Author/Authors :
Boonman، A. M. S. نويسنده , , Tak، F. F. S. van der نويسنده , , Braakman، R. نويسنده , , van Dishoeck، E. F. نويسنده ,
Abstract :
The sulphur chemistry in nine regions in the earliest stages of high-mass star formation is studied through single-dish submillimeter spectroscopy. The line profiles indicate that 10-50% of the SO and SO 2 emission arises in high-velocity gas, either infalling or outflowing. For the low-velocity gas, excitation temperatures are 25 K for H 2S, 50 K for SO, H 2CS, NS and HCS +, and 100 K for OCS and SO 2, indicating that most observed emission traces the outer parts ( T<100 K) of the molecular envelopes, except high-excitation OCS and SO 2 lines. Abundances in the outer envelopes, calculated with a Monte Carlo program, using the physical structures of the sources derived from previous submillimeter continuum and CS line data, are ~10 -8 for OCS, ~10 -9 for H 2S, H 2CS, SO and SO 2, and ~10 -10 for HCS + and NS. In the inner envelopes ( T>100 K) of six sources, the SO 2 abundance is enhanced by a factor of ~100-1000. This region of hot, abundant SO 2 has been seen before in infrared absorption, and must be small, <0 “2 (180 AU radius). The derived abundance profiles are consistent with models of envelope chemistry which invoke ice evaporation at T ~ 100 K. Shock chemistry is unlikely to contribute. A major sulphur carrier in the ices is probably OCS, not H 2S as most models assume. The source-to-source abundance variations of most molecules by factors of ~10 do not correlate with previous systematic tracers of envelope heating. Without observations of H 2S and SO lines probing warm ( >100 K) gas, sulphur-bearing molecules cannot be used as evolutionary tracers during star formation.
Keywords :
ISM: molecules , molecular processes , stars: formation , stars: circumstellar matter