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Effect of Processing Parameters on theMechanical Properties of Injection MoldedThermoplastic Polyolefin (TPO) Cellular Foams
Steven Wong, John W. S. Lee, Hani E. Naguib,* Chul B. Park
In this study, the effects of processing parameters on the mechanical properties of injectionmolded thermoplastic polyolefin (TPO) foams are investigated. Closed cell TPO foams wereprepared by injection molding process. The microstructure of these foamed samples wascontrolled by carefully altering the processing parameters on the injection molding machine.The foammorphologies were characterized in terms of skin thickness, surface roughness, andrelative foam density. Tensile properties andimpact resistance of various injection moldedTPO samples were correlated with various foammorphologies. The findings show that the mech-anical properties are significantly affected byfoam morphologies. The experimental resultsobtained from this study can be used to predictthe microstructure and mechanical properties ofcellular injection molded TPO foams preparedwith different processing parameters.
Introduction
Structural foams are plastic foams manufactured by
using conventional preplasticating-type injection molding
machines. A physical blowing agent (PBA), a chemical
blowing agent (CBA), or both are employed in the process
to produce a cellular (foam) structure. The structural foam
molding technology was first invented and improved by
Angell et al.[1–3] Low-pressure preplasticating-type struc-
tural foam molding machines are most commonly used to
create structural foams, since the required size of the
S. Wong, J. W. S. Lee, H. E. Naguib, C. B. ParkDepartment of Mechanical and Industrial Engineering, Universityof Toronto, 5 King’s College Road, Toronto, ON, M5S 3G8, CanadaFax: (þ1) 416 978 7753; E-mail: [email protected]
Macromol. Mater. Eng. 2008, 293, 605–613
� 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
molding system for producing large products is smaller
than that of conventional injection molding due to lower
cavity pressure.[4] The advanced structural foam molding
technology[5,6] guarantees uniform gas dispersion and
complete (or substantial) dissolution in the polymer melt,
despite the non-steady molding process.
Since the generated cells compensate for the shrinkage
of injection molded parts during cooling, structural foams
typically have outstanding geometric accuracy. The
advantages of foam injection molding include the absence
of sink marks on the part surface, reduced weight, low
back pressure, faster production cycle time, and high
stiffness-to-weight ratio.[7–9] Due to this unique set of
advantages, low-pressure preplasticating-type structural
foam molding technology has been widely used for manu-
facturing large products that require geometric accuracy.
Poly(propylene) (PP) is widely used inmany engineering
applications. It has excellent physical and mechanical
DOI: 10.1002/mame.200700362 605
S. Wong, J. W. S. Lee, H. E. Naguib, C. B. Park
Figure 1. Schematic of advanced structural foammoldingmachine.
606
properties as well as good recycling ability. It is also
inexpensive. However, PP has poor mechanical properties
on impact and at low temperatures.[10] Therefore, polymer
alloys are used to enhance thesemechanical properties. For
instance, the addition of poly(ethylene terephthalate) (PET)
in PP could enhance the stiffness at higher tempera-
tures[11] and the addition of rubber, such as ethylene–
propylene rubber (EPR) or ENGAGE, could result in the
improvement of impact properties and scratch resistance
of the thermoplastic polyolefin (TPO) materials. Rubber
toughened PP is called TPO.[12,13]
The automotive industry has been increasingly using
TPO alloys in exterior and interior applications, such as
bumper fascias, claddings, and wire insulation, because of
their excellent weatherability, low density, and low
cost.[10,12,14] However, TPO foams have not been utilized
because the technologies for foaming TPO materials using
batch or injection foaming processes have not been
developed yet. Nonetheless, there is a significant amount
of interest in developing foamed TPO products since
replacing solid TPO with a foamed counterpart could
considerably reduce material costs and fuel consumption.
The tensile properties and impact resistance of cellular
polymeric foams are rarely reported. Sun and Mark[15]
studied the effect of cell morphology on mechanical
properties of microcellular polysulfone, polyethersulfone,
and polyphenylsulfone foams. They found that the tensile
modulus of these polysulfone foams increased with the
square of their relative densities. The tensile strengths
were proportional to foam densities. More research also
proved that the relative foam density is by far, the most
influential parameter over mechanical properties of
cellular liner low-density polyethylene (LLDPE),[16] poly-
(methyl methacrylate) (PMMA),[17] polyurethane,[18] poly-
carbonate,[19–21] glass fiber reinforced polycarbonate,[22]
polystyrene,[23] poly(phenylene oxide),[24] and poly(vinyl
chloride) (PVC).[25,26]
Matuana et al.[27] found that the impact resistance
increases as the relative density of the cellular PVC foams
decreased. The cellular structure in the foams improves the
impact resistance of the material. In addition, Doroudiani
and Kortschot[28] investigated the effect of cellmorphology
on the impact strength of polystyrene foams. They found
that the cell size does not affect the impact strength of the
foams. However, the impact strength is dominated by
the relative density of the foam. They also concluded
that the plastic and viscoelastic deformation in the cell
walls are the major sources of energy dissipation in these
materials. Other research also investigated the impact
strength of polystyrene[29] and polyethylene[30–32] foams,
which led to similar results.
Recently, the tensile behaviors of various unfoamed TPO
composites were investigated by Lee et al.,[33] Mehta
et al.,[12] Mishra et al.,[10] and Liu and Kontopouloua.[34]
Macromol. Mater. Eng. 2008, 293, 605–613
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However, the relationships of cell morphologies and
tensile properties, and the impact resistance of injection
molded TPO foams have not been previously studied.
The purpose of this study is to investigate the relation-
ships of the processing, structure, and properties for
injectionmolded TPO foams. Cellular closed-cell TPO foams
were successfully processed using injection molding
process. Nitrogen was used as the PBA to process the
injection molded TPO foams. By altering the processing
parameters, different foam morphologies of the injection
molded TPO foams could be successfully controlled. Tensile
and impact testing were conducted in order to investigate
the relationships between the foaming parameters, foam
morphologies, mechanical properties, and impact resis-
tance. The injectionmolded TPO foamswere preparedwith
different processing parameters in order to examine their
effects on the mechanical properties of the foam structure.
Elastic modulus, tensile strength, elongation at breaks, and
impact resistance of the foamed TPO samples were
characterized as functions of foam morphologies. The
results of this study will allow designers to predict the
microstructure and mechanical properties of microcellular
TPO foams prepared from different sets of processing
parameters for their specific applications.
Experimental Part
Material and Preparation of TPO Foams
The polymer material used in this study was TPO (Hifax TYC735C
from Basell). It had a density of 0.96 g � cm�3 and an MFI of
25 dg �min�1. The specimens of fine-celled TPO foams were
processed. An 80-ton injection molding machine (TR80EH) from
Sodick Plustech Inc. was modified into an advanced structural
foam molding machine.[5,6] Figure 1 shows a schematic of the
advanced foam injection machine. The ASTM standard (D638
type IV) foamed TPO specimens and a 3 mm thick foamed TPO
plate were produced with this injection molding machine for
tensile and impact testing, respectively. The information on the
processing parameters of injection molded TPO foamed samples
are listed in Table 1. Three major process parameters that are
controllable, including the amount of gas content in the molten
DOI: 10.1002/mame.200700362
Effect of Processing Parameters on the Mechanical Properties . . .
Table 1. Processing information of injection molded TPO foams.
Run
Number
N2 Gas
Content (%)
Relative
Density
GCP Mold
Opening
0 (Unfoamed) 0 1 N/A N/A
1 0.5 0.90 No No
2 0.5 0.85 No No
3 0.5 0.80 No No
4 0.5 0.75 No No
5 0.5 0.90 Yes No
6 0.5 0.85 Yes No
7 0.5 0.80 Yes Yes
8 0.5 0.75 Yes Yes
gas/polymer mixture, use of the gas counter pressure, and use of
mold opening, can be altered in this injection molding machine.
The PBA used was N2, supplied by BOC Canada.
Foam Characterization
The TPO foam morphology was characterized by utilizing a
scanning electron microscope (SEM, JOEL JSM-6060). The samples
were cooled in liquid nitrogen and fractured to produce a clean
and intact surface with minimum plastic deformation. They were
then gold-coated by using a sputter coater for enhanced
conductivity. The average cell size and density were analyzed
by utilizing ImageJ software from the National Institutes of
Health, USA. The cell density was calculated as the number of cells
per unit volume with respect to the unfoamed polymer. The cell
density was calculated from the ImageJ software by using the
following equation:
Macrom
� 2008
N ¼ n
A
� �3=2�rPrf
(1)
where n is the number of cells in the defined area A, rp, and rf is
the density of the unfoamed and foamed polymers, respectively.
The foam density was measured by the buoyancy method. The
relative foam density is defined as the ratio of the foamed density
to the unfoamed polymer density. The volume expansion ratio is
defined as the ratio of the unfoamed polymer density to the
foamed density.
Figure 2. Cell density obtained from low pressure structural foammolding and gas counter pressure molding.
Mechanical Testing
The tensile mechanical testing of injection molded TPO foams
were conducted following the ASTM D638 on an Instron 4465
mechanical testing machine at room temperature. The capacity of
the load cell was 5 kN. All TPO foamed samples used for tensile
testing had a thickness ranging from 3 to 4 mm, depending on the
expansion ratio of the sample under processing parameters. The
ol. Mater. Eng. 2008, 293, 605–613
WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
displacement rate of the crosshead was 50 mm �min�1.[35] The
tensile strength was calculated as the load force divided by
the initial cross-sectional area of the specimen. The strain was
calculated as the elongation divided by the initial length of a
specimen. Three tensile properties were determined from the
resulting stress–strain curves for each foaming condition:
modulus of elasticity, stress at break, and strain at break. The
modulus of elasticity was obtained by calculating the slope of the
stress–strain curves in the elastic region. The elongation at break
of a sample was calculated in terms of percent elongation. A
minimum of five specimens were tested for each set of foaming
conditions. The surface roughness of TPO foamed samples was
measured by using a roughness tester (Times Inc. TR200). The
elastic modulus, tensile strength, and elongation at break of the
foamed TPO specimens were characterized as functions of foam
morphologies and surface roughness. The average value of each
foaming condition is reported in this study.
The impact testing was carried out in accordance to ASTM
standard D5420[36] by using a Gardner impact tester (Qualitest
IG-1142). This method determines the impact energy and impact
resistance of rigid polymers. The impact energy is defined as the
minimum energy that is required to fracture the TPO specimen.
The impact resistance is defined as the impact energy to fracture
the sample per unit thickness. Aminimum20 sampleswere tested
for each processing condition. The average value of each foaming
condition is reported in this study.
Results and Discussion
Effect of Processing Parameter on the Cell Densityand Skin Thickness
Figure 2 shows the cell density obtained from low pressure
structural foam molding and gas counter pressure
molding. The overall trend of the cell density in the two
processes is very similar. The cell density is the lowest at a
relative density of 0.9 and increases as the relative density
decreases to 0.75. Above a relative density of 0.8, the
increase in the cell density is not significant. An interesting
observation is that the cell densities obtained from the two
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S. Wong, J. W. S. Lee, H. E. Naguib, C. B. Park
Figure 3. Skin thickness obtained from low pressure structuralfoam molding and gas counter pressure molding.
Figure 4. Engineering stress–strain curves of injection moldedTPO foams.
608
processes are almost the same. Usually, the cell density
obtained from low pressure structural foam molding is
significantly higher than that from gas counter pressure
molding because of higher pressure drop rates at the
gate.[37,38] There are two possibilities that explain this
phenomenon. The first possibility is that the mold cavity
pressure in low pressure structural foam molding might
have been higher than the solubility pressure, thereby
preventing cell nucleation at the gate with a high pressure
drop rate as the cells should have nucleated along themold
cavitywith a low pressure drop rate. The second possibility
is that there might have been some cell coalescence during
filling, thereby decrease in the final cell density.
Figure 3 shows the skin thickness obtained from low
pressure structural foammolding and gas counter pressure
molding. For low pressure structural foam molding, the
skin thickness decreases as the relative density is
decreased. The decrease in skin thickness in low pressure
structural foam molding might have been caused by a
shorter injection time and lower mold cavity pressure due
to the smaller shot size. The lower mold cavity causes the
cells to nucleate during filling and the nucleated cells are
able to be located more closely to the mold surfaces,
thereby decrease in the skin thickness. On the other hand,
in gas counter pressure molding, there are no significant
changes in skin thickness with respect to the set relative
density of the foams. This is because in gas counter
pressure molding, cell nucleation always occurs after the
counter pressure is released. Since the counter pressure is
released after injection is completed, regardless of the shot
sizes, the set relative density does not have any effect on
the skin thickness.
Figure 5. The effect of skin thickness on tensile modulus ofinjection molded TPO foams.
Effect of Foam Morphology on Mechanical Properties
The effect of cell morphology on mechanical properties of
injection molded TPO foams is presented in this section.
Macromol. Mater. Eng. 2008, 293, 605–613
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Figure 4 shows the engineering stress–strain curves of TPO
foams prepared under various processing parameters
which are listed in Table 1. The effects of the relative
density, skin thickness, and surface roughness on tensile
and impact properties will be discussed in the following
sub-sections in detail.
Effect of Skin Thickness
The skin thickness is defined as the thickness of the
unfoamed skin layer in the foamed specimen. The
unfoamed skin layer exists in foams which were produced
by the injection molding technique. As the molten gas/
polymer mixture is injected into the mold, the rapid
decrease in pressure in the mold causes the gas molecules,
which are close to the surface, to diffuse very quickly from
the material, resulting in no cells nucleating at the surface
of the sample. As a result, the solid skin on the sample is
created and therefore, the skin thickness could affect the
mechanical properties of the polymeric foams.
DOI: 10.1002/mame.200700362
Effect of Processing Parameters on the Mechanical Properties . . .
Figure 6. The effect of skin thickness on tensile strength ofinjection molded TPO foams.
Figure 7. The effect of skin thickness on the % elongation ofinjection molded TPO foams.
Figure 8. The effect of skin thickness on impact energy of injec-tion molded TPO foams.
Figure 9. The effect of surface roughness on tensile modulus ofinjection molded TPO foams.
Figure 5–7 show the effects of skin thickness on the
tensile properties of injection molded TPO foams. Obser-
vation of the figures show that the tensile modulus,
tensile strength, and percent elongation increase with
the skin thickness. The tensile modulus and strength have
an increase of approximately 10%. The percent
strain increases rapidly from 100 to 600% as the skin
thickness increases from 100 to 500 mm. These are
expected results since as the unfoamed region increases,
the amount of material per unit area increases, which
causes the tensile properties of the foams to increase. The
increasing elongation at break possibly results from
the small bubbles blunting the crack tips which increased
the energy needed to propagate the crack.[17]
The effect of skin thickness on impact resistance is
shown in Figure 8. In this figure, the impact resistance of
the injection molded TPO foams increases with skin
thickness. The impact resistance of the foams increases
approximately three-fold as the skin thickness increases
from 90 to 450 mm. When the impact occurred directly on
the face of the unfoamed skin layer, this solid skin layer
acted as an energy absorber in the first zone. The foamed
Macromol. Mater. Eng. 2008, 293, 605–613
� 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
structure in the core of the sample was the second zone in
absorbing the impact energy. A thicker skin layer resulted
in more energy that can be absorbed and it was harder to
fracture. Therefore, the impact property increases with the
skin thickness of the foams.
Effect of Surface Roughness
The effects of surface roughness on tensile properties of
injection molded TPO foams are shown in Figure 9–11. The
tensile modulus and strength did not change noticeably as
the average surface roughness increases from 0 to 2.5 mm.
This finding shows that the effect of surface roughness
on tensile modulus and strength is negligible. However,
the percent strain decreases as the surface roughness
increases. The percent strain decreases significantly from
700 to 100% as the average surface roughness of the TPO
foams increases from 0 to 2.5 mm. Similarly, the impact
resistance decreases as the surface roughness increases as
shown in Figure 12. The impact resistance decreases from
approximately 6 to 3 kJ �m�1 as the surface roughness
increases from 0 to 2.5 mm. This is attributed to the
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S. Wong, J. W. S. Lee, H. E. Naguib, C. B. Park
Figure 10. The effect of surface roughness on tensile strength ofinjection molded TPO foams.
Figure 11. The effect of surface roughness on the % elongation ofinjection molded TPO foams.
Figure 13. The effect of relative density on relative tensilemodulus of injection molded TPO foams.
610
increase in stress concentration on the surface of the
samples as the surface roughness increases. Therefore, less
energy is needed to initiate cracks on the surface of the
sample under impact loading, thus causing the percent
Figure 12. The effect of surface roughness on impact energy ofinjection molded TPO foams.
Macromol. Mater. Eng. 2008, 293, 605–613
� 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
strain and impact resistance to decrease. Therefore, the
percent strain and impact resistance are also affected by
the surface roughness of the injection molded TPO foams.
Effect of Relative Density
The effect of relative density on tensile properties of
injection molded TPO materials is shown in Figure 13–15.
Similarly, both tensile modulus and strength decrease
with relative density. By observing the figures, the
tensile modulus decreases from 420 to 320 MPa and the
tensile strength decreases from 18 to 15MPa as the relative
density decreases from 1 to 0.7%. This is attributed to the
material reduction per unit volume of the foams. However,
the tensile strength only decreases 16.7% as the material
weight is reduced by 30% as shown in Figure 14. Therefore,
the introduction of the cellular structure by the injection
molding technique successfully improves the mechanical
strength of the material. By observing Figure 15, the effect
of relative density on percent elongation is not noticeable.
The effects of relative density on the impact resistance
of injection molded TPO foams are shown in Figure 16. By
Figure 14. The effect of relative density on relative tensile strengthof injection molded TPO foams.
DOI: 10.1002/mame.200700362
Effect of Processing Parameters on the Mechanical Properties . . .
Figure 15. The effect of relative density on the % elongation ofinjection molded TPO foams.
Figure 16. The effect of relative density on impact energy ofinjection molded TPO foams.
observing the figures, the impact energy decreases with
the relative density of the foams. The impact energy
decreases by approximately half at 10% weight reduction
of the TPO materials. For a 25% weight reduction of the
foamed samples which were produced without using gas
counter pressure, the impact resistance further decreases
to one sixth of the unfoamed material.
By using gas counter pressure, the impact resistance
remains at approximately 5 kJ �m�1 at a 25% weight
reduction of the foamed TPO materials. Since the foamed
samples which had better surface roughness can be
produced by using gas counter pressure, the stress
concentration on the surface of the samples was reduced,
causing the impact resistance to increase.
For unfoamed TPOmaterials, rubber that was treated as
a second phase in the PP matrix contributes to the overall
energy absorption in an impact loading. Thus, incorporat-
ing rubbery particles can toughen the unfoamed PP
polymer. However, the interfacial adhesion between the
rubber and PP phase is relatively weak. For TPO foams, the
Macromol. Mater. Eng. 2008, 293, 605–613
� 2008 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
cells in the structure reduce the crack length between two
regions of the second phase. As the crack of the cells is
initiated by impact loading, less energy is required to
propagate the crack. Therefore, the impact resistance of the
TPO foams are significantly reduced in comparison to the
unfoamed TPO materials.
Overall, the results show that the impact resistance is
very sensitive to the relative density, skin thickness, and
surface roughness. The cellular structure of the foams
significantly reduces the ability of the TPO materials to
withstand the shock loading.
Constitutive Model for Injection Molded TPO Foams
The structure–mechanical property of microcellular TPO
foams was experimentally obtained in the previous
section. In this section, constitutive models are proposed
to correlate the structure–mechanical relationship of
microcellular TPO foams. Most of these studies attempt
to relate the mechanical properties to the relative density
of the foam. Gibson and Ashby[39] suggested that the
tensile modulus and strength could be related to the
relative foam density in the following equations:
EfEp
� C1 frfrp
!2
þ C01 1� fð Þ rf
rp
!(2)
sf
sp� C5 f
rfrp
!3=2
þ C005 1� fð Þ rf
rp
!(3)
where Ef is the tensile modulus of the foams, Ep the tensile
modulus of the unfoamed polymer, sf the tensile strength
of the foams, sp the tensile strength of the unfoamed
polymer,rf the density of the foam, rp the density of the
unfoamed polymer, f the fraction of solid in cell struts, and
C1, C01, C5, and C 0
5 are constants representing the micro-
structure of the foams. These constitutivemodelswould be
able to assist engineers in predicting the mechanical
properties through knowledge of the relative density of the
polymeric foams.
The Effect of Relative Density on Tensile Modulus
The effect of relative foam density on relative tensile
modulus of injection molded TPO foams is shown in
Figure 13. Similarly, the tensilemodulus is found to be very
closely related to the relative density of the foams. The dots
are the data obtained experimentally from the previous
section. The constitutive model based on Gibson and
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S. Wong, J. W. S. Lee, H. E. Naguib, C. B. Park
612
Ashby is proposed in accordance to the experimental data
of the following:
Macrom
� 2008
EfEp
� 0:8 0:5rfrp
!1=2
þ 0:6 0:5ð Þ rfrp
!(4)
In Equation (4), the constants that fit the experimental
data were C1¼ 0.8, C 01¼ 0.6, and f is 0.5. The formula is
plotted as the solid line in Figure 13. This constitutive
model fits the experimental data very well.
The Effect of Relative Density on Tensile Strength
Figure 14 presents the effect of relative foam density on
relative tensile strength of injection molded TPO foams.
The dots plotted on Figure 14 are the experimental data.
The proposed constitutive model based on Gibson and
Ashby is plotted as the dashed line on the figures shown in
the following equation:
sf
sp� 0:9
rfrp
!3=2
þ 0:1ð Þ rfrp
!(5)
where the constants are C5¼ 1, C05¼ 1, and f is 0.9. The
suggested use of the values of these constants was based
on the experimental data obtained from convectional
foam.
By observing Figure 14, the constitutive model (Equa-
tion 5) suggested by Gibson and Ashby has under-
estimated the performance of the TPO foams. Similarly,
this is due to the estimation of the constants used in
Equation (5) being based on low density conventional
foams which have a relative density between 0.4 and 0.7.
Since all the injection molded TPO foams have a relative
density above 0.75, the constitutive model from Gibson
and Ashby had underestimated the tensile strength of the
injection molded TPO foams.
As a result, an empirical formula is proposed in
accordance to the experimental data as follows:
sf
sp� 0:8 0:8
rfrp
!1=2
þ 0:2ð Þ rfrp
!(6)
where the constants are C5¼ 0.8, C05¼ 1, and f¼ 0.8. The
formula is plotted as the solid line in Figure 14 and fits the
experimental data very well.
Conclusion
The mechanical properties and impact resistance of
injection molded TPO foams are examined. The effects
ol. Mater. Eng. 2008, 293, 605–613
WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
of relative density, skin thickness, cell density, and surface
roughness on tensile and impact properties of injection
molded TPO foams are correlated. Several conclusions are
made in this study: (i) the tensile strength only decreases
16.7% at a 30% weight reduction of injection molded TPO
foams. Therefore, the tensile strength is successfully
improved by introducing the cellular structure in the
TPO material by injection molding method. (ii) The tensile
properties and impact resistance increase with the skin
thickness of the foams. (iii) The percent strain is only
affected by the surface roughness of the TPO foams due to
the stress concentration on the surface of the foamed
samples. (iv) The impact resistance is very sensitive to the
relative foam density, skin thickness, and surface rough-
ness of the foams. (v) For foamed TPO materials that are
rubber toughened, the impact resistance is significantly
decreased by the cellular structure. (vi) The impact
resistance and surface roughness of the foams can be
improved by using the gas counter pressure.
Acknowledgements: The authors would like to acknowledge thefinancial support of the AUTO21 Network of Centres of Excellenceand the Government of Ontario.
Received: November 8, 2007; Revised: March 12, 2008; Accepted:March 13, 2008; DOI: 10.1002/mame.200700362
Keywords: cellular foam; impact resistance; injection moldingprocess; mechanical properties; processing parameters; tensiletesting; thermoplastic polyolefin; TPO
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