(509d) Optimization of Reaction Conditions in the Epoxidation and Hydroxylation of High-Oleic Palm Oil
AIChE Annual Meeting
2021
2021 Annual Meeting
Catalysis and Reaction Engineering Division
Poster Session: Catalysis and Reaction Engineering (CRE) Division
Wednesday, November 10, 2021 - 3:30pm to 5:00pm
The higher content of unsaturated fatty acid chains confers this oil suitable properties for further valorization, in particular, it could be used as feedstock in the production of epoxides and polyols, which have a large demand in the manufacture of polymers and resins.
Polyols are produced from vegetable oils by epoxidation of the double bounds in the unsaturated fatty acid chains, followed by hydroxylation with a proton donor. Epoxidation is generally carried out by mean of reaction with H2O2, with acid catalysts. Under these conditions, water can drive oxirane ring opening resulting in polyols with less reactive secondary hydroxyl groups. Generally, polyols with primary hydroxyl groups are commercially referred, so there is need to reduce the simultaneous ring opening reaction and to improve selectivity towards the epoxide. In this regard, a simplex algorithm was experimentally implemented to identify the operating conditions that improve conversion and that maximize the oxygen oxirane content.
In a subsequent stage, and to assess the main characteristics of natural oil polyols (hydroxyl value, molecular weight, viscosity, functionality), different ring opening agents were used during hydroxylation, namely diethylene glycol, ethylene glycol and glycerol. Simplex algorithm was used to enhance the reaction yield and the hydroxyl value.