Abstract
The mechanism of natural organic matter (NOM) removal by AlCl 3 and polyaluminum chloride (PACl) was investigated through bench-scale tests. The fraction distributions of NOM and residual Al after coagulation in solution, colloid and sediment were analyzed as changes of coagulant dosage and pH. The influence of NOM, coagulant dose and pH on coagulation kinetics of AlCl 3 was investigated using photometric dispersion analyzer compared with PACl. Monomeric Al species (Al a) shows high ability to satisfy some unsaturated coordinate bonds of NOM to facilitate particle and NOM removal, while most of the flocs formed by Al a are small and difficult to settle. Medium polymerized Al species (Al b) can destabilize particle and NOM efficiently, while some flocs formed by Al b are not large and not easy to precipitate as compared to those formed by colloidal or solid Al species (Al c). Thus, Al c could adsorb and remove NOM efficiently. The removal of contaminant by species of Al a, Al b and Al c follows mechanisms of complexation, neutralization and adsorption, respectively. Unlike preformed Al b in PACl, in-situ-formed Al b can remove NOM and particle more efficiently via the mechanism of further hydrolysis and transfer into Al c during coagulation. While the presence of NOM would reduce Al b formed in-situ due to the complexation of NOM and Al a.
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