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Transition metal nitrides ternary compounds

We have included not only pure nitride materials but also many amides, azides, oxynitrides (but not nitrates and nitrites), nitride chalcogenides, and nitride halides. Specifically excluded are polymeric compounds (e.g. SxNy), cluster compounds (e.g. Sc2C12N), coordination compounds (e.g. [Pd(NS3)2]), ternary azides and amides, as well as ternary interstitial transition-metal nitrides. We have attempted to include all important structures and all type compounds. This review is also unique in that we attempt to evaluate the... [Pg.309]

Kumta and co-workers [20] have used a three-step sol-gel-based procedure to prepare ternary transition metal nitrides involving heat treatment under ammonia of a metal organic hydroxide precursor. This route consists in the hydrolysis of a polymeric liquid precursor to form a metal-organic hydroxide. Thermochemical decomposition of the metal-organic hydroxide precursor under ammonia leads to ternary nitrides such as NijMOjN, FeWN and Ti AIN. DiSalvo and co-workers incorporated alkaU metal ions to increase the stability of the nitrides compared to binary compounds. They used a sol-gel-based route to prepare ternary alkali and alkaline-earth metal nitrides such as NaTaN, KTaN and NaNbN [21, 22]. [Pg.154]

Ternary phases with structures different from those of the phases of the binary boundary systems are more the exception than the rule. Such phases have been reported in the systems Nb-Mo-N, Ta-Mo-N, Nb-Ta-N, Zr-V-N, Nb-Cr-N, and Ta-Cr-N. Information about ternary transition metal-nitrogen systems is often available for specific temperatmes only. This is even more the case for quaternary nitride systems, which play a role in the production of carbonitride cermets where quaternary compounds of the types (Ti,Mo)(C,N) and (Ti,W)(C,N) are of interest (see Carbides Transition Metal Solid-state Chemistry), as well as in layer technology where titanium nitride-based coatings of the type Ti(C,B,N) are prepared by magnetron sputtering. Layers consisting of ternary compounds of the type (Ti,Al)N and (Ti,V)N also have favorable properties with respect to abrasion resistance. [Pg.3014]

Metallic nitrides, sometimes termed interstitial compounds, are formed from combinations of N with transition metals of groups IVA, VA, and VIA. As the name implies, they exhibit electrical conductivity and most of the general characteristics associated with standard metals. They are also refractory and hard, and usually depart from the ideal stoichiometry ratios displayed above (see 17.3.9, Table 1). They readily form solid solutions with carbides and oxides, which gives rise to problems when it is necessary to obtain nitrides in pure form. Included in this category are numerous ternary nitrides of a transition metal with a group B metal. [Pg.444]

By far the largest class of ternary lithium nitrides are those with the antifluorite structure, prepared largely by Juza, and reviewed by him [42], The ternaries are more thermally stable than the binaries which would seem to indicate a relaxation of the internal strain (both cation- cation and anion-anion repulsions) of binary nitrides. Many of these compounds are in fact ordered superstructures of antifluorite and it is remarkable that most of the transition metals are observed in high oxidation states--much higher than those in the binaries (e.g. Li7Mn + N4 vs Mn5 + N2). They are Li+ conductors at elevated... [Pg.314]

While most of the binary carbides and nitrides considered above form unlimited homogeneous solid solutions, some other 5 and p elements (B, Be, Al, Mg, etc.) have only a low solubility in these phases. As their content in carbides and nitrides increases, ternary compounds with very specific crystal structures are formed which were reviewed by Alyamovsky et al (1981) and Goldschmidt (1967). It is well known (see Samsonov, Serebryakov and Neronov (1975)) that B or transition metal borides do not form unlimited solid solutions, when interacting with MX phases (X = C, N) and single-phase TiNjBj, compounds exist over a narrow composition range for example, when z + y = 0.62-0.94, y < 0.03 (see Alyamovsky, Zainulin and Shveikin (1976)). As the B/N ratio increases. [Pg.147]

Ceramic superconducting films are divided into three classes, Bl-type compounds, ternary compounds, and high-temperature oxide superconductors. The Bl-type (NaCl-type structure) compound superconductors consist of nitrides and carbides with 5A, 6A, and 7A transition metals, such as TiN, ZrN, HfN, VN, NbN TaN, MoN, WN, TiC, ZrC, HfC, VC, NbC, TaC, MoC, WC, NbNi tC t, hex-MoN, and hex-MoC. Regarding the thin-film material, it is notable that NbN and NbN] (C ( (x = 0.08 and 0.15) have superconducting critical temperature, T, values of 17.3 and 17.8 K, respectively. The deposition method used is almost always sputtering or CVD. The properties of films deposited by the former method are superior. A highly reliable Josephson device was realized with an NbN film. [Pg.78]

Quaternary boro-nitrides. The well-known magnetic properties of R2T14B ternary borides (T=transition metal) are typified by the neodymium iron compound Nd[2Fei4B, discovered in 1983. Several studies aimed at introducing interstitial nitrogen in the composition of such permanent-magnet materials in order to improve their characteristics, in particular the Curie temperature. [Pg.69]


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Nitride compounds

Nitrides ternary compounds

Nitrides, ternary

Ternary transition metal nitrides

Transition compounds

Transition metal nitrides

Transition nitrides

Transition-metal compounds

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