Charging of Materials Non-Metallic Used in Underground Mines Endangered by Firedamp and/or Coal Dust

The expansion parts and components of non-metallic in devices have become a fait accompli. In the case parts, components of non-metallic are used in atmospheres explosive and may be a potential source of ignition [1]. Ignition hazards due to static electricity from the charged non-conductive non-metallic materials are well known [2]. The prevalence protection metal parts and components of anti-corrosion exist in any device equipped with a metal casing. Inherent risks associated services are caused by static electricity. Electrostatic phenomena arise in many situations, in a variety of environments and industries. The occurrence of charge static in many cases unexpected is unwanted and requires the use of expensive preventive measures. Brush discharge and propagating brush discharge (e.g. composite coating about non-conductive electrostatic properties of an isolated base conductive) create explosion hazard in underground endangered by firedamp and/or coal dust [3].

Research on toughening mechanisms of alumina matrix ceramic composite materials improved by rare earth additive

Mixed rare earth elements were incorporated into alumina ceramic materials. Hot-pressing was used to fabricate alumina matrix composites in nitrogen atmosphere protection. Microstructures and mechanical properties of the composites were tested. It was indicated that the bending strength and fracture toughness of alumina matrix ceramic composites sintered at 1550 ℃ and 28 MPa for 30 min were improved evidently. Besides mixed rare earth elements acting as a toughening phase, AlTiC master alloys were also added in as sintering assistants, which could prompt the formation of transient liquid phase, and thus nitrides of rare earth elements were produced. All of the above were beneficial for improving the mechanical properties of alumina matrix ceramic composites.

A Novel Uniplanar Multi-Electrode Capacitive Sensor for In-Situ Weathering Damage Detection of Nonmetallic Materials

A uniplanar capacitive sensor with 5-electrodes on one plane substrate and a large reflector electrode,was designed to get the corresponding capacitance information for weathering damage detection of non-metallic materials exposed to a service environment.A 2-D finite-element method was employed to simulate the electric potential distribution and capacitance measurements for the sensor.2 marble slabs,one was healthy and the other was notched,were experimentally detected.Both the simulation and the preliminary experimental results show that the measured capacitances decrease after weathering damage occurs in nonmetallic material.The reflector can enlarge the sensitive depth.The weathering assessment of nonmetallic materials can be done by processing the measured capacitances.The proposed approach can effectively detect the weathering damage of nonmetallic material and can be practically used for in-situ weathering damage evaluation.

Characterization of the negative thermal expansion material Zr_(1-x)Hf_xW_2O_8

The oxide ZrW_2O_8 displays unusual property of isotropic negative thermalexpansion in a large wide temperature range, which makes it have a number of important potentialapplications. The cubic Zr_(1-x)Hf_xW_2O_8 (x velence 0,0.3, 0.5, 0.7, and 1.0) were synthesized bystandard solid state reaction technique. The high and low temperature X-ray diffraction analysisindicate that the substitution of the Hf^(4+) for Zr^(4+) only leads to reducing the latticeconstants, and the changes of negative thermal expansion coefficients are not obvious. The linearexpansion coefficients of Zr_(1-x)Hf_xW_2O_8 (x velence 0,0.3, 0.5, 0.7, and 1.0) are about -6 X 10^(-6) K^(-1) in the temperature range of 298 to 973 K, while that of Zr_(0.5)Hf_(0.5)W_2O_8 is -9.6X 10^(-6) K_(-1) from 83 to 298 K. The phase transition temperatures from alpha-ZrW_2O_8 tobeta-ZrW_2O_8 structure were also determined by X-ray diffraction method. Thermogravimetric analysis(TGA) exhibits that Zr_(1-x)Hf_xW_2O_8 is not hygroscopic in air.

无铅压电陶瓷研究的新进展

综述了近年来国内外无铅压电陶瓷材料方面的研究进展。主要介绍了钛酸钡基、铌酸盐系、含铋层状结构以及含铋钙钛矿型无铅压电陶瓷体系中所开展的研究工作。同时对近年来无铅压电陶瓷在粉体制备以及晶粒定向新工艺方面的进展也进行了简要的评述。

Influence of processing parameters on the phase composition of ZrN-Si_3N_4 synthesized from zircon

The optimum parameters were determined for synthesizing ZrN-Si3N4 composite powder from zircon by carbothermal reduction-nitridation （CTRN） process. The samples were prepared by mixing the carbon black of an average particle size less than 30 μm and the zircon of 40 μm with C/ZrSiO4 mass ratios of 0.2, 0.3, 0.4, and 0.5. The prepared samples were subjected to the CTRN process at temperatures of 1673, 1723, 1753, and 1773 K for 6, 9, and 12 h. The CTRN process was conducted in an atmosphere-controlled tubular furnace in a nitrogen gas flow of 1.0 L/rain. All the products were examined by X-ray powder diffraction to determine the transformation. The results showed that the proper transformation of ZrN-Si3N4 occurred at 1773 K for 12 h with a C/ZrSiO4 mass ratio of 0.4.

Influence of cerium ions on the anatase-rutile phase transition of TiO_2 prepared by sol-gel auto-igniting synthesis

The anatase-rutile phase transformation of TiO_2 doped cerium up to 5 molpercent was studied by X-ray diffraction and X-ray photoelectron spectroscopy. The samples wereprepared by sol-gel auto-igniting synthesis process from a TiO(NO_3)_2-Ce(NO_3)_2-NH_4NO_3-citricacid complex compound system. The combusted amorphous powders were calcined at differenttemperatures. Significant structural changes were observed during the various stages of the phasetransformation. It was concluded that at low dopant contents, cerium ions were incorporated into theTiO_2 structure, and the anatase phase was stabilized; but at larger amounts, part of the dopantwas segregated on the surface of TiO_2 and the rutile formation was accelerated at elevatedcalcination temperature.

Preparation and characterization of the TiO_2-V_2O_5 photocatalyst with visible-light activity

Visible-light responsive TiO2-V2O5 catalyst was prepared using a binary sol-gel and in-situ intercalation method. The TiO2 sol and V2O5 sol were mixed to disperse the V2O5 species in the TiO2 phase at molecular level. The binary sol was then intercalated into interspaces of polyaniline （PANI） by means of in-situ polymerization of aniline. Conglomeration of the TiO2-V2O5 dusters during the calcination process was avoided because of the wrap of polyaniline. The surface mor- phology, the crystal phases, the structure, and the absorption spectra of （PANI）,/TiO2-V2O5 and the composite catalyst were studied using SEM, XRD, FT-IR, and UV-Vis. The photoactivity of the prepared catalyst under UV and visible light irradiation were evaluated by decolorization of methylene blue （MB） solution. The results showed that the composite catalyst displayed a homogeneous anatase phase, and the vanadium pentoxide species was highly dispersed in the TiO2 phase. The composite catalyst responded to visible light because of the narrowed band gap. In this study, the catalyst with the sol volume ratio of TiO2： V2O5 = 10：1 presented the best photocatalytic activity.

TiO_2 thin film photocatalyst

It is well known that the photocatalytic activity of TiO_2 thin filmsstrongly depends on the preparing methods and post-treatment conditions, since they have a decisiveinfluence on the chemical and physical properties of TiO_2 thin films. Therefore, it is necessary toelucidate the influence of the preparation process and post-treatment conditions on thephoto-catalytic activity and surface microstructures of the films. This review deals with thepreparation of TiO_2 thin film photo-catalysts by wet-chemical methods (such as sol-gel,-reversemicellar and liquid phase deposition) and the comparison of various preparation methods as well astheir advantage and disadvantage. Furthermore, it is discussed that the advancement ofphotocatalytic activity, super-hydrophilicity and bactericidal activity of TiO_2 thin filmphotocatalyst in recent years.

Rapid communication Preparation of TiO_2 nanometer thin films with high photocatalytic activity by reverse micellar method

Two kinds of TiO_2 nanometer thin films were prepared on stainless steel bythe reverse micellar and sol-gel methods, respectively. The calcined TiO_ 2 thin films werecharacterized by X-ray diffraction (XRD), atomic force microscopy (AFM), BET surface area and X-rayphotoelectron spectroscopy (XPS). Photocatalytic activity was evaluated by photocatalyticdecoloration of methyl orange aqueous solution. The results showed that the TiO_2 thin filmsprepared by reverse micellar method (designated as RM-TiO_2 films) showed higher photocatalyticactivity than those by sol-gel method (designated as SG-TiO_2 films). This is attributed to the factthat the former is composed of smaller monodispersed spherical particles with a size of about 15 nmand possesses higher surface areas.

Effect of growth time on morphology and photovoltaic properties of ZnO nanowire array films

Single-crystalline ZnO nanowire arrays with different aspect ratios and nanowire densities were prepared by the hydrothermal growing method using polyethyleneimine （PEI） as a surfactant. PEI can only hinder the lateral growth of the ZnO nanowires, which is observed by high resolution transmission electron microscopy （HRTEM） analysis. Dye-sensitized solar cells were assembled by the ZnO nanowire arrays with different thicknesses, which can be controlled by the growing time and characterized using photocurrent-voltage measurements. Their photocurrent densities and energy allover conversion efficiencies increased with increasing ZnO nanowire lengths. Short-circuit current density of 4.31 mA.cm-2 and allover energy conversion efficiency of 0.87% were achieved with 12.9-μm-long ZnO nanowire arrays.

Experimental Investigation on Transmission of Stress Waves in Sandwich Samples Made of Foam Concrete

A series of impact tests of sandwich samples were completed using a large-diameter split Hopkinson pressure bar (SHPB)device at different velocities. The interlayer is made of foam concrete, loess or sand. The stress peak value decay, energy decay and waveform dispersion characters are studied by comparing the incident waves with the transmission waves. The tests indicate that the foam concrete has the best capabilities of shock resistance and energy absorption, the loess comes second, and the sand takes third place.

Effects of argon gas flow rate and guide shell on oxygen concentration in Czochralski silicon growth

φ200 mm silicon single crystals were grown in the φ450 mm hot zone of a Czochralski （CZ） furnace. By modifying the pattern and the velocity of the argon flow, the silicon single crystals with different oxygen concentrations were obtained. Through numerical simulation, the velocity of the argon gas flow was plotted for the first time. The experiment resuits were analyzed and the optimum condition of the argon flow with the lowest oxygen concentration was obtained.

Roles of crystal defects in the persistent luminescence of Eu^(2+), Dy^(3+) co-doped strontium aluminate based phosphors

The roles of different point defects in persistent luminescence of SrAl2O4：Eu,Dy phosphors were investigated. The research results showed that Dyer plays an important role in the persistent luminescence of SrA1EO4：Eu, Dy phosphors. It can serve as the electron trap of suitable depth for persistent luminescence. V~ does not serve as the electron trap of suitable depth, but its existence can increase the depth of electron traps. There is interaction between the Dy^3＋（ DySr ） and the Eu^2＋（Eu^x Sr ）, and only if the distance between the Dy^3＋（DySr） and the Eu^2＋ （Eu^x Sr） is close enough, the Dyer can work as an effective electron trap. The point defect of V＂ Sr can be hole trap, but the change of its density in crystal matrix does not arouse the obvious change of persistent luminescence.

Mechanical Behaviors of ZrO_2-Al_2O_3 Ceramic Composites with Y_2O_3 as Stabilizer

The ZrO2-Al2O3 ceramic composites were prepared by appropriate techniques with commercial ZrO2 and Al2O3 powders as raw materials and Y2O3 as stabilizer. The results indicate that with the introduction of Al2O3 into the ZrO2 matrix where the quantity of additive Y2O3 is 3.5% (mole fraction), the growth of ZrO2 grains is efficiently inhibited, which helps the ZrO2 grains exist in a metastable tetragonal manner; thus higher strength and toughness are acquired. When the content of alumina is 20% (mass fraction), the bending strength and fracture toughness of the composites are 676.7 MPa and 10 MPa·m1/2 respectively, the mechanical behaviors are close to those prepared with ZrO2 and Al2O3 powders synthesized through wet chemical approach. The mechanical behaviors of the composites are well improved owing to the dispersion toughening of alumina grains and phase transformation toughening of zirconia grains.

Synthesis of Long Afterglow Phosphors MAl_2O_4∶Eu^(2+), Dy~ (3+)(M=Ca, Sr, Ba) by Microemulsion Method and Their Luminescent Properties

Long afterglow phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） were synthesized by microemulsion method, and their crystal structure and luminescent properties were compared and investigated. XRD patterns of samples indicate that phosphors CaAl2O4：Eu^2＋, Dy^3＋ and SrAl2O4 ： Eu^2＋, Dy^3＋ are with monoelinie crystal structure and phosphor BaAl2O4：Eu^2＋ , Dy^3＋ is with hexagonal crystal structure. The wide range of excitation spectrum of phosphors MAl2O4： Eu^2 ＋ , Dy^3＋ （M = Ca,Sr, Ba） indicates that the luminescent materials can he excited by light from ultraviolet ray to visible light and the maximum emission wavelength of phosphors MAl2O4：Eu^2＋ , Dy^3＋ （M = Ca, Sr, Ba） is found mainly at λem of 440 nm （M = Ca）, 520 nm （M = Sr） and 496 nm （M = Ba） respectively, the corresponding colors of emission light are blue, green and eyna-green respectively. The afterglow decay tendency of phosphors can he summarized as three processes： initial rapid decay, intermediate transitional decay and very long slow decay. Afterglow decay curves coincide with formula I = At^ - n, and the sequence of afterglow intensity and time is Sr 〉 Ca 〉 Ba.

Facile synthesis of La_2Mo_2O_9 nanoparticles via an EDTA complexing approach

A facile EDTA （ethylene diamine tetraacetic acid） complexing technique has been successfully employed to prepare La2Mo2O9 nanoparticles. The as-synthesized products are characterized by X-ray diffraction （XRD）, scanning electron microscopy （SEM）, transmission electron microscopy （TEM）, and Fourier transform infrared spectroscopy （FT-IR）. The results show that a homogeneous transparent gel can be obtained with EDTA as the organic complexing reagent under the pH value of 3.0. Further thermal decomposition of the as-synthesized transparent gel by increasing the temperature up to 600℃ for 3 h results in the formation of La2Mo2O9 nanoparticles with a crystal size of about 30 nm. Moreover, the nanoparticles tend to form micrometer-sized aggregates with a three-dimensional network structure, which shows promising applications in solid oxide fuel cells （SOFC）, catalysts and so on.

Investigation of Loss Weight and Densification of SiC-Al_2O_3-Y_2O_3 Ceramic Composite on Sintering

α-SiC, Al_2O_3 and Y_2O_3 powders were all used as raw materials. The SiC-Al_2O_3-Y_2O_3 ceramic composites were made by pressureless liquid phase sintering technology. The effects of sintering temperature, loss weight and coordination number on sintering densification were studied. The reason for producing loss weight on sintering was analysed. The results show that the primary reason for producing loss weight on sintering in SiC-Al_2O_3-Y_2O_3 ceramic composite was that chemical reactions between SiC and Al_2O_3 are happened during sintering, and given out volatile gases. If sintering temperature is excessively lower, grain size would be finer, and coordination number would be higher, well then material would be on no sintering densification. If sintering temperature is excessively higher, grains would grow up, though small coordination number would benefit to make pore eliminate and shrink, but coarse microstructure would also block gliding and resetting of grains, together affected by expansion stress from volatile gas, the material densification would instead go down. Only under the sintering process of 1850 ℃ for 30 min, material densification is better, and the mechanical property of ceramic composites is also improved.

Preparation of CuInSe_2 thin films by paste coating

Precursor pastes were obtained by milling Cu-In alloys and Se powders. CulnSe2 thin films were successfully prepared by precursor layers, which were coated using these pastes, and were annealed in a H2 atmosphere. The pastes were tested by laser particle diameter analyzer, simultaneous thermogravimetric and differential thermal analysis instruments （TG-DTA）, and X-ray diffractometry （XRD）. Selenized films were characterized by XRD, scanning electron microscopy （SEM）, and energy dispersive spectroscopy （EDS）. The results indicate that chalcopyrite CuInSe2 is formed at 180℃ and the crystallinity of this phase is improved as the temperature rises. All the CuInSe2 thin films, which were annealed at various temperatures, exhibit the preferred orientation along the （112） plane. The compression of precursor layers before selenization step is one of the most essential factors for the preparation of perfect CuInSe2 thin films.

Magnetic and Magnetoresistance Properties in (La_(0.67)Ca_(0.33)MnO_3)_x / (ZrO_2 )_(1-x) Composite System

La_(0.67)Ca_(0.33)MnO_3)_x /(ZrO_2)_(1-x) (x is the volume fraction ratio) percolated composites were fabricated by combining La_(0.67)Ca_(0.33)MnO_3 (LCMO) powders with ZrO_2 particles, where LCMO powders were prepared by sol-gel process. Low field magnetoresistance ( LFMR ) is greatly enhanced at low temperature when the system is close to the metallic percolation threshold of x=0.4. The magnetoresistance ratio of ( LCMO)_(0.4) /( ZrO_2 )_(0.6) in a 10 mT magnetic field at 77 K is 7.8 %, about 7.12 times larger than that of pure LCMO compound. The enhancement of spin-dependent tunneling of electrons at the interfaces between LCMO and ZrO_2 grains is responsible for the enhanced LFMR. With increasing ZrO_2 addition, Curie temperature T_C decreases firstly and then remains constant at about 220 K when (x<60%), showing limited substitution effect of Zr ions on B sites.