@article {2090,
	title = {Reactive uptake of NO3, N2O5, NO2, HNO3, and O-3 on three types of polycyclic aromatic hydrocarbon surfaces},
	journal = {Journal of Physical Chemistry A},
	volume = {112},
	number = {14},
	year = {2008},
	note = {Gross, Simone Bertram, Allan K.},
	month = {Apr},
	pages = {3104-3113},
	abstract = {We investigated the reactive uptake of NO3, N2O5, NO2, HNO3, and O-3 on three types of solid polycyclic aromatic hydrocarbons (PAHs) using a coated wall flow tube reactor coupled to a chemical ionization mass spectrometer. The PAH surfaces studied were the 4-ring systems pyrene, benz[a]anthracene, and fluoranthene. Reaction of NO3 radicals with all three PAHs was observed to be very fast with the reactive uptake coefficient, gamma, ranging from 0.059 (+0.11/-0.049) for benz[a]anthracene at 273 K to 0.79 (+0.21/-0.67) for pyrene at room temperature. In contrast to the NO3 reactions, reactions of the different PAHs with the other gas-phase species (N2O5, NO2, HNO3, and O-3) were at or below the detection limit (gamma <= 6.6 x 10(-5)) in all cases, illustrating that these reactions are at best slow. For NO3 we also investigated the time dependence of the reactive uptake to determine if the surface-bound PAH molecules were active participants in the reaction (i.e., reactants). Reaction of NO3 on all three PAH surfaces slowed down at 263 K after long NO3 exposure times, suggesting that the PAH molecules were reactants. Additionally, NO2 and HNO3 were identified as major gas-phase products. Our results show that under certain atmospheric conditions, NO3 radicals can be a more important sink for PAHs than NO2, HNO3, N2O5, or O-3 and impact tropospheric lifetimes of surface-bound PAHs.},
	isbn = {1089-5639},
	url = {<Go to ISI>://000254659700015},
	author = {Gross, S. and Bertram, A. K.}
}
