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Secondary organic aerosols (SOA) play an important role in global climate change and air quality, and SOA tracers can directly characterize the source and reaction mechanism of SOA. However, it is not well known that whether the tracers can be oxidized or how the instability of the tracers in the atmosphere. In this paper,  in-situ  FTIR was used to analyze the chemical structure changes of erythritol, analogue of 2-methyl erythritol (AME) that is, a tracer of isoprene SOA, and 2, 3-dihydroxy-4-oxopentanoic acid (DHOPA), a tracer of toluene SOA, when exposed to high concentration of ozone for short periods. Under the condition of 20 ppm ozone exposure for 30 min, the change rate of absorption area of AME at 3,480 and 1700 cm −1  was −0.0134 and 0.00117 int.abs/s, respectively, and the change rate of the absorption area of DHOPA at 1,640 and 3340cm −1  was −0.00191 and 0.00218 int.abs/s, respectively. The pseudo-first-order reaction rate constant  k   app   were 1.89 × 10 −8  and 2.12 × 10 −7  s −1 , and the uptake coefficients of ozone on the surface of AME and DHOPA were (1.3 ± 0.8) × 10 −8  and (4.5 ± 2.7) × 10 −8 , respectively. These results showed the oxidation processes of AME and DHOPA were slow in the presence of high concentrations of ozone, which implied that AME and DHOPA could be considered to be stable in the atmospheric environment with ozone as the main oxidant.

In-Situ FTIR Study of Heterogeneous Oxidation of SOA Tracers by Ozone