The NO3−- and Cl−-containing layered double hydroxides (LDHs) of Mg with Al interact weakly with anions in solution under equilibrated conditions and yield a type V isotherm. The uptake of anions under nonequilibrated conditions varies monotonically with the layer charge when the outgoing anion is NO3−, whereas it goes through a maximum when the outgoing anion is Cl−. These observations suggest that Coulombic interactions play a dominant role in Cl−-LDHs, whereas weak interactions governing the mode of intercalation of NO3− ions influence the exchange reactions of NO3−-LDHs. These studies have significant implications for the remediation of insidious anions by LDHs.
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Prasanna et al. (2009) studied this question.
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