Although microplastics are ubiquitous in today’s natural environments, our understanding of the materials, quantities, and particle sizes involved remains limited. The recovery of microplastics from different types of environmental matrices requires standardized matrix digestion protocols that allow inter-laboratory comparisons and that have no effect on the polymers themselves. A number of commonly used digestion methods rely on oxidation with concentrated hydrogen peroxide solutions to remove organic matter from the matrix. However, this can alter the nature of polymers through hydrolysis and often does not lead to a complete matrix removal. We have therefore investigated the use of two altered matrix digestion protocols, an acidic (Fenton) protocol and a new alkaline (Basic Piranha) protocol, focusing mainly on the effect on biodegradable polymers (polylactide, polybutylene adipate terephthalate, polybutylene succinate) and polymers with known degradation pathways via hydrolysis (thermoplastic polyurethanes, polyamide). Comparing the initial surface textures, chemical compositions, and particle size distributions with those obtained after digestion revealed that the Fenton protocol left most of the polymers unchanged. The ferrous residue that remains following Fenton digestion had no effect on either the polymer composition or the particle size distribution, but could disturb further analytics (e.g. Raman microscopy due to auto-fluorescence). While increasing the chance of complete matrix removal, the more powerful Basic Piranha protocol is also more likely to affect the polymer properties: Polylactide polymers in particular showed signs of degradation under alkaline digestion (reduced polylactide content, holes in the polymer matrix), indicating the unsuitability of the Basic Piranha protocol in this specific case. Polyamide, however, remained stable during the Basic Piranha treatment, and the surface chemistry, the particle size as well as the molar mass distribution of the investigated thermoplastic polyurethanes were also not affected. Hence, this protocol offers a powerful alternative for microplastic analysis with focus on particle size in more complex environmental matrices (e.g. removal of cellulose in soil), while avoiding ferrous Fenton residue. Unexpectedly, also tire rubber, a frequent target analyte in microplastic monitoring, was found to be susceptible to artefact structures by both oxidation protocols. In summary, controls for the specific combination of polymer and sample preparation protocol are highly recommended to select the most fitting protocol. Here selected suitable combinations are reported.

No abstract

The application of copper‐catalyzed azide/alkyne cycloaddition to monomers containing a ferrocene unit leads to polyferrocenes with ferrocene in the backbone. Catalyst performance and kinetic studies of a model system comprising 1,1'‐bis(azidoethyl)ferrocene and propargyl ether revealed the usage of CuI and DBU as the catalyst in DMF at 50 °C as efficient reaction conditions for the synthesis. The resulting polymers display molecular weight‐averages up to $\overline {M} _{{\rm n}} $ = 10 000 and $\overline {M} _{{\rm w}} $ = 33 000. The polyaddition of monomers both containing ferrocene units led to polyferrocenes with $\overline {M} _{{\rm n}} $ between 4 000 and 11 000 ($\overline {M} _{{\rm w}} $ up to 78 000). The present study thus provides a pathway to polyferrocenes based on modular ligation chemistry. magnified image

We introduce an avenue for the structural elucidation of bio-inspired functional poly(catecholamines) via high-resolution electrospray ionization mass spectrometry.