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Wyszukujesz frazę "Redaoui, D." wg kryterium: Autor


Wyświetlanie 1-2 z 2
Tytuł:
Mechanism and kinetic parameters of the thermal decomposition of gibbsite Al(OH)₃ by thermogravimetric analysis
Autorzy:
Redaoui, D.
Sahnoune, F.
Heraiz, M.
Raghdi, A.
Powiązania:
https://bibliotekanauki.pl/articles/1057886.pdf
Data publikacji:
2017-03
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
81.70.Pg
81.05.Je
81.05.Mh
81.30.Mh
07.85.Nc
Opis:
In this study, the mechanism and the kinetic parameters of the thermal decomposition of gibbsite Al(OH)₃ were studied by differential thermogravimetry technique under non-isothermal conditions, between room temperature and 1200 K at heating rates of 5, 10, 15 and 20°C min¯¹. The obtained differential thermogravimetry curves show clearly three distinct peaks. The first peak is due to the partial dehydroxylation of gibbsite. Among the 32 types of differential equations of non-isothermal kinetics, we have found that the most suitable mechanism is (A_{3/2}: g(x)=[-ln(1-x)]^{2/3}) also called Avrami-Erofeev equation of order 2/3. The values of the activation energy E_{A} and of the pre-exponential factor K are 157 kJ mol¯¹ and 7.58×10¹⁵ s¯¹, respectively. The second peak corresponds to the decomposition of gibbsite to boehmite. Decomposition is controlled by the rate of second-order reaction (F₂: g(x)=(1-x)¯¹-1), under the applied conditions. The activation energy E_{A} and pre-exponential factor K correspond to 243 kJ mol¯¹ and 3.73×10²² s¯¹, respectively. The third peak is due to transformation of boehmite to alumina. However the mechanism for such transformation is better described by the 3/2 rate order reaction (F_{3/2}: g(x)=(1-x)^{-1/2}-1). In addition, the values of E_{A} and K were determined to be around 296 kJ mol¯¹ and 1.82×10¹⁹ s¯¹, respectively. The results of differential thermogravimetry were supplemented by the differential thermal analysis. X-ray powder diffraction analysis was carried out for samples of gibbsite treated at different temperatures between 200 and 1200°C in 200°C steps.
Źródło:
Acta Physica Polonica A; 2017, 131, 3; 562-565
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Thermal Decomposition Kinetics of Algerian Tamazarte Kaolin by Differential Thermal Analysis (DTA)
Autorzy:
Sahnoune, F.
Heraiz, M.
Belhouchet, H.
Saheb, N.
Redaoui, D.
Powiązania:
https://bibliotekanauki.pl/articles/1033455.pdf
Data publikacji:
2017-03
Wydawca:
Polska Akademia Nauk. Instytut Fizyki PAN
Tematy:
82.30.Lp
81.05.Je
81.05.Mh
81.70.Pg
Opis:
In the present study, the kinetics of meta-kaolinite (Al₂O₃·2SiO₂) formation from Algerian Tamazarte kaolin was investigated by using differential thermal analysis. The differential thermal analysis and the thermogravimetric experiments were carried out on samples between room temperature and 1400°C, at heating rates from 10 to 40°C min¯¹. X-ray diffraction was used to identify the phases present in the samples. The activation energies measured by differential thermal analysis from isothermal and non-isothermal treatments using Johnson-Mehl-Avrami methods with Ligero approximation and using Kissinger-Akahira-Sunose methods were around 145 and 159 kJ/mol, respectively. The Avrami parameter n which indicates the growth morphology parameters were found to be almost equal to 1.60, using non-isothermal treatments, and equal to 1.47 using isothermal treatments. The numerical factor which depends on the dimensionality of crystal growth was 1.60 obtained using Matusita et al. equation. The frequency factor calculated using the isothermal treatment is equal to 1.173× 10⁷ s¯¹. Analysis of the results have shown that bulk nucleation was dominant during kaolinite transformation, followed by three-dimensional growth of meta-kaolinite with polyhedron-like morphology, controlled by diffusion from a constant number of nuclei.
Źródło:
Acta Physica Polonica A; 2017, 131, 3; 382-385
0587-4246
1898-794X
Pojawia się w:
Acta Physica Polonica A
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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