In the Rohrschneider-McReynolds method of constants used in gas chromatogra
phy for estimating polarity and selectivity of stationary phases, the stand
ard stationary nonpolar phase and the standard set of paraffin hydrocarbons
were excluded. A method for separating the dispersion and polar (specific)
components of the experimentally determined differential heats of adsorpti
on of polar organic molecular tests on the studied surfaces was suggested,
The electron and proton donor and acceptor abilities of the surface of lign
osulfonate (LS) powders of various molecular and cationic compositions were
estimated. The differential specific heats of adsorption were correlated w
ith the donor and acceptor numbers of test adsorbate molecules (benzene, di
ethyl ether, nitromethane, methyl ethyl ketone, pyridine, and ethanol) on t
he surface of LSs. The dependences of the specific and nonspecific differen
tial heats of adsorption on the electronic polarizability of singly charged
surface cations and the molecular weight of LS were determined. The conclu
sion was drawn that electron acceptor properties prevailed on the surface o
f lignosulfonates.