241,994 research outputs found
Transport of ferrihydrite nanoparticles in saturated porous media: role of ionic strength and flow rate
The use of nanoscale ferrihydrite particles, which are known to effectively enhance microbial degradation of a wide range of contaminants, represents a promising technology for in situ remediation of contaminated aquifers. Thanks to their small size, ferrihydrite nanoparticles can be dispersed in water and directly injected into the subsurface to create reactive zones where contaminant biodegradation is promoted. Field applications would require a detailed knowledge of ferrihydrite transport mechanisms in the subsurface, but such studies are lacking in the literature. The present study is intended to fill this gap, focusing in particular on the influence of flow rate and ionic strength on particle mobility. Column tests were performed under constant or transient ionic strength, including injection of ferrihydrite colloidal dispersions, followed by flushing with particle-free electrolyte solutions. Particle mobility was greatly affected by the salt concentration, and particle retention was almost irreversible under typical salt content in groundwater. Experimental results indicate that, for usual ionic strength in European aquifers (2 to 5 mM), under natural flow condition ferrihydrite nanoparticles are likely to be transported for 5 to 30 m. For higher ionic strength, corresponding to contaminated aquifers, (e.g., 10 mM) the travel distance decreases to few meters. A simple relationship is proposed for the estimation of travel distance with changing flow rate and ionic strength. For future applications to aquifer remediation, ionic strength and injection rate can be used as tuning parameters to control ferrihydrite mobility in the subsurface and therefore the radius of influence during field injection
Friction and wear behavior of glasses and ceramics
Adhesion, friction, and wear behavior of glasses and ionic solids are reviewed. These materials are shown to behave in a manner similar to other solids with respect to adhesion. Their friction characteristics are shown to be sensitive to environmental constituents and surface films. This sensitivity can be related to a reduction in adhesive bonding and the changes in surficial mechanical behavior associated with Rehbinder and Joffe effects. Both friction and wear properties of ionic crystalline solids are highly anisotropic. With metals in contact with ionic solids the fracture strength of the ionic solid and the shear strength in the metal and those properties that determine these will dictate which of the materials undergoes adhesive wear. The chemical activity of the metal plays an important role in the nature and strength of the adhesive interfacial bond that develops between the metal and a glass or ionic solid
Deposition and transport of graphene oxide in saturated and unsaturated porous media
In this work, sand and bubble column experiments were conducted to explore the deposition mechanisms of graphene oxide (GO) particles in porous media with various combinations of moisture content and ionic strength. Sand column experimental results indicated that retention and transport of GO in porous media were strongly dependent on solution ionic strength. Particularly, GO showed high mobility under low ionic strength conditions in both saturated and unsaturated porous media. Increasing ionic strength dramatically increased the retention of GO particles in porous media, mainly through secondary-minimum deposition as indicated in the XDLVO interaction energy profiles. Recovery rates of GO in unsaturated sand columns were lower than that in saturated columns under the same ionic strength conditions, suggesting moisture content also played an important role in the retention of GO in porous media. Findings from the bubble column experiments showed that the GO did not attach to the air–water interface, which is consistent with the XDLVO predictions. Additional retention mechanisms, such as film straining, thus could be responsible to the reduced mobility of GO in unsaturated porous media. The experimental data of GO transport through saturated and unsaturated porous media could be accurately simulated by an advection–dispersion-reaction model
Isotropic-nematic phase transition in suspensions of filamentous virus and the neutral polymer Dextran
We present an experimental study of the isotropic-nematic phase transition in
an aqueous mixture of charged semi-flexible rods (fd virus) and neutral polymer
(Dextran). A complete phase diagram is measured as a function of ionic strength
and polymer molecular weight. At high ionic strength we find that adding
polymer widens the isotropic-nematic coexistence region with polymers
preferentially partitioning into the isotropic phase, while at low ionic
strength the added polymer has no effect on the phase transition. The nematic
order parameter is determined from birefringence measurements and is found to
be independent of polymer concentration (or equivalently the strength of
attraction). The experimental results are compared with the existing
theoretical predictions for the isotropic-nematic transition in rods with
attractive interactions.Comment: 8 Figures. To be published in Phys. Rev. E. For more information see
http://www.elsie.brandeis.ed
Liquid-liquid interfacial tension of electrolyte solutions
It is theoretically shown that the excess liquid-liquid interfacial tension
between two electrolyte solutions as a function of the ionic strength I behaves
asymptotically as O(- I^0.5) for small I and as O(+- I) for large I. The former
regime is dominated by the electrostatic potential due to an unequal
partitioning of ions between the two liquids whereas the latter regime is
related to a finite interfacial thickness. The crossover between the two
asymptotic regimes depends sensitively on material parameters suggesting that,
depending on the actual system under investigation, the experimentally
accessible range of ionic strengths can correspond to either the small or the
large ionic strength regime. In the limiting case of a liquid-gas surface where
ion partitioning is absent, the image chage interaction can dominate the
surface tension for small ionic strength I such that an Onsager-Samaras
limiting law O(- I ln(I)) is expected. The proposed picture is consistent with
more elaborate models and published measurements.Comment: Accepted for publication in Physical Review Letter
Three-phase contact line and line tension of electrolyte solutions in contact with charged substrates
The three-phase contact line formed by the intersection of a liquid-vapor
interface of an electrolyte solution with a charged planar substrate is studied
in terms of classical density functional theory applied to a lattice model. The
influence of the substrate charge density and of the ionic strength of the
solution on the intrinsic structure of the three-phase contact line and on the
corresponding line tension is analyzed. We find a negative line tension for all
values of the surface charge density and of the ionic strength considered. The
strength of the line tension decreases upon decreasing the contact angle via
varying either the temperature or the substrate charge density
Effect of dipolar moments in domain sizes of lipid bilayers and monolayers
Lipid domains are found in systems such as multi-component bilayer membranes
and single component monolayers at the air-water interface. It was shown by
Andelman et al. (Comptes Rendus 301, 675 (1985)) and McConnell et al. (Phys.
Chem. {\bf 91}, 6417 (1987)) that in monolayers, the size of the domains
results from balancing the line tension, which favors the formation of a large
single circular domain, against the electrostatic cost of assembling the
dipolar moments of the lipids. In this paper, we present an exact analytical
expression for the electric potential, ion distribution and electrostatic free
energy for different problems consisting of three different slabs with
different dielectric constants and Debye lengths, with a circular homogeneous
dipolar density in the middle slab. From these solutions, we extend the
calculation of domain sizes for monolayers to include the effects of finite
ionic strength, dielectric discontinuities (or image charges) and the
polarizability of the dipoles and further generalize the calculations to
account for domains in lipid bilayers. In monolayers, the size of the domains
is dependent on the different dielectric constants but independent of ionic
strength. In asymmetric bilayers, where the inner and outer leaflets have
different dipolar densities, domains show a strong size dependence with ionic
strength, with molecular-sized domains that grow to macroscopic phase
separation with increasing ionic strength. We discuss the implications of the
results for experiments and briefly consider their relation to other two
dimensional systems such as Wigner crystals or heteroepitaxial growth.Comment: 13 pages, 5 figues in eps Replaced with new version, one citation
added and a few statements corrected. The results of the paper are unchange
- …