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Pyrolysis of sulfonic acid substituted benzenes and investigation of CO2 capture capability of resulting carbons

dc.contributor.authorZaman, Ali Can
dc.date.accessioned2026-06-27T14:35:24Z
dc.date.issued2021
dc.description.abstractAromatic organic compounds: 5-sulfosalicylic acid (SSA) and p-toluenesulfonic acid (TsOH) were used to prepare sulfur doped ultramicropore (pores smaller than 0.7 nm) containing carbons by pyrolysis under Argon atmosphere. SSA derived carbon processed at 1000 degrees C showed the best CO2 (carbon dioxide) adsorption performance. CO2 sorption capacity of SSA1000 is 3.91 mmol g(-1)at 1 bar at 273 K and 2.88 mmol g(-1)at 1 bar at 298 K. Remarkably, at typical flue gas conditions (0.15 bar@298 K) SSA1000 takes up 0.95 mmol g(-1) CO2. SSA1000 possessed good gas sorption properties, recyclability for regeneration, and Ideal Adsorbed Solution Theory (IAST)based selectivity of 14.7 (1 bar, CO2/N-2:0.15/0.85). This work shows the possibility of production of ultramicropore containing sulfur and oxygen doped carbons exhibiting high CO2 uptake capability via simple pyrolysis method from molecular precursors.en
dc.description.urihttps://doi.org/10.1016/j.jssc.2021.122546
dc.identifier.doi10.1016/j.jssc.2021.122546
dc.identifier.eissn1095-726X
dc.identifier.issn0022-4596
dc.identifier.urihttps://hdl.handle.net/20.500.14981/62409
dc.identifier.volume303
dc.identifier.wos000700860100082
dc.language.isoeng
dc.publisherACADEMIC PRESS INC ELSEVIER SCIENCE
dc.relation.ispartofJOURNAL OF SOLID STATE CHEMISTRY
dc.subjectCO2 capture
dc.subjectSulfur doped carbon
dc.subjectUltramicroporous
dc.subjectSubstituted benzene
dc.subjectMolecular precursor
dc.subjectMETAL-ORGANIC FRAMEWORKS
dc.subjectACTIVATED CARBON
dc.subjectMESOPOROUS CARBON
dc.subjectDOPED CARBONS
dc.subjectPORE-SIZE
dc.subjectMICROPOROUS CARBONS
dc.subjectSURFACE-CHEMISTRY
dc.subjectAMORPHOUS-CARBON
dc.subjectDIOXIDE CAPTURE
dc.subjectISOSTERIC HEATS
dc.subjectChemistry
dc.titlePyrolysis of sulfonic acid substituted benzenes and investigation of CO2 capture capability of resulting carbons
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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