A&A 464, 393-398 (2007)
DOI: 10.1051/0004-6361:20066275
Photodissociation of organic molecules in star-forming regions
III. Methanol
S. Pilling1, R. Neves2, A. C. F. Santos3, and H. M. Boechat-Roberty21 Laboratório Nacional de Luz Síncrotron, Caixa Postal 6192, CEP 13084-971, Campinas, SP, Brazil
e-mail: spilling@lnls.br
2 Observatório do Valongo, Universidade Federal do Rio de Janeiro, Ladeira Pedro Antônio 43, CEP 20080-090, Rio de Janeiro, RJ, Brazil
3 Instituto de Física, Universidade Federal do Rio de Janeiro, Caixa Postal 68528, CEP 21941-972, Rio de Janeiro, RJ, Brazil
(Received 18 August 2006 / Accepted 11 December 2006 )
Abstract
The presence of methyl alcohol or methanol (CH3OH) in several
astrophysical environments has been characterized by its high abundance that depends on
both the production rate and the destruction rate. In the present work, the
photoionization and photodissociation processes of methanol have been experimentally
studied, employing soft X-ray photons (100-310 eV) from a toroidal grating monochromator
(TGM) beamline of the Brazilian Synchrotron Light Laboratory (LNLS). Mass spectra were
obtained using the photoelectron photoion coincidence (PEPICO) method. Kinetic energy
distribution and abundances for each ionic fragment have been obtained from the analysis
of the corresponding peak shapes in the mass spectra. Absolute photoionization and
photodissociation cross sections were also determined. We have found, among the channels
leading to ionization, about 11-16% of CH3OH survive the soft X-rays photons. This
behavior, together with an efficient formation pathways, may be associated with the high
column density observed in star-forming regions. The three main photodissociation
pathways are represented by COH+ (or HCO+) ion release (with ejection of H2 +
H), the dissociation via C-O bond rupture (with strong charge retention preferentially
on the methyl fragment) and the ejection of a single energetic (2-4 eV) proton. Since
methanol is very abundant in star forming regions, the produced protons could be an
alternative route to molecular hydrogenation or a trigger for secondary dissociation
processes or even to promote extra heating of the environment.
Key words: astrochemistry -- methods: laboratory -- ISM: molecules -- X-rays: ISM -- molecular data -- molecular processes
© ESO 2007

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