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DOE OSTI · 3002463

Catalytic Oxygen Reduction for Deep O 2 Removal from CO 2 Streams

Abstract

Streams of CO 2 from various capture processes may contain several impurities of which O 2 is often overlooked as a problematic impurity. Because of its reactivity, the National Energy Technology Laboratory has recommended a stringent limit, less than 10 ppm, for the O 2 level in treated CO 2 products for safe transport, storage, and utilization. Here, in this study, a variety of catalytic oxygen reduction approaches using commercial automotive exhaust emission catalysts are evaluated for O 2 removal from CO 2 streams using different reducing agents, including H 2 , CO, CH 3 OH, and CH 4 . When the amount of reductant added into the feed is carefully controlled, H 2 , CO, or CH 3 OH can effectively remove O 2 from 1.5% to below 10 ppm with a single-reactor design (>99.93% removal efficiency), while simultaneously meeting the impurity limits for other species. With CH 4 as a reductant, it is challenging to simultaneously meet the the O 2 and CO specifications in a single-reactor design because CH 4 also reacts with CO 2 to produce high levels of CO in the stream (at several hundred ppm). A dual-reactor design is developed to enable the use of CH 4 , a readily available and low-cost reductant, for the purification of CO 2 streams to meet the specifications for O 2 and other impurities.

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BibTeXRIS

Park, Yensil [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)], Toops, Todd J. [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)] (ORCID:0000000231638539), Majumdar, Sreshtha Sinha [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)] (ORCID:0000000203942672), Sholl, David S. [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)] (ORCID:0000000227719168), Chen, Hai-Ying [Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)] (ORCID:0000000341162607). 2025-09-16. Catalytic Oxygen Reduction for Deep O 2 Removal from CO 2 Streams. https://doi.org/10.1021/acsestengg.5c00491

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