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    Wyświetlanie 1-8 z 8
    Tytuł:
    The Effect of Detonator Shell Materials on Detonation Calorimetry Results
    Autorzy:
    Němec, Ondřej
    Musil, Tomáš
    Künzel, Martin
    Powiązania:
    https://bibliotekanauki.pl/articles/1062738.pdf
    Data publikacji:
    2020
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    detonation calorimetry
    detonator
    PETN
    heat of detonation
    bomb calorimetry
    Opis:
    Detonation calorimetry is a method for the determination of the heat released by the detonation of an explosive charge. Compared to classical combustion calorimetry, detonation calorimetry requires an inert atmosphere, a large sample mass and a detonator for its initiation. This detonator releases some energy for which the results must be corrected. Four types of detonator have been tested in the calorimeter alone and also in combination with explosive charges of PETN. It was found that the aluminium shell of the detonator considerably increases the apparent heat of detonation of the PETN samples in a vacuum, while the presence of combustible (polymeric) components has the opposite effect. Pressurization of the calorimetric vessel with nitrogen gas only partially suppresses these effects. The preferred technique is to use copper or glass confinement in a high pressure inert atmosphere.
    Źródło:
    Central European Journal of Energetic Materials; 2020, 17, 4; 552-565
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Synthesis and Characterization of the Energetic Compounds Aminoguanidinium-, Triaminoguanidiniumand Azidoformamidinium Perchlorate
    Autorzy:
    Klapötke, T. M.
    Stierstorfer, J.
    Powiązania:
    https://bibliotekanauki.pl/articles/358855.pdf
    Data publikacji:
    2008
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    perchlorates
    energetic salts
    calorimetry
    X-ray
    DSC
    Opis:
    Aminoguanidinium perchlorate (2, AGClO4) was formed by the reaction of aminoguanidinium bicarbonate (1) with aqueous perchloric acid solution. Triaminoguanidinium perchlorate (3, TAGClO4) was synthesized by nucleophilic attack of aqueous hydrazine solution on aminoguanidinium perchlorate under release of ammonia. The new and highly explosive azidoformamidinium perchlorate (4, AFClO4) was formed by the reaction of aminoguanidinium perchlorate with potassium nitrite under acidic conditions. The structures of the perchlorate salts in the crystalline state were determined using low temperature single crystal X-ray diffraction yielding monoclinic as well as orthorhombic structures. The compounds were characterized comprehensively using vibrational spectroscopy (IR and Raman), multinuclear (1H, 13C and 15N) NMR spectroscopy, elemental analysis and mass spectrometry. The thermal behavior as well as the decompositions were investigated using DSC (differential scanning calorimetry) and the heats of formation were calculated using heats of combustion determined by bomb calorimetric measurements. In addition, the sensitivities were evaluated using BAM methods (drophammer and friction tester), whereby the perchlorate salts are all sensitive towards impact as well as friction.
    Źródło:
    Central European Journal of Energetic Materials; 2008, 5, 1; 13-30
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Purification of Hexabenzylhexaazaisowurtzitane
    Autorzy:
    Gołofit, T.
    Maksimowski, P.
    Powiązania:
    https://bibliotekanauki.pl/articles/358605.pdf
    Data publikacji:
    2016
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    HBIW
    CL-20
    purification
    differential scanning calorimetry
    cryometric method
    Opis:
    Hexabenzylhexaazaisowurtzitane (HBIW) is produced by a condensation reaction of benzylamine with glyoxal in suitable organic solvents in the presence of protonic acid catalysts. Impurities have to be removed prior to the subsequent stages of the synthesis of CL-20. The effectiveness of HBIW purification by recrystallization from a variety of solvents has been studied here. This method was compared with a novel approach suggested for HBIW purification that consists of prolonged heating of the crude product in boiling methanol. This new purification method allows the product to be prepared in satisfactory purity, it is simple and easily performed on a large-scale.
    Źródło:
    Central European Journal of Energetic Materials; 2016, 13, 4; 1038-1050
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Synthesis and Study of the Thermal and Ballistic Properties of SMX
    Autorzy:
    Sizov, V. A.
    Pleshakov, D. V.
    Asachenko, A. F.
    Topchiy, M. A.
    Nechaev, M. S.
    Powiązania:
    https://bibliotekanauki.pl/articles/358831.pdf
    Data publikacji:
    2018
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    tetranitrate ester
    burning rate
    differential scanning calorimetry
    decomposition
    thermogravimetric analysis
    Opis:
    The high-density tetranitrate ester 1,4-dinitrato-2,3-dinitro-2,3-bis(nitratomethylene)butane (SMX) was synthesized. The methods of obtaining and isolating the intermediates were optimized. The differences between the syntheses of SMX by a four- and five-step scheme were investigated. Combustion of SMX and its catalysis was studied. The possibility of replacing NG as the main plasticizer in a double-base propellant composition was demonstrated. SMX particles were shown to have pronounced crystal faceting using scanning electron microscopy. The decomposition rate equation was determined. The amount of SMX decomposed under isothermal conditions (90 °C) was 0.8 wt.% after 60 min. Thermogravimetric analysis demonstrated that heating SMX results in two different processes – decomposition and evaporation, with SMX evaporating faster than it decomposes.
    Źródło:
    Central European Journal of Energetic Materials; 2018, 15, 1; 30-46
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Phase Stability of Ammonium Nitrate with Organic Potassium Salts
    Autorzy:
    Xu, Z.-X.
    Fu, X.-Q.
    Wang, Q.
    Powiązania:
    https://bibliotekanauki.pl/articles/358264.pdf
    Data publikacji:
    2016
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    ammonium nitrate(V)
    phase transition
    organic compounds
    differential scanning calorimetry
    Opis:
    A study has been undertaken on the effect of additives on the phase transition of ammonium nitrate(V) (AN). Results obtained using Differential Scanning Calorimetry (DSC) showed that organic compounds and potassium salts of organic compounds have an effect on the phase transition behavior of AN. The samples were further analyzed using infrared (IR) and powder X-ray diffraction (XRD). The mechanism of phase stabilization of AN by compounds of this kind was examined. The present study showed that the influence of additives on the phase transition of AN occurs through the polar groups that are involved in intermolecular interactions of orbital and electrostatic types that form new hydrogen bonds. AN exists in only one phase in the temperature range from 30 °C to +100 °C, when a potassium salt of organic compounds was added. However, with organic compounds, the III→II phase transition was changed. IR and XRD of composites are characterized by new intermolecular interactions. Compacted samples of AN containing potassium salts of organic compounds exhibited better stability than AN containing organic compounds to multiple cyclic changes within a temperature range. This we named ‘freezing and thawing analysis’. Additives have two functions on the AN phase transition. First, solid solutions of AN mixture were formed for K+ replacement of NH4+. Second, hydrogen bonds formed, which caused AN and salts of organic compounds to interact intimately.
    Źródło:
    Central European Journal of Energetic Materials; 2016, 13, 3; 736-754
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Kinetics of Polymorphic Transitions in Energetic Compounds
    Autorzy:
    Chukanov, N. V.
    Zakharov, V. V.
    Korsunskiy, B. L.
    Chervonnyi, A. D.
    Vozchikova, S. A.
    Powiązania:
    https://bibliotekanauki.pl/articles/358796.pdf
    Data publikacji:
    2016
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    polymorphic transitions
    energetic compounds
    molecular crystals
    kinetics
    calorimetry
    IR spectroscopy
    Opis:
    Available data on the kinetics of polymorphic transitions (PTs) in energetic compounds under isothermal conditions are summarized and discussed. It is shown that the general kinetic regularities of these processes (stepwise and continuous regimes) depend on their topotactic mode (frontal or quasi-homogeneous, respectively). In reverse PTs, a nucleation stage is not observed, which is explained by the presence of nuclei of the low-temperature polymorph in the preheated sample. The influence of mechanical effects on the kinetics of PTs in molecular crystals is discussed.
    Źródło:
    Central European Journal of Energetic Materials; 2016, 13, 2; 483-504
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Thermal Degradation Behaviour and Kinetics of aged TNT-based Melt Cast Composition B
    Autorzy:
    Singh, Arjun
    Sharma, Tirupati Chander
    Singh, Vasundhara
    Mukherjee, Niladri
    Powiązania:
    https://bibliotekanauki.pl/articles/358256.pdf
    Data publikacji:
    2019
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    composition B
    thermal degradation
    thermogravimetry
    Differential Scanning Calorimetry
    kinetics
    thermodynamic parameters
    Opis:
    In the present paper, three kinds of aged and freshly prepared 2,4,6-trinitrotoluene (TNT) based Composition B stockpiled, for a period of 20 and 32 years, were investigated for the effect of natural ageing on their thermal degradation behaviour and kinetic parameters. The properties investigated indicated that there was no significant change in the thermal stability of the samples aged under natural environmental conditions. The kinetic parameters were studied by means of the Kissinger method using the peak temperature at maximum reaction rate from DSC data, and the isoconversional Kissinger-Akahira-Sunnose (KAS) and ASTM E689 methods from TGA data. The apparent activation energies calculated by the Kissinger method were 173.8 kJ·mol–1 for fresh, 170.4 kJ·mol–1 for 20 y old and 187.1 kJ·mol–1 for 32 y old Composition B, respectively. The values calculated by the KAS method were found to be in the range 77.2-235.8 kJ·mol–1 for fresh Composition B, 75.7-224.0 kJ·mol–1 for 20 y old and 70.4-196.0 kJ·mol–1 for 30 y old Composition B, respectively. The activation energies obtained from the KAS methods are in good agreement and consistent with the isoconversional ASTM E689 kinetic method. The thermodynamic parameters, such the Gibbs free energy of activation (ΔG#), activation enthalpy (ΔH#) and activation entropy (ΔS#) for the formation of activated complexes were also studied and are discussed.
    Źródło:
    Central European Journal of Energetic Materials; 2019, 16, 3; 360-379
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Bomb Calorimetric Correlation Study between Chemical Structure and Enthalpy of Formation for a Linear Energetic Polyphosphazene
    Autorzy:
    Bellamy, A. J.
    Contini, A. E.
    Golding, P.
    Powiązania:
    https://bibliotekanauki.pl/articles/358199.pdf
    Data publikacji:
    2013
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    PBX technology
    energetic polyphosphazenes
    bomb calorimetry
    enthalpy of combustion
    enthalpy of formation
    Opis:
    Energetic polyphosphazenes constitute a novel class of insensitive binders which potentially outperform conventional carbon-based systems in terms of their energy-densities and glass transition temperatures. To facilitate the calculation of energetic performance for these materials, we report here on the use of bomb calorimetry to determine the standard enthalpies of combustion (ΔcH°) and formation (ΔfH°) of 2,2,2-trifuoroethan-1-oxy-/2,3-dinitratopropan-1-oxy-polyphosphazene (I) as the proportion of (energetic) 2,3-dinitratopropan-1-oxy substituents (% Energetic Substitution, % ES) is varied between 31% and 78%. Similar data is presented for the parent polymer bis(2,2,2-trifuoroethan-1-oxy)-polyphosphazene (II) (% ES = 0). ΔcH° was found to vary between -2275 kJ·mol-11for the parent polymer II (% ES = 0) and -3415 kJ·mol-1 for I with % ES = 78. The corresponding values for ΔfH° were -3184 kJ·mol-1 and -1566 kJ·mol-1. These data indicate that, as expected, the polymer heats of formation become more favourable – with respect to the energetic performance of the polymer – as the percentage of energetic side chain functionalities (% ES) increases.
    Źródło:
    Central European Journal of Energetic Materials; 2013, 10, 1; 3-15
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-8 z 8

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