梨园戏《井边会》与南音“指”《照见》的比照

文章以小梨园的传统剧目《刘智远》第四出《井边会》与福建南音《刘智远与李三娘》中的李三娘唱段《照见》,做一个初浅的比照。通过二者的形成年代、人文背景、唱词、音乐结构、曲调、调式调性等来找寻梨园戏与福建南音之间千丝万缕的关系。

照见

看着镜中的自己 突然感到吃惊 这个陌生的人 怎么会是我 他的名字 也令人不解

Hydrothermal Synthesis and Efficient Visible Light Photocatalytic Properties of InVO4 Hierarchical Microspheres and InVO4 Nanowires

In this work, InVO4 hierarchical microspheres and InVO4 nanowires were successfully synthesized by a facile hydrothermal method. Field emission scanning electron microscopy showed that InVO4 crystals can be fabricated in different morphologies by simply manipulating the reuction parameters of hydrothermal process. The as-prepared InVO4 photocatalysts exhibited higher photocatalytic activities in the degradation of rhodamine B under visible-light irradiation （λ〉420 nm） compared with commercial P25 TiO2. Furthermore, the as-synthesized InVO4 hierarchical microspheres showed higher photocatalytic activity than that of InVO4 nanowires. Up to 100% Rh B （3 μmol/L） was decolorized after visible-light irradiation for 40 min. In addition, the reason for the difference in the photocatalytic activities for InVO4 hierarchical microspheres and InVO4 nanowires was studied based on their structures and morphologies.

Visible-Light Activities of Erbium Doped BiVO4 Photocatalysts

Er-doped BiVO4 composite photocatalyst was hydrothermal synthesized and characterized by X-ray powder diffraction, scanning electron microscopy, energy-dispersive X-ray Spectroscopy, X-ray photoelectron spectroscopy, and UV-Vis diffuse reflectance spectra techniques. The activity of the catalyst was determined by oxidative decomposition of methyl orange in aqueous solution under visible-light irradiation. X-ray photoelectron spectroscopy and energy-dispersive X-ray Spectroscopy analysis revealed that the doped Er existed in the form of Er2O3. It also showed that the Er doping can enhance the visible-light absorption abilities of catalysts and their visible-light-driven photocatalytic activities in comparison with those of pure BiVO4.

Fast electron transfer and enhanced visible light photocatalytic activity by using poly-o-phenylenediamine modified AgCl/g-C_3N_4 nanosheets

Exfoliation of bulk graphitic carbon nitride(g‐C3N4)into two‐dimensional(2D)nanosheets is one of the effective strategies to improve its photocatalytic properties so that the 2D g‐C3N4 nanosheets(CN)have larger specific surface areas and more reaction sites.In addition,poly‐o‐phenylenediamine(PoPD)can improve the electrical conductivity and photocatalytic activity of semiconductor materials.Here,the novel efficient composite PoPD/AgCl/g‐C3N4 nanosheets was first synthesized by a precipitation reaction and the photoinitiated polymerization approach.The obtained photocatalysts have larger specific surface areas and could achieve better visible‐light response.However,silver chloride(AgCl)is susceptible to agglomeration and photocorrosion.The PoPD/AgCl/CN composite exhibits an extremely high photocurrent density,which is three times that of CN.Obviously enhanced photocatalytic activities of PoPD/AgCl/g‐C3N4 are revealed through the photodegradation of tetracycline.The stability of PoPD/AgCl/CN is demonstrated based on four cycles of experiments that reveal that the degradation rate only decreases slightly.Furthermore,.O2^-and h+are the main active species,which are confirmed through a trapping experiment and ESR spin‐trap technique.Therefore,the prepared PoPD/AgCl/CN can be considered as a stable photocatalyst,in which PoPD is added as a charge carrier and acts a photosensitive protective layer on the surface of the AgCl particles.This provides a new technology for preparing highly stable composite photocatalysts that can effectively deal with environmental issues.

Formation of active radicals and mechanism of photocatalytic degradation of phenol process using eosin sensitized TiO_2 under visible light irradiation

The role of oxygen and the generation of active radicals in the photocatalitic degradation of phenol were investigated using the eosin sensitized TiO2 as photocatalyst under visible light irradiation. Diffuse reflectance spectra show that the absorbancy range of eosin/TiO2 is expanded from 378 nm (TiO2 ) to about 600 nm. The photocatalitic degradation of phenol is almost stopped when the eosin/TiO2 system is saturated with N2 , which indicates the significance of O2 . The addition of NaN 3 (a quencher of single oxygen) causes about a 62% decrease in the phenol degradation. The phenol degradation ratio is dropped from 92% to 75% when the isopropanol (a quencher of hydroxyl radical) is present in the system. The experimental results show that there are singlet oxygen and hydroxyl radical generated in the eosin/TiO2 system under visible light irradiation. The changes of absorbancy indicate that the hydrogen peroxide might be produced. Through the analysis and comparison, it is found that the singlet oxygen is the predominant active radical for the degradation of phenol.

Synthesis and Antimicrobial Activity of Boron-doped Titania Nano-materials

Antibacterial activity of boron-doped TiO2(B/TiO2) nano-materials under visible light irradiation and in the dark was investigated. A simple sol-gel method was used to synthesize TiO2 nano-materials. X-ray diffraction pattern of B/TiO2 nano-materials represents the diffraction peaks relating to the crystal planes of TiO2(anatase and rutile). X-ray photoelectron spectroscopy result shows that part of boron ions incorporates into TiO2 lattice to form a possible chemical environment like Ti O B and the rest exist in the form of B2O3. The study on antibacterial effect of B/TiO2 nano-materials on fungal Candida albicans(ATCC10231), Gram-negative Escherichia coli(ATCC25922) and Gram-positive Staphylococcus aureus(ATCC6538) shows that the antibacterial action is more significant on Candida albicans than on Escherichia coli and Staphylococcus aureus. Under visible light irradiation, the antibacterial activity is superior to that in the dark.

Photorheologically reversible micelle composed of polymerizable cationic surfactant and 4-phenylazo benzoic acid

A photorheologically reversible micelle composed of polymerizable cationic surfactant n-cetyl dimethylallyl am- monium chloride （CDAAC） and trans-4-phenylazo benzoic acid （trans-ACA） was prepared. The effects of molar ratio of CDAAC/trans-ACA, time of UV and visible light irradiation and temperature on the rheological properties of micellar system were investigated. The results show that before UV irradiation the system with an optimum CDAAC/trans-ACA molar ratio of 1.4 forms viscoelastic micelles at 45 ℃. After 365 nm UV irradiation, the viscos- ities of micelle systems with different concentrations at fixed molar ratio of 1.4 are decreased by 85%-95%. The CDAAC/trans-ACA （14 mmol. L- 1/10 mmol. L- 1 ） micelle system exhibits shear thinning property and its viscos- ity is decreased obviously with the increases of UV irradiation time less than I h. The rheological process during LIV irradiation for CDAAC/trans-ACA （14 mmol- L- 1/10 mmol. L 1） micelle proves that viscosity, elastic modulus G＇ and viscous modulus G＂ will reduce quickly with the UV light. Furthermore, the micelle system after 1 h UV- irradiation is able to revert to its initial high viscosity with 460 nm visible light irradiation for 4 h, and the micelle can be cycled between low and high viscosity states by repetitive UV and visible light irradiations. The LIV-Vis spectra of CDAAC/trans-ACA micelle indicate that its photosensitive theological properties are related closely to photoisomerization of trans-ACA to c/s-ACA.

Chemical Composition of Summertime PM_(2.5) and Its Relationship to Aerosol Optical Properties in Guangzhou,China

Urban aerosols have a large effect on the deterioration of air quality and the degradation of atmospheric visibility.Characterization of the chemical composition of PM 2.5 and in situ measurements of the optical properties of aerosols were conducted in July 2008 at an urban site in Guangzhou,Southern China.The mean PM 2.5 concentration for the entire period was 53.7±23.2 μg m 3.The mean PM 2.5 concentration (82.7±25.4 μg m 3) on hazy days was roughly two times higher than that on clear days (38.8±8.7 μg m 3).The total water-soluble ion species and the total average carbon accounted for 47.9%±4.3% and 35.2%±4.5%,respectively,of the major components of PM 2.5.The increase of secondary and carbonaceous aerosols,in particular ammonium sulfate,played an important role in the formation of haze pollution.The mean absorption and scattering coefficients and the single scattering albedo over the whole period were 53±20 M m 1,226±111 M m 1,and 0.80±0.04,respectively.PM 2.5 had a high linear correlation with the aerosol extinction coefficient,elemental carbon (EC) was correlated with aerosol absorption,and organic carbon (OC) and SO 4 2 were tightly linked to aerosol scattering.

Preparation of TiO_2 photocatalyst loaded with V_2O_5 for O_2 evolution

TiO2 photocatalysts loaded with V2O5 were prepared via a modified hydrolysis process,and characterized by X-ray diffraction,transmission electron microscopy,Raman spectra and diffuse reflectance UV-Vis spectra measurements. The photocatalytic activity of V2O5/TiO2 was investigated by employing splitting of water for O2 evolution. The results indicate that V2O5 loading can pronouncedly improve the photocatalytic activity of TiO2 with Fe3+ as an electron acceptor under UV or visible light irradiation. The optimum mass fraction of the loaded V2O5 is 8%,and the largest speed of O2 evolution for 8%V2O5 (mass fraction) loaded TiO2 catalyst is 118.2 μmol/(L.h) under UV irradiation,and 83.7 μmol/(L.h) under visible light irradiation.

Photocatalytic Denitrogenation over Modified Waste FCC Catalyst

The strontium modified waste FCC catalyst was prepared by magnetic stirring method and characterized by Xray diffractometry(XRD),UV-Vis diffuse reflectance spectrometry(DRS),X-ray photoelectron spectroscopy(XPS)and scanning electron microscopy(SEM).Meanwhile,its photocatalytic denitrogenation performance was evaluated in terms of its ability to degrade the N-containing simulation oil under visible light.A mixture of strontium nitrate solution(with a concentration of 0.5 mol/L)and waste FCC catalyst was calcined at 400℃for 5 h prior to taking part in the photocatalytic denitrogenation reaction.The test results showed that the photocatalytic degradation rate of pyridine contained in simulation oil in the presence of the strontium modified FCC catalyst could reach 92.0% under visible light irradiation for 2.5 h.

Photocatalytic Degradation of Methylene Blue with Side-glowing Optical Fiber Deliverying Visible Light

The side-glowing optical fibers (SOFs) were chosen as the conducting medium of endogenous light; and 20 mg·L-1 methylene blue was chosen as the target to be degraded. The SOF is made up of quartz core with a silicon cladding, which can emit light through side surface more uniformly and transmit light for longer distance to avoid attenuation of light by liquid medium. The filament lamp was chosen as visible light source. Different reaction conditions, such as the presence of optical fiber or not, the quantity of SOF, light irradiation intensity were tested by measuring the methylene blue degradation of methylene blue. The results show that suitable reaction conditions were 1.167 g·L-1 Ag + /TiO 2 with 7% (by mass) of Ag + doped in TiO 2 , and 500 roots of SOF (30 cm length in solution). The photocatalytic degradation efficiency under 300W lamp irradiation for 8h was about 97%. And the photocatalytic degradation efficiency of methylene blue degradation was proportional to SOF quantity, light irradiation intensity and catalytic dosage within a certain range. Compared with general UV and visible light SOFs could save a huge amount of energy and cost, in the potential applications in dealing with organic pollutants on a large scale.

Synthesis of Ordered Multivalent Mn-TiO2 Nanospheres with Tunable Size： A High Performance Visible-Light Photocatalyst

A facile and reproducible method has been developed for the synthesis of ordered anatase Mn-TiO2 nanospheres with controllable sizes in the range 200-300 nm by simply varying the amount of manganese（lI） chloride added. The samples were characterized by X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, scanning electron microscope （SEM）, and transmission electron microscope （TEM） measurements, and it was found that the manganese exists in multivalent forms （Mn4＋/Mn3＋） and substitutes for some of the Ti4＋ in the anatase TiO2 lattice. The presence of Mn significantly influences the morphology and high-temperature stability of TiO2, and extends its light absorption range. Surface photovoltage and photocurrent measurements revealed that an electronic interaction between the Mn and TiO2 was present, in which Mn served as an electron acceptor and effectively inhibited the charge recombination in TiO2; this is thought to be responsible for the highly efficient photocatalytic activity of the material in the degradation of rhodarnine B （RhB） under visible-light irradiation （λ 〉 420 nm）.

A High Performance Cobalt-Doped ZnO Visible Light Photocatalyst and Its Photogenerated Charge Transfer Properties

Highly photocatalytically active cobalt-doped ZnO （ZnO：Co） nanorods have been prepared by a facile hydrothermal process. X-ray diffraction, X-ray photoelectron spectroscopy, Raman scattering and UV-vis diffuse reflectance spectroscopy confirmed that the dopant ions substitute for some of the lattice zinc ions, and furthermore, that Co〉 and Co〉 ions coexist. The as-prepared ZnO：Co samples have an extended light absorption range compared with pure ZnO and showed highly efficient photocatalytic activity, only requiring 60 rain to decompose -93% of alizarin red dye under visible light irradiation （λ 〉 420 nm）, The photophysical mechanism of the visible photocatalytic activity was investigated with the help of surface photovoltage spectroscopy. The results indicated that a strong electronic interaction between the Co and ZnO was present, and that the incorporation of Co promoted the charge separation and enhanced the charge transfer ability and, at the same time, effectively inhibited the recombination of photogenerated charge carriers in ZnO, resulting in high visible light photocatalytic activity.

Heterogeneous degradation of toxic organic pollutants by hydrophobic copper Schiff-base complex under visible irradiation

A hydrophobic complex of Cu2＋[bis-salicylic aldehyde-o-phenylenediamine], Cu-SPA, was prepared and used as a heterogeneous photocatalyst to degrade organic pollutants in water under visible irradiation （λ≥420 nm） at neutral pH. The structure of complex was characterized by using nuclear magnetic resonance （NMR）, elemental analysis, IR and UV-vis spectrometries. Degradation of Rhodamine B （RhB）, Sulforhodamine B （SRB） and Benzoic acid （BA） in water were used as model reactions to evaluate the photocatalytic activities of Cu-SPA. The results indicated that RhB and SRB were easily adsorbed on the hydrophobic surface of Cu-SPA from aqueous solution （the maximum adsorption amount： Qmax = 11.09 and 8.05 μmol/g, respectively）. Under visible irradiation, RhB and SRB were decolorized completely after 210 and 240 min, respectively, and BA was removed completely after 5 h. The efficiency of H202 was 〉 95%, in contrast to that of the reaction without catalyst or light （〈 20%）. In water soluble medium, the hydrophobic Cu-SPA can be used more than 6 cycles. ESR results and the behavior of cy- clic voltammetry showed that, in the reaction process, Cu2＋-SPA was reduced to intermediate state Cu＋-SPA firstly, which was extremely unstable and reacted rapidly with H2O2, leading to high reactive oxygen species （.OH radical ） to degrade the substrate.

Preparation,characterization of Mo,Ag-loaded BiVO_4 and comparison of their degradation of methylene blue

Two types of metal-loaded visible-light-driven photocatalysts,Mo-BiVO4and Ag-BiVO4,were synthesized by wet impregnation method.Material poperties were characterized by UV-vis diffuse reflectance spectroscopy,X-ray diffraction,field emission scanning electron microscopy,X-ray photoelectron spectroscopy and low temperature nitrogen adsorption-desorption.Photocatalytic activity of the obtained materials was investigated through degrading methylene blue(MB) solution under visible-light irradiation.The results reveal that both metal loaded-BiVO4catalysts have monoclinic scheelite structure.Mo and Ag exist as oxides on the surface of the particles.The changes of absorption in visible-light region,band gap(E g) and specific surface area(A BET) caused by loading Ag are more obvious than those caused by loading Mo.But the isoelectric point of Ag-BiVO4decreases less than that of Mo-BiVO4does.Both catalysts show higher photocatalytic activity than pure BiVO4,resulting in the significantly improved efficiency of degradation of MB.And the degradation efficiency of these two metal-loaded BiVO4photocatalysts is similar to each other.However,mechanisms of such enhancement are different.The decrease of isoelectric point helps Mo-BiVO4improve the degradation efficiency.As for Ag-BiVO4,the augmentation of absorption in visible-light region as well as the abatement of E g plays more important roles.

Photocatalytic remediation of ionic pollutant

Recently, the photocatalysts have attracted lots of attention and efforts due to their great potential for environmental remediation application. Toxic ions in water are an increasing environmental pollutant with the fast development. Numerous researches have been made to develop photocatalysts to treat ionic pollutants under the illumination of ultraviolet light and visible light. Here, photocatalytic remediation of toxic ionic pollutants has been reviewed. This review summarized and discussed various photocatalysts including TiO〉 modified TiO2, metal oxides, metalsulfides, and nitrides and their recent progress in removing ionic pollutants such as heavy metal ion. The latest achievements and their future prospects of photocatalytic remediation of ion pollutant have also been reviewed.

Microemulsion synthesis and photocatalytic activity of visible light-active BiVO_4 nanoparticles

A water-in-oil microemulsion made up of a cyclohexane/n-hexyl alcohol/Polyethylene glycol tertoctylphenyl/aqueous solution including Bi3+ and VO+3 ions yields the spherical BiVO4 precursors with the size from 5 to 300 nm. Well-crystallized monoclinic scheelite BiVO4 particles with nanometer or micrometer size are fabricated in control by heating microemulsion precursors under various temperatures. The corresponding nucleation and growth process of as-prepared samples has also been investigated via TEM,which demonstrates the detailed morphological evolution of nuclei inside the precursors. As-prepared BiVO4 photocatalysts exhibit enhanced photocatalytic activity under visible-light irradiation in comparison with the bulk BiVO4 prepared by solid-state reaction. The highest RB degrading efficiency of 98% in 180 min under visible-light irradiation is observed for the sample calcined at 600 °C.

Microwave-assisted hydrothermal synthesis of cube-like Ag-Ag_2MoO_4 with visible-light photocatalytic activity

Cube-like Ag-Ag2MoO4 composite has been successfully prepared in the presence of PVP （potyvinylpyrrolidone） via a facile microwave-assisted hydrothermal process. Studies of its photocatalytic performance in the decomposition of RhB indicate that the cube-like Ag-Ag2MoO4 composite exhibits good catalytic activities under visible-light irradiation. The face that Ag pro- motes the absorption of visible light may be attributed to the surface plasmon resonance. Further XRD characterization after recycle photocatalytic tests confirms that partial Ag~ ions in Ag2MoO4 have been reduced to metallic Ag. Reaction temperature, reaction time and the amount of PVP have also been studied and found to play crucial roles in the formation of the cube-like microstructures.

Flower-like Au/Ag/TiO2 nanocomposites with enhanced photocatalytic efficiency under visible light irradiation

Uniform flower-like TiO2 coated Au nanostars and core-shell Au@Ag nanostars with different amounts of Ag coating were prepared through a facile method by hydrolysis of TiF4 under an acidic environment. The photocatalytic capability of these flower-like nanocomposites under visible light irradiation was found to be enhanced by up to 4.7-fold compared to commercial P25 TiO2 nanoparticles. The enhanced photocatalytic activity was ascribed to improved light absorption and hot electron inj ection from the photo-excited Au@Ag core to the TiO2 shell.