New research could extend the lifetime of key carbon-capture materials

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New research could extend the lifetime of key carbon-capture materials

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Atomistic simulations, machine learning potential and accelerated degradation experiments reveal the complex role of CO2 in the oxidation kinetics of amine-functional sorbents for carbon capture. Credit: Illustration concept: Sichi Li/LLNL; Illustration: Jacob Long and Adam Samuel Connell/LLNL

Researchers at Lawrence Livermore National Laboratory (LLNL), in collaboration with the Georgia Institute of Technology, have made a significant breakthrough in understanding the impact of carbon dioxide (CO₂) on the stability of amine-functionalized porous solid materials, a crucial component in direct air capture (DAC) carbon-capture technologies.

This new research,

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in the Journal of the ********* Chemical Society and featured on the journal cover, sheds light on the complex interactions between CO₂ and poly(ethylenimine) sorbents, offering important insights that could enhance the efficiency and durability of DAC systems.

“This study underscores the importance of considering all atmospheric components in the design of DAC processes and materials,” said Simon Pang, corresponding author and principal investigator of the project. “Our findings will be instrumental in developing next-generation sorbents with enhanced durability, contributing to more efficient and cost-effective carbon-capture solutions.”

Amine-based sorbents are at the forefront of DAC technology due to their exceptional ability to efficiently capture CO₂ even at ultra-dilute conditions. However, the long-term stability of these materials has been a significant challenge, primarily due to oxidative degradation.

The research team investigated the previously unresolved role of CO₂ in the oxidative degradation process of these sorbents, reconciling conflicting data in existing literature. The study reveals that CO₂ exerts a non-monotonic effect on the oxidation kinetics of poly(ethylenimine) sorbents, with its impact varying significantly depending on temperature and CO₂ concentration.

“Our research highlights the dual role of CO₂ in the oxidation process,” said Sichi Li, lead author of the paper and co-investigator of the project. “On one hand, CO₂ catalyzes critical oxidation reactions, while on the other, it reduces polymer branch mobility, which slows down ******** propagation. These contrasting effects are key to understanding the complex degradation profiles we observed.”

The study’s conclusions extend beyond reconciling existing literature, offering practical implications for the future of DAC technology. By identifying polymer side chain mobility and the presence of acidic environments as major factors accelerating oxidation, the research suggests new strategies to enhance sorbent longevity. Potential solutions include the introduction of functional groups, additives or oxide supports with surface chemistry designed to reduce polymer mobility or neutralize acidic conditions, thereby mitigating the rate of oxidative degradation.

More information:
Sichi Li et al, Competing Kinetic Consequences of CO₂ on the Oxidative Degradation of Branched Poly(ethylenimine), Journal of the ********* Chemical Society (2024).

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Provided by
Lawrence Livermore National Laboratory

Citation:
New research could extend the lifetime of key carbon-capture materials (2024, September 26)
retrieved 26 September 2024
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