Post-Synthesis Strategies to Prepare Mesostructured and Hierarchical Silicates for Liquid Phase Catalytic Epoxidation

Olefin epoxidation is an important transformation for the chemical valorization of olefins, which may derive from renewable sources or domestic/industrial waste. Different post-synthesis strategies were employed to introduce molybdenum species into mesostructured and hierarchical micro-mesoporous catalysts of the type TUD-1 and BEA, respectively, to confer epoxidation activity for the conversion of relatively bulky olefins (e.g., biobased methyl oleate, DL-limonene) to epoxide products, using tert-butyl hydroperoxide as an oxidant. The influences of (i) the type of metal precursor, (ii) type of post-synthesis impregnation method, (iii) type of support and (iv) top-down versus bottom-up synthesis methodologies were studied to achieve superior catalytic performances. Higher epoxidation activity was achieved for a material prepared via (post-synthesis) incipient wetness impregnation of MoO2(acac)(2) (acac = acetylacetonate) on (pre-treated) siliceous TUD-1 and calcination; for example, methyl oleate was converted to the corresponding epoxide with 100% selectivity at 89% conversion (70 degrees C). Catalytic and solid-state characterization studies were conducted to shed light on material stability phenomena.

Automated summary

Olefin epoxidation is a significant chemical transformation that converts olefins, derived from renewable sources or waste, into valuable chemicals. Various strategies were used to introduce molybdenum species into catalytic materials, allowing efficient epoxidation of bulky olefins. The study investigated the effects of metal precursor, impregnation method, support type, and synthesis methodology on catalytic performance. The results demonstrated that the use of MoO2(acac)(2) on pre-treated siliceous TUD-1 achieved the highest epoxidation activity and selectivity for methyl oleate conversion.