Control of Structural Hydrophobicity and Cation Solvation on Interlayer Water Transport during Clay Dehydration

• Published in: Nano letters 2022-04, Vol.22 (7), p.2740-2747
• Main Authors: Ho, Tuan A, Coker, Eric N, Jové-Colón, Carlos F, Wang, Yifeng
• Format: Article
• Language: English
• Subjects: Cations; chemomechanical coupling effect; Clay; Dehydration; evaporation; Humans; hydration; Hydrophobic and Hydrophilic Interactions; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; ions; layered materials; molecules; nuclear waste repositories; phyllosilicates; Water - chemistry; water transport
• ISSN: 1530-6984; 1530-6992
• DOI: 10.1021/acs.nanolett.1c04609

Swelling clay hydration/dehydration is important to many environmental and industrial processes. Experimental studies usually probe equilibrium hydration states in an averaged manner and thus cannot capture the fast water transport and structural change in interlayers during hydration/dehydration. Using molecular simulations and thermogravimetric analyses, we observe a two-stage dehydration process. The first stage is controlled by evaporation at the edges: water molecules near hydrophobic sites and the first few water molecules of the hydration shell of cations move fast to particle edges for evaporation. The second stage is controlled by slow desorption of the last 1–2 water molecules from the cations and slow transport through the interlayers. The two-stage dehydration is strongly coupled with interlayer collapse and the coordination number changes of cations, all of which depend on layer charge distribution. This mechanistic interpretation of clay dehydration can be key to the coupled chemomechanical behavior in natural/engineered barriers.