadays providing opportunity of manufacturing a variety of industrial items, for instance automobile interior components. Among these fibers, ramie (Boehmeria nivea) is one of the least investigated and only recently was studied as polymeric composite reinforcement. Therefore, the objective of this work was to evaluate the possibility of ramie waste reinforced polyester composites to replace conventional building materials, such as plywood, plastic boards and gypsum panels in terms of a cost-benefit analysis.IntroductionThere is a growing concern over the environmental questions that are presently affecting our society in a global sale such as climate changes and generalized pollution. Among the solutions for these questions, the replacement of energy intensive materials, especially those long term degradable such as the synthetic fibers, is already being considered [1]. As a consequence, the past decades have witnessed an increase in research devoted to new biodegradable materials obtained from natural resources mainly the biomass. Important examples are the renewable natural fibers as well as composites incorporated with them [2,3]. In addition to their friendly status with respect to the environment, well know natural fibers like jute, sisal, wood, coir, hemp and flax are relatively low cost and recyclable. In recent works [4,5], the use of these cultivated and abundant lignocellulosic fibers was investigated as the reinforcement phase in polymeric composites.Other less know lignocellulosic fibers have also been recently investigated [6,7]. These are fibers that likewise show a potential of incorporation into the polymeric matrix of composite materials. Most of these less know fibers are typical of tropical regions and, in principle, their application in industrialized composites would represent job opportunities for developing countries in Africa, South Asia and Latin America."

Jan 1, 2008

By S. W. Ip

Over the years, the importance of surface and interfacial phenomena has been neglected by the copper-nickel industry. As a result, little data on the surface and interfacial tension of the Ni matte and slag system are available in the literature. In view of the scarcity of information in this area, the surface tensions of the Ni-Fe-S system together with the Ni-Fe-S and fayalite type slag system were measured using the sessile drop technique. Drop images were obtained by X-ray radiography. For the Ni-Fe-S system, the results showed that the surface tension of the matte increases with matte grade. The surface tension behavior with changing matte grade showed a slight negative deviation from ideality. This indicated that FeS is slightly surface active in the nickel matte system. Results also indicated that small increase in sulphur content in the matte can decrease the surface tension quite significantly. The measured surface tension of the Ni-Cu-S system showed a linear relationship with the Cu2S content in the matte. The surface tension decreased with Cu2S content. Interfacial tension measurements showed a similar trend. That is, interfacial tension increased with increasing matte grade. The presence of MgO (-1.5%) and A12O3 (-6%) in the slag does not affect the interfacial tension value. Effects of matte surface tension on phenomena such as entrainment of matte in slag and infiltration of matte into refractory pores are discussed. The calculated flotation coefficients indicated that flotation of nickel mattes cannot be avoided by changing the matte grade. Filming of matte on bubbles can occur below a matte grade of about 19% Ni3S2. As for infiltration, refractory bricks containing high Cr2O3 will be easily wetted by matte regardless of matte grade. Therefore, bricks containing high Cr2O3 can easily be infiltrated by liquid matte.

Jan 1, 1993

By Na Wang, Chao Du, Hongmin Zhu, Kai Huang, Shuqiang Jiao

"Niobium aluminides were directly synthesized by a sodiothermic reduction process of NbC15 - AlCb which was dispersed into LiCl - KCl - NaCl - CaCb melts. The melt supplied a homogenous reaction medium which was substantially beneficial to the co-reduction of Nb and Al to form niobium aluminides in situ. The reduction was performed at 500°C for 4 hours. The products were analyzed by X-ray diffraction (XRD) and scanning electron microscope (SEM). The corresponding results indicated that niobium aluminides powders were successfully synthesized.1. IntroductionNiobium aluminides have received considerable attention as high-temperature structural materials, due to their high melting points, relatively low density, high strength, excellent oxidation and creep resistance [1-4]. Figure 1 shows that there are three intermetallic compounds in the Nb - Al binary [5], which includes Nb3Al (A15 structure, Cr3Si type), Nb2Al (D8b structure, cr-CrFe type) and NbAb (D022 structure, TiAb type). These niobium aluminides have been used in turbine blades or in stationary gas turbines [6-8]. However, despite their attractive features, the ir applications are still limited by the long and costly fabrication process [9, 10].Niobium aluminides were industrially fabricated by the mechanically alloyed process [11-13]. Traditionally, niobium is extracted from Nb2O 5 or K2NbF7 by a metallothermic reduction process while aluminum is produced by the Hall-Heroult process of Ah03 electrolysis. Based on the extraction of Nb and Al, respectively, niobium aluminides is synthesized by a mechanical powder alloying process. The present process for making niobium aluminides requires a set of complicated equipment, has high production cost and time consuming [14, 15].The purpose of this work is to present the simple, economic and direct synthesis of niobium aluminides powders utilizing a sodiothermic reduction from NbC15 - Al Cb dispersed into molten salts."

Jan 1, 2011

By Thomas J. O'Keefe, Pu Yu, George Houlachi, Xuewen Tang

"Impedance measurements were used to investigate the electrochemical characteristics of acidic zinc sulphate electrolytes containing Sb3+, gelatin and their mixtures. The data were correlated with cyclic voltammetry curves made using synthetic as well as industrial electrolytes. The cyclic voltammetry results were similar to those obtained in previous studies in that antimony caused a depolarizing effect while gelatin gave an increase in the potential for zinc nucleation on an aluminum substrate.The electrochemical impedance spectroscopy (ElS) evaluations were conducted on electrodeposited zinc at three overpotential values. The potentials were chosen to represent various current density regions in the zinc polarization curves. The antimony and gelatin gave characteristic impedance plots which correlated with expected behavior, particularly current efficiency. Both antimony and glue appear to modify the intermediate zinc reaction sequence, but in different ways. The data strongly suggest that film formation and stability are major factors in the zinc ion reduction mechanism.IntroductionThe zinc electrodeposition process is sensitive to the presence of a variety of organic and inorganic chemical species in the electrolyte [I]. Such components can produce either beneficial or harmful effects, depending on their relative concentrations and electrochemical behavior. Extensive investigations have been made to gain a better understanding of the changes occurring during zinc deposition in the presence of such additives. Techniques employed include microscopy, x-ray diffraction, dynamic voitammetry, current imd energy efficiency studies [2-5]. Ultimately, the objectives are to identify the factors which most affect the efficiency of the process and to provide a means to effectively control them.One of the most harmful impurities is antimony, which can be detrimental when present at concentrations as low as 10 to 20 parts per billion. Dramatic changes in zinc polarization behavior, deposition structure and current efficiency have been observed with antimony in the electrolyte. Antimony appears to lower the hydrogen overpotential by hydride formation or a similar catalytic mechanism, which allows an increase in localized corrosion and zinc dissolution [6-8]."

Jan 1, 1997