RESUMO
Blended organic copolymer (or homopolymer) and inorganic nanoparticles have been widely used (separately or simultaneously) for optimizing membrane pore structure and surface functionality. However, the prepared membranes suffer from degraded stability and insufficient integrity due to the high solubility or incompatibility of the blending additives. In this work, an organic-inorganic nanocomposite (i.e., PLA-TiO2) was designed, and employed for PSF membrane preparation. The Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) analysis confirmed that bidentate chelating dominated the bonding mechanism between PLA and TiO2. The resultant PSF/PLA-TiO2 membranes possessed a highly porous surface with narrowed pore size distribution, demonstrating the strong pore forming ability of PLA-TiO2 for membrane preparations. Moreover, owing to the distinct inorganic-organic molecular conformation, the PLA-TiO2 exhibited enhanced stability and dispersibility within the PSF substance, which endowed the membrane with long-acting hydrophilicity and UV responsiveness. Given the UV responsiveness that is introduced by PLA-TiO2, UV-assisted strategies (UV-F and UV-C) were designed to further mitigate membrane fouling. The fouling analysis indicated that both reversible fouling and irreversible fouling were reduced in the UV-C process, signifying the synergistic effect between photocatalysis and hydraulics in membrane fouling mitigation. The enhanced membrane performance and the efficient preparation process highlight the potential of PLA-TiO2 in membrane modifications.