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A green sorbent for CO(2) capture: α-cyclodextrin-based carbonate in DMSO solution

Cyclodextrin (α-CD)/KOH pellet dissolved in DMSO was utilized to capture CO(2). KOH has a dual function of enhancing the nucleophilicity of the hydroxyl groups on the α-CD rims and acting as a desiccant. (13)C NMR spectroscopy provided evidence for the chemisorption of CO(2) through the formation of...

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Detalles Bibliográficos
Autores principales: Eftaiha, Ala'a F., Qaroush, Abdussalam K., Alsoubani, Fatima, Pehl, Thomas M., Troll, Carsten, Rieger, Bernhard, Al-Maythalony, Bassem A., Assaf, Khaleel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089425/
https://www.ncbi.nlm.nih.gov/pubmed/35558579
http://dx.doi.org/10.1039/c8ra08040b
Descripción
Sumario:Cyclodextrin (α-CD)/KOH pellet dissolved in DMSO was utilized to capture CO(2). KOH has a dual function of enhancing the nucleophilicity of the hydroxyl groups on the α-CD rims and acting as a desiccant. (13)C NMR spectroscopy provided evidence for the chemisorption of CO(2) through the formation of organic carbonate (RO-CO(2)(−)·K(+)). This was supported by the spectral changes obtained using ex situ ATR-FTIR spectroscopy upon bubbling CO(2). Activation of α-CD with NaH or bubbling with (13)CO(2) verified that chemisorption occurred solely via RO-CO(2)(−)·K(+) rather than inorganic bicarbonate. Volumetric gas uptake demonstrated a sorption capacity of 21.3 wt% (4.84 mmol g(−1)). To the best of our knowledge, this is the highest chemisorption value reported to date for CD-based sorbents. DFT calculations of the Gibbs free energies indicated that the formation of RO-CO(2)(−)·K(+) was more favoured at the primary carbinol rather than its secondary counterpart.