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Ti 3 C 2 MXenes-based catalysts for the process of α-pinene isomerization.
- Source :
-
RSC advances [RSC Adv] 2023 Oct 16; Vol. 13 (43), pp. 30281-30292. Date of Electronic Publication: 2023 Oct 16 (Print Publication: 2023). - Publication Year :
- 2023
-
Abstract
- In this study, the catalytic performance of Ti <subscript>3</subscript> C <subscript>2</subscript> MXene materials in the reaction of α-pinene isomerization was demonstrated. The influence of etching agents (HF, HF/H <subscript>2</subscript> SO <subscript>4,</subscript> and HF/HCl; weight ratios of mixed acids: 1 : 3, 1 : 4, and 1 : 5) on removing Al atoms from MAX phase, creation of an accordion-like structure typical for MXenes and catalytic activity of the produced samples have been revealed. The MXene HF obtained by MAX phase HF treatment exhibited the highest activity (conversion of α-pinene 74.65 mol%), while materials produced with the mixed acids (HF/H <subscript>2</subscript> SO <subscript>4</subscript> and HF/HCl) showed a significant reduction in the conversion of α-pinene (on average about 28-fold). However, these last samples displayed an increase of about 10 mol% in the selectivity to the most desirable product-camphene. The high activity of MXene HF is a result of a high concentration of acid sites (11.62 mmol g <superscript>-1</superscript> ) - the concentration of acid sites in the samples obtained by MAX phase mixed acids treatment was about 2.5-5.5 times smaller. This work proposes possible mechanisms for the α-pinene isomerization reaction on the MXene HF and on the MXene HF/H <subscript>2</subscript> SO <subscript>4</subscript> X : Y and MXene HF/HCl X : Y in connection with their structure.<br />Competing Interests: There are no conflicts to declare.<br /> (This journal is © The Royal Society of Chemistry.)
Details
- Language :
- English
- ISSN :
- 2046-2069
- Volume :
- 13
- Issue :
- 43
- Database :
- MEDLINE
- Journal :
- RSC advances
- Publication Type :
- Academic Journal
- Accession number :
- 37849709
- Full Text :
- https://doi.org/10.1039/d3ra05055f