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Trivalent thulium ions (Tm3+) doped GdAlO3 (Gd1-xTmxAlO3) phosphors which show a blue luminescence of high color purity have been synthesized by using solid-state reaction method starting from nanosized powders. X-ray diffraction (XRD) measurements were used to analyze the phase transformations that take place during the preparation of the phosphors. The morphologies of the powders calcined at different temperatures were studied by using scanning electron microscopy (SEM). The luminescence properties of the compounds were investigated. Pure phase of orthorhombic type GdAlO3 (GAP) was yielded by calcining the phosphors at 1200°C for 8 h. The PL spectra showed representative Tm3+ emission. The strong band centered at ~488 nm and the weak one centered at 697 nm were attributed to the 1D2-3F4 and 1G4-3F4 transitions of Tm3+, respectively. The quenching concentration of Tm3+ was estimated to be ~0.75at.% (x=0.0075), for which can be ascribed to the exchange interactions. The decay curve was fitted to be a single exponent and the estimated fluorescent lifetime of the GdAlO3:Tm3+ phosphor was 1.73±0.08 ms.

The metastable garnet lattice of Gd3Al5O12 (GdAG) was effectively stabilized via doping with significantly smaller Lu3+, and based on which (Gd,Lu)AG:Yb/Ho was developed in this work as a new type of upconversion phosphor. The phosphor particles calcined from the precursors synthesized via carbonate precipitation were observed to have good dispersion and fairly uniform morphologies. Optical spectroscopy found that the [(Gd1-xLux)0.948Yb0.05Ho0.002]3Al5O12 (x=0.1-0.5) garnet powders exhibit a green emission centered at ~543 nm (the 5F4,5S25I8 transition of Ho3+) and a red emission centered at ~668 nm (the 5F55I8 transition of Ho3+) under laser excitation at 978 nm. The upconversion emission intensity was found to decrease with increasing Lu3+ doping. Meanwhile, the dependence of up-conversion emission intensity on the pumping power was measured and the up-conversion mechanism was discussed in detail. The Yb/Ho codoped (Gd,Lu)AG garnet system developed herein may potentially be used as a new type of luminescent material.

Yb rare earth doped YAG ultrafine particles were synthesized by the stearate melting method using yttrium stearate, ytterbium stearate and aluminum tristearate as starting materials. The phase formation of Yb:YAG, the properties and the sintering activity of the powders were investigated by means of XRD, SEM, dilatometry and vacuum sintering. The results show that pure Yb:YAG nanopowders can be obtained by calcining the co-melted precursor at a relatively low temperature of 800 °C for 4 h. The powders calcined at 1000°C have better sintering activity than the powders calcined at other temperatures. For the Yb:YAG powders doping with 0.5% TEOS, the compact can be sintered to 99.2% of the theoretical density at 1600 °C and 99.7% at 1700 °C. The transparent Yb:YAG ceramics obtained by vacuum sintering at 1700 °C for 5 h exhibit a pore-free and uniform microstructure.

Direct coagulation casting (DCC) is a relatively new ceramic near-net-shape forming process which can form homogeneous ceramic green body with complex shape and high density. Direct coagulation casting of aqueous alumina slurries by adding Y3+ions, which have been frequently used as additive for the sintering of alumina ceramics, were studied. Two different kinds of Y3+-ion releasing substances, Y2O3powder and Y(NO3)3, were used as coagulants and were introduced into stabilized alumina suspensions directly after dispersing. Compared with that of Y2O3powder, both the coagulation time and the added amount required for a reasonable shaping were significantly reduced for using Y(NO3)3as coagulant. The effects of the two coagulants on the properties of the consolidated green bodies and sintered ceramics were studied. The mechanisms of coagulation induced by the addition of Y3+-ions were discussed on the basis of interactions between Y3+ions and the added polyelectrolyte dispersant.

To suppress the thermal decomposition and to stabilize the crystal structure of Gd3Al5O12 (GdAG) garnet, doping GdAG with smaller Ln3+ (Ln=Tb, Dy, Ho, Er, Tm, Yb, Lu, and Y, respectively) to form (Gd,Ln)AG solid solutions was proposed in work. Carbonate precursors of (Gd,Ln)AG with an approximate composition of (NH4)x(Gd,Ln)3Al5(OH)y(CO3)z•nH2O were synthesized via coprecipitation from a mixed solution of ammonium aluminum sulfate and rare earth nitrate, using ammonium hydrogen carbonate as the precipitant. The precursors and the calcination derived oxides were characterized using FT-IR spectroscopy, DTA/TG, XRD, BET and FE-SEM. The results showed that smaller Ln3+ doping can indeed stabilize GdAG against its thermal decomposition to a mixture of GdAlO3 (GdAP) and Al2O3 phases at elevated temperatures and at the same time effectively lowers the temperature for garnet crystallization. The carbonate precursors are loosely agglomerated and the resultant (Gd,Ln)AG powders show good dispersion and a fairly uniform particle morphology. The (Gd,Ln)AG solid solutions exhibit decreasing lattice parameters along with decreasing radius of the dopant ions at the same dopant content of 50 at%. Photoluminescence properties of some of the garnet solid solutions are also studied. The materials developed herein may potentially be used for photoluminescent and scintillation applications.

Ca3Co4O9 powders were synthesized by a solid-state reaction method. Porous Ca3Co4O9 ceramics with parallel sheet shaped pores were prepared by a template sacrifice method using epispastic polystyrend (EPS) hollow spheres as the templates. During compaction of the green body, the EPS hollow spheres change into EPS discs due to the pressing force. After sintering, the pores in the Ca3Co4O9 ceramics are sheet shaped, well distributed and parallel to the pressing surface of compaction. The value of ZT merit of the porous Ca3Co4O9 sample obtained with 10 wt% EPS spheres is 0.0489. It was found that the ZT merit value can be improved by changing the density of sample to achieve a high ratio of electrical conductivity to thermal conductivity.

Fine yttrium stearate powder was produced at a relatively low temperature using yttrium nitrate hexahydrate, ammonia and stearic acid as the raw materials. Dispersed Y2O3 nanopowder was synthesized by calcining the yttrium stearate. The formation mechanism of the precursor and the Y2O3 nanopowder was studied by means of XRD, TG-DTA, FT-IR, BET, FE-SEM and HR-TEM. Pure and dispersed Y2O3 nanopowder with an average particle size of 30 nm was produced by calcining the precursor at 600 °C. The particle size increases to about 60 nm with the increase of the calcination temperature to 1000 °C. In the preparation of Y2O3 from yttrium stearate, no water medium is involved, thus capillarity force and bridging of adjacent particles by hydrogen bonds can be avoided, resulting in good dispersion of the particles. The dispersed Y2O3 nanopowder prepared in this work has potential application in phosphors and transparent ceramic materials.

A series of layered rare-earth hydroxides (LRHs) of (Y,Ln)2(OH)5NO3•nH2O ( Ln=Tb,Eu), have been synthesized via a hydrothermal route. Crystal structures and optical properties of the materials have been investigated in detail by the combined techniques of XRD, FT-IR, FE-SEM, HR-TEM, and PLE/PL spectroscopies. It is shown that Tb3+ and Eu3+ are successfully incorporated into the Y-LRH host lattice to form solid solutions. Under UV excitation, the binary (Y0.97Tb0.03)- and (Y0.97Eu0.03)-LRHs exhibit their respective characteristic photoluminescence of the Eu3+ and Tb3+ activators. The ternary (Y0.965Eu0.005Tb0.03)-LRH simultaneously shows red and green emissions and both the intensity and emission color can be adjusted by changing the excitation wavelength. Compared with (Y0.995Eu0.005)-LRH, the ternary (Y0.965Eu0.005Tb0.03)-LRH exhibits appreciably enhanced 615nm red-emission, which indicates the existence of non- radiative energy transfer from Tb3+ to Eu3+. The ternary (Y0.965Eu0.005Tb0.03)-LRH also readily undergoes anion exchange with a series of inorganic and organic anions at room temperature.

Nano-porous bilayers structure antireflection films on glass substrate were prepared by sol-gel method, tetraethyl orthosilicate(TEOS) and tetrabutyl titanate(TEOT) as the main raw materials, cetyl trimethyl ammonium bromide(CTAB) and polyethylene glycol(PEG) as template. The relation of the template agent addition, pH, and aging time to surface morphology and optical properties were analyzed. When the CTAB/TEOS = 1/30, the average spectral transmittance in the visible wavelength is 93.69% and the peak transmission is up to 97.37%. All the bilayers antireflection films are amorphous structure, uniform surface morphology, dense nano-porous size distribution, pore size is about 10nm.

Oxyfluoride tellurite glass with the composition of TeO2-AlF3-LaF3-ZnO/ZnCl2/ZnF2 was prepared successfully. The thermal stability and structure of TeO2-AlF3-LaF3 system tellurite glass were studied bySubscript text DSC and IR spectra. The results indicated that glass transition temperature of TeO2-AlF3-LaF3-ZnO/ZnCl2/ZnF2 glass was higher than that of (1-x)TeO2-xAlF3 (x=10%, 20%, 30%, 40%, 50%, in mol%) binary glass system slightly. A small number of ZnF2/ZnCl2/ZnO (5mol%) improved glass thermal stability. After adding 5mol% ZnF2/ZnO/ZnCl2 into fluoride tellurite glass respectively, glass transition temperature increased in turn. The introduction of 5mol% different zinc compounds had a little impact on the glass network structure.

Transparent oxyfluoride tellurite glass with the composition of TeO2-SiO2-AlF3-CaO-KF system were prepared by conventional melting and annealing technique, and the transparent oxyfluoride glass-ceramics containing CaF2 nano-crystallines were obtained by controlled heat-treatment. The effect of heat-treatment schedules on the crystallization behavior and the microstructure of the glass-ceramics were analyzed by differential scanning caborimetry (DSC) analysis, X-ray diffraction (XRD) analysis, infrared (IR) spectrum and scanning electron microscopy (SEM). The sole CaF2 crystalline phase was confirmed by XRD, the spherical CaF2 nano-crystallines at about 20~100nm embed homogeneously among the glassy matrix after crystallization by SEM observation. The size of CaF2 grains grew with the increase of crystallization temperature and holding time. Te and Si atoms existed in [TeO3] and [SiO4] forms. Part of Al atoms existed in the form of [AlO4] and formed network together with [SiO4] tetrahedron. The other Al atoms acted as modifiers in the form of [AlO6]. The transmittance of glass-ceramics can reach 85% in visible light and 90% in infrared waveband. The novel transparent oxyfluoride tellurite glass-ceramics are excellent matrix materials in up-conversion luminescence field.

Nano-Cordierite powders used for high frequency chip inductors (MLCIs) were prepared by the sol-emulsion-gel method. The samples derived from these powders could be sintered at 900°C to be cordierite ceramics having a low dielectric constant and dielectric loss (ε=3.18, tgδ=0.00011; 1GHz). Effects of precursor concentration, treating temperature, and [H2O]/[Si] ratio of this material were studied. The pseudo-ternary phase diagram of sol/TritonX-100/n-hexanol/cy- clohexane was constructed and the influences of each variable on the phase diagram were discussed. Results showed that the optimal precursor concentration, treating temperature, and [H2O]/[Si] ratio for qualifying the gelation of the material were 1.5 mol/L, 45°C, and 4, respectively. Results also showed that for qualifying cordierite powders, the use of TritonX-100 as a surfactant together with n-hexanol as a co-surfactant could dissolve more magnesium nitrate and aluminium nitrate, and obtain a wider W/O micro-emulsion region than when other reagents were used. The samples derived from this method can be co-fired with a silver electrode, an ideal dielectric material for high frequency MLCIs.

Hydroxyapatite (HA) nanopowder was synthesized by reverse microemulsion technique using calcium nitrate and phosphoric acid as starting materials in aqueous phase. Cyclohexane was used as organic solvents, TX-100 as surfactants and n-butyl alcohol to make the emulsion. Synthesized powder was characterized by X-ray diffraction (XRD) and scanning electron microscopy(SEM). The results showed that different pH values and temperatures had significant effect on the purity and crystallinity of HA by using the reverse microemulsion. When the pH value is 11 and at 700°C, high purity and well crystallinity HA was obtained. There is a dicalcium phosphate phase present at pH 9, which is easily disassembled to CPP at 700°C. This HA powders have a rapid Cu2+ and Cd2+ sorption rate and good removal efficiency. The removal rates for heavy metal ions were Cd2+＞Cu2+.

Nano-hydroxyapatite (HAP) were prepared by sol-gel method with Ca(NO3)2•4H2O and H3PO4 precursors. The result was shown that the powder was spherical with very little reunion and the particle size was around 50nm. The HAP adsorbent was utilized for copper removal from aqueous solutions using the batch technique. Some parameters that determine copper ion uptake including contact time, adsorbent dose, the solution temperature and initial concentration of the copper in the aqueous solution were evaluated. The experimental results shown that the removal efficiency was about 99.27% at pH 7, 40°C, contact time 60 min, adsorbent dose of 5g/L and initial concentration of 60mg/L.

Fault diagnosis is a key technology to ensure safe and reliable operation of large electromechanical equipments. Fault feature extraction is important in fault diagnosis process. For non-stationary vibration signal, energy normalization method based on wavelet packet is used to make signal processing with signals decomposed into different frequency bands to perform energy normalization process in corresponding frequency band so as to extract fault feature. Flue Gas Turbine is chosen as research object and analysis shows that energy normalization processing method based on wavelet packet can effectively extract non-stationary signal characteristic parameters and make effective nondestructive testing analysis of equipments condition.

Preparation technology and sintering characteristics of the CaO-Al2O3-B2O3-SiO2 system glass ceramics were investigated. Results showed that the glass ceramics of this system could be sintered at 850oC; the material has fine sintering properties, outstanding dielectric properties including low dielectric constant (about 4.85, 1GHz) and low dielectric loss (about 0.1%, 1GHz). XRD analysis indicated that the crystalline phases in the sintered body are mainly Al5(BO3)O6, a trace amount of SiO2 and CaSiO3.

The development of a virtual axis cutter grinder was introduced. The main contents of this paper include layout design, parameters design method, control system and program system. The purpose of the development of the parallel machine tools is for cutter grinding. The dimension of the cutter and the translation workspace for cutter grinding usually is small and is therefore suitable for the parallel machine tool application. The new machine tool has high rigidity and good precision.