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Calcination
Terms modified by Calcination Selected AbstractsCrystal growth of mixed-valence ammonium vanadatesCRYSTAL RESEARCH AND TECHNOLOGY, Issue 4 2007Tie-Zhen Ren Abstract A new method has been developed for the synthesis of mixed-valence ammonium vanadate crystals. Single crystals of (NH4)2V3O8 were synthesized on a large scale by hydrothermal reduction of NH4VO3 in ethanol-H2O solutions in the presence of triblock copolymer Pluronic P123. The crystals are shining thin plates with (001) cleavage planes. Calcination of the (NH4)2V3O8 crystals at 300°C or above resulted in pure phases of V2O5. (© 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Synthesis of Nd-YAG material by citrate-nitrate sol-gel combustion route,ADVANCED ENGINEERING MATERIALS, Issue 4 2007L. Costa Polycrystalline, Neodymium doped, yttrium aluminum garnet Nd:YAG is a functional materials for solid-state lasers. The synthesis of Nd:YAG powders requires a strict control of the precursor reactivity and composition. Sol-gel citrate-based methods increase the chemical homogeneity and reactivity of the precursor powder. Calcination performed around 900,°C leads to the formation of pure YAG phase at temperatures much lower than the temperature required for the solid-state reaction (1600,°C). [source] Separation of light gas mixtures using SAPO-34 membranesAICHE JOURNAL, Issue 4 2000Joseph C. Poshusta Continuous SAPO-34 membranes were prepared on porous alumina tubular supports, and shown to be useful for light gas separations at low and high temperatures. Single-gas permeances of CO2, N2 and CH4 decreased with increasing kinetic diameter. For the best membrane at 300 K, the He and H2 permeances were less than that of CO2, because He, H2, and CO2 were small compared to the SAPO-34 pore, and differences in the heat of adsorption determined the permeance order. The smaller component permeated the fastest in CO2/CH4, CO2/N2, N2/CH4, H2/CH4 and H2/N2 mixtures between 300 and 470 K. For H2/CO2 mixtures, which were separated by competitive adsorption at room temperature, the larger component permeated faster below 400 K. The CO2/CH4 selectivity at room temperature was 36 and decreased with temperature. The H2/CH4 mixture selectivity was 8 and constant with temperature up to 480 K. Calcination, slow temperature cycles, and exposure to water vapor had no permanent effect on membrane performance, but temperature changes of approximately 30 K/min decreased the membrane's effectiveness. [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] Effect of Calcination on Crystallinity for Nanostructured Development of Wormhole-Like Mesoporous Tungsten OxideJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2007Wei Hao Lai The effects of calcination on the crystallinity and grain growth model for microstructure development of wormhole-like mesoporous tungsten oxide are investigated in this study. We found that residual mesopores of wormhole-like tungsten oxide can be seen calcined above 500°C, as evidenced by retention of a wormhole-like mesostructure of tungsten oxide. A model was proposed to combine grain growth with wormhole-like mesoporous behavior and to investigate whether the formation of wormhole-like mesoporous tungsten oxide can retard the collapse rate of mesopores during the calcination process. [source] Synthesis, Densification, and Phase Evolution Studies of Al2O3,Al2TiO5,TiO2 Nanocomposites and Measurement of Their Electrical PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 8 2007Vikas Somani Alumina,aluminum titanate,titania (Al2O3,Al2TiO5,TiO2) nanocomposites were synthesized using alkoxide precursor solutions. Thermal analysis provided information on phase evolution from the as-synthesized gel with an increase in temperature. Calcination at 700°C led to the formation of an Al2O3,TiO2 nanocomposite, while at a higher temperature (1300°C) an Al2O3,Al2TiO5,TiO2 nanocomposite was formed. The nanocomposites were uniaxially compacted and sintered in a pressureless environment in air to study the densification behavior, grain growth, and phase evolution. The effects of nanosize particles on the crystal structure and densification of the nanocomposite have been discussed. The sintered nanocomposite structures were also characterized for dielectric properties. [source] Synthesis of Gallium Oxide Hydroxide Crystals in Aqueous Solutions with or without Urea and Their Calcination BehaviorJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 6 2002A. Cüneyt Ta Gallium oxide hydroxide (GaOOH·xH2O) single crystals were synthesized in aqueous solutions by using two different precipitation techniques: homogeneous decomposition of urea and forced hydrolysis in pure water. Precipitation of crystals started at exactly the same pH value (i.e., 2.05 at 85°C) in both cases. The morphology of crystals turned out to be quite different (zeppelin-like with urea, rodlike without urea) in each of the above methods. Calcination of these gallium oxide hydroxide crystals in air at temperatures ,500°C transformed them into Ga2O3. Characterization of the samples was performed by X-ray diffractometry, scanning electron microscopy, thermogravimetry/differential thermal analysis, Fourier transform infrared spectroscopy, and ICP, carbon, and nitrogen analyses. [source] ChemInform Abstract: Phase Formation and Solid State Structure on Calcination of a Nickel Ferrite Acetate Precursor.CHEMINFORM, Issue 2 2001H. Heegn Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] A Study of the Influence of Composition on the Microstructural Properties of ZnO/Al2O3 Mixed Oxides,EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 7 2009Shaojun Miao Abstract A series of ZnO/Al2O3 mixed oxide samples with varyingZn/Al ratio is prepared by coprecipitation, ageing, drying, and calcination. Samples are investigated in the state after drying and calcination. The applied methods include X-ray diffraction, solid-state 27Al magic-angle spinning nuclear magnetic resonance spectroscopy, transmission electron microscopy and thermogravimetric experiments coupled with evolved gas analysis. Phases present in the dried precursor samples include hydrozincite, zaccagnaite, and an unknown phase. After calcination zinc oxide and spinel can be found. All results indicate the substitution of Al ions for Zn ions in zinc oxide of zinc-rich samples. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Incorporation of Aluminium and Iron into the Zeolite MCM-58EUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 6 2005Gabriela Ko Abstract The hydrothermal synthesis of zeolite MCM-58 is investigated with N -benzylquinuclidinium bromide as a structure-directing agent in order to isomorphously substitute aluminium or iron for silicon. Al-MCM-58 was synthesised in a wide range of nSi/nAl ratios (from 19 to 56), and Fe-MCM-58 was successfully prepared in a narrower range of nSi/nFe ratios (from 18 to 36). The obtained products were characterised by XRD, SEM, 27Al MAS NMR, 29Si MAS NMR, FTIR, and ESR spectroscopy. Two different calcination procedures, viz. in a stream of nitrogen and air or in a stream of ammonia, were used in order to modify the acid sites in the zeolite. FTIR spectroscopy before and after the adsorption of [D3]acetonitrile and pyridine was employed to determine the concentration and type of the acid sites. The acid forms of Al(Fe)-MCM-58 are characterised by the vibrations of bridging Si,OH,Al(Fe) groups at 3628 cm,1 and 3564 cm,1 (Al-MCM-58) or 3646 cm,1 and 3520 cm,1 (Fe-MCM-58). The acid sites of both zeolites Al-MCM-58 and Fe-MCM-58 are accessible for [D3]acetonitrile and pyridine, and all materials contain substantial numbers of Lewis sites (Al-MCM-58: 50,% of the total acid sites; Fe-MCM-58: 90,%) over the whole range of nSi/nAl (nSi/nFe) ratios studied. Only a small increase in the concentration of Brønsted acid sites was achieved after calcination of the as-synthesised samples in a flow of ammonia. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] Microwave Assisted Synthesis of Yb:Y2O3 Based Materials for Laser Source Application,ADVANCED ENGINEERING MATERIALS, Issue 3 2010Anna Luisa Costa Yb:Y2O3 submicrometric particles were synthesized through co-precipitation of Yb and Y nitrate in water. Microwave heating and controlled release of ammonia through urea decomposition at reaction temperature leaded to the formation of disaggregated, monosized spherical particles of carbo-hydroxy-nitrate precursors. Pure crystalline Yb:Y2O3 powder that preserved the described morphology was obtained after calcination in air at 800,°C for 30,min. This powder mixed with commercial alumina powder was used to produce transparent Yb:YAG ceramics. Improved properties in terms of powder morphology and reactivity were presented in comparison with powders obtained by traditional heating. [source] The Synthesis of Novel Porous Functional Materials for use as Nitrosamine Traps,ADVANCED FUNCTIONAL MATERIALS, Issue 11 2004Y. Xu Abstract Two novel porous nitrosamine traps have been synthesized in order to eliminate carcinogens from the environment. A functional mesoporous material, CuO/SBA-15, has been synthesized by using an in-situ coating method, with the addition of a guest salt to the reaction system to modify the porous materials before the particles of SBA-15 were incubated; the synthesis and modification processes were performed in a single step. The resulting mesoporous composites selectively adsorb N -nitrosopyrrolidine (NPYR), a typical volatile nitrosamine, and are potential cigarette additives that can be used for the removal of nitrosamines from cigarette smoke, thereby protecting public health and the environment. In another reaction, silica gel is modified by being coated with magnesia and then corroded by NaOH solution. The magnesia is dispersed onto the silica by impregnating it with a magnesium acetate solution, followed by calcination. After corrosion of the calcined sample with caustic soda, only the silica particles that are completely covered by magnesia remain. This material exhibits a similar ability to SBA-15 and zeolite NaY in its selective adsorption of NPYR. [source] Hydrothermal Synthesis of Rare Earth (Tb, Y) Hydroxide and Oxide Nanotubes,ADVANCED FUNCTIONAL MATERIALS, Issue 12 2003Y.-P. Fang Abstract In this paper, Tb(OH)3 and Y(OH)3 single-crystalline nanotubes with outer diameters of 30,260,nm, inner diameters of 15,120,nm, and lengths of up to several micrometers were synthesized on a large scale by hydrothermal treatment of the corresponding oxides in the presence of alkali. In addition, Tb4O7 and Y2O3 nanotubes can be obtained by calcination of Tb(OH)3 and Y(OH)3 nanotubes at 450,°C. X-ray diffraction (XRD), field-emission scanning electron microscopy, transmission electron microscopy (TEM), electron diffraction (ED), energy-dispersive X-ray spectroscopy (EDS), thermogravimetry, and differential scanning calorimetry (DSC) have been employed to characterize these nanotube materials. The growth mechanism of rare earth hydroxide nanotubes can be explained well by the highly anisotropic crystal structure of rare earth hydroxides. These new types of rare earth compound nanotubes with open ends have uses in a variety of promising applications such as luminescent devices, magnets, catalysts, and other functional materials. Advantages of this method for easily realizing large-scale production include that it is a simple and unique one-pot synthetic process without the need for a catalysts or template, is low cost, has high yield, and the raw materials are readily available. The present study has enlarged the family of nanotubes available, and offers a possible new, general route to one-dimensional single-crystalline nanotubes of other materials. [source] A New Method for Post-Synthesis Coating of Zirconia on the Mesopore Walls of SBA-15 Without Pore Blocking,ADVANCED MATERIALS, Issue 11 2008Cheralathan Kanakkampalayan Krishnan Zirconia coating of the mesopore walls of the mesoporous silica material SBA-15 is achieved by internal hydrolysis of a zirconia precursor, which is loaded inside the mesopores, using NH3/H2O vapor at elevated temperature and subsequent calcination (see figure). High loadings of zirconia, more than 30 wt%, can be coated on the mesopore walls without any pore blocking. [source] Size-Dependent Catalytic Activity of Supported Palladium Nanoparticles for Aerobic Oxidation of AlcoholsADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 3 2008Jing Chen Abstract Silica-alumina (SiO2 -Al2O3)-supported palladium catalysts prepared by adsorption of the tetrachloropalladate anion (PdCl42,) followed by calcination and reduction with either hexanol or hydrogen were studied for the aerobic oxidation of alcohols. The mean size of the Pd particles over the SiO2 -Al2O3 support was found to depend on the Si/Al ratio, and a decrease in the Si/Al ratio resulted in a decrease in the mean size of the Pd nanoparticles. By changing the Si/Al ratio, we obtained supported Pd nanoparticles with mean sizes ranging from 2.2 to 10,nm. The interaction between the Pd precursor and the support was proposed to play a key role in tuning the mean size of the Pd nanoparticles. The Pd/SiO2 -Al2O3 catalyst with an appropriate mean size of Pd particles could catalyze the aerobic oxidation of various alcohols to the corresponding carbonyl compounds, and this catalyst was particularly efficient for the solvent-free conversion of benzyl alcohol. The intrinsic turnover frequency per surface Pd atom depended significantly on the mean size of Pd particles and showed a maximum at a medium mean size (3.6,4.3,nm), revealing that the aerobic oxidation of benzyl alcohol catalyzed by the supported Pd nanoparticles was structure-sensitive. [source] High resistance to aerial oxidation of an amorphous NiB/SiO2 catalyst: TP-XRD, TPR and related investigationsJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 6 2004Yong-Zhen Wang Abstract An amorphous NiB/SiO2 catalyst, prepared by a reductive,impregnation method, was thoroughly studied as to its behavior in air and in benzene hydrogenation in a fixed-bed reactor at atmospheric pressure. The results showed that the amorphous NiB/SiO2 catalyst possessed long life and excellent resistance to aerial oxidation. Even after calcination at 400 °C, TP-XRD and TPR measurements revealed that the amorphous NiB/SiO2 catalyst was not oxidized, and could retain its activity in benzene hydrogenation. Copyright © 2004 Society of Chemical Industry [source] Controlled-release systems based on the intercalation of polymeric metribuzin onto montmorilloniteJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 14 2002Ahmed Rehab Abstract A series of polymer,clay composites carrying metribuzin as herbicide moieties were prepared. Linear copolymers containing metribuzin via an imide linkage were prepared by the free-radical polymerization of metribuzin monomer (N,N -diacryloyl metribuzin) with different comonomers. The intercalation of the copolymers onto montmorillonite through a cationic exchange process was carried out and yielded metribuzin composite products. The prepared materials were characterized with a wide variety of analytical techniques, including gel permeation chromatography, NMR, IR, elemental microanalysis, gravimetric analysis (calcination), and swelling measurements. The release rates for the prepared materials were investigated in media of different pHs with an ultraviolet spectrophotometer. Also, these compounds were studied for the control of herb growth. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2513,2525, 2002 [source] Preparing titania aerogel monolithic chromatography columns using supercritical carbon dioxideJOURNAL OF SEPARATION SCIENCE, JSS, Issue 11 2010Ruohong Sui Abstract The search for a method to fabricate monolithic inorganic columns has attracted significant recent attention due to their unique ability in separation applications of various biomolecules. Silica and polymer based monolithic columns have been prepared, but titania and other metal oxide monoliths have been elusive, primarily due to their fragility. This article describes a new approach for preparing nanostructured titania based columns, which offer better performance over conventional particle packed columns for separating a wide variety of biomolecules including phosphopeptides. TiO2 monolithic aerogels were synthesized in separation columns using in situ sol-gel reactions in supercritical carbon dioxide (scCO2) followed by calcination, and compared to those prepared in heptanes. The characterization results show that scCO2 is a better solvent for the sol-gel reactions, providing lower shrinkage with the anatase TiO2 monolith composed of nanofibers with very high surface areas. The monolithic columns show the ability to isolate phosphopeptides with little flow resistance compared to conventional titania particle based microcolumns. [source] Synthesis and Characterization of Silver Nanoparticles and Titanium Oxide Nanofibers: Toward Multifibrous NanocompositesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2010Fredrick O. Ochanda A new method was investigated to produce new multiscale fibrous nanocomposites comprised of titanium oxide (TiO2) nanofibers and silver (Ag) nanoparticles (NPs). The process involved electrospinning TiO2 precursor solution containing colloidal solution of Ag NPs, and organic solvent (dimethyl- n,n -formamide) to fabricate a porous, nonwoven, free-standing nanofiber mesh. Postprocess heating of the electrospun nanofibers entailed calcination in air environment at 500°C for 3 h. Microemulsion processing was used to generate NPs of Ag in a monodispersed distribution throughout the colloidal solution. X-ray diffraction data were consistent with the anatase phase of TiO2, while transmission electron microscopy and hydrogen desorption measurements revealed a very porous microstructure. It was demonstrated that NP colloidal stability is solvent dependent. It is anticipated that incorporation of metal particles in nanofibers will lead to enhanced photocurrent generation, when used in functional devices. [source] Al3BC3 Powder: Processing and Synthetic MechanismJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2009Sea-Hoon Lee The processing parameters for the synthesis of Al3BC3 powder were optimized, and the synthetic mechanism was investigated. The mechanical mixing of the raw powders promoted the formation of secondary phases due to mechanical alloying effect and contamination. Nearly X-ray pure Al3BC3 powder was obtained after the calcination of the raw powder mixture at 1800°C for 2 h in Ar by suppressing the vaporization of aluminum. During calcination, Al4C3 layer was formed at the surface of aluminum powder by the reaction with carbon, which maintained the morphology of the aluminum powder above its melting temperature. The nucleation and growth of Al3BC3 within aluminum melt began to occur at 1000°C, and became the main synthetic mechanism of Al3BC3 at 1100°C. The Al3BC3 particles synthesized at 1100°C were porous and were composed of fine hexagonal crystals. The main synthetic mechanism of A3BC3 changed into solid,solid reaction above 1100°C, and a gas,solid reaction promoted the densification of the porous Al3BC3 powder above 1340°C. [source] Fabrication and Luminescent Properties of Nd3+ -Doped Lu2O3 Transparent Ceramics by Pressureless SinteringJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 10 2009Ding Zhou The fabrication of transparent Nd3+ ion-doped Lu2O3 ceramics is investigated by pressureless sintering under a flowing H2 atmosphere. The starting Nd-doped Lu2O3 nanocrystalline powder is synthesized by a modified coprecipitant processing using a NH4OH+NH4HCO3 mixed solution as the precipitant. The thermal decomposition behavior of the precipitate precursor is studied by thermogravimetric analysis and differential thermal analysis. After calcination at 1000°C for 2 h, monodispersed Nd3+:Lu2O3 powder is obtained with a primary particle size of about 40 nm and a specific surface area of 13.7 m2/g. Green compacts, free of additives, are formed from the as-synthesized powder by dry pressing followed by cold isostatic pressing. Highly transparent Nd3+:Lu2O3 ceramics are obtained after being sintered under a dry H2 atmosphere at 1880°C for 8 h. The linear optical transmittance of the polished transparent samples with a 1.4 mm thickness reaches 75.5% at the wavelength of 1080 nm. High-resolution transmission electron microscopy observations demonstrate a "clear" grain boundary between adjacent grains. The luminescent spectra showed that the absorption coefficient of the 3 at.% Nd-doped Lu2O3 ceramic at 807 nm reached 14 cm,1, while the emission cross section at 1079 nm was 6.5 × 10,20 cm2. [source] Solid-State Synthesis of Nanocrystalline BaTiO3: Reaction Kinetics and Powder PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 9 2008Maria Teresa Buscaglia The formation of BaTiO3 nanoparticles by a solid-state reaction between nanocrystalline raw materials BaCO3 and TiO2 was studied as a function of temperature (400°,800°C), time (1,24 h), and titania particle size (15 and 30 nm). The reaction starts at 500°C and a high reaction rate is already observed at 600°C for the finest titania, with up to 90% conversion after 2 h. Two main reaction stages were observed at 600°,700°C. The first step is dominated by nucleation and growth of BaTiO3 at the TiO2,BaCO3 contact points and at the TiO2 surface. Surface diffusion of BaCO3 is, most likely, the prevailing mass transport mechanism responsible for the rapid formation of BaTiO3, even in the absence of a significant contribution from lattice diffusion. The second stage begins when the residual TiO2 cores are completely covered by the product phase. For longer times, the reaction can only proceed by the slower lattice diffusion, resulting in a strong decrease of the reaction rate. Single-phase BaTiO3 nanopowders with a specific surface area of 12,15 m2/g, an average particle size of 70,85 nm, a relative density of 96.5%,98.3%, and a tetragonality of 1.005 were obtained by calcination at 700°,800°C. Critical parameters in the preparation of ultrafine powders by solid-state reactions are the particle size of both raw materials, the absence of large hard agglomerates, and the homogeneity of the mixture. The use of fine raw materials and optimization of the reaction conditions make mechanical activation unnecessary. [source] Preparation of Porous Tin Oxide Nanobelts Using the Electrospinning TechniqueJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2008An Yang The electrospinning method is adopted to prepare utralong PEO/stannic hydroxide composite nanofibers. Tin-oxide nanobelts can be obtained by calcination of the composite nanofibers in an open atmosphere. The nanobelts were characterized by a field emission scanning electron microscope, X-ray diffraction, a transmission electron microscope, a Raman spectromicroscope, and Fourier transform infrared spectroscopy. Microstructural analysis has shown that the nanobelts prepared consist of a continuous network of interconnected SnO2 grains. As a result, the SnO2 nanobelts possess a high surface area and continuous porosity, which may be applied for the fabrication of sensitive gas sensors. [source] Effect of Calcination on Crystallinity for Nanostructured Development of Wormhole-Like Mesoporous Tungsten OxideJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2007Wei Hao Lai The effects of calcination on the crystallinity and grain growth model for microstructure development of wormhole-like mesoporous tungsten oxide are investigated in this study. We found that residual mesopores of wormhole-like tungsten oxide can be seen calcined above 500°C, as evidenced by retention of a wormhole-like mesostructure of tungsten oxide. A model was proposed to combine grain growth with wormhole-like mesoporous behavior and to investigate whether the formation of wormhole-like mesoporous tungsten oxide can retard the collapse rate of mesopores during the calcination process. [source] Effect of Calcination Conditions and Excess Alkali Carbonate on the Phase Formation and Particle Morphology of Na0.5K0.5NbO3 PowdersJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 5 2007Pornsuda Bomlai Sodium-potassium niobate [Na0.5K0.5NbO3] powders were prepared following the conventional mixed oxide method. An orthorhombic XRD pattern, consistent with single-phase Na0.5K0.5NbO3, was obtained after calcination at 900°C for 6 h. Introducing 5 mol% excess Na2CO3 and K2CO3 into the starting mixture allowed milder calcination conditions to be used, for example 800°C for 2 h. Primary particles in 5 mol% excess samples were cuboid, with maximum sizes of ,2.5 ,m. Equiaxed 0.3,0.4-,m particles were formed for non-excess powders, and also for powders prepared with 1 and 3 mol% excess alkali carbonates. The results suggest liquid formation during calcination of the excess 5-mol% starting powders. [source] Cation Ordering and Dielectric Characteristics in Barium Zinc NiobateJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2007Chun-Te Lee Barium zinc niobate (Ba(Zn1/3Nb2/3)O3) (BZN) complex perovskite has been reported to have special microwave dielectric properties with close relation of its ordered structure. This study investigated the effect of calcination on the evolution of ordered structure and on quality factor with Raman spectroscopy, X-ray diffractometry, and transmission electron microscopy. The results revealed that single calcination at a lower temperature inhibited the growth of the ordered domain during sintering. In contrast, the 1:2-ordered domain in double-calcined BZN powder grew significantly with a higher sintering temperature and a longer soaking time. It is attributed that double calcination caused a higher degree of 1:2 ordering and better homogeneity. At the same time, the quality factor of the sintered ceramic body was highly promoted when using double-calcined powder. A close relation of the quality factor with the size of ordered domain, the degree of 1:2 ordering, and the relative density of BZN ceramics was presented. [source] Preparation of Molybdenum, Vanadium, and Tungsten Oxide Thin Films from Self-Assembly Deposited Polyoxometalate,Alkylamine-Layered Hybrid FilmsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2007Tetsuya Kida A novel, simple, and efficient route for preparing MoO3, V2O5, and WO3 films has been developed from layered polyoxometallate (POM)-alkylamine hybrid films by calcination. The highly ordered hybrid films were self-assembly deposited in a one-step process using clear precursor POM solutions, prepared by reacting layered MoO3, V2O5, and WO3·H2O powders with hexylamine in the presence of water. The morphology of the resulting films can be tuned by removing the intercalated hexylamine molecules from the as-prepared hybrid films through UV irradiation before calcination. [source] Influence of a Ceramic Substrate on Aqueous Precipitation and Structural Evolution of Alumina Nano-Crystalline CoatingsJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 1 2007Marie Mahé Either boehmite (,-AlOOH) or gibbsite (,-Al(OH)3) nanocrystalline thin films (h,100 nm) can be precipitated from AlCl3 solution at fixed pH and temperature onto different substrates. It depends on the nature of the substrate (mica flakes, SiO2 flakes, or ,-Al2O3 flakes), on their crystallographic properties (crystalline or amorphous), and on some experimental parameters (agitation rate, addition rate). According to the surface charge of the substrates, different alumina species are involved in the precipitation process. When negative charges are present on the substrate, the [Al3O(OH)3(OH2)9]4+ polycation is promoted, leading to the formation of the (Al4) tetramer ([Al4O(OH)10(OH2)5]o) and then to the precipitation of bohemite. When positive charges are present, a ligand bridge containing complex ([Al3O(OH)3(O2H3)3(OH2)9]+) is likely favored, giving rise to hexagonal ring structures or amorphous solids that lead to the formation of gibbsite. Besides the surface effects, crystalline substrates can act as a template during precipitation of aluminum species as shown for the formation of gibbsite on muscovite. Finally, calcination at 850°C of boehmite samples leads to porous ,-Al2O3 layers, while calcination of gibbsite leads to ,-Al2O3 layers. [source] Synthesis of Nanocrystalline Lanthanum Strontium Manganite Powder by the Urea,Formaldehyde Polymer Gel Combustion RouteJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2006Kuttan Prabhakaran Nanocrystalline lanthanum strontium manganite (LSM) powder has been synthesized by combustion of a transparent gel obtained by the polymerization of methylol urea and urea in a solution containing La3+, Sr2+, and Mn2+ (LSM ions). Chemistry of the transparent urea,formaldehyde (UF) polymer gel formation and structure of the gel have been proposed such that the LSM ions act in between the growing UF polymer chains by interacting through NH, OH, and CO groups by co-ordination and prevent polymer self-assembly through inter-chain hydrogen bonding as evidenced from infrared spectrum. Thermally stable structures formed by the decomposition of UF polymer below 300°C undergo combustion in the presence of nitrate oxidant in a temperature range from 350°,450°C. A perovskite LSM phase has been formed by self-sustained combustion of the dried gel initiated with little kerosene. The powder obtained after deagglomeration and calcination at 600°C for 2 h has a D50 value of 0.19 ,m, and the particles are aggregates of crystallites 10,25 nm in size. [source] Chemical Synthesis of Nanocrystalline Strontium Bismuth Tantalate Powders Using Tantalum,Tartarate ComplexJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2006Asit Baran Panda Nanocrystalline strontium bismuth tantalate (SrBi2Ta2O9; SBT) powders have been synthesized through complete dehydration of an aqueous solution mixture of tantalum tartarate, strontium salt of ethylenediaminetetraacetic acid, and bismuth,triethanolamine complex. Single-step calcination of the fluffy, mesoporous, carbonaceous dehydrated precursor mass at 700°C/2 h results in nanosized SBT powders, with average particle size ,15 nm. When palletized and sintered at 950°C/4 h these powders show a relative density of 97.6% of theoretical value, and a maximum dielectric constant value of 1387 at Tc (Curie temperature)=279°C, when measured at 100 kHz. [source] | |||||||||||||||||||||||||||||||