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  • Chemistry  (13)
  • Poly(ethylene terephthalate)  (1)
  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Propellants, Explosives, Pyrotechnics 15 (1990), S. 77-80 
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Rapid-scan FTIR/temperature profiling studies of the fast thermal decomposition of alkanediammonium dinitrate salts [H3N(CH2)nNH3](NO3)2, n = 1-4 and 6, are described. All of the salts liberate HNO3 and NH3 early in the first stage. When n = 1-3, small molecule products from redox reactions occur in the second stage of decomposition. When n = 4, 6, the second stage involves cycloclimination to form pyrrolidine (n = 4) and α-ethlypyrrolidine (n = 6). The temperature of the onset of thermal decomposition is lower when n = 1 than when n is larger. Intra- and intermolecular hydrogen bonding are proposed to play a significant role in these decomposition patterns.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 12
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Fast thermolysis/FTIR spectroscopy of [H3NCH2CH2NH3]-(NO3)2 (EDD), [H2N(CH2CH2)2NH2](NO3)2 (PIPDN), and [HN(CH2CH2)3NH](NO3)2(DABCOD) and new oxonium nitrate (H3O+NO-3) double salts of PIPDN and DABCOD is described. EDD initially yields HNO3 and then small molecule decomposition products from redox reactions when heated at ≥ 100°C (dcc.). PIPDN initially yields HNO3, but then generates a significant amount of N,N′-dinitrosopiperazine along with small molecule fragments. DABCOD produces no HNO3(g), but instead gives CH2O, N,N′-dinitrosopiperazine and small molecule products. These patterns are entirely consistent with the behavior observed for primary, secondary and teritary ammonium mononitrate salts in our previous work. The presence of nitrosamines strongly increases the health hazard of the matcrials upon heating. No nitramines were detected as thermolysis products. Thermolysis of the oxonium nitrate double salts liberates HNO3 and H2O at a relatively low temperature (≥ 60 °C). Above this temperature, the thenmolysis proceeds in the same way as that of pure PIPDN and DABCOD. The crystal structure of PIPDN is described.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Propellants, Explosives, Pyrotechnics 15 (1990), S. 66-72 
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Fast thermolysis (〉 100°C/s)/FTIR spectroscopy of alkylammonium mononitrate salts is described in terms of the gas products and the temperature and time correlations of their evolution. The salts studied are [(CH3)nNH4-n]NO3, n = 1-3; [(CH3CH2)nNH4-n]NO3, n = 1-4; and [CH3(CH2)nNH3]NO3, n = 0-3. In addition to the patterns among the small molecule thermolysis products, the tendency to form nitrosamines, amides, and alkylnitrates is presented. The release of HNO3 qualitatively correlates with the basicity of the parent amine. The tertiary ammonium nitrate salts did not release HNO3(g). The release of NH3(g) appears only to occur when the residue can stabilize itself. Otherwise, the parent alkylamine is released. The formation of nitrosamines upon fast thermolysis of di- and trialkylammonium nitrate salts makes these materials a potential health risk in formulations. There is no evidence that the nitrate salts convert to nitrosamines through a nitramine intermediate.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Propellants, Explosives, Pyrotechnics 15 (1990), S. 123-126 
    ISSN: 0721-3115
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The fast thermolysis of N-methyl substituted ethanediam-monium dinitrate salts is described by temperature profiling/FTIR spectroscopy. The salts described are [CH3NH2CH2CH2NH3](NO3)2 (MEDD), [CH3NH2CH2CH2NH2CH3](NO3)2 (SDMEDD), [(CH3)2NHCH2CH2NH3](NO3)2 (UDMEDD), [(CH3)2NHCH2CH2NH2CH3](NO3)2 (TRMEDD) und [(CH3)2NHCH2CH2NH(CH3)2](NO3)2 (TMEDD). MEDD, UDMEDD, SDMEDD and TRMEDD more closely resemble the behavior of alkylammonium mononitrate salts than primary alkanediammonium dinitrates in terms of the temperature at which HNO3 is released. However, TMEDD resembles the dinitrates. Both C-C and C-N bond fission occur based on the nature of the alkylamine products that are liberated.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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