Transient liquid phase sintering of high-purity mullite for high-temperature structural ceramics

High-purity mullite ceramics, promising engineering ceramics for high-temperature applications, were fabricated using transient liquid phase sintering to improve their high-temperature mechanical properties. Small amounts of ultrafine alumina or silica powders were uniformly mixed with the mullite precursor depending on the silica-alumina ratio of the resulting ceramics to allow for the formation of a transient liquid phase during sintering, thus, enhancing densification at the early stage of sintering and mullite formation by the reaction between additional alumina and the residual glassy phase (mullitization) at the final stage of sintering. The addition of alumina powder to the silica-rich mullite precursor resulted in a reaction between the glassy silica and alumina phases during sintering, thereby forming a mullite phase without inhibiting densification. The addition of fine silica powder to the mullite single-phase precursor led to densification with an abnormal grain growth of mullite, whereas some of the added silica remained as a glassy phase after sintering. The resulting mullite ceramics prepared using different powder compositions showed different sintering behaviors, depending on the amount of alumina added. Upon selecting an optimum process and the amount of alumina to be added, the pure mullite ceramics obtained via transient liquid phase sintering exhibited high density (approximately 99%) and excellent high-temperature flexural strength (approximately 320 MPa) at 1500 °C in air. These results clearly demonstrate that pure mullite ceramics fabricated via transient liquid phase sintering with compositions close to those of stoichiometric mullite could be a promising process for the fabrication of high-temperature structural ceramics used in an ambient atmosphere. The transient liquid phase sintering process proposed in this study could be a powerful processing tool that allows for the preparation of superior high-temperature structural ceramics used in the ambient processing atmosphere.     

On A Maximum Likelihood Method for Clustering

Behaviormetrika - In this paper, we propose a new clustering method based on the concept of maximum likelihood (ML) estimation. In general, the problem of local minima arises when we try to use the...     

Hierarchical Clustering Method Using Probabilistic Similarity Measure

In this paper, we propose a new hierarchical clustering method, which is useful to find appropriate clusters of attributes from given dichotomous or frequency data. Important features of our method are 1) the similarity between two attributes is defined as a probability of their pattern vectors being observed under the hypothesis of independence, 2) for each generated cluster, one pattern vector is defined in a natural manner, and 3) it can be used freely without distinguishing the frequency data from the dichotomous one.

A typical frequency data is analyzed to illustrate how our method works effectively. The discussion on similarities among objects is also included to propose a new similarity measure based on our clustering method.

     

Relationship Between Local Atomic Arrangements and Properties of High-T c Superconductive Copper Oxides

Here various approaches to understanding the complex relationship among the local atomic arrangements, the distribution of charge/holes and the superconductivity characteristics are discussed for a variety of multi-layered copper-oxide superconductors. Regarding the structural parameters, i.e. bond lengths and angles, no single parameter is revealed to control the superconductivity characteristics alone. As a matter of fact, superconductivity properties are found to be correlated with the whole delicately balanced fine-structure that is described by a set of multiple parameters: it is shown that T _c and H_irr are enhanced in somewhat opposite ways. Expressing the delicately balanced fine-structure through the charge/hole distribution, it is concluded that the more homogeneously distributed the charge carriers are the more enhanced is the H_irr characteristics, while the opposite is likely to apply to the T _c value.     

Preparation and characterization of porous and electrically conducting carbon-clay composites

Porous and electrically conducting carbon-clay composites were prepared by firing mixtures of carbon powder (0 to 20 wt%) and clay minerals. They showed porosity of 50 to 65% and had high mechanical strength (compressive strength = 130 to 400 kg cm^–2) as well as high resistance against thermal oxidation in air. Their electrical conductivity, , increased with increasing carbon content levelling off at about 20 wt% of carbon content to give a value of about 2 S cm^–1. Formation of carbon chains is considered to be responsible for the electrical conduction in the composite, and a model to correlate the electrical conductivity with the carbon content has been proposed by modifying a model previously proposed by Scarisbrick.     

Preparation of fine particles of carnegieite by a mist decomposition method

A mist of a hydrosol consisting of silica, alumina/NaAlO₂ and sodium hydroxide was produced by a supersonic atomization, and treated successively in three furnaces of different temperatures. The temperatures of the furnaces were adjusted for the evaporation of water, the dehydration and the crystallization of the mixed oxide, respectively. The spherical particles ( 0.5m) of carnegieite were found to be formed in a narrow composition range of the raw materials at temperatures of 650 to 900° C. The factors affecting the properties of the particles were investigated.     

Gas permeation property of polyaniline films

We examined the influence of polyaniline (PAn)'s unit sequence and doping with low molecular weight dopants or polymer dopants on permeation property. It was found that CO₂ permeability was increased by the formation of a quinonediimine unit in PAn with the oxidation. CO₂ sorption amount of PAn was decreased by oxidation. The increase of CO₂ permeability with oxidation, therefore, resulted from the increase of diffusivity, which was attributable to morphological variation by the increase of a quinonediimine unit. The permselectivity of PAn films was found to be remarkably improved by doping. In particular, the selectivity value of the PAn film doped with polyvinyl sulphonic acid as a polymer dopant went up to over 2,000. This remarkable increase of selectivity was found to result in the increase of selectivity, depending on diffusivity. It was also found that the permselectivity of the PAn film doped by polymer dopants was surpassed, as compared with that doped by low molecular dopants. © 1995 John Wiley & Sons, Inc.     

Effects of support and additive on oxidation state and activity of Pt catalyst in propane combustion

The effects of support and additive on the oxidation state and catalytic activity of Pt catalyst in the low temperature propane combustion were systematically investigated on Pt/MgO, Pt/Al₂O₃ and Pt/SiO₂–Al₂O₃. The catalytic activity varied much with both support materials and additives. The catalyst on the more acidic support showed higher activity, and the catalytic activity on every support materials increased as the electronegativity of additives increased, while some additives decreased the activity. The oxidation state of platinum, estimated by white line intensity of Pt L_III-edge XANES spectrum, also varied with the support and additives, and additives with higher electronegativity greatly prevented the platinum from its oxidation under oxidising atmosphere. Among almost all the catalysts with various supports and various additives, a clear relationship was observed between the oxidation state of platinum and the catalytic activity; the more metallic platinum showed higher activity. Thus, it was concluded that the total electrophilic/electrophobic property derived from those of the support and additive controls the oxidation state of platinum, which intensively affects the catalytic activity; i.e. higher electrophilic property provides less oxidised platinum, resulting in high catalytic activity. The mechanism of this effect was also discussed on the basis of thermochemical data, and it was proposed that the electrophobic materials promote the noble metal oxidation since the noble metal oxo-anion such as PtO^δ− is more stabilised with electrophobic cation.     

Microstructure of TiO2 and ZnO Films Fabricated by the Sol-Gel Method

Titanium dioxide and zinc oxide films were fabricated by spin-on and dip-coating methods. Both types of films exhibited columnar grains when the single coating was thin, ∼10 nm. The columnar TiO₂ films were dense, as confirmed by their density values calculated from the refractive index and TEM results. The addition of Al cations into the ZnO suppressed grain growth, because Zn had a lower diffusivity in the doped films. The doped ZnO films had nearly the same electrical resistivity as that of the undoped films.     

Prolonged degradation of end-capped polyelectrolyte multilayer films

Cationic chitosan (CT) and anionic dextran sulfate (Dex) were layer-by-layer (LbL) assembled from aqueous solutions containing 1 M NaCl on a quartz crystal microbalance (QCM) substrate, and the original films ((CT-Dex)₃-CT)) were end-capped with LbL assembly from CT solutions containing 1 M NaCl and Dex solutions without NaCl. The enzymatic degradation of films by chitosanase was quantitatively analyzed by QCM in terms of numbers of end-capping steps. The degradation of films end-capped with (Dex-CT)₃ was considerably prolonged when compared to those end-capped with other end-capping steps. A mechanism for the prolonged degradation was proposed by quantitative QCM data and zeta potential results.