We have investigated the effect of solution parameters on the adsorption of phosphate ions and on charges and structures, i.e., on the nature of species, at the alpha-Al(2)O(3) colloid/solution interface by using the batch method, zeta potential measurements, and in situ ATR-FTIR spectroscopy. The uptake of phosphate decreases with the extent of surface deprotonation (i.e., pH), imparts negative charges to the colloid surface, and induces IEP shifts showing chemical sorption. Use of complementary techniques provides evidence that phosphate is sorbed at low pH (3.3) by a combination of surface reactions of complexation and precipitation, whose relative contributions depend on phosphate loading. Surface complexation includes fast reactions of ligand exchange with single coordinated hydroxyls, and electrostatic attraction of H(2)PO(4)(-) ions at positively charged surface sites. This is supported by experiments at low coverage showing sharp and linear decrease of zeta potential (i.e., surface charge) with amount of phosphate sorbed. At high coverage, zeta potential values are low and independent of phosphate loading. Formation of surface precipitates of Al-phosphate is inferred from the assignment of the ATR-FTIR absorption band at 1137cm(-1), whose intensity increases with phosphate solution content and reaction time, to the P-O-stretching vibration mode for phosphate sorbed at high concentrations on alpha-Al(2)O(3). In situ ATR-FTIR spectroscopy reveals also structural reorganizations of surface hydroxyls with time, due to surface hydration and to surface precipitation continuing over extended periods along alumina dissolution.
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