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The dynamics of charged and hard-sphere silica colloidal suspensions are measured using diffusing wave spectroscopy and are interpreted by the Generalized Stokes–Einstein Relation (GSER). At high concentration, the resulting moduli are in good qualitative agreement with bulk rheology, including the frequency response, but are higher by a quantitative factor. We show that the "two-point" GSER, which derives from the correlated motion of the colloidal particles, provides a better quantitative agreement between bulk and microrheology. The two-point GSER applies generally when the average scattering vector sampled by the multiple scattering events corresponds to a length scale greater than the scatterer diameter. We discuss applications for characterizing colloid interactions by measuring the high-frequency moduli of suspensions and extend the two-point analysis to tracer particle microrheology measurements of a semiflexible biopolymer network. [ABSTRACT FROM AUTHOR]

Novel measurements of the spatiotemporal microstructure of a continuous shear thickening colloidal suspension under shear cessation and reversal using small angle neutron scattering in a 1–2 shear cell are presented for moderate to high Péclet numbers. In the shear cessation experiments from high Péclet shear flow, two-step relaxation mechanism is found. Particles first readily diffuse on a characteristic timescale of single particle Brownian motion, followed by slower relaxation dynamics on a timescale of short-time self-diffusion when caging effects start dominating. In the shear reversal experiment, the unchanged scattering intensity and the quick flip in anisotropic structure around the shear thickened state suggest the persistence of hydroclusters without transitioning through the equilibrium structure, at least in a time resolution of 0.01 s. Access to the time evolution of microstructure provides valuable insights into the spatiotemporal details of interparticle interactions governing colloidal suspension rheology, such as Brownian, hydrodynamic, and nanotribological forces. [ABSTRACT FROM AUTHOR]

Two colloidal suspensions of paucidisperse, spherical silica particles with different surface chemistries leading to extreme limits of surface contact friction are studied to identify experimental differences in shear rheology and microstructure and quantitatively test theory and simulation models. The nonequilibrium microstructure in the plane of shear is measured by flow-small angle neutron scattering for steady shear states spanning the shear thinning and shear thickening regimes. The shear rheology and microstructure are compared against predictions from theory for Brownian hard sphere suspensions and state-of-the-art simulation methods that incorporate either contact friction or enhanced lubrication hydrodynamics. The first normal stress differences are confirmed to distinguish between these micromechanical mechanisms for stress enhancement in the shear thickened regime. The nonequilibrium microstructure in the plane of shear shows more anisotropy for the suspension with higher interparticle friction. A significant fourfold symmetry is confirmed and found to be amplified with increasing surface contact friction in the shear thickened state. The differences in shear-induced microstructures between suspensions with varying contact friction demonstrate that the nonequilibrium microstructure can distinguish between nanotribological interactions in the shear thickened state. Statistical comparison of experiments with simulations indicates that better resolution of microstructures in simulation models is required to be validated by the experimental data presented. Implications for the development of theories for colloidal suspension rheology are discussed. [ABSTRACT FROM AUTHOR]

BACKGROUND: Human blood is a thixo-elasto-visco-plastic (TEVP) material that exhibits unique fluctuations in mechanical properties based on physiology, and shear rate. We demonstrate new visual tools to help visualize and characterize these varied mechanical properties. OBJECTIVE: Our objective is to demonstrate contemporary visual and numerical tools to help visualize and characterize the varied mechanical properties of human blood. METHODS: Using the ARESG2 strain-controlled rheometer with double wall couette geometry and eight human blood donors, with lab test results, elastic and viscous properties are investigated using Series of Physical Processes (SPP) and MITLaos to both analyze and visualize the mechanical signatures of the blood. RESULTS: Variations of mechanical properties are shown via SPP generated Cole-Cole plots and MITLaos analysis. These variations are a function of physiological properties of blood on the day of the blood draw based on hematocrit, fibrinogen, cholesterol, triglycerides, and a host of other proteins and constituents. Each rheological experiment with blood is replicated with an analogous experiments with 0.04 wt% xanthan in glycerol, and water to demonstrate that the mechanical properties of the human blood, and its rheological signatures are unique to human blood. CONCLUSIONS: Human blood is proven to be a TEVP material, as shown on a series of Cole-Cole plots for eight different donors, at two different frequency and strain amplitude combinations. Variations in Cole-Cole plots for each donor are shown. MITLaos average mechanical properties are calculated and shown. Aggregated elastic and viscous projections and a Cole-Cole plot is shown for Donors 1–8, along with 95% confidence interval. [ABSTRACT FROM AUTHOR]

Rheological experiments on model and industrial colloidal dispersions that exhibit reversible shear thickening are compared to a recent model that correlates simulation results for the shear rheology of bidisperse suspensions of particles with varying levels of contact friction. Comparisons are presented with rheological results for a variety of colloidal dispersions varying from model systems to industrially relevant, commercial dispersions where both shear and first normal stress differences are available. Particle-scale measurements of particle friction coefficients are provided through a survey of the literature. The comparisons show under which conditions the model can quantitatively describe the measured rheology and how the model can be used to correlate data for systems with more complex interactions when allowances are made for effective volume fractions and adjustments in friction coefficients. Discrepancies evident in comparisons for the first normal stress differences highlight the importance of enhanced hydrodynamic friction in many systems, especially for continuous shear thickening, in qualitative agreement with recent simulations that incorporate enhanced lubrication hydrodynamics due to elastohydrodynamics or particle roughness. Finally, a literature survey of measurements of jamming volume fractions and particle friction coefficients indicates that the model overestimates the experimentally observed jamming volume fraction. The comparisons presented in this work provide quantitative information valuable for those modeling suspension processing as well as suggestions for further model improvement. [ABSTRACT FROM AUTHOR]

Electrophoretic and electroosmotic motion of a charged spherical particle within a cylindrical pore filled with a Debye-Bueche-Brinkman (DBB) polymeric solution is investigated theoretically, which is of high relevance in capillary electrophoresis as well as micro- and nanofluidic applications involving polymeric solutions in a micro- or nanopore. The DBB model describes the rheological response of a polymeric solution with a linear polymer dissolved in a homogeneous solvent. It is a well-known non-Newtonian model in liquid physics based on rigorous theoretical derivations. By Debye and Bueche, corresponding governing fundamental electrokinetic equations are solved numerically with a patched pseudo-spectral method based on Chebyshev polynomials. We found that the double-layer polarization effect reduces the particle mobility severely when the Debye parameter, κa, is around unity, especially in narrow pores. This is attributed to the extra confinement effect from the nearby wall, which tends to sweep the predominant counterions within the double layer to the wake of the moving particle, resulting in a motion-deterring induced electric field. The electrophoretic mobility in a polymer solution is smaller than that in an aqueous electrolyte solution in general as a result of the much stronger viscous drag effect in a polymer solution. Moreover, electroosmotic flow (EOF) as a result of a charged pore wall is found to exhibit a highly non-Newtonian behavior. Unlike the corresponding plug-like flow for a Newtonian solution, an axisymmetric flow with a large local maximum in the velocity profile in the region near the pore wall is observed. This radial-varying velocity profile offers a potential extra separation mechanism, which favors the elution of smaller particles in general. The results obtained here provide fundamental understandings and insights of the electrophoresis and electroosmosis phenomena in a cylindrical pore filled with polymeric solution.