Study on Industrial Application of Hydrogen Sulfide Removal by Wet Oxidation Method with High Gravity Technology

The removal of hydrogen sulfide from gas plays an important role in rational utilization of resources and environ- mental protection. In this paper, the process of hydrogen sulfide removal by wet oxidation method in a rotating packed bed was investigated in a scale for treating 10 000 Nm3/h of gas. On the basis of studying the influence of the species and con- centration of alkali source, the liquid/gas volume ratio, the high gravity factor, and the hydrogen sulfide content in feed gas on the desulfurization effect, the suitable technological conditions were obtained. The hydrogen sulfide removal efficiency could reach 98.0% under these conditions. The results of continuous operation of process facilities showed that the high gravity method has many merits including higher desulfurization rate, good stability in operation, lower liquid/gas volume ratio, greater operation elasticity, and apparent energy saving effects.

A kind of double-sided porous anodic alumina membrane fabricated with the three-step anodic oxidation method

The porous anodic alumina membranes （PAAMs） have been successfully used as templates for the fabrication of functional nano-materials due to their outstanding regularity and physicochemical properties. In this paper, a transparent double-sided anodic alumina membrane with ultra-thin aluminum substrate was fabricated with the three-step anodic oxidation method in the oxalic acid electrolyte. The characters such as the top-surface morphology, membrane thickness, and depth of nanopores of this three-layer （A1203-A1-A1203） sandwiched nano-structure were controllable through regulating the main anodic oxidation conditions, e.g., anodic oxidation time of various steps, coating remove process. The experiments data revealed that the aluminum substrate is exponential declined with the oxidation time when it was approximately reduced by a few micrometers. This new double-sided anodic alumina membrane can be used as the high-quality functional field emission materials and templates.

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.

Corrosion Behavior of Anodic Oxidized TiO_2 Film in Seawater

TiO2 films were formed on metallic titanium substrates by the anodic oxidation method in H2SO4 solution under the 80V D.C..Phase component and microstructure were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM).Water contact angles on titanium oxide film surface were measured under both dark and sunlight illumination conditions.Corrosion tests were carried out in seawater under different illumination conditions by electrochemistry impedance spectrum (EIS) and polarization curves.The result showed that the TiO2 film prepared by the anodic oxidation method was anatase with a uniform structure and without obvious pores or cracks on its surface.The average water contact angle of the film was 116.4? in dark, in contrast to an angle of 42.7? under the UV illumination for 2 hours, which demonstrates good hydrophobic property.The anti-corrosion behavior of the TiO2 film was declining with the extended immersion time.Under dark conditions, however, the hydrophobic TiO2 film retarded the water infiltrating into the substrate.The impedance changed slowly and the corrosion current density was 2 orders of magnitude lower than that with the film illuminated by sunlight.All of those mentioned above indicate that the TiO2 film possesses much better performance under dark condition, and it can be applied as an engineering material under dark seawater environment.

Biodegradation of Lubricating Oil in Wastewater with Zoogloea sp.

The purpose of this study was to identify microbial strains that have a strong ability to biodegrade lubricating oil. No. 20 lubricating oil was used as the sole carbon source in an isolation medium to screen bacteria from sludge that had been contaminated with crude oil. Through both morphological and biochemical methods, the bacterial strain that had the highest biodegrading capacity was identified as Zoogloea sp. On the basis of these preliminary results, a biological contact oxidation method was employed to further assess the ability of the Zoogloea sp. strain to treat wastewater contaminated by No. 20 lubricating oil using three oxidation cabins and two hydraulic retaining times （HRT）. Results showed that the concentration of No. 20 lubricating oil with a 12 h hydraulic retaining time and 16.5 L h^-1 inflow rate was reduced by 99.3% in 15 d, and with a 6 h hydraulic retaining time and 33 L h%^-1 inflow rate it decreased by 98.6070 in 12 d. The results from this study indicated that Zoogloea sp. had a strong potential to be utilized in biodegradation of lubricating oil.

Preparation and photoelectric effect of Zn^(2+)-TiO_2 nanotube arrays

Zn 2+-TiO2 nanotube arrays were prepared by anodic oxidation method.The current-time curves were used to investigate their growth mechanism.Scanning electron microscopy and X-ray diffractometry were applied to characterizing their structures and properties.The photoelectrochemical properties were studied by electrochemical impedance spectrum(EIS).The optimised working conditions for TiO2 nanotube arrays were found to be pH 1,0.5%HF(mass fraction),20 V oxidation voltage and for 2 h.The produced sample was in anatase form,with length of 70-100 nm,thickness of 10 nm,uniform diameter and structure that does not collapse under the preparation conditions.The EIS results show that TiO2 nanotube arrays prepared with 0.5%HF(mass fraction) present a low impedance and TiO2 nanotube arrays loaded by Zn 2+could have a decreased resistance.This decrease could likely accelerate the transfer of carriers and even increase photoelectric conversion.

Ligand Size Effect on PdLn Oxidative Addition with Aryl Bromide： A DFT Study

The process and mechanism of the ligand volume controlled Pd（PR3）2 （PR3=PH3, PMe3, and PtBu3） oxidative addition with aryl bromide were investigated, using density functional theory method with the conductor-like screening model. Association pathway and dissocia-tion pathway were investigated by the comparison of several energies. The cleavage energy of Pd（PR3）2 complex was calculated, as well as the oxidative addition reaction barrier energy of Pd（PR3）n （n=1,2） with aryl bromide in N,N-dimethylformamide solvent. This study proved that the ligands volume possessed a great impact on the mechanism of oxidative addition： less bulky ligand palladium associated with aryl bromide via two donor ligands,but larger bulky ligand palladium coordinated via monoligand.

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.

THE PREPARATION AND PHOTOCATALYTIC ABILITY OF LEAD TITANATE

he perovskite-type PbTiO3 has been synthesized by the method of mixed oxides. The appropriate conditions for preparing have been reported. The obtained PbTiO3 powder is pure and fine. The decolorization of dyes in a PbTiO3 suspension system is over 90%. In this paper the photocatalytic ability of PbTiO3 and the factors of influence are discussed.

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.

Simple and cost-effective methods for precise analysis of trace element abundances in geological materials with ICP-MS

Inductively coupled plasma mass spectrometry （ICP-MS） is the most commonly used technique to deter- mine the abundances of trace elements in a wide range of geological materials. However, incomplete sample digestion, isobaric interferences and instrumental drift remain obvious problems that must be overcome in order to obtain precise and accurate results, For this reason, we have done many experi- ments and developed a set of simple, cost-effective and practical methods widely applicable for precise and rapid determination of trace element abundances in geological materials using ICP-MS. Commonly used high-pressure digestion technique is indeed effective in decomposing refractory phases, but this inevitably produces fluoride complexes that create new problems. We demonstrate that the fluoride complexes formed during high-pressure digestion can be readily re-dissolved using high-pressure vessel at 190 ℃ for only 2 h for 50 mg sample. In the case of isobaric interferences, although oxide （e.g., MO^＋/M^＋） and hydroxide （e.g., MO^＋/M^＋） productivity is variable between runs, the （MO^＋/M^＋）/（CeO^＋/Ce^＋） and （MOH^＋/M^＋）/（CeO^＋/Ce^＋） ratios remain constant, making isobaric interference correction for all other elements of interest straightforward, for which we provide an easy-to-use off-line procedure. We also show that mass-time-intensity drift curve is smooth as recognized previously, for which the correction can be readily done by analyzing a quality-control （QC） solution and using off-line Excel VBA procedure without internal standards. With these methods, we can produce data in reasonable agreement with rec- ommended values of international rock reference standards with a relative error of 〈8% and precision generally better than 5%. Importantly, compared to the widely used analytical practice, we can effectively save 〉60% of time （e.g., 〈24 h vs. 〉60 h）.