Sunlight-Driven Photochemical Removal of Polypropylene Microplastics from Surface Waters Follows Linear Kinetics and Does Not Result in Fragmentation.

Floating microplastics are susceptible to sunlight-driven photodegradation, which can convert plastic carbon to dissolved organic carbon (DOC) and can facilitate microplastic fragmentation by mechanical forces. To understand the photochemical fate of sub-millimeter buoyant plastics, ∼0.6 mm polypropylene microplastics were photodegraded while tracking plastic mass, carbon, and particle size distributions. Plastic mass loss and carbon loss followed linear kinetics. At most time points DOC accumulation accounted for under 50% of the total plastic carbon lost. DOC accumulation followed sigmoidal kinetics, not the exponential kinetics previously reported for shorter irradiations. Thus, we suggest that estimates of plastic lifespan based on exponential DOC accumulation are inaccurate. Instead, linear plastic-C mass and plastic mass loss kinetics should be used, and these methods result in longer estimates of photochemical lifetimes for plastics in surface waters. Scanning electron microscopy revealed that photoirradiation produced two distinct patterns of cracking on the particles. However, size distribution analyses indicated that fragmentation was minimal. Instead, the initial population of microplastics shrank in size during irradiations, indicating photoirradiation in tranquil waters (i.e., without mechanical forcing) dissolved sub-millimeter plastics without fragmentation.

Plastic-Rock Complexes as Hotspots for Microplastic Generation.

Discarded plastics and microplastics (MPs) in the environment are considered emerging contaminants and indicators of the Anthropocene epoch. This study reports the discovery of a new type of plastic material in the environment─plastic-rock complexes─formed when plastic debris irreversibly sorbs onto the parent rock after historical flooding events. These complexes consist of low-density polyethylene (LDPE) or polypropylene (PP) films stuck onto quartz-dominated mineral matrices. These plastic-rock complexes serve as hotspots for MP generation, as evidenced by laboratory wet-dry cycling tests. Over 1.03 × 108 and 1.28 × 108 items·m-2 MPs were generated in a zero-order mode from the LDPE- and PP-rock complexes, respectively, following 10 wet-dry cycles. The speed of MP generation was 4-5 orders of magnitude higher than that in landfills, 2-3 orders of magnitude higher than that in seawater, and >1 order of magnitude higher than that in marine sediment as compared with previously reported data. Results from this investigation provide strong direct evidence of anthropogenic waste entering geological cycles and inducing potential ecological risks that may be exacerbated by climate change conditions such as flooding events. Future research should evaluate this phenomenon regarding ecosystem fluxes, fate, and transport and impacts of plastic pollution.

Preliminary Study on the Role of Mangroves in Entrapping Microplastics in Tuticorin Coast of Gulf of Mannar, Southeast Coast of India.

Mangroves constitute a unique and important type of coastal wetlands in tropical and subtropical zones worldwide. The abundance of microplastics (MPs) in the mangrove sediments is poorly understood. This study aimed to quantify the role of mangrove root systems in effectively entrapping MPs in the mangrove areas of Tuticorin and Punnakayal Estuary. It investigated the abundance, characteristics, and weathering patterns of MPs in different mangrove sediments. Sediment samples were collected from ten mangrove sites and two control sites without mangroves. Microplastics were extracted from mangrove sediments by density separation method, and then counted and categorized according to their shape, size, and colour. Microplastics were identified in all ten sampling sites. Punnakayal Estuary has a greater MPs concentration (27 ± 2.65 items/kg dw) than Tuticorin (9.33 ± 2.52 items/kg dw). Also, microplastic concentrations are higher in the mangrove sites than in the control sites. Most MPs are fibres with size ranges of 1-2 mm and 2-3 mm dominating. Blue and transparent are the predominant colours. Four polymers were identified, namely polyethylene (PE), polypropylene (PP), polymethyl methaacrylate (PMMA), and polyurethane (PUR). The degree of weathering was confirmed by carbonyl index and the values vary between 0.28 and 1.25 for PE and 0.6 and 1.05 for PP.

Distribution, characterization and contamination risk assessment of microplastics in the sediment from the world's top sediment-laden estuary.

Microplastics (MPs) have gained a serious attention as an emerging contaminant throughout the world because of their persistence and possible risks to aquatic ecosystems and human well-being. However, knowledge on MPs contamination from sub-tropical coastal systems is limited, and no study has been conducted on the MPs contamination in sediment from one of the highest sediment-laden estuaries, Meghna River, in the world. This is the first study to examine the quantity, morpho-chemical characteristics and contamination risk level of MPs from this large scale river. MPs were extracted from the sediment samples of 10 stations along the banks of the estuary by density separation, and then characterized using a stereomicroscope and Fourier Transform Infrared (FTIR) spectroscopy. The incidence of MPs varied from 12.5 to 55 item/kg dry sediment with an average of 28.67 ± 10.80 item/kg. The majority (78.5%) of the MPs were under 0.5 mm in size, with fibers being the most (74.1%) prevalent MPs type. Polypropylene (PP) was found to be the predominant polymer (53.4%), followed by polyethylene (PE, 20%), polystyrene (PS, 13.3%), and polyvinyl chloride (PVC, 13.3%). The highest occurrence of PP indicted the MPs in the estuary might be originated from clothing and dying industries, fishing nets, food packages, and pulp industries. The sampling stations were contaminated with MPs as shown by the contamination factor (CF) values and pollutant load index (PLI), both of which were >1. This study exposed new insights on the status of MPs in the sediments of the Meghna River, laying the groundwork for future research. The findings will contribute to estimate the global share of MPs to the marine environment.

Recycling of polypropylene by supercritical carbon dioxide for extraction of contaminants from beverage cups. A comparison with polyethylene terephthalate and polylactic acid.

BACKGROUND: EU policies towards a circular economy address plastic packaging as one of the significant concerns and sets ambitious recycling targets. Polyolefins (POs) cannot be recycled for food contact using conventional polyethylene terephthalate (PET) recycling approaches. Thermal degradation prevents the use of high temperatures and, consequently, decontamination of POs may be insufficient when using lower temperatures. Polypropylene (PP) beverage cups were decontaminated using supercritical fluid extraction with carbon dioxide (scCO2 ). Decontamination efficiencies (DEs) of selected markers were determined in challenge tests following European Food Safety Authority guidelines. The effects of time (10-60 min) for PET, polylactic acid (PLA), and PP and temperature (60-80 °C) for PP were studied at constant pressure. The physical properties, sensorial properties, and overall migration of treated scCO2 PP were analysed and compared with virgin PP. RESULTS: PP showed the highest average DE, and PET the lowest, for all the surrogates and in all time conditions. A relative increase in the DE with the increase in process time, particularly for PET and to some extent for PLA, was seen. For PP, no significant impact of time and temperature was observed under the conditions tested. The DE of volatile surrogates was higher than that of semi-volatiles. Results indicate that the scCO2 treatment did not affect the physical and sensorial properties, nor the overall migration of PP, although it contributes to a considerable reduction in extractable n < C24 alkanes. CONCLUSIONS: Results indicate that scCO2 can be used to decontaminate post-consumption PP beverage cups with higher DEs than those for PET and PLA, applying mild processing conditions. © 2022 Society of Chemical Industry.

Investigating biodegradation of polyethylene and polypropylene microplastics in Tehran DWTPs.

Microplastic (MP) pollution is a growing concern and various methods are being sought to alleviate the level of pollution worldwide. This study investigates the biodegradation capacity of MPs by indigenous microorganisms of raw water from Tehran drinking water treatment plants. By exposing polypropylene (PP) and polyethylene (PE) MPs to selected microbial colonies, structural, morphological, and chemical changes were detected by scanning electron microscope (SEM), cell weight measurement, Fourier transform infrared (FTIR), Raman spectroscopy test, and thermal gravimetric analysis (TGA). Selected bacterial strains include Pseudomonas protegens strain (A), Bacillus cereus strain (B), and Pseudomonas protegens strain (C). SEM analysis showed roughness and cracks on PP MPs exposed to strains A and C. However, PE MPs exposed to strain B faced limited degradation. In samples related to strain A, the Raman spectrum was completely changed, and a new chemical structure was created. Both TGA and FTIR analysis confirmed changes detected by Raman analysis of PP and PE MPs in chemical changes in this study. The results of cell dry weight loss for microbial strains A, B, and C were 13.5, 38.6, and 25.6%, respectively. Moreover, MPs weight loss was recorded at 32.6% for PP MPs with strain A, 13.3% for PE MPs with strain B, and 25.6% for PP MPs with strain C.

Identification and Quantification of Microplastics in the Marine Environment Using the Laser Direct Infrared (LDIR) Technique.

Here, we evaluate for the first time the performances of the newly developed laser direct infrared (LDIR) technique and propose an optimization of the initial protocol for marine microplastics (MPs) analysis. Our results show that an 8 µm porosity polycarbonate filter placed on a Kevley slide enables preconcentration and efficient quantification of MPs, as well as polymer and size determination of reference plastic pellets of polypropylene (PP), polyethylene (PE), polystyrene (PS), polyvinyl chloride (PVC), and polyethylene terephthalate (PET), with recoveries ranging from 80-100% and negligible blank values for particle sizes ranging from 200 to 500 µm. A spiked experiment using seawater, sediment, mussels, and fish stomach samples showed that the method responded linearly with significant slopes (R2 ranging from 0.93-1.0; p < 0.001, p < 0.01). Overall, 11 polymer types were identified with limited handling and an analysis time of ca. 3 h for most samples and 6 h for complex samples. Application of this technique to Mediterranean marine samples (seawater, sediment, fish stomachs and mussels) indicated MP concentrations and size distribution consistent with the literature. A high predominance of PVC (sediment, fish stomachs) and PE and PP (seawater, mussels) was observed in the analyzed samples.

Identification and Quantification of Nanoplastics in Surface Water and Groundwater by Pyrolysis Gas Chromatography-Mass Spectrometry.

Nanoplastics (NPs) are currently considered an environmental pollutant of concern, but the actual extent of NP pollution in environmental water bodies remains unclear and there is not enough quantitative data to conduct proper risk assessments. In this study, a pretreatment method combining ultrafiltration (UF, 100 kDa) with hydrogen peroxide digestion and subsequent detection with pyrolysis gas chromatography-mass spectrometry (Py-GC/MS) was developed and used to identify and quantify six selected NPs in surface water (SW) and groundwater (GW), including poly(vinylchloride) (PVC), poly(methyl methacrylate) (PMMA), polypropylene (PP), polystyrene (PS), polyethylene (PE), and poly(ethylene terephthalate) (PET). The results show that the proposed method could detect NPs in environmental water samples. Nearly all selected NPs could be detected in the surface water at all locations, while PVC, PMMA, PS, and PET NPs were frequently below the detection limit in the groundwater. PP (32.9-69.9%) and PE (21.3-44.3%) NPs were the dominant components in both surface water and groundwater, although there were significant differences in the pollution levels attributed to the filtration efficiency of riverbank, with total mass concentrations of 0.283-0.793 µg/L (SW) and 0.021-0.203 µg/L (GW). Overall, this study quantified the NPs in complex aquatic environments for the first time, filling in gaps in our knowledge about NP pollution levels and providing a useful methodology and important reference data for future research.

Alcohol Pretreatment to Eliminate the Interference of Micro Additive Particles in the Identification of Microplastics Using Raman Spectroscopy.

Raman spectroscopy is an indispensable tool in the analysis of microplastics smaller than 20 µm. However, due to its limitation, Raman spectroscopy may be incapable of effectively distinguishing microplastics from micro additive particles. To validate this hypothesis, we characterized and compared the Raman spectra of six typical slip additives with polyethylene and found that their hit quality index values (0.93-0.96) are much higher than the accepted threshold value (0.70) used to identify microplastics. To prevent this interference, a new protocol involving an alcohol treatment step was introduced to successfully eliminate additive particles and accurately identify microplastics. Tests using the new protocol showed that three typical plastic products (polyethylene pellets, polyethylene bottle caps, and polypropylene food containers) can simultaneously release microplastic-like additive particles and microplastics regardless of the plastic type, daily-use scenario, or service duration. Micro additive particles can also adsorb onto and modify the surfaces of microplastics in a manner that may potentially increase their health risks. This study not only reveals the hidden problem associated with the substantial interference of additive particles in microplastic detection but also provides a cost-effective method to eliminate this interference and a rigorous basis to quantify the risks associated with microplastic exposure.

A comparative study on the distribution behavior of microplastics through FT-IR analysis on different land uses in agricultural soils.

Plastic materials have been variously exposed to arable land for decades through soil mulching, plastic housing, and sewage sludge composting. Their mechanical abrasion and biochemical degradation induce the proliferation of myriad microplastics that can further be broken into smaller nano-sized pieces that can be further accumulated in living organisms (including soil invertebrates, fruits, and vegetables); they can also be widely dispersed in neighboring environments. Despite the intensive use of plastics in agriculture, little is known about their origin of occurrence and environmental fate, especially with a size below 100 µm. Therefore, in this study, microplastics with a size in the range of 20-2,000 µm were investigated in soil samples obtained from three different conditions of land uses: tilled with plastic mulch, bare ground (i.e., uncultivated land), and in between the greenhouses of the farmland D located in Namyangju-si, Gyeonggi-do, Republic of Korea. They were primarily identified using Fourier transform infrared (FT-IR) spectroscopy coupled with a microscope. Prior to performing the analysis, microplastic extraction from the soil samples was validated using standardized high-density polyethylene (HDPE) microplastics of various sizes ranging from 20 to 500 µm. As a result, the number of microplastics was estimated to be (241 ± 52), (195 ± 37), and (306 ± 56) particles per kg of dry soil in tillage, bare ground, and in between greenhouses, respectively. They consist of polyethylene (PE), polypropylene (PP), and poly(ethylene terephthalate) (PET), which are the basic constituents of commonly used agricultural products. The particle size distribution depends on the type of plastic, the time elapsed since their usage, and the degree and duration of environmental exposure; the plastic particle sizes were smaller in tillage and around the greenhouses since agricultural films have been weathered for a long time, whereas those with relatively large sizes were found in the uncultivated.

Migration of Microplastics and Phthalates from Face Masks to Water.

Since the outbreak of COVID-19, face masks have been introduced in the complex strategy of infection prevention and control. Face masks consist of plastic polymers and additives such as phthalates. The aim of this study was to evaluate the migration of microplastics (MP) and phthalates from face masks to water. Four types of masks including FFP2 masks and surgical were studied. Masks were first characterized to determine the different layers and the material used for their fabrication. Then, masks were cut into 20 pieces of 0.5 cm2, including all their layers, placed in water, and the migration of MP and phthalates was evaluated according to the conditions stated in EU Regulation No 10/2011 on plastic materials and articles intended to come into contact with food. For MP, the morphological analysis (shape, dimension, particle count) was performed using a stereomicroscope, while the identification of both masks and MP released was conducted using µ-Fourier-transform infrared spectroscopy (µ-FT-IR). Migration of phthalates was assessed by ultra-high-performance liquid chromatography coupled to triple quadrupole mass spectrometer (UPLC-MS/MS). Face masks analyzed in the present study were made of atactic polypropylene (PP) as stated by the manufacturer. The µ-FT-IR confirmed that PP and polyamide (PA) were released as fragments, while both PP and polyester (PES) were released as fibers. In addition, 4 phthalates were identified at concentrations between 2.34 and 21.0 µg/mask. This study shows that the migration study can be applied to evaluate the potential release of MP and phthalates from face masks to water and could give a hint for the potential impact of their incorrect disposal on the aquatic resources.

Spatial and seasonal distribution of microplastic in surface water of Bueng Boraphet Wetland-a Ramsar wetland in Thailand.

This study sought to assess microplastic contamination in the surface water of the inland freshwater wetland, Bueng Boraphet Wetland, Thailand, which is a lentic system with various land-use patterns, including community areas, agricultural areas, and natural resource conservation areas. In 2019, water samples were collected during the wet and dry periods from the three land-use zones at depths of 0-30 cm using a plankton net with 333 µm in mesh size. The water samples were digested via a wet peroxide oxidation process prior to the identification of microplastic morphology using a stereomicroscope. The polymer types of microplastic were analyzed using Fourier transform infrared spectrophotometry. Microplastic was found to range from 0.00 to 4.61 particles/m2 (0.34 ± 0.81 particles/m2) or 0.0 to 19.57 particles/m3 (1.44 ± 3.4 particles/m3). Furthermore, significantly high amounts of microplastics were found in samples from the community area. No microplastic was detected in the sample from the natural resource conservation area. The quantity of microplastic did not significantly differ between the sampling periods. Polymer types, including polyester, polypropylene, and polyethylene terephthalate, were identified in this study. The microplastics were predominantly small and were colored black or red. Microplastic with a fiber shape (93.8%) was observed. Besides the specific gravity of the microplastic and hydrological characteristics, the high concentration of microplastics found in samples from the community area (0.62 ± 0.79 particles/m2 or 2.63 ± 3.36 particles/m3) is likely related to the high human pressure. As microplastic contamination can impact aquatic animals and wetland ecosystems, appropriate control measures for human activities and plastic waste management are required.

Seasonal variation and complex analysis of microplastic distribution in different WWTP treatment stages in Lithuania.

Industrial wastewater, domestic wastewater, and stormwater are the three entry points for microplastics (MP) in wastewater treatment plants. Extreme weather conditions, such as rising temperatures and heavy rainfall caused by climate change, can alter the rate at which MP enters wastewater treatment plants. In this study, wastewater and sludge samples from different treatment stages were collected during a 12-month sampling campaign (seasonal) to determine the efficiency of a municipal wastewater treatment plant in removing microplastic particles. MP ranging from 20 to 1000 µm were detected and classified by shape, color, size, and chemical composition. All samples contained MP particles, with concentration ranging from 1964 ± 50-2982 ± 54 MP/L in influent to 744 ± 13-1244 ± 21 MP/L in effluent and 91.1 ± 8-61.9 ± 5 MP/g in sludge; 71.6-90.1% identified particles were fragment-type with black, white, and transparent colors. Most of the microplastic particles were removed in the activated sludge tank, while the average removal rate in the wastewater treatment plant was 57%. The total concentration of MP was 27% higher in spring than in other seasons. The most common microplastic particles were polyethylene terephthalate (PET), polystyrene (PS), and polypropylene (PP). These results demonstrate the value of long-term monitoring and MP quantification, which would provide a more accurate estimate of MP pollution from wastewater treatment plants.

Effects of Water and Chemical Solutions Ageing on the Physical, Mechanical, Thermal and Flammability Properties of Natural Fibre-Reinforced Thermoplastic Composites.

Biocomposites comprising a combination of natural fibres and bio-based polymers are good alternatives to those produced from synthetic components in terms of sustainability and environmental issues. However, it is well known that water or aqueous chemical solutions affect natural polymers/fibres more than the respective synthetic components. In this study the effects of water, salt water, acidic and alkali solutions ageing on water uptake, mechanical properties and flammability of natural fibre-reinforced polypropylene (PP) and poly(lactic acid) (PLA) composites were compared. Jute, sisal and wool fibre- reinforced PP and PLA composites were prepared using a novel, patented nonwoven technology followed by the hot press method. The prepared composites were aged in water and chemical solutions for up to 3 week periods. Water absorption, flexural properties and the thermal and flammability performances of the composites were investigated before and after ageing each process. The effect of post-ageing drying on the retention of mechanical and flammability properties has also been studied. A linear relationship between irreversible flexural modulus reduction and water adsorption/desorption was observed. The aqueous chemical solutions caused further but minor effects in terms of moisture sorption and flexural modulus changes. PLA composites were affected more than the respective PP composites, because of their hydrolytic sensitivity. From thermal analytical results, these changes in PP composites could be attributed to ageing effects on fibres, whereas in PLA composite changes related to both those of fibres present and of the polymer. Ageing however, had no adverse effect on the flammability of the composites.

Toxicological risk assessment of bisphenol a released from dialyzers under simulated-use and exaggerated extraction conditions.

Bisphenol A (BPA) belongs to a group of chemicals used in the production of polycarbonate, polysulfone, and polyethersulfone which are used, among other applications, in the manufacture of dialyzers. While exposure to BPA is widespread in the general population, dialysis patients represent a population with potentially chronic parenteral BPA exposures. To assess the potential risk of BPA exposure to dialysis patients through dialyzer use, exposure estimates were calculated based on BPA levels measured by ultra-high performance liquid chromatography-quadrupole time-of-flight mass spectrometry following extractions from dialyzers manufactured by Fresenius Medical Care. Extraction conditions included both simulated-use leaching and exaggerated extractions to evaluate possible leachable and extractable BPA, respectively, from the devices. The mean BPA concentrations were 3.6 and 108.9 ppb from simulated-use and exaggerated extractions, respectively, from polycarbonate-containing dialyzers. No BPA was detected from polypropylene-containing dialyzers. Margins of Safety (MOS) were calculated to evaluate the level of risk to patients from estimated BPA exposure from the dialyzers, and the resulting MOS were 229 and 45 for simulated-use and exaggerated extractions, respectively. The findings suggest that there is an acceptable level of toxicological risk to dialysis patients exposed to BPA from use of the dialyzers tested in the current study.

Current research and perspective of microplastics (MPs) in soils (dusts), rivers (lakes), and marine environments in China.

In this study, we first reviewed the current research progress regarding the presence of environmental microplastics (MPs) in environment in China from 2010 to 2019. Results showed that: (1) current research has primarily focused on river and marine environments rather than soils and dusts, mainly located in eastern China, i.e., the Yangtze river, Poyang lake, Dongting lake, Yellow sea, and Bohai sea; (2) the abundance of MPs found in water bodies (sediments) of the rivers in China ranged from 3.9 to 7900 items·m-3 (19.0 × 103-13600.5 × 103 items·km-2), and 20-24300 items·kg-2 (170-5500 × 106 items·km-2) in the sediments, respectively; in lake water the range was 340-8900 items·m-3 (5 × 103-340 × 105 items·km-2) and 8 to 1200 items·m-2/25-300 items·kg-1 in the sediments, respectively; in marine water the range was 0.003-540 items·m-3 (0-380,100 item·km-2) and 1.3-14700 item·kg-1 in the sediments, respectively; in fish, shellfish, and natural planktons from ocean and freshwater, the range was 0-57 items·individuals-1 (0-168 items·g-1); (3) The absorption and toxicological effects of MPs in freshwater and oceans have mainly focused on polyethylene (PE), polypropylene (PP), and polystyrene (PS); (4) the sources of microplastics in soils and dusts primarily come from urban/town activities; for rivers and lakes (estuary), they primarily come from urban activities; for coastal waters, fishing gear and nets, and the maritime activities were the main sources.

Microplastics in Salt of Tuticorin, Southeast Coast of India.

Microplastics (< 5 mm) are considered to be global environmental pollutants. This study investigates the occurrence, physical properties, polymer composition and surface morphology, and element composition of MPs present in food-grade salts produced from seawater and bore-well water in Tuticorin, Tamil Nadu, Southeast coast of India. Fourteen different brands of sea salts and bore-well salts were collected from the salt manufacturing units. The mean abundance of microplastics was 35 ± 15 to 72 ± 40 items/kg in sea salt and 2 ± 1 to 29 ± 11 items/kg in bore-well salt. Four types of polymers viz. polyethylene (51.6%), polypropylene (25%), polyester (21.8%), and polyamide (1.6%) were found in salt. Polyethylene fibers of size ranging from 100 to 500 µm were observed commonly. Being manufactured from seawater, sea salt had the highest quantities of different microplastic particles. The study reveals that people consume approximately 216 particles of MPs per year via sea salt and 48 items per year via bore-well salt if the average person has a daily salt intake of 5 g. The surface morphology of MPs as exhibited in the SEM-EDAX images obtained in the study revealed the different weathering features of MPs, such as pits, cracks, and particles adhering to the surface. The presence of the elements Fe, As, and Ni on the surfaces as identified by energy-dispersive x-ray spectroscopy indicates that these elements exist in the environment as contaminants and have become associated with the MPs. The trace metals adsorbed onto MPs increase the risks of human exposure and may cause some adverse effects in humans.

Distribution and Characterization of Microplastics in Surface Waters and the Southern Caspian Sea Coasts Sediments.

The Caspian Sea is the largest enclosed aquatic ecosystem in the world. The combinations of the toxic pollutants with microplastics endanger the Caspian Sea ecosystem. In this work, the distribution of microplastics was studied in surface waters and southern Caspian Sea coasts sediments. The samples were collected from eight stations, including the Tonakabon, Chalos, Nowshahr, Noor, Mahmood Abad, Babolsar, Sari, and Neka coasts. The average concentrations of microplastics in the coastal waters and sediments were 34,490 particles per km2 and 210 particles per kg, respectively. Isolated microplastics were characterized using ATR-FTIR and energy dispersive X-ray (EDS) techniques. The samples exhibited a strong carbon peak in the EDS spectra, which was screened as microplastic particles. The microplastics were mainly fragments and foams and identified as polyethylene, polypropylene, and polystyrene by means of ATR-FTIR spectra. This is the first study to determine the distribution of microplastics in southern Caspian coastal regions.

Exploitation of nitric oxide donors to control bacterial adhesion on ready-to-eat vegetables and dispersal of pathogenic biofilm from polypropylene.

BACKGROUND: Nitric oxide (NO) donors have been used to control biofilm formation. Nitric oxide can be delivered in situ using organic carriers and acts as a signaling molecule. Cells exposed to NO shift from biofilm to the planktonic state and are better exposed to the action of disinfectants. In this study, we investigate the capability of the NO donors molsidomine, MAHAMA NONOate, NO-aspirin and diethylamine NONOate to act as anti-adhesion agents on ready-to-eat vegetables, as well as dispersants for a number of pathogenic biofilms on plastic. RESULTS: Our results showed that 10 pM molsidomine reduced the attachment of Salmonella enterica sv Typhimurium 14 028 to pea shoots and coriander leaves of about 0.5 Log(CFU/leaf) when compared with untreated control. The association of 10 pmol L-1 molsidomine with 0.006% H2 O2 showed a synergistic effect, leading to a significant reduction in cell collection on the surface of the vegetable of about 1 Log(CFU/leaf). Similar results were obtained for MAHMA NONOate. We also showed that the association of diethylamine NONOate at 10 mmol L-1 and 10 pmol L-1 with the quaternary ammonium compound diquat bromide improved the effectiveness of biofilm dispersal by 50% when compared with the donor alone. CONCLUSIONS: Our findings reveal a dual role of NO compounds in biofilm control. Molsidomine, MAHMA NONOate, and diethylamine NONOate are good candidates for either preventing biofilm formation or dispersing biofilm, especially when used in conjunction with disinfectants. Nitric oxide compounds have the potential to be developed into a toolkit for pro-active practices for good agricultural practices (GAPs), hazard analysis and critical control points (HACCP), and cleaning-in-place (CIP) protocols in industrial settings where washing is routinely applied. © 2020 Society of Chemical Industry.

Microplastic abundance, distribution and composition in water, sediments, and wild fish from Poyang Lake, China.

Microplastic pollution in global aquatic environments has aroused increasing concern in recent years. In this study, the occurrence of microplastics in multiple environmental compartments was investigated in Poyang Lake, the largest freshwater lake of China. The abundance of microplastics was respectively 5-34 items/L for surface waters, 54-506 items/kg for sediments, and 0-18 items per individual for wild crucians (Carassius auratus). The distribution of microplastics in Poyang Lake varied heterogeneously in space, with the highest abundance being observed in the middle region of the lake for surface waters and in the northern region for sediments. Anthropogenic and topographic factors were speculated to be the major factors affecting the abundance and distribution of microplastics. The majority of the detected microplastics were found with a size of < 0.5 mm, with fibrous and coloured being the predominant characteristics. Polypropylene (PP) and polyethylene (PE) were the major polymer types of the selected plastic particles, indicating that domestic sewage and fishing activities might be the main sources of microplastics in the lake. No significant correlation was observed between microplastic abundance in surface water and sediment samples. Our results demonstrated the wide occurrence of microplastics in water, sediment and biota of the Poyang Lake, which may assist in extending our knowledge regarding microplastics pollution in inland freshwater systems.