Impact of alkali on the passivation of silicate glass

Marie Collin (1) , Maxime Fournier (1) , Thibault Charpentier (2) , Mélanie Moskura (2) , S. Gin (1)

1 DPME - Département de recherche sur les Procédés et Matériaux pour les Environnements complexes
2 LSDRM - Laboratoire Structure et Dynamique par Résonance Magnétique (LCF)

Amorphous silica-rich surface layers, also called gels, can passivate silicate glass and minerals depending on environmental conditions. However, several uncertainties remain on the mechanisms controlling the formation of these layers. In this paper, the influence of exogenous ions supplied by solutions is studied, both on the formation and on the properties of the gel formed on international simple glass (ISG). ISG was altered at 90 °C, pH$_{90°C}$ 7, in silica-saturated solutions containing various alkaline cations separately (Li$^+$ , Na$^+$ , K$^+$ , and Cs$^+$). The alteration kinetics observed with Li and Na in the solution is similar to that observed with no ions, while K and Cs in the solution tend to decrease glass alteration. Furthermore, for K or Cs ions, the kinetics decreases as the ionic strength of the solution increases. The passivation layer formed in these solutions shows a selectivity toward cations following the series K > Cs > Na >> Li. These alkalis replace Ca from pristine glass in the altered structures, leading to differences in [AlO$_4$] − units charge compensation. Importantly, exchange between Ca and alkali also affects the total quantity of water inside each gel and this effect is well correlated with the observed drop in glass alteration.

Domains: Material chemistry

Marie Collin, Maxime Fournier, Thibault Charpentier, Mélanie Moskura, S. Gin. Impact of alkali on the passivation of silicate glass. npj Materials Degradation, 2018, 2, pp.16. ⟨10.1038/s41529-018-0036-3⟩. ⟨cea-01800770⟩