Aggregation and Colloidal Stability of Commercially Available Al(2)O(3) Nanoparticles in Aqueous Environments

The aggregation and colloidal stability of three, commercially-available, gamma-aluminum oxide nanoparticles (γ-Al(2)O(3) NPs) (nominally 5, 10, and 20–30 nm) were systematically examined as a function of pH, ionic strength, humic acid (HA) or clay minerals (e.g., montmorillonite) concentration using dynamic light scattering and transmission electron microscopy techniques. NPs possess pH-dependent surface charges, with a point of zero charge (PZC) of pH 7.5 to 8. When pH < PZC, γ-Al(2)O(3) NPs are colloidally stable up to 100 mM NaCl and 30 mM CaCl(2). However, significant aggregation of NPs is pronounced in both electrolytes at high ionic strength. In mixed systems, both HA and montmorillonite enhance NP colloidal stability through electrostatic interactions and steric hindrance when pH ≤ PZC, whereas their surface interactions are quite limited when pH > PZC. Even when pH approximates PZC, NPs became stable at a HA concentration of 1 mg·L(−1). The magnitude of interactions and dominant sites of interaction (basal planes versus edge sites) are significantly dependent on pH because both NPs and montmorillonite have pH-dependent (conditional) surface charges. Thus, solution pH, ionic strength, and the presence of natural colloids greatly modify the surface conditions of commercial γ-Al(2)O(3) NPs, affecting aggregation and colloidal stability significantly in the aqueous environment.