Daytime isoprene nitrates under changing NOx and O3

被引:0
|
作者
Mayhew, Alfred W. [1 ]
Edwards, Peter M. [1 ]
Hamilton, Jaqueline F. [1 ,2 ]
机构
[1] Univ York, Dept Chem, Wolfson Atmospher Chem Labs, York, England
[2] Univ York, Natl Ctr Atmospher Sci, York, England
基金
英国自然环境研究理事会;
关键词
GAS-PHASE CHEMISTRY; ATMOSPHERIC OXIDATION; RADICAL CHEMISTRY; OZONE; REGION; FOREST; MODEL; POLLUTION; PRODUCTS; SEASON;
D O I
10.5194/acp-23-8473-2023
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Organonitrates are important species in the atmosphere due to their impacts on NOx, HOx, and O-3 budgets, and their potential to contribute to secondary organic aerosol (SOA) mass. This work presents a steady-state modelling approach to assess the impacts of changes in NOx and O-3 concentrations on the organonitrates produced from isoprene oxidation. The diverse formation pathways to isoprene organonitrates dictate the responses of different groups of organonitrates to changes in O-3 and NOx. For example, organonitrates predominantly formed from the OH-initiated oxidation of isoprene favour formation under lower-ozone and moderate-NOx concentrations, whereas organonitrates formed via daytime NO3 oxidation show the highest formation under high-O-3 concentrations with little dependence on NOx concentrations. Investigating the response of total organonitrates reveals complex and nonlinear behaviour with implications that could inform expectations of changes to organonitrate concentrations as efforts are made to reduce NOx and O-3 concentrations, including a region of NOx-O-3 space where total organonitrate concentration is relatively insensitive to changes in NOx and O-3. These conclusions are further contextualised by estimating the volatility of the isoprene organonitrates revealing the potential for high concentrations of low-volatility species under high-ozone conditions.
引用
收藏
页码:8473 / 8485
页数:13
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