Characterisation of porous solids using integrated nitrogen sorption and mercury porosimetry

Abstract

The two different techniques of nitrogen sorption and mercury porosimetry, which are generally utilised completely separately, have been integrated into the same experiment to improve upon the information obtained from both methods. Nitrogen sorption isotherms have been run both before and after a mercury porosimetry experiment on the same sample. This experiment has revealed that for a particular type of sol–gel silica catalyst support the entrapped mercury is confined to only the very largest pores in the material. Light micrograph studies have shown that the spatial distribution of entrapped mercury is highly heterogeneous. These results suggest that mercury entrapment within the material is caused by a mechanism involving macroscopic ( >0.1 mm ) heterogeneities in the pore structure. These findings conflict with the usual assumptions generally made in simulations of porosimetry based on random pore bond network models. The new work has shown that, in conjunction with computer simulations involving the correct mercury retraction mechanism, mercury porosimetry and nitrogen sorption can be used to study the spatial distribution of all pore sizes within a mesoporous material. A percolation analysis of the nitrogen sorption data, obtained both before and after mercury entrapment, allowed broad features of the spatial disposition of variously sized pores to be determined. The results reported here also support the use of new, semi-empirical alternatives to the Washburn Equation to analyse raw mercury porosimetry data, rather than the traditional approach.