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In relation to this article, we declare that there is no conflict of interest.
Publication history
Received November 8, 2024
Revised December 29, 2024
Accepted January 15, 2025
Available online July 25, 2025
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Removal of Carbon Dioxide from Natural Gas Using a Zeolite-Based Pressure Swing Adsorption Process

Center for Low Carbon Chemical Process and Chemical and Process Technology Division 1Department of Advanced Materials and Chemical Engineering , University of Science and Technology (UST) 2Department of Chemical Engineering , Hanyang University
jhshin@krict.re.kr, kwkim@krict.re.kr
Korean Journal of Chemical Engineering, July 2025, 42(8), 000042
https://doi.org/10.1007/s11814-025-00398-0

Abstract

Natural gas processing consists of pretreatment, acid gas removal, N 2 rejection, and distillation. Among these, acid gas

removal requires signifi cant energy, and thus, there is a need for effi cient CO 2 separation technology to replace conventional

amine scrubbing. To develop CO 2 -adsorption technology for natural gas, a vacuum pressure swing adsorption (VPSA) process

was developed using a Cu-modifi ed zeolite adsorbent. Adsorption isotherms for CO 2 , N 2 , and CH 4 on the Cu-modifi ed

zeolite adsorbent were measured, and adsorption equilibrium parameters were estimated using dual-site Langmuir isotherms.

Single-component breakthrough experiments subsequently were performed and mass transfer rate parameters were estimated

using these measured dynamic data, yielding values of 0.35, 0.5, and 0.5 s −1 for CO 2 , N 2 , and CH 4 , respectively. The VPSA

process based on the modifi ed Skarstrom cycle was constructed, and for feed conditions of CH 4 , CO 2 , and N 2 ratio of 80, 10,

and 10 vol%, the CO 2 recovery and CH 4 recovery rates were confi rmed to be 70.1% and 90.0%, respectively. Subsequently,

multi-objective optimization was performed on CO 2 recovery and CH 4 recovery to obtain the Pareto frontier curve. The

results indicated that achieving a CO 2 removal rate of over 90% yields a CH 4 recovery rate of 85%.

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