Probing Carbon Mineralization Mechanisms in Pore and Bulk Fluids by Harnessing Architected Calcium Silicates

Journal Article · Mon May 05 00:00:00 UTC 2025 · Energy and Fuels

DOI: https://doi.org/10.1021/acs.energyfuels.5c00121 · OSTI ID:3001181

Asgar, Hassnain  ^[1]; Dasgupta, Nabankur ^[2]; Yin, Tianhe ^[1]; Hahn, Seung Ho  ^[3]; Kuzmenko, Ivan ^[4]; van Duin, Adri C. T.  ^[3]; Gadikota, Greeshma  ^[1]

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1. Cornell Univ., Ithaca, NY (United States)
2. Univ. of Southern California, Los Angeles, CA (United States)
3. Pennsylvania State Univ., University Park, PA (United States)
4. Argonne National Laboratory (ANL), Argonne, IL (United States). Advanced Photon Source (APS)

The ability to synthesize materials with well-controlled pore structures gives us unprecedented control over probing fluid interactions with reactive interfaces and advancing calibrated insights into coupled chemo-morphological interactions. One of the primary challenges in developing crystalline silicate materials lies in achieving ordered pore structures. Existing approaches of producing amorphous mesoporous metal silicates via sol–gel methods and heat-treatment of these materials to produce crystalline phases cause the pore structures in the amorphous phases to collapse. To overcome this challenge, carbon coating of amorphous mesoporous calcium silicate particles is carried out to retain the pore structure, while the material is heated to produce crystalline calcium silicate with calcium sulfate inclusions. The pore diameter in these materials is about 3.9 nm, with a surface area and a pore volume of 28.75 m²/g and 0.092 cm²/g, respectively. The mechanisms of carbon mineralization are investigated by reacting architected calcium silicate with 1 M Na₂CO₃ and monitoring the evolution in the structural phases using operando wide-angle X-ray scattering (WAXS) measurements. Formation of stable calcium carbonate polymorph or calcite and metastable calcium carbonate polymorph or vaterite in pore and bulk fluids, respectively, resulting from the reaction between Na₂CO₃ and CaSiO₃, are noted. The mechanisms associated with carbon mineralization are delineated using ReaxFF molecular dynamics (MD) simulations. The surface dissolution reaction is initiated by 2H⁺ ions that replace a Ca²⁺ ion in the Ca–silicate matrix. Ca²⁺ ions in the solution initially react with water to form calcium hydroxide and eventually form calcium (bi)carbonate. A slow and gradual increase in the formation of sodium silicate in the solution resulting from the reactions of silicic acid or the silicon dioxide reaction with sodium hydroxide is noted. When carbon mineralization occurs in environments bearing interfacial fluids, calcite is the dominant calcium carbonate polymorph, as determined using experiments with pore fluids and molecular-scale simulations. In conclusion, these studies provide fundamental insights into the mechanisms underlying the carbon mineralization of calcium silicate informed by experiments and molecular-scale simulations.

• Research Organization: Argonne National Laboratory (ANL), Argonne, IL (United States)
• Sponsoring Organization: National Science Foundation (NSF); USDOE Office of Science (SC), Basic Energy Sciences (BES). Scientific User Facilities (SUF)
• Grant/Contract Number: AC02-06CH11357; SC0019285; SC0020263
• OSTI ID: 3001181
• Journal Information: Energy and Fuels, Journal Name: Energy and Fuels Journal Issue: 19 Vol. 39; ISSN 1520-5029; ISSN 0887-0624
• Publisher: American Chemical Society (ACS)Copyright Statement
• Country of Publication: United States
• Language: English