The vacuum assisted thermoforming process for heavy gauge thermoplastic sheets follows a sequential series of steps, beginning with the loading and clamping of a flat sheet. The material is then heated using a radiative heater bank, typically from both the top and bottom side of the sheet. This heating step brings the sheet to a soft, formable state. This heating phase is attentively controlled by setting a specific temperature, which is precisely measured using an infrared (IR) sensor. Despite the symmetrical arrangement of the heating elements aiming for uniform in plane heat distribution, the temperature across the sheet is almost inevitably uneven [
1]. When a uniform heating pattern is applied, the center of the sheet often reaches a higher temperature compared to the clamped edges, resulting in a temperature gradient from the center to the edges [
2]. Adjusting the in-plane temperature pattern of the sheet according to the mould shape is a method to enhance the quality of the thermoformed part [
3]. During the heating process, the material also experiences thermal strain, leading to warpage. This warpage typically manifests as concave deformations both upward and downward which is caused by the material being constrained at its edges, thus hindering its ability to thermally expand freely [
4]. In the pursuit of capturing intricate details of the mould shape, a common practice is to set a high temperature. However, the use of elevated temperature set points can induce sag deformation [
5]. This occurs because of the lower stiffness of the material at high temperatures. The material loses its ability to support its own weight, resulting in sagging or off-sagging deformations[
6]. This concave sag deformation can intensify the variation in heat flux distribution across the sheet, caused by the altered view factor relative to the heater bank. This might also lead to uneven heat flux on both the upper and lower sides of the sheet, thereby creating temperature gradients both across the surface of the sheet and through its thickness [
7]. While increasing the temperature is essential for capturing intricate mould details, it comes with the trade-off of potential sag deformation. To tackle the challenges associated with thermal expansion-induced warpage and sag deformation during heating, a commonly employed technique involves the creation of a pre-forming bubble. This is achieved by applying air pressure within a sealed cabinet to transform the thermoplastic sheet into a bubble-like configuration[
8]. Through the generation of a pre-forming bubble, the onset of contact between the positive mould and the material is postponed. This intentional delay allows the material to stretch uniformly, contributing to a more consistent thickness distribution in the final part. Therefore, the creation of a pre-forming bubble serves as a dual-purpose solution, fostering both uniform stretching and controlled contact, ultimately enhancing the overall quality of the thermoforming process. The height of the preforming bubble is a critical parameter in this context, requiring careful matching with the mould height and precise consideration of its location within the forming process. During the subsequent forming stage, the positive mould moves upwards to make contact with the softened thermoplastic sheet. In this phase of thermoforming, the mould and polymer interact at various times and locations, depending on the mould shape, aided by vacuum in between the mould and the sheet to achieve the desired shape. Here the friction between material and mould, which is highly temperature dependent itself [
9], exhibits the highest friction load in the region with initial contact [
10,
11]. This differential in contact timing, combined with the temperature nonuniform distribution field, and material cooling rate across different regions during forming, leads to non-uniform stretching of the polymeric sheet during forming, consequently resulting in an inevitable thickness variation in the final product [
1,
12].
In thermoforming, the uniformity of wall thickness, or its distribution, is considered as a key factor in determining the quality of a formed product [
13,
14]. To evaluate this aspect of quality during the thermoforming process and to fine-tune the process parameters for industrial applications, in-situ stereo Digital Image Correlation (DIC) as a non-contact method synchronized with a thermal camera, significantly enhances the real-time monitoring of 3D surface large deformations and temperature variations across the entire field in industrial thermoforming applications [
15]. This method commonly entails applying a random speckle pattern to the surface of the object and contrasting subsets of images, both ‘deformed’ and ‘undeformed’, along with performing camera calibration focused on the region of interest. In experimental setups, a stereo camera system captures these speckled patterns as the sample undergoes deformation. The technique involves correlating images taken from various angles, enabling the tracking of alterations in the 3D surface geometry throughout the deformation process [
16,
17,
18]. Given the substantial nonlinear deformation inherent in vacuum forming processes, it is crucial to employ more than one camera to capture the out-of-plane movements [
19,
20]. Seefried and Drummer [
21] utilized DIC to investigate the effects of radiation cross-linking and various process parameters. Their research focused on analyzing strain distributions in thermoformed parts, particularly examining how sheet thickness and processing parameters influence these distributions. The implementation of DIC method on an actual vacuum-forming industrial machine, as demonstrated by Van Mieghem et al., [
15] was a significant advancement in this field. Their work effectively highlighted the practicality and feasibility of applying stereo DIC in vacuum forming, contributing valuable insights and methodologies to the industry. Building upon this, Van Mieghem et al [
22,
23] introduced a methodology for determining wall thickness in thermoformed products in negative vacuum-assisted semi-sphere mould. This method, utilizing in-situ surface strain DIC measurements, effectively validated various strain definition equations, thereby enhancing the precision of thickness calculations in thermoforming processes [
22,
23]. Later on, the complexities involved in accurately measuring pressure-induced mechanical strains during bubble-assisted thermoforming of thin gauge thermoplastic sheets were thoroughly examined by Ayadi et al. using DIC techniques [
2,
24].