Poly (L-lactic acid) (PLLA) is a biodegradable polymer typically used as the base material for manufacturing bioresorbable vascular scaffolds (BVS) [1,2,3,4,5]. PLLA based BVS offer significant advantages over permanent metal scaffolds due to their ability to provide a temporary scaffold that resorbs once the artery has healed. These properties enable the scaffold to reduce the risk of late stent thrombosis and provides more options for future potential repeated interventional treatment [6, 7]. One weakness of PLLA BVS is the poor mechanical performance due to the inadequate stiffness, strength and ductility of PLLA, resulting in thicker struts (∼150 μm) compared to metal stents (∼80 μm), which significantly limits its clinical applications [8,9,10]. One widely used approach to fabricate PLLA BVS is to perform laser cutting on a PLLA tube to obtain the scaffold pattern by a femtosecond laser [11, 12], achieving very high resolution (< 100 nm) with negligible formation of a heat-affected zone (HAZ) [13] hence the mechanical properties of PLLA tubes have a primary influence on the final performance of products [5].

PLLA material processed by melting or solution state usually has low tensile modulus, strength and elongation to break. However, its mechanical properties can be significantly improved by altering the morphology by a secondary mechanical stretch in its semi-solid state above the glass transition temperature (Tg) (>60 °C) [14,15,16,17]. In order to take advantage of this feature, stretch blow moulding (SBM) was introduced in the fabrication of PLLA BVS [2, 18, 19]. In this operation, thick walled tubes were prepared by extrusion [18, 20] or dip coating [19, 21, 22] and subsequently processed into a parison (or preform) shape. The tube parison was heated in a mould to temperatures just above the glass transition temperature (Tg) but below the thermal crystallisation temperature (Tcc) and biaxially deformed by applying internal pressure and axial stretch [23]. The biaxial deformation altered the material morphology and microstructure [24] and hence enhanced the mechanical properties (stiffness, strength and ductility) [18, 25, 26].

A combination of temperature, pressure, and stretch is needed for the application of stretch blow moulding. Of these conditions, processing temperature (Tp) for stretch blow moulding of PLLA scaffolds has typically been performed at 10~20 °C or 20~40 °C above Tg (~60 °C) [18]. The tube parison can be heated inside a hot mould by convection [26] or radiation [24] at a controlled heating time. Processing temperature has previously been observed to influence the tensile modulus and strength when compared at the same hoop strain level [27] and the strain level mainly determined the final orientation [26]. The operational sequence is another influence factor, i.e. supplying axial stretch and pressure simultaneously (SIM) or sequentially where the material was initially stretched in the axial direction and subsequently inflated in the hoop direction (SEQ). It was found that there was less anisotropy in the SEQ process indicated by balanced hoop and axial modulus and yield strength at low axial strain rate (~0.2 s−1) [26, 28]. Although the literature highlights the relevance of processing conditions with the blown tubes, there is little information on the actual strain rate occurring during blowing and the evolution of hoop and axial strain during forming.

Previous research on stretch blow moulding has offered different approaches to better understand the forming process. By using a transparent mould, the shape evolution of preforms in the blowing process was recorded by high speed cameras for PET bottles [29] and PA-12 angioplasty balloons [30]. The disadvantage of inspecting blowing inside the mould is the lack of accurate quantitative data during deformation. An approach that removes the mould to perform ‘free blow’ was subsequently proposed [31] and enabled the measurement of surface strain by digital image correlation (DIC) [32,33,34]. The stress during deformation was calculated based on the measured processing parameters (pressure, reaction force) during stretching [35]. In free blow, the preforms were heated firstly to the desirable temperature, transferred to a blowing station and blown in air without the mould. However the time dependent temperature profile of preforms need to be accounted for due to the complexity of the coupling between the thermal and mechanical properties [32, 34].

Based on the successful investigation of stretch blow moulding by free stretch blow for PET bottles [32,33,34,35,36], this article describes a technique for characterising the behaviour of PLLA tubes for stretch blow moulding of BVS. A novel experimental setup by processing tubes within a water bath has been introduced to ensure isothermal conditions, overcoming the surface cooling problems from exposure in the atmosphere during transfer from heating station to blow station. Along with this approach, a test rig was developed to conduct the stretching and blowing operation whilst recording processing parameters (axial force, inflation pressure) with incorporated sensors. Digital image correlation (DIC) was employed to acquire accurate evaluation of the surface strain by analysing deforming images of the tube parison. With a combination of the pressure, force and strain field, the stress-strain relationship of the PLLA material can be acquired directly from the tube and provide an insight into how this stress-strain behaviour changes with processing conditions. Thus a methodology to characterise the behaviour of the PLLA material directly from the parison is developed.

Experimental setup

Tube preparation

Pellets of PLLA (Tradename: PURAPOL LX175) were supplied by Corbion PURAC (Amsterdam, The Netherlands) with 96% L-isomer of stereochemical purity and weight-average molecular weight (Mw) of 14.25 × 104 g/mol. The PLLA pellets were melted and extruded into tubes by a KILLION single screw extruder with a pin of 5.4 mm and die of 10.5 mm. The temperature of the extrusion barrel ranged from 175 °C to 194 °C whilst the rotation speed of the extruder was set at 15.0 rad·min−1. The extruded tubes were precisely calibrated by a vacuum calibrator and by a drawing machine operating at a speed of 7.26 m·min−1. They were quenched by a water bath in a long (~2m) tank to ensure an amorphous state which was confirmed by an initial crystallinity of 3.0% via a DSC test. The final extruded tubes had dimensions of 4.0 ± 0.1 mm outside diameter (OD) and 1.00 ± 0.03 mm wall thickness (WT).

In the lab operation, the extruded PLLA tubes (OD: 4 mm, WT: 1 mm) were cut into pieces with a length of 105 mm, producing specimens with a central part of 20 mm and two ends of length equal to 60 mm and 20 mm (Fig. 1a). The extruded PLLA tubes were further processed into a parison shape with two pre-stretched ends as is typically done for the stretch blow moulding of angioplasty balloons [37, 38]. Each end of the tube was immersed in a silicone oil bath of 100 °C for two minutes and then stretched to a ratio of 5.0 within 10 s. The stretched tube was trimmed at each end to leave 60 mm at one end and 20 mm at the other end to create a tube parison (Fig. 1b). The purpose of this preparation was to leave an effective length of the tube at the original dimension that ultimately was stretched and blown. Orientation and crystallization (~30%) were introduced at the two ends with enhanced stiffness to avoid these sections being inflated.

Fig. 1
figure 1

Dimensions of PLLA tubes (unit: mm), (a) original tube, (b) tube parison

Experiment design

A schematic diagram of the equipment for the free stretch blow of the PLLA tubes is shown in Fig. 2. The PLLA tube parison was heated and formed inside a water bath in a glass tank. A thermostatic heating circulator with temperature display and control was employed to heat the water to the desired temperature. Compressed air was supplied with the pressure regulated to a desirable level. The pressure activation was controlled by a solenoid valve. A test rig capable of standing vertically in the water tank was built to conduct the stretching operation without a mould to visualize the forming process. The pressure and axial force were measured by a pressure sensor at working pressure from 0.0 to 1.2 MPa and a load cell with a maximum force limit of 250 N respectively. A programmable microcontroller (Arduino Mega 2560) with a user interface (LCD terminal) was used to conduct the process control and data collection. The tube forming process was monitored by two high speed cameras.

Fig. 2
figure 2

Experimental setup

The details of the test rig are shown in Fig. 3. The tube parison was installed between two grips where the top end grip was connected to a motion table mounted on the shaft and driven by a stepper motor whilst the bottom grip was fixed on a support frame. An initial axial stretch (~6 mm) within 0.3 s was used to provide axial tension on tubes to avoid sagging as the sample heated. The maximum stretching distance of the motion table from the stepper motor was 60 mm whilst a maximum speed of 25 mm·s−1, allowing for a total forming time of 2.5 s. Considering the initial effective length of 20 mm of the tube parison, the stepper motor was able to provide a maximum possible axial strain of 2.0 at an average strain rate of 1.3 s−1. The amount of initial axial stretch was varied by modifying the timing of the application of the pressure. In order to provide a simultaneous deformation process (SIM), the timing of the onset of pressure was set at a value of 0.3 s, following the initial axial deformation whilst the timing was increased to a value of 1.3 s to supply a sequential (SEQ) deformation process by applying an initial larger axial strain (~1.7). During the pressure supply, a constant pressure value of 6.0 bar was provided for a time of 2.0 s, accomplishing the inflation process without the specimen bursting. Two processing temperatures (Tp) were selected at Tp = 72 °C and Tp = 77 °C, within the range of 10~20 °C above Tg (~60 °C) [23]. Overall 4 blowing cases, which were defined as T72SIMP6, T72SEQP6, T77SIMP6, T77SEQP6 were studied in the free stretch blow experiment.

Fig. 3
figure 3

Test rig arrangement in water bath

Digital image correlation

The technique of digital image correlation (DIC) calculates the strain field on the external surface of an object by comparing the grayscale of captured images during the deformation process, where a subset with points is tracked by building a correlation on the grey values [39]. To employ this technique, the surface of PLLA tubes along the 20 mm effective length was painted thoroughly with a white background by a permanent paint marker. A random black speckle pattern in the foreground was applied by an acrylic spraying aerosol (Fig. 4a). A black rubber O-ring was installed on the top cone region of the tube parison to mark the effective height of tube. Two Photon Fastcam SA1.1 high speed cameras with resolution of 1024 × 1024 pixels at a frame rate of 1000 frames per second (fps) were used to set up a stereo DIC on a fixed support. LED panels were used to provide the necessary lighting. A Tokina 100 mm F2.8 AT-X Macro Lens was installed on each camera to adequately observe the scale of the speckle pattern. The lens had a full coverage of 35 mm with the closest focusing distance of 300 mm that yields a 1:1 reproduction ratio. A calibration process was performed after setting up the configuration of DIC by using the painted plate with 3 mm dots immersed in water to obtain the configuration parameters before experiment (Fig. 4b). The commercial software Vic-3D (Correlated Solutions, US) was used to analyse the captured images during forming, based on the parameters in the DIC setup (Table 1).

Fig. 4
figure 4

Preparation of DIC, (a) speckle patterns on the tube, (b) calibration in water bath

Table 1 DIC setup details

Deformation assessment

Strain extraction

Only the effective length of the tube parison was subjected to deformation and a section of this length equal to 15 mm was selected for the strain measurement (Fig. 5a). The contours on Fig. 6a represent the vertical distance in mm (Y) from a reference point on the middle of the specimen marked with a label of zero. The time dependent nominal hoop and axial strain history was extracted at the zero point and at a distance of plus and minus 5 mm from it. In addition to DIC measurement, the average hoop and axial strain were calculated by measuring the length and diameter of tube images before and during forming manually (Fig. 5b). The deformed images at processing time of t = 0.2, 0.6, 1.0, 1.4, 1.8 and 2.2 s were selected to investigate the shape evolution and perform subsequent measurement. The average hoop strain is calculated by Eq. (1) based on the initial diameter (D0) and deformed diameter (D1). The average axial strain is calculated by Eq. (2) based on the initial length (L0) and deformed length (L1).

$$ {\varepsilon}_{\mathrm{h}}^{\mathrm{ave}}=\frac{D_1-{D}_0}{D_0} $$
$$ {\varepsilon}_a^{\mathrm{ave}}=\frac{L_1-{L}_0}{L_0} $$
Fig. 5
figure 5

Strain extract, (a) initial tube length (t = 0) and data points extracted by DIC, (b) average strain by measurement

Fig. 6
figure 6

Stress state of the middle surface for the cylindrical part of the tube parison

To obtain the average values of hoop strain through the wall thickness, the measured strains on the external surface were converted to the results on the middle surface based on a number of assumptions, (1) the deformation was perfectly axisymmetric [40, 41], (2) the axial strain was uniform through the thickness [40, 41] and (3) the material was assumed incompressible, which is a reasonable assumption for a deforming polymer with finite strain above Tg [42]. The average hoop strain on the middle surface can be calculated by Eq. (3) and the unknown wall thickness was calculated based on the equivalent volume before and after deformation by Eq. (4). The updated external radius can be solved by the measured surface strain by Eq. (5).

$$ {\varepsilon}_{\mathrm{h}}^{\mathrm{mid}}=\frac{R-\frac{t}{2}}{R_0-\frac{t_0}{2}}-1 $$
$$ \pi \left[{R}_0^2-{\left({R}_0-{t}_0\right)}^2\right]=\pi \left[{R}^2-{\left(R-t\right)}^2\right]\left(1+{\varepsilon}_{\mathrm{a}}^{\mathrm{ext}}\right) $$
$$ R={R}_0\left(1+{\varepsilon}_{\mathrm{h}}^{\mathrm{ext}}\right) $$

Where, εhmid is the hoop strain on the middle surface; R0 and t0 are the initial external radius and wall thickness of tubes before deformation; R and t are the external radius and wall thickness of deformed tubes during deformation respectively; εaext and εhext are the hoop and axial strain on the external surfaces extracted by DIC respectively.

Stress calculation

It has been reported that the contribution of inertia during forming is negligible compared to the elastic and viscous effect [43]. When the tube is long enough, the stress state of the tube can be estimated by an analytical approach without considering the boundary effect [40, 41]. It is considered to be a closed end cylinder under internal pressure and an axial stretch (Fig. 6). Before blowing, the tube has a diameter to thickness ratio of 2.0, placing it in a thick-walled cylinder category. This ratio changes significantly however when the tube begins to blow. It has been found that even during stretch blow moulding of PET bottles for preforms with diameter to thickness ratio of 3.0, the hoop stress can be calculated by thin walled theory due to the low initial stress values [35]. To confirm this conclusion, the stress on the middle surface is computed by two methods. Eq. (6) and (7) calculate the hoop and axial stress by the thin-walled shell theory whilst Eq. (8) and (9) calculate the hoop and axial stress based on thick-walled shell theory [44].

$$ {\sigma}_{\mathrm{h}}^{\mathrm{thn}}=\left(\frac{P{R}_{\mathrm{mid}}}{t}\right) $$
$$ {\sigma}_{\mathrm{a}}^{\mathrm{thn}}=\frac{1}{2{R}_{\mathrm{mid}}t}\left[P{R}_{\mathrm{mid}}^2+\frac{F}{\pi}\right] $$
$$ {\sigma}_{\mathrm{h}}^{\mathrm{thk}}=\frac{P{\left(R-t\right)}^2}{R^2-{\left(R-t\right)}^2}\left[1+\frac{R^2}{R_{\mathrm{mid}}^2}\right] $$
$$ {\sigma}_{\mathrm{a}}^{\mathrm{thk}}=\frac{1}{R^2-{\left(R-t\right)}^2}\left[P{\left(R-t\right)}^2+\frac{F}{\pi}\right] $$

Where, σh and σa are the hoop and axial stress on the middle surface, with a subscript ‘thk’ for thick walled cylinder theory and ‘thn’ for thin walled theory; F is the axial force induced by the mechanical stretch; Rmid, R and t are the middle radius, external radius and wall thickness of the tube respectively.


Influence of paint on forming process

For the case of T72SIMP6, the forming process of the original tube parison without paint was investigated and compared with the parison with the painting required for DIC (Fig. 7). It can be seen that for the original tube parison (Fig. 7a), after pressure supply at t = 0.3 s, between 0 and 1 s the tube is stretched axially with little or no hoop deformation however after 1 s an initial homogenous expansion along the tube length was observed. The formed product at t = 2.2 s had a cylindrical shape with a diameter of 8.2 mm. A similar evolution process was found for the tube parison with paint (white background and speckle patterns in the foreground) (Fig. 7b). The onset of inflation occurred at the same time point as the original tube (t = 1.0 s) and further expansion showed the same characteristics. The blown product with painting at t = 2.2 s exhibited a cylindrical length with a diameter of 8.7 mm, indicating a small deviation of 6% when compared with the tube without paint. This comparison displayed the repeatability of the free stretch blow test in the experiment and the irrelevance of speckle painting to the forming process.

Fig. 7
figure 7

Shape evolution at T72SIMP6, (a) original tube parison, (b) tube parison with speckle pattern

Influence of mode of deformation

As stated in section 3, two different modes of deformation were analysed in the free stretch blow test, (1) the case where the axial stretching and pressure were applied simultaneously – referred to as simultaneous stretching (SIM) and the case where there was an initial axial strain of 1.7 before blowing commenced, referred to as sequential stretching (SEQ). Figure 8 shows the shape evolution of the parison when stretched sequentially at Tp = 72 °C and 6 bar (T72SEQP6). In contrast to the onset of inflation for the SIM process (~1.0 s), it can be clearly seen that all the hoop deformation in the SEQ process occurs after a time of 1.8 s after the axial deformation has completed.

Fig. 8
figure 8

Shape evolution at T72SEQP6

The measured pressure and axial force data during the forming process were extracted and compared for the two tests (T72SIMP6 and T72SEQP6) (Fig. 9). The difference between the SIM and SEQ mode of deformation was clearly evident by the time shift of 1.0 s from the pressure supply. This is deliberate to enable a reasonable difference in the level of axial strain applied before pressurisation to initiate the SIM and SEQ deformation modes. The small drop of pressure measured after t = 2.3 s in the SIM process is due to a pressure release after stopping the air supply at the point when the experiment had finished.

Fig. 9
figure 9

Pressure (P), displacement (D) and force history (F), (a) T72SIMP6, (b) T72SEQP6

A linear increase of axial force was observed before t = 0.7 s for T72SIMP6 (Fig. 9a) and T72SEQP6 (Fig. 9b). This indicated the initial elastic stage of the PLLA material in the small strain regime [23, 45]. There was an initial higher axial force at T72SEQP6 as the stretch was exclusively from the motor movement whilst the stretching load was shared with the axial force from the internal pressure for T72SIMP6.

Quantitative information of the forming process was provided by analysing the tube images with digital image correlation (DIC) and average strain from manual measurement. The strain vs time in the axial and hoop directions for 3 points on the surface of the tube (as highlighted in Fig. 5a) are shown in Fig. 10. For the T72SIMP6 test (Fig. 10a), it can be seen that the evolution of strain for each location was similar. The deformation resulted in a final hoop and axial nominal strain of approximately 1.3 on the external surface. In contrast to the linear increase of axial strain at a rate of 0.5 s−1, three stages were observed in the hoop direction, which can be described by (1) onset of pressurisation time (t = 0.3 s), (2) onset of rapid inflation (t = 1.1 s), and (3) cessation of rapid inflation (t = 1.7 s). Before t = 0.3 s, the axial stretch introduced a decreasing diameter, i.e. negative hoop strain. After pressurisation (~0.3 s), a short duration of 0.1 s was required for the pressure to reach the desirable level characterised by a fast increase of hoop strain. Deformation continued at low strain rate (~0.2 s−1) until yielding at t = 1.1 s, after which a rapid inflation occurred at a maximum strain rate of 1.9 s−1. At the latter stage of inflation, the hoop strain rate decreased gradually towards zero until t = 1.7 s, where the deformation in the hoop direction significantly reduced due to the material strain hardening [23].

Fig. 10
figure 10

Strain history of external surface by DIC (purple: −5 mm, green: 0 mm, magenta: 5 mm) and average manual measurement, (1) onset of pressurisation time, (2) onset of rapid inflation and (3) cease of rapid inflation; (a) T72SIMP6, (b) T72SEQP6

At T72SEQP6 (Fig. 10b), the axial strain data by DIC showed a linear increase over time but that the strain rate and the final strain was strongly dependent on the location thus indicating a non-uniform stretch along the tube in the case of large initial stretch. The average axial strain by measurement (blank circle) was found to be similar to the result at position 3 (−5 mm). The agreement of hoop strain at the three positions was observed by strain data from DIC, showing a maximum deviation of 7% with the average results by measurement. The deformation can be split into 3 distinct regions, i.e. uniaxial stretching for t < 1.3 s which was indicated by the increasing axial strain with decreasing hoop strain, followed by rapid inflation (strain rate = 3 s−1) between t = 1.3 s and t = 2.3 s and strain hardening beyond this time point.

Based on the assumption of uniform axial strain throughout the wall thickness and consideration of constant volume, the point strain data from DIC similar to average measurement strain was selected to calculate the hoop and axial strain on the middle surface at Tp = 72 °C (Fig. 11). The hoop strain vs time for both the SIM and SEQ process showed similar qualitative behaviour to the result of the external surface but both had significantly different magnitudes. A final hoop strain of 2.1 on the middle surface was displayed for T72SIMP6 and T72SEQP6, a 50% increase compared to the result of the external surface (~1.4). The maximum hoop strain rate during inflation reached 2.8 s−1 for the SIM process and 4.2 s−1 for the SEQ process, approximately 40% higher than the results as calculated from the external surface (SIM: 1.9 s−1, SEQ: 3.0 s−1).

Fig. 11
figure 11

Average strain history on the middle surface, (a) T72SIMP6, (b) T72SEQP6

Increase of temperature

At the elevated processing temperature of Tp = 77 °C, the shape evolution of the PLLA tubes was inspected for both simultaneous and sequential mode of deformation (Fig. 12). At T77SIMP6 (Fig. 12a), after the pressure was supplied at t = 0.3 s, the inflation occurred at t = 0.6 s, a time interval of 0.3 s smaller than the T72SIMP6 test. The external diameter reached a stable size (no further increase in hoop strain) at t = 1.0 s and a ‘banana’ shaped tube was observed. Since the balloon is acting as a closed end pressure vessel and hence has both an axial and hoop stress it is clear that the cause of the “banana” shape is due to the axial deformation contribution from the internal pressure deforming the tube axially at a faster rate than that capable of being produced by the stepper motor (~1.0 s−1). Beyond this time point, the axial deformation from the internal pressure became stable. The elongation from the motor acted on the top end of the tube, enabling it to recover to a straight state at t = 1.4 s. At T77SEQP6 (Fig. 12b) however, the distortion of the tube parison was prevented. By comparing the results at 72 °C and 77 °C, the effect of temperature can be clearly seen for both the SIM and SEQ deformation mode, with an earlier onset and more rapid blowing process for the higher temperature tests.

Fig. 12
figure 12

Shape evolution, (a) T77SIMP6, (b) T77SEQP6

A different evolution of axial force was illustrated between the SIM and SEQ process at 77 °C in Fig. 13. An initial elastic stage was observed before t = 0.6 s and subsequent slow increase of force at T77SIMP6 from t = 0.6 s to 1.7 s. This was similar to the evolution of T72SIMP6 at the same time interval but showed smaller axial force due to the reduced material stiffness at high temperature [23]. Beyond 0.6 s (T77SIMP6) and 1.7 s (T77SEQP6), a rapid decrease of the axial force was observed, which was caused by the increase of axial force from internal pressure at a higher rate than the axial elongation from the stepper motor. The negative axial force at t = 1.0 s at T77SIMP6 highlighted the more significant influence and overrode the axial stretch completely, corresponding to the ‘banana’ shaped tube parison. Comparatively, the axial force remained positive at this stage before t = 1.9 s at T77SEQP6. After the accomplishment of hoop inflation, the axial force remained constant from t = 1.0 to 1.4 s at T77SIMP6, implying a duration of 0.4 s to re-engage the axial stretch from the stepper motor. This re-engagement became faster at T77SEQP6 taking place between t = 1.9 to 2.0 s. In the subsequent axial stretching stage, there was a stronger sequentially secondary stretch effect at T77SIMP6 than T77SEQP6 due to the early accomplishment of the hoop deformation for the SIM process.

Fig. 13
figure 13

Pressure (P), displacement (D) and force history (F), (a) T77SIMP6, (b) T77SEQP6

The hoop and axial strain for the T77SIMP6 and T77SEQP6 tests are shown in Fig. 14. A big influence on the strain history from processing temperature was observed in both processes. After pressure supply at 0.3 s (T77SIMP6) and 1.3 s (T77SEQP6), a hoop strain rate of 0.8 s−1 (SIM) and 2.5 s−1 (SEQ) was found before yielding, which is approximately four times the respective values at 72 °C (0.2 s−1 (SIM), 0.6 s−1 (SEQ)). The strong time dependency was attributed to the dramatic change in moduli in this temperature range, which has been highlighted in DMA tests in previous research [23, 46]. After the rapid inflation occurs at t = 0.5 s (T77SIMP6) and t = 1.4 s (T77SEQP6), the maximum hoop strain rate reached 6.5 s−1 (T77SIMP6) and 11.8 s−1 (T77SEQP6) respectively, which was 240% and 290% higher than that at 72 °C. This finding confirmed the significant change of the viscoelastic behaviour as a function of processing temperature at finite strain [23]. After rapid inflation at 0.5 s (T77SIMP6) and 1.4 s (T77SEQP6), the axial strain history showed a significant difference with much more evidence of nonlinear behaviour than the axial strain history at 72 °C. This implied that the axial load from the internal pressure increased more quickly after the onset of inflation and dominated the axial deformation. A maximum axial strain rate of 3.5 s−1 (T77SIMP6) and 5.0 s−1 (T77SEQP6) was exhibited in the nonlinear stage, which was much higher than the maximum possible axial strain rate from elongation of the motor (~1 s−1). At the end of the forming period, an average hoop strain of 2.0 on the outer surface was observed in both processes whilst the average axial strain reached 1.6~1.8.

Fig. 14
figure 14

Strain history of external surface by DIC (purple: −5 mm, green: 0 mm, magenta: 5 mm) and average manual measurement, (a) T77SIMP6, (b) T77SEQP6

In Fig. 15, it was found the final hoop strain on the middle surface increased to approximately 3.0 for both T77P6SIM and T77P6SEQ. The maximum hoop strain rate was found to be 9.1 s−1 for the SIM process and 16.8 s−1 for the SEQ process and was 40% greater than the rate on the external surface (SIM: 6.5 s−1, SEQ: 11.8 s−1). The maximum hoop strain rate on the middle surface during inflation at 77 °C showed a significant increase of 225% and 300% compared to the results at 72 °C.

Fig. 15
figure 15

Strain history on the middle surface, (a) T77SIMP6, (b) T77SEQP6

Stress state

Since the strain is available via the DIC, the evolution of the corresponding stress is also of interest thus providing an opportunity to obtain the constitutive behaviour of PLLA directly from the inflating parison. The ratio between the internal diameter (Din) and wall thickness (t) as the tube inflates for all tests was initially calculated to evaluate whether thick walled or thin walled shell theory was the most appropriate for calculating the stress (Fig. 16). As the inflation progressed over time it can be seen the Din/t increased and that it reached a critical value of 10 at t = 0.95 s for the T72SIMP6 and at t = 1.5 s for T72SEQP6 (Fig. 16(a)). In both cases this time corresponded to the onset of rapid inflation. At Tp = 77 °C (Fig. 16(b)), the characteristic time for the change of Di/t to reach greater than 10.0 was t = 0.55 s (T77SIMP6) and t = 1.44 s (T77SEQP6), approximately 40~50 ms beyond the onset of rapid inflation. The results showed that the tube behaved as a thick-walled shell before inflation with non-uniform hoop stress through the wall thickness and a membrane after the onset of rapid inflation due to the big increase of Din/t.

Fig. 16
figure 16

Geometrical evolution of (Din/t) in the deformation process, (a) Tp = 72 °C, (b) Tp = 77 °C

The case of a slow geometric transformation (T72SIMP6) before Di/t = 10 (t = 1.0 s) was selected to calculate the stress history on the middle surface using Eq. (6) ~ (9). The resulting hoop stress from thin-walled shell (σhthn) was slightly higher than that by thick walled-shell (σhthk) with a deviation of ~0.3 MPa (Fig. 17(a)). The small deviation between σhthk and σhthn confirmed that the assumption of membrane state was valid [35]. The axial stress calculated by the thin (σathn) and thick (σathk) walled cylinder shell on the middle surface showed a similar stress shift (~0.3 MPa) (Fig. 17(b)), proving the reliability of the assumption of uniformly distributed axial stress. Based on these investigations, the simplified σhthn and σathn (Eq. (6) and (7)) were used in the following section to characterise the average stress state along the cross section in the inflating tube.

Fig. 17
figure 17

Stress history at T72SIMP6 (a) hoop, (b) axial

Before rapid inflation (t = 1.1 s) at T72SIMP6, a consistent hoop and axial stress response was observed in Fig. 18a. This was attributed to the consistent hoop and axial strain history (Fig. 15a) at the early stage. The uniaxial stretch for the T72SEQP6 process led to a smaller axial stress compared to the biaxial stretch in the SIM processes. A more rapid increase of hoop stress occurred after the onset of inflation due to the growth of diameter of the tube. In the SIM process, this resulted in the hoop stress being higher than the axial stress. The increase of hoop stress due to rapid inflation introduced an intersection between the hoop and axial stress at (t = 1.8 s) in the SEQ process. The final hoop stress (~25 MPa) in the SEQ process was approximately 5 MPa higher than the result in the SIM process (~20 MPa) whilst a similar axial stress (~15 MPa) was found for both modes of deformation. These stresses are similar to those observed from previous studies by the authors on biaxially stretching of planar sheets at similar temperature conditions (~70 °C), e.g. a stress value of 30 MPa was measured from an equal biaxial (EB) test stretched to a final stretch ratio of 2.5 at a constant strain rate of 4 s−1 [23].

Fig. 18
figure 18

Stress evolution on the middle surface, (a) Tp = 72 °C, (b) Tp = 77 °C

A similar stress history was found when the processing temperature increased to Tp = 77 °C (Fig. 18b). At T77SIMP6, the axial and hoop stress evolved at a similar level in a very short time period from t = 0.3 to 0.6 s due to the early onset of rapid inflation. The axial stress had a slower increase in the SEQ process at uniaxial stretch due to the smaller stiffness at high temperature [23]. The intersection point of hoop and axial stress (SEQ) was observed earlier due to the rapid inflation. After inflation, the hoop stress in the SIM and SEQ continuously increased to reach a final stress of 38 MPa (SIM) and 45 MPa (SEQ). The axial stress experienced a nonlinear rapid increase during inflation but returned to a linear increase after that, giving a final value of 20 MPa (SIM) and 25 MPa (SEQ). The effect from processing temperature by comparing Fig. 18a, b indicated a high stress level at high Tp due to the higher stretch of material. A higher stress difference (~20 MPa) between the hoop and axial direction was observed at high Tp compared to the result (~5 MPa) at low Tp.

The stress-strain relationships on the middle surface curves were created based on the strain and stress history (Fig. 19). As shown in Fig. 19a, isotropic stress-strain relations below a strain of 0.6 was found for T72SIMP6 due to an equal biaxial strain and stress response. For the SIM stretch condition, the strain evolution showed different levels vs. time during the inflation, showing a primary hoop deformation due to the higher inflation rate, leading to a higher axial stress than hoop stress at the same strain. For T72SEQP6 however, no initial coincidence of axial and hoop stress-strain relationship was found due to the deliberate sequential effect of the primary axial stretch. At the same strain, the hoop stress in the SEQ process was higher than that in the SIM process for the initial secondary hoop deformation. For strains less than 1.1, the axial stress (SEQ) was smaller than the hoop stress, corresponding to the stage before the intersection point. After that, the hoop inflation dominated, and the secondary axial stretch introduced higher axial stress than hoop stress.

Fig. 19
figure 19

Stress-strain relationship on the middle surface, (a) Tp = 72 °C, (b) Tp = 77 °C

At Tp = 77 °C (Fig. 19b), the stress-strain response for T77SIMP6 displayed similar characteristics as the results at 72 °C, with an overlap in behaviour in the small strain regime (< 0.3) and a higher axial stress after that. At a strain level of 2.0, the material behaved softer in the hoop direction at high temperature condition, i.e. a hoop stress of 15 MPa at 77 °C in comparison to 20 MPa at 72 °C (SIM). A large final hoop strain of 3.7 created a high stress level value of 38 MPa for the test at 77 °C. The early onset of inflation at 77 °C and the fact that hoop strain rate exceeded the axial strain rate enhanced the sequential effect by secondary stretch in the axial direction. For T77SEQP6, higher hoop stress than the SIM process was observed by the effect of delayed hoop deformation. An intersection between axial and hoop stress curves occurred at a strain level of 0.7, which was smaller than that (~1.0) in the SEQ process at 72 °C. In general, it can be seen that both the temperature and operational sequence had a great influence on the stress-strain relationship by changing the evolution process and final values.


In this study a new apparatus has been designed and built enabling a new load-controlled test for measuring the stress-strain behaviour of PLLA directly from a parison under blow moulding conditions. It provides valuable data on typical strain rates experienced by the material during forming along with its response when subjected to nonlinear loading paths, which enables a good experimental idealisation of the blow moulding process.

The data presented in this paper highlights the strong influence of temperature and mode of deformation on the blowing characteristics of the PLLA tubes and the corresponding stress-strain behaviour. The sensitivity to temperature is strong with only a 5 °C increase in temperature from 72 °C to 77 °C, resulting in an increase in maximum strain rate from 4 s−1 to 17 s−1, an increase in final strain from 2.0 to 3.0 and an increase in final stress from 25 MPa to 45 MPa. Since the maximum temperature tested here was 77 °C, additional work is required to evaluate how this effect evolves as the temperature increases further towards the cold crystallisation temperature (maximum forming temperature) of ~100 °C [23].

Although the influence is not as strong as the temperature, the mode of deformation also has an influence on the blowing characteristics and the stress strain behaviour with an increase in the final stress from 38 MPa to 45 MPa and a reduction in final hoop strain from 3.8 to 3.2 observed for tests conducted at 77 °C for the two conditions investigated. In this paper only one scenario of a sequential test is provided (initial strain equal to 0.5) but further work exploring the influence of the magnitude of the strain in the axial direction on the subsequent behaviour in the hoop direction should be investigated. The other factor that is able to influence the deforming sequence is the magnitude of the pressure however this parameter has not been part of this study.

The test method provides a major step forward for characterising the behaviour of PLLA for stretch blow moulding. Whilst previous studies have produced stress strain behaviour at different temperatures and strain rates [23, 45, 47, 48], these have been performed on planar sheets which by default have a different processing history to the tube. In addition, this new test method has the benefit that the properties are measured at conditions directly comparable to stretch blow moulding i.e. with varying strain rates and modes of deformation. One weakness of the test is that due it being a load-controlled test the individual contribution of strain rate and temperature is difficult to detect since the strain rate varies significantly during each test and for tests conducted at different temperatures. For this reason, the rig provides important complementary data to the data already presented in the previous study from displacement controlled tests [23, 45, 47, 48]. One anomaly compared to previous published data stress-strain behaviour of PLLA is that no obvious yield point is observed in the stress strain results. This is also due to the load-controlled nature of the test since the material rather than being forced to stretch at a specific speed regulates itself resulting in variable strain rate and no obvious yield point.

One potential criticism of the test method that it was conducted in a water bath given that it is known that hydrolysis and water absorption of PLLA can have a major effect on the mechanical properties [49,50,51,52]. However it should be noted that the timescale of the experiment is orders of magnitude smaller than the timescale for hydrolysis to have an influence [53,54,55,56,57]. To verify this, additional experiments have been performed where PLLA tubing was uniaxially stretched after heating in a wet environment for 8 min (similar to the timescale of the experiments in this paper) and after heating in a dry environment with no significant difference observed [58].

There is an opportunity to further explore the effect of both temperature and mode of deformation by conducting corresponding mechanical property measurements on the blown tubes to assess the influence of the processing history on the modulus, yield and strain at break - although given the dimensions of the blown tubes this provides its own challenges, especially in the hoop direction. With this data in addition to the stress strain data it would be feasible to fit it to a previously developed material model of PLLA [23] and create a forming simulation that has the capability of optimising the parison dimensions and corresponding process conditions to produce a BVS with optimal properties. Even without such a model the raw data presented from the test is a valuable design aid for engineers in the design and manufacture of BVS where the natural draw ratio of a material as a function of temperature is readily available enabling appropriate nominal parison dimensions and processing temperature values to be chosen.


By a novel experimental setup, a tube forming process for characterising the behaviour of PLLA tubes for stretch blow moulding of BVS has been developed. The experimental scheme was highlighted by the forming process at isothermal conditions in a water bath and measurement of surface strain by digital image correlation (DIC). Operations at designed processing temperature and blowing sequence revealed the deformation behaviour of PLLA materials by the qualitative results on evolution of tube shape and quantitative data of strain and stress. Quantitative results reveal the strong dependence of the stress strain behaviour on strain history experienced by the inflating tube as well as the processing temperature. The unique test rig and methodology developed and the corresponding results offer the ability to characterise materials and understand the influence of processing on material behaviour and provide stress strain data at conditions relevant to forming that is critical for forming simulation development. As a result, the research output has great potential to benefit industry in the development and optimisation of stretch blow moulding of PLLA.