Abstract

(Calcium,alkali)-aluminosilicate gel frameworks are the basis of modern cements and alkali-activated materials for sustainable infrastructure and radioactive waste immobilization and also find application in glass alteration, mineral weathering, and zeolite synthesis. Here, we resolve the nanostructure of these gels that dictates mass transport, solubility, and mechanical properties. The key structural motifs comprising hydrous (calcium,alkali)-aluminosilicate gels are identified via 17O, 23Na, and 27Al triple-quantum magic angle spinning and 29Si magic angle spinning nuclear magnetic resonance spectroscopy of a novel class of stoichiometrically controlled 17O-enriched multiphase gels. Increased Ca content promotes low-Al, high-Ca chain-structured “C-S-H-type” products exhibiting significant nanostructural ordering, low levels of chain cross-linking, predominant Ca coordination of nonbridging oxygen atoms, and an increase in proton association with CaO layers to form Ca–OH sites. Al substitution is identified in multiple sites in the silicate chains, including cross-linking, bridging, and pairing tetrahedra. Increased Al content increases the proportion of cross-linking sites and gel disorder. The large increase in SiIV–O–AlIV sites increases the relative amounts of Na+ and AlV species charge-balancing AlO4– tetrahedra and results in the formation of an additional disordered low-calcium, framework-structured alkali aluminosilicate (“N-A-S-H-type”) gel, with high Al and Na contents. Changes in bulk composition significantly alter the nanostructures of the C-S-H-type and N-A-S-H-type gels. Mean SiIV–O–AlIV bond angles for each type of AlIV site environment are highly consistent, with compositional changes dictating the relative proportions of individual AlIV species but not altering the local structure of each AlIV site. These findings reveal the molecular interactions governing the (calcium,alkali)-aluminosilicate gel nanostructure, which are crucial in controlling material properties and durability.

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