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Intracrystalline Transport Barriers Affecting the Self-Diffusion of CH4 in Zeolites vertical bar Na-12 vertical bar-A and vertical bar Na12-xKx vertical bar-A
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).ORCID-id: 0000-0002-7284-2974
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).ORCID-id: 0000-0003-3185-3535
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för material- och miljökemi (MMK).
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Antal upphovsmän: 52019 (Engelska)Ingår i: Langmuir, ISSN 0743-7463, E-ISSN 1520-5827, Vol. 35, nr 40, s. 12971-12978Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Carbon dioxide must be removed from biogas or natural gas to obtain compressed or liquefied methane, and adsorption-driven isolation of CO2 could be improved by developing new adsorbents. Zeolite adsorbents can select CO2 over CH4, and the adsorption of CH4 on zeolite vertical bar Na12-xKx vertical bar-A is significantly lower for samples with a high K+ content, i.e., x > 2. Nevertheless, we show, using H-1 NMR experiments, that these zeolites adsorb CH4 after long equilibration times. Pulsed-field gradient NMR experiments indicated that in large crystals of zeolites vertical bar Na12-xKx vertical bar-A, the long-time diffusion coefficients of CH4 did not vary with x, and the upper limit of the mean-square displacement was about 1.5 mu m, irrespective of the diffusion time. Also for zeolite vertical bar Na-12 vertical bar-A samples of three different particle sizes (similar to 0.44, similar to 2.9, and similar to 10.6 mu m), the upper limit of the mean-square displacement of CH4 was 1.5 mu m and largely independent of the diffusion time. This similarity provided further evidence for an intracrystalline diffusion restriction for CH4 within the medium- and large-sized zeolite A crystals and possibly of clustering and close contact among the small zeolite A crystals. The upper limit of the long-time diffusion coefficient of adsorbed CH4 was (at 1 atm and 298 K) about 10(-10) m(2)/s irrespective of the size of the zeolite particle or the studied content of K+ in zeolites and vertical bar Na-12 vertical bar-A. The T-1 relaxation time for adsorbed CH4 on zeolites vertical bar Na12-xKx vertical bar-A with x > 2 was smaller than for those with x < 2, indicating that the short-time diffusion of CH4 was hindered.

Ort, förlag, år, upplaga, sidor
2019. Vol. 35, nr 40, s. 12971-12978
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Kemi
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URN: urn:nbn:se:su:diva-175812DOI: 10.1021/acs.langmuir.9b02574ISI: 000489678500010PubMedID: 31510744OAI: oai:DiVA.org:su-175812DiVA, id: diva2:1371779
Tillgänglig från: 2019-11-20 Skapad: 2019-11-20 Senast uppdaterad: 2019-11-29Bibliografiskt granskad

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Hedin, NiklasRzepka, PrzemyslawJasso-Salcedo, Alma BereniceChurch, Tamara L.Bernin, Diana
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