BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to a heat resistant Mg-Al-Zn-rare earth element magnesium
alloy which is superior in heat resistance and strength characteristics.
Description of the Related Art
[0002] Magnesium (Mg) has a specific gravity of 1.74, it is the lightest metal among the
industrial metallic materials, and it is as good as aluminum alloy in terms of the
mechanical properties. Therefore, Mg has been observed as an industrial metallic material
which can be used in aircraft, automobiles, or the like, and which can satisfy the
light-weight requirements, the fuel-consumption reduction requirements, or the like.
[0003] Among the conventional magnesium alloys, an Mg-Al alloy, for instance AM60B, AM50A,
AM20A alloys, etc., as per ASTM, includes 2 to 12% by weight of aluminum (Al), and
a trace amount of manganese (Mn) is added thereto. In the phase diagram of the Mg-Al
alloy, there is a eutectic system which contains alpha-Mg solid solution and beta-Mg₁₇Al₁₂
compound in the Mg-rich side. When the Mg-Al alloy is subjected to a heat treatment,
there arises age-hardening resulting from the precipitation of the Mg₁₇Al₁₂ intermediate
phase. Further, the Mg-Al alloy is improved in terms of the strength and the toughness
by a solution treatment.
[0004] Further, there is an Mg-Al-Zn alloy, for instance an AZ91C alloy or the like as per
ASTM, which includes 5 to 10% by weight of Al, and 1 to 3% by weight of zinc (Zn).
In the phase diagram of the Mg-Al-Zn alloy, there is a broad alpha solid solution
area in the Mg-rich side where Mg-Al-Zn compounds crystallize. The as-cast Mg-Al-Zn
alloy is tough and excellent in corrosion resistance, but it is further improved in
terms of the mechanical properties by age-hardening. In addition, in the Mg-Al-Zn
alloy, the Mg-Al-Zn compounds are precipitated like pearlite in the boundaries by
quenching and tempering.
[0005] In an as-cast Mg-Zn alloy, a maximum strength and elongation can be obtained when
Zn is added to Mg in an amount of 2% by weight. In order to improve the castability
and obtain failure-free castings, Zn is added more to Mg. However, an Mg-6% Zn alloy
exhibits a tensile strength as low as 17 kgf/mm² when it is as-cast. Although its
tensile strength can be improved by the T6 treatment (i.e., an artificial hardening
after a solution treatment), it is still inferior to that of the Mg-Al alloy. As the
Mg-Zn alloy, a ZCM630A (e.g., Mg-6% Zn-3% Cu-0.2% Mn) has been available.
[0006] Furthermore, a magnesium alloy has been investigated which is superior in heat resistance
and accordingly which is suitable for high temperature applications. As a result,
a magnesium alloy with rare earth element (hereinafter abbreviated to "R.E.") added
has been developed. This magnesium alloy has mechanical properties somewhat inferior
to those of aluminum alloy at an ordinary temperature, but it exhibits mechanical
properties as good as those of the aluminum alloy at a high temperature of from 250
to 300 °C. For example, the following magnesium alloys which include R.E. have been
put into practical application: an EK30A alloy which is free from Zn (e.g., Mg-2.5
to 4% R.E.-0.2% Zr), and a ZE41A alloy which includes Zn (e.g., Mg-1% R.E.-2% Zn-0.6%
Zr).
[0007] Among the above-described magnesium alloys, the Mg-Al or Mg-Al-Zn alloy is less expensive
in the costs, it can be die-cast, and it is being employed gradually in members which
are used at a low temperature of 60 °C at the highest. However, since the Mg-Al alloy
has a low melting point and since it is unstable at elevated temperatures, its high
temperature strength deteriorates and its creep resistance degrades considerably at
high temperatures.
[0008] For example, AZ91D alloy, one of the Mg-Al-Zn alloys similar to the AZ91C alloy,
is good in terms of castability, corrosion resistance and tensile strength at room
temperature and up to 150 °C, but it is inferior in terms of creep resistance at temperatures
of 100 °C or more. In the case that the creep resistance is low at elevated temperatures,
there arises a problem in that component parts made of such alloys exhibit deteriorating
tightening forces (i.e., axial forces) at the portions, for instance at the portions
tightened with a bolt, when the temperature is raised during their service. When the
component parts are produced by die casting, this problem is particularly notable.
[0009] The aluminum contained in the magnesium alloys forms Mg₁₇Al₁₂ crystals during the
solidification. When the cooling rate is as fast as die casting, there arise the areas
(i.e., the dendritic cells) adjacent to the grain boundaries, areas which contain
the solute atoms (e.g., aluminum atoms) prior to the crystallization in high concentrations.
Due to the presence of these unstable aluminum atoms, the grain boundary diffusion
is active in the environment where the temperature is elevated, and accordingly it
is believed that the unstable aluminum atoms facilitate the creep deformations.
SUMMARY OF THE INVENTION
[0010] The present invention has been developed in order to solve the aforementioned problems
of the conventional Mg-Al magnesium alloy for die casting, e.g., their inferior creep
resistance. It is therefore an object of the present invention to provide a heat resistance
magnesium alloy whose creep properties are improved at 150 °C, which securely exhibits
a predetermined tensile strength at room temperature and up to 100 °C, and whose castability
and corrosion resistance are enhanced.
[0011] In order to achieve the object, the present inventors investigated the aluminum concentrations
in magnesium alloys at which no dendritic cells are formed. As a result, they found
that the dendritic cells can be inhibited from forming by restricting the aluminum
concentration in a range of from 1.0 to 3.0% by weight. Further, they found that zinc
can be added effectively to magnesium alloys in an amount of from 0.25 to 3.0% by
weight to securely give the resulting products a predetermined tensile strength and
elongation at room temperature and up to 100 °C. Furthermore, they found that a rare
earth element, for example cerium (Ce) and neodymium (Nd), capable of forming crystals
of high melting points in grain boundaries of magnesium alloys can be added to magnesium
alloys in an amount of from 0.5 to 4.0% by weight to strengthen the grain boundaries
of the resulting magnesium alloys. Moreover, they found that manganese (Mn) can be
added to magnesium alloys in an amount of from 0.1 to 1.0% by weight to enhance the
proof stress, and that it can be added in a limited amount of from 0.2 to 0.3% by
weight thereto to enhance the corrosion resistance as well. Thus, the present inventors
completed a heat resistant magnesium alloy according to the present invention.
[0012] The present heat resistant magnesium alloy has excellent elongation and strength
properties, and it is expressed by a general formula, Mg-("a"% by weight)Al-("b"%
by weight)Zn-("c"% by weight)rare earth element, in which:
"a" stands for an aluminum content in a range of from 1.0 to 3.0% by weight;
"b" stands for a Zinc content in a range of from 0.25 to 3.0% by weight; and
"c" stands for a rare earth element content in a range of from 0.5 to 4.0% by weight;
and
when "b" is in a range, 0.25 ≦ "b" ≦ 1.0, "a" and "c" satisfy a relationship,
"c" ≦ "a" + 1.0; and
when "b" is in a range, 1.0 ≦ "b" ≦ 3.0, "a," "b" and "c" satisfy a relationship,
"c" ≦ "a" + "b" ≦ (1/2)"c" + 4.0.
[0013] Further, the present heat resistant magnesium alloy is enhanced, if necessary, in
terms of the proof stress by including Mn in an amount of from 0.1 to 1.0% by weight.
Furthermore, it is improved, if required, in terms of the corrosion resistance as
well by limitedly including Mn in an amount of from 0.2 to 0.3% by weight.
[0014] In the present heat resistant magnesium alloy, since the aluminum concentration is
restricted in the range of from 1.0 to 3.0% by weight where no dendritic cells are
formed, the resulting products made of the present heat resistant magnesium alloy
are improved in terms of the creep resistance at elevated temperatures of 100 °C or
more. Further, since Zn is added in the amount of from 0.25 to 3.0% by weight, the
resulting products made thereof are enhanced in terms of the tensile strength and
elongation at room temperature and up to 100 °C, and they are simultaneously upgraded
in terms of the castability. Furthermore, since a rare earth element, for example
Ce and Nd, is added in the amount of from 0.5 to 4.0% by weight, there are formed
the high melting point crystals in the grain boundaries of the present heat resistance
magnesium alloy so as to strengthen the grain boundaries, and thereby the resulting
products made thereof are improved in terms of the creep properties at 150 °C.
[0015] In particular, when Mn is added to the present heat resistant magnesium alloy in
the amount of 0.1 to 1.0% by weight, the resulting products made thereof exhibit an
improved proof stress and a less degrading initial bolt tightening axial force. Mn
can dissolve into grains even in a small addition amount, thereby effecting the solution
strengthening or hardening. As a result, Mn improves the proof stress of the resulting
products made thereof at room temperature and at elevated temperatures. Since the
deterioration of the initial axial force depends on the proof stress of materials
(i.e., members to be tightened), the addition of Mn is believed to result in the improvement.
Moreover, when Mn is added thereto in the limited amount of 0.2 to 0.3% by weight,
the resulting products made thereof exhibit enhanced corrosion resistance as well.
[0016] The reasons why the alloying elements of the present heat resistant magnesium alloy
are added and the composition ranges thereof are limited as set forth above will be
hereinafter described.
1.0 to 3.0% by weight of Al:
The axial force retention rate of products made of magnesium alloys decreases as
the Al content increases. Figure 1 illustrates the results of an evaluation on the
variation in the axial force retention rate of the test specimen made of a magnesium
alloy which comprised Zn in an amount of 2.0% by weight, R.E. in an amount of 2.9%
by weight, Mn in an amount of 0.2% by weight and balance of Mg and inevitable impurities,
and to which Al was added in amounts of from 0 to 4.0% by weight. A target value of
the axial force retention rate was designed to be 50% after degrading the test specimen
at 150 °C for 300 hours. Thus, the Al content of 3.0% by weight satisfying the target
value was taken as the upper limit. Figure 2 illustrates the results of an evaluation
on the hot tearings occurrence rate of the test specimen made of the same magnesium
alloy. As can be appreciated from the drawing, when the Al content was less than 1.0%
by weight, the hot tearings were more likely to occur. Thus, the Al content of 1.0%
by weight was taken as the lower limit. It is further preferred that the present heat
resistant magnesium alloy includes Al in an amount of from 1.5 to 2.5% by weight.
[0017] In the evaluation of the axial force retention rate, a tensile creep test was carried
out in order to measure the creep deformation amounts of the test specimens. Here,
the magnesium alloys were melted and processed into a cylindrical test specimen having
an inside diameter of 7 mm, an outside diameter of 15 mm and a length of 25 mm by
die casting with a hot chamber at a casting temperature of 690 °C, at mold temperatures
of 80 to 120 °C and under a casting pressure of 300 kgf/cm². This cylindrical test
specimen was tightened with a bolt and a nut at the ends under a surface pressure
of 6.5 kgf/mm² at ordinary temperature, it was held in an oven whose temperature was
raised to 150 °C for 300 hours, and thereafter an elongation of the bolt was measured
in order to examine for an axial force retention rate of the test specimen.
[0018] In the evaluation of the hot tearings occurrence rate, a hot tearings occurrence
test was carried out in order to observe the hot tearings occurred in the test specimens.
Here, the magnesium alloys were processed into a square-shaped box test specimen having
corners of predetermined radii hereinafter described in detail. As illustrated in
Figure 17, the test specimen 10 for die cast hot tearings occurrence test was a cylindrical
body which had a square shape in a cross section, it had a thickness of 3 to 4 mm,
and each of whose side had a length of 200 mm. A sprue 12 was disposed on a side 14,
and a heat insulator 18 was disposed on a side 16 which was opposite to the side 14
with the sprue 12 disposed. One end of the side 16 was made into a round corner 20
having a radius of 1.0 mm, and the other end of the side 16 was made into a round
corner 22 having a radius of 0.5 mm. This die cast hot tearings test specimen was
intended for examining the hot tearings which were caused either in the round corner
20 or 22 by the stress resulting from the solidification shrinkage. The solidification
shrinkage resulted from the solidification time difference between the portion covered
with the heat insulator 18 and the other portions.
0.25 to 3.0% by weight of Zn:
Figure 4 illustrates the results of an evaluation on the variation in the room
temperature tensile strength of the test specimen made of a magnesium alloy which
comprised Al in an amount of 2.0% by weight, R.E. in an amount of 2.9% by weight,
Mn in an amount of 0.2% by weight and balance of Mg and inevitable impurities, and
to which Zn was added in amounts of from 0 to 4.0% by weight. Figure 5 illustrates
the results of an evaluation on the variation in the elongation of the test specimen
made of the same magnesium alloy at 100 °C. Here, the tensile strength test was carried
out onto the test specimens which had a dumbbell-shaped configuration and dimensions
in accordance with ASTM "80-91," paragraph 12.2.1. As can be readily seen from Figures
4 and 5, the test specimen was improved not only in the room temperature tensile strength
but also in the 100 °C elongation by adding Zn in an amount of 0.25% by weight or
more. In view of the room temperature tensile strength alone, Zn is added preferably
in a range of 10% by weight or more. However, as can be seen from Figure 3 which illustrates
the results of an evaluation on the variation in the axial force retention rate of
the test specimen made of the same magnesium alloy, when Zn was added in a large amount,
the axial force retention rate was deteriorated. Therefore, the Zn content of 3.0%
by weight satisfying the aforementioned target axial force retention rate was taken
as the upper limit. It is further preferred that the present heat resistant magnesium
alloy includes Zn in an amount of from 0.5 to 1.5% by weight.
[0019] In particular, when Zn is added in a small amount, it dissolves into the grains of
magnesium alloys and forms compounds of high melting points together with Mg, Al and
R.E., thereby improving the tensile strength, the elongation and the creep resistance.
However, when Zn is added in a large amount, there also arise compounds of low melting
points which are comprised of Mg, Al and Zn but free from R.E. in the grain boundaries,
thereby deteriorating the creep resistance.
0.5 to 4.0% by weight of R.E.:
Figure 6 illustrates the results of an evaluation on the variation in the axial
force retention rate of the test specimen made of a magnesium alloy which comprised
Al in an amount of 2.0% by weight, Zn in an amount of 2.0% by weight, Mn in an amount
of 0.2% by weight and balance of Mg and inevitable impurities, and to which R.E. was
added in amounts of from 0 to 4.0% by weight. As can be readily understood from Figure
6, the test specimen was sharply improved in the axial force retention rate by adding
R.E. in an amount of 0.5% by weight or more. However, as can be seen from Figure 7
which illustrates the results of an evaluation on the variation in the room temperature
tensile strength of the test specimen made of the same magnesium alloy, when R.E.
was added in an amount of more than 4.0% by weight, the room temperature tensile strength
was deteriorated. Therefore, the R.E. content of 4.0% by weight was taken as the upper
limit. It is further preferred that the present heat resistant magnesium alloy includes
R.E. in an amount of from 2.5 to 3.5% by weight.
[0020] As for R.E., a misch metal containing cerium (Ce) as a major component can be employed
preferably, but magnesium alloys in which neodymium (Nd) substituted for the misch
metal equally produced the advantageous effects.
[0021] In particular, it is furthermore preferred that R.E. is a misch metal which includes
cerium (Ce) at least. It is moreover preferred that the misch metal includes Ce in
an amount of 45 to 55% by weight.
0.1 to 0.1% by weight of Mn:
Mn dissolves into grains, thereby effecting the solution strengthening or hardening.
As a result, the resulting products made of magnesium alloys containing Mn can be
inhibited from deteriorating in the initial axial force. In order to obtain this advantageous
effect, it is necessary to add Mn to magnesium alloys in an amount of 0.1% by weight
or more. The advantageous effect of inhibiting the initial axial force deterioration
is saturated by adding Mn thereto in an amount of around 0.4% by weight. However,
when Mn is added thereto in an amount of more than 1.0% by weight, the Mn-Al-R.E.
crystals are produced, thereby causing the hot tearings. Hence, the upper limit of
the Mn addition is set at 1.0% by weight. In particular, when Mn is added thereto
in an amount of 0.2% by weight or more, Mn and Al simultaneously operate so as to
remove Fe which adversely affects the corrosion resistance of the resulting products.
However, when Mn is added thereto in an amount of more than 0.3% by weight, no improvement
can be appreciated in the corrosion resistance. Therefore, when improved corrosion
resistance is desired, it is preferable to set the upper limit of the Mn addition
at 0.3% by weight.
[0022] In addition, in the present heat resistant magnesium alloy, the aluminum content
"a," the zinc content "b" and the R.E. content "c" are arranged so as to satisfy the
relationship, "c" ≦ "a" + 1.0, when "b" is in the range, 0.25 ≦ "b" ≦ 1.0, and the
relationship "c" ≦ "a" + "b" ≦ (1/2)"c" + 4.0, when "b" is in the range, 1.0 ≦ "b"
≦ 3.0. They are designed so as to satisfy the relationships because the resulting
products are degraded in the room temperature tensile strength when R.E. is added
in an amount of more than an amount calculated from the Al content, i.e., the Al content
with a factor of 1.0 added thereto (e.g., "a" + 1.0), and because the resulting products
are deteriorated in the creep properties at elevated temperatures when Al and Zn are
added in total more than an amount calculated from the R.E. content, i.e., the R.E.
content multiplied by half and a factor of 4.0 added thereto (e.g., (1/2)"c" + 4.0).
[0023] Thus, the present heat resistance magnesium alloy is expressed by the general formula,
Mg-("a"% by weight)Al-("b"% by weight)Zn-("c"% by weight) rare earth element, in which:
"a" stands for an aluminum content in a range of from 1.0 to 3.0% by weight; "b" stands
for a zinc content in a range of from 0.25 to 3.0% by weight; and "c" stands for a
rare earth element content in a range of from 0.5 to 4.0% by weight; and when "b"
is in a range, 0.25 ≦ "b" ≦ 1.0, "a" and "c" satisfy a relationship, "c" ≦ "a" + 1.0;
and when "b" is in a range, 1.0 ≦ "b" ≦ 3.0, "a," "b" and "c" satisfy a relationship,
"c" ≦ "a" + "b" ≦ (1/2)"c" + 4.0. Since the aluminum content is restricted in the
range of from 1.0 to 3.0% by weight where no dendritic cells are formed, the resulting
products made of the present heat resistant magnesium alloy can be improved in terms
of the creep resistance at elevated temperatures of 100 °C or more. Since Zn is added
in the amount of from 0.25 to 3.0% by weight, the resulting products made thereof
can securely exhibit the tensile strength and elongation at room temperature and up
to 100 °C and it can be simultaneously enhanced in terms of the castability. Since
a rare earth element, for example Ce and Nd, is added in the amount of from 0.5 to
4.0% by weight, there are formed the high melting point crystals in the grain boundaries
of the present heat resistance magnesium alloy so as to strengthen the grain boundaries,
and thereby the resulting products made thereof are upgraded in terms of the creep
properties at 150 °C. In the case that Mn is further added in the amount of from 0.1
to 1.0% by weight, the resulting products can be inhibited from deteriorating in terms
of the initial axial force, and, in particular, in the case that Mn is further added
in the limited amount of from 0.2 to 0.3% by weight, the resulting products can be
further enhanced in terms of the corrosion resistance as well.
BRIEF DESCRIPTION OF THE DRAWINGS
[0024] A more complete appreciation of the present invention and many of its advantages
will be readily obtained as the same becomes better understood by reference to the
following detailed description when considered in connection with the accompanying
drawings and detailed specification, all of which forms a part of the disclosure:
Figure 1 is a graph illustrating the relationship between the axial force retention
rate and the Al contents of the present heat resistant magnesium alloy;
Figure 2 is a graph illustrating the relationships between the hot tearings occurrence
rate and the Al contents of the present heat resistant magnesium alloy;
Figure 3 is a graph illustrating the relationship between the axial force retention
rate and the Zn contents of the present heat resistant magnesium alloy;
Figure 4 is a graph illustrating the relationship between the tensile strength at
room temperature and the Zn contents of the present heat resistant magnesium alloy;
Figure 5 is a graph illustrating the relationship between the elongation at 100 °C
and the Zn contents of the present heat resistant magnesium alloy;
Figure 6 is a graph illustrating the relationship between the axial force retention
rate and the R.E. contents of the present heat resistant magnesium alloy;
Figure 7 is a graph illustrating the relationship between the tensile strength at
room temperature and the R.E. contents of the present heat resistant magnesium alloy;
Figure 8 is a scatter diagram illustrating the compositions of the present heat resistant
magnesium alloys which contain Zn in an amount of 1.0% by weight and which exhibit
a tensile strength and axial force retention rate of a predetermined value or more;
Figure 9 is a scatter diagram illustrating the compositions of the present heat resistant
magnesium alloys which contain Zn in an amount of 2.0% by weight and which exhibit
a tensile strength and axial force retention rate of a predetermined value or more;
Figure 10 is a scatter diagram illustrating the compositions of the present heat resistant
magnesium alloys which contain Zn in an amount of 3.0% by weight and which exhibit
a tensile strength and axial force retention rate of a predetermined value or more;
Figure 11 is a scatter diagram illustrating the compositions of the present heat resistant
magnesium alloys which contain Zn in an amount of 0.25% by weight and which exhibit
a tensile strength and axial force retention rate of a predetermined value or more;
Figure 12 is a trace of a microphotograph showing a comparative magnesium alloy containing
Al and Zn more than the composition range of the present heat resistant magnesium
alloy;
Figure 13 is a trace of a microphotograph showing the present heat resistant magnesium
alloy;
Figure 14 is a graph illustrating the results of the tensile creep test to which the
present heat resistant magnesium alloy, a comparative magnesium alloy and a conventional
magnesium alloy were subjected;
Figure 15 is a graph illustrating the relationship between the initial axial force
retention rate and the Mn contents of the present heat resistant magnesium alloy;
Figure 16 is a graph illustrating the relationships between the hot tearings occurrence
rate and the Mn contents of the present heat resistant magnesium alloy; and
Figure 17 is a perspective view of the test specimen which was prepared for the die
cast hot tearings occurrence test.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0025] Having generally described the present invention, a further understanding can be
obtained by reference to the specific preferred embodiments which are provided herein
for purposes of illustration only and are not intended to limit the scope of the appended
claims.
[0026] Preferred embodiments of the present heat resistant magnesium alloy will be hereinafter
described together with the conventional magnesium alloys or comparative examples
in order to demonstrate the advantageous effects of the present invention.
First Preferred Embodiment
[0027] The following four magnesium alloys were prepared:
a first magnesium alloy containing Zn in an amount of 1.0% by weight, Al in an
amount of from 0 to 4.0% by weight, R.E. in an amount of from 0 to 4.0% by weight,
and balance of Mg and inevitable impurities (hereinafter referred to as "Alloys "A"");
a second magnesium alloy containing Zn in an amount of 2.0% by weight, Al in an
amount of from 0 to 4.0% by weight, R.E. in an amount of from 0 to 5.0% by weight,
and balance of Mg and inevitable impurities (hereinafter referred to as "Alloys "B"");
a third magnesium alloy containing Zn in an amount of 3.0% by weight, Al in an
amount of from 0 to 4.0% by weight, R.E. in an amount of from 0 to 5.0% by weight,
and balance of Mg and inevitable impurities (hereinafter referred to as "Alloys "C"");
and
a fourth magnesium alloy containing Zn in an amount of 0.25% by weight, Al in an
amount of from 0 to 4.0% by weight, R.E. in an amount of from 0 to 5.0% by weight,
and balance of Mg and inevitable impurities (hereinafter referred to as "Alloys "D"").
[0028] The four alloys, i.e., the Alloys "A" through "D," were melted and processed into
the aforementioned cylindrical test specimens and the dumbbell-shaped test specimens
designated in ASTM "80-91," paragraph 12.2.1. The cylindrical test specimens were
examined for their axial force retention rate after they were left in the 150 °C oven
for 300 hours, and the dumbbell-shaped test specimens were examined for their tensile
strength at room temperature. The obtained results are illustrated in Figures 8, 9,
10 and 11 on the Alloys "A," "B," "C" and "D," respectively. In the drawings, magnesium
alloys are marked with "x" which produced the cylindrical test specimens exhibiting
an axial force retention rate of 50% or less, magnesium alloys are marked with solid
triangles ( ▲ ) which produced the dumbbell-shaped test specimens exhibiting a room
temperature tensile strength of 200 MPa or less, and magnesium alloys are marked with
solid circles ( ● ) which produced the cylindrical test specimens exhibiting an axial
force retention rate of 50% or more and the dumbbell-shaped test specimens exhibiting
a room temperature tensile strength of 200 MPa or more.
[0029] Figure 8 illustrates the examination results on the Alloys "A" which are expressed
by a general formula, Mg-("a"% by weight)Al-("b(=1.0)"% by weight)Zn-("c"% by weight)R.E.
In Figure 8, among the Alloys "A," alloys which are marked with solid circles ( ●
) and whose aluminum content "a," zinc content "b" and R.E. content "c" satisfied
the following conditions: 1.0 ≦ "a" ≦ 3.0; 1.0 ≦ "b" ≦ 3.0; 0.5 ≦ "c" ≦ 4.0; and "c"
≦ "a" + "b" ≦ (1/2)"c" + 4.0; lie in the area enclosed by the quadrangle "ABCD" thereof,
and they produced the cylindrical test specimens and the dumbbell-shaped test specimens
which exhibited an axial force retention rate of 50% or more, and a room temperature
tensile strength of 200 MPa or more, respectively. On the other hand, among the Alloys
"A," alloys which are marked with "x" or solid triangles ( ▲ ) and whose aluminum
content "a," zinc content "b" and R.E. content "c" did not satisfy the aforementioned
conditions lie outside the quadrangle "ABCD" area, and they produced the cylindrical
test specimens and the dumbbell-shaped test specimens which exhibited an axial force
retention rate of 50% or less, or a room temperature tensile strength of 200 MPa or
less, respectively. Thus, the alloys whose compositions satisfied the aforementioned
conditions were verified to effect the advantageous effects of the present invention.
[0030] Figure 9 illustrates the examination results on the Alloys "B" which are expressed
by a general formula, Mg-("a"% by weight)Al-("b(=2.0)"% by weight)Zn-("c"% by weight)R.E.
In Figure 9, among the Alloys "B," alloys which are marked with solid circles ( ●
) and whose aluminum content "a," zinc content "b" and R.E. content "c" satisfied
the following conditions: 1.0 ≦ "a" ≦ 3.0; 1.0 ≦ "b" ≦ 3.0; 0.5 ≦ "c" ≦ 4.0; and "c"
≦ "a" + "b" ≦ (1/2)"c" + 4.0; lie in the area enclosed by the hexagon "ABCDEF" thereof,
and they produced the cylindrical test specimens and the dumbbell-shaped test specimens
which exhibited an axial force retention rate of 50% or more, and a room temperature
tensile strength of 200 MPa or more, respectively. On the other hand, among the Alloys
"B," alloys which are marked with "x" or solid triangles ( ▲ ) and whose aluminum
content "a," zinc content "b" and R. E. content "c" did not satisfy the aforementioned
conditions lie outside the hexagon "ABCDEF" area, and they produced the cylindrical
test specimens and the dumbbell-shaped test specimens which exhibited an axial force
retention rate of 50% or less, or a room temperature tensile strength of 200 MPa or
less, respectively. Thus, the alloys whose compositions satisfied the aforementioned
conditions were verified to effect the advantageous effects of the present invention.
[0031] Figure 10 illustrates the examination results on the Alloys "C" which are expressed
by a general formula, Mg-("a"% by weight)Al-("b(=3.0)"% by weight)Zn-("c"% by weight)R.E.
In Figure 10, among the Alloys "C," alloys which are marked with solid circles ( ●
) and whose aluminum content "a," zinc content "b" and R.E. content "c" satisfied
the following conditions: 1.0 ≦ "a" ≦ 3.0; 1.0 ≦ "b" ≦ 3.0; 0.5 ≦ "c" ≦ 4.0; and "c"
≦ "a" + "b" ≦ (1/2)"c" + 4.0; lie in the area enclosed by the quadrangle "ABCD" thereof,
and they produced the cylindrical test specimens and the dumbbell-shaped test specimens
which exhibited an axial force retention rate of 50% or more, and a room temperature
tensile strength of 200 MPa or more, respectively. On the other hand, among the Alloys
"C," alloys which are marked with "x" or solid triangles ( ▲ ) and whose aluminum
content "a," zinc content "b" and R.E. content "c" did not satisfy the aforementioned
conditions lie outside the quadrangle "ABCD" area, and they produced the cylindrical
test specimens and the dumbbell-shaped test specimens which exhibited an axial force
retention rate of 50% or less, or a room temperature tensile strength of 200 MPa or
less, respectively. Thus, the alloys whose compositions satisfied the aforementioned
conditions were verified to effect the advantageous effects of the present invention.
[0032] Figure 11 illustrates the examination results on the Alloys "D" which are expressed
by a general formula, Mg-("a"% by weight)Al-("b(=0.25)"% by weight)Zn-("c"% by weight)R.E.
In Figure 11, among the Alloys "D," alloys which are marked with solid circles ( ●
) and whose aluminum content "a," zinc content "b" and R.E. content "c" satisfied
the following conditions: 1.0 ≦ "a" ≦ 3.0; 0.25 ≦ "b" ≦ 1.0; 0.5 ≦ "c" ≦ 4.0; and
"c" ≦ "a" + 1.0; lie in the area enclosed by the quadrangle "ABCD" thereof, and they
produced the cylindrical test specimens and the dumbbell-shaped test specimens which
exhibited an axial force retention rate of 50% or more, and a room temperature tensile
strength of 200 MPa or more, respectively. On the other hand, among the Alloys "D,"
alloys which are marked with "x" or solid triangles ( ▲ ) and whose aluminum content
"a," zinc content "b" and R.E. content "c" did not satisfy the aforementioned conditions
lie outside the quadrangle "ABCD" area, and they produced the cylindrical test specimens
and the dumbbell-shaped test specimens which exhibited an axial force retention rate
of 50% or less, or a room temperature tensile strength of 200 MPa or less, respectively.
Thus, the alloys whose compositions satisfied the aforementioned conditions were verified
to effect the advantageous effects of the present invention.
Second Preferred Embodiments
[0033] Magnesium alloys having the following chemical compositions as set forth in Table
1 below were melted and processed into the aforementioned cylindrical test specimens
and the dumbbell-shaped test specimens designated in ASTM "80-91," paragraph 12.2.1
by die casting with a cold chamber. I.D. No. 1 is the present heat resistant magnesium
alloy. I.D. No. 2 is a comparative magnesium alloy which included Al and Zn in amounts
more than the present composition range. I.D. No. 3 is a conventional magnesium alloy
which is equivalent to the AZ91D alloy.
[0034] Figures 12 and 13 are traces of microphotographs showing the comparative magnesium
alloy and the present heat resistant magnesium alloy, respectively. As illustrated
in Figure 12, in the comparative magnesium alloy, there existed the areas containing
the solute atoms, which did not produce the crystals, in high concentrations adjacent
to the grain boundaries, because the cooling rate was faster. When these areas are
present, the solute atoms are facilitated to diffuse in the vicinity of the grain
boundaries, and the high temperature creep properties are believed to be adversely
affected. On the other hand, as illustrated in Figure 13, in the present heat resistant
magnesium alloy, there existed no such areas, because the Al and Zn concentrations
were kept low. Accordingly, the present heat resistant magnesium alloy are superior
in terms of the high temperature creep properties.
[0035] The cylindrical test specimens were examined for their axial force retention rate
after they were left in the 150 °C oven for 300 hours, and the dumbbell-shaped test
specimens were examined for their tensile strength at room temperature. The results
obtained are summarized in Table 1 below and illustrated in Figure 14.
TABLE 1
| Classification |
I.D. No. |
Alloying Elements (% by weight) |
Axial Force Retention Rate after 300 hrs. at 150 °C (%) |
R.T. Tensile Strength (MPa) |
| |
|
Al |
Zn |
R.E. |
Mn |
|
|
| Pref. Embodiment |
1 |
2 |
2 |
3 |
0.2 |
70 |
220 |
| Comp. Ex. |
2 |
4 |
4 |
2 |
0.2 |
30 |
220 |
| Conventional Alloy |
3 |
9 |
1 |
0 |
0.2 |
30 |
260 |
[0036] As can be appreciated from Table 1 and Figure 14, the dumbbell-shaped test specimens
made of the comparative magnesium alloy exhibited a room temperature tensile strength
of 220 MPa which was almost equivalent to that of the dumbbell-shaped test specimens
made of the conventional AZ91D alloy. However, the cylindrical test specimens made
of the comparative magnesium alloy were inferior in the bolt loosening characteristic
which was associated with the high temperature creep properties, and thereby they
exhibited an axial force retention rate of 30%.
[0037] Likewise, in the conventional AZ91D alloy, there were the areas containing the solute
atoms, which did not produce the crystals, in high concentrations adjacent to the
grain boundaries, because the conventional AZ91D alloy was processed into the cylindrical
test specimens by die casting. Accordingly, the cylindrical test specimens made thereof
exhibited an axial force retention rate of 30%.
[0038] On the other hand, the dumbbell-shaped test specimens made of the present heat resistant
magnesium alloy also exhibited a room temperature tensile strength of 220 MPa which
was almost equivalent to that of the dumbbell-shaped test specimens made of the conventional
AZ91D alloy. Moreover, the cylindrical test specimens made thereof exhibited an axial
force retention rate of 70%. Thus, the present heat resistant magnesium alloy was
improved in terms of the high temperature creep properties without loss of the tensile
properties.
Third Preferred Embodiments
[0039] A magnesium alloy was melted which comprised 2% by weight of Al, 2% by weight of
Zn, 3% by weight of R.E., and balance of Mg and inevitable impurities, and Mn was
added to the resulting molten metal in an amount which varied in a range of 0 to 1.0%
by weight. The thus prepared magnesium alloys were processed into the aforementioned
cylindrical test specimens by die casting with a cold chamber. The resulting test
specimens were subjected to the bolt loosening test, in which they were left in the
150 °C oven for 1 hour, in order to examine for their initial axial force retention
rates. The results obtained are illustrated in Figure 15 as a relationship between
the Mn contents and the initial axial force retention rates.
[0040] Further, except that the amount of Mn addition was varied in a range of 0 to 1.6%
by weight, the magnesium alloys prepared as above were melted and cast into the square-shaped
box test specimens for the die cast hot tearings occurrence test illustrated in Figure
17. The resulting test specimens were subjected to the die cast hot tearings occurrence
test in order to examine for their hot tearings occurrence rates at the round corner
20 having a radius of 1.0 mm as set forth above. The results obtained are illustrated
in Figure 16 as a relationship between the Mn contents and the hot tearings occurrence
rates.
[0041] Furthermore, another magnesium alloy was melted which comprised 3% by weight of Al,
2% by weight of Zn, 3% by weight of R.E., and balance of Mg and inevitable impurities,
and Mn was added to the resulting molten metal in an amount which varied in a range
of 0 to 1.6% by weight. The thus prepared another magnesium alloys were cast into
the square-shaped box test specimens for the die cast hot tearings occurrence test,
and they were similarly examined for their hot tearings occurrence rates at the round
corner 20 having a radius of 1.0 mm. The results obtained are also illustrated in
Figure 16 as another relationship between the Mn contents and the hot tearings occurrence
rates.
[0042] It is apparent from the results illustrated in Figure 15 that the initial axial force
retention rate was improved appreciably when Mn was added in an amount of 0.1% by
weight or more, and that the effect of the initial axial force improvement saturated
when Mn was added in an amount of up to 0.4% by weight. However, as can be seen from
Figure 16, the hot tearings occurred when the Mn content exceeded 1.0% by weight,
because there were formed the Mn-Al-R.E. crystals. According to these results, it
was verified that the present heat resistant magnesium alloy could produce the advantageous
effects more favorably when it contained Mn in an amount of from 0.1 to 1.0% by weight.
[0043] Having now fully described the present invention, it will be apparent to one of ordinary
skill in the art that many changes and modifications can be made thereto without departing
from the spirit or scope of the present invention as set forth herein including the
appended claims.
[0044] A magnesium alloy includes 1.0 to 3.0% by weight of Al ("a"), 0.25 to 3.0% by weight
of Zn ("b") and 0.5 to 4.0% by weight of R.E.: wherein when "b" is in a range, 0.25
≦ "b" ≦ 1.0, "a" and "c" satisfy a relationship, "c" ≦ "a" + 1.0; and when "b" is
in a range, 1.0 ≦ "b" ≦ 3.0, "a," "b" and "c" satisfy a relationship, "c" ≦ "a" +
"b" ≦ (1/2)"c" + 4.0; in order to further improve creep properties at elevated temperatures
while maintaining enhanced tensile strength at room temperature and up to 100 °C at
least.