An investigation on the influence of support type for Ni catalysed vapour phase hydrogenation of aqueous levulinic acid to g-valerolactone

Velisoju, V, Gutta, N, Medak, S, Anjaneyulu, C, Bhargava, S, Tardio, J, Reddy, V, Padmasri, A and Venugopal, A 2016, 'An investigation on the influence of support type for Ni catalysed vapour phase hydrogenation of aqueous levulinic acid to g-valerolactone', RSC Advances, vol. 6, pp. 9872-9879.


Document type: Journal Article
Collection: Journal Articles

Title An investigation on the influence of support type for Ni catalysed vapour phase hydrogenation of aqueous levulinic acid to g-valerolactone
Author(s) Velisoju, V
Gutta, N
Medak, S
Anjaneyulu, C
Bhargava, S
Tardio, J
Reddy, V
Padmasri, A
Venugopal, A
Year 2016
Journal name RSC Advances
Volume number 6
Start page 9872
End page 9879
Total pages 8
Publisher Royal Society of Chemistry
Abstract Ni (20 wt%) supported on SiO2, γ-Al2O3 and ZrO2 catalysts was examined for hydrogenation of aqueous levulinic acid (LA) to γ-valerolactone (GVL) at 270 °C and ambient pressure. The band intensities of Brønsted (BAS: 1540 cm-1) and Lewis acid sites (LAS: 1450 cm-1) estimated by pyridine adsorbed DRIFT spectra revealed a lower ratio of BAS/LAS over the Ni/SiO2 catalyst than over the Ni/ZrO2 and Ni/γ-Al2O3 catalysts. The rate of angelica lactone (AL) formation was lower than the rate of AL hydrogenation over the Ni/SiO2 catalyst. The poisoning and regeneration of the Ni/SiO2 catalyst using pyridine and 2,6-dimethylpyridine demonstrated that Lewis acid sites influenced the conversion of LA to AL and subsequent hydrogenation of AL to GVL occurred on surface Ni sites. In contrast, Brønsted acid sites were responsible for the ring opening of GVL to valeric acid (VA). Kinetic data emphasized that the hydrogenation activity and product distribution were dependent on the type of acid site, and the Ni sites in close proximity to Brønsted acid sites are prone to hydrogenolysis of GVL to valeric acid and hydrocarbons.
Subject Chemical Sciences not elsewhere classified
DOI - identifier 10.1039/C5RA24199E
Copyright notice © The Royal Society of Chemistry 2016
ISSN 2046-2069
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