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Ceramic mixture

Preceramic polymer precursors (45,68) can be used to make ceramic composites from polymer ceramic mixtures that transform to the desired material when heated. Preceramic polymers have been used to produce oxide ceramics and are of considerable interest in nonoxide ceramic powder processing. Low ceramic yields and incomplete burnout currently limit the use of preceramic polymers in ceramics processing. [Pg.309]

Iron(II) oxide occurs in the mineral, wustite. It is used in the manufacture of heat-ahsorhing green glasses. It also is used in ceramic mixtures and enamels and as a catalyst. [Pg.431]

All of the steps preceding "Shape", step 10, Figure 1, are intended to make magnesium oxide and zirconia particles smaller and to mix them evenly. Figure 2 contains an illustration of what a classical "well mixed" pre-ceramic mixture might look like. Figures 3 and 4 are represenations of the crystal structures of magnesium oxide and zirconium (IV) oxide. [Pg.87]

A composite biomaterial formed by Pd metal, carbon-ceramic mixture and oxidoreductase enz3ones constitutes a new t3rpe of renewable smface biosensor with a controllable size reaction layer [198]. The carbon provides the electrical conductivity, the enzymes are used for biocatalyst process, metallic palladimn is used for electrocatalysis of biochemical reaction product and the porous silica provides a rigid skeleton. The hydrophobicity of this composite material allows only a limited section of the electrode to be wetted by the aqueous analyte, thus providing a controlled thickness reactive layer. Another biocomposite material containing enzyme-modifled boron-doped diamond was used in the development of biosensors for the determination of phenol derivatives [199], alcohol [200] and glucose [201]. [Pg.518]

Rheology and Mixing of Ceramic Mixtures Used in Plastic Molding... [Pg.239]

UN is a ceramic mixture of uranium and nitrogen. It has a melting point in the range of 3100 K, well above the likely peak fuel temperatures (1300 K) [Tagawa, 1974]. The maximum theoretical density is 14.32 g/cc [Johnson, 1976]. The core will use a 1-to-1 atomic ratio mixture. A phase diagram for UN can be found in Figure 3-1. [Pg.13]

A noteworthy statement is that the inception of a reaction coincides almost always with the temperature at which one or the other of the reactants undergoes recrystallization. This may occur by partial fusion on the surface (sintering) that can take place (as proved by Hedvall) below actual fusion temperature accompanied by diffiisicm processes, sintering, and recrystallization with consequent shrinkage. These observations appear to derive from ceramic mixtures but may be applicable to pyrochemical combinations. [Pg.290]

About 80 % of the hot-melt adhesive was added into the mixing chamber and allowed to melt. After that, the powder was slowly added. The rest 20 % hot-melt adhesive was used upon saturation of the powder, followed by the addition of all powder. Finally, the thermoplastic-ceramic melt was mixed for additional 15 min and then the mixture was allowed to cool down. The hardened melt was treated one more time to ensure homogeneity. Before extrusion, the thermoplastic-ceramic mixture was degassed at 110 °C for 2 h and at a vacuum level of about 10 Torr. [Pg.274]

Extrusion was conducted by using a ram extrusion machine with a spider die of 31 mm in diameter. Figure 4.50 shows a schematic of the extruder and spider extrusion die. Before extmsion was started, the extmsion die was preheated to 140 °C. The granulated thermoplastic-ceramic mixture was then added into the die. The bottom of the die was blocked, while the ram was pressed to a pressure of 2.3 MPa. The die was cooled to 50 °C, while the stop was removed from the end of the die. A smaller heati ng mantle was then used to heat the spider region of the die. As the spider was heated to 120-130 °C, mbes with length of up to 0.7 m could be extmded out at a rate of about 2 mm min, at die pressures of about 1 MPa. [Pg.274]

The ceramic materials used consisted of lead zirconate—lead titanate mixtures. These materials have relatively square hysteresis loops and can be prepared in large thin plates. Tlie thickness of the ceramic layer was of the order of 100 jum, that of the liquid crystal about 10 Mm. With a thickness of about 50 jum, these ceramic mixtures have a sufficient transparency, so that a matrix which also operates in transmitted light can be realized. [Pg.153]

Metal-ceramic mixture Grain size too small for dislocation Cluster coating Multi-shell particles... [Pg.141]

After removing the polymeric binder during sintering, strong adhesion between the layers is built up by forming grain boundaries of ceramic materials. From this viewpoint, a ceramic mixture seems to be a more feasible choice. For example, one layer is composed of A and B, and the adjacent layer is made of B and C, the adhesion between these two layers can be formed by the continnous phase of B at the interface. [Pg.325]

FC304 and Fe304+ Ni were added to graphite paste, and Mn + Ni were added to a graphite-ceramic mixture to make anodes used in sediment fuel cells using the same procedure employed by Park and Zeikus (2002). These anodes produced 1.7- to 2.2-foId greater current than plain graphite electrodes under similar conditions Lowy et al. 2006). The Mn -based electrode, which performed best in these laboratory tests, was also field-tested in sediment MFCs and produced 105 mW/m, versus 20 mW/m obtained in previous tests. [Pg.67]


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See also in sourсe #XX -- [ Pg.278 ]




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