Influence of amino acids on the mobility of iodide in hydrocalumite

In the cement system, hydrocalumite is a candidate adsorbent for low-level¹²⁹ I anionic species. However, the stability of hydrocalumite after immobilizing I⁻ is unclear when they are exposed to pedosphere characterized by organic substances derived from living organisms. In the present work, five amino acids were selected as simplified models of natural organic substances under alkaline conditions. L-cysteine (H₂ Cys) and L-aspartic acid (H₂ Asp) accelerated the release of I⁻ from I-hydrocalumite through ion-exchange. Ion-exchange of Cys²⁻ with I⁻ in I-hydrocalumite was faster than Asp²⁻, and the interlayer spacing (d₀₀₃ ) of Cys-hydrocalumite was smaller than that of Asp-hydrocalumite. DFT simulations not only supported the above results but also predicted that there was a positive correlation between the formation energies and interlayer spacings of amino acids intercalated hydrocalumite, depending on the configurations. Moreover, in the DFT predictions, the interaction between amino acids and metallic hydroxide layers was responsible for the formation of hydrogen bonds and Ca-O chemical bonds between the-COO⁻ groups and [Ca₂ Al(OH)₆ ]⁺ . The other three amino acids did not show intercalation through ion-exchange. The stability of I-hydrocalumite is influenced differently by coexisting amino acids, depending on the ionic sizes, charge numbers, and hydrophilicity, which cause the second contamination.