Enhanced photo-Fenton activity and stability for sulfamethoxazole degradation by FeS2@TiO2 heterojunction derived from MIL-125.

FT-x composites with core-shell structure (FT = FeS2@TiO2, x represents the mass ratio of the used FeCl3·6H2O to MIL-125) were fabricated by a hydrothermal method using MIL-125(Ti) as a self-sacrificing template. Both the photo-Fenton activity and stability of the FT-1 were improved greatly in comparison with its counterparts due to the unique core-shell structure and synergistic effect between FeS2 and TiO2. Especially, the Fe leaching concentration of FT-1 was approximately 1/10 of the individual FeS2, benefiting from the protection effect of TiO2 shell. Under dark condition, the formed FeOOH occupied active sites and inhibited iron cycle as well as H2O2 decomposition, leading to the inactivation of FT-1. UV light irradiation not only boosted the catalytic activity but also prevented the FT-1 from reactivity decline owning to the regeneration of Fe2+ by photogenerated electrons and continuous generation of ·OH. Experimental and DFT calculation results indicated that a type-II heterojunction was formed, in which photogenerated electrons were transferred from FeS2 core to TiO2 shell, accelerating charge separation and further boosting sulfamethoxazole (SMX) degradation. FT-1 displayed outstanding photo-Fenton activity in wide pH ranged from 2 to 6 and good anti-interfering ability toward impurities in water matrix. Besides, the reusability of FT-1 was good, in which 90% SMX degradation was maintained even after 5 runs. Noteworthy, the photo-Fenton activity was recovered via a revulcanization process, in which FeOOH was completely transformed into FeS2. This founding provided insights for the design and construction of heterojunction with both excellent photo-Fenton activity and stability.

Enhanced catalytic peroxymonosulfate activation for sulfonamide antibiotics degradation over the supported CoSx-CuSx derived from ZIF-L(Co) immobilized on copper foam.

The CoSx-CuSx was firmly immobilized on copper foam (CF) substrate to fabricate supported CoSx-CuSx/CF using ZIF-L(Co)/CF as a self-sacrificing template, in which CF substrate played an important role in improving the adhesion between CF and target catalyst as well as the interfacial interaction between CoSx and CuSx. The CoSx-CuSx/CF performed well in catalytic peroxymonosulfate (PMS) activation, which can accomplish 97.0% sulfamethoxazole (SMX) degradation within 10 min due to the special structure and Co2+ regeneration promoted by S2- and Cu+. The influences of pH, PMS dosage, catalyst dosage, co-existing anions and natural organic matter (NOM) on SMX removal were studied in detail. CoSx-CuSx/CF presented excellent catalytic activity and reusability, which might be fascinating candidate for real wastewater treatment. The possible pathway of SMX degradation was proposed, and the toxicity of the intermediates during the degradation process were evaluated. It is noteworthy that long-term continuous degradation of sulfonamide antibiotics was achieved using a self-developed continuous-flow fixed-bed reactor. This work demonstrated that CF as a substrate to fabricate supported catalysts derived from MOF had great potential in actual wastewater remediation.

Selective adsorption activities toward organic dyes and antibacterial performance of silver-based coordination polymers.

Two silver-based coordination polymers, [Ag2(bpy)2(cbda)] (BUC-51) and [Ag3(bpy)3(cpda)]·(NO3)·9H2O (BUC-52), have been successfully prepared by slow evaporation at room temperature. These coordination polymers exhibited good adsorptive performances toward series organic dyes with sulfonic groups, which could be ascribed to the AgcdotsO interaction between the silver(I) atoms in CPs and the oxygen atoms from sulfonic groups attached to organic dyes. Both BUC-51 and BUC-52 favoured slow release of Ag+ ions resulting into outstanding long-term antibacterial abilities toward Gram-negative bacteria, Escherichia coli (E. coli), which was tested by a minimal inhibition concentration (MIC) benchmark and an inhibition zone testing method. Both scanning electron microscope (SEM) and transmission electron microscope (TEM) images demonstrated that these two Ag-based coordination polymers could destroy the bacterial membrane and further cause death. Additionally, the excellent stability in common solvents and good optical stability under UV-visible light facilitated their adsorptive and antibacterial applications.