Issue 11, 2024

Selective hydrogenolysis of furfural to 1,2-pentanediol over a Pt–Fe/MT catalyst under mild conditions

Abstract

Furfural is a large-volume and widely available biomass-derived platform compound, and its transformation into valuable pentanediols is important for the sustainable production of bio-based polymers. Herein, we report a new catalyst system composed of Pt–Fe bimetallic nanoparticles highly dispersed on a commercial magnesium titanate (MT) support. HAADF-STEM, CO-DRIFTS and XPS characterization studies revealed that Pt was in the metallic state with a particle size of 1–2 nm, while Fe existed as Fe2+ and was decorated on the Pt particles. The electron transfer from Fe to Pt weakened the hydrogenation activity of the furan ring and meanwhile promoted selective ring-opening to 1,2-pentanediol (1,2-PeD). Reaction kinetics studies revealed the reaction rate with respect to hydrogen pressure was close to zero order, which allowed the reaction to proceed at a hydrogen pressure as low as 0.1 MPa. Under mild conditions of 140 °C and 0.1 MPa, the 0.1Pt0.05Fe/MT catalyst offered by far the highest production rate of 178 mol 1,2-PeD per mol Pt per hour, and the Pt–Fe bimetallic catalyst was stable during 200 h of time-on-stream, showing great potential for practical applications.

Graphical abstract: Selective hydrogenolysis of furfural to 1,2-pentanediol over a Pt–Fe/MT catalyst under mild conditions

Supplementary files

Article information

Article type
Paper
Submitted
04 2 2024
Accepted
17 4 2024
First published
30 4 2024

Green Chem., 2024,26, 6511-6519

Selective hydrogenolysis of furfural to 1,2-pentanediol over a Pt–Fe/MT catalyst under mild conditions

C. Cao, W. Guan, Q. Liu, L. Li, Y. Su, F. Liu, A. Wang and T. Zhang, Green Chem., 2024, 26, 6511 DOI: 10.1039/D4GC00642A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements