Pyrolysis-atmospheric pressure chemical ionization was used to study the thermal decomposition of the energetic material cyclotrimethylenetrinitramine (RDX) and characterization of the individual molecular ion products was accomplished by tandem mass spectrometry. The analysis was aided with pyrolysis mass spectra of the (''N)-and perdeuterated RDX isotopes, and molecular formulae were derived for the m/z 46, 60, 74, 75, 85 and 98 molecular ions in the RDX pyrolysis mass spectrum. Equivalent fragments between the daughter ion mass spectra of the unlabeled and labeled RDX were determined in order to define a structure for each pyrolysis feature. Daughter ion mass spectra of pure reference compounds confirmed the identity of five of the six molecular ions, Perdeuterated RDX analyses provided evidence that m/z 74 and 75 are N,N-dimethylformamide and N-nitrosodimethylamine, respectively; m/z 46, 60 and 85 were identified as the protonated forms of formamide, N-methylformamide and dimethylaminoacetonitrile, respectively.
A concerted study of poly(vinyl chloride), chlorinated poly(vinyl chloride), and poly(vinylidene chloride) polymers by spectroscopy, thermal analysis, and pyrolysis‐gas chromatography resulted in a proposed mechanism for their thermal degradation. Polymer structure with respect to total chlorine content and position was determined, and the influence of these polymer units on certain of the decomposition parameters is presented. Distinguishing differences were obtained for the kinetics of decomposition, reactive macroradical intermediates, and pyrolysis product distributions for these systems. It was determined that chlorinated poly(vinyl chloride) systems with long‐chain CHCI units were more thermally stable than the unchlorinated precursor, exhibited increasing activation energy for the dehydrochlorination, and produced chlorine‐containing macroradical intermediates and chlorinated aromatic pyrolysis products. The poly(vinyl chloride) polymer was relatively less thermally stable, exhibited decreasing activation energy during dehydrochlorination, and produced polyenyl macro‐radical intermediates and aromatic pyrolysis products.
Significant effort has been made in the past by many workers to investigate the mechanism of thermal decomposition of poly(vinyl chloride) (PVC). The presence and role of free radicals has been controversial in this regard. Our data on PVC and chlorinated PVC systems demonstrate the existence of macroradicals in the early stage of thermal decomposition under inert and oxidative atmospheres. Data from conventional thermogravimetric experiments are used in conjunction with the electron spin resonance findings.
Macromolecules derived from hydrogen cyanide (HCN) may be major components of the dark matter observed in bodies in the outer Solar System, which include comets and asteroids. HCN oligomers and polymers are readily formed at room temperature and react with water to produce polypeptides and alpha-amino acids or undergo pyrolysis to produce nitrogen heterocycles. Electron spin resonance (ESR) spectroscopy shows that HCN polymer mixtures contain a significant amount of long-lived organic free radicals that are primarily carbon-based. For comparison, we have also examined samples of tholins produced from experimental analogs of Titan aerosols, which has been shown by trace organic analysis to consist partly of HCN polymer. The "Titan tholin" exhibits at least two ESR signals that can be assigned to nitrogen- and carbon-centered radicals, although heating the sample eliminates the nitrogen centers and increases the signal from the carbon centers. This result suggests that the nitrogen-centered radicals may be thermodynamically less stable, but are kinetically trapped during the spark-discharge reactions that produce tholins from mixtures of gases such as methane and nitrogen. The results strongly support previous proposals of free radical mechanisms for HCN polymerization.
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