Synergistic catalyst enables targeted cleavage of ethane C–H bonds in tandem with CO₂ activation

Synergistic sites over the ZnxZrO catalyst for targeted cleavage of the C–H bonds of ethane in tandem with CO2 activation
The tandem reaction achieved by the synergistic effect of Zn-O-Zr sites and oxygen vacancies, the ethane C–H bond was selectively clipped over the Zn-O-Zr sites and the CO2 C=O bonds was activated over the oxygen vacancies. Credit: Chinese Journal of Catalysis

Ethylene, as one of the most important light olefins, serves as a fundamental feedstock for producing various high-value-added chemical products. Industrial ethylene production primarily relies on steam cracking of ethane and naphtha feedstock, which suffers from several drawbacks including excessive energy consumption, significant carbon emissions, and severe coke deposition.

The CO2-assisted oxidative dehydrogenation of (CO2-ODHE) represents an eco-friendly process that enables resource utilization of ethane with the greenhouse gas CO2. This technology demonstrates significant potential for advancing carbon neutrality initiatives and establishing sustainable chemical production systems.

The current catalyst systems exhibit inherent limitations originating from the activity-selectivity trade-off and insufficient stability. The design of catalysts capable of simultaneously achieving selective C–H bond scission of ethane and efficient CO2 activation represents a key challenge in CO2-ODHE.

The ZnxZrO bifunctional catalyst developed in a recent study exhibits synergistic effects in the simultaneous activation of C–H and C=O bonds. Comprehensive characterization techniques were employed to probe the surface chemical states of ZnxZrO catalysts during CO2-ODHE, identifying distinct functions of active sites.

The findings are published in the Chinese Journal of Catalysis.

The Zn-O-Zr sites selectively cleave C–H bonds of ethane, while oxygen vacancies effectively activate CO2 C=O bonds, enabling synergistic conversion of ethane and CO2. In situ FTIR further elucidated the tandem reaction mechanism involving ethane dehydrogenation and reverse water-gas shift (RWGS).

This study provides fundamental insights into developing cost-effective, highly active, and stable catalysts for CO2-ODHE, while establishing a novel design strategy for targeting alkane C–H scission in olefin production and CO2 utilization.

More information: Wenjun Qiang et al, Synergistic sites over the Zn ZrO catalyst for targeted cleavage of the C–H bonds of ethane in tandem with CO2 activation, Chinese Journal of Catalysis (2025). DOI: 10.1016/S1872-2067(24)60235-4

Citation: Synergistic catalyst enables targeted cleavage of ethane C–H bonds in tandem with CO₂ activation (2025, April 21) retrieved 16 May 2025 from https://phys.org/news/2025-04-synergistic-catalyst-enables-cleavage-ethane.html
This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no part may be reproduced without the written permission. The content is provided for information purposes only.

Explore further

Researchers tailor main-group catalyst with atomically dispersed In sites for highly efficient oxidative dehydrogenation

0 shares

Feedback to editors