Synthesis and Characterisation of Self-Cleaning TiO2/PES Mixed Matrix Membranes in the Removal of Humic Acid

Membranes (Basel). 2023 Mar 24;13(4):373. doi: 10.3390/membranes13040373.

Abstract

Membrane application is widespread in water filtration to remove natural organic matter (NOM), especially humic acid. However, there is a significant concern in membrane filtration, which is fouling, which will cause a reduction in the membrane life span, a high energy requirement, and a loss in product quality. Therefore, the effect of a TiO2/PES mixed matrix membrane on different concentrations of TiO2 photocatalyst and different durations of UV irradiation was studied in removing humic acid to determine the anti-fouling and self-cleaning effects. The TiO2 photocatalyst and TiO2/PES mixed matrix membrane synthesised were characterised using attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy, X-ray powder diffraction (XRD), scanning electron microscope (SEM), contact angle, and porosity. The performances of TiO2/PES membranes of 0 wt.%, 1 wt.%, 3 wt.%, and 5 wt.% were evaluated via a cross-flow filtration system regarding anti-fouling and self-cleaning effects. After that, all the membranes were irradiated under UV for either 2, 10, or 20 min. A TiO2/PES mixed matrix membrane of 3 wt.% was proved to have the best anti-fouling and self-cleaning effect with improved hydrophilicity. The optimum duration for UV irradiation of the TiO2/PES mixed matrix membrane was 20 min. Furthermore, the fouling behaviour of mixed matrix membranes was fitted to the intermediate blocking model. Adding TiO2 photocatalyst into the PES membrane enhanced the anti-fouling and self-cleaning properties.

Keywords: antifouling; membrane fouling; photocatalytic; self-cleaning membrane.

Grants and funding

The research was funded by Ministry of Higher Education, Malaysia (MOHE) Fundamental Research Grant Scheme (FRGS) under grant number FRGS/1/2015/TK02/UNIMAP/02/3 and the APC was funded by Universiti Malaysia Perlis (UniMAP) scientific publication fund.