Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9605438 | Journal of Photochemistry and Photobiology A: Chemistry | 2005 | 5 Pages |
Abstract
Long-path length FT-IR-smog chamber techniques were used to study the title reactions in 700 Torr of N2 or N2/O2, diluent at 296 K. There was no discernable effect of CxF2x + 1-group size on the reactivity of CxF2x + 1CHCH2 towards Cl atoms and OH radicals. Values of k(Cl + CxF2x + 1CHCH2) = (9.07 ± 1.08) Ã 10â11 cm3 moleculeâ1 sâ1 and k(OH + CxF2x + 1CHCH2) = (1.36 ± 0.25) Ã 10â12 cm3 moleculeâ1 sâ1 were measured. Ozone reacts more rapidly with CF3CHCH2 than with larger members of the series; k(O3 + CF3CHCH2) = (3.5 ± 0.3) Ã 10â19 cm3 moleculeâ1 sâ1 and k(O3 + CxF2x + 1CHCH2) = (2.0 ± 0.4) Ã 10â19 cm3 moleculeâ1 sâ1 (x â¥Â 2). The atmospheric lifetime of CxF2x + 1CHCH2 (x â¥Â 2) is approximately 8 days with 90% of removal occurring via reaction with OH and 10% via reaction with O3.
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Authors
M.P. Sulbaek Andersen, O.J. Nielsen, A. Toft, T. Nakayama, Y. Matsumi, R.L. Waterland, R.C. Buck, M.D. Hurley, T.J. Wallington,