Influence of Sc^3＋ on LiMn2O4 cathode materials at elevated temperature

Sc^3＋-doped lithium manganese oxides were synthesized by solid-state reaction. The influences of doping element on structure, mean valence of manganese, and electrochemical performances were studied by X-ray diffraction （XRD）, galvanostatic charge-discharge and cyclic voltammetric tests, and also electrochemical impedance spectroscopy （EIS）. XRD tests showed that doped lithium manganese oxides were pure spinel structure without other phases. Redox titration and visible spectrophotometry tests indicated that the mean valence of manganese in doped lithium manganese oxides was higher than that of pure one. LiSc0.02Mn1.9804 remained 92.9% of the initial specific discharge capacity after 50th cycle at a constant current of 50 m/g, and the reversibility of LiSc0.02Mn1.98O4 was improved in comparison with pure LiMn2O4 at 50 ℃. EIS indicated that film deposition on spinel particles was suppressed because of Sc^3＋ doping, and the charge transfer between the surface film and spinel particles with increasing temperature for Sc^3＋-doped materials became easier as compared with undoped one.     

Grain refinement of AZ31 magnesium alloy by AI-Ti-C-Y master ahoy

Al-Ti-C-Y master alloy was prepared by combining SHS technique and melting-casting method. The microstructure of master alloy and its grain-refining effect on AZ31 alloy were investigated by means of OM, XRD, SEM and EDS. Experimental results indicated that the prepared master alloy consisted of α-Al, TiAl3, TiC and Al3Y phases, and exhibited good grain-refining performance of AZ31 alloy. Morphology of α-Mg changed from coarse dendritic to free equiaxed and the average grain size of α-Mg matrix reduced from the original 580 to 170 μm after adding 1.0 wt.% master alloy. The grain refining efficiency of Al-Ti-C-Y master alloy on AZ31 alloy was mainly attributed to heterogeneous nucleation of TiC particles and grain growth restriction of Al-Y compound or TiC at grain boundaries.     

Surface ξ potential and photocatalytic activity of rare earths doped TiO2

The iso-electric point of different rare earths （La, Ce, Y） doped anatase TiO2 was set out, and three organisms with different sur- face electrical properties （methylene blue trihydrate-positive electricity, methyl orange-negative electricity, methyl red-neutral electricity） were selected as photodegradable models. The result showed that the photocatalytic activity of 0.5wt.%Y ions doped anatase TiO2 was better than those of the others. The relationship between Zeta （ξ） potential and the photocatalytic activity of different RE doped anatase TiO2 were also investigated. The Y-doped anatase TiO2 was found with the special two iso-electric points and three ξ potential values.     

Preparation and photoluminescence of Tb^3＋ doped SrAl2O4 phosphor by composite combustion method

High-efficient Tb^3＋ activated SrAl2O4 phosphor was synthesized by a combined combustion-solid-state reaction method. The precursor of SrAl2O4：Th^3＋ phosphor was prepared via a combustion process, and then the as-prepared powder was heated in a reductive ambient of activated carbon at 1250 ℃ for 1 h. The results of X-ray diffraction, scanning electron microscopy, and photoluminescence spectra revealed the influence of the dosage of urea and heated process on the crystallinity, morphology, and photoluminescence of the phosphor. Comparing with traditional solid-sate reaction, the crystallinity and emission intensity of the SrAl2O4：Tb^3＋ phosphor were improved by this two-step process.     

湿法炼锌尾气治理控制技术的生产实践

叙述了蒙自矿冶有限责任公司铟锌冶炼厂低浓度S02烟气脱硫的生产实践,介绍了吸收过程的运行控制技术和吸收液对炼锌系统危害的解决办法,并成功将制酸尾气和挥发窑尾气合并处理,取得了显著的环保治理成效。     

Thermodynamic optimization and calculation of phase diagrams of YbCl3-MCl （M=Na,K, Rb,Cs）

YbCl3-MCl （M = Na, K, Rb, Cs） systems were optimized and calculated using the CALPHAD （CALculation of PHAse Diagram） technique. The modified quasi-chemical model in the pair-approximation for short-range ordering was used to describe the Gibbs energies of liquid phase in the systems. On the basis of the measured phase diagram data and experimental thermodynamic properties, a series of thermodynamic functions were optimized and calculated through an interactive computer-assisted analysis. Furthermore, some reasonable discussions on the thermodynamic parameters for these strong interaction binary systems were carded out. The results showed that the optimized parameters and experimental data are thermodynamically self-consistent.     

Optical properties of Eu^2＋-doped strontium borate glasses containing F-and Li^＋ ions

In this experiment, strontium borate glasses were prepared using the conventional quenching method in air atmosphere. Optical absorption, photoluminescence excitation and emission spectra, X-ray excited luminescence （XEL）, and luminescence decay curve of the as-prepared glasses were investigated at room temperature. The as-prepared glasses had two kinds of Eu ions, i.e., Eu^2＋ and Eu^2＋. Compared with the reported results of strontium borate glasses, Eu^2＋ luminescence was enhanced in the studied strontium borate glasses coprepared with F^- and Li^＋ ions. The coexisting of Li^＋ or F^- in the borate glasses could create more negative defect Vsr″ and stabilize Eu^2＋ ions, which might act as donor of electrons; For the F^- doping, the new center of B（O, F）4 （or BO3F） and BO2F2 units could be considered to be the distorted （BO4）, which were needed as a rigid framework to stabilize the divalent rare earth ions.     

Application of monodispersive anion exchangers in sorption and separation of Y^3＋ from Nd^3＋ and Sm^3＋ complexes with dcta

Rare earth complexes with trans-1,2-diaminocyclohexane-N,N,N ,N -tetraacetic acid （DCTA） of the Ln（dcta） type exhibited an unusual sequence of affinity on the polystyrene anion exchangers： pm^3＋〉Nd^3＋〉Sm^3＋〉Pr^3＋〉Ce^3＋〉Eu^3＋〉Gd^3＋〉La^3＋〉Sc^3＋〉Tb^3＋〉Dy^3＋〉 Ho^3＋〉Y^3＋〉Er^3＋〉Tm^3＋〉Yb3＋〉Lu^3＋[1]. Taking into account the position of Y^3＋, Sm^3＋, and Nd^3＋ in this affinity series, for the monodispersive polystyrene anion exchangers, Lewatit MonoPlus M 500, Lewatit MonoPlus M 600, Lewatit MonoPlus MP 500, Lewatit MonoPlus MP 64, and for the heterodispersive anion exchanger, Lewatit MP 62, the weight （Dg） and bed （Dv） distribution coefficients of these complexes and working ion exchange capacities （Cw） were determined. Based on these values, purifications of Y^3＋ from Nd^3＋ and Y^3＋ from Sm^3＋ in the macro-micro component system on these anion exchangers were studied. The application potential of this method was highlighted for the separation of Y^3＋ in the presence of Nd^3＋ and Sm^3＋. With 1 L of monodispersive and strongly basic polystyrene gel anion exchanger Lewatit MonoPlus M 500 in the acetate form, it is possible to obtain approximately 79 g Y2O3 purified from Nd2O3 and 70 g Y2O3 purified from Sm2O3 in the same process condition.     

Application of high-temperature permanent magnets Sm（Co,Fe, Cu,Zr）z in PPM focusing system

Rare earth permanent magnets Sm（Co, Fe, Cu, Zr）z with outstanding performance and high-temperature thermal stability were fabricated. Optimized by Fe content and process, Sm（Co0.72Fe0.15Cu0.1Zr0.03）7.5 magnet with B1〉0.75 T and Hci〉1300 kA/m at 300 ℃ can be obtained. According to the performance data of Sm（Co0.72Fe0.15Cu0.1Zr0.03）7.5, the magnetic field along central axis Bz in periodic permanent magnet （PPM） focusing system was simulated using electromagnetic field analysis software Maxwell 2D/3D. The Bz exhibited typical cosine curve along central axis, and the peak value of Bz was high enough to meet the demand of PPM focusing system at room temperature even at 200±20 ℃. Additionally, a kind of simple cooling structure for PPM focusing system was designed by setting cooling pipe between polepieces. Simulated results showed that smooth cosine curve of Bz was successfully achieved with good control of the thickness of cooling pipe.     

Preparation of neodymium-doped yttrium aluminum garnet powders and fibers

Using nitrate precursors, a novel spray-drying assisted citrate gel process for the preparation of neodymium-doped yttrium alumi- num garnet （YAG） phase was developed. Synthesis of single-phase polycrystalline YAG was achieved at temperatures as low as 800 ℃ using the spray-drying methodology whilst conventional approaches currently available require 1000 ℃. Initially, a solution was prepared by mixing aluminum and yttrium nitrates, citric acid, etilenglycol and neodymium oxide. This solution was dried by pulverization （spray dryer） to obtain aggregated precursor powders of the compound. These aggregates were calcined at 800, 850 and 900 ℃ to determine the phase evolution from amorphous to crystalline by X-ray diffraction （XRD）. The morphology of aggregates was characterized by scanning electron microscopy （SEM） and transmission electron microscopy （TEM）. Moreover, through XRD it was determined that the crystallization of YAG phase started at about 800 ℃ without any intermediate phases. The powders were composed of spherical aggregates with an average diameter of 1 um. From these powders, ceramic fibers with additions of 2at.% and 5at.% Nd, were extracted from the melt with diameters ranging from 30 um to 50 um.     

Synthesis,spectroscopic characterization,and thermal decomposition kinetics of some lanthanide（Ⅲ） nitrate complexes of 2-（N-o-hydroxyacetophenone） amino-3-carboxyethyl-4,5,6,7-tetrahydrobenzo[b]thiophene

Complexes of La（Ⅲ）, Ce（Ⅲ）, Pr（Ⅲ）, Nd（Ⅲ）, Sm（Ⅲ）, Eu（Ⅲ）, Gd（Ⅲ）, Dy（Ⅲ）, Yb（Ⅲ）, and Lu0ID with 2-（N-o- hydroxyacetophenone）amino-3-carboxyethyl-4,5,6,7-tetrahydrobenzo[b]thiophene （HAAT） formed by the condensation of o-hydroxyacetophenone and 2-amino-3-carboxyethyl-4,5,6,7-tetrahydrobenzo[b]thiophene were synthesized and characterized on the basis of elemental analyses, molar conductance measurements, magnetic susceptibility data, UV-Visible, IR, and NMR spectral studies. The spectral data revealed that the ligand acted as a neutral tridentate coordinating to the metal ion through ONO donor sequence. A coordination number nine was proposed for the complexes. Thermal decomposition studies of the ligand and lanthanum（Ⅲ） complex were carried out and kinetic parameters were calculated using Coats-Redfem equation. The decomposition reactions followed random nucleation mechanism with one nucleus on each particle.     

Calculation of AlN and MnS Precipitation in Non-Oriented Electrical Steel Produced by CSP Process

Combining with the study of analogue experiments and test analysis, the kinetics of precipitation and growth of AlN and MnS in non-oriented electrical steel produced by the CSP process is calculated. The results show that the precipitate phase particles of AlN and MnS in typical non-oriented electrical steel grades produced by the CSP process have grown to some extent in the soaking stage, but the precipitation contents are less than 20% of the total contents of nitride and sulfide. The precipitate phase particles of AlN and MnS have precipitated almost after the hot rolling process. The precipitation contents are more than 80% of the total contents of nitride and sulfide, but it is very late for the precipitate phase particles to grow at the end of the hot rolling process.     

Magnetic and magnetostrictive properties of amorphous TbFefFeAl multilayer thin film

Exchange coupling multilayer thin films, which combined giant magnetostriction and soft magnetic properties, were of growing interest for applications. The TbFe/FeAl multilayer thin films were prepared by dc magnetron sputtering onto glass substrates. The microstructure, magnetic, and magnetostrictive properties of TbFe/FeAl multilayer thin film was investigated at different annealing temperatures. The results indicated that the soft magnetic and magnetostrictive properties for TbFe/FeAlmultilayer thin film compared with TbFe single layer film were obviously improved./n comparison with the intrinsic coercivity JHo of 59.2 kA/m for TbFe single layer film, the intrinsic coercivity jHc for TbFe/FeAl multilayer thin films rapidly dropped to 29.6 kA/m. After optimal annealing （350 ℃×60 min）, magnetic properties of Hs=96 kA/m and jHc=16 kA/m were obtained, and magnetostrictive coefficient could reach to 574×10^-6 under an external magnetic field of 400 kA·m^-1 for the TbFe/FeA1 multilayer thin film.     

A white long-lasting phosphor Y2O2S： Tb^3＋ , Sm^3＋： an improvement of Y2O2S：Tb3＋

As an improvement of reported Y2O2S：Tb^3＋, a white-light long-lasting phosphor： Y2O2S：Tb^3＋, Sm^3＋ was prepared by the solid-state reaction. The photo-luminescence spectra showed that the position and shape of Tb^3＋ and Sm^3＋ emissions under UV excitation were similar in this host, which ensured a stable white emission color （daylight standard of IEC） under different excitations. The decay curves of co-doped samples indicated that the decay times of emissions of the two ions were close. The thermo-luminescence measurement suggested that the traps created by the doped Sm^3＋ ions were helpful to postpone the white afterglow of co-doped samples. Therefore, the function of co-doped Sm^3＋ ions was confirmed as improving the white emission colors of samples and acting as new trap centers.     

Synthesis,crystal structure,and fluorescence of two dimeric europium（Ⅲ） complexes with 2-（trifluoromethyl）benzoate

Two complexes [Eu2（2-TFMBA）6（2,2′-bipy）2]·2H2O （1） and Eu2（2-TFMBA）6（1,10-phen）2 （2） （2-TFMBA=2-（Trifluoromethyl） benzoate; 2,2′-bipy=2,2′-bipyridine; 1,10-phen= 1,10-phenanthroline） were synthesized by solvent method and determined by X-ray diffraction analysis. Complex 1 crystallizes in monoclinic system with space group P21/c, whereas complex 2 crystallizes in triclinic system with space group Pi. Both are binuclear molecules with an inversion center. In complex 1, two center Eu^3＋ ions are linked together by four 2-TFMBA ligands in bidentate-bridging mode. Each Eu^3＋ ion is eight-coordinated with six O atoms from five 2-TFMBA ligands and two N atoms from one 2,2′-bipy molecule. In complex 2, two center Eu^3＋ ions are linked together by four 2-TFMBA ligands in two modes, namely, bidentate-bridging and tridentate-bridging. Each Eu^3＋ ion is nine-coordinated with seven O atoms from five 2-TFMBA ligands and two N atoms from one 1,10-phen molecule. The two complexes both exhibited strong red fluorescence under ultraviolet light, and the ^5D0→^7Fj （j=0-4） transition emissions of Eu^3＋ ion were observed in their emission spectra.     

Phase structure and magnetocaloric effect of （Tb1-xDyx）Co2 alloys

Phase structure and magnetocaloric effect of （Tb1-xDyx）Co2 alloys with x=0, 0.2, 0.4, 0.6, 0.8, and 1.0 were investigated using X-ray diffraction analysis, differential thermal analysis, and magnetization measurement. The samples were single phase with cubic MgCu2- type structure; with the increase of Dy content, Tc decreased from 240 K （TbCo2） to 130 K （DyCo2）, and the maximum magnetic entropy change ｜ △SM,max｜ increased from 3.133 to 8.176 J/kg-K under low magnetic field of 0-2 T. The Arrott plot and the change of ｜△SM,max｜ showed that magnetic phase transition from second order to first order occured with the increase of Dy content between x=-0.6 and 0.8.     

Effects of AIMnCa and AIMnFe Alloys on Deoxidization of Low Carbon and Low Silicon Aluminum Killed Steels

To confirm the effects of AlMnCa and AlMnFe alloys on the deoxidization and modification of Al2O3 inclusions, experiments of 4-heat low carbon and low silicon aluminum killed steels deoxidized by AlMnCa and AlMnFe alloys were done in a MoSi2 furnace at 1 873 K. It is found that the 1^# AlMnCa alloy has the best ability of deoxidization and modification of Al2O3 inclusions than 2^# AlMnCa and AlMnFe alloys. Steel A deoxidized by 1^# AlMnCa alloy has the lowest total oxygen content in the terminal steel, which is 37× 10^-6. Most of the inclusions in the steel deoxidized by 1^# AlMnCa alloy are spherical CaO-eontaining compound inclusions, and 89.1% of them are smatter than 10 μm. The diameter of the inclusion bigger than 50 μm is not found in the final steels deoxidized by AlMnCa alloys. Whereas, for the steels deoxidized by AlMnFe alloys, most inclusions in the terminal steel are Al2O3 or Al2O3-MnO inclusions, and a few of them are spherical, and only 76.8% of them are smaller than 10 μm. Some in- clusions bigger than 50μm are found in the steel D deoxidized by AlMnFe alloy.     

A new polyoxometalate based on mono-lacunary Dawson polyoxoanion： molecular structure of [{Nd（H2O）3（α2-P2W17O61）}2]^14-

A new polyoxometalate dimer based on lacunary Wells-Dawson anion and lanthanide cation, Na14[{Nd（H2O）3 （α2-PeWt7O61）2]·17H2O, was isolated as a sodium salt under ambient conditions and characterized by IR, TG, and X-ray single crystal structure analysis and electrochemistry. It belonged to the triclinic, space group Pi with a=1.26738 （15） nm, b=1.41464 （17） nm, c=2.3254 （4） nm, α=103.142 （2）°, β = 95.122 （2）°, γ=113.9690 （10）°, V=3.6317 （8）nm^3, Z=2, Dc=4.274 mg/m^3, and μ=27.695 mm^-1. The Nd^3＋ ion was substituted for a [W=O]^4＋ unit in the ＂cap＂ site of the tungsten-oxygen framework of the parent Wells-Dawson ion. The cyclic voltammograms of the title compound exhibited nearly chemically reversible one-step one-electron transfer process and two-step irreversible reduction processes. Thermogravimetric showed a one-step slow weight loss stage in the range of 25-850 ℃.     

Influence of Chemical Composition on Phase Transformation Temperature and Thermal Hot Work Expansion Coefficient of Die Steel

On the basis of the uniform design method, six kinds of martensitic hot work die steels were designed. The phase transformation temperatures including Ac1 , Ac3 , and Ms were measured by DIL805A quenching dilatometer. The influences of the main elements on phase transformation temperatures were analyzed by quadratic stepwise regression analysis, and three corresponding equations were obtained. These equations, in which the interactions of the elements were considered, showed more effectiveness than the traditional ones. In addition, the thermal expansion coefficients of these steels in annealed state and quenched state were also obtained during the tests. The influences of chemical composition and temperature on the thermal expansion coefficient were analyzed; the equations obtained were verified by using several kinds of steels. The predicted values were in accordance with the results of the experiments.     

Kinetic Model of ε-Cu Particle Dissolution in Welding- Induced HAZ of Copper-Containing Steel

The kinetics of ε-Cu particle dissolution in the matrix of heat affected zone （HAZ） during welding of a copper-containing steel was determined by assembling the welding temperature-time program into a modified Whelan＇s solution. The particle dissolution dependence on the degree of ＂superheating＂ above the equilibrium transformation is demonstrated from the model. In terms of volume fraction of particle dissolution, the HAZ may he classified into three zones, including the undissolving zone, the partially dissolving zone, and the completely dissolving zone, respectively. The numerical solution was in good agreement with the experimental examination finding. The results of model can be used to quantitatively map the ε-Cu dissolution zone dependence on the peak temperature of welding thermal cycles and understand the evolution of this transformation during welding.