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By L. Z. Villanueva

An investigation and evaluation has been performed to determine the potential utilization of electron beam irradiation technology for sulfur oxides removal from reduced-S02-strength metallurgical gases from copper smelters. These off-gases, though too weak to be converted to usable, concentrated: sulfuric acid by conventional means, are characterized by SO2 content higher than 2,000 ppm and a complex chemical composition, including high oxygen content and its generation occurring in a cyclical, fluctuating pattern. This work was based on information supplied by principal smelter companies in Chile. A laboratory facility with flow rate of 20 Nm3/h and equipped with an electron accelerator of beam energy 8.00 keV, has been used for testing. Influence on SO2 removal efficiency of operational parameters such as gas temperature, water vapor content, ammonia feed ratio and irradiation dose was established. The main conclusion of this work, from experimental laboratory tests as well as engineering studies, is that the Electron Beam Process (EBDS) is a cost-effective, simple and appropriate chemical process means for emission abatement. EBDS can, on a site-specific basis, adequately augment SO2 removal to upgrade overall abatement as required and in an optimal manner.

Jan 1, 1999

By William K. Tolley

The U.S. Bureau of Mines (USBM) is investigating hydrometallurgical processing techniques to recycle metals from semiconductors and other advanced materials. Cadmium and tellurium were recovered from mixed CdTe/CdS scrap produced in the manufacture of thin-film photovoltaic devices. Cadmium and tellurium dissolution was achieved using hydrogen peroxide in dilute sulfuric acid. Leaching the scrap in 2.2 N H2SO4 yielded 99% Cd extraction and 98% Te extraction. Sulfur remained in the leach residue primarily in the elemental form. Elemental tellurium was precipitated from the leach liquor by adding Na2S2O5. Cadmium sulfate was recovered by evaporation. A preliminary process evaluation suggests that the process may have economic potential. Alternative recovery schemes are discussed.

Jan 1, 1995

By J. P. Downey, L. G. Twidwell

"The high density sludge process (HDS) is a commercially proven acid rock drainage wastewater treatment process that is based on acid neutralization and metal precipitation. Previous studies have established that metal removal efficiencies in precipitation-based wastewater treatment applications can be improved through metal ion adsorption on ferrihydrite and/or aluminummodified ferrihydrite. This study was conducted specifically to determine whether the metals removal efficiencies at an existing industrial facility could be improved by promoting ferrihydrite and/or aluminum-modified ferrihydrite precipitation during the pH adjustment stages of the HDS process. The metal tenors of the treated wastewater samples are compared with those obtained through baseline experiments, which were designed to simulate the conventional HDS operation. The subject metals were: aluminum, arsenic, cadmium, copper, iron, manganese, nickel, and zinc.IntroductionThe HDS process is commercially proven ARD wastewater treatment technology that involves raising the wastewater pH by adding hydrated lime, caustic soda, or another alkaline substance. In addition to neutralizing the acidity, many dissolved metals precipitate as pH is elevated. Waste volume is minimized by capturing and immobilizing the precipitated solids.However, ARD streams characteristically contain multiple dissolved metal species. The response of various metals to pH adjustment in the HDS process is neither uniform nor quantitative, so minor to trace concentrations typically remain in the treated wastewater following solid-liquid separation. The effectiveness and applicability of the process would be improved if a means were found to further reduce the metal concentrations.Previous research and industrial applications have proven that metal ion adsorption on ferrihydrite (FH) and/or aluminum-modified ferrihydrite (AMF) increase metal removal efficiencies. Ferrihydrite and AMF are considered ideal for cation and anion adsorption from an aqueous solution at the appropriate pH [1]. Ferrihydrate adsorption of dissolved heavy metals is widely practiced throughout the world [2, 3]. It is established that FH and AMF effectively adsorb As contained in aqueous solutions [4]. Arsenic removal by adsorption on FH is the U.S. Environmental Protection Agency’s (EPA) Best Demonstrated Available Technology [5]. Twidwell and Leonhard also demonstrated that heavy metals (Cd, Cu, Ni, and Zn) are effectively removed from solution by coprecipitation/adsorption using AMF and FH [6]."

Jan 1, 2008

By De-qing Zhu, Jian Pan, Tie-jun Chun, Dong Chen, Yu Cui

"A study of processing pyrite cinder and metallurgical slag using “one step” technology in strand grate - rotary kiln is presented, which aims to efficiently recover the valuable metals of iron, lead, zinc and copper. The effect of chloridizing roasting parameters including roasting time and temperature on the removal rates of nonferrous metals was investigated. It is shown that copper and zinc are difficult to remove and lead is removed more easily. The preheated pellets were reduced in a rotary kiln, where zinc and lead can be removed easily and high iron grade and good metallurgical performance prereduced pellets can be obtained. Furthermore, the chlorination and the reduction mechanisms of copper, lead and zinc are discussed. It is revealed that the phases of copper, lead and zinc in slag are complex and ferrite and silicate of metals are difficult to remove.IntroductionAs two kinds of significant secondary resources, metallurgical slag and pyrite cinder contain not only abundant iron but also considerable copper, lead, zinc and so on. Several tens of millions of tons of metallurgical slag and pyrite cinder are discharged in nonferrous metal and chemical industries annually in China [1, 2]. In addition, the accumulated waste slag in storage is more than one hundred million tons, which not only occupies much land but also pollutes the environment [3]. However, because the metallurgical slag and pyrite cinder are treated by high temperature processing, the properties are distinctly different from the properties of natural ores, and iron is in close association with copper, lead and zinc. So, metallurgical slag and pyrite cinder are difficult to efficiently utilize and only a small amount is used as additives in cement, paving, brickmaking and auxiliary additives [4-7]."

Jan 1, 2011

By Wander. L. Vasconcelos, Virgínia. S. T. Ciminelli, Angela. M. F. Guimarães

"The present work was aimed at synthesizing nanostructured hybrid materials derived from the functionalization of smectite clays with ligands containing thiol (-SH) groups for application in cadmium adsorption processes. An in nature Brazilian bentonite was investigated. The modification route was based on the grafting reaction between hydroxyl groups present on clay surface and the hydrolyzable alkoxy group of the (3-mercaptopropyl)trimethoxysilane in dry toluene under reflux. The present work showed that the proposed modification route was effective for the grafting of the thiol groups in the clay structure. The thiol-functionalized bentonite samples showed average binding capacities 160% higher with respect to Cd2+ to those obtained with the ungrafted material. These results support a mechanism of adsorption involving primarily ion complexation by the thiol groups (specific) instead of cation exchange (unspecific). The proposed modification processes are suggested for the preparation of novel adsorbent materials with controlled selectivity and specificity and therefore with good potential for separation and pre-concentration purposes.IntroductionMany efforts have recently been devoted to the design and preparation of inorganic-organic nanomaterials because of their potential application in novel functional materials. The intercalation of organic species within the spaces between interlayers of inorganic layered crystals provides nanostructures consisting of alternating layers of inorganic and organic compound. The intercalation reactions occur by insertion of mobile guest species (neutral, molecules, or ions) into the accessible crystallographic-defined vacant sites located between the layers (interlayer spacing) of the layered host structure [1}.Silane coupling agents, used widely for the modification of silica surfaces, have also been employed more recently for modification of layered silicates [2,3,4,5]. Modification with organosilane involves grafting reactions by establishing covalent bonds between the reactive groups of the layer, normally hydroxyl groups, and silane molecules. These reactions can be restricted to the external surface (the basal spacing remains unchanged) or to the interlayer surface, in which case an interlayer expansion occurs. The resulting material can be defined as a hybrid material or, more specifically, functionalized inorganic layered material [1]."

Jan 1, 2008

By N. L. Piret, E. N. Mounsey

Ausmelt technology is successfully used to process primary and secondary materials to produce lead in large-scale commercial operations and to meet stringent environmental standards. The development and commercial data covering these applications and the results with respect to metallurgical, cost and environmental performance are reviewed in commercial operations. A new smelter is scheduled for commissioning in 2000 at Korea Zinc's Onsan site to process lead fume and other secondary materials to produce 50,000 tonnes per annum of lead bullion. The unique features of Ausmelt technology also allow for the efficient processing of polymetallic concentrates and secondary materials, particularly copper and lead, through the effective separation of these elements into metal, slag and fume species. This capability has been successfully demonstrated at a commercial scale and the results and implications for the industry are discussed.

Jan 1, 2000

By Lin Yang, Minjun Tang, Shuishi Liu, Jianfeng Zhou, Linjiang Qing, Xiaolei Song, Yufeng Guo, Tao Jiang

"The dynamics of oolitic hematite magnetic roasting was studied. The results show that oolitic hematite magnetic roasting was controlled by the internal diffusion, and the diffusion coefficient was 9.018x10-7 m2·s-1when the oolitic hematite was roasted at 650°C. Magnetic susceptibility improves when temperature increases and roasted time prolonges under the condition of roasting at 650°Cfor 50min, with the magnetic susceptibility is 39.88%. CaF2 and Na2C03 can significantly improve the magnetic susceptibility at the same roasting condition, and the magnetic susceptibility was 63.35% and 57.99% respectively, thus the reduction of oolimic hematite was promoted.IntroductionWith the continual depletion of free-milling iron ores and its rising price, developing the abundant resources of oolitic hematite has become one of the main research areas. The oolitic hematite accounts for 10% of China's iron ore reserve, and it also accounts for 30% of red ore reserve in China [1]. In order to exploit the oolitic hematite, there are many beneficiation research methods, including fine grinding/selective flocculation/high intensity magnetic separation or flotation, high-gradient magnetic separation, low intensity magnetic separation/high intensity magnetic separation/reverse flotation, chloridizing roasting/acid pickling, magnetic roasting/leaching process etc [2]. However, the oolitic hematite is easy to slim and the valuable mineral is covered by the slim, because of the tiny granule of value mineral, then the ooides are formed due to the state of layer morphology formed by iron ore and ganaue minerals [3, 4]. Fairly good separation indexes were hard to be obtained by traditional separation due to its structural features, so the magnetic property of the iron minerals will be changed with the use of the magnetic roasting [5, 6], which result in hematite variably altered to magnetite and simplified technological process so that a good separation indexes will be obtained by using the low intensity magnetic separation. Therefore, in order to provide theoretical direction of how to use the oolitic hematite effectively through the magnetic roasting, the oolitic hematite of GuiZhou province was studied, which emphasized on researching the dynamics of oolitic hematite magnetic roasting."

Jan 1, 2013

By Keizo Uematsu, Satoshi Tanaka, Nozomu Uchida, Yutaka Saito

"Effect of moisture content must be fully understood for controlling the granule compaction of ceramics. It changes the mechanical behavior of spray-dried granules applied for compaction process, and governs the structure and properties of .ceramics. To understand the time-dependent change in processing, the kinetics was examined for change of moisture content for granules placed in a die and the pressed compacts also. The results were explained in terms of apparent moisture diffusion coefficients. They varied non-linearly with the PVA content in the granules. The results were explained through the non-uniform PVA distribution in the granules.IntroductionMoisture must be controlled in compaction process to produce the green compacts having uniform structure. It affects glass transition temperature of binder and thus the deformation behavior of powder granules under an applied stress. Several studies [1-7] have clarified the effect of moisture content on the compaction behavior of granules and the structure of resultant compacts for both die pressing and cold isostatic pressing (CIP) of pre-formed compacts. In these studies, the moisture contents in the system were equilibrated with the humidity in the atmosphere before compaction. In practice, however, the moisture content in the system may vary with time if the relative humidity of surrounding atmosphere is different from what the granules were equilibrated previously. This is very likely case in real production processes. However, the kinetics of moisture change in the granules as well as in the pre-formed powder compacts have not been well studied. For controlling the microstructure in a system, it is necessary to fully understand the kinetics of moisture change and its relevance to packing structure of powders."

Jan 1, 2000

By S. A. Platias

Large amounts of dunile tailings can be recycled for olivine produdion from the existing beneficiation adivity of chromite ore in northern Greece. This olivine production aims at the preparation of a material suitable for the substitution of the environmental hazardous quartz sand in the foundries of Europe In smelting of chromite ore the losses that occur ore usually of the order of 6-8% Cr that report in the slag. Most of this is in the form of oxides that cannot be recovered, but usually 30-35% is in the form of FeCr alloy that can be recovered by gravity methods. About 90% of the produced slag is sold for road construdion after crushing to a desired grain size. Finally, recycling of chromites sludges from the ferrochrome produdion plant, through the preparation of pellets, improved the total chromite yield by 2%.

Jan 1, 1996

By Shivendra Sinha

Total pressure oxidation (TPOX) is widely outreached leaching practice for base metals from sulfide minerals, wherein high temperature (T ∼ 200 °C) and oxygen pressure (pO2 ∼ 25 bar) are required. These aggressive conditions intensify the oxygen mass transfer, and therefore facilitate metal dissolution. However, challenging-cum-negative aspects of such practice are energy and material intensive requirements and high oxygen demand. Thus, the present study explores the novel emulsified medium for enhancement of oxygen mass transfer, which assists faster metal dissolution at significantly lower temperature and pressure condition. It is possible to achieve quantitative dissolution (>95%) of Cu, Ni and Co from mixed sulfide minerals at T ∼ 95 °C and pO2 ∼ 2 bar using an emulsion of 2.5% (v/v) n-Hexadecane in dilute sulfuric acid. In addition, n-Hexadecane was found to be inert, stable and immiscible in a pressurized leaching system, thus can be easily separated and recycled in subsequent leaching stages. Thus, this study offers an energy efficient route for low temperature-pressure leaching of sulfides.

By Igor Rojkovic

The most important uranium mineralization in the Western Carpathians occurs in the Permian rocks. Low grade stratiform uranium mineralization was formed during the Permian due to adsorbtion and reduction by organic matter, titanium oxides, iron hydroxides, pyrite and clay minerals. During the Alpine orogeny uranium (± molybdenum and copper) remobilized stratabound ores were formed. Dominant ore minerals are uraninite, U-Ti oxides, molybdenite, pyrite and chalcopyrite Two generations of ore minerals are reflected by their textures and chemical composition.

Jan 1, 1995

By Himaki Nakano, Kenji Hara, Toshiaki Tsuru, Shunsuke Kawano, Takeshi Ohgai, Hisaaki Fukushima, Shigeo Kobayashi, Tetsuya Akiyama

"Electrodeposition of Fe-Ni and Zn-Ni alloys from aqueous solutions is one of the well-known examples of anomalous codeposition in which less noble metal deposits preferentially. In this paper, the electrodeposition behavior of these alloy systems was compared between the methanol and aqueous baths. In Fe-Ni system, the significant suppression of the deposition rate of more noble Ni was observed over a wide range of electrolysis conditions in both methanol and aqueous baths. However, the electrodeposition of Zn-Ni alloys showed the typical feature of normal type codeposition in the methanol baths, which was completely different from that in aqueous sulfate baths. The difference in the electrodeposition mechanism between Fe-Ni and Zn-Ni alloys was discussed on the basis of the alloy deposition behavior in the baths in which the activity of water was varied:INTRODUCTION'It has been well known that Fe-Ni alloys show an excellent soft magnetic property. Therefore, thin films of this alloy have been used to fabricate the'-various magnetic devices. For the production of Fe-Ni thin films, dry processes such as sputtering, PVD and CVD are 'employed frequently and the resulting films showed a preferable property as a magnetic material. Electrolyses as a production technique of thin films, on the other hand, has the advantage over other processes in its cheaper production cost due to the simplicity of the production unit The Zn-iron-group metal alloys such as Zn-Ni and Zn-Fe electrodeposited on a steel sheet ale known to exhibit excellent corrosion resistance and therefore the electrodeposition of these, alloys has been applied to the production of surface treated steel sheets mainly for automotive body panels.According to Brenner (1), the electrodeposition behavior of Fe-Ni and Zn-Ni alloys was' classified into the' 'anomalous type. In this type of codeposition, less noble metal, i.e. Fe for Fe-Ni and Zn for Zn-Ni system, deposits preferentially and the change in -the alloy composition- with the variation of electrolysis conditions was unpredictable because of their obscure deposition mechanism. Since most properties of the alloys mainly depend on their composition, the composition of the deposited' alloys must be controlled strictly. Therefore, it is neces5al)' to clarify the mechanism of anomalous codepasition in Fe-Ni and Zn-Ni systems: Several mechanisms have been proposed so fur, and among them the hydroxide .suppression mechanism (2), (3) has been regarded most plauslble depend on their composition, the composition of the deposited' alloys must be controlled strictly. Therefore, it is necessary to clarify the mechanism of anomalous codeposition in Fe-Ni and Zn-Ni systems: Several mechanisms have been proposed so far, and among them the hydroxide suppression mechanism (2), (3) has been regarded most plausible. According to this mechanism, it can be predicted that the codeposition behavior depends greatly on the characteristic of water solvent in this study, using methanol as a solvent, the electrodeposition behavior of the anomalous codeposition was investigated to discuss the validity of the hydroxide suppression mechanism."

Jan 1, 2000

By B. Farouk, D. Apelian

"A numerical model has been developed to predict the temperature history of particles injected in a low pressure d.c. plasma jet. The temperature and velocity fields of the plasma jet are predicted as a free jet by solving the parabolized compressible Navier-Stokes equations using a spatial marching scheme. Particle trojectories and heat transfer characteristics are calculated using the predicted plasma jet temperature and velocity fields. Correction factors have been introduced to take into account non-continuum effects encountered in the low pressure environment. The plasma jet profiles as well as the particle/plasma interactions under different jet pressure ratios (from underexpanded to overexpanded) have been investigated.I. IntroductionIn the plasma spraying process a d.c. plasma jet is used as a heat source to melt and accelerate powder particles which subsequently impinge and solidify on a given substrate. During low pressure plasma deposition (LPPD) prooess, the plasma jet is expanded into a low pressure environment (40-80 Corr) which results in high plasma jet velocities with Mach numbers ranging from 2 to 3. Previous efforts to predict heat transfer and fluid flow in plasmas have made use of incompressible flow formulation employing turbulence models [1-3] for atmospheric plasma spraying. However, these theoretical calculations have been limited to the subsonic flow regime; hence, the compressibility effects and viscous heat dissipation were neglected. In the LPPD process, the plasma jet is operated at the supersonic flow regime, therefore, the compressibility effects and viscous heat dissipation are no longer negligible. This is the main motivation of this work.In addition, production of high quality dense deposits requires that a large fraction of the injected particles be in a molten state when they impact the substrate. An additional motivation for this work is that it is important to understand the plasma/particle heat and momentum transfer since these phenomena dictate both the particle thermal history and particle trajectory.Early computational works in supersonic nozzle field flow [4,5,6] consisted of patching methods that divided the flow field into an invisoid free stream and a viscous boundary and. mixing layers. Each was analyzed independently and coupled through appropriate boundary conditions. Later schemes [7,8] involved solving time-dependent, compressible Navier-Stokes equations over the entire computational domain. These schemes show a great promise in predicting flows with complex structure, and where the viscous effects became prevalent."

Jan 1, 1986

By Jie Li, Thomas A. Rawdanowicz, W. J. Collis, S. Venkatraman, S. Iyer

"InSb being the lowest band gap. material amongst the 111-V semiconductors with low effective mass has long attracted research interest, due to its potential application in far infrared devices and for high speed circuit elements. In this paper, we report, for the first time, Te-doping of InSb on GaAs substrate using SnTe doping source with molecular beam epitaxy (MBE) technique and its electrical characterization. The undoped epilayers are n-type in the temperature range of 10 K to 300 K investigated. The room temperature (RT) mobility as high as 64,810 cm2/V·s (1.9x1016 cm-3) have been measured on a 4.8 µm thick epilayer. Sn Te doping at different doping levels were investigated. 5. 7 µm thick doped layers with RT carrier concentrations ranging from 2x1016 cm-3 to 3.2x1018 cm-3 with corresponding full width at half maximum (FWHM) of x-ray (400) rocking curve varying from 170-200 arc-seconds have been achieved. The Hall mobility of 20,000 cm2/V·s at 1.3xl018 cm-3 carrier concentration was obtained indicating that SnTe is a good candidate as source material for n-type doping of InSb.IntroductionThe thin films of InSb and InSb-based alloys have found considerable interest because of potential applications in III-V semiconductor-based infrared optoelectronic devices1• In addition, the advantage of the small effective mass and the consequent high mobility can be utilized in high frequency and high-speed circuit devices2 InSb can also be used in magnetoresistive sensors for position sensing3. Epitaxial InSb films grown by MBE may be doped n-type with Si or Sn, or with the group VI elements, namely, S, Se, or Te. Of the group VI elements, Te may be advantageous because of its relatively low vapor pressure. However, the vapor pressure is high enough to have sufficient memory effect during MBE growth. Hence different telluride compounds such as GaTe45, PbTe6 and Sb2Te37 have been used as the dopant source for Sb-based compounds. SnTe has also been used as a successful n-type dopant in the MBE growth ofGaSb8 But, to our knowledge, there is no report on the investigation of SnTe doping of InSb. In this paper, we report the first doping characteristics of SnTe in InSb layers grown on GaAs substrate."

Jan 1, 1998

By J. C. Agarwal

Most metals are produced from minerals containing one or more of the desired metals, some contaminating metals, silicate, oxides, carbonates, and sulfides. Therefore, in the production of metals, there is generally a gaseous effluent in pyrometallurgical processes and a liquid effluent in hydrometallurgical processes. There are also solid residues such as waste ore, tailings, dust, and slag, created by the metal recovery processes. There are two important distinctions between the effluents and the residues: I. Effluents ? gases and liquids ? affect the neighboring environment for miles from the point of emission, while residues affect only the soil on which they are stored or dumped. 2. The environmental and economic effects of effluents are known and felt essentially immediately. By contrast, the environmental effects of the residues may not be known for a long time. For these reasons, the economic impact and the potential corrective actions required are very different for effluents and residues.

Jan 1, 1992

By Hiroshi Ono

"By newly developed ICP method, trace amounts of As(III), As(V) .,Sb(III) and Sb(V) were precisely determined within accuracy of sub ng/ml. As(III) and Sb(III) were separated from As(V) and Sb(V) by extracting into ·xylene as diethyldithiocarbamate complexes using diethylammonium diethyldithiocarbamate (DDDC), and then back-extracted into nitric acid for a quantitative determiruition by ICP-AES equipped with hydridegeneration system The recoveries of As(III) and Sb(III) were satisfactory throughout the extraction with 0.04mol/l DDDC in xylene from lmol/l hydrochloric acid solution and the back-extraction with 7 mol/l nitric acid. As(V) and Sb(V) were reduced to As(III) and Sb(III) by ascorbic acid and potassium iodide, and their quantities were determined as mentioned above. The detection limits were found to be 0.58ng/ml for As(III), 0.63ng/ml for Sb(III) using 50ml of a sample. The proposed method was applied to analysis of the real sample.Introduction In drain, arsenic(AS) concentration is prescribed below 0.lmg/l, so As must be removed. As is existed at .the form of As(III) or As(V) in solution. For t1Jeir difference of chemic;µ property, it is not easy to remove As in solution. So it is an urgent necessity to develop for determining concentration of As(III) and As(V). Antimony( Sb) has resemblance .chemical property to As. So Sb was experimented the same as As.The separation and determination of As(III) and As(V) have been carried out using several methods, such as ICP after copreclpitating separation, HPLC, direct hydride generation atomic absorption. However these methods have some problems. One of main problems is that HPLC and direct hydride generation atomic absorption methods are influenced by coexisting elements."

Jan 1, 2000

By J. R. Goode

There are at least a dozen methods of selectively removing cerium from a mixture of the rare earth elements (REE) including separation techniques based on the oxidation of cerium to the quadrivalent state. Several of the oxidation processes have been operated on a commercial scale, others have been tested and in some cases are part of proposed flowsheets. In this paper, we describe and compare the various methods. We also present preliminary estimates of the costs of early Ce removal and discuss recovery and purity aspects of the options.

By James L. Whitlock

Biological treatment of mining and industrial effluents reached full scale commercialization around 1980. These proven, low cost, technologies have been limited in application due to a number of factors, including extended periods of time and cost required for pilot testing as compared to chemical treatment technologies, lack of biological expertise in metallurgical personnel, longer treatment periods in some cases, and performance failures based on improper application. Renewed interest in biological treatment technologies is being driven by permits with lower effluent concentration criteria, permits with bioassay evaluation, the need to remove thiocyanate, nitrates, sulfates and? other parameters. Chemical treatment processes, in general, have not been able to meet these present requirements, or require elaborate? combinations of processes, in terms of effluent quality and treatment economics. This paper addresses biologieal treatment of mining and industrial waste waters and selected recent advances in these technologies. The future looks very bright for application of these low capital and operating cost technologies,

Jan 1, 1998

By Suleyman Tekeli, Serdar Salman, Bulent Aktas

"The effect of La2O3 content up to 15 wt% on phase stability, sintering and microstructure of cubic zirconia (8YSZ) was investigated. XRD results showed that the specimens containing up to 15 wt% La2O3 were composed of only cubic structure. Also, the specimens doped up to 5 wt% La2O3 revealed no La2O3 peaks, indicating that La2O3 was completely solubilized in the cubic structure. However, when> 5 wt% La2O3 was added, the peak of La2Zr2O7 compound emerged, showing that the overdoped La2O3 was not solubilized in the 8YSZ matrix. The lattice parameter of the 8YSZ slightly decreased with the increasing La2O3 content up to 1 wt% but further increase in the La203 amount resulted in an increased lattice parameter. The comparison of grain size of the 8YSZ specimens with various La2O3 content showed that grain size slightly increased with the increasing La2O3 content up to 1 wt% but further increase in the La2O3 amount resulted in a decreased grain size.IntroductionAt atmospheric pressures, three polymorphic forms of Zr02 are stable at different temperatures i.e. monoclinic, tetragonal and cubic. A high-pressure orthorhombic form of Zr02 has also been reported[l]. The successful production of pure Zr02 bodies is not possible all the time due to the large volume expansion associated with the martensitic tetragonal-monoclinic transformation. This fact restricts the applications of zirconia, in spite of its excellent mechanical and thermal properties. However, the stabilization of the high temperature polymorphs at room temperature as stable phases is made possible by addition of suitable dopants. Fully stabilized cubic Zr02 and partially stabilized tetragonal Zr02 show interesting properties and are widely used as ionic conductors, coatings and gas sensors in solid oxide fuel cells and structural applications[2]. Most frequently used dopants include Y203, CaO, MgO and Ce02, although other oxides, such as those of rare earth elements, can also act as stabilizers of the high temperature structures. The incorporation of aliovalent cations to the lattice, forming substitutional solid solutions, allows to control the concentration of anionic vacancies in the structure. This aspect is particularly important in designing ionic conductors[3], and is also determinant in the stabilization process[ 4]. The process of stabilization with larger ionic radii dopants is rationalized by the crystal chemistry model[ 5], that describes the dopant cations as typical stabilizer when they have larger ionic size, lower charged state and higher ionicity than Zr4+ The ionic radius of Zr4+ is 0.84 Å and that for La3+ is 1.016 Å [6]."

Jan 1, 2012

By Lucas Barbosa de Souza Martins, Felipe Perissé Duarte Lopes, Nathalia Carneiro Garcia Rosa, Lucas Lopes da Costa, Sergio Neves Monteiro, Rubén Jesus Sanchez Rodriguez

"The fibers extracted from the stem of the banana plant are relatively stronger and have been used as reinforcement of polymer matrix composites. In addition to quasi-static mechanical properties, there is a need to characterize the dynamic behavior of banana fiber composites subjected to thermal and mechanical constraints. In this work, the temperature variation of the dynamicmechanical parameters of polyester composites incorporated with up 30% in volume of banana fibers were investigated by DMA tests. The storage and loss moduli as well as the tangent delta were measured from 20 to 200°C in a TA Instrument operated with the flexural mode at 1 Hz. The results showed that the incorporation of banana fibers tends to increase the viscoelastic stiffness of the polyester matrix. It was also observed changes in the T g and the structure dumping capacity of the composites with increasing fraction of banana fibers.IntroductionNatural fibers with high amount of cellulose, also known as lignocellulosic fibers, have been used from primeval times by our civilization. In the last century, synthetic fibers such as nylon, carbon, aramid and glass fibers gained interest owing to superior strength and precise dimensional control. Natural fibers were then replaced by synthetics in many fields such as textiles and appliances. In the past decades, however, environmental issues drawn, once again, the attention to lignocellulosic fibers as possible substitute for intensive energy-consuming and long term polluting synthetics, specially the glass fiber [1]. In particular, research works have disclosed the potential advantages associated with the use of lignocellulosic fibers as the reinforcing phase in polymer composites [2-7]. Among the advantages it is worth mentioning the renewability, recyclability, biodegradability and the fact that natural fibers are neutral with respect to C02 emissions responsible for global warming. Moreover, as compared to synthetics, lignocellulosic fibers present lower density and cost as well as reduced wear caused to the processing equipment. On the other hand, in terms of composite reinforcement, hydrophilic lignocellulosic fibers present drawbacks such as weak adhesion to hydrophobic polymeric matrices in addition to dimensional limitations and non-uniform properties."

Jan 1, 2011