Degradation Of Films Research Articles

A General Physics Model of Oxygen Vacancy Dynamics for Ferroelectricity Enhancement and Degradation in Hafnia-Based Thin Films

A General Physics Model of Oxygen Vacancy Dynamics for Ferroelectricity Enhancement and Degradation in Hafnia-Based Thin Films

Effect of thermal shock on energy density of biaxially oriented polypropylene films for pulsed power capacitors

In this paper, thermal shock experiments are performed on the biaxially oriented polypropylene (BOPP) films, and the changes in dielectric and energy storage properties before and after the experiments are explored. The experimental results show that the films have reduced comprehensive performance with the thermal shock time and frequency increasing. After the thermal shock, both the permittivity and the dielectric loss increase slightly. And, the direct current (DC) conductivity has risen by 73.6%–714.2%. The lowest DC breakdown strength of film is 604.4 kV mm−1, showing a 13.5% reduction compared to that of pristine film. In addition, energy storage performance has also deteriorated. The maximum discharge energy density decreased from 4.62 J cm−3 of pristine film to 3.26 J cm−3 of treated film. There is a decrease in charge and discharge efficiency under the same electric field. The metallization layer of the film receives less influence; the capacitance is reduced by only 0.37%. The causes and mechanisms of performance changes are analyzed and discussed. The disruption of molecular chains during thermal shock is the most important factor leading to the degradation of films. This paper provides a powerful perspective and reference for studying the performance degradation and failure of polymer dielectrics under extreme operating conditions.

Rapid Microwave Annealing for Improved Crystallinity and Morphology of Perovskite Materials

Perovskite solar cells are gaining significant attention for their remarkable power conversion efficiency, cost‐effective processing, and material abundance. This study investigates the impact of rapid microwave annealing on the crystallinity and morphology of MAPbI3 films on FTO glass substrates. Multifaceted characterization techniques, including field emission scanning electron microscopy (FESEM), X‐ray diffraction (XRD), UV–Vis spectroscopy, photothermal deflection spectroscopy (PDS), and steady‐state photoluminescence (PL) measurements are used to compare microwave‐annealed samples with traditional hotplate‐annealed samples. Microwave annealing yields significantly larger crystals in shorter processing times, suggesting enhanced crystallinity, as evidenced by SEM analysis and XRD data. UV‐Vis and PDS measurements indicate improved optical properties and reduced sub‐bandgap states, while PL results suggest diminished nonradiative recombination in microwave‐annealed samples. However, a partial film detachment has been observed at higher microwave powers, a phenomenon explained by COMSOL simulations. These findings demonstrate rapid microwave annealing as an energy‐efficient and cost‐effective alternative while highlighting the need for further optimization to address film degradation issues, which remain a significant challenge. This research supports the potential for scalable, high‐quality perovskite material production, facilitating large‐scale production and commercialization of next‐generation solar cells.

Study of Factors Affecting UV-Induced Photo-Degradation in Different Types of Polyethylene Sheets.

Enhancing the degradability of polyethylene plastics could provide a potential solution to the overwhelming crisis of plastic waste. Conventional studies have focused on the degradation of polyethylene thin films. This study investigated UV-induced photo-degradation according to ASTM D5208-14 in polyethylene sheets with thicknesses ranging from 0.4 to 1.2 mm. The impacts of sample thickness, metal pro-oxidants, polyethylene resin types and foaming were explored through the characterization of the carbonyl index, molecular weight, tensile properties and crystallinity. As pro-oxidants, single iron or manganese stearate demonstrated a concentration-dependent trend in accelerating the photo-degradation of polyethylene sheets. The thickness, foaming and resin type-such as low-density polyethylene (LDPE) and high-density polyethylene (HDPE)-significantly impacted the rate of photo-oxidation. Thick polyethylene sheets (1.2 mm) exhibited a heterogenous and depth-dependent degradation profile. As the photo-degradation progressed, the enhanced crystallinity, reduced UV transmittance and formation of crosslinks were able to prevent further oxidative cleavage of the polyethylene chain. This study investigated the time course and factors affecting the photo-degradation of polyethylene sheets, which could provide insights into the formulation design of photo-degradable polyethylene plastics.

Appropriate flame-spraying treatment exacerbates thermal oxidative degradation of residual polyethylene films

In dryland farming, plastic film mulching can significantly increase crop yields, but the resulting residues impair soil health. Heretofore, only few studies had examined how heat treatment facilitates the rapid degradation of polyethylene (PE) residual films. Herein, we characterized the variations in micro-morphology, functional groups, and crystallinity of PE residual films after moderate heat exposure using a self-made flame-spraying equipment. The results revealed that solid residues (SR) obtained from flame-spraying showed a gravimetric weight loss of 9.39 %–15.35 % compared with untreated PE residual films (UPF). Scanning electron microscope equipped with energy dispersive X-ray spectroscopy revealed considerable pits, cracks, and visible roughness in appearance and an increase in the oxygen-to‐carbon (O/C) atomic ratio. Fourier-transform infrared spectroscopy identified characteristic oxygen-containing functional groups and double bonds. X-ray diffraction showed that flame-spraying treatments did not alter the crystal form of polymer, but increased the crystallinity. Higher flame-spraying temperatures resulted in larger oxygen-containing bond indices and lower crystallinity, suggesting a more severe decomposition of PE residual film. The possible volatile gaseous products at different reaction temperatures were predicted using thermogravimetric analysis coupled with Fourier transform infrared spectroscopy (TG-FTIR). Degradation of the PE residual film started at 220 °C, and concentrated release of major products such as long-chain aliphatic hydrocarbons, ketones, and CO2, occurred in the temperature range of 340 °C–440 °C. These results highlighted the effectiveness of the moderate flame-spraying method in accelerating rapid decomposition of residual films, and a flame-spraying temperature range of 220 °C–340 °C should be recommended to avoid potential environmental risks induced by the release of large quantities of degradation products. This study will contribute to enhance our understanding of the thermal oxidative degradation behavior of PE waste and provide a scientific basis for the rapid and clean establishment of PE residual films mitigation in agricultural fields.

Degradation of nitrocellulose film under aerobic conditions by a newly isolated Rhodococcus pyridinivorans strain

The explosive and biorefractory nature of nitrocellulose (NC) poses major risks to both humans and the environment. Expanding the range of microorganisms capable of degrading NC is essential, though the most effective known microorganisms, Desulfovibrio genera and Fusarium solani, achieve degradation rates of 5%-25%. Here, a novel strain, Rhodococcus pyridinivorans LZ1 was isolated, demonstrating the ability to degrade NC, with its growth potentially enhanced by the presence of NC. The degradation process was monitored by assessing changes in nitrate, nitrite, and ammonium. Notably, the –OH strength of NC increased over time, whereas the energetic functional groups (–NO2 and O-NO2) diminished. Furthermore, the presence of NC enhanced nitrate esterase activity 1–2-fold, indicating that ammonification was the primary pathway for NC biodegradation. By converting the nitrate ester of NC into hydroxyl, R. pyridinivorans LZ1 mitigates the harmful effects of NC, offering a promising approach for the treatment of NC waste and wastewater.

Ageing behavior of starch-based food packaging bioplastics in riparian sediments and sediment-derived dissolved organic matter in the soil environment

Riparian sediment (RS) is a translational zone separating aquatic and terrestrial ecosystems. To this date, the bioplastic's UV ageing and biodegradation features in these contaminated sediments remain unknown. It is a considerable concern to investigate whether a food packaging film can interact with RS and riparian sediment-derived Dissolved Organic Matter (RS-DOM) during biodegradation and UV ageing respectively, after disposal in a natural environmental setting. To address this research gap, for the first time, this study investigates the biodegradation and UV ageing of starch/PPst/GTR films intended for food packaging applications in RS and RS-DOM respectively. The findings revealed that RS comprises major fulvic acid DOM components. Remarkably, research demonstrates the leaching of humic acid-like DOM from the film promotes aromaticity and humification as UV ageing progresses from the third to the tenth day. Comparable DOM samples were darkly analysed, revealing aromatic proteins I and II. Furthermore, an elevated carbonyl carboxyl index confirmed significant degradation of films during UV ageing. Lesser humification, aromaticity, and higher biological activity were confirmed by a HI < 10 and BIX > 0.6 respectively. In comprehension, these findings reveal that the starch/PPst/GTR food packaging film will have a lesser adverse environmental impact after disposal, offering a hopeful outlook for the future of bioplastics.

Green synthesis of Bio-CuS quantum dots by sulfate reducing bacteria for solid-phase photocatalytic degradation of polyethylene film

In this study, CuS quantum dots (QDs) synthesized through biological method were used as photocatalysts for the photocatalytic degradation of polyethylene (PE) plastics. Bio-CuS QDs were synthesized through a green process using sulfate reducing bacteria, while Che-CuS QDs were prepared by chemical precipitation for comparison. The crystal structure, surface morphology, microstructure and optical properties of the samples were detected by XRD, SEM, TEM and UV–Vis DRS. The green synthesis mechanism of Bio-CuS was inferred by analyzing changes in amino acid concentration and the three-dimensional fluorescence spectra of extracellular polymeric substances before and after synthesis. The photocatalytic degradation of PE films by Che-CuS and Bio-CuS was investigated. The weight loss rates of PE+Che-CuS and PE+Bio-CuS were 9.1 % and 12.8 % after 14 d irradiation, respectively, while pure PE was only 1.7 %. Furthermore, SEM, UV–Vis DRS, contact angle, TGA, GPC and FTIR were adopted to characterize the PE film. The results revealed that PE+Che-CuS and PE+Bio-CuS underwent major changes in morphology, transparency, hydrophilicity, thermal stability, molecular weight and functional groups compared with PE, with more pronounced changes observed for PE+Bio-CuS. The quenching experiments of active species showed that h+ and·OH were critical to the PE degradation. The intermediate products of PE degradation were analyzed by GC–MS, and a possible degradation pathway was proposed. In addition, the possible mechanism of photocatalytic degradation of PE films by CuS QDs was proposed. This work provides a green remediation approach to addressing the growing plastic pollution in the environment.

Enhanced degradation of phototreated recycled and unused low-density polyethylene films by Pleurotus ostreatus.

Polyethylene, one of the most used petroleum-derived polymers, causes serious environmental pollution. The ability of Pleurotus ostreatus to degrade UV-treated and untreated recycled and unused (new) low-density polyethylene (LDPE) films was studied. We determined the fungal biomass production, enzyme production, and enzyme yield. Changes in the chemical structure and surface morphology of the LDPE after fungal growth were analyzed using FTIR spectroscopy and SEM. Functional group indices and contact angles were also evaluated. In general, the highest Lac (6013 U/L), LiP (2432 U/L), MnP (995 U/L) and UP (6671 U/L) activities were observed in irradiated recycled LDPE (IrRPE). The contact angle of all samples was negatively correlated with fermentation time; the smaller the contact angle, the longer the fermentation time, indicating effective biodegradation. The IrRPE samples exhibited the smallest contact angle (49°) at 4 weeks, and the samples were fragmented (into two pieces) at 5 weeks. This fungus could degrade unused (new) LDPE significantly within 6 weeks. The biodegradation of LDPE proceeded faster in recycled than in unused samples, which can be enhanced by exposing LDPE to UV radiation. Enzymatic production during fungal growth suggest that LDPE degradation is initiated by laccase (Lac) followed by lignin peroxidase (LiP), whereas manganese peroxidase (MnP) and unspecific peroxygenase (UP) are involved in the final degradation process. This is the first experimental study on the fungal growth and its main enzymes involved in LDPE biodegradation. This fungus has great promise as a safe, efficient, and environmentally friendly organism capable of degrading LDPE.

Field-based assessment of the effect of conventional and biodegradable plastic mulch film on nitrogen partitioning, soil microbial diversity, and maize biomass

In an agricultural context, the use of conventional low-density polyethylene (LDPE) and biodegradable plastic mulch film has been actively promoted, however, the effects on physical and biochemical soil properties, crop growth dynamics, yield, and nutrient cycling of conventional and biodegradable mulch film use in a temperate climate remain largely undetermined. Here, we conducted a field experiment, exploring the effects of no mulch (control), conventional (LDPE), and biodegradable (PLA/PBAT) plastic mulch film on soil and crop (Zea mays L.) nitrogen (N) partitioning after application of 15N-labelled ammonium-nitrate fertiliser. Further, we also investigated the treatment effects on soil physical and biochemical properties (e.g., microbial diversity, compound-specific microbial 15N incorporation, N dynamics), plant development, as well as monitoring the biotic and abiotic degradation of the plastic mulch films. We found that conventional mulch film increased crop yield by 25 % and 15N uptake by 34 % compared to the control, simultaneously reducing 15N retention by 40 % in the topsoil (0–10 cm), but not affecting microbial N use efficiency and N transformation and incorporation into the protein pool. Biodegradable film application resulted in similar biomass (306 ± 14 g plant−1) to both control (275 ± 14 g plant−1) and conventional mulch (344 ± 20 g plant−1) treatments, but significantly reduced 15N crop uptake by 63 % compared to the conventional mulch film. We ascribe this to the accelerated mechanical breakdown and faster degradation of the biodegradable mulch film during the growing season. These findings suggest that current biodegradable plastic mulch film polymer blends may not be a suitable alternative to conventional mulch film in terms of short-term productivity and N use efficiency in a temperate climate for maize production.

Photocatalytic performance of copper ferrite/polypyrrole nanohybrids: studies on visible light induced degradation of urea and microwave-assisted degradation of polyethylene films

Photocatalytic performance of copper ferrite/polypyrrole nanohybrids: studies on visible light induced degradation of urea and microwave-assisted degradation of polyethylene films

Unveiling the potential of bacterial isolates from plastic-polluted environments: enhancement of polyhydroxybutyrate biodegradation

This study explores the biodegradation potential of microbial isolates focusing on their ability to utilize biopolymers as sole carbon source. Previously described isolates have been investigated through agar-based screen for the ability to degrade plastic-related substrates in powder form, and four strains have been selected for further assessment. Polyhydroxybutyrate (PHB) films degradation was examined through liquid culture, soil burial, and respirometry assays. Structural and chemical alterations in PHB were analysed using scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC). The most successful strains were tested for the ability to degrade PHB/bacterial nanocellulose (BNC) blends. Bacillus sp. DG90 excelled in PHB degradation, achieving 60% weight loss in liquid culture, while Streptomyces sp. DG19 exhibited a notable degradation rate of 51 ± 1.7%. Soil burial assays underscored the impact of environmental factors on degradation rates, emphasizing the role of soil composition and nitrogen availability. In respirometry assay, PHB films were severely defragmented by Streptomyces sp. DG19 with overall weight loss of 83%, while for Bacillus sp. DG90, this percentage reached 39%. FTIR and DSC analyses suggested potential hydrolysis and structural alterations in treated samples. This study observed rapid PHB degradation (83% in 3 weeks) while, considering the complex composition of modern biomaterials, also showcased the potential of examined strains to degrade PHB-BNC blends up to 85%.

High toughness and fast home-compost biodegradable packaging films derived from polylactic acid/thermoplastic starch/para-rubber ternary blends

This research aims to formulate biobased and biodegradable packaging films with high toughness and fast home-compost biodegradation using ternary blends of polylactic acid (PLA), Para rubber (NR), and thermoplastic starch (TPS) through blown-film extrusion. The TPS content in this work ranges from 5 to 20 wt%, while the PLA: NR ratio is fixed at 70:30. At this PLA: NR ratio, the blend with 10 wt% TPS (PNT10) exhibited the highest % elongation at break and tensile toughness. Peroxide radical initiator was investigated as a potential additive for improving the properties of the ternary blend. Our binary interaction study indicated that peroxide initiated grafting reactions of PLA–NR and NR–TPS pairs, while no grafting occurred between PLA and TPS. In ternary blends, the highest peroxide content (0.5 wt%) increased the % elongation at break up to 120%, with the tensile toughness reaching 7255 MJ/m3. The improved compatibility induced by peroxide addition was supported by enhanced dispersion of TPS in the PLA/NR matrices. Results from the room-temperature soil burial test indicated that the presence of TPS could significantly accelerate the home-compost degradation of PNT films compared to films produced from neat PLA and PLA/NR. This suggests its potential as both a cost reducer and a biodegradation accelerator.

Impact of Residual Strains on the Carrier Mobility and Stability of Perovskite Films.

Solution-based inorganic-organic halide perovskites are of great interest to researchers because of their unique optoelectronic properties and easy processing. However, polycrystalline perovskite films often show inhomogeneity due to residual strain induced during the film's post-processing phase. In turn, these strains can impact both their stability and performance. An exhaustive study of residual strains can provide a better understanding and control of how they affect the performance and stability of perovskite films. In this work, we explore this complex interrelationship between residual strains and electrical properties for methylammonium CH3NH3PbI3-xClx films using grazing incidence X-ray diffraction (GIXRD). We correlate their resistivity and carrier mobility using the Hall effect. The sin2(ψ) technique is used to optimize the annealing parameters for the perovskite films. We also establish that temperature-induced relaxation can yield a significant enhancement of the charge carrier transports in perovskite films. Finally, we also use Raman micro-spectroscopy to assess the degradation of perovskite films as a function of their residual strains.

Establishing a biodegradable film with gluten and tea polyphenols: Structure, properties, and function

Film packaging is a common method to extend the shelf life of food during storage. But the non degradability and potential toxicity of some synthetic films are gradually limiting their usage in food packaging. In present study, gluten and tea polyphenols were utilized to prepare a packaging film, and the properties of this film were determined. With addition of tea polyphenols, thickness and tensile properties of film were improved. By using scanning electron microscope, fourier transform infrared spectra and molecular docking, this film showed a dense network structure, which was due to the strong interactions between tea polyphenols and gluten. Hydrogen bonds and hydrophobic interactions were the main molecular forces during the interactions. Meanwhile, the film showed the good thermal stability and barrier properties. In addition, this film exhibited the remarkable capability to scavenge free radicals and inhibited the increase of peroxide value of oil during storage. Moreover, this film had the slow-release properties of tea polyphenols, and could be biodegradable in nature. All present results suggested that tea polyphenols improved the properties and functions of gluten film effectively, and this complex film showed the potential for food preservation in food industry.

Multigenerational toxicity of microplastics derived from two types of agricultural mulching films to Folsomia candida

Degradation and fragmentation of mulching films represents an increasing source of microplastics (MPs, plastic particles 1 μm to 5 mm in size) to agricultural soils. MPs have been shown to affect many soil invertebrates, including springtails. However, these studies typically use test materials representing less environmentally relevant particle types, such as pristine uniform MPs, which do not represent the large range of particle sizes and morphologies found in the field. This study aimed at providing insight into the adverse effects of MPs originating from agricultural mulching films, by using artificially aged MPs derived from both biodegradable (starch-polybutadiene adipate terephthalate (PBAT)) blend, as well as conventional (linear low-density polyethylene (LLDPE)) plastic polymers. The soil dwelling springtail Folsomia candida was exposed to these MPs for five generations in order to elucidate population effects due to possible reproduction toxicity, endocrine disruption, mutagenesis or developmental toxicity. F. candida were exposed to 0, 0.0016, 0.008, 0.04, 0.2, 1, 2, 3, 4 and 5 % (w/w dry soil) MPs in Lufa 2.2 soil, which includes concentrations within the range of environmental relevance. Juveniles produced at each concentration were transferred to the next generation, with the parental, F2 and F4 generations being exposed for four weeks and F1 and F3 generations for five weeks. No concentration-dependent effects on F. candida survival or reproduction were observed in exposures to either of the MPs, in any of the generations. These results suggest that the particular MPs used in this study, derived from mulching films used on agricultural soils, may not be potent toxicants to F. candida, even after long-term exposure and at elevated concentrations.

Reactively Processed Poly(butylene adipate terephthalate) Composite–Based Multilayered Films with Improved Properties for Sustainable Packaging Applications: Structural Characterization and Biodegradation Mechanism

AbstractIn this study, it is attempted to enhance the properties and biodegradability of poly(butylene adipate terephthalate) (PBAT) using nanocomposite technology to meet the demand for sustainable packaging applications. Two nanoclays containing PBAT composites are reactively processed and integrated into the multilayered films. Reactive processing facilitates the dispersion and distribution of nanoclay particles in the PBAT matrix. The multilayered films comprising reactively processed PBAT composites exhibited a 24.5%–31.5% reduction in the oxygen transmission rate and improved dimensional stability and tensile properties. Moreover, the degradability of the multilayered film comprising reactively processed PBAT composites reached 82% in 180 days. In contrast, a neat PBAT film of similar thickness attained only 53% degradation in the same period. The biodegradation mechanism is proposed based on the topology of the disintegrated films studied using scanning electron microscopy, chemical bond vibrations determined by Fourier‐transform infrared spectroscopy, and structural evolution by small‐ and wide‐angle X‐ray scattering (SWAXS). The SWAXS analysis is used to understand the changes in the degree of crystallinity, long‐range periodic order, and crystalline and amorphous layer thickness of the multilayered films before and after degradation. Such multilayered films can find applications where packaging or biomedical devices cannot be recycled.

Degradation of Polymer Films of Sodium Alginate during Prolonged Irradiation with X-ray under Ultra-High Vacuum.

Sodium alginate (NaAlg) is widely used as a food additive. To study the effect of irradiation with X-ray quanta with energies of 1253.6 eV and 1486.6 eV on the composition of NaAlg, thick films with a smooth surface were prepared, which did not differ in IR spectra from the original powders. The films were irradiated in a high vacuum (3 × 10-10 mbar) in the chamber of a Specs PHOIBOS 150 MCD9 XPS spectrometer with an X-ray source power of 150 W and an irradiation duration of up to 300 min, which significantly exceeded the time required to obtain an XPS spectrum. This made it possible to use XPS to monitor changes in the composition of the NaAlg surface directly during irradiation. As a result of the research, it has been established that NaAlg degrades with prolonged irradiation, which is accompanied by a significant decrease in the O/C ratio. When analyzing the dependence of the intensities of individual peaks in the C1s spectrum on the irradiation time, it was found that after 100 min of irradiation, a peak due to the carbonate group appears in the spectrum. The decomposition was also accompanied by a change in the color of NaAlg from white to yellow-brown. In the IR spectrum of the NaAlg film irradiated for 300 min, an absorption band was detected at 1910 cm-1, which is usually associated with the presence of allene groups.

Salinity effect on corrosion inhibition of 2-mercaptopyrimidine as an inhibitor in CO2-containing solution

In this work, the effects of Cl-, Ca2+, and Mg2+ on the corrosion inhibition performance of 2-mercaptopyrimidine (2-MP) were investigated. The analysis reveals a marked reduction in the inhibition efficiency of 2-MP, from 91.24 % to 76.29 %, as the NaCl content in the solution rises from 1 wt% to 20 wt%. UV–visible absorption spectroscopy and quartz crystal microbalance measurements indicate that the desorption of 2-MP worsens with an increasing content of corrosive ions. Molecular dynamics simulations reveal the inhibitor desorption mechanism. This work enhances understanding of ion effects on corrosion inhibition and film degradation in high salinity environments.

Insulator Polymer Matrix Construction on All-Small-Molecule Photoactive Blend Towards Extrapolated 15000 Hour T80 Stable Devices.

To boost the stability of all-small-molecule (ASM) organic photovoltaic (OPV) blends, an insulator polymer called styrene-ethylene-butylene-styrene (SEBS) as morphology stabilizer is applied into the host system of small molecules BM-ClEH:BO-4Cl. Minor addition of SEBS (1mg/ml in host solution) provides a significantly enhanced T80 value of 15000 hours (extrapolated), surpassing doping-free (0mg/ml) and heavy doping (10mg/ml) counterparts (900 hours, 30 hours). The material reproducibility and cost-effectiveness of the active layer will not be affected by this industrially available polymer, where the power conversion efficiency (PCE) can be well maintained at 15.02%, which is still a decent value for non-halogen solvent-treated ASM OPV. Morphological and photophysical characterizations clearly demonstrate SEBS's pivotal effect on suppressing the degradation of donor molecules and blend film's crystallization/aggregation reorganization, which protects the exciton dynamics effectively. This work pays meaningful attention to the ASM system stability, performs a smart strategy to suppress the film morphology degradation, and releases a comprehensive understanding of the mechanism of device performance reduction.