Abstract

2-methyl furan (MF) is a fuel additive with improved fuel characteristics compared to bio-ethanol. Unfortunately, the production of MF (from furfural (FF) hydrogenation) is not economically feasible. Interestingly, molten salts in biomass pyrolysis have shown to promote the formation of furans (mainly FF). Because molten salts hydropyrolysis could be an alternative route to both produce FF and convert it into MF, an assessment is indispensable. Molten salts pyrolysis and hydropyrolysis of pinewood and wheat straw and related model compounds were studied in a micro-reactor. The effect of hydropyrolysis process variables was assessed on the total detectable condensable vapors and MF formation.At low pressures (0.4 MPa), the chloride salts favored the production of FF and acetic regardless of the reaction atmosphere. Under a high pressure of hydrogen though (1.6 and 3.0 MPa), the conversion of FF to MF was enhanced through hydrogenation, hydrodeoxygenation and demethylation reactions. Molten salts hydropyrolysis at 350 °C and pressures of either 1.6 MPa (biomass mass fraction of 0.09) or 3.0 MPa (biomass mass fraction of 0.24) were optimal and yielded ca. 8 wt% to 9 wt% MF. Reaction temperatures >350 °C were unfavorable for the MF yield and instead promoted furfural decarbonylation to furan.

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