Correction: Migration of nanoparticles across a polymer-polymer interface: theory and simulation.

Correction for 'Migration of nanoparticles across a polymer-polymer interface: theory and simulation' by Nigel Gibbions , , 2021, , 7294-7310, https://doi.org/10.1039/D1SM00671A.

Efficient polynomial analysis of magic-angle spinning sidebands and application to order parameter determination in anisotropic samples.

Chemical shift tensors in C solid-state NMR provide valuable localized information on the chemical bonding environment in organic matter, and deviations from isotropic static-limit powder line shapes sensitively encode dynamic-averaging or orientation effects. Studies in C natural abundance require magic-angle spinning (MAS), where the analysis must thus focus on spinning sidebands. We propose an alternative fitting procedure for spinning sidebands based upon a polynomial expansion that is more efficient than the common numerical solution of the powder average.

Migration of nanoparticles across a polymer-polymer interface: theory and simulation.

We proposed recently a theoretical description for hydrodynamic flows in inhomogeneous liquids in the vicinity of solid interfaces, consistent with current theoretical descriptions of the thermodynamical equilibrium of liquids in the vicinity of solid surfaces and with the Onsager formalism for linear response theory in out-of-equilibrium liquids. We showed that these equations allow for describing diffusio-osmosis along a capillary and also wetting/dewetting dynamics of liquids on a solid substrate. We now apply this physical model to the wetting/dewetting dynamics of nano-particles in polymer blends, showing how they reach equilibrium at the interface between two liquids at rest and how they migrate from the non-preferred polymer to the preferred one under applied flow.

Mechanical properties of amorphous and semi-crystalline semi-aromatic polyamides.

We investigate the mechanical properties of amorphous and semi-crystalline semi-aromatic polyamides, polyphthalamides (PPA). Three relaxation processes have been identified by DMTA which is consistent with literature for polyamide. PPA exhibit a brittle-to-ductile transition from a low impact strength to a high impact strength.

Diffusio-osmosis and wetting on solid surfaces: a unified description based on a virtual work principle.

In order to account for diffusio-osmosis, Derjaguin proposed long ago that there is an excess pressure confined within a layer of typically a few nanometers in the vicinity of a solid surface immersed in a liquid and resulting from the interaction between the liquid and the surface. In the presence of a composition gradient in the liquid a confined pressure gradient parallel to the surface is therefore responsible for the diffusio-osmotic flow. This picture appears in contradiction with the contact theorem of colloidal science according to which such excess pressure does not exist.

Mechanical and ultimate properties of injection molded cellulose acetate/plasticizer materials.

The mechanical properties of injection molded plasticized cellulose acetate polymers processed with two different plasticizers (Triacetine and Diethyl phthalate) and various weight fractions comprised between 15 and 30 wt % have been investigated. Plasticized cellulose acetate exhibit a brittle-to-ductile transition from a low impact strength to a high impact strength of order 40 kJ/m². Obtaining a high impact resistance at room temperature requires plasticizer content larger than 25 wt.

Dielectric relaxation of thin films of polyamide random copolymers.

We investigate the relaxation behavior of thin films of a polyamide random copolymer, PA66/6I, with various film thicknesses using dielectric relaxation spectroscopy. Two dielectric signals are observed at high temperatures, the α process and the relaxation process due to electrode polarization (the EP process). The relaxation time of the EP process has a Vogel-Fulcher-Tammann type of temperature dependence, and the glass transition temperature, T(g), evaluated from the EP process agrees very well with the T(g) determined from the thermal measurements.

Nucleation and Growth of Ordered Copolymer Structures at Reactive Interfaces between PA6 and MA--HDPE.

We have studied the effect of the interfacial chemical reaction between PA6 and MA--HDPE in static conditions at a macroscopically flat interface. Interface destabilization and the growth of instabilities, somehow similar to myelin figures observed in surfactants put in the presence of water, are observed. For the first time in this system, it is shown that ordered microphase-separated copolymer domains, whose morphologies depend on the architecture of the copolymer, namely, essentially on the relative length of the blocks on each side of the interface, may nucleate and grow at a static interface between reactive polymers.

Miscibility and dynamical properties of cellulose acetate/plasticizer systems.

Due to its biodegradability and renewability, a great interest has been devoted to investigating cellulose acetate in order to expand its potential applications. In addition, secondary cellulose acetate (CDA) could also be considered as a model system for strongly polar polymer system. The dynamical behavior of CDA is supposed to be governed by H-bonding and dipolar interaction network.