Limonene oxidation over Ti-MCM-41 and Ti-MWW catalysts with t-butyl hydroperoxide as the oxidant

This paper presents the method of limonene epoxidation over Ti-MCM-41 and Ti-MWW catalysts in the presence of t-butyl hydroperoxide as an oxidant. Natural limonene used in the epoxidation process was obtained via steam distillation (97% purity). The purpose of the research was to obtain the highest yield of 1,2-epoxylimonene, but the performed studies showed that the process of limonene epoxidation is more complex because in addition to epoxidation products (1,2-epoxylimonene and its diol which were formed usually in small amount) also the following oxygenated derivatives of limonene are formed: carvone, carveol, and perillyl alcohol (products of allylic oxidation (hydroxylation) at positions 6 and 7 in limonene molecule). Therefore, ultimately, the most favorable conditions for the limonene oxidation process were selected at the highest conversion of limonene and at high values of perillyl alcohol and carveol or one of these two products. Perillyl alcohol and carveol have found numerous applications in medicine, among others, therefore this direction seems to be the most beneficial. This also work presents the short characteristization of the titanium silicate Ti-MCM-41 and Ti-MWW catalysts used in the research, taking into account their structure, properties and applications are presented.