Developing membranes with superior antifouling properties is crucial for efficient and sustainable water treatment. In this study, polysulfone (PSM) composite membranes were fabricated by incorporating hydroxylated titanium nanotubes (TNT@OH) via the non-solvent-induced phase separation method. The hydroxylation of TNTs enhanced their dispersion in the polymer matrix and promoted strong polymer–nanoparticle interactions. Comprehensive characterization using FTIR, XRD, TGA, FESEM, and AFM confirmed the successful integration of TNT@OH, resulting in membranes with improved hydrophilicity, porosity, and thermal stability. The contact angle decreased from ~88° for neat PSM to ~50° at 7 wt% TNT@OH, while surface free energy increased significantly. Mechanical strength and flexibility were also enhanced at optimal TNT@OH loadings (3–5 wt%), owing to uniform dispersion and strong interfacial bonding. Filtration experiments using humic acid (HA) and natural organic matter (NOM) demonstrated remarkable improvements in water flux, rejection efficiency, and fouling resistance. The composite membranes achieved HA rejection rates of up to 98%, with reduced irreversible fouling and higher flux recovery ratios across multiple filtration–cleaning cycles. The proposed antifouling mechanism is attributed to the formation of a stable hydration layer by surface hydroxyl groups, which prevents foulant adhesion and facilitates cleaning. These findings suggest that incorporating TNT@OH into polysulfone membranes is a promising approach for developing high-performance ultrafiltration membranes with enhanced permeability, mechanical robustness, and long-term antifouling stability, thereby making them suitable for advanced water purification applications.

This study centers on the development and characterization of an innovative electrochemical sensing probe composed of a sensing mesoporous functional sol–gel coating integrated onto a glassy carbon electrode (sol–gel/GCE) for the detection of NH₃ and/or NH₄⁺ in water. The main interest for integrating a functional sol–gel coating onto a GCE is to increase the selective and sensing properties of the GCE probe towards NH₃ and/or NH₄⁺ ions. The structure and surface morphology of the newly developed sol–gel/GCE probe were characterized employing scanning electron microscopy (SEM), atomic force microscopy (AFM), dynamic light scattering (DLS), and Fourier-transform infrared (FTIR), while the electrochemical sensing properties were evaluated by Berthelot’s reaction, cyclic voltammetry (CV), and adsorptive square wave–anodic striping voltammetry (Ads SW–ASV). It is shown that the newly developed sol–gel coating is homogeneously deposited on the GCE with a sub-micron and uniform thickness close to 630 nm and a surface roughness of 25 nm. The sensing testing of the sol–gel/GCE probe showed limits of detection and limits of quantitation of 1.7 and 5.56 nM of NH₄⁺, respectively, as well as a probe sensitivity of 5.74 × 10⁻¹ μA/μM cm⁻². The developed probe was fruitfully validated for the selective detection of NH₃/NH₄⁺ in fresh and sea water samples. Computed Student t_exp (0.45–1.25) and F_exp (1.69–1.78) (n = 5) tests were less than the theoretical t_tab (2.78) and F_tab (6.39) at 95% probability.

An ultrasensitive, simple and highly selective spectrofluorometric strategy for quantifying traces of mercury(II) in environmental water has been established using the fluorescent probe procaine hydrochloride (PQ+.Cl−). The procedure was based upon the formation of the ternary ion associate complex [(PQ+)2.(HgI4)2−] between PQ+.Cl− and mercury(II) in iodide media at pH 9.0–10.0 with its subsequent extraction onto dichloromethane accompanied by a change in fluorescence intensity at λex/em = 268/333 nm. The developed strategy exhibited a linear range of 1–114 μg L−1 with lower limit of detection (LOD) and quantification (LOQ) of mercury(II) 1.3 and 3.98 nM, respectively. Intra and inter-day laboratory accuracy and precision for trace analysis of mercury(II) in water were performed. Complexed mercury(II) in environmental water, chemical speciation and successful literature comparison was performed. The proposed system offered excellent selectivity towards mercury(II) ions examined in the presence of competent ions in excess, relevant to real water samples. The method was applied for analysis of mercury(II) in tap water samples. Statistical comparison (Student’s t and F tests) of the proposed method with the reference ICP-OES method revealed no significant differences in the accuracy and precision.