Astron. Astrophys. 325, 1264-1279 (1997)
2. Model of the accretion disk
We use in this paper the same semi-analytical model for a thin
stationary accretion disk as in Duschl et al. (1996, henceforth called
Paper II)
1 and in Paper I. The
details of the model are described in Paper II. The resulting basic
equations for the disk structure are
![[EQUATION]](img4.gif)
where s is the radial distance from the protosun in units
AU, is the surface density, h the (half)
thickness of the disk, M the mass of the protostar,
the solar mass, the
constant accretion rate in units of , and
P and T are the pressure and temperature in the midplane
of the disk, respectively. is the mass
absorption coefficient and µ the mean molecular weight.
The opacity is determined by the opacity of the dust and the gas (see
Sect. 2.1).
Illumination due to the accreting star and/ or the disk-star
boundary layer may lead to modifications of the disk structure, even
to self induced warping (Pringle 1996). In the present investigation
such effects are not accounted for.
The inwards directed drift velocity of the disk material is
![[EQUATION]](img10.gif)
Integrating this with respect to time yields the radial position of
a fixed gas parcel at each instant t
![[EQUATION]](img11.gif)
is the initial position of the parcel at
.
The vertical component of the gas velocity
accounting for the decrease of the height h of the accretion
disk with decreasing s is
![[EQUATION]](img15.gif)
In the one zone approximation, the vertically averaged gradient of
the vertical velocity is
![[EQUATION]](img16.gif)
The basic parameters of the disk model used in our calculation are
listed in Table 1.
![[TABLE]](img27.gif)
Table 1. Model parameters of the accretion disk used in the computation of disk structure
2.1. Opacity
In our model calculation, the opacity of the disk material is
determined for each time step simultaneously with the temperature in
the central plane of the disk. The temperature dependent Rosseland
mean opacity of the two main dust components (silicate and graphite)
is calculated using the dust extinction model of Draine and Lee (1984)
and Draine (1985) (see Paper I for more details). This is probably a
strong oversimplification for the true absorption properties of dust
in protoplanetary accretion disks since coagulation will modify the
dust properties (e.g. Henning and Stognienko 1996), but this process
presently cannot be coupled to our type of model calculation.
For the Rosseland mean of the mass extinction coefficient of the
gas, , we use the analytical approximations to
tabular values given by Lin and Papaloizou (1985) and Bell and Lin
(1994):
(i) Once the whole dust has disappeared, the absorption is
dominated by molecules (mainly H2 O and TiO, see for
instance the Figs. in Alexander 1975 or Sharp 1992). In the region
where molecular extinction dominates the mass extinction coefficient
of the gas can be approximated by
![[EQUATION]](img18.gif)
(ii) In the temperature regime between K and
K the H ions dominate
the extinction. In this region the mass extinction coefficient can be
approximated by
![[EQUATION]](img22.gif)
We note the high power of the temperature in this case: a small
change in the temperature dramatically modifies the opacity. This
strong temperature dependence of is the cause of
the so called viscous instability in accretion disks. Test
calculations for the time evolution of a protoplanetary disk using
this opacity law, indeed, showed this type of instability triggered by
the steep temperature raise of to occur (cf.
Bell and Lin 1994).
(iii) For higher temperatures and
transitions of atoms and ions dominate the
extinction of the gas. The mass extinction coefficient can be
approximated in this case by
![[EQUATION]](img25.gif)
Temperatures above K where this
approximation becomes valid are usually not encountered in a
protoplanetary accretion disk. For our set of accretion disk
parameters (cf. Table 1) such high temperatures occur only at the
smallest radii of the disk (Eq. 3) and in the transition layer to the
stellar surface. Our model approximations for the disk break down in
this transition zone (see, e.g., Duschl and Tscharnuter 1991).
The total gas opacity is calculated from the interpolation formula
![[EQUATION]](img28.gif)
which smoothly interpolates between the different cases. In
Fig. 1 the different opacity approximations are displayed for a
value of the mean density of 10-8 g
cm-3 together with the interpolated value of the total
opacity. The total mass extinction coefficient of the disk material
(dust + gas) finally is obtained by the simple summation
![[FIGURE]](img31.gif) |
Fig. 1. Interpolation of the extinction coefficient. The dashed curves show the extinction by the indicated opacity sources for a mass density of g/ cm3. The full line is the interpolated extinction coefficient according to the prescription (12).
|
![[EQUATION]](img33.gif)
and are the mass
density of the carbon and silicon dust in the gas-dust mixture and
and are their extinction
coefficients. This simple addition of the different opacities is
surely not very precise but it should be sufficient for our present
more explorative calculation.
Fig. 2 shows as an example the temperature structure in the
inner part of the disk for AU resulting from
this opacity law. The dust vapourisation and the dissociation are
calculated here not by solving the corresponding rate equations but
from thermodynamic equilibrium as in Paper II. The disk equations with
the opacity law (13) have multiple valued solutions for T and
P in the radius interval AU
AU which results from the steep increase of
opacity in the region of hydrogen dissociation. If one starts at large
s and moves inwards one first moves on the lower branch of the
solution into the multiple valued region. In the stationary case there
results a strong upwards jump in the temperature if one reaches the
lower critical radius at 0.0728 AU where
becomes singular. As one moves further inwards
the solution then continues on the high temperature branch.
![[FIGURE]](img43.gif) |
Fig. 2. Structure of a stationary accretion disk with opacity law (12) for the gas component.
|
For time dependent models of an accretion disk it is known that the
very strong temperature dependence of the H
opacity ( , Eq. 10), resulting in the
multi-valued solution for the stationary case, gives rise to an
unstable structure of the disk (Meyer and Meyer-Hofmeister 1981,
Duschl 1991). This instability, however, is not destructive to the
disk but rather gives rise a limit-cycle behaviour. This introduces an
inherent time dependence into the problem and thus leads beyond the
scope of our present work. While the basic features of the instability
and the time dependent disk evolution due to it have been investigated
and are understood fairly well, not very much is known how a proper
treatment of the chemical evolution influences the overall evolution
of such an unstationary accretion disk. In this context it is
important to note that not only steep opacity gradients due to
hydrogen ionisation/ recombination can give rise to an instability.
Also steep gradients due to destruction of molecular absorbers (e.g.,
H2 O) can lead to similar consequences. We will address the
question of the chemical evolution of unstationary accretion disks in
a forthcoming paper.
In the present models of the chemistry of the disk we perform the
inwards integrations of the rate equations only down to a radius
slightly above the critical radius at AU where
the solution of the disk equations becomes singular. The calculation
is stopped at this point since the high temperature branch of the
solution is of no interest for the chemistry.
The opacity law (13) is used to determine for each time step the
temperature from Eq. (3) and pressure from Eq. (4) which is equivalent
to determine the zeros of the two following functions F and
G:
![[EQUATION]](img48.gif)
The extremely non-linearity of these functions results in
considerable numerical problems if coupled to the system of rate
equations for the chemistry and dust destruction, but the numerical
method presented in Paper I is well suited to handle such
problems.
© European Southern Observatory (ESO) 1997
Online publication: April 28, 1998
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