Issue 1, 2025

Study of supported heteropolyacid catalysts for one-step DME synthesis from CO2 and H2

Abstract

Dimethyl ether (DME) is a versatile molecule, gaining increasing interest as a viable hydrogen and energy storage solution, pivotal for the transitioning from fossil fuels to environmentally friendly and sustainable energy supply. This research explores a novel approach for the direct conversion of CO2 to DME in a fixed-bed reactor, combining the Cu/ZnO/Al2O3 methanol synthesis catalyst with supported heteropolyacids (HPAs). First, various HPAs, both commercially available and custom-synthesized, were immobilized on Montmorillonite K10. Using a wet impregnation procedure an almost ideal mono-layer of HPA on the support was achieved. The catalysts were further evaluated for their efficiency in direct synthesis of DME from CO2/H2 in combination with the Cu/ZnO/Al2O3 catalyst. Among the catalysts tested, tungstosilicic acid (HSiW) supported on K10 exhibited the most promising performance, achieving a DME yield (YDME) of 7.06% and a molar productivity (Pmol) of 77.84 molDME molHPA−1 h−1. In a subsequent step, further tests using HSiW on various support materials identified ZrO2 as the most effective support, increasing the molar productivity to 125.44 molDME molHPA−1 h−1, while maintaining the DME yield. The results highlight the potential of applying HPA-based catalysts for sustainable DME synthesis directly from CO2, emphasizing the critical role of the catalyst support for optimizing catalytic performance.

Graphical abstract: Study of supported heteropolyacid catalysts for one-step DME synthesis from CO2 and H2

Supplementary files

Article information

Article type
Paper
Submitted
08 Nov 2024
Accepted
16 Dec 2024
First published
02 Jan 2025
This article is Open Access
Creative Commons BY license

RSC Adv., 2025,15, 38-47

Study of supported heteropolyacid catalysts for one-step DME synthesis from CO2 and H2

A. Wesner, N. Herrmann, L. Prawitt, A. Ortmann, J. Albert and M. J. Poller, RSC Adv., 2025, 15, 38 DOI: 10.1039/D4RA07964G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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