Low-density Polyethylene Films Research Articles

Mechanical and Tribological Characterization of Microporous Low Density Polyethylene Films Obtained in Blown Extrusion

Mechanical and Tribological Characterization of Microporous Low Density Polyethylene Films Obtained in Blown Extrusion

Enrichment of LDPE-degrading bacterial consortia: Community succession and enhanced degradation efficiency through various pretreatment methods

Low-density polyethylene (LDPE) is a widely used plastic that significantly contributes to environmental pollution, and its biodegradation remains challenging. This study investigates the dynamics of bacterial communities in consortia enriched with LDPE as the sole carbon source. The potential for microbial diversity to adapt to polluted environments underscores its role in bioremediation. Community analysis identified Actinobacteria and Proteobacteria as key contributors to LDPE degradation, with dominant genera including Mycobacterium, Cupriavidus, Gordonia, Ochrobactrum, Nocardia, Agromyces, Amycolatopsis, and Cellulosimicrobium. The biodegradation of untreated and pretreated LDPE films was also examined, revealing that UV pretreatment significantly enhances degradation, with weight losses of 2.22–5.17% after 120 days. In contrast, sunlight and thermal treatments resulted in lower weight losses of 1.67–4.56% and 1.42–3.22%, respectively, while untreated LDPE showed only 1.32–2.80% weight loss. These findings underscore the importance of UV pretreatment in facilitating plastic biodegradation. Furthermore, potential LDPE-degrading Actinobacteria and Proteobacteria were isolated, identified as key players in the communities and co-occurrence networks, suggesting promising candidates for developing sustainable plastic waste management solutions. Moreover, this study is the first to reveal the potential LDPE degradation abilities of several genera, including Mesorhizobium, Agromyces, Amycolatopsis, Olivibacter, Aquamicrobium, Pseudaminobacter, and others.

Different metal-doped NiO nanoparticles for sunlight-mediated degradation of low-density polyethylene microplastic films.

Due to the widespread use and incorrect handling of plastics, we need to find a practical and effective way to eliminate plastic waste from the environment. Different metal-doped nickel oxide (DMD-NiO) nanoparticles (NPs) were synthesized using a sol-gel technique and were used to degrade low-density polyethylene (LDPE) microplastic (MP) films when exposed to sunlight. The optical and structural properties of sol-gel method synthesized materials were investigated using a variety of characterization methods (Fourier transform infrared (FT-IR), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), X-ray diffractometer (XRD) analysis, X-ray photoelectron spectroscopy (XPS), high-resolution transmission electron microscopy (HR-TEM), scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) analysis, and thermogravimetric analysis (TGA). Degradation study results suggest that the photocatalytic activity of DMD-NiO-LDPE nanocomposites (NCs) films was greater than that of pure LDPE and undoped NiO-LDPE films. Because of their increased optical absorption and efficient suppression of photo-produced charge carriers' recombination, the DMD-NiO NPs showed higher photocatalytic degradation of LDPE films. Thus, LDPE films with 2% wt Fe-NiO (iron-doped nickel oxide) nanomaterials showed a degradation of around 38.16% among DMD-NiO-LDPE NCs films under visible light over a short period of 30 days (240 h). The formation of carbonyl groups in the degradation product of LDPE was confirmed by Fourier transform infrared (FT-IR) analysis. When compared to the original LDPE film, the Fe-NiO-LDPE NCs films showed a significant decrease in crystallinity and carbonyl indexes, as much as 8.4% lower. The current project proposes the development of eco-friendly photocatalysts using a sol-gel technique for combating MP pollution in the environment.

Rapid Generation of Microplastics and Plastic-Derived Dissolved Organic Matter from Food Packaging Films under Simulated Aging Conditions.

In this study, we show that low-density polyethylene films, a prevalent choice for food packaging in everyday life, generated high numbers of microplastics (MPs) and hundreds to thousands of plastic-derived dissolved organic matter (DOM) substances under simulated food preparation and storage conditions. Specifically, the plastic film generated 66-2034 MPs/cm2 (size range 10-5000 μm) under simulated aging conditions involving microwave irradiation, heating, steaming, UV irradiation, refrigeration, freezing, and freeze-thaw cycling alongside contact with water, which were 15-453 times that of the control (plastic film immersed in water without aging). We also noticed a substantial release of plastic-derived DOM. Using ultrahigh-resolution mass spectrometry, we identified 321-1414 analytes with molecular weights ranging from 200 to 800 Da, representing plastic-derived DOM containing C, H, and O. The DOM substances included both degradation products of polyethylene (including oxidized forms of oligomers) and toxic plastic additives. Interestingly, although no apparent oxidation was observed for the plastic film under aging conditions, plastic-derived DOM was more oxidized (average O/C increased by 27-46%) following aging with a higher state of carbon saturation and higher polarity. These findings highlight the future need to assess risks associated with MP and DOM release from plastic wraps.

Biodegradation Study of Food Packaging Materials: Assessment of the Impact of the Use of Different Biopolymers and Soil Characteristics

In this article, the relationship between the properties of different membranes (agar, chitosan, and agar + chitosan) and biodegradability in natural and sterilized soil was investigated. The membranes under investigation exhibited variations in the biodegradation process, a phenomenon closely linked to both the soil microbiota composition and their water affinity. Higher solubility in water and greater swelling tendencies correlated with shorter initiation times for the biodegradation process in soil. Overall, all tested membranes began biodegradation within 14 days, as assessed through thickness and morphological analysis parameters, demonstrating a superior degradation rate compared to low-density polyethylene films.

From multilayer LDPE/EVOH flexible film scraps to new multilayer films

This study explores the mechanical and optical properties of multilayer films incorporating recycled materials, mimicking the structure of industrial films. Using a coextrusion blown film line with a three-layer ABC configuration extrusion head, films were produced using two different recycled multilayer films, from post-industrial scraps, in layers A and B and virgin low-density polyethylene (LDPE) in one of the external layers (C). These recycles result from multilayer films mainly constituted of LDPE; one has also linear-LDPE (LLDPE) Metallocene, and the other has Ethylene Vinyl Alcohol (EVOH). Both recycled materials enabled to maintain blown film extrusion process stability during film production. The multilayer films produced with the incorporation of recycles were characterized using scanning electron microscopy (SEM), haze and gloss measurements, and tensile tests. Films with Recycled EVOH presented haze values much higher than those obtained for the Recycled Metallocene. However, all films presented good mechanical properties when compared to single layer virgin LDPE film. Anisotropic behaviour was observed, emphasizing the directional dependence of mechanical properties. The findings provide insights into the behaviour of multilayer films with recycled content, offering valuable information for the development of sustainable packaging solutions.

Toward mechanical recyclability of high barrier food packaging films through filler incorporation on the EVOH layer

AbstractTo preserve food from moisture and oxygen, polymers, such as ethylene vinyl alcohol (EVOH) are used in multilayer structures to provide oxygen barrier, while low‐density polyethylene (LDPE) is used for a water vapor barrier. While this material combination is functionally ideal, it may not comply with the new packaging recycling guidelines. Some European markets have implemented rules that limit the weight percentage of EVOH in LDPE films. One way to increase recyclability is by reducing the amount of EVOH in the film structure while maintaining the packaging's oxygen barrier properties. To achieve this, it is necessary to improve the barrier properties of EVOH. With this objective in mind, this study evaluated the incorporation of nanoclays (NC), cellulose microcrystals (MCC), silicon dioxide nanoparticles (SiO2), and cellulose nanocrystals (CNC) into an EVOH matrix. The results indicate that NC and MCC facilitate a stable blown film extrusion process and have a better dispersion in the EVOH matrix. Based on this finding, three‐layer films (with an ABA configuration) consisting of LDPE (A) and EVOH (7 μm layer) with 0.5 or 1 wt.% MCC or NC (B) were produced to protect the EVOH from moisture and enable blown film processing. The oxygen transmission rate (OTR) values were lowest for 0.5 wt.% NC and 1 wt.% MCC incorporation. Although the films with micro and nanoparticles had increased haze, this did not affect the visibility of the packaged food.

Water-Polymer Slide Electrification in Polyethylene Films Coated with Amphiphilic Compounds and Its Connection to Surface Properties Dependent on Water-Polymer Interactions.

Slide electrification experiments were performed on low-density polyethylene films (PE) and PE sprayed with five amphiphilic compounds, including antistatic and slip additives. Drops of aqueous solutions were delivered on the films and after sliding spontaneously acquired a net electrical charge (Qdrop), which is dependent on the pH and ionic strength. The slide electrification was detected in pristine PE films and those with five additives. An acid-base equilibrium model, based on the adsorption of hydroxides and protons on surface sites, accounted for the dependence of Qdrop on pH, allowing recovery of the acid-base equilibrium constants and the density of adsorption sites. The model was modified to account for ionic strength effects through activity factors. The surface conductivity, wettability, and friction coefficients were strongly modified by the additives. However, the observed trends are different from those observed in slide electrification, which better correlated with zeta potential determinations. This suggests that the interaction mechanisms among surface water, the considered additives, and the polymer, which are involved in slide electrification and the generation of zeta potential, are different from those associated with other surface processes involving surface water. Although additives are required for changing surface resistivity, friction coefficients, and wettability, the generation of sliding electrical charges in polyethylene is a spontaneous and highly effective process. For one specific additive, a simultaneous decrease in friction coefficients, zeta potential, and Qdrop was observed, assigned to the blockade of hydroxide adsorption sites and water repulsion by the compound.

Synthesis of ion exchange film based on chemical grafting of styrene onto polyethylene/EPDM rubber blend for thorium removal.

Chemical grafting of low-density polyethylene film blended with ethylene propylene diene monomer rubber (PE/EPDM) using styrene monomer followed by a sulfonation process was investigated. Different factors affecting the grafting process, such as monomer and initiator concentrations, time of reaction, and grafting temperature, were studied. Sulfonation of the grafted films was carried out using chlorosulfonic acid in dichloromethane. Characterization of the grafted and sulfonated films was performed using ATR-FTIR, SEM, TGA, and XRD instruments. The grafting was successfully performed in aqueous media using sodium bisulfite as initiator, reaching a grafting yield of 130% and an ion exchange capacity of 1.2 meq/g. The removal of thorium ions from aqueous solution was studied using the obtained ion exchange films. The results showed that the maximum adsorption capacity of Th(IV) was 177.5 mg. g-1 (pH = 3, 298 K and 60 min). Removal isotherm and Kinetics were investigated, and the results revealed that the adsorption process was chemisorption homogeneous monolayer adsorption, exothermic, and spontaneous.

Tannic acid-loaded halloysite clay grafted with silver nanoparticles improved the mechanical, antimicrobial, and degradation properties of linear low-density polyethylene films

Synthetic polymers used for food packaging contribute to plastic pollution due to poor degradability. While they prevent the entry of microorganisms, they may not protect against spoilage microorganisms in the packed food. Nanofillers have been used to improve such properties, but end-of-life degradation remains an issue, making plastic a persistent pollutant. Here, we tested a nanocomposite (Nc) of tannic acid-loaded halloysite nanotubes grafted with silver nanoparticles as a reinforcement to enhance the mechanical, antimicrobial, and degradation properties of Linear low-density polyethylene (LLDPE) films. LLDPE films incorporated with Nc significantly improved tensile strength (TS), elongation at break (EB), and oxygen permeability rate. Nc incorporated (at 5%-and 10%) LLDPE films exhibited a 1.89–2.85 log10 reduction in multi-drug resistant Staphylococcus aureus 1158c in chicken fillets. Both film types demonstrated silver migration below the European Food Safety Authority-mandated acceptable limit. Nc/LLDPE films disintegrated faster when exposed to incandescent light for 6 h, evidenced by significant reduction of weight, TS, and EB. Fourier-transform infrared spectroscopy, scanning electron microscopy, and X-ray photoelectron spectroscopy suggested oxidative degradation and breakdown of the polymer. Conclusively, Nc improved the functional properties and degradation rate of LLDPE films when exposed to light, showing potential for enhancing the sustainability of synthetic polymers.

Effects of Titanium Dioxide (TiO2) on Physico-Chemical Properties of Low-Density Polyethylene.

Hazardous chemicals are transported on rail and road networks. In the case of accidental spillage or terror attack, civilian and military first responders must approach the scene equipped with appropriate personal protective equipment. The plausible manufacturing of chemical protective polymer material, from photocatalyst anatase titanium dioxide (TiO2) doped low-density polyethylene (LDPE), for cost-effective durable lightweight protective garments against toxic chemicals such as 2-chloroethyl ethyl sulphide (CEES) was investigated. The photocatalytic effects on the physico-chemical properties, before and after ultraviolet (UV) light exposure were evaluated. TiO2 (0, 5, 10, 15% wt) doped LDPE films were extruded and characterized by SEM-EDX, TEM, tensile tester, DSC-TGA and permeation studies before and after exposure to UV light, respectively. Results revealed that tensile strength and thermal analysis showed an increasing shift, whilst CEES permeation times responded oppositely with a significant decrease from 127 min to 84 min due to the degradation of the polymer matrix for neat LDPE, before and after UV exposure. The TiO2-doped films showed an increasing shift in results obtained for physical properties as the doping concentration increased, before and after UV exposure. Relating to chemical properties, the trend was the inverse of the physical properties. The 15% TiO2-doped film showed improved permeation times only when the photocatalytic TiO2 was activated. However, 5% TiO2-doped film exceptionally maintained better permeation times before and after UV exposure demonstrating better resistance against CEES permeation.

A comparative study on biodegradation of low density polyethylene bags by a Rhizopus arrhizus SLNEA1 strain in batch and continuous cultures.

Biodegradation poses a challenge for environmentalists and scientific community, offering a potential solution to the plastic waste problem. This study aims to investigate the biological degradation of low-density polyethylene (LDPE) bags by a fungus in both batch and continuous cultures, with the goal of identifying an eco-friendly and cost-effective waste management strategy. The fungal strain Rhizopus arrhizus SLNEA1, isolated from a landfill located in northeastern Algeria, was tested for its capability to degrade LDPE films and utilize them as a sole carbon source in batch (α-LDPE) and continuous (γ-LDPE) cultures. The results indicated a higher rate of weight loss for γ-LDPE (29.74%) compared to α-LDPE (23.77%). The biodegradation effect was examined using scanning electron microscopy (SEM), Energy Dispersive X-ray Spectroscopy (EDS) and Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) to evaluate morphological and chemical changes in LDPE samples, highlighting alterations of LDPE films through cracks, veins and holes under SEM and chemical transformation and appearance of new functional groups in the FTIR data. Rhizopus arrhizus SLNEA1 demonstrated the ability to break down and utilize LDPE films as a carbon source. This isolate shows promise for LDPE biodegradation applications, which may be leveraged for the development of future plastic degradation systems involving fungi.

Simulation of the effect of temperature on space charge transport in LDPE under DC electric field stress

Polymers are considered essential materials used in high-voltage direct current (HVDC) applications due to their excellent insulating properties. They are widely employed in various electrical equipment such as cables, transformers, and station insulators, providing effective protection against high currents and voltages. One of the main challenges in these applications is the effect of temperature on the performance of these insulators, as elevated temperatures can alter the electrical properties of polymers, potentially impacting the dynamics of electric charges within the material. In this work, bipolar charge transport (BCT) was used to study the effect of temperature on the dynamics of space charge in LDPE under a DC electric field. The model includes processes such as injection, migration, trapping, detrapping, and recombination. We applied a DC electric field of 50 kV/mm to low-density polyethylene (LDPE) films for 2 hours under different temperatures. The results indicate that higher temperatures significantly enhance charge mobility, leading to improved charge flux, reduced trapping, and increased detrapping of charges. This results in a more uniform distribution of the electric field within the material and a quicker transition to a steady-state condition. The increase in temperature within the applied electric field created a relative balance between trapped charge and mobile charge, indicating a positive effect of higher temperatures on the electrical insulation properties of LDPE.

Application of interlayer perforation and installation of transparent elements in the technology of duplicated decorative polymer films

Objectives. To develop technologies for producing multilayer films of transparent thermoplastic polymers; to study methods of modifying their supramolecular structure; and to determine their optical properties by means of optical-polarization methods for the use of modified films as decorative and design materials in modern architecture.Methods. Industrial samples of polystyrene, low-density polyethylene, polypropylene, and polyvinyl chloride films from various manufacturers (Don Polimer, Vektor, and Sibur) were the objects of the study. The optical properties of the films were studied by means polarized-light spectrophotometry. In order to modify the supramolecular structure of the polymers, the surfaces of the films were treated under isometric conditions with volatile solvents or their aqueous solutions. Parts of the layers of multilayer films were removed by cutting with a punching knife using a press or with a manual device for perforating printing materials.Results. The spectral characteristics of multilayer films of several transparent thermoplastic polymers in polarized light were determined. The study showed that a wide palette of colors and contrasting images can be obtained by mechanically removing part of the layers of multilayer films. The phenomenon of pseudo-disappearance of the outermost layer was discovered after treatment of a stack of films under isometric conditions with volatile solvents or their aqueous solutions.Conclusions. Based on the example of large-scale production thermoplastics, it was shown that a combination of technological methods of stacking, perforation, and local plasticization of films of transparent thermoplastic polymers can produce pleochroic multicolor materials for a range of human activities. The possibility of hidden coding of information on multilayer packaging materials, and its visualization and instrumental reading in polarized light was confirmed by color differential and contrast of 150 and 60 units, respectively. It was also shown that several monochrome tones of different lightness and brightness can be obtained by varying the number of layers or perforating the films in multilayer materials.

Development of fish gelatin film for anti-fogging mushroom packaging

Mushrooms are extremely perspiring and transpiring commodities. The commonly used plastic films for packaging fresh mushrooms have lower water vapour permeability compared to the rate at which mushrooms transpire, resulting in excessive moisture accumulation inside the package which leads to fogging. This study aimed to investigate the properties of a fish scale gelatin-based film and its correlation with antifogging properties. To produce the gelatin-based film, gelatin was extracted from fish scales using chemical pretreatment and thermal denaturation of collagen. A film-forming solution (FFS) was prepared by dissolving 2% (w/v) gelatin in a solvent, with the addition of glycerol. The solution was then cast to form the film, which underwent tests for mechanical strength, thermal behaviour, barrier properties, and antifogging performance. The resulting film (G-Gly) exhibited reduced tensile strength (13.21 MPa) but increased elongation at break (82.4%). Differential scanning calorimetry revealed a lower glass transition temperature (59.91 °C) for G-Gly. Both gelatin films displayed high water vapour permeability (1.69–3.09x10-6 g m/m2.day.Pa), preventing condensation. Notably, the G and G-Gly films remained fog-free even under varying temperatures, unlike linear low-density polyethylene film (LLDPE). In conclusion, the gelatin-based films demonstrated strong barrier properties and effective antifogging capabilities, making them suitable for moisture-sensitive commodities like mushrooms.

Biodegradation of low-density polyethylene by mixed fungi composed of Alternaria sp. and Trametes sp. isolated from landfill sites

With the development of industry and modern manufacturing, nondegradable low-density polyethylene (LDPE) has been widely used, posing a rising environmental hazard to natural ecosystems and public health. In this study, we isolated a series of LDPE-degrading fungi from landfill sites and carried out LDPE degradation experiments by combining highly efficient degrading fungi in pairs. The results showed that the mixed microorganisms composed of Alternaria sp. CPEF-1 and Trametes sp. PE2F-4 (H-3 group) had a greater degradation effect on heat-treated LDPE (T-LDPE). After 30 days of inoculation with combination strain H-3, the weight loss rate of the T-LDPE film was approximately 154% higher than that of the untreated LDPE (U-LDPE) film, and the weight loss rate reached 0.66 ± 0.06%. Environmental scanning electron microscopy (ESEM) and Fourier transform infrared spectroscopy (FTIR) were used to further investigate the biodegradation impacts of T-LDPE, including the changes on the surface and depolymerization of the LDPE films during the fungal degradation process. Our findings revealed that the combined fungal treatment is more effective at degrading T-LDPE than the single strain treatment, and it is expected that properly altering the composition of the microbial community can help lessen the detrimental impact of plastics on the environment.

Comprehensive study of plasma polymerization parameters on thiol-coated LDPE films for effective fibronectin adsorption targeting biomedical applications

In the realm of biomedical applications, biocompatible materials with optimized surface properties are crucial for facilitating cellular interactions. To attain the perfect balance of these properties, surface modification of non-toxic and stable bulk materials is often required. Within this context, this research aimed to improve the physiochemical and cell-responsive properties of a low-density polyethylene film. This was achieved by depositing thiol-rich coatings using a dielectric barrier discharge plasma reactor operating at medium pressures, with 1-propanethiol serving as polymerization precursor. The study systematically investigated the impact of key plasma polymerization parameters, including DBD chamber pressure, treatment time, and the combination of precursor flow rate and discharge power represented by the Yasuda parameter, to identify optimal plasma processing conditions for the formation of thiol-rich coatings. To characterize the coating thickness, hydrophilicity and surface chemical composition, atomic force microscopy, water contact angle measurements, and X-ray photoelectron spectroscopy were employed. The findings indicated that reducing the chamber pressure to 10 kPa led to more hydrophilic and thicker deposits possessing a higher sulphur content. Deposition time (5 to 15 min) also significantly impacted coating thickness and surface chemistry, where long times increased thickness, but also led to a reduced sulphur and increased oxygen content because of more pronounced etching. The optimal deposition time was therefore set at 10 min resulting in the deposition of dense coatings possessing a high number of sulphur-containing functionalities. The Yasuda parameter (W/FM) analysis demonstrated optimal thiol incorporation in combination with high coating stability at an intermediate W/FM value of 72 MJ/kg. Following the determination of the optimal plasma polymerization parameters, the effectiveness of thiol plasma polymerization and subsequent fibronectin immobilization for enhancing cell adhesion and proliferation was investigated. The thiol-coated substrates were found to exhibit superior protein immobilization, because of the high affinity for protein binding of the available thiol groups. To assess cellular responses, Schwann cells were cultured on uncoated and coated samples before and after fibronectin immobilization. The results revealed a superior cellular response of the thiol-coated samples after fibronectin immobilization, showing the highest cell viability and significantly enhanced cell adhesion and proliferation. Collectively, these results underscore the synergistic effect of thiol plasma polymerization and fibronectin immobilization in promoting the cellular response of LDPE substrates, thus highlighting their potential as a surface modification strategy of biomaterials.

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.

Preparation and application of waste cigarette butts-derived mulch film with excellent mechanical properties and optical transparency

Abstract The small waste cigarette butts every year worldwide added up is a significant threat to the environment. The main component of cigarette butts is cellulose acetate, which is an excellent film-forming material. Here, a one-step phase transition method was employed to successfully convert waste cigarette butts into a transparent film. This film (160×18×0.5 mm) derived from waste cigarette butts (CB) has high mechanical strength (fracture stress 23.5 MPa, Young’s modulus 13.1 MPa), good thermal stability, and excellent optical transmittance (91.8%), and low haze (40.3%). Its properties rival those of traditional low-density polyethylene (PE) film. Meanwhile, the CB film displayed fascinating bending-ability and folding resistance. The cigarette butt-derived film with low cost and excellent properties exhibits a promising application as agricultural mulch and provides recycle solution for waste cigarette butts.