Biphasic solvents for post-combustion CO2 capture from natural gas flue Gas

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Abstract

Fossil fuel fired power plants are generally expected to remain one of the most significant global sources of electricity for decades to come. Consequently, carbon management technologies are needed to reduce or eliminate ongoing emissions from these sources. Amongst the many techniques for carbon capture, aqueous amine-based absorbents (monoethanolamine, MEA, in particular) are, presently, considered the leading technology for post-combustion CO2 point-source capture. These technologies are nevertheless limited by their high capital and regeneration energy costs. Biphasic solvents have been identified as an attractive alternative to traditional MEA based absorbents due to their potential energy savings. Thus far, however, the research on biphasic solvents has largely focused on their performance in coal flue gas while more dilute natural gas flue gas applications have received relatively little attention. This work examines the performances of two novel biphasic solvent blends, diethylenetriamine (DETA) and triethylenetetramine (TETA), in CO2 capture from a natural gas flue gas simulant. Across several regeneration tests, both solvents achieved considerable energy savings over the benchmark MEA solution. Specifically, the energy consumption per mol CO2 recovered for the DETA-based and TETA-based solvents was 46 % and 35 % less than that of the benchmark MEA solution, respectively. Molecular dynamics simulations were also performed to gain a deeper understanding of the phase separation phenomena that occur as a consequence of CO2 absorption. These simulations indicated that phase change was driven by the strong interaction between the absorption products and water, while the degree of separation depended on the CO2 loading.

Original languageEnglish
Article number163351
JournalChemical Engineering Journal
Volume514
DOIs
StatePublished - Jun 15 2025

Funding

This work was supported by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory (ORNL), which is managed by UT-Battelle, LLC, for the US Department of Energy (DOE) under contract DE-AC05-00OR22725. This research used resources from the Compute and Data Environment for Science (CADES) at the Oak Ridge National Laboratory, which is supported by the Office of Science of the U.S. Department of Energy under Contract No. DE-AC05-00OR22725 and National Energy Research Scientific Computing Center (NERSC), a DOE Office of Science User Facility for access to additional supercomputing resources. This work is a part of a user project at the Center for Nanophase Materials Sciences (CNMS), a US Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory.

Keywords

  • Biphasic solvents
  • CO capture
  • DETA
  • Post-combustion capture
  • TETA

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