Surface chemistry-mediated porewater fluctuations boost CO2 docking in calcium silicate hydrates
Abstract While CO2 mineralization using carbonatable binders and solid waste has become an overwhelming trend in laboratory and industrial trials, a lack of fundamental understanding of the underlying carbonation mechanisms hinders advancement of carbonation technology for large-scale applications....
Saved in:
| Main Authors: | , , , , , , |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-08-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-62580-6 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
| Summary: | Abstract While CO2 mineralization using carbonatable binders and solid waste has become an overwhelming trend in laboratory and industrial trials, a lack of fundamental understanding of the underlying carbonation mechanisms hinders advancement of carbonation technology for large-scale applications. This study addresses this gap by employing Grand Canonical Monte Carlo simulations to unravel the optimal CO2 sequestration conditions within the mesopores of calcium silicate hydrates, a ubiquitous component of construction materials. Here we show that CO2-surface interactions dominate at low relative humidity (RH), while CO2-water interactions prevail at high RH, maximizing CO2 uptake during capillary condensation, where the metastable porewater boosts CO2 dissolution. Furthermore, we reveal the influence of surface hydrophilicity on the critical RH for optimal carbonation, indicating that less hydrophilic minerals require higher optimal carbonation RH. These insights into the complex CO2-water-surface interactions within minerals’ mesopores provide a foundation for developing effective CO2 mineralization strategies and advancing our understanding of geochemical carbonation processes. |
|---|---|
| ISSN: | 2041-1723 |