Suppressing transmembrane-pressure rise by pulse dosing of submicron super-fine powdered activated carbon: Effects of filtration flux, coagulant types, and coagulant-dose timing during precoating

Submicron-sized powdered activated carbon (SSPAC, diameter 200 nm) dosed in a pulse after coagulation pretreatment has recently been found to effectively mitigate membrane fouling and thus to suppress the rise of transmembrane pressure (TMP) in the microfiltration process because SSPAC has a higher capacity to adsorb membrane foulants, such as natural organic matter, than conventional PAC and a precoat layer formed by SSPAC on the membrane surface retards membrane fouling. This study investigated the effects of the filtration flux during precoating, the timing of coagulant dosing, and the types of coagulants on the suppression of TMP rise by pulse-dosed SSPAC. The TMP rise was insensitive to the filtration flux during precoating. However, the efficacy of the SSPAC was sensitive to the use of the coagulant polyaluminum-chloride (PACl). Unlike pulse dosing of SSPAC, pulse dosing of coagulant led to excessive aggregation and settling of SSPAC and insufficient formation of a precoating layer. The best filterability was achieved when the coagulant was dosed continuously in the entire operation period. It is also effective to use treated water for feeding during the preparation stage. For sulfated PACl, high basicity (70 %), with its high charge neutralization capacity, was preferred to medium basicity (50 %). Meanwhile, the TMP rise was more effectively suppressed by non-sulfated PACl with a low-to-medium basicity (20 & ndash;40 %) than zero or high basicity (70 %). This behavior was explained by the fact that, as the basicity increases, hydrolysis of the coagulants is lessened, but the charge neutralization effect becomes stronger

Automated summary

Submicron-sized powdered activated carbon has been found to effectively mitigate membrane fouling and suppress the rise of transmembrane pressure. This study investigated the effects of filtration flux, timing of coagulant dosing, and types of coagulants on the suppression of pressure rise.