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Ceramics, nitrogen

In nonoxide ceramics, nitrogen (N) or carbon (C) takes the place of oxygen in combination with silicon or boron. Specific substances are boron nitride (BN), boron carbide (B4C), the silicon borides (SiB4 and SiBg), silicon nitride (SisN4), and silicon carbide (SiC). All of these compounds possess strong, short covalent bonds. They are hard and strong, but brittle. Table 22.5 lists the enthalpies of the chemical bonds in these compounds. [Pg.910]

Davidge R.W. Economic and energetic considerations for nitrogen ceramics. Nitrogen Ceram. Prac. NATO Adv. Study Inst.7 Oanterburu, 1976. - Noordhof-Leuden.- 1977.-... [Pg.127]

Figure 12, Thermal conductivity of packed beds of hollow cylinders at various temperatures according to Ref. and Equation 23. (a) Ceramic- nitrogen (h) steelnfiitrogen. Figure 12, Thermal conductivity of packed beds of hollow cylinders at various temperatures according to Ref. and Equation 23. (a) Ceramic- nitrogen (h) steelnfiitrogen.
Pe 0 , o according to Equation 23, Dotted line calculated for lOOO K, how-ever, heat transfer by radiation dropped, Ceramic-nitrogen. [Pg.144]

R. Kat2 and G. Quinn in F. Riley, ed.. Progress in Nitrogen Ceramics, Martinus Nijhoff Pubhshers, The Hague, Netherlands, 1983, p. 491. [Pg.326]

Alternatively, tows of fibers can be passed through a Hquid metal bath, where the individual fibers are wet by the molten metal, wiped of excess metal, and a composite wine is produced. A bundle of such wines can be consoHdated by extmsion to make a composite. Another pressureless Hquid metal infiltration process of making MMCs is the Prim ex process (Lanxide), which can be used with certain reactive metal alloys such as Al—Mg to iafiltrate ceramic preforms. For an Al—Mg alloy, the process takes place between 750—1000°C ia a nitrogen-rich atmosphere (2). Typical infiltration rates are less than 25 cm/h. [Pg.195]

Nickel—beryllium casting alloys are readily air melted, in electric or induction furnaces. Melt surface protection is suppHed by a blanket of argon gas or an alumina-base slag cover. Furnace linings or cmcibles of magnesia are preferred, with zirconium siUcate or mullite also adequate. Sand, investment, ceramic, and permanent mold materials are appropriate for these alloys. Beryllium ia the composition is an effective deoxidizer and scavenger of sulfur and nitrogen. [Pg.73]

Beryllium Nitride. BeryUium nitride [1304-54-7], Be N2, is prepared by the reaction of metaUic beryUium and ammonia gas at 1100°C. It is a white crystalline material melting at 2200°C with decomposition. The sublimation rate becomes appreciable in a vacuum at 2000°C. Be2N2 is rapidly oxidized by air at 600°C and like the carbide is hydrolyzed by moisture. The oxide forms on beryllium metal in air at elevated temperatures, but in the absence of oxygen, beryllium reacts with nitrogen to form the nitride. When hot pressing mixtures of beryUium nitride and sUicon nitride, Si N, at 1700°C, beryllium sUicon nitride [12265-44-0], BeSiN2, is obtained. BeSiN2 may have appHcation as a ceramic material. [Pg.76]

Electrical and Electronic Applications. Silver neodecanoate [62804-19-7] has been used in the preparation of a capacitor-end termination composition (110), lead and stannous neodecanoate have been used in circuit-board fabrication (111), and stannous neodecanoate has been used to form patterned semiconductive tin oxide films (112). The silver salt has also been used in the preparation of ceramic superconductors (113). Neodecanoate salts of barium, copper, yttrium, and europium have been used to prepare superconducting films and patterned thin-fHm superconductors. To prepare these materials, the metal salts are deposited on a substrate, then decomposed by heat to give the thin film (114—116) or by a focused beam (electron, ion, or laser) to give the patterned thin film (117,118). The resulting films exhibit superconductivity above Hquid nitrogen temperatures. [Pg.106]

Vapor—sohd reactions (13—17) are also commonly used ia the synthesis of specialty ceramic powders. Carbothermic reduction of oxides, ia which carbon (qv) black mixed with the appropriate reactant oxide is heated ia nitrogen or an iaert atmosphere, is a popular means of produciag commercial SiC, Si N, aluminum nitride [24304-00-3], AIN, and sialon, ie, siUcon aluminum oxynitride, powders. [Pg.306]

Using 2eohte catalysts, the NO reduction takes place inside a molecular sieve ceramic body rather than on the surface of a metallic catalyst (see Molecularsieves). This difference is reported to reduce the effect of particulates, soot, SO2/SO2 conversions, heavy metals, etc, which poison, plug, and mask metal catalysts. ZeoHtes have been in use in Europe since the mid-1980s and there are approximately 100 installations on stream. Process applications range from use of natural gas to coal as fuel. Typically, nitrogen oxide levels are reduced 80 to 90% (37). [Pg.511]

Superconductivity The physical state in which all resistance to the flow of direct-current electricity disappears is defined as superconductivity. The Bardeen-Cooper-Schriefer (BCS) theoiy has been reasonably successful in accounting for most of the basic features observed of the superconducting state for low-temperature superconductors (LTS) operating below 23 K. The advent of the ceramic high-temperature superconductors (HTS) by Bednorz and Miller (Z. Phys. B64, 189, 1989) has called for modifications to existing theories which have not been finahzed to date. The massive interest in the new superconductors that can be cooled with liquid nitrogen is just now beginning to make its way into new applications. [Pg.1127]

Creep of polymers is a major design problem. The glass temperature Tq, for a polymer, is a criterion of creep-resistance, in much the way that is for a metal or a ceramic. For most polymers, is close to room temperature. Well below Tq, the polymer is a glass (often containing crystalline regions - Chapter 5) and is a brittle, elastic solid -rubber, cooled in liquid nitrogen, is an example. Above Tq the Van der Waals bonds within the polymer melt, and it becomes a rubber (if the polymer chains are cross-linked) or a viscous liquid (if they are not). Thermoplastics, which can be moulded when hot, are a simple example well below Tq they are elastic well above, they are viscous liquids, and flow like treacle. [Pg.193]

Martensite transformations are not limited just to metals. Some ceramics, like zirconia, have them and even the obscure system of (argon + 40 atom% nitrogen) forms martensite when it is cooled below 30 K. Helical protein crystals in some bacteria undergo a martensitic transformation and the shape change helps the bacteria to burrow into the skins of animals and people ... [Pg.86]

They are, potentially or actually, cheap. Most ceramics are compounds of oxygen, carbon or nitrogen with metals like aluminium or silicon all five are among the most plentiful and widespread elements in the Earth s crust. The processing costs may be high, but the ingredients are almost as cheap as dirt dirt, after all, is a ceramic. [Pg.162]

There are two further processes. Silicon-based ceramics can be fabricated by sintering or by hot-pressing. But a new route, reaetion bonding (Fig. 19.6), is cheaper and gives good precision. If pure silicon powder is heated in nitrogen gas, or a mixture of silicon and carbon powders is sintered together, then the reactions... [Pg.197]

Adding large quantities of pozzolan, ceramic microspheres or nitrogen. These materials lighten the slurry because they have lower specific gravities than the cement. [Pg.1186]

I would like to take this opportunity to thank my colleagues, with whom I have had the pleasure to work. I would like to extend my gratitude to the brilliant professionals at the Institute of Chemistry at the Kola Science Center of the Russian Academy of Sciences (Apatity, Russia), Institute of Common and Inorganic Chemistry of the Ukraine Academy of Science (Kiev, Ukraine), Karpov Institute of Physical Chemistry (Moscow, Russia), Institute of Chemistry of Nitrogen (Moscow, Russia), Technion - Israel Institute of Technology (Haifa, Israel), Chemistry of Solids Laboratory of CNRS (Bordeaux, France), Tan Ceramics Ltd. (Migdal Haemek, Israel). [Pg.398]


See other pages where Ceramics, nitrogen is mentioned: [Pg.241]    [Pg.276]    [Pg.91]    [Pg.322]    [Pg.399]    [Pg.136]    [Pg.240]    [Pg.241]    [Pg.50]    [Pg.56]    [Pg.172]    [Pg.251]    [Pg.124]    [Pg.156]    [Pg.54]    [Pg.211]    [Pg.212]    [Pg.214]    [Pg.4]    [Pg.330]    [Pg.635]    [Pg.279]    [Pg.375]    [Pg.378]    [Pg.417]    [Pg.418]    [Pg.1183]    [Pg.235]    [Pg.1100]    [Pg.174]   
See also in sourсe #XX -- [ Pg.27 ]

See also in sourсe #XX -- [ Pg.27 ]




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