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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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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 |
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. |
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