[0001] The present invention relates to titanium-based alloy compositions designed for enhanced
superplastic formability during sheet metal-forming processes which have lower cost
than current alloys and improved cold formability.
[0002] Examples of typical compositions of α+β Ti-alloys which are superplastic and which
are often used for the manufacture of superplastically-formed components are listed
in Table 1.
Table 1: Nominal composition in wt.% of commercially used titanium alloys for superplastic
forming applications.
| Alloy |
Al |
V |
Fe |
Mo |
Ti |
| Ti-6Al-4V |
6 |
4 |
- |
- |
Bal. |
| Ti54M |
5.1 |
3.9 |
0.5 |
0.7 |
Bal. |
| ATI425 |
4 |
2.5 |
1.5 |
- |
Bal. |
| SP700 |
4.5 |
3 |
2 |
2 |
Bal. |
[0003] These alloys suffer from relatively poor superplastic and cold formability and a
relatively narrow formability window - in terms of temperature, flow stress and strain-rate.
[0004] It is an aim of the invention to provide a α+β Ti-alloy which has equivalent or improved
superplastic formability in comparison with the superplastic alloys listed in Table
1. A comparable or lower raw cost and improved or comparable machinability and cold
formability are desired.
[0005] The present invention provides a titanium-based alloy composition consisting, in
weight percent, of: between 0.5 and 2.5% aluminium, between 0.5 and 1.5% vanadium,
between 0.0 and 3.0% iron, between 0.0 and 1.0% chromium, between 0.0 and 3.0% nickel,
between 1.0 and 4.0% molybdenum, between 0.0 and 1.0% silicon, between 0.0 and 0.2%
boron, between 0.0 and 0.5% tin, between 0.0 and 0.5% zirconium, between 0.0 and 1.0%
niobium, between 0.0 and 1.0% tantalum, between 0.0 and 0.5% calcium, between 0.0
and 0.5% carbon, between 0.0 and 0.5% manganese, the balance being titanium and incidental
impurities, wherein one of iron and nickel is present in an amount of at least 2.0%
and the other of iron and nickel is present in an amount of 1.0% or less.. This composition
provides a good balance between cost, density, optimal mechanical performance at service
temperature and low-stress and low-temperature superplastic formability and adequate
microstructural stability.
[0006] In an embodiment the titanium-based alloy consists of at least 1.0% aluminium. This
helps keep the density of the alloy low and helps increase the diffusivity merit index
and thereby formability and the strength of the alloy.
[0007] In an embodiment the titanium-based alloy composition consists of at most 2.25% or
less than 2.25% or 2.0% or less aluminium. This is advantageous as this improves the
cold formability of the alloy and helps reducing further the temperature for superplastic
forming.
[0008] In an embodiment the titanium-based alloy consists, in weight percent, of 0.5% or
less iron. This is advantageous as it increases the stability of the alloy avoiding
the formation of the ω-phase - or so-called 'beta fleck'.
[0009] In an embodiment the titanium-based alloy consists, in weight percent, of 0.5% or
less chromium, preferably 0.4%, or less chromium. This is advantageous as it increases
the stability of the alloy avoiding the formation of the ω-phase - or so-called 'beta
fleck'.
[0010] In an embodiment the titanium-based alloy composition consists, in weight percent,
of 0.1% or more Si, preferably 0.2% or more Si, more preferably 0.5% or more silicon.
This is advantageous as it increases strength and creep resistance.
[0011] In an embodiment the titanium-based alloy composition consists, in weight percent,
of 0.05% or more boron, preferably 0.1% or more boron. This is advantageous as it
improves the ductility of the alloy.
[0012] In an embodiment the titanium-based alloy composition consists, in weight percent,
of 0.25% or more nickel. This ensures a higher diffusivity merit index.
[0013] The term "consisting of" is used herein to indicate that 100% of the composition
is being referred to and the presence of additional components is excluded so that
percentages add up to 100%. Unless otherwise stated, all amounts are in weight percent.
[0014] The invention will be more fully described, by way of example only, with reference
to the accompanying drawings in which:
Figure 1 is a flow diagram illustrating the process by which the titanium-based alloy
composition was determined;
Figure 2 illustrates for each of aluminium, vanadium, chromium, iron, nickel and molybdenum
how composition affects the temperature for optimal superplastic forming and density;
Figure 3 illustrates for aluminium, vanadium, chromium, iron, nickel and molybdenum
how composition affects the temperature for optimal superplastic forming and cost;
Figure 4 illustrates for aluminium, vanadium, chromium, iron, nickel and molybdenum
the effect of composition on optimal temperature for superplastic forming versus normalised
diffusivity;
Figure 5 illustrates the trade offs in alloy characteristics apparent from Figures
2-4 and the trade offs in the alloy of the present invention compared to the four
commercially available alloys of Table 1;
Figures 6-8 illustrate the effect of varying composition on optimal superplastic forming
temperature with Fe and Ni fixed at zero in Figure 6, Cr and Ni fixed at zero in Figure
7 and Cr and Fe fixed at zero in Figure 8;
Figures 9-11 illustrate the variation in density as a function of composition for
the alloy system with Ni and Fe fixed at zero in Figure 9, Ni and Cr fixed at zero
in Figure 10 and Fe and Cr fixed at zero in Figure 11;
Figures 12-14 illustrate the effect of composition on cost with Ni and Fe fixed at
zero on Figure 12, Ni and Cr fixed at zero in Figure 13 and Fe and Cr fixed to zero
in Figure 14;
Figures 15-17 illustrate the effect of composition on diffusivity with Fe and Ni fixed
at zero in Figure 15, Cr and Ni fixed at zero in Figure 16 and Cr and Fe fixed at
zero in Figure 17;
Figure 18 illustrates the constraints used in the computer software to find the optimum
alloy composition and the target properties; and
Figure 19 illustrate graphs of temperature for optimal superplastic forming on the
y axis versus cost, density, normalised diffusivity and stability showing the variation
throughout the alloy design space and the location of the alloy of the present invention.
[0015] Traditionally, titanium-based alloys have been designed through empiricism. Thus
their chemical compositions have been isolated using time consuming and expensive
experimental development, involving small-scale processing of limited quantities of
material and subsequent characterisation of their behaviour. The alloy composition
adopted is then the one found to display the best, or most desirable, combination
of properties. The large number of possible alloying elements indicates that these
alloys are not entirely optimised and that alloys with more desirable properties are
likely to exist.
[0016] In titanium alloys, generally additions of aluminium (Al) are added as an α-stabiliser
to improve the mechanical strength. However, large additions of Al lead to cold workability
deterioration - machining particularly. Also, excess content of Al leads to stability
problems: loss of ductility and stress corrosion occurs due to reordering reaction
of α
2 formation after long-time exposure at high-temperature.
[0017] General additions of vanadium (V) are added as a β-stabiliser to increase the mechanical
strength without forming brittle intermetallic compounds. V makes a solid solution
with the β phase.
[0018] Additions of nickel (Ni), cobalt (Co), iron (Fe) and chromium (Cr) are added as β-stabiliser
elements to reduce the flow stress during superplastic forming and to maximise the
strain-rate sensitivity. These elements have a diffusivity higher than that of V,
hence tend to increase the diffusivity of Ti-6AI-4V.
[0019] Small additions of silicon (Si) are added to increase the strength and creep resistance.
At high-temperatures, Si dissolves in the α phase and precipitates as silicides that
pin mobile dislocations from climb and glide. Silicon was not part of the calculations
described hereinafter, but experience shows that additions of silicon of up to 1.0%,
but preferably 0.1 % or more, more preferably 0.2% or more and most preferably at
least 0.5% are beneficial for increased strength and ductility and so are included
in the inventive alloy.
[0020] Small additions of boron (B) are added to improve the ductility due to enhancement
of the prior-β grain-boundary cohesion by boron segregation at the grain boundaries.
Boron was not part of the calculations described hereinafter, but experience shows
that additives of up to 0.2%, but preferably limited to 0.1% are beneficial and so
are included in the inventive alloy. Small amounts of boron of 0.05% or more or 0.1%
or more are beneficial for improved ductility. The present inventors have not modelled
the effect of low levels of other commonly used alloying elements such as tin, zirconium,
niobium, tantalum, calcium, carbon and manganese.
[0021] Neutral phase elements such as zirconium and tin may be added in quantities of 0.5
% or less -- these won't change the α-β phase proportion. The density of Zr and Sn
is close to that of Mo therefore the following limitation may be introduced in order
to keep the density below the imposed constrain (
Zr wt. %
+ Sn wt. %
+ Mo wt.% ≤ 4.0 wt. %). Niobium and tantalum have similar effects in titanium alloys and each may be
added in quantities of 1% or below as a β-stabiliser. Nb and Ta do not affect the
stability of the alloy and have a density and price comparable to that of Mo - Nb
and/or Ta may act as a substitute to Mo. Therefore, preferably the amount of Nb and
Ta are limited in the following manner:
Nb wt. % +
Ta wt.% +
Mo wt. % ≤ 4.0 wt. %. Preferably Nb wt% + Ta wt.%<1.0 wt.%.
[0022] Manganese is a β-eutectoid stabiliser therefore further additions of Mn will reduce
the SPF temperature but it will promote formation of unwanted phases similarly to
Cr, Ni and Fe. Due to a very similar density and cost to Cr, one may substitute an
amount of Cr (up to 0.5 wt. %) by Mn. So preferably
Cr wt. % + Mn wt.% ≤ 1.0 wt. %,
more preferably ≤ 0.5 wt.%.
[0023] Calcium and carbon may be present at levels of up to 0.5% each and are not expected
greatly to change the character of the alloy at this level.
[0024] A modelling-based approach used for the isolation of new grades of titanium based
alloys is described here, termed the "Alloys-By-Design" (ABD) method. This approach
utilises a framework of computational materials models to estimate design relevant
properties across a very broad compositional space. In principle, this alloy design
tool allows the so called inverse problem to be solved; identifying optimum alloy
compositions that best satisfy a specified set of design constraints.
[0025] The first step in the design process is the definition of an elemental list along
with the associated upper and lower compositional limits. The compositional limits
for each of the elemental additions considered in this invention - referred to as
the "alloy design space" - are detailed in Table 2.
Table 2: Alloys design space in wt.% searched using the 'Alloy-by-Design' method.
| |
Al |
V |
Fe |
Cr |
Ni |
Mo |
Si |
B |
| Min. |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
0.0 |
| Max. |
8.0 |
8.0 |
4.0 |
4.0 |
4.0 |
6.0 |
0.5 |
0.1 |
[0026] The design process comprises discretising the alloy design space into different compositions
covering the complete alloy design space (for example with amounts of each given element
varying by 0.01 or 0.001 between different compositions with the amounts of the other
added elements remaining constant. Thus, a huge member of specific alloy compositions
within the alloy design space are determined. For each alloy composition a property
is calculated.
[0027] The second step relies upon thermodynamic calculations used to calculate the phase
diagram and thermodynamic properties for each of the specific alloy compositions.
Often this is referred to as the CALPHAD method (CALculate PHAse Diagram). These calculations
are conducted for those temperatures where an optimal phase architecture of the new
alloy is found: temperatures in excess of 40% the melting point of the alloy and where
the ratio of α-to-β phase is approximately 0.6.
[0028] A third stage involves isolating specific alloy compositions which have the desired
microstructural architecture. In the case of titanium alloys which require maximum
formability
via the exploitation of superplasticity, the enhanced regime is found when the volume
fraction of the β-phase lies between 30%-50% at temperatures where the thermally-activated
deformation is active:
i.e. above 0.4 of the melting temperature of the alloy (0.4
T/
Tm). This can be measured experimentally by differential scanning calorimetry or by
quenching from the temperature so that β-phase transforms to martensite not α-phase,
observable by metallographic examination.
[0029] Rejection of a specific alloy composition on the basis of unsuitable microstructural
architecture is also made from estimates of susceptibility to form unstable precipitates.
The present calculations predict the formation of the α
2 precipitates using CALPHAD modelling. Moreover, the susceptibility of the alloy to
form the deleterious segregation phase called 'beta fleck' is calculated in terms
of molybdenum equivalent weight percent.
[0030] The model rejects all specific alloy compositions not meeting these design criteria
and only maintains those specific alloy compositions in the design space which are
calculated to result in a volume fraction of β of between 30 and 50% at temperatures
of creep (>0.4
T/
Tm) which form experience are expected to have a low tendency to form the unstable segregation
phase 'beta fleck'.
[0031] In the fourth stage, merit indices are estimated for the remaining isolated alloy
compositions in the dataset. A merit index is a value calculated according to a formula
(described below) which is indicative of a desired property of the alloy. Examples
of the merit indices include: β-diffusivity merit index (which describes an alloy's
superplastic formability based solely on mean composition), superplastic forming temperature
merit index, density, cost and diffusivity.
[0032] At the end of the process only those alloy compositions which have passed the thermodynamic
requirements and all of the merit indices remain and this is the optimized alloy composition.
[0033] The first merit index is the temperature at which superplasticity is optimal; or
the temperature where the microstructure is composed by 40% β-phase and 60% α-phase.
Equilibrium thermodynamic calculations were carried out in order to determine the
temperature of 40% β-phase for each single composition within the proposed design
space. The lower this superplastic forming (SPF) temperature, the better as less energy
is needed for forming and less damage (e.g. due to oxidation occurs at lower forming
temperatures.
[0034] The second merit index is the diffusivity of the β-phase; this is strongly linked
to the stress necessary to activate superplastic deformation. A faster diffusivity
of β is translated directly into a decrease of the flow stress of superplastic titanium.
This is accomplished by addition of small percentages of elements with tracer diffusivity
higher than that of titanium on β-Ti -
e.g. Fe, Ni and Cr - since the diffusivity is controlled by the faster diffusing species,
consistent with

where
xi is the concentration of element
i and D
i is its tracer diffusivity as shown in Table 3. The forming resistance merit index
is related directly to this diffusivity, for clarity, the forming resistance merit
index is written as a function of the diffusivity of V on β titanium - see Table 3.
Table 3: diffusivity (D) of beta stabilising elements at 870C
| Diffusivity (D) of β-stabilising elements at 870°C |
| Element |
D (cm2s) |
D of element / D of V |
| Ni |
220 x 10-10 |
63.7 |
| Co |
190 x 10-10 |
55.3 |
| Fe |
78 x 10-10 |
22.6 |
| Cr |
11 x 10-10 |
3.22 |
| β-Ti |
3.36 x 10-10 |
1.0 |
| V |
2.4 x 10-10 |
0.69 |
| Nb |
1.7 x 10-10 |
0.49 |
| Al |
1.44 x 10-10 |
0.43 |
| Mo |
0.6 x 10-10 |
0.173 |
| W |
0.2 x 10-10 |
0.063 |
[0035] The third merit index is density. The density,
ρ, was calculated using a simple rule of mixtures and a correctional factor of 5% as
has been shown practically to give a more accurate prediction, where,
ρi is the density for a given element and
xi is the atomic fraction of the alloy element.

[0036] The fourth merit index is cost. In order to estimate the cost of each alloy a simple
rule of mixtures was applied, where the weight fraction of the alloy element,
xi, was multiplied by the current (2015) raw material cost for the alloying element,
ci.

[0037] The estimates assume that processing costs are identical for all alloys,
i.e. that the product yield is not affected by composition.
[0038] The fifth merit index is the β-phase stability. In order to avoid the formation of
the ω-phase - or so-called 'beta fleck' - one must keep the amount of non-solid solutioning
β stabilisers below a maximum. This sum is defined in terms the addition of the wt.%
of Ni, Fe and Cr as

[0039] If the stability merit index exceeds a value of 3 to 3.5, the alloy is likely to
be susceptible to form the ω segregation phase upon melting and solidification of
the alloy-this would translate into a loss of ductility under service conditions.
However, this index is related directly to the forming resistance of the alloy: the
lower the resistance, the higher the stability merit index will become. For optimal
formability and microstructural stability, this fifth merit index is assumed optimal
between a value of 2 to 3.
[0040] The sixth merit index is the aluminium content. This is related directly to the machinability,
strength and stability of the alloy. High values (>7 wt. %) of aluminium will cause
a brittle behaviour in the alpha phase. Medium aluminium content (3-6 wt. %) provides
good strength but the machinability is difficult. No aluminium content facilitates
greatly the cold machinability but the strength is decreased substantially. This led
to a maximum aluminium content of 2.5%. Reducing the aluminium concentration to 2.25%
or less, less than 2.25% or to 2.0% or less improves cold formability and helps in
further reducing the temperature for superplastic forming.
[0041] The ABD method described above was used to isolate the inventive alloy composition.
The design intent for this alloy was to isolate a composition of a new titanium alloy
which exhibits a combination of superplastic formability, strength and ductility which
is comparable or better than equivalent grades of alloy. The density, cost and processing
of the alloy have also been considered in the design of the new alloy. A thermoformed
product made of the alloy composition preferably has an equiaxed alpha-beta microstructure
with a grain size below 10 microns - more preferably below 6 or 7 microns.
[0042] The material properties - determined using the ABD method - for the commercially
available superplastic titanium alloys are listed in Table 4. The design of the new
alloy was considered in relation to the predicted properties listed for these alloys.
The method was used to propose a novel alloy composition which targets different properties.
The calculated material properties for the ABD-SPTi alloys with nominal compositions
according to Table 5 and in accordance with the present invention are also given.
Table 4: Calculated phase fractions and merit indices made with the "Alloys-by-Design" software.
Results for four commonly used SPF Ti alloys as listed in Table 1 and the compositions
of the new alloys ABD-SPTi listed in Table 5.
| |
β phase |
Diff. Merit Index |
Density |
Cost |
Cold formability |
| Alloy |
SPF temp. (°C) |
Wt.% Mo equivalent |
(Deff/DβTi) |
(g/cm3) |
($/lb) |
Wt. % Al content |
| Ti-6Al-4V |
876 |
0 |
0.81 |
4.29 |
5667 |
6 |
| Ti54M |
815 |
1.5 |
1.18 |
4.34 |
5692 |
5 |
| ATI425 |
802.8 |
0.5 |
1.65 |
4.36 |
5309 |
4 |
| SP700 |
725 |
2 |
1.96 |
4.39 |
5500 |
4.5 |
| ABD-SPTi |
672 |
3.0 |
4.61 |
4.51 |
5277 |
1.5 |
| ABD-SPTi LC |
715 |
3.0 |
2.55 |
4.46 |
4788 |
1 |
| ABD-SPTi LD |
723 |
3.0 |
2.52 |
4.41 |
4955 |
2.5 |
| ABD-SPTi LT |
631 |
3.0 |
2.49 |
4.52 |
5243 |
1.5 |
| ABD-SPTi HD |
713 |
3.0 |
5.37 |
4.47 |
5268 |
2 |
Table 5: Compositions of the titanium alloys derived using the proposed methodology.
| |
Comments |
Al |
V |
Fe |
Cr |
Ni |
Mo |
Si |
B |
| ABD-SPTi |
Nominal |
1.5 |
1.0 |
0.5 |
0.0 |
2.5 |
3.0 |
0.5 |
0.1 |
| ABD-SPTi LC |
Lowest cost |
1.0 |
0.5 |
3.0 |
0.0 |
0.0 |
1.0 |
0.5 |
0.1 |
| ABD-SPTi LD |
Lowest density |
2.5 |
1.0 |
3.0 |
0.0 |
0.0 |
1.0 |
0.5 |
0.1 |
| ABD-SPTi LT |
Lowest temp. |
1.5 |
1.5 |
3.0 |
0.0 |
0.0 |
3.0 |
0.5 |
0.1 |
| ABD-SPTi HD |
Highest diff. |
2.0 |
1.0 |
0.0 |
0.0 |
3.0 |
2.0 |
0.5 |
0.1 |
[0043] The method described above was used to isolate the inventive alloy composition. The
design intent for this alloy was to achieve good cold formability, superplastic forming
at relatively low temperatures and with low stress. The cost of the alloy was to be
comparable to or lower than those currently commercially available. Those properties
were given more importance than the density and stability merit index.
[0044] The material properties, determined using the above described method, for the commercially
used alloys of Table 1 are listed in Table 4 along with those of an alloy falling
within the present invention. This shows a greatly reduced superplastic forming temperature
along with a greatly increased diffusivity merit index (meaning a lower stress is
required for superplastic forming) along with a low amount of aluminium allowing good
cold formability. The cost of the alloy is also lower than the majority of the commercially
available alloys and at least comparable to the cheapest commercially available alloys.
The density of the alloy is a little greater than those of the commercial alloys and
the stability merit index is also higher.
[0045] Because of the lower amounts of aluminium and vanadium than the commercially available
alloys, the alloy of the present invention can also be expected to be less strong
than the commercially available alloys. The lower stability means that the alloy is
also more prone to martensite formation.
[0046] Figure 1 is a flow diagram of the process for designing the alloy of the present
invention. As a first step a design space is defined. The design space is shown in
Table 2. The design space is then discretised into many different individual alloy
compositions and for each of those individual alloy compositions thermodynamic calculations
as described above are performed.
[0047] Based on the thermodynamic calculations and calculated merit indices, the effect
of each alloying element on the import design parameters may be plotted. Figures 2-4
are such plots.
[0048] Figure 2 shows the effect of alloying components on the alloy density along the x
axis and the superplastic forming temperature along the y axis. What this shows is
that generally as alloys increase in density the superplastic forming temperature
decreases.
[0049] Figure 3 plots the effect of alloy composition against cost along the x axis and
superplastic forming temperature along the y axis. This shows that there is not such
a strong correlation between cost and superplastic forming temperature as between
density and superplastic forming temperature.
[0050] Figure 4 illustrates along the x axis the normalised diffusivity versus superplastic
forming temperature along the y axis for different compositions. What is striking
about these results is the strong influence of nickel on the normalised diffusivity.
[0051] The next stage of the design process was to determine the properties required of
the alloy. This is illustrated with the help of Figure 5. In Figure 5 the influences
from Figures 2-4 are plotted one against each other around the outside of the triangle.
Plotted inside the triangle is the position of the four commercial alloys of Table
1 and their relative performance in terms of cost, formability and density. Also plotted
is the balance of properties achieved by the present invention, namely relatively
low cost compared to the commercially available alloys, a similar density to the commercially
available alloys and better formability compared to the commercially available alloys.
[0052] Figures 6-17 are plots showing variations in certain merit indices with variation
in aluminium content along the x axis and vanadium content along the y axis for different
fixed amounts of other elements. Elements not mentioned are present at zero percent.
[0053] On the basis of the data in Figures 6-17 and on the calculated merit indices in Table
4 for existing commercial alloys, desired merit indices for the inventive alloy were
devised. These are shown in Figure 18 pictorially.
[0054] The strongest variation in a merit indices with composition is the variation in normalised
diffusivity with nickel content (Figure 4). In order to achieve as high diffusivity
as possible, as high an amount of nickel as possible whilst meeting the remainder
of the merit indices, is required. The strong effect of diffusivity of nickel can
be seen in Figure 4 and is also illustrated in Figure 17. Also as can be seen from
Figure 8, increasing nickel content also has the beneficial effect of reducing superplastic
forming temperature (a decrease in superplastic forming temperature in the graphs
going from the left to the right of Figure 8). Therefore a preferably minimum level
of nickel is set at 0.25% or more. In order to meet the requirement of a stability
merit index of 3.0 or less (see equation 4) whilst dramatically increasing diffusivity
merit index, the amount of nickel is limited to 3.0%. The nickel content may be replaced
by iron. This would advantageously further decrease the cost and the forming temperature
(see figures 13 and 14 and figures 7 and 8) at expense of reducing the normalised
diffusivity (see figures 16 and 17), but still maintain the diffusivity merit index
above 2.
[0055] One of nickel and iron (but not both) is present at 2.0% or more, to ensure that
the diffusivity merit index of at least 2 is met. The other of nickel and iron is
present at up to 1.0% to preserve microstructural stability. A desired minimum level
of nickel of 2.0% is chosen in order to meet a minimum of normalised diffusivity of
greater than 3.0 (see the central column of graphs in Figure 17).
[0056] A nickel content of up to 3.0% means that the lower levels of iron and chromium which
are also present in equation 4 is set at 0.0% to increase stability as much as possible.
At the lowest level of nickel of 2.0%, one of iron and chromium may be present at
up to 1.0%, thereby setting the upper limit for the amount of iron and chromium. If
both iron and chromium are present, they may be present at up to 0.5%, thereby setting
the preferred upper limit for iron and chromium. In the case of, an iron content of
up to 3.0%, the lower levels of nickel and chromium which are also present in equation
4, is set at 0.0% to increase stability as much as possible. At the lowest level of
iron of 2.0%, one of iron and chromium may be present at up to 1.0%, thereby setting
the upper limit for the amount of iron and chromium. If both nickel and chromium are
present, they may be present at up to 0.5%, thereby setting the preferred upper limit
for nickel and chromium. In any case, a preferred upper level of chromium is 0.5%
or less, preferably 0.4% or less to increase stability.
[0057] As can be seen from Figures 10 and 11, high levels of iron and nickel are generally
detrimental to density of the alloy. As can be seen from Figures 9-11, aluminium is
the element with the strongest influence on density. Therefore, the alloy contains
as much aluminium as possible to compensate for the high levels of iron or nickel.
[0058] However, aluminium is detrimental for most other properties which are intended to
be optimised in the inventive alloy. For a maximum level of nickel of 3.0%, Figure
11 shows that a minimum amount of aluminium of 0.5%, even with a maximum amount of
vanadium of 0.5% and a maximum amount of molybdenum of 4.0% (explained below) substantially
limits the density of the alloy to below 4.6 g/cm
3. If nickel is substituted by iron, density decreases. Thus, the minimum level of
aluminium is set to 0.5%, preferably 1.0% as this further reduces density.
[0059] Increasing levels of molybdenum beyond 4.0% deleteriously increases the density and
cost of the alloy so the maximum amount of molybdenum is set to 4.0%. However, increasing
levels of molybdenum help in reducing the superplastic forming temperature (see the
right hand column of Figure 8) without reducing the stability (molybdenum does not
appear in equation 4), whereas the other elements which are useful for reducing the
superplastic forming temperature are limited for other reasons. For example, iron
and chromium are limited by equation 4 and vanadium is limited by cost (see Figures
12-14). Therefore a minimum amount of molybdenum is set at 1.0% in order to reduce
the superplastic forming temperature substantially below 725°C (with maximum amounts
of aluminium of 2.5%, minimum amounts of vanadium of 0.5% (described below) and minimum
amounts of nickel of 2.0% (described above)). Desirably Mo is present in an amount
of at least 1.5% or even 2.5% as increasing levels reduce the superplastic forming
temperature. Most preferably Mo is present at least at 2.75% in order further to reduce
the superplastic forming temperature while keeping an stable microstructure. Desirably
Mo is present in an amount below 3.25% in order to keep the cost, diffusivity and
density of the alloy well within the design constrains.
[0060] Vanadium is beneficial in increasing the superplastic forming temperature (see Figures
6-8) whilst is substantially neutral in terms of its effect on density. Vanadium is
deleterious for the normalised diffusivity (see Figures 4 and 15-19). However, the
effect of vanadium on cost of the alloy is the largest factor in limiting the amount
of vanadium to 1.5%. By limiting the amount of vanadium to 1.5% the cost of the alloy
can be kept to 5300 or below (see Figures 12-14).
[0061] In order to benefit from the effect of vanadium in improving the superplastic forming
temperature without effecting stability (equation 4), a minimum level of vanadium
of at least 0.5% is chosen. This means that even at the lowest levels of molybdenum
and nickel and highest levels of aluminium, a superplastic deformation temperature
of substantially at most 725°C is achievable. Desirably V is present in an amount
of at least 1.0% in order to increase the strength of the alloy and to reduce further
the superplastic temperature.
[0062] Aluminium is limited due to its deleterious effect on cold formability, superplastic
formation temperature and diffusivity. Limiting aluminium content to 2.5% or less
enables the merit indices of Figure 18 to be achieved at the extremes of the alloy
range while also achieving a cold formability index lower than any of the commercially
available alloys of Table 1. Desirably Al is present in an amount of at least 1.0%
in order provide alloy strength and to help reducing the total density of the alloy.
[0063] On the basis of these considerations the composition of the alloy is determined in
accordance with Figure 19. The table shows that the amount of aluminium lying between
0.5 and 2.5% is much lower than that of the previous alloys. This manifests itself
in particular in the good cold formability of the inventive alloy as illustrated by
Table 4.
[0064] The amount of vanadium being between 0.5 and 1.5% is also much lower than that of
the commercial alloys of Table 1. This helps maintain the cost of the alloy low.
[0065] The amount of iron and chromium is also relatively limited when the amount of nickel
lies between 2.0 and 3.0% (which is relatively high). The high amount of nickel is
substantially responsible for the very high diffusivity merit index and low SPF temperature.
Desirably Ni and Fe are present in amounts below 2.5% in order provide good alloy
stability reducing the risk of brittle behaviour. Ni is preferable to Fe due to its
higher diffusivity but if cost and density are a primary concern one may substitute
Ni for Fe in amounts between 2.0 to 2.5 wt. % so that low SPF temperatures are achieved
but the alloy still offers a good microstructural stability.
[0066] The allowable amount of molybdenum and the preferred higher minimum levels are also
high compared to the commercially available alloys of Table 1. A combination of high
amounts of nickel and molybdenum are largely responsible for the low superplastic
forming temperature of the alloy of the present invention.
[0067] The amounts of silicon and boron are not arrived at from thermodynamic calculations
but instead are added from knowledge that they will increase the strength and creep
resistance and enhance the ductility of the alloy.
1. A titanium-based alloy composition consisting, in weight percent, of: between 0.5
and 2.5% aluminium, between 0.5 and 1.5% vanadium, between 0.0 and 3.0% iron, between
0.0 and 1.0% chromium, between 0.0 and 3.0% nickel, between 1.0 and 4.0% molybdenum,
between 0.0 and 1.0% silicon, between 0.0 and 0.2% boron, between 0.0 and 0.5% tin,
between 0.0 and 0.5% zirconium, between 0.0 and 1.0% niobium, between 0.0 and 1.0%
tantalum, between 0.0 and 0.5% calcium, between 0.0 and 0.5% carbon, between 0.0 and
0.5% manganese, the balance being titanium and incidental impurities, wherein one
of iron and nickel is present in an amount of at least 2.0% and the other of iron
and nickel is present in an amount of 1.0% or less.
2. The titanium-based alloy composition of claim 1, consisting of at least 1.0% aluminium.
3. The titanium-based alloy composition of claim 1 or 2, consisting of at most 2.25%
or less than 2.25% or 2.0% or less aluminium.
4. The titanium-based alloy composition of claim 1, 2 or 3, consisting of 0.5% or less
iron.
5. The titanium-based alloy composition of any of claims 1-4, consisting of 0.5% or less
chromium, preferably 0.4% or less chromium.
6. The titanium-based alloy composition of any of claims 1-5, consisting of 0.1% or more
Si, preferably 0.2% or more Si, more preferably 0.5% or more Si.
7. The titanium-based alloy composition of any of claims 1-6, consisting of 0.05% or
more boron, preferably 0.1% or more boron.
8. The titanium-based alloy composition of any of claims 1-7, consisting of 1.0% or more
vanadium.
9. The titanium-based alloy composition of any of claims 1-8, consisting of 1.5% or more
Molybdenum, preferably 2.5% or more molybdenum, more preferably 2.75% or more molybdenum.
10. The titanium-based alloy composition of any of claims 1-9, consisting of 3.25% or
less Molybdenum.
11. The titanium-based alloy composition of any of claims 1-10, wherein the microstructure
of the alloy composition is 30-50 vol % β-phase at SPF temperatures with the remainder
being a-phase.
12. The titanium-based alloy composition of any of claims 1-11, wherein Fe wt. % + Ni wt. % + Cr wt. % ≤ 3.5, preferably ≤ 3.0, and/or
wherein Fe wt.% + Ni wt.% < 2.5%..
13. The titanium-based alloy composition of any of claims 1-12, wherein Nb wt. % + Mo wt. % ≤ 4.0, and/or
wherein Zr wt. % + Sn wt. % + Mo wt.% ≤ 4.0, and/or
wherein Cr wt.% + Mn wt.% ≤ 0.5.
14. The titanium-based alloy composition of any of claims 1 - 13, consisting of 0.25%
or more nickel.
15. A thermoformed product made of the alloy composition of any of claims 1-14.
1. Legierungszusammensetzung auf Titanbasis, die in Gewichtsprozent aus Folgendem besteht:
zwischen 0,5 und 2,5 % Aluminium, zwischen 0,5 und 1,5 % Vanadium, zwischen 0,0 und
3,0 % Eisen, zwischen 0,0 und 1,0 % Chrom, zwischen 0,0 und 3,0 % Nickel, zwischen
1,0 und 4,0 % Molybdän, zwischen 0,0 und 1,0 % Silizium, zwischen 0,0 und 0,2 % Bor,
zwischen 0,0 und 0,5 % Zinn, zwischen 0,0 und 0,5 % Zirkonium, zwischen 0,0 und 1,0
% Niob, zwischen 0,0 und 1,0 % Tantal, zwischen 0,0 und 0,5 % Calcium, zwischen 0,0
und 0,5 % Kohlenstoff, zwischen 0,0 und 0,5 % Mangan, wobei der Rest Titan und zufällige
Verunreinigungen ist, wobei eines aus Eisen und Nickel in einer Menge von mindestens
2,0 % und das andere aus Eisen und Nickel in einer Menge von 1,0 % oder weniger vorhanden
ist.
2. Legierungszusammensetzung auf Titanbasis nach Anspruch 1, bestehend aus mindestens
1,0 % Aluminium.
3. Legierungszusammensetzung auf Titanbasis nach Anspruch 1 oder 2, bestehend aus höchstens
2,25 % oder weniger als 2,25 % oder 2,0 % oder weniger Aluminium.
4. Legierungszusammensetzung auf Titanbasis nach Anspruch 1, 2 oder 3, bestehend aus
0,5 % oder weniger Eisen.
5. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-4, bestehend aus
0,5 % oder weniger Chrom, bevorzugt 0,4 % oder weniger Chrom.
6. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-5, bestehend aus
0,1 % oder mehr Si, bevorzugt 0,2 % oder mehr Si, bevorzugter 0,5 % oder mehr Si.
7. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-6, bestehend aus
0,05 % oder mehr Bor, bevorzugt 0,1 % oder mehr Bor.
8. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-7, bestehend aus
1,0 % oder mehr Vanadium.
9. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-8, bestehend aus
1,5 % oder mehr Molybdän, bevorzugt 2,5 % oder mehr Molybdän, bevorzugter 2,75 % oder
mehr Molybdän.
10. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-9, bestehend aus
3,25 % oder weniger Molybdän.
11. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-10, wobei die
Mikrostruktur der Legierungszusammensetzung 30-50 Vol-% β-Phase bei SPF-Temperaturen
ist, wobei der Rest a-Phase ist.
12. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-11, wobei Fe Gew.-% + Ni Gew.-% + Cr Gew.-% ≤ 3,5, bevorzugt ≤ 3,0 und/oder
wobei Fe Gew.-% + Ni Gew.-% < 2,5 %.
13. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-12, wobei Nb Gew.-% + Mo Gew.-% ≤ 4,0 und/oder
wobei Zr Gew.-% + Sn Gew.-% + Mo Gew.-% ≤ 4,0 und/oder
wobei Cr Gew.-% + Mn Gew.-% ≤ 0,5.
14. Legierungszusammensetzung auf Titanbasis nach einem der Ansprüche 1-13, bestehend
aus 0,25 % oder mehr Nickel.
15. Warmgeformtes Produkt, das aus der Legierungszusammensetzung nach einem der Ansprüche
1-14 hergestellt ist.
1. Composition d'alliage à base de titane constituée, en pourcentage en poids, par :
entre 0,5 et 2,5% d'aluminium, entre 0,5 et 1,5% de vanadium, entre 0,0 et 3,0% de
fer, entre 0,0 et 1,0% de chrome, entre 0,0 et 3,0% de nickel, entre 1,0 et 4,0% de
molybdène, entre 0,0 et 1,0% de silicium, entre 0,0 et 0,2% de bore, entre 0,0 et
0,5% d'étain, entre 0,0 et 0,5% de zirconium, entre 0,0 et 1,0% de niobium, entre
0,0 et 1,0% de tantale, entre 0,0 et 0,5% de calcium, entre 0,0 et 0,5% de carbone,
entre 0,0 et 0,5% de manganèse, le reste étant du titane et des impuretés accidentelles,
dans laquelle l'un parmi le fer et le nickel est présent en une quantité d'au moins
2,0% et l'autre parmi le fer et le nickel est présent en une quantité de 1,0% ou moins.
2. Composition d'alliage à base de titane selon la revendication 1, constituée par au
moins 1,0% d'aluminium.
3. Composition d'alliage à base de titane selon la revendication 1 ou 2, constituée par
au plus 2,25% ou moins de 2,25% ou 2,0% ou moins d'aluminium.
4. Composition d'alliage à base de titane selon la revendication 1, 2 ou 3, constituée
par 0,5% ou moins de fer.
5. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 4, constituée par 0,5% ou moins de chrome, de préférence 0,4% ou moins de chrome.
6. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 5, constituée par 0,1% ou plus de Si, préférablement 0,2% ou plus de Si, plus préférablement
0,5% ou plus de Si.
7. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 6, constituée par 0,05% ou plus de bore, préférablement 0,1% ou plus de bore.
8. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 7, constituée par 1,0% ou plus de vanadium.
9. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 8, constituée par 1,5% ou plus de molybdène, préférablement 2,5% ou plus de molybdène,
plus préférablement 2,75% ou plus de molybdène.
10. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 9, constituée par 3,25% ou moins de molybdène.
11. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 10, dans laquelle la microstructure de la composition d'alliage est de 30 à 50%
en volume de phase β aux températures SPF, le reste étant une phase a.
12. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 11, dans laquelle Fe % en poids + Ni % en poids + Cr% en poids ≤ 3,5, de préférence
≤ 3,0, et / ou
dans laquelle Fe% en poids + Ni % en poids < 2,5%.
13. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 12, dans laquelle Nb % en poids + Mo % en poids ≤ 4,0, et / ou
dans laquelle Zr % en poids + Sn % en poids + Mo % en poids ≤ 4,0, et / ou
dans laquelle Cr % en poids + Mn % en poids ≤ 0,5.
14. Composition d'alliage à base de titane selon l'une quelconque des revendications 1
à 13, constituée par 0,25% ou plus de nickel.
15. Produit thermoformé fabriqué à partir de la composition d'alliage selon l'une quelconque
des revendications 1 à 14.