Journal
FUEL
Volume 263, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2019.116750
Keywords
Biofuel; Metal oxide catalyst; Hydrocarbon; Deoxygenation; Waste cooking oil
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Funding
- Eppley Foundation
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The present work explores the potential to upgrade waste cooking oil (WCO) via deoxygenation using inexpensive, unsupported metal oxide catalysts (CaO, TiO2, Mn(IV)O, and ZnO) in the absence of a hydrogen feedstock. WCO was mixed with 5 wt% catalyst material in a stainless steel reactor and heated to 300 degrees C for 60 min. The relative concentration of fatty acids increased upon heating in the absence of any catalyst, from similar to 15% of the total identifiable compounds for WCO to 64% for the Organic Liquid Products as a result of the nearly complete conversion of aldehyde and ester groups to organic acids, alkanes and aromatics. The inorganic catalysts shifted the product distributions significantly. CaO and ZnO slightly increased the concentration of acidic groups (versus WCO) but produced less acids than OLP alone, while Mn(IV)O and TiO2 resulted in overall decreases of free fatty acids. Mn(IV)O showed a slight preference for alkene formation, whereas TiO2 was selective toward alkanes. All catalysts - and uncatalyzed heating - showed significant deoxygenation in terms of ridding the WCO of C-O groups. Thermal treatment of WCO (with and without catalysts) resulted in a 25% increase in higher heating values, in line with those of commercial jet fuels. While the one-pot catalytic upgrading of WCO would not result in a direct substitute for aviation fuel, this work demonstrated the potential to significantly upgrade WCO using an inexpensive catalyst without relying on copious amounts of hydrogen gas to affect a hydrodeoxygenation reaction.
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