The natures of the pyrogenic alumina/silica (AS) surface and water
adsorbed on AS were studied by 1H
NMR, infrared (IR), dielectric relaxation (DRS), and optical
spectroscopies, thermally stimulated
depolarization (TSD), and quantum chemical methods. An influence
of the alumina content on the AS
characteristics is nonlinear and stronger for the boundary of
air/adsorbed water/oxide than for the liquid
water/oxide interface. The 1H NMR study shows that the
AS particles in aqueous suspension can strongly
disturb 6−14 monolayers of interfacial water unfrozen at 200 K <
T < 273 K. The alumina content does
not have potent effects on the IR spectra independently of pretreatment
temperatures, but other experiments
exhibit the marked influence of the AS constitution on the oxide
properties that is caused by both the
alumina phase and the phase boundary of
Al2O3/SiO2. The theoretical
simulation demonstrates that
adsorbed water can promote dissociative adsorption and associative
desorption of water molecules especially
in the regions of contact between the alumina and silica fragments in
the AS particles, where the Brønsted
acid sites are located and the adsorbed water clusters have a maximum
size according to DRS and TSD
data.