Molecularly imprinted polymers for per- and polyfluoroalkyl substances enrichment and detection.

Per- and polyfluoroalkyl substances (PFAS) are highly toxic pollutants of significant concern as they are being detected in water, air, fish and soil. They are extremely persistent and accumulate in plant and animal tissues. Traditional methods of detection and removal of these substances use specialised instrumentation and require a trained technical resource for operation. Molecularly imprinted polymers (MIPs), polymeric materials with predetermined selectivity for a target molecule, have recently begun to be exploited in technologies for the selective removal and monitoring of PFAS in environmental waters. This review offers a comprehensive overview of recent developments in MIPs, both as adsorbents for PFAS removal and sensors that selectively detect PFAS at environmentally-relevant concentrations. PFAS-MIP adsorbents are classified according to their method of preparation (e.g., bulk or precipitation polymerization, surface imprinting), while PFAS-MIP sensing materials are described and discussed according to the transduction methods used (e.g., electrochemical, optical). This review aims to comprehensively discuss the PFAS-MIP research field. The efficacy and challenges facing the different applications of these materials in environmental water applications are discussed, as well as a perspective on challenges for this field that need to be overcome before exploitation of the technology can be fully realised.

Electropreconcentration with charge-selective nanochannels.

We report on the systematic investigation of electropreconcentration phenomena in hybrid micro/nanofluidic devices. The competition between the electroosmotic dragging force and the highly nonlinear electrophoretic forces induced by the polarization effect is responsible for four preconcentration regimes within such structures that can arise at both cathodic and anodic sides of the nanochannel. Numerical calculations on the spatiotemporal concentration of charged molecules confirm such a classification, showing a general agreement with the reported experimental data at low and moderate ionic strengths. The results also suggest that both the mobility and the valence of the species of interest are important parameters in the determination of the preconcentration rates.