Epoxidation of Methyl Esters as Valuable Biomolecules: Monitoring of Reaction

Abstract

The paper is focused on the epoxidation of methyl esters prepared from oil crops with various profiles of higher fatty acids, especially unsaturated, which are mainly contained in the non-edible linseed and Camelina sativa oil (second generation). The novelty consists in the separation and identification of all products with oxirane ring formed through a reaction and in the determination of time course. Through the epoxidation, many intermediates and final products were formed, i.e., epoxides with different number and/or different position of oxirane rings in carbon chain. For the determination, three main methods (infrared spectroscopy, high-pressure liquid chromatography and gas chromatography with mass spectrometry) were applied. Only gas chromatography enables the separation of individual epoxides, which were identified on the base of the mass spectra, molecule ion and time course of products. The determination of intermediates enables: (i) control of the epoxidation process, (ii) determination of the mixture of epoxides in detail and so the calculation of selectivity of each product. Therefore, the epoxidation will be more environmentally friendly especially for advanced applications of non-edible oil crops containing high amounts of unsaturated fatty acids.

Versatile Polyoxometalates of Different Structural Dimensionalities for Liquid Phase Catalytic Oxidation

“…In the transition to a bio-based economy, the epoxidation of olefins such as fatty acid methyl esters (FAMEs) has attracted much attention because the epoxidized FAMEs (EFAMEs) have broad application profiles, e.g., for plasticizers, lubricants, polyurethanes, painting, coatings and adhesives, and improving the oxidation stability of biodiesel [1][2][3][4][5][6].…”