Abstract

The effect of membrane surface charge on demulsification and fouling resistance during emulsion separation is investigated. By grafting poly(2-dimethylaminoethyl methacrylate) (pDMAEMA) and poly(oligo(ethylene glycol) methacrylate) (pOEGMA) onto polypropylene (PP) membrane via ultraviolet (UV)-initiated polymerization, the obtained membranes PP-g-pDMAEMA and PP-g-pOEGMA present positive and negative surface charges in water, respectively. During the emulsion separation, PP-g-pOEGMA and PP-g-pDMAEMA membranes exhibit different separation efficiencies and pollutant resistant behaviors to the emulsions prepared from anionic surfactant (sodium dodecyl sulfate, SDS) and cationic surfactant (cetyltrimethylammonium bromide, CTAB). Comparing to PP-g-pOEGMA, the separation efficiency of PP-g-pDMAEMA was 15% (SDS emulsion) and 300% (CTAB emulsion) higher. But the flux recovery ratio of PP-g-pOEGMA was raised 30% (SDS emulsion) and 16% (CTAB emulsion). Hence, the membrane surface positive charges assist demulsification, but aggravate the membrane fouling. The mechanism obtained is beneficial to construct membranes with high separation efficiency and long-term durability.

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