![]() | ![]() |
Astron. Astrophys. 336, 309-314 (1998) 2. ModelIf the telescope beam includes a number of unresolved clumps then
the difference in emission may be due to the differences in the
physical, and hence chemical, evolution between them. We proposed in
Paper 1 that all clumps had collapsed from a relatively diffuse state,
in which only hydrogen is predominantly molecular. As the gas
collapses, a large amount of free carbon is available to form
molecules such as CS, before the carbon is swallowed up in CO. These
`early-time' carbon-based molecules (like CS) exhibit a peak in
fractional abundance (= n(X)/ appear to be considerably slower at 10K than other comparable reactions. Only cores that are stable upon the initial collapse will be detectable in these molecules. Other cores, perhaps dispersed quickly because they are too small or are not in pressure equilibrium with the external medium, will not be detectable in "late-time" species. Our chemical model is described in detail in Paper 1; the important
points are reiterated here. In a single point calculation chemical
abundances are followed from initial conditions typical of a diffuse
cloud ( The observations pertinent to Paper 1 could only be explained if the effective freezeout parameter, FR, was low. This parameter accounts for the efficiency of adsorption of gas molecules onto dust grain surfaces and for the grain size distribution (which affects the surface area available for gas species to stick to), and its low value may be an indication of effective desorption rather than inefficient sticking. There are a number of methods of desorption, described e.g. in Williams & Taylor (1996), and amongst the more recent to be considered are desorption due to the heat emitted from the exothermic formation of molecular hydrogen on the grain surface (Willacy, Williams & Duley 1994), and the desorption of CO by transfer of energy from the O-H vibration at 3.1 µm (Dzegilenko & Herbst 1995). As in Paper 1 we normally take FR=0.01, and we also use the same elemental abundances. However, the chemical data has been updated, and also extended, by increasing the carbon chain chemistry to include species as complex as HC3N (there are now 138 gas phase species and 1996 reactions), and the revised UMIST ratefile has also been used (Millar, Farquhar & Willacy 1997). ![]() ![]() ![]() ![]() © European Southern Observatory (ESO) 1998 Online publication: July 7, 1998 ![]() |