On The Measurement of True Fracture Strain of Thermoplastics Materials
On The Measurement of True Fracture Strain of Thermoplastics Materials
POLYMER
TESTING
Polymer Testing 27 (2008) 284–295
www.elsevier.com/locate/polytest
Test Method
Abstract
In tensile testing, engineering thermoplastic materials can sustain large deformation after necking. This property can be
advantageous to the manufacturing process and mechanical performance. However, it causes difficulties in strain
measurement and in the determination of true stress and true strain, particularly at higher strain rates. This paper
discussed the measurement of true fracture strain. The true fracture strain was estimated using three different methods: the
area reduction, elongation over the necked zone, and elongation over the gage length. With strain localization, strain
measured by an extensometer becomes gage length dependent. To address the issue, an algorithm was formulated that
estimates the average fracture strain over an arbitrary gage length from the fracture strain measured over the necked zone.
The proposed algorithm provides a way to estimate the mesh dependence of the fracture strain for finite element (FE)
analysis. This paper also presents an analysis-based two-step correction scheme for the crosshead extension to be used to
supplement the strain measurement from the extensometer.
r 2007 Elsevier Ltd. All rights reserved.
Keywords: Strain measurement; Strain rates; Tensile testing; Necking; True fracture strain; Thermoplastics
0142-9418/$ - see front matter r 2007 Elsevier Ltd. All rights reserved.
doi:10.1016/j.polymertesting.2007.11.007
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Engineering Stress (MPa) X. Xiao / Polymer Testing 27 (2008) 284–295 285
Dl l l 0
¼ ¼ . (3.1)
l0 l0
r = 20
Since the data from the extensometer were only
Fig. 2. ISO 8256 type-3 specimen (unit in mm), the tensile valid up to a certain range, the crosshead data were
specimen used at Axel Product Lab. used to supplement the strain data. Assuming that
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X. Xiao / Polymer Testing 27 (2008) 284–295 287
the entire deformation occurred within the gage method. Nevertheless, such corrections resulted in
length of the specimen, the engineering strain can be discontinuities in the strain rate-history plot, as
estimated from the crosshead extension. shown in Fig. 6. In high strain rate testing, using
Fig. 4 compares the engineering stress–strain specimens with different gage lengths can modify
curves using strain obtained from the extensometer the dynamic response of the test [17,18]. In a
and the strain calculated directly from the crosshead previous work [19], a one-step correction method
extension for a test conducted at a nominal strain was used which simply shifts the strain measured by
rate of 0.1 s1. The strain value calculated from crosshead extension vertically to supplement the
crosshead extension is larger because it includes not extensometer data, as illustrated in Fig. 7. The one-
only the gage length elongation but also the step method results in a discontinuity in the strain-
displacement due to the compliance of the load history curve and the estimated fracture strain was
train and the extension in the area of the specimen also lower [19].
outside the gripping area. To eliminate the unwanted contribution from the
The effect of the compliance of the load train may additional compliances and deformation outside the
be corrected by testing specimens with different gage length, a two-step correction scheme was
gage lengths [16]. Fig. 5 plots the engineering stress– proposed.
strain curves constructed using a similar correction
3.2. Two-step correction for crosshead extension
strain from CH
20 0.20
15
Strain rate (1/s)
0.15
10
0.10
5
0.05
0
0 0.5 1 1.5 2 2.5 0.00
Engineering Strain 0 0.2 0.4 0.6 0.8 1 1.2 1.4
Strain
Fig. 4. Engineering stress–strain curves obtained by strain
measurement from the extensometer (EX) and crosshead exten- Fig. 6. The strain rate versus strain plot corresponding to curve 1
sion (CH). in Fig. 5.
30 1.0 1.0
1
25 2 0.8 0.8
3
Stress (MPa)
20 0.6 0.6
Load (kN)
Strain
15
0.4 0.4
10 StrainZimmer
Strain Zimmer
0.2 Strain(cross
(crosshead) 0.2
Strain head)
5 Load
Load
0.0 0.0
0 0.0035 0.004 0.0045 0.005 0.0055 0.006
0 0.2 0.4 0.6 0.8 1 1.2 1.4 1.6 -0.2 -0.2
Strain Time (s)
Fig. 5. Typical engineering stress–strain curves obtained by Fig. 7. Supplement the strain measured by the optical extens-
combining strain measurement from the extensometer and ometer (Strain Zimmer) with the strain calculated from crosshead
crosshead extension using the conventional correction method. displacement.
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288 X. Xiao / Polymer Testing 27 (2008) 284–295
Strain
linear range, the difference in the compliance of the
0.4 ε2CH’
two stress–strain curves is
1CH 1EX 0.2 ε2EX
a ¼ cCH cEX ¼ , (3.2)
s1 s1 0.0
0 10 20 30 40 50
where e1EX and e1CH are the strains measured by TIME (s)
extensometer and by crosshead extension at an
arbitrary stress s1. cEX and cCH are the compliances Fig. 9. Two-step correction scheme: step 2—determining the
of the stress–strain curve measured by the extens- strain values corresponding to the last valid point of extens-
ometer measurement for the calculation of scale factor b. It
ometer and by the crosshead extension, respectively.
illustrates the crosshead strain after correction 1 and correction 2.
a is the difference in compliance between the two
measurements and, hence, can be used as a
compliance correction factor. value is obtained by a second correction via a scale
The strain from the crosshead is corrected by factor b. b is the ratio of the strain values:
subtracting the contribution of the additional 2EX
compliance b¼ , (3.4)
02CH
0CH ¼ CH as, (3.3)
where e2EX is the strain measured by extensometer
where eCH is the strain calculated directly from the and 02CH is the strain from the crosshead after
crosshead extension and 0CH is the corrected strain. correction 1. To fully utilize the measurement from
Fig. 9 compares the strain from extensometer, the extensometer, the values corresponding to the
crosshead and correction 1 (compliance correction). last valid point of extensometer measurement
Fig. 9 shows that the curve labeled as ‘‘correction 1’’ should be used, as indicated in Fig. 9.
is much closer to the curve labeled as ‘‘strain from The second correction is obtained by
EX’’ as compared to the curve without correction,
00CH ¼ b0CH , (3.5)
but the two curves are not overlapping. The reason
is that Eq. (3.2) provides an averaged value over a where 0CH and 00CH are the respective strains after
range rather than as a function representing the correction 1 and correction 2. Correction 2 ensures
instantaneous values in terms of difference in that the combined curve is smooth, i.e. maintains its
compliance. The adjustment for the instantaneous continuity in terms of the first derivative at the last
valid point of extensometer measurement.
25 The strain after two-step correction is labeled as
σ1
‘‘correction 2’’ in Fig. 9. As seen, the correction 2
Engineering Stress (MPa)
0.15 _ ¼ , (3.6)
l0
0.10 where v is the loading rate of the testing frame and l0
is the nominal gage length of the testing specimen. In
0.05 dynamic testing, the actual strain rate in the specimen
is not constant because the specimen must experience
0.00 acceleration when being loaded from rest to the
0 0.5 1 1.5
Strain
targeted rate. To standardize the definition of strain
rate in high rate tensile tests of polymeric material,
Fig. 11. The strain rate versus strain plot corresponding to the the SAE draft Standard J2749 [21] recommends the
combined curve in Fig. 10. use of the average strain rate within the range of 10–
20% plastic strain. This definition was used in the
current study.
Fig. 13 plots the typical engineering stress–strain
80 curves at five rates. Table 1 provides a summary of
70
Engineering Stress (MPa)
60 40
0.017
Engineering Stress (MPa)
50 0.17
40 30 3
30
30 120
strain from EX 20
20
strain from CH
10 2-step correction
UDRI data 10
0
0 0.2 0.4 0.6 0.8 1
Engineering Strain 0
0.0 0.2 0.4 0.6 0.8 1.0 1.2 1.4
Fig. 12. Tensile stress–strain curves of PC/ABS, tested at 40 s1. Engineering Strain
The curves were obtained by strain measurement from the
extensometer (EX), crosshead extension (CH), by combining the Fig. 13. Engineering stress–strain curves of HDPE. The nominal
strain from EX and the corrected CH strain (two-step correc- strain rates are 0.01, 0.1, 1, 10, 100 s1. The plastic strain rates are
tion), and by direct measurement (UDRI). 0.017, 0.17, 3, 30 and 120 1s, determined according to Ref. [20].
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290 X. Xiao / Polymer Testing 27 (2008) 284–295
Table 1
Tensile properties of the HDPE material
Nominal strain rate Strain rate (10–20% ep) Peak stress (MPa) Modulus (MPa) Engineering failure strain
the mechanical properties including the peak tion, the Poisson’s ratio is derived to be 0.5. For a
engineering stress, the Young’s modulus and the metallic tensile specimen, as long as the deformation
engineering failure strain measured at different is homogeneous along the gage length, the constant
rates. As mentioned in Section 1, the strain mea- volume condition yields [13]:
sured by extensometer is an average strain over the
gage length and, therefore, the strain measured after Ai l i ¼ A0 l 0 (4.4)
necking becomes gage length dependent. The failure and the following relationships hold between
strain values listed in Table 1 correspond to a gage the engineering and the true stress and strain
length of 11–12 mm. values [13]:
Table 2
True fracture strain estimated using various methods
three methods to estimate the true tensile fracture Fig. 14. Viscoelastic recovery observed from the shape change of
strain: a specimen after three-point bending test.
Table 3
Tensile test specimen gage length measurements
Strain rate Sample ID Engineering Gage length Final gage True fracture Necked zone True fracture
(s1) fracture (mm) length (mm) strain over (mm) strain over
strain gage length necked zone
zone is shown in Fig. 15. The mathematical Based on Eqs. (5.1)–(5.3), the failure strain for an
expressions are arbitrary gage length l (l4ln) is derived as
Dl ¼ Dl 1 þ Dl 2 , (5.1) Dl ðl l n Þ 0:3 þ nf l n
f ¼ ¼ . (5.4)
l l
Dl 1 ¼ ðl l n Þ 0:3, (5.2) Eq. (5.4) allows one to estimate the true failure
strain at an arbitrary gage length, i.e. for an
Dl 2 ¼ nf l n , (5.3) arbitrary mesh size. As an example, Fig. 17 plots
the mesh size dependence of the true fracture strain
where ln is the size of the necked zone, nf is the estimated using Eq. (5.4) for a strain rate of 3 s1.
failure strain measured over the necked zone. Fig. 18 plots the true fracture strain as a function of
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294 X. Xiao / Polymer Testing 27 (2008) 284–295
11mm measured
on measurements with ruptured specimens that did
not include the viscoelastic strain. This affected the
1.0 strain rate dependence of fracture strain obtained by
these two methods, particularly at lower rates.
0.5
Nevertheless, these measurements provided addi-
tional information needed in the formulation of an
algorithm that relates the fracture strain measured
0.0 over the necked zone to the average value over an
0.01 0.1 1 10 100 1000 arbitrary gage length larger than the necked zone
Strain Rate (1/s) for materials exhibiting uniform necking. The
Fig. 18. Rate dependence of true fracture strain as a function of
proposed algorithm provides a method to estimate
strain rate and mesh size, determined by the algorithm discussed the mesh dependence of the fracture strain for FE
in Section 5. analysis.
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Acknowledgments [11] Q.Z. Fang, T.J. Wang, H.M. Li, Large tensile deformation
behavior of PC/ABS/alloy, Polymer 47 (2006) 5174–5181.
The author would like to thank Zohir Molhem, [12] Standard Test Methods for Tensile Properties of Plastics,
ASTM Designation: D7638-03, ASTM International, Phila-
Hamid Kia of General Motors Corporation for delphia, USA, 2002.
helpful discussions and valuable suggestions; Andi [13] G.E. Dieter, Mechanical Metallurgy, third ed., McGraw-
Poli and Kurt Miller of Axel Products for tensile Hill, New York, 1986.
testing and photos; Susan Hill of UDRI for sharing [14] I.M. Ward, Mechanical Properties of Solid Polymers, Wiley/
high rate testing data. InterScience, London, UK, 1971.
[15] J.D. Ferry, Viscoelastic Properties of Polymers, Wiley, New
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