Issue 15, 2024

Cycloaddition–dehydration continuous flow chemistry for renewable para-xylene production from 2,5-dimethylfuran and ethylene over phosphorous-decorated zeolite beta

Abstract

Continuous manufacturing of platform chemicals from lignocellulose is highly desirable for a fossil fuel independent future. We demonstrate highly selective production of para-xylene (pX) from ethylene and 2,5-dimethylfuran (DMF) in a packed bed microreactor using phosphorous-decorated zeolite beta (P-BEA), with pX selectivity up to 97% at 80% DMF conversion. We map the effect of reactor temperature, space velocity, concentration, gas-to-liquid ratio, and process pressure. Time-on-stream (TOS) and in situ regeneration studies show minimal productivity degradation over ∼5 h TOS and full productivity restoration upon regeneration for multiple cycles. Most non-selective Brønsted acidity occurs at low TOS and is attributed to the remaining trace Al bridge site. External mass transfer limitations are implicated at low space velocities. We combine the TOS data with NMR, XRD, and Raman to develop structure–performance insights into the catalyst behavior. A comparison with mesoporous P-supported materials illustrates that P-BEA is an excellent catalyst for size selectivity and long-term stability.

Graphical abstract: Cycloaddition–dehydration continuous flow chemistry for renewable para-xylene production from 2,5-dimethylfuran and ethylene over phosphorous-decorated zeolite beta

Supplementary files

Article information

Article type
Paper
Submitted
18 4月 2024
Accepted
29 6月 2024
First published
03 7月 2024
This article is Open Access
Creative Commons BY license

Green Chem., 2024,26, 8831-8839

Cycloaddition–dehydration continuous flow chemistry for renewable para-xylene production from 2,5-dimethylfuran and ethylene over phosphorous-decorated zeolite beta

Z. Wang, T. Goculdas, Y. W. Hsiao, W. Fan and D. G. Vlachos, Green Chem., 2024, 26, 8831 DOI: 10.1039/D4GC01904K

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