Polystyrene Research Articles

Photoaging of polystyrene-based microplastics amplifies inflammatory response in macrophages

The continuous release of municipal and industrial products into the environment poses a growing concern for public health. Among environmental pollutants, polystyrene (PS) stands out as a primary constituent of environmental plastic waste, given its widespread use and high production rates owing to its durability and user-friendly properties. The detection of polystyrene microparticles (PS-MPs) in various living organisms has been well-documented, posing a serious threat due to their potential passage into the human ecosystem. In this manuscript, we aimed to study the toxicological effects of low concentrations of pristine and photoaged PS-MPs in a murine macrophage cell line. To this purpose, PS-MPs were photoaged by indoor exposure to visible light to simulate environmental weathering due to solar irradiation (PS-MPs3h). Physical characterization revealed that the irradiation treatment results in particle degradation and the possible release of nanoparticles. Monocultures of the RAW264.7 cell line were then exposed to PS-MPs and PS-MPs3h at concentrations comparable to experimental measurements from biological samples, to assess cytotoxicity, intracellular oxidative stress, primary genotoxicity, and inflammatory effects. Significant toxicity-related outcomes were observed in cells treated with both pristine PS-MPs and PS-MPs3h even at low concentrations (0,10 μg/ml and 1 μg/ml). PS-MPs3h exhibited greater adverse effects compared to PS-MPs, including reduced cell viability, increased ROS production, elevated DNA damage, and upregulation of IL-6 and NOS2 gene expression. Therefore, we can conclude that changes induced by environmental aging in the physicochemical composition of PS microplastics play a crucial role in the adverse health outcomes associated with microplastic exposure.

Orientation of Antibody Modified and Reacted on Carboxy-Functionalized Polystyrene Particle Revealed by Zeta Potential Measurement.

The comprehensive understanding of the orientation of antibodies on a solid surface is crucial for affinity-based sensing mechanisms. In this study, we demonstrated that the orientation of primary antibodies modified on carboxy-functionalized polystyrene (PS) particles can be analyzed using zeta potential behavior at different pH based on the combined Gouy-Chapman-Stern model and the acid dissociation of carboxy groups and antibodies. We observed that at low surface concentrations of the primary antibody, a side-on orientation was predominant. However, at higher concentrations (approximately 30000 antibodies per PS particle), the orientation shifted to an end-on type due to steric hindrance. Furthermore, the reaction mechanism of the secondary antibody exhibited pH-dependent behavior. At pH > 7, the zeta potential changes were attributed to the antibody-antibody reaction, whereas at pH < 7, adsorption of secondary antibody onto the PS particle was observed, leading to a change in the orientation of the primary antibody modified on the PS particle to an end-on type. The change in zeta potential due to secondary antibody binding indicated a detection limit of 37000 antibodies per PS particle. As a result, we revealed that the analysis of zeta potential behavior enables the evaluation of antibody orientation and the detection of zeptomole order antibodies. This study represents the first demonstration of this capability. We anticipate that the present concept and results will broaden the quantitative application of zeta potential measurements and have significant implications for research areas, including physical chemistry and analytical chemistry.

Assessment of plastic debris and biofouling in a specially protected area of the Antarctic Peninsula region

The aim of this paper is to characterize the plastic and to study a potential relationship between plastic debris characteristics and the presence of fouling biota in an Antarctic Specially Protected Area Robert Island, on the Antarctic peninsula region. A combination of lab-based sorting, advanced spectral analysis and general linear modelling was used to assess the abundance and type of plastic debris washed up on the shore. Observations recorded 730 debris items, with 85 % being plastic. Polystyrene (PS) and Polyethylene terephthalate (PET) were the dominant plastics (61 %). Biofouling was observed on 25 % of plastic debris, with debris complexity and degradation significantly increasing the likelihood of fouling occurring. There was no correlation found between biofouling type and plastic polymer type. Findings raise concerns that even with the highest level of environmental protection, an external marine-based source of pollution can intrude the coastal habitat, with uncertain consequences to local flora and fauna.

Suspended whispering gallery mode resonators made of different polymers and fabricated using drop-on-demand inkjet printing for gas sensing applications

Investigation of drop-on-demand inkjet printing as a fabrication method for an optical gas sensor reveals its potential to incorporate multiple sensing materials on a single microchip. Through this additive method, three distinct polymers—SU-8, polystyrene (PS), and polyhexamethylene biguanide (PHMB)—were deposited onto a silicon substrate and suspended, allowing the polymer microdroplets to expand freely. The coupling to these whispering gallery mode resonators with a tapered optical fiber allows measuring high quality factors exceeding 106. The gas sensing capabilities of all three polymers were studied for three different gases: isopropanol, water, and carbon dioxide. Sensitivities of up to 0.25pm/ppmv and limits of detection as low as 14ppmv were achieved.

Microplastic exposure reduced the defecation rate, altered digestive enzyme activities, and caused histological and ultracellular changes in the midgut tissues of the ground beetle (Blaps polychresta)

Concerns about microplastic (MP) pollution in terrestrial systems are increasing. It is believed that the overall amount of MPs in the terrestrial system could be 4–23 times higher than that in the ocean. Agricultural ecosystems are among the most polluted areas with MPs. Terrestrial organisms such as ground beetles, will be more vulnerable to MPs in various agricultural soil types because they are common in garden and agricultural areas. Therefore, this work aims to assess for the first time the potential adverse effects of chronic exposure for 30 days of ground beetles to a field-realistic concentration of 2 % (w/w) of three different irregularly shaped MPs polymers: Polystyrene (PS), polyethylene terephthalate (PET), and polyamide 6 (PA; i.e., nylon 6) on their health. The results showed no effect on beetle survival; nevertheless, there was a decrease in beetle defecation rate, particularly in beetles exposed to PS-MPs, and a change in the activity of midgut digestive enzymes. The effects on digestive enzymes (amylase, protease, lipase, and α-glucosidase) were polymer and enzyme specific. Furthermore, histological and cytological studies demonstrated the decomposition of the midgut peritrophic membrane, as well as abnormally shaped nuclei, vacuolation, disordered microvilli, necrosis of goblet and columnar cells, and necrosis of mitochondria in midgut cells. Given the importance of ground beetles as predators in most agricultural and garden settings, the reported adverse impacts of MPs on their health may impact their existence and ecological functions.

Enrichment characteristics of microplastics in Antarctic benthic and pelagic fish and krill near the Antarctic Peninsula

Global microplastic pollution has garnered widespread attention from researchers both domestically and internationally. However, compared to other regions worldwide, little is known about microplastic pollution in the marine ecosystems of the Antarctic region. This study investigated the abundance and characteristics of microplastics (MPs) in the gills and intestines of 15 species of Antarctic fish and Antarctic krill (Euphausia superba). The results indicate that the abundance of MPs in Antarctic fish and E. superba ranged from 0.625 to 2.0 items/individual and 0.17 to 0.27 items/individual, with mean abundances of 0.93 ± 0.96 items/individual and 0.23 ± 0.44 items/individual, respectively. Antarctic fish ingested significantly more MPs than E. superba. There was no significant difference in the abundance of MPs between the gills and intestines of Antarctic fish. However, the quantity of pellet-shaped MPs in the gills was significantly higher than in the intestines. The depth of fish habitat influenced the quantity and size of MPs in their bodies, with benthic fish ingesting significantly fewer MPs than pelagic fish. Pelagic fish ingested significantly more MPs sized 1–5 mm than benthic fish. Additionally, analysis of the characteristics of MPs revealed that fiber-shaped MPs were predominant in shape, with sizes generally smaller than 0.25 mm and 0.25–0.5 mm. The predominant colors of MPs were transparent, red, and black, while the main materials were polypropylene (PP), polystyrene (PS), polyamide (PA), and polyvinyl chloride (PVC). Compared to organisms from other regions, the levels of MPs in Antarctic fish and E. superba were relatively low. This study contributes to a better understanding of the extent of MP pollution in Antarctic fish and E. superba, aiding human efforts to mitigate its impact on the environment.

Contribution of gut microbiota to biodegradation of polystyrene in Tenebrio molitor larvae: Microbiome under antibiotic suppression of Gram-positive, Gram-negative, and fungal microbes

The discovery of plastic biodegradation by insects such as Tenebrio molitor larvae has been well known, however, understanding of the roles of larval gut microorganisms is still very limited. The contribution of the gut microbes belonging to respective Gram-positive (G+), Gram-negative (G−), and fungal (F) groups remains unclear. In this study, we tested polystyrene (PS) biodegradation by T. molitor larvae under three selective antibiotics i.e., gentamicin sulfate (GMS) against G− bacteria, ampicillin (AMP) against G+ bacteria and nystatin (NS) against fungi. The larvae consumed and biodegraded PS foams with Mn 86.381 kDa and Mw 181.176 kDa under antibiotic suppressions at reduced rates versus control (CK) with a sequence of CK>GMS>AMP>NS group. Specifically, only NS group showed a significant decreased in consumption compared to the control. The gut microbial counts decreased with GMS, AMP, or NS addition during the PS feeding. The respective gut microbial counts decreased by 103 to 104 with GMS, AMP, or NS addition PS feeding. Analyses of DSC, TGA, FTIR confirmed oxidation and biodegradation in the presence of antibiotics. The ingested PS polymers were depolymerized and mass reduction with negative influence in the order of NS<AMP<GMS. The negative impact of antibiotic suppression on PS biodegradation process was as follows: anti-fungi reagent > anti-G+ bacteria > anti- G− bacteria. Changes in chemical functional groups are probably related to certain gut microbes, such as the fungal genus of Candida, and bacterial genera of unclassified Enterobacteriaceae and Lactobacillus. Our findings provided new insights into the mechanisms of the biodegradation of plastics in insects.

Assessing the impact of simulated ocean acidification on the photodegradation of selected microplastics

This study investigated the impact of ocean acidification on the photodegradation of three microplastics (MPs): polypropylene (PP), expanded polystyrene (EPS), and ethylene-vinyl acetate (EVA), under accelerated UV radiation at three pH levels (i.e., 8.1, 7.8, and 7.5), simulating marine conditions. The acidification system simulated current and projected future environmental conditions. As expected, an increase in partial pressure of CO2, total inorganic carbon, bicarbonate ion, and CO2 resulted in more acidic pH levels, with the reverse being true for the carbonate ion. Structural changes of MPs were evaluated, revealing that all weathered samples underwent higher degradation rate compared to the virgin samples. The oxidation state and crystallinity of PP and EVA MPs were higher in samples exposed to the lowest pH, whereas no significant increase in the degradation rate of EPS samples was observed. Saltwater acidification in this study contributed to enhance the photo-oxidation of MPs depending on their polymeric composition.

Impact of Nanoplastic Particles on Macrophage Inflammation and Intestinal Health in a Mouse Model of Inflammatory Bowel Disease.

The increasing presence of plastics in the human diet is raising public concern about the potential risks posed by nanoplastic (NP) particles, which can emerge from the degradation of plastic debris. NP ingestion poses particular risks to individuals with inflammatory bowel disease (IBD), as compromised epithelial barriers may facilitate NP translocation. In vitro, bone-marrow-derived macrophages (BMDMs) were exposed to 25 nm polymethacrylate (PMMA) or 50 nm polystyrene (PS) particles to assess morphological changes and alterations in pro- and anti-inflammatory gene expression. In vivo, mice received PMMA NP particles for 6 months before acute dextran sodium sulfate (DSS) colitis was induced to investigate NP impacts on intestinal health and inflammation. PMMA and PS NP exposure in BMDMs induced morphological changes indicative of a proinflammatory phenotype characterized by enlarged amoeboid cell shapes. It also triggered an inflammatory response, indicated by increased expression of proinflammatory cytokines such as Tnfa and Il6. Unexpectedly, long-term PMMA NP administration did not affect the intestinal epithelial barrier or exacerbate acute DSS-induced colitis in mice. Colonoscopy and histological analysis revealed no NP-related changes, suggesting adverse effects on intestinal health or inflammation. Our findings from animal models offer some reassurance to IBD patients regarding the effects of NP ingestion. However, variations in lifestyle and dietary habits may lead to significantly higher plastic intake in certain individuals, raising concerns about potential long-term gastrointestinal effects of lifelong plastic consumption.

Separation of microplastics from deep-sea sediment using an affordable, simple to use, and easily accessible density separation device

Microplastics accumulate in the environment but methods to extract particles from sediment for quantification and identification often lack accuracy and reproducibility. Existing methods vary greatly and many do not achieve adequate microplastic separation. During method development for extraction procedures, spike-recovery experiments (positive controls) are essential to ensure accurate and reproducible results from each sample matrix. Furthermore, the large variability in grain size and organic matter can affect the extraction of microplastics from the matrix. Scientists have used density separation to separate microplastics from matrices for decades, but apparatuses are often made of plastic, need to be custom made, and require multiple sample transfers from one apparatus to another. This study presents an affordable, easily accessible, and simple to use Density Separation Device (DSD) to remove plastics from deep-sea sediments. Eight polymers were spiked into replicates of environmental sediment, including six fragments: high density polyethylene (HDPE), polypropylene (PP), polyvinyl chloride (PVC), polystyrene (PS), nylon (PA6), and crumb rubber (CR) and two fibers: cellulose acetate (CA) and polyester (PEST). Two size classes of polymers were used: 100 μm to 300 μm and > 300 μm. Using a sodium polytungstate solution at a density of 1.9 g/mL and reflectance FTIR microscopy for particle identification, mean recoveries of all fragments exceeded 78% (CR: 92.7% ± 30.8%, PP: 78.4% ± 34.0%, HDPE: 93.8% ± 13.5%, PS: 86.9% ± 25.7%, PA6: 98.4% ± 63.2%, PVC: 100.0% ± 12.4%). Fiber recovery was much lower (PEST: 28.1% ± 28.1% and CA: 25.9% ± 17.3%) because they aggregated, passed through sieves vertically, or were obscured under other particles. The fragment recovery success, accessibility (available online, all parts under $200) and ease of use of this DSD should facilitate widespread use, thus helping to standardize sample preparation methods for microplastic metrology.

A study on the effect of fluorescently stained micro(nano)plastics on the full life history of Skeletonema costatum

As a new type of environmental pollutant, micro(nano)plastics have become a research hotspot in recent years, and their effects on the full life history of marine microalgae have not been studied. To investigate the effects of micro(nano)plastics on the growth, photosynthesis, physiological morphology and interaction of microalgae during the full life cycle, we selected fluorescently stained polystyrene (PS) plastic microbeads as the target pollutant. By sampling and testing the growth rate, photosynthesis and physiological morphology parameters of algal species, the influence of different concentrations of PS (10, 50 and 100 mg/L) and different particle sizes (0.1, 0.5 and 1 μm) on the full life history of Skeletonema costatum (S. costatum) was investigated. The results showed that after adding PS (particle sizes of 0.5 and 1 μm), the response of S. costatum showed a dual character, while adding the same kind of microplastics (MPs) with a particle size of 0.1 μm inhibited S. costatum throughout the full life cycle. Compared with previous studies, short-term experimental data may overestimate the true ecological risks of MPs. In addition, 0.1 μm fluorescent-stained MPs obviously accumulated around the microalgae, indicating that MPs mainly adhered to the surface of algal cells and may enter the food chain by direct or indirect ways, which can cause negative effects on the aquatic ecosystem. This study supports a more accurate assessment of the true risk of MPs to marine aquatic ecosystems.

Adsorption behavior of heavy metals onto microplastics derived from conventional and biodegradable commercial plastic products

This study extensively explored the adsorption behavior of heavy metals (Pb+2, Ni+2, Cu+2, Zn+2, and Cd+2) onto microplastics (MPs). The particle sizes of MPs ranged from 0.149 to 0.25 mm. The microplastics were generated from commercial products manufactured from both conventional (polyethylene (PE) bottle, polystyrene (PS) spoon, and polyethylene terephthalate (PET) egg carton) and biodegradable (polylactic acid (PLA) spoon, and polylactic acid (PLA) egg carton) plastics. The study also considered the influence of solution pH on the adsorption capacity of heavy metals. Regarding the adsorption potential for Cu+2, the ranking was as follows: PLA-egg (1408 μg·g−1) > PLA-spoon (735 μg·g−1) > PE-bottle (315 μg·g−1) > PET-egg (283 μg·g−1) > PS-spoon (237 μg·g−1). PLA MPs showed the highest adsorption capacity due to the lower thermal stability and higher presence of surface oxygen functional groups. Moreover, the adsorption capacities of the five metals onto PLA-spoon and PLA-egg decreased in the following order: Pb (1785 μg·g−1) > Zn (1267 μg·g−1) > Cd (748 μg·g−1) > Cu (735 μg·g−1) > Ni (722 μg·g−1), and Pb (1520 μg·g−1) > Ni (1412 μg·g−1) > Cu (1408 μg·g−1) > Zn (1118 μg·g−1) > Cd (423 μg·g−1), respectively. The SEM-EDS, FTIR and XPS results demonstrated that surface oxygen-containing functional groups play an important role during the adsorption process. This study extended its analysis to quantify the metal content of the post-adsorption MPs, revealing uneven adsorption of heavy metals onto the MPs. This implies that the diversity of commercial plastic products may result in significant variations in their ability to adsorb heavy metals, underscoring the importance of effectively managing discarded commercial plastic products.

Synthesis and Characterization of Polycarbonate/Polystyren/Polyethylene Oxide/Zinc Sulfide Nanocomposites: Gamma Ray Induced Changes in their Optical and Color Properties

Amorphous polycarbonate (PC), amorphous polystyrene (PS), semicrystalline polyethylene oxide (PEO) and zinc sulfide (ZnS) nanoparticles (NP) were used to fabricate PC/PS/PEO/ZnS nanocomposite (NC) films. We believe that this study is novel in the area of the effect of γ ray radiation on such NC. The synthesized ZnS NP had an average particle size of 18 nm, as indicated from the Rietveld refinement of the X-ray diffraction (XRD) scans. Samples of the PC/PS/PEO/ZnS NC films were irradiated with γ ray doses ranging from 20 to 180 kGy. UV-vis spectroscopy and the International Commission on Illumination (CIE) color changes technique were used to investigate the resulting effects of the γ ray irradiation on the optical and color properties of the prepared films. The light absorbance of the NC films increased as it was irradiated with the γ ray doses up to 180 kGy, the maximum dose used. The increase in absorbance was associated with a decrease in the direct bandgap from 5.88 to 4.92 eV, and an increase of Urbach energy from 0.43 to 0.81 eV. This was attributed to the dominance of chain crosslinks. The γ ray effects on the absorbance, extinction coefficient, refractive index and optical conductivity of the NC films were studied. The modifications in the optical properties indicated that the γ radiation is a useful tool that allows the application of the resulting PC/PS/PEO/ZnS NC films in optoelectronic devices. Furthermore, the color differences between the pristine and irradiated films were evaluated using the CIE color differences technique. The pristine film was uncolored but showed significant color changes when irradiated with γ radiation up to 180 kGy, the maximum dose used.

Constructing highly thermally conductive polystyrene-based composites by introducing multi-walled carbon nanotubes into melamine foam-supported boron nitride network

High-density 3D thermally conductive nanofiller network plays a vital role in the fabrication of polymer-based composites with high thermal conductivity (TC) for thermal management systems. In this work, highly thermally conductive polystyrene (PS)-based composites were prepared by introducing boron nitride nanosheets-coated melamine foam (MF@BNNSs) and carboxylated multi-walled carbon nanotubes (MWCNT–COOH). In this unique structure, MF@BNNSs can provide a 3D thermally conductive network, while MWCNT–COOH is embedded into the MF@BNNSs skeleton to improve the network-density. Specifically, the TC of PS/MWCNT/MF@BNNSs composite with 0.6 wt% MWCNT–COOH loading reaches 5.33 W /m· K, about 4.4-fold as high as that of the PS/MF@BNNSs. Moreover, the PS/MWCNT/MF@BNNSs composite exhibits effective heat dissipation capacity after assembling the power LED chip. Due to the isolation effect of MF@BNNSs skeleton, the PS/MWCNT/MF@BNNSs maintain electrical insulation properties. Consequently, the design of the thermal conductive network based on MF@BNNSs and MWCNT–COOH offered a substantial potential avenue for the preparation of polymer-based composites with high TC and insulating properties.

Regulation of Brightness Attributes of High-Stability Carbon Quantum Dots Applicable in LED Digital Color Display.

Fluorescent carbon dots (CDs) attract much attention due to high stability and low toxicity. For high brightness, multi-color emission and fluorescence stability, polystyrene (PS)/CDs composite films were prepared. First, three types of CDs and three PS/CDs films were prepared. Then, three light-emitting-diode (LED) devices were achieved. Compared to CDs solutions, CDs filled films show almost unchanged photoluminescence (PL) spectra. PL peaks of blue, green and red films appear at 462nm, 544nm and 603nm, separately. Blue CDs lead to highest photoluminescence quantum yields (PLQYs) of 76% (solution) and 49% (film). A certain level of thermal stability and fluorescent reversibility of blue film were verified. After 60 days of air exposure, PL intensities of blue and green films reach 97% and 93% of original values, separately. Improving work time cannot vary PL wavelengths of devices. For blue-emitted device, PL intensity reaches 55% of original value after working for 600min. For green-emitted device, PL intensity reaches 80% after working for 300min. The novelty is effective PS encapsulation and uniform dispersion of CDs to yield favorable fluorescence properties of devices. This work inspires ideas for large-scale preparation of fluorescent films for LED digital color display.

Polarizability inversion suspension for nonlinear optical limiting with a low limiting threshold.

We propose what we believe to be a novel nonlinear optical limiting (NOL) method with a low limiting threshold based on a light intensity-controlled polarizability inversion suspension (PIS). This suspension has negative polarizability under weak light, allowing stable propagation of weak light with a low loss. Nevertheless, the suspension reverses into positive polarizability due to the optical Kerr effect under strong light, resulting in enhanced scattering that rapidly attenuates the intense light. In a proof-of-concept experiment, PS (polystyrene)-CS2-CCl4 suspension is used as the example suspension. We experimentally verify the NOL performance of several samples. Among them, 4 g/L PS-CS2-CCl4 suspension with a volume ratio of 0.15 has the best optical limiting effect, with a high limiting capacity coefficient of 0.48 and a very low limiting threshold of 14.80 kW/cm2, which is an order magnitude lower than that of most common NOL materials. Therefore, the proposed method provides a new promising approach to achieve NOL of continuous wave laser with a low limiting threshold.

Effects of Contamination with Selected Polymers on the Mechanical Properties of Post-Industrial Recycled Polypropylene.

The effect of contamination of polypropylene (PP) with selected polymers is studied to simulate the effect of mis-sorting in recycling streams. Polystyrene (PS), polyethylene terephthalate (PET), polycarbonate (PC), acrylonitrile butadiene styrene (ABS), and polylactic acid (PLA) were compounded with PP at different concentrations varying between 3 and 10%. Infrared spectroscopy proved the absence of chemical bonds between the constituents. Generally, melt flowability, except for the PP/PLA blend, and crystallinity were only slightly affected by the incorporation of the contaminating polymers. Samples of the polymer blends were injection moulded and further tested for their tensile and impact properties. Critical behaviour was induced by the introduction of a weld line as a result of the application of multiple gating points during injection moulding. Results generally show the applicability of PP mixtures within the investigated range of contamination, without much sacrifice in mechanical performance. However, in the case of ABS and PLA, more care should be taken when designing complex parts with weld lines, due to reduced toughness.

Effect of interaction between different plastics and polyvinyl chloride on the chlorine transformation behavior in volatiles during low-temperature pyrolysis

To reduce the pollution during the pyrolysis recovery of chlorine-containing plastic waste from different sources, effects of the interaction between different plastics and polyvinyl chloride (PVC) on the transformation of chlorine at low temperature were investigated by thermogravimetry-Fourier transform infrared (TG-FTIR) and fixed-bed pyrolysis experiments. Results showed that the proportions of chlorine in chars were all <0.04 %, indicating that almost all chlorine was released after pyrolysis. However, the chlorine forms in volatiles were significantly changed with mixing different plastics. HCl production was significantly inhibited due to the addition of other plastics, while the organic chlorinated compounds (OCCs) formation was promoted, which increased the distribution of chlorine in liquid products. During PVC pyrolysis, chlorine was mainly distributed in gas (93.09 %) in the form of HCl, only a small amount of aliphatic chlorides were generated and distributed in liquid (6.89 %). After the addition of polystyrene (PS), polyethylene (PE) and polyethylene terephthalate (PET), the chlorine distribution in liquid increased to 8.86 %, 11.98 % and 25.99 %, respectively. The formation of OCCs was significantly affected by the difference in thermochemical reaction characteristics of plastics. Specifically, the production of aromatic chlorides was promoted by PS, while the generation of aliphatic chlorides and aromatic chloroesters was significantly promoted by PE and PET, respectively. Therefore, the release form of chlorine could be significantly altered by the interaction between PVC and other waste plastics, which provides a reference for the regulation of chlorine-containing pollutants in the recovery and utilization of plastic waste.

New insights on the degradation of polystyrene and polypropylene by larvae of the superworm Zophobas atratus and gut bacterial consortium enrichments obtained under different culture conditions

This study aims to deepen knowledge of the biodegradation of plastics, focusing on polypropylene (PP) fabric from surgical masks and polystyrene (PS) by larvae of Zophobas atratus as well as of specialized bacterial consortia from their gut, which were obtained in different enrichment conditions (aerobic, anaerobic, presence or absence of combined nitrogen). Plastics ingested by larvae obtained in Spain did not show any signs of oxidation but only limited depolymerization, preferably from the lowest molecular weight chains. Gut microbiota composition changed as an effect of plastic feeding. Such differences were more evident in bacterial enrichment cultures, where the polymer type influenced the composition more than by culture conditions, with an increase in the presence of nitrogen-fixers in anaerobic conditions. PS and PP degradation by different enrichment cultures was confirmed under aerobic and anaerobic conditions by respirometry tests, with anaerobic conditions favouring a more active plastic degradation. In addition, exposure to selected bacterial consortia in aerobiosis induced limited surface oxidation of PS. This possibly indicates that different biochemical routes are being utilized in the anaerobic gut and in aerobic conditions to degrade the polymer.

Epsilon‐negative materials with lower percolation threshold derived from segregated structures

AbstractEpsilon‐negative materials (ENM) at radio frequency, usually designed based on percolation theory, recently drew much attention because of their potential applications in capacitors, transistors, and antennas. However, randomly distributed conductive functional materials cannot achieve directional long‐range electron transportation within the material, resulting in decreased utilization efficiency. The morphology design of the substrate material can change the distribution state and electron transfer pathway of conductive fillers. By controlling the size of the polystyrene (PS) and the content of multi‐walled carbon nanotubes (MWCNTs), PS/MWCNTs composites with random structures and segregated structures were designed, both of which exhibited negative permittivity with increasing MWCNTs content. Further investigation revealed that negative permittivity behavior is due to the establishment of the conductive network and the plasma oscillation of free electrons. Moreover, components with segregated structures have lower percolation thresholds, as directional electron transport is achieved and conductive fillers are efficiently utilized. This work provides a new method for guiding the electron transport pathway and effectively changing the distribution state of conductive fillers in ENM.Highlights Negative permittivity is achieved by plasma oscillation at radio frequency. The segregated structure leads to a decrease in the percolation threshold. Epsilon‐negative materials have good prospects in inductive components.