Effect of preheat temperature, pressure, and residence time on methanation performance

Cristian Mejía-Botero, Camilo Echeverri-Uribe, Juan E. Ferrer-Ruiz and Andrés A. Amell

Energy, 2023, vol. 269, issue C

Abstract: The present work studies the effect of reagent preheat temperature on methanation while maintaining the initial temperature of the catalytic bed constant. An adiabatic packed bed reactor was used with 193 g of commercial 10% Ni/Al2O3 catalyst. The tested preheat temperatures were 25 °C, 100 °C, 180 °C, and 280 °C, while the initial catalytic bed temperature was 280 °C. Two tests were performed in which the effect of preheat temperature was evaluated: the first comparing gas hourly space velocities (GHSVs) of 935 h−1 and 1559 h−1, and the second comparing gauge pressures of 0 bar, 1 bar, and 4 bar. Similar behavior was observed for the temperature inside the reactor and final CO2 conversion for preheating temperatures of 100 °C, 180 °C, and 280 °C at a gauge pressure of 0 bar. However, at this pressure, conversion was considerably reduced for the preheat temperature of 25 °C, due to a large part of the catalytic bed serving to preheat the reactants to the minimum reaction temperature. This effect can be partially attenuated by decreasing the GHSV, due to the increased residence time. Finally, increased pressure significantly improved the final CO2 conversion for all preheating temperatures (Tin), and attenuates the effect of Tin. These results show that certain operating conditions do not require as high a reactant preheat temperature for methanation, which offers energy savings in certain processes such as power-to-gas (P2G), where the hydrogen is produced from electrolysis and can leave the process at a lower temperature than that required for methanation.

Keywords: Methanation reactor; Hydrogen; Carbon dioxide; Reagent preheating temperature (search for similar items in EconPapers)
Date: 2023
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Persistent link: https://EconPapers.repec.org/RePEc:eee:energy:v:269:y:2023:i:c:s0360544223000877

DOI: 10.1016/j.energy.2023.126693

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