Search arXivSearch

arXiv · 1005.0730

Capillary Rise and Imbibition of Liquids in Nanoporous Matrices: Rheological Concepts and Experiments

Abstract

Liquid flow propelled by capillary forces is one of the most important transport mechanisms in porous environments. It is governed by a fascinating interplay of interfacial, viscous drag as well as gravitational forces which liquids encounter upon invasion into geometries with often complex topologies, such as capillary networks of trees or interconnected fractures in soils and ice. Here, we present fundamentals, concepts and an experimental, gravimetric study on the capillarity-driven invasion dynamics of liquids in networks of pores a few nanometers across in monolithic, nanoporous silica glass (porous Vycor). A variation of the complexity of the building blocks of the liquids investigated along with a variation of the humidity and the temperature upon spontaneous imbibition allows us to gain information regarding the fluidity and capillarity of liquids in such nanoporous environments. We observe square-root of time imbibition dynamics for all liquids applied, which we can quantitatively describe by both a conserved bulk fluidity in the pore center and bulk capillarity at the advancing menisci, if we assume a sticky boundary layer (negative velocity slip length). Moreover, pecularities of nanopore-confined liquids, such as transport via the vapor phase leading to preadsorbed liquid layers, have to be properly accounted for. Upon increasing the chain-length in the case of the n-alkanes, we found hints towards a transition from stick- to slip-flow at the pore walls with increasing chain-length and thus polymeric behavior. Meniscus freezing is reported for n-tetracosane confined in porous Vycor. For the rheology of a rod-like liquid nematogen (8OCB) we found no hints of the viscosity drop upon entering into the nematic phase, typical of the bulk rheology of this liquid crystal.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Simon Gruener, Patrick Huber. 2010-05-05. Capillary Rise and Imbibition of Liquids in Nanoporous Matrices: Rheological Concepts and Experiments. https://arxiv.org/abs/1005.0730

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Deformation and organization of droplet-encapsulated soft beads

Many biological, culinary, and engineering processes lead to the co-encapsulation of several soft particles within a liquid interface. In these situations the particles are bound together by the capillary forces that deform them and influence their biological or rheological properties. Here, we introduce an experimental approach to encapsulate a controlled number of soft beads within aqueous droplets in oil. These droplet-encapsulated gels are manipulated in a deformable microfluidic device to merge them and modify the liquid fraction. In the dry limit the contact surface between the hydrogels is found to be determined by the elastocapillary number $E_c$, with the contact radius following a $E_c^{1/3}$ dependence, indicating that the deformation increases for soft or small particles. When multiple beads are co-encapsulated within a single droplet they can be arranged into linear or three-dimensional aggregates that remain at a local energy minimum.

cond-mat.soft

Flexoelectricity-driven softening of bend elasticity leads to spontaneous chiral symmetry breaking in a polar fluid

The origin of the recently observed spontaneous chiral symmetry breaking in polar fluids composed of achiral molecules is an unsolved problem, raising fundamental questions about how heliconical structures emerge in such systems. Here, we investigate the pretransitional fluctuations leading to the formation of the spontaneously chiral twist-bend ferroelectric nematic phase using dielectric spectroscopy, light scattering, and small-angle X-ray scattering. We observe simultaneous softening of the bend elastic constant and the emergence of a collective dielectric mode on approaching the transition. By developing a theoretical model, we show that these phenomena are signatures of a flexoelectricity-driven transition arising from the coupling between electric polarization and bend deformation.

cond-mat.soft

Taylor dispersion in a soft tube

Diffusion of a solute along a tube is enhanced by hydrodynamic flow, a phenomenon known as Taylor dispersion. In microfluidic applications, the compliance of the tube boundaries modifies the hydrodynamic flow and thus solutal transport. Here, we develop the theory of solutal dispersion in a soft, axisymmetric tube where the tube walls respond to the hydrodynamic pressure through a Winkler response. By deriving the modified macro-transport equation for the solutal concentration dynamics based on multiple-time-scale analysis, we explore the influence of softness on solutal transport for steady and pulsatile configurations. Our main finding is that softness enhances the effective advection velocity and dispersion coefficient, which might have practical implication in biology and microfluidic technology.

cond-mat.soft