HONO chemistry affected by relative humidity and ammonia in the North China Plain during winter

Nitrous acid (HONO) is a critical precursor of the hydroxyl radical (OH) and plays a pivotal role in atmospheric photochemistry . Although nitrogen dioxide (NO 2 ) heterogeneous reactions (HET) on ground and aerosol surfaces are widely recognized as major paths of HONO production, their influencing factors are not well characterized in air quality models, limiting the understanding of HONO formation and the quantification of their regional impact. In this study, a novel parameterization scheme for the NO 2 uptake coefficient, including the effects of solar radiation, relative humidity (RH) and ammonia (NH 3 ), was developed and coupled into the Weather Research and Forecasting model with Chemistry. Nine simulation scenarios were designed to assess the impacts of RH and NH 3 on HONO chemistry and O 3 levels in the North China Plain (NCP). The results showed that the RH-impacted HET contributed 10−25% of HONO, with a significant increase of more than 35% during the haze periods; whereas the NH 3 -impacted HET contributed 15% of nighttime HONO and <5% of noontime HONO, playing a more significant role in rural areas. Vertically, the RH-impacted HET contribution to nighttime HONO concentrations remained 26−31% at an altitude of 700–900 m due to the higher RH levels (50−60%) during the haze periods; whereas the NH 3 -impacted HET contribution was minor above 500 m owing to the fast-decreasing NH 3 concentrations with height. When RH exceeded the turning point (70%), nighttime HONO was suppressed by up to 1 ppb in eastern NCP. The combination of RH and NH 3 produced a ground daily maximum 8h averaged O 3 enhancement of 6–14 μg m −3 during the haze periods, exceeding the effect of solar radiation. These findings deepen our understanding of the role of RH and NH 3 in HONO chemistry and imply the importance of reasonably expressing HET in air quality models. • NO 2 heterogeneous reactions (HET) were newly parameterized and coupled into WRF-Chem. • HET contained impacts of solar radiation, relative humidity and NH 3 concentrations. • The relative humidity-impacted HET could contribute >35% of HONO on the haze days. • The NH 3 -impacted HET played a more significant role in HONO formation in rural areas. • The inhibited nighttime HONO via HET approached to 1 ppb when RH > 70%.

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Publication Details

Journal
Atmospheric Environment
Published
2025-02-16
DOI
https://doi.org/10.1016/j.atmosenv.2025.121114
Citations
6
Primary Topic
Atmospheric chemistry and aerosols
Type
article
Field-Weighted Citation Impact
7.80
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article

HONO chemistry affected by relative humidity and ammonia in the North China Plain during winter

Chaoyang Xue, Yele Sun, Yang Juan, Yong Chen et al.
6 citations
Atmospheric Environment
Atmospheric chemistry and aerosols
7.80
article

HONO chemistry affected by relative humidity and ammonia in the North China Plain during winter

Chaoyang Xue, Yele Sun, Yang Juan, Yong Chen, Yujing Mu, Haiyan Ran, Jingwei Zhang, Yu Qu
article en
6 citations

Abstract

Nitrous acid (HONO) is a critical precursor of the hydroxyl radical (OH) and plays a pivotal role in atmospheric photochemistry . Although nitrogen dioxide (NO 2 ) heterogeneous reactions (HET) on ground and aerosol surfaces are widely recognized as major paths of HONO production, their influencing factors are not well characterized in air quality models, limiting the understanding of HONO formation and the quantification of their regional impact. In this study, a novel parameterization scheme for the NO 2 uptake coefficient, including the effects of solar radiation, relative humidity (RH) and ammonia (NH 3 ), was developed and coupled into the Weather Research and Forecasting model with Chemistry. Nine simulation scenarios were designed to assess the impacts of RH and NH 3 on HONO chemistry and O 3 levels in the North China Plain (NCP). The results showed that the RH-impacted HET contributed 10−25% of HONO, with a significant increase of more than 35% during the haze periods; whereas the NH 3 -impacted HET contributed 15% of nighttime HONO and <5% of noontime HONO, playing a more significant role in rural areas. Vertically, the RH-impacted HET contribution to nighttime HONO concentrations remained 26−31% at an altitude of 700–900 m due to the higher RH levels (50−60%) during the haze periods; whereas the NH 3 -impacted HET contribution was minor above 500 m owing to the fast-decreasing NH 3 concentrations with height. When RH exceeded the turning point (70%), nighttime HONO was suppressed by up to 1 ppb in eastern NCP. The combination of RH and NH 3 produced a ground daily maximum 8h averaged O 3 enhancement of 6–14 μg m −3 during the haze periods, exceeding the effect of solar radiation. These findings deepen our understanding of the role of RH and NH 3 in HONO chemistry and imply the importance of reasonably expressing HET in air quality models. • NO 2 heterogeneous reactions (HET) were newly parameterized and coupled into WRF-Chem. • HET contained impacts of solar radiation, relative humidity and NH 3 concentrations. • The relative humidity-impacted HET could contribute >35% of HONO on the haze days. • The NH 3 -impacted HET played a more significant role in HONO formation in rural areas. • The inhibited nighttime HONO via HET approached to 1 ppb when RH > 70%.

Atmospheric EnvironmentVol. 348
Yunnan University (CN), Chinese Academy of Sciences (CN), Max Planck Institute for Chemistry (DE), Research Center for Eco-Environmental Sciences (CN), Institute of Atmospheric Physics (CN), University of Chinese Academy of Sciences (CN)
Life below water
Openalex Percentile: Top 2%
Atmospheric chemistry and aerosols
7.80
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