We've updated our Privacy Policy to make it clearer how we use your personal data. We use cookies to provide you with a better experience. You can read our Cookie Policy here.


Conversion Process Turns Greenhouse Gas Into Ethylene

Smoke coming from factory chimneys.
Credit: Johannes Plenio / Unsplash.
Listen with
Register for free to listen to this article
Thank you. Listen to this article using the player above.

Want to listen to this article for FREE?

Complete the form below to unlock access to ALL audio articles.

Read time: 2 minutes

Engineers at the University of Cincinnati created a more efficient way of converting carbon dioxide into valuable products while simultaneously addressing climate change.

In his chemical engineering lab in UC’s College of Engineering and Applied Science, Associate Professor Jingjie Wu and his team found that a modified copper catalyst improves the electrochemical conversion of carbon dioxide into ethylene, the key ingredient in plastic and a myriad of other uses.

Ethylene has been called “the world’s most important chemical.” It is certainly among the most commonly produced chemicals, used in everything from textiles to antifreeze to vinyl. The chemical industry generated 225 million metric tons of ethylene in 2022.

Want more breaking news?

Subscribe to Technology Networks’ daily newsletter, delivering breaking science news straight to your inbox every day.

Subscribe for FREE

Wu said the process holds promise for one day producing ethylene through green energy instead of fossil fuels. It has the added benefit of removing carbon from the atmosphere.

“Ethylene is a pivotal platform chemical globally, but the conventional steam-cracking process for its production emits substantial carbon dioxide,” Wu said. “By utilizing carbon dioxide as a feedstock rather than depending on fossil fuels, we can effectively recycle carbon dioxide.”

The study was published in the journal Nature Chemical Engineering.

Wu’s students, including lead author and UC graduate Zhengyuan Li, collaborated with Rice University, Oak Ridge National Laboratory, Brookhaven National Laboratory, Stony Brook University and Arizona State University. Li received a prestigious graduate student award last year from the College of Engineering and Applied Science.

The electrocatalytic conversion of carbon dioxide produces two primary carbon products, ethylene and ethanol. Researchers found that using a modified copper catalyst produced more ethylene.

“Our research offers essential insights into the divergence between ethylene and ethanol during electrochemical CO2 reduction and proposes a viable approach to directing selectivity toward ethylene,” lead author Li said.

“This leads to an impressive 50% increase in ethylene selectivity,” Wu said. “Ideally, the goal is to produce a single product rather than multiple ones.”

Sponsored by the U.S. Department of Energy’s Office of Energy Efficiency and Renewable Energy. Its Industrial Efficiency and Decarbonization Office is leading efforts to reduce fossil fuels and carbon emissions in industry wherever possible.

Li said the next step is refining the process to make it more commercially viable. The conversion system loses efficiency as byproducts of the reaction such as potassium hydroxide begin forming on the copper catalyst.

“The electrode stability must be improved for commercial deployment. Our next focus is to enhance stability and extend its operation from 1,000 to 100,000 hours,” Li said.

Wu said these new technologies will help make the chemical industry greener and more energy efficient.

“The overarching objective is to decarbonize chemical production by utilizing renewable electricity and sustainable feedstock,” Wu said. “Electrifying the conversion of carbon dioxide to ethylene marks a significant stride in decarbonizing the chemical sector.”

Reference: Li Z, Wang P, Lyu X, et al. Directing CO2 electroreduction pathways for selective C2 product formation using single-site doped copper catalysts. Nat Chem Eng. 2024;1(2):159-169. doi: 10.1038/s44286-023-00018-w

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.