Related Experiment Video
Updated: Dec 7, 2025

Reducing Willow Wood Fuel Emission by Low Temperature Microwave Assisted Hydrothermal Carbonization
Published on: May 19, 2019
Synergizing Sulfonated Hydrothermal Carbon and Microwave Irradiation for Intensified Esterification Reaction
Laddawan Tumkot1, Armando T Quitain2,3, Panatpong Boonnoun4
1Bio-Circular-Green-economy Technology & Engineering Center, BCGeTEC, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.
Abstract:
The synergy of sulfonated hydrothermal carbon and microwave (MW) irradiation was applied for the esterification of oleic acid with methanol (MeOH) to produce biodiesel. The effects of temperature, reaction time, ratio of oleic acid to methanol, and catalyst loading were investigated at a fixed MW power of 400 W. The addition of hexane, serving as a co-solvent and separator, was also investigated. The optimum conditions for the proposed process were oleic acid-to-methanol molar ratio of 1:5 and hexane-to-methanol ratio of 0.5 (v/v) in the presence of a 5 wt % catalyst, at 100 °C for 60 min, obtaining a 97% yield of oleic acid methyl ester. The addition of slight amounts of hexane resulted into an eightfold reduction in the amount of MeOH needed to obtain a yield above 90%, which normally required a MeOH-to-oil ratio of 40:1. This proposed novel approach could provide a more cost-effective method for the esterification of oil to produce biodiesel, that is, reactive separation utilizing carbon-based catalysts under MW irradiation.
Related Concept Videos
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
Esters to Carboxylic Acids: Saponification
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Regioselectivity and Stereochemistry of Acid-Catalyzed Hydration
Alkylation of β-Diester Enolates: Malonic Ester Synthesis

