When a microparticle is trapped at a fluid interface, particle's electrical charge and weight combine to deform the interface. Such deformation is expected to affect the particle diffusion via hydrodynamics boundary conditions. Using available models of particle-induced electrostatic deformation of the interface and particle dynamics at the interface, we are able to analytically predict particle diffusion coefficient values in a large range of particle's contact angle and size. This might offer a solid background of numerical values to compare with for future experimental studies in the field of particle diffusion at a fluid interface.

Supramolecular associations provide a promising route to functional materials with properties such as self-healing, easy recyclability or extraordinary mechanical strength and toughness. The latter benefit especially from the transient character of the formed network, which enables dissipation of energy as well as regeneration of the internal structures. However, recent investigations revealed intrinsic limitations in the achievable mechanical enhancement. This manuscript presents studies of a set of telechelic polymers with hydrogen-bonding chain ends exhibiting an extraordinarily high, almost glass-like, rubbery plateau. This is ascribed to the segregation of the associative ends into clusters and formation of an interfacial layer surrounding these clusters. An approach adopted from the field of polymer nanocomposites provides a quantitative description of the data and reveals the strongly altered mechanical properties of the polymer in the interfacial layer. These results demonstrate how employing phase separating dynamic bonds can lead to the creation of high-performance materials.

We propose a novel model for a glass-forming liquid which allows to switch in a continuous manner froma standard three-dimensional liquid to a fully connected mean-field model. This is achieved by introducingk additional particle-particle interactions which thus augments the effective number of neighbors of eachparticle. Our computer simulations of this system show that the structure of the liquid does not changewith the introduction of these pseudo neighbours and by means of analytical calculations, we determine thestructural properties related to these additional neighbors. We show that the relaxation dynamics of thesystem slows down very quickly with increasing k and that the onset and the mode-coupling temperaturesincrease. The systems with high values of k follow the MCT power law behaviour for a larger temperaturerange compared to the ones with lower values of k. The dynamic susceptibility indicates that the dynamicheterogeneity decreases with increasing k whereas the non-Gaussian parameter is independent of it. Thus weconclude that with the increase in the number of pseudo neighbours the system becomes more mean-field like.By comparing our results with previous studies on mean-field like system we come to the conclusion that thedetails of how the mean-field limit is approached are important since they can lead to different dynamicalbehavior in this limit.

We investigate the structure of gluten polymer-like gels in a binary mixture of water/ethanol, $50/50$ v/v, a good solvent for gluten proteins. Gluten comprises two main families of proteins, monomeric gliadins and polymer glutenins. In the semi-dilute regime, scattering experiments highlight two classes of behavior, akin to standard polymer solution and polymer gel, depending on the protein composition. We demonstrate that these two classes are encoded in the structural features of the proteins in very dilute solution, and are correlated with the presence of proteins assemblies of typical size tens of nanometers. The assemblies only exist when the protein mixture is sufficiently enriched in glutenins. They are found directly associated to the presence in the gel of domains enriched in non-exchangeable H-bonds and of size comparable to that of the protein assemblies. The domains are probed in neutron scattering experiments thanks to their unique contrast. We show that the sample visco-elasticity is also directly correlated to the quantity of domains enriched in H-bonds, showing the key role of H-bonds in ruling the visco-elasticity of polymer gluten gels.

The thin film of life that inhabits all plastics in the oceans, so-called “plastisphere,” has multiple effects on the fate and impacts of plastic in the marine environment. Here, we aimed to evaluate the relative influence of the plastic size, shape, chemical composition, and environmental changes such as a phytoplankton bloom in shaping the plastisphere abundance, diversity and activity. Polyethylene (PE) and polylactide acid (PLA) together with glass controls in the forms of meso-debris (18 mm diameter) and large-microplastics (LMP; 3 mm diameter), as well as small-microplastics (SMP) of 100 μm diameter with spherical or irregular shapes were immerged in seawater during 2 months. Results of bacterial abundance (confocal microscopy) and diversity (16S rRNA Illumina sequencing) indicated that the three classical biofilm colonization phases (primo-colonization after 3 days; growing phase after 10 days; maturation phase after 30 days) were not influenced by the size and the shape of the materials, even when a diatom bloom (Pseudo-nitzschia sp.) occurred after the first month of incubation. However, plastic size and shape had an effect on bacterial activity (3H leucine incorporation). Bacterial communities associated with the material of 100 μm size fraction showed the highest activity compared to all other material sizes. A mature biofilm developed within 30 days on all material types, with higher bacterial abundance on the plastics compared to glass, and distinct bacterial assemblages were detected on each material type. The diatom bloom event had a great impact on the plastisphere of all materials, resulting in a drastic change in diversity and activity. Our results showed that the plastic size and shape had relatively low influence on the plastisphere abundance, diversity, and activity, as compared to the plastic composition or the presence of a phytoplankton bloom.

Using cyclic shear to drive a two dimensional granular system, we determine the structural char-acteristics for different inter-particle friction coefficients. These characteristics are the result of acompetition between mechanical stability and entropy, with the latter’s effect increasing with fric-tion. We show that a parameter-free maximum-entropy argument alone predicts an exponential cell order distribution, with excellent agreement with the experimental observation. We show thatfriction only tunes the mean cell order and, consequently, the exponential decay rate and the pack-ing fraction. We further show that cells, which can be very large in such systems, are short-lived,implying that our systems are liquid-like rather than glassy..