α-苯基邻硝基苄类保护基酯化方法的选择及其光解性质

研究了α 苯基邻硝基苄类光致保护基的合成方法和酯化方法,探讨了其光解性质并同α 甲基邻硝基苄类保护基的光解性质进行了比较,为实现多波长正交光致脱保护的研究寻求技术上的支持。

光解性塑料户外暴露试验方法的验证试验

本试验选取多种光降解膜对标准ASTM D5272-08《光解性塑料户外曝露试验标准规则》中的试验方法和条件进行必要的验证和对比,为修订我国国家标准提供技术依据。

二氰蒽醌的水解、光解和挥发性

为研究二氰蒽醌的水解、光解和挥发3种环境行为特性,采用室内模拟实验方法,测定二氰蒽醌的水解性、光解性和挥发性,并对此3种特性分别进行评价。结果表明:二氰蒽醌的水解半衰期t1/2为42.5d[pH值5,(25±1)℃]、84.5h[pH值7,(25±1)℃]、19.3h[pH值5,(50±1)℃]、85.6min[pH值7,(50±1)℃],在pH值9缓冲液中迅速水解而无法测定其半衰期;该农药在纯水中光解t1/2为52.1min(平均光强为4313lx,平均紫外强度为92.3μw/cm2);其挥发性表现为在空气、水和云南黏土表面3种介质中均未有挥发。按《化学农药环境安全评价试验准则》规定,二氰蒽醌水解性为较易水解和易水解,在纯水中光解特性为易光解,在空气、水和云南黏土表面挥发性属难挥发。

BiOBr/ATP的制备及光催化降解四环素性能研究

通过湿式机械化学合成法一步制备了BiOBr/ATP复合光催化剂,利用扫描电子显微镜(SEM)、X射线衍射仪(XRD)、红外光谱(FT-IR)和X射线能谱(XPS)等对所制备催化剂的微观结构和形貌进行表征,通过在可见光照射下光催化降解四环素评价催化剂的活性,并考察了其降解四环素类抗生素的性能和机理.结果表明,凹凸棒土棒晶(ATP)与溴氧铋(BiOBr)纳米片之间形成了插层结构,且在ATP质量分数为5%时,复合材料的光催化效果最佳,四环素降解率达到88.23%.通过自由基抑制实验推测主要作用是(·O^(2−)),并提出了可能的四环素降解机制.根据活性物种捕获实验,·O^(2−)和·OH是主要活性物种,h^(+)和e^(−)是次要活性物种.瞬态光电流测试表明,BiOBr/ATP复合光催化剂的光电流增强是BiOBr的1.24倍.

Synthesis and highly efficient photocatalytic activity of mixed oxides derived from ZnNiAl layered double hydroxides

ZnO/NiO/ZnAl2O4 mixed-metal oxides were successfully synthesized through a hydrotalcite-like precursor route, in which appropriate amounts of metal salts solutions were mixed to obtain a new series of ZnNiAl layered double hydroxides（LDHs） as precursors, followed by calcination under different temperatures. The as-obtained samples were characterized by SEM, HRTEM, TEM, XRD, BET, TG-DTA, and UV-Vis spectra techniques. The photocatalytic activities of the samples were evaluated by degradation of methyl orange（MO） under the simulated sunlight irradiation. The effects of Zn/Ni/Al mole ratio and calcination temperature on the composition, morphology and photocatalytic activity of the samples were investigated in detail. The results indicated that compared with ZnNiAl-LDHs, the mixed-metal oxide showed superior photocatalytic performance for the degradation of MO. A maximum of 97.3% photocatalytic decoloration rate within 60 min was achieved from the LDH with the Zn/Ni/Al mole ratio of 2：1：1 and the calcination temperature of 500 ℃, which much exceeded that of Degussa P25 under the same conditions. The possible mechanism of photocatalytic degradation over ZnO/NiO/ZnAl2O4 was discussed.

Neutral Dissociation of Superexcited Nitric Oxide Induced by Intense Laser Fields

Superexcited states of NO molecule and their neutral dissociation processes have been studied both experimentally and theoretically. Neutral excited N^＊ and O^＊ atoms are detected by fluorescence spectroscopy for the NO molecule upon interaction with 800 nm intense laser radiation of duration 60 fs and intensity 0.2 PW/cm^2. Intense laser pulse causes neutral dissociation of superexcited NO molecule by way of multiphoton excitation, which is equivalent to single photon excitation in the extreme-ultraviolet region by synchrotron radiation. Potential energy curves （PECs） are also built using the calculated superexcited state of NO^＋. In light of the PECs, direct dissociation and pre-dissociation mechanisms are proposed respectively for the neutral dissociation leading to excited fragments N^＊ and O^＊.

Synthesis and photoluminescence properties of single-crystal ZnO hexagonal pyramids by PEG400-assisted thermal decomposition route

Large-scale synthesis of ZnO hexagonal pyramids was achieved by a simple thermal decomposition route of precursor at 240 oC in the presence of PEG400. The precursor was obtained by room-temperature solid-state grinding reaction between Zn（CH3COO）2-2H2O and Na2CO3. Crystal structure and morphology of the products were analyzed and characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM） and high-resolution transmission electron microscopy （HRTEM）. The results of further experiments show that PEG400 has an important role in the formation of ZnO hexagonal pyramids. Difference between the single and double hexagonal pyramid structure may come from the special thermal decomposition reaction. The photoluminescence （PL） spectra of ZnO hexagonal pyramids exhibit strong near-band-edge emission at about 386 nm and weak green emission at about 550 nm. The Raman-active vibration at about 435 cm-1 suggests that the ZnO hexagonal pyramids have high crystallinity.

Influence of Triarylamine and Indoline as Donor on Photovoltaic Performance of Dye-Sensitized Solar Cells Employing Cobalt Redox Shuttle

Two organic dyes XSS1 and XS52 derivated from triarylamine and indoline are synthesized for dye-sensitized solar ceils （DSCs） employing cobalt and iodine redox shuttles. The effects of dye structure upon the photophysical, electro-chemical characteristics and cell perfor- mance are investigated. XS51 with four hexyloxyl groups on triarylamine performs better steric hindrance and an improvement of photovoltage. X852 provides higher short-circuit photocurrent density due to the strong electron-donating capability of indoline unit. The results from the redox electrolyte on cell performances indicate that the synthesized dyes are more suitable for tris（1,10-phenanthroline）cobalt（II/III） redox couple than I-/I3- redox couple in assembling DSCs. Application of X852 in the cobalt electrolyte yields a DSC with an overall power conversion efficiency of 6.58% under AM 1.5 （100 mW/cm2） irradiation.

Characterization of V_2O_5/MoO_3 composite photocatalysts prepared via electrospinning and their photodegradation activity for dimethyl phthalate

Vanadium pentoxide（V2O5）/molybdenum trioxide（MoO 3） composites with different molar ratios of vanadium（V） to molybdenum（Mo） were synthesized via a simple electrospinning technique. The photocatalytic activity of the composites were evaluated by their ability to photodegrade methylene blue and dimethyl phthalate（DMP） under visible-light irradiation. Compared with pure V2O5 and MoO 3,the V2O5/MoO 3 composites showed enhanced visible-light photocatalytic activity because of a V 3d impurity energy level and the formation of heterostructures at the interface between V2O5 and MoO 3. The optimal molar ratio of V to Mo in the V2O5/MoO 3 composites was found to be around 1/2. Furthermore,high-performance liquid chromatographic monitoring revealed that phthalic acid was the main intermediate in the photocatalytic degradation process of DMP.

Purification and Characterization of Flammulin,a Basic Protein with Anti-tumor Activities from Flammulina velutipes

Aim To purify and characterize flammulin, a basic protein with anti-tumoractivities. Methods Ammonium sulfate, ethanol fractionation and column chromatography were used forseparation and purification. Electrophoretic analysis, amino acid analysis, and MS of flammulin werecarried out. Results Flammulin was purified to electrophoretic homogeneity and crystallized. With amolecular mass of 19891.13 Da, pI 8.9, λ_(max) = 276 - 278 nm, λ_(min) = 250 nm, flammulin wascharacterized by its lack of methionine. Fingerprint mapping of flammulin was determined by MALDI-MSfollowing in-gel protease digestion; no close matches were identified. Conclusion Flammulin waspurified to electrophoretic homogeneity, and its characteristics are discussed for the first time.

Preparation, Characterization, Photocatalytic Activity of S and Ag co-Doped Mesoporous Titania Photocatalysts

In order to improve the photocatalytic performance of mesoporous titania under visible light, a series of photocatalysts of S and Ag co-doped mesoporous titania have been successfully prepared by template method using thiourea, AgNO3 and tetrabutyl titanate as precursors and Pluronic P123 （EO20PO70EO20） as template. Scanning electron microscopy （SEM）, X-ray diffraction （XRD）, nitrogen adsorption-desorption measurements, and UV-visible spectroscopy （UV-Vis） were employed to characterize the morphology, crystal structure, surface structure, and optical absorption properties of the samples. The microcrystal of the photocatalysts consisted of anatase phase and was approximately present in the form of spherical particle. The photocatalytic performance was studied by photodegradation methyl orange （MO） in water under UV and visible light irradiation. The calcination temperature and the doping content influenced the photoactivity. In addition, the possibility of cyclic usage of co-doped mesoporous titania was also confirmed, the photocatalytic activity of mesoporous titania remained above 89% of that of the fresh sample after being used four times. It was shown that the co-doped mesoporous titania could be activated by visible light and could thus be potentially applied for the treatment of water contaminated by organic pollutants. The synergistic effect of sulfur and silver co-doping played an important role in improving the photocatalytic activity.

Modification of Reflectron Time-of-Flight Mass Spectrometer for Photodissociation of Mass-Selected Cluster lons

We introduce a modification of reflectron time-of-flight mass spectrometer for laser photodissociation of mass-selected ions. In our apparatus, the ions of interests were selected by a mass gate near the first space focus point and decelerated right after the mass gate, were then crossed by a laser beam for dissociation. The daughter ions and surviving parent ions were re-accelerated and analyzed by the reflectron time-of-flight mass spectrometer. Compared to the designs reported by other research groups, our selection-deceleration-dissociation-reacceleration approach has better daughter-parent-ions-separation, easier laser timing, and better overlapping between the ion beam and laser beam. We also conducted detailed cal- culations on the parent ion and daughter ion flight times, and provided a simplified formula for the calibration of daughter ion mass.

Synthesis and Photocatalytic Activity of One-dimensional ZnO-Zn2SnO4 Mixed Oxide Nanowires

Mixed oxide photocatalysts, ZnO-Zn2SnO4 （ZnO-ZTO） nanowires with different sizes were prepared by a simple thermal evaporation method. The ZnO-ZTO nanowires were characterized with a scanning electron microscope, X-ray diffraction, high-resolution transmission electron microscopy, energy-dispersive spectrom- eter, and X-ray photoelectron spectra. The photocatalytic activity of the ZnO-ZTO mixed nanowires were studied by observing the photodegradation behaviors of methyl orange aqueous solution. The results suggest that the ZnO-ZTO mixed oxide nanowires have a higher photocatalytic activity than pure ZnO and Zn2SnO4 nanowires. The photocatalyst concentration in the solution distinctly affects the degradation rate, and our results show that higher photodegradation efficiency can be achieved with a smaller amount of ZnO-ZTO nanowire catalyst, as compared to the pure ZnO and ZTO nanowires. Moreover, the photocatalytic activity can also be enhanced by reducing the average diameter of the nanowires. The activity of pure ZnO and ZTO nanowires are also enhanced by physically mixing them. These results can be explained by the synergism between the two semiconductors.

Tannins from Canarium album with potent antioxidant activity

The contents of total phenolics and extractable condensed tannins in the leaves, twigs and stem bark of Canarium album were determined. The structural heterogeneity of condensed tannins from stem bark was characterized by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry （MALDI-TOF MS） and nuclear magnetic resonance （NMR） analyses The results show the predominance of signals representative of procyanidins and prodelphinidins. In addition, epicatechin and epigallocatechin polymers with galloylated procyanidin or prodelphinidin were also observed. The tannins were screened for their potential antioxidant activities using l,l-diphenyl-2-picrylhydrazyl （DPPH） and ferric reducing/antioxidant power （FRAP） model systems. Tannins extracted from leaves, twigs and stem bark all showed a very good DPPH radical scavenging activity and ferric reducing power.

Linearity optimization of edge filter demodulators in FBG_s

A kind of electric circuit is improved to optimize the linearity of edge filter demodulators in FBG .By using a logarithm amplifier and an extraction operation, the linear range of optimized edge filter demodulators has been broadened effectively, and the requirement of optical filter＇s linear range has been reduced. Theoretical analyses and the simulation results indi-cated that the linear range of optimized edge fdter demodulator＇s covers the whole transition region of the edge filter, while a strict linearity of the optical filter is not necessary.

Preparation of TiO_2/SiO_2 Aerogels by Non-supercritical Drying Method and Their Photocatalytic Activity for Degradation of Pyridine

TiO2/SiO2 aerogels with different molar ratio of SiO2/TiO2 were prepared via non-supercritical method using tetrabutyl titanate and silica sols as raw materials. The samples were characterized by TEM, SEM, BET, IR, XRD and so on. The results indicate that the BET surface area of TiO2/SiO2 aerogels calcined at 550℃ which consisted of anatase structure of TiO2 with narrow distribution pores of 5-25 nm is as high as 357.89 m2·g-1. For the photocatalytic degradation of pyridine, the catalytic activities of TiO2/SiO2 aerogels are much higher than that of TiO2 powder. The photocatalytic activity of TiO2/SiO2 aerogels calcined at 800℃ is the optimum. The higher the content of SiO2, the higher the photocatalytic activity of TiO2/SiO2 aerogels. The cost for preparation of the aerogels is greatly reduced by using non-supercritical drying method, and the aerogels are hopefully applied in the treatment of industrial waste water such as coking effluent treatment.

Photocatalytic degradation of textile dyeing wastewater through microwave synthesized Zr-AC,Ni-AC and Zn-AC

The novel zirconium oxide, nickel oxide and zinc oxide nanoparticles supported activated carbons（Zr-AC, Ni-AC, Zn-AC） were successfully fabricated through microwave irradiation method. The synthesized nanoparticles were characterized using XRD, HR-SEM, XPS and BET. The optical properties of Zr-AC, Ni-AC and Zn-AC composites were investigated using UV–Vis diffuse reflectance spectroscopy. The photocatalytic efficiency was verified in the degradation of textile dyeing wastewater（TDW） in UV light irradiation. The chemical oxygen demand（COD） of TDW was observed at regular intervals to calculate the removal rate of COD. Zn-AC composites showed impressive photocatalytic enrichment, which can be ascribed to the enhanced absorbance in the UV light region, the effective adsorptive capacity to dye molecules, the assisted charge transfer and the inhibited recombination of electron-hole pairs. The maximum TDW degradation（82% COD removal） was achieved with Zn-AC. A possible synergy mechanism on the surface of Zn-AC was also designed. Zn-AC could be reused five times without exceptional loss of its activity.

Stabilizing CuO photocathode with a Cu_(3)N protection shell

CuO,as a promising photocathode material,suffers from severe photocorrosion in photoelectrochemical water splitting applications.Herein,a Cu_(3)N protection shell was used to protect the CuO photocathode for the first time to effectively suppress the photocorrosion of CuO.Consequently,the Cu_(3)N‐protected CuO photocathode shows improved stability,retaining 80% of its initial current density in a 20‐min test,while only 10%of the initial current density can be retained for the bare photocathode.This work may provide an important strategy for using Cu_(3)N shells to stabilize unstable photocathodes.

Design of metal-organic frameworks(MOFs)-based photocatalyst for solar fuel production and photo-degradation of pollutants

Metal organic frameworks(MOFs)is a research hotspot in the solar fuel production and photo-degradation of pollutants field due to high surface area,rich metal/organic species,large pore volume,and adjustability of structures and compositions.Therefore,in this review,we first summarized the design factors of photocatalytic materials based on MOF from the perspective of"star"MOF.The modification strategies of MOFs-based photocatalysts were discussed to improve its photocatalytic activity and specific applications were summarized as well,including photocatalytic CO_(2)reduction,photocatalytic water splitting and photo-degradation of pollutants.Finally,the advantages and disadvantages of MOFs-based photocatalysts were discussed,the current challenges were highlighted,and suggestions for future research directions were proposed.

Photocatalytic degradation of 2,4-dichlorophenol with V_2O_5-TiO_2 catalysts: Effect of catalyst support and surfactant additives

Binary oxide catalysts with various weight percentage V2O5 loadings were prepared by solid‐state dispersion and the nanocomposites were modified with surfactants. The catalysts were analyzed using X‐ray diffraction, diffuse‐reflectance spectroscopy, Fourier‐transform infrared spectroscopy, scanning electron microscopy, and N2 adsorption‐desorption. The photocatalytic activities of the catalysts were evaluated in the degradation of 2,4‐dichlorophenol under ultraviolet irradiation. The photocatalytic activity of 50 wt%V2O5‐TiO2 （50V2O5‐TiO2） was higher than those of pure V2O5, TiO2, and P25. Interactions between V2O5 and TiO2 affected the photocatalytic efficiencies of the binary oxide catalysts. Cetyltrimethylammonium bromide （CTAB） and hexadecyltrimethylammonium bromide （HTAB） significantly enhanced the efficiency of the 50V2O5‐TiO2 catalyst. The highest per‐centage of 2,4‐dichlorophenol degradation （100%） and highest reaction rate （2.22 mg/（L·min）） were obtained in 30 min with the （50V2O5‐TiO2）‐CTAB catalyst. It is concluded that the addition of a surfactant to the binary oxide significantly enhanced the photocatalytic activity by modifying the optical and electronic properties of V2O5 and TiO2.