Micro- and nanoplastic (pMP and pNP, respectively) release is an emerging issue since these particles constitute a ubiquitous and growing pollutant, which not only threatens the environment but may have potential consequences for human health. In particular, there is concern about the release of secondary pMP and pNP from the degradation of plastic consumer products. The phenomenon is well-documented in relation to plastic waste in the environment but, more recently, reports of pMP generated even during the normal use of plastic food contact materials, such as water bottles, tea bags, and containers, have been published. So far, a validated and harmonized strategy to tackle the issue is not available. In this study, we demonstrate that plastic breakdown to pMP and pNP can occur during the normal use of polyethylene (PE) rice cooking bags and ice-cube bags as well as of nylon teabags. A multi-instrumental approach based on Raman microscopy, X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and particular attention on the importance of sample preparation were applied to evaluate the chemical nature of the released material and their morphology. In addition, a simple method based on Fourier transform infrared (FT-IR) spectroscopy is proposed for pNP mass quantification, resulting in the release of 1.13 ± 0.07 mg of nylon 6 from each teabag. However, temperature was shown to have a strong impact on the morphology and aggregation status of the released materials, posing to scientists and legislators a challenging question: are they micro- or nanoplastics or something else altogether?

Hydrophobicity is an important parameter for the risk assessment of chemicals, but standardised quantitative methods for the determination of hydrophobicity cannot be applied to nanomaterials. Here we describe a method for the direct quantification of the surface energy and hydrophobicity of nanomaterials. The quantification is obtained by comparing the nanomaterial binding affinity to two or more engineered collectors, i.e. surfaces with tuned hydrophobicity. In order to validate the concept, the method is applied to a set of nanoparticles with varying degrees of hydrophobicity. The technique described represents an alternative to the use of other methods such as hydrophobic interaction chromatography or water–octanol partition, which provide only qualitative values of hydrophobicity.

Since nanoplastics are currently considered potentially hazardous to the environment and human health, reliability of studies on nanoplastic exposure becomes crucial. However, analytical challenges limit our understanding of their formation and detection, thus hampering their biological interactions assessment. Here we provide a combined approach to quantitatively and qualitatively detect the release of nanoplastics in water matrix and, in particular, to measure direct exposure of consumers by simulated use of drinking water plastic bottles. We measured that the polyethylene sealing of the bottles released particles with a size distribution ranging from few hundreds nanometers up to about one micron and estimated a mass release in the order of few tenths of nanograms per opening/closing cycle. We observe that mechanical stress alters the physical-chemical characteristics of the generated secondary nanoplastics and degrades the material properties compared to the original bulk source, thus complicating their spectroscopic chemical identification. Our findings demonstrate that understanding material degradation processes is therefore crucial for identifying and quantifying nanoplastics in real samples. Moreover, methods allowing quantitative studies on the release of nanoplastic as a source of exposure are considered essential for proper assessment of their potential health hazards and to promote improvements in consumer products plastic packaging design.

Overview of natural and engineered material-binding peptides and the molecular forces crucial for their (material-specific) binding to material surfaces.

Plastic particulates in the environment pose an increasing concern for regulatory bodies due to their potential risk to higher organisms (including humans) as they enter the food chain. Nanoplastics (defined here as smaller than 1 μm) are particularly challenging to detect and analyze at environmentally relevant concentrations and in biological matrices. The tunicate Ciona Robusta is an effective bioindicator for microplastics and nanoplastic contamination in the marine environment, due to its capacity to filter substantial volumes of water and to accumulate particulates. In this proof-of-principle study that demonstrates a complete methodology, following controlled exposure using spiked samples of a model nanoplastic (100 nm diameter polystyrene spheres) the nanoparticles were separated from an enzymatically digested biological matrix, purified and concentrated for analysis. The described method yields an approximate value for nanoplastic concentration in the organism (with a limit of detection of 10⁶ particles/organism, corresponding to 1 ng/g) and provides the chemical composition by Raman spectroscopy. Furthermore, this method can be extended to other biological matrices and used to quantitatively monitor the accumulation of nanoplastics in the environment and food chain.

This review paper reports a detailed characterization of some combustion or incineration residues and by-products produced in a medium-sized city in Northern Italy. The municipal solid waste incineration (MSWI) generates fly ash, which is a toxic waste. Coal fly ash (CFA) and flue gas desulfurization (FGD) derive from the thermoelectric coal plant located in the same city. Along with these ashes, silica fume and rice husk ash are also considered for the stabilization of fly ash based on their amorphous silica content with the aim to convert them into an inert material. The characterization of all the investigated ashes was performed using different techniques: X-ray diffraction, total reflection X-ray fluorescence, scanning electron microscopy, and transmission electron microscopy. The aim of this work is to describe the reuse possibilities that were proposed for these ashes, which were determined also on the basis of their structural properties. Several possible applications of the investigated ashes are proposed, and the most suitable reuse of stabilized fly ash samples seems to be the production of sustainable plastic composites. This paper shows that the reuse of the by-product materials can allow natural resources to be preserved following the principles of a circular economy.