Фазовая диаграмма системы Ta-Ti
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Ta-Ti (Tantalum-Titanium)
J.L. Murray
The Ti-Ta phase diagram is of the simple isomorphous type, but data are
lacking on the liquidus, and data on the solid phase boundaries are both
mutually contradictory and inconsistent with thermodynamic properties of pure
Ti. Thermodynamic calculations therefore played a major role in the
construction of the assessed diagram.
[52Sum] measured the temperature of the solid-liquid interface and suggested
that these data represented points about midway between the solidus and
liquidus. On the Ti-rich side, the data of [53May] were obtained by optical
observation of melting; other data were obtained from microscopic examination
of quenched alloys. [65Bru], [69Rud], and [67Bud] obtained solidus data by
optical methods. Discrepancies in the melting temperatures are nearly 500 C
for Ta contents exceeding 40 at.%. Alloy contamination at high temperature is
thus a predominating effect. Because of the large discrepancies, the assessed
solidus is based on the pure metal melting points and the approximate
linearity of the solidus.
The (aTi) solvus [52Sum, 53May, 67Bud] and (bTi) transus [53May, 67Bud, 69Nik]
were examined by metallographic and X-ray techniques, supplemented by
resistivity [53May] and physical and mechanical property [67Bud] measurements.
There is agreement that the maximum solubility of Ta in (aTi) is about 3 с 0.2
at.% at 600 C.
The absence of compounds strongly suggests that excess Gibbs energies are
positive and that the (bTi) transus lies everywhere above a metastable (bTi)
miscibility gap. The appearance of two bcc phases in tempered (bTi,Ta)
supports the existence of a metastable miscibility gap with approximate tie
line compositions of 20 and 70 at.% Ta at 400 C [72Byw2]. Gibbs energy
functions were constructed that reproduce the (aTi) solvus and the approximate
metastable bcc miscibility gap, and the calculation was used to draw the
assessed diagram.
The martensite transformation of (bTi) was reported to be partly suppressed in
alloys containing more than 9 at.% Ta [52Sum] or 15 at.% Ta [53May] and fully
suppressed in alloys containing more than 14 at.% Ta [52Sum], 15 at.% Ta [
58Bag], or 21 at.% Ta [53May]. [72Byw1] showed that prior heat treatment can
influence the product structures and also that samples which showed no optical
evidence of martensite may nevertheless be fully transformed.
In alloys containing up to 7 at.% Ta, the martensite has the cph structure; in
alloys containing more than 7 at.% Ta, the martensite has an orthorhombic
structure. The start temperature of the martensite transformation was measured
by [53Duw] for alloys containing up to 5 at.% Ta; it varies approximately
linearly with composition and reaches 750 C at 5 at.% Ta.
In Ti-Ta alloys, w phase is not found in quenched specimens of any composition,
but only forms during tempering of the bcc phase near 400 C [58Bag, 72Byw2].
52Sum: D.J. Summers-Smith, J. Inst. Met., 81, 73 (1952).
53Duw: P. Duwez, Trans. ASM, 45, 934-940 (1952).
53May: D.J. Maykuth, H.R. Ogden, and R.I. Jaffee, Trans. AIME, 197, 231-237 (
1953).
58Bag: Yu.A. Bagariatskii, G.I. Nosova, and T.V. Tagunova, Dokl. Akad. Nauk
SSSR, 122, 593-596 (1958) in Russian; TR: Sov. Phys. Dokl., 3, 1014-1018 (1958)
.
65Bru: C.E. Brukl et al., unpublished work (1965); cited in [69Rud].
67Bud: P.B. Budberg and K.K. Shakova, Izv. Akad. Nauk SSSR Neorg. Mat., 3(4),
656-660 (1967) in Russian; TR: Russ. J. Inorg. Mater., 3(4), 577-580 (1967).
69Nik: P.N. Nikitin and V.S. Mikheyev, Fiz. Met. Metalloved., 28(6), 1127-1129
(1969) in Russian; TR: Phys. Met. Metallogr., 28(6), 190-192 (1969).
69Rud: E. Rudy, USAF Tech. Rep. AFML-TR-65-2, Part V (1969).
72Byw1: K.A. Bywater and J.W. Christian, Philos. Mag., 25, 1249-1273 (1972).
72Byw2: K.A. Bywater and J.W. Christian, Philos. Mag., 25, 1275-1289 (1972).
Published in Phase Diagrams of Binary Titanium Alloys, 1987. Complete
evaluation contains 5 figures, 3 tables, and 17 references.