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Cited by 184

The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.

Ultrahigh CO2 adsorption capacity on carbon molecular sieves at room temperature

Silvestre-Albero, Joaquín, Wahby, Anass, Sepúlveda-Escribano, Antonio, Martínez-Escandell, Manuel, Kaneko, Katsumi, Rodríguez-Reinoso, Francisco·2011·Chemical Communications

Abstract

Although metal-organic framework (MOF) materials have been postulated as superior to any other sorbent for CO(2) adsorption at room temperature, here we prove that the appropriate selection of the raw material and the synthesis conditions allows the preparation of carbon molecular sieves (CMSs) with adsorption capacity, on a volumetric basis, highly exceeding those reported in the literature for MOFs. Furthermore, the excellent sorption properties of CMSs over the whole pressure range (up to 50 bar) are fully reversible after different adsorption/desorption cycles.

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Crossref · 10.1039/c1cc11618e

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Metadata

Authors
Silvestre-Albero, J., Wahby, A., Sepúlveda-Escribano, A., Martínez-Escandell, M., Kaneko, K., & Rodríguez-Reinoso, F.
Venue
Chemical Communications
Published
2011
Volume
47
Issue
24
Pages
6840
ISSN
  • 1359-7345 (ISSN-L)
  • 1364-548X
OpenAlex
W2083397962
Cited by
184
References
3
FWCI
29.60
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Ultrahigh CO2 adsorption capacity on carbon molecular sieves at room temperature. https://app.cochat.ai/papers/10.1039/c1cc11618e
The paper
Silvestre-Albero, J., Wahby, A., Sepúlveda-Escribano, A., Martínez-Escandell, M., Kaneko, K., & Rodríguez-Reinoso, F. (2011). Ultrahigh CO2 adsorption capacity on carbon molecular sieves at room temperature. Chemical Communications. https://doi.org/10.1039/c1cc11618e

Data sources

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.