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The efficient treatment of oil–water emulsions in extreme environments, such as strongly acidic and alkaline media, remains a widespread concern. Poly(phenylene sulfide) (PPS)-based porous membranes with excellent resistance to chemicals and solvents are promising for settling this challenge. However, the limited hydrophilicity and the poor hydrated ability of the hydrophilic PPS (h-PPS) membranes reported in the literature prevents them from separating oil–water emulsions with high efficiency, large fluxes, and good antifouling performances. In this study, a firm rough TiO 2 layer is constructed on a h-PPS membrane via electrostatic assembly to improve the surface hydrophilization. The introduction of the TiO 2 layer increases the wetting selectivity and decreases the oil adhesion, which makes it capable to efficiently treat oil-in-water emulsions (efficiency > 98%). Most importantly, the underwater critical oil intrusion pressure almost doubled after the incorporation of the TiO 2 layer, which allows the membrane to withstand pressurized filtration, achieving a high flux of ∼4000 L m –2 h –1 . This is more than 2 orders of magnitude larger than the flux of the reported h-PPS. Furthermore, the TiO 2 @h-PPS membrane displays long-term stability in separating oil–water emulsions in strong acid and strong alkali, showing a promising prospect for the treatment of strongly corrosive emulsions.
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Han et al. (2019) studied this question.
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