Thermal Analysis of Turbine Blades with Thermal Barrier Coatings Using Virtual Wall Thickness Method

Avirtual wall thicknessmethod is developed to simulate the temperature field of turbine bladeswith thermal barrier coatings(TBCs),to simplify the modeling process and improve the calculation efficiency.The results show that the virtualwall thickness method can improve themesh quality by 20%,reduce the number ofmeshes by 76.7%and save the calculation time by 35.5%,compared with the traditional real wall thickness method.The average calculation error of the two methods is between 0.21%and 0.93%.Furthermore,the temperature at the blade leading edge is the highest and the average temperature of the blade pressure surface is higher than that of the suction surface under a certain service condition.The blade surface temperature presents a high temperature at both ends and a low temperature in themiddle height when the temperature of incoming gas is uniformand constant.The thermal insulation effect of TBCs is the worst near the air film hole,and the best at the blade leading edge.According to the calculated temperature field of the substrate-coating system,the highest thermal insulation temperature of the TC layer is 172.01 K,and the thermal insulation proportions of TC,TGO and BC are 93.55%,1.54%and 4.91%,respectively.

A modified single edge V-notched beam method for evaluating surface fracture toughness of thermal barrier coatings

The surface fracture toughness is an important mechanical parameter for studying the failure behavior of air plasma sprayed(APS)thermal barrier coatings(TBCs).As APS TBCs are typical multilayer porous ceramic materials,the direct applications of the traditional single edge notched beam(SENB)method that ignores those typical structural characters may cause errors.To measure the surface fracture toughness more accurately,the effects of multilayer and porous characters on the fracture toughness of APS TBCs should be considered.In this paper,a modified single edge V-notched beam(MSEVNB)method with typical structural characters is developed.According to the finite element analysis(FEA),the geometry factor of the multilayer structure is recalculated.Owing to the narrower V-notches,a more accurate critical fracture stress is obtained.Based on the Griffith energy balance,the reduction of the crack surface caused by micro-defects is corrected.The MSEVNB method can measure the surface fracture toughness more accurately than the SENB method.

Fluorescence and preparation of Sr_2(P_2O_7 ):Ce,Tb phosphate by co-precipitation method

The micron-sized Sr2（P2OT）：Ce,Tb green phosphors were prepared by being annealed at different temperatures with its precursors synthesized by co-pre-cipitates of （NH4）2HPO4 at ambient temperature. The phase structure, grain size, surface morphology, and luminescent properties of phosphors were investigated by X-ray diffraction, scanning electron microscope, trans-mission electron microscope, and fluorescence spectrum. The results show that the product of precursor annealed at 1,100 ℃ is Sr2（P2O7）：Ce,Tb, which belongs to ortho-rhombic phase. The powder is spherical and the size dis-tribution is in micron grade. The sample with the molar ratio of Sr/Tb/Ce of 100.0：0.4：0.6 shows the best fluores-cence effect annealed at 1,100 ℃ for 3 h. The phosphors produce green fluorescence by being excitated with ultra-violet radiation of 254 nm wavelength, and the main emission peak is at 547 nm. The Sr2（P2O7）：Ce,Tb phos-phors synthesized by co-precipitation method of precursors at ambient temperature is a kind of efficient green-emitting phosphors.

Effects of synthesis conditions on the structural and electrochemical properties of layered LiNi_(1/3)Co_(1/3)Mn_(1/3)O_2 cathode material via oxalate co-precipitation method

The uniform layered LiNi1/3Co1/3Mn1/3O2 cathode material for lithium ion batteries was prepared by using （Ni1/3Co1/3Mn1/3）C2O4 as precursor synthesized via oxalate co-precipitation method in air. The effects of calcination temperature and time on the structure and electrochemical properties of the LiNi1/3Co1/3Mn1/3O2 were systemically studied. XRD results revealed that the optimal calcination conditions to prepare the layered LiNi1/3Co1/3Mn1/302 were 950℃ for 15 h. Electrochemical measurement showed that the sample prepared under the such conditions has the highest initial discharge capacity of 160.8 mAh/g and the smallest irreversible capacity loss of 13.5% as well as stable cycling performance at a constant current density of 30 mA/g between 2.5 and 4.3 V versus Li at room temperature.

An electrochemical method for evaluating the resistance to cathodic disbondment of anti-corrosion coatings on buried pipelines

Methods for evaluating the resistance to cathodic disbondment （RCD） of anti-corrosion coatings on buried pipelines were reviewed. It is obvious that these traditional cathodic disbondment tests （CDT） have some disadvantages and the evaluated results are only simple figures and always rely on the subjective experience of the operator. A new electrochemical method for evaluating the RCD of coatings, that is, the potentiostatic evaluation method （PEM）, was developed and studied. During potentiostatic anodic polarization testing, the changes of stable polarization current of specimens before and after cathodic disbonding （CD） were measured, and the degree of cathodic disbondment of the coating was quantitatively evaluated, among which the equivalent cathodic disbonded distance AD was suggested as a parameter for evaluating the RCD. A series of testing parameters of the PEM were determined in these experiments.

A Finite Difference Method for Determining Interdiffusivity of Aluminide Coating Formed on Superalloy

A numerical method has been developed to extract the composition-dependent interdiffusivity from the concentration profiles in the aluminide coating prepared by pack cementation. The procedure is based on the classic finite difference method (FDM). In order to simplify the model, effect of some alloying elements on interdiffusivity can be negligible. Calculated results indicate the interdiffusivity in aluminide coating strongly depends on the composition and give the formulas used to calculate interdiffusivity at 850, 950 and 1050癈. The effect on interdiffusivity is briefly discussed.

Preparation and Characterization of Y_3Sc_2Ga_3O_(12) Nano-Polycrystalline Powders by Co-Precipitation Method

In order to grow high-quality gallium garnet crystals,polycrystalline materials were used as starting materials.YSGG precursor was synthesized by co-precipitation method using aqueous ammonia as a precipitator,and the precursor was then sintered at different temperatures.The results showed that the feasible pH range was 8.3～9.84 in the process of co-precipitation reaction.The YSGG precursor and the powders sintered at different temperatures were characterized by IR,XRD and TEM methods.It was found that the precursor transformed to pure YSGG polycrystalline phase at 800 ℃.YSGG nano-polycrystalline powders sintered at 800～1000 ℃ were well dispersed and the sizes of the YSGG grains were about 40～100 nm.

Synthesis of LaPO_4:Ce,Terbium by Co-Precipitation Method

The synthesis of precursor of green phosphors, LaPO4:Ce, Tb, by means of co-precipitation with cocurrent flow feed was studied. The effects of the reaction temperature, the kind and concentration of the acid in the bottom water, and the charging rate on the physical properties, such as particle size, were investigated. It is found that the particle size of the powder is controllable by adjusting acidity in bottom water and charging rate. The powder with diameter size of 3 to 5 μm was obtained. Its XRD and SEM were analyzed. XRD patterns of the as-prepared green phosphor powders display the typical peaks of CePO4. SEM shows that the morphology of powders is ball-shaped.

Preparation and Magnetic Properties of Mn-Zn Ferrites by the Co-precipitation Method

Mn-Zn ferrites （Mn1-xZnxFe2O4） with different compositions were prepared by the coprecipitation method, and the influences of such synthesis conditions as pH value, composition and volume ratio （R） of the mixed solution and NH4HCO3 solution on their microstructures and magnetic properties were discussed. The samples were characterized by X-ray diffraction （XRD） and magnetization measurement instrument. Lattice parameters and average crystalline size of the synthesized materials were calculated from the corresponding XRD patterns with the related software Jade.5. For samples of different pH values, only one phase was found when pH values were 7.0, 8.0 and 9.0. The sample with pH value of 7.0 exhibited the highest saturation magnetic induction, the lowest coercive force, and crystallized best. For samples of different R values with pH value of 7.0, only one phase was observed in all samples, and the sample with R value of 2.3 exhibited the highest saturation magnetic induction and the lowest coercive force. The composition has mainly afected the magnetic properties, and the saturation magnetic induction increases with the increase of the content of Zn （x）, but decreases when x is beyond 0.6. The trend of coercive force is on the contrary. However, no magnetism is exhibited when the x value is up to 0.8.

Characterization and ultraviolet-visible shielding property of samarium-cerium compounds containing Sm_(2)O_(2)S prepared by co-precipitation method

Since ultraviolet(UV)light,as well as blue light,which is part of visible light,is harmful to skin,samarium-cerium compounds containing Sm_(2)O_(2)S were synthesized by co-precipitation method.This kind of compounds blocks not only UV light,but also blue light.The minimum values of average transmittance(360-450 nm)and band gap of samarium-cerium compounds were 8.90%and 2.76 eV,respectively,which were less than 13.96%and 3.01 eV of CeO_(2).Elemental analysis(EA),X-ray diffraction(XRD),Fourier transformation infrared(FTIR),and Raman spectra determined that the samples contained Ce_(4)O_(7),Sm_(2)O_(2)S,Sm_(2)O_(3),and Sm_(2)O_(2)SO_(4).The microstructure of samples was analyzed by scanning and transmission electron microscopies(SEM and TEM).X-ray photoelectron spectrum(XPS)showed that cerium had Ce^(3+)and Ce^(4+) valence states,and oxygen was divided into lattice oxygen and oxygen vacancy,which was the direct cause of the decrease of average transmittance and band gap.

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.

Yttrium-Doped SnO_2 Prepared by Co-Precipitation Method for Lithium-Ion Battery Anodes

SnO2 doped with Y were prepared by co-precipitation method and tested in lithium-ion cells. The structure and morphology of the materials were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). XRD patterns presented that the all the as-prepared materials had tetragonal rutile structure but a second phase (Y2O3) was observed when Y content reached 4%. TEM micrograph indicated that Y doped SnO2 had a small particle size ranging from 20 to 25 nm. The electrochemical properties for an anode active material in lithium-ion batteries were investigated at room temperature, including the observed capacity involved in the first-discharge and the reversible capacity values during subsequent charge-discharge cycles. The as-prepared Y-doped SnO2 exhibited promising electrochemical properties as anodes for lithium-ion batteries.

THE INTERIOR TRANSMISSION EIGENVALUE PROBLEM FOR AN ANISOTROPIC MEDIUM BY A PARTIALLY COATED BOUNDARY

We consider the interior transmission eigenvalue problem corresponding to the scattering for an anisotropic medium of the scalar Helmholtz equation in the case where the boundary?Ωis split into two disjoint parts and possesses different transmission conditions.Using the variational method,we obtain the well posedness of the interior transmission problem,which plays an important role in the proof of the discreteness of eigenvalues.Then we achieve the existence of an infinite discrete set of transmission eigenvalues provided that n≡1,where a fourth order differential operator is applied.In the case of n■1,we show the discreteness of the transmission eigenvalues under restrictive assumptions by the analytic Fredholm theory and the T-coercive method.

Preparation of Se-based solar cell using spin-coating method in ambient condition

A new hybrid organic-inorganic structure of FTO/TiO2/Se/HTL/Au based selenium solar cell has been fabricated through a low-cost spin-coating process in air. In this process, selenium is completely dissolved in hydrazine, to fk）rm a homogeneous precursor solution. After spin-coating the precursor solution on the TiO2 substrates, following by sintering at 200 ℃ for 5rain, a uniform selenium film with crystalline grains is formed. The selenium based solar cell exhibits an efficiency of 1.23% under AM1.5 illumination （100 mW.cm-2）, short-circuit current density of 8 mA.cm 2, open-circuit voltage of 0.55 V, and fill factor of 0.37. Moreover, the device shows a stable ability with almost the same performance alter 60 days.

Synthesis of M1-3xAl2O4:Eu2+x/Dy3+ 2x(M^2+= Sr^2+, Ca^2+ and Ba^2+) phosphors with long-lasting phosphorescence properties via co-precipitation method

The long afterglow fluorescent material of M1-3xAl2O4:Eu2+ x/Dy3+2x(M2+= Sr2+, Ca2+ and Ba2+) phosphors are successfully synthesized by calcining precursor obtained via co-precipitation method at 1300oC for 4 h with reducing atmosphere (20% H2 and 80% N2). The phase evolution, morphology and afterglow fluorescent properties are systematically studied by the various instruments of XRD, FE-SEM, PLE/PL spectroscopy and fluorescence decay analysis. The PL spectra shows that the Sr1-3xAl2O4:Eu2+x/Dy3+ 2x phosphors display vivid green emission at s519 nm (4f65d1!4f7 transition of Eu2+) with monitoring of the maximum excitation wavelength at s334 nm (8S7=2!6IJ transition of Eu2+), among which the optimal concentration of Eu2+ and Dy3+ is 15 at.% and 30 at.%, respectively. The color coordinates and temperature of Sr1-3xAl2O4:Eu2+ x/Dy3+ 2x phosphors are approximately at (s0.27, s0.57) and s6700 K, respectively. On the above basis, the M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors is obtained by the same method. The PL spectra of these phosphors shows the strongest blue emission at s440 nm and cyan emission at s499 nm under s334 nm wavelength excitation, respectively, which are blue shifted comparing to Sr1??3xAl2O4:Eu2+ x/Dy3+ 2x phosphors. The color coordinates and temperatures of M0:55Al2O4:Eu2+ 0:15/Dy3+ 0:3 (M2+= Ca2+ and Ba2+) phosphors are approximately at (s0.18, s0.09), s2000 K and (s0.18, s0.42), s11600 K, respectively. In this work, long afterglow materials of green, blue and cyan aluminates phosphors with excellent properties have been prepared, in order to obtain wide application in the field of night automatic lighting and display.

Green Emitting Phosphor M_3(PO_4)_2∶Ce, Tb (M=Mg, Ca, Sr, Ba) Prepared by Co-Precipitation Method

The M3-3x(PO4)2∶2xCe, xTb(M=Mg, Ca, Sr, Ba) phosphors were prepared by coprecipitation in this paper. Their phase structures, morphologies and luminescent properties were investigated by X-ray diffractometer, field emission scanning electron microscopy and fluorospectrophotometer. The results indicate that the Ce3+ and Tb3+ enteres the host lattice because the XRD patterns of alkaline earth phosphate show no impurity phase, the SEM shows the spherical particles with an average size about 1 μm. The emission and excitation spectra are similar to rare earth phosphate. Concentration quenching of the Sr3(PO4)2∶Ce, Tb emission intensity was not observed even when the Tb3+ increases to 0.05, while the maximum emission intensity appears when x=0.04 in M3-3x(PO4)2∶2xCe, xTb(M=Ca, Ba) emission spectrum.

Constitutive parameters identification of thermal barrier coatings using the virtual fields method

Thermal barrier coatings (TBCs) are widely applied in thermal components to protect metallic components. Owing to the complex layered structure of TBCs and difficult preparation of coating, the mechanical characterization of TBCs should be of primary importance. With regard to TBCs, this study deals with the constitutive parameters identification of bi-material. Considering the complex construction and boundary of bi material, the virtual fields method (VFM) was employed in this study. A methodology based on the optimized virtual fields method combined with moire interferometry was proposed for the constitutive parameters identification of bi-material. The feasibility of this method is verified using simulated deformation fields of a two-layer material subjected to three point ben ding loading. As an application, the deformation fields of the TBC specimens were measured by moire interferometry. Then, lhe mechanical parameters of the coating were identified by the proposed method. The identification results indicate that Young's modulus of the TBC top coating is 89.91 GPa, and its Poisson's ratio is 0.23.

Structural and Optical Properties of Mg<SUB>1-x</SUB>Zn<SUB>x</SUB>Fe<SUB>2</SUB>O<SUB>4</SUB>Nano-Ferrites Synthesized Using Co-Precipitation Method

In this work, the Mg1-x Znx Fe2 O4 Nanoferrites (where x = 0.0, 0.2, 0.4, 0.6 and 0.8) was synthesized using co-precipitation method. The investigation of structural and optical properties was carried out for the synthesized samples using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and Ultraviolet visible spectrophotometer (UV-Vis). XRD revealed that the structure of these nanoparticles is spinel with space group Fd3m and crystallite size lies in the range 21.0 - 42.8 nm. Lattice parameter was found to increases with Zn concentration and this may be due to the larger ionic radius of the Zn2+?ion. FTIR spectroscopy confirmed the formation of spinel ferrite and showed the characteristics absorption bands around 612, 1146, 1404, 1649 and 3245 cm-1. The energy band gap was calculated for samples with different ratio and was found to be 4.77, 4.82, 4.86, 4.87 and 4.95 eV. The substitution was resulted in slight increased in the lattice constant and that sequentially may lead to the slightly decreased in the energy gap.

An efficient nano-adsorbent via surfactants/dual surfactants assisted ultrasonic co-precipitation method for sono-removal of monoazo and diazo anionic dyes

To preserve the environment for civilization,we should remove the pollutants like toxic dyes by friendly and cost efficacious method.In this study,the effect of surfactants or mixed surfactants on physicochemical,optical and adsorption properties of ternary mixed oxide CeO_(2)-ZrO_(2)-Al_(2) O_3(CZA) are investigated.The ternary mixed oxide CZA was prepared by surfactants or mixed surfactants assisted ultrasonic coprecipitation method.The physicochemical and optical properties are estimated by different techniques like XRD,TEM,EDX,FTIR,S_(BET) and UV-Vis/DR.The CZA_T and CZA_C have hybrid shapes and high surface area.The adsorption properties of ternary mixed oxides adsorbents were characterized by sono-removing anionic dyes such as Congo red(CR) and Remazol red RB-133(RR).The different factors like contact time,different dye concentrations and temperatures also studied.The kinetics and isotherms applications showed that,the adsorption process was followed pseudo second order kinetics and the Freundlich isotherm model.Also,the adsorption is spontaneous and endothermic process through the thermodynamic study.Finally,the results showed that the ternary mixed oxide nano-adsorbent(CeO_(2)-ZrO_(2)-Al_(2) O_3) is promising and functional materials for anionic dye sweep from wastewater.

Preparation Nano-Diamond Film by Sol-Gelled Coating Method for Field Emission Display

The mixture of Nano-graphite and organic vehicles doped to Nano-diamond paste. The suitable paste proportion was found. Nano-diamond film (NDF) was prepared by sol-gel coating method on ITO glass at 3000/min. The field emission characteristics of luminance-current, luminance-voltage and luminance-power of Nano-diamond film were analyzed and tested. Comparing these tested curves, the luminance was well proportional to current was got. Theoretic, the inner resistance of NDF field emission display (FED) consumes electric energy and real voltage change between the cathode and the anode of NDF-FED was very small after electrons emit. So the characteristic of NDF-FED was preferable to describe by luminance-current linear relationship, which was advantageous to device tested and designed.