Polystyrene Research Articles

Study on the elimination characteristics of smoke particles with different materials using electric agglomeration technology

ABSTRACT Fire smoke, consisting of solid particles and liquid droplets, poses risks of asphyxiation, poisoning, making it a significant contributor to fire-related fatalities and environmental pollution. The exploration of effective smoke control methods represents a vital approach to reducing the threat of fire smoke to public health and safety. This study aims to determine the characteristics of elimination for the fire smoke generated from burning four typical materials, thereby validating the universality of electric agglomeration smoke elimination technology. The results indicate that the elimination efficiency of electric agglomeration varies with the material type of the smoke. The rate of change in smoke transmittance from fast to slow is: polyvinyl chloride (PVC), polystyrene (PS), wood, and styrene butadiene rubber (SBR), respectively. With an external potential of 4 kV, PVC smoke reaches the safe threshold after 12.1 s, while SBR smoke achieves it in just 4.9 s. Analysis of the microscopic morphology of agglomerates with scanning electron microscopy (SEM) reveals that particle size distribution is an important factor affecting electric agglomeration elimination. This is because larger initial particles carry a greater charge, enabling the formation of larger agglomerates for more efficient removal. This study provides theoretical guidance for the practical application of electric agglomeration in eliminating smoke particles.

Experimental study of interception effect by submerged dam on microplastics

Submerged dam can alter microplastic (MP) transport, and act as a sink for MPs. In this paper, we investigated the interception rates of Polyvinyl chloride (PVC) and Polystyrene (PS) by an artificial submerged dam in a flow flume at first, and found that most of the un-intercepted PVC and PS particles by the dam accumulated behind it under the subcritical (Fr < 1) and turbulent (Re > 500) flows. PVC particles behind the dam mainly concentrated within two dam widths, and the concentration of PS particles decreased with the distance behind the dam lengthening. Then, we performed linear regression fitting and Redundancy Analysis (RDA) between the interception rates collected in 162 experiment tests and environmental factors, including flow velocity, distance to dam and MP concentration. The results showed that the interception rate of PVC and PS particles increased with the distance to dam lengthening, but decreased with the flow velocity and MP concentration heightening. RDA revealed that the interception rate was influenced by flow velocity, distance to dam, and MP concentration from the most to the least. Our findings are believed to contribute to understanding the mechanism of the interception effect of submerged dam on microplastics.

ACFs-NH2 developed for dispersive solid phase extraction combined with Py-GC/MS for nanoplastic analysis in ambient water samples

Accurate determination of nanoplastics (NPs) in aquatic ecosystems constitutes a challenge for which highly sensitive analytical methods are necessitated. Herein, a sample pretreatment based on self-made amino-functionalized activated carbon fibers (ACFs-NH2) dispersive solid-phase extraction (DSPE) allows for high-recovery, followed by high-sensitivity detection of NPs by pyrolysis-gas chromatography/mass spectrometry (Py-GC/MS). The developed methodology allowed low detection limits (20–100 μg/L) to be achieved quickly in a few steps. Under optimal conditions, ACFs-NH2 (12.5 mg) was able to recover ≥98.45 % of polystyrene (PS) nanoplastics at high concentration (100 mg/L) in 10 mL seawater. Based on the high adsorption performance of materials, the adsorption dynamics and isotherms were determined to infer the interaction mechanism of PSNPs on ACFs-NH2. After adsorption, the target on the surface of the adsorbent can be directly pyrolyzed, which can simplify the operation steps and avoid the elution of organic solvents, making the process more environmentally friendly. This strategy is feasible for the analysis of trace NPs in water systems.

Impact of seasonal changes and environmental conditions on suspended and inhalable microplastics in urban air

Microplastics (MPs) are ubiquitous environmental pollutants extensively detected in atmospheric environments. Airborne MPs have raised concerns due to their transport and potential health risks of inhalation exposure. However, the factors influencing airborne MPs, particularly their concentrations and shapes suspended in urban air, remain unclear. We investigated MPs in total suspension particles with one-year measurements in Taipei City and identified their features using Nile Red staining combined with fluorescence microscopy and micro-Fourier transform infrared (μFTIR) spectroscopy. This study quantified the mean number concentration of total MPs as approximately 6.0 #/m³. We observed that MP abundance varied seasonally, with higher levels in the warm season than in the cold. A similar trend was noted for polymer types. Fragment-like MPs were the predominant shape, mainly found in polystyrene (PS), polyethylene (PE), and polypropylene (PP), while fibrous MPs, detected mostly as polyethylene terephthalate (PET) and polyamide (PA), were primarily observed at sizes greater than 300 μm. Both fiber and fragment-like MPs were positively associated with particle mass concentration, temperature, ultraviolet (UV) index, and wind speed, but negatively correlated with relative humidity and rainfall. Fibrous MPs were more affected by environmental factors than fragment-like MPs. Meteorological changes significantly influenced suspended MPs more than human activity within the city.

Exceptional anisotropic superhydrophobicity of sword-lily striated leaf surface and soft lithographic biomimicking using polystyrene replica

Herein, we report unusually high anisotropic superhydrophobicity, unidirectional self-cleaning, and biomimicking of adaxial sword-lily (Gladiolus hortulanus) leaf comprising three distinct levels of surface textures. Observably, the static anisotropic wetting and rolling of water droplets are more favourable in the parallel (or, striation) direction than in the perpendicular direction. Inspired from such water repellency of the sword lily leaf surface, here bio-mimicked polystyrene (PS) leaf construct is developed through a soft lithographic technique. Considering different water droplet sizes (4–10 μl) on natural lily leaf and bio-mimicked PS construct surfaces, the respective parallel (θ ||) and perpendicular (θ ⊥) water contact angles (WCAs) stand at, θ || ∼143°–147°, θ ⊥ ∼156°–169°; and θ || ∼130°–139°, θ ⊥ ∼142°–145°. Moreover, the specimens under study exhibit roll-off angles ranging, α || ∼8°–23° (α ⊥ ∼16°–41°) and α || ∼21°–49° (α ⊥ ∼40°–55°) along parallel (and perpendicular) directions; respectively. A noticeable difference in α ⊥ and α || values can be ascribed to the profound three-phase contact line (TCL) pinning along the perpendicular direction taking advantage of striation as means of barrier. The roll-off angles can also alter due to a variation in the droplet volume. The unusual anisotropic superhydrophobicity and unidirectional droplet roll-off can be attributed to the entrapped air within the micro-nano texture beneath the water droplet along with the pinning effect in the perpendicular direction caused by the striated heights.

Increased Static Charge‐Induced Threshold Voltage Shifts and Memristor Activity in Pentacene OFETs Comprising Polystyrene‐Based Gate Dielectrics Containing Electroactive Small Molecule Crystallites

AbstractTop‐contact bottom‐gate pentacene OFETs are fabricated with single layer dielectrics comprised of either polystyrene (PS), poly(4‐methylstyrene) (P4MS), or poly(4‐tert‐butylstyrene) (P4TBS). The polystyrenes are blended with varying concentrations of two different small molecules, dibenzotetrathiafulvalene (DBTTF) and 2,8‐difluoro‐5,11‐bis(triethylsilylethynyl)anthradithiophene (diF‐TES‐ADT), to form small, separated crystallites contained throughout the polymer dielectric layer. The OFET characteristics of these devices are investigated and their threshold voltage shifts are measured after −70 V static charging for 5 min. Two‐terminal measurements are conducted using multiple different gate biases in the range of −50 to +50 V to investigate memristor behavior in the devices. OFETs containing DBTTF exhibited ΔVth increases as large as 330% relative to control OFETs containing no DBTTF, while OFETs containing at least 7.5 wt.% DBTTF exhibited memristor activity, with currents ranging from 20 nA to 44 µA depending on the applied bias. This work demonstrates that including small, separated crystallites in polymer dielectrics enhances their charge storage ability and can be promising for creating nonbinary memory devices for data processing. Additionally, the observed memristor activity indicates the OFETs in this work can be used in development of neuromorphic systems that aim to mimic the synaptic behavior of the human nervous system.

Unclonable Encryption-Verification Strategy Based on Bilayer Shape Memory Photonic Crystals.

The ability to reversibly exhibit structural color patterns has positioned photonic crystals (PCs) at the forefront of anti-counterfeiting. However, the security offered by the mere reversible display is susceptible to illicit alteration and disclosure. Herein, inspired by the electronic message captcha, bilayer photonic crystal (BPC) systems with integrated decryption and verification modules, are realized by combining inverse opal (IO) and double inverse opal (DIO) with polyacrylate polymers. When the informationized BPC is immersed in ethanol or water, the DIO layer displayed encrypted information due to the solvent-induced ordered rearrangement of polystyrene (PS) microspheres. The verification step is established based on the different structural colors of the IO layer pattern, which result from the deformation or recovery of the macroporous skeleton induced by solvent evaporation. Moreover, through the evaporation-induced random self-assembly of PS@SiO2 and SiO2 microspheres, unclonable structurally colored identifying codes are created in the IO layer, ensuring the uniqueness upon the verification. The decrypted code in the DIO layer is valid only when the IO layer displays the pattern with the predetermined structural color; otherwise, it is a pseudo-code. This structural color-based "decryption-verification" approach offers innovative anti-counterfeiting applications in nanophotonics.

Supercritical CO2-promoted degradation of polystyrene to aromatic oils with NiO@C catalyst

Exploring new system for chemical recycling of plastic is an effective way to convert plastic waste into energy. Herein, the use of supercritical CO2 (ScCO2) to promote the catalytic degradation of polystyrene (PS) with high yield of aromatic oils was proposed. ScCO2 provided a homogeneous environment for the reaction, which not only facilitated the swelling of PS, but also inhibited the formation of coke, beneficial for the degradation of PS to aromatic oils. In addition, CO2 as an oxidant reacted with PS or intermediates to generate new products. NiO@C catalyst prepared by doping carbon material in NiO had a simple preparation process, an abundance of porous structure and strong acidic sites, thus improving the catalytic activity. Under the co-action of ScCO2 and NiO@C, the yield of aromatic oils produced from PS was up to 89.3 ± 0.6 wt% at 300 °C with a reaction time of 2 h and a catalyst loading amount of 10 wt%. Moreover, the NiO@C catalyst was used for three cycles without obvious change in the catalytic performance. The efficient catalytic degradation of PS to aromatic oils by ScCO2 promoted NiO@C catalysis provides a potential route for simultaneously recycling plastic and sequestering carbon.

Development of immunochromatographic and homogeneous assay based on quantum dot-functionalized polystyrene nanoprobes for the qualitative and quantitative screening of respiratory viruses

Accurately differentiating respiratory diseases caused by viruses is challenging because of the similarity in their early or clinical symptoms. Moreover, different infection sources require different treatments. However, the current diagnostic methods have limited differentiating efficiency and sensitivity. We developed a dual-system immunosensor with a bilayer fluorescent label as a signal amplifier for the on-site, sensitive, and accurate identification of multiple respiratory viruses (RVs). The nanomaterial, comprising a polystyrene (PS) nanosphere core encapsulated by two layers of CdSe@ZnS-COOH quantum dots (QDs), outperforms the conventional color and fluorescent labels in RV detection. The dual-system detection platform, comprising a PS@DQD-based lateral flow immunoassay (LFIA) and a PS@DQD-based homogeneous sensor, enables qualitative and quantitative screening of multiple respiratory viruses within 10 and 30 min, respectively, depending on the specific detection requirements for different application scenarios. This remarkable method provides 51.2 to 1000 times sensitivity improvement over commercial antigen detection kits and greater than 12.5 to 100 times improvement over QD-based immunosensors. Furthermore, we comprehensively evaluated the specificity, reproducibility, and stability of the integrated dual-system detection platform, demonstrating its reliability. Remarkably, the respiratory viral testing was validated using biological samples, thus illustrating its promise and convenience in the detection of respiratory viruses.

Antimicrobial Functionalization of Surfaces by a Chimeric Adhesive Protein.

The main aim of this work is to account for the prevention and control of microbial growth on surfaces of interest in medical technology. Surface modification is often achieved by physiotherapy or chemical treatments that can involve time-consuming steps, hazardous reagents, and harsh conditions. One of the ways to overcome these drawbacks is the use of surface-active proteins such as hydrophobins. They can form stable protein layers on different surfaces, serving as anchoring points for other molecules of interest. The fungal hydrophobin Vmh2, already exploited for its adhesive ability, has been fused with the antimicrobial peptide GKY20, forming the chimeric protein used herein for functionalizing polystyrene (PS) and bacterial cellulose (BC). As a natural biomass, BC has multiple advantages, including biodegradability, low cost, renewability, high purity, and excellent mechanical properties. The chimeric protein has been proven to successfully adhere to both surfaces. A strong decrease in biofilm formation on PS and a good bactericidal effect of BC have been demonstrated. These findings provide evidence of an alternative strategy to obtain functional composites using a green, easy process.

Immunotoxic response of bio-based plastic on early life stage zebrafish (Danio rerio): A safe alternative to petroleum-based plastics?

Bio-based plastics are marketed as environmentally friendly alternatives to petroleum-based plastics, although they require specific composting conditions for degradation, which leads to their accumulation in the environment and potential risks to aquatic organisms. We hypothesized that the accumulation of bio-based plastics may induce immunotoxic responses in fish. Our research focused on the accumulation and immunotoxicity of 80 nm polylactic acid (PLA) and polystyrene (PS) (0.1–10 mg/L) on early life stage zebrafish (Danio rerio) exposed for 7 days. Compared to PS, there was a higher accumulation of PLA in larvae. Exposure to PLA resulted in a significant increase in neutrophils and macrophages, while immune protein levels such as Complement 3 (C3), Immunoglobulin M (IgM), and C-reactive protein (CRP) were significantly reduced. Furthermore, the mRNA expression of pro-inflammatory cytokines, including tnf-α and il-6, were significantly elevated in PLA treatments. Additionally, PLA-exposed zebrafish were more susceptible to infection by Vibrio parahaemolyticus. Interestingly, at the same concentration, exposures to PS did not induce significant changes in macrophages or immune protein levels, C3 and IgM. This suggests that PLA has a greater immunotoxic response relative to PS. Our research findings contradict the popular belief that bio-based plastics are non-toxic and harmless, which may have potential risk to aquatic organisms.

Low-voltage organic field-effect transistors by using solution-processable high-κ inorganic-polymer hybrid dielectrics

Organic field-effect transistors (OFETs) incorporating hybrid high-κ inorganic Al2O3 and polymer dielectrics, including polyvinyl alcohol (PVA), polystyrene (PS), or polymethyl methacrylate (PMMA), through solution-processing techniques were fabricated. The analyses revealed that the high surface energy and hydrophilicity property of Al2O3 and PVA, and the relatively hydrophobic property of PS surface, hindered the performance of corresponding OFETs. The Al2O3/PMMA-based OFET achieved the optimized performance, with a threshold voltage of −2.7 V, a hole carrier mobility of 0.056 cm2/Vs, and a current on/off ratio of 1.0 × 104 at a low operating voltage of −5 V. Through analyzing the characteristics of leakage current, capacitance, contact resistance, and trap density of OFETs, we found that the PMMA-engaged films possessed the optimized electrical properties. The introduction of PMMA eliminated the interfacial trapping, thereby lowering the threshold voltage and enhancing the performance of the device. The COMSOL Multiphysics simulation was conducted to confirm the physical mechanism. The strategy of utilizing Al2O3/PMMA hybrid dielectric could simultaneously ensure the low operating voltage and good performance of OFET, while guaranteeing the low leakage current by the thick PMMA.

Integrating Metal-Phenolic Networks-Mediated Separation and Machine Learning-Aided Surface-Enhanced Raman Spectroscopy for Accurate Nanoplastics Quantification and Classification.

Increasing accumulation of nanoplastics across ecosystems poses a significant threat to both terrestrial and aquatic life. Surface-enhanced Raman scattering (SERS) is an emerging technique used for nanoplastics detection. However, the identification and classification of nanoplastics using SERS faces challenges regarding sensitivity and accuracy as nanoplastics are sparsely dispersed in the environment. Metal-phenolic networks (MPNs) have the potential to rapidly concentrate and separate various types and sizes of nanoplastics. SERS combined with machine learning may improve prediction accuracy. Herein, we report the integration of MPNs-mediated separation with machine learning-aided SERS methods for the accurate classification and high-precision quantification of nanoplastics, which is tailored to include the complete region of characteristic peaks across diverse nanoplastics in contrast to the traditional manual analysis of SERS spectra on a singular characteristic peak. Our customized machine learning system (e.g., outlier detection, classification, quantification) allows for the identification of detectable nanoplastics (accuracy 81.84%), accurate classification (accuracy > 97%), and sensitive quantification of various types of nanoplastics (polystyrene (PS), poly(methyl methacrylate) (PMMA), polyethylene (PE), and poly(lactic acid) (PLA)) down to ultralow concentrations (0.1 ppm) as well as accurate classification (accuracy > 92%) of nanoplastic mixtures at a subppm level. The effectiveness of this approach is substantiated by its ability to discern between different nanoplastic mixtures and detect nanoplastic samples in natural water systems.

Polystyrene Chain Geometry Probed by Ion Mobility Mass Spectrometry and Molecular Dynamics Simulations.

Polystyrene (PS) is a thermoplastic polymer commonly used in various applications due to its bulk properties. Designing functional polystyrenes with well-defined structures for targeted applications is of significant interest due to the rigid and apolar nature of the polymer chain. Progress is hindered to date by the limitations of current analytical methods in defining the atomistic-level folding of the polymer chain. The integration of ion mobility spectrometry and molecular dynamics simulations is beneficial in addressing these challenges. However, data on gas-phase polystyrene ions are rarely reported in the literature. We herein investigate the gas phase structure of polystyrene ions with different end groups to establish how the nature and the rigidity of the monomer unit affect the charge stabilization. We find that, in contrast to polar polymers in which the charges are located deep in the ionic globules, the charges in the PS ions are rather located at the periphery of the polymer backbone, leading to singly and doubly charged PS ions adopting dense elliptic-shaped structures. Molecular dynamics (MD) simulations indicate that the folding of the PS rigid chain is controlled by phenyl ring interactions with the charge ultimately remaining excluded from the core of the globular ions, whereas the folding of polyether ions is initiated by the folding of the flexible polyether chain around the sodium ion that remains deeply enclosed in the core of the ions.

Studies on particleboard production using Expanded Polystyrene (EPS) waste as a binder for construction applications

This study explored the potential of using EPS waste as a substitute for synthetic resin in particleboard production. The objectives were to assess the impact of various processing parameters, including board density, EPS waste percentage, and pressing temperature, on the properties of the board. For this purpose, lab-scale particleboards were fabricated by combining kelempayan wood particles with EPS waste powders. Subsequently, the physical, mechanical, and thermal stability properties of the board were assessed. The results indicated that the board density, EPS waste percentage, and pressing temperature influenced the physical, mechanical, and thermal stability properties of the board. The bending properties, internal bond (IB) strength, and thickness swelling (TS) of the board exhibited an upward trend with increasing board density. At the same time, the TS decreased while bending properties and IB strength increased with rising EPS waste percentages and pressing temperatures. Notably, the board fabricated with a target density of 0.70 g/cm3, comprising 20 % EPS waste and pressed at 180°C, met the standard requirements for particleboard designated for construction purposes, except the modulus of rupture (MOR), which is slightly lower than the standard requirement. In addition, the thermal stability of the board increased with higher pressing temperatures. Conversely, increasing the density and EPS waste percentage to 40 % appeared to decrease the thermal stability of the board. These findings underscore the significant potential of EPS waste as a binder in particleboard production.

Effects of microplastic interaction with persistent organic pollutants on the activity of the aryl hydrocarbon and estrogen receptors

Environmental microplastics (MPs) are complex mixtures of plastic polymers and sorbed chemical pollutants with high degrees of heterogeneity, particularly in terms of particle size, morphology and degree of weathering. Currently, limitations exist in sampling sufficient amounts of environmental particles for laboratory studies to assess toxicity endpoints with statistical rigor and to examine chemical pollutant interactions. This study seeks to bridge this gap by investigating environmental plastic particle mimetics and pollutant-polymer interactions by mixing polymer particles with persistent organic pollutants (POPs) at set concentrations over time. Solutions containing combinations of polymers including polystyrene (PS), polypropylene (PP), polyethylene terephthalate (PET), and polyamide (PA) and POPs including 2,3,7,8 -Tetrachlorodibenzo-p-dioxin (TCDD), bisphenol A (BPA), and atrazine, were stirred for up to 19 weeks and monitored using assays to test for aryl hydrocarbon (AhR) and estrogen receptor (ER) activity which are cell signaling pathways impacted by environmental pollutants. TCDD induced AhR activity decreased over time in the presence of PS in a surface area dependent manner. BPA and atrazine also exhibited AhR antagonist activity in the presence of TCDD. The addition of BPA slowed the loss of activity but atrazine did not, suggesting that polymer chemistry impacts interactions with POPs. We also observed potential differences in TCDD sorption with different plastic polymers and that higher concentrations of PS particles may inhibit BPA-induced estrogen receptor activation. These results emphasize the need for additional understanding of how POPs and polymer chemistry impact their interaction and toxicity.

NiO/AgNPs nanowell enhanced SERS sensor for efficient detection of micro/nanoplastics in beverages

The ubiquity of plastic products has led to an increased exposure to micro and nano plastics across diverse environments, presenting a novel class of pollutants with substantial health implications. Emerging research indicates their capacity to infiltrate human organs, posing risks of tissue damage and carcinogenesis. Given the prevalent consumption of beverages as a primary vector for these plastics' entry into the human system, there is an imperative need for the advancement of precise detection methodologies in liquids. In this study, we introduce a substrate comprising a Nickel Oxide (NiO) nanosheet array decorated with Silver Nanoparticles (AgNPs) for the Surface-Enhanced Raman Spectroscopy (SERS) analysis of micro//nano plastics. This configuration, leveraging a unique nanowell architecture alongside silver plasmonic enhancement, demonstrates unparalleled sensitivity and repeatability in signal, facilitating the accurate quantification of these contaminants. Through the application of a portable Raman apparatus, this study successfully identifies prevalent micro/nano plastics including polystyrene (PS), polyethylene (PE), and polypropylene (PP), achieving detection sensitivities of 5 μg/mL, 25 μg/mL, and 25 μg/mL, respectively. Moreover, the substrate's efficacy extends to the detection of PS within commonly consumed beverages such as water, milk, and liquor with sensitivities of 25 μg/mL, 50 μg/mL, and 50 μg/mL, respectively. These findings highlight the substrate's potential as an expedient and effective sensor for the real-time monitoring of micro/nano plastic pollutants.

Emergence of microplastics in African environmental drinking water sources: A review on sources, analysis and treatment strategies

The emergence of microplastics (MPs) as microcontaminants in environmental drinking water sources is a problem in Africa that requires immediate action. Therefore, this review focused on understanding the sources of MPs in African water systems, treatment strategies, analytical methods for identification and quantification, and Africa's pollution index. From the findings, the source of MPs in African water systems was attributed to unregulated importation of plastic products, poor waste management, lack of awareness, poor environmental value system and the inability of local polymer industries to adjust to new policies on plastic management. Most studies identified microfibers and microbeads to be the primary sources of plastics that break down to MPs in African drinking water sources, with polystyrene (PS), polypropylene (PP), and polyethylene (PE) being frequently detected. Current methods for identification, and quantification of MPs in most studies conducted in Africa were not developed in Africa but was adopted from developed countries and, in some cases, modified to meet specific analytical requirements. More studies are necessary for in-depth understanding of the fate and pollution index of MP in African environmental water systems. Furthermore, the interaction between MP and other pollutants in the water system still needs to be better understood. This review suggests membrane and rapid sand filtration methods as promising methods that may be considered for removing MPs from water systems in Africa.

Mitogenomic profiling and gut microbial analysis of the newly identified polystyrene-consuming lesser mealworm in Kenya

Plastic waste has recently become a major global environmental concern and one of the biggest challenges has been seeking for alternative management options. Several studies have revealed the potential of several coleopteran species to degrade plastics, and this is the first research paper on plastic-degradation potential by lesser mealworms from Africa. This study evaluated the whole mitogenomic profile of the lesser mealworm to further identify the insect. The ability of the mealworm to consume Polystyrene (PS) was also evaluated alongside its associated gut microbiota diversity. Our results showed a complete circular mitochondrial genome which clustered closely to the Alphitobius genus but also suggested that our insect might be a new subspecies which require further identification. During the PS feeding trials, overall survival rates of the larvae decreased when fed a sole PS diet while PS intake was observed to increase over a 30-day period. The predominant bacteria observed in larvae fed PS diets were Kluyvera, Lactococcus, Klebsiella, Enterobacter, and Enterococcus, while Stenotrophomonas dominated the control diet. These findings demonstrated that the newly identified lesser mealworm can survive on a PS diet and has a consortium of important bacteria strongly associated with PS degradation. This work provides a better understanding of bioremediation applications, paving the way for further research into the metabolic pathways of plastic-degrading microbes and bringing hope to solving plastic waste pollution while providing high-value insect protein towards a circular economy.

Enhanced microplastics removal from sewage effluents via CTAB-modified magnetic biochar: Efficacy and environmental impact

Sewage treatment plants (STPs) are identified as a significant pathway of microplastics (MPs) re-entry into the environment through effluent discharge, thereby emphasizing the need for reliable and efficient treatment methods. This study investigated MPs removal from sewage effluents using cetyl trimethyl ammonium bromide (CTAB)-modified magnetic biochar (RH-MBC-CTAB) as an adsorbent. Biochars from different biomass were synthesized, surface modified, characterized, and compared for their MPs removal efficacy from aqueous matrices. Batch adsorption studies were initially conducted on synthetic water with 1 μm sized polystyrene (PS) MPs using different MP concentrations (1–10 mg/L) and varying adsorbent dosages (1–10 mg/50 mL) to assess the effect of different process parameters, viz. pH (2–10), humic acid (6–25 mg/L), and competitive ions (0.01–0.2 M). The maximum MPs removal (98%) was achieved at the favorable conditions: initial MPs concentration: 10 mg/L, RH-MBC-CTAB dose: 7 mg/50 mL, pH 4, mixing speed: 180 rpm, and contact time: 3 min. Electrostatic attraction and hydrogen bonding were likely to remove MPs while the MPs adsorption was best fitted by the pseudo-second-order kinetics model (R2 = 0.91) and Langmuir isotherm model (R2 = 0.94) with the maximum adsorption capacity of 247.52 mg/g. Further, the application of RH-MBC-CTAB on the real-time sewage effluents from sequencing batch reactor (SBR) and moving bed biofilm reactor (MBBR)-based STPs spiked with MPs showed up to 96% MPs removal. The reusability results revealed that developed RH-MBC-CTAB could maintain good stability for up to three reusability cycles, therefore offering extensive potential for the removal of MPs from sewage effluents.