This paper reports on investigations about the adsorption at the air-water surface, and for the sake of comparison at the silica-solution interface, of two 1-2 electrolytes, Pb(NO3)(2) and PbCl2, at first alone and then from a mixture with carbofuran or with benzene; all of them were at concentrations below 10(-2) M. The limited domain, where the Debye and Huckel formalism for solutions and the Wagner-Onsager-Samaras (WOS) model for surfaces are correct, is then respected. This study was aimed at trying to identify the part played in the surface by the different particles of the system components and in particular the role of water. When aqueous solutions of nonorganic salts are dilute enough, their surface tensions are known to be salt concentration-independent; however, the zero value of the resulting relative adsorption has never been the subject of analysis about water behavior. By combining experimental relative adsorptions and Gibbs excesses calculated from the WOS theory, we will show that, in well-known solutions such as KCl ones, where the negative excess in salt can be very precisely modeled by the WOS theory, the resulting water excess W is negative. The same result can be obtained by taking into account the Ray-Jones effect. This observation drove us to wonder about the results of a similar analysis done on solutions of unsymmetrical electrolytes and on mixtures of salt and organic molecules. Experiments showed that, for all of the systems, W was negative. For a given salt, W was more negative in the presence of organic molecules, and carbofuran was a more efficient water repellent than benzene; water repulsion was greater with nitrates than with chlorides. From these data, it seems that water was repelled toward the solution bulk, whereas ions probably took place between the bulk and a layer of organic molecules. These observations called for a more detailed modeling.