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Aqueous high-temperature chemistry of carbo- and heterocycles. 14. Mercaptans and sulfonic acids

Journal Article · · Energy and Fuels; (USA)
DOI:https://doi.org/10.1021/ef00023a028· OSTI ID:6088897
; ; ;  [1];  [2]
  1. Univ. of Florida, Gainesville (USA)
  2. Exxon Research and Engineering Company, Annandale, NJ (USA)
Phenylmethanethiol and phenylethanethiol are highly reactive under both thermolytic and aquathermolysis conditions. 3-Phenylpropanethiol shows some conversion, but 75% or more remains after 5 days at 250{degree}C. Initial coupling reactions of such mercaptans to form disulfides which then lose H{sub 2}S provide facile pathways for the formation of H{sub 2}S during the steam stimulation process used to recover heavy bitumens. 2-(2-Pyridyl)- and 2-(4-pyridyl)ethanesulfonic acids give a wide variety of derivatives under both thermal and aqueous conditions, with 2- and 4-methylpyridines as major products. By contrast 2-phenylethanesulfonic acid is unreactive, and its sodium salt gives only traces of styrene under aquathermolysis conditions.
OSTI ID:
6088897
Journal Information:
Energy and Fuels; (USA), Journal Name: Energy and Fuels; (USA) Vol. 4:5; ISSN 0887-0624; ISSN ENFUE
Country of Publication:
United States
Language:
English