Revolutionizing Carbon Capture: Berkeley’s Breakthrough Tackles Industrial Emissions Head-On

Researchers have developed a metal-organic framework that effectively captures CO₂ at temperatures typical of industrial exhausts, such as those from cement and steel plants.

Unlike traditional methods, which require cooling of exhausts, this new material operates efficiently at up to 300 °C (570 °F), offering a promising solution for hard-to-decarbonize industries.

High-Temperature CO₂ Capture Challenges

Industrial plants, like those that manufacture cement or steel, release large amounts of carbon dioxide, a powerful greenhouse gas. However, their exhaust is often too hot for current carbon removal technologies, which require a lot of energy and water to cool down these hot gas streams. This cooling requirement has made it difficult for some of the highest-emitting industries to adopt CO₂ capture.

Now, chemists at the University of California, Berkeley, have discovered that a porous material can act like a sponge to capture CO₂ at temperatures close to those of many industrial exhaust streams. The material — a type of metal-organic framework, or MOF — will be described in a paper that will be published in the November 15 print edition of the journal Science.

The dominant method for capturing carbon from power or industrial plant emissions employs liquid amines to absorb CO₂, but the reaction only works efficiently at temperatures between 40 and 60 °C (100–140 °F). Cement manufacturing and steelmaking plants produce exhaust that exceeds 200 °C (400 °F), and some industrial exhaust approaches 500 °C (930 °F). New materials that are now being piloted, including a subclass of MOFs with added amines, break down at temperatures above 150 °C (300 °F) or work far less efficiently.

Advantages of MOFs in Carbon Capture

“A costly infrastructure is necessary to take these hot gas streams and cool them to the appropriate temperatures for existing carbon capture technologies to work,” said UC Berkeley postdoctoral fellow Kurtis Carsch, one of two co-first authors of the paper. “Our discovery is poised to change how scientists think about carbon capture. We’ve found that a MOF can capture carbon dioxide at unprecedentedly high temperatures — temperatures that are relevant for many CO₂ emitting processes. This was something that was previously not considered as possible for a porous material.”

“Our work moves away from the prevalent study of amine-based carbon capture systems and demonstrates a new mechanism for carbon capture in a MOF that enables high-temperature operation,” said UC Berkeley graduate student and co-first author Rachel Rohde.

Experimental Success and Future Potential

Like all MOFs, the material features a porous, crystalline array of metal ions and organic linkers, with an internal area equivalent to about six football fields per tablespoon — a huge area for adsorbing gases.

“As a result of their unique structures, MOFs have a high density of sites where you can capture and release CO₂ under the appropriate conditions,” Carsch said.

Under simulated conditions, the researchers showed that this new type of MOF can capture hot CO₂ at concentrations relevant to the exhaust streams of cement and steel manufacturing plants, which average 20% to 30% CO₂, as well as less concentrated emissions from natural gas power plants, which contain about 4% CO₂.

Moving Beyond Traditional Carbon Capture

Removing CO₂ from industrial and power plant emissions, after which it is either stored underground or used to make fuels or other value-added chemicals, is a key strategy for reducing greenhouse gases that are warming Earth and altering the climate globally. While renewable energy sources are already reducing the need for CO₂-emitting, fossil fuel-burning power plants, industrial plants that make intense use of fossil fuels are harder to make sustainable, so flue gas capture is essential.

“We need to start thinking about the CO₂ emissions from industries, like making steel and making cement, that are hard to decarbonize, because it’s likely that they’re still going to be emitting CO_2, even as our energy infrastructure shifts more toward renewables,” Rohde said.

The Future of Carbon Capture Technology

Rohde and Carsch conduct research in the lab of Jeffrey Long, UC Berkeley professor of chemistry, chemical and biomolecular engineering, and of materials science and engineering. Long has been conducting research on CO₂-adsorbing MOFs for more than a decade. His lab created a promising material in 2015 that was further developed by Long’s startup company, Mosaic Materials, which in 2022 was acquired by the energy technology company Baker Hughes. This material features amines that capture the CO₂; next-generation variants are being tested as alternatives to aqueous amines for CO₂ capture in pilot-scale plants, and as a way to capture CO₂ directly from ambient air.

But those MOFs, like other porous adsorbents, are ineffective at the elevated temperatures associated with many flue gases, Carsch said.

Amine-based adsorbents, like those developed by Long, have been the focus of carbon capture research for decades. The MOF studied by Rohde, Carsch, Long and their colleagues instead features pores decorated with zinc hydride sites, which also bind CO₂. These sites turned out to be surprisingly stable, Rohde said.

Stability and Effectiveness of New MOF Material

“Molecular metal hydrides can be reactive and have low stability,” Rohde said. “This material is highly stable and does something called deep carbon capture, which means it can capture 90% or more of the CO₂ that it comes into contact with, which is really what you need for point-source capture. And it has CO₂ capacities comparable to the amine-appended MOFs, though at much higher temperatures.”

Once the MOF is filled with CO₂, the CO₂ can be removed, or desorbed, by lowering the partial pressure of CO₂, either by flushing with a different gas or putting it in a vacuum. The MOF is then ready to be reused for another adsorption cycle.

High-Temperature Performance and Research Directions

“Because entropy favors having molecules like CO₂ in the gas phase more and more with increasing temperature, it was generally thought to be impossible to capture such molecules with a porous solid at temperatures above 200 C,” Long said. “This work shows that with the right functionality — here, zinc hydride sites — rapid, reversible, high-capacity capture of CO₂ can indeed be accomplished at high temperatures such as 300 °C.”

Rohde, Long and their colleagues are exploring variants of this metal hydride MOF to see what other gases they can adsorb, and also modifications that will allow such materials to adsorb even more CO₂.

“We’re fortunate to have made this discovery, which has opened up new directions in separation science focused on the design of functional adsorbents that can operate at high temperatures,” said Carsch, who has taken a faculty position in the Department of Chemistry at The University of Texas at Austin. “There’s a tremendous number of ways we can tune the metal ion and linker in MOFs, such that it may be possible to rationally design such adsorbents for other high-temperature gas separation processes relevant to industry and sustainability.”

Reference: “High-temperature carbon dioxide capture in a porous material with terminal zinc hydride sites” by Rachel C. Rohde, Kurtis M. Carsch, Matthew N. Dods, Henry Z. H. Jiang, Alexandra R. McIsaac, Ryan A. Klein, Hyunchul Kwon, Sarah L. Karstens, Yang Wang, Adrian J. Huang, Jordan W. Taylor, Yuto Yabuuchi, Nikolay V. Tkachenko, Katie R. Meihaus, Hiroyasu Furukawa, Danielle R. Yahne, Kaitlyn E. Engler, Karen C. Bustillo, Andrew M. Minor, Jeffrey A. Reimer, Martin Head-Gordon, Craig M. Brown and Jeffrey R. Long, 14 November 2024, Science.
DOI: 10.1126/science.adk5697

Other authors of the paper are Jeffrey Reimer, a UC Berkeley professor of chemical and biomolecular engineering, whose lab provided evidence from NMR spectroscopy to support the unique mechanism of CO₂ capture by the zinc hydride sites in the MOF; Craig Brown of the National Institute of Standards and Technology in Gaithersburg, Maryland, who also provided critical structural data supporting the proposed mechanism; and UC Berkeley chemistry professor Martin Head-Gordon, whose lab provided a computational understanding of the high-temperature CO₂ capture behavior. Other UC Berkeley authors include Andrew Minor, a UC Berkeley professor of materials science and engineering, and Matthew Dods, Henry Jiang, Alexandra McIsaac, Hyunchul Kwon, Sarah Karstens, Yang Wang, Adrian Huang, Jordan Taylor, Yuto Yabuuchi, Nikolay Tkachenko, Katie Meihaus, Hiroyasu Furukawa and Kaitlyn Engler.

Rohde was supported by a graduate fellowship from the National Aeronautics and Space Administration, while Carsch was supported by a postdoctoral fellowship from the Arnold O. Beckman Foundation.

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