Influences of polarity and hydration cycles on imbibition hysteresis in silica nanochannels.

Spontaneous liquid imbibition is a dominant mechanism for moving fluids in confinements with extremely high hydrodynamic resistance; i.e. nanopores.

Subsurface to substrate: dual-scale micro/nanofluidic networks for investigating transport anomalies in tight porous media.

Micro/nanofluidic experiments in synthetic representations of tight porous media, often referred to as "reservoir-on-a-chip" devices, are an emerging approach to researching anomalous fluid transport trends in energy-bearing and fluid-sequestering geologic porous media. We detail, for the first time, the construction of dual-scale micro/nanofluidic devices that are relatively large-scale, two-dimensional network representations of granular and fractured nanoporous media. The fabrication scheme used in the development of the networks on quartz substrates (master patterns) is facile and replicable: transmission electron microscopy (TEM) grids with lacey carbon support film were used as shadow masks in thermal evaporation/deposition and reactive ion etch (RIE) was used for hardmask pattern transfer.

Anomalous liquid imbibition at the nanoscale: the critical role of interfacial deformations.

We observed that imbibition of various Rhodamine B-doped wetting liquids in an array of different-sized, horizontal, two-dimensional silica nanochannels terminated within the channels as a function of hydraulic diameter and liquid type. This front termination is not predicted by the classic Washburn equation for capillary flow, which establishes diffusive dynamics in horizontal channels. Various explanations for the anomalous static imbibition measurements were negated; hydrodynamics, thermodynamics, surface chemistry and mechanics were all taken into consideration for this analysis.

Quantification of bulk solution limits for liquid and interfacial transport in nanoconfinements.

Liquid imbibition, the capillary-pressure-driven flow of a liquid into a gas, provides a mechanism for studying the effects of solid-liquid and solid-liquid-gas interfaces on nanoscale transport. Deviations from the classic Washburn equation for imbibition are generally observed for nanoscale imbibition, but the identification of the origin of these irregularities in terms of transport variables varies greatly among investigators. We present an experimental method and corresponding image and data analysis scheme that enable the determination of independent effective values of nanoscale capillary pressure, liquid viscosity, and interfacial gas partitioning coefficients, all critical transport variables, from imbibition within nanochannels.