Helium separation from gas mixtures using a temperature-regulated trapdoor zeolite

Alternative methods of recovering helium from natural gas such as adsorption processes are often more cost-effective than cryogenic distillation approaches for small-scale reserves. However, conventional adsorbents tend to selectively adsorb bulk components like nitrogen and methane rather than the minor helium component, increasing overall gas production costs. Here we show that a trapdoor potassium chabazite, K-CHA, can selectively capture helium from a helium‑nitrogen mixture. Isobaric measurements of helium adsorption capacities on K-CHA were found to exhibit a distinctive bell shape indicative of a trapdoor guest admission rather than a monotonic increase of adsorption capacity with decreasing temperature. The threshold temperature for helium admission on K-CHA was determined to be 100.6 K from these measurements, which is lower than that for nitrogen (254 K). Helium trapped inside the zeolite cavities was observed to escape slowly over an extended period even when the temperature remained well below the threshold, which is an observation not previously reported for trapdoor zeolites. The time constant of the exponential associated with this helium release was 5.5 h at 77 K when the K-CHA was used to encapsulate 1.8 mol/kg with approximately 4 % of the total encapsulated helium released during the first hour. Nevertheless, it was possible to use the trapdoor mechanism within encapsulation cycles lasting 1 h to enrich helium from an initial 4.5 mol% to 80 mol% with a helium recovery rate of 60 %, achieving a helium‑nitrogen separation factor of 89. Our results highlight a potential new process with selectivity for inert, minor components in gas mixtures. • Helium encapsulation using trapdoor zeolites demonstrated for first time • Threshold temperature for helium admission into K-CHA measured to be 101 K • High-pressure helium trapped in zeolite cavities at 77 K escaped slowly. • N 2 separated from He using temperature cycle with K-CHA despite slow leak • 4.5 mol% helium enriched to 80 mol% purity in single encapsulation cycle

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Publication Details

Journal
Chemical Engineering Journal
Published
2025-11-13
DOI
https://doi.org/10.1016/j.cej.2025.170692
Primary Topic
Zeolite Catalysis and Synthesis
Type
article
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article

Helium separation from gas mixtures using a temperature-regulated trapdoor zeolite

Eric F. May, Gongkui Xiao, Michael L. Johns, Ehsan Sadeghi Pouya et al.
Chemical Engineering Journal
Zeolite Catalysis and Synthesis
article

Helium separation from gas mixtures using a temperature-regulated trapdoor zeolite

Eric F. May, Gongkui Xiao, Michael L. Johns, Ehsan Sadeghi Pouya, Arash Arami‐Niya, Gang Li, Libin Liu, Yang Wang
article en

Abstract

Alternative methods of recovering helium from natural gas such as adsorption processes are often more cost-effective than cryogenic distillation approaches for small-scale reserves. However, conventional adsorbents tend to selectively adsorb bulk components like nitrogen and methane rather than the minor helium component, increasing overall gas production costs. Here we show that a trapdoor potassium chabazite, K-CHA, can selectively capture helium from a helium‑nitrogen mixture. Isobaric measurements of helium adsorption capacities on K-CHA were found to exhibit a distinctive bell shape indicative of a trapdoor guest admission rather than a monotonic increase of adsorption capacity with decreasing temperature. The threshold temperature for helium admission on K-CHA was determined to be 100.6 K from these measurements, which is lower than that for nitrogen (254 K). Helium trapped inside the zeolite cavities was observed to escape slowly over an extended period even when the temperature remained well below the threshold, which is an observation not previously reported for trapdoor zeolites. The time constant of the exponential associated with this helium release was 5.5 h at 77 K when the K-CHA was used to encapsulate 1.8 mol/kg with approximately 4 % of the total encapsulated helium released during the first hour. Nevertheless, it was possible to use the trapdoor mechanism within encapsulation cycles lasting 1 h to enrich helium from an initial 4.5 mol% to 80 mol% with a helium recovery rate of 60 %, achieving a helium‑nitrogen separation factor of 89. Our results highlight a potential new process with selectivity for inert, minor components in gas mixtures. • Helium encapsulation using trapdoor zeolites demonstrated for first time • Threshold temperature for helium admission into K-CHA measured to be 101 K • High-pressure helium trapped in zeolite cavities at 77 K escaped slowly. • N 2 separated from He using temperature cycle with K-CHA despite slow leak • 4.5 mol% helium enriched to 80 mol% purity in single encapsulation cycle

Chemical Engineering JournalVol. 526
The University of Melbourne (AU), The University of Western Australia (AU), Department of Mines and Petroleum (AU)
Openalex Percentile: Top 71%
Zeolite Catalysis and Synthesis
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