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Tantalum nitride nanoparticles were produced from a (K2TaF7 +5NaN3) exothermic mixture under the combustion regime. The effects of the K2TaF7/NaN3 ratio and KF and NH4F concentrations on the combustion parameters, product composition, and size of the tantalum nitride particles were studied. Depending on the synthesis conditions, the combustion temperature was maintained in the 700–1200°C range, resulting in hexagonal ε-TaN, TaN0.8, and Ta2N phases. The dominant phases were TaN and TaN0.8 in the 1000–1200°C range, whereas only the Ta2N phase was present in the 700–100°C range. Pure-phase cubic tantalum nitride (δ-TaN) was produced with 4.0mol of NH4F at a combustion temperature of ~800°C. Under controlled reaction conditions, the size of the tantalum nitride particles was about 10–50nm. We also found that during the synthesis, the stainless steel tube located inside of the reaction mixture was partially coated with fine TaN crystals. The mechanism of the combustion process is discussed in regards to the experimental results. [ABSTRACT FROM AUTHOR]

Abstract: Quasi-aligned, high-aspect-ratio AlN micro- and nanostructures were synthesized under high nitrogen pressure by the exothermic reaction of an Al+0.015mol (C2F4) n mixture. Structurally uniform AlN micro- and nanofibers with hexagonal and cylindrical morphologies were obtained when the system temperature was maintained within the range of 1600–1700°C. The fibers had aspect ratios as high as 2000, diameters in the range of ∼0.05–20μm, and were ∼100–1000μm in length. High-resolution transmission electron microscopic and selected area diffraction analyses indicated that the as-synthesized AlN micro- and nanostructures are perfectly single crystalline with preferential growth along the [001] direction. Branching was also observed in some of the micro-fibers, giving rise to randomized, two-dimensional comb textures. Based on the results obtained in the present study, a mechanism for the formation of AlN micro- and nanostructures under combustion conditions was proposed. [Copyright &y& Elsevier]

Abstract: An experimental study on the preparation of zirconium silicides was conducted using ZrSiO4–Mg, ZrSiO4–SiO2–Mg and ZrSiO4–ZrO2–Mg powder mixtures by the combustion synthesis (CS) technique. Test specimens having different composition ratios including Zr:Si=1:2, 1:1, 5:4, 5:3, 2:1, and 3:1 were employed in this study. Temperature profiles relative to all the starting compositions were measured using thermocouples, and the values of the combustion parameters (combustion temperature and wave velocity) were estimated using the same. The formation of ZrSi, ZrSi2, Zr5Si3, and Zr3Si2 phases was confirmed by X-ray analysis; however, only ZrSi was produced as a single-phase product. The proposed method was also extended to synthesize spherical ZrSi particles having mean diameters of 0.2–3.0μm. A comprehensive chemical pathway to describe the sequence of chemical reactions in the combustion wave was also proposed. [ABSTRACT FROM AUTHOR]