Impacts of water advection and CO 2 exchanges on the carbon dioxide removal potential of ocean alkalinity enhancement
Open accessPreprint — published as 10.5194/bg-23-7523-2026
Abstract
Abstract. Ocean alkalinity enhancement is a carbon dioxide removal strategy with high CO2 uptake potential and rather low cost. Long term modelling studies have focused on this strategy, but most laboratory experiments focus on shorter term with strong advection, which may not be representative of natural systems. Hence, the long-term fate of alkalinity is yet to be addressed. Also, the role of CO2 ingassing is still largely overlooked. In a new setup, 6-month experiments using solid Ca(OH)2 and Mg(OH)2, and liquid NaOH have been conducted with a constant supply of CO2. Bottles were either kept stagnant or exposed to slow advection. All experiments revealed lower measured TA compared to expected, but bottles subjected to advection led to nearly twice as much TA generation in some cases and significantly faster CO2 ingassing rates. This led to a quicker equilibration, decreasing the low CO2 period, lately identified as a potential threat to living organisms, and a decreased critical alkalinity period (CAP) for CaCO3 formation. Yet, CaCO3 precipitated in most bottles, either as needles with Ca(OH)2 or as “broccolis” with Mg(OH)2. Such broccoli resulted most likely from precipitation on slowly dissolving Mg(OH)2 particles. Once the CAP was over, conditions remained stable with no redissolution of the CaCO3 precipitates. Using NaOH revealed buffering by Mg(OH)2 precipitation, which ultimately redissolved in the bottles exposed to advection. Finally, the bottles exposed to advection represented open ocean conditions with wind speeds of ~3 m s-1, which, given the calm state of the ocean, may serve as a lower threshold for implementation in global models.
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In the ocean, advection energy is typically lower than in a stirred reactor, resulting in higher Ω at the mineral surface and slower dissolution rates.
“In the ocean however, advection energy is typically lower than in a stirred reactor, resulting in higher Ω at the mineral surface and slower dissolution rates. 11”
From A framework for understanding efficiency losses of Ocean Alkalinity Enhancement (2026) · cites this paper as [11]
Such precipitation may enter a runaway process, where more alkalinity is lost than the amount added.
“Such precipitation may enter a runaway process, where more alkalinity is lost than the amount added. 11,14,15,30,48,49”
From A framework for understanding efficiency losses of Ocean Alkalinity Enhancement (2026) · cites this paper as [11]
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A framework for understanding efficiency losses of Ocean Alkalinity Enhancement
Lunstrum, A., Keller, D., Hartmann, J., & Moras, C. (2026) · CDRxiv · doi:10.70212/cdrxiv.2026517.v1 · Cited by 1 · see citing works
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- Authors
- Moras, C. A., Saez Moreno, M., Bartsch, P., & Hartmann, J.
- Affiliations
- Universität Hamburg (DE)
- Venue
- Biogeosciences
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- Copernicus GmbH
- Published
- 2026-01-16
- Volume
- 23
- Issue
- 20
- Pages
- 7523-7544
- ISSN
- 1726-4170 (ISSN-L)
- OpenAlex
- W7124470142
- Cited by
- 1
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- 2026: 1
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- Helmholtz Centre for Ocean Research Kiel (GEOMAR) (submittedVersion)
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- Topics
- Physical Sciences › Environmental Science › Environmental Engineering › CO2 Sequestration and Geologic Interactions
- Physical Sciences › Earth and Planetary Sciences › Oceanography › Marine and coastal ecosystems
- Physical Sciences › Environmental Science › Global and Planetary Change › Climate Change and Geoengineering
- Keywords
- ocean alkalinity enhancement, carbon dioxide removal, water advection, total alkalinity, calcium hydroxide, magnesium hydroxide, sodium hydroxide, calcium carbonate precipitation
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