U.S. patent number 3,622,406 [Application Number 04/710,631] was granted by the patent office on 1971-11-23 for dispersoid titanium and titanium-base alloys.
This patent grant is currently assigned to Titanium Metals Corporation of America. Invention is credited to Milton B. Vordahl.
| United States Patent |
3,622,406 |
| Vordahl |
November 23, 1971 |
DISPERSOID TITANIUM AND TITANIUM-BASE ALLOYS
Abstract
As a new article of manufacture a base metal of the group
titanium and titanium base alloys containing a dispersoid of the
group consisting of thorium, boron, rare earth elements having an
atomic number of 57-71, and elements of groups IIIb and IIIc of the
periodic table of elements, which are substantially insoluble in
solid titanium but soluble in molten titanium, and combinations and
compounds thereof, preferably in proportions of about 0.1 to 6
percent by weight of the total, and wherein said dispersoid is
preferably dispersed in a particle size of several microns and
under, said article being characterized by high-elevated
temperature creep strength.
|
Inventors: |
Vordahl; Milton B. (Henderson,
NV) |
|
Assignee: |
Titanium Metals Corporation of
America (New York, NY)
|
| Family
ID: |
24854867 |
| Appl.
No.: |
04/710,631 |
| Filed: |
March 5, 1968 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
Issue Date |
|
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558589 |
Jun 20, 1966 |
3379522 |
|
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| Current U.S.
Class: |
148/401; 75/252;
75/255; 148/421; 419/12; 428/338; 428/546; 75/254; 148/407; 419/10;
420/419 |
| Current CPC
Class: |
C22C
14/00 (20130101); C22C 1/0458 (20130101); Y10T
428/12014 (20150115); Y10T 428/268 (20150115) |
| Current International
Class: |
C22C
14/00 (20060101); C22C 1/04 (20060101); C22c
015/00 (); C22c 031/04 () |
| Field of
Search: |
;75/175.5,201,202
;148/32,32.5 ;29/182,182.5,182.7 |
References Cited
[Referenced By]
U.S. Patent Documents
Foreign Patent Documents
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726,203 |
|
Mar 1955 |
|
GB |
|
594,813 |
|
Mar 1960 |
|
CA |
|
Other References
Titanium Abstracts Bulletin, Vol. 4, Imperical Chemical Ind.
Limited, July 1958-June 1959, pg. 122.
|
Primary Examiner: Lovell; Charles N.
Parent Case Text
This application is a continuation-in-part of my copending
application Ser. No. 558,589, filed June 20, 1966, now U.S. Pat.
No. 3,379,522.
Claims
What is claimed is:
1. As a new article of manufacture, a base metal selected from the
group consisting of titanium and titanium base alloys containing a
dispersion of a dispersoid selected from the group consisting of
boron, thorium, rare earth elements having an atomic number of 57
to 71, scandium, yttrium, actinium, and compounds and combinations
thereof which are substantially insoluble in solid titanium but
soluble in molten titanium, the particle size of said dispersoid
being predominantly of the order of one micron and under.
2. An article according to claim 1 wherein said dispersoid
comprises 0.1 to 6 percent by weight of the total.
3. The article of claim 2 wherein the dispersoid is boron, titanium
boride, thorium, cerium, cerium sulfide, lanthanum, or lanthanum
sulfide.
4. The article of claim 1 wherein the dispersoid is boron.
5. The article of claim 1 wherein the dispersoid is thorium.
6. The article of claim 1 wherein the dispersoid is cerium.
7. The article of claim 1 wherein the dispersoid is cerium
sulfide.
8. The article of claim 1 wherein the dispersoid is lanthanum
sulfide.
9. A cast article according to claim 2.
10. A wrought article according to claim 2.
11. An article according to claim 1 consisting essentially of
about: 6 percent aluminum, 4 percent vanadium, 0.25 to 1 percent
boron and the balance substantially titanium.
Description
This invention pertains to titanium and titanium-base alloys
containing dispersions of particles essentially insoluble in solid
titanium at any temperature but soluble in molten titanium, and to
methods of producing such dispersoid alloys.
More particularly the invention pertains to titanium-base alloys
containing finely divided particle dispersions of one or more
dispersoids selected from the group consisting of boron, thorium,
groups IIIb and IIIc of the periodic table of elements set forth
inside the forth cover of "The Merck Index," seventh edition, 1960,
published by Merck & Co., Inc., Rahway, New Jersey elements
having atomic numbers 57 through 71 which may be designated rare
earth elements, and compounds of the foregoing such as the sulfides
as well as combinations of any of them, which are substantially
insoluble in solid titanium at any temperature but soluble in
molten titanium. The preferred dispersoids are boron, cerium,
thorium, lanthanum and combinations and compounds thereof, such as
TiB, CeS, LaS, misch metal and other mixed rare earth sulfides, and
the like. The rare earths and especially cerium and lanthanum are
most preferably used as the sulfides whereas the boron and thorium
are preferably used in the elemental form. The method for producing
dispersions of the present invention involves melting the
components to form a homogeneous liquid preferably thence extreme
chill-casting the liquid as by splashing it in thin layers against
a cold solid surface or by spraying the liquid into a cold chamber
wherein it freezes as fine shot, and finally consolidating the shot
and splashings by pressure, heat and plastic deformation into a
product of essentially theoretically full density.
In the extreme chill-casting described, the dispersoid particle
components, although soluble in the liquid titanium, are
substantially insoluble in solid titanium and are thus forced by
freezing of the liquor to separate as particle of extreme fineness
because of the very short time available for growth. Thus the
dispersoid particles ordinarily appear as submicron-sized
dispersions within the shot or splashed flakes which, although fine
themselves relative to any standard ingots, are very coarse
relative to the dispersoid particles. That is, the shot or flakes
may be from perhaps 50 to 100 microns to several hundred microns in
mean section, and the dispersed particles therein will be on the
order of several microns to less than 1 microns in particles
size.
The dispersoid as present in the final solid alloy may appear as a
compound with one or more of the materials present in the base
alloy. Thus, for example, when elemental boron is added, the final
solid alloy may contain the boron as TiB. As used herein, reference
to the novel base metal alloys of the present invention as
including a given dispersoid is to be understood as meaning the
dispersoid as added irrespective of the form in which it appears in
the final product.
The advantages of fine particles dispersions in alloys for elevated
temperature use are well-known, as are several methods for
producing them. Most commonly, dispersions of particles in a base
metal are formed as precipitates therein by suitable heat treatment
of alloys containing components which are soluble in the solid
alloy at high temperatures and less soluble at low. Such systems
are very numerous and of great usefulness. Since the precipitate
components are soluble at high temperatures, however, they tend to
be of limited elevated temperature usefulness generally, and for
use beyond their temperature range, dispersoids substantially
insoluble in the solid matrix are required.
Alloys containing substantially insoluble, stable and inert
particles dispersions, and certain methods of making them are also
well-known. The most used conventional method consists of mixing
extremely fine powders of base metal and of dispersoids,
compacting, sintering and working the mixtures to solidify them. In
the case of titanium, the high reactivity of submicron powders
thereof and the ready solubility of contaminants, as for example,
oxygen and nitrogen from the air, make the powder approach
impractical. Shot and flake as described herein have several
hundred times less surface per unit mass than conventional powders,
and handling is therefore not difficult. The micron or submicron
particles exist in the shot and flake as made according to the
invention and titanium powder of such small particle size is
unnecessary.
Another known method of making stable dispersoid systems consists
of internal oxidation of solid solutions of active metals in a less
reactive base metal, such for example as titanium containing in
solid solution, certain rare earth metals which can be oxidized in
situ to form stable particles of oxide. The combined requirements
of solid solubility of the metallic component of the dipersoid,
plus greater reactivity then titanium, essentially limits the
possibilities for this approach to the rare earths which are
soluble in solid titanium. Also such rare earth oxides are stable
only in titanium which of itself contains a substantial oxygen
content, which is in some instances undesirable.
The dispersoids above-mentioned with reference to this invention,
are all substantially insoluble in solid titanium, and when present
as micron or submicron dispersions as produced in accordance with
the methods of the invention, impart outstanding elevated
temperature creep properties operable to higher temperature levels
than is attainable with dispersoid type titanium and titanium-base
alloy materials heretofore available insofar as I am aware.
Additionally, compositions of the present invention, especially
those containing boron as the dispersoid display a substantial
resistance to hot salt corrosion cracking. Quick satisfactory
results are obtained in this regard at boron inclusions of about
0.25 to about 1 percent.
EXAMPLE
In the practice of the invention, titanium or titanium alloys in
the molten state containing about 0.1 to 6 percent in total amounts
of one or more elements, compounds or mixtures as aforesaid which
are soluble in the molten base metal but insoluble in the solid
state thereof, are shotted as described for example, in U.S. Pat.
No. 2,897,539. The shot are then consolidated into billets by known
methods such as canning and hot pressing. Mill products are made
from the hot pressed billets by conventional means as by forging,
rolling, extruding, etc.
Maximum usefulness of inert dispersoid-containing alloys as
described herein occurs under conditions of very long time and/or
high-temperature exposure.
The following table I shows for a Ti-6A1-2Sn-4Zr-2Mo alloy, creep
strength with long-term aging without and with an inert submicron
dispersoid according to the invention.
Table I
Creep Deformation of Cast Alloys Aged 200 Hours at 1,100.degree. F.
And
---------------------------------------------------------------------------
Stressed to 30 Ks.i. at 1,000.degree. F. for 150 Hours
Alloy Deformation %
__________________________________________________________________________
Ti-6Al-2Sn-4Zr-2Mo 0.421 Ti-6Al-2Sn-4Zr-2Mo-1.7 Ce-0.5S 0.167
__________________________________________________________________________
inclusion of the dispersoid thus reduces the creep deformation
approximately 60 percent in this alloy.
The effects of dispersoid particle size variation in titanium and
titanium base alloys is shown by the following comparative tests.
In table II below a dispersoid was produced in a very
coarse-grained condition in the two titanium base alloys shown, and
the creep deformation measured for the alloy without and with the
dispersoid. ##SPC1##
It is thus shown that extremely coarse grained dispersoids are
damaging to creep. In contrast in the following table III, there is
shown the effect of a fine dispersoid on the order of 1 micron in
particle size.
TABLE III
Deformation Alloy 1,000.degree. F.-30 Kp.s.i.-150 Hr. Ti-8A1 0.06
Ti-8A1. and dispersoid 0.005
Thus the presence of an inert dispersoid in particle size on the
order of several microns and under greatly improves the creep
properties.
The following table IV gives the elevated temperature creep
properties of various "as cast" base metal and dispersoid alloys
according to the invention, wherein the base metal or base metal
plus dispersoid additions were melted up and cast into test
specimens. The specimens were then aged for about 24 hours at about
1,100.degree. F. before testing. ##SPC2##
It will be seen from the test results of table IV that the
dispersoid additions have in each instance greatly increased the
creep strength of the base alloy in cast specimens produced as
above.
The following table V shows the effects on creep properties of
taking as cast alloys produced as above and subsequently working
the same as by forging or rolling and thence aging prior to
testing. It has been found in this connection that creep properties
of such wrought products are developed by working in the alpha-beta
temperature field at about 1,700-1,800.degree. F. followed by a
lower temperature aging treatment at about 1,100.degree. F. for
about 24 hours, although the benefits are not limited to such
processing. The specimens for the following table V data were
prepared in this way. ##SPC3##
It will thus be seen from the table V data that the dispersoid
additions greatly increase the creep properties of these alloys in
wrought and aged conditions.
Typical room temperature tensile properties of dispersoid alloys
according to the invention after creep testing in wrought form, as
in table V supra, are given in the following table VI. ##SPC4##
It will be seen from table VI that the dispersoid alloys according
to the invention have good strength and ductility after creep
testing.
I have further discovered as an additional feature of the present
invention that the alloy thereof containing about 6 percent
aluminum, 4 percent vanadium, 1 percent boron and the balance
substantially titanium, is substantially more resistant to hot salt
corrosion cracking than is the alloy without the boron addition.
The boron free, 6 percent Al-4 % V alloy shows severe cracking in
less than 100 hours of exposure to salt, NaCl, at 800.degree. F.
and under 25 Ks.i. stress. As compared to this, the above boron
containing alloy showed no visible cracking such as degraded
ductility in tensile tests after 100 hours at 800.degree. F. and at
30, 35, 40 and 50 Ks.i. stresses in separate tests. The following
table VII gives the results of a series of creep tests on the
aforesaid Ti-6Al-4V-1B alloy both as conducted in an air and in a
salt or chloride containing atmosphere. ##SPC5##
* * * * *