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  • 1
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Materials Research 19 (1989), S. 145-164 
    ISSN: 0084-6600
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Solid State Communications 63 (1987), S. 141-145 
    ISSN: 0038-1098
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Tetrahedron Letters 35 (1994), S. 3901-3904 
    ISSN: 0040-4039
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Bioorganic & Medicinal Chemistry Letters 4 (1994), S. 2851-2856 
    ISSN: 0960-894X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology , Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 102 (1971), S. 1234-1244 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die manganreiche Seite der Systeme Mn−V und Mn−Cr wurde hochtemperatur-röntgenographisch untersucht. Im System Mn−V treten bei 90 At% Mn zwei bisher nicht beobachtete Phasen, α′ und β′, mit α-bzw. β-Manganstruktur auf. Diese gehören möglicherweise der Klasse der χ-bzw. π-Phasen an. Die γ-Mischphase besitzt einen größeren Existenzbereich als in der Literatur angegeben. Die Existenz der σ-Phase Mn3V, sowie die Phasenzustände bis 80 At% Mn und bei manganreicheren Legierungen unterhalb 700°C werden bestätigt. Das lineare thermische Ausdehnungsverhalten der Phasen σ, α′ und β′ sowie des α-und δ-Mischkristalls werden angegeben. Für den manganreichen Teil wird ein vorläufiges Zustandsdiagramm entworfen. Im System Mn−Cr konnte in großen Zügen Über-einstimmung mit Literaturangaben gefunden werden. Es wird das lineare thermische Ausdehnungsverhalten der σ-Phase Mn3Cr angegeben.
    Notes: Abstract The manganese rich portions of the phase diagrams Mn−V and Mn−Cr have been investigated by means of a high temperature X-ray technique. In the system Mn−V two new phases, α′ and β′, have been observed with α-manganese and β-manganese type structure, resp. These phases are probably to be classified as χ-and π-phase. The γ-manganese solid solution with vanadium has a wider range of homogeneity as compared with previous work. The existence of a σ-phase Mn3V and phase equilibria below 700°C reported previously could be confirmed. The linear thermal expansion of the intermetallic compounds σ, α′, β′, the α-and δ-manganese solid solutions with vanadium has been evaluated. A tentative phase diagram for the manganese rich portion is given. The main features of the system Mn−Cr according to previous investigations could be confirmed. The linear thermal expansion of the σ-phase Mn3Cr is reported.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 101 (1970), S. 65-82 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract The stability of the following transition element carbides TiC, ZrC, HfC, VC1−x , NbC, TaC, Cr3C2, Mo2C, WC against nitrogen (1–300 at) at temperatures 1100–1800° C has been investigated. The carbides of IVa group metals react with nitrogen within the above mentioned temperature range and very likely even at higher temperature forming carbonitrides. The monocarbides of the Va metal group with exception of the vanadium carbide VC1−x are much more stable as compared with the IVa metal carbides. Tantalum carbide withstands any attack of nitrogen under the above mentioned conditions. A similar behavior has been observed for WC. Cr3C2 reacts with nitrogen at 1450° C and 270 at forming a ternary compound Cr3(C,N)2 already previously reported. Likewise a reaction takes place between Mo2C and N2 (1100° C, 30 at; 1450° C, 270 at) a ternary phase Mo(C, N) being formed. The latter seems to be structurally related to WC.
    Notes: Zusammenfassung Die Beständigkeit der Carbide: TiC, ZrC, HfC, VC1−x , NbC, TaC, Cr3C2, Mo2C und WC gegen Stickstoff von Normaldruck, 30 at und 300 at bei Temperaturen von 1100° C, 1400° C, 1700° C und 1800° C wurde untersucht. Die Carbide der IVa-Gruppe reagieren im obigen Temperaturbereich und vermutlich noch weit darüber hinaus unter Carbonitridbildung. Vergleichsweise zeichnen sich die Monocarbide der Va-Metalle (mit Ausnahme von VC1−x ) durch wesentlich größere Stabilität gegen N2 aus. Tantalcarbid erwies sich bei allen Versuchsbedingungen als vollkommen inert gegen N2. Von den untersuchten Carbiden der VIa-Gruppe (Cr3C2, Mo2C, WC) zeigte nur WC eine mit TaC vergleichbare Stabilität gegen N2. Cr3C2 setzt sich mit N2 bei 1450° C und 270 at zu der früher beschriebenen Phase Cr3(C,N)2 um. Eine bemerkenswerte Reaktion mit N2 (1100° C, 30 at und 1450° C, 270 at) zeigt Mo2C, wobei eine dem WC strukturell ähnliche Mo(C,N)-Phase entsteht.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 103 (1972), S. 1130-1137 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Das pseudoternäre System TiC−TiN−TiO wurde mit röntgenographischen und metallographischen Methoden untersucht. Im Temperaturbereich von 1100–1500°C herrscht vollständige Mischbarkeit der Komponenten. Der Verlauf der Gitterparameter in Abhängigkeit von der Zusammensetzung zeigt in der Nähe des Randsystems TiN−TiO Anomalien.
    Notes: Abstract The pseudoternary system TiC−TiN−TiO has been investigated by X-ray and metallographic technique within the temperature range 1100–1500°C. Complete miscibility was proved to exist. The variation of lattice parameters with sample composition shows anomalies near the boundary system TiO−TiN.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 101 (1970), S. 1098-1103 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Abstract The occurence of η-carbides of typeA 3B3C,A 2B4C, andA 6B6C (A=Fe, Co, Ni), (B=Mo, W) has been investigated. With the exception of the system Fe−Mo−C the formation of a phaseA 6B6C could be observed in all systems. The phase Co6Mo6C is not stable at temperatures exceeding 1000°C, but undergoes a decomposition to Co3Mo3C and μ-phase (Co7Mo6). Three structurally related η-phases are observed in the system Co−W−C in the temperature range 1100 to 1350° C: Co6W6C, Co3W3C, and Co2W4C. Below 1100° C the phase Co3W3C is unstable and decomposes, forming Co6W6C, WC, and Co. Isothermal sections of the systems Co−W−C are drawn for the temperatures 1100 and 1300° C.
    Notes: Zusammenfassung Das Auftreten von η-Carbiden vom TypusA 3B3C,A 2B4C undA 6B6C (A=Fe, Co, Ni,B=Mo, W) wurde untersucht. Mit Ausnahme des Systems Fe−Mo−C konnten in allen Systemen η-Carbide des TypsA 6B6C beobachtet werden. Im System Co−Mo−C ist die Phase Co6Mo6C oberhalb 1000° C thermisch nicht mehr stabil, sondern zerfällt in Co3Mo3C+μ-Phase (Co7Mo6). Im System Co−W−C treten im Temperaturbereich 1100–1350° C drei strukturell eng verwandte η-Carbide der Zusammensetzungen CO6W6C, Co3W3C und Co2W4C auf. Unterhalb 1000° C ist Co3W3C nicht beständig und zerfällt in Co6W6C, WC und Kobalt. Isotherme Schnitte durch das System Co−W−C bei 1100° C und 1300° C werden entworfen.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 106 (1975), S. 823-832 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pseudoternary system “ZrO”−ZrN−ZrC and the corresponding pseudobinary systems “ZrO”−ZrN, “ZrO”−ZrC and ZrC−ZrN have been investigated by X-ray and metallographic techniques at 1600 and 2000°C. There is a considerable solid solubility of “ZrO”, which as a pure phase is not existent, in ZrC, ZrN and Zr(C, N). At 1600°C the boundary solubility of “ZrO” decreases from ZrC0.45O0.55 to ZrN0,65O0.35. The solubility of the oxide increases with the temperature to ZrC0.25O0.75 and ZrN0.45O0.55 at 2000°C.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 106 (1975), S. 973-981 
    ISSN: 1434-4475
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The pseudoternary system “HfO”−HfN−HfC and the corresponding pseudobinary systems “HfO”−HfN, “HfO”−HfC and HfC−HfN have been examined by metallographic and X-ray methods within the temperature range of 1600 to 2000°C. The field of homogeneity for the hafniumoxicarbonitrides is not extended. The oxygen content of the solid solutions decreases from hafniumoxicarbides to hafniumoxinitrides. The miscibility ends at 1600°C for HfC0.75O0.25 and HfN0,80O0.20 and at 2000°C for HfC0.70O0.30 and HfN0.75O0.25 resp.
    Type of Medium: Electronic Resource
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