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Methyl laurate was synthesized from lauric acid (LA) and methanol via an esterification reaction using ionic liquids (ILs) as catalysts. The efficiencies of three different catalysts, 1-methylimidazole hydrogen sulfate ([Hmim]HSO 4 ), 1-methyl-2-pyrrolidonium hydrogen sulfate ([Hnmp]HSO 4 ) and H 2 SO 4 , were compared. The effect of the methanol/LA molar ratio, reaction temperature, reaction time and catalyst dosage on the esterification rate of LA was investigated by single-factor experiments. Based on the single-factor experiments, the esterification of LA and methanol was optimized using response surface methodology. The results showed that the most effective catalyst was the IL [Hnmp]HSO 4 . The optimal conditions were as follows: [Hnmp]HSO 4  dosage of 5.23%, methanol/LA molar ratio of 7.68 : 1, reaction time of 2.27 h and reaction temperature of 70°C. Under these conditions, the LA conversion of the esterification reached 98.58%. A kinetic study indicated that the esterification was a second-order reaction with an activation energy and a frequency factor of 68.45 kJ mol −1  and 1.9189 × 10 9  min −1 , respectively. The catalytic activity of [Hnmp]HSO 4  remained high after five cycles.

Optimization and kinetic study of methyl laurate synthesis using ionic liquid [Hnmp]HSO 4 as a catalyst

Optimization and kinetic study of methyl laurate synthesis using ionic liquid [Hnmp]HSO ₄ as a catalyst