4.2 Article

Electrolytic Seawater Mineralization and the Mass Balances That Demonstrate Carbon Dioxide Removal

Journal

ACS ES&T ENGINEERING
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsestengg.3c00004

Keywords

Carbon dioxide mineralization; calcium carbonate; hydrated magnesium carbonate; brucite; electrolysis

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This study presents the mass balances of carbon dioxide removal (CDR) using seawater through electrolysis. The process leads to the durable immobilization of CO2 and can remove approximately 4.6 kg of CO2 per m3 of seawater catholyte processed. The research provides quantifications of the Equatic process as a technological CDR method to mitigate the worst effects of climate change.
We present the mass balances associated with carbon dioxide (CO2) removal (CDR) using seawater as both the source of reactants and as the reaction medium via electrolysis following the Equatic (formerly known as SeaChange) process. This process, extensively detailed in La Plante, E.C.; et al. ACS Sustain. Chem. Eng. 2021, 9, (3), 1073-1089, involves the application of an electric overpotential that splits water to form H+ and OH- ions, producing acidity and alkalinity, i.e., in addition to gaseous coproducts, at the anode and cathode, respectively. The alkalinity that results, i.e., via the continuous electrolytic pH pump results in the instantaneous precipitation of calcium carbonate (CaCO3), hydrated magnesium carbonates (e.g., nesquehonite: MgCO3 center dot 3H2O, hydromagnesite: Mg5(CO3)4(OH)2 center dot 4H2O, etc.), and/or magnesium hydroxide (Mg(OH)2) depending on the CO32- ion-activity in solution. This results in the trapping and, hence, durable and permanent (at least similar to 10 000-100 000 years) immobilization of CO2 that was originally dissolved in water, and that is additionally drawn down from the atmosphere within: (a) mineral carbonates, and/or (b) as solvated bicarbonate (HCO3-) and carbonate (CO32-) ions (i.e., due to the absorption of atmospheric CO2 into seawater having enhanced alkalinity). Taken together, these actions result in the net removal of similar to 4.6 kg of CO2 per m3 of seawater catholyte processed. Geochemical simulations quantify the extents of net CO2 removal including the dependencies on the process configuration. It is furthermore indicated that the efficiency of realkalinization of the acidic anolyte using alkaline solids depends on their acid neutralization capacity and dissolution reactivity. We also assess changes in seawater chemistry resulting from Mg(OH)2 dissolution with emphasis on the change in seawater alkalinity and saturation state. Overall, this analysis provides direct quantifications of the ability of the Equatic process to serve as a means for technological CDR to mitigate the worst effects of accelerating climate change.

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