Catalytic COS formation on ion-exchanged LTA zeolites during adsorption

In this study, the catalytic reaction of H 2 S and CO 2 to COS and H 2 O during the adsorptive treatment of a model natural gas on modified Linde type-A (LTA) zeolites is investigated. Breakthrough curves of all 4 components were measured at 25 °C in a fixed bed adsorber on eight NaA and CaNaA zeolites with different calcium exchange ratios. The COS breakthrough curves are discussed with regard to the properties of the materials in the exchange series (number of cations, cation position, cation type). The COS curves reveal that catalytic formation of COS occurs at cation positions II and III, whereas no COS formation occurs at position I. Ca 2+ -ions are more catalytically active than Na + -Ions due to their higher ionic charge. The quantities of COS formed prove that the reaction water plays a significant role in the termination of the reaction. The reaction water adsorbs on the catalytically active cations so that no further COS formation can occur. The feed water, on the other hand, mainly leads to a displacement of the previously adsorbed components (CO 2 , H 2 S, COS). • Catalytic COS formation on LTA zeolites during adsorptive treatment of natural gas. • Catalytic activity depends on cation position and cation type. • Ca 2+ ions in Linde type A zeolites are more catalytically active than Na + ions. • CaNaA zeolites with a high ion exchange ratio reduce the formation of COS. • Adsorption of water extinguishes catalytic activity.

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Publication Details

Journal
Microporous and Mesoporous Materials
Published
2024-11-12
DOI
https://doi.org/10.1016/j.micromeso.2024.113408
Citations
5
Primary Topic
Industrial Gas Emission Control
Type
article
Field-Weighted Citation Impact
1.06

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article

Catalytic COS formation on ion-exchanged LTA zeolites during adsorption

Christian Bläker, Nele Klinkenberg, Dieter Bathen, Jakob G. Eggebrecht et al.
5 citations
Microporous and Mesoporous Materials
Industrial Gas Emission Control
1.06
article

Catalytic COS formation on ion-exchanged LTA zeolites during adsorption

Christian Bläker, Nele Klinkenberg, Dieter Bathen, Jakob G. Eggebrecht, Sebastian Pfeifer, Tobias Eckardt, Christoph Pasel, Kristin Gleichmann
article en
5 citations

Abstract

In this study, the catalytic reaction of H 2 S and CO 2 to COS and H 2 O during the adsorptive treatment of a model natural gas on modified Linde type-A (LTA) zeolites is investigated. Breakthrough curves of all 4 components were measured at 25 °C in a fixed bed adsorber on eight NaA and CaNaA zeolites with different calcium exchange ratios. The COS breakthrough curves are discussed with regard to the properties of the materials in the exchange series (number of cations, cation position, cation type). The COS curves reveal that catalytic formation of COS occurs at cation positions II and III, whereas no COS formation occurs at position I. Ca 2+ -ions are more catalytically active than Na + -Ions due to their higher ionic charge. The quantities of COS formed prove that the reaction water plays a significant role in the termination of the reaction. The reaction water adsorbs on the catalytically active cations so that no further COS formation can occur. The feed water, on the other hand, mainly leads to a displacement of the previously adsorbed components (CO 2 , H 2 S, COS). • Catalytic COS formation on LTA zeolites during adsorptive treatment of natural gas. • Catalytic activity depends on cation position and cation type. • Ca 2+ ions in Linde type A zeolites are more catalytically active than Na + ions. • CaNaA zeolites with a high ion exchange ratio reduce the formation of COS. • Adsorption of water extinguishes catalytic activity.

Microporous and Mesoporous MaterialsVol. 383
Basys (Germany) (DE), Institut für Energie- und Umwelttechnik (DE), TCM-Klinik Bad Kötzting (DE), University of Duisburg-Essen (DE)
BASF
Openalex Percentile: Top 26%
Industrial Gas Emission Control
1.06
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