Abstract

Recently, deteriorating ozone (O3) pollution in China brought the precise diagnosis of O3 sensitive chemistry to the forefront. As a dominant precursor of OH radicals, atmospheric nitrous acid (HONO) plays an important role in O3 production. However, its measurement unavailability in many regions especially for second- and third-tier cities may lead to the misjudgment of the O3 sensitivity regime derived from observation-based models. Here, we systematically assess the potential impact of HONO on diagnosing the sensitivity of O3 production using a 0-dimension box model based on a comprehensive summer urban field campaign. The results indicated that the default mode (only the NO + OH reaction is included) in the model could underestimate ∼87% of observed HONO levels, leading to an obvious decrease (∼19%) of net O3 production in the morning, which was in line with the previous studies. The unconstrained HONO in the model was found to significantly push O3 production toward the VOC-sensitive regime. Additionally, it is unrealistic to change NO x but constrain HONO in the model due to the dependence of HONO formation on NO x . Assuming that HONO varied proportionally with NO x , a stronger NO x -sensitive condition could be achieved. Therefore, effective reduction of NO x should be given more attention together with VOC emission control for O3 mitigation.

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