TECHNICAL FIELD
[0001] The present invention is one which relates to a magnesium alloy for casing, magnesium
alloy which is suitable for service under high temperature.
BACKGROUND ART
[0002] Magnesium alloy, which is much more light weight than aluminum alloy is, is about
to come to be used widely for aircraft material, vehicle material, and the like, from
the viewpoint of weight saving. However, in magnesium alloy, since the strength and
heat resistance are not sufficient depending on applications, further improvement
of the characteristics has been sought.
[0003] For example, as a general magnesium alloy, AZ91D (ASTM code) is present, for instance.
Since the heat conductivity of AZ91D is 73 W/mK approximately, when it is used in
member whose service environment is high temperature, or in member that generates
heat in service, the radiation of heat cannot be carried out satisfactorily, and thereby
thermal deformation might occur in the member. In particular, when a magnesium alloy
whose heat conductivity is low is used as a magnesium alloy that is used in a cylinder
head or cylinder block of internal combustion engine, the cylinder head undergoes
thermal deformation, or heat dwells within the cylinder block so that the cylinder
bores deform, and thereby adverse affects, such as increased friction and declined
air tightness, occur. Consequently, a magnesium alloy has been sought, magnesium alloy
in which the radiation of heat is carried out satisfactorily by possessing a high
heat conductivity, and magnesium alloy which is thereby suitable for usage under high
temperature.
[0004] For example, the heat conductivity of a magnesium alloy that has an alloy composition
of Mg-3%Cu-1%Ca (the units being "% by mass") is higher than the heat conductivity
of AZ91D, because Cu whose heat conductivity is high is included. However, there might
be a case where the creep resistance at high temperature is not sufficient, depending
on service conditions.
[0005] In Japanese Unexamined Patent Publication (KOKAI) Gazette No.
6-25, 791, a magnesium alloy is disclosed, magnesium alloy which includes calcium (Ca) in an
amount of 0.8-5% by mass, copper (Cu) in an amount of 0-10% by mass, and zinc (Zn)
in an amount of 3-8% by mass. Although the magnesium alloy set forth in Japanese Unexamined
Patent Publication (KOKAI) Gazette No.
6-25,791 exhibits high strength at room temperature and high temperature, nothing is set forth
on the heat conductivity, and accordingly it is unclear whether the addition of zinc
influences the heat conductivity of magnesium alloy or not.
DISCLOSURE OF THE INVENTION
[0006] In view of the aforementioned problematic issues, it is an object for the present
invention to provide a magnesium alloy for casting, magnesium alloy which is suitable
for usage under high temperature. Moreover, it is an object to provide a cast product,
which comprises that magnesium alloy for casting.
[0007] As a result of wholehearted studies, the present inventors found out that it is possible
to improve the creep resistance of magnesium alloy at high temperature by adding tin
along with copper and calcium as another alloying element of the magnesium alloy,
without ever affecting the heat conductivity adversely, and then arrived at completing
the present invention based on this.
[0008] Specifically, a magnesium alloy for casting according to the present invention is
characterized in that, when the entirety is taken as 100% by mass, it includes:
copper (Cu) in an amount of from 1% by mass or more to 5% by mass or less;
calcium (Ca) in an amount of from 0.1% by mass or more to 5% by mass or less;
tin (Sn) in an amount of from 0.1 or more to 3 or less by mass ratio with respect
to the Ca (Sn/Ca); and
the balance comprising magnesium (Mg) and inevitable impurities.
[0009] Since the magnesium alloy for casting according to the present invention includes
Cu, Ca and Sn, crystallized substances of Mg-Ca-Sn compounds crystallize in crystalline
grain boundaries between Mg crystalline grains as network shapes (three-dimensionally
mesh shapes), along with Mg-Cu compounds. By means of the three-dimensionally mesh
constructions, grain-boundary sliding, which becomes active especially when becoming
high temperature, is suppressed, and thereby high-temperature strength and creep resistance
at high temperature improve. Moreover, Mg-Ca compounds are brittle comparatively;
however, since strength is high in the Mg-Ca-Sn compounds in which Sn substitutes
for a part of Ca of the Mg-Ca compounds, the strength of the three-dimensionally mesh
constructions and eventually the strength of the magnesium alloy improve.
[0010] Moreover, it will be detailed later that, since Sn forms compounds with Ca preferentially,
it influence less on the heat conductivity, compared with the other additive elements
such as aluminum.
[0011] Note that, in the present description, the expressions such as "X-Y compounds" are
compounds, in which "X" and "Y" make the major components, like those which are represented
with such a compositional formula as "X
2Y," for instance.
[0012] Moreover, a magnesium-alloy cast product according to the present invention is a
cast product that comprises the magnesium alloy for casting according to the present
invention. The magnesium-alloy cast product according to the present invention is
characterized in that it is obtainable by way of the following:
a molten-metal pouring step of pouring an alloy molten metal into a casting mold,
the alloy molten metal including: copper (Cu) in an amount of from 1% by mass or more
to 5% by mass or less; calcium (Ca) in an amount of from 0.1% by mass or more to 5%
by mass or less; tin (Sn) in an amount of from 0.1 or more to 3 or less by mass ratio
with respect to the Ca (Sn/Ca) ; and the balance comprising magnesium (Mg) and inevitable
impurities; when the entirety is taken as 100% by mass; and
a solidifying step of solidifying the alloy molten metal after the molten-metal pouring
step by cooling it.
BRIEF DESCRIPTION OF THE DRAWINGS
[0013] Fig. 1 is a graph for illustrating the heat conductivities of magnesium alloys whose
alloy compositions differ.
[0014] Fig. 2 is a graph for illustrating the stress lowering magnitudes from the beginning
of testing to 40 hours later in a stress relaxation test on magnesium alloys whose
alloy compositions differ.
[0015] Fig. 3 is a graph in which compression stresses being applied to test specimens are
plotted with respect to the testing time of the stress relaxation test for every 10
minutes.
[0016] Fig. 4A and Fig. 4B are photographs for substituting for drawings that show the metallic
structure of Mg-3%-by-mass Cu-1%-by-mass Ca alloy (#01).
[0017] Fig. 5A and Fig. 5B are photographs for substituting for drawings that show the metallic
structure of Mg-3%-by-mass Cu-1%-by-mass Ca-0.1%-by-mass Sn alloy (#02).
[0018] Fig. 6A and Fig. 6B are photographs for substituting for drawings that show the metallic
structure of Mg-3%-by-mass Cu-1%-by-mass Ca-1%-by-mass Sn alloy (#03).
[0019] Fig. 7A and Fig. 7B are photographs for substituting for drawings that show the metallic
structure of Mg-3%-by-mass Cu-1%-by-mass Ca-2%-by-mass Sn alloy (#04).
[0020] Fig. 8A and Fig. 8B are photographs for substituting for drawings that show the metallic
structure of Mg-3%-by-mass Cu-1%-by-mass Ca-4%-by-mass Sn alloy (#05).
Best Mode for Carrying Out the Invention
[0021] Hereinafter, the best mode for carrying out the magnesium alloy for casting according
to the present invention will be explained.
[0022] The magnesium alloy for casting according to the present invention is characterized
in that it includes copper (Cu), calcium (Ca), tin (Sn), and the balance comprising
magnesium (Mg) and inevitable impurities.
[0023] In the magnesium alloy for casting according to the present invention, the crystallized
substances of Mg-Ca-Sn compounds crystallize as network shapes (three-dimensionally
mesh shapes) in crystalline grain boundaries between Mg crystalline grains, along
with Mg-Cu compounds, by setting the contents of Cu, Ca and Sn to appropriate amounts.
Since they are network shapes with less discontinuous parts, the effect of suppressing
grain-boundary slip is high.
[0024] When the entire magnesium alloy for casting is taken as 100% by mass, the content
of Cu is from 1% by mass or more to 5% by mass or less. When the content of Cu is
1% by mass or more, the Mg-Cu compounds crystallize sufficiently in the crystalline
grain boundaries. When the content of Cu is less than 1% by mass, the strength is
low because the crystallization of the Mg-Cu compounds to the crystalline grain boundaries
is insufficient. A preferable content of Cu can be 2% by mass or more. Meanwhile,
the greater the content of Cu is, the more excessive the amount of the Mg-Cu compounds
that crystallize in the crystalline grain boundaries becomes, thereby turning into
brittle structures so that the strength lowers. A preferable content of Cu can be
4% by mass or less.
[0025] The magnesium alloy for casting according to the present invention includes Ca and
Sn along with Cu. Ca and Sn exist in the crystalline grain boundaries along with Cu,
and thereby contribute to the formation of three-dimensionally mesh constructions.
To be concrete, the Mg-Ca-Sn compounds crystallize in the crystalline grain boundaries
along with the Mg-Cu compounds, and then favorable three-dimensionally mesh constructions
with less discontinuous parts are formed.
[0026] When the entire magnesium alloy for casting is taken as 100% by mass, the content
of Ca is from 0.1% by mass or more to 5% by mass or less. When the content of Ca is
0.1% by mass or more, the Mg-Ca-Sn compounds crystallize sufficiently in the crystalline
grain boundaries. Moreover, since the ignition temperature of magnesium alloy rises
when adding Ca to the magnesium alloy, the combustion that might occur when making
the magnesium alloy into a molten metal is prevented. A preferable content of Ca can
be 0.5% by mass or more. Meanwhile, when the content proportion of Ca surpasses 5%
by mass, problems might arise in post-processing because the generation amount of
the grain-boundary crystallized substances has become too much so that the mechanical
strengths, such as the tensile strength and the elongation, lower. A preferable content
of Ca can be 3% by mass or less, further preferably 2% by mass or less.
[0027] The content of Sn is from 0.1 or more to 3 or less by mass ratio with respect to
calcium (Ca) (Sn/Ca). When the content of Sn is 0.1% by mass or more, the Mg-Ca-Sn
compounds crystallize in the crystalline grain boundaries sufficiently. Meanwhile,
when the content proportion of Sn becomes great, the Mg-Ca-Sn compounds separate from
the three-dimensionally mesh constructions so that they come to crystallize even within
the crystalline grains, and thereby favorable three-dimensional mesh constructions
become less likely to be formed. As a result, the creep resistance tends to lower.
Moreover, in the case of adding Sn excessively, not only the Mg-Ca-Sn compounds but
also Mg-Sn compounds arise. Since the Mg-Sn compounds are compounds with low melting
points, they degrade the creep resistance. Consequently, the content of Sn is set
to 3 or less by Sn/Ca. When Sn/Ca is 3 or less, the formation of the low-melting-point
compounds is suppressed. Further, when Sn/Ca is 2 or less, favorable three-dimensionally
mesh constructions with less discontinuous parts are formed so that the high-temperature
strength and the creep resistance at high temperature improve. Specifically, a preferable
content of Sn can be 2 or less, further preferably 1.5 or less, by Sn/Ca.
[0028] Note that the Sn makes compounds with Ca more preferentially than with Mg and Cu.
Consequently, it does not have a bad influence on Cu and the Mg-Cu compounds whose
heat conductivities are high; and, as a result of this, it is believed that the heat
conductivity of magnesium alloy becomes less likely to lower. Considering this fact,
namely, in view of the stoichiometric ratio of Sn/Ca in the Mg-Ca-Sn compounds, it
is preferable to set the mass ratio of Sn with respect to Ca (Sn/Ca) to 3 or less,
further preferably from 0.1 or more to 2 or less; there is hardly any Sn that forms
compounds with the Mg-Cu compounds, and accordingly the crystallization of above-described
low-melting-point compounds is also suppressed.
[0029] Beginning with the fields of space, military and aviation, the magnesium alloy for
casting according to the present invention being explained as above can be used in
various fields, such as automobiles and electric instruments. Moreover, as a member
comprising the magnesium alloy for casting according to the present invention, the
following can be given, taking advantage of its characteristics at high temperature:
products being utilized in high-temperature environments, for example, component parts
constituting compressor, pumps and various cases that become high temperatures in
service; moreover, engine component parts being used under high temperature and high
load, especially, cylinder heads, cylinder blocks and oil pans of internal combustion
engine, impellers for turbocharger of internal combustion engine, transmission cases
being used for automobile and the like, and so forth.
[0030] Moreover, the magnesium-alloy cast product according to the present invention is
a cast product that comprises the magnesium alloy for casting according to the present
invention being detailed as above. Specifically, the magnesium-alloy cast product
according to the present is a cast product that is obtainable by way of a molten-metal
pouring step, and a solidifying step; the molten-metal pouring step is a step of pouring
an alloy molten metal into a casting mold, the alloy molten metal including: copper
(Cu) in an amount of from 1% by mass or more to 5% by mass or less; calcium (Ca) in
an amount of from 0.1% by mass or more to 5% by mass or less; Sn in an amount of from
0.1 or more to 3 or less by mass ratio with respect to the Ca (Sn/Ca) ; and the balance
comprising magnesium (Mg) and inevitable impurities; when the entirety is taken as
100% by mass; and the solidifying step is a step of solidifying the alloy molten metal
after the molten-metal pouring step by cooling it.
[0031] The magnesium-alloy cast product according to the present invention is not limited
to those made by ordinary gravity casting and pressure casting, but can even be those
made by die-cast casting. Moreover, even the casting mold being utilized for the casting
does not matter if it is sand molds, metallic molds, and the like. Since even the
solidification rate (cooling rate) in the solidifying step is not limited in particular,
it is allowable to properly select such an extent of solidification rate, which permits
to form the three-dimensionally mesh constructions, depending on the size of ingots.
Note that, when it is solidified at a usual solidification rate, the network-shaped
metallic structure is obtainable.
[0032] Moreover, it is desirable that themagnesiumalloy for casting and magnesium-alloy
cast product according to the present invention can be an as-cast material. It is
even allowable to improve the characteristics of the cast product by means of heat
treating it after casting.
[0033] So far, the embodimentmodes of themagnesiumalloy for casting and magnesium-alloy
cast product according to the present invention have been explained, however, the
present invention is not one which is limited to the aforementioned embodiment modes.
It can be conducted in various modes to which modifications, improvements, and the
like, which one of ordinary skill in the art can carry out, are performed, within
a range not departing from the scope of the present invention.
[0034] Hereinafter, while giving specific examples, the present invention will be explained
in detail.
[0035] Test specimens whose contents of alloying elements in magnesium alloys were varied
were made in a quantity of plural pieces, and then the evaluation of their characteristics
and the observation of their metallic structures were carried out.
[0036] (Making of Test Specimens #01-#05)
[0037] A chloride-system flux was coated onto the inner surface of a crucible being made
of iron that had been preheated within an electric furnace, and then a weighed pure
magnesium base metal, pure Cu, and pure Ag, if needed, were charged into it and were
then melted. Further, weighed Ca was added into this molten metal that was held at
750 °C (i.e., a molten-metal preparing step).
[0038] After fully stirring this molten metal to melt the raw materials completely, it was
held calmly at the same temperature for a while. The thus obtained various alloy molten
metals were poured into a metallic mold with a predetermined configuration (i.e.,
a molten-metal pouring step), and were then solidified in air atmosphere (i.e., a
solidifying step), thereby casting test specimens (i.e., magnesium-alloy cast products)
being labeled #01-#05. Note that the obtained test specimens had a size of 30 mm ×
30 mm × 200 mm. The chemical compositions of the respective test specimens were specified
in Table 1.
[0039] (Measurement of Heat Conductivity)
[0040] In addition to regarding the test specimens being labeled #01-#05 that were made
with the aforementioned procedures, regarding similar test specimens that were made
from the commercially available AZ91D (the composition is set forth in Table 1), the
heat conductivities were found by means of laser flash method. The test results are
specified in Table 1 and Fig. 1.
[0041] (Stress Relaxation Test)
[0042] Onto test specimens being made from Test Specimens #01-#05 and AZ91D that are specified
in Table 1, a stress relaxation test was carried out, thereby examining the creep
resistances of the magnesium alloys. In the stress relaxation test, processes of how
stresses decreased with time were measured, stresses which arose when a load was applied
to the test specimens in the course of testing time until they exhibited a predetermined
deformation magnitude. To be concrete, in 200 °C air atmosphere, a compression stress
of 100 MPa was loaded to the test specimens, and then the compression stress was lowered
in agreement with the elapse of time so as to keep the displacements of the test specimens
at that time constant. The stress lowering magnitudes from the beginning of testing
to 40 hours later are specified in Table 1 and Fig. 2. Moreover, a graph is illustrated
in Fig. 3, graph which was prepared by plotting the compression stresses, which were
applied to the test specimens, for every 10 minutes.
[0043] (Observation of Metallic Structure)
[0044] The surfaces of Test Specimens #01-#05 given in Table 1 were observed. The surface
observation was carried out by observing cross sections, which were cut out of the
respective test specimens, with a metallographic microscope. Although the metallic
structures in the surfaces being labeled #01-#05 are shown in Fig. 4A-Fig. 8A and
in Fig. 4B-8B, respectively, Fig. 4A-Fig. 8A are for observing identical cross sections
with (a) lowmagnification; and Fig. 4B-Fig. 8B are for observing identical cross sections
with (b) high magnification, in the respective drawings.
[0045] In Test Specimen #01, the three-dimensionally mesh constructions were confirmed,
three-dimensionally mesh constructions which comprised intermetallic compounds that
crystallized in crystalline grain boundaries, as can be appreciated from Fig. 4A.
Moreover, it was ascertained by means of EPMA (electron probe microanalyzer) and XRD
(X-ray diffraction) that, in Fig. 4B, those looking bright at the crystalline grain
boundaries are CuMg
2 and those looking dark thereat are Mg
2Ca . Moreover, in Test Specimens #02 and #03, the three-dimensionally mesh constructions
were confirmed, three-dimensionally mesh constructions whose meshes were finer and
continuities were higher than those of #01, as can be appreciated from Fig. 5A and
Fig. 6A. Moreover, it was ascertained by means of EPMA and XRD that, in Fig. 5B and
Fig. 6B, those looking bright at the crystalline grain boundaries are CuMg
2 and those looking dark thereat are Mg
2Ca and MgCaSn. Meanwhile, in Test Specimens #04 and #05, the three-dimensionally mesh
constructions were not formed completely because of the fact that the crystallized
substances crystallized even inside the crystalline grains, as canbe appreciated from
the other respective diagrams, namely, Fig. 7A as well as Fig. 7B and Fig. 8A as well
as Fig. 8B. Here, in Fig. 7B and Fig. 8B, the crystallized substances that crystallized
at the grain boundaries and within the grains are designated with the arrows for one
of their locations at least. In Fig. 7B and Fig. 8B, "Ga" is the crystallized substances
within a grain, and "Gb" is the crystallized substances at a grain boundary. It was
ascertained by means of EPMA and XRD that those crystallizing within the grains were
MgCaSn. Further, in Test Specimen #05, Mg
2Sn being a low-melting-point compound was detected by means of XRD.
[0046]
(TABLE 1)
No. |
Alloy Composition (% by mass) |
Heat Conductivity (W/mK) |
Stress Lowering Magnitude (MPa) |
#01 |
Mg-3%Cu-1%Ca |
155 |
65 |
#02 |
Mg-3%Cu-1%Ca-0.1%Sn |
163 |
54 |
#03 |
Mg-3%Cu-1%Ca-1%Sn |
154 |
52 |
#04 |
Mg-3%Cu-1%Ca-2%Sn |
148 |
59 |
#05 |
Mg-3%Cu-1%Ca-4%Sn |
122 |
67 |
AZ91D |
Mg-9%Al-1%Zn |
73 |
60 |
[0047] Any one of the test specimens being labeled #01-#05 were better than AZ91D in terms
of the heat conductivity. Although the heat conductivity of the test specimens being
labeled #01 that did not include any Sn was 155 W/mK, lowering of the heat conductivity
that resulted from the addition of Sn was not seen in test specimens being labeled
#02-#04. Meanwhile, in #05 in which the content of Sn was excessive, although the
heat conductivity was better than that of AZ91D, the difference was great between
the heat conductivity and that of #01.
[0048] Moreover, in the test specimens being labeled #02-#04, the stress lowering magnitudes
were less than that of Test Specimen #01 from the beginning of testing to 40 hours
later in the stress relaxation test at 200 °C. Specifically, the creep resistance
at high temperature was improved by adding Sn to an Mg-Cu-Ca alloy (i.e., #01). This
is presumed that #02-#04 had the three-dimensionally mesh constructions with high
continuities more, compared with #01 in which discontinuous parts are present more
in the three-dimensionally mesh constructions. On the contrary, in #04 including Sn
in an amount of 2% by mass, although the creep resistance after 40 hours was better
than that of #01 that did not include any Sn, it was inferior to those of #02 and
#03. It is believed that the metallic structure of #04 was more incomplete than those
of #02 and #03. In #05 including Sn in an amount of 4% by mass, it is believed that
the creep resistance degraded because the three-dimensionally mesh constructions were
incomplete and included Mg
2Sn being a low-melting-point compound.
[0049] Further, in test specimens being labeled #02 and #03, although the stress lowering
magnitudes were greater than that of #01 from the beginning of testing to about 3
hours later, the changing magnitudes of the stress from 3 up to 40 hours were small
and stabilized. Moreover, in test specimens being labeled #04, although the stress
lowering magnitude was greater than those of #01 and AZ91D from the beginning of testing
to about 3 hours later, the changing magnitude of the stress from 3 up to 40 hours
was small and stabilized. (Fig. 3).
[0050] Note that, in the aforementioned respective test specimens, the content of Cu was
kept constant at 3% by mass and the content of Ca was kept constant at 1% by mass.
Even in any one of the test specimens, they exhibit the heat conductivity and creep
resistance to the same extent as those of the aforementioned respective test specimens
when they fall in a range of from 2.7% by mass or more to 3.3% by mass or less for
the case of being the content of Cu, and in a range of from 0.7% by mass or more to
1.3% by mass or less for the case of being the content of Ca.
[0051] Specifically, a magnesium alloy that includes Cu, Ca and Sn in the appropriate amounts
does not show any lowering of the heat conductivity resulting from the addition of
Sn, and is good in terms of the creep resistance at high temperature.