@ARTICLE{Gajda_Aleksandra_Adsorption_2024, author={Gajda, Aleksandra and Jodłowski, Przemysław and Kozieł, Katarzyna and Kurowski, Grzegorz and Hyjek, Kornelia and Skoczylas, Norbert and Pajdak, Anna}, volume={50}, number={4}, pages={51-63}, journal={Archives of Environmental Protection}, howpublished={online}, year={2024}, publisher={Polish Academy of Sciences}, abstract={Thermal effects accompanying gas sorption on micro- and mesoporous materials provide unique insights into the type, course, and efficiency of sorption. In this study, metal-organic frameworks (MOFs) with different topologies and chemical structures were synthesized and investigated: HKUST-1, Ni-MOF-74, UiO-66, and MIL-140A. These MOFs were characterized structurally and sorptively with respect to selected greenhouse gases (GHGs). Sorption capacities for CO2 and CH4 were determined at several temperatures and measurement pressures, and the maximum sorption capacity was determined using the Langmuir-Freundlich model. Thermal effects accompanying adsorption were quantified through the isosteric heat of adsorption parameter. For each MOF, the values of isosteric heat of adsorption were higher for CO2 than for CH4. The values of this parameter was determined in the following order: HKUST-1 > Ni-MOF-74 > UiO-66 > MIL-140A. Energy homogeneity of the adsorbent surface was observed in nearly all cases, except for UiO-66 during CO2 adsorption. Changes in the determined isosteric heat of adsorption of CO2 with increasing sorption capacity were in the range of 5-15 kJ/mol, while for CH4 they ranged from 1.4 to 17 kJ/mol, respectively. The level of thermal selectivity of CO2 over CH4 was determined in the following order: UiO-66 (1.9) > Ni-MOF-64 (1.7) > MIL-140A (1.5) > HKUST-1 (1.1).}, title={Adsorption of selected GHG on metal-organic frameworks in the context of accompanying thermal effects}, type={Article}, URL={http://journals.pan.pl/Content/133557/PDF/Archives50no4pp51_63.pdf}, doi={10.24425/aep.2024.152895}, keywords={Metal-organic frameworks;, CO2 and CH4 adsorption;, isosteric heat of adsorption;, thermal selectivity;}, }