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dc.contributor.authorLing, Huajuan
dc.contributor.authorWang, Zichun
dc.contributor.authorWang, Leizhi
dc.contributor.authorStampfl, Catherine
dc.contributor.authorWang, Dan
dc.contributor.authorChen, Jianfeng
dc.contributor.authorHuang, Jun
dc.date.accessioned2021-02-01T01:15:45Z
dc.date.available2021-02-01T01:15:45Z
dc.date.issued2020en
dc.identifier.urihttps://hdl.handle.net/2123/24385
dc.description.abstractKetonization can efficiently convert carboxylic acids into ketones, promising in bio-oil upgrading. For economic-sustainable bio-refining, Ca/Zn/AlOx (CZA) metal oxides with various Ca/Zn/Al ratios have been prepared by the low-cost and natural abundant metals and are applied in the process here. Mechanistic study on the ketonization of acetic acid revealed the reaction pathways strongly depends on “composition-structure-function” correlation of the Ca/Zn/AlOx catalysts. The reaction is mainly performed on strong base sites (e.g. CaO and ZnO) via thermal decomposition of carboxylates at high temperature (≥375 °C), but depends on acid-base pairs (e.g. amorphous calcium aluminates) significantly at low temperature (≤350 °C). CZA(331) (Ca/Zn/Al = 3/3/1) obtained the highest acetone yield of 97.1% at 425 °C hitherto and retained for over 100 h with simple regeneration process. Adding major bio-oil model compounds (e.g. phenol) into the reaction mixture has minor effect on the CZA catalysts. Therefore, current highly active and stable CZA catalysts are promising in boosting the efficiency and economy of bio-oil upgrading process in future.en
dc.publisherElsevieren
dc.relation.ispartofCatalysis Todayen
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivatives 4.0en
dc.titleComposition-structure-function correlation of Ca/Zn/AlOx catalysts for the ketonization of acetic aciden
dc.typeArticleen
dc.identifier.doi10.1016/j.cattod.2019.01.057
dc.relation.arcDP150103842
dc.relation.arcDP140102432
usyd.facultySeS faculties schools::Faculty of Engineeringen
usyd.citation.volume351en
usyd.citation.spage58en
usyd.citation.epage67en
workflow.metadata.onlyNoen


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