Enhancement of Cr(VI) removal efficiency via adsorption/photocatalysis synergy using electrospun chitosan/g-C3N4/TiO2 nanofibers.

Chitosan/g-C3N4/TiO2 (CS/CNT) nanofibers were fabricated by electrospinning technique for Cr(VI) removal through the adsorption and photocatalytic processes. The effects of crucial factors in the adsorption process including contact time (0-1440 min), pH (1-7), initial concentration of Cr(VI) (20-800 mg/L) were investigated. The photocatalytic experiment was executed in a photochemical reactor with an 800 W xenon lamp to simulate visible light. In adsorption process, at pH = 2, the adsorption capacities of chitosan (CS) nanofibers, CS/CNT10:1 (CS : g-C3N4/TiO2 = 10:1) nanofibers and CS/CNT5:1 nanofibers were 20.8, 165.3 and 68.9 mg/g, respectively, suggesting the addition of g-C3N4/TiO2 (CNT) could notably enhance the acid resistance of CS and widen its practical application. Under visible-light irradiation, the removal efficiency of Cr(VI) using CS/CNT nanofibers was appreciably improved, which was about 50 % higher than that of pure adsorption, indicating that the CS/CNT nanofibers exhibited the effective synergistic effect of adsorption and photocatalysis.

One Step In Situ Loading of CuS Nanoflowers on Anatase TiO2/Polyvinylidene Fluoride Fibers and Their Enhanced Photocatalytic and Self-Cleaning Performance.

CuS nanoflowers were loaded on anatase TiO2/polyvinylidene fluoride (PVDF) fibers by hydrothermal treated electrospun tetrabutyl orthotitanate (TBOT)/PVDF fibers at low temperature. The results indicated that the amount of copper source and sulfur source determined the crystallization and morphology of the resultant products. It was found that the composite of CuS narrowed the band gap energy of TiO2 and enhanced the separation efficiency of the photogenerated electron-hole pairs of TiO2. The photocatalytic reaction rate of CuS/TiO2/PVDF fibers to rhodamine B was 3 times higher than that of TiO2/PVDF fibers under visible light irradiation. Besides, owing to the preparation process was carried out at low temperature, the flexibility of CuS/TiO2/PVDF fibers was ensured. In addition, the self-cleaning performance of the dye droplets on the resultant product surface was demonstrated under visible light. Meanwhile, the resultant product can automatically remove dust on the surface of the material under the rolling condition of droplets due to its hydrophobicity. Therefore, the as-prepared CuS/TiO2/PVDF fibers can not only degrade the contaminated compounds, but also depress the maintenance cost owing to its self-cleaning performance, which means a very practical application prospect.

Flexible TiO2/PVDF/g-C3N4 Nanocomposite with Excellent Light Photocatalytic Performance.

As the world faces water shortage and pollution crises, the development of novel visible light photocatalysts to purify water resources is urgently needed. Over the past decades, most of the reported photocatalysts have been in powder or granular forms, creating separation and recycling difficulties. To overcome these challenges, a flexible and recyclable heterostructured TiO2/polyvinylidene fluoride/graphitic carbon nitride (TiO2/PVDF/g-C3N4) composite was developed by combining electrospinning, sintering and hydrothermal methods. In the composite, PVDF was used as a support template for removing and separating the photocatalyst from solution. Compared with pure TiO2, the TiO2/PVDF/g-C3N4 composite exhibited the extended light capture range of TiO2 into the visible light region. The photogenerated carriers were efficiently transferred and separated at the contact interface between TiO2 and g-C3N4 under visible light irradiation, which consequently increased the photocatalytic activity of the photocatalyst. In addition, the flexible composites exhibited excellent self-cleaning properties, and the dye on the photocatalysts was completely degraded by the as-prepared materials. Based on the intrinsic low cost, recyclability, absorption of visible light, facile synthesis, self-cleaning properties and good photocatalytic performances of the composite, the photocatalyst is expected to be used for water treatment.

High levels of testosterone inhibit ovarian follicle development by repressing the FSH signaling pathway.

The effect of high concentrations of testosterone on ovarian follicle development was investigated. Primary follicles and granulosa cells were cultured in vitro in media supplemented with a testosterone concentration gradient. The combined effects of testosterone and follicle-stimulating hormone (FSH) on follicular growth and granulosa cell gonadotropin receptor mRNA expression were also investigated. Follicle growth in the presence of high testosterone concentrations was promoted at early stages (days 1-7), but inhibited at later stage (days 7-14) of in vitro culture. Interestingly, testosterone-induced follicle development arrest was rescued by treatment with high concentrations of FSH (400 mIU/mL). In addition, in cultured granulosa cells, high testosterone concentrations induced cell proliferation, and increased the mRNA expression level of FSH receptor (FSHR), and luteinized hormone/choriogonadotropin receptor. It was concluded that high concentrations of testosterone inhibited follicle development, most likely through regulation of the FSH signaling pathway, although independently from FSHR downregulation. These findings are an important step in further understanding the pathogenesis of polycystic ovary syndrome.

[Emissions of methyl halides from coastal salt marshes: A review].

Methyl halides are the major carrier of halogens in the atmosphere, and they play an important role in tropospheric and stratospheric ozone depletion. Meanwhile, methyl halides can act as greenhouse gases in the atmosphere, and they are also environmentally significant because of their toxicity. Coastal salt marshes, the important intertidal ecosystems at the land-ocean interface, have been considered to be a large potential natural source of methyl halides. In this paper, the research status of the natural source or sink of methyl halides, the mechanisms of their emission from coastal salt marshes and affecting factors were summarized. In view of this, the following research fields need to be strengthened in the future: 1) Long time-scale and large region-range researches about the emission of methyl halides and the evaluation of their source and sink function, 2) Accurate quantification of contribution rates of different plant species and various biological types to fluxes of methyl halides, 3) Further researches on effects of the tidal fluctuation process and flooding duration on methyl halides emission, 4) Effects of the global change and human activities on methyl halides emission.

[Research advances in methyl bromide in the ocean].

Methyl bromide is an important atmospheric trace gas, which plays significant roles in the global warming and atmospheric chemistry. The ocean plays important and complex roles in the global biogeochemical cycles of methyl bromide, not only the source of atmospheric methyl bromide, but also the sink. Therefore, developing the chemical research of the soluble methyl bromide in the ocean, will not only have a certain guiding significance to the atmospheric ozone layer protection, but also provide a theoretical basis for estimating methyl bromide's contribution to the global environmental change on global scale. This paper reviewed the research advances on methyl bromide in the ocean, from the aspects of the biogeochemical cycle of methyl bromide in the ocean, the analysis and determination method, the concentration distribution, the sea-to-air flux and its sources and sinks in the atmosphere. Some deficiencies in the current studies were put forward, and the directions of the future studies were prospected.