This work deals with electrical properties of nanosurfaces in contact with electrolyte solutions. Single halide ion solutions were studied by streaming potential (SP) measurements and observed retention (R-obs) of the F-, Cl-, and Br- ions across nanofiltration (NF) membranes. The detailed understanding of an electrolyte solution mass transfer requires an intimate knowledge of the physicochernical interactions occurring between nanoporous, materials and electrolyte solutions across the first-generation composite membranes called NF5.5, NF70 and NF90. These membranes are composed of a polysulfone mesoporous sublayer and a microporous skin layer in polyamide. In order to get a better understanding of these effects, it seems attractive to compare the mass transfer permeation of the monovalent ions F-, Cl-, and Br- with the. electrokinetic characterizations deduced from a properly developed SP apparatus. SP measurements is a very simple method to show the intrinsinc charges on membrane pore walls. The membrane's electrical properties are studied with SP design modeling pH, ionic strength and kind of electrolyte solutions. We have observed that the isoelectric point (IEP) of the membrane materials is both dependent on the ionic strength and on the kind of electrolyte solution. The IEP in the presence of KCl is 4.4 at 0.0001 mol/L and 5.8 at 0.001 mol/L, showing an increasing adsorption of the cation K by increasing its solution concentration. For a fixed concentration, the effect of the electrolyte solution has shown that a higher adsorption of Ca++ occurs in comparison to K+ and Na+. But the adsorption of these electrolyte solutions is essentially reversible as observed under dilution conditions. Furthermore SP measurements were used for the first time to characterize the transmembrane pressure ranges where a convective and/or a diffusional mass transfer occurs. Such an approach was developed to correlate the R-obs of the halide ions F-, Cl- and Br- with the kind of mass transfer (diffusional and/or convective) occurring predominantly under transmembrane pressure variations. Thus the NF70 membrane shows at low pressure (under 3 bar) the order of R., following the hydrated ionic radius: R-obs.(F-)>R-obs.(Cl-)>R-obs.(Br-). For a higher pressure (> 3 bar) an inversion occurs between Cl- and Br-, but F was not affected. These results open a new prospective area for selective defluorination of brackish drinking Waters using NF membranes under low transmembrane pressure.