Lignin monomer conversion into biolubricant base oils

Despite progress in the depolymerization of lignin, only a few studies convert the obtained monomers to value-added products. Here we introduce a strategy to synthesize branched benzene lubricant (BBL) and branched cyclic lubricant (BCL) base oils from lignin-derived monomers and aldehyde. We perform carbon-carbon coupling via Bronsted acid-catalyzed hydroxyalkylation/alkylation (HAA) then hydrodeoxygenation (HDO). Optimum HAA reaction conditions achieve up to 90% guaiacol conversion and an HAA product containing 76% BBL and 24% enal condensation product over a P-SiO2 catalyst. Subsequent HDO of HAA products over an Ir-ReOx/SiO2 catalyst produces a lubricant-ranged mixture of BCL (C-24) up to yield (82%) and small fractions of dodecyl cyclohexane and C-10 and C-15 carbons alkanes. The kinematic viscosity, viscosity index, and Noack volatility of these base oils are comparable to commercial petroleum-derived poly alpha-olefin Group IV and refrigerant base oils. This approach provides a sustainable pathway for replacing petroleum-derived base oils.

Automated summary

This study introduces a strategy to synthesize branched benzene lubricant (BBL) and branched cyclic lubricant (BCL) base oils from lignin-derived monomers and aldehyde, providing a sustainable pathway for replacing petroleum-derived base oils. The base oils produced show comparable properties to commercial petroleum-derived poly alpha-olefin Group IV and refrigerant base oils in terms of kinematic viscosity, viscosity index, and Noack volatility.