Polymer Degradation Research Articles

Visible-Light-Induced Divergent Oxygenation of Methylbenzene Utilizing Aryl Halides.

The selective oxidation of methylbenzene to value-added products is of indisputable importance in organic synthesis. Although photocatalytic oxidation reactions of toluene have achieved great success for the preparation of its oxidative products, such as carboxylic acids, benzaldehyde, and benzoate, there remains a lack of a unified photocatalytic system for the selective preparation of these oxidation products. Herein, we report a metal- and additive-free photocatalytic protocol enabled by aryl halides using O2 as a green oxidant for the selective synthesis of the above-mentioned three oxidation products by adjusting the reaction solvent. This strategy features many advantages, including environmentally friendly and mild reaction conditions, broad substrate applicability and functional group tolerance, and potential practical application for the synthesis of aromatic carboxylic drugs and polymer materials and degradation of polystyrene waste. The continuous-flow system was utilized for the oxidation of toluene, which resulted in a reduced reaction time and increased production efficiency. Detailed mechanistic investigation revealed that the hydrogen atom transfer process was facilitated by the bromine radical from aryl halides for further oxidation, and an electron donor-acceptor complex of methylbenzene and aryl halides may exist.

Polymer Degradation via a Mechanochemical Gating Strategy

AbstractThe extensive use of plastics, valued for their lightweight, durability, and cost‐effectiveness, has led to severe environmental pollution, with 72% of plastic waste ending up in landfills or natural habitats. Traditional methods for plastic decomposition, including both mechanical and chemical approaches, often face challenges such as incomplete degradation and stability concerns. The innovative concept of mechanical gating presents a promising solution by incorporating mechanophores into polymer structures, enabling controlled degradation. Recent advancements have focused on utilizing mechanophores, such as cyclobutane, as "door locks" to regulate the degradation process. This perspective highlights recent progress in this field, demonstrating the potential of mechanophore‐based strategies for achieving on‐demand polymer degradation. It addresses the limitations of conventional recycling methods and explores how this approach can balance polymer stability with environmental degradability, paving the way for more sustainable plastic management solutions.Early Day Record

Understanding, Mimicking, and Mitigating Radiolytic Damage to Polymers in Liquid Phase Transmission Electron Microscopy.

Advances in liquid phase transmission electron microscopy (LP-TEM) have enabled the monitoring of polymer dynamics in solution at the nanoscale, but radiolytic damage during LP-TEM imaging limitsits routine use in polymer science. This study focuses on understanding, mimicking, and mitigating radiolytic damage observed in functional polymers in LP-TEM. It is quantitatively demonstrated how polymer damage occurs across all conceivable (LP-)TEM environments,and the key characteristics and differences between polymer degradation in water vapor and liquid water are elucidated. Importantly, it is shown that the hydroxyl radical-rich environment in LP-TEM can be approximated by UV light irradiation in the presence of hydrogen peroxide, allowing the use of bulk techniques to probe damage at the polymer chain level. Finally, the protective effects of commonly used hydroxyl radical scavengers are compared, revealing that the effectiveness of graphene's protection is distance-dependent. The work provides detailed methodological guidance and establishes a baseline for polymer degradation in LP-TEM, paving the way for future research on nanoscale tracking of shape transitions and drug encapsulation of polymer assemblies in solution.

On the Non-Catalytic Role of Lytic Polysaccharide Monooxygenases in Boosting the Action of PETases on PET Polymers.

Synthetic polymers are resistant to biological attack, resulting in their long-term accumulation in landfills and in natural aquatic and terrestrial habitats. Lytic polysaccharide monooxygenases (LPMOs) are enzymes which oxidatively cleave the polysaccharide chains in recalcitrant polysaccharides such as cellulose. It has been widely hypothesised that LPMOs could be used to aid in the enzymatic breakdown of synthetic polymers. Herein, through the use of biochemical assays, X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) we show that LPMOs can bind to polyethylene terephthalate (PET), and - in doing so - the hydrophobic surface of PET becomes more hydrophilic such that product release is boosted by subsequent treatment with classical PETases. The boosting effect is however, only observed in reactions when the LPMO and the PETase are added sequentially rather than simultaneously to the PET. Moreover, the same boosting effect is also seen when a catalytically-inactive mutant of LPMO is used, showing that the principal means by which AA9 LPMOs boost the degradation of synthetic polymers is through their role as a "hydrophobin" rather than as an oxygenase. Indeed, in accord with this role of LPMOs, we further show that this effect can be extended to other ostensibly 'non-catalytic' proteins beyond LPMOs, such as bovine serum albumin and lactate dehydrogenase.

Unveiling the Potential of Ultraviolet Fluorescence Imaging as a Versatile Inspection Tool: Insights from Extensive Photovoltaic Module Inspections in Multi‐MWp Photovoltaic Power Stations

UV fluorescence imaging (UVF) has the potential to grow into a powerful, informative, and economically attractive inspection method for photovoltaic (PV) power stations. UVF demonstrates the ability to indicate differences in polymer types and degradation states in backsheets and encapsulation materials of PV modules. The data acquisition rate of UVF measurements is 10 to 15 times higher than that achieved by state‐of‐the‐art near‐infrared spectroscopy, enabling the mapping of the bill of materials (BoMs) and degradation state for every module in large PV arrays. Combinations of UVF with vibrational spectroscopies allow the polymer BoMs to be recognized and correlated with aging phenomena such as metal corrosion or potential induced degradation. UVF imaging can also be used for conventional visualization of nonmaterial‐related anomalies, such as hot cells or cell cracks. The low purchase cost of the equipment makes UVF an affordable and high‐throughput diagnostic method yielding comprehensive information that would otherwise only be accessible by combining several slower and more laborious methods. Automated UVF image analysis and refinements of correlations between different BoMs and UVF pattern geometry can further unlock the potential of UVF as a straightforward tool accessible to all stakeholders and promote proactive strategies for the optimization of the reliability and performance of PV power stations.

Laser-Induced Decomposition and Mechanical Degradation of Carbon Fiber-Reinforced Polymer Subjected to a High-Energy Laser with Continuous Wave Power up to 120 kW

Carbon fiber-reinforced polymer (CFRP), noted for its outstanding properties including high specific strength and superior fatigue resistance, is increasingly employed in aerospace and other demanding applications. This study investigates the interactions between CFRP composites and high-energy lasers (HEL), with continuous wave laser powers reaching up to 120 kW. A novel automated sample exchange system, operated by a robotic arm, minimizes human exposure while enabling a sequence of targeted laser tests. High-speed imaging captures the rapid expansion of a plume consisting of hot gases and dust particles during the experiment. The research significantly advances empirical models by systematically examining the relationship between laser power, perforation times, and ablation rates. It demonstrates scalable predictions for the effects of high-energy laser radiation. A detailed examination of the damaged samples, both visually and via micro-focused computed X-ray tomography, offers insights into heat distribution and ablation dynamics, highlighting the anisotropic thermal properties of CFRP. Compression after impact (CAI) tests further assess the residual strength of the irradiated samples, enhancing the understanding of CFRP’s structural integrity post-irradiation. Collectively, these tests improve the knowledge of the thermal and mechanical behavior of CFRP under extreme irradiation conditions. The findings not only contribute to predictive modeling of CFRP’s response to laser irradiation but enhance the scalability of these models to higher laser powers, providing robust tools for predicting material behavior in high-performance settings.

Unclicking the Click: A Depolymerizable Clicked Polymer via Two Consecutive Single-Crystal-to-Single-Crystal Reactions.

We report here a clicked polymer that can be depolymerized by a declicking reaction. A designed dipeptide monomer, upon heating its crystals, underwent a single-crystal-to-single-crystal topochemical ene-azide cycloaddition polymerization to form a triazoline-linked polymer, which upon further heating, underwent a remarkable SCSC denitrogenation, resulting in an imine-linked polymer quantitatively. As both the TEAC polymerization and the denitrogenation occurred in SCSC fashion, the structures of the triazoline-linked polymer and the imine-linked polymer could be determined at atomic resolution by SCXRD. Acid hydrolysis of the imine-linked polymer leads to quantitative depolymerization, yielding a dipeptide, showcasing the degradability and depolymerizability of such polymers. This solid-state click polymerization and denitrogenation yielding depolymerizable polymer is attractive over the usual click polymers that cannot be unclicked.

Unclicking the Click: A Depolymerizable Clicked Polymer via Two Consecutive Single‐Crystal‐to‐Single‐Crystal Reactions

AbstractWe report here a clicked polymer that can be depolymerized by a declicking reaction. A designed dipeptide monomer, upon heating its crystals, underwent a single‐crystal‐to‐single‐crystal topochemical ene‐azide cycloaddition polymerization to form a triazoline‐linked polymer, which upon further heating, underwent a remarkable SCSC denitrogenation, resulting in an imine‐linked polymer quantitatively. As both the TEAC polymerization and the denitrogenation occurred in SCSC fashion, the structures of the triazoline‐linked polymer and the imine‐linked polymer could be determined at atomic resolution by SCXRD. Acid hydrolysis of the imine‐linked polymer leads to quantitative depolymerization, yielding a dipeptide, showcasing the degradability and depolymerizability of such polymers. This solid‐state click polymerization and denitrogenation yielding depolymerizable polymer is attractive over the usual click polymers that cannot be unclicked.

HRMAS NMR for Studying Solvent-Induced Mobility of Polymer Chains and Metallocene Migration Into Low-Density Polyethylene (LDPE).

HRMAS (high-resolution magic angle spinning) nuclear magnetic resonance (NMR) spectroscopy of low-density polyethylene (LDPE) affords 1H and 13C NMR spectra with superior resolution. For acquiring HRMAS NMR spectra, the polymer is first swollen with representative organic solvents. Then, the samples are measured with a conventional solid-state NMR spectrometer in the wideline mode or at the low spinning speed of 2 kHz. Anisotropic interactions like CSA (chemical shift anisotropy) and dipolar interactions are reduced due to the additional mobility of the polymer chains in the presence of the solvent within the polymer network. The combined effect of this mobility and MAS leads to signals with substantially reduced halfwidths as compared to classic MAS of the dry polymer. With HRMAS, all signals of the polymer become visible, and the spectra can be used for a quick and easy assessment of the polymer swelling behavior in diverse solvents. Being able to characterize polymers on the molecular level, and identifying the solvents that penetrate the polymer network best, enables the study of post-synthesis modifications of the polymers. It is demonstrated by paramagnetic HRMAS that the metallocene nickelocene (Cp2Ni) penetrates the LDPE network along with the solvent and is homogeneously dispersed in the polymer. SEM images prove that the structure of the polymer is not altered by the presence of a solvent and Cp2Ni. The impact of the paramagnetic Cp2Ni on the 1H signal halfwidth and T1 time of LDPE is studied. HRMAS allows a quick assessment of metal complexes regarding their ability to penetrate the LDPE network and therefore supports future studies of catalytic polymer degradation.

Antioxidation and rheological modification of polylactide by gallic acid at chain end and stereocomplex formation

Abstract This study offers a novel approach that enables both functionalization of degradable polymers and modification of polymer properties during processing and use. By utilizing degradable polylactide, it was copolymerized with polyethylene glycol with the aim to facilitate processing and blending by heating. Moreover, L,L- and D,D-lactide were employed for the possible stereocomplexation, with the aim to enhance physical properties during use after processing. Additionally, the gallic acid was introduced at both chainends, which exhibits antioxidant properties as functionalization.

Metaproteomics identifies key cell wall degrading enzymes and proteins potentially related to inter-field variability in fiber quality during flax dew retting

In this study, metaproteomics and biochemical analyses were used to identify for the first time specific proteins and associated micro-organisms responsible for cell wall degrading enzyme activity during dew retting of flax in two adjacent fields in northern France. This approach identified 6032 non-redundant proteins present at 4 key retting stages (R0/day 1, R2/day 6, R4/day 13, and R7/day 25), of which 75 contained CAZy (Carbohydrate Active Enzyme) motifs belonging to 31 different families from all 5 CAZy classes. 19 families were putatively related to the degradation of different plant cell wall polymers including lignin (AA1), pectins (CE13, CE8, PL1, PL3, GH28, GH35), hemicellulose (GH2, GH10, GH26, GH35, GH55, GH3, GH5, GH17) and cellulose (GH5, GH7, GH3, GH94, AA3). Taxonomy of identified proteins indicated that 85 % come from bacteria, 13 % from fungi, and 2 % from plants; however, ∼60 % of CAZymes involved in the degradation of plant wall polymers are of fungal origin. Although 88 % of total proteins and almost 65 % of cell wall degrading CAZymes were similar between the two investigated fields, certain differences in the abundance and dynamics of certain CAZymes might be related to observed inter-field variability in cell wall degrading enzyme activities, stem/fiber yield and industrial qualities of fibers harvested from the two fields. Overall, these results highlight the interest of using metaproteomics for improving our biological understanding of how retting impacts fiber quality. In addition, the identification of several new bacterial and fungal species in this study demonstrates that such an approach is also extremely powerful for generating novel taxonomic data.

Measurement of Acrylamido Tertiary Butyl Sulfonate Polymer Retention on Limestone by Three Methods Under Varying Temperature and Oil Presence

Summary Polymer retention poses a significant challenge in polymer flooding applications, emphasizing the importance of accurately determining retention levels for successful project design. In carbonate reservoirs of the Middle East, where temperatures exceed 90°C, conducting adsorption tests under similar temperature conditions becomes crucial for the precise determination of adsorption values. The choice of analytical method potentially impacts the accuracy of retention measurements from effluent analysis. This study investigates the effect of temperature on the performance of a polymer, specifically its rheological behavior and retention. Rheological and polymer flooding experiments were carried out using an acrylamido tertiary butyl sulfonate (ATBS)-based polymer in formation water (167,114 ppm) at different temperatures (25°C, 60°C, and 90°C) with required oxygen control measures. Dynamic polymer retention was conducted in both the absence of oil (single-phase tests) and the presence of oil (two-phase tests). In addition, different analytical techniques were evaluated, including viscosity measurements, ultraviolet (UV)-visible spectroscopy, and total organic carbon-total nitrogen (TOC-TN) analysis, to determine the most accurate method for measuring the polymer concentration with the least associated uncertainty. Furthermore, the study investigates the effects of these uncertainties on the final dynamic polymer retention values by applying the propagation of error theory. The effluent polymer concentration was determined using viscosity correlation, UV spectrometry, and TOC-TN analysis, all of which were reliable methods with coefficient of determination (R2) values of ~0.99. The study analyzed the effects of flow through porous media and backpressure regulator on polymer degradation. The results showed that the degradation rates were around 2% for flow through porous media and 16% for mechanical degradation due to the backpressure regulator for all temperature conditions. For the effluent sample, the concentration of polymer was lower when using the viscosity method due to polymer degradation. However, the TOC-TN and UV methods were unaffected as they measured the TN and absorbance at a specific wavelength, respectively. Therefore, all viscosity results were corrected for polymer degradation effects in all tests. During the two-phase coreflooding experiment conducted at 25°C, the accuracy of the UV spectrometry and viscosity measurements was affected by the presence of oil, rendering these methods unsuitable. However, the TOC-TN measurements were able to determine effluent polymer concentration and, subsequently, the retention value. Moreover, the use of glycerin preflush to inhibit oil production during polymer injection in the two-phase studies showed that all three methods were appropriate. The error range was obtained using the propagation of error theory for all the methods. Accordingly, it was noted that the temperature did not affect the dynamic retention values in both single-phase and two-phase conditions. The findings of this study highlight that when adequate oxygen control measures are implemented, the temperature does not exhibit a statistically significant impact on the retention of the ATBS-based polymer under investigation. Furthermore, TOC-TN has been identified as the optimal analytical method due to its minimal uncertainties and ease of measuring polymer concentration under varying experimental conditions.

A novel “reinforcing-foaming-recovering” strategy for achieving thermally insulating green foams with ultrafast degradation

Lightweight porous materials have garnered increasing attention in application domains of intelligent construction and flexible thermal insulation, owing to their customizable 3D porous structures and outstanding performances. Nonetheless, the severe environmental pollution resulting from the accumulation of non-degradable plastic waste in the ecosystem has sparked significant interest in developing bio-degradable thermal insulation foams. The preparation of biodegradable foam, however, typically requires operating specialized equipment for long periods under extreme conditions, which diminishes its environmental friendliness as claimed. Herein, we present a pioneering "Reinforcing-Foaming-Recovering" strategy to achieve ultralight and recyclable green foams with excellent thermal insulation properties. This innovative strategy, involving materials reinforcing and low-pressure foaming complemented by nitrogen-assisted gas recovering enables the preparation of low-density (0.08 g/cm3) biodegradable foams with restricted shrinkage ratio (<5%). Thanks to the easy-to-control foaming method, combined with the improved 3D network cellular structures caused by nitrogen-assisted gas exchange, the achieved green foams exhibit favorable thermal insulation (39.8 mW/m·K) and superior biodegradation efficiency (11.5%/2 months). The approach of energy-efficient nitrogen-assisted low-pressure foaming of degradable polymers offers a promising and practical solution for producing eco-friendly and multifunctional porous materials with economic advantages.

Structuring of particle-associated bacterial communities along the extracellular polymeric substance gradient of sinking and suspended particles in an oligotrophic, subtropical region of the western North Pacific Ocean

Extracellular polymeric substances, such as transparent exopolymer particles (TEP) composed of acidic polysaccharides, are important particulate organic carbon (POC) components of marine environments that affect particle dynamics and ocean carbon export. However, how polymeric substances interact with and shape bacterial communities associated with marine particles is poorly understood. This study investigated whether the composition of particle-associated bacterial communities differs between sinking and suspended particles, which differ in their polymeric substance contents, in the upper water column of the subtropical, oligotrophic Kuroshio region. Bacterial taxa likely involved in polymer degradation (Alphaproteobacteria, Gammaproteobacteria, and Bacteroidia) were enriched on sinking particles with a lower TEP: POC ratio, indicating that bacterial degradation of polymeric substances promotes particle sinking by removing positively buoyant polymers. By contrast, suspended particles were increasingly enriched for Bdellovibrionota and Desulfobacterota as the TEP: POC ratio increased. These taxa, which include predatory microbes, seem to prefer polymer-rich environments with a high density of potential prey. Planctomycetota were not significantly related to the TEP: POC ratio, indicating their broad niche breadth on particles’ polymeric substance contents. The results suggest that the bacterial niche differentiation associated with the particle polymeric-substance gradient shapes bacterial communities in a subtropical ocean.

Anodic Commodity Polymer Recycling: The Merger of Iron-Electrocatalysis with Scalable Hydrogen Evolution Reaction.

Plastics are omnipresent in our everyday life, and accumulation of post-consumer plastic waste in our environment represents a major societal challenge. Hence, methods for plastic waste recycling are in high demand for a future circular economy. Specifically, the degradation of post-consumer polymers towards value-added small molecules constitutes a sustainable strategy for a carbon circular economy. Despite of recent advances, chemical polymer degradation continues to be largely limited to chemical redox agents or low energy efficiency in photochemical processes. We herein report a powerful iron-catalyzed degradation of high molecular weight polystyrenes through electrochemistry to efficiently deliver monomeric benzoyl products. The robustness of the ferraelectrocatalysis was mirrored by the degradation of various real-life post-consumer plastics, also on gram scale. The cathodic half reaction was largely represented by the hydrogen evolution reaction (HER). The scalable electro-polymer degradation could be solely fueled by solar energy through a commercially available solar panel, indicating an outstanding potential for a decentralized green hydrogen economy.

Associative analysis of sludge microbiota and wastewater degradation efficacy within swine farm sludge systems

Industrial wastewater management is a significant global challenge. Sludge microbiota from swine farms may play a crucial role in enhancing wastewater treatment processes, thereby reducing water pollution from industrial activities. A deeper understanding of this complex community could lead to innovative approaches for improving wastewater treatment methods. Sludge samples were collected from the anaerobic, sedimentation, and thickening tanks of ten swine farms. The microbiota communities were analyzed using 16S rRNA full-length sequencing on the PacBio platform, with subsequent data analysis conducted on the QIIME2 platform utilizing the SILVA database. Compared to anaerobic and thickening tanks, the sedimentation tanks exhibited a unique profile of sludge microbiota, with higher abundances of the phyla Proteobacteria, Bacteroidota, and Caldatribacteriota. Additionally, sludges from farms already utilized in processing industrial water—specifically farms B, G, and J—contained higher concentrations of bacteria (>20 ng/μL), indicating the robustness of the bacterial load for practical industrial use. Furthermore, sludge from farms with higher alpha diversity, such as E, G, I, and J, exhibited enriched degradation profiles, including the degradation of aromatic compounds, polymers, industrial compounds, toluene, and vanillin. The farms were categorized based on wastewater ammonia nitrogen degradation levels, revealing a clustering effect of the microbiota from the sedimentation tanks in the Principal Coordinates Analysis (PCoA) plot. A higher relative abundance of the families Rhodocyclaceae, AKYH767, and Comamonadaceae, and a lower abundance of the families Anaerolineaceae and Christensenellaceae, were found in groups with high ammonia nitrogen reduction, suggesting potential targets for bioaugmentation strategies. In conclusion, this study underscores the critical role of microbial abundance, composition, and biodiversity in optimizing wastewater treatment and advocates for comprehensive microbiota analysis to identify suitable sludge for industrial applications.

Mechanical Properties of 3D Printed PLA Scaffolds for Bone Regeneration

Abstract The growing interest in biodegradable scaffolds for bone regeneration created a need to investigate new materials suitable for scaffold formation. Poly(lactic acid) (PLA) is a polymer commonly used in biomedical engineering, e.g. in tissue engineering as a biodegradable material. However, the mechanical behavior of PLA along its degradation time is still not explored well. For this reason, the mechanical properties of PLA scaffolds affected by incubation in physiological medium needs to be investigated to show the potential of PLA to be used as a material for biodegradable scaffold formation. The purpose of this research is to determine the mechanical properties of PLA scaffolds before and after incubation, and to apply constitutive material models for further behavior prediction. Two sets of PLA scaffolds were printed by the 3D printer “Prusa i3 MK3S” and sterilized by ultraviolet light and ethanol solution. The first set of specimens was incubated in DMEM (Dulbecco’s Modified Eagle Medium) for 60, 120, and 180 days maintaining 36.5 °C temperature. The mechanical properties of the scaffolds were determined after performing the compression test in the “Mecmesin MultiTest 2.5-i” testing stand with a force applied at two different speed modes. The obtained data was curve fitted with the hyperelastic material models for a model suitability study. The second set of specimens was incubated in PBS (Phosphate Buffered Saline) for 20 weeks and used in a polymer degradation study. The obtained results show that the mechanical properties of PLA scaffolds do not decrease during incubation in physiological medium for a predicted new bone tissue formation period, though hydrolysis starts at the very beginning and increases with time. PLA as a material seems to be suitable for the use in bone tissue engineering as it allows to form biocompatible and biodegradable scaffolds with high mechanical strength, required for effective tissue formation.

Crystallization-Controlled Structure and Thermal Properties of Biobased Poly(Ethylene2,5-Furandicarboxylate).

Crystallization-controlled structure and thermal properties of biobased poly(ethylene 2,5-furandicarboxylate) (PEF) were studied. The cold-crystallization temperature controlled the structure and thermal properties of the biobased PEF. The melting was complex and evidenced the presence of a significant fraction of less-stable crystals with a low melting temperature that linearly increased with Tc, which formed already during the early stages of crystallization, together with those melting at a higher temperature. Low Tc resulted in the α'-phase formation, less crystallinity, and greater content of the rigid amorphous phase. At high Tc, the α-phase formed, higher crystallinity developed, the rigid amorphous phase content was lower, and the melting temperature of the less-stable crystals was higher; however, slight polymer degradation could have occurred. The applied thermal treatment altered the thermal behavior of PEF by shifting the melting of the less stable crystals to a significantly higher temperature. SEM examination revealed a spherulitic morphology. A lamellar order was evidenced with an average long period and small average lamella thickness, the latter about 3-3.5 nm, only slightly increasing with Tc.

Anodisches Recycling von gängigen Polymeren: Die Kombination von Eisen‐Elektrokatalyse und skalierbarer Wasserstoffentwicklungsreaktion

AbstractKunststoffe sind in unserem Alltag allgegenwärtig, und die Akkumulation von Kunststoffabfällen in unserer Umwelt stellt ein großes gesellschaftliches Problem dar. Daher sind Methoden für das Recycling von Kunststoffabfällen im Hinblick auf eine künftige Kreislaufwirtschaft von hohem Interesse. Insbesondere der Abbau von Polymeren nach Nutzung durch Verbraucher hin zu wertschöpfenden kleinen Molekülen stellt eine nachhaltige Strategie für eine Kohlenstoff‐Kreislaufwirtschaft dar. Trotz jüngster Fortschritte ist der chemische Polymerabbau nach wie vor weitgehend auf chemische Redox‐Reagenzien beschränkt oder durch eine geringe Energieeffizienz photochemischer Prozesse limitiert. In dieser Arbeit berichten wir über einen leistungsstarken eisenkatalysierten Abbau von Polystyrolen mit hohem Molekulargewicht durch Elektrochemie, um effizient monomere Benzoylprodukte zu liefern. Die Robustheit der Ferraelektrokatalyse wurde durch den Abbau von verschiedenen realen Nach‐Gebrauchs‐Kunststoffen, ebenfalls im Gramm‐Maßstab, bestätigt. Die kathodische Halbreaktion wurde weitgehend durch die Wasserstoffentwicklungsreaktion (HER) dargestellt. Der skalierbare elektrolytische Polymerabbau konnte ausschließlich mit Solarenergie über ein handelsübliches Solarpanel betrieben werden, was auf ein herausragendes Potenzial für eine dezentralisierte, grüne Wasserstoffwirtschaft hinweist.

Recent Advance of Sustainable Polymers for Packaging Applications

The extensive application of non-renewable polymers has brought about deep environmental concerns, demonstrating the immediate requirement for new biodegradable and biobased packaging choices. The work offers an in-depth look at a wide array of degradable and biobased polymers like Polylactic Acid (PLA), Polyhydroxyalkanoates (PHA), and Polyvinyl Alcohol (PVOH), as well as starch and cellulose materials, discussing their qualities, uses, and the issues faced in food packaging. These types of green polymers, either in new ways or from renewable sources, offer great advances not only from decomposition into harmless parts but also from the reduction of environmental damage. The essay covers the exploitation side of this material, be it the role of PLA in enzymatic, hydrolytic, or microbial degradations, or the main tactical function of PHA in terms of a water barrier aimed at preserving the quality of stored food. Additionally, the multifunctionality of these substances is represented anew in packaging dairy goods, such as fruits, and vegetables, and specialized applications like edible films or water-soluble bags. The participation of compostable polymers has become increasingly vital in the area of food packaging to meet consumers’ demands and to upgrade the present science technologies aimed at guiding food producers who are looking for more sustainability in their business.