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Oxide Mixture (oxide + mixture)
Selected AbstractsThe Remarkable Reaction of N2O with a Binary Component Lanthanide Oxide Mixture.CHEMINFORM, Issue 52 2006M. T. Harrington Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Design of Ceramic Materials for Chemical Sensors: Effect of SmFeO3 Processing on Surface and Electrical PropertiesJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 2 2001Hiromichi Aono Perovskite-type SmFeO3 powders were prepared by the thermal decomposition of a heteronuclear complex, Sm(Fe(CN)6)·4H2O and by solid-state reaction between the corresponding single oxides, Sm2O3 and Fe2O3. The thermal decomposition behavior of the complex was studied by thermogravimetric analysis. X-ray diffractometry was used to investigate the structure of the products from the complex thermal decomposition and the formation of SmFeO3 from the oxide mixture. Powders prepared by both methods were used to deposit thick films onto alumina substrates with comb-type gold electrodes. The microstructure and chemical homogeneity of the film surfaces were investigated by scanning electron microscopy and Auger electron spectroscopy. Thick SmFeO3 single-phase films having a homogeneous elemental distribution on the surface were obtained when powder prepared by thermal decomposition of the complex was used for deposition, even when the powder was fired at low temperature (800°C). Surface chemical analysis was performed by X-ray photoelectron spectroscopy (XPS). The O 1s XPS line was deconvoluted into two peaks, attributed to adsorbed oxygen (Oad) and oxygen in the lattice (Olattice). Quantitative analysis showed that the surface coverage of iron, expressed as Fe/(Fe + Sm), was larger for the films prepared using the solid-state reacted powder. Although the Olattice/(Fe + Sm) atomic ratio was not influenced by the processing procedures (and, thus, by iron surface coverage), the amount of Oad decreased with increasing iron surface coverage. A model of the SmFeO3 surface was used to determine that the outermost layer of the perovskite-type SmFeO3 prepared from the complex consisted mainly of samarium ions that could each bond four adsorbed oxygen ions. A single oxygen ion could adsorb onto an iron ion, and therefore, the content of adsorbed oxygen was lower for the film prepared from the solid-state reacted powders, which showed larger iron surface coverage. Electrical conductance measurements, performed with increasing temperature in different gaseous environments, confirmed these findings. Higher conductances and lower activation energies were observed for the films with larger samarium surface coverage. [source] Mechanical Activation-Assisted Synthesis of Pb(Fe2/3W1/3)O3JOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 7 2000Seok Khim Ang Perovskite Pb(Fe2/3W1/3)O3 (PFW) was prepared via a mechanical activation-assisted synthesis route from mixed oxides of PbO, Fe2O3, and WO3. The mechanically activated oxide mixture, which exhibited a specific area of >10 m2/g, underwent phase conversion from nanocrystalline lead tungstate (PbWO4) and pyrochlore (Pb2FeWO6.5) phases on sintering to yield perovskite PFW, although the formation of perovskite phase was not triggered by mechanical activation. When heated to 700°C, >98% perovskite phase was formed in the mechanically activated oxide mixture. The perovskite phase was sintered to a density of ,99% of theoretical density at 870°C for 2 h. The sintered PFW exhibited a dielectric constant of 9800 at 10 kHz, which was ,30% higher than that of the PFW derived from the oxide mixture that was not subjected to mechanical activation. [source] Investigation on the oxidation behaviour of gamma titanium aluminides coated with thermal barrier coatingsMATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 7 2008R. Braun Abstract In the present study, the applicability of thermal barrier coatings (TBCs) on ,-TiAl alloys was investigated. Two alloys with the chemical compositions of Ti-45Al-8Nb-0.2B-0.15C and Ti-45Al-1Cr-6Nb-0.4W-0.2B-0.5C-0.2Si were used. Before TBC deposition, the specimens were pre-oxidised in laboratory air or low partial pressure oxygen atmosphere. Yttria partially stabilised zirconia top coats were then deposited using electron-beam physical vapour deposition (EB-PVD). The oxidation behaviour of the ,-TiAl specimens with TBC was studied by cyclic oxidation testing in air at 850 and 900,°C. Post-oxidation analysis of the coating systems was performed using scanning electron microscopy with energy-dispersive X-ray spectroscopy (EDS). No spallation of the TBC was observed for pre-oxidised specimens of both alloys when exposed to air at 850,°C for 1100 cycles of 1,h dwell time at high temperature. SEM micrographs of the thermally grown oxide scale revealed outer mixed TiO2/Al2O3 protrusions with a columnar structure. The protrusions contained small particles of zirconia and a low amount of about 0.5 at% zirconium was measured by EDS analysis throughout this outer oxide mixture. The TBCs exhibited excellent adherence on the oxide scale. Intercolumnar gaps and pores in the root area of the TBC were filled with titania and alumina. Below the outer columnar oxide scale, a broad porous zone of predominant titania was observed. The transition region between the oxide scale and substrate consisted of a discontinuous nitride layer intermixed with alumina particles and intermetallic phases rich in niobium formed at the nitride layer/substrate interface. When thermally cycled at 900,°C, the oxide scales on the alloy Ti-45Al-8Nb-0.2B-0.15C pre-oxidised in low partial pressure oxygen spalled off after 540 cycles. For the sample with TBC, spallation was observed after 810 cycles. Failure occurred in the thermally grown oxide near the oxide/nitride layer interface. Microstructural examinations revealed again oxide scales with columnar structure beneath the zirconia top coat and good adherence of the TBC on the thermally grown oxides formed at 900,°C. [source] | ||||||||||