CO(2) Adsorption Enhanced by Tuning the Layer Charge in a Clay Mineral

[Image: see text] Due to the compact two-dimensional interlayer pore space and the high density of interlayer molecular adsorption sites, clay minerals are competitive adsorption materials for carbon dioxide capture. We demonstrate that with a decreasing interlayer surface charge in a clay mineral, the adsorption capacity for CO(2) increases, while the pressure threshold for adsorption and swelling in response to CO(2) decreases. Synthetic nickel-exchanged fluorohectorite was investigated with three different layer charges varying from 0.3 to 0.7 per formula unit of Si(4)O(10)F(2). We associate the mechanism for the higher CO(2) adsorption with more accessible space and adsorption sites for CO(2) within the interlayers. The low onset pressure for the lower-charge clay is attributed to weaker cohesion due to the attractive electrostatic forces between the layers. The excess adsorption capacity of the clay is measured to be 8.6, 6.5, and 4.5 wt % for the lowest, intermediate, and highest layer charges, respectively. Upon release of CO(2), the highest-layer charge clay retains significantly more CO(2). This pressure hysteresis is related to the same cohesion mechanism, where CO(2) is first released from the edges of the particles thereby closing exit paths and trapping the molecules in the center of the clay particles.