In 1987, van Oss, Chaudhury and Good introduced the Lewis acid (or hyd
rogen-bond acidic) component, gamma(+), and Lewis base (or hydrogen-bo
nd basic) component, gamma(-), and assumed the ratio of gamma(+) and g
amma(-) for water at 20 degrees C to be 1.0. With that ratio, the base
components, gamma(-), for other liquids and polymers appeared to be o
verestimated. Recently, we unexpectedly found a correlation between ga
mma(+) and gamma(-) and the linear solvation energy relationship (LSER
) parameters alpha (hydrogen-bond-donating ability, HBD) and beta (hyd
rogen-bond-accepting ability, HBA), introduced by Taft and Kamlet in 1
976. Interestingly, we found the ratio for the normalized alpha and be
ta for water at ambient temperature to be 1.8 instead of 1.0. Based on
this new ratio for the corresponding gamma(+) and gamma(-), the calcu
lated total surface tensions for other liquids and polymers at 20 degr
ees C are generally unchanged, as expected, despite the favorable chan
ges in the gamma(+) and gamma(-) ratio to make them less basic. In add
ition, the implications of other LSER parameters, e.g. Pi and delta(H
)(2) on surface properties will be briefly mentioned.