Abstract
AbstractBACKGROUNDRecently, nanocarbons (e.g. carbon nanotubes, nanodiamond and mesoporous carbon) were found to be efficient catalysts in dehydrogenation reactions. However, the preparation of these nanocarbons is costly, complicated and time‐consuming. The goal of this study is to exploit a biomass‐derived carbon for propane dehydrogenation.RESULTSBiomass‐derived carbons with hierarchical porous structures and high surface area are prepared via carbonization of bean dregs with NaOH, and operated as metal‐free catalysts for direct dehydrogenation of propane to propylene. The properties of the prepared carbon catalysts are characterized by SEM, TEM, XRD, N2 sorption and XPS techniques, revealing the presence of many nanopores and oxygenated functional groups. The catalytic results show that the resultant carbons exhibit high catalytic activity, selectivity and stability for direct dehydrogenation of propane. The activation temperature can significantly affect the textural properties and surface functional groups of the carbons, and thus, affect their catalytic performance.CONCLUSIONThe excellent catalytic performance can be attributed to the high content of oxygenated functional groups combined with hierarchical porous structure and large surface area of the obtained porous carbons which could provide more accessible active sites. This work demonstrates the flexible utilization of bean dregs‐derived carbons in propane dehydrogenation to propylene. © 2018 Society of Chemical Industry
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Chemical Technology & Biotechnology
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.