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Article: Active-site engineering of a frustrated-Lewis-pair Au-loaded Zn-Al catalyst for the highly stable synthesis of glycerol carbonate from co-utilisation of CO2 and glycerol

TitleActive-site engineering of a frustrated-Lewis-pair Au-loaded Zn-Al catalyst for the highly stable synthesis of glycerol carbonate from co-utilisation of CO2 and glycerol
Authors
KeywordsCarbon dioxide
FLPs
Glycerol
Glycerol Carbonate
Hydrotalcite
Issue Date5-Aug-2024
PublisherElsevier
Citation
Applied Catalysis A: General, 2024, v. 683 How to Cite?
AbstractSolid frustrated-Lewis-pair catalysts, based on Zn-Al composite oxide modified loaded with Au (Aux/ZnAl-CHT), were prepared by calcination of hydrotalcite precursors and tested for the direct synthesis of glycerol carbonate using CO2 as the carbon source. An Au5/ZnAl-CHT catalyst shows the highest catalytic performance with the glycerol carbonate yield of 19.5 % and the selectivity of 50.5 % at 170 °C and 4.0 MPa CO2, while maintaining good thermal stability and excellent regeneration ability. A series of characterization results and density functional theory (DFT) calculations indicated the introduction of Au leads to more frustrated-Lewis-pairs in Zn-Al composite oxide (ZnAl-CHT), which improve the adsorption and activation of CO2. Meanwhile, FTIR analysis indicates that glycerol is activated by Zn2+ for the formation of zinc glycerolate intermediates. The above dual synergistic activation processes effectively enhance the catalytic performance. And the reaction pathway is proposed for the synthesis of glycerol carbonate from CO2 and glycerol.
Persistent Identifierhttp://hdl.handle.net/10722/353803
ISSN
2023 Impact Factor: 4.7
2023 SCImago Journal Rankings: 0.967
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorZhang, Shizheng-
dc.contributor.authorWu, Gongde-
dc.contributor.authorWang, Xiaoli-
dc.contributor.authorDeng, Lin-
dc.contributor.authorCao, Zhangjin-
dc.contributor.authorWan, Jie-
dc.contributor.authorZhang, Jin-
dc.contributor.authorLiu, Yanjun-
dc.contributor.authorKan, Jianfei-
dc.contributor.authorXu, Wei-
dc.contributor.authorHu, Lihua-
dc.contributor.authorShang, Congxiao-
dc.contributor.authorGuo, Zhengxiao-
dc.date.accessioned2025-01-25T00:35:23Z-
dc.date.available2025-01-25T00:35:23Z-
dc.date.issued2024-08-05-
dc.identifier.citationApplied Catalysis A: General, 2024, v. 683-
dc.identifier.issn0926-860X-
dc.identifier.urihttp://hdl.handle.net/10722/353803-
dc.description.abstractSolid frustrated-Lewis-pair catalysts, based on Zn-Al composite oxide modified loaded with Au (Aux/ZnAl-CHT), were prepared by calcination of hydrotalcite precursors and tested for the direct synthesis of glycerol carbonate using CO2 as the carbon source. An Au5/ZnAl-CHT catalyst shows the highest catalytic performance with the glycerol carbonate yield of 19.5 % and the selectivity of 50.5 % at 170 °C and 4.0 MPa CO2, while maintaining good thermal stability and excellent regeneration ability. A series of characterization results and density functional theory (DFT) calculations indicated the introduction of Au leads to more frustrated-Lewis-pairs in Zn-Al composite oxide (ZnAl-CHT), which improve the adsorption and activation of CO2. Meanwhile, FTIR analysis indicates that glycerol is activated by Zn2+ for the formation of zinc glycerolate intermediates. The above dual synergistic activation processes effectively enhance the catalytic performance. And the reaction pathway is proposed for the synthesis of glycerol carbonate from CO2 and glycerol.-
dc.languageeng-
dc.publisherElsevier-
dc.relation.ispartofApplied Catalysis A: General-
dc.subjectCarbon dioxide-
dc.subjectFLPs-
dc.subjectGlycerol-
dc.subjectGlycerol Carbonate-
dc.subjectHydrotalcite-
dc.titleActive-site engineering of a frustrated-Lewis-pair Au-loaded Zn-Al catalyst for the highly stable synthesis of glycerol carbonate from co-utilisation of CO2 and glycerol-
dc.typeArticle-
dc.identifier.doi10.1016/j.apcata.2024.119843-
dc.identifier.scopuseid_2-s2.0-85195814299-
dc.identifier.volume683-
dc.identifier.eissn1873-3875-
dc.identifier.isiWOS:001256921000001-
dc.identifier.issnl0926-860X-

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