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A Lewis acid-base paired InBO 3 catalyst: synthesis and high selectivity for isopropanol dehydrogenation.

Authors :
Sun Y
Gao W
Yang T
Source :
Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2023 Jun 06; Vol. 52 (22), pp. 7538-7543. Date of Electronic Publication: 2023 Jun 06.
Publication Year :
2023

Abstract

Whilst metal borates are well known as optical materials, their potential in solid catalysis has been less investigated. The calcite structured InBO <subscript>3</subscript> was selected as the target borate and was prepared using a solvothermal method. High-resolution transmission electron microscopy and powder X-ray diffraction prove that the material has a nanoparticle morphology with an average size ∼50 nm and high crystallinity. Intrinsic surface oxygen vacancies, which are beneficial to catalysis, were detected using X-ray photoelectron spectroscopy. Lewis acidity and basicity were both observed using NH <subscript>3</subscript> -/CO <subscript>2</subscript> -temperature-programmed desorption experiments, and the total acid and base amounts were found to be 46.6 and 123.8 μmol g <superscript>-1</superscript> , respectively. Catalytic dehydration and dehydrogenation reactions for isopropanol at elevated temperatures were conducted in a fixed bed reactor to evaluate the catalytic performance of InBO <subscript>3</subscript> . InBO <subscript>3</subscript> exhibits a high conversion rate (>90.5%) and, most importantly, a high dehydrogenation selectivity (acetone selectivity >92.5%), whilst the optimal acetone yield achieved was 121.3 mmol h <superscript>-1</superscript> g <superscript>-1</superscript> <subscript>cat</subscript> at 350 °C. This study on InBO <subscript>3</subscript> strongly suggests that metal borates have promising applications in heterogeneous catalysis.

Details

Language :
English
ISSN :
1477-9234
Volume :
52
Issue :
22
Database :
MEDLINE
Journal :
Dalton transactions (Cambridge, England : 2003)
Publication Type :
Academic Journal
Accession number :
37183950
Full Text :
https://doi.org/10.1039/d3dt00941f