THERMAL BEHAVIOR OF RAW OIL SHALE AND ITS COMPONENTS

Oil Shale ◽  
2015 ◽  
Vol 32 (2) ◽  
pp. 160 ◽  
Author(s):  
S S PALAYANGODA ◽  
Q P NGUYEN
Keyword(s):  
2017 ◽  
Vol 120 ◽  
pp. 19-25 ◽  
Author(s):  
Hong Qin ◽  
Wanli Wang ◽  
Hongpeng Liu ◽  
Lidong Zhang ◽  
Qing Wang ◽  
...  

2014 ◽  
Vol 118 (2) ◽  
pp. 891-899 ◽  
Author(s):  
Tiit Kaljuvee ◽  
Igor Štubňa ◽  
Peeter Somelar ◽  
Valdek Mikli ◽  
Rein Kuusik

2021 ◽  
Author(s):  
Sepehr Mozaffari ◽  
Zachariah Baird ◽  
Oliver Järvik

A kukersite oil shale sample from Estonia was pyrolyzed using a Fischer assay method under N2, N2/steam, CO2 and CO2/steam environments. The thermal behavior of the oil shale sample was also studied using TGA and DSC with similar conditions. Also, several properties of produced oils were measured and FTIR analysis was carried out to compare the molecular structure of the derived oils. The presence of steam increased the liquid and gaseous yields, and also caused a greater weight loss in the oil shale. The pyrolysis tests in both the CO2 and N2 atmospheres produced oils with relatively similar properties however, the molecular structure was different.


ACS Omega ◽  
2021 ◽  
Author(s):  
Wei Guo ◽  
Qinchuan Yang ◽  
Xu Zhang ◽  
Shaotao Xu ◽  
Sunhua Deng ◽  
...  

2016 ◽  
Vol 127 (1) ◽  
pp. 33-45 ◽  
Author(s):  
Tiit Kaljuvee ◽  
Igor Štubňa ◽  
Tomáš Húlan ◽  
Rein Kuusik

2016 ◽  
Vol 109 ◽  
pp. 413-422 ◽  
Author(s):  
Hong-peng Liu ◽  
Wen-Xue Liang ◽  
Hong Qin ◽  
Qing Wang
Keyword(s):  

Processes ◽  
2021 ◽  
Vol 10 (1) ◽  
pp. 46
Author(s):  
Tiit Kaljuvee ◽  
Igor Štubňa ◽  
Tomáš Húlan ◽  
Mai Uibu ◽  
Marve Einard ◽  
...  

The thermal behavior of green clay samples from the Arumetsa and Füzérradvány deposits (Hungary) and the influence of two new types of Estonian oil shale (OS) ashes and cement bypass dust (clinker dust) additives on it were the objectives of this study. Thermal and thermo-dilatometric analysis methods were applied using a Setaram Setsys 1750 thermoanalyzer coupled with a Pfeiffer Omnistar spectrometer and a Setaram Setsys 1750 CS Evolution dilatometer. The kinetic parameters were calculated based on the differential isoconversional method of Friedman. The results of the thermal analysis of clays and blends indicated the emission of physically bound water at 200–250 °C. At temperatures from 200–250 °C to 550–600 °C the release of water is caused by oxidation of organic matter and dehydroxylation of different clay minerals like illite, illite-smectite, mica and kaolin. From blends, in addition, also from the decomposition of portlandite. The emission of CO2 at these temperatures was a result of the oxidation of organic matter contained in the clays. In the temperature range from 550–600 °C to 800–900 °C, the mass loss was caused by ongoing dehydroxylation processes in clay minerals but was mainly due to the decomposition of the carbonates contained in the OS ashes and clinker dust. These processes were accompanied by contraction and expansion of the ceramic bodies with the corresponding changes in the SSA and porosity values of the samples. Therefore, the decomposition of the clays took place in one step which blends in two steps. At first, dehydroxylation of the clay minerals occurs, followed by decomposition of the carbonates. The value of the conversion-dependent activation energy E along the reaction progress α varied for the Arumetsa and illitic clay between 75–182 and 9–206 kJ mol−1, respectively. For the blends based on Arumetsa and illitic clay, the activation energy of the first step varied between 14–193 and 5–205 kJ mol−1, and for the second step, it was between 15–390 and 135–235 kJ mol−1, respectively, indicating the complex mechanism of the processes.


2020 ◽  
Vol 40 (suppl 2) ◽  
pp. 597-604
Author(s):  
Zahra NILCHIAN ◽  
Mohamad Reza EHSANI ◽  
Zahra PIRAVI-VANAK ◽  
Hossein BAKHODA

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