Microplastics In Aquatic Environments Research Articles

Enhancing the degradation of microplastics through combined KMnO4 oxidation and UV radiation

The pervasive issue of microplastics in aquatic environments presents a formidable challenge to traditional water treatment methodologies, including those utilizing KMnO4. This study pioneers advanced oxidation processes (AOPs) method aimed at improving the degradation of PE microplastics by employing a dual treatment strategy that combines KMnO4 oxidation with UV irradiation. Detailed analysis of the surface modifications and chemical functional groups of the treated PE microplastics revealed the establishment of Mn-O-Mn linkages on their surfaces. Weight reductions of 3.9%, 4.9%, and 7.5% were observed for the KMnO4/UVA, KMnO4/UVB, and KMnO4/UVC treatments over seven days, respectively. The emergence of carboxyl and hydroxyl groups played a crucial role in accelerating the degradation process. Notably, the combined application of UVC rays and KMnO4 resulted in the most effective degradation of PE microplastics observed in our study. The process significantly enhanced the formation of MnO2 particles from KMnO4 oxidation, with concentrations ranging from 0.036 to 0.070 mM for KMnO4/UVA, 0.066–0.097 mM for KMnO4/UVB, and 0.086–0.180 mM for KMnO4/UVC. Furthermore, the influence of varying pH levels, KMnO4 concentrations, and different water sources on the degradation efficacy was investigated. The pivotal role of free radicals and reactive manganese species in promoting the degradation of PE microplastics was identified. A comparative evaluation with treatments solely utilizing KMnO4 or UV light highlighted the enhanced effectiveness of the combined approach, demonstrating its potential as an efficient solution for reducing microplastic contamination in aquatic systems.

Quantitative Raman analysis of microplastics in water using peak area ratios for concentration determination

This study presents a novel analytical method for the quantitative and qualitative analysis of microplastics (MPs) in deionized (DI) water using Raman spectroscopy. Raman peak area ratios of 1295 cm−1 for polyethylene (PE) and 637 cm−1 for polyvinylchloride (PVC) to the broad H2O peak were utilized to establish a calibration model for the concentration of MPs dispersed in DI water at 0.1 wt% to 1.0 wt%. The calibration model demonstrated R2 values of 0.98537 for PE and 0.99511 for PVC, indicating high linearity between the peak area ratio and concentration. The calibration model was validated using mixed PE and PVC samples to confirm its applicability to real-world water bodies, where multiple types of MPs are present. The calculated standard error of calibration (SEC) and relative standard error of calibration (%RSEC) values further confirmed the accuracy of the predictions, providing a robust approach for detecting and quantifying MPs in aquatic environments.

Influence of Aging and the Presence of Dissolved Organic Matter on Caffeine Adsorption onto Microplastics in Aquatic Environments

Influence of Aging and the Presence of Dissolved Organic Matter on Caffeine Adsorption onto Microplastics in Aquatic Environments

The Study of Removal of Polyvinyl Chloride (PVC) Particles from Wastewater through Electrocoagulation

Plastic was produced massively, especially using polyvinyl chloride (PVC) as a raw material. Unfortunately, this condition cause affects the environment, which creates a new pollutant issue. It is essential to study the removal of PVC microplastics in current water treatment processes. The study of wastewater treatment can be achieved using electrocoagulation, which has several benefits, including low-cost, simple chemicals, and accessible equipment operation. This research investigated the study of the removal of PVC microplastics from wastewater by electrocoagulation. The new potential of the electrocoagulation technique using Al-Al electrodes was studied systematically at various variations, i.e., electrolysis time, electrolyte concentration, initial pH, coagulation speed, and electrolyte type. The results showed that the PVC microplastics removal efficiency reached 100% after electrolysis for 60 min, electrolyte concentration of 0.01 mol/L, initial pH of 7, coagulation speed of 500 rpm, the type of electrolyte used was NaCl at a flocculation speed. These optimum conditions also reduced the value of turbidity of wastewater samples from 1.39 ± 0.02 to 1.10 ± 0.05 NTU. The results of this study provide an engineering perspective in optimizing operational parameters for removing PVC microplastics in aquatic environments.

Assessing the contribution of sewing threads to microfiber release during domestic laundering

Environmental science studies from the past decade have emphasized that microplastics in aquatic environments are mostly caused by domestic laundering of synthetic textiles. Although many studies have explored the microfiber release behavior of fabrics washed in laundry, attempts to witness microfiber release from sewing threads, which are an inevitable part of any finished garment, are meager. With this research gap, this study attempted to analyze the potential of sewing threads to release microfibers during washing and the extent to which they can contribute to the overall microfiber release during domestic laundering. The study's findings revealed an average release of 2.65 ± 0.70 (n = 33) microfibers/m from the sewing thread sewn on the fabric during laundering. The sewing process was noted to cause damage to the sewing thread, which led to a comparatively higher microfiber release (∼114%) compared with the sewing threads that were washed before sewing. Among the selected sewing threads, higher microfiber emissions were reported with spun threads, followed by twistless filaments, and twisted filament threads. The results showed that coarser sewing threads with higher Tex values released more microfibers than finer Tex threads. Compared to the 20 Tex spun thread, the 80 Tex spun thread showed a 22–150% increase in microfiber release. In the case of filament sewing thread, a similar impact was noted, whereas the role of twist was found to be efficient in reducing microfiber emission. Compared to the untwisted filaments, the ply twisted filaments exhibited approximately 76% lower microfiber emissions. The findings of this study showed that sewing thread contributed approximately 1.09% of the total microfiber emissions from apparel during laundry.

Recreational activities as a major source of microplastics in aquatic environments

Recreational activities as a major source of microplastics in aquatic environments

Advanced understanding of the natural forces accelerating aging and release of black microplastics (tire wear particles) based on mechanism and toxicity analysis

Currently, tire wear particles (TWPs), a typical type of black microplastics (MPs), are frequently overlooked as the major source of MPs in aquatic environments. TWPs are widely distributed and exhibit complex environmental behaviors. However, how natural forces affect the aging and release behavior of TWPs at the nano(micro)scale remains inadequately explored. This study systematically investigated the aging behavior and mechanism of TWPs under the action of simulated natural light and high-temperature in both dry and wet environments, as well as the effect of aging treatment on the released leachate. The findings demonstrated that aging treatment significantly altered the physicochemical properties of TWPs, including chain scission and surface oxidation, and facilitated the release of heavy metals and organic additives in the meantime. In particular, the leaching concentration of Zn exhibited a positive linear relationship with exposure time. In the thermal-aging process, the oxidation of TWPs was primarily caused by superoxide anion (O2•−). During the photo-aging exposure, TWPs exhibited heightened electron-donating capacity, resulting in the formation of more O2•− and singlet oxygen (1O2) to attack TWPs. Moreover, the analysis of leachate produced under light and high-temperature conditions suggested that heavy metals exerted low ecological risks in water. Nonetheless, the photo-aging process enhanced the toxicity of released leachate to L929 cells, which could be attributed to highly toxic additive transformation products (such as HMMM-411 and 6PPD-Q) and more heavy metals. These findings shed light on the fate of TWPs and the ecological risks posed by aged TWPs in aquatic environments.

The conversion of metal ions to metals particles contributes the photoaging of microplastics in aquatic environments

Metals ions enriched on the surface of Microplastics (MPs) may undergo redox reactions under UV irradiation to promote its photoaging. However, there is a paucity of information on studies of the aging behavior of MPs mediated by different metal ions. This study aims to investigate the effects of three different metal ions (Ag+, Cu2+ and Al3+) on the photoaging properties of polypropylene (PP) to enhance our comprehension of their aging in water contaminated by heavy metals. Physicochemical analyses, like the ratio of O/C and carbonyl index (CI), suggested that metal ions accelerated the aging of PP. The correlation model was established between CI and aging time to confirm that the aging sequence of PP in three metal ions solution was Ag+-PP>Cu2+-PP>Al3+-PP. Electron Paramagnetic Resonance (EPR) results showed metal ions enhanced the generation of reactive oxygen species (•O2–, HO• and 1O2) to accelerate aging through free radical pathways. Electronic exchange capability (EEC) and X-Ray Photoelectron Spectroscopy (XPS) confirmed metal particles were on PP, leading to the e-bridge for electronic relays that altered the EEC of PP and accelerated its protonation process. It needs to note the surface plasmon resonance (SPR) effect of metal nanoparticles may also accelerated the photoaging of MPs in UV–vis illumination. For the first time, the study establishes a connection between different valence states metal ion and PP aging, shedding light on interfacial and free radical aging process of MPs. The finding also proposes the potential e-bridge or SPR effect of metal particles may exist in accelerating photoaging reaction of PP in special water bodies contaminated with heavy metals. The environmental implications and ecological risks of this phenomenon warrant greater consideration.

Innovative Approaches for Microplastic Pollution Detection and Remediation in Aquatic Ecosystems

Microplastic pollution in aquatic ecosystems is a pressing environmental issue, posing significant threats to marine life and human health. Traditional detection and remediation methods are often inadequate, necessitating the development of innovative approaches. This research aims to explore and evaluate novel techniques for detecting and mitigating microplastics in aquatic environments. The study investigates advanced detection technologies, including spectroscopy and sensor-based methods, that offer higher accuracy and efficiency compared to conventional approaches. Additionally, it explores innovative remediation techniques such as bioremediation and the use of advanced filtration systems. Field and laboratory experiments were conducted to test the effectiveness of these methods in various aquatic settings. The results indicate that these innovative approaches significantly enhance the detection and removal of microplastics, demonstrating superior performance over traditional methods. This research provides critical insights into the potential of advanced technologies in addressing microplastic pollution, highlighting their applicability and benefits for environmental conservation. By integrating these innovative solutions, we can better safeguard aquatic ecosystems and promote sustainable environmental practices.

Occurrence and emission characteristics of microplastics in agricultural surface runoff under different natural rainfall and short-term fertilizer application

Land-based microplastics (MPs) are considered the primary source of MPs in aquatic environments, with runoff being a major pathway for their transfer from soil to surface water. However, the transportation characteristics of MPs via agricultural surface runoff remain unclear. In this study, we investigated the occurrence and emission characteristics of MPs in agricultural surface runoff under various short-term fertilizer applications and natural rainfall events using laser direct infrared imaging analysis (LDIR). MPs from fertilizers and soils co-migrated with the agricultural runoff. The abundance and concentration of MPs in runoff were 145.90 ± 22.48–2043.38 ± 89.51 items·L−1 and 39.17 ± 21.94–523.04 ± 47.85 µg·L−1, respectively. Small and low-density MPs, such as polyethylene (PE), chlorinated polyethylene (CPE), and polyurethane (PU) in film/fragment form with 20–50 µm exhibited a higher mobility. No statistical differences were observed in the distribution of runoff MPs with the application of different fertilizers. There was a significant positive relationship between runoff MP abundance and rainfall intensity. The annual emission load in this study area was 116.73 g·hm−2, indicating that the transportation of MPs via agricultural surface runoff cannot be ignored. This study is conducive to understanding the migration behavior of MPs in soil-water environments in a better manner.

Combined effects of polyethylene terephthalate and abamectin on enzymatic activity and histopathology response in juvenile zebrafish (Danio rerio).

One of the most pressing global environmental issues is the widespread abundance and distribution of microplastics (MPs). MPs can act as vectors for other contaminants in the environment making these small plastic particles hazardous for ecosystems. The presence of MPs in aquatic environments may pose threats to aquatic organisms that ingest them. This study examined effects of abamectin (ABM) and polyethylene terephthalate (PET) MP fragments on histopathological and enzymatic biomarkers in zebrafish (Danio rerio). Zebrafish were exposed for 96 h to pristine PET-MPs at concentrations of 5 mg/L and 10 mg/L, ABM alone at 0.006 mg/L, and the same concentration of ABM in the presence of PET-MPs in aquaria. Histopathological analysis revealed tissue content changes in liver and kidney in the presence of ABM individually and in combination with MPs. Results of enzymatic analysis showed that MPs increased the bioavailability and toxicity of pesticides due to inhibition of catalase (CAT) and acid phosphatase (ACP) enzymes. However, MPs did not affect the toxicity of ABM for glutathione s-transferase (GST) enzyme. Despite the inhibition of acetylcholinesterase (AChE) in MPs or ABM treatments, and some neurotoxicity, no change in activity of this enzyme and neurotoxicity was observed in the combined MPs and ABM treatments, although toxicity effects of MPs and ABM on zebrafish require more detailed studies.

Simulation of the dynamic processes of microplastic suspension and deposition in a lake sediment-water system.

The occurrence of microplastics in aquatic environments has attracted increasing interest from both the public and scientists, especially their migration behaviors. Although several environmental behaviors of microplastics have been studied, the issue of microplastic suspension and deposition in lake sediment-water systems remains to be elucidated. In this study, we built an indoor sediment-water system with input and output rivers that simulated the actual situations in lakes, and aimed to explore the suspension and deposition behavior of microplastics using eight group experiments. The abundance of microplastics in overlying water and sediments in different periods was analyzed, and the characteristics of hydrodynamic disturbance on microplastic suspension and deposition were identified. Importantly, the exchange of microplastics in sediments and water under dynamic flow conditions was assessed. The results showed that the middle-scale experiment designed in this study effectively simulated the dynamic transport process of microplastics in lakes, and the hydrodynamic force had a significant impact on the suspension and deposition behaviors of microplastics. The average abundance of polystyrene, polyethylene terephthalate and polyamide microplastics was 1.07, 0.60 and 0.83 particles/L in overlying water during the suspension experiments, respectively. This showed a pattern of first rising and then falling with the extension of suspension time. Even in the environment with the maximum input water volume (8000 ml/min) in this study, only microplastics at a depth of 0 to 2 cm from the sediment were suspended. The average abundance of microplastics was 313.02 particles/kg during the deposition experiments, which gradually increased with the extension of deposition time in sediments. Finally, microplastic sizes in water of the suspension experiments and in sediments of the deposition experiments were concentrated in the range of 500 to 1500 μm and 300 to 1000 μm, respectively.

Aging and Small-sized Particles Release Characteristics of Tire Microplastics in Various Environmental Media

In recent years, research on microplastics has mostly focused on thermoplastic materials, and there is a lack of research on the pollution status and environmental behavior of tire microplastics, a type of rubber elastomers. In order to investigate the aging and small-sized particles release characteristics of tire microplastics in various environmental media, the aging process of two different tire microplastics, one for cars and the other for electric bicycles, was simulated in dry and aquatic environments under laboratory conditions. The results showed that the tire microplastics would be aged after 30 d of UV illumination, which was manifested by the roughness of the surface and the appearance of cracks and flaking. The Fourier infrared spectra showed that the carbonyl index of the surface also increased. In addition, tire microplastics released a large number of small sub-micron particles under the influence of UV illumination and hydrodynamic action, and the number of particles released from car tire microplastics in aquatic environments reached 694.8 million particles per milliliter of solution at 30 d of the UV light condition, among which 694.6 million particles with a particle size of less than 1 μm were released, which was approximately 100 times of that in the dark condition. The study showed that tire microplastics in aquatic environments were more susceptible to aging and released more small particles under light conditions and that car tire microplastics released more small particles than electric bicycle tire microplastics, posing ecological and environmental risks.

How plastic waste management affects the accumulation of microplastics in waters: a review for transport mechanisms and routes of microplastics in aquatic environments and a timeline for their fate and occurrence (past, present, and future)

An increasing global problem is the buildup of improperly handled plastic garbage in the environment. One of the biggest environmental issues facing aquatic ecosystems today is contamination from bulk plastics and plastic detritus. Specifically, microplastics (MPs) and nanoplastics, which are small-scale plastic waste, are now the main causes of pollution in freshwater and marine environments. On the other hand, contamination of aquatic systems is now acknowledged as one of the major environmental hazards facing our world. Currently, concerns have been raised regarding the breakdown of plastic products into micro and nanosized particles, because of the ineffective plastic waste management. To prioritize regions for mitigation policy implementation, it is critical to pinpoint the precise MPs’ transport mechanisms and the locations where trash is created. In order to show the historical and contemporary circumstances as well as forecasts and scenarios of global plastic waste management from now until 2060, we used continent-level data on trash management. This study, finally, presents a potential future scenario of estimates on the destiny, transport, and occurrence of plastic waste in aquatic habitats, highlighting the different factors that trigger the transport of MPs into water and the necessity of rational management of plastic waste.

Adsorption of Macrolide Antibiotics and a Metabolite onto Polyethylene Terephthalate and Polyethylene Microplastics in Aquatic Environments.

Microplastics (MPs) and antibiotics are emerging pollutants widely found in aquatic environments, potentially causing environmental harm. MPs may act as carriers for antibiotics, affecting their environmental distribution. This study investigates the adsorption of four macrolide antibiotics and a metabolite onto two types of MPs: polyethylene terephthalate (PET) and polyethylene (PE). Results revealed a linear isotherm adsorption model, with higher adsorption to PET than to PE (R2 > 0.936 for PE and R2 > 0.910 for PET). Hydrophobic interactions and hydrogen bonding could be the main adsorption mechanisms, with pore filling potentially involved. Reduced particle size enhances adsorption due to the increase of active adsorption sites. This increasement is more pronounced in PE than in PET, leading to an 11.6% increase in the average adsorption of all macrolides to PE, compared to only 5.1% to PET. Dissolved organic matter inhibits adsorption (azithromycin adsorption to PE was reduced from 12% to 5.1%), while salinity enhances it just until 1% salinity. pH slightly influences adsorption, with maximal adsorption at neutral pH. Results in real samples showed that complexity of the matrix decreased adsorption. Overall, these findings indicate that PE and PET MPs can be a vector of macrolides in aquatic environments.

Polystyrene microplastics enhance microcystin-LR-induced cardiovascular toxicity and oxidative stress in zebrafish embryos

The health risks associated with combined exposure to microplastics (MPs) and cyanobacteria toxins have gained increasing attention due to the large-scale prevalence of cyanobacterial blooms and accumulation of MPs in aquatic environments. Therefore, we explored the cardiovascular toxic effects of microcystin-LR (MC-LR, 1, 10, 100 μg/L) in the presence of 5 μm polystyrene microplastics (PS-MPs, 100 μg/L) and 80 nm polystyrene nanoplastics (PS-NPs, 100 μg/L) in zebrafish models. Embryos were exposed to certain PS-MPs and PS-NPs conditions in water between 3 h post-fertilization (hpf) and 168 hpf. Compared to MC-LR alone, a significant decrease in heart rate was observed as well as notable pericardial edema in the MC-LR + PS-MPs/NPs groups. At the same time, sinus venosus and bulbus arteriosus (SV-BA) distances were significantly increased. Furthermore, the addition of PS-MPs/NPs caused thrombosis in the caudal vein and more severe vascular damage in zebrafish larvae compared to MC-LR alone. Our findings revealed that combined exposure to PS-NPs and MC-LR could significantly decreased the expression of genes associated with cardiovascular development (myh6, nkx2.5, tnnt2a, and vegfaa), ATPase (atp1a3b, atp1b2b, atp2a1l, atp2b1a, and atp2b4), and the calcium channel (cacna1ab and ryr2a) compared to exposure to MC-LR alone. In addition, co-exposure with PS-MPs/NPs exacerbated the MC-LR-induced reactive oxygen species (ROS) production, as well as the ROS-stimulated apoptosis and heightened inflammation. We also discovered that astaxanthin (ASTA) treatment partially attenuated these cardiovascular toxic effects. Our findings confirm that exposure to MC-LR and PS-MPs/NPs affects cardiovascular development through calcium signaling interference and ROS-induced cardiovascular cell apoptosis. This study highlights the potential environmental risks of the co-existence of MC-LR and PS-MPs/NPs for fetal health, particularly cardiovascular development.

Modeling of microplastics degradation in aquatic environments using an experimental plan

The aim of this article is to apply advanced predictive modeling techniques to understand the degradation process of microplastics in aquatic environments. Utilizing a Fractional Factorial Central Composite Experimental Plan, this study seeks to develop precise predictive statistical models that enable forecasting the quantity of pollutants generated during the degradation of microplastics under various environmental conditions. This tool was applied to model changes in DOC (dissolved organic carbon) and DEHP (bis(2-ethylhexyl) phthalate) values during the degradation of microplastics in aquatic ecosystems. The methods were developed using data derived from laboratory tests conducted using the GC-MS technique. The obtained approximating functions, considering factors such as degradation time, water temperature, and particle size, significantly reduced the analysis time. A two-stage verification of the approximating functions was conducted, considering the accuracy of the function form, its adequacy, the statistical significance of input variables, and their correlation with DOC and DEHP. The employed a Fractional Factorial Central Composite Experimental Plan allowed for the simultaneous reduction in the number of experiments and prediction of the influence of variables on the output values. Precise predictive models support understanding of the microplastic degradation process, facilitating the development of effective strategies for managing this pollution.

Study of Advanced Techniques for Inquisition, Segregation and Removal of Microplastics from Water Streams: Current Insights and Future Directions

The present research covers different analytical methods utilized for the diagnosis and characterization of microplastics (MPs) in water and wastewater, such as particle size distribution analysis, and focuses on the sources and forms of MPs in receiving environments. First, we look at the most recent collection techniques, which include a variety of spectroscopic, chromatographic, and microscopic approaches used to identify and measure microplastics in water samples. We then investigate separation techniques designed to separate microplastics from diverse environmental matrices. This involves applying existing methods of separation based on density, such as centrifugation, flotation, and sedimentation, as well as more recent ones, like the use of microfluidic devices and materials for selective adsorption. Lastly, we look into removal methods aimed to reduce the buildup of microplastics in aquatic environments. These include enzymatic breakdown, coagulation/flocculation, and filtering, among other physical, chemical, and biological techniques.

Size-selective attachment of polyvinyl chloride microplastics on iron oxides in aqueous environments

The interaction of microplastics (MPs) with mineral particles is a crucial process determining the fate of MPs in aquatic environments, but potential size-selective interaction of MPs with minerals is unknown. In this work, strong and multi-layered attachment of a mix of heterogeneously size of polyvinyl chloride (PVC) MPs was observed on all the four types of iron oxides, following an order of Fe3O4-i > Fe3O4-s > γ-Fe2O3 > Fe3O4-n. Electrostatic attraction dominated their strong attachment, while hydrogen bonding and halogen bonding also contributed to MPs-mineral interaction. Importantly, both attachment rates and capacities were more favorable for large-sized PVC MPs (> 1.0 μm) than small-sized MPs (0.6–1.0 μm), due to more available attachment sites and stronger electrostatic attraction. Large-sized MPs preferred to detach from iron oxides before small-sized MPs, confirming by configuration analysis. The attachment accelerated the sedimentation of PVC MPs, while a fraction (i.e., 26.7 %, PVC/iron oxide ratio at 0.2:1) of heteroaggregates floated at the air–water interface associated with bubbles. Natural organic matter decreased MPs-mineral interaction due to competitive adsorption, electrostatic repulsion, and steric hindrance, while the attachment was enhanced with increasing ionic strengths (0–200 mM). These findings contribute to a better understanding of the transport and fate of MPs in aquatic systems.

Understanding microplastic aging driven by photosensitization of algal extracellular polymeric substances

The aging of microplastics (MPs) is extremely influenced by photochemically-produced reactive intermediates (PPRIs), which are mediated by natural photosensitive substances. Algal extracellular polymeric substances (EPS) can produce PPRIs when exposed to sunlight. Nonetheless, the specific role of EPS in the aging process of MPs remains unclear. This work systematically explored the aging process of polystyrene (PS) MPs in the EPS secreted by Chlorella vulgaris under simulated sunlight irradiation. The results revealed that the existence of EPS accelerated the degradation of PS MPs into particles with sizes less than 1 µm, while also facilitating the formation of hydroxy groups on the surface. The release rate of dissolved organic matter (DOM) from PS MPs was elevated from 0.120 mg·L-1·day-1 to 0.577 mg·L-1·day-1. The primary factor contributing to the elevated levels of DOM was humic acid-like compounds generated through the breakdown of PS. EPS accelerated the aging process of PS MPs by primarily mediating the formation of triplet excited states (3EPS*), singlet oxygen (1O2), and superoxide radicals (O2∙-), resulting in indirect degradation. 3EPS* was found to have the most substantial impact. This study makes a significant contribution to advance understanding of the environmental fate of MPs in aquatic environments impacted by algal blooms.