The environmental and economic challenges currently faced by the wax market may be addressed by the use of sustainable bio-based alternatives. Hereto, ketonization of vegetable oils and animal fats is...
TiO2 is one of the most promising catalysts
for liquid-phase
ketonization of carboxylic acids. As recently reported, its use significantly
contributes to the overall environmental impact of the fatty acid
ketonization process. Therefore, postsynthetic modifications such
as metal addition and thermal treatment under inert and reducing atmospheres
were studied to enhance the catalytic activity of anatase TiO2 for the ketonization of lauric acid. Although more active
surfaces can be generated by the additional metal through hydrogen
spillover effects, its presence led to substantial decarboxylation
rather than ketonization. Interestingly, metal-free anatase TiO2 is also substantially activated after thermal treatment in
nitrogen or hydrogen gas, while maintaining its full ketonization
selectivity. Ascertained by X-ray analysis, this was not related to
polymorphism but due to a higher content of Lewis acid sites, of which
the hydrogen-treated catalysts possessed the largest density. A quadratic
relationship appears between the ketonization rate and surface acid
site density, a defining characteristic of rate-determining bimolecular
C–C coupling in the ketonization mechanism. In contrast to
studies on short-chain carboxylic acids, this liquid-phase study renders
hydrogenated TiO2 as the most promising catalyst, while
metal addition is less suitable for selectivity reasons. Although
less essential for bio-oil upgrading, high selectivity is of utmost
importance for on-purpose fatty acid ketonization.
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