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A ceria loaded carbon nanotubes (CeO2/CNTs) nanocomposites photocatalyst was prepared by chemical precipitation, and the preparation conditions were optimized using an orthogonal experiment method. HR-TEM, XRD, UV-Vis/DRS, TGA and XPS were used to characterize the photocatalyst. Nitrogen adsorption-desorption was employed to determine the BET specific surface area. The results indicated that the photocatalyst has no obvious impurities. CeO2 was dispersed on the carbon nanotubes with a good loading effect and high loading efficiency without agglomeration. The catalyst exhibits a strong ability to absorb light in the ultraviolet region and some ability to absorb light in the visible light region. The CeO2/CNTs nanocomposites photocatalyst was used to degrade azo dye Acid Orange 7 (40 mg/L). The optical decolorization rate was 66.58% after xenon lamp irradiation for 4 h, which is better than that of commercial CeO2 (43.13%). The results suggested that CeO2 loading on CNTs not only enhanced the optical decolorization rate but also accelerated the separation of CeO2/CNTs and water.

To enhance the photocatalytic degradation efficiency and selectivity of di(2-ethyl)hexyl phthalate (DEHP), molecularly imprinted TiO2 (MIP-TiO2) was synthesized with di(2-ethylhexyl) phthalate as template molecule. The as-prepared MIP-TiO2 was characterized by Field emission scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier infrared spectroscopy (FI-IR), UV-Visible diffuse reflection spectroscopy (UV-Vis) and photoluminescence spectroscopy (PL). The selective adsorption and photocatalytic activity of MIP-TiO2 for DEHP were studied. The results show that DEHP molecularly imprinted polymer was coated on the surface of TiO2. The light-response of MIP-TiO2 was broadened. The photo-generated electron/hole recombination on the surface of TiO2 decreased. The selective recognition to DEHP was improved. Compared with TiO2, MIP-TiO2 exhibited higher photocatalytic activity and selectivity to DEHP. The photocatalytic degradation efficiency of DEHP (5mg/L) by MIP-TiO2 was 89%. The photocatalytic degradation rate of DEHP by MIP-TiO2 is 1.5 times that by TiO2. MIP-TiO2 could be reused.

Aiming at effectively controlling nonylphenol (NP) pollution, three bacterial strains were isolated from activated sludge and landfill leachate, which could grow with nonylphenol as sole carbon and energy source. The three nonylphenol-degrading bacteria isolated were named as WN6, SLY9 and SLY10, respectively. The morphological observation and 16S rDNA identification revealed that the strains belonged to Serratia sp., Klebsiella sp. and Pseudomonas putida, respectively. WN6 and SLY9 contained ALK gene, while WN6 and SLY10 harbored C12O genes. The three strains were combined together to form complex microorganisms ZJF. The ratio of Serratia sp. to Klebsiella sp. to Pseudomonas putida was 2:1:2 (volume ratio of bacterial suspension). Under the conditions that temperature was 30 ℃, pH was 6, inoculation amount was 10% (volume ratio), initial concentration of NP solutions was 20 mg/L, NP degradation rate by ZJF reached 73.82%, compared with any single strain of the three bacteria, NP degradation rate by ZJF increased more than 15% during 6 days. Bioremediation of nonylphenol-polluted the Yangtze River and the Ancient Canal water by ZJF ware simulated. After a 6-day incubation period, the degrading rate of nonylphenol in Ancient Canal water was close to 80%, and the degrading rate of nonylphenol in Yangtze River water was 72.84%.

BACKGROUND: Ferrocene (Fc) is a chemically stable, safe and non‐toxic substance with excellent redox performance and is often used to activate various oxidants. However, Fc is a nanoscale non‐magnetic material, which needs a suitable carrier such as chitosan (CS) to be fixed and being compounded with magnetic material for recycling. RESULTS: A new magnetic catalyst, Fc/CS@Fe3O4, was prepared for activating persulfate (PS) to degrade tetracycline (TC) in water. The catalyst prepared was characterized by X‐ray powder diffraction, Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy and vibrating sample magnetometry, and the effects of the dosage of PS and catalyst, pH, temperature, coexisting anions and fulvic acid on TC degradation were investigated. The results showed that the removal of TC could be promoted by increasing the temperature, and acidic conditions are more beneficial to TC degradation than alkaline conditions. Cl−, CO32−, HCO3− and fulvic acid could all inhibit the degradation of TC. Light and catalyst had a synergistic activation effect on PS. Under conditions of PS and catalyst dosage all 400 mg L−1, temperature 25° C, TC concentration 30 mg L−1 and initial pH 5, TC could be completely degraded within 60 min. Both SO4−• and HO• contributed to TC degradation, and SO4−• was the main active species in the degradation system. CONCLUSION: The results indicate that Fc/CS@Fe3O4 has good catalytic activity and stability, and has potential application in the treatment of antibiotics in water. © 2022 Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

BACKGROUND: Bismuth tetraoxide (Bi2O4) has attracted increasing interest as a novel visible‐light‐driven photocatalyst. It suffers from some drawbacks, such as quick recombination of photogenerated electrons and holes, small specific surface area and few active sites due to submicron rod structure. RESULTS: A novel and efficient binary heterojunction photocatalyst, in which zero‐dimensional (0D) SnO2 nanoparticles was anchored on the surface of one‐dimensional (1D) Bi2O4 micrometer rods, was successfully synthesized. The as‐prepared samples were characterized by X‐ray diffraction (XRD), scanning electron microscopy, transmission electron microscope, Fourier transform infrared spectroscopy and X‐ray photoelectron spectroscopy. The photocatalytic activity of the synthesized photocatalysts was evaluated by photodegradation of tetracycline (TC) under visible‐light irradiation. The prepared 30‐SB composite (30 wt% SnO2/Bi2O4) exhibits the highest photocatalytic activity toward TC degradation. The removal efficiency of TC was up to 84.3% within 120 min. The rate constant k for the reaction of 30‐SB composite is 0.029017 min−1, which is 13.4 and 1.8 times as high as that of SnO2 and Bi2O4, respectively. CONCLUSION: The significantly boosted photocatalytic activity is attributed to the formation of Z‐scheme heterojunctions between SnO2 and Bi2O4. Z‐scheme charge transfer promoted the effective separation of photogenerated carriers and ensured that the holes with higher oxidative activity and electrons with stronger reducibility participate in the production of •OH and •O2− as well as direct degradation of TC. This work will provide a new modification strategy for the potentially excellent photocatalyst Bi2O4. © 2022 Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]

A novel ternary heterojunction composite photocatalyst g-C3N4/TiO2/NiWO4 was fabricated using a simple hydrothermal method. The synthesized samples were characterized using X-ray diffraction (XRD), scanning electronic microscopy (SEM), energy-dispersive spectrum (EDS), Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), ultraviolet–visible (UV–Vis) absorption spectra, photoluminescence (PL) spectra, transient photocurrent responses, and electrochemical impedance spectroscopies (EIS). The results indicated that the composite of g-C3N4/TiO2/NiWO4 had been successfully synthesized. By constructing a ternary heterojunction, the electron migration rate and light absorption of the material are further improved; the photogenerated electron–hole recombination is inhibited. The ternary composite photocatalyst shows the highest photocatalytic activity for the degradation of rhodamine B (RhB) than that of g-C3N4, TiO2, NiWO4, and g-C3N4/TiO2 photocatalyst. The degradation efficiency of RhB using g-C3N4/TiO2/NiWO4 can reach 99% after visible-light irradiation for 40 min. Finally, the migration mechanism of charge carriers in the ternary system has been schematically illustrated by the active species capture experiment. Our research can pave the way for the fabrication of ternary heterojunction composite photocatalyst with high photocatalytic activity for the environmental contaminants treatment. [ABSTRACT FROM AUTHOR]

BACKGROUND: A Z‐scheme structured photocatalyst is a highly efficient photocatalyst for hydrogen evolution and degradation of pollutants. RESULTS: An indirect Z‐scheme heterojunction g‐C3N4/CQDs/InVO4 with carbon quantum dots (CQDs) as electron mediator was constructed and was successfully synthesized using a facile hydrothermal method. The photocatalytic activity of the as‐prepared composite was evaluated in terms of hydrogen generation and degradation of rhodamine B (RhB) dye. The as‐prepared sample CV20/CQDs2 (g‐C3N4/2 wt% CQDs/20 wt% InVO4) exhibits the best photocatalytic activity towards hydrogen production and RhB degradation. Within 90 min, 99.6% of RhB is removed, and the degradation rate constant of RhB over CV20/CQDs2 is 0.06491 min−1, which is 43.9, 6.64 and 3.3 times as high as that of InVO4, g‐C3N4 and binary composite g‐C3N4/InVO4. CV20/CQDs2 exhibits H2 evolution rate of 2.169 mmol g−1 h−1, which is 26.07, 2.65 and 1.6 times as high as that of InVO4, g‐C3N4 and g‐C3N4/InVO4. CONCLUSIONS: The enhanced photocatalytic activity is attributed to two aspects. First, CQDs, as electron mediator, promote the effective separation of photogenerated electrons and holes through Z‐scheme charge transfer pathway, preserving the high redox ability of electrons and holes. Second, g‐C3N4/CQDs/InVO4 shows strong optical absorption in the full visible‐light region. © 2021 Society of Chemical Industry (SCI). [ABSTRACT FROM AUTHOR]