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    Wyświetlanie 1-11 z 11
    Tytuł:
    Research on the Mechanism and Kinetics of Polymorphic Transitions of ε CL-20 in Composite Systems
    Autorzy:
    Guo, X.-Y.
    Zhang, P.
    Xu, J.-J.
    Wang, Z.-H.
    Jiao, Q.-J.
    Powiązania:
    https://bibliotekanauki.pl/articles/358032.pdf
    Data publikacji:
    2015
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    polymorphic transition
    kinetics
    activation energy
    transition temperature
    Opis:
    In order to explore the polymorphic transition law for ε-CL-20 in composite systems, the polymorphic transition process of pure ε-CL-20 crystals stimulated by heat was investigated by the X-ray Diffraction (XRD) method, and the kinetic parameters of the polymorphic transition process were calculated (including the apparent activation energy Ea and the pre-exponential factor lnA). Meanwhile the effects of different additives on the polymorphic transition process and kinetics of ε-CL-20 were explored in detail. The experimental results showed that the ε-form tends to transform into the γ- form on heating and that the Ea and lnA for the transition process were 209.97 kJ/mol and 57.47, respectively. The first group of additives clearly promoted the polymorphic transition of ε-CL-20 and lowered the initial transition temperature and the activation energy. The second and third groups of additives inhibited the polymorphic transition of ε-CL-20 and raised the initial transition temperature and the activation energy.
    Źródło:
    Central European Journal of Energetic Materials; 2015, 12, 4; 689-702
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Ethylene Glycol Dinitrate (EGDN): from Commercial Precursors, Physicochemical and Detonation Characterization
    Autorzy:
    Fettaka, H.
    Lefebvre, M.
    Powiązania:
    https://bibliotekanauki.pl/articles/358286.pdf
    Data publikacji:
    2015
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    EGDN
    liquid explosive
    precursor
    activation energy
    detonation tests
    Opis:
    Currently, liquid explosives pose a potential threat. An important phase in the assessment of this threat is to investigate the various synthesis paths leading to their manufacture and to evaluate the potential use of readily purchasable precursors. The aim of this work was to assess the synthesis of Ethylene Glycol Dinitrate (EGDN), a liquid nitrate ester explosive, using commercially available precursors. The characteristics of the synthetic process (ease, yield), the chemical properties of the synthesized product (purity, spectra) and its explosive properties (sensitivities, detonability) were investigated. Comparisons are drawn between these products and the product obtained using laboratory ingredients. Three ingredients have been used: 1) ethylene glycol, laboratory grade, 2) ready to use, commercial coolant fluid, and 3) ethylene glycol extracted from commercial coolant fluid. The chemical composition and purity of the synthesized liquid explosive was analyzed by Gas Chromatography-Mass Spectrometry (GCMS), and infrared spectroscopy (IR). Differential Scanning Calorimetric (DSC) analysis allowed the heat of decomposition and activation energies to be assessed. The Ozawa and Kissinger models were used. The explosive properties of the pure synthesized products and comparable other explosives, have been tested. The potential use as a priming charge or as a main charge was assessed.
    Źródło:
    Central European Journal of Energetic Materials; 2015, 12, 2; 287-305
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    The Influence of the Semtex Matrix on the Thermal Behavior and Decomposition Kinetics of Cyclic Nitramines
    Autorzy:
    Yan, Q. L.
    Zeman, S.
    Elbeih, A.
    Zbyněk, A.
    Powiązania:
    https://bibliotekanauki.pl/articles/357984.pdf
    Data publikacji:
    2013
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    cyclic nitramines
    thermal decomposition
    activation energy
    Semtex
    PBX
    Opis:
    The thermal behavior and decomposition kinetics of Semtex 10 polymeric matrix (Semtex) bonded PBXs containing RDX (1,3,5-trinitro 1,3,5-triazinane), HMX (1,3,5,7-tetranitro-1,3,5,7-tetrazocane), BCHMX (cis-1,3,4,6tetranitrooctahydroimidazo [4,5-d] imidazole), HNIW (2,4,6,8,10,12-hexanitro2,4,6,8,10,12-hexaazaisowurtzitane) have been investigated by means of nonisothermal TG and DSC techniques. It is shown that only a single decomposition process occurs for RDX-SE and HMX-SE whilst an obvious two-step process occurs for CL-20-SE and BCHMX-SE. The onset of the exotherms were observed at 210.6, 239.7, 279.2 and 229.4 °C with the peak maxima at 232.2, 249.4, 280.4 and 240.2 °C, and energy changes of 1808, 2140, 612 and 1757 J·g-1 for RDX-SE, BCHMX-SE, HMX-SE and CL-20-SE, respectively. It has been found that the Semtex matrix has little influence on the activation energy distribution for RDX, BCHMX and ε-CL-20. The activation energies for BCHMX-SE and CL-20-SE decomposition are almost independent of the degree of conversion, with mean values of 159.6 ±1.9 and 187.3 ±1.8 kJ·mol-1. It has been proved that Semtex and Viton A are better binders than C4 and Formex for ε-CL-20 and RDX based PBXs in terms of their greater thermal stability, and Formex is a poor binder for BCHMX.
    Źródło:
    Central European Journal of Energetic Materials; 2013, 10, 4; 509-528
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Non-isothermal Studies on the Thermal Decomposition of C4 Explosive Using the TG/DTA Technique
    Autorzy:
    Pouretedal, H. R.
    Damiri, S.
    Ghaemi, E. F.
    Powiązania:
    https://bibliotekanauki.pl/articles/358520.pdf
    Data publikacji:
    2014
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    C4 explosive
    non-isothermal
    decomposition
    activation energy
    Opis:
    The thermal behaviour of energetic materials is very important for their safe production, storage, handling and even demilitarization. In this work, the thermal behaviour and decomposition kinetics of conventional C4 plastic explosive has been studied experimentally by a non-isothermal thermogravimetric (TG)/differential thermal analysis (DTA) technique at different heating rates (2, 4, 6 and 8 °C·min-1). The kinetic triplet of activation energy, frequency factor and model of thermal decomposition of this compound has been evaluated via model-fitting and model-free methods. The results show a single thermal decomposition process for C4, with the model of integral function (g(α)) of [(1−α)-1/3 −1]2 and differential function (f(α)) of [(1−α)2/3(3α−3)/2(1−α)1/3−2], indicating a 3-dimensional diffusion mechanism. In addition, Ea values of 207.1 ± 17.3, and 241 kJ·mol-1, by using the isoconversional model-free modified Kissinger-Akahira-Sunose (KAS) and the Kissinger method, respectively, were obtained for the conversion interval of 0.3-0.7. The C4 matrix shows a significant effect on the activation energy distribution of pure RDX.
    Źródło:
    Central European Journal of Energetic Materials; 2014, 11, 3; 405-416
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Synthesis and Kinetic Study of a PCL-GAP-PCL Tri-block Copolymer
    Autorzy:
    Chizari, M.
    Bayat, Y.
    Powiązania:
    https://bibliotekanauki.pl/articles/358140.pdf
    Data publikacji:
    2018
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    poly(glycidyl azide)
    poly(caprolactone)
    copolymer
    kinetic study
    activation energy
    Opis:
    An energetic tri-block copolymer PCL-GAP-PCL (Mn = 1794) was synthesized by a ring-opening polymerization of ε-caprolactone with glycidyl azide polymer (GAP) of low molecular weight (Mn = 1006 g/mol) as initiator, in the presence of dibutyltin dilaurate (DBTDL) as catalyst, at 100 °C in the absence of solvent. The products obtained in high yield were characterized by FTIR, gel permeation chromatography (GPC), and 1H and 13C NMR spectroscopy. Thermogravimetric analysis (TG) and differential scanning calorimetry (DSC) were used to study the thermal behaviour of the polymers. An advanced isoconversional method has been applied for kinetic analysis. The activation energy, calculated by the Flynn-Wall-Ozawa (FWO) and Kissinger methods, and thermal analysis revealed that the tri-block copolymer has greater thermal stability than homopolymer GAP. The results of the activation energies from the Kissinger method for the first and second steps were 180.3 kJ·mol−1 and 209.8 kJ·mol−1, respectively. Furthermore, for the copolymer, the activation energy versus the level of conversion was calculated by the FWO method. The glass transition temperature (Tg) for GAP was influenced by the PCL blocks; as a result the copolymer (Tg = −64 °C) showed better thermal properties than homopolymer GAP (Tg = −48 °C).
    Źródło:
    Central European Journal of Energetic Materials; 2018, 15, 2; 243-257
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Studies on the Effect of a Covalently Bonded PGN Based Reactive Plasticizer on the Thermal Decomposition Behaviour of Glycidyl Azide Polymer
    Autorzy:
    Bodaghi, Asghar
    Shahidzadeh, Mansour
    Powiązania:
    https://bibliotekanauki.pl/articles/358381.pdf
    Data publikacji:
    2019
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    plasticizer
    reactive plasticizer
    glycidyl azide polymer
    kinetic study
    activation energy
    Opis:
    Plasticizers are one of the additives that are added to polymers to increase the plasticity or decrease the viscosity of the material. Here, we have synthesized and characterized a new PGN-based reactive energetic plasticizer that has an oligomeric structure. The reactive energetic plasticizer can be grafted onto glycidyl azide polymer via a Cu-free Huisgen azide-alkyne 1,3-dipolar cycloaddition. The effect of the covalently bonded PGN-based plasticizer on the thermal properties of GAP-g-PGN copolymer has been investigated through thermogravimetric analysis and differential scanning calorimetry. The results indicate that the glass transition temperature of the prepolymer is decreased from –47.8 to –50.7 °C. Also, the kinetics of the thermal behaviour of GAP-g-PGN copolymer was determined by the application of the Kissinger and FWO kinetic models. The activation energies calculated by the Kissinger method were 165 and 188 kJ/mol for peak 1 and peak 2, respectively. Furthermore, the critical temperature (Tb) of thermal explosion for this energetic copolymer was estimated to be 182 °C.
    Źródło:
    Central European Journal of Energetic Materials; 2019, 16, 2; 259-280
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Recent Advances in the Study of the Initiation of Energetic Materials Using the Characteristics of Their Thermal Decomposition Part II. Using Simple Differential Thermal Analysis
    Autorzy:
    Zeman, S.
    Yan, Q.-L.
    Elbeih, A.
    Powiązania:
    https://bibliotekanauki.pl/articles/358712.pdf
    Data publikacji:
    2014
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    activation energy
    detonation velocity
    DTA
    explosives
    initiation
    nitramines
    PBX
    thermal decomposition
    Opis:
    Simple Differential Thermal Analysis (DTA), with evaluation of its output by the Kissinger method, was used in the case of emulsion explosives and, as an advanced application, for several plastic bonded explosives (PBXs). In both of these kinds of explosive the square of their detonation velocities, D2, is used as their performance characteristic. A relationship between the slope of the Kissinger equation, EaT-1, and the D2 values makes it possible to formulate a possible mechanism for the initiation of emulsion explosives. Regarding PBXs, it would seem possible to postulate a change in the detonation chemistry of plastic bonded nitramines, depending on the pressure and temperature in the zone of the detonation wave, particularly in the case of CL-20 fillers. Binders with aromatic building units in their macromolecular structure seem to be less-favoured in terms of their thermal reactivity and performance than the final PBXs. These findings document the advantages of the above-mentioned application of simple DTA.
    Źródło:
    Central European Journal of Energetic Materials; 2014, 11, 3; 395-404
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Toluene Mono-nitration in a Semi-batch Reactor
    Autorzy:
    Chen, L. P.
    Chen, W. P.
    Liu, Y.
    Peng, J. H.
    Liu, R. H.
    Powiązania:
    https://bibliotekanauki.pl/articles/358853.pdf
    Data publikacji:
    2008
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    toluene mono-nitration
    apparent activation energy
    semi-batch reaction
    thermal hazard
    Opis:
    Toluene mono-nitration in a semi-batch reactor was investigated with reaction calorimeter (RC1). The mixed acid HNO3/H2SO4/H2O (wt%) was used in proportion 13/66/21, which is similar to industrial parameters. The exothermic rates at different reaction temperatures were compared, and then the curves of heat generation rate after dosing were analyzed. The Maximal Temperature attainable by runaway of the desired Synthetic Reaction (MTSR) under different conditions were calculated for the course hazard evaluation. The results showed that the average reaction heat of mono-nitration was between 169.07~177.11 kJ mol-1, and the special heat of reactant was about 2 kJ kg-1 K-1. Average Ea of second order kinetic was about 30 kJ mol-1, and reaction rate was 10-4 mol s-1 l-1 order of magnitude when the strength of sulphuric acid was about 73.5%. It was also found that when temperature or stirring speed increases, the potential heat accumulation decreases.
    Źródło:
    Central European Journal of Energetic Materials; 2008, 5, 2; 37-47
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    Determination of the activation energy of a gasless pyrotechnic composition
    Wyznaczanie energii aktywacji kompozycji pirotechnicznej bezgazowej
    Autorzy:
    Zakusylo, Daryna
    Powiązania:
    https://bibliotekanauki.pl/articles/27787705.pdf
    Data publikacji:
    2021
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    activation energy
    gasless
    pyrotechnic composition
    flashpoint
    energia aktywacji
    bezgazowa
    skład pirotechniczny
    temperatura zapłonu
    Opis:
    This article presents the determining of some parameters of a gasless pyrotechnic composition. Thermo-analytical studies have been carried out. The activation energy of the gasless pyrotechnic composition was determined experimentally and by calculation. The flashpoint was 100 °C. The value of the activation energy of the pyrotechnic composition was 369.39 kJ/mol, which exceeds the activation energy of standard solid and liquid explosives by 2.4-2.8 times and makes it more stable. The change in the mass of the pyrotechnic composition during heating did not exceed 1%.
    Artykuł dotyczy zagadnień wyznaczania niektórych parametrów bezgazowej kompozycji pirotechnicznej. Przeprowadzono badania derywatograficzne. Energię aktywacji bezgazowej kompozycji pirotechnicznej wyznaczono doświadczalnie i obliczeniowo. Temperatura zapłonu wynosiła 100 °C. Wartość energii aktywacji kompozycji pirotechnicznej wyniosła 369,39 kJ/mol, co przewyższa energię aktywacji standardowych materiałów wybuchowych stałych i ciekłych 2,4-2,8 razy i czyni ją bardziej stabilną. Zmiany masy kompozycji pirotechnicznej pod wpływem temperatury nie przekraczają 1%.
    Źródło:
    Materiały Wysokoenergetyczne; 2021, 13; 96--100
    2083-0165
    Pojawia się w:
    Materiały Wysokoenergetyczne
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    E-Smoking Liquids as Precursors for Liquid Nitroesters
    Autorzy:
    Fettaka, H.
    Lefebvre, M. H.
    Powiązania:
    https://bibliotekanauki.pl/articles/358051.pdf
    Data publikacji:
    2016
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    E-smoking liquid
    nitroesters
    nitroglycerin
    1,2-propylene glycol dinitrate
    brisance test
    activation energy
    Opis:
    Currently, E-smoking cigarettes are widely used and occur within all classes of society. This work investigated the use of E-smoking liquids for the synthesis of Nitroglycerin (NG) and 1,2-Propylene Glycol Dinitrate (PGDN), both considered as nitroester liquid high explosives. Two kinds of E-smoking liquids (10 mL) were investigated: nicotine free and with nicotine (10 mg/mL). Quantitative analysis of the glycerin and propylene glycol (PG) present in the E-smoking liquids was carried out by gas chromatography-mass spectrometry (GCMS), with calculation of the accuracy and precision parameters. The percentage of glycerin was (10-13 wt.%) and percentage of propylene glycol was (40-70 wt.%) The synthesis of pure NG and pure PGDN were performed with laboratory grade glycerin and propylene glycol and compared to the samples obtained from the E-smoking liquid. Differential Scanning Calorimetry (DSC) was used for the determination of the activation energy and the heat of decomposition for each synthesized explosive, using the Ozawa and Kissinger models. The brisance index was assessed by the witness plate test and compared with some conventional explosives (TNT and C4). Finally, the influence of nicotine (less than 2 wt.%) on the synthetic process and the detonic properties of the explosive mixture was studied.
    Źródło:
    Central European Journal of Energetic Materials; 2016, 13, 1; 199-216
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
    Tytuł:
    The Applicability of Chromatographic Methods in the Investigation of Ageing Processes in Double Base Rocket Propellants
    Autorzy:
    Matečić-Muśanić, S.
    Sućeska, M.
    Čuljak, R.
    Powiązania:
    https://bibliotekanauki.pl/articles/358695.pdf
    Data publikacji:
    2013
    Wydawca:
    Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
    Tematy:
    activation energy
    artifcial ageing
    DB rocket propellants
    decomposition
    Ethyl Centralite (EC)
    Gel Permeation Chromatography (GPC)
    High Performance Liquid Chromatography (HPLC)
    kinetics of degradation
    mean molecular mass of NC
    Opis:
    The ageing of double base (DB) rocket propellants is the result of chemical decomposition reactions and physical processes, causing degradation of a number of relevant propellant properties (such as reduction in stabilizer and nitroglycerine (NG) content, reduction of the mean molecular mass of nitrocellulose (NC) etc.), which is refected in a decrease in the reliable service life time of DB propellants. This is the reason why the study of processes of ageing and their consequences (effects) is so important. In this paper we have studied the kinetics of DB rocket propellant decomposition during their artifcial ageing, i.e. at elevated temperatures. The kinetic parameters were obtained by measurements of the stabilizer/Ethyl Centralite (EC) content and the mean molecular mass reduction of NC, during artifcial ageing at temperatures of 80, 85 and 90 °C. Consumption of the EC was observed using High Performance Liquid Chromatography (HPLC), whilst the reduction in the mean molecular mass of NC was monitored using Gel Permeation Chromatography (GPC). It has been shown that artifcial ageing of DB propellant causes signifcant EC consumption and a reduction in the mean molecular mass of NC, from the very beginning of ageing. EC is entirely consumed after 120 days at 80 °C, and is followed by the intensive reactions of NC decomposition. Signifcant changes in the mean molecular mass of NC starts after 60 days of ageing at 90 °C (or ~250 days at 80 °C). The results obtained from the kinetic data have shown that the activation energy of DB propellant decomposition, determined on the basis of changes in the mean molecular mass of NC is 145.09 kJ•mol-1 , whilst the activation energy of decomposition obtained on the basis of EC consumption is 142.98 kJ•mol-1 , which is consistent with available literature values [1, 2].
    Źródło:
    Central European Journal of Energetic Materials; 2013, 10, 2; 245-262
    1733-7178
    Pojawia się w:
    Central European Journal of Energetic Materials
    Dostawca treści:
    Biblioteka Nauki
    Artykuł
      Wyświetlanie 1-11 z 11

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