Regularities of Metallurgical Reactions of Ti1 –n\({\text{Me}}_{n}^{{\text{V}}}\)C0.5N0.5 Carbonitrides with the Ni–Mo Melt
- Authors: Zhilyaev V.A.1, Patrakov E.I.2
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Affiliations:
- Institute of Solid-State Chemistry, Ural Branch, Russian Academy of Sciences
- Institute of Metal Physics, Ural Branch, Russian Academy of Sciences
- Issue: Vol 59, No 6 (2018)
- Pages: 664-670
- Section: Refractory, Ceramic, and Composite Materials
- URL: https://journal-vniispk.ru/1067-8212/article/view/226651
- DOI: https://doi.org/10.3103/S1067821218060196
- ID: 226651
Cite item
Abstract
The influence of alloying TiC0.5N0.5 carbonitride by transition metals of Group V (V, Nb, and Ta) on the contact interaction mechanism with the Ni–25%Mo melt (T = 1450°C, τ = 1 h, rarefaction is 5 × 10–2 Pa) is systematically studied by X-ray spectral microanalysis and scanning electron microscopy for the first time. It is established that the dissolution of single-type Ti1 –n\({\text{Me}}_{n}^{{\text{V}}}\)C0.5N0.5 carbonitrides (n = 0.05) is an incongruent process (alloying metal and carbon preferentially transfer into the melt), and the relative rate and degree of incongruence of the dissolution process of carbonitrides in a series of alloying metals V–Nb–Ta vary nonmonotonically. An explanation for the discovered effects is proposed. The causal-effect relation between the initial composition of Ti0.95\({\text{Me}}_{{0.05}}^{{\text{V}}}\)C0.5N0.5 carbonitride (the grade of the alloying metal) and composition of the Ti1 – n – mMon\({\text{Me}}_{m}^{{\text{V}}}\)Cx K-phase that is precipitated from the melt upon system cooling is analyzed. It is shown that the factor determining the composition of the forming K-phase is the ΔT factor (the degree of exceeding crystallization temperatures of carbide eutectics Ni/MeVC over the crystallization temperature of the Ni/Mo2C eutectic that is the lowest melting in these systems). The conclusion is argued that the interrelation between the initial carbonitride composition and the composition of the K-phase is a consequence of a microinhomogeneous structure of metallic alloys. It is shown that this interrelation is rather common and manifests itself in all studied systems irrespective of the type of alloying Group V metal and presence or absence of molybdenum in the melt.
About the authors
V. A. Zhilyaev
Institute of Solid-State Chemistry, Ural Branch, Russian Academy of Sciences
Author for correspondence.
Email: zhilyaev@ihim.uran.ru
Russian Federation, Yekaterinburg, 620990
E. I. Patrakov
Institute of Metal Physics, Ural Branch, Russian Academy of Sciences
Author for correspondence.
Email: patrakov@imp.uran.ru
Russian Federation, Yekaterinburg, 620137
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