S/N/O-Enriched Carbons from Polyacrylonitrile-Based Block Copolymers for Selective Separation of Gas Streams
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Abstract
A series of polyacrylonitrile (PAN)-based block copolymers with poly(methyl methacrylate) (PMMA) as sacrificial bock were synthesized by atom transfer radical polymerization and used as precursors for the synthesis of porous carbons. The carbons enriched with O- and S-containing groups, introduced by controlled oxidation and sulfuration, respectively, were characterized by Raman spectroscopy, scanning electron microscopy, and X-ray photoelectron spectrometry, and their surface textural properties were measured by a volumetric analyzer. We observed that the presence of sulfur tends to modify the structure of the carbons, from microporous to mesoporous, while the use of copolymers with a range of molar composition PAN/PMMA between 10/90 and 47/53 allows the obtainment of carbons with different degrees of porosity. The amount of sacrificial block only affects the morphology of carbons stabilized in oxygen, inducing their nanostructuration, but has no effect on their chemical composition. We also demonstrated their suitability for separating a typical N2/CO2 post-combustion stream
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Gómez-Díaz, D.; Domínguez-Ramos, L.; Malucelli, G.; Freire, M.S.; González-Álvarez, J.; Lazzari, M. S/N/O-Enriched Carbons from Polyacrylonitrile-Based Block Copolymers for Selective Separation of Gas Streams. Polymers 2024, 16, 269. https://doi.org/10.3390/ polym16020269
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https://doi.org/10.3390/polym16020269Sponsors
This research was funded by the Ministerio de Ciencia, Innovación y Universidades, AEI PID2021-122923NB-I00 and by the Xunta de Galicia (Centro Singular de Investigación de Galicia, accreditation 2019–2022; ED431G2019/03, Consolidación e estructuración ED431B 2021/23) and the European Regional Development Fund
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© 2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license
Attribution 4.0 International
Attribution 4.0 International








