Liquid transport through nanopore is central into many applications, from water purification to biosensing or energy harvesting. Ultimately thin nanopores are of major interest in these applications to increase driving potential and reduce as much as possible dissipation sources. We investigate here the efficiency of the electrical power generation through an ultrathin nanoporous membrane by means of streaming current (electrical current induced by ionic flow in the vicinity of the liquid/solid interface) or electroosmosis (flow rate induced by an electrical potential). Upscaling from one unique pore to a nanoporous membrane is not straightforward when we consider low aspect ratio nanopore because of 3D entrance effects, which lead to interactions between the pores. Whereas these interactions have already been considered for direct transport (hydrodynamic permeability of the membrane, ionic conductance), specific effects appear when coupled transports are considered. We obtain here the expression of the electroosmotic mobility for a nanoporous membrane including surface conduction, and by a numerical evaluation of our results, we show that (i) it depends mainly of the distance between the pores and (ii) it is sublinear with the number of pores. Varying the pore spatial organization (square, hexagonal, disordered structure) reveals that these transport properties are only dependent on one parameter, the porosity of the membrane (if other parameters such as membrane material/thickness are kept constant). Finally, when considering energy conversion yield, it is shown that increasing the number of pores is deleterious, and a nonmonotonic behavior with salt concentration is reported.
We present an efficient and robust numerical model for simulation of electrokinetic phenomena in porous networks over a wide range of applications including energy conversion, desalination, and lab-on-a-chip systems. Coupling between fluid flow and ion transport in these networks is governed by the Poisson-Nernst-Planck-Stokes equations. These equations describe a wide range of transport phenomena that can interact in complex and highly nonlinear ways in networks involving multiple pores with variable properties. Capturing these phenomena by direct simulation of the governing equations in mult…
We present a numerical study of nonlinear electrokinetic transport in porous media, focusing on the role of heterogeneity in a porous microstructure on ion concentration polarization and over-limiting current. For simplicity, the porous medium is modeled as a network of long, thin charged cylindrical pores, each governed by one-dimensional effective transport equations. For weak surface conduction, when sufficiently large potential is applied, we demonstrate that electrokinetic transport in a porous network can be dominated by electroconvection via internally induced flow loops, which is not p…
Electrokinetic in-situ recovery is an alternative to conventional mining, relying on the application of an electric potential to enhance the subsurface flow of ions. Understanding the pore-scale flow and ion transport under electric potential is essential for petrophysical properties estimation and flow behavior characterization. The governing physics of electrokinetic transport is electromigration and electroosmotic flow, which depend on the electric potential gradient, mineral occurrence, domain morphology, and electrolyte properties. Herein, mineral occurrence and its associated zeta potent…
Correlation effects arising during liquid infiltration into hydrophobic porous medium are considered. On the basis of these effects a mechanism of energy absorption at filling porous medium by nonwetting liquid is suggested. In accordance with this mechanism, the absorption of mechanical energy is a result expenditure of energy for the formation of menisci in the pores on the shell of the infinite cluster and expenditure of energy for the formation of liquid-porous medium interface in the pores belonging to the infinite cluster of filled pores. It was found that in dependences on the porosity …
Our Society is in high need of alternatives to fossil fuels. Nanoporous systems filled with aqueous electrolytes show great promises for harvesting the osmotic energy of sea water or waste heat. At the core of energy conversion in such nanofluidic systems lie the so-called electrokinetic effects, coupling thermodynamic gradients and fluxes of different types (hydrodynamical, electrical, chemical, thermal) at electrified water-solid interfaces. This chapter starts by introducing the framework of linear irreversible thermodynamics, and how the latter can be used to describe the direct and couple…
It has been shown that changes in the energy of a system of nonwetting-liquid clusters confined in a random nanoporous medium in the process of relaxation can be written in the quasiparticle approximation in the form of the sum of the energies of local (metastable) configurations of liquid clusters interacting with clusters in the connected nearest pores. The energy spectrum and density of states of the local configuration have been calculated. It has been shown that the relaxation of the state of the system occurs through the scenario of self-organized criticality (SOC). The process is charac…
When a macroscopic droplet spreads, a thin precursor film of liquid moves ahead of the advancing liquid-solid-vapor contact line. Whereas this phenomenon has been explored extensively for planar solid substrates, its presence in nanostructured geometries has barely been studied so far, despite its importance for many natural and technological fluid transport processes. Here we use porous photonic crystals in silicon to resolve by light interferometry capillarity-driven spreading of liquid fronts in pores of few nanometers in radius. Upon spatiotemporal rescaling the fluid profiles collapse on …
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 gl…
We present heterodyne detected transient grating measurements on water filled Vycor 7930 in the range of temperature 20 - 90 degrees C. This experimental investigation enables to measure the acoustic propagation, the average density variation due the liquid flow and the thermal diffusion in this water filled nano-porous material. The data have been analyzed with the model of Pecker and Deresiewicz which is an extension of Biot model to account for the thermal effects. In the whole temperature range the data are qualitatively described by this hydrodynamic model that enables a meaningful insigh…
A physical mechanism has been proposed to describe the formation of a stable state of a nonwetting liquid after filling of a porous medium at an increased pressure with the subsequent reduction of the overpressure to zero. It has been shown that the observed transition of the system of nonwetting-liquid nanoclusters to the stable state in a narrow range of filling factors and a narrow temperature interval is due to a decrease in the surface free energy without change in the chemical potential owing to the collective interactions between liquid nanoclusters in the neighboring pores. This effect…
The sorption-desorption hysteresis observed in many nanoporous solids, at vapor pressures low enough for the the liquid (capillary) phase of the adsorbate to be absent, has long been vaguely attributed to changes in the nanopore structure, but no mathematically consistent explanation has been presented. The present work takes an analytical approach to account for discrete molecular forces in the nanopore fluid and proposes two related mechanisms that can explain the hysteresis at low vapor pressure without assuming any change in the nanopore structure. The first mechanism, presented in Part I,…
Spatial confinement in nanoporous media affects the structure, thermodynamics and mobility of molecular soft matter often markedly. This article reviews thermodynamic equilibrium phenomena, such as physisorption, capillary condensation, crystallisation, self-diffusion, and structural phase transitions as well as selected aspects of the emerging field of spatially confined, non-equilibrium physics, i.e. the rheology of liquids, capillarity-driven flow phenomena, and imbibition front broadening in nanoporous materials. The observations in the nanoscale systems are related to the corresponding bu…
During spontaneous imbibition a wetting liquid is drawn into a porous medium by capillary forces. In systems with comparable pore length and diameter, such as paper and sand, the front of the propagating liquid forms a continuous interface. Sections of this interface advance in a highly correlated manner due to an effective surface tension, which restricts front broadening. Here we investigate water imbibition in a nanoporous glass (Vycor) in which the pores are much longer than they are wide. In this case, no continuous liquid-vapor interface with coalesced menisci can form. Anomalously fast …
Based on the capillary pore model (space-charge theory) for combined fluid and ion flow through cylindrical nanopores or nanotubes, we derive the continuum equations modified to include wall slip. We focus on the ionic conductance and streaming conductance, cross-coefficients of relevance for electrokinetic energy conversion and electro-osmotic pumping. We combine the theory with a Langmuir-Stern 1-pK charge regulation boundary condition resulting in a non-monotonic dependence of the cross-coefficients on salt concentration.
We present measurements on the spontaneous imbibition (capillary rise) of water, a linear hydrocarbon (n-C16H34) and a liquid crystal (8OCB) into the pore space of monolithic, nanoporous Vycor glass (mean pore radius 5 nm). Measurements on the mass uptake of the porous hosts as a function of time, m(t), are in good agreement with the Lucas-Washburn square root of time prediction, typical of imbibition of liquids into porous hosts. The relative capillary rise velocities scale as expected from the bulk fluid parameters.
Apparent liquid permeability (ALP) in ultra-confined permeable media is primarily governed by the pore confinement and fluid-rock interactions. A new ALP model is required to predict the interactive effect of the above two on the flow in mixed-wet, heterogeneous nanoporous media. This study derives an ALP model and integrates the compiled results from molecular dynamics (MD) simulations, scanning electron microscopy, atomic force microscopy, and mercury injection capillary pressure. The ALP model assumes viscous forces, capillary forces, and liquid slippage in tortuous, rough pore throats. Pre…
We experimentally explore pressure-driven flow of water and n-hexane across nanoporous silica (Vycor glass monoliths with 7 or 10 nm pore diameters, respectively) as a function of temperature and surface functionalization (native and silanized glass surfaces). Hydraulic flow rates are measured by applying hydrostatic pressures via inert gases (argon and helium, pressurized up to 70 bar) on the upstream side in a capacitor-based membrane permeability setup. For the native, hydrophilic silica walls, the measured hydraulic permeabilities can be quantitatively accounted for by bulk fluidity provid…
