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On the reduction of CO2 footprint via selective hydrodeoxygenation by ZnO–Ti3C2Tx catalyst under solvent-free conditions.

Authors :
Saini, Bhagirath
Krishnapriya, R.
Yadav, Meena
Singhal, Rahul
Sharma, Rakesh K.
Source :
Green Chemistry; 7/21/2023, Vol. 25 Issue 14, p5470-5482, 13p
Publication Year :
2023

Abstract

Biomass-derived fatty acids are essential feedstock for producing liquid fuels and value-added chemicals with significantly low CO<subscript>2</subscript> footprints. Herein, Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript> and ZnO–Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript> catalysts were synthesized and demonstrated for the selective hydrodeoxygenation reaction (HDO) of methyl oleate (MO) as a model compound. The synthesized ZnO–Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript> catalyst showed 100% conversion of MO with >90% selectivity for the HDO product (n-C18). In addition, the pure Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript> demonstrated 100% conversion with a selectivity of 67% for n-C17 hydrocarbon via the decarboxylation route. The highest reduction of CO<subscript>2</subscript> footprint is achieved at 280 °C and 30 bar H<subscript>2</subscript> pressure under solvent-free conditions using ZnO–Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript>. The catalyst is recyclable and reusable for five test cycles. The high catalytic selectivity of the ZnO–Ti<subscript>3</subscript>C<subscript>2</subscript>T<subscript>x</subscript> catalyst towards HDO is attributed to the synergic effect of the Ti and ZnO active sites and the thermally stable structure. This study offers an efficient route for converting edible and non-edible vegetable oils to biofuels by controlling CO<subscript>2</subscript> production. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14639262
Volume :
25
Issue :
14
Database :
Complementary Index
Journal :
Green Chemistry
Publication Type :
Academic Journal
Accession number :
164957874
Full Text :
https://doi.org/10.1039/d3gc01260c