Rivers are a major pathway for plastics between lands and the ocean. At the land-ocean interface, estuaries make the transfer dynamic of plastics complex and nonlinear. That is why very little is known about this dynamic. In this respect, a specific marker (i.e. Microlax packaging) showing date-prints was systematically investigated in different riverbanks of the Seine estuary to identify the share of "old" and "recent" litter transiting through the estuary toward the ocean. Up to 70% of Microlax were "old" plastic items probably related to the meandering dynamic of the river over large time and space scales, and hydrodynamic conditions (tides) at smaller scales. This contributes together to increase the residence time of plastics into the estuary up to decades with almost endless transport, deposit and remobilization cycles. Consequently, the Seine estuary may function as a "microplastic factory" resulting from the fragmentation of macroplastics into microplastics well before they reach the ocean.
Global estimations state that between 0.5 and 12.7 million metric tons of plastic enter the oceans each year. They are, however, associated with great uncertainties due to methodological difficulties to accurately quantify land-based plastic fluxes into the oceans. New studies at basin scale are thus needed for better model calibrations. Here, a modeling approach based on Jambeck's statistical method and a field approach are compared in order to (i) quantify plastic fluxes in the Seine River and (ii) characterize and constrain uncertainties of both approaches. Despite the simplicity of the statistical approach and rough extrapolations, both methods yield similar results, i.e., between 1,100 and 5,900 t/yr of plastic litter flowing into the Sea of which about 88-128 t/yr are removed by cleaning operations. According to the marine strategy framework directive (2008/56/EC), actions are required to quantify plastic fluxes entering the oceans. Among different methods, a better use of the data from the waste collection should be considered. The development of a national and homogenous platform listing all the collects would be a first step in that direction.
The aim of this work is to study the transport of small molecules through the hybrid systems polyamide 12 (PA12)/organo-modified montmorillonite (Cloisite 30B, C30B) prepared by melt blending, using two blending conditions. The transport mechanisms were investigated by using three probe molecules: nitrogen, water, and toluene. While a barrier effect appears clearly with nitrogen, this effect changes with the amount of fillers for water and disappears for toluene. The reduction of permeability for nitrogen is mainly due to the increase of tortuosity. For water and toluene, the permeation kinetics reveals many concomitant phenomena responsible for the permeation behavior. Despite the tortuosity effect, the toluene permeability of nanocomposites increases with C30B fraction. The water and toluene molecules interact differently with fillers according to their hydrophilic/hydrophobic character. Moreover, the plasticization effect of water and toluene in the matrix, involving a concentration-dependent diffusion coefficient, is correctly described by the law D = D(0)e(gammaC). On the basis of Nielsen's tortuosity concept, we suggest a new approach for relative permeability modeling, not only based on the geometrical parameters (aspect ratio, orientation, recovery) but also including phenomenological parameters deduced from structural characterization and permeation kinetics.
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