Abstract
Non-acyl peroxy nitrates, RO2NO2, act as a reservoir species for NOx in the upper troposphere. The low thermal stability of these compounds means that they only become a significant sink of NOx at the low temperatures observed in the upper troposphere. The chemical processes involved with the formation and degradation of methyl peroxy nitrate (CH3O2NO2) and an additional forty-four RO2NO2 have been incorporated into the global 3-D chemical transport model, STOCHEM-CRI. The study investigates the effect of the addition of RO2NO2 chemistry on the budget of NOx, which in turn impacts the ozone, hydroxyl radical (OH) and nitrate radical (NO3) formation. This investigation found that the addition of CH3O2NO2 led to an increase in the tropospheric burdens of NOx (+3.0%), ozone (+2.0%), OH (+4.0%) and NO3 (+8.8%). However, the other 44 RO2NO2 contribute a significant increment of tropospheric global burdens of NOx (+4.4%), ozone (+3.4%), OH (+5.5%) and NO3 (+11.1%) with largest mixing ratios of NOx up to 25%, ozone up to 14%, OH up to 20% and NO3 up to 50%. The increase in the global burden of oxidizing species like OH due to the addition of 44 other RO2NO2, led to a significant decrease in the lifetimes of greenhouse gases such as methane (~6%). The modelled mixing ratios of CH3O2NO2 were in reasonable agreement with measurements, the only extensive dataset available.
Original language | English |
---|---|
Pages (from-to) | 1201-1212 |
Number of pages | 12 |
Journal | ACS Earth and Space Chemistry |
Volume | 4 |
Issue number | 7 |
Early online date | 16 Jun 2020 |
DOIs | |
Publication status | Published - 16 Jul 2020 |
Keywords
- upper troposphere
- chemical transport model
- surface distribution
- zonal distribution
- global budget
- oxidation cycle
- atmospheric life-time
- global fluxes
- greenhouse gases