Formation of nearly monodiperse MnO nanocrystals by simple heating of Mn stearate in octadecene was studied systematically and quantitatively as a model for non-injection synthesis of nanocrystals. For controlling the shape of the nanocrystals, that is, rice, rods, peanuts, needles, and dots, either an activation reagent (ocadecanol) or an inhibitor (stearic acid) might be added prior to heating. The quantitative results of this typical non-injection system reveal that the formation of nearly monodisperse nanocrystals did not follow the well-known "focusing of size distribution" mechanism. A new growth mechanism, self-focusing enabled by inter-particle diffusion, is proposed. Different from the traditional "focusing of size distribution", self-focusing not only affects the growth process of the nanocrystals, but may also play a role in controlling nucleation. Because of the simplicity of the reaction system, it was possible to also identify the chemical reactions associated with the growth and ripening of MnO nanocrystals with a variety of shapes. Through a recycling reaction path, water was identified as a decisive component in determining the kinetics for both growth and ripening in this system, although the reaction occurred at around 300 degrees C.
The synthesis, physical properties, and calculated performances of six stereo-and regioisomeric cyclobutane nitric ester materials are described. While the calculated performances of these isomers, as expected, were similar, their physical properties were found to be extremely different. By alteration of the stereo-and regiochemistry, complete tunability in the form of low-or high-melting solids, stand-alone melt-castable explosives, melt-castable explosive eutectic compounds, and liquid propellant materials was obtained. This demonstrates that theoretical calculations should not be the main factor in driving the design of new materials and that stereo-and regiochemistry matter in the design of compounds of potential relevance to energetic formulators.
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