Issue 15, 2018

Supported gold- and silver-based catalysts for the selective aerobic oxidation of 5-(hydroxymethyl)furfural to 2,5-furandicarboxylic acid and 5-hydroxymethyl-2-furancarboxylic acid

Abstract

The sustainable synthesis of two important intermediates relevant for the production of bio-based polymers, 2,5-furandicarboxylic acid (FDCA) and 5-hydroxymethyl-2-furancarboxylic acid (HFCA), via oxidation of 5-(hydroxymethyl)furfural (HMF) was investigated using supported gold- and silver-based catalysts in water with air as the oxidant. High yields and selectivities for the production of FDCA (89%) and HFCA (≥98%) were achieved under the optimized reaction conditions with Au/ZrO2 and Ag/ZrO2 catalysts, respectively. While FDCA was mainly formed in the presence of gold catalysts at a maximum productivity of 67 molFDCA h−1 molAu−1, silver catalysts showed a remarkably high activity in aldehyde oxidation producing HFCA in almost quantitative yields with a maximum productivity of 400 molHFCA h−1 molAg−1. By variation of the reaction parameters, the Au/ZrO2 catalyst could be tuned to produce also HFCA, whereas the Ag/ZrO2 catalyst exclusively produced HFCA in a wide range of reaction parameters. The observed differences in catalyst selectivities can be taken as a starting point for further mechanistic investigation on the oxidation of HMF, contributing to a fundamental understanding of this reaction which is particularly important for establishing the production of bio-based polymers.

Graphical abstract: Supported gold- and silver-based catalysts for the selective aerobic oxidation of 5-(hydroxymethyl)furfural to 2,5-furandicarboxylic acid and 5-hydroxymethyl-2-furancarboxylic acid

Supplementary files

Article information

Article type
Paper
Submitted
28 abr 2018
Accepted
20 jun 2018
First published
03 jul 2018
This article is Open Access
Creative Commons BY-NC license

Green Chem., 2018,20, 3530-3541

Supported gold- and silver-based catalysts for the selective aerobic oxidation of 5-(hydroxymethyl)furfural to 2,5-furandicarboxylic acid and 5-hydroxymethyl-2-furancarboxylic acid

O. R. Schade, K. F. Kalz, D. Neukum, W. Kleist and J. Grunwaldt, Green Chem., 2018, 20, 3530 DOI: 10.1039/C8GC01340C

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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