Polyethylene Terephthalate Research Articles

Direct laser writing of curved SERS for light-guided enhancement

Flexible SERS substrates, typically used on irregular surfaces, have unexplored optomechanical effects that could enhance performance. We developed a micromechanically bending structure, i.e. microbender, to study how bending affects SERS substrates’ performance. Optical simulations of nanopillar arrays on micro-curved surfaces showed a 25–134 % improvement in mean-field localization at the pillar tips for arrays with pillar diameters of 0.4–1 μm, pitches of 0.5–0.8 μm, and heights of 0.5–4.5 μm. Raman measurements showed that SERS intensity increases when in a curved state due to enhanced light scattering, guiding, and field localization. A curved array of 6 μm tall pillars (0.5 μm diameter, 1 μm spacing) produced Raman intensities similar to dense single-voxel arrays with shorter 0.8 μm pillars (0.2 μm diameter, 0.2 μm gaps) in the planar state. This finding suggests that low resolution fabrication technologies can produce curved SERS substrates with similar performance to high resolution planar SERS, offering an alternative to the current “smaller is better” trend through post-fabrication manipulation.

Analysis of fatigue degradation process and modelling of an elliptical crack in the locking system of a PET bottle blower

In the dynamic world of Polyethylene Terephthalate (PET) bottle production, ensuring the reliability of blow molding machines is paramount, particularly the locking mechanisms that endure significant cyclic loads during operation. This study investigates the fatigue degradation and crack propagation within the locking system of a two-cavity, 2-liter PET bottle blow molder. By modeling an elliptical crack in the most stressed component, we explore the complex stress distribution and the impact of repeated opening and closing cycles on the system’s integrity. Utilizing advanced finite element analysis (FEA), our research provides a comprehensive understanding of the stress intensity factors and safety margins under varying loading conditions. The results not only enhance predictive maintenance strategies but also offer valuable insights into extending the operational lifespan of these machines, thereby improving safety and reliability in industrial applications. This study opens new avenues in the field of component lifespan prediction. By combining artificial intelligence, machine learning, and innovative materials, it aims to improve the reliability and lifespan of PET blow molders.

Lost in the Dark: Current Evidence and Knowledge Gaps About Microplastic Pollution in Natural Caves

In this study, a systematic review of the scientific literature was carried out to summarize the emerging evidence on microplastic pollution in natural caves. After the screening of 655 papers on the topic from a combined search on the Web of Knowledge and the Scopus databases, we found only 14 studies reporting quantitative data on microplastics from a total of 27 natural caves. Most of the assessments focused on water and sediment, with very limited investigations concerning the cave biota. Overall, the most common types of particles found in caves were small (<1 mm) fibers (~70–90% of items), transparent or light-colored, mostly made of polyethylene and polyethylene terephthalate. Anthropogenic cellulosic materials, however, represented a non-negligible portion of particles (i.e., ~20–30%). Microplastic concentrations in caves varied between 0.017 and 911 items/L for water and 7.9 and 4777 items/kg for sediment, thus falling within the levels of microplastic pollution found in other terrestrial, freshwater, and marine environments. Levels of microplastic pollution appear largely variable among caves, stressing the need to extend the geographic and environmental ranges of the assessments, which are currently concentrated on Italian caves on land, with very few case studies from other regions of the world and from marine caves. Despite their putative isolation, natural caves have a high vulnerability to microplastic contamination, requiring much more research effort to understand the potential risk that plastics pose to these fragile ecosystems.

A new mechanism for the kinetics of simultaneous depolymerization reaction inside and outside poly (ethylene terephthalate) particles

The depolymerization and recycling of PET is important for waste reduction, resource efficiency and production cost reduction. However, among the industrialized methods for recycling waste PET, the main challenge applicable to the PET glycolysis strategy is the low efficiency and low purity in recovering polyester, which is mainly due to the imperfections in the reaction kinetics model. In this study, we developed a kinetic model for PET glycolysis at different reaction temperatures by investigating the glycolysis process of PET chips at different reaction temperatures to discover new PET glycol depolymerization mechanisms. It was found that the zinc acetate-catalyzed PET glycolysis followed a first-order reversible kinetic model at higher temperature (206–210 °C). However, at lower temperatures (180 °C–205 °C), the experimental curve of the kinetic model is similar to the theoretical curve of the nucleation-controlled model, and in this temperature range, EG depolymerized PET in a manner that internal and external depolymerization proceeded simultaneously. This finding is expected to guide the establishment of a more efficient PET depolymerization process, which is an important guide for recycling waste PET.

A Three-Dimensional Surface-Adaptive Stretchable Sensor for Online Monitoring of Composite Materials Curing.

Recently, rigid sensors have been commonly applied to online monitoring of the core curing processes of composite materials to prevent both overcuring and under-curing. However, conventional rigid sensors are prone to causing cracks and bubbles in composite materials during the curing process, thereby affecting both the mechanical performance and the overall reliability of the materials. Herein, stretchable interdigital dielectric sensors with flexible substrates and electrodes are designed to conform to complex 3D surfaces, thus enabling embedded nondestructive monitoring of composite curing processes. The sensors obtained can endure 1000 cycles of bending from 0° to 180° and 1000 cycles of stretching at 30% strain while still conforming perfectly to complex 3D surfaces, thus overcoming the inability of traditional curing monitoring sensors to bend. Additionally, sensor integration with an electronic circuit enables real-time data collection and transmission, which makes the device more portable, compact, and lightweight. Moreover, after atmospheric exposure for 5 months, the unit sensitivity of the sensor decreased by only 0.1%, thus demonstrating its excellent reliability and stability. Furthermore, during curing monitoring of the complex three-dimensional surfaces of the Fendouzhe deep-sea submersible, the unit's sensitivity is close to that of conventional planar monitoring equipment, decreasing by only 0.4%. The proposed online nondestructive monitoring technology demonstrates high sensitivity, high monitoring accuracy, and high reliability during surface monitoring, thus enabling long-term curing monitoring under complex nonplanar conditions.

Fast and label-free detection of procalcitonin in human serum for sepsis using a WTex-based extended-gate field-effect transistor biosensor

In this article, we present the first instance of depositing WTex-sensitive films with varying thicknesses (3, 4, and 5 nm) onto flexible polyimide substrates using radio-frequency sputtering. These films were used to create an extended-gate field-effect transistor (EGFET) for pH sensing and detecting procalcitonin (PCT) in the sera of patients with sepsis or bacterial infections. Among the films, the 4 nm WTex film exhibited high sensitivity (59.57 mV/pH), minimal hysteresis (∼0.8 mV), and a low drift rate (0.14 mV/h). Additionally, this WTex-based EGFET sensor retained a pH sensitivity of 59.2 mV/pH even after 180 days of operation and exhibited excellent mechanical flexibility, enduring 500 bending cycles without degradation. Moreover, PCT antibodies, activated using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-hydroxysuccinimide, were immobilized on the WTex film functionalized with 3-aminopropyl triethoxysilane. This effective immobilization enabled the specific binding of PCT antigens. The WTex-based EGFET biosensor demonstrated high sensitivity (18.12 mV/pCPCT) across a wide dynamic range (1 fg/mL to 1 μg/mL). Furthermore, the PCT concentrations in patient sera, whether from individuals with or without sepsis or bacterial infections, measured by our biosensor were comparable to results obtained using clinical enzyme-linked immunosorbent assay kits.

A Star‐Nose‐Inspired Bionic Soft Robot for Nonvisual Spatial Detection and Reconstruction

The star‐nosed mole is recognized as a tactilely sensitive mammal due to its unique nose, which facilitates spatial detection in dark environments through touch using its appendages enveloped in numerous sensory receptors. This article introduces a bionic soft robot inspired by the star‐nosed mole, which combines a pneumatic soft platform with a polydimethylsiloxane–polyethylene terephthalate cylindrical tactile sensor array based on bilayer single‐electrode triboelectric nanogenerators, mimicking the muscle tissue of the mole's nose and the cylindrical appendages surrounded by Eimer's organs. The cylindrical sensor array enables multiangle spatial detection without an external power supply and remains unaffected by external materials. By implementing a constant curvature model for robot motion control, positional information is provided for the contact points between the cylindrical sensor array and the external environment. The robot effectively discriminates the distance and shape of various objects and achieves nonvisual 3D spatial detection and reconstruction in real‐world scenarios. This work presents a novel bionic approach for 3D spatial detection in nonvisual environments.

Comparative study of virgin and recycled polyethylene terephthalate and polypropylene intermingled thermoplastic composites

AbstractIn this study, a comparative analysis of the use of recycled PET (R‐PET) in synthetic and natural fiber blended composites was made. PET, R‐PET, and PP yarns were folded with reinforcing fibers by commingling technique and then fabrics were prepared using weaving technology. Hot compression molding technology was used for composite fabrication. Tensile and impact characterization revealed the significant influence of reinforcing and TP fibers on mechanical properties. R‐PET matrix glass fiber reinforced composites exhibited 41.77% higher tensile strength than virgin PET and 20.41% higher than PP. In terms of tensile strength for linen reinforced samples, R‐PET shows an impressive 181% improvement over virgin PET and 154% over PP. According to the drop weight test results, glass fiber reinforced R‐PET matrix sample exhibited a peak load value 53% higher than that of the virgin PET matrix, although it was 9.47% lower than the PP matrix. In linen fiber reinforced samples, R‐PET demonstrated a 57.73% improvement over virgin PET but lower by 9.47% compared to the PP matrix. During this time, DSC, TGA, FTIR, and flammability tests were also performed on the composite samples. The results showed that R‐PET has easy processability as a matrix material and provides better wetting of the reinforcing fibers. For this reason, it has been shown that R‐PET matrix samples provide better mechanical properties than both PET and PP matrix samples. It has also been determined that R‐PET is a more suitable matrix material compared with natural fiber reinforced composites.Highlights Commingled yarns were used for preparing composites. R‐PET yarns were used as matrix in preparing glass and linen reinforced composites. R‐PET was compared with virgin PET and PP yarns. R‐PET showed great potential in easy preparation of TP composites. Composites made with R‐PET showed improved thermal and mechanical properties.

Fusion of Hydrophobic Anchor Peptides Promotes the Hydrolytic Activity of PETase but not the Extent of PET Depolymerization

Enzymatic recycling of polyethylene terephthalate (PET) has attracted significant attention in recent years. While the fusion of anchor peptides to PET hydrolases is believed to enhance PET hydrolytic activity, a quantitative analysis is yet lacking. Here, we construct four fusion enzymes by fusing anchor peptides (including hydrophobic LCI, LCIM1 and TA2, and hydrophilic EK4) to the C terminus of HotPETase, one of the most active PET hydrolases for high‐crystallinity PET (HC‐PET). Single‐molecule force spectroscopy (SMFS) demonstrates that hydrophobic anchor peptides promote adhesive interactions between the fusion enzymes and the PET surface. This is also validated by the adsorption kinetics and isotherms, and the saturated adsorption capacity remains unaltered compare to HotPETase. At low substrate loadings, the apparent hydrolytic activity of these fusion enzymes is positively related to the hydrophobicity of the anchor peptides. Among them, HotPETase‐LCI stands out as the most effective enzyme for HC‐PET degradation, demonstrating a 1.5‐fold increase in hydrolytic activity. At high substrate loadings, the advantages of fusion with anchor peptides diminish. We conclude that fusion enzymes only facilitate the hydrolytic rates of HC‐PET but have little effect on the final conversion extent.

Quality changes of durian pulp (Durio ziberhinus Murr.) in cold storage

Abstract In this study, the effects of four types of polystyrene (PS) plastic box with polyethylene terephthalate (PET) lid (PSPET), PS tray with polyethylene (PE) bag (PSPE), PS tray with a vacuumed PE bag (PSVPE), and PET box with a sealed lid (PET) on the quality of durian fruit during storage at 10°C were investigated. The analysis results showed that in all four types of packaging, the total aerobic bacteria count in the durian pulp ranged from 101 to 105 CFU/mL after storage. However, total yeast and mold count was not detected. During the same survey period, PET packaging for the product had the lowest weight loss of 0.58–3.07%. Next, the impact of temperature, at 0 and 10°C, on the quality stability of durian fruit during storage was also studied and evaluated. Durian pulp preserved in PET at two different cold temperatures did not show any significant difference in microbial content and phytochemical composition. Total aerobic bacteria count in the samples was recorded at about 104 CFU/g after storage; total yeast and mold count was not detected, and the weight loss reached 1.82 and 1.72% at temperatures of 0 and 10°C, respectively.

Reinforcing the Efficiency of Plastic Upgrading through Full-Spectrum Photothermal Effect Integration of Heat Isolator.

Photoreforming of polyethylene terephthalate (PET) to H2 is practically attractive strategy for upgrading waste plastics. The major challenge is to utilize the infrared energy in the solar spectrum to improve the efficiency for photoreforming of PET to H2. Herein, through the ingenious integration of tungsten phosphide nanoparticles and tungsten single atoms (WP/W SAs) with carbon nitride (g-C3N4), the constructed hybrid inherits both the desirable properties and structural merits of the respective building blocks. Specifically, the photothermal effect of WP/W SAs couples with the "heat isolator" role of g-C3N4 due to its low thermal conductivity, thereby forming localized high-temperature regions, reducing the activation energy and improving the kinetics in the photoreforming of PET to H2. Additionally, the green pretreatment of PET using alkali-free hydrothermal strategy is reported, achieving direct separation of the ethylene glycol and terephthalic acid. This work not only provides an alkali-free hydrothermal pretreatment for PET, but also integrates the photothermal effect with the thermal insulation and opens a new avenue for harnessing solar energy into to convert plastics into H2.

Upcycling of waste polyethylene terephthalate (PET) into CoFe@C for highly efficient PV-driven bifunctional seawater splitting via a “waste materialization” strategy

Developing green and efficient techniques to convert plastic wastes into functional materials is attractive and remains highly challenging. This study employs a hydrothermal combining with pyrolysis process for constructing a Co3Fe1@C heterostructure from the polyethylene terephthalate (PET) waste-mediated metal-organic frameworks. The as-obtained Co3Fe1@C shows a core-shell structure and possesses good performance towards water electrolysis. The Co3Fe1@C can attain the current density of 100 mA cm−2 with an overpotential of 250 mV for oxygen evolution reaction (OER). In addition, the bifunctional Co3Fe1@C can realize the overall seawater electrolysis at 50 mA cm−2 with good stability for 280 h driven by a 2.2 V commercial silicon solar cell. Overall, this study demonstrates a green chemistry approach to simultaneous plastic waste upcycling and cost-effective electrocatalyst fabrication, which may stimulate further research on the “waste materialization” approach to converting solid waste into highly efficient catalysts for various chemistry and energy industry applications.

Field-free spin–orbit torque magnetization switching in Pt/CoTb devices grown on flexible substrates for neuromorphic computing

Flexible spintronic devices based on spin–orbit torque (SOT)-induced perpendicular magnetization switching (PMS) have attracted increasing attention due to their high storage intensity and good programming capability. However, to achieve deterministic PMS, an in-plane auxiliary magnetic field is required, which greatly limits its application. Here, we show that “robust” magnetic field-free SOT-driven PMS is realized in the oblique sputtered Pt/CoTb multilayers grown on a flexible polyimide substrate. “Robust” means the magnetic field-free SOT switching is highly repeatable and stable after 100 bending cycles under various bending conditions. Additionally, the fabricated flexible multilayers exhibit nearly linear and nonvolatile multistate plasticity as synapses and a nonlinear sigmoid activation function when acting as neurons. We construct a fully connected neural network for handwritten digit recognition, achieving an over 96.27% recognition rate. Our findings may spur further investigations on the SOT-based flexible spintronic devices for wearable artificial intelligence applications.

Flexible Supercapacitor Device Based on Laser‐Synthesized Nanographene for Low‐Power Applications

Laser‐induced graphene (LIG) and laser‐induced reduced graphene oxide (LIrGO) are two relatively recent graphene‐based nanoscale materials suitable for miniaturized flexible supercapacitors. This study employs direct laser engraving techniques to generate patterns on flexible substrates, such as paper and polyamide (PI). This methodology allows fine control over the formed nanographene structures to fabricated LIG and LIrGO supercapacitors. The LIG on PI exhibits a distinctive porous structure and high surface area, adsorption, and transportation of ions. Furthermore, paper‐based LIrGO electrodes are recyclable and are formed in a single step. The morphological study is done using scanning electron microscopy, Raman spectroscopy, X‐ray photoelectron spectroscopy, and X‐ray diffraction. Galvanostatic charge–discharge studies at 0.05 mA cm−2 current density show an areal capacitance of 3.69 mF cm−2 for LIG and 1.61 mF cm−2 for LIrGO. The comparable energy densities for LIG and LIrGO are 0.32 and 0.16 μWh cm−2, respectively. From the calculative analysis of both types, the variation in specific areal capacitance enabling effective is 56.3% from GCD, indicating that the LIG device performs better. Finally, a portable potentiostat is employed to investigate the viability of utilizing supercapacitors to operate self‐powered sensors in a portable and integrable fashion.

Color/Transparent Bi‐Customizable Solar Antifogging Nanofilms

AbstractAlmost all reported solar anti‐/defogging surfaces are black and opaque. However, aesthetics and transparency are preferred to enhance security, privacy, and visual experience without sacrificing antifogging in some practical scenarios, such as automotive windshields, architectural glass facades, and sports goggles. Herein, a color and transparency bi‐customizable solar antifogging heterostructure nanofilms is reported, which only consists of a Ti–TiOx layer for partial visible light transmission and a narrow bandgap Ti2O3 layer for broadband sunlight absorption. By precisely controlling each monolayer thickness, various vibrant structural colors (covering yellow/green/purple/blue) through interference effects, along with tunable visible light transparency (from 0% to 30%), and broadband solar absorption (up to 90%) are obtained, providing personalized options for various applications. Simultaneously, the nanofilms exhibit remarkable photothermal performance (110.3 °C under 1 kW m−2 irradiation) compared to blank samples, demonstrating sustained and superior defogging (3.5‐fold improvement) and antifogging capabilities, even in extremely cold (–20 °C) or high temperature and high humidity (50 °C, 100%) conditions. Importantly, the nanofilms are just 174 nm thick, and can be easily upgraded and scalable fabricated by sputtering on various rigid, flexible and portable substrates, such as glass, metals, textiles, plastics, enabling a wide range of direct applications.

The comparison of echocardiographic and serum parameters between Sapien 3 Ultra Resilia and Sapien 3 at one month

Abstract Background Sapien 3 Ultra Resilia (S3UR) is the latest balloon-expandable valve for transcatheter aortic valve replacement (TAVR). Compared to Sapien 3 (S3), previous model of balloon-expandable valve, the leaflets are modified to anti-calcification tissue and the outer skirt becomes 40% higher with textured polyethylene terephthalate. However, it is unknown how these structural changes affect echocardiographic and serum parameters after TAVR. Purpose To compare impacts of these design changes on relevant echocardiographic and serum parameters between S3UR and S3 in the short term. Methods Patients with severe aortic valve stenosis who underwent TAVR with S3 or S3UR were included in this study. Echocardiographic parameters and blood samples were retrospectively collected at discharge and at 1 month post-procedure. Echocardiographic outcomes included mean pressure gradient (PG), effective orifice area index (EOAi), and paravalvular leak (PVL) grade. Hemolytic anemia indicators, specifically lactate dehydrogenase (LDH) and hemoglobin (Hb), were also assessed. Findings suggestive of hemolytic anemia at 1 month were defined as "an increase in LDH level of ≧200 IU/L as well as a decrease in Hb level of ≧1.0 g/dL from pre-procedure." Results Among 443 patients (S3: April 2020-March 2023, S3UR: April 2023-December 2023), 339 patients (S3: n=270, S3UR: n=69) were available for this study. The mean PG was significantly lower in the S3UR group compared to the S3 group at discharge and at 1 month (Figure 1A). On the other hand, the EOAi was similar between the two groups at discharge and at 1 month (Figure 1B). Although the prevalence of none/trace PVL was significantly higher in the S3UR group at discharge, this difference disappeared at 1 month (Figure 1C). LDH levels were significantly increased from pre-procedure to 1 month in both groups (Figure 2A). The median of ΔLDH (1 month – pre-procedure) and %change of LDH (ΔLDH/ pre-procedure) were significantly higher in the S3UR group. The prevalence of hemolytic anemia at 1 month was also significantly higher in this group (Figure 2B). Conclusion At 1 month, S3UR demonstrated superiority in mean PG but equivalence in EOAi and PVL grade compared with S3. Although both S3UR and S3 showed significant increase in LDH from pre-procedure to 1 month, hemolytic anemia was experienced more frequently in S3UR cases. Further evaluation will be needed to assess the potential clinical impacts of these differences.

One-pot Hydrogenolysis of Polyethylene Terephthalate (PET) to p-xylene over CuZn/Al2O3Catalyst.

Chemical upcycling of plastic wastes into valuable chemicals is a promising strategy for resolving plastic pollution, but economically viable methods currently are still lacking. Here, we report one-pot hydrogenolysis of PET plastic into p-xylene with an excellent yield (99.8 %) over a robust non-precious Cu-based catalyst, CuZn/Al2O3, in the absence of alcohol solvents. The presence of Zn species promotes the dispersion of Cu0 and increases the ratio of Cu+/Cu0, whereas the synergistic effect of Cu0 and Cu+ leads to a superior performance in the conversion of PET. The combination of GC-MS, 13C CP MAS NMR, 2D 1H-13C CP HETCOR NMR spectroscopy and kinetic studies for the first time demonstrates 4-methyl benzyl alcohol as an important reaction intermediate in the hydrogenolysis of PET. Mechanistic studies indicate that the conversion of PET mainly follows a hydrogenolysis process, involving the cleavage of ester bonds to alcohols and the C-O bond cleavage of alcohols to alkanes. This work not only brings new insight for understanding the upgrading pathway of PET, but also provides a guidance for the design of high-performance non-precious catalysts for the chemical upcycling of plastic wastes.

Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.

A growing number of hydrolase enzymes show promiscuous acyltransferase activity, even under aqueous conditions. Here we report, for the first time, the ability of Pyrobaculum calidifontis VA1 esterase (PestE) to catalyse the formation of a wide range of amides in buffer, where the acyl donor forms a significant structural component in the amide product. The reactions occur under mild conditions and can achieve conversions up to 97% in 6 h for formation of N-benzylfuranamide as the model reaction. We demonstrate PestE's potential in enzyme cascades to make amides from waste PET plastic and the conversion of the terephthalic acid product to tamibarotene, a drug with activity against acute leukemia. Rational mutagenesis led to identification of PestE variants F33L_F289A and F33L. F33L_F289A increased conversion of N-benzylfuranamide by 1.2-fold, and F33L gave a 4-fold increase in conversion to tamibarotene.

Development of the esterase PestE for amide bond synthesis under aqueous conditions: Enzyme cascades for converting waste PET into tamibarotene.

A growing number of hydrolase enzymes show promiscuous acyltransferase activity, even under aqueous conditions. Here we report, for the first time, the ability of Pyrobaculum calidifontis VA1 esterase (PestE) to catalyse the formation of a wide range of amides in buffer, where the acyl donor forms a significant structural component in the amide product. The reactions occur under mild conditions and can achieve conversions up to 97% in 6 h for formation of N‐benzylfuranamide as the model reaction. We demonstrate PestE’s potential in enzyme cascades to make amides from waste PET plastic and the conversion of the terephthalic acid product to tamibarotene, a drug with activity against acute leukemia. Rational mutagenesis led to identification of PestE variants F33L_F289A and F33L. F33L_F289A increased conversion of N‐benzylfuranamide by 1.2‐fold, and F33L gave a 4‐fold increase in conversion to tamibarotene.

Effect of rPET Content and Preform Heating/Cooling Conditions in the Stretch Blow Molding Process on Microcavitation and Solid-State Post-Condensation of vPET-rPET Blend: Part I—Research Methodology and Results

Polyethylene terephthalate (PET) is widely used in bottle production due to its cost-effectiveness and low environmental impact. The first part of this article describes the research and statistical analysis methodology of the influence of the virgin PET (vPET) and recycled PET (rPET) content in the vPET-rPET blend, as well as the preform heating/cooling conditions in the stretch blow molding (SBM) process on the microscopic bottle properties. Microscopic properties such as crystallinity, density, viscosity, relaxation degree of the amorphous phase, and microcavitation in PET were examined. This study reveals that microcavity and solid-state post-condensation effects occur during PET deformation in the SBM process. The increase in free volume, indicating microcavitation, was confirmed by measuring positron annihilation lifetime spectroscopy (PALS). PALS and density of the amorphous phase studies prove a reduction in the dimensions of the free volumes, with a simultaneous significant increase in their number and ellipsoidization. It can be associated with crystallite rotation in a temperature-dependent non-crystalline matrix. The occurrence of solid-state post-condensation effects was confirmed by measuring the intrinsic viscosity. The conclusions resulting from the analysis of the microstructure affecting the mechanical strength of the material were validated by pressure resistance tests of the bottles.