Using chitosan as a raw material, 1,8-naphthimide as the fluorescent chromophore, and sulfur-containing compounds as the recognition groups, a novel naphthimide-functionalized chitosan probe, CS-BNS, for the detection of ClO⁻ was successfully synthesized. The modification of chitosan was verified by SEM, XRD, FTIR, mapping, ¹³C-NMR, TG and the structure of the probe molecule was characterized. The identification performance of the probes was studied using UV and fluorescence spectrophotometers. The results show that CS-BNS exhibits a specific response to ClO⁻ based on the oxidative reaction of ClO⁻ to the recognition motifs, as well as a good resistance to interference. And the probe has high sensitivity and fast response time, and can complete the detection of ClO⁻ in a pure water system within 60 s. The probe can also quantify ClO⁻ (y = 30.698x + 532.37, R² = 0.9833) with a detection limit as low as 0.27 μM. In addition, the combination of the probe with smartphone technology enables the visualization and real-time monitoring of ClO⁻. Moreover, an identification system for ClO⁻ was established by combining the probe with smartphone technology, which realized the visualization and real-time monitoring of ClO⁻.

A boron-doped BiOBr photocatalytic nanosheet was synthesized using a one-step hydrothermal method. The effects of solvent, temperature, and boron doping content on the morphology and photocatalytic performance were investigated. The boron-doped samples synthesized with acetic acid at 180 °C (1B-AB) showed optimal photocatalytic performance, achieving 80% efficiency in degrading sulfanilamide (SN) within 6 h. After five cycles, the degradation rate decreased by 21%. The 10% boron doping reduced BiOBr’s bandgap (from 2.90 to 2.88 eV), improving visible light utilization and reducing electron–hole pair recombination. The 1B-AB photocatalyst also demonstrated excellent activity against anionic dyes like methyl orange (MO) and malachite green (MG). Hydroxyl radicals (·OH) and superoxide anions (·O₂⁻) were identified as the main active species in the SN degradation process.

To comparatively study the effects of cold plasma activation and chemical treatment on the adsorption capacities of biomass carbon nanofiber membranes (BCNMs), microcrystalline cellulose (MCC) and chitosan (CS) were used to fabricate porous BCNMs by electrospinning and carbonization. Two modification methods, including oxygen (O₂) plasma activation and chemical treatment using nitric acid (HNO₃), sulfuric acid (H₂SO₄), hydrogen peroxide (H₂O₂), and urea, were further employed to enhance their adsorption performance. Various carbonyl group (C=O), ether bond (C-O), carboxyl group (O-C=O) and pyridinic nitrogen (N), pyrrolic N, and quaternary N functional groups were successfully introduced onto the surface of the BCNMs by the two methods. The BCNM-O₂ showed optimal formaldehyde absorption capacity (120.67 mg g⁻¹), corresponding to its highest contents of N, O-containing functional groups, and intact network structure. However, chemical treatment in strong acid or oxidative solutions destructed the microporous structures and changed the size uniformity of fibers in the BCNMs, resulting in a decline in formaldehyde adsorption capacity. A synergistically physical–chemical adsorption took place during formaldehyde adsorption by the modified biomass nanofiber membranes, due to the coexistence of suitable functional groups and porous structures in the membranes.