Esterification of levulinic acid to ethyl levulinate: optimization of process conditions using commercial levulinic acid and extension to the use of levulinic acid derived from depithed sugarcane bagasse

The need for sustainability necessitates intensive research on using renewable resources to produce biofuels and biochemicals. The esterification of commercial levulinic acid (LA) into ethyl levulinate (EL) was first optimized using methanesulfonic acid (MsOH) and response surface methodology (RSM). The optimum condition for the esterification of commercial LA into EL was 5.25 h, 90 degrees C and 2.75 g of MsOH loading. The EL yield and selectivity obtained were 92.2% and 94%, respectively, at a LA conversion of 98%. The effect of various catalysts which are less corrosive and environmentally friendly, namely MsOH and ionic liquids (ILs), was investigated under fixed conditions to determine the best catalyst for the production of EL from LA. The alkyl levulinate ester selectivity from LA conversion was also studied by using linear and branched chain alcohols. The alkyl levulinate ester, ethyl levulinate, was produced from depithed sugarcane bagasse (DSB)-derived LA using a less corrosive homogenous catalyst (methanesulfonic acid). The reaction conditions of 5.25 h, 90 degrees C and 2.75 g of MsOH loading were used to produce EL from DSB-derived LA with an EL yield of 75%.

Automated summary

The need for sustainable development requires extensive research on the use of renewable resources for the production of biofuels and biochemicals. This study optimized the esterification of commercial levulinic acid into ethyl levulinate using methanesulfonic acid as the catalyst. The researchers also investigated the effect of different catalysts, including methanesulfonic acid and ionic liquids, on the production of ethyl levulinate. Additionally, the selectivity of alkyl levulinate ester from levulinic acid conversion was studied.