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R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 386 | P a g e
FABRICATION AND TESTING OF ULTRASONICALLY
ASSISTED STIR CAST AA 5083-Sicp COMPOSITES
R. S. Rana*, Rajesh Purohit* and S. Das**
*Department of Mechanical Engineering,Maulana Azad National Institute of Technology, Bhopal, (MP)
**Scientist, AMPRI, Bhopal, (MP)
ABSTRACT
Aluminum Matrix composites (AMCs) are light weight, high-strength materials with potential application in
areas such as automobile, aerospace, defence, engineering and other industries. AMCs are projected to
significantly reduce the overall weight of the vehicles and aircraft while maintaining satisfactory structural
strength. Reinforcement of micron or nano-sized range particles with aluminium matrix yields improved
mechanical and physical properties in composite materials. The distribution of nano sized reinforcing particles
also changes morphology and interfacial characteristics of nanocomposites. In this study, AA 5083 alloy micron
and nano SiC composites have been fabricated by Ultrasonic assisted stir casting. Different weight % of SiC
particles Micron (3, 5, 8, and 10 wt%) and Nano (1, 2, 3 and 4 wt%) were used for synthesis of composites.
SEM microstructure shows uniform distribution of SiC particles with agglomeration at some places. Various
properties of composites like tensile strength, compressive strength, hardness, ductility, density were measured.
Results revealed that the tensile strength, compressive strength and hardness of composites increases with
increase the weight % of SiC particles and particle size reduction. However ductility of composites with micron
SiC particles reduced in large value with increasing the weight % of SiC however with addition of nano SiC
particles only a small reduction in ductility was observed. The application of ultrasonic vibration on the
composite during melting not only refined the grain structure of the matrix, but also improved the distribution of
nano-sized reinforcement.
Keywords: Aluminum Matrix Composites, Ultrasonic Assisted Casting, Agglomeration, Nanocomposites.
I. INTRODUCTION
The engineering sector is always on the
search for newer materials with superior properties
combined with ease of fabrication, reproducibility
and ability to vary the composition to attain a range
of desired properties. The properties attainable in any
alloy system are limited to a certain extent and reach
a saturation limit; further improvement can be done
by strengthening mechanism, controlling
microstructure, alloying constituents, addition of
modifiers etc. [1]. Aluminium matrix composites
have drawn immense interest for various applications
in making aerospace and automobile components due
to their light weight, high strength, high stiffness,
lower cost, easy of fabrication and high dimensional
stability. Particulate–reinforced Aluminum matrix
composites (AMCs) are of particular interest due to
their ease of fabrication, lower costs, recyclability
and isotropic properties. Overall strength of such
particle reinforced AMCs depends on size of the
particles, the inter-particle spacing, volume fraction
of the particles and the nature of matrix and
reinforcement interface. Zhao et. al. [2] characterized
the properties and deformation behaviour of
aluminum matrix nano-composites. It was reported
that the ultimate tensile strength and yield strength of
nano-composites are enhanced with increasing the
particulate volume fraction, which are markedly
higher than those of Al composites synthesized by
micro size particles. Mazahery A. et. al. [3] reported
that incorporation of nano-particles into the
aluminum matrix could enhance the yield and
ultimate tensile strength considerably, while the
ductility is retained. A. Sakthivel, et. al. [4] studied
the mechanical properties of 2618 aluminum alloy
MMCs reinforced with two different sizes (7 and 33
µm) and wt. % of SiCp ( 0, 5 and 10 %) were
fabricated by stir casting method. The results show
that tensile strength of the composites increases with
decreasing size and increasing weight fraction of the
particles. The tensile strength of the forged
composites was higher than those of the cast
composites.
S. A. Sajjadi, et. al. [5] studied the
mechanical properties of A356 aluminum alloy
micron and nano Al2O3 composites fabricated by
liquid metallurgy route. Results revealed that by
increasing in Al2O3 percentage, the compressive
strength shows an increasing trend. The results also
show that the compressive strength of
nanocomposites is greater than that of micro-
composites. The compressive strength of composite
can primarily be attributed to the significant grain
refinement, the presence of reasonably distributed
hard particulates, dislocation generation due to elastic
modulus mismatch, coefficient of thermal expansion
RESEARCH ARTICLE OPEN ACCESS
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 387 | P a g e
mismatch between the matrix and reinforcement
phase, load transfer from matrix to reinforcement
phase and Orowan strengthening mechanism. Zhao
et. al. [2] characterized the properties and
deformation behavior of aluminum matrix nano-
composites. It was reported that the elongation
enhanced with increasing particulate volume fraction,
which are markedly higher than those of Al
composites synthesized by micro size particles. Ali
Mazahery et. al. Ali Mazahery, et. al. [6]
characterized cast A356 alloy reinforced with nano
SiCp composites and reported that hardness of the
composites is higher than that of the un-reinforced
alloy. It is maximum at 3.5 % of SiCp nanoparticles.
The higher hardness of the composites could be
attributed to the fact that SiCp particles act as
obstacles to the motion of dislocation. The hardness
increment can also be attributed to the reduced grain
size. In this study, AA 5083 alloy micron and nano
SiC composites has been fabricated by Ultrasonic
assisted Stir casting. Different weight % of SiC
particles Micron (3, 5, 8, and 10 wt%) and Nano (1,
2, 3, and 4 wt%) were used for synthesis of
composites. SEM microstructure shows uniform
distribution of SiC particles with some places
agglomeration. Varies properties of composites like
tensile strength, compressive strength, hardness,
ductility, density were studied.
II. EXPERIMENTAL PROCEDURES
Aluminum alloy 5083 has been selected as
matrix alloy for synthesis of AMCs. The chemical
compositions are shown in Table 1. Micron and Nano
size Silicon Carbide particulates have been used as
reinforcement material. SiC micron size particles
average particles size was 35 µm SiCp (99% Pure).
SiC Nano particles of average particle size 40 nm
(SiCp-b, 99+% pure). SEM micrograph of micron SiC
particles and TEM micrograph nano SiC particles are
shown in Fig. 1 and 2 respectively.
Table 1 Composition of AA 5083 Al alloy
Element Zn Fe Ti Cu Si Pb Mn Mg Cr Al
Percent 0.03 0.173 0.04 0.0181 0.16 0.014 0.526 5.13 0.097 Balance
Fig.1 SEM analysis of Micron size SiC particles
Fig. 2 TEM analysis of Nano SiC Particles
Synthesis of Aluminum alloy SiCp Composites
The steps involved for synthesizing Al-SiCp
composites are as follows:
 Cutting the aluminium ingot into small pieces
and placing them into a graphite crucible. The
graphite crucible was placed in electric
resistance furnace.
 Melting the aluminium alloy to a temperature
760o
C, added flux coveral 11 and degassed with
dry nitrogen gas of grade I.
 Addition of the pre-heated micron SiC particles
with different wt. % in the melt and stirring the
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 388 | P a g e
alloy melt with the help of a mechanical stirrer.
After stirring ultrasonification of the composites
with ultrasonic probe for about 5 minutes was
done. Composites have been prepared for 3, 5, 8
and 10 wt. % of SiC particles separately.
Similarly composites were prepared for 1, 2, 3
and 4 wt% of Nano SiC particles through
ultrasonic assisted stir casting.
 After successful addition of particles, the
composite melt was poured and solidified into a
mild steel die in the form of cylindrical rods (20
mm diameter and 200 mm length).
 Standard samples were prepared for tensile test,
compression tests, hardness test and
microstructural analysis.
III. RESULTS AND DISCUSSIONS
3.1 Microstructure: Fig. 3 shows the micrograph of
Al-2 wt. % SiCp composites which shows uniform
distribution of Nano SiCp particles. The
microstructure shows two phases one is α- Al and
intermetallic phases (Mg2Si). By comparing it with
phase diagram the possible intermetallic compound
could be Mg2Si, Al3Mg2 as well as SiCp. The
intermetallic phase was formed by precipitation on
the grain boundaries.
Fig. 3 SEM Micrograph of composite with 2 % nano SiCp
3.2 Density Measurement: The experimental density
of Al-SiCp composites were measured according to
Archimedes principle. The small pieces were cut
from alloy and composites and weighted first in air
and then in water. The theoretical densities were
calculated using the rule of mixture according to the
mass fraction of micron and nano particles. Porosities
were reported by difference between theoretical
density and experimental density. Density of
aluminium alloy is 2.66 gm/cc and density of SiC
particles is 3.22 gm/cc.
Fig.4 Variation of porosity of alloy and composites with different wt. % of micron SiC
0
0.5
1
1.5
2
2.5
0 3 5 8 10
%porosity
weight % of micron SiC
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 389 | P a g e
Fig.5 Variation of porosity of composites with different wt. % of Nano SiC
Porosity increases with increasing SiC weight percent
and decreasing particle size. This is due to the effect
of low wettability and agglomeration at high
reinforcement content and pore nucleation at the
matrix–SiC interfaces. Moreover, decreasing liquid
metal flow associated with the particle clusters leads
to the formation of porosity.
3.3 Tensile and compressive Strength: From the
Fig. 6, 7, 8 and 9 following observations were made:
(i) The Alloy have the lower tensile strength and
compressive strength.
(ii) The tensile strength and compressive strength of
composites with 10 % micron SiCp is higher than 1 &
2 % Nano SiCp.
(iii) The tensile strength and compressive strength of
composites with 3% nano SiCp is higher than 10 %
Micron SiCp.
(iv) The highest tensile strength and compressive
strength was observed in the case of 4% nano SiCp.
Fig. 10 shows the tensile strength and Compression
Strength of Alloy, composites with Micron SiCp and
Composites with Nano SiCp.
Fig.6 Variation of Tensile strength of alloy and composites with different wt. % of micron SiCp
0
0.5
1
1.5
2
2.5
1 2 3 4
%porosity
weight % of Nano SiC
225
230
235
240
245
250
255
0 2 4 6 8 10 12
Tensilestrength(MPa)
weight % of micron SiC
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 390 | P a g e
Fig.7 Variation of Tensile strength of composites with different wt. % of Nano SiC
Fig 8 Variation of compressive strength of alloy and composites with different wt. % of micron SiC
Fig.9 Variation of compressive strength of alloy and composites with different wt. % of nano SiC
235
240
245
250
255
260
265
270
275
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5
Tensilestrength(MPa)
weight % of Nano SiC
320
325
330
335
340
345
350
0 2 4 6 8 10 12
Compressivestrength(Mpa)
weight % of micron SiC
335
340
345
350
355
360
365
0 0.5 1 1.5 2 2.5 3 3.5 4 4.5
Compressivestrength(Mpa)
weight % of Nano SiC
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 391 | P a g e
Fig. 10 Tensile strength and Compression Strength of Alloy, composites with 10 % Micron SiCp and
Composites with Nano SiCp
Tensile strength and compressive strength of Nano
composites is higher because of two reasons- First,
each larger-sized particle has larger interface area
with the matrix, and thus endures higher stress
concentration. Second, the particle fracture strength
is controlled by the intrinsic SiCp flaws within the
particle. Since the size and number of flaws are
limited by the size of the particle, larger particles are
more likely to fracture because they have a greater
statistical probability of containing a flaw that is
greater than the critical size [7]. Since the fractured
particles cannot withstand any load, but act as
preferential failure sites, the composites with larger
SiCp particle size show lower tensile and compressive
strength as compared to that with smaller particle
size. The grain refinement and strong multidirectional
thermal stress at the Al/SiC interface are also
important factors which play a significant role in the
high strength of the composites. SiC particles have
grain-refined strengthening effect, which is improved
with increasing volume fraction since they act as the
heterogeneous nucleation catalyst for aluminum [8].
The difference between the coefficient of thermal
expansion (CTE) values of matrix and ceramic
particles generates thermally induced residual
stresses and increases dislocations density upon rapid
solidification during the fabrication process. The
interaction of dislocations with the non-sharable nano
particles increases the strength level of the composite
samples. According to the Orowan mechanism, the
nano-SiC particles act as obstacles to hinder the
motion of dislocations near the particles in the
matrix. This effect of particles on the matrix is
enhanced gradually with the increase of particulate
volume fraction [9, 10].
3.4. Elongation: Fig.11 shows the comparison of %
elongation of alloy, composites with micron SiCp and
composites with nano SiCp particles. Normally,
micron-sized particles are used to improve the
ultimate tensile and the compressive strength of the
alloy. However, the ductility of the MMCs
deteriorates significantly with high ceramic particle
concentration in the case of composites with micron
size SiCp. It is of interest to use nano-sized ceramic
particles to strengthen the metal matrix while
maintaining good ductility. It is noted from
observation that the elongation remains almost same
with the addition of nano particles. This is one of the
advantages of nano composites. The application of
ultrasonic vibration on the composite melt during the
casting not only refined the grain structure of the
matrix, but also improved the distribution of nano-
sized reinforcement.
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 392 | P a g e
Fig.11 Percentage elongation of Alloy, composites with Micron SiCp and Composites with Nano SiCp
3.5 Hardness: Fig.12 shows the comparison of
hardness of alloy, composites with micron SiCp and
composites with nano SiCp. From the graph it is
observed that (1)-The Alloy have lower hardness.
(2)-The hardness of composites with 10 % micron
SiCp is higher than 1 and 2 % Nano SiCp. (3)- The
hardness of composites with 3 % nano SiCp is
slightly higher than 10 % Micron SiCp composites.
(4)-The highest hardness was observed in the case of
4% nano SiCp composites. The hardness of the
composites is higher than that of the alloy and
hardness of the composites increases with increasing
weight percent of the particles and with decreasing
particles size. The higher hardness of the composite
samples relative to that of the Al-alloy matrix could
be attributed to the reducing grain size and existence
of SiCp hard particles acting as obstacles to the
motion of dislocation [11]. Also, the hardness of 3 &
4 % nano SiCp composites was greater than that of
micron SiCp composites because of the more
influence of nano particles on the strengthening
mechanism (Orowan mechanism). At higher SiC
weight percent, scattering of hardness results
increases because of non-uniform distribution of the
reinforcement particles. It should be mentioned that
agglomeration occurs as a result of higher viscosity
of the molten metal and increasing tendency to clump
the particles together due to high surface tension and
poor wetting between the particles and the melt.
Fig.12 Comparison of Hardness of Alloy, composites with Micron SiCp and Composites with
Nano SiCp
0
0.5
1
1.5
2
2.5
3
3.5
4
4.5
% Elongation
0
10
20
30
40
50
60
70
80
90
Hardness (BHN)
R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com
Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393
www.ijera.com 393 | P a g e
IV. CONCLUSIONS
(1) Aluminium matrix micron (3, 5, 8 and 10 wt. %)
and nano (1, 2, 3 and 4 wt. %) SiCp composites
have been successfully fabricated by ultrasonic
assisted stir casting process.
(2) Porosity of composites could be decreased
significantly by the ultrasonic treatment and
nitrogen degassing. Moreover the porosity was
controlled below 2.14 % after of 5 minutes of
ultrasonic treatment, proposing an effective
method for degassing particulate reinforced
aluminum alloy composites.
(3) Tensile strength increases with increase in wt. %
of SiCp particles. Al-4 % nano SiCp composites
have the maximum tensile strength of 270 MPa.
(4) The compressive strength increases with increase
in wt. % of SiCp particles. Al-4% nano SiCp
composites have the maximum compressive
strength of 361 MPa.
(5) Composites with 10 % micron SiCp have higher
hardness (77 BHN) among all the micron SiCp
composites. However, Al- 4% nano SiCp
composite shows highest value of hardness (79
BHN).
(6) The elongation of composites with micron SiCp
particles decreases considerably with increasing
weight % of micron SiC particles. In case of
composites with nano SiCp the elongation remain
almost same.
REFERENCES
[1] Rupa Dasgupta, Humaira Meenai, “SiC
particulate dispersed composites of an Al–
Zn–Mg–Cu alloy: Property comparison with
parent alloy”, Materials Characterization,
54, 2005, 438-445.
[2] Y Zhao T, S L Zhang, G Chen, X N Cheng,
C Q Wang, “In situ (Al2O3+Al3Zr) NP /Al
nano composites synthesized by magneto-
chemical melt reaction”, Composite Science
Technology, 68, 2008, 1463-1470
[3] 3.A.Mazahery, H.Abdizadeh., H.R.
Baharvandi, “Development of high-
performanceA356/nano-Al2O3 composites”,
Material Science Engineering A 518, 2009,
61–64.
[4] A. Sakthivel, R. Palaninathan, R.
Velmurugan, P. Raghothama Rao,
“Production and mechanical properties of
SiCpp particle-reinforced 2618 aluminum
alloy composites”, Journal of Material
Science 43, 2008, 7047–7056.
[5] S. A. Sajjadi, H.R. Ezatpour, H. Beygi,
“Microstructure and mechanical properties
of Al–Al2O3 micro and nano composites
fabricated by stir casting”, Materials Science
and Engineering A 528, 2011, 8765– 8771.
[6] Ali Mazahery, Mohsen Ostad Shabani,
“Characterization of cast A356 alloy
reinforced with nano SiCp composites”,
Transactions Nonferrous Metallurgical
Society, China 22, 2012, 275-280.
[7] Y. L. Shen, E. Fishencord, and N. Chawla,
“Correlating Macrohardness and Tensile
Behavior in Discontinuously Reinforced
Metal Matrix Composites”, Scripta Materila,
42, No. 5, 2000, 427–432.
[8] M. C. Watson, T. W. Cline, “The use of
single fibre push out testing to explore
interfacial mechanics in SiC monofilament-
reinforced Ti: A photoelastic study of the
test”, Acta Metall Mater, 40, 1992, 131-
139.
[9] FM Hosking, Portillo Folgar F, R
Wonderlin, R Mehrabian, “Composite of
aluminium alloys: fabrication and wear
behaviour”, Journal of Material Science, 17,
1982, 477–98
[10] M Habibnejad-Korayema, R Mahmudia, W
J Pooleb, “Enhanced properties of Mg-based
nano-composites reinforced with Al2O3
nano-particles”, Material Science &
Engineering A, 519 (1-2), 2009, 198-203.
[11] P S Cooke, P S Werner, “Pressure
infiltration casting of metal matrix
composites”, Journal of Material Science
Engineering A, 144, 1991, 189-193.

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Bq35386393

  • 1. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 386 | P a g e FABRICATION AND TESTING OF ULTRASONICALLY ASSISTED STIR CAST AA 5083-Sicp COMPOSITES R. S. Rana*, Rajesh Purohit* and S. Das** *Department of Mechanical Engineering,Maulana Azad National Institute of Technology, Bhopal, (MP) **Scientist, AMPRI, Bhopal, (MP) ABSTRACT Aluminum Matrix composites (AMCs) are light weight, high-strength materials with potential application in areas such as automobile, aerospace, defence, engineering and other industries. AMCs are projected to significantly reduce the overall weight of the vehicles and aircraft while maintaining satisfactory structural strength. Reinforcement of micron or nano-sized range particles with aluminium matrix yields improved mechanical and physical properties in composite materials. The distribution of nano sized reinforcing particles also changes morphology and interfacial characteristics of nanocomposites. In this study, AA 5083 alloy micron and nano SiC composites have been fabricated by Ultrasonic assisted stir casting. Different weight % of SiC particles Micron (3, 5, 8, and 10 wt%) and Nano (1, 2, 3 and 4 wt%) were used for synthesis of composites. SEM microstructure shows uniform distribution of SiC particles with agglomeration at some places. Various properties of composites like tensile strength, compressive strength, hardness, ductility, density were measured. Results revealed that the tensile strength, compressive strength and hardness of composites increases with increase the weight % of SiC particles and particle size reduction. However ductility of composites with micron SiC particles reduced in large value with increasing the weight % of SiC however with addition of nano SiC particles only a small reduction in ductility was observed. The application of ultrasonic vibration on the composite during melting not only refined the grain structure of the matrix, but also improved the distribution of nano-sized reinforcement. Keywords: Aluminum Matrix Composites, Ultrasonic Assisted Casting, Agglomeration, Nanocomposites. I. INTRODUCTION The engineering sector is always on the search for newer materials with superior properties combined with ease of fabrication, reproducibility and ability to vary the composition to attain a range of desired properties. The properties attainable in any alloy system are limited to a certain extent and reach a saturation limit; further improvement can be done by strengthening mechanism, controlling microstructure, alloying constituents, addition of modifiers etc. [1]. Aluminium matrix composites have drawn immense interest for various applications in making aerospace and automobile components due to their light weight, high strength, high stiffness, lower cost, easy of fabrication and high dimensional stability. Particulate–reinforced Aluminum matrix composites (AMCs) are of particular interest due to their ease of fabrication, lower costs, recyclability and isotropic properties. Overall strength of such particle reinforced AMCs depends on size of the particles, the inter-particle spacing, volume fraction of the particles and the nature of matrix and reinforcement interface. Zhao et. al. [2] characterized the properties and deformation behaviour of aluminum matrix nano-composites. It was reported that the ultimate tensile strength and yield strength of nano-composites are enhanced with increasing the particulate volume fraction, which are markedly higher than those of Al composites synthesized by micro size particles. Mazahery A. et. al. [3] reported that incorporation of nano-particles into the aluminum matrix could enhance the yield and ultimate tensile strength considerably, while the ductility is retained. A. Sakthivel, et. al. [4] studied the mechanical properties of 2618 aluminum alloy MMCs reinforced with two different sizes (7 and 33 µm) and wt. % of SiCp ( 0, 5 and 10 %) were fabricated by stir casting method. The results show that tensile strength of the composites increases with decreasing size and increasing weight fraction of the particles. The tensile strength of the forged composites was higher than those of the cast composites. S. A. Sajjadi, et. al. [5] studied the mechanical properties of A356 aluminum alloy micron and nano Al2O3 composites fabricated by liquid metallurgy route. Results revealed that by increasing in Al2O3 percentage, the compressive strength shows an increasing trend. The results also show that the compressive strength of nanocomposites is greater than that of micro- composites. The compressive strength of composite can primarily be attributed to the significant grain refinement, the presence of reasonably distributed hard particulates, dislocation generation due to elastic modulus mismatch, coefficient of thermal expansion RESEARCH ARTICLE OPEN ACCESS
  • 2. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 387 | P a g e mismatch between the matrix and reinforcement phase, load transfer from matrix to reinforcement phase and Orowan strengthening mechanism. Zhao et. al. [2] characterized the properties and deformation behavior of aluminum matrix nano- composites. It was reported that the elongation enhanced with increasing particulate volume fraction, which are markedly higher than those of Al composites synthesized by micro size particles. Ali Mazahery et. al. Ali Mazahery, et. al. [6] characterized cast A356 alloy reinforced with nano SiCp composites and reported that hardness of the composites is higher than that of the un-reinforced alloy. It is maximum at 3.5 % of SiCp nanoparticles. The higher hardness of the composites could be attributed to the fact that SiCp particles act as obstacles to the motion of dislocation. The hardness increment can also be attributed to the reduced grain size. In this study, AA 5083 alloy micron and nano SiC composites has been fabricated by Ultrasonic assisted Stir casting. Different weight % of SiC particles Micron (3, 5, 8, and 10 wt%) and Nano (1, 2, 3, and 4 wt%) were used for synthesis of composites. SEM microstructure shows uniform distribution of SiC particles with some places agglomeration. Varies properties of composites like tensile strength, compressive strength, hardness, ductility, density were studied. II. EXPERIMENTAL PROCEDURES Aluminum alloy 5083 has been selected as matrix alloy for synthesis of AMCs. The chemical compositions are shown in Table 1. Micron and Nano size Silicon Carbide particulates have been used as reinforcement material. SiC micron size particles average particles size was 35 µm SiCp (99% Pure). SiC Nano particles of average particle size 40 nm (SiCp-b, 99+% pure). SEM micrograph of micron SiC particles and TEM micrograph nano SiC particles are shown in Fig. 1 and 2 respectively. Table 1 Composition of AA 5083 Al alloy Element Zn Fe Ti Cu Si Pb Mn Mg Cr Al Percent 0.03 0.173 0.04 0.0181 0.16 0.014 0.526 5.13 0.097 Balance Fig.1 SEM analysis of Micron size SiC particles Fig. 2 TEM analysis of Nano SiC Particles Synthesis of Aluminum alloy SiCp Composites The steps involved for synthesizing Al-SiCp composites are as follows:  Cutting the aluminium ingot into small pieces and placing them into a graphite crucible. The graphite crucible was placed in electric resistance furnace.  Melting the aluminium alloy to a temperature 760o C, added flux coveral 11 and degassed with dry nitrogen gas of grade I.  Addition of the pre-heated micron SiC particles with different wt. % in the melt and stirring the
  • 3. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 388 | P a g e alloy melt with the help of a mechanical stirrer. After stirring ultrasonification of the composites with ultrasonic probe for about 5 minutes was done. Composites have been prepared for 3, 5, 8 and 10 wt. % of SiC particles separately. Similarly composites were prepared for 1, 2, 3 and 4 wt% of Nano SiC particles through ultrasonic assisted stir casting.  After successful addition of particles, the composite melt was poured and solidified into a mild steel die in the form of cylindrical rods (20 mm diameter and 200 mm length).  Standard samples were prepared for tensile test, compression tests, hardness test and microstructural analysis. III. RESULTS AND DISCUSSIONS 3.1 Microstructure: Fig. 3 shows the micrograph of Al-2 wt. % SiCp composites which shows uniform distribution of Nano SiCp particles. The microstructure shows two phases one is α- Al and intermetallic phases (Mg2Si). By comparing it with phase diagram the possible intermetallic compound could be Mg2Si, Al3Mg2 as well as SiCp. The intermetallic phase was formed by precipitation on the grain boundaries. Fig. 3 SEM Micrograph of composite with 2 % nano SiCp 3.2 Density Measurement: The experimental density of Al-SiCp composites were measured according to Archimedes principle. The small pieces were cut from alloy and composites and weighted first in air and then in water. The theoretical densities were calculated using the rule of mixture according to the mass fraction of micron and nano particles. Porosities were reported by difference between theoretical density and experimental density. Density of aluminium alloy is 2.66 gm/cc and density of SiC particles is 3.22 gm/cc. Fig.4 Variation of porosity of alloy and composites with different wt. % of micron SiC 0 0.5 1 1.5 2 2.5 0 3 5 8 10 %porosity weight % of micron SiC
  • 4. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 389 | P a g e Fig.5 Variation of porosity of composites with different wt. % of Nano SiC Porosity increases with increasing SiC weight percent and decreasing particle size. This is due to the effect of low wettability and agglomeration at high reinforcement content and pore nucleation at the matrix–SiC interfaces. Moreover, decreasing liquid metal flow associated with the particle clusters leads to the formation of porosity. 3.3 Tensile and compressive Strength: From the Fig. 6, 7, 8 and 9 following observations were made: (i) The Alloy have the lower tensile strength and compressive strength. (ii) The tensile strength and compressive strength of composites with 10 % micron SiCp is higher than 1 & 2 % Nano SiCp. (iii) The tensile strength and compressive strength of composites with 3% nano SiCp is higher than 10 % Micron SiCp. (iv) The highest tensile strength and compressive strength was observed in the case of 4% nano SiCp. Fig. 10 shows the tensile strength and Compression Strength of Alloy, composites with Micron SiCp and Composites with Nano SiCp. Fig.6 Variation of Tensile strength of alloy and composites with different wt. % of micron SiCp 0 0.5 1 1.5 2 2.5 1 2 3 4 %porosity weight % of Nano SiC 225 230 235 240 245 250 255 0 2 4 6 8 10 12 Tensilestrength(MPa) weight % of micron SiC
  • 5. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 390 | P a g e Fig.7 Variation of Tensile strength of composites with different wt. % of Nano SiC Fig 8 Variation of compressive strength of alloy and composites with different wt. % of micron SiC Fig.9 Variation of compressive strength of alloy and composites with different wt. % of nano SiC 235 240 245 250 255 260 265 270 275 0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 Tensilestrength(MPa) weight % of Nano SiC 320 325 330 335 340 345 350 0 2 4 6 8 10 12 Compressivestrength(Mpa) weight % of micron SiC 335 340 345 350 355 360 365 0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 Compressivestrength(Mpa) weight % of Nano SiC
  • 6. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 391 | P a g e Fig. 10 Tensile strength and Compression Strength of Alloy, composites with 10 % Micron SiCp and Composites with Nano SiCp Tensile strength and compressive strength of Nano composites is higher because of two reasons- First, each larger-sized particle has larger interface area with the matrix, and thus endures higher stress concentration. Second, the particle fracture strength is controlled by the intrinsic SiCp flaws within the particle. Since the size and number of flaws are limited by the size of the particle, larger particles are more likely to fracture because they have a greater statistical probability of containing a flaw that is greater than the critical size [7]. Since the fractured particles cannot withstand any load, but act as preferential failure sites, the composites with larger SiCp particle size show lower tensile and compressive strength as compared to that with smaller particle size. The grain refinement and strong multidirectional thermal stress at the Al/SiC interface are also important factors which play a significant role in the high strength of the composites. SiC particles have grain-refined strengthening effect, which is improved with increasing volume fraction since they act as the heterogeneous nucleation catalyst for aluminum [8]. The difference between the coefficient of thermal expansion (CTE) values of matrix and ceramic particles generates thermally induced residual stresses and increases dislocations density upon rapid solidification during the fabrication process. The interaction of dislocations with the non-sharable nano particles increases the strength level of the composite samples. According to the Orowan mechanism, the nano-SiC particles act as obstacles to hinder the motion of dislocations near the particles in the matrix. This effect of particles on the matrix is enhanced gradually with the increase of particulate volume fraction [9, 10]. 3.4. Elongation: Fig.11 shows the comparison of % elongation of alloy, composites with micron SiCp and composites with nano SiCp particles. Normally, micron-sized particles are used to improve the ultimate tensile and the compressive strength of the alloy. However, the ductility of the MMCs deteriorates significantly with high ceramic particle concentration in the case of composites with micron size SiCp. It is of interest to use nano-sized ceramic particles to strengthen the metal matrix while maintaining good ductility. It is noted from observation that the elongation remains almost same with the addition of nano particles. This is one of the advantages of nano composites. The application of ultrasonic vibration on the composite melt during the casting not only refined the grain structure of the matrix, but also improved the distribution of nano- sized reinforcement.
  • 7. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 392 | P a g e Fig.11 Percentage elongation of Alloy, composites with Micron SiCp and Composites with Nano SiCp 3.5 Hardness: Fig.12 shows the comparison of hardness of alloy, composites with micron SiCp and composites with nano SiCp. From the graph it is observed that (1)-The Alloy have lower hardness. (2)-The hardness of composites with 10 % micron SiCp is higher than 1 and 2 % Nano SiCp. (3)- The hardness of composites with 3 % nano SiCp is slightly higher than 10 % Micron SiCp composites. (4)-The highest hardness was observed in the case of 4% nano SiCp composites. The hardness of the composites is higher than that of the alloy and hardness of the composites increases with increasing weight percent of the particles and with decreasing particles size. The higher hardness of the composite samples relative to that of the Al-alloy matrix could be attributed to the reducing grain size and existence of SiCp hard particles acting as obstacles to the motion of dislocation [11]. Also, the hardness of 3 & 4 % nano SiCp composites was greater than that of micron SiCp composites because of the more influence of nano particles on the strengthening mechanism (Orowan mechanism). At higher SiC weight percent, scattering of hardness results increases because of non-uniform distribution of the reinforcement particles. It should be mentioned that agglomeration occurs as a result of higher viscosity of the molten metal and increasing tendency to clump the particles together due to high surface tension and poor wetting between the particles and the melt. Fig.12 Comparison of Hardness of Alloy, composites with Micron SiCp and Composites with Nano SiCp 0 0.5 1 1.5 2 2.5 3 3.5 4 4.5 % Elongation 0 10 20 30 40 50 60 70 80 90 Hardness (BHN)
  • 8. R. S. Rana et al. Int. Journal of Engineering Research and Application www.ijera.com Vol. 3, Issue 5, Sep-Oct 2013, pp.386-393 www.ijera.com 393 | P a g e IV. CONCLUSIONS (1) Aluminium matrix micron (3, 5, 8 and 10 wt. %) and nano (1, 2, 3 and 4 wt. %) SiCp composites have been successfully fabricated by ultrasonic assisted stir casting process. (2) Porosity of composites could be decreased significantly by the ultrasonic treatment and nitrogen degassing. Moreover the porosity was controlled below 2.14 % after of 5 minutes of ultrasonic treatment, proposing an effective method for degassing particulate reinforced aluminum alloy composites. (3) Tensile strength increases with increase in wt. % of SiCp particles. Al-4 % nano SiCp composites have the maximum tensile strength of 270 MPa. (4) The compressive strength increases with increase in wt. % of SiCp particles. Al-4% nano SiCp composites have the maximum compressive strength of 361 MPa. (5) Composites with 10 % micron SiCp have higher hardness (77 BHN) among all the micron SiCp composites. However, Al- 4% nano SiCp composite shows highest value of hardness (79 BHN). (6) The elongation of composites with micron SiCp particles decreases considerably with increasing weight % of micron SiC particles. In case of composites with nano SiCp the elongation remain almost same. REFERENCES [1] Rupa Dasgupta, Humaira Meenai, “SiC particulate dispersed composites of an Al– Zn–Mg–Cu alloy: Property comparison with parent alloy”, Materials Characterization, 54, 2005, 438-445. [2] Y Zhao T, S L Zhang, G Chen, X N Cheng, C Q Wang, “In situ (Al2O3+Al3Zr) NP /Al nano composites synthesized by magneto- chemical melt reaction”, Composite Science Technology, 68, 2008, 1463-1470 [3] 3.A.Mazahery, H.Abdizadeh., H.R. Baharvandi, “Development of high- performanceA356/nano-Al2O3 composites”, Material Science Engineering A 518, 2009, 61–64. [4] A. Sakthivel, R. Palaninathan, R. Velmurugan, P. Raghothama Rao, “Production and mechanical properties of SiCpp particle-reinforced 2618 aluminum alloy composites”, Journal of Material Science 43, 2008, 7047–7056. [5] S. A. Sajjadi, H.R. Ezatpour, H. Beygi, “Microstructure and mechanical properties of Al–Al2O3 micro and nano composites fabricated by stir casting”, Materials Science and Engineering A 528, 2011, 8765– 8771. [6] Ali Mazahery, Mohsen Ostad Shabani, “Characterization of cast A356 alloy reinforced with nano SiCp composites”, Transactions Nonferrous Metallurgical Society, China 22, 2012, 275-280. [7] Y. L. Shen, E. Fishencord, and N. Chawla, “Correlating Macrohardness and Tensile Behavior in Discontinuously Reinforced Metal Matrix Composites”, Scripta Materila, 42, No. 5, 2000, 427–432. [8] M. C. Watson, T. W. Cline, “The use of single fibre push out testing to explore interfacial mechanics in SiC monofilament- reinforced Ti: A photoelastic study of the test”, Acta Metall Mater, 40, 1992, 131- 139. [9] FM Hosking, Portillo Folgar F, R Wonderlin, R Mehrabian, “Composite of aluminium alloys: fabrication and wear behaviour”, Journal of Material Science, 17, 1982, 477–98 [10] M Habibnejad-Korayema, R Mahmudia, W J Pooleb, “Enhanced properties of Mg-based nano-composites reinforced with Al2O3 nano-particles”, Material Science & Engineering A, 519 (1-2), 2009, 198-203. [11] P S Cooke, P S Werner, “Pressure infiltration casting of metal matrix composites”, Journal of Material Science Engineering A, 144, 1991, 189-193.