Ultraviolet Survey of CO and H_2 in Diffuse Molecular Clouds: The Reflection of Two Photochemistry Regimes in Abundance Relationships

Details Ultraviolet Survey of CO and H_2 in Diffuse Molecular Clouds: The Reflection of Two Photochemistry Regimes in Abundance Relationships Ultraviolet Survey of CO and H_2 in Diffuse Molecular Clouds: The Reflection of Two Photochemistry Regimes in Abundance Relationships

2008-07-07

arxiv.org/abs/0807.0940v1

Astronomy and Astrophysics

Astrophysics

40 pages in emulateapj style, to appear in the Astrophysical Journal

Scientific paper

10.1086/591484

(Abridged) We carried out a comprehensive far-ultraviolet (UV) survey of ^12CO and H_2 column densities along diffuse molecular Galactic sight lines in order to explore in detail the relationship between CO and H_2. We measured new CO abundances from HST spectra, new H_2 abundances from FUSE data, and new CH, CH^+, and CN abundances from the McDonald and European Southern Observatories. A plot of log N(CO) versus log N(H_2) shows that two power-law relationships are needed for a good fit of the entire sample, with a break located at log N(CO, cm^-2) = 14.1 and log N(H_2) = 20.4, corresponding to a change in production route for CO in higher-density gas. Similar logarithmic plots among all five diatomic molecules allow us to probe their relationships, revealing additional examples of dual slopes in the cases of CO versus CH (break at log N = 14.1, 13.0), CH^+ versus H_2 (13.1, 20.3), and CH^+ versus CO (13.2, 14.1). These breaks are all in excellent agreement with each other, confirming the break in the CO versus H_2 relationship, as well as the one-to-one correspondence between CH and H_2 abundances. Our new sight lines were selected according to detectable amounts of CO in their spectra and they provide information on both lower-density (< 100 cm^-3) and higher-density diffuse clouds. The CO versus H_2 correlation and its intrinsic width are shown to be empirically related to the changing total gas density among the sight lines of the sample. We employ both analytical and numerical chemical schemes in order to derive details of the molecular environments. In the low-density gas, where equilibrium-chemistry studies have failed to reproduce the abundance of CH^+, our numerical analysis shows that nonequilibrium chemistry must be employed for correctly predicting the abundances of both CH^+ and CO.

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