Technical Field
[0001] This invention relates to a method of preparing improved hyper-eutectic alloys and
metal matrix composites containing such alloys.
Background Art
[0002] Metal matrix composite materials have gained increasing acceptance as structural
materials. Such composites typically are composed of reinforcing particles, such as
fibres, grit, powder or the like that are embedded within a metallic matrix. The reinforcement
imparts strength, stiffness and other desirable properties to the composite, while
the matrix protects the fibres and transfers load within the composite. The two components,
matrix and reinforcement, thus cooperate to achieve results which are improved over
what either could provide on its own. A typical composite is an aluminum alloy reinforced
with particles of silicon carbide or alumina.
[0003] A major difficulty in the production of good quality metal matrix composites is segregation
of the reinforcing particles. The segregation of particles occurs in the liquid state
as well as during solidification. The segregation in the liquid state can be overcome
by a proper mixing of the liquid. However, even if the particles are uniformly distributed
in the liquid state, they may still segregate during solidification. When metal matrix
composites are in the process of solidifying, the reinforcing particles can be rejected
ahead of the solidification interface, and may agglomerate in the interdendritic liquid
which solidifies last. For instance, in aluminum matrix composites, solid α-aluminum
dendrites are formed and the reinforcing particles are pushed ahead of the growing
dendrites to be finally trapped in the last to solidify interdendritic liquid. The
reinforcing particles are not found inside the aluminum dendrites and, in this sense,
it can be said that the aluminum dendrites do not "wet" the reinforcing particles.
This results in a highly inhomogeneous distribution of reinforcing particles in the
as-cast materials.
[0004] Whether reinforcement particles are pushed by the solidification interface or are
engulfed is primarily dependent upon the degree of wetting between the particles and
the solid surface. If the solid surface wets the particles, they are engulfed by the
solid surface. In this case the particle distribution in the solidified material is
as uniform as it was in the liquid state. On the other hand, if the solid surface,
e.g. aluminum dendrite surface, does not wet the particles, they are pushed away,
resulting in interdendritic segregation.
[0005] In certain alloy systems, such as eutectic or hyper-eutectic systems, intermetallic
compounds may precipitate directly from a melt of the alloy. These intermetallic compounds
often tend to be coarse, brittle particles, and these particles tend to segregate
due to density difference, particularly when the solidification rate is slow.
[0006] There is some evidence in the prior art of a degree of wetting between refractory
particles and intermetallic surfaces. For instance P.K. Rohatgi, "Interfaces in Metal
Matrix Composites", p. 185, The Metallurgical Society/AIME, New Orleans, 2-6 March
1986, has shown an example of primary NiAl
3 nucleating on graphite particles during the solidification of a hyper-eutectic Al-Ni
alloy. He also noted that there is a tendency for primary Si to nucleate on graphite
and alumina particles during the solidification of a hyper-eutectic Al-Si alloy.
[0007] Solidification studies of grain refining Al-Ti-B alloys are described in K. Kuisalaas
and L. Backerud, Solidification Process 1987, p. 137, Institute of Metals, Sheffield,
U.K., 21-24 September, 1987. These studies noted that TiAl
3 inter-metallics tended to adhere to the surface of TiB
2 particles.
[0008] A study on aluminum alloys far elevation temperature applications is described in
D.A. Granger et al.,
[0009] "Aluminum Alloys for Elevated Temperature Applications" p. 777-778, AFS Transactions,
86-143. Traditionally, casting alloys for elevated temperature applications were made
by adding large amounts of Cu or Ni, e.g. up to about 8 wt% Cu and 5.5 wt% Ni. It
has been generally understood that high volume fractions of the intermetallics so
formed improve the high temperature properties. However, the amount of these elements
which could be added was restricted because they formed large brittle intermetallic
primaries on solidification if the addition was beyond a certain limit. The amount
of Mn that could be added was limited to less than 0.5 wt%.
[0010] U.S. Patent No. 3,951,651 issued April 20, 1976 describes aluminum-silicon-iron alloys
which can also contain reinforcing particles. However, the US patent does not describe
a system where the excess elements from a hyper-eutectic alloy solidify first thereby
engulfing the reinforcing particles by the intermetallics thus formed.
[0011] In S. Das et al., "Some Modified Structures of the Matrix in Cast Al-Alloy-Graphite
Particle Composites", Z. Metallkde., Vol. 80 (1989) 6, p. 444-446, a hypereutectic
LM30 Al-Si alloy containing 3 wt.% of graphite particles is analyzed. The LM30 alloy
specification defines an alloy composition which contains,among others, from 16 to
18 wt.% Si, from 0.3 to 0.7 wt.% Mg, up to 1.1 wt.% Fe, and up to 0.3 wt.% Mn. Fig.
2 shows a preferential nucleation of primary silicon on the surface of the graphite.
[0012] It is the object of the present invention to provide a technique for improving hyper-eutectic
alloys and for solving the problem of the segregation of the reinforcement particles
in metal matrix composites made from hyper-eutectic alloys which tends to occur during
solidification. It is a further object of the invention to produce new alloy products
having improved high temperature properties.
Disclosure of the Invention
[0013] According to the present invention, it has now been discovered that non-metallic
refractory particles when added to a molten hyper-eutectic Al-Si-Mn alloy can be engulfed
durina solidification by an intermetallic phase which solidifies first from the molten
hypereutectic alloy during solidification thereof such that the refractory particles
are engulfed by the intermetallic phase as it grows during solidification. Because
the intermetallics engulf the refractory particles, there is no longer a tendency
for the refractory particles to segregate to the interdendritic regions and they remain
homogeneously distributed throughout an as-solidified ingot. The presence of excess
alloying elements in the hyper-eutectic alloy beyond eutectic amounts is the mechanism
for the formation of the desired intermetallic phase and this intermetallic phase
forms automatically during cooling provided the alloy being cooled is a hyper-eutectic
alloy.
[0014] One embodiment of the invention is a method for preparing a composite of an aluminum
alloy and particles of a non-metallic refractory material, which comprise melting
an aluminum alloy; adding particles of non-metallic refractory material to the molten
aluminum matrix; mixing together the molten aluminum alloy and the particles of refractory
material; and casting the resulting mixture. According to the novel feature, the aluminum
alloy is a hyper-eutectic aluminum alloy comprising, in percentages by weight, 7-16%
silicon, 0.5-3.0% manganese, 0-5.0% copper, 0-5.0% nickel, 0-1.0% iron, 0-0.2% titanium
and 0.3-2.0% magnesium and the balance of the alloy being aluminum and inevitable
impurities and the excess alloying element or elements of the hyper-eutectic molten
aluminum alloy solidify first from the molten aluminum matrix during solidification
thereof to form intermetallics comprising Mn
3Si
2Al
15 which engulf said refractory particles and keep them homogeneously distributed throughout
the solidified product.
Best Modes For Carrying Out the Invention
[0015] In one preferred embodiment of the invention, the refractory particles act as a refiner
for precipitating intermetallics. The use of unreinforced hyper-eutectic alloys is
very restricted because they often form coarse, brittle intermetallic particles on
solidification, and the intermetallic particles tend to segregate due to the density
difference, particularly when the solidification rate is not rapid. For instance,
in commercial hyper-eutectic Al-Si alloys, such as A390 alloy, used for engine block
applications, phosphorus additions and fluxing have previously been required to refine
the primary silicon to a size suitable for good wear properties. However, the efficiency
of phosphorus to refine primary silicon decreases with increasing holding time of
the melt, complicating the casting practice. On the other hand, the addition of refractory
particles, such as silicon carbide particles, according to the present invention can
nucleate and refine these intermetallics, as well as modify their morphology, so that
the deleterious effect of coarse intermetallics is reduced. This is of particular
value for alloys that are intended for high temperature use.
[0016] There is a need for aluminum alloy products capable of extended use at high temperatures.
Such high temperature alloys may be used in casting applications, or as wrought products,
such as forgings and extrusions. The alloy composites of this invention in which the
refractory particles act as a refiner for precipitating intermetallics have superior
high temperature strength, making them useful for applications such as cast brake
rotors.
[0017] According to a further preferred embodiment, the refractory particles may also serve
as reinforcing particles in a composite with a hyper-eutectic alloy. Thus, they may
be used not only to refine a hyper-eutectic alloy, but also to form a composite therewith.
When the particles are used solely to refine an alloy, they are typically used in
very small sizes, e.g. less than 1
µm. On the other hand, when they are used also for reinforcing the alloy, they may
be used in much larger sizes, e.g. up to 20
µm. For reinforcing, they are typically used in sizes in the range of 5-20
µm and preferably 10-15
µm. When the particles are used in reinforcing sizes, the wetting and engulfment of
them by the intermetallic phase prevent the problem of segregating to the interdendritic
regions during cooling.
[0018] The non-metallic refractory material is preferably a metal oxide, metal nitride,
metal carbide or metal silicide. The most preferred refractory material is silicon
carbide or aluminum oxide particulate.
[0019] The procedure of the present invention for making a composite functions best with
reinforcing particles which are relatively equi-dimensional, e.g. having an aspect
ratio in any direction of no more than 5:1. The reinforcing particles are typically
added in amounts of 5-40% by volume, preferably 10-25% by volume. It has been found
that silicon carbide reinforcing particles are engulfed by silicon crystals formed
during solidification of the composite.
[0020] The invention also relates to new aluminum alloy products having improved high temperature
properties. One of the novel products is a particle reinforced aluminum alloy casting
in which the alloy is a hyper-eutectic alloy and the excess alloying element or elements
of the hypereutectic alloy have solidified first from the molten metal matrix and
have formed intermetallics during solidification which have engulfed the refractory
particles and kept them homogeneously distributed throughout the solidified product.
Another novel product is a refined aluminum alloy casting in which intermetallics
formed during solidification are uniformly dispersed as fine particles because of
the refining effect of particles of non-metallic refractory material contained in
the alloy.
[0021] The alloy of the novel products is a hyper-eutectic aluminum alloy containing silicon,
magnesium and manganese, preferably in the amounts 7-16 wt% silicon, 0.5-3.0 wt% manganese,
0-5.0 wt% copper, 0-5.0 wt% nickel, 0-1.0 wt% iron, 0-0.2 wt% titanium and 0.3-2.0
wt% magnesium and the balance of the alloy being aluminum and inevitable impurities.
The silicon assists fluidity and stabilizes the refractory particles; below 7% silicon
the refractory material tends to be unstable while above 16% coarse intermetallics
are formed and the composite becomes embrittled. The magnesium improves wetting and
provides strengthening; below 0.3% magnesium the wetting is poor, while above 2% there
is shrinkage porosity. The manganese forms intermetallics providing uniform refractory
particle distribution and improved high temperature strength; below 0.5% manganese
there is no improvement in high temperature strength and above 3.0% the casting temperature
becomes too high.
[0022] The alloy also preferably contains up to 5.0 wt% copper. This improves elevated temperature
strength with amounts above 5.0% providing poor casting fluidity and embrittlement.
Another optional component is nickel which may also be present in amounts up to 5.0
wt%. It also improves elevated temperature strength, although amounts above 5.0% cause
coarse intermetallics and embrittlement.
[0023] A further common optional element is iron which may be present in amounts up to 1.0
wt%. At amounts above 1.0 wt% there is the danger of forming coarse intermetallics
which cannot be refined by the refractory particles.
[0024] The alloy may also contain up to 0.2 wt%, preferably 0.1-0.2 wt%, titanium as a grain
refiner.
[0025] A series of aluminum alloys and the intermetallic phases that precipitate therefrom
are shown in Table 1 below:
Table I
| Alloy |
Intermetallic |
| Al - 16 wt% Si --- |
Si |
| Al - 12 wt% Si - 1.5 wt% Fe |
FeSiAl5 |
| Al - 7 wt% Si - 2 wt% Fe |
Fe2SiAl8 |
| Al - 12 wt% Si - 1.5 wt% Mn |
Mn3Si2Al15 |
| Al - 11 wt% Si - 5 wt% Ni |
NiAl3 |
| Al - 10 wt% Si - 10 wt% Mg |
Mg2Si |
| Al - 10 wt% Si - 2 wt% Cr |
Cr5Si8Al2 |
| Al - 16 wt% Si - 0.3 wt% Ti |
Ti(AlSi)2 |
| Al - 10 wt% Si - 0.5 wt% Zr |
ZrAl3 |
[0026] Alloys of particular interest for high temperature applications are those containing
substantial amounts of Mn. Such alloys may be produced by adding Mn to traditional
high temperature alloy compositions until the hyper-eutectic range is reached. This
is mixed with refractory particles, e.g. which refine the intermetallics and distribute
the particles uniformly throughout the matrix.
[0027] Examples of new composites thus produced are given in Table II below:
Table II
| Alloy |
| Al-10 wt% Si-1.2 wt% Mn-0.4 wt% Mg-15 vol% SiC |
| Al-10 wt% Si-1.2 wt% Mn-0.4 wt% Mg-5 wt% Ni-15 vol% SiC |
| Al-10 wt% Si-1.2 wt% Mn-1.0 wt% Mg-5 wt% Ni-2.5 wt% Cu -15 vol% SiC |
[0028] While a typical intermetallic is a compound formed of at least two metallic components,
within the process of this invention, silicon behaves in the manner of an intermetallic
in its ability to wet and engulf refractory particles. Accordingly, the term "intermetallic"
as used in this invention includes silicon.
Brief Description of the Drawings
[0029] In the drawings which illustrate the present invention:
Figure 1 is a photomicrograph of an A-356 alloy casting with refractory particles,
Figures 2-7 are photomicrographs of hyper-eutectic castings with refractory particles,
Figure 8 is a photomicrograph of a hyper-eutectic alloy casting without refractory
particles,
Figure 9 is a photomicrograph of a hyper-eutectic alloy casting with refractory particles,
Figure 10 is a photomicrograph of a further hyper-eutectic alloy casting without refractory
particles,
Figure 11 is a photomicrograph of a casting of the alloy of Fig. 10 with refractory
particles,
Figure 12 is bar graphs showing yield strengths of different matrix alloys and composites
of the invention, and
Figures 13-15 are plots of stress as a function of soak time for three different cast
composites of the invention.
Example 1 (Comparative)
[0030] An aluminum matrix composite was prepared by mixing 15% by volume of silicon carbide
particles having sizes in the range of 10-15
µm with a melt of A356 aluminum alloy containing 6.5 to 7.5% Si and 0.3 to 0.45% Mg.
This was cast and solidified to form an ingot having the microstructure shown in Figure
1. It will be seen that the reinforcing particles have been pushed ahead of the solidification
interface and are not uniformly dispersed throughout the ingot.
Example 2 (a) (Comparative)
[0031] Another ingot was prepared from a melt of Al - 16% Si alloy and 15% by volume of
silicon carbide particles having particle sizes in the range of 10-15
µm. These were thoroughly mixed and the mixture was then cast and solidified to form
an ingot. The ingot formed had the microstructure shown in Figure 2 and it will be
seen that the reinforcing particles are uniformly spaced and are engulfed by silicon
crystals. The silicon carbide particles also refined the silicon.
Example 2 (b) (Comparative)
[0032] The above procedure was repeated using a melt of Al-12 Si-1.5 Mn, to which was added
15% by volume of the same silicon carbide particles. The results in Figure 3 show
particle engulfment by Mn
3Si
2Al
15 crystals.
Example 2 (c) (Comparative)
[0033] The above procedure was again repeated using a melt of Al-7Si-2Fe, to which was added
15% by volume of the same silicon carbide particles. The results in Figure 4 show
particle engulfment by α-AlFeSi crystals (Fe
2SiAl
8).
Example 2 (d) (Comparative)
[0034] The above procedure was again repeated using a melt of Al-12Si-1.5 Fe, to which was
added 15% by volume of the same silicon carbide particles. The results in Figure 5
show particle engulfment by β-AlFeSi crystals (FeSiAl
5).
Example 2 (e) (Comparative)
[0035] The above procedure was again repeated using a melt of Al-11Si-5Ni, to which was
added 15% by volume of the same silicon carbide particles. The result in Figure 6
show particle engulfment by NiAl
3 crystals.
Example 2 (f) (Comparative)
[0036] The above procedure was again repeated using a melt of Al-10Si-10Mg, to which was
added 15% by volume of the same silicon carbide particles. The results in Figure 7
show particle engulfment by Mg
2Si crystals.
Example 3 (Comparative)
[0037] Two melts were prepared by heating aluminum containing 16 wt% silicon to a temperature
of 750°C. One melt was cast "as is" to form an ingot and a second melt was mixed with
15% by volume of silicon carbide particles having sizes in the range of 10-15 microns
and then cast to form an ingot. The ingots were identical in size and were cooled
and solidified under identical conditions. Figure 8 shows the microstructure of the
ingot without the refractory particles, while Figure 9 shows the microstructure of
the ingot with the refractory particles. The refinement of the silicon is clearly
evident.
Example 4 (Comparative)
[0038] To illustrate the effectiveness of the refinement according to this invention, the
procedure of Example 2 was repeated using a melt of Al - 7% Si - 2% Mn alloy. One
cast ingot was made from the alloy itself and a second cast ingot was made from a
composite of the alloy and 15% by volume of silicon carbide particles. Fig. 10 shows
the microstructure of the cast alloy and Fig. 11 shows the microstructure of the cast
composite. It can be seen that the primary Mn
3Si
2Al
15 intermetallic dendrites in the cast alloy are completely refined by the SiC particles.
Example 5
[0039] Three aluminum matrix composites were prepared by mixing 15% by volume of silicon
carbide particles having sizes in the range of 10-15
µm with three different aluminum alloy melts. The matrix alloys had the following compositions:
- Alloy A:
- Al - 10 wt% Si - 1.2 wt% Mn - 0.4 wt% Mg
- Alloy B:
- Al - 10 wt% Si - 1.2 wt% Mn - 0.4 wt% Mg - 5 wt% Ni
- Alloy C:
- Al - 10 wt% Si - 1.2 wt% Mn - 1.0 wt% Mg - 5 wt% Ni - 2.5 wt% Cu
[0040] The composites so formed were cast and solidified in the form of 12.7 mm diameter
as-cast test bars and 57 mm diameter ingots. The as-cast test bars were held for 100
hours at 250°C, and tensile tested at the soak temperature. The 57 mm diameter ingots
were extruded at 450°C to 9.5 mm diameter rod. Test bars were machined from the rod,
and held at between 200 and 400°C for various times to examine the effect of long
time exposure on the high temperature strength. The results are shown in Figure 12-15.
[0041] High temperature composite alloys may be used in casting applications, or as wrought
products such as forgings and extrusions. Figure 12 shows the strength retention of
as-cast material after 100 hrs at 250°C, which is relevant for applications such as
cast brake rotors. The figure shows that the new alloy composites have superior high
temperature strength to the presently used A356-SiC composite. It is also apparent
that adding SiC reinforcement to the unreinforced alloys adds to the high temperature
performance of these materials.
[0042] In wrought products additional softening mechanisms, such as sub-structure and grain
size coarsening, may operate which are usually absent in as-cast material. Figures
13-15 show the time dependence of the softening at 250, 300 and 400°C. All 3 alloys
show rapid softening in the first 10 hours of exposure, but beyond this are relatively
stable. This initial softening is due to normal, precipitate coarsening and resolution,
while after this has occurred the alloys have excellent long term stability. Comparing
the extrusion results with those for as-cast test bars in Figure 12, the extruded
composites have somewhat superior strength.
Industrial Applicability
[0043] It will be apparent from the above disclosure that the invention provides techniques
for improving hyper-eutectic alloys, which alloys can be used for the manufacture
of a variety of industrial products by conventional techniques.
1. A method for preparing a composite of an aluminum alloy and particles of a non-metallic
refractory material, comprising:
melting an aluminum alloy;
adding particles of non-metallic refractory material to the molten aluminum matrix;
mixing together the molten aluminum alloy and the particles of refractory material;
and
casting the resulting mixture;
characterized in that the aluminum alloy is a hyper-eutectic metal alloy comprising,
in percentages by weight, 7-16% silicon, 0.5-3.0% manganese, 0-5.0% copper, 0-5.0%
nickel, 0-1.0% iron, 0-0.2% titanium and 0.3-2.0% magnesium and the balance of the
alloy being aluminum and inevitable impurities and the excess alloying element or
elements of the hyper-eutectic molten aluminum alloy solidify first from the molten
aluminum matrix during solidification thereof to form intermetallics which comprise
Mn
3Si
2Al
15 and which engulf said refractory particles and keep them homogeneously distributed
throughout the solidified product.
2. A method according to claim 1 characterized in that the refractory particles are selected
from the group consisting of a metal oxide, metal nitride, metal carbide and metal
silicide.
3. A method according to claim 2 characterized in that the refractory particles comprise
silicon carbide.
4. A method according to any one of claims 1-3 characterized in that the refractory particles
are reinforcing particles and have sizes up to 20 µm.
5. A method according to any one of claims 1-3 characterized in that the refractory particles
are reinforcing particles having sizes in the range of 10 - 15 µm.
6. A method according to any one of claims 1-3 characterized in that the refractory particles
have sizes of less than 1 µm.
7. A method according to claim 6 characterized in that the refractory particles nucleate
and refine the intermetallics.
8. An aluminum alloy composite casting comprising a matrix of aluminum alloy having dispersed
therethrough particles of non-metallic refractory material,
characterized in that the aluminum alloy is an Al-Si-Mn hyper-eutectic alloy comprising,
in percentage by weight, 7-16% silicon, 0.5-3.0% manganese, 0-5.0% copper, 0-5.0%
nickel, 0-1.0% iron, 0-0.2% titanium and 0.3-2.0% magnesium and the balance of the
alloy being aluminum and inevitable impurities, in which the excess alloying element
or elements of the hyper-eutectic alloy have solidified first from the molten aluminum
matrix and have formed intermetallics comprising Mn3Si2Al15 during solidification which have engulfed the refractory particles and kept them
homogenerously distributed throughout the solidified product.
9. A casting according to claim 8 characterized in that the refractory particles are
selected from the group consisting of a metal oxide, metal nitride, metal carbide
and metal silicide.
10. A casting according to claim 8 characterized in that the refractory particles comprise
silicon carbide.
11. A casting according to any one of claims 8-10 characterized in that the refractory
particles have sizes up to 20 µm.
12. A casting according to any one of claims 8-10 characterized in that the refractory
particles have sizes in the range of 10 - 15 µm.
13. A casting according to any one of claims 8-10 characterized in that the refractory
particles have sizes of less than 1 µm.
14. A casting according to any one of claims 8-13 characterized in that the particles
have an aspect ratio in any direction of no more than 5:1.
15. A casting according to any one of claims 8-14 characterized in that the particles
are present in an amount of 5-40% by volume.
16. A casting according to any one of claims 8-15 characterized in that titanium is present
in the alloy in an amount of 0.1-0.2%.
1. Verfahren zur Herstellung eines Verbundwerkstoffs aus einer Aluminium-Legierung und
Teilchen aus einem nichtmetallischen, feuerfesten Material, umfassend:
Schmelzen einer Aluminium-Legierung;
Zugeben von Teilchen aus nicht-metallischem, feuerfestem Material zur geschmolzenen
Aluminiummatrix;
Vermischen der geschmolzenen Aluminium-Legierung und der Teilchen aus feuerfestem
Material; und
Gießen der resultierenden Mischung;
dadurch
gekennzeichnet, daß
die Aluminium-Legierung eine übereutektische Metall-Legierung ist, die in Gew.-% 7-16
% Silicium, 0,5-3,0 % Mangan, 0-5,0 % Kupfer, 0-5,0 % Nickel, 0-1,0 % Eisen, 0-0,2
% Titan und 0,3-2,0 % Magnesium umfaßt, wobei der Restanteil der Legierung Aluminium
und unvermeidbare Verunreinigungen sind, und das überschüssige Legierungselement oder
die -elemente der übereutektischen geschmolzenen Aluminium-Legierung zuerst aus der
geschmolzenen Aluminiummatrix während deren Festwerdens erstarren, um intermetallische
Verbindungen zu bilden, die Mn
3Si
2Al
15 umfassen und die feuerfesten Teilchen einhüllen und sie durch das erstarrte Produkt
hindurch homogen verteilt halten.
2. Verfahren gemäß Anspruch 1,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen ausgewählt sind aus der Gruppe, die aus einem Metalloxid,
Metallnitrid, Metallcarbid und Mitallsilicid besteht.
3. Verfahren gemäß Anspruch 2,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Siliciumcarbid umfassen.
4. Verfahren gemäß einem der Ansprüche 1 bis 3,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Verstärkungsteilchen sind und Größen von bis zu 20 µm aufweisen.
5. Verfahren gemäß einem der Ansprüche 1 bis 3,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Verstärkungsteilchen mit Größen im Bereich von 10 bis 15
µm sind.
6. Verfahren gemäß einem der Ansprüche 1 bis 3,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Größen von weniger als 1 µm aufweisen.
7. Verfahren gemäß Anspruch 6,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Kristallkeime bilden und die intermetallischen Verbindungen
raffinieren.
8. Aluminiumlegierungs-Verbundwerkstoff-Gußstück, umfassend eine Matrix aus Aluminium-Legierung
mit darin dispergierten Teilchen aus nicht-metallischem, feuerfestem Material,
dadurch gekennzeichnet, daß
die Aluminium-Legierung eine übereutektische Al-Si-Mn-Legierung ist, umfassend in
Gew.-% 7-16 % Silicium, 0,5-3,0 % Mangan, 0-5,0 % Kupfer, 0-5,0 % Nickel, 0-1,0 %
Eisen, 0-0,2 % Titan und 0,3-2,0 % Magnesium, wobei der Restanteil der Legierung Aluminium
und unvermeidbare Verunreinigungen sind, worin das überschüssige Legierungselement
oder die -elemente der übereutektischen Legierung zuerst aus der geschmolzenen Aluminiummatrix
erstarrten und intermetallische Verbindungen, umfassend Mn3Si2Al15, während des Erstarrens bildeten, welche die feuerfesten Teilchen eingehüllt und
sie durch das erstarrte Produkt hindurch homogen verteilt gehalten haben.
9. Gußstück gemäß Anspruch 8,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen ausgewählt sind aus der Gruppe, die aus einem Metalloxid,
Metallnitrid, Metallcarbid und Metallsilicid besteht.
10. Gußstück gemäß Anspruch 8,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Siliciumcarbid umfassen.
11. Gußstück gemäß einem der Ansprüche 8 bis 10,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Größen von bis zu 20 µm aufweisen.
12. Gußstück gemäß einem der Ansprüche 8 bis 10,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Größen im Bereich von 10 bis 15 µm aufweisen.
13. Gußstück gemäß einem der Ansprüche 8 bis 10,
dadurch gekennzeichnet, daß
die feuerfesten Teilchen Größen von weniger als 1 µm aufweisen.
14. Gußstück gemäß einem der Ansprüche 8 bis 13,
dadurch gekennzeichnet, daß
die Teilchen ein Längenverhältnis in jede Richtung von nicht mehr als 5:1 aufweisen.
15. Gußstück gemäß einem der Ansprüche 8 bis 14,
dadurch gekennzeichnet, daß
die Teilchen in einer Menge von 5 bis 40 Vol.-% vorhanden sind.
16. Gußstück gemäß einem der Ansprüche 8 bis 15,
dadurch gekennzeichnet, daß
Titan in der Legierung in einer Menge von 0,1 bis 0,2 % vorhanden ist.
1. Procédé de préparation d'un composite d'un alliage d'aluminium et de particules d'une
matière réfractaire non métallique comprenant:
la fusion d'un alliage d'aluminium;
l'addition de particules de matière réfractaire non métallique à la matrice d'aluminium
fondue,
le mélange ensemble de l'alliage d'aluminium fondu et des particules de matière réfractaire;
et
le coulage du mélange résultant;
caractérisé en ce que l'alliage d'aluminium est un alliage métallique hyper-eutectique
comprenant, en pourcentage en poids, 7-16% de silicium, 0,5-3,0% de manganèse, 0-5,0%
de cuivre, 0-5,0% de nickel, 0-1,0% de fer, 0-0,2% de titane et 0,3-2,0% de magnésium
et le complément de l'alliage étant de l'aluminium et des impuretés inévitables, et
le ou les éléments d'alliage en excès de l'alliage d'aluminium hyper-eutectique fondu
se solidifiant d'abord dans la matrice d'aluminium fondue pendant sa solidification
pour former des composés intermétalliques qui comprennent du Mn
3Si
2Al
15 et qui engloutissent lesdites particules réfractaires et les maintiennent uniformément
distribués dans tout le produit solidifié.
2. Procédé selon la revendication 1, caractérisé en ce que les particules réfractaires
sont choisies dans le groupe constitué d'un oxyde métallique, un nitrure métallique,
un carbure métallique et un siliciure métallique.
3. Procédé selon la revendication 2, caractérisé en ce que les particules réfractaires
comprennent du carbure de silicium.
4. Procédé selon l'une quelconque des revendications 1-3, caractérisé en ce que les particules
réfractaires sont des particules de renfort et ont des tailles allant jusqu'à 20 µm.
5. Procédé selon l'une quelconque des revendications 1-3, caractérisé en ce que les particules
réfractaires sont des particules de renfort ayant des tailles dans la gamme de 10
- 15 µm.
6. Procédé selon l'une quelconque des revendications 1-3, caractérisé en ce que les particules
réfractaires ont des tailles inférieures à 1 µm.
7. Procédé selon la revendication 6, caractérisé en ce que les particules réfractaires
assemblent en noyau et affinent les composés intermétalliques.
8. Coulée de composite d'un alliage d'aluminium comprenant une matrice d'aluminium dans
laquelle sont dispersées des particules de matière réfractaire non métallique,
caractérisée en ce que l'alliage d'aluminium est un alliage hyper-eutectique Al-Si-Mn
comprenant, en pourcentage en poids, 7-16% de silicium, 0,5-3,0% de manganèse, 0-5,0%
de cuivre, 0-5,0% de nickel, 0-1,0% de fer, 0-0,2% de titane et 0,3-2,0% de magnésium
et le complément de l'alliage étant de l'aluminium et des impuretés inévitables, dans
lequel le ou les éléments d'alliage en excès de l'alliage hyper-eutectique se solidifient
d'abord dans la matrice d'aluminium fondue et forment des composés intermétalliques
comprenant du Mn3Si2Al15 pendant la solidification qui engloutissent les particules réfractaires et les maintiennent
uniformément distribués dans tout le produit solidifié.
9. Coulée selon la revendication 8, caractérisée en ce que les particules réfractaires
sont choisies dans le groupe constitué d'un oxyde métallique, un nitrure métallique,
un carbure métallique et un siliciure métallique.
10. Coulée selon la revendication 8, caractérisée en ce que les particules réfractaires
comprennent du carbure de silicium.
11. Coulée selon l'une quelconque des revendications 8-10, caractérisée en ce que les
particules réfractaires ont des tailles allant jusqu'à 20 µm.
12. Coulée selon l'une quelconque des revendications 8-10, caractérisée en ce que les
particules réfractaires ont des tailles dans la gamme de 10 - 15 µm.
13. Coulée selon l'une quelconque des revendications 8-10, caractérisée en ce que les
particules réfractaires ont des tailles inférieures à 1 µm.
14. Coulée selon l'une quelconque des revendications 8-13, caractérisée en ce que les
particules ont un rapport des côtés dans n'importe quelle direction inférieur à 5:1.
15. Coulée selon l'une quelconque des revendications 8-14, caractérisée en ce que les
particules sont présentes en une proportion de 5-40% en volume.
16. Coulée selon l'une quelconque des revendications 8-15, caractérisée en ce que du titane
est présent dans l'alliage en une proportion de 0,1-0,2%.