Triple-point wetting is a well-known phenomenon of many simple adsorbates o
n solid substrates. It implies that in the liquid phase above the triple-po
int temperature, T-3, complete wetting with the formation of arbitrarily th
ick films is observed, whereas below T-3 only a few monolayers of the solid
phase are adsorbed at saturated vapour pressure. This effect is usually as
cribed to substrate-induced strain in the solid film, which occurs due to l
attice mismatch and/or the strong van der Waals pressure in the first monol
ayers. Molecular hydrogen is a suitable system to investigate this phenomen
on, in particular by tailoring the adsorbate-substrate interaction by means
of thin preplating layers of other adsorbates, and by introducing disorder
into the system by using not only the pure systems H-2 and D-2, but also m
ixtures thereof. In particular the dependence of T-3 of the mixture on the
mass ratio of its components is measured and deviations from the simple van
der Waals law are discussed. The experiments show that triple-point wettin
g is a rather dominating effect, which in contrast to expectation persists
even if the system parameters are widely varied, indicating that the presen
t picture of this effect is incomplete.