The pressure applied in liquid chromatography (LC) can influence the capaci
ty factor of analytes. Using commercial equipment, column (33 x 4.6 mm) and
1.5 mu m non-porous, tetradecyl (C-14) coated silica particles, a moderate
but significant change in the capacity factor was observed with increasing
pressure. Depending on the experimental conditions the relationship was fo
und to be either linear or non-linear. In the latter case the retention inc
reased at first, but later tended to decrease at still higher pressure. The
results direct attention to the role of the pressure (and hence of flow ra
te and heat of friction) in determing capacity factors.