Synthesis of Y_2O_3 phosphor by a hydrolysis and oxidation method

A novel and convenient hydrolysis and oxidation method was first used in preparation of carbon contained Y2O3 phosphor powders. The alloy was hydrolyzed in deionized water and the obtained Y（OH）3 powders were heat treated in air atmosphere. The final products - Y2O3 powders were micron clusters which were aggregated by hundreds of nanoparticles with the size of about 5 nm. The chemical composition, structural and morphological features of the samples were characterized by means of X-ray powder diffraction （XRD） analysis, transmission electron microscopy （TEM）, Fourier-transform infrared （FT-IR） spectra, X-ray photoelectron spectra （XPS） and carbon sulfur analyzer. The obtained powders showed good bluish-white photoluminescence （PL） emissions （ranging from 430 to 600 nm, peaking at 468 nm and 578 nm） under the xenon light excitation. The luminescent mechanism was ascribed to the carbon impurities in the Y2O3 host.

Preparation of Hydroxyapatite-titanium Dioxide Coating on Ti6Al4V Substrates using Hydrothermal-electrochemical Method

Ti6Al4V substrates were anodized in a 0.5 mol/L H_2SO_4 solution at applied voltages of 90-140 V.A hydroxyapatite-titanium oxide（HA-TiO2）coating was then deposited on the anodized Ti6Al4 V substrates via a hydrothermal-electrochemicalmethod at a constant current.The obtained films and coatings were characterized by X-ray diffraction,scanning electron microscopy,energy-dispersive X-ray spectroscopy,and Fourier-transform infrared spectrometry.The microstructures of the porous films on the Ti6Al4 V substrates were studied to investigate the effect of the anodizing voltage on the phase and morphology of the HATiO_2 coating.The results indicated that both the phase composition and the morphology of the coatings were significantly influenced by changes in the anodizing voltage.HA-TiO_2 was directly precipitated onto the surface of the substrate when the applied voltage was between 110 and 140 V.The coatings had a gradient structure and the HA exhibited both needle-like and cotton-like structures.The amount of cotton-like HA structures decreased with an increase in voltage from 90 to 120 V,and then increased slightly when the voltage was higher than 120 V.The orientation index of the（002）plane of the coating was at a minimum when the Ti6Al4 V substrate was pretreated at 120 V.

Prediction of Superconductivity for Oxides Based on Structural Parameters and Artificial Neural Network Method

Superconductive properties for oxides were predicted by artificial neural network (ANN) method with structural and chemical parameters as inputs. The predicted properties include superconductivity for oxides, distributed ranges of the superconductive transition temperature (Tc) for complex oxides, and Tc values for cuprate superconductors. The calculated results indicated that the adjusted ANN can be used to predict superconductive properties for unknown oxides.

Nanostructure and Formation Mechanism of Pt-WO_3/C Nanocatalyst by Ethylene Glycol Method

Pt-WO3 nanoparticles uniformly dispersed on Vulcan XC-72R carbon black were prepared by an ethylene glycol method.The morphology,composition,nanostructure,electrochemical characteristics and electrocatalytic activity were characterized,and the formation mechanism was investigated.The average particle size was 2.3 nm,the same as that of Pt/C catalyst.The W/Pt atomic ratio was 1/20,much lower than the design of 1/3.The deposition of WO3·xH2O nanoparticles on Vulcan XC-72R carbon black was found to be very difficult by TEM.From XPS and XRD,the Pt nanoparticles were formed in the colloidal solution of Na2WO4,the EG insoluble Na2WO4 resulted in the decreased relative crystallinity and increased crystalline lattice constant compared with those of Pt/C catalyst and,subsequently,the higher specific electrocatalytic activity as determined by CV.The Pt-mass and Pt-electrochemically-active-specific-surface-area based anodic peak current densities for ethanol oxidation were 422.2 mA·mg-1Pt and 0.43 mA·cm-2Pt,1.2 and 1.1 times higher than those of Pt/C catalyst,respectively.

Chemical Analysis Method for Carbon Bearing Refractory Products——Determination of Magnesium Oxide Content by CyDTA Volumetric Method

This standard specifies the method summary, reagents, apparatus, sampling, procedure, test results calculation and permissible tolerance of the determination of magnesium oxide by CyDTA volumetric method.

Chemical Analysis of Magnesia and Magnesia-Alumina Refractory Materials——Flame atomic absorption spectrometric method for determination of calcium oxide content

1 Scope This standard specifics the determination of calcium oxide coutent by flame atomic absorption spectrometric method.

Preparation and photocatalytic activity of PANI/TiO_2 composite film

A PANI/TiO2 composite film deposited on the glass surface was successfully prepared using sol-gel dip-coating technique and chemical oxidation method. The film was characterized using XRD, AFM, and UV. The result showed that the TiO2 film consists of both cuboid-shaped and anatase-phased TiO2 nanoparticles. The average grain size of TiO2 in the film was approximately 20 nm. After coating with PANI, the particle was changed into irregular spherical-shaped and the size was increased up to approximately 35 nm in diameter. UV-Vis spectroscopy analysis indicated that the coating of TiO2 with PANI would result in an enhancement of photocatalytic efficiency and an extension of the photoresponse of TiO2. The band gap of the PANI/TiO2 film was 3.18 eV. The photocatalytic property of the film was evaluated by the degradation of rhodamine-B. It was found that 67.1% and 83.2% of rhodamine-B could be degraded under sunlight and UV irradiation within 120 min using the PANI/TiO2 composite t-tim as photocatalyst.

Gas Absorption and Mass Transfer in a Pore-Array Intensified Tube-in-Tube Microchannel

A pore-array intensified tube-in-tube microchannel(PA-TMC),which is characterized by high throughput and low pressure drop,was developed as a gas–liquid contactor.The sulfite oxidation method was used to determine the oxygen efficiency(φ)and volumetric mass transfer coefficient(k_(L)a)of PA-TMC,and the mass transfer amount per unit energy(ε)was calculated by using the pressure drop.The effects of structural and operating parameters were investigated systematically,and the twophase flow behavior was monitored by using a charge-coupled device imaging system.The results indicated that the gas absorption efficiency and mass transfer performance of the PA-TMC were improved with increasing pore number,flow rate,and number of helical coil turns and decreasing pore size,row number,annular size,annular length,and surface tension.Theφ,εand k La of PA-TMC could reach 31.3%,1.73×10^(-4) mol/J,and 7.0 s-1,respectively.The Sherwood number was correlated with the investigated parameters to guide the design of PA-TMC in gas absorption and mass transfer processes.

Configuration interaction studies on the spectroscopic properties of PbO including spin-orbit coupling

Lead oxide（Pb O）, which plays the key roles in a range of research fields, has received a great deal of attention. Owing to the large density of electronic states and heavy atom Pb including in Pb O, the excited states of the molecule have not been well studied. In this work, high level multireference configuration interaction calculations on the low-lying states of Pb O have been carried out by utilizing the relativistic effective core potential. The effects of the core-valence correlation correction, the Davidson modification, and the spin–orbital coupling on the electronic structure of the Pb O molecule are estimated. The potential energy curves of 18 Λ-S states correlated to the lowest dissociation limit（Pb（~3P_g） ＋ O（~3P_g）） are reported. The calculated spectroscopic parameters of the electronic states below 30000 cm^（-1）, for instance, X^1Σ~＋, 1~3Σ~＋,and 1~3Σ^-, and their spin–orbit coupling interaction, are compared with the experimental results, and good agreements are derived. The dipole moments of the 18 Λ-S states are computed with the configuration interaction method, and the calculated dipole moments of X^1Σ~＋and 1~3Σ~＋are consistent with the previous experimental results. The transition dipole moments from 1~1Π, 2~1Π, and 2~Σ to X^1Σ~＋and other singlet excited states are estimated. The radiative lifetime of several low-lying vibrational levels of 1~1Π, 2~1Π, and 2~1Σ~＋ states are evaluated.

Rietveld refinement, microstructure and high-temperature oxidation characteristics of low-density high manganese steels

Three forged low-density high manganese steels Mn28Al10,Mn28Al8 and Mn20Al10 were used as experimental materials in this study.The forged microstructure and external oxidation characteristics at 1323 K and 1373 K for 5-25 h in air were investigated by microstructural observation and X-ray diffraction（XRD）technique.The phase compositions and abundance in the forged and oxidized samples were quantitatively obtained by Rietveld method on the basis of XRD pattern analysis.The results showed that an austenitic microstructure formed in steels Mn28Al10 and Mn28Al8,and 18.02 wt%ferrite could be found in Mn20Al10.The relative amount of ~5.28 wt%-carbide（Fe_3AlC_（0.5））in Mn28Al10 was far greater than that in Mn28Al8 and Mn20Al10.The oxidation kinetics of forged steels oxidized at 1323 K for 5-25 h had two-stage parabolic rate laws;and the oxidation rate of the first stage was lower than that of the second stage.When they were oxidized at 1373 K for 5-25 h,the oxidation kinetics followed only a parabolic law and the oxidation rates were respectively greater than those at 1323 K for 5-25 h.When they were oxidized at 1323 K for 25 h,detached external scales contained Fe_2MnO_4and-Fe_2O_3oxides.-Al_2O_3and（Fe,Mn）_2O_3oxides could only be indexed in steels Mn28Al8 and Mn28Al10,respectively.When they were oxidized at 1373 K for 25 h,Fe_2MnO_4,Fe_3O_4,-Fe_2O_3 and-Al_2O_3oxides could all be indexed in the external detached scales.The main phase of detached external scales was Fe_2MnO_4;and the relative amount of-Al_2O_3in steel Mn28Al8 was higher than that in steels Mn28Al10 and Mn20Al.The external oxidation layers of these three forged steels oxidized at 1323 K and 1373 K for 25 h were essentially followed the sequence of-Al_2O_3,Fe_2MnO_4,Fe_3O_4,FeMnO_3,and Fe_2O_3from the substrate to the outside surface.The forged Mn28Al10 steel with austenitic microstructure and a certain amount of-carbide（~5.28 wt%in the present work）possessed a better combination of strength,ductility,specific strength,and oxidation rate when compared to that of the forged Mn28Al8 and Mn20Al10 steels.

Catalytic oxidation of formaldehyde over CeO2-Co3O4 catalysts

A series of CeO2-Co3O4 mixed oxide catalysts with different Co/（Co＋Ce） atomic ratios were synthesized by citric acid sol-gel method and used for catalytic oxidation of formaldehyde（HCHO）. Many techniques such as Brumauer-Emmett-Teller（BET）, X-ray diffraction（XRD）, scanning electron microscopy（FE-SEM）, temperature programmed reduction（H_2-TPR）, temperature-programmed desorption（O_2-TPD） and X-ray photoelectron spectroscopy（XPS） were used to characterize catalysts. The results of catalytic performance tests showed that the catalyst CeO_2-Co_3O_4 with Co/（Co＋Ce） ratio of 0.95 exhibited the best performance, and the temperature of complete oxidation of HCHO was 80 oC. The analytical results indicated that the addition of CeO_2 enhanced the specific surface area of Co_3O_4 and the fine dispersion of both of them. Moreover, the strong interaction between CeO_2 and Co_3O_4 resulted in the unique redox properties, which enhanced the available surface active oxygen and led to high valence state of cobalt oxide species. All those effects played crucial roles in the excellent performance of CeO_2-Co_3O_4 for the HCHO oxidation.

Rietveld refinement,microstructure,mechanical properties and oxidation characteristics of Fe-28Mn-xAl-1C(x=10 and 12 wt.%)low-density steels

The quantitative relationship between microstructure and properties of austenitic Fe-28Mn-xAl-1C（x=10 and 12 wt.%）low-density steels was evaluated using Rietveld method to refine X-ray diffraction（XRD）patterns.The results showed that a typical three-phase austenitic steel was obtained in the forged Mn28Al10（i.e.Fe-28Mn-10Al-1C）steel,which included about 92.85 wt.% γ-Fe（Mn,Al,C）（austenite）,5.28 wt.%（Fe,Mn）_3AlC_（0.5）（κ-carbide）,and 1.87 wt.% α-Fe（Al,Mn）（ferrite）.For the forged Mn28Al12（i.e.Fe-28Mn-12Al-1C）steel,nevertheless,only about 76.64 wt.% austenite,9.63 wt.%κ-carbide,9.14 wt.%ferrite and 4.59 wt.% Fe_3Al（DO_3）could be obtained.Nanometerκ-carbide and DO_3 were mainly distributed in austenite grains and at the interface between austenite and ferrite,respectively.The forged Mn28Al10 steel had a better combination of strength,ductility and specific strength as compared with the forged Mn28Al12 steel.The ductility of the forged Mn28Al12 steel was far lower than that of the forged Mn28Al10 steel.The oxidation kinetics of Mn28Al10 steel oxidized at 1323 Kfor 5-25 h had two-stage linear rate laws,and the oxidation rate of the second stage was faster than that of the first stage.Although the oxidation kinetics of Mn28Al12 steel under this condition also had two-stage linear rate laws,the oxidation rate of the second stage was slower than that of the first stage.When the oxidation temperature increased to 1373K,the oxidation kinetics of the two steels at 5-25 hhad only onestage linear rate law,and the oxidation rates of the two steels were far faster than those at 1323K for5-25 h.The oxidation resistance of Mn28Al12 steel was much better than that of Mn28Al10 steel.Ferrite layer formed between the austenite matrix and the oxidation layer of the two Fe-Mn-Al-C steels oxidized at high temperature.

Oxidation kinetics of ilmenite concentrate by non-isothermal thermogravimetric analysis

The non-isothermal oxidation experiments of ilmenite concentrate were carried out at various heating rates under air atmosphere by thermogravimetry.The oxidation kinetic model function and kinetic parameters of apparent activation energy（Ea）were evaluated by Málek and Starink methods.The results show that under air atmosphere,the oxidation process of ilmenite concentrate is composed of three stages,and the chemical reaction（G（α）=1-（1-α）~2,whereαis the conversion degree）plays an important role in the whole oxidation process.At the first stage（α=0.05-0.30）,the oxidation process is controlled gradually by secondary chemical reaction with increasing conversion degree.At the second stage（α=0.30-0.50）,the oxidation process is completely controlled by the secondary chemical reaction（G（α）=1-（1-α）~2）.At the third stage（α=0.50-0.95）,the secondary chemical reaction weakens gradually with increasing conversion degree,and the oxidation process is controlled gradually by a variety of functions;the kinetic equations are G（α）=（1-α）^（-1）（β=10K·min^（-1）,whereβis heating rate）,G（α）=（1-α）^（-1/2）（β=15-20K·min^（-1））,and G（α）=（1-α）^（-2）（β=25K·min^（-1））,respectively.For the whole oxidation process,the activation energies follow a parabolic law with increasing conversion degree,and the average activation energy is 160.56kJ·mol^（-1）.

Enhanced catalytic complete oxidation of 1,2-dichloroethane over mesoporous transition metal-doped γ-Al_2O_3

High-surface-area mesoprous powders of γ-Al2O3 doped with Cu^2＋, Cr^3＋, and V^3＋ ions were prepared uia a modified sol-gel method and were investigated as catalysts for the oxidation of chlorinated organic compounds. The composites retained high surface areas and pore volumes comparable with those of undoped γ-Al2O3 and the presence of the transition metal ions enhanced their surface acidic properties. The catalytic activity of the prepared catalysts in the oxidation of 1,2-dichloroethane （DCE） was studied in the temperature range of 250-400℃. The catalytic activity and product selectivity were strongly dependent on the presence and the type of dopant ion. While Cu^2＋- and Cr^3＋-containing catalysts showed 100% conversion at 300℃ and 350℃, V3＋-containing catalyst showed considerably lower conversion. Furthermore, while the major products of the reactions over γ-alumina were vinyl chloride （C2H3Cl） and hydrogen chloride （HCl） at all temperatures, Cu- and Cr-doped catalysts showed siguiticantly stronger capability for deep oxidation to CO2.

Influence of Forming Pressure on Properties of Yttrium Iron Garnet Ferrite

The Ca-Sn co-substituted yttrium iron garnet(YIG)ferrite materials were prepared by the traditional oxide solid-state reaction method,and the influence of forming pressure on the density,morphology and magnetic properties of YIG ferrite was systematically studied.The results show that the density of YIG ferrite green body increases with the increase of the forming pressure,while the density of its sintered body shows a trend of first increasing and then decreasing.At the same time,the ferromagnetic resonance(FMR)linewidth of YIG sample first decreases and then increases.Meanwhile,the effects of forming pressure on the saturation magnetization,remanence and coercivity of the sample can be ignored.This study proves that the density and FMR linewidth of YIG materials can be controlled by regulating the forming pressure and the best performance is obtained for the sample prepared under a forming pressure of 5 MPa.

Analysis of Carbaryl Pesticide Residues in Environmental Samples with Spectrophotometry

A facile, rapid and sensitive spectrophotometric method was developed for the determination of carbaryl in its formulations, water and grain （rice and wheat） samples with newly synthesised reagent. The proposed method was based on the alkaline hydrolysis of carbaryl pesticide and thus resulted 1-naphthol was coupled with diazotised 4,4＇-methylene-bis-m-nitroaniline in basic medium （pH 9） to give red colored product having λmax 480 nm for diazonium method （DM） or 1-naphthol reacts with 4,4＇-methylene-bis-m-nitroaniline in the presence of oxidising agent potassium dichromate （K2Cr2O7） to give red colored product having λmax 510 nm for oxidation method （OM）. The formation of colored derivatives with the coupling agent is instantaneous and stable for 48 h （DM） and 32 h （OM） respectively. Beer＇s law was obeyed in the concentration range of 0.2--10.0 μg·mL ^-1 for DM and 0.2--0.150 μg·mL^-1 for OM. The proposed methods are sensitive, easy to operate and permitted for the determination of carbaryl with detection limits of 0.028 μg·mL^-1 for DM and 0.024 μg·mL^-1 for OM respectively. The experimental results indicate that the procedure can eliminate the fundamental interferences caused by other pesticides and non-target ions, which made the methods more sensitive and selective. The method was applicable to the determination of carbaryl residue in water and food grain samples up to μg level.

Effect of Ce doping of TiO_2 support on NH_3-SCR activity over V_2O_5–WO_3/CeO_2–TiO_2 catalyst

CeO2–TiO2composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5–WO3/CeO2–TiO2catalysts for the selective catalytic reduction（SCR） of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV–Vis,Raman and XPS techniques. The results showed that the catalytic activity of V2O5–WO3/TiO2 was greatly enhanced by Ce doping（molar ratio of Ce/Ti = 1/10） in the TiO2 support.The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning.

Nitric Oxide Signaling Molecules in Acupoints:Toward Mechanisms of Acupuncture

Recent clinical trial studies have demonstrated that the effects of acupuncture on pain improvement are small and no difference between acupoints and non-points. Whether acupuncture needles must be inserted in specific points depends on whether acupoint specificity exists that is still not resolved, and is now urgent. Previous anatomical studies have demonstrated that acupoints exist higher number of nerve fibers/trunks, blood vessels, hair follicles, and sweat glands as well as density of the gap junction. Recent evidence shows that nitric oxide（NO） level is elevated in the acupoints/meridians and is associated with an enhanced expression of NO synthase endowed with transient receptor potential vanilloid type-1. There is growing evidence from international groups showing that acupuncture induces NO-mediated vasodilatation, which increases local blood flow and allows for a flush of algesic or sensitizing substances, leading to pain relief. Previous studies, using a novel biocapture system, have demonstrated that NOx–（total nitrite and nitrate） and cyclic guanosine monophosphate（c GMP） concentrations are consistently increased over skin acupoints compared to non-meridian control regions（NMCR） in humans. Dermal microdialysis in humans showed that NO-c GMP releases in the subcutaneous tissue of acupoint are higher than those in NMCR and increased by electroacupuncture（EA）. Recent studies have demonstrated that low-frequency electrical stimulation and manual acupuncture with low stimulating force and rate produce an elevation of NO release predominantly over acupoints. In contrast, NO levels over the areas of the skin regions are moderately reduced by high-frequency EA stimulation. The results from anatomical and biochemical studies consistently show that acupoints exist higher levels of NO signaling molecules, and stimulus-evoked NO release is also with a higher level at acupoints. Results suggest that NO signaling molecules contribute to the specificity of acupoints, and selecting well-trained acupuncturetists for using correct acupoints and appropriate parameters should improve acupuncture clinical trial studies.

Metal-free synthesis of substituted phenols from arylboronic acids in water at room temperature

A convenient,efficient and practical metal-free method for the synthesis of substituted phenols from arylboronic acids has been developed.The protocol uses hydrogen peroxide as a hydroxylating agent ammonium bicarbonate as an additive,and the reactions were conveniently performed in water at room temperature.The method shows an excellent tolerance of functional groups,so it will find a wide variety of applications in academic and industrial research.

Synthesis,Crystal Structural and Electrical Conductivity Properties of Fe-Doped Zinc Oxide Powders at High Temperatures

The synthesis,crystal structure and electrical conductivity properties of Fe-doped ZnO powders（in the range of 0.25-15 mol%） were reported in this paper.I-phase samples,which were indexed as single phase with a hexagonal（wurtzite） structure in the Fe-doped ZnO binary system,were determined by X-ray diffraction（XRD）.The solubility limit of Fe in the ZnO lattice is 3 mol% at 950℃.The above mixed phase was observed.And the impurity phase was determined as the cubic-ZnFe 2 O 4 phase when compared with standard XRD data using the PDF program.This study focused on single I-phase ZnO samples which were synthesized at 950℃ because the limit of the solubility range is the widest at this temperature.The lattice parameters a and c of the I-phase decreased with Fe-doping concentration.The morphology of the I-phase samples was analyzed with a scanning electron microscope.The grain size of the I-phase samples increased with heat treatment and doping concentration.The electrical conductivity of the pure ZnO and single I-phase samples was investigated using the four-probe dc method at 100-950℃ in air atmosphere.The electrical conductivity values of pure ZnO,0.25 and 3 mol% Fe-doped ZnO samples at 100℃ were 2×10-6,1.7×10-3 and 6.3×10-4 S.cm-1,and at 950℃ they were 3.4,8.5 and 4 S.cm-1,respectively.