We combine high resolution isotherms measurements and light scattering technics to study over a broad temperature range collective effects during the condensation and evaporation of helium from Vycor, a prototypic disordered porous material. For evaporation, our results provide the first direct evidence for a crossover from a percolation collective mechanism at low temperature to a local cavitation mechanism at high temperature. No long range collective effects are detected during condensation. We compare these results to recent theoretical predictions emphasizing the specific role of disorder, and discuss their relevance for determining pores sizes distributions in disordered porous materials.

Sorption isotherm measurement is a standard method for characterizing porous materials. However, such isotherms are generally hysteretic, differing between condensation and evaporation. Quantitative measurement of pore diameter distributions requires proper identification of the mechanisms at play, a topic which has been and remains the subject of intensive studies. In this paper, we compare high-precision measurements of condensation and evaporation of helium in Vycor, a prototypical disordered porous glass, to a model incorporating mechanisms on the single pore level through a semimacroscopic description and collective effects through lattice simulations. Our experiment determines both the average of the fluid density through volumetric measurements and its spatial fluctuations through light scattering. We show that the model consistently accounts for the temperature dependence of the isotherm shape and of the optical signal over a wide temperature range as well as for the existence of thermally activated relaxation effects. This demonstrates that the evaporation mechanism evolves from pure invasion percolation from the sample’s surfaces at the lowest temperature to percolation from bulk cavitated sites at larger temperatures. The model also shows that the experimental lack of optical signals during condensation does not imply that condensation is unaffected by network effects. In fact, these effects are strong enough to make most pores to fill at their equilibrium pressure, a situation deeply contrasting the behavior for isolated pores. This implies that, for disordered porous materials, the classical Barrett–Joyner–Halenda approach, when applied to the condensation branch using an extended version of the Kelvin equation, should properly measure the true pore diameter distribution. Our experimental results support this conclusion.

High resolution measurements reveal that condensation isotherms of (4)He in high porosity silica aerogel become discontinuous below a critical temperature. We show that this behavior does not correspond to an equilibrium phase transition modified by the disorder induced by the aerogel structure, but to the disorder-driven critical point predicted for the athermal out-of-equilibrium dynamics of the random-field Ising model. Our results evidence the key role of nonequilibrium effects in the phase transitions of disordered systems.