FIELD OF THE INVENTION
[0001] This invention relates to a Mn-based alloy of nonequilibrium austenite phase which
possesses excellent tensile strength and high ductility.
BACKGROUND OF THE INVENTION
[0002] Conventional Mn-based alloy assumes an A-12 type a-Mn structure containing 58 atoms
in the unit cell at room temperature. Therefore, the alloy is too brittle to be normally
worked or formed. Therefore, an inexpensive Mn-Al powder alloy has been found to have
a small amount of utility as a material for a.magnet. None of the Mn-based alloys
existing today possess any appreciable degree of strength, elongation and high ductility.
SUMMARY OF THE INVENTION
[0003] An object of this invention is to provide a Mn-based alloy which is very rich in
ductility and workability, capable of being cold worked, and excellent in mechanical
properties including tensile strength. Another object of this invention,is to provide
a Mn-based alloy which is useful in a great variety of products such as nonmagnetic
electromagnetic parts, composite materials, and textile materials.
[0004] As a result of diligent efforts to meet the objects .described above, the present
inventors have found that a Mn-based alloy of a specific composition, when solidified
by quenching, retains intact (even at room temperature) an austenite phase which is
stable only at elevated temperatures. The Mn-based alloy having a nonequilibrium austenite
phase at room temperature is very rich in ductility and workability and capable of
being cold worked.
[0005] More specifically, the invention is directed to providing a Mn-based alloy having
a nonequilibrium austenite phase. The alloy is produced by solidifying by quenching
an alloy comprising 4 to 30 atomic % of at least one element selected from the group
consisting of Al, Ni, and Cr, 1 to 15 atomic % of C, not more than 30 atomic % of
at least one element selected from the group consisting of Co, Mo, W, Ta, Nb, V, Ti,
and Zr. The balance of the alloy making up 100 atomic % is comprised substantially
of Mn. The Mn-based alloy of a nonequilibrium austenite phase provided by this invention
is very rich in ductility and workability. Furthermore, the alloy is capable of being
cold worked, excellent in mechanical properties including tensile strength, inexpensive
and, therefore, is highly useful in nonmagnetic electromagnetic parts, composite materials
textile materials, etc.
DETAILED DESCRIPTION OF PREFERRED EIMBODIMENT
[0006] The Mn-based alloy of a nonequilibrium austenite phase according to this invention
is obtained by quenching and solidifying a molten alloy which comprises 4 to 30 atomic
% of at least one element selected from the group consisting of Al, Ni, and Cr, 1
to 15 atomic % of C, not more than 30 atomic % of at least one element selected from
the group consisting of Co, Mo, W, Ta, Nb, V, Ti, and Zr, and the balance to make
up 100 atomic % being comprised substantially of Mn.
[0007] The Mn-based alloy of this invention will now be described. It contains at least
one element selected from the group consisting of Al, Ni, and Cr in a concentration
of 4 to 30 atomic %. The elements and percentage amounts described above represent
the metallic elements and the amounts which are essential for the purpose of enabling
a Mn-alloy in a molten state to be solidified by quenching into a tough Mn-based alloy,
whereby the austenite phase which is stable only at elevated temperatures is supercooled
intact to room temperature. If the atomic % amount of these elements is less than
4 atomic %, the alloy produced will have very high brittleness because it can no longer
be expected to enjoy the effect described above and further because the alloy suffers
precipitation of an α-Mn phase.
[0008] An alloy which does not contain the indicated atomic % amounts of metals cannot be
used to produce continuous ribbons and thin wires of fixed shapes. If the concentration
exceeds 30 atomic %, the alloy to be produced is rigid and brittle due to the precipitation
of an intermetallic compound MnX (X denoting Ni, A1, or Cr). Thus, the alloy lacks
practicability. The elongation of the alloy material is effected by the amounts of
A1, Ni and/or Cr to be present. As the amount of these components increases, the elongation
of the alloy decreases. The tensile strength is not affected much by the content of
Al and is liable to increase with the content of Ni and/or Cr. The Mn-based alloy
of this invention further contains C in a concentration in the range of 1 to 15 atomic
%. The carbon must be present in this amount to enable the austenite phase to be cooled
down intact to room temperature when the molten Mn-based alloy is solidified by quenching.
If the concentration is less than 1 atomic %, the alloy obtained produces the nonequilibrium
austenite phase at room temperature with difficulty and shows very high brittleness
because the quenching does not easily manifest its effect. If the concentration exceeds
15 atomic %, the produced alloy is brittle due to the precipitation of a carbide Mn
23C
6.
[0009] When at least one element selected from the group consisting of Co, Mo, W, Ta, Nb,
V, Ti, and Zr is contained in a concentration of not more than 30 atomic %, the Mn
in the austenite phase which is stable only at elevated temperatures improves the
mechanical properties of the alloy such as tensile strength. This improvement is brought
about without impeding the conversion of the austenite phase, by quenching, into the
nonequilibrium austenite phase which is stable even at room temperature. However,
if the concentration of the elements exceeds 30 atomic %, the Mn-based alloy will
be too brittle to be useful due to the precipitation of a MnY (Y denoting Co, Mo,
W, Ta, Nb, V, Ti, and/or Zr) type compound. Particularly in the aforementioned alloy
composition, an alloy composed of 7 to 26 atomic % of at least one element selected
from the group consisting of Al, Ni and Cr, 3 to 10 atomic % of C, not more than 30
atomic % of at least one element selected from the group consisting of Co, Mo, W,
Ta, Nb, V, Ti and Zr (providing that Co have concentration not exceeding 30 atomic
%, Mo and/or W have concentration not exceeding 20 atomic % and the at least one element
selected from the group consisting of Ta, Nb, V, Ti and Er have concentration not
exceeding 10 atomic %), and the balance to make up 100 atomic % being comprised substantially
of Mn (e.g., 25 to 95 atomic % of Mn), when converted from its molten state by quenching
into a solid state, assumes a highly tough austenite phase.
[0010] The Mn-based alloy of the present invention is highly desirable because uniform ribbons
or thin wires of a circular cross section can be manufactured from this alloy. Moreover,
the Mn-based alloy of this composition is capable of being cold rolled or cold drawn.
Particularly with respect to wire drawing, it should be noted that the workability
such as cold drawing of this alloy can be effected to more than 90% of reduction of
area. The alloy is advantageous in that the tensile strength at fracture notably increases
proportionally with respect to increases in the area of reduction. The alloy has been
found to be highly suitable for economic production of nonferrous and nonmagnetic
heavy-duty metal fibers having diameters not exceeding about 150 um,preferably 50
um or more. The reduction ratio of area is represented by the following equation:

wherein D is a diameter of wire before the wire drawing and d is a diameter of the
thin wire after repeatedly wire drawing. That is, it shows the reduction ratio of
the cross section of thin wire to be reduced in accordance with subjecting to the
drawing workability.
[0011] An alloy of the present invention may include additional elements such as Si, B,
P, Ge, Cu, and Hf in addition to the essential elements of this invention provided
in that these additional elements are only present within a range in which the objects
and effects of this invention are not impaired by their presence.
[0012] The particle diameter of microcrystals in the nonequilibrium austenite phase varys
with the alloy composition and cooling speed. However, it should be pointed out that
it is the successful formation of the austenite phase and not the magnitude of the
particle diameter of the crystals which is important.
[0013] The alloy of this invention is produced by preparing a molten alloy in the aforementioned
composition and quenching this molten alloy. Various methods are available for effecting
this quenching. For example, the single roll method, the double roll method, and the
submerged rotary spinning method which are liquid quenching methods are particularly
effective. Plates of the alloy may be produced by the piston-anvil method, the splat
etching method, etc.. The aforementioned liquid quenching methods (single roll method,
double room method, or submerged rotary spinning method) have a cooling speed in the
range of about 10
4 to 10
5°C/sec., while the piston-anvil method or the splat etching method has a cooling speed
in the range of about 10 to 10
6°C/sec. By using some of these quenching methods, therefore, the quenching of the
molten alloy can be efficiently carried out. The term "submerged rotary spinning method"
refers to a method as disclosed in Japanese Patent Application (OPI) No. 64948/80
(The term "OPI" as used herein refers to a "published unexamined Japanese patent application.).
The "submerged rotary spinning method is a method for obtaining a thin wire of a circular
cross section by placing water in a rotary drum in motion thereby centrifugally forming
a film of water on the inner wall surface of the drum and extruding molten alloy through
a spinning nozzle into the water film. To produce a continuous thin wire uniformly
by this method, the peripheral speed of the rotary drum is preferably equal to or
greater than the speed of the flow of molten alloy being thrown out of the spinning
nozzle. Particularly, the peripheral speed of the rotary drum is preferably 5 to 30%
high than the speed of the flow of molten alloy extruded through the spinning nozzle.
The angle formed between the flow of molten metal extruded through the spinning nozzle
and the water film formed on the inner wall surface of the rotary drum is preferably
greater than 20°.
[0014] The Mn-based alloy of this invention has a wider range of equilibrium austenite phase
at elevated temperatures than the Fe-based alloy. It, therefore, acquires the nonequilibrium
austenite phase at room temperature over a wide range of alloy compositions. At the
same time, it enjoys stability because it is capable of keeping the austenite phase
from converting into martensite. Particularly, the alloy acquires-a large thick austenite
phase as compared with the Fe-X-C (X denoting Cr, Mo, W, or Al) alloy..This fact is
profoundly significant from the industrial point of view. When the Mn-based alloy
incorporates Cr, among other elements of the same group, it becomes highly resistant
to corrosion. Therefore, the alloy may be used in nonmagnetic corrosion- proofing
materials.
[0015] Moreover, the Mn-based alloy of this invention is capable of being cold worked continuously.
For the production of thin wires, for example, this Mn-based alloy can be cold drawn
to economically form wires of high tensile strength having diameters in the range
of 1 to 200 um. It is noteworthy that the tensile strength of the Mn-based alloy can
be improved to even more than 150 kg/mm
2. Such strength has not been previously attained using any of the nonferrous materials
developed to date.
[0016] Because the Mn-based alloy of this nvention has the quality and structure described
above, it can be readily used in the production of a variety of products including,
nonmagnetic high resistance materials, nonmagnetic springs, nonmagnetic switch relays,
belts, tires and other rubber reinforcements, plastics, concretes and other similar
composite materials, and knit and woven fabrics such as fine mesh filters.
[0017] The present invention will now be described more specifically below with reference
to working examples. However, the present invention is not limited to be following
examples.
Example 1
[0018] An alloy composed of 85 atomic % of Mn, 10 atomic % of A1, and 5 atomic % of C and
prepared in a molten state was extruded, under argon gas pressure of 2.5 kg/mm
2, through a spinning nozzle of a varying diameter of 0.1 to 1 mm. The extrusion was
made onto the surface of a steel roll having a diameter of 20 cm, rotating at a varying
speed of 1000 to 5000 rpm, cooled and solidified to produce ribbons of 10 to 500 µm
in thickness.
[0019] The ribbons thus obtained were noted to trend toward gradual loss of toughness in
proportion to growth in thickness. Up to about 500 µm of thickness, however, the ribbons
were capable of being bent by 180° and folded fast over themselves without fracture.
When the ribbons were tested for texture by observation through an optical microscope,
an X-ray diffraction meter and a transmission electron microscope, they were found
to be-composed of microcrystals of nonequilibrium austenite phase in the structure
of a face centered cubic lattice. The crystals measured about 1 to 5 µm. The crystals
showed a trend toward gradual growth in particle diameter in proportion to growth
in ribbon thickness.
[0020] The tough alloy ribbon having a nonequilibrium austenite phase and measuring 200
µm in thickness was tested for tensile strength by an Instron tension tester over
a test distance of 2.0 cm at a strain rate of 4.17 x 10
-4/sec. The ribbon was found to be a very tough material having tensile strength of
35kg/mm
2, yield strength of 15 kg/mm
2, and elongation of 22%.
Example 2
[0021] An alloy composed of 75 atomic % of Mn, 18 atomic % of A1, and 7 atomic % of C was
melted. The molten alloy was extruded, under argon gas pressure of 3.0 kg/cm , through
a spinning nozzle 150 µm in orifice diameter into a cooling water bath 2.5 cm in depth
formed centrifugally (350 rpm)
' within a rotary cylinder 50 cm in diameter, there to be cooled and solidified with
the rotating body of cooling water. As the thin wire of alloy of a circular cross
section was cooled and solidified, it was continuously wound up on the inner wall
of the rotary cylinder. (At this time, the speed of the cooling water (V
W) inside the rotary cylinder and the speed of the flow of molten alloy (V
J) extruded through the spinning nozzle were adjusted, thus V
W/V
J = 1.15.)
[0022] This operation produced a continuous thin wire of a substantially circular cross
section having a uniform diameter of 130 um.
[0023] When this thin wire was tested for texture in the same way as in Example 1, it was
found to have a nonequilibrium austenite phase in the structure of a fcc. The particle
diameter of the crystals was about 3 um.
[0024] This thin wire was found to be a highly tough material having tensile strength of
40 kg/mm2, yield strength of 25 kg/mm
2 and elongation of 4%.
[0025] This thin wire was cold drawn, without any process annealing, through a commercially
available diamond die up to 79% of reduction of area. During the cold drawing, the
wire sustained no damage of any sort. Thus, the cold drawing produced a very strong
thin wire having a highly uniform tensile strength of 160 kg/mm
2, a yield strength of 135 kg/ mm
2, and an elongation of 1.1%.
Example 3
[0026] By following the procedure of Example 2, a very tough continuous thin wire having
a circular cross section 130 µm in diameter was obtained from an alloy composed of
62 atomic % of Mn, 18 atomic % of Al, 8 atomic % of Cr, 7 atomic % of C, and 5 atomic
% of Ta.
[0027] When this thin wire was tested for texture by observation through an X-ray diffraction
meter and a transmission electron microscope, it was found to have a nonequilibrium
austenite phase of crystals Z to 3 µm in particle diameter. The thin wire had tensile
strength of 50 kg/mm
2, yield strength of 30 kg/mm
2, and elongation of 3.8%. These test results indicate that the addition of Cr and
Ta enabled the produced alloy to acquire enhanced toughness and improved tensile strength.
[0028] This thin wire was cold drawn, without'any process annealing, through a commercially
available diamond die to 79% of reduction of area. When the cold drawn wire was tested
for tensile strength under the same conditions, it was found to be a heavy-duty wire
having tensile strength of 190 kg/mm
2, yield strength of 140 kg/mm
2, and elongation of 0.
8 %.
[0029] While the invention has been described in detail and.with reference to specific embodiments
thereof, it will be apparent to one skilled in the art that various changes and modifications
can be made therein without departing from the spirit and scope thereof.
1. An Mn-based alloy, comprising:
4 to 30 atomic % of at least one element selected from the group consisting of Al,
Ni, and Cr;
1 to 15 atomic % of C;
30 atomic % or less of at least one element selected from the group consisting of
Co, Mo, W, Ta, Nb, V, Ti, and Zr; and
the balance of the alloy to make up 100 atomic % being comprised substantially of
Mn, the alloy having a nonequilibrium austenite phase.
2. An Mn-based alloy as claimed in Claim 1, wherein the alloy is comprised of from
25 to 95 atomic % of Mn.
3. An Mn-based alloy as claimed in Claim 1, wherein the alloy is comprised of from
7 to 26 atomic % of at least one element selected from the group consisting of Al,
Ni and Cr.
4. An Mn-based alloy as claimed in Claim 1, wherein the alloy is comprised of from
3 to 10 atomic % of C.
5. An Mn-based alloy as claimed in Claim 1, wherein the alloy is comprised of 30 atomic
% or less of at least one elemen-t selected from the group consisting of Co, Mo, W,
Ta, Nb, V, Ti, and'Zr.
6. An Mn-based alloy as claimed in Claim 5, wherein the alloy is comprised of 20 atomic
% or less of at least one element selected from the group consisting of Mo and W.
7. An Mn-based alloy as claimed in Claim 5, wherein the alloy is comprised of 10 atomic
% or less of at least one element selected from the group consisting of Ta, Nb, V,
Ti and Zr.