Related Experiment Video
Updated: Aug 10, 2025

Experimental Protocol for Biodiesel Production with Isolation of Alkenones as Coproducts from Commercial Isochrysis Algal Biomass
Published on: June 24, 2016
Enzymatic Transesterification of Atlantic Salmon (Salmo salar) Oil with Isoamyl Alcohol
Milda Gumbytė1, Violeta Makareviciene1, Egle Sendzikiene1
1Agriculture Academy, Vytautas Magnus University, K. Donelaicio Str. 58, LT-44248 Kaunas, Lithuania.
Abstract:
In this experimental study, biodiesel was synthesized from the salmon oil using the Lipozyme®RM IM (Bagsværd, Denmark) as a biocatalyst. Isoamyl alcohol was used as an acyl acceptor in the transesterification process. The aim of this study is to select the best process conditions, aiming to obtain the highest transesterification degree that meets the requirements of the EN 14214 standard. Response surface methodology (RSM) was used for statistical analysis and optimization of process parameters. A four-factor experimental design was modelled by central compositional design (CCD) to investigate the effects of biocatalyst concentration, isoamyl alcohol-to-oil molar ratio, temperature, and duration on transesterification degree. It was determined that the optimal parameters for biodiesel synthesis were the following: an enzyme concentration of 11% (wt. of oil mass); a process temperature of 45 °C; a process duration of 4 h; and an alcohol-to-oil molar ratio of 6:1. The transesterification degree of biodiesel reached 87.23%. The stepwise addition of isoamyl alcohol during the transesterification process further increased the degree of transesterification to 96.5%.
Related Concept Videos
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
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...
Alkylation of β-Diester Enolates: Malonic Ester Synthesis
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide

