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A spectroscopic identification of the products formed in the gas-phase reaction of OH with the atmospheric sulfur compounds: CH/sub 3/SH, CH/sub 3/SSCH/sub 3/ and SO/sub 2/

Conference · · Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States)
OSTI ID:5655503

The mechanism for the conversion of naturally occurring atmospheric sulfur compounds to sulfur dioxide is not yet established. The sulfur dioxide produced during degradation of sulfur compounds can undergo further chemical and/or physical interactions to form sulfuric acid, which is one of the components of acid rain. A number of sulfur compounds have been detected in the atmosphere; COS (carbonyl sulfide), CS/sub 2/ (carbon disulfide), H/sub 2/S (hydrogen sulfide), CH/sub 3/SH (methyl mercaptan), CH/sub 3/SCH/sub 3/ (dimethyl sulfide) and CH/sub 3/SSCH/sub 3/ (dimethyl disulfide). It is generally believed that the biological reduction of sulfur compounds is a major natural source for these atmospheric sulfur compounds. The chemical degradation of sulfur compounds of the type X-S-Y (X = H or CH/sub 3/, Y = H, CH/sub 3/ or SCH/sub 3/) is proposed to be initiated by their reactions with OH radicals. The proposed mechanisms for the sulfur compounds used in this study (CH/sub 3/SH, CH/sub 3/SSCH/sub 3/ and SO/sub 2/) are: a) the OH radical forms a weak complex with CH/sub 3/SH which further reacts with O/sub 2/ before decomposing to form sulfur dioxide; b) an adduct is formed between CH/sub 3/SSCH/sub 3/ and OH radical which decomposes to yield CH/sub 3/S and CH/sub 3/SOH. These mechanisms have been proposed to account for the pressure-dependence and temperature-dependence of the observed reaction rates. The mercaptyl radical thus formed could undergo further chemical reactions.

Research Organization:
School of Geophysical Sciences, Georgia Institute of Technology, Atlanta, GA 30332
OSTI ID:
5655503
Report Number(s):
CONF-860425-
Journal Information:
Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States), Journal Name: Am. Chem. Soc., Div. Pet. Chem., Prepr.; (United States) Vol. 31:2; ISSN ACPCA
Country of Publication:
United States
Language:
English