276
IONISATION, DIFFUSION, ROTATION
lighter elements—not quite so abruptly-—drop from the surface to the
centre. Hydrogen lags behind the others, the reversal occurring when
¿i 0 /3 0 = 0-5, i.e. in extremely massive stars with 1 — )S 0 > 0-75. Helium
leaves the surface in stars of more than 10 times the mass of the sun—
just the stars which show its spectrum most conspicuously. The other light
elements reverse at smaller masses.
It would be difficult to reconcile these results with the observed spectra
at the surfaces of the stars where light and heavy elements appear to
gether. For some elements the exponent of T is so large as to leave not a
single atom anywhere near the surface. If we believed these results we
might have to consider important modifications in the theory of the stellar
interior—for example, its constitution of heavy elements in small stars
and light elements in great stars. We must now point out that these
formulae give the ultimate steady state of the material ; and the question
arises whether the approach to this steady state is sufficiently rapid to
effect appreciable separation in the life-time of a star or to overcome the
mixing tendencies which may be retarding it.
Thermal Diffusion,
194. It is desirable to give a warning against possible misuse of (191-3)
and similar formulae. In a star <f> is proportional to T by (58-3) so that
gimi-mj) <t>/RT p as the same value at all parts. We might be tempted to
infer that $j/s 2 is constant so that no separation of the different sorts of
atoms occurs. This is very far from true. The formulae (191-1) refer to
thermodynamical equilibrium, and there is no justification for employing
them even as an approximation in material at non-uniform temperature.
Our procedure is to differentiate these formulae keeping T constant
because the formulae apply only to uniform temperature. Thus (191-2)
gives
i <‘°g *) -
m x d<f>
RT dz
.(194-1).
This gives us the density gradients of the different kinds of atoms required
to keep the composition steady when the material is under a pressure
gradient but no temperature gradient; that is to say, it gives us the density
gradients set up to prevent further pressure diffusion. If now we superpose
a temperature gradient this will set up diffusion on its own account known
as thermal diffusion. Hence, in general, the required density gradient
consists of two parts, the one set up by pressure diffusion, and the other
by thermal diffusion.
If thermal diffusion can be shown to be negligible the differential
formula (194-1), but not the integral formula, is valid for non-uniform
temperature. We then re integrate it allowing T to vary.