氢化物分离SAF—CTMAB光度法测定钨产品中的锡

通过对锡的氢化分离，吸收条件和Sn－SAF－CTMAB显色条件的研究，制定了氢化物分离，水杨基荧光酮──溴化十六烷基三甲胺光度法测定钨产品中锡的分析方法．方法具有灵敏度高，选择性强，分高效果好，测量范围宽等优点。

A method for calculation of ion distribution in reaction system forming hydroxide

A formula was proposed to calculate the distribution of metal ions quantitatively in chemical reaction system forming hydroxide where precipitation and complex are formed together. The effects of some factors on formation of precipitation and complex were investigated, and the corresponding precipitation rates of zinc, iron （III）, aluminum, copper and magnesium were calculated. As a result, it shows that the proposed formula is reliable. By the proposed formula, the existence state of metal ions in hydroxides reaction system with any metal ions can be well described and the effects of some factors on the distribution of metal ions were determined.

Separation and analysis of aromatic hydrocarbons from two Chinese coals

Separation and analysis of aromatic hydrocarbons (AHs) from coals is of considerable significance for both fuel and non-fuel use of the coals. In present work two Chinese bituminous coals were selected for separation of AHs by ultrasonic extrac-tion with CS2 followed by column chromatography using hexane as eluent. A series of AHs were separated from the two coals and analyzed by GC/MS. FTIR was employed to characterize the raw coals and the extracted residues. The results of GC/MS analysis show that the separated AHs are mono- to tetracyclic arenes, among which the principle AHs are alkyl naphthalenes and phenan-threnes. Obvious differences in the composition and the structure of AHs exist between the two coals, i.e., the AHs from Tongting coal tend to be higher rings compared to those from Pingshuo coal both from the variety and from the abundance of the AHs. FTIR analysis shows that the raw and extracted coals are similar in terms of functional groups, suggesting that the composition and structure of CS2 extract, especially the AHs, from coals can be used to interpret the coal structure to some extent.

The roles and mechanism of cocatalysts in photocatalytic water splitting to produce hydrogen

Photocatalytic hydrogen(H2)evolution via water spilling over semiconductors has been considered to be one of the most promising strategies for sustainable energy supply in the future to provide non-pollution and renewable energy.The key to efficient conversion of solar-chemical energy is the design of an efficient structure for high charge separation and transportation.Therefore,cocatalysts are necessary in boosting photocatalytic H2 evolution.To date,semiconductor photocatalysts have been modified by various cocatalysts due to the extended light harvest,enhanced charge carrier separation efficiency and improved stability.This review focuses on recent developments of cocatalysts in photocatalytic H2 evolution,the roles and mechanism of the cocatalysts are discussed in detail.The cocatalysts can be divided into the following categories:metal/alloy cocatalysts,metal phosphides cocatalysts,metal oxide/hydroxide cocatalysts,carbon-based cocatalysts,dual cocatalysts,Z-scheme cocatalysts and MOFs cocatalysts.The future research and forecast for photocatalytic hydrogen generation are also suggested.

Purification technology of molten aluminum

Various purification methods were explored to eliminate the dissolved hydrogen and nonmetallic inclusions from molten aluminum alloys. A novel rotating impeller head with self-oscillation nozzles or an electromagnetic valve in the gas circuit was used to produce pulse gas currents for the rotary impeller degassing method. Water simulation results show that the size of gas bubbles can be decreased by 10%20% as compared with the constant gas current mode. By coating ceramic filters or particles with active flux or enamels, composite filters were used to filter the scrap A356 alloy and pure aluminum. Experimental results demonstrate that better filtration efficiency and operation performance can be obtained. Based on numerical calculations, the separation efficiency of inclusions by high frequency magnetic field can be significantly improved by using a hollow cylinder-like separator or utilizing the effects of secondary flow of the melt in a square separator. A multi-stage and multi-media purification platform based on these methods was designed and applied in on-line processing of molten aluminum alloys. Mechanical properties of the processed scrap A356 alloy are greatly improved by the composite purification.

Latest progress in hydrogen production from solar water splitting via photocatalysis,photoelectrochemical,and photovoltaic-photoelectrochemical solutions

Hydrogen production via solar water splitting is regarded as one of the most promising ways to utilize solar energy and has attracted more and more attention. Great progress has been made on photocatalytic water splitting for hydrogen production in the past few years. This review summarizesthe very recent progress (mainly in the last 2–3 years) on three major types of solar hydrogenproduction systems: particulate photocatalysis (PC) systems, photoelectrochemical (PEC) systems,and photovoltaic‐photoelectrochemical (PV‐PEC) hybrid systems. The solar‐to‐hydrogen (STH)conversion efficiency of PC systems has recently exceeded 1.0% using a SrTiO3:La,Rh/Au/BiVO4:Mophotocatalyst, 2.5% for PEC water splitting on a tantalum nitride photoanode, and reached 22.4%for PV‐PEC water splitting using a multi‐junction GaInP/GaAs/Ge cell and Ni electrode hybrid system.The advantages and disadvantages of these systems for hydrogen production via solar watersplitting, especially for their potential demonstration and application in the future, are briefly describedand discussed. Finally, the challenges and opportunities for solar water splitting solutions are also forecasted.

Highly enhanced visible-light photocatalytic hydrogen evolution on g-C_3N_4 decorated with vopc through π-π interaction

Photocatalytic H2 evolution reactions on pristine graphitic carbon nitrides(g-C3N4),as a promising approach for converting solar energy to fuel,are attractive for tackling global energy concerns but still suffer from low efficiencies.In this article,we report a tractable approach to modifying g-C3N4 with vanadyl phthalocyanine(VOPc/CN)for efficient visible-light-driven hydrogen production.A non-covalent VOPc/CN hybrid photocatalyst formed viaπ-πstacking interactions between the two components,as confirmed by analysis of UV-vis absorption spectra.The VOPc/CN hybrid photocatalyst shows excellent visible-light-driven photocatalytic performance and good stability.Under optimal conditions,the corresponding H2 evolution rate is nearly 6 times higher than that of pure g-C3N4.The role of VOPc in promoting hydrogen evolution activity was to extend the visible light absorption range and prevent the recombination of photoexcited electron-hole pairs effectively.It is expected that this facile modification method could be a new inspiration for the rational design and exploration of g-C3N4-based hybrid systems with strong light absorption and high-efficiency carrier separation.

Engineering piezoelectricity and strain sensitivity in CdS to promote piezocatalytic hydrogen evolution

Piezocatalytic hydrogen evolution has emerged as a promising direction for the collection and utilization of mechanical energy and the efficient generation of sustainable energy throughout the day.Hexagonal CdS,as an established semiconductor photocatalyst,has been widely investigated for splitting water into H_(2),while its piezocatalytic performance has attracted less attention,and the relationship between the structure and piezocatalytic activity remains unclear.Herein,two types of CdS nanostructures,namely CdS nanorods and CdS nanospheres,were prepared to probe the above‐mentioned issues.Under ultrasonic vibration,the CdS nanorods afforded a superior piezocatalytic H_(2) evolution rate of 157μmol g^(−1)h^(−1)in the absence of any co‐catalyst,which is nearly 2.8 times that of the CdS nanospheres.The higher piezocatalytic activity of the CdS nanorods is derived from their larger piezoelectric coefficient and stronger mechanical energy harvesting capability,affording a greater piezoelectric potential and more efficient separation and transfer of intrinsic charge carriers,as elucidated through piezoelectric response force microscopy,finite element method,and piezoelectrochemical tests.This study provides a new concept for the design of efficient piezocatalytic materials for converting mechanical energy into sustainable energy via microstructure regulation.

Studies on Recovery Efficiencies of Phenols from Phenol Fraction Using Alkali Treatment

Experiments were conducted for the extraction of phenols from the phenol fraction obtained from the coal tar distillate. The phenol fraction for the present investigation has been procured from Visakhapatnam Steel Plant, Visakhapatnam whose composition is known. The phenol fraction from coal tar distillate can be treated for extracting phenols using caustic soda. An attempt has been made to find out whether the existing practice of using only 8%-15% can be modified by increasing the strength of sodium hydroxide and also explore the possibilities of substituting the sodium hydroxide with KOH as an extractant. The different streams of liquids obtained during experimentation have been analyzed by gas chromatograph. Salient features of the study are that higher concentrations of the alkali significantly improved the separation efficiencies of phenols and also regenerate the phenolate with higher phenol content. Increase in the alkali strength has greatly improved the separation as well as the phenol content in the regenerated phenols. Disposal of effluents containing phenols may lead to environmental problem of ground water pollution and the study throws a light on the removal of phenols from the effluents to the extent possible by using higher strength alkali solutions.

Photocatalytic hydrogen evolution activity over MoS_2/ZnIn_2S_4 microspheres

MoS2/ZnIn2S4composites with MoS2anchored on the surface of ZnIn2S4microspheres were synthesized by a two‐step hydrothermal process.The obtained samples were characterized by X‐ray diffraction,field emission scanning electron microscopy,energy dispersive X‐ray spectroscopy,high‐resolution transmission electron microscopy,X‐ray photoelectron spectroscopy,Raman spectroscopy,ultraviolet–visible diffuse reflectance absorption spectroscopy,nitrogen adsorption–desorption measurements,photoluminescence spectroscopy,and photoelectrochemical tests.The influence of the loading of MoS2on the photocatalytic H2evolution activity was investigated using lactic acid as a sacrificial reagent.A H2evolution rate of343μmol/h was achieved under visible light irradiation over the1wt%MoS2/ZnIn2S4composite,corresponding to an apparent quantum efficiency of about3.85%at420nm monochromatic light.The marked improvement of the photocatalytic H2evolution activity compared with ZnIn2S4can be ascribed to efficient transfer and separation of photogenerated charge carriers and facilitation of the photocatalytic H2evolution reaction at the MoS2active sites.

Enantiomeric Separation of Meptazinol Hydrochloride by Capillary Electrophoresis

Aim To establish a capillary electrophoresis method for enantiomericseparation of meptazinol hydrochlo-ride. Methods The separation conditions such ascyclodextrin(CD)type, buffer pH, concentration of 2,3,6-O-trimethyl-β-cyclodextrin and organicadditives were optimized. An optimum concentration was 30 mmol· L^(-1) phosphate (pH 7.02) with 10%(W/V) TM-β-CD and 2% acetonitrile. Results Baseline resolution of the enantiomer was readilyachieved using 2, 3, 6-O-trimethyl-β-cyclodextrin. Conclusion This is a convenient method for fastenantiomeric resolution of meptazinol hydrochloride.

Analysis of H_2S Tolerance of Pd-Cu Alloy Hydrogen Separation Membranes

The presence of a limited amount of H2S in H2-rich feed adversely affects the Pd-Cu membrane permeation performance due to the sulphidization of the membrane surface. A theoretical model was proposed to predict the S-tolerant performance of the Pd-Cu membranes in presence of H2S under the industrial water-gas-shift(WGS) reaction conditions. The ideas of surface coverage and competitive adsorption thermodynamics of H2S and H2 on Pd-Cu surface were introduced in the model. The surface sulphidization of the Pd-Cu membranes mainly depended on the pressure ratio of H2S to H2, temperature and S-adsorbed surface coverage, i.e., the occurrence of sulphidization on the surface was not directly related with the bulk compositions and structures [body centered cubic and face centered cubic(bcc or fcc)] of Pd-Cu alloy membranes because of the surface segregation phenomena. The resulting equilibrium equations for the H2S adsorption/sulphidization reactions were solved to calculate the pressure ratio of H2S to H2 over a wide range of temperatures. A validation of the model was performed through a comparison between lots of literature data and the model calculations over a rather broad range of operating conditions. An extremely good agreement was obtained in the different cases, and thus, the model can serve to guide the development of S-resistant Pd alloy membrane materials for hydrogen separation.

Deep Hydrodesulfurization of Diesel Fuel over Diatomite-dispersed NiMoW Sulfide Catalyst

Diatomite-dispersed NiMoW catalyst was prepared and characterized,and the activity of catalyst samples was tested during the HDS reaction of FCC diesel.Sulfur compounds in the feedstock and the hydrogenated products obtained over different catalysts were determined by GC-PFPD.The test results showed that the diatomite-dispersed NiMoW catalyst had high hydrodesulfurization activity for FCC diesel,which could be contributed to the excellent hydrogenation performance of the said catalyst.Characterization of catalyst by TEM and XRD indicated that the diatomite-dispersed NiMoW catalyst possessed higher layer stacking,larger curvature of MoS2or WS2,and segregated Ni3S2crystals relative to the supported catalyst.This kind of structure leads to high hydrogenation activity of the diatomite-dispersed NiMoW catalyst.

Novel Cu_3P/g-C_3N_4 p-n heterojunction photocatalysts for solar hydrogen generation

Developing efficient heterostructured photocatalysts to accelerate charge separation and transfer is crucial to improving photocatalytic hydrogen generation using solar energy. Herein, we report for the first time that p-type copper phosphide（Cu3P） coupled with n-type graphitic carbon nitride（g-C3N4） forms a p-n junction to accelerate charge separation and transfer for enhanced photocatalytic activity.The optimized Cu3P/g-C3N4 p-n heterojunction photocatalyst exhibits 95 times higher activity than bare g-C3N4, with an apparent quantum efficiency of 2.6% at 420 nm. A detail analysis of the reaction mechanism by photoluminescence,surface photovoltaics and electrochemical measurements revealed that the improved photocatalytic activity can be ascribed to efficient separation of photo-induced charge carriers. This work demonstrates that p-n junction structure is a useful strategy for developing efficient heterostructured photocatalysts.

Three-dimensional ordered macroporous g-C_(3)N_(4)-Cu_(2)O-TiO_(2) heterojunction for enhanced hydrogen production

In this study,a g-C_(3)N_(4)-Cu_(2)O-TiO_(2) photocatalyst with a novel three-dimensional ordered macroporous(3DOM)structure was successfully prepared using a sacrificial template strategy and a photodeposition method.The influence of the special porous structure with cross pore channels on the photocatalytic properties of the as-prepared sample was studied in detail.Compared with the original photocatalyst(TiO_(2) with 3 wt%Pt),g-C_(3)N_(4)-Cu_(2)O-TiO_(2) exhibited a higher specific surface area and more active sites,thus accelerating the separation efficiency of the photogenerated electron-hole pair.Consequently,the as-prepared photocatalyst showed good photocatalytic performance,reaching a maximum hydrogen production rate of 12,108μmol g^(-1) h^(-1) and approximately five times higher than that of the pristine comparison sample.The enhanced photoactivity of the g-C_(3)N_(4)-Cu_(2)O-TiO_(2) heterojunction can be ascribed to its double p-n heterojunction and robust porous structure,where the photodeposited Cu_(2)O plays a synergistic catalytic role in the photocatalytic process and the outer clad g-C_(3)N_(4) layer prevents Cu_(2)O oxidation.Additionally,the possible photocatalytic mechanism was briefly discussed based on the experimental results.This work identifies viable pathways for developing low-cost heterojunction photocatalysts with highly efficient photocatalytic activity toward improved solar energy conversion.

Carbon nitride with encapsulated nickel for semi-hydrogenation of acetylene: pyridinic nitrogen is responsible for hydrogen dissociative adsorption

A new mechanism of catalyst has been demonstrated in this article. With the interaction between carbon nitride(CN) and encapsulated nickel, the CN in the catalyst has been endowed with new active sites for the adsorption and activation of hydrogen while nickel itself is physically isolated from the contact with reactive molecules. For the selective hydrogenation of acetylene in large amount of ethylene, the catalyst shows excellent ethylene selectivity than the nickel catalyst itself, which is almost totally unselective. Meanwhile, the CN itself is inactive for the reaction. The results of characterization demonstrate that pyridinic nitrogen doped in the carbon matrix should be the active sites for hydrogen dissociative adsorption. The theoretical calculations further confirm the results and provide with the detail in the electron transfer between nickel and CN in the catalyst. The current results supply a new concept for design of high performance catalyst.