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Improving the separation efficiency of photo-generated electron–hole pair is a key issue in the field of photocatalytic hydrogen production. In this work, we successfully improved the efficiency of photo-generated carrier separation using the synergistic action of sulfur (S) vacancies and a Ni2P co-catalyst. Vs-Zn0.5Cd0.5S (Vs-ZCS) with S vacancies was designed and constructed, and Vs-ZCS/Ni2P photocatalysts were prepared with non-precious metal Ni2P as a co-catalyst. Among all the produced materials, Vs-ZCS/Ni2P-5% has a photocatalytic characteristic of 40.81 mmol g−1 h−1, which is 7.88, 3.08 and 3.75 times greater than those of ZCS (5.18 mmol g−1 h−1), Vs-ZCS (13.25 mmol g−1 h−1) and ZCS/Ni2P-5% (10.88 mmol g−1 h−1), respectively. The results of transient photo-current, electrochemical impedance spectroscopy, photoluminescence and time-resolved fluorescence show that the synergistic effect of S vacancies and Ni2P significantly promotes the separation and transfer efficiency of photo-generated carriers, as well as the photocatalytic hydrogen production reaction. Superoxide radicals and electrons are the active species for photocatalytic hydrogen generation, which is confirmed by active species capture tests and EPR. This study presents an innovative approach for developing photocatalysts with low cost and good catalytic performance. [ABSTRACT FROM AUTHOR]

BaFe12O19-polypyrrolenanocomposites were prepared via the in situ chemical oxidative polymerization of pyrrole monomers in the presence of BaFe12O19 powder, with ammonium persulfate as an oxidant and sodium dodecyl benzene sulfonate as a dopant. X-ray diffraction measurements and Fourier-transform infrared spectroscopy indicated that there were no chemical interactions between BaFe12O19 and polypyrrole. In addition, scanning electron microscopy showed that the composites exhibited a core–shell structure. Subsequently, the prepared nanocomposite was used as a filler to prepare a coating suitable for ultraviolet curing. The performance of the coating was investigated by evaluating its hardness, adhesion, absorbance, and resistance to acids and alkalis. Importantly, the addition of BaFe12O19-polypyrrole nanocomposites not only improved the coating hardness and adhesion but also produced a coating with a good microwave absorption performance. The results suggested that BaFe12O19/PPy composite has a lower reflection loss peak and a larger effective bandwidth at the X band when the proportion of the absorbent sample is 5–7%, when the absorption performance is the best. The reflection loss is in the range of 8.88–10.92 GHz below −10 dB. [ABSTRACT FROM AUTHOR]

In the process of using photocatalysts to treat tetracycline (TC) wastewater, the degradation efficiency of soybean powder carbon material (SPC) can be improved by loading it with cerium oxide (CeO2). In this study, firstly, SPC was modified by phytic acid. Then, the CeO2 was deposited on modified SPC using the self-assembly method. Catalyzed cerium (III) nitrate hexahydrate (CeH3NO4) was treated with alkali and calcined at 600 °C under nitrogen. XRD, XPS, SEM, EDS, UV-VIS /DRS, FTIR, PL and N2 adsorption–desorption methods were used to characterize the crystal structure, chemical composition, morphology, surface physical and chemical properties. The effects of catalyst dosage, monomer contrast, pH value and co-existing anions on TC oxidation degradation were investigated, and the reaction mechanism of a 600 Ce-SPC photocatalytic reaction system was discussed. The results show that the 600 Ce-SPC composite presents uneven gully morphology, which is similar to the natural "briquettes". The degradation efficiency of 600 Ce-SPC reached about 99% at 60 min under light irradiation when the optimal catalyst dosage and pH were 20 mg and 7. Meanwhile, the reusability of the 600 Ce-SPC samples showed good stability and catalytic activity after four cycles. [ABSTRACT FROM AUTHOR]

Photocatalysis is a hopeful technology to solve various environmental problems, but it is still a technical task to produce large-scale photocatalysts in a simple and sustainable way. Here, nano-flower β-Bi2O3/TiO2 composites were prepared via a facile solvothermal method, and the photocatalytic performances of β-Bi2O3/TiO2 composites with different Bi/Ti molar ratios were studied. The nano-flower Bi2O3/TiO2 composites were studied by SEM, XRD, XPS, BET, and PL. The PL result proved that the construction of staggered heterojunction enhanced the separation efficiency of carriers. The degradation RhB was applied to study the photocatalytic performances of prepared materials. The results showed that the degradation efficiency of RhB increased from 61.2% to 99.6% when the molar ratio of Bi/Ti was 2.1%. It is a mesoporous approach to enhance photocatalytic properties by forming heterojunction in Bi2O3/TiO2 composites, which increases the separation efficiency of the generated carriers and improves photocatalytic properties. The photoactivity of the Bi2O3/TiO2 has no evident changes after the fifth recovery, indicating that the Bi2O3/TiO2 composite has distinguished stability. [ABSTRACT FROM AUTHOR]

Heterojunction photocatalytic materials show excellent performance in degrading toxic pollutants. This study investigates the influence of calcination temperature on the performances of floral Bi2O3/TiO2 composite photocatalyst crystal, which was prepared with glycerol, bismuth nitrate, and titanium tetrachloride as the major raw materials via the solvothermal method. XRD, SEM/TEM, BET, Uv-vis, and XPS were employed to analyze the crystal structure, morphology, specific surface area, band gap, and surface chemical structure of the calcined temperature catalysts. The calcination temperature influence on the catalytic performance of composite photocatalysis was tested with rhodamine B (RhB) as the degradation object. The results revealed the high catalytic activity and higher photocatalytic performance of the Bi2O3/TiO2 catalyst. The degradation efficiency of the Bi2O3/TiO2 catalyst to RhB was 97%, 100%, and 91% at 400 °C, 450 °C, and 500 °C calcination temperatures, respectively, in which the peak degradation activity appeared at 450 °C. The characterization results show that the appropriate calcination temperature promoted the crystallization of the Bi2O3/TiO2 catalyst, increased its specific surface area and the active sites of catalytic reaction, and improved the separation efficiency of electrons and holes. [ABSTRACT FROM AUTHOR]

Senecavirus A (SVA), an important emerging porcine virus, has outbreaks in different regions and countries each year, becoming a virus with global prevalence. SVA infection has been reported to induce macroautophagy/autophagy; however, the molecular mechanisms of autophagy induction and the effect of SVA on autophagy remain unknown. This study showed that SVA infection induced the autophagy process in the early stage of SVA infection, and the rapamycin-induced autophagy inhibited SVA replication by degrading virus 3 C protein. To counteract this, SVA utilized 2AB protein inhibiting the autophagy process from promoting viral replication in the late stage of SVA infection. Further study showed that SVA 2AB protein interacted with MARCHF8/MARCH8 and LC3 to degrade the latter and inhibit the autophagy process. In addition, we found that MARCHF8 was a positive regulator of type I IFN (IFN-I) signaling. During the autophagy process, the SVA 2AB protein targeted MARCHF8 and MAVS forming a large complex for degradation to deactivate IFN-I signaling. Together, our study reveals the molecular mechanisms of selective autophagy in the host against viruses and reveals potential viral strategies to evade the autophagic process and IFN-I signaling for successful pathogenesis. Abbreviations: Baf A1: bafilomycin A1; Co-IP: co-immunoprecipitation; CQ: chloroquine; DAPI: 4′,6-diamidino-2-phenylindole; hpi: hours post-infection; IFN: interferon; ISG: IFN-stimulated gene; MAP1LC3/LC3: microtubule associated protein 1 light chain 3; MARCHF8/MARCH8: membrane associated ring-CH-type finger 8; MAVS: mitochondrial antiviral signaling protein; MOI: multiplicity of infection; Rapa: rapamycin; RT: room temperature; siRNA: small interfering RNA; SVA: Senecavirus A; TCID50: 50% tissue culture infectious doses. [ABSTRACT FROM AUTHOR]

Functionalized silicon dioxide nanoparticles (nano-fSiO2) were uniformly deposited on the surface of carbon fibers (CFs) using a coating process which consisted of immersing the fibers directly in a suspension of nano-fSiO2 particles and epoxy monomers in 1-methyl-2-pyrrolidinone (NMP). The 0° flexural properties, 90° flexural properties, and Interlaminar shear strength (ILSS) mechanical properties of unidirectional epoxy composites made with nano-fSiO2+epoxy sized carbon fibers, with control fibers, and with epoxy-only sized fibers were measured and compared. An obvious increase of the fiber/matrix adherence strength was obtained with the nano-fSiO2+epoxy coating. The nano-fSiO2+epoxy sized CF/epoxy composites showed a relative increase of 15%, 50%, and 22% in comparison to control fibers, for the Interlaminar shear strength, the 90° flexural strength and the 90° flexural modulus, respectively, but little e difference was measured between the different systems for the 0° flexural properties. The observation of the fracture surfaces by scanning electron microscopy of composite fracture confirmed the improvement of the interfacially dependent mechanical properties. POLYM. COMPOS., 38:1474-1482, 2017. © 2015 Society of Plastics Engineers [ABSTRACT FROM AUTHOR]