ZnSe-石墨烯/TiO_2声催化剂上罗丹明B降解与反应氧物种生成(英文)

Nanostructured ZnSe-graphene/TiO2 was synthesized by a hydrothermal-assisted approach. ZnSe-graphene/TiO2 exhibited favorable adsorption of rhodamine B, a wide wavelength absorption range, and efficient charge separation. Reactive oxygen species were generated by the oxidation of 1,5-diphenyl carbazide to 1,5-diphenyl carbazone. The sonocatalytic reaction mechanism was pro-posed. These findings potentially broaden the applications of sonocatalytic technologies.     

紫外光照射下 Fe-碳纳米管/TiO2 复合材料降解罗丹明 B

 The composites comprising Fe-carbon nanotubes (CNTs) on TiO2 were prepared by a modified sol-gel method and characterized by nitrogen adsorption, scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and energy dispersive X-ray analysis. The photocatalytic decomposition of rhodamine B (Rh.B) under UV irradiation and air aeration catalyzed by the composites was measured. The photocatalytic activity of TiO2 nanoparticles was significantly enhanced by the large CNT network that facilitated electron transfer between adsorbed Rh.B molecules and the catalyst substrate and the simultaneous occurrence of the photo-Fenton reaction in the presence of Fe particles. A marked acceleration of the decomposition rate was observed with aeration by flowing air aeration due to the formation of the circulatory photo-Fenton system. Chemical oxygen demand of piggery waste was measured at regular intervals to evaluate the mineralization of wastewater.     

Rhodamine B degradation and reactive oxygen species generation by a ZnSe-graphene/TiO2 sonocatalyst

Nanostructured ZnSe-graphene/TiO2 was synthesized by a hydrothermal-assisted approach. ZnSe-graphene/TiO2 exhibited favorable adsorption of rhodamine B, a wide wavelength absorption range, and efficien...     

Surface Modification Effect and Electrochemical Performance of LiOH-High Surface Activated Carbon as a Cathode Material in EDLC

This study aimed to improve the performance of the activated carbon-based cathode by increasing the Li content and to analyze the effect of the combination of carbon and oxidizing agent. The crystal structure and chemical structure phase of Li-high surface area activated carbon material (Li-HSAC) was analyzed by X-ray diffraction (XRD) and Raman spectroscopy, the surface state and quantitative element by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) and the surface properties with pore-size distribution by Brunauer–Emmett–Teller (BET), Barrett–Joyner–Halenda (BJH) and t-plot methods. The specific surface area of the Li-YP80F is 1063.2 m²/g, micropore volume value is 0.511 cm³/g and mesopore volume is 0.143 cm³/g, and these all values are higher than other LiOH-treated carbon. The surface functional group was analyzed by a Boehm titration, and the higher number of acidic groups compared to the target facilitated the improved electrolyte permeability, reduced the interface resistance and increased the electrochemical properties of the cathode. The oxidizing agent of LiOH treated high surface area of activated carbon was used for the cathode material for EDLC (electric double layer capacitor) to determine its electrochemical properties and the as-prepared electrode retained excellent performance after 10 cycles and 100 cycles. The anodic and cathodic peak current value and peak segregation of Li-YP80F were better than those of the other two samples, due to the micropore-size and physical properties of the sample. The oxidation peak current value appeared at 0.0055 mA/cm² current density and the reduction peak value at –0.0014 mA/cm², when the Li-YP80F sample used to the Cu-foil surface. The redox peaks appeared at 0.0025 mA/cm² and –0.0009 mA/cm², in the case of using a Nickel foil, after 10 cycling test. The electrochemical stability of cathode materials was tested by 100 recycling tests. After 100 recycling tests, peak current drop decreased the peak profile became stable. The LiOH-treated high surface area of activated carbon had synergistically upgraded electrochemical activity and superior cycling stability that were demonstrated in EDLC.     

The characteristic study and sonocatalytic performance of CdSe–graphene as catalyst in the degradation of azo dyes in aqueous solution under dark conditions

The sonocatalytic degradation of azo dyes; methyl orange (MO) and rhodamine B (RhB) were studied catalyzed by cadmium selenide (CdSe)-graphene in dark ambiance. The CdSe–graphene composites were prepared by simple hydrothermal method. The characterizations of composites were studied by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), specific surface area (BET) and with energy dispersive X-ray (EDX). The UV-spectroscopic analysis of the dyes was done by measuring the change in absorbance. The degradation of the organic dyes was calculated based on the decrease in concentration of the dyes with respect to regular time intervals. The rate coefficients for the sonocatalytic process were successfully established and the reusability tests were done to test the stability of the used catalysts.     

还原氧化石墨烯-硒化银纳米复合材料的水热合成与表征及其活性氧物种产生(英文)

A visible-light photocatalyst containing Ag2Se and reduced graphene oxide(RGO) was synthesized by a facile sonochemical-assisted hydrothermal method. X-ray diffraction, scanning electron mi-croscopy with energy-dispersive X-ray analysis, and ultraviolet-visible diffuse reflectance spectros-copy results indicated that the RGO-Ag2Se nanocomposite contained small crystalline Ag2Se nano-particles dispersed over graphene nanosheets and absorbed visible light. The high crystallinity of the nanoparticles increased photocatalytic activity by facilitating charge transport. N2 adsorp-tion-desorption measurements revealed that the RGO-Ag2Se nanocomposite contained numerous pores with an average diameter of 9 nm, which should allow reactant molecules to readily access the Ag2Se nanoparticles. The RGO-Ag2Se nanocomposite exhibited higher photocatalytic activity than bulk Ag2Se nanoparticles to degrade organic pollutant rhodamine B and industrial dye Texbrite BA-L under visible-light irradiation(λ 420 nm). The generation of reactive oxygen spe-cies in RGO-Ag2Se was evaluated through its ability to oxidize 1,5-diphenylcarbazide to 1,5-diphenylcarbazone. The small size of the Ag2Se nanoparticles in RGO-Ag2Se was related to the use of ultrasonication during their formation, revealing that this approach is attractive to form po-rous RGO-Ag2Se materials with high photocatalytic activity under visible light.     

简单水热法合成石墨-CdSe复合材料及其光催化降解有机染料(英文)

A graphene-CdSe composite was synthesized by a facile hydrothermal method,and characterized by X-ray diffraction,scanning electron microscopy with energy dispersive X-ray analysis,transmission electron microscopy and UV-vis diffuse reflectance spectrophotometry.The graphene-CdSe composite efficiently catalyzed the photodegradation of methylene blue(MB),methyl orange(MO) and rhodamine B(Rh.B) in aqueous solution under UV or visible light irradiation.The graphene-CdSe composite exhibited a higher photocatalyt...     

Fabrication and Characterization of Tailored TiO_2 and WO_3/MWCNT Composites for Methylene Blue Decomposition

A sol-gel method was used to prepare WO3/MWCNT-TiO2 composites.Their photocatalytic activities were evaluated by the degradation of methylene blue (MB) solution under UV light.The catalysts were characterized by X-ray diffraction,specific surface area measurement,energy-dispersive X-ray analysis,transmission and scanning electron microscopy.Aqueous MB solutions of 100 ml were photodegraded by a small amount of the WO3/MWCNT-TiO2 composite under UV light irradiation.The photocatalytic data showed that the WO...     

CoS2-碳(C60,石墨,碳纳米管)/TiO2复合光敏剂光降解有机染料（英文）

CoS2,CoS 2-C60 /TiO2,CoS2-CNT/TiO2,and CoS2-Graphene/TiO2 were prepared.The TiO2 products had the anatase phase structure and interesting surface compositions.X-ray diffraction patterns of the CoS2-carbon/TiO2 composites showed a single and clear anatase phase and the CoS2 structure.Scanning electron microscopy characterization of the texture on the CoS 2-carbon/TiO2 composites showed a homogenous composition.Energy-dispersive X-ray spectra for elemental identification showed the presence of C and Ti with strong Co and S peaks from the CoS2-carbon/TiO2 composites.The composites obtained were also characterized by transmission electron microscopy and UV-Vis spectroscopy.CoS2-carbon/TiO2 composites showed excellent photocatalytic activity for the degradation of methylene blue under visible light irradiation.This was attributed to both photocatalysis on the TiO2 support and charge transfer by the carbon nanomaterial,and the introduction of CoS2 to enhance transfer of photogenerated electrons.     

Sonocatalytic degradation of Rhodamine B in the presence of C60 and CdS coupled TiO2 particles

CdS-TiO₂ and CdS-C₆₀/TiO₂ were prepared using C₆₀, cadmium acetate dehydrate [(CH₃COO)₂Cd·2H₂O], sodium sulfide (Na₂S·5H₂O) and titanium (IV) n-butoxide by a sol-gel method. The prepared sonocatalysts were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) and transmission electron microscopy (TEM). A rhodamine B (RhB) solution under ultrasonic irradiation was used to determine the catalytic activity. Excellent catalytic degradation of an RhB solution was observed using the CdS-C₆₀/TiO₂ composites under ultrasonic irradiation. C₆₀ coupled CdS-TiO₂ can enhance the Brunauer-Emmett-Teller (BET) surface area and increase the decolorization rate for rhodamine B solution. The results also shows that increase the content of CdS can enhance the catalytic activity.