Flocculation kinetics of low-turbidity raw water and the irreversible floc breakup process

Abstract

ABSTRACTThe main objective of this study was to propose an improvement to the flocculation kinetics model presented by Argaman and Kaufman, by including a new term that accounts for the irreversible floc breakup process. Both models were fitted to the experimental results obtained with flocculation kinetics assays of low turbidity raw water containing Microcystis aeruginosa cells. Aluminum sulfate and ferric chloride were used as coagulants, and three distinct average velocity gradient (G) values were applied in the flocculation stage (20, 40 and 60 s-1). Experimental results suggest that the equilibrium between the aggregation and breakup process, as depicted by Argaman and Kaufman’s original model, might not be constant over time, since the residual turbidity increased in various assays (phenomenon that was attributed to the irreversible floc breakup process). In the aluminum sulfate assays, the residual turbidity increase was visible when G = 20 s-1 (dosages of 60 and 80 mg L-1). For the ferric chloride assays, the phenomenon was noticed when G = 60 s-1 (dosages of 60 and 80 mg L-1). The proposed model presented a better fit to the experimental results, especially at higher coagulant dosages and/or higher values of average velocity gradient (G).