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The Application of Hollow Carbon Nanofibers Prepared by Electrospinning to Carbon Dioxide Capture

Coaxial electrospinning has been considered a straightforward and convenient method for producing hollow nanofibers. Therefore, the objective of this study was to develop hollow activated carbon nanofibers (HACNFs) for CO(2) capture in order to reduce emissions of CO(2) to the atmosphere and mitigat...

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Detalles Bibliográficos
Autores principales: Chiang, Yu-Chun, Chin, Wei-Ting, Huang, Chih-Cheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8512053/
https://www.ncbi.nlm.nih.gov/pubmed/34641091
http://dx.doi.org/10.3390/polym13193275
Descripción
Sumario:Coaxial electrospinning has been considered a straightforward and convenient method for producing hollow nanofibers. Therefore, the objective of this study was to develop hollow activated carbon nanofibers (HACNFs) for CO(2) capture in order to reduce emissions of CO(2) to the atmosphere and mitigate global warming. Results showed that the sacrificing core could be decomposed at carbonization temperatures above 900 °C, allowing the formation of hollow nanofibers. The average outer diameters of HACNFs ranged from 550 to 750 nm, with a shell thickness of 75 nm. During the carbonization stage, the denitrogenation reactions were significant, while in the CO(2) activation process, the release of carbon oxides became prominent. Therefore, the CO(2) activation could increase the percentages of N=C and quaternary N groups. The major nitrogen functionalities on most samples were O=C–NH and quaternary N. However, =C and quaternary N groups were found to be crucial in determining the CO(2) adsorption performance. CO(2) adsorption on HACNFs occurred due to physical adsorption and was an exothermic reaction. The optimal CO(2) adsorption performance was observed for HACNFs carbonized at 900 °C, where 3.03 mmol/g (1 atm) and 0.99 mmol/g (0.15 atm) were measured at 25 °C. The degradation of CO(2) uptakes after 10 adsorption−desorption cyclic runs could be maintained within 8.9%.