Selective hydrogenation of oleic acid to fatty alcohols on Rh-Sn-B/Al2O3 catalysts. Influence of Sn content

[Display omitted] •New heterogenous Rh-Sn-B/Al2O3 catalysts for selective hydrogenation of oleic acid to fatty alcohol were studied.•Sn and Rh were found to be in interaction, activity of the metal function and TPR traces being modified by tin addition.•Higher yields to oleyl alcohol as compared to...

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Veröffentlicht in:Applied catalysis. A, General General, 2019-08, Vol.584, p.117149, Article 117149
Hauptverfasser: Fonseca Benítez, Cristhian A., Mazzieri, Vanina A., Sánchez, María A., Benitez, Viviana M., Pieck, Carlos L.
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Sprache:eng
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Zusammenfassung:[Display omitted] •New heterogenous Rh-Sn-B/Al2O3 catalysts for selective hydrogenation of oleic acid to fatty alcohol were studied.•Sn and Rh were found to be in interaction, activity of the metal function and TPR traces being modified by tin addition.•Higher yields to oleyl alcohol as compared to other reported catalysts were obtained.•Sn addition limits the Rh activity for hydrogenation of the CC double bond thus increasing the formation of oleyl alcohol. The influence of tin loading of Rh-Sn-B/γ-Al2O3 catalysts on the selective hydrogenation of oleic acid to fatty alcohol was studied. The catalysts were characterized by N2 sorptometry, temperature programmed reduction and X-ray photoelectron spectroscopy. Cyclohexane dehydrogenation and cyclopentane hydrogenolysis were also used to evaluate the metal function. Sn and Rh are in interaction since the conversion values of the cyclohexane, cyclopentane, and TPR profiles are modified by tin addition. Moreover, XPS analysis showed that Sn modifies the amount of Rh on the surface and its reduction state. The yield to oleyl alcohol was maximum for the Rh(1 wt%)-Sn(4 wt%)-B/γ-Al2O3 and Rh(1 wt%)-Sn(5 wt%)-B/γ-Al2O3 catalysts. This behavior could be explained considering that the Sn addition limits the Rh activity for hydrogenation of the CC double bond, thus increasing the formation of oleyl alcohol. At low Sn content, high selectivity to octadecane appears due to the total hydrogenation of the CC, COH and CO bonds.
ISSN:0926-860X
1873-3875
DOI:10.1016/j.apcata.2019.117149