Common Polymers Research Articles

Tunable Late-Transition-Metal-Catalyzed Polymerization for Controlled Polymer Synthesis

As a powerful protocol for the preparation of common polymers, such as polyolefins, polyesters, and polycarbonates, late-transition-metal-catalyzed polymerization can be carried out by controlling the reaction conditions or developing dynamic catalytic systems that use external stimuli to influence the performance of the active sites, resulting in well-defined polymeric materials. In particularly, under the latter conditions, ‘one catalyst’ can provide more than one kind of polymer with a controlled sequence from the monomer mixture, making full use of the prepared catalyst. In this review, tunable modes, including reaction conditions, redox, light or electrochemical properties, Lewis acids, and alkali metal cations, of late-transition-metal-complex (especially iron, cobalt, and nickel)-catalyzed polymerization were collected and thoroughly discussed.

The Pd-catalyzed precise synthesis of self-assembled fluorescent nanoprobes with different molecular weights for enhancing the permeability of cell membrane and targeting lysosomes

As a common polymer, poly (dimethylaminoethyl methacrylate) (PDMAEMA) is mainly used to synthesize medical materials. However, there are few reports about the related polymer fluorescent probes. Moreover, as far as we know, no one has studied the effect of its molecular weight on the performance of polymer probes. In this work, polymer probes (NapNH2(1)-PDM(4), NapNH2(1)-PDM(9), NapNH2(1)-PDM(23), NapNH2(1)-PDM(34)) with different molecular weights were accurately constructed based on 1,8-naphthalimide fluorophore and poly(N,N-dimethylaminoethyl methacrylate) and their photophysical properties were systematically studied. The test results showed that they all showed good photophysical properties. Moreover, the polymer probe NapNH2(1)-PDM(23), which had the best self-assembly effect and good cell permeability, was successfully screened by confocal fluorescence imaging technology. Not only that, the probe NapNH2(1)-PDM(23) could also label lysosomes in cells quickly and accurately. Therefore, this work provided important reference to construct relevant polymer probes with good cell permeability in the future.

Microplastic Accumulation in Catfish and Its Effects on Fish Eggs from Songkhla Lagoon, Thailand

Microplastics have been found to accumulate in freshwater, marine ecosystems, and biological organisms. The frequency of studies on microplastic contamination in organs has increased recently, although there have been relatively fewer investigations on fish eggs in Thailand. To extract microplastics from catfish samples for laboratory analysis (Osteogeneiosus militaris), we used 10% potassium hydroxide in the digestion process. A needle penetrated the fish eggs to investigate microplastic contamination. We examined microplastics under a stereomicroscope and used Fourier transform infrared spectroscopy to determine the type of polymer. We found microplastic contamination in organs, most commonly in the stomach (0.91 ± 0.13 items/g), followed by tissue (0.53 ± 0.09 items/g), and gills (0.30 ± 0.03 items/g) at the level of significance p < 0.01. We found a total of 349 fish eggs with 27 items of microplastic. The dominant microplastic we found in the stomach, tissue, and gills of the fish, as well as in fish eggs, was of fiber shape. We noted that fragments were found only in the stomach and tissue of fish. The dominant color of microplastics was black in organs and blue in fish eggs. The common polymer types in organs and fish eggs were polyethylene terephthalate, polypropylene, and cellulosic fiber.

Microplastic distribution and characteristics across a large river basin: Insights from the Neuse River in North Carolina, USA

While microplastics (MP) have been found in aquatic ecosystems around the world, the understanding of drivers and controls of their occurrence and distribution have yet to be determined. In particular, their fate and transport in river catchments and networks are still poorly understood. We identified MP concentrations in water and streambed sediment at fifteen locations across the Neuse River Basin in North Carolina, USA. Water samples were collected with two different mesh sizes, a trawl net (>335 μm) and a 64 μm sieve used to filter bailing water samples. MPs >335 μm were found in all the water samples with concentrations ranging from 0.02 to 221 particles per m3 (p m−3) with a median of 0.44 p m−3. The highest concentrations were observed in urban streams and there was a significant correlation between streamflow and MP concentration in the most urbanized locations. Fourier Transform Infrared (FTIR) analysis indicated that for MPs >335 μm the three most common polymer types were polyethylene, polypropylene, and polystyrene. There were substantially more MP particles observed when samples were analyzed using a smaller mesh size (>64 μm), with concentrations ranging from 20 to 130 p m−3 and the most common polymer type being polyethylene terephthalate as identified by Raman spectroscopy. The ratio of MP concentrations (64 μm to 335 μm) ranged from 35 to 375, indicating the 335 μm mesh substantially underestimates MPs relative to the 64 μm mesh. MPs were detected in 14/15 sediment samples. Sediment and water column concentrations were not correlated. We estimate MP (>64 μm) loading from the Neuse River watershed to be 230 billion particles per year. The findings of this study help to better understand how MPs are spatially distributed and transported through a river basin and how MP concentrations are impacted by land cover, hydrology, and sampling method.

Effect of synovial fluid temperature on wear resistance of different polymer acetabular materials.

In order to investigate the effect of frictional heat on the wear resistance characteristics of polymeric acetabular materials, the tribological tests and wear numerical analysis of three common polymer acetabular materials were carried out under different synovial fluid temperatures. The study results show that XLPE and VE-XLPE exhibit superior wear resistance compared to UHMWPE in high-temperature, heavy load environments. The coefficient of friction of three materials gradually decreases as the temperature of the synovial fluid increases. The wear depth and wear volume of the three materials increased with the increase of the temperature of the synovial fluid, and the forms of wear at 46°C and 55°C were mainly adhesive wear and plastic deformation. The higher temperature of the synovial fluid accelerates the oxidative degradation of the material surface and generates oxidation functional groups, which leads to the breakage of C-C bonds in the surface molecular chains under the sliding shear effect, thus reducing the mechanical properties of the material. Specifically, the surface of the polymer material will soften at a higher ambient temperature, mainly due to the decrease of hardness, and then deteriorate in the friction property, and finally increase the wear rate. Ansys results showed that the volume wear of the three materials increased with the increase of synovial fluid temperature, and the trend could be approximately linear. Numerical calculations predict that VE-XLPE has the highest wear of 0.693mm3 among the three materials at 37°C, followed by XLPE at 0.568mm3 and UHMWPE with the lowest wear of 0.478mm3. At higher synovial fluid temperatures (46°C, 55°C), VE-XLPE still has the largest wear volume among the three materials, while XLPE and UHMWPE have similar wear. The wear cloud pictures showed that the maximum wear volume occurred near the edge of the acetabulum.

Plastic occurrence in fish caught in the highly industrialized Gulf of İzmit (Eastern Sea of Marmara, Türkiye)

Occurrence of micro- (<5 mm) and mesoplastics (5–25 mm) in twelve fish species caught off Gulf of İzmit in the Sea of Marmara was investigated. Plastics were found in the gastrointestinal tracks of all the analysed species: Trachurus mediterraneus, Chelon auratus, Merlangius merlangus, Mullus barbatus, Symphodus cinereus, Gobius niger, Chelidonichthys lastoviza, Chelidonichthys lucerna, Trachinus draco, Scorpaena porcus, Scorpaena porcus, Pegusa lascaris, Platichthys flesus. From a total of 374 individuals examined plastics were found in 147 individuals (39%). The average plastic ingestion was 1.14 ± 1.03 MP. fish−1 (considering all the analysed fish) and 1.77 ± 0.95 MP. fish−1 (considering only the fish with plastic). Fibres were the primary plastic types found in GITs (74%), followed by films (18%) and fragments (7%), no foams and microbeads were found. A total of ten different colours of plastics were found with blue (62%) being the most common colour. Length of plastics ranged from 0.13 to 11.76 mm with an average of 1.82 ± 1.59 mm. A total of 95.5% of plastics were microplastics, and 4.5% as mesoplastics. The mean frequency of plastic occurrence was higher in pelagic fish species (42%), followed by demersal (38%) and bentho-pelagic species (10%). Fourier-transform infrared spectroscopy confirmed that 75% of polymers were synthetic with polyethylene terephthalate being the most common polymer. Our results indicated that carnivore species with a preference for fish and decapods were the highest impacted trophic group in the area. Fish species in the Gulf of İzmit are contaminated with plastics, representing a potential risk to ecosystem and human health. Further research is needed to understand the effects of plastic ingestion on biota and possible pathways. Results of this study also provide baseline data for the implementation of the Marine Strategy Framework Directive Descriptor 10 in the Sea of Marmara.

Architecture-Controllable Single-Crystal Helical Self-assembly of Small-Molecule Disulfides with Dynamic Chirality.

Beyond the common supramolecular helical polymers in solutions, controlling single-crystal helical self-assembly with precisely defined chirality and architectures has been challenging. Here, we report that simply merging static homochiral amino acids with dynamic chiral disulfides can produce a class of building blocks featuring supramolecular helical single-crystal self-assembly with unusual stereodivergency. Analysis of 20 single-crystal structures of 1,2-dithiolanes gives an atom-precision understanding of the chirality transfer from the molecular to supramolecular level, featuring homochiral and heterochiral helical supramolecular self-assembly in the solid state. The underlying structure-assembly relationship reveals that the synergistic interplay of intermolecular H-bonds and the 1,2-dithiolane ring with adaptive chirality plays a key role in determining the assembly pathway, also involving the effects of residue groups, substituents, molecular stacking, and solvents. The confinement effect in the solid state can stabilize the dynamic stereochemistry of disulfide bonds and selectively result in specific conformers that can minimize the energy of global supramolecular systems. We envision that these results represent a starting point to use dynamic chiral disulfide as a functional entity in supramolecular chemistry and may inspire a new class of supramolecular helical polymers with dynamic functions.

PEO-based polymer blend electrolyte for composite structural battery

ABSTRACT High mechanical strength and ionic conductivity of solid-state electrolyte (SSE) are currently conflicting targets that are very difficult to achieve. Polyethylene oxide (PEO) is one of the most common polymers adopted for SSE because of its very high ionic conductivity, but its mechanical strength is very low. This work discusses the manufacturing and testing of PEO blends using polysulfone (PSf) and Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) to assess the mechanical response under microtensile testing and the ionic conductivity with electrochemical impedance spectroscopy (EIS). Mechanical tests demonstrated a beneficial effect of LiTFSI with significant increase in maximum stress and ductility measured as strain at failure. The blending of PEO and PSf showed promising conductivity values at room temperature with the 90–10 PEO-PSf composition achieving the highest value (1.06 × 10−6 S/cm) and for the 70–30 composition achieving the highest maximum stress (3.5 MPa) with a conductivity of 3.12 × 10−7 S/cm.

Micro(nano)plastics in the atmosphere of the Atlantic Ocean

The occurrence, long-range atmospheric transport and deposition of micro and nano plastics (MNPLs) remains un-quantified for the oceanic atmosphereopen ocean. Here we show the characterisation of MNPLs and the aerosol composition (PM10) in a north-south Atlantic transect from Vigo (Spain) to Punta Arenas (Chile). The analytical procedure to assess the composition of MNPLs consisted of a double suspect screening approach of the polymers and additives, the two constituents of plastics. Polymers were analysed by size exclusion chromatography coupled with high-resolution mass spectrometry using an atmospheric pressure photoionization source operated in positive and negative conditions (HPLC(SEC)-APPI(+/-)-HRMS). Plastic additives were screened with high-performance liquid chromatography coupled to high-resolution mass spectrometry using an electrospray ionisation source (HPLC-ESI(+/-)-HRMS). The most common polymers were polyethylene (PE), polypropylene (PP), polyisoprene (PI), and polystyrene (PS), with the highest polymer concentration being 51.7 ng·m−3 of PI. The air mass back trajectories showed the variable influence of oceanic and terrestrial air masses. These differences were reflected in the aerosol composition with different contributions of Saharan dust, sea spray aerosol, organic/elemental carbon, and MNPLs. Results showed that samples largely influenced by sea-spray and air masses originating from coastal South America and the north Atlantic subtropical gyre were more contaminated by MNPLs. Moreover, this information was complemented by the characterisation of the largest particles using scanning electron microscopy (SEM) and µ-Fourier Transform Infrared Spectroscopy (µ-FTIR). This work provides the first field evidence of the long-range transport of MNPLs in most of the Atlantic Ocean, as the result of dynamic coupling between the lower atmosphere and the surface ocean. Sea-spray formation arises as a key driver for the aerosolisation of MNPLs, and atmospheric transport followed by dry deposition may modulate the occurrence of MNPLs in large oceanic regions, issues that will require future research efforts.

High-Strength, Degradable and Recyclable Epoxy Resin Based on Imine Bonds for Its Carbon-Fiber-Reinforced Composites

Carbon fiber (CF) is widely used in the preparation of carbon-fiber-reinforced polymer composites (CFRP) in which it is combined with epoxy resin due to its good mechanical properties. Thermosetting bisphenol A epoxy resin, as one of the most common polymer materials, is a non-renewable resource, leading to a heavy environmental burden and resource waste. To solve the above problems and achieve high mechanical and thermal properties comparable to those of bisphenol A, herein, a high-performance, degradable and recyclable bio-based epoxy resin was developed by reacting the lignin derivative vanillin with 4-amino cyclohexanol via Schiff base. This bio-based epoxy resin showed a Young's modulus of 2.68 GPa and tensile strength of 44 MPa, 36.8% and 15.8% higher than those of bisphenol A epoxy, respectively. Based on the reversible exchange reaction of the imine bond, the resin exhibited good degradation in an acidic environment and was recoverable by heat treatment. Moreover, the prepared epoxy resin could be used to prepare carbon fiber (CF)-reinforced composites. By washing off the epoxy resin, the carbon fiber could be completely recycled. The recovered carbon fiber was well preserved and could be used again for the preparation of composite materials to realize the complete recovery and utilization of carbon fiber. This study opens a way for the preparation of high-performance epoxy resin and the effective recycling of carbon fiber.

Glycoproteins as a Platform for Making Proton-Conductive Free-Standing Biopolymers.

Biopolymers are an attractive environmentally friendly alternative to common synthetic polymers, whereas primarily proteins and polysaccharides are the biomacromolecules that are used for making the biopolymer. Due to the breadth of side chains of such biomacromolecules capable of participating in hydrogen bonding, proteins and polysaccharide biopolymers were also used for the making of proton-conductive biopolymers. Here, we introduce a new platform for combining the merits of both proteins and polysaccharides while using a glycosylated protein for making the biopolymer. We use mucin as our starting point, whereas being a waste of the food industry, it is a highly available and low-cost glycoprotein. We show how we can use different chemical strategies to target either the glycan part or specific amino acids for both crosslinking between the different glycoproteins, thus making a free-standing biopolymer, as well as for introducing superior proton conductivity properties to the formed biopolymer. The resultant proton-conductive soft biopolymer is an appealing candidate for any soft bioelectronic application.

Lignin-based composites with enhanced mechanical properties by acetone fractionation and epoxidation modification

Epoxy resin is widely used in various fields of the national economy due to its excellent chemical and mechanical properties. Lignin is mainly derived from lignocelluloses as one of the most abundant renewable bioresources. Due to the diversity of lignin sources and the complexity as well as heterogeneity of its structure, the value of lignin has not been fully realized. Herein, we report the utilization of industrial alkali lignin for the preparation of low-carbon and environmentally friendly bio-based epoxy thermosetting materials. Specifically, epoxidized lignin with substituted petroleum-based chemical bisphenol A diglycidyl ether (BADGE) in various proportions was cross-linked to fabricate thermosetting epoxies. The cured thermosetting resin revealed enhanced tensile strength (4.6MPa) and elongation (315.5%) in comparison with the common BADGE polymers. Overall, this work provides a practicable approach for lignin valorization toward tailored sustainable bioplastics in the context of a circular bioeconomy.

Recent Progress of the Preparation and Application of Electrospun Porous Nanofibers.

Electrospun porous nanofibers have gained a lot of interest recently in various fields because of their adjustable porous structure, high specific surface area, and large number of active sites, which can further enhance the performance of materials. This paper provides an overview of the common polymers, preparation, and applications of electrospun porous nanofibers. Firstly, the polymers commonly used to construct porous structures and the main pore-forming methods in porous nanofibers by electrospinning, namely the template method and phase separation method, are introduced. Secondly, recent applications of electrospun porous nanofibers in air purification, water treatment, energy storage, biomedicine, food packaging, sensor, sound and wave absorption, flame retardant, and heat insulation are reviewed. Finally, the challenges and possible research directions for the future study of electrospun porous nanofibers are discussed.

Distribution of microplastics in freshwater systems in an urbanized region: A case study in Flanders (Belgium)

Microplastics (MPs) are an emerging pollutant of concern in all known aquatic ecosystems. However, studies at a regional scale on MP pollution in freshwater systems and the necessary risk assessments are limited. Therefore, in this study, we examined microplastic concentrations, size distributions, and polymer types in surface waters and sediments in the geographic region Flanders (Belgium), as a case study for a densely populated region and one of the most developed parts of Europe. Samples have been taken on nine different locations, of which five were repeated in a different weather condition. In total 43 aqueous and nine sediment samples have been collected. The quantity and identity of the microplastics in the samples were determined with μFTIR spectroscopy in the range of 25–1000 μm. The MPs' abundances in surface waters and sediments ranged from 0 to 4.8 MP L−1 (average = 0.48 MP L−1) and from 0 to 9558 MP kg−1 dry weight (average = 2774.57 ± 2317.93 MP kg−1 DW), respectively. Polystyrene and polypropylene were the most common polymer compositions found. No correlations were observed between microplastic concentrations in the sediment/the surface water samples and the measured environmental variables rainfall, conductivity, pH, dissolved oxygen content, waterway flow rate and width, and surrounding land use. Risk assessment results for the measured surface water concentrations through the risk quotient (RQ) method and the probabilistic risk assessment framework suggest that most of the sampled sites in Flanders posed negligible risks to freshwater biota, while this was not the case for some of the sediment concentrations. Our results illustrate the need to urgently develop analytical methods that can routinely measure the full size range of MP in environmental samples to adequately assess risks for the environment.

Qualitative and quantitative contaminants assessment in recycled pellets from post‐consumer plastic waste by means of spectroscopic and thermal characterization

AbstractThe complexity of any plastic recycling initiative lies in the heterogeneous nature of the post‐consumer commingled plastic waste stream: recycling treatments are challenging without prior reliable sorting. A suitable identification system should be able to recognize different plastics and blends. Nowadays, the main technique used as quality control in plastic waste sorting centers is differential scanning calorimetry, whose result can be purely qualitative or semi‐quantitative, since only the crystalline fraction is evaluated. Moreover, the time required for data acquisition is relatively long. Infrared spectroscopy is an alternative, faster technique extensively used in applied research, but not widely utilized in industry. In this work, the cross‐use of infrared spectroscopy and calorimetry is tested in a real, practical case: the quality control of recycled pellets (namely composed of polyolefins only), which represent the output of a commingled plastic recycling plant and are used as secondary raw materials for different applications. Appropriate infrared spectroscopy calibration curves were built to allow the quantitative analysis with respect to the most common polymers found in the commingled plastic waste stream; the composition and contaminants in the recycled pellets were thereby determined and tracked through different production batches through the cross‐use of the two techniques outlined above.

First Evidence of Microplastic Occurrence in the Marine and Freshwater Environments in a Remote Polar Region of the Kola Peninsula and a Correlation with Human Presence

Microplastics (MPs) have even been detected in remote environments, including high-latitude regions, where human activities are restricted or strongly limited. We investigated the surface water of the bays of the Barents Sea and the freshwater lakes that are located close to and several kilometers from a year-round resident field station in the remote tundra region of the Kola Peninsula. The microplastics' presence in aquatic environments in this region has not been indicated yet. Microplastics were detected in all samples collected from the Barents Sea (<4800 items·m-3) and the lakes (<3900 items·m-3). Fibers made from polyethylene terephthalate (PET)-the most common thermoplastic polymer of the polyester family-and semi-synthetic cellulosic rayon were the most dominant. This indicated that the source of fiber contamination may come from protective clothes, ropes, ship equipment, and fishing nets. Small microplastics can spread through current and atmospheric transport. The Norwegian Current is likely responsible for the lack of correlations found between MP contamination and the distance from the field station between the studied bays of the Barents Sea. On the contrary, a significant correlation with human presence was observed in the concentration of microfibers in the water of the tundra lakes. The number of MP fibers decreased with an increase in the distance from the field station. This is the first study, to the best of our knowledge, that reports such a correlation in a remote region. We also discuss implications for animals. Our results show that even the most isolated ecosystems are not free from microplastic pollution.

Biodegradation of low-density polyethylene plastic waste by a constructed tri-culture yeast consortium from wood-feeding termite: Degradation mechanism and pathway

Polyethylene (PE) is one of the most common synthetic polymers, and PE waste pollution has been an environmental and health concern for decades. Biodegradation is the most eco-friendly and effective approach for plastic waste management. Recently, an emphasis has been placed on novel symbiotic yeasts isolated from termite guts as promising microbiomes for multiple biotechnological applications. This study might be the first to explore the potential of a constructed tri-culture yeast consortium, designated as DYC, isolated from termites for the degradation of low-density polyethylene (LDPE). The yeast consortium DYC stands for the molecularly identified species Sterigmatomyces halophilus, Meyerozyma guilliermondii, and Meyerozyma caribbica. The LDPE-DYC consortium showed a high growth rate on UV-sterilized LDPE as a sole carbon source, resulting in a reduction in tensile strength (TS) of 63.4% and a net LDPE mass reduction of 33.2% compared to the individual yeasts. All yeasts, individually and in consortium, showed a high production rate for LDPE-degrading enzymes. The hypothetical LDPE biodegradation pathway that was proposed revealed the formation of several metabolites, including alkanes, aldehydes, ethanol, and fatty acids. This study emphasizes a novel concept for using LDPE-degrading yeasts from wood-feeding termites for plastic waste biodegradation.

Physics-Based and Data-Driven Polymer Rheology Model

Summary Polymer flooding is a common enhanced oil recovery (EOR) method used to increase aqueous phase sweep efficiency by increasing viscosity. Estimating polymer viscosity for given reservoir conditions (i.e., oil viscosity, temperature, and brine composition) requires intensive laboratory work. There are existing empirical models to estimate polymer bulk rheology without prior laboratory work; however, they have many coefficients, simple brine composition, and lack physics-based regression boundaries. This study benchmarks the existing polymer empirical and machine learning (ML) models against a new data-driven model with some physics basis for common synthetic polymers. We cover a broad range of polymer concentrations, temperature, salinity, and hardness with an upper limit of 5,000 ppm, 120℃, 290,000 ppm, and 33,000 ppm, respectively. The data were preprocessed through data analytics techniques, and a model was developed with some physics basis by fitting Martin’s equation for Carreau model coefficients. Our regression boundaries obey flexible polymers’ physical and laboratory behavior. We benchmarked the bulk rheological model with existing models in the literature. We used the published models’ coefficients and then tuned their coefficients for our data set for a fair comparison. We then investigated ML as a predictive tool without compromising overfitting the data using the simplest ML model (linear regression) all the way to artificial neural network (ANN) and hybrid ML models. This is the first study that comprehensively benchmarks polymer rheology models and proposes a simple, least number of coefficients, and tunable polymer-rheology model. We provide a predictive bulk rheology model that enables the user to accurately predict polymer viscosity without laboratory measurements and for a wide range of temperatures and brine compositions. Moreover, our study includes the recently common polymer SAV-10 that was not previously studied. We present a simple water viscosity model for a broad brine salinity and temperature range. Our study shows that ML techniques might provide deceptively high accuracy for small data sets, unless due diligence is done to avoid a high-variance model.

A comparative characterisation of commercially available lipid-polymer nanoparticles formed from model membranes

From the discovery of the first membrane-interacting polymer, styrene maleic-acid (SMA), there has been a rapid development of membrane solubilising polymers. These new polymers can solubilise membranes under a wide range of conditions and produce varied sizes of nanoparticles, yet there has been a lack of broad comparison between the common polymer types and solubilising conditions. Here, we present a comparative study on the three most common commercial polymers: SMA 3:1, SMA 2:1, and DIBMA. Additionally, this work presents, for the first time, a comparative characterisation of polymethacrylate copolymer (PMA). Absorbance and dynamic light scattering measurements were used to evaluate solubilisation across key buffer conditions in a simple, adaptable assay format that looked at pH, salinity, and divalent cation concentration. Lipid-polymer nanoparticles formed from SMA variants were found to be the most susceptible to buffer effects, with nanoparticles from either zwitterionic DMPC or POPC:POPG (3:1) bilayers only forming in low to moderate salinity (< 600 mM NaCl) and above pH 6. DIBMA-lipid nanoparticles could be formed above a pH of 5 and were stable in up to 4 M NaCl. Similarly, PMA-lipid nanoparticles were stable in all NaCl concentrations tested (up to 4 M) and a broad pH range (3–10). However, for both DIBMA and PMA nanoparticles there is a severe penalty observed for bilayer solubilisation in non-optimal conditions or when using a charged membrane. Additionally, lipid fluidity of the DMPC-polymer nanoparticles was analysed through cw-EPR, showing no cooperative gel-fluid transition as would be expected for native-like lipid membranes.

Understanding the aggregation, consumption, distribution and accumulation of nanoparticles of polyvinyl chloride and polymethyl methacrylate in Ruditapes philippinarum

Plastic products have become an integral part of our life. A widespread usage, high stability, uncontrolled disposal and slow degradation of plastics in the environment led to the generation and accumulation of nanoparticles of polymers (NPs) in the marine environment. However, little is known about the aggregation, consumption and distribution of NPs from common polymers such as polyvinyl chloride (NP-PVC) and polymethyl methacrylate (NP-PMMA) inside marine animal physiologies. In the current study, two types of polymers (PVC and PMMA) × four exposure concentrations (1, 5, 15 and 25 mg/L) × four times (4, 8, 12 and 24 h) exposure studies were conducted to understand the consumption and distribution of luminescent NP-PVC (98.6 ± 17.6 nm) and NP-PMMA (111.9 ± 37.1 nm) in R. philippinarum. Under laboratory conditions, NP-PVC showed a higher aggregation rate than NP-PMMA in seawater within a period of 24 h. Aggregations of NPs increased with an increase in initial NP concentrations, leading to significant settling of nanoparticles within 24 h exposure. Such aggregation and settling of particles enhanced the consumption of NPs by benthic filter-feeding R. philippinarum at all exposure concentrations during 4 h exposure. More interestingly, NP-PVC and NP-PMMA were observed in large amounts in both liver and gills (22.6 % - 29.1 %) of the clams. Furthermore, NP-PVC was detected in most organs of R. philippinarum as compared to NP-PMMA. This study demonstrates that different polymers distribute and accumulate differently in the same biological model under laboratory exposure conditions based on their chemical nature.