Abstract
We present gravimetrical, optical, and neutron imaging measurements of the capillarity-driven infiltration of mesoporous silica glass by hydrocarbons. Square-root-of-time Lucas-Washburn invasion kinetics are found for linear alkanes from n-decane (C10) to n-hexacontane (C60) and for squalane, a branched alkane, in porous Vycor with 6.5 nm or 10 nm pore diameter, respectively. Humidity-dependent experiments allow us to study the influence on the imbibition kinetics of water layers adsorbed on the pore walls. Except for the longest molecule studied, C60, the invasion kinetics can be described by bulk fluidity and bulk capillarity, provided we assume a sticking, pore-wall adsorbed boundary layer, i.e. a monolayer of water covered by a monolayer of flat-laying hydrocarbons. For C60, however, an enhanced imbibition speed compared to the value expected in the bulk is found. This suggests the onset of velocity slippage at the silica walls or a reduced shear viscosity due to the transition towards a polymer-like flow in confined geometries. Both, light scattering and neutron imaging indicate a pronounced roughening of the imbibition fronts. Their overall shape and width can be resolved by neutron imaging. The fronts can be described by a superposition of independent wetting fronts moving with pore size-dependent square-root-of-time laws and weighted according to the pore size distributions obtained from nitrogen gas sorption isotherms. This finding indicates that the shape of the imbibition front in a porous medium, such as Vycor glass, with interconnected, elongated pores, is solely determined by independent movements of liquid menisci. These are dictated by the Laplace pressure and hydraulic permeability variations and thus the pore size variation at the invasion front. Our results suggest that pore size distributions can be derived from the broadening of imbibition fronts.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have