Abstract

Surface energetic characterization of porous solids usually requires the determination of the contact angle. This quantity is deduced by imbibition experiments carried out in such media with high surface tension liquids. Now then, this methodology needs the geometrical characterization of the porous medium by means of the deduction of its effective radius. Normally, this is made by imbibition experiments with n-alkanes, liquids whose surface tension is low enough as to suppose their contact angles with the solid surface are null. However, this last procedure is not free from some criticisms. Among them, the possible influence of the imbibition velocity on the contact angle, the effect of the precursor liquid film ahead the advancing liquid front on the driving force that gives rise to the movement, or the dependence of the effective radius on the length of the hydrocarbon chain of the n-alkanes. In an attempt of going deeply in these questions, imbibition experiments with n-alkanes have been carried out in porous columns of powdered calcium fluoride. These experiments have consisted of the measurement of the increase in the weight of the columns caused by the migration of the liquids through their interstices. The analysis of their results has been carried out by means of a new procedure based on the study of the velocity profile associated to the weight increase. This analysis has permitted us to conclude that, at least in the calcium fluoride columns, the contact angle of the n-alkane is not influenced by the capillary rise velocity, it taking in fact a null value during the process. On the other hand, it has been also proved that the driving force of the movement is caused by the replacement of the solid–vapour interface by the solid–liquid interface that happens during the imbibition, which means that only the Laplace's pressure, and not the precursor liquid film, contributes to the development of the phenomenon. Finally, it has been compared the values of the effective radius associated to each n-alkane, similar values being found independently from the particular liquid employed in the experiments, fact that indicates that the porous solid can be considered as a bunch of cylindrical and parallel capillaries of the same radius.

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