scholarly journals Analysis of the Influence of Coal Petrography on the Proper Application of the Unipore and Bidisperse Models of Methane Diffusion

Energies ◽  
2021 ◽  
Vol 14 (24) ◽  
pp. 8495
Author(s):  
Marcin Karbownik ◽  
Jerzy Krawczyk ◽  
Katarzyna Godyń ◽  
Tomasz Schlieter ◽  
Jiří Ščučka

The analysis of phenomena related to gas transport in hard coal is important with regard to the energetic use of coal bed methane (CBM), the reduction of greenhouse gas emissions to the atmosphere (CO2) and the prevention of natural hazards such as methane hazards and gas and rock outbursts. This article presents issues concerning the feasibility and scope of applying the unipore and bidisperse diffusion models to obtain knowledge concerning the kinetics of methane sorption and its diffusion in the carbon structure, depending on its petrography. Laboratory tests were carried out on coal samples which varied in terms of petrography. Quantitative point analyses were carried out, based on which content of groups of macerals was determined. The degree of coalification of coal samples was also determined based on measurements of vitrinite reflectivity R0 and the volatile matter content Vdaf. Sorption kinetics were also investigated, and attempts were made to adjust the unipore and bidisperse models to the real sorption kinetic courses. This allowed the identification of appropriate coefficients controlling the course of sorption in mathematical models. An attempt was also made to assess the possibility of applying a given model to properly describe the phenomenon of methane sorption on hard coal.

2014 ◽  
Vol 59 (2) ◽  
pp. 509-516
Author(s):  
Andrzej Olajossy

Abstract Methane sorption capacity is of significance in the issues of coalbed methane (CBM) and depends on various parameters, including mainly, on rank of coal and the maceral content in coals. However, in some of the World coals basins the influences of those parameters on methane sorption capacity is various and sometimes complicated. Usually the rank of coal is expressed by its vitrinite reflectance Ro. Moreover, in coals for which there is a high correlation between vitrinite reflectance and volatile matter Vdaf the rank of coal may also be represented by Vdaf. The influence of the rank of coal on methane sorption capacity for Polish coals is not well understood, hence the examination in the presented paper was undertaken. For the purpose of analysis there were chosen fourteen samples of hard coal originating from the Upper Silesian Basin and Lower Silesian Basin. The scope of the sorption capacity is: 15-42 cm3/g and the scope of vitrinite reflectance: 0,6-2,2%. Majority of those coals were of low rank, high volatile matter (HV), some were of middle rank, middle volatile matter (MV) and among them there was a small number of high rank, low volatile matter (LV) coals. The analysis was conducted on the basis of available from the literature results of research of petrographic composition and methane sorption isotherms. Some of those samples were in the form (shape) of grains and others - as cut out plates of coal. The high pressure isotherms previously obtained in the cited studies were analyzed here for the purpose of establishing their sorption capacity on the basis of Langmuire equation. As a result of this paper, it turned out that for low rank, HV coals the Langmuire volume VL slightly decreases with the increase of rank, reaching its minimum for the middle rank (MV) coal and then increases with the rise of the rank (LV). From the graphic illustrations presented with respect to this relation follows the similarity to the Indian coals and partially to the Australian coals.


2021 ◽  
Vol 3 (3) ◽  
Author(s):  
Munique Gonçalves Guimarães ◽  
Rafael Benjamin Werneburg Evaristo ◽  
Augusto César de Mendonça Brasil ◽  
Grace Ferreira Ghesti

AbstractThe present work analyzed the energy generation potential of Buriti (Mauritia flexuosa L. f.) by thermochemical reactions. The experimental part of the study performed immediate analyses, elemental analyses, lignocellulosic analysis, thermogravimetric analysis, calorific values, and syn gas concentrations measurements of the gasification of Buriti in a fixed-bed reactor. Additionally, numerical simulations estimated the syn gas concentrations of the gasification reactions of Buriti. The immediate analysis showed that Buriti has the highest ash content (4.66%) and highest volatile matter content (85%) compared to other Brazilian biomass analyzed, but the higher heating value was only 18.28 MJ.kg−1. The elemental analysis revealed that the oxygen to carbon ratio was 0.51 while hydrogen to carbon ratio was 1.74, indicating a good thermal conversion efficiency. The Lignocellulosic analysis of Buriti resulted in a high content of holocellulose (69.64%), a lignin content of 28.21% and extractives content of 7.52%. The thermogravimetry of the Buriti indicated that the highest mass loss (51.92%) occurred in a temperature range between 150 °C and 370 °C. Lastly, the experimental gasification study in a fixed-bed updraft gasifier resulted in syn gas concentrations of 14.4% of CO, 11.5% of CO2 and 17.5% of H2 while the numerical simulation results confirmed an optimal equivalence ratio of 1.7 to maximize CO and H2 concentrations. Therefore, based on the results presented by the present work, the gasification process is adequate to transform Buriti wastes into energy resources. Graphic abstract


2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Veniamin Zheleznov ◽  
Aleksey Golikov ◽  
Tatiana Sokolnitskaya ◽  
Sergey Ivannikov

Abstract The sorption kinetics of uranyl ions micro-quantities from fluoride solutions by nanostructured materials with anatase mesoporous structures has been studied. Using the model of competitive sorption of ions and positively charged complexes of uranyl ion on deprotonated hydroxyl groups of an anatase, kinetic curves of changes in the ratio of ionic forms of uranium in solution were calculated. Modeling was carried out under the assumption of a two-stage mechanism of uranium complex ions sorption. The modeling considered the influence of the uranyl ion carbonate complexes formation. The shift in equilibrium among ionic forms of uranyl correlates with the stability of the complexes in solution.


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