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Piperazine-modified activated carbon as a novel adsorbent for CO 2 capture: modeling and characterization
In this study, activated carbon and piperazine-modified activated carbon adsorbents were prepared and used for CO adsorption. The effect of various parameters including adsorbent particle size, adsorbent amount, piperazine weight percent, pressure, and temperature were investigated on the CO adsorpt...
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Published in: | Environmental science and pollution research international 2022-01, Vol.29 (4), p.5134 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | In this study, activated carbon and piperazine-modified activated carbon adsorbents were prepared and used for CO
adsorption. The effect of various parameters including adsorbent particle size, adsorbent amount, piperazine weight percent, pressure, and temperature were investigated on the CO
adsorption capacity. The adsorbents were characterized using nitrogen adsorption/desorption isotherms and FTIR analyses. The results showed that the adsorption capacity decreases with temperature increasing and increases with pressure increasing. In addition, the surface modification of activated carbon improved the CO
adsorption capacity more than the unmodified adsorbent, and the highest CO
adsorption was obtained 203.842 mg/g at 25 °C and 8 bar. Additionally, to determine the adsorbent behavior, CO
adsorption experimental data were fitted by isotherm and kinetic models. CO
adsorption isotherm modeling was studied up to 8 bar at 25 °C, and kinetic modeling was investigated up to 85 °C at 6 bar. The results show that Hill isotherm model and Elovich kinetic models have a good agreement with the adsorption data. Finally, thermodynamic modeling was carried out for modified and unmodified adsorbents, and enthalpy, entropy, and Gibbs free energy changes of adsorption for piperazine-modified activated carbon at 25 °C and 6 bar obtained 17.078 kJ/mol, - 0.039 kJ/mol.K, and - 5.318 kJ/mol, respectively. |
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ISSN: | 1614-7499 |
DOI: | 10.1007/s11356-021-16040-5 |