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Powder Materials (powder + material)
Selected AbstractsThin films of Co3O4, MnCo2O4 and their solid solution as electrocatalyst: study of their magnetic propertiesPHYSICA STATUS SOLIDI (C) - CURRENT TOPICS IN SOLID STATE PHYSICS, Issue S1 2004E. Ríos Abstract We present magnetic measurements performed on the MnxCo3,xO4 (0 , x , 1) solid solution, prepared by spray pyrolysis. Thin films of about 20 ,m thickness were obtained after depositing aqueous metal nitrates precursors on Ti or conducting glass substrates. Powder material scratched from the substrate's surface was used for physico-chemical characterization. Presence of two oxidation states for each metal ion (Mn3+,Mn4+; Co2+,Co3+) triggers specific conduction mechanisms and double-exchange magnetic interactions. The ferromagnetic components are enhanced when x(Mn) increases, in detriment of the antiferromagnetic interactions. The ordering temperature Tc changes with x (from 22 K up to room temperature, for x = 0 up to x = 1). Based in the paramagnetic moment ,eff obtained at T > Tc, we propose a cationic distribution which can be nicely compared to the one obtained from crystallographic analyses. (© 2004 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim) [source] Physico-chemical properties of protein-bound polysaccharide from Agaricus blazei Murill prepared by ultrafiltration and spray drying processINTERNATIONAL JOURNAL OF FOOD SCIENCE & TECHNOLOGY, Issue 1 2007Joo Heon Hong Summary This study was conducted to develop the powder material and investigate the various physico-chemical properties of protein-bound polysaccharide with different molecular weight from Agaricus blazei Murill using ultrafiltration and spray-drying process. Powder properties of the three spray-dried powders were very different based on their molecular weights. The inlet temperature had less influence than pump rate on particle size of spray-dried powders. The moisture content of powders was increased with increasing pump rate and decreasing inlet temperature. Among these powders, SD-1, the molecular weight of which is below 10 kDa, was less flowable by internal cohesion. The decomposition temperature for the powders was in the range of 200,400 °C and showed relatively good enough for their thermal stabilities. [source] Comparison of particle sizing techniques in the case of inhalation dry powdersJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 12 2001Cynthia Bosquillon Abstract The objectives of this work were (i) to validate electrical zone sensing and laser diffraction for the analysis of primary particle size in the case of inhalation dry powders and (ii) to study the influence of the aggregation state of the powder on the sizing techniques. Free-flowing dry powders were prepared by spray-drying with a combination of albumin, lactose, and dipalmitoylphosphatidylcholine. The replacement of lactose by mannitol, the removal of albumin, and the atomization at high relative humidity all increased powder cohesion. Automated measurements were compared with primary particle sizes collected by light and electron microscopy. The mass mode obtained by electrical zone sensing and the mass median diameter measured by laser diffraction following dispersion with compressed air at a pressure of 3 bar or following suspension in water and ultrasonic dispersion at a power of 60 W for 30 s each provided primary particle sizes close to microscopy measurements. However, these conditions only applied in the case of slightly to moderately aggregated powders. For strongly agglomerated powders, an exact measurement of the size was only collected by laser diffraction in the wet state combined with ultrasonic dispersion. Our study underlies how measurement of primary particle size highly depends on both powder material and proper particle dispersion. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:2032,2041, 2001 [source] In1.06Ho0.94Ge2O7: a thortveitite-type compoundACTA CRYSTALLOGRAPHICA SECTION C, Issue 2 2004Erick A. Juarez-Arellano A new indium holmium digermanate, In1.06Ho0.94Ge2O7, with a thortveitite-type structure, has been prepared as a polycrystalline powder material by high-temperature solid-state reaction. This new compound crystallizes in the monoclinic system (space group C2/c, No. 15). The structure was characterized by Rietveld refinement of powder laboratory X-ray diffraction data. The In3+ and Ho3+ cations occupy the same octahedral site, forming a hexagonal arrangement on the ab plane. In their turn, the hexagonal arrangements of (In/Ho)O6 octahedral layers are held together by sheets of isolated diortho groups comprised of double tetrahedra sharing a common vertex. In this compound, the Ge2O7 diortho groups lose the ideal D3d point symmetry and also the C2h point symmetry present in the thortveitite diortho groups. The Ge,O,Ge angle bridging the diortho groups is 160.2,(3)°, compared with 180.0° for Si,O,Si in thortveitite (Sc2Si2O7). The characteristic mirror plane in the thortveitite space group (C2/m, No. 12) is not present in this new thortveitite-type compound and the diortho groups lose the C2h point symmetry, reducing to C2. [source] In1.08Gd0.92Ge2O7: a new member of the thortveitite familyACTA CRYSTALLOGRAPHICA SECTION C, Issue 10 2002Erick-Adrian Juarez-Arellano Indium gadolinium digermanium heptaoxide, In1.08Gd0.92Ge2O7, with a thortveitite-type structure, has been prepared as a polycrystalline powder material by a high-temperature solid-state reaction. As in the mineral thortveitite, the crystal structure belongs to the monoclinic system, with space group C2/m (No. 12). The precise structural parameters were obtained by applying the Rietveld method of refinement to the X-ray powder diffraction data. This layered structure presents, on one side, a honeycomb-like arrangement of the unique octahedral site, which is occupied randomly by In and Gd atoms, and, on the other side, sheets of isolated Ge2O7 diortho-groups made up of double tetrahedra sharing a common vertex and displaying C2h point symmetry. This compound showed a remarkable photoluminescence effect when it was irradiated with the X-ray beam during the X-ray diffraction measurements, and with the , beam during the Rutherford back-scattering spectrometry experiments employed to analyze the chemical stoichiometry. [source] Organometallic Access to Intermetallic , -CuE2 (E = Al, Ga) and Cu1,xAlx PhasesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 21 2008Mirza Cokoja Abstract In this work, we compare different precursor approaches for the mild decomposition to copper,aluminum and ,gallium powder materials in nonaqueous solution. Referring to previous work on the preparation of Cu,Al alloy materials from [(AlCp*)4] and [CpCu(PMe3)], the amine-stabilized metal trihydrides [(Me3N)AlH3] and [(quinuclidine)GaH3] were used as alternative sources for Al and Ga. In a comparative study, [(Me3N)AlH3] and [(AlCp*)4] were treated with the Cu precursors [CpCu(PMe3)] and [{Cu(mesityl)}5] in mesitylene solution in various molar ratios at 150 °C and 3 bar H2 to give metallic precipitates of the composition Cu1,xAlx (x = 0.67, 0.50, 0.31). Whereas the combination [(AlCp*)4] with [{Cu(mesityl)}5] did not yield an intermetallic phase, all other Cu/Al precursor combinations led to alloyed Cu,Al materials. For x = 0.67, the ,-CuAl2 phase formed, as shown by X-ray powder diffraction (XRD) and solid-state magic-angle-spinning (MAS)NMR spectroscopic studies. Similarly, the reaction of [{Cu(mesityl)}5] with [(quinuclidine)GaH3] immediately led to the precipitation of a gray powder, without the addition of hydrogen. The powder was identified by means of XRD as ,-CuGa2. At x = 0.50 and below, the reactions were less phase selective depending on the precursor combination. [CpCu(PMe3)] combined with both Al precursors afforded a mixture of several Cu,Al phases, whereas [{Cu(mesityl)}5] was treated with [(Me3N)AlH3] to yield a material whose X-ray signature was assigned to the monoclinic Cu0.51Al0.49 phase. The ,-Cu9Al4 phase could not be obtained from [CpCu(PMe3)]; instead, solid solutions of ,-Cu were obtained. The treatment of [{Cu(mesityl)}5] with [(Me3N)AlH3] in the Cu/Al molar ratio of 9:4 (x = 0.31) gave a gray powder, which could be identified by XRD as ,-Cu9Al4.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] A mathematical model of powder components oxidation during thermal spray processISRAEL JOURNAL OF CHEMISTRY, Issue 3-4 2007Alexey Kossenko A model developed on the basis of kinetic principles of mass transfer allows performing computer simulation of the oxidation of powder materials during the thermal spray process. Such simulation enables one to determine the oxidation degree of the powder. The calculation is based on determining quasi-stationary oxygen diffusion flow on a flying particle. Calculations performed for various spray powders and various flammable gases demonstrate a significant decrease of the oxidation degree with the growth of the particle diameter and density of a spray powder. The calculation results were confirmed by experiments. [source] Development of the powder reaction moulding processJOURNAL OF CHEMICAL TECHNOLOGY & BIOTECHNOLOGY, Issue 3 2009Lei Zhao Abstract BACKGROUND: The powder reaction moulding process uses a reactive monomer as carrier and binder for the moulding of metal or ceramic powders. De-binding is achieved using thermal depolymerisation which is followed by sintering to give the finished component. Binder can be recovered for re-use. RESULTS: Moulding compounds, with various powder volume fractions, have been prepared using stainless steel, silicon nitride and alumina with n-butyl cyanoacrylate as binder, and the stability of the compounds established. Rheological properties of the compounds have been measured using both pressure flow and drag flow methods. Compounds are strongly pseudoplastic. Comparison of experimental results with theoretical models, describing suspension flow behaviour shows that experimental maximum volume fractions are close to the theoretical volume fraction of 0.42 for silicon nitride, 0.68 for alumina and 0.7 for stainless steel. Differential scanning calorimetry and thermogravimetry have been used to simulate de-binding and show a rapid loss of binder through depolymerisation. Post-sintering porosity of the ceramic materials is high but this is thought to arise from the low pressure moulding techniques used. Porosity of the stainless steel mouldings is much lower. CONCLUSIONS: The results validate the powder reaction moulding idea and demonstrate applicability to three widely different powder materials. Copyright © 2008 Society of Chemical Industry [source] Impact of Thermal Diffusion on Densification During SPSJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2009Eugene A. Olevsky Spark-plasma sintering (SPS) has the potential for rapid (with heating rates reaching several hundred K/min) and efficient consolidation of a broad spectrum of powder materials. Possible mechanisms of the enhancement of consolidation in SPS versus conventional techniques of powder processing are categorized with respect to their thermal and athermal nature. This paper analyzes the influence of thermal diffusion, which is an SPS consolidation enhancement factor of a thermal nature. The Ludwig,Soret effect of thermal diffusion causes concentration gradients in two-component systems subjected to a temperature gradient. The thermal diffusion-based constitutive mechanism of sintering results from the additional driving force instigated by spatial temperature gradients, which cause vacancy diffusion. This mechanism is a commonly omitted addition to the free-surface curvature-driven diffusion considered in conventional sintering theories. The interplay of three mechanisms of material transport during SPS is considered: surface tension- and external stress-driven grain-boundary diffusion, surface tension- and external stress-driven power-law creep, and temperature gradient-driven thermal diffusion. It is shown that the effect of thermal diffusion can be significant for ceramic powder systems. Besides SPS, the results obtained are applicable to the ample range of powder consolidation techniques, which involve high local temperature gradients. The case study conducted on the alumina powder SPS demonstrates the correlation between the modeling and experimental data. It is noted that this study considers only one of many possible mechanisms of the consolidation enhancement during SPS. Further efforts on the modeling of field-assisted powder processing are necessary. [source] Characterization of Powder Beds by Thermal Conductivity: Effect of Gas Pressure on the Thermal Resistance of Particle Contact PointsPARTICLE & PARTICLE SYSTEMS CHARACTERIZATION, Issue 4 2004Michael Shapiro Abstract The thermal conductivity of ceramic powder packed beds was measured at temperatures below 100,°C for various powder sizes and compositions and under different gas atmospheres. Measurements at low pressures (down to 10,Pa) combined with a theoretical model allowed the elucidation of geometrical and thermal resistance parameters for the contact points between granules. The gap thickness and contact point size were found to be well correlated with the mean particle size. The thermal conductivities of all powders at low pressure were found to differ at most by a factor of two, whereas the solid-phase conductivities of the powder materials differed by more than one order of magnitude. A theoretical model accounting for the size-dependence of contact point conductivity is incorporated to rationalize this trend. [source] | |||||||||||||