Polyethylene Terephthalate Research Articles

Flexible substrate based wideband polarization converter with extremely high polarization conversion ratio

In this article an anticipated reflection-mode cross-polarization converters (CPCs) are designed on a polydimethylsiloxane (PDMS) based flexible substrate operating in the GHz region. The proposed CPC metasurface comprises three layers where a flexible substrate is endwise between the resonating layer and ground layers. The converter can convert linear to circular and circular to cross-polarized waves at the frequency range of 5–8 GHz, as evidenced by the identical amplitude of Rxx and Ryx and a phase difference of 90°. More than 99 % of the polarization conversion ratio (PCR) was performed between the 6.75 and 9.07 GHz frequency range, while more than 80 % of the PCR was performed between the 6.0 and 10.73 GHz frequency range. The highest PCR values show nearly flawless energy conversion from an x-polarized incident wave to a y-polarized reflected wave. The PCR ratio of 80 % is achieved by this ultra-wideband linear-to-cross- and circular-to-cross-polarization converter. The anticipated converter's spectrum for all incidence angles between 0◦ and 60°. The PCR remained higher than 99 % over a wide incidence angle range to 60° without much performance degradation. The bending stability of the PDMS-based flexible substrate is also investigated up to 60°. The structure is fabricated on a flexible substrate, and the measured performance is compared with simulated results. Radar, antenna, and communications systems, as well as other cross-polarization converters, can utilize the transmitted wave's very high polarization purity result.

Porous biochar supported PET plastic waste MOF heterostructure as a novel, efficient and recyclable catalyst for acetaminophen degradation

Herein, the innovative hybrid photocatalyst PET-based Zn-MOF on orange peel biochar (BC)(PZM/BC) was designed and synthesized via the hydrothermal method. Electrochemical methods have been used to demonstrate the action of the PET-MOF in the PZM/BC photocatalyst as a medium for electron transfer. The latter involved the synthesis of a zinc-containing metal–organic framework (MOF) in which the linkers were derived from the depolymerization of polyethylene terephthalate (PET) originating from plastic wastes. According to research, the catalytic reactions are sped up when porous BC and linker PET are assimilated into PZM/BC photocatalyst hetero-junction. Furthermore, BC stored electrons under light and released these electrons under dark conditions. When BC was combined with PET-MOF, the electrons on the biochar activated the catalytic redox activity of acetaminophen. Additionally, it lowers the reassimilation rate due to the combined meshed nanostructures and functionality of PET-MOF and PZM/BC. UV–Vis DRS, Mott-Schottky, Photoluminescence(PL), and Electrochemical Impedance spectra(EIS) results showed that the PZM/BC exhibited efficient spatial separation and transportation of photogenerated charge carriers and exhibited superior photocatalytic ability. Electron spin resonance(ESR) analysis confirmed that ⋅OH and h+ were the predominant radical species responsible for the degradation of acetaminophen(ACT). The optimum conditions for ACT removal were observed at pH 6.07, with a PZM/BC dosage of 0.1 g L−1, and an initial ACT concentration of 50 mg L−1, highlighting the pivotal role of the PZM/BC system in ACT degradation. Furthermore, potential photocatalytic degradation pathways of ACT were inferred renders on the identified intermediates which are responsible for the degradation of refractory intermediates. Regeneration trials were carried out to assess the stability of the photocatalyst. Additionally, the degraded intermediates generated during the degradation processes were examined, providing a comprehensive elucidation of the degradation mechanism.Graphical

Fungal microbiota of biodamages of various polymeric materials.

Data on microbial fouling of various synthetic polymer materials, including those used in space technology, are summarized. It has been established that the dominant groups of microbiota of polymer fouling are the genera of mitosporous fungi Aspergillus, Penicillium, Alternaria, Trichoderma. The enzymatic properties of fungal strains from the collection of microbial cultures of the Microbial Depository Center of the National Academy of Sciences of Armenia were studied. It has been shown that Aspergillus fumigatus, Penicillium chrysogenum, P. steckii, Juxtiphoma eupyrena and a number of other fungi have biofouling activity towards polyethylene, polyethylene terephthalate and some other synthetic polymers. New fungal kits have been developed and proposed to evaluate the fungal resistance of polymeric materials. They include fungi isolated from bio-damaged polymers used in space technology and contain 2 to 5 fungal strains instead of 7 to 9 strains in previously used kits. Taking into account the obtained data, a comparative assessment of the fungal resistance of samples of synthetic polymeric materials of various classes that passed accelerated climatic tests has been carried out. It has been established that the kits of biodegradant fungi, composed of cultures of bio-damaged space technology, generally exceeded the activity of the previously used kits, based on which one can judge the obvious advantages of strains isolated from bio-damaged space technology. In the future, these kits could find application not only for biodegradation of polymers, but also for testing the biostability of various polymers, to use for the construction of aviation and space techniques. Moreover, new optimized kits may be developed based on the strains involved in this study.

ATR-FTIR characterisation of daily-use plastics mycodegradation

Synthetic polymers, such as plastics, have permeated all aspects of modern life, and nowadays plastic pollution is a major environmental problem. Mycodegradation of these polymers could represent part of the solution to this problem since it calls on a broad toolbox of enzymes and applies non-enzymatic mechanisms to degrade and deteriorate recalcitrant materials. However, not enough is known about this ability for most of the representatives of the fungal kingdom. Another bottleneck is the harmonisation of technologies to analyse plastic degradation. This work involved the design of a biodegradation experiment, where the potential of four fungi representative of Dikarya and Penicillia (Funalia floccosa, Trametes versicolor, Pycnoporus cinnabarinus and Penicillium oxalicum) were tested on their ability to deteriorate the six most used plastics based on gravimetry and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). The following correlation between changes in the band signals and the loss of mass after treatment was determined using polyethylene terephthalate, polypropylene, polyethylene, poly vinyl chloride, high density polyethylene, low density polyethylene and nylon. After treatment, the decrease in absorbance of the characteristic bands of the plastics was taken as an indication of the degradation of the corresponding bonds/functionalities. The four fungi used could transform CH, CH2, CH3, CO, CO, CN, NH and CCl bonds. The best result was obtained using the fungus F. floccosa with 90-day treatments for high density polyethylene (∼ 62.0 %), low density polyethylene (∼ 23.6 %) and nylon (∼ 35.6 %). Therefore, mycodegradation could open up new doors in the fight against plastic pollution.

Unscrambling why plastics aren’t detectable in chicken eggs

Several food groups have been reported to contain varying concentrations of plastics. This study was designed to quantitatively investigate for the first time in Australia the presence of plastics in store-bought chicken eggs. Three commonly consumed brands of free-range, free-range organic, barn-laid and backyard (home-laid) chicken egg samples were analyzed for seven common polymers (i.e., polypropylene, polyethylene, polyvinyl chloride, polyethylene terephthalate, polystyrene, poly-(methylmethacrylate) and polycarbonate)). Samples were extracted by enzyme digestion and pressurized liquid extraction, followed by quantitative analysis through double-shot microfurnace pyrolysis coupled to gas chromatography-mass spectrometry. No plastics were detected at concentrations >limit of detection (LOD) (from 0.04 μg/g for PS to 0.22 μg/g for PVC) in the egg samples analyzed, regardless of brand and category, suggesting limited exposure of Australians to plastics from consuming eggs This study provides valuable baseline data and underscores the importance of continued monitoring to ensure the safety and integrity of food supplies in the face of rising environmental plastic pollution.

A low-profile dual-band millimeter wave patch antenna for high-speed wearable and biomedical applications

This paper presents a low-profile, dual-band patch antenna designed for the mmWave frequency range. The antenna, fed by a microstrip line, is fabricated on a thin, flexible substrate (Rogers 3003) with dimensions of 12 × 3 × 0.25 mm³. The radiating patch includes two circular slots, enabling dual-band operation at 28 GHz and 38 GHz. Key performance metrics, including realized gain, efficiency, and radiation patterns, are analyzed across these frequency bands, with measured results compared to simulations performed using CST Microwave Studio. Furthermore, the antenna's parameters are evaluated in a bent configuration, demonstrating its suitability for wearable applications. The study also assesses the antenna's impact on human tissues, calculating average SAR values of 0.914 W/Kg and 1.140 W/Kg at 28 GHz, and 0.720 W/Kg and 1.360 W/Kg at 38 GHz, for 1/10 gm tissue. Furthermore, the link margin is calculated to verify effective wireless communication over distances up to 80 m. This antenna effectively covers key millimeter-wave frequency bands, making it ideal for high-speed 5 G and biomedical applications.

Self-Assembly Hybrid Manufacture of Nanoarrays for Metasurfaces.

The development of metasurfaces necessitates the rapid fabrication of nanoarrays on diverse substrates at large scales, the preparation of patterned nanoarrays on both planar and curved surfaces, and even the creation of nanoarrays on prefabricated structures to form multiscale metastructures. However, conventional fabrication methods fall short of these rigorous requirements. In this work, a novel self-assembly hybrid manufacturing (SAHM) method is introduced for the rapid and scalable fabrication of shape-controllable nanoarrays on various rigid and flexible substrates. This method can be easily integrated with other fabrication techniques, such as lithography and screen printing, to produce patterned nanoarrays on both planar and non-developable surfaces. Utilizing the SAHM method, nanoarrays are fabricated on prefabricated micropillars to create multiscale pillar-nanoarray metastructures. Measurements indicate that these multiscale metastructures can manipulate electromagnetic waves across a range of wavelengths. Therefore, the SAHM method demonstrates the potential of multiscale structures as a new paradigm for the design and fabrication of metasurfaces.

Upconversion Phosphor-Driven Photodegradation of Plastics.

Plastic waste poses a profound threat to ecosystems and human health, necessitating novel strategies for effective degradation in nature. Here, we present a novel approach utilizing upconversion phosphors as additives to significantly accelerate plastic photodegradation in nature via enhancing ultraviolet (UV) radiation. Pr-doped Li2CaGeO4 (LCGO:Pr) upconversion phosphors readily converting blue light into deep-UV radiation, dramatically improve photodegradation rates for polyethylene (PE) and polyethylene terephthalate (PET) microplastics. In situ spectroscopic studies show that upconversion fluorescence initiates the photophysical cleavage of C-C and C-O bonds in the backbones of PE and PET, resulting in plastic degradation. Moreover, incorporating LCGO:Pr into polypropylene (PP) sheets realizes markedly enhanced photodamage, with the cracking area increasing by nearly 38-fold under simulated sunlight for 10 days. This underscores the potential of employing this approach for the construction of light-driven destructible polymers. Further optimization and exploration of material compatibility hold promise for developing sustainable photodegradable plastics.

Oriented artificial nanofibers and laser induced periodic surface structures as substrates for Schwann cells alignment

People with injuries to the peripheral nervous system suffer from paralysis of the facial muscles, fingers and hands or toes and feet, often for the rest of their lives, due to its poor functional regeneration. Therefore, to improve patients’ quality of life, there is an urgent need for conduits that effectively support the healing of large defects in nerve pathways through specific guidance of nerve cells. This paper describes two specific methods for achieving directed growth of Schwann cells, a type of glial cells that can support the regeneration of the nerve pathway by guiding the neuronal axons in the direction of their alignment. One method uses aligned polyamide-6 (PA-6) nanofibers produced via electrospinning on a very fast rotating structured collector, which enables easy nanofiber detachment, without additional effort. The other method implies the exposure of a poly(ethylene terephthalate) (PET) foil to a KrF* laser beam, that renders a nanorippled surface topography. Schwann cell growth on these substrates was inspected after one week of cultivation by means of scanning electron microscopy (SEM). For both methods we show that Schwann cells grow in a certain direction, predetermined by nanofiber and nanoripple orientation. In contrast, cells cultivated on randomly oriented nanofibers or unstructured surfaces, show an omnidirectional growth behavior. These two methods can be used to produce nerve conduits for the treatment of injuries to the peripheral nervous system.

Novel Bioreactor Design for Non-invasive Longitudinal Monitoring of Tissue-Engineered Heart Valves in 7T MRI and Ultrasound.

The development of cardiovascular implants is abundant, yet their clinical adoption remains a significant challenge in the treatment of valvular diseases. Tissue-engineered heart valves (TEHV) have emerged as a promising solution due to their remodeling capabilities, which have been extensively studied in recent years. However, ensuring reproducible production and clinical translation of TEHV requires robust longitudinal monitoring methods.Cardiovascular magnetic resonance imaging (MRI) is a non-invasive, radiation-free technique providing detailed valvular imaging and functional assessment. To facilitate this, we designed a state-of-the-art metal-free bioreactor enabling dynamic MRI and ultrasound imaging. Our compact bioreactor, tailored to fit a 72mm bore 7T MRI coil, features an integrated backflow design ensuring MRI compatibility. A pneumatic drive system operates the bioreactor, minimizing potential MRI interference. The bioreactor was digitally designed and constructed using polymethyl methacrylate, utilizing only polyether ether ketone screws for secure fastening. Our biohybrid TEHV incorporates a non-degradable polyethylene terephthalate textile scaffold with fibrin matrix hydrogel and human arterial smooth muscle cells.As a result, the bioreactor was successfully proven to be MRI compatible, with no blooming artifacts detected. The dynamic movement of the TEHVs was observed using gated MRI motion artifact compensation and ultrasound imaging techniques. In addition, the conditioning of TEHVs in the bioreactor enhanced ECM production. Immunohistology demonstrated abundant collagen, α-smooth muscle actin, and a monolayer of endothelial cells throughout the valve cusp. Our innovative methodology provides a physiologically relevant environment for TEHV conditioning and development, enabling accurate monitoring and assessment of functionality, thus accelerating clinical acceptance.

Sintering of Copper Nanoparticles using Intense Pulsed Light for screen-printed films on flexible substrate

Abstract Rapid growth in applications involving large area flexible electronics has led to wide adoption of the technique of sintering printed films using intense pulsed light (IPL) due to its pulse mode operation and ability to reach high sintering temperatures without affecting the underlying substrate significantly. We study sintering mechanisms of screen-printed thin films of copper nanoparticles on polyethylene terephthalate (PET) plastic substrate by varying irradiance energy over a wide range to monitor conductivity and associated microstructure changes. We obtain optimized parameters which indicate existence of a sharp threshold irradiance energy to kickstart sintering, and two distinct regimes beyond that. The low temperature regime has a high energy barrier while the high temperature regime has a substantially reduced energy barrier with change of phase due to local melting.

The emission and physicochemical properties of airborne microplastics and nanoplastics generated during the mechanical recycling of plastic via shredding

This study examined the emission and physicochemical properties of microplastics and nanoplastics (MPs/NPs) generated during shredding, which is regularly used in mechanical recycling. Waste and new polyethylene terephthalate, polypropylene, and high-density polyethylene were investigated herein for a total of six categories. The concentration and size distribution of particles were measured using two spectrometer instruments, and morphology and elemental composition of emitted particles were analyzed with microscopy and spectroscopy. This study found that number concentrations in both submicron and micron sizes of respirable particles were 3–2910× higher during periods of shredding than pre-shredding background concentrations. Maximum concentrations of particles within 10–420 nm, across all six categories, ranged from 22,000- to 1,300,000-particles/cm3 during shredding, compared to average background levels of 700 particles/cm3. Maximum concentrations of particles within 0.3 to 10 μm, across all six categories, ranged from 24- to 2000-particles/cm3 during shredding, compared to average background levels of 2 particles/cm3. Waste plastics consistently generated higher emissions than their new counterparts, which is attributed to the labels, adhesives, and increased additives incorporated into the waste plastic. Morphology varied drastically between particles and an elemental composition analysis found that the samples consisted primarily of C and O, representing the polymer material, as well as Na, Mg, Al, Si, Cu, Cl, K, Ca, Ti, Fe, Rb, and Br representing additives, label, and other contaminates. The shredding of plastic has the potential to expose workers to elevated concentrations of airborne MPs/NPs, especially those between 10 and 100 nm.

Structure and Energetics of PET-Hydrolyzing Enzyme Complexes: A Systematic Comparison from Molecular Dynamics Simulations.

Discovered in 2016, the enzyme PETase, secreted by bacterial Ideonella Sakaiensis 201-F6, has an excellent hydrolytic activity toward poly(ethylene terephthalate) (PET) at room temperature, while it decreases at higher temperatures due to the low thermostability. Many variants have been engineered to overcome this limitation, which hinders industrial application. In this work, we systematically compare PETase wild-type (WT) and four mutants (DuraPETase, ThermoPETase, FastPETase, and HotPETase) using standard molecular dynamics (MD) simulations and unbinding free energy calculations. In particular, we analyze the enzymes' structural characteristics and binding to a tetrameric PET chain (PET4) under two temperature conditions: T1─300 K and T2─350 K. Our results indicate that (i) PET4 forms stable complexes with the five enzymes at room temperature (∼300 K) and (ii) most of the interactions are localized close to the active site of the protein, where the W185 and Y87 residues interact with the aromatic rings of the substrate. Specifically, (iii) the W185 side-chain explores different conformations in each variant (a phenomenon known in the literature as "W185 wobbling"). This suggests that the binding pocket retains structural plasticity and flexibility among the variants, facilitating substrate recognition and localization events at moderate temperatures. Moreover, (iv) PET4 establishes aromatic interactions with the catalytic H237 residue, stabilizing the catalytic triad composed of residues S160-H237-D206, and helping the system achieve an effective configuration for the hydrolysis reaction. Conversely, (v) the binding affinity decreases at a higher temperature (∼350 K), retaining moderate interactions only for HotPETase. Finally, (vi) MD simulations of complexes formed with poly(ethylene-2,5-furan dicarboxylate) (PEF) show no persistent interactions, suggesting that these enzymes are not yet optimized for binding this alternative semiaromatic plastic polymer. Our study offers valuable insights into the structural stability of these enzymes and the molecular determinants driving PET binding onto their surfaces, sheds light on the mechanistic steps that precede the onset of hydrolysis, and provides a foundation for future enzyme optimization.

Structure and Properties of Thin Films Prepared on Flexible Substrates from SnCl4-Derived Solutions

Thin transparent films of SnO2 were obtained from aqueous–alcohol solutions of SnCl4 on a flexible polyethylene terephthalate (PET) substrate by spray pyrolysis at 100 °C. The influence of the addition of aqueous ammonia to the film-forming solution on the different properties has been studied. Properties studied include surface morphology, phase composition and transparency of the formed films and the crystallization processes and band gap of the film material. It was found that the addition of aqueous ammonia causes the formation of skeletal crystals (NH4)2[SnCl6] with a perovskite structure in the film structure. The resulting films are promising for use in the technology of manufacturing flexible solar cells.

Recycled PET Fibers with Dopamine Surface Modification for Enhanced Interlayer Adhesion in 3D Printed Concrete.

Three-dimensional printed concrete (3DPC) is increasingly recognized in the construction industry for its high design flexibility and the elimination of conventional formwork. However, weak interlayer adhesion remains a significant challenge. The potential of recycled polyethylene terephthalate (PET) fibers for reinforcing 3DPC is being explored, driven by their environmental sustainability and economic advantages. However, there is an inadequate interfacial adhesion between these recycled fibers and the 3DPC matrix. This study investigated the use of dopamine modification to address this issue and enhance the interlayer adhesion of fiber-reinforced 3DPC. Recycled PET fibers were surface-modified using dopamine treatment, forming a polydopamine (PDA) film that improved surface roughness and hydrophilicity. Both unmodified and modified fibers were incorporated into 3DPC at various volume fractions (0.1%, 0.3%, 0.5%). The effects on interlayer adhesion strength, compressive strength, and flexural strength were systematically evaluated and compared. The results showed that the inclusion of 0.3 vol% dopamine-modified fibers resulted in a 22.5% increase in interlayer adhesion strength compared to the control group, and a 14.8% improvement over unmodified fibers at the same content. Additionally, the compressive strength and flexural strength of 3DPC with 0.3 vol% MPET fibers increased by 22.5% and 27.6%, respectively, compared to the control group. Microstructural analysis using SEM and XRD revealed that the dopamine modification significantly improved the interfacial adhesion between fibers and the concrete matrix, explaining the superior performance of modified fibers. This study demonstrates that recycled PET fibers modified with dopamine can effectively enhance the interlayer adhesion of 3DPC. The findings affirm that surface modification techniques can significantly elevate the utility of recycled PET fibers in 3DPC, contributing to the sustainable advancement of construction materials.

Strain-Induced Tunable and Field-Free Spintronic THz Emitters Based on Flexible Substrate Heterostructures.

Spintronic THz emitters have been widely studied due to their advantages of broadband frequency, high efficiency, and easy fabrication. The spintronic THz signal is proportional to the magnetization of the ferromagnetic (FM) layer and requires an external magnetic field to maximize the THz signal intensity. Recently, a field-free emitter was designed based on a CoFeB/IrMn3 heterostructure via the exchange bias between two films. However, field-free spintronic THz emitters based on a common FM/nonmagnetic metal structure are rare. Here, we fabricate a tunable and field-free THz emitter with giant THz emission modulation ability based on a polyimide/CoFeB/Pt heterostructure. The THz emission can be modulated by changing the curvature radius of the polyimide substrate. After the emitter is forward bent, the THz radiation without an external magnetic field is stronger than in the flat state with a field, which we attribute to in-plane magnetic anisotropy on the FM layer induced by the tensile strain. When we curve the emitter backward, the THz intensity decreases sharply. Moreover, the modulation (ΔS/Smax) of the THz wave from the forward-curved and backward-curved emitter is over 95%, and the device shows good cyclic repeatability. We provide a novel way to design field-free spintronic THz sources, and flexible devices are promising for application in THz devices.

Decision-analytics-based PET plastic recycling selection - a hesitant fuzzy comprehensive ratio assessment model

Decision-analytics-based PET plastic recycling selection - a hesitant fuzzy comprehensive ratio assessment model

Overcoming barriers to proactive plastic recycling toward a sustainable future

The plastics sector, accounting for a significant portion of global emissions, presents a challenge and an opportunity in achieving carbon neutrality. Despite Japan's commendable polyethylene terephthalate (PET) bottle recycling rates, most plastics are thermally recycled, creating environmental issues. This study proposes an evaluation framework to enhance recycling, aligned with end-user preferences and fostering a circular plastics economy. Employing a mixed-methods approach, this study conducts fieldwork including interviews with plastic recyclers and analysis of industry data. A weighted sum multicriteria analysis integrating end-user preferences, recycling effectiveness, and market dynamics is utilized. Systemic, process, and policy challenges were shown to hinder sustainable recycling practices, while varying willingness to pay, emission and cost reduction potentials, among acceptability and sectoral diversity informed priority plastic types for recycling. Multicriteria analysis showed that although PET is favored by end users, Polyoxymethylene (POM) emerges as a potential priority target for manufacturers and recyclers. Sensitivity analysis underscores the potential impact of establishing or enhancing willingness to pay (WTP) toward certain plastic types. Moreover, manufacturer and recycler evaluations suggest a broader willingness to recycle plastics than previously assumed. The proposed evaluation framework offers insights toward plastic recycling strategies. Policy interventions such as sustained subsidies for recyclers, market incentives leveraging WTP preferences, and technological advances, including chemical recycling and the broadening of plastic type recycling in line with user and manufacturer preferences, could all contribute to promoting sustainable plastic recycling practices.

Microplastic Transport and Accumulation in Rural Waterbodies: Insights from a Small Catchment in East China.

Microplastic (MP) pollution in agricultural ecosystems is an emerging environmental concern, with limited knowledge of its transport and accumulation in rural waterbodies. This study investigates the distribution and sources of MP in drainage ditches influenced by pond connectivity, land use, and soil properties within a small catchment in Nanjing, East China. Sediment was collected from ditches in 18 sites across forest, agricultural, horticultural, and urban areas. Using laser-directed infrared spectroscopy (LDIR), 922 MP particles were identified. Six materials were dominant: fluororubber (FR), polyethylene terephthalate (PET), polyurethane (PU), acrylonitrile (ACR), chlorinated polyethylene (CPE), and polyethylene (PE). MP concentrations varied by land use and pond connectivity, with ditches above ponds exhibiting higher counts (1700 particles/kg) than those below (1050 particles/kg), indicating that ponds act as MP sinks. The analysis revealed site-specific MP sources, with FR linked to road runoff and PET associated with agricultural practices. Correlations between MP shape and soil properties showed that more compact and filled shapes were more commonly associated with coarser soils. PE particle size was negatively correlated with organic matter. This study highlights the need for targeted strategies to reduce MP pollution in rural landscapes, such as reducing plastic use, ditch maintenance, and improved road runoff management.

Evaluating microplastic emission from takeaway containers: A Micro-Raman approach across diverse exposure scenarios

Based on inconsistencies observed in literature regarding microplastic levels released by takeaway plastic containers, this study investigates the release from takeaway containers composed of polypropylene (PP), polystyrene (PS), and polyethylene terephthalate (PET). To simulate real-world conditions, experiments were conducted using Milli-Q water at room temperature, 100 °C, and at pH 4.5. Containers were subjected to 20-min exposure with agitation, and microplastics were quantified via optical microscopy, with micro-Raman spectroscopy to confirm the particle polymeric nature. The results indicate that PET and PS containers released microplastic in varying quantities: 9 and 1 at room temperature, 7 and 3 in acidified water, and 17 and 30 at 100 °C, respectively. The particle sizes ranged between 13 and 32 μm. Notably, no microplastics were detected from PP containers under any tested conditions. This study underscores the significant release of microplastics from PET and PS containers, particularly at elevated temperatures, suggesting that PP may represent a safer alternative.