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Wyszukujesz frazę "kinetic decomposition" wg kryterium: Temat


Wyświetlanie 1-4 z 4
Tytuł:
Synthesis and Characterization of Polyethylene Glycol Dinitrates
Autorzy:
Matyáš, R.
Šelešovský, J.
Jalový, Z.
Roháčová, J.
Powiązania:
https://bibliotekanauki.pl/articles/358415.pdf
Data publikacji:
2011
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
polyethylene glycol dinitrate
synthesis
properties
decomposition
kinetic decomposition
Opis:
Polyethylene glycol dinitrates (PEGN) with molecular weights between 400 and 20 000 gźmol-1 were prepared from polyethylene glycols by esterifcation with nitric acid/sulfuric acid in dichloromethane. The products were characterized by gel permeation chromatography. The yield of PEGN increases with increasing reaction temperature (0-40 °C) however large liberation of nitrogen oxides was observed at 40 °C. No infuence of reaction temperature (0-40 °C) on the cleavage of the polyethylene glycol chain during esterifcation was observed. The dependence of melting point on the molecular weight of PEGN was determined. Polyethylene glycol dinitrates with molecular weights Mn above 454 are not sensitive to impact. Heat of combustion of PEGN increases with increasing molecular weight. All samples tested decompose in a similar way during thermal exposition.
Źródło:
Central European Journal of Energetic Materials; 2011, 8, 3; 145-155
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
Tytuł:
Improved understanding of Sodium hydroxide concentration role and kinetic model of cryolite reactive extraction in cathode Spent Pot Linings
Autorzy:
Tropenauer, Blaž
Klinar, Dušan
Golob, Janvit
Powiązania:
https://bibliotekanauki.pl/articles/1849329.pdf
Data publikacji:
2021
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
spent pot lining
NaOH concentration role
cryolite decomposition
reaction mechanism
kinetic model
Opis:
Spent Pot Lining (SPL) cathode pot, waste from the aluminium smelting process needs detoxification from cyanides, washing out water-soluble salts and extraction of the cryolite (Na3AlF6) decomposition products to be recycled. Revealed cryolite decomposition mechanism with NaOH opens possibilities to explore its critical role in the reactive extraction process. Common Na+ ion from NaOH hinders the solubility of the product but also drives mass transfer to the reaction site. Reaction mass balance provides adequate liquid to solid ratio (L/S) and NaOH concentration range. A newly developed kinetic model based on Whitman film theory and NaOH mass flow enables prediction of the reaction time to decompose cryolite to a low enough level. Results show that the internal particle resistance to transport (1/ks) is 19 times larger than the external (1/kl) one and governs the whole process.
Źródło:
Polish Journal of Chemical Technology; 2021, 23, 1; 37-44
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Role of Thermochemical Decomposition in Energetic Material Initiation Sensitivity and Explosive Performance
Autorzy:
Shackelford, S. A.
Powiązania:
https://bibliotekanauki.pl/articles/358845.pdf
Data publikacji:
2008
Wydawca:
Sieć Badawcza Łukasiewicz - Instytut Przemysłu Organicznego
Tematy:
energetic material
thermochemical decomposition
kinetic deuterium isotope effect
KDIE
initiation sensitivity
performance
Opis:
Catastrophic initiation of an energetic material consists of a complex, interactive, sequential train of mechanistic mechanical, physical, and chemical processes which occur over a finite time period and proceed from macroscopic into sub-microscopic composition levels (bulk > crystalline > molecular > atomic). Initiation results when these processes proceed at a rate which generates sufficient energy (heat) to reach a threshold stage within this finite time period. Thus, the rate at which these mechanistic processes occur defines initiation sensitivity and affects performance. Thermochemical decomposition processes regulate the rate at which heat energy is released at the molecular level, and therefore to some extent, control energetic material initiation sensitivity and performance characteristics. Kinetic deuterium isotope effect (KDIE) data, obtained during the ambient pressure thermochemical decomposition process, identifies the mechanistic rate-controlling bond rupture which ultimately regulates the energy release rate of a given energetic material. This same rate-controlling bond rupture also appears as a significant rate-limiting feature in higher order deflagration, combustion, and explosion phenomena. The effect the KDIE-determined rate-controlling bond rupture exerts on initiation sensitivity, and its potential influence in combustion and explosion performance is delineated.
Źródło:
Central European Journal of Energetic Materials; 2008, 5, 1; 75-101
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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