Related Experiment Video
Updated: Jul 4, 2025

Author Spotlight: Employing Green-Chemistry Principles for Safe and Sustainable Synthesis of Biodiesels
Published on: April 19, 2024
Engine Performance of High-Acid Oil-Biodiesel through Supercritical Transesterification
1Department of Marine Engineering, National Taiwan Ocean University, Keelung 20224, Taiwan.
Abstract:
Relatively cheaper high-acid oil was used to make biodiesel through supercritical methanol transesterification, where high FFA contents in feedstock might conversely enhance the reaction extent. A direct-injection diesel engine and a dynamometer were used to analyze the engine characteristics of the high-acid oil-biodiesel. The experimental results show that the biodiesel made in this study had adequate fuel properties. This present biodiesel from high-acid oil was found to bear a lower heating value and equivalence ratio, with higher exhaust gas temperature, brake-specific fuel consumption (bsfc), and excess air ratio, than super-low sulfur diesel (SLSD). The biodiesel appeared to have larger-sized carbon residue left after the burning process in comparison with that of SLSD. The higher engine speed resulted in higher exhaust gas temperature and equivalence ratio, while lower bsfc, excess air ratio, was observed for the biodiesel. Supercritical methanol transesterification has been successfully proven to convert those low-cost feedstocks to renewable biodiesel products which own competitive engine performance in this study.
More Related Videos
09:10Experimental Protocol for Biodiesel Production with Isolation of Alkenones as Coproducts from Commercial Isochrysis Algal Biomass
Published on: June 24, 2016
11:28Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating
Published on: December 25, 2016
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...
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
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 Methylesters: Alkylation using Diazomethane
Alkylation of β-Ketoester Enolates: Acetoacetic Ester Synthesis