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Wyświetlanie 1-4 z 4
Tytuł:
The Catalytic Effect of Mn2O3 Nanoparticles on the Ignition Reaction of Pyrotechnic of Ammonium Nitrate(V)/Thiourea
Autorzy:
Pouretedal, H. R.
Ravanbod, M.
Powiązania:
https://bibliotekanauki.pl/articles/358302.pdf
Data publikacji:
2017
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
ammonium nitrate(V)
thiourea
non-isothermal kinetic
ignition reaction
Mn2O3 nanoparticles
Opis:
The non-isothermal TG/DSC technique has been used to study the kinetic triplet and heat of ignition reaction of ammonium nitrate(V) (AN)/thiourea (TU) pyrotechnic in the presence of Mn2O3 catalyst nanoparticles under an argon atmosphere at different heating rates (5 K·min−1, 10 K·min−1, 15 K·min−1 and 20 K·min−1). The activation energies for the ignition reaction of AN/TU were calculated using the non-isothermal isoconversional Kissinger-Akahira-Sunose (KAS) and Friedman equations for different conversion fraction (α) values in the range 0.1-0.9. The pre-exponential factor and kinetic model were determined by means of the compensation effect and the selected model was confirmed by a nonlinear fitting method. The average activation energies in the absence and presence of 5 wt.% Mn2O3 nanoparticles were 110.1 kJ·mol−1 to 117.3 kJ·mol−1 for the reaction model A3 (g(α) = [−ln(1−α)]1/3), and 86.5 kJ·mol−1 to 101.8 kJ·mol−1 for the reaction model A4 (g(α) = [−ln(1−α)]1/4). The evolved heat (ΔH) of ignition reaction in the presence of Mn2O3 was about 4 times that in the absence of the nano-sized Mn2O3.
Źródło:
Central European Journal of Energetic Materials; 2017, 14, 2; 430-447
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:
Statistical Optimization and Selective Separation of RDX and HMX Explosives by Using Binary Solvent Mixtures Containing Ethyl Acetate and Water
Autorzy:
Damiri, S.
Pouretedal, H. R.
Panahi, H.
Dris, A.
Powiązania:
https://bibliotekanauki.pl/articles/358250.pdf
Data publikacji:
2017
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
RDX and HMX
explosive
ethyl acetate
solubility
separation
Opis:
The present study introduces the application of a binary solvent of ethyl acetate and water for the selective separation of 1,3,5-trinitroperhydro-1,3,5-triazine (RDX) and octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (HMX). The effect of temperature and weight percent of ethyl acetate in water on the solubility of RDX and HMX over a temperature range of 273.15 K to 363.15 K and 70.0 wt.% to 100.0 wt.% ethyl acetate in water mixtures were modelled and optimized using a central composite design (CCD) and response surface methodology (RSM) in Minitab (ver. 16) software. Multiple regression analysis and analysis of variance (ANOVA) showed that the predicted results were in good agreement with the experimental data. The enthalpies of dissolution and mixing of the materials were determined experimentally from the solubility data. The experimental results showed that the solubility ratio of RDX to HMX can change 6.53- to 16.55-fold, indicating a much lower solubility of HMX in this binary solvent, for a relatively selective separation of RDX and HMX mixtures. Separation experiments under optimized conditions showed that 98.3% of the RDX impurity in HMX was recovered in the first precipitation with an HMX purity of > 99.5% as characterized by high performance liquid chromatography (HPLC).
Źródło:
Central European Journal of Energetic Materials; 2017, 14, 2; 391-402
1733-7178
Pojawia się w:
Central European Journal of Energetic Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Kinetic Study of the Thermal Decomposition of Potassium Chlorate Using the Non-isothermal TG/DSC Technique
Autorzy:
Ravanbod, M.
Pouretedal, H. R.
Amini, M. K.
Ebadpour, R.
Powiązania:
https://bibliotekanauki.pl/articles/358772.pdf
Data publikacji:
2016
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
potassium chlorate
thermal decomposition
kinetic triplet
non-isothermal TG/DSC
Opis:
The non-isothermal TG/DSC technique has been used to study the kinetic triplet of the thermal decomposition of potassium chlorate at different heating rates (5, 10, 15 and 20 °C•min−1). The DSC results showed two consecutive broad exothermic peaks after melting. The first peak contains a shoulder indicating the presence of at least two processes. The overlapped peaks were resolved by a peak fitting procedure, and the three resolved peaks were used for evaluation of the kinetic triplet for each step. The TG results also showed two consecutive mass losses after melting. The kinetics of the mass loss processes were studied using resolved DTG peaks. The activation energies were calculated using the KAS model-free method. The pre-exponential factor and the best kinetic model for each step were determined by means of the compensation effect, and the selected models were confirmed by the nonlinear model fitting method. The average activation energies obtained from the DSC results were 237.3, 293.8, and 231.3 kJ•mol−1 for the three consecutive steps of thermal decomposition of KClO3. The activation energies were 231.0 and 239.9 kJ•mol−1 for the first and second mass loss steps. The Avrami-Erofeev of Ax/y with the function of g(α) = [−ln(1−α)]x/y (x/y = 5/4 and 3/2) was the most probable model for describing the reaction steps.
Źródło:
Central European Journal of Energetic Materials; 2016, 13, 2; 505-525
1733-7178
Pojawia się w:
Central European Journal of Energetic Materials
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

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