Selective decarboxylation of biobased fatty acids using a Ni-FSM-16 catalyst
[Display omitted] •Novel catalyst Ni-FSM-16 was successfully synthesized and fully characterized.•Ni-FSM-16 exhibited high efficiency in decarboxylation of biobased carboxylic acids.•Bifunctional action of the Ni-FSM-16 is proposed to give high selectivity and reactivity.•Ni-FSM-16 is promising for...
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Published in | Applied catalysis. B, Environmental Vol. 291; p. 120050 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.08.2021
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
•Novel catalyst Ni-FSM-16 was successfully synthesized and fully characterized.•Ni-FSM-16 exhibited high efficiency in decarboxylation of biobased carboxylic acids.•Bifunctional action of the Ni-FSM-16 is proposed to give high selectivity and reactivity.•Ni-FSM-16 is promising for converting waste materials into renewable products.
A novel catalyst based on nickel supported on a folded sheet material (FSM) was synthesized and fully characterized. The resulting Ni-FSM-16 catalyst showed a high reactivity and selectivity in decarboxylation of plant-based carboxylic acids to yield the corresponding linear alkenes and alkanes in up to 75 % yield and less than 5 % of undesired cracking products. In addition, lignin-derived vanillic acid was smoothly converted to guaiacol. A comparative investigation showed that both the support and the metal of the Ni-FSM-16 catalyst proved to be pivotal for the reactivity. Particularly, substituting Ni with Fe, Pd or Al or replacing the FSM-16 support with MCM-41 or SBA-15 led to lower reactivity and selectivity towards linear decarboxylated products. The superior catalytic performance of Ni-FSM-16 was driven by a higher and more even metal distribution, more acidic silanol-group and an electron-rich, thus softer Ni, that promote coordination by the carbon-carbon double-bond of the fatty acid. |
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ISSN: | 0926-3373 1873-3883 1873-3883 |
DOI: | 10.1016/j.apcatb.2021.120050 |