Production of green jet fuel from furanics via hydroxyalkylation-alkylation over mesoporous MoO3-ZrO2 and hydrodeoxygenation over Co/γ-Al2O3: Role of calcination temperature and MoO3 content in MoO3-ZrO2

Kunamalla, Alekhya and Maity, Sunil Kumar (2023) Production of green jet fuel from furanics via hydroxyalkylation-alkylation over mesoporous MoO3-ZrO2 and hydrodeoxygenation over Co/γ-Al2O3: Role of calcination temperature and MoO3 content in MoO3-ZrO2. Fuel, 332. ISSN 0016-2361

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Abstract

Green biofuels are equivalent to hydrocarbon-based motor fuels and compatible with existing refinery in-frastructures and combustion engines. Therefore, sustainable production of green biofuels is essential to circumvent the construction of expensive biorefinery infrastructures. This study thus presents the production of green jet fuel from biomass-derived furanic compounds via hydroxyalkylation-alkylation (HAA) reaction coupled with hydrodeoxygenation (HDO) of the C15 biofuel precursor. MoO3-promoted ZrO2 is a promising solid acid catalyst with excellent thermal stability. The HAA reaction of 2-methylfuran with furfural was thus investigated over a novel MoO3-promoted mesoporous ZrO2 catalyst. This work elucidated the role of calcination temperature and MoO3 loading on the structural variation of MoO3-promoted mesoporous ZrO2 and the evolution of acid sites. The highest acid density and consequently best catalytic performance was observed at 873 K calcination temperature with 20 wt% MoO3 loading. About 85 % 2-methylfuran conversion was achieved over 1.25 g of this optimum catalyst at 2:1 2-methylfuran/furfural mole ratio, 323 K, and 5 h. The HAA reaction was further investigated at various reaction temperatures, catalyst loadings, and 2-methylfuran/furfural mole ratios to obtain optimum reaction conditions. HDO of biofuel precursor was examined over Co/gamma-Al2O3 catalyst at various re-action temperatures, initial hydrogen pressure, and Co metal loading on gamma-Al2O3 to understand the reaction mechanism and identify the optimum reaction conditions. HDO of biofuel precursor progressed through suc-cessive furan ring saturation and opening reactions, followed by a combination of HDO, decarbonylation, and cleavage of tertiary-carbon bonds. C9-C15 alkanes were observed as products, with C11 and C14 hydrocarbons being dominant at 573 K and 30 bar. The elevated hydrogen pressure and reaction temperature boosted the conversion of oxygen-containing intermediate compounds at the cost of C-C cracking reactions. The conversion of oxygen-containing intermediate compounds was enhanced with rising Co metal loading on gamma-Al2O3 up to 20 wt % due to the enhancement of metal dispersion.

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