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 inApplied catalysis. B, Environmental Vol. 291; p. 120050
Main Authors Jiraroj, Duangkamon, Jirarattanapochai, Orhathai, Anutrasakda, Wipark, Samec, Joseph S.M., Tungasmita, Duangamol N.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 15.08.2021
Elsevier BV
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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.
ISSN:0926-3373
1873-3883
1873-3883
DOI:10.1016/j.apcatb.2021.120050