Impact of ozone and inlet design on the quantification of isoprene-derived organic nitrates by thermal dissociation cavity ring-down spectroscopy (TD-CRDS)

Abstract

We present measurements of isoprene-derived organic nitrates (ISOP-NITs) generated in the reaction of isoprene with the nitrate radical (NO3) in a 1gm3 Teflon reaction chamber. Detection of ISOP-NITs is achieved via their thermal dissociation to nitrogen dioxide (NO2), which is monitored by cavity ring-down spectroscopy (TD-CRDS). Using thermal dissociation inlets (TDIs) made of quartz, the temperature-dependent dissociation profiles (thermograms) of ISOP-NITs measured in the presence of ozone (O3) are broad (350 to 700gK), which contrasts the narrower profiles previously observed for, for example, isopropyl nitrate (iPN) or peroxy acetyl nitrate (PAN) under the same conditions. The shape of the thermograms varied with the TDI's surface-to-volume ratio and with material of the inlet walls, providing clear evidence that ozone and quartz surfaces catalyse the dissociation of unsaturated organic nitrates leading to formation of NO2 at temperatures well below 475gK, impeding the separate detection of alkyl nitrates (ANs) and peroxy nitrates (PNs). The use of a TDI consisting of a non-reactive material suppresses the conversion of isoprene-derived ANs at 473gK, thus allowing selective detection of PNs. The potential for interference by the thermolysis of nitric acid (HNO3), nitrous acid (HONO) and O3 is assessed.