Open AccessA study of the NO x dependence of isoprene oxidation
Author(s) -
Barket Dennis J.,
Grossenbacher John W.,
Hurst Julia M.,
Shepson Paul B.,
Olszyna Kenneth,
Thornberry Troy,
Carroll Mary Anne,
Roberts James,
Stroud Craig,
Bottenheim Jan,
Biesenthal Thomas
Publication year - 2004
Publication title -
journal of geophysical research: atmospheres
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.67
H-Index - 298
eISSN - 2156-2202
pISSN - 0148-0227
DOI - 10.1029/2003jd003965
Subject(s) - isoprene , methyl vinyl ketone , national laboratory , environmental chemistry , chemistry , ozone , environmental science , organic chemistry , physics , catalysis , polymer , engineering physics , copolymer
A large set of isoprene and isoprene oxidation product concentration data from four North American sites was examined to assess the NO x dependence of the daytime oxidation of isoprene. Sites that represent a wide range of NO x (50 ppt to 30 ppb) were studied and include the Dickson, Tennessee, and Cornelia Fort Air Park sites during the 1999 Southern Oxidants Study, the Pellston, Michigan, site during the 1998 PROPHET summer intensive, and the Kejimkujik National Park site during the Atlantic 1996 study. Knowledge of NO x and HO x concentrations were critical for this evaluation. While NO x data are readily available at all sites, HO x data are limited. We employed a simple 10‐reaction HO x model to calculate steady state OH radical concentrations as a function of [NO x ] to enable analysis of the data from all sites. Here, we use methyl vinyl ketone (MVK) concentrations to quantify the extent of isoprene‐OH oxidation. Making use of the MVK/isoprene ratio, we show that the rate of production of isoprene oxidation products at various North American sites, although highly variable, exhibits the crossover from NO x ‐dependent to VOC‐dependent conditions at ∼8 ppb [NO x ], in agreement with what is calculated from HO x measurements and our calculations.