Risk assessment framework for microplastic in marine environments.

Constantly raising microplastic (MP) contamination of water sources poses a direct threat to the gentle balance of the marine environment. This study focuses on a multifactor hazard evaluation of conventional (polyethylene - PE, polypropylene - PP, and polystyrene - PS) and alternative (polyethylene terephthalate with 25 % or 50 % recycled material and polylactic acid) plastics. The risk assessment framework explored included MP abundance, water acidification potential, surface oxidation, fragmentation, and bacterial growth inhibition. Based on MP monitoring campaigns worldwide, we conclude that PE-based plastics are the most abundant MPs in water samples (comprise up to 82 % the MP in those samples). A year-long weathering experiment showed that PS-based and PP-based plastics were oxidized to a higher extent, resulting in the highest water acidification with pH reduction of up to three orders of magnitude. Finally, our laboratory experiments showed that weathered PS was the most fragile plastic during mechanical degradation, while both PP- and PS-based plastic extracts showed a significant growth inhibition toward the marine microorganisms (Bacillus sp. and Pseudoaltermonas sp). Using the examined factors as weighted inputs into our framework, this holistic evaluation of hazards suggest that PP-based plastic products were the most hazardous compared to the other conventional and alternative plastic types.

Mediterranean microplastic contamination: Israel's coastline contributions.

This study provides an analysis of the current state of microplastic (MP) contamination along the Mediterranean coastline of Israel. Six strategic sites were monitored in this study - each representing a unique coastal environment. We conclude that Tel Aviv and Hadera, both located near stream estuaries, were highly contaminated (18,777 particles/m3) with MP compared to the other locations. The MP detected included both secondary MP and pristine polymeric pellets. In-depth characterization of the MP illustrated a large percentage of both fragmented and film MP morphologies and the most common MP polymers were polyethylene and polypropylene. Further particle analysis showed that MPs were contaminated with biofilm, including microorganisms such as diatoms, as well as metal residues. Through the spatial analysis presented herein we suggest that local rivers are significant contributors to MP contamination along the Mediterranean Sea coastline of Israel and may pose a direct threat to environment and human health.

1,4-Dioxane as an emerging water contaminant: State of the science and evaluation of research needs.

1,4-Dioxane has historically been used to stabilize chlorinated solvents and more recently has been found as a contaminant of numerous consumer and food products. Once discharged into the environment, its physical and chemical characteristics facilitate migration in groundwater, resulting in widespread contamination of drinking water supplies. Over one-fifth of U.S. public drinking water supplies contain detectable levels of 1,4-dioxane. Remediation efforts using common adsorption and membrane filtration techniques have been ineffective, highlighting the need for alternative removal approaches. While the data evaluating human exposure and health effects are limited, animal studies have shown chronic exposure to cause carcinogenic responses in the liver across multiple species and routes of exposure. Based on this experimental evidence, the U.S. Environmental Protection Agency has listed 1,4-dioxane as a high priority chemical and classified it as a probable human carcinogen. Despite these health concerns, there are no federal or state maximum contaminant levels for 1,4-dioxane. Effective public health policy for this emerging contaminant requires additional information about human health effects, chemical interactions, environmental fate, analytical detection, and treatment technologies. This review highlights the current state of knowledge, key uncertainties, and data needs for future research on 1,4-dioxane.

Reactive, Self-Cleaning Ultrafiltration Membrane Functionalized with Iron Oxychloride Nanocatalysts.

Self-cleaning, antifouling ultrafiltration membranes are critically needed to mitigate organic fouling in water and wastewater treatment. In this study, we fabricated a novel polyvinylidene fluoride (PVDF) composite ultrafiltration membrane coated with FeOCl nanocatalysts (FeOCl/PVDF) via a facile, scalable thermal-treatment method, for the synergetic separation and degradation of organic pollutants. The structure, composition, and morphology of the FeOCl/PVDF membrane were extensively characterized. Results showed that the as-prepared FeOCl/PVDF membrane was uniformly covered with FeOCl nanoparticles with an average diameter of 1-5 nm, which greatly enhanced membrane hydrophilicity. The catalytic self-cleaning and antifouling properties of the FeOCl/PVDF membrane were evaluated in the presence of H2O2 at neutral pH. Using a facile H2O2 cleaning process, we showed that the FeOCl/PVDF membrane can achieve an excellent water flux recovery rate of ∼100%, following organic fouling with a model organic foulant (bovine serum albumin). Moreover, the in situ catalytic production of active hydroxyl radicals by the FeOCl/PVDF membrane was elucidated by electron spin resonance (ESR) and UV analysis. The catalytic performance of the FeOCl/PVDF membrane was further demonstrated by the complete degradation of bisphenol A when H2O2 was dosed in the feed solution at neutral pH. Our results demonstrate the promise of utilizing this novel membrane for the treatment of waters with complex organic pollutants.

Enhanced antibacterial activity through the controlled alignment of graphene oxide nanosheets.

The cytotoxicity of 2D graphene-based nanomaterials (GBNs) is highly important for engineered applications and environmental health. However, the isotropic orientation of GBNs, most notably graphene oxide (GO), in previous experimental studies obscured the interpretation of cytotoxic contributions of nanosheet edges. Here, we investigate the orientation-dependent interaction of GBNs with bacteria using GO composite films. To produce the films, GO nanosheets are aligned in a magnetic field, immobilized by cross-linking of the surrounding matrix, and exposed on the surface through oxidative etching. Characterization by small-angle X-ray scattering and atomic force microscopy confirms that GO nanosheets align progressively well with increasing magnetic field strength and that the alignment is effectively preserved by cross-linking. When contacted with the model bacterium Escherichia coli, GO nanosheets with vertical orientation exhibit enhanced antibacterial activity compared with random and horizontal orientations. Further characterization is performed to explain the enhanced antibacterial activity of the film with vertically aligned GO. Using phospholipid vesicles as a model system, we observe that GO nanosheets induce physical disruption of the lipid bilayer. Additionally, we find substantial GO-induced oxidation of glutathione, a model intracellular antioxidant, paired with limited generation of reactive oxygen species, suggesting that oxidation occurs through a direct electron-transfer mechanism. These physical and chemical mechanisms both require nanosheet penetration of the cell membrane, suggesting that the enhanced antibacterial activity of the film with vertically aligned GO stems from an increased density of edges with a preferential orientation for membrane disruption. The importance of nanosheet penetration for cytotoxicity has direct implications for the design of engineering surfaces using GBNs.