Carbon capture from steam methane reforming (SMR) stream by Supported Ionic Liquids (SILPs) using commercial supports

The selective capture of CO 2 from reforming stream for H 2 productions was evaluated in fixed-bed columns using Supported Ionic Liquid Phases (SILP) based on commercial ionic liquid 1-butyl-3-methylimidazolium acetate ([Bmim][Acetate]). Thirteen different commercial supports were evaluated, varying in particle size, porosity and surface chemistry. Selected supports were used to prepare SILP materials via incipient wetness impregnation, incorporating ~40 wt% IL. Supports and SILP sorbent characterization were performed using scanning electron microscopy, nitrogen adsorption-desorption isotherms and thermogravimetric and elemental analysis. A synthetic gas mixture modeling a Steam Methane Reforming (SMR) stream with composition of H 2 /CO 2 /CH 4 (70/25/5%) was used to evaluate the CO 2 capture performance of the six different SILP materials by means of fixed-bed experiments. Measured breakthrough curves at 30 ºC under various operating pressures (1, 5, and 10 bar) allowed to estimate thermodynamic and kinetic parameters on CO 2 sorption from SMR gas model. The experimental fixed-bed tests revealed CO 2 sorption capacities of 0.4–0.6 mol·kg⁻¹, with pre-breakthrough times up to 20 min and CO 2 removal efficiencies above 90% at 10 bar. Thermodynamics (sorption capacity) was maintained independently of the support, while particle size governed sorption/desorption kinetics, with smaller particles exhibiting faster mass transfer and more efficient use of the sorbent. Increasing CO 2 partial pressure enhanced both sorption capacity and kinetic constants, leading to improved process performance. The LDF model successfully described the experimental breakthrough curves, using K MTC as reference kinetic parameter. Additionally, regeneration tests, using a N 2 stripping stream and pressure-swing, were conducted on one selected SILP material over seven sorption-desorption cycles. So, experimental results highlighted the improved performance of SILP materials with smaller particle sizes, with high effective CO 2 sorption capacity and enhanced sorption and desorption rates, enabling treating SMR streams by a simple two-fixed bed configuration. • 13 supports of very different nature were evaluated as SILP in CO 2 capture from SMR streams • The amount of IL in SILP determined the CO 2 sorption capacity • Higher IL loadings were reported in supports with high BET surfaces and mesopore volumes • The support particle size is the key parameter of the CO 2 sorption kinetics • The reusability of the SILP was demonstrated by 7 sorption/desorption cycles preserving CO 2 sorption capacity

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Publication Details

Journal
Journal of environmental chemical engineering
Published
2025-10-23
DOI
https://doi.org/10.1016/j.jece.2025.119869
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
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article

Carbon capture from steam methane reforming (SMR) stream by Supported Ionic Liquids (SILPs) using commercial supports

Journal of environmental chemical engineering
Carbon Dioxide Capture Technologies
article

Carbon capture from steam methane reforming (SMR) stream by Supported Ionic Liquids (SILPs) using commercial supports

article en

Abstract

The selective capture of CO 2 from reforming stream for H 2 productions was evaluated in fixed-bed columns using Supported Ionic Liquid Phases (SILP) based on commercial ionic liquid 1-butyl-3-methylimidazolium acetate ([Bmim][Acetate]). Thirteen different commercial supports were evaluated, varying in particle size, porosity and surface chemistry. Selected supports were used to prepare SILP materials via incipient wetness impregnation, incorporating ~40 wt% IL. Supports and SILP sorbent characterization were performed using scanning electron microscopy, nitrogen adsorption-desorption isotherms and thermogravimetric and elemental analysis. A synthetic gas mixture modeling a Steam Methane Reforming (SMR) stream with composition of H 2 /CO 2 /CH 4 (70/25/5%) was used to evaluate the CO 2 capture performance of the six different SILP materials by means of fixed-bed experiments. Measured breakthrough curves at 30 ºC under various operating pressures (1, 5, and 10 bar) allowed to estimate thermodynamic and kinetic parameters on CO 2 sorption from SMR gas model. The experimental fixed-bed tests revealed CO 2 sorption capacities of 0.4–0.6 mol·kg⁻¹, with pre-breakthrough times up to 20 min and CO 2 removal efficiencies above 90% at 10 bar. Thermodynamics (sorption capacity) was maintained independently of the support, while particle size governed sorption/desorption kinetics, with smaller particles exhibiting faster mass transfer and more efficient use of the sorbent. Increasing CO 2 partial pressure enhanced both sorption capacity and kinetic constants, leading to improved process performance. The LDF model successfully described the experimental breakthrough curves, using K MTC as reference kinetic parameter. Additionally, regeneration tests, using a N 2 stripping stream and pressure-swing, were conducted on one selected SILP material over seven sorption-desorption cycles. So, experimental results highlighted the improved performance of SILP materials with smaller particle sizes, with high effective CO 2 sorption capacity and enhanced sorption and desorption rates, enabling treating SMR streams by a simple two-fixed bed configuration. • 13 supports of very different nature were evaluated as SILP in CO 2 capture from SMR streams • The amount of IL in SILP determined the CO 2 sorption capacity • Higher IL loadings were reported in supports with high BET surfaces and mesopore volumes • The support particle size is the key parameter of the CO 2 sorption kinetics • The reusability of the SILP was demonstrated by 7 sorption/desorption cycles preserving CO 2 sorption capacity

Journal of environmental chemical engineeringVol. 13(6)
Universidad Nacional de Educación a Distancia (ES), Universidad Rey Juan Carlos (ES), Técnicas Reunidas (Spain) (ES), Universidad Autónoma de Madrid (ES)
Openalex Percentile: Top 51%
Carbon Dioxide Capture Technologies
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