Direct propylene epoxidation with molecular oxygen over titanosilicate zeolites.

Natl Sci Rev

Key Laboratory of Advanced Energy Materials Chemistry of Ministry of Education, College of Chemistry, Nankai University, Tianjin 300071, China.

Published: November 2024

AI Article Synopsis

  • The direct conversion of propylene to propylene oxide (PO) using molecular oxygen offers a highly efficient production method, known as aerobic epoxidation, but faces challenges in balancing conversion rates and PO selectivity.
  • Researchers have found that Ti-Beta zeolites with isolated titanium species can effectively catalyze this reaction, achieving a consistent propylene conversion of 25% along with a PO selectivity of up to 90%, comparable to industrial methods for ethylene.
  • The study highlights that specific titanium sites in the zeolite frameworks facilitate the reaction; these findings may lead to more sustainable practices in PO production within the chemical industry.

Article Abstract

The direct epoxidation of propylene with molecular oxygen represents a desired route for propylene oxide (PO) production with 100% theoretical atomic economy. However, this aerobic epoxidation reaction suffers from the apparent trade-off between propylene conversion and PO selectivity, and remains a key challenge in catalysis. We report that Ti-Beta zeolites containing isolated framework Ti species can efficiently catalyze the aerobic epoxidation of propylene. Stable propylene conversion of 25% and PO selectivity of up to 90% are achieved at the same time, matching the levels of industrial ethylene aerobic epoxidation processes. H-terminated pentacoordinated Ti species in Beta zeolite frameworks are identified as the preferred active sites for propylene aerobic epoxidation and the reaction is initiated by the participation of lattice oxygen in Ti-OH. These results are expected to spark new technology for the industrial production of PO toward more sustainable chemistry and chemical engineering.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11493086PMC
http://dx.doi.org/10.1093/nsr/nwae305DOI Listing

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