Promotional effect of H2O on the activity of In2O3‐doped Ga2O3–Al2O3 for the selective reduction of nitrogen monoxide

Effect of metal oxide additives on the catalytic performance of Ga₂O₃–Al₂O₃ prepared by the sol–gel method for the selective reduction of NO with propene in the presence of oxygen was studied. Of several metal oxide additives, the addition of In₂O₃ enhanced drastically the activity of Ga₂O₃–Al₂O₃ for NO reduction by propene in the presence of H₂O. In addition, the activity of In₂O₃‐doped Ga₂O₃–Al₂O₃ catalyst was extremely intensified by the presence of H₂O below 350°C. The promotional effect of H₂O was interpreted by the suppression of undesirable propene oxidation and the removal of carbonaceous materials deposited on the catalyst surface. We also found that close interaction of In₂O₃ and Ga₂O₃ is necessary for the enhancement of activity by H₂O. A lot of hydrocarbons except methane and oxygenated compounds served as good reducing agents, among which propene and 2‐propanol were the most efficient ones. In₂O₃‐doped Ga₂O₃–Al₂O₃ catalyst was capable of reducing NO into N₂ quite efficiently in the presence of H₂O at a very high space velocity. This revised version was published online in July 2006 with corrections to the Cover Date.     

Effect of Tungsten Oxide on the Crystallization Properties of Glasses of the B2O3–La2O3–Nb2O5 System

Glass Physics and Chemistry - The effect of tungsten oxide on the crystallization properties of glasses of the 37.5B2O3 22.5La2O3 (40 – x)Nb2O5 xWO3 (where x = 10, 15, 20, 30, 40 mol %)...     

Possibility of Initiation of Combustion of CH4–O2 (Air) Mixtures with Laser‐Induced Excitation of O2 Molecules

The possibility of initiation of combustion of CH₄–O₂ mixtures with excitation of O₂ molecules to the states a¹_g and b¹⁺ _g by laser radiation with wavelengths of 1.268 m and 762 nm is considered. It is shown that excitation of O₂ molecules significantly decreases the induction period and ignition temperature because of accelerated formation of active atoms and radicals and intensification of the chain mechanism of the process. Even if the specific energy of laser radiation absorbed by the gas is low ( 0.1 eV per molecule), the ignition temperature of the CH₄–O₂ mixture with a ratio of 1:2 can be reduced from 1000 to 300 K.     

Effect of P2O5 on evolution of microstructure of MgO–Al2O3–SiO2 glass ceramics

Abstract

MgO–Al₂O₃–SiO₂ (MAS) cordierite based glass ceramics were prepared by volume crystallisation. X-ray diffraction, Scanning electron microscopy and Energy diffraction scanning were used to investigate crystallisation behaviour and the influence of P₂O₅ on microstructure MAS based glass ceramics. The results showed that P⁵⁺ could promote the phase separation of MAS glass and that the glass was divided into two areas, such as Mg₄Al₂Ti₉O₂₅ and the containing P⁵⁺ area at <900°C. Mg₄Al₂Ti₉O₂₅ and Mg₃(PO₄)₂ in the area were both advantageous to the precipitation of μ cordierite, which further transformed to α cordierite due to P⁵⁺ in the residual glassy phase. However, P⁵⁺ inhibited the presence of cordierite when the heat treatment temperature was >900°C.     

Sintering behavior of Cr2O3–Al2O3 ceramics

We investigated the sintering behavior of Cr₂O₃–Al₂O₃ ceramic materials. In our observation of the isothermal shrinkage behavior of Cr₂O₃–Al₂O₃ ceramic, the activation energy of sintering reaction was measured to be 102 kJ/mol, that is, the near value of the activation energy of diffusion of Al ions in Al₂O₃ single crystal. Therefore the diffusion of cations is believed to control the sintering behavior of this material. With the addition of TiO₂, (the compound chosen to accelerate the diffusion of cations) to Cr₂O₃–Al₂O₃, the sintering behavior was accelerated.     

Load-dependence of Knoop hardness of Al2O3–TiC composites

Nine samples of Al₂O₃–30 wt.% TiC composites were prepared by hot-pressing the Al₂O₃ powder mixed with TiC particles. The average sizes of the TiC particles used for preparing the nine samples were different with each other. Knoop hardness measurements were conducted on these nine samples, respectively, in the indentation load range from 1.47 to 35.77 N. For each sample, the measured Knoop hardness decreases with the increasing indentation load. The classical Meyer's power law and an empirical equation proposed originally by Bückle were verified to be sufficiently suitable for describing the observed load-dependence of the measured hardness. Analysis based on Meyer's law can not provide any useful information about the cause of the observed ISE while true hardness values, which are load-independent, can be deduced from the Bückle's equation. It was found that the deduced true hardness increases with the average size of TiC particles existing in the sample.     

Catalytic behavior of V2O5 in rechargeable Li–O2 batteries

The possibility of using vanadium pentoxide (V₂O₅) as a catalyst in rechargeable lithium–oxygen (Li–O₂) batteries was studied. A V₂O₅-carbon composite was cast onto Ni foam to form a cathode. Electrochemical cells designed based on the flat cell manufactured by Hohsen Corporation were fabricated. The initial discharge capacity was 715 mA?h?g^?1, and the maximum discharge capacity reached 2,260 mA?h?g^?1 during the twelfth cycle. The cell had high capacity retention during cycling (1.24?% during cycles 2–8). V₂O₅ acted as a catalyst as well as an active material, improving the specific capacity and capacity retention of the non-aqueous Li–O₂ cell more effectively than do other materials.     

On the Possibility of Forming Complexes with the Participation of O2– Ions in Melts and Glasses of the Na2O–SiO2–Cu2O System

The structural role of copper ions in melts (glasses) of the Na₂O–SiO₂–Cu₂O–CuO system is analyzed in the framework of the acid–base concept with due regard for the geometric (the radius ratio for Cu²⁽¹⁾⁺ and O^2– ions) and energy (the mean enthalpies of the Cu²⁽¹⁾⁺–O bonds) factors. It is demonstrated that copper ions in the structure fulfill the function of modifier cations. In these melts, the Cu¹⁺–Cu²⁺ redox equilibrium can be described without regard for the formation of [Cu²⁽¹⁾⁺O_4/2]^2(3)– ionic complexes (which could be incorporated into the structure of silicon–oxygen anions) and [Cu²⁺O _b/k ]^{2 – b/k} polyhedra providing the interaction between Cu²⁺ ions and anions. The influence of the formation of these polyhedra on the redox equilibrium is considered within the formalism of chemical thermodynamics. The composition dependence of the oxygen ion exponent pO is measured by an electromotive force (emf) technique. The ratio between the numbers of copper atoms with different valences is determined by chemical analysis. The experimental data obtained are in agreement with the theoretical inferences.     

The Effect of Al2O3（Mul.） on Phase Compositions of O′—Sialon Cermics

O′-Sialon Cermics are formed by reaction sintering of silicon nitride and silica with Al2O3(Y2O3) additive,The phase compositions of O′-Sialon Cermics are highly affected by addition of Al2O3( mul.) and are measured by X-ray diffraction techinque.The range of additions which could impaire the stucture of O′-Sialon Cermics is given in this article.     

Influence of annealing treatment on magnetic properties of Fe2O3/SiO2 and formation of ε-Fe2O3 phase

Magnetic properties of Fe₂O₃/SiO₂ samples were studied after being produced by sol-gel synthesis and formation of ε-Fe₂O₃ polymorph. Samples were thermally treated, using different annealing temperatures and annealing times. The size and morphological characteristics of the iron oxide nanoparticles were examined using a TEM microscope. We used the “ellipticity of shapes”, which is a measure of how much the shape of a nanoparticle differs from a perfect ellipse, in order to quantitatively describe morphological properties of nanoparticles. Coercivity measurements were used to identify and monitor the formation of the epsilon-iron oxide phase during the thermal treatments (annealing). Coercivity values were in the range from 1.2 to 15.4 kOe, which is in accordance with previous experience regarding the existence of ε-Fe₂O₃. We have determined the optimal formation conditions for the ε-Fe₂O₃ polymorph (t=1050 °C for 7 h, H_C=15.4 kOe), as well as the narrow temperature interval (1050–1060 °C) in which the polymorph abruptly vanished (H_C=2300 Oe), on the basis of results of the magnetic properties. The threshold temperature for the ε-Fe₂O₃ phase transformation was measured as 1060 °C. We found that different annealing temperatures and annealing times significantly affected magnetic properties of the examined samples.     

The characteristics of ZnO–Bi2O3-based varistor ceramics doped with Y2O3 and varying amounts of Sb2O3

ZnO–Bi₂O₃-based varistor samples doped with 0.45 mol% of Y₂O₃ and varying amounts of Sb₂O₃ in the range from 1.8 to 0.0 mol% were fired at 1230 °C. Only in the samples co-doped with Sb₂O₃ did doping with Y₂O₃ resulted in the formation of a fine-grained Bi–Zn–Sb–Y–O phase (the Y₂O₃-containing phase) at the grain boundaries, which very effectively hinders the grain growth. Despite of a decrease in the amount of added Sb₂O₃ from 1.8 to 0.45 mol% and a significant decrease in the amount of spinel phase the samples had a similar ZnO grain size and a threshold voltage of 200 V/mm. The results confirmed that doping with Y₂O₃ is a very promising route for the production of fine-grained high-voltage ZnO–Bi₂O₃-based varistor ceramics, and determining the proper amounts of added Sb₂O₃ and Y₂O₃ is of great importance.     

Effect of Additives on Sintering of Cr2O3 in Reductive Atmosphere

The influence of additives TiO2,Y2O3 and composite rare earth on sintering of Cr2O3 in reductive atmosphere was studied.Results show that TiO2 can effectively increase the sinteed density at low temperature,As the increase of sintering temperature,such kind of effect becomes more and more unobvious and finaly disappear at 1550℃.Moreover,Y2O3 and composite rare earth have negative effect on sintering.     

Rh–Sr/Al2O3 Catalyst for N2O Decomposition in the Presence of O2

The improving effect of Sr in the catalytic activity of Rh for N₂O decomposition has been studied under 1,000 ppm N₂O/He and 1,000 ppm N₂O/5% O₂/He (GHSV = 10,000 h^?1). Different techniques have been used for catalysts characterization: TEM, SEM-EDX, XRD, N₂ adsorption at ?196 °C and in situ XPS. Sr favours the Rh dispersion and reduction under reaction conditions, and allows the low temperature removal of N₂O in the presence of O₂ (100% decomposition at 350 °C).     

Influence of Raw Material on the Properties of MgO—Al2O3—Cr2O3 Ramming Mixes

MgO-Al2O3-Cr2O3 ramming mixes made of different raw materials have different mineral structure and different physical properties though with the identical particle size distribution, the same amount of binder and chemical composition. The residual carbon content of the fused magnesia-chrome material made in reducing atmosphere is very high, if this materials is used in the MgO-Al2O3-Cr2O3 ramming mix, it would cause spalling of the furnace lining during drying-out.     

Sintering of α-Al2O3-seeded nanocrystalline γ-Al2O3 powders

This paper demonstrates that seeding nanocrystalline transition alumina powders is a viable option for producing high quality, alumina-based ceramics. By using α-Al₂O₃ concentrations of ⩾1.25 wt.% α-Al₂O₃ seed particles (equivalent to 5 ×10¹⁴ seeds/cm³ of γ-Al₂O₃) the sintering temperature is reduced from 1600°C for unseeded γ-Al₂O₃ to 1300–1400°C in dry pressed powders. The scale of the sintered microstructure is related to N_v^−1/3 and thus a 100-nm grain size is obtained. It is apparent that seeding is necessary for producing dense, alumina-based ceramics from nanocrystalline transition alumina powders.     

Effects of Cr2O3 on Properties of Alumina—spinel Castable

The effects Cr2O3 on properties of alumina-spinel castable has been discussed in this paper,The results show that modulus of rupture(MOR) and cold crushing strength(CCS) of the alumina-spinel castable can be improved when Cr2O is added to this material.At higher temperature,Cr2O3 moves into the melt and raises its viscosity,forming high creep resistance bonding phase,so the thermal shock resistance and slag corrosion resistance are improved.     

Synthesis of O＇-SiAION-BN Composite by Reaction Sintering

By using micron α-SisN4, SiO2, Al2O3 and h-BN as starting materials, O＇ -SiAION-BN （ Si2-z AlzO1 ＋z N2-z, z= 0. 3） composite was synthesized by reaction sintering. According to theoretical proportion ratio： n（ SiO2）/n（ α-Si3N4） = 1, the effects of two sintering aid composites, Y2O3 ＋ B2O3 and Y2O3 ＋ TiO2 at 1700℃ for 2h, were studied. The results indicate that Y2 O3 ＋ TiO2 as sintering aid can accelerate reaction sintering of O＇ -SiAION-BN more effectively than Y2O3 ＋ B2O3, and the relative density of the composites declined with the increase of BN addition （10%, 20% and 30% respectively）; XRD analysis found that excessive β-Si3N4 existed in the O＇ -SiAION-BN composite. Therefore, in order to get more pure O＇ -SiAION and BN phases in the composites ore SiO2 is needed. When Y2O3 ＋ TiO2 was used as sintering aid and addition of BN was 10%, the result of cross experiment on condition of A- n（SiO2）/n（α-Si3N4） was 1.05, 1.1 and 1.2; B-- addition of sintering aid was 2%, 4% and 6% ; C-- firing temperature was 1600℃, 1650℃ and 1700℃ ; D--soaking time was 1h, 2h and 3h, shows that the sintering properties were influenced by factors of firing temperature, soaking time, addition of sintering aid and n（ SiO2 ）/n（α-SisN4） in order of importance. In addition, the technical parameter A s B 3 C s D3 can achieve the highest relative density. Besides, using Pattern Recognition method, the optimized parameter range to form pure O＇ -SiAION and BN without β-Si3N4 remained was determined as Y 〉 1024X^2 - 230. 400X ＋ 11.088 （ X = 0. 9999A -0. 0006C - 0. 0163D, Y = 0. 0163A ＋ 0. 009B -0. 0014C ＋0. 9999D）.     

Synthesis of O’-SiAlON-BN Composite by Reaction Sintering

1 IntroductionO’-SiAlON is a solid solution made from Si2N2Oand Al2O3, and its crystal structure is similar toSi2N2O. Chemical formula of O’-SiAlON can be ex-pressed as Si2 -ZAlZO1 ZN2 -Z, which solid solubilitychanges depending on temperature, e.g. z …     

Melt extraction processing of structural Y2O3–Al2O3 fibers

Compounds in the system Y₂O₃-Al₂O₃ are promising materials for optical, electronic and structural applications. In this study, a melt extraction process with a new approach to making ceramic fibers was used to produce amorphous fibers in the Y₂O₃–Al₂O₃ system within the 20–30-micron size range. Smooth and uniform cross section fibers with relatively high tensile strength were obtained depending on the wheel velocity. X-ray diffraction of as-extracted fibers revealed the non-crystalline nature of the yttria-alumina compositions. The crystallization and glass transition temperatures of non-crystalline fibers were determined using differential thermal analysis (DTA). Crystalline phases were identified by X-ray diffraction in the fibers after heat treatment.     

Effect of adding Y2O3 on structural and mechanical properties of Al2O3–ZrO2 ceramics

The effects of adding 1–8 wt% Y₂O₃ on phase formation and fracture toughness of Al₂O₃–xZrO₂–Y₂O₃(AZY) ceramics were studied. Phase formations of the samples were characterized by the X-ray diffraction (XRD) technique. It was found that the major phase was rhombohedral-Al₂O₃, while the minor phase consisted of the monoclinic-ZrO₂, tetragonal-ZrO₂ and monoclinic-Y₂O₃. It was found that Y₂O₃ contents did not clearly influence grain shape of AZY ceramics. The results obtained from the microhardness test could be used to evaluate the fracture toughness. It was found that the smaller grains had high fracture toughness. The maximum fracture toughness of 4.827 MPa m^1/2 was obtained from 4 wt% Y₂O₃. Refinement of lattice parameters using Rietveld analysis revealed the quantitative phases of AZY ceramics. This shows that under adding Y₂O₃ conditions the proportion of tetragonal-ZrO₂ phase plays an important role for the mechanical properties of AZY ceramics.