Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

Wyszukujesz frazę "thermogravimetric" wg kryterium: Temat


Wyświetlanie 1-4 z 4
Tytuł:
Thermal decomposition characterization of supergene potassium-jarosite and sodium-jarosite minerals from the northern Tibetan Plateau, China
Autorzy:
Chen, L.
Powiązania:
https://bibliotekanauki.pl/articles/949691.pdf
Data publikacji:
2018
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
potassium-jarosite
sodium-jarosite
thermogravimetric analysis
X-ray diffraction
Opis:
The thermal decomposition of supergene potassium-jarosite and sodium-jarosite samples from the weathering profiles of sulfide deposits in the northern Tibetan Plateau, China, was investigated. Electron microprobe, scanning electron microscopy, and X-ray diffraction analyses indicated the presence of nearly pure potassium-jarosite and sodium-jarosite. Thermogravimetric analysis of the potassium-jarosite sample revealed mass losses of 11.39 wt% at 443.0 °C, 20.99 wt% at 688.3 °C, and 3.18 wt% at 779.3 °C. The thermogravimetric analysis of sodium-jarosite revealed mass losses of 11.72 wt% at 447.5 °C, 21.32 wt% at 682.6 °C, and 3.70 wt% at 716.5 °C. The results provide no evidence for water-molecule loss below 400 °C, as has been reported previously for natural potassium-jarosite and sodium-jarosite. Thermal-decomposition mechanisms have been proposed for potassium-jarosite and sodium-jarosite based on X-ray diffraction analyses of samples obtained at distinct points along the respective thermal decomposition processes. A comparison of the thermal analysis patterns of potassium-jarosite and sodium-jarosite indicates that sodium-jarosite undergoes the initiation of lattice destruction at a higher temperature.
Źródło:
Physicochemical Problems of Mineral Processing; 2018, 54, 2; 459-466
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Halloysite intercalated by potassium acetate
Autorzy:
Mariusz, Adamczyk
Katarzyna, Małycha
Karol, Kułacz
Michał, Pocheć
Kazimierz, Orzechowski
Powiązania:
https://bibliotekanauki.pl/articles/1450347.pdf
Data publikacji:
2020
Wydawca:
Politechnika Wrocławska. Oficyna Wydawnicza Politechniki Wrocławskiej
Tematy:
clay minerals
electron microscopy
XRD
X-ray diffraction
TGA
thermogravimetric analysis
dielectric spectroscopy
Opis:
Halloysite was intercalated by the mechanochemical technique from dry components. The process efficiency of 50% was achieved. The obtained intercalate differed from the material acquired using an aqueous solution of potassium acetate. The material was analyzed employing electron microscopy, thermogravimetry, X-ray powder diffraction, and dielectric spectroscopy. It was found that the molecules and/or ions present in the interlayer spaces retain some possibility of movement. This property of the material is promising for potential application as low expensive absorbers of electromagnetic radiation.
Źródło:
Physicochemical Problems of Mineral Processing; 2020, 56, 6; 235-243
1643-1049
2084-4735
Pojawia się w:
Physicochemical Problems of Mineral Processing
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
The Behavior of Jordanian Oil Shale during Combustion Process from the El-Lajjun Deposit
Autorzy:
Gougazeh, Mousa
Alsaqoor, Sameh
Borowski, Gabriel
Alsafasfeh, Ashraf
Hdaib, Ismail I.
Powiązania:
https://bibliotekanauki.pl/articles/2173323.pdf
Data publikacji:
2022
Wydawca:
Polskie Towarzystwo Inżynierii Ekologicznej
Tematy:
El-Lajjun oil shale
combustion
X-ray diffraction
thermogravimetric
fourier transform infrared spectroscopy
X-ray fluorescence
Opis:
The results of X-ray diffraction, thermogravimetric and FTIR spectroscopy analyses of mineral composition indicated that the El-Lajjun oil shale is principally composed of calcite, quartz with minor amounts of kaolinite), gypsum, and apatite. The obtained oil shale ash products at 830 °C and 1030 °C are dominated by lime, quartz, anhydrite, portlandite, gehlenite, and amorphous phases. The TGA weight loss curves clearly indicate that it occurred in the temperature range from 310 to 650 °C. The decomposition of oil shale carbonates was detected above 750°C. The functional groups in the organic material of oil shale are dominated by the aliphatic hydrocarbons, the semi-ash of which had diverse structures of polycyclic aromatic hydrocarbons. The most intensive of combustion occurred in the temperature range of 400–750 °C. In this temperature range, about 75 wt.% was accounted for the total mass loss.
Źródło:
Journal of Ecological Engineering; 2022, 23, 8; 133--140
2299-8993
Pojawia się w:
Journal of Ecological Engineering
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Kinetics of nanocrystalline iron nitriding
Autorzy:
Arabczyk, W.
Zamłynny, J.
Moszyński, D.
Powiązania:
https://bibliotekanauki.pl/articles/778372.pdf
Data publikacji:
2010
Wydawca:
Zachodniopomorski Uniwersytet Technologiczny w Szczecinie. Wydawnictwo Uczelniane ZUT w Szczecinie
Tematy:
azotki żelaza
materiały mikroporowate
synteza chemiczna
analiza termograwimetryczna
dyfrakcja promieniowania rentgenowskiego
iron nitrides
microporous materials
chemical synthesis
thermogravimetric analysis
X-ray diffraction
Opis:
Nitriding of nanocrystalline iron was studied under the atmosphere of pure ammonia and in the mixtures of ammonia - hydrogen - nitrogen at temperatures between 350°C and 500°C using thermogravimetry and x-ray diffraction. Three stages of nitriding were observed and have been ascribed to the following schematic reactions: (1) α-Fe → γ-Fe4N, (2) γ- Fe4N → ε - Fe3N and (3) ε - Fe3N → ε - Fe2N. The products of these reactions appeared in the nitrided nanocrystalline iron not sequentially but co-existed at certain reaction ranges. The dependence of a reaction rate for each nitriding stage on partial pressure of ammonia is linear. Moreover, a minimal ammonia partial pressure is required to initiate the nitriding at each stage.
Źródło:
Polish Journal of Chemical Technology; 2010, 12, 1; 38-43
1509-8117
1899-4741
Pojawia się w:
Polish Journal of Chemical Technology
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-4 z 4

    Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies