In order to improve the photocatalytic performance of g-C₃N₄, the g-C₃N₄/Ti₃C₂/Ag₃PO₄ S-type heterojunction catalyst was prepared by electrostatic assembly method, and then the g-C₃N₄/Ti₃C₂/Ag₃PO₄/PAN composite nanofiber membrane was prepared by electrospinning technology. The morphology and chemical properties of the nanofiber membrane were characterized by SEM, FTIR, and XRD, and the photocatalytic degradation of tetracycline hydrochloride (TC) in water by the nanofiber membrane was investigated. The results showed that g-C₃N₄/Ti₃C₂/Ag₃PO₄ could be successfully loaded on PAN and uniformly distributed on the surface of composite nanofiber membrane by electrospinning technology. Increasing the amount of loading and catalyst, lowering the pH value and TC concentration of the system were conducive to the oxidation and degradation of TC. The nano-fiber catalytic membrane had been recycled five times and found to have excellent photocatalytic stability and reusability. The study of catalytic mechanism showed that h⁺, •OH and •O₂⁻ were produced and participated in the oxidation degradation reaction of TC, and •O₂⁻ plays a major role in catalysis. Therefore, this work provides a new insight into the construction of high-performance and high-stability photocatalytic system by electrospinning technology.

Herein, poly (allylamine hydrochloride) (PAH)/ poly (styrene sulfonic acid) sodium salt (PSS) microcapsules of (PAH/PSS)₂PAH (P2P MCs) and (PAH/PSS)₂ (P2 MCs) were obtained by a layer-by-layer method. The P2 MCs show high adsorption capacity for Rhodamine B (642.26 mg/g) and methylene blue (909.25 mg/g), with an extremely low equilibrium adsorption time (~20 min). The P2P MCs exhibited high adsorption capacities of reactive orange K-G (ROKG) and direct yellow 5G (DY5G) which were 404.79 and 451.56 mg/g. Adsorption processes of all dyes onto microcapsules were best described by the Langmuir isotherm model and a pseudo-second-order kinetic model. In addition, the P2P MCs loaded with reactive dyes (P2P–ROKG), could further adsorb rhodamine B (RhB) dye, and P2 MCs that had adsorbed cationic MB dyes could also be used for secondary adsorption treatment of direct dye waste-water, respectively. The present work confirmed that P2P and P2 MCs were expected to become an excellent adsorbent in the water treatment industry.

Cotton fabric was modified with Na(2)EDTA using a hydrothermal method to introduce surface hydroxyl groups, and subsequent coordination of Fe(III) ions to produce an Na(2)EDTA modified cotton-fiber-Fe complex (Fe-EDTA-Cotton). After characterization by SEM and FTIR, Fe-EDTA-Cotton was used as a heterogeneous photocatalyst to reduce Cr(VI) and degrade Reactive Red 195 oxidatively, to evaluate its catalytic activity. The results indicated that high Na(2)EDTA and/or NaH2PO4 concentrations, and/or high hydrothermal temperature increased the carboxyl group content (Q(COOH)) of the cotton fiber; high Fe content and elevated temperature could enhance coordination. Fe-EDTA-Cotton had a significant photocatalytic function in reducing Cr(VI). Increasing the Q(Fe) value of the complex or stronger irradiation favored photocatalytic reduction of Cr(VI) species. Increasing the system's pH did not help the reduction reaction. Fe-EDTA-Cotton could also remove Cr(VI) and Reactive Red 195 simultaneously from aqueous solution, and showed strong photocatalytic capacity. The reduction or oxidation reaction could be regulated by changing Na2S2O8 concentration in the reaction system, which might provide a new way to treat wastewater containing organic pigments and Cr(VI) species.

Hemin possesses great potential in eliminating organic pollutants due to its mild reaction condition, light-harvesting efficiency, and environmental friendliness. However, it has drawbacks such as being easy to aggregate and hard to recycle, and poor stability should be improved in practical application. Herein, the subject developed an electrospinning approach to enable the hemin particulates to be immobilized onto polyacrylonitrile (PAN) nanofibers stably. Hydrogen peroxide (H₂O₂) was adopted as an oxidant in the system to simulate the enzymatic catalysis of hemin in an organism. Scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), UV-Vis diffuse reflection spectroscopy (DRS), and electron spin resonance spectroscopy (ESR) analysis was employed to discuss the morphology, structure, and mechanism of the prepared n-hemin/PAN nanocomposite membranes, and 0.02 mmol L⁻¹ of the rhodamine B (RhB) removal activity in different conditions was also verified with these membranes. The kinetic studies showed that n-hemin/PAN nanocomposite membranes maintained excellent properties both in adsorption and degradation. Around 42% RhB could be adsorbed in the dark, while 91% RhB decolorized under xenon lamp irradiation in 110 min, suggesting the catalytic performance of n-hemin/PAN was greatly driven by light irradiation. Differing from the axial coordinated hemin complexes, n-hemin/PAN would catalyze hydrogen peroxide into •OH radicals rather than •OOH and high-valent metal-oxo species. This work provides an effective way to support hemin as nanocomposite membranes, in which the molecular interaction between polymer and hemin made their light adsorption an obvious red shift.