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.

The severe water pollution from effluent dyes threatens human health. This study created pH-magnetic-photocatalytic polymer microspheres to conveniently separate the photocatalyst nanoparticles from the treated water by applying an external magnetic field. While fabricating magnetic nanoparticles’ (MNPs) microspheres, incorporating 0.5 wt.% iron oxide (Fe₃O₄) showed the best magnetophoretic separation ability, as all the MNPs microspheres were attracted toward the external magnet. Subsequently, hybrid organic–inorganic polyoxometalates (HPOM), a self-synthesized photocatalyst, were linked with the functionalized magnetic nanoparticles (f-MNPs) to prepare augmented magnetic-photocatalytic microspheres. The photodegradation dye removal efficiency of the augmented magnetic-photocatalytic microspheres (f-MNPs-HPOM) was then compared with that of the commercial titanium dioxide (TiO₂) photocatalyst (f-MNPs-TiO₂). Results showed that f-MNPs-HPOM microspheres with 74 ± 0.7% photocatalytic removal efficiency better degraded methylene orange (MO) than f-MNPs-TiO₂ (70 ± 0.8%) at an unadjusted pH under UV-light irradiation for 90 min. The excellent performance was mainly attributed to the lower band-gap energy of HPOM (2.65 eV), which required lower energy to be photoactivated under UV light. The f-MNPs-HPOM microspheres demonstrated excellent reusability and stability in the photo-decolorization of MO, as the microspheres retained nearly the same removal percentage throughout the three continuous cycles. The degradation rate was also found to follow the pseudo-first-order kinetics. Furthermore, f-MNPs-HPOM microspheres were pH-responsive in the photodegradation of MO and methylene blue (MB) at pH 3 (acidic) and pH 9 (alkaline). Overall, it was demonstrated that using HPOM photocatalysts in the preparation of magnetic-photocatalytic microspheres resulted in better dye degradation than TiO₂ photocatalysts.

Driven by the urgent need for a solution to tackle the surge of rice husk (RH) and waste frying oil (WFO) waste accumulation at a global scale, this report highlights the use of calcium silicates (CS) extracted from acid-pre-treated rice husk ash (RHA) for free fatty acid (FFA) removal from WFO as conventional RHA shows limited FFA adsorption performance. A novel alkaline earth silicate extraction method from acid-pre-treated RHA was outlined. The structural and behavioural attributes of the synthesised CS were identified through BET, SEM-EDS, and XRD analyses and compared to those of RHA. Notable morphology and structural modification were determined, including reducing specific surface areas, mitigating from amorphous to crystalline structure with regular geometric forms, and detecting Si-O-Ca functional groups exclusive to CS adsorbents. A comparison study showed superior lauric acid (LA) adsorption performance by CS absorbents over acid-pre-treated RHA, with a significant increase from 0.0831 ± 0.0004 mmol LA/g to 2.5808 ± 0.0011 mmol LA/g after 60 min. Recognised as the best-performing CS adsorbent, CS-1.0 was used for further investigations on the effect of dosage, LA concentration, and temperature for efficient LA adsorption, with up to 100% LA removal and 5.6712 ± 0.0016 mmol LA/g adsorption capacity. The adsorption isotherm and kinetic studies showed LA adsorption onto CS-1.0 followed Freundlich isotherm with K_F = 0.0598 mmol^(1-1/n) L^(1/n) g^-1 & Q_e,cal = 3.1696 mmol g^-1 and intraparticle diffusion model with k_id = 0.1250 mmol g^-1 min^0.5 & C_i = 0.9625 mmol g^-1, indicating rapid initial adsorption and involvement of carboxylate end of LA and the calcium ions on the CS-1.0 in the rate-limiting step. The high equilibrium adsorption capacity and LA adsorption rate indicated that the proposed CS-1.0 adsorbent has excellent potential to recover FFA from WFO effectively.