Photoenhanced NO2 loss on simulated urban grime

RACHID AMMAR; MARIA EUGENIA MONGE; CHRISTIAN GEORGE; BARBARA D'ANNA

Chemphyschem

WILEY-V C H VERLAG GMBH

Lugar: Weinheim; Año: 2010 vol. 11 p. 3956 - 3961

1439-4235

The present study focuses on the heterogeneous reaction between gaseous NO2 and solid pyrene/KNO3 films, used as a simplified proxy of urban grime. This reaction is investigated under simulated atmospheric conditions with respect to relative humidity, NO2 concentration and irradiation in a coated-wall flow-tube reactor. The geometric steady-state uptake coefficients gamma(geo) for pyrene/KNO3 films exposed to 50 ppbv of NO2 ranged from 1.12 x 10(-7) in the dark to 2.67 x 10(-6) under near-UV irradiation (300-420 nm) and decreased with increasing NO2 concentration in the range 30-120 ppbv. NO2 removal is linearly dependent on light intensity, with release of gas-phase NO and HONO. Analysis of the solid film by ion chromatography and GC-MS showed the formation of nitrite ions and traces of 1-nitropyrene. A light-induced reaction mechanism is proposed. The results discussed herein suggest that PAH-containing urban grime on windows and buildings may be a key player in urban air pollution.