Demonstration-scale CO2 capture and liquefaction at the Amager Bakke waste-to-energy facility with monoethanolamine, Part one: Efficiency, CO2 purity, and emission control

The integration of CO 2 capture at waste-to-energy (WtE) facilities can provide carbon-neutral electricity and district heating, and treat residual waste streams. However, before full-scale implementation, a better understanding of the production of liquid CO 2 and emissions from the capture process is required. This study investigates the performance of a CO 2 capture demonstration-scale unit, including CO 2 liquefaction at the Amager Bakke WtE facility, covering topics including efficiencies, CO 2 purity, and emission control. The demonstration unit has a capacity of 4 t CO 2 d − 1 and is capable of capturing and conditioning CO 2 to food-grade-compliant purity for utilization by local consumers. The unit was operated for five months, using 35 wt% monoethanolamine (MEA) solvent. During the five months of operation, seven experimental campaigns with different objectives were conducted to optimize energy performance, evaluate flue-gas emissions, and monitor the quality of the produced CO 2 . Across 2002 h of on-stream time the specific reboiler duty (SRD) averaged 3.73–4.18 GJ t CO 2 − 1 , fully consistent with the best values reported for 30–35 wt% MEA systems. Production of liquid CO 2 totalled 193 t CO 2 , corresponding to an 84 % overall recovery, while a 12 % loss was observed between absorber and storage tank. The specific solvent consumption was 2.43 kg MEA t CO 2 − 1 . The most significant contributor to solvent loss was oxidative degradation to NH 3 . Peak NH 3 slip reached 75 ppmv and showed a positive correlation with both absorber temperature and dissolved‑iron level (up to 600 mg L − 1 ). Lastly, the effect of thermal reclaiming is qualitatively reported. Finally, the purity of the produced liquid CO 2 for export was measured and compared with the degradation of the solvent. All consignments met Northern Lights transport limits and EIGA beverage-grade specifications; typical impurities were <5 ppmv O 2 , <1 ppmv SO x , and <0.05 ppmv amine. We produced high-purity liquid CO 2 , with impurity levels in compliance with commercial CO 2 specifications, but found significant challenges related to amine degradation that must be solved before full-scale implementation. • Demonstration-scale CO 2 capture and liquefaction at Amager Bakke WtE • Achieved solvent consumption of 2.43 kg MEA per ton of CO 2 captured • Produced CO 2 met commercial purity standards for industrial use • Oxidative degradation was the main cause of solvent loss. • A correlation was found between solvent degradation and NH 3 slip.

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Publication Details

Journal
Chemical Engineering Journal
Published
2025-08-29
DOI
https://doi.org/10.1016/j.cej.2025.167465
Citations
2
Primary Topic
Carbon Dioxide Capture Technologies
Type
article
Field-Weighted Citation Impact
1.43
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article

Demonstration-scale CO2 capture and liquefaction at the Amager Bakke waste-to-energy facility with monoethanolamine, Part one: Efficiency, CO2 purity, and emission control

Christian Riber, Brian Elmegaard, Jonas Nedenskov, Jens Kristian Jørsboe et al.
2 citations
Chemical Engineering Journal
Carbon Dioxide Capture Technologies
1.43
article

Demonstration-scale CO2 capture and liquefaction at the Amager Bakke waste-to-energy facility with monoethanolamine, Part one: Efficiency, CO2 purity, and emission control

Christian Riber, Brian Elmegaard, Jonas Nedenskov, Jens Kristian Jørsboe, Jannik Kappel, Isaac Appelquist Løge, Philip Loldrup Fosbøl, Ebbe Hauge Jensen, Søren Holdt Jensen, Peter Volsing Rahbek
article en
2 citations

Abstract

The integration of CO 2 capture at waste-to-energy (WtE) facilities can provide carbon-neutral electricity and district heating, and treat residual waste streams. However, before full-scale implementation, a better understanding of the production of liquid CO 2 and emissions from the capture process is required. This study investigates the performance of a CO 2 capture demonstration-scale unit, including CO 2 liquefaction at the Amager Bakke WtE facility, covering topics including efficiencies, CO 2 purity, and emission control. The demonstration unit has a capacity of 4 t CO 2 d − 1 and is capable of capturing and conditioning CO 2 to food-grade-compliant purity for utilization by local consumers. The unit was operated for five months, using 35 wt% monoethanolamine (MEA) solvent. During the five months of operation, seven experimental campaigns with different objectives were conducted to optimize energy performance, evaluate flue-gas emissions, and monitor the quality of the produced CO 2 . Across 2002 h of on-stream time the specific reboiler duty (SRD) averaged 3.73–4.18 GJ t CO 2 − 1 , fully consistent with the best values reported for 30–35 wt% MEA systems. Production of liquid CO 2 totalled 193 t CO 2 , corresponding to an 84 % overall recovery, while a 12 % loss was observed between absorber and storage tank. The specific solvent consumption was 2.43 kg MEA t CO 2 − 1 . The most significant contributor to solvent loss was oxidative degradation to NH 3 . Peak NH 3 slip reached 75 ppmv and showed a positive correlation with both absorber temperature and dissolved‑iron level (up to 600 mg L − 1 ). Lastly, the effect of thermal reclaiming is qualitatively reported. Finally, the purity of the produced liquid CO 2 for export was measured and compared with the degradation of the solvent. All consignments met Northern Lights transport limits and EIGA beverage-grade specifications; typical impurities were <5 ppmv O 2 , <1 ppmv SO x , and <0.05 ppmv amine. We produced high-purity liquid CO 2 , with impurity levels in compliance with commercial CO 2 specifications, but found significant challenges related to amine degradation that must be solved before full-scale implementation. • Demonstration-scale CO 2 capture and liquefaction at Amager Bakke WtE • Achieved solvent consumption of 2.43 kg MEA per ton of CO 2 captured • Produced CO 2 met commercial purity standards for industrial use • Oxidative degradation was the main cause of solvent loss. • A correlation was found between solvent degradation and NH 3 slip.

Chemical Engineering JournalVol. 524
Amager Hospital (DK), Chr. Hansen (Denmark) (DK), NeuroSearch (Denmark) (DK), Technical University of Denmark (DK)
Affordable and clean energy
Openalex Percentile: Top 18%
Carbon Dioxide Capture Technologies
1.43
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