Advances in Chemical Propulsion (auth unkn) [No TOC]

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1990. Complete assignment of the 1 H and 13 C NMR spectra of Thiele’s Ester. Magnetic Resonance Chemistry 28:623–26. 27. Peters, D. 1959. Cyclopentadienecarboxylic acid. The structure of the monomer and the dimers. J. Chemical Society. 1761–65. 28. Marchand, A. , I. N. N. Namboothiri, S. B. Lewis, and W. H. Watson. Unpublished results. 29. Cady, H. H. 1979. Estimation of the densities of organic explosives from their structural formulas. Report LA-7760-MS. Los Alamos Scientific Laboratory, Los Alamos, NM.

J. Kabo and his colleagues at Belarussian State University, Minsk, Belarus. © 2002 by CRC Press LLC In the course of this study, several new candidate fuel systems have been synthesized in gram quantities. In the future, it is planned to undertake largescale syntheses of those new hydrocarbons, like 5, whose combustion properties suggest that they might excel as energetic fuels or as fuel additives. It is also planned to continue crystal density modeling studies in collaboration with Prof. Ammon with the expectation that comparison of predicted with experimental (X-ray derived) crystal density values will permit further refinement of the MOLPAK/WMIN computational approach.

Temperature curves discussed below (“breakdown curves”), curve fit of the variable-temperature CI data was made using two different methods. , spectra for individual molecular components), where each basis spectrum was assumed to be temperature independent. In the factor analysis method [23, 24], eigenvectors capable of describing the data were extracted directly, and no assumptions are required regarding the nature or number of components contributing to the signal. , nonnegative) basis spectra that describe the contribution, of each molecular component, to the mixture exiting the flow tube reactor.

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