Abstract
Utilization of cellular materials is an effective strategy for enhancing energy efficiency and reducing emissions in the construction sector. Incorporating CO2 into aqueous foam bubbles to fabricate porous cement materials offers a new pathway for carbon sequestration. However, for CO2 gas-entraining foamed cement (CFC), stabilizing CO2-aqueous foam precursors remains a major challenge due to the high water-solubility of CO2 molecules. This study pioneered a polymer sol-based modification for producing ultra-stable CO2 foam bubbles with lifespans exceeding 8 h—20 ∼ 50 times longer than conventional foaming agents. The self-assembled 3D colloidal networks within the foam films exhibited high viscosity, modulus, and low CO2 gas permeability, significantly improving CO2 foam stability. Two new indices, drainage and coalescence factors, were first proposed to guide CO2 foam design. Accordingly, the engineered CO2 foams successfully created CFC with ultra-low density (∼300 kg/m3), excellent strength (superior to normal foamed concrete), low thermal conductivity, and considerable CO2 storage capacity. The CO2 foams also facilitated internal CO2 mineralization effect by in-situ growing micro calcite and nano aragonite on pore walls. The findings of this study resolve the critical issue of CO2 foam stability and provide new insights for the design and fabrication of carbon-sink construction materials.
| Original language | English |
|---|---|
| Article number | 163477 |
| Journal | Chemical Engineering Journal |
| Volume | 515 |
| DOIs | |
| State | Published - 1 Jul 2025 |
| Externally published | Yes |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 7 Affordable and Clean Energy
Keywords
- CO foams
- Foam stability
- Internal CO mineralization
- Physicochemical dynamics
- Pore structure
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