1. Introduction
In light of the proper identification and subsequent evaluation of the material deformation behaviour, so-called stress–strain curves represent a truly very important characteristic. In general, their measurement and knowledge are some of the most important parts of material testing, and that is why there are quite a lot of books and standards on how their computation and determination should be carried out, e.g., [
1,
2,
3]. In addition to that, there are quite a lot of parameters (mainly temperature and strain rate) that can influence them. Last but not least, they also differ in light of the used stress states. Very often, the tensile test is used, so the uniaxial stress–strain curve is determined. However, a proper description of the overall material deformation behaviour, e.g., for advanced yield conditions to be used in Finite Element Analysis (FEA), also requires their determination under other states of stress. Among them, the so-called equi-biaxial state of stress is one of the most important ones. That is why, in this paper, two quite different materials (high-strength steel and deep-drawing material) were tested using the hydraulic bulge test (HBT), and biaxial stress–strain curves were determined according to standard ČSN EN ISO 16808 [
4]. Moreover, different loading modes were applied at their measurement to reveal the deformation behaviour at HBT under a continuous increase in pressure as well as under the so-called ramp test, where, at the chosen pressure values, a holding time of 90 s was always applied.
As was already mentioned before, very often, biaxial stress–strain curves are required for solving different mechanical engineering problems. These are especially important in applications of the yield locus for the utilisation of FEA. Generally, almost all the theoretical aspects of FEA that are needed in the engineering industry, that is, the basic concept, math equations, mechanics of materials, and so on, are given in the work of Kim et al. [
5]. Suitable examples of the application of FEA in structural mechanics are shown, e.g., in [
6,
7]. Regarding the focus of this paper, a numerical model to investigate the influence of different parameters (e.g., stress and strain distribution) is discussed in Reis et al. [
8]. Other authors use numerical simulations mostly to incorporate different yield loci [
9,
10], increase the accuracy of FEA and even neural networks [
11,
12], or, e.g., to compare the strain distribution from numerical simulations and experiments [
13]. After that, basic theoretical approaches and methods of determining stress–strain curves and constitutive equations taking into account the strain, strain rate, and temperature are described in [
14,
15,
16,
17].
Because the testing of material properties via the HBT generally means that, in light of the state of stress, there is equi-biaxial stretching (thus, biaxial stress–strain curves), there exists an effort to achieve another state of stress. Very often, the so-called elliptical HBT is used, so the plain strain is achieved [
18,
19,
20,
21]. Moreover, a modified Nakajima test without inverse parameter identification was proposed by Eder et al. [
22] to increase the accuracy of the given equi-biaxial flow curves. Very important research in this branch is about testing the influence of used hardening models, e.g., Lezen et al. [
23] used the HBT to characterise kinematic hardening under nonlinear strain paths. The final results revealed higher accuracy than the data from the cyclic tensile–compression tests. Sometimes, instead of the HBT, cruciform specimens are used, which also makes it possible to achieve biaxial loading (and sometimes unloading is required as well) of specimens [
24,
25]. In addition to that, the HBT can be used to evaluate, e.g., fracture [
26,
27] or even fatigue [
28] characteristics.
Quite a lot of interest in this area of testing is also devoted to the influence of temperature on stress–strain curves. For example, Mulder et al. [
29] proposed the analytical temperature compensation model with respect to the flow stress. Boyer [
30,
31] studied and already proposed a new testing device, which enables the HBT to be carried out at high temperatures. The influence of higher temperatures on the effective stress–strain behaviour and modified Johnson–Cook model for strain hardening was developed by Ashrafian and Hosseini [
32]. Some authors also studied the effect of warm forming temperatures or elevated temperatures on the flow curves [
33,
34,
35].
The influence of different strain rates on the biaxial stress–strain curves has also been of great interest in recent years. Jocham et al. [
36] investigated the strain rate sensitivity of material DC06 both at HBT and tensile test. Suttner and Merklein [
37] applied the constant strain rate at hydraulic bulge test for different materials. From the strain rate point of view, great research interest is also devoted to the application of quite high strain rates [
38,
39,
40,
41], sometimes also for the pneumatic bulge test [
42]. However, regarding the application of different loading modes, already with the holding times (or just keeping constant stress), there are just a few articles [
43,
44], but these are about testing the superplastic materials.
Additionally, the lack of knowledge about the deformation behaviour of common materials used in car-body design under the equi-biaxial stress state depending on the different loading modes was the major reason to carry out the study described in this paper. In the previously mentioned studies, the right holding times at the relevant pressure values were not applied during the HBT; thus, their influence on the final position of the stress–strain curves was not monitored. Furthermore, because these results are especially important, e.g., for the proper computation of the yield locus or just for FEA, two commonly used materials (high-strength steel as well as deep-drawing material) were selected to be tested at HBT. That is why, besides the classical measuring of HBT performed in accordance with ISO 16808, also, so-called ramp tests at HBT were carried out, where, for every integer multiple of actual pressure values, a holding time of a duration of 90 s was applied. Generally, the major aim of this paper was to find out if there is such an influence of different loading modes, especially in light of the final comparison between continuous “classical” measurement and ramp tests. In addition to that, there was also the possibility to reveal the influence of the own magnitude of holding time on the final position of stress–strain curves. Moreover, there was also a presumption that the evaluation of microstructure with the help of scanning electron microscopy (SEM) should be suitable for such research.
2. Materials and Methods
In selecting the materials to be tested, there was an effort to take into account their different deformation behaviour and also their different microstructures. For this reason, representatives of high-strength and deep-drawing materials, commonly used in car body design, were selected. Specifically, two-phase steel CR290Y490T with a martensitic-ferritic structure and a thickness of 0.55 mm, later referred to as DP500, was tested. As a deep-drawing material, the ferritic steel CR4EG29-29-E-P-O with a thickness of 0.70 mm, further referred to as CR4, was then chosen. The actual carried out experiments and the methods used to evaluate them are described in the following chapters.
2.1. Static Tensile Test
At first, the static tensile test was used to determine the basic material properties of the tested materials. Taking into account the anisotropic behaviour of both materials, three basic directions relative to the rolling direction (RD) were used in the test—0°, 45°, and 90°. Five specimens were tested for each measured rolling direction. The actual tensile tests were carried out in accordance with EN ISO 6891-1 [
45] on a modernised testing device TIRA Test 2300 (Schalkau, Germany) using software Labtest v.4 (LabControl, Opava, Czech Republic) for evaluation, which allows the required basic material properties (proof yield strength
σp0.2, ultimate tensile strength
σm, total ductility
A80mm, uniform ductility
Ag, and Young’s modulus of elasticity
E) to be accurately determined. The required measured values are summarised in
Table 1. Engineering stress–strain curves from the static tensile test of both tested materials are plotted in
Figure 1. In this case, averaged curves from 5 measurements are shown.
Concerning the main focus of this paper, which is to determine the effect of loading mode on the position of the stress–strain curve at HBT (i.e., under equi-biaxial stress state), the true stress–strain curves determined by the static tensile test (uniaxial tensile stress state) were not important. However, these data have been also processed as part of the planned further research, where one of the areas to be investigated is the accurate definition of the yield conditions.
Table 1.
Basic material properties of the tested materials DP500 and CR4.
Table 1.
Basic material properties of the tested materials DP500 and CR4.
Material | RD (°) | σp0.2 (MPa) | σm (MPa) | Ag (%) | A80mm (%) | E (MPa) |
---|
DP500 | 0 | 318.5 | 514.6 | 17.79 | 22.97 | 199,180 |
45 | 319.6 | 521.3 | 18.62 | 25.55 | 212,450 |
90 | 314.2 | 528.9 | 18.59 | 26.15 | 221,569 |
CR4 | 0 | 157.7 | 301.1 | 26.76 | 46.12 | 183,920 |
45 | 156.7 | 306.7 | 26.06 | 45.46 | 205,239 |
90 | 154.6 | 300.6 | 26.16 | 46.55 | 191,942 |
Figure 1.
Engineering stress–strain curves from the static tensile test for tested material.
Figure 1.
Engineering stress–strain curves from the static tensile test for tested material.
2.2. Hydraulic Bulge Test (HBT)
The values from the static tensile test represent the basic material properties. However, the focus of this research was to determine biaxial stress–strain curves. For this reason, all further experiments were carried out using the hydraulic bulge test (HBT), in which the specimen is subjected to an equi-biaxial stress state. The initial workpiece for the tests is a rounded blank with a diameter of 210 mm, made by shearing. Since the optical system GOM Correlate Pro (Carl Zeiss GOM Metrology GmbH, Germany) was used for strain analysis, it was necessary to first degrease the specimens and then apply a stochastic pattern. For the actual test and subsequent evaluation, rolling direction (RD) was also marked on each specimen before testing. During the test, the values of pressure and deformation induced on the specimen surface were recorded synchronously by cameras (DIC—Digital Image Correlation). From these input data, the required stress–strain curves can be determined and calculated. The following equations were used.
Following
Figure 2, which shows the effect of fluid pressure on the stress distribution for the selected element, Equation (1) can then be derived using the equilibrium equation to calculate the biaxial true stress
σBT in the specimen wall.
where:
p—hydraulic pressure (MPa);
R—radius of curvature (mm);
t—actual thickness of specimen (mm).
Values of major and minor true strains
ε1 and
ε2 are determined by means of contactless optical system. Using the law of volume constancy and neglecting the elastic deformation, true thickness strain
ε3 can be calculated according to Equation (2):
In terms of deformation, the plastic work principle is used for the resulting biaxial stress–strain curves according to standard ČSN EN ISO 16808 to express the (true) plastic strain
εpl—see Equation (3). Final biaxial stress–strain curves were plotted as
σBT vs. −(
εpl).
where:
ν—Poisson’s ratio (1)
E—Young’s modulus (MPa)
Figure 2.
Principle and stress state at the hydraulic bulge test (HBT).
Figure 2.
Principle and stress state at the hydraulic bulge test (HBT).
As was already written above, to determine the biaxial stress–strain curves during the hydraulic bulge test, a contactless optical system for measurement deformation was used—in this case, GOM Correlate Pro from German company ZEISS GOM. The schematic layout of the actual test is shown in
Figure 3.
Figure 3.
Scheme of the measurement of the biaxial stress–strain curve at HBT via DIC.
Figure 3.
Scheme of the measurement of the biaxial stress–strain curve at HBT via DIC.
During the measurement of deformation characteristics, the given jig was placed on the bolster of hydraulic press CBA 300/63. The magnitude of the applied clamping force was 2000 kN, which is, for the tested materials, high enough to prevent the specimen from sliding out of the clamping area. The diameter of the die was 100 mm and, thus, the surface radius values were as follows: r1 = 12.5 mm (for determining curvature) and r2 = 5 mm (for determining strain). It is necessary to vent the whole system before every measurement. As external equipment for this press, there was a programmable and own press-independent hydraulic unit that controlled the pressure courses in the jig. A precision Proportional Integral Derivative (PID)-controlled hydraulic servo valve with an achievable accuracy of pressure 0.002 MPa ensured the accurate adjustment and progression during the pressure loading of the specimen. The actual deformation process was scanned by a pair of synchronised 12 MPx resolution digital cameras with 20 mm lenses. These cameras were positioned at the required distance from the specimen to be measured (450 mm) using aluminium profiles. The distance between the cameras was 220 mm. Since the optical system operates with a fixed focal length, it is always necessary to accurately adjust not only the lighting conditions but, also, for example, the aperture size in the given measuring volume. Last but not least, it is important to focus the optical system carefully on the surface of the test specimen. Before performing the HBT itself, it is then always necessary to calibrate the used optics, which, in this case, was conducted using a relevant calibration plate (CP40/170/44142), whose position in space was scanned by cameras during calibration. Depending mainly on the used calibration plate point spacing, the distance of cameras from the object to be measured and from each other, a so-called calibration volume was then obtained, which, in this case, was as follows: 160 mm × 120 mm × 100 mm (length × width × depth). The system also automatically evaluated the calibration quality. The measurement error according to the calibration protocol was, in this case, 0.049 Px. When measuring the biaxial stress–strain curves (generally when external data also need to be processed), it is necessary to have the actual value of applied pressure for each pair of images during the test.
The major focus of this paper was to find the influence of loading mode on the position of the biaxial stress–strain curve. Because of this, these curves were measured under two different loading modes, which are shown in
Figure 4 and were as follows:
Continuous tests—“classical” type of loading that was carried out according to ISO 16808;
Ramp tests—at every pressure step, there was always applied a holding time of 90 s.
In light of ramp tests, it has subsequently proved appropriate to divide these tests into several subgroups, which were as follows:
Ramp test without HT (holding time)—without the influence of applied holding time;
Ramp tests with HT —three important time moments were taken into account
—start of HT (0 s); half of HT (45 s); and end of HT (90 s).
So, during so-called continuous tests, a constant increase in pressure depending on time was used. For both tested materials (DP500 and CR4), these kinds of tests were always carried out up to fracture because of Forming Limit Diagrams (FLC).
However, besides the common continuous tests, so-called ramp tests were investigated as well. In this case, it meant that, on every integer multiple of pressure value (from 1 MPa up to 7 MPa), a holding time (HT) was used—step duration of 90 s. The last applied pressure was 7.5 MPa. In the case of the ramp test, a pressure of 8 MPa was not used because there was a risk of specimen failure during the holding time. Subsequently, all determined stress–strain curves were fitted by the Hollomon equation—see Equation (4)—up to a pressure value of 7.5 MPa, although the actual failure of the material under continuous measurement occurred at approximately 8.5 MPa (see
Figure 4).
where:
K—strength coefficient (MPa);
n—strain hardening exponent (1).
From
Figure 4, it is also evident that the ramp test itself was very time-consuming; in this case, one test lasted up to about 900 s. Given the resulting size of the measurement (due to the large number of acquired frames), it was suitable to set the frame rate to 3 fps. An example of observed time moments for 2 MPa is also shown in
Figure 4.
Figure 4.
Comparison of used loading modes—continuous measurement and ramp test.
Figure 4.
Comparison of used loading modes—continuous measurement and ramp test.
As can be seen, the selected loading modes were quite very different in terms of time course. For these reasons, it was clear that the selection of loading method would result in different strain rate evolutions, with a gradual increase in the case of continuous measurement (slowly at first to relatively high values just before the failure) and then only certain “peaks” at moments of increasing pressure values during the ramp tests. The actual strain rate courses for two applied loading methods are shown below. In addition to that, ramp tests themselves were very time-consuming. Because of that, 5 continuous as well as 5 ramp tests for both tested materials were carried out and resulting stress–strain curves were taken as average curves from these measurements.
4. Discussion
Most stress–strain curves in materials testing are determined by the static tensile test. However, for a reliable description of deformation behaviour, they must be also determined under an equi-biaxial stress state, which is essential, e.g., for the accuracy of the yield conditions used in FEA. These biaxial stress–strain curves are currently measured mainly by contactless optical analysis (DIC) according to EN ISO 16808, where pressure loading is continuously increased during the measurement. However, in the case of the real stamping process, it is sometimes necessary to know the influence of the loading history, which may affect the resulting position of the biaxial stress–strain curves. One of these parameters may be, e.g., the utilisation of holding time under a given loading (e.g., at hydroforming or by using the programable servo-presses).
Therefore, in this work, the effect of such time variation of loading has been investigated at the measurement of the biaxial stress–strain curves using contactless optical deformation analysis. As a reference position for this stress–strain curve (and its subsequent approximation by the Hollomon equation), a common hydraulic bulge test was used, performed in accordance with EN ISO 16808. Because of the subsequent change in loading mode, this test was referred to as a continuous measurement. After that, the influence of holding time at loading was determined as well. To be specific, a holding time of 90 s was applied at the following pressure values: 1; 2; 3; 4; 5; 6; 7; and 7.5 MPa. The actual method of computing the biaxial stress–strain curves was then carried out again in accordance with EN ISO 16808 and these tests were subsequently referred to as ramp tests. The first comparisons of such curves are shown in
Figure 9 (DP500) and
Figure 15 (CR4).
The first results obtained from the performed tests concerned the change in geometry of the specimen during the holding (dwell) time itself, i.e., within 90 s at each monitored pressure value. In this case, a sphere was first fitted by the best-fit method for the relevant scanned area using the GOM Correlate Pro system to monitor the actual radius of curvature R (mm). The next observed value was always the current maximum position of the sample in the
Z-axis (thus, height of the dome). Therefore, in the case of the radius of curvature, it was always a certain best approximation within the relevant surface area, while, in the case of the maximum
Z-axis position value, it was always a single point. The results for the two tested materials are shown in
Figure 7 and
Figure 8. Based on these results, the deformation behaviour of the tested materials during the holding times can then be explained to some extent. At lower values of pressure (up to about 3 MPa), it is mainly influenced by the change in the radius of curvature so that there is a decrease mainly in the stress values (change in the negative vertical direction within the biaxial stress–strain curve—
Y-axis). However, there is an increasing influence of the change in the maximum Z position with increasing pressure values, which is observed on the biaxial stress–strain curve by increasing strain magnitude under almost the same stress value (change in the positive horizontal direction +
X-axis). These increments in terms of ∆R and ∆Z are given in
Table 2 and
Table 3.
Nevertheless, the main objective of this research was to compare the deformation behaviour of the tested materials in light of continuous measurement and ramp tests. However, it proved useful to divide the ramp test data into several subgroups. Probably the most important approach was to consider only those parts of the biaxial stress–strain curves that were not affected by the regulation and holding time itself. Thus, at this ramp test, only data measured during increasing pressure values were considered, as in the continuous measurement. Graphical examples of this approach are shown in
Figure 12 and
Figure 18. Here, the different deformation behaviour between the two tested materials is shown. It is clear that the DP500 shows almost no difference between the continuous measurement and the ramp test without the influence of holding times. However, this is not valid for the deep-drawing material CR4, where the difference between the loading methods is evident. These results are subsequently graphically shown in Figures 30 and 31. However, much more clearly and for both tested materials together, these results are shown in
Figure 29. The different deformation behaviour regarding the influence of loading mode is evident.
On the other hand, for DP500, it can be seen that the HT at a given pressure value has almost no effect on the subsequent deformation behaviour of this material at the equi-biaxial stress state. It is obvious that two monitored stress–strain curves practically overlap. In contrast, in the case of deep-drawing material CR4, a decrease in the strength coefficient value can be observed. So, in this case, the resulting stress–strain curve for the ramp test without the influence of HT is below the values measured in continuous measurement. For clarity, the values of all fitting constants are shown in
Table 6.
Figure 29.
Overview of stress–strain curves for both tested materials.
Figure 29.
Overview of stress–strain curves for both tested materials.
Moreover, in addition to such basic comparison between continuous measurement and ramp test without the influence of HT, the influence of the course of HT was also evaluated. More precisely, the effect of the actual time course of the holding time was monitored using three selected time moments—0 s (start), 45 s (half), and 90 s (end) of HT. It is interesting to note that the same time intervals do not have the same effect on the strain response. To describe this effect more accurately, these points were then also approximated using the Hollomon equation, with graphical dependencies shown in
Figure 14 and
Figure 20. The final values of the fitting constants of all performed analyses are summarised in
Table 6.
Table 6.
Final overview of the fitting constants.
Table 6.
Final overview of the fitting constants.
Material/ Measuring Mode | DP500 | CR4 |
---|
K (MPa) | n (1) | K (MPa) | n (1) |
---|
Continuous measurement | 904.5 | 0.2013 | 716.8 | 0.2809 |
Ramp test—without HT | 907.4 | 0.2053 | 689.5 | 0.2770 |
0 s (start of HT) | 884.3 | 0.1963 | 690.9 | 0.2866 |
45 s (half of HT) | 876.6 | 0.2025 | 667.0 | 0.2862 |
90 s (end of HT) | 874.6 | 0.2036 | 659.8 | 0.2838 |
Graphically, these results for material DP500 are shown in
Figure 30. If the values obtained from the continuous measurement are taken as a basis (100%), it is interesting to note that the change in the magnitude of strain hardening exponent is not so significant depending on the used loading and evaluation modes and almost all the values (with the minor exception of the start of HT, where there is a decrease of 2.5%) are within a maximum change of 2%. The situation is slightly different for the strength coefficient. The ramp test itself, without the effect of holding times, is almost the same as the continuous measurement (change + 0.3%), while the effect of HT itself is reflected in a gradual decrease in these values up to −3.3% at the end of HT.
The same graphical overview of such major results, in this case for the deep-drawing material CR4, is shown in
Figure 31. The values given in
Table 6 can be again used for a quick comparison of changes that have occurred under the influence of applying the different loading methods to the material under test. Again, the values of the fitting constants (C and n) obtained from the continuous measurement can be used as reference ones. The most important comparison is again between the continuous measurement and ramp test without HT. There is a decrease of up to 3.8% for the strength coefficient and 1.3% for the strain hardening exponent. A significant decrease in the strength coefficients can also be observed for the time moments during HT—start, half, and end. Specifically, these decreases are as follows: 3.6%; 6.9%; and 8.0%. Regarding the strain hardening exponents, these values then increase slightly by 2.0%, 1.9%, and 1.0%, respectively.
The results described above regarding the effect of loading mode on the final position of stress–strain curves for both tested materials are probably the most important results of this research. It can be seen that there is a relatively large difference between the influence of used loading mode on the deformation behaviour of high-strength steel DP 500 and deep-drawing material CR4. For the DP500 material, it turns out that the application of the holding times has almost no influence on the resulting stress–strain curve, more precisely, its comparison just with the continuous measurement. In contrast, in this comparison, the CR4 material shows a notable decrease in the final stress–strain curve. Numerically, these trends are then evaluated by the Hollomon equation, particularly concerning the resulting strength coefficient values. However, such different deformation behaviour was already observable not only using the changes in radius of curvature R and the maximal dZ position (see chapter 3.2) but also with respect to the results of the strain rates—see chapter 3.1. From this measurement, it can be seen that, in the case of DP500, the strain rate value decreases towards zero, even at higher pressures—already at 7 MPa. On the other hand, in the case of CR4, it can be seen that almost from 5 MPa, the strain rate does not drop to zero during the holding time and, therefore, deformation is still spreading. The higher the applied pressure, the higher the values of strain rate at the end of the applied holding time for the material CR4.
To analyse the microstructure of the tested material before and after deformation, EBSD and IPF analyses were carried out via scanning electron microscope. Due to the HBT, for both materials, the formation of deformation texture was observed. However, already from this measurement, it was evident that a higher directionality was found for material CR4. Moreover, it can be seen that there is almost not any effect of loading mode on the grain size of DP500, which is not valid for material CR4, where differences can be observed in grain sizes concerning used loading mode. It seems that the ferritic-martensitic structure of DP500 can greatly reduce the motion of a dislocation, while the pure ferritic structure of CR4 allows the dislocations to reach to some extent the equilibrium state during the holding time, which results in a reduction in its strengthening. However, this fact was not investigated further in this paper and it would be appropriate to carry out separate material research in this area.
From SEM figures, the formation of deformation texture caused by the biaxial stress state at HBT is evident. In order to evaluate the intensity of plastic deformation, which is in the case of HBT determined by the magnitude of plastic deformation in the thickness direction, it is useful to observe the grain sizes after deformation. A general overview of the important grain dimensions (breadth × length) both before and after deformation as well as the used loading mode (continuous measurement and ramp test) is shown in
Table 7. A graphical illustration of these results is given in
Figure 32.
Table 8 shows percentage representations of individual grain orientations of tested materials. It is again evident that initial structures have typical grain orientations corresponding to the rolling technology. Material DP500 has a significantly lower grain orientation related to the rolling direction and the percentage representation of each direction is almost uniform in this case. The initial state of grain orientation for material CR4 is significantly anisotropic, with a predominant orientation of (111) in the direction of the material thickness (X-direction)—up to 82%. The different deformation behaviours of these two tested materials arises from their different structures (ferritic-martensitic structure of DP500 and pure ferritic structure of CR4). As can be seen also from
Table 8, in the case of material DP500 after deformation, there is only a minimal change in the orientation of the crystal lattice caused by the blocking motion of dislocation by martensite grains. On the other hand, in the case of the CR4 material, the pure ferritic structure does not prevent such motion of dislocations in the predominant directions and, therefore, deformation of the grains occurs only and not their rotation. From
Table 8, it can be seen that, for material DP500, the loading mode does not affect the resulting percentage representation of grains with (111) orientation. In contrast, in the case of material CR4, it can be seen that there is a further increase in this proportion of grain orientation after the ramp test. These results confirm the different deformation behaviour of both tested materials at HBT when comparing continuous measurements and ramp tests.
From
Table 7 and
Table 8, it is evident that, in the case of material DP500, there is almost no difference in grain size for both loading modes used (continuous measurement and ramp test). The grain shape and size are almost identical. On the other hand, for material CR4, it is possible to observe the effect of used loading mode on the grain size after deformation, where the ramp test revealed a higher plastic deformation of grains, which is consistent with the measured deformation behaviour during determination of the stress–strain curves. For the material CR4, a secondary plastic deformation (plastic creep) occurs during the holding time under the given pressure loading. This phenomenon can be explained by the different structures of tested materials, where, in DP500, the dislocation motion is resisted by the martensitic grains combined with a finer structure. In comparison, material CR4 has a purely ferritic structure, so dislocation motions to achieve the equilibrium state during the holding time are not limited. This phenomenon, observed in the submitted research, is especially important for numerical simulation of low strain rate technological processes, such as hydroforming.
Figure 32.
Grain dimensions for all monitored loading modes and tested materials.
Figure 32.
Grain dimensions for all monitored loading modes and tested materials.
It is important to note that only two materials (DP500 and CR4) with different deformation behaviour were tested in this paper. In addition, due to the considerable time and hardware requirements of the measurements, especially in the case of ramp tests, five specimens were always used for each tested material to obtain biaxial stress–strain curves. Further research in this area is currently focused on obtaining more material data to assist in the necessary verification of the presented results. On the other hand, this paper has already shown a relatively good agreement with the already made measurements. Much attention is also being given to the use of these results as input data for numerical simulations of sheet metal forming and their verification on real stampings.
Given the planned further research about the influence of loading modes on the biaxial stress–strain curves, it would be advisable to test specimens also of other important material groups, such as stainless steels or aluminium alloys. Based on the measurements made so far, the length of HT also appears to be an important characteristic, as it has already been shown in this paper that this is certainly not a directly proportional dependence. The deformation behaviour over the time course of these HTs was also somewhat different for the two materials. However, to monitor the influence of the various parameters on the test presented, it would be useful to also consider, e.g., PID control settings for decelerating and accelerating the time change of pressure around HT, the influence of strain rate, or, for example, the grain size of used materials.