Classically, stable covalent bonding cannot occur between heavy metal cations and clay surface O atoms. However, the classical theory ignores the effect of the electric field arising from clay surface charges on the orbitals of surface O atoms. This article studies the adsorption behavior of heavy metal cations (Pb2+, Cd2+, Cu2+, and Zn2+) on charged montmorillonite surfaces from a new theoretical foundation based on the quantum mechanics analysis of surface O atoms in this electric field, which reveals that polarization-induced covalent bonding is a strong adsorption force. The strength of polarization-induced covalent bonding can be controlled by regulating the energy of the lone-pair electrons of surface O atoms, which depends on solution pH, electrolyte type, electrolyte concentration, temperature or dielectric constant of medium, etc. The mathematic relationship between the energy of lone-pair electrons of surface O atoms and electric field arising from surface charges was established through quantum mechanics analysis; and correspondingly the mathematical relationship between the polarization-induced covalent bonding energy and surface potential also was established for different heavy metal cations. The finding of the new adsorption force will have important impact on both theoretical research and removal/deactivation approaches of heavy metal cations.
Keywords: Asymmetric hybridization orbitals; Charged colloidal surface; Heavy metal cation; Polarization induced covalent bonding; Regulation of chemical bonding energy.
Copyright © 2021 The Authors. Published by Elsevier B.V. All rights reserved.