Viscoelastic liquids are characterized by a finite static viscosity and a zero yield stress, whereas soft solids have an infinite viscosity and a non-zero yield stress. The rheological nature of viscoelastic materials has long been a challenge, and it is still a matter of debate. Here, we provide for the first time the constitutive equations of linear viscoelasticity for magnetic wires in yield stress materials, together with experimental measurements using Magnetic Rotational Spectroscopy (MRS). With MRS, the wires are submitted to a rotational magnetic field as a function of frequency and the wire motion is monitored by time-lapse microscopy. The soft solids studied are gel-forming polysaccharide aqueous dispersions (gellan gum) at concentrations above the gelification point. It is found that soft solids exhibit a clear and distinctive signature compared to viscous and viscoelastic liquids. In particular, the wire average rotation velocity equals zero over a broad frequency range. We also show the MRS technique is quantitative. From the wire oscillation amplitudes, the equilibrium elastic modulus is retrieved and agrees with polymer dynamics theory.
One major concern in the fate of nanomaterials in aquatic systems is the lack of data on nanomaterial transformations under relevant environmental conditions. The disagglomeration of aggregates composed of manufactured anatase titanium dioxide nanoparticles is investigated here in the presence of alginate and Suwannee River humic acids at varying concentrations using dynamic light scattering and electrophoretic measurements. Stability of TiO 2 nanoparticle agglomerates at typical environmental concentrations of natural organic matter is discussed at a pH value corresponding to the point of zero charge of TiO 2 nanoparticles. In this scenario, the surface charge of TiO 2 is neutralized, allowing the nanoparticles to form large agglomerates. Alginate and Suwannee River humic acids exhibit a negative structural charge under this pH condition and adsorption of both natural polyelectrolytes on the surface of nanoparticle agglomerates leads to disagglomeration and significant redispersion of TiO 2 nanoparticles into fragments. Results indicate that both electrostatic forces and steric interactions play key roles during the disagglomeration process and that the physicochemical properties of natural organic matter are found to influence the kinetics and importance of fragmentation in the disagglomeration process. Most importantly, our data indicate that the presence of natural organic matter at typical environmental concentrations induces significant disagglomeration of large submicron nanoparticle agglomerates. Such a result constitutes an important outcome with regards to the risk associated with manufactured nanoparticles by including the possible transformations of the micron size range structures they can form.
Nano impactOne of the main problems in the ecological risk assessment of nanomaterials is the lack of important information on their environmental (bio)physicochemical transformations. The disagglomeration of manufactured titanium dioxide nanoparticles is investigated here in the presence of alginate and Suwannee River humic acids at realistic environmental concentrations. Under such concentration conditions, the adsorption of these compounds is found to induce disagglomeration and significant redispersion of TiO 2 nanoparticles into fragments. Such a result constitutes an important outcome with regards to the risk associated with manufactured nanoparticles by considering one important life-cycle transformation of micron size range structures composed of nanoparticles in aquatic systems.
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