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Calcination Temperature (calcination + temperature)
Selected AbstractsEffects of Calcination Temperature and A/B Ratio on the Dielectric Properties of (Ba,Ca)(Ti,Zr,Mn)O3 for Multilayer Ceramic Capacitors with Nickel ElectrodesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2000Wen-Hsi Lee The electrical performance of multilayer ceramic capacitors (MLCCs) with Ni inner electrodes, made from (Ba,Ca)(Ti,Zr,Mn)O3 (BCTZM), is closely related to the calcination temperature and the A/B ratio of the powder. For materials showing A/B = 1.000, the lifetime, the breakdown voltage, and the RC increase with higher calcination temperatures. No significant effect of the calcination temperature on RC and lifetime was found for materials showing A/B = 0.991. The isoelectric point of BCTZM is shifted toward higher pH values when the calcination temperature is decreased. The above results are attributed to the colloidal stability of aqueous BCTZM suspensions and the resulting green density of powder compacts. [source] Preparation and characterization of ZnO nanofibers by electrospinningCRYSTAL RESEARCH AND TECHNOLOGY, Issue 5 2006R. Siddheswaran Abstract Electrospun ZnO nanofibers were obtained by calcinating PVA/Zinc Acetate composite fibers at various temperatures. Atomic Force Microscopy (AFM) revealed that the ZnO fibers have diameters in the range of 100-200 nm. The fibers were characterized by FT- IR, TGA-DTA, and XRD studies. The XRD results showed that the crystal structure and the morphology of the fibers were largely dependent on the calcination temperature (© 2006 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Assembly and Formation of Biomorphic Tin Dioxide by a Biomimetic Sol,Gel Approach Involving GlycoproteinEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 16 2007Qun Dong Abstract Three diverse layers of eggshell membrane (ESM) were introduced in a biogenic sol,gel technique for the synthesis of hierarchical SnO2 nanomaterials with corresponding configurations. Typically, the biomorphic replication of the interwoven inner eggshell membrane was systematically investigated by controlling synthesis conditions such as pH value, dipping time, and calcination temperature. The as-prepared SnO2 tubes consisting of interconnected 5-nm nanocrystallite units were successfully interwoven into ESM-morphic films. Herein, the biomaterial ESM served both as the physical substrate and the functional macromolecule template to realize the precision replication, by the interactions between ESM macromolecules (containing carboxyl, hydroxy, amino groups, etc.) and Sn colloid ingredients. Moreover, some biomacromolecules also acted as the surfactant to yield small-scaled and well-distributed SnO2 nanocrystallites based on the strong bondage of short-chained amino acids within ESM glycoprotein with SnO2 nuclei. This technique can be attributed to a biomimetic sol,gel process and is widely applicable to the synthesis of other functional material systems. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] Tailored Mesoporosity Development in Zeolite Crystals by Partial Detemplation and DesilicationADVANCED FUNCTIONAL MATERIALS, Issue 1 2009Javier Pérez-Ramírez Abstract Partial detemplation of zeolites followed by desilication in alkaline medium is demonstrated as a powerful and elegant approach to design hierarchical zeolites with tailored degree of mesoporosity. This achievement, illustrated for large beta crystals, is based on the fact that the template-containing zeolite is virtually inert to Si leaching upon treatment in aqueous NaOH solutions. Partial removal of the structure-directing agent creates regions in the crystal susceptible to mesopore formation by subsequent desilication, while template-containing regions are protected from silicon extraction. Variation of the calcination temperature in the range 230,550,°C determines the amount of template removed and enables control of the extent of mesopore formation in the zeolite (20,230,m2,g,1) upon alkaline treatment. The functionality of the introduced mesoporosity in the hierarchical beta crystals is demonstrated by the improved performance in the catalytic pyrolysis of low-density polyethylene. The partial detemplation,desilication treatment enhances the tuning options of this demetallation method. [source] Structure of nanoporous zirconia-based powders synthesized by different gel-combustion routesJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007Jorge R. Casanova Zirconia-based ceramics that retain their metastable tetragonal phase at room temperature are widely studied due to their excellent mechanical and electrical properties. When these materials are prepared from precursor nanopowders with high specific surface areas, this phase is retained in dense ceramic bodies. In this work, we present a morphological study of nanocrystalline ZrO2,2.8 mol% Y2O3 powders synthesized by the gel-combustion method, using different organic fuels , alanine, glycine, lysine and citric acid , and calcined at temperatures ranging from 873 to 1173,K. The nanopore structures were investigated by small-angle X-ray scattering. The experimental results indicate that nanopores in samples prepared with alanine, glycine and lysine have an essentially single-mode volume distribution for calcination temperatures up to 1073,K, while those calcined at 1173,K exhibit a more complex and wider volume distribution. The volume-weighted average of the nanopore radii monotonically increases with increasing calcination temperature. The samples prepared with citric acid exhibit a size distribution much wider than the others. The Brunauer,Emmett,Teller technique was used to determine specific surface area and X-ray diffraction, environmental scanning electron microscopy and transmission electron microscopy were also employed for a complete characterization of the samples. [source] Clean synthesis of propylene carbonate from urea and 1,2-propylene glycol over zinc,iron double oxide catalystJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 5 2006Xinqiang Zhao Abstract A series of zinc,iron double oxide catalysts has been prepared. The suitable preparation conditions are as follows: zinc nitrate and iron nitrate as precursors, molar ratio of Zn/Fe 2:1, ammonia as the precipitant, precipitation end-point pH 8.04, and calcination temperature 450 °C. The clean synthesis of propylene carbonate (PC) via urea and 1,2-propylene glycol (PG) over the zinc,iron double oxide catalyst has been studied. The optimal reaction conditions are as follows: reaction temperature 170 °C, reaction time 2 h, catalyst concentration 1.4% (wt), and molar ratio of urea to PG 1:4. The highest yield of PC was 78.6%. XRD, CO2 -TPD and XPS techniques have been employed for catalyst characterization. Two kinds of crystal phase, ZnO and ZnFe2O4, have been detected and their synergistic effect promotes the catalytic activity of the oxide catalysts. Copyright © 2006 Society of Chemical Industry [source] Structure, texture and surface acidity studies of a series of mixed zinc,aluminum (60,90 molar % Al) phosphate catalystsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 2 2001Karim Mtalsi Abstract A series of mixed zinc,aluminum phosphate (ZnAlP) catalysts containing 40,90 aluminum molar % were synthesized by a coprecipitation method and characterized by nitrogen adsorption,desorption, X-ray diffraction, FTIR spectroscopy, thermogravimetric analysis (TGA), differential thermal analysis (DTA), diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and temperature programmed desorption (TPD) of ammonia. The presence of aluminum greatly affected the surface properties of Zn3(PO4)2 by delaying the crystallization process of Zn3(PO4)2. All amorphous samples were shown to be mesoporous and they contained two types of aluminum surface hydroxyl groups and one type of phosphorus hydroxyl group, as shown by DRIFT spectra. The specific surface area and the acidity of ZnAlP increased on increasing the aluminum content. On the other hand, a great difference in the texture and the concentration of surface acid sites was found by changing the precipitating agent and calcination temperature. Thus these factors also play an important role in the final properties of these catalysts. © 2001 Society of Chemical Industry [source] Monolithic Ceramic Foams for Ultrafast Photocatalytic Inactivation of BacteriaJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2009Pinggui Wu Palladium-modified nitrogen-doped titanium dioxide (TiON/PdO) foams were synthesized by a sol,gel process on a polyurethane foam template. The TiON/PdO foam was tested for microbial killing using Escherichia coli cells as a target. Under visible-light illumination, the TiON/PdO foam displayed a strong antimicrobial effect on the bacteria cells in water. The antimicrobial effect was found to be dependent on the palladium content and the calcination temperature. In a flow-through dynamic photoreactor, the new photocatalyst efficiently inactivated E. coli within a short contact time (<1 min), the shortest ever reported for the photocatalytic killing of bacteria. The strong antimicrobial functions of the TiON/PdO foam were related to charge trapping by PdO and the high contact efficiency of the foam structure. [source] Phase Morphology in Electrospun Zirconia MicrofibersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 4 2008Erin Davies Electrospinning of sol,gels has been used to produce zirconium-doped polymer microfibers from zirconyl chloride and poly(vinylpyrollidone) precursors. Calcination of these structures between temperatures of 370° and 930°C resulted in the formation of zirconia nanograined microfibers whose diameters ranged from 1200 to 800 nm at the higher temperatures and whose average grain size ranged from 9 to 33 nm. X-ray diffraction analysis revealed varying amounts of monoclinic and tetragonal zirconia present in the fibers and established how this varied with calcination temperature and time. The tetragonal phase was shown to be unstable and disappeared on heating the material beyond around 750°C. The amount of zirconia yielded from the precursor material was measured and was found to be consistently greater than the theoretical yield. Average grain size within the microfibers increased with increasing calcination temperature and is effectively doubled when a 10 kPa pressure was applied. The effect of pressure also results in the creation of new crystal structures within the nanofibers and, as with traditional zirconia processing, the addition of impurity ions was found to stabilize the tetragonal phase. [source] A Novel Hybrid Method of Sol,Gel and Ultrasonic Atomization Synthesis and Piezoelectric Properties of SrBi4Ti4O15 CeramicsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 3 2008Zhijun Xu SrBi4Ti4O15(SBTi) powders were synthesized by a novel hybrid method of sol,gel and ultrasonic atomization. TiO2 particle was used as a starting material to replace other expensive soluble titanium salts. X-ray diffraction results showed that the pure-phase SBTi powders were obtained at 700°C for 2 h, which is much lower than the calcination temperature (800°,850°C) required in solid-state reactions. The ceramics sintered at 1100°C for 1 h exhibited 94.5% of relative density and a piezoelectric coefficient of 21 pC/N. The results showed that this hybrid method could lead to an attractive method for the industrial fabrication of SBTi materials. [source] Phase Evolution During Formation of SrAl2O4 from SrCO3 and ,-Al2O3/AlOOHJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2007Yu-Lun Chang Through the execution of experimental investigation, thermogravimetry, X-ray diffractometry, Fourier transform-infrared spectrometry, transmission electron microscopy, and energy-dispersive spectrometry, a variant reaction mechanism model was proposed for the solid-state reaction between SrCO3 and Al2O3/AlOOH for formation of SrAl2O4 material. The solid-state reaction is observed to be dependent on the calcination temperature. At temperatures lower than the transformation temperature of SrCO3 from orthorhombic to hexagonal (920°C), the reaction is attributed to the interfacial reaction between SrCO3 and alumina. Conversely, at temperatures higher than that, the solid-state reaction is dominated by the diffusion of Al3+ ions into the SrCO3 lattice. In this mechanism, two metastable species, hexagonal SrCO3 and hexagonal SrAl2O4, were observed. The activation energies of SrCO3 decomposition in the solid-state reaction also support these results. The interfacial reaction at low temperatures is characterized by a high activation energy of ,130 kJ/mol; whereas, in the reaction at higher temperatures, the activation energy of SrCO3 decomposition decreases to 34 kJ/mol. [source] Low-Temperature Synthesis of Fully Crystallized Spherical BaTiO3 Particles by the Gel,Sol MethodJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2004Un-Yeon Hwang The synthesis of spherical BaTiO3 particles was attempted by a new technique, the "gel,sol method," at 45°C. The (Ba,Ti) gel used as a starting material was prepared by aging mixtures of titanyl acylate with a barium acetate aqueous solution ([glacial acetic acid (AcOH)]/[titanium isopropoxide (TIP)] = 4, [barium acetate]/[TIP] = 1) at 45°C for 48 h. Potassium hydroxide (KOH) was used as a catalyst for the formation of BaTiO3. Powder X-ray diffractometry (XRD) results and Fourier-transform infrared (FT-IR) measurements for the (Ba,Ti) gel showed that the gel was amorphous, but the spatial arrangement of barium and titanium in the (Ba,Ti) gel is similar to that in crystalline BaTiO3 particles. Fully crystallized spherical BaTiO3 powder with a particle size of 40,250 nm formed at the very low reaction temperature of 45°C. Scanning electron microscopy images showed that the final particles formed via aggregation of the fine particles that seem to be the primary particles of bulk (Ba,Ti) gel. From the XRD, FT-IR, and Raman spectroscopy analysis, it was found that the crystal structure of the as-prepared particles continuously transformed from cubic to tetragonal as the calcination temperature increased, and high crystalline tetragonal BaTiO3 phase was obtained at 1000°C after 1 h of heat treatment. [source] Low-Temperature Synthesis of Nanocrystalline Yttrium Aluminum Garnet Powder Using TriethanolamineJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2003Yangqiao Liu Nanocrystalline yttrium aluminum garnet (YAG, Y3Al5O12) was synthesized by pyrolysis of complex compounds of aluminum and yttrium with triethanolamine [(HOCH2CH2)3N, (TEA)]. Loose and porous precursor was obtained on complete dehydration of the metal ion,triethanolamine complexes. Pure YAG powder was obtained by calcination of the precursor at 950°C. The precursor was characterized by simultaneous thermogravimetry, differential scanning calorimetry, and mass spectra analyses (TG,DSC,MS). The heat-treated powders were characterized by X-ray diffractometry (XRD), specific surface area measurements, and transmission electron microscopy (TEM). The average crystallite size as determined from X-ray line broadening and transmission electron microscopy studies was ,40 nm. The effects of the calcination temperature and the ratio of triethanolamine to mixed metal ions were also studied. [source] Sintering Behavior and Surface Microstructure of PbO-Rich PbNi1/3Nb2/3O3,PbTiO3,PbZrO3 CeramicsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 11 2001Masao Kondo The sintering behavior and surface microstructure of PbNi1/3Nb2/3O3,PbTiO3,PbZrO3 (PNiNb-PT-PZ) ceramics were investigated. The PNiNb-PT-PZ ceramics with the stoichiometric composition and the addition of excess lead oxide (PbO-rich ceramics) were sintered by liquid-phase sintering in accordance with the solution-reprecipitation mechanism at temperatures below the melting point of PbO. The temperature at which the liquid phase forms fell to near the eutectic point of the PbO,Nb2O5 and the PbO,TiO2 system (868°C) with the addition of 5 mol% PbO. As the calcination temperature influenced the sinterability of the stoichiometric PNiNb-PT-PZ ceramic, unreacted PbO was considered to be the source of the liquid phase in the sintering of the stoichiometric powder. The secondary phase was observed at the surface of PbO-rich ceramics and was suggested to be a liquid phase expelled from inside the ceramic. A sintering scheme of PNiNb-PT-PZ ceramics was proposed, and the high sinterability of PNiNb-PT-PZ ceramics was attributed to the low formation temperature of the liquid phase. [source] Single-Source Sol-Gel Synthesis of Nanocrystalline ZnAl2O4: Structural and Optical PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2001Sanjay Mathur Nanometer-sized zinc aluminate (ZnAl2O4) particles were synthesized from heterometal alkoxides, [ZnAl2(OR)8], possessing an ideal cation stoichiometry for the ZnAl2O4 spinel. ZnAl2O4 is formed at 400°C, which is the lowest temperature reported for the formation of monophasic ZnAl2O4. 27Al magic-angle spinning nuclear magnetic resonance spectroscopy revealed that ZnAl2O4 possesses an inverse structure at <900°C, while the normal spinel phase is observed at higher temperatures. The homogeneity of the in-depth composition and Zn:Al stoichiometry (1:2) was confirmed by electron spectroscopy for chemical analysis. Evaluation of the valence-band spectra of ZnAl2O4 and ZnS suggested that the hybridization of O 2p and Zn 3d orbitals is responsible for lowering the bandgap in the latter. The average crystallite size showed an exponential relationship to the calcination temperature (X-ray diffractometry and transmission electron microscopy data). The optical spectra of different spinel powders (average particle sizes, 20,250 nm) showed that the absorption edge exhibits a blue shift as particle size decreases. [source] Effects of Calcination Temperature and A/B Ratio on the Dielectric Properties of (Ba,Ca)(Ti,Zr,Mn)O3 for Multilayer Ceramic Capacitors with Nickel ElectrodesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2000Wen-Hsi Lee The electrical performance of multilayer ceramic capacitors (MLCCs) with Ni inner electrodes, made from (Ba,Ca)(Ti,Zr,Mn)O3 (BCTZM), is closely related to the calcination temperature and the A/B ratio of the powder. For materials showing A/B = 1.000, the lifetime, the breakdown voltage, and the RC increase with higher calcination temperatures. No significant effect of the calcination temperature on RC and lifetime was found for materials showing A/B = 0.991. The isoelectric point of BCTZM is shifted toward higher pH values when the calcination temperature is decreased. The above results are attributed to the colloidal stability of aqueous BCTZM suspensions and the resulting green density of powder compacts. [source] Li-doped nanosized TiO2 powder with enhanced photocalatylic acivity under sunlight irradiationAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 10 2010Soraa Bouattour Abstract This work reports on the synthesis of Li-doped TiO2 nanoparticles using the sol,gel process and solid-state sintering, and investigates their potential use as a photocatalyst for degradation under sunlight excitation of different organic model compounds in aqueous solution. The structure of the nanocrystals was examined by X-ray diffraction, UV-vis ground state diffuse reflectance absorption spectra and X-ray photoelectron emission spectroscopy. Results showed that samples prepared by sol,gel process and calcined at 400 °C are composed of a mixture of anatase and rutile phases, in contrast to the one prepared by solid-state sintering, which exhibits an anatase phase with Li being involved in a spinel phase. The photocatalytic degradation of aqueous solutions of different aromatic compounds was successfully achieved under sunlight excitation in presence of Li-doped TiO2 prepared via sol,gel process. It was shown that the calcination temperature and the preparation mode greatly affect the photocatalytic efficiency. Copyright © 2010 John Wiley & Sons, Ltd. [source] Synthetic hydrotalcites from different routes and their application as catalysts and gas adsorbents: a reviewAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 9 2009M. R. Othman Abstract In this paper, widely accepted methods of hydrotalcite preparation such as co-precipitation, urea hydrolysis, hydrothermal, sol,gel, microwave irradiation, steam activation and solvothermal have been selected and reviewed. Our review indicates that the nature of the divalent cations, the synthesis method, the calcination temperature and the nature of the interlayer species are determinant factors in shaping the surface properties of the layered double hydoxides. The basic strength of the surface base site and structural changes produced in the mixed oxides can be adjusted conveniently by varying the Al content during the synthesis. The combination of sol,gel with microwave irradiation during the gelling and crystallization steps has also been found to increase the surface area of the hydrotalcite-like compound. Copyright © 2009 John Wiley & Sons, Ltd. [source] A novel route to perovskite lead zirconate titanate from glycolate precursors via the sol,gel processAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 2 2008N. Tangboriboon Abstract A perovskite lead zirconate titanate was synthesized by the sol-gel process, using lead glycolate, sodium tris(glycozirconate) and titanium glycolate as the starting precursors. For the mole ratio Pb:Zr:Ti of 1:0.5:0.5 [Pb(Zr0.5Ti0.5)O3], TGA-DSC thermal analysis indicated that the percentage of ceramic yield was 55.8, close to the calculated chemical composition value of 49.5. The exothermic peak occurred at 268 °C below the theoretical Curie temperature of 400 °C. The pyrolysis of Pb(Zr0.5Ti0.5)O3 of the perovskite phase was investigated in terms of calcination temperature and time. The structure obtained was of the tetragonal form when calcined at temperatures below 400 °C; it transformed to the tetragonal and the cubic forms of the perovskite phase on calcination above the Curie temperature, as verified by X-ray data. The lead zirconate titanate synthesized and calcined at 400 °C for 1 h had the highest dielectric constant, the highest electrical conductivity and the dielectric loss tangent of 10 190, 0.803 × 10,3 (,.m),1 and 1.513 at 1000 Hz, respectively. The lead zirconate titanate powder synthesized has potential applications as an electronic material. Copyright © 2008 John Wiley & Sons, Ltd. [source] A novel route to perovskite lead titanate from lead and titanium glycolates via the sol,gel processAPPLIED ORGANOMETALLIC CHEMISTRY, Issue 12 2006N. Tangboriboon Abstract Pure perovskite lead titanate powder (PbTiO3) is successfully produced via the sol,gel process using lead and titanium glycolates as starting precursors and has been synthesized by the oxide one spot synthesis process. The obtained lead titanate is of the tetragonal form of the perovskite phase, with high purity and nearly zero moisture content. From high-resolution mass spectra, the XRD technique, Raman-FTIR and TGA-DTA analysis, the lead,titanium glycolates undergo sol,gel transition through the formation of PbOTi bonds. From the SEM micrographs, the PbTiO3 particle shape transforms from an agglomerate sphere to a needle and fiber-like shapes as the calcination temperature is varied above Tc. The corresponding molecular structural transformation, from the tetragonal form to the cubic form, occurs at 430 °C. The lead titanate powder calcined at 300 °C for 3 h has the highest dielectric constant and electrical conductivity values, namely 17470 and 1.83 × 10,3, respectively. Copyright © 2006 John Wiley & Sons, Ltd. [source] Catalytic decomposition of methane over supported Ni catalysts with different particle sizesASIA-PACIFIC JOURNAL OF CHEMICAL ENGINEERING, Issue 5 2009Sun Yunfei Abstract Methane decomposition on ,-Al2O3 -supported Ni catalysts, as a method for the production of carbon nanofibers (CNFs) and CO-free hydrogen, has been investigated to show the effect of catalyst particle size on the rate and yield of CNFs formation. The catalysts were prepared by deposition,precipitation with different calcination temperature ranging from 725 to 1025 K so as to have different initial particle sizes. The results show that catalysts with smaller initial particle sizes had higher initial growth rate but experienced fast deactivation. The lifetime of the catalyst, ending at the inflection point on the rate curve of CNFs growth, could well represent the yield of CNFs of the catalyst, and the maximal yield of CNFs was achieved on the Ni catalysts calcinated at 823 K and with a particle size of around 56 nm. However, the diameters of the grown CNFs were not directly related to the initial size of the catalysts, because of particle sintering and breaking during catalyst reduction or CNFs formation. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd. [source] Zeta Potential Measurement in Catalyst PreparationsCHEMICAL ENGINEERING & TECHNOLOGY (CET), Issue 2 2005J. B. Stelzer Abstract Oxide surfaces are covered with hydroxyl groups. In contact with water, positive or negative surface charges can be developed. The surface charge of oxide particles can be fine-tuned by changing the calcination temperature of the oxides before dispersion in water or by variation of the suspension pH. Strong negative or positive surface charges stabilize a suspension and avoid particle aggregation. Nano-structured catalysts suspended in water show surface charges different from those of compact TiO2. For spray drying, the cationic or anionic additives used have to be strongly attached via electrostatic forces to the surface of the suspended oxide particles. When noble metal complexes have to be brought to the support surface, the positively or negatively charged complexes must have an opposite charge relative to the surface charge. Zeta potential measurements can solve these problems. [source] Structure of nanoporous zirconia-based powders synthesized by different gel-combustion routesJOURNAL OF APPLIED CRYSTALLOGRAPHY, Issue 2007Jorge R. Casanova Zirconia-based ceramics that retain their metastable tetragonal phase at room temperature are widely studied due to their excellent mechanical and electrical properties. When these materials are prepared from precursor nanopowders with high specific surface areas, this phase is retained in dense ceramic bodies. In this work, we present a morphological study of nanocrystalline ZrO2,2.8 mol% Y2O3 powders synthesized by the gel-combustion method, using different organic fuels , alanine, glycine, lysine and citric acid , and calcined at temperatures ranging from 873 to 1173,K. The nanopore structures were investigated by small-angle X-ray scattering. The experimental results indicate that nanopores in samples prepared with alanine, glycine and lysine have an essentially single-mode volume distribution for calcination temperatures up to 1073,K, while those calcined at 1173,K exhibit a more complex and wider volume distribution. The volume-weighted average of the nanopore radii monotonically increases with increasing calcination temperature. The samples prepared with citric acid exhibit a size distribution much wider than the others. The Brunauer,Emmett,Teller technique was used to determine specific surface area and X-ray diffraction, environmental scanning electron microscopy and transmission electron microscopy were also employed for a complete characterization of the samples. [source] UV Raman spectroscopic study on the phase transformation of ZrO2, Y2O3,ZrO2 and SO42,/ZrO2JOURNAL OF RAMAN SPECTROSCOPY, Issue 5 2002Can Li The phase evolution of zirconia (ZrO2), sulfated zirconia (SO42,/ZrO2) and yttrium oxide incorporated zirconia (Y2O3,ZrO2) from the tetrahedral phase to the monoclinic phase was studied using UV Raman spectroscopy, visible Raman spectroscopy and x-ray diffraction (XRD). It is clearly observed that there are discrepancies between the results from the UV Raman spectra, visible Raman spectra and XRD patterns. The phase change from tetragonal to monoclinic is always earlier or at lower calcination temperatures as observed by UV Raman spectroscopy than by visible Raman spectroscopy and XRD. UV Raman spectroscopy is found to be more sensitive at the surface region while visible Raman spectroscopy and XRD supply the information mainly from the bulk. The inconsistency in the results from the three techniques suggests that the phase transformation of zirconia starts from its surface region and then gradually develops into its bulk. For SO42,/ZrO2 and Y2O3,ZrO2, the transformation from the tetragonal to the monoclinic phase is significantly retarded owing to the presence of the sulfated groups and the yttrium oxide. Particularly, the tetragonal phase of Y2O3,ZrO2 can be maintained up to 800 °C although its phase at the surface region changed into monoclinic at 500 °C. Copyright © 2002 John Wiley & Sons, Ltd. [source] Mechanochemical Activation-Assisted Low-Temperature Synthesis of CaZrO3JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2007Guotian Ye Calcium zirconate (CaZrO3, CZ) was prepared using a solid-state reaction with mechanochemical activation through vibro-milling, aiming at completing the reaction CaO+ZrO2=CaZrO3 at relatively low calcination temperatures. Changes in the crystallite size and homogeneity of the mixed components CaO and ZrO2 in the starting mixtures were observed with different milling times. The influence of milling on the incipient temperature of CZ formation and completion of CZ formation was investigated. It is concluded that milling of the reactants for 20 h lowered the incipient temperature of CZ formation from 800° to 600°C, and the temperature of complete CZ formation from above 1100° to 800°C. [source] Control of Phase and Pore Structure of Titania Powders Using HCl and NH4OH CatalystsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2001Ki Chang Song Porous titania powders were prepared by hydrolysis of titanium tetraisopropoxide (TTIP) and were characterized at various calcination temperatures by nitrogen adsorption, X-ray diffraction, and microscopy. The effect of HCl or NH4OH catalysts added during hydrolysis on the crystallinity and porosity of the titania powders was investigated. The HCl enhanced the phase transformations of the titania powders from amorphous to anatase as well as anatase to rutile, while NH4OH retarded both phase transformations. Titania powders calcined at 500°C showed bimodal pore size distributions: one was intra-aggregated pores with average pore diameters of 3,6 nm and the other was interaggregated pores with average pore diameters of 35,50 nm. The average intra-aggregated pore diameter was decreased with increasing HCl concentration, while it was increased with increasing NH4OH concentration. [source] Effects of Calcination Temperature and A/B Ratio on the Dielectric Properties of (Ba,Ca)(Ti,Zr,Mn)O3 for Multilayer Ceramic Capacitors with Nickel ElectrodesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2000Wen-Hsi Lee The electrical performance of multilayer ceramic capacitors (MLCCs) with Ni inner electrodes, made from (Ba,Ca)(Ti,Zr,Mn)O3 (BCTZM), is closely related to the calcination temperature and the A/B ratio of the powder. For materials showing A/B = 1.000, the lifetime, the breakdown voltage, and the RC increase with higher calcination temperatures. No significant effect of the calcination temperature on RC and lifetime was found for materials showing A/B = 0.991. The isoelectric point of BCTZM is shifted toward higher pH values when the calcination temperature is decreased. The above results are attributed to the colloidal stability of aqueous BCTZM suspensions and the resulting green density of powder compacts. [source] The Effect of Trivalent Cations on the Performance of Mg-M-CO3 Layered Double Hydroxides for High-Temperature CO2 CaptureCHEMSUSCHEM CHEMISTRY AND SUSTAINABILITY, ENERGY & MATERIALS, Issue 8 2010Qiang Wang Dr. Abstract The effect of trivalent cations on the performance of Mg-M-CO3 (M=Al, Fe, Ga, Mn) layered double hydroxides (LDHs) for high-temperature CO2 capture is systematically investigated for the first time. We demonstrate that the M3+ determines the structure evolution of LDH derivatives under thermal treatment, and finally influences the CO2 capture capacity. Very different calcination temperatures are required for the different LDHs to obtain their maximum CO2 capture capacities. To have a clear understanding of the reason behind these big differences the physicochemical properties, thermal stability, and memory effect of the LDHs were investigated. Both the thermal stability and the memory effect of LDHs are greatly influenced by the type of trivalent cation. The CO2 capture capacities were also evaluated under various conditions. Another important finding of this work is that the quasi-amorphous phase obtained by thermal treatment at the lowest possible temperature gives the highest CO2 capture capacity. [source] | |||||||||||||