Contribution of nitrous acid to the atmospheric oxidation capacity in an industrial zone in the Yangtze River Delta region of China

Abstract

Abstract. A suite of instruments was deployed to simultaneously measure nitrous acid (HONO), nitrogen oxides (NOx = NO + NO2), carbon monoxide (CO), ozone (O3), volatile organic compounds (VOCs – including formaldehyde, HCHO) and meteorological parameters near a typical industrial zone in Nanjing in the Yangtze River Delta (YRD) region of China from 1 to 31 December 2015. High levels of HONO were detected using a wet-chemistry-based method. HONO ranged from 0.03 to 7.04 ppbv with an average of 1.32±0.92 ppbv. Elevated daytime HONO was frequently observed with a minimum of several hundred parts per trillion by volume (pptv) on average, which cannot be explained by the homogeneous OH + NO reaction (POH+NO) and primary emissions (Pemission), especially during periods with high particulate matter (PM2.5) loadings. HONO chemistry and its impact on the atmospheric oxidation capacity in the study area were further investigated using a Master Chemical Mechanism (MCM) box model. The results show that the average hydroxyl radical (OH) production rate was dominated by the photolysis of HONO (7.13×106 molec. cm−3 s−1), followed by the ozonolysis of alkenes (3.94×106 molec. cm−3 s−1), the photolysis of O3 (2.46×106 molec. cm−3 s−1) and the photolysis of HCHO (1.60×106 molec. cm−3 s−1) during the campaign period, especially within plumes that originated from the industrial zone. Model simulations indicated that heterogeneous chemistry played an important role in HONO formation. The average nighttime NO2 to HONO conversion rate was determined to be ∼0.8 % h−1. A good correlation between nocturnal HONO∕NO2 and the product of particle surface area density (S∕V) and relative humidity (RH), S/V⋅RH, supports the heterogeneous NO2∕H2O reaction mechanism. The other HONO source, designated as Punknonwn, was about twice as high as POH+NO on average and displayed a diurnal profile with an evidently photo-enhanced feature, i.e., photosensitized reactions of NO2 may be an important daytime HONO source. Nevertheless, our results suggest that daytime HONO formation was mostly due to the light-induced conversion of NO2 on aerosol surfaces, whereas heterogeneous NO2 reactions on the ground surface dominated nocturnal HONO production. Our study indicated that an elevated PM2.5 level during haze events can promote the conversion of NO2 to HONO by providing more heterogeneous reaction sites, thereby increasing the atmospheric oxidation capacity, which may further promote the formation of secondary air pollutants. Highlights: High levels of HONO, with an average of 1.32±0.92 ppbv, were observed near one of the largest industrial zones in the YRD region of China. HONO photolysis and alkene ozonolyses contributed the most to OH production and, hence, the atmospheric oxidation capacity. High loading of PM2.5 provided additional reaction surfaces for HONO formation. Heterogeneous formation mechanisms were the most important daytime HONO sources and were further enhanced by sunlight.

Enhanced atmospheric oxidation capacity and associated ozone increases during COVID-19 lockdown in the Yangtze River Delta

“…Limited studies have related to AOC changes with O 3 formation. Recent studies modeled the highest ever-reported concentrations of OH at urban site in the YRD ( Zheng et al, 2020 ; Zhu et al, 2020 ), which indicates AOC is strong in this region. Therefore, it is necessary to study the changes of AOC due to NO x emission and O 3 elevation during the COVID-19 lockdown period.…”

“…Previous studies on AOC only focused on radical chemistry ( Keywood et al, 2004 ; von Sonntag, 2007 ; Xue et al, 2016 ; Zheng et al, 2020 ). Limited studies have related to AOC changes with O 3 formation.…”

Measurement report: Fast photochemical production of peroxyacetyl nitrate (PAN) over the rural North China Plain during cold-season haze events

“…But it is slightly higher than most observations in other southern China (2.1−5.6) ppb (Guo et al, 2016;Wang et al, 2017;Yang et al, 2019;Zeng et al, 2019b) and the background NCP region (3.5−3.7 ppb) conducted 3−6 years before our experiments (Yang et al, 2017;Wang et al, 2020). The HCHO photolysis rate of 8.3×10 6 molec cm -3 s -1 at noon on pollution days is higher than pervious results in a suburban site of Beijing during winter (~6.7×10 6 molec cm -3 s -1 at noon) (Tan et al, 2018) and an industrial zone of southeastern China during winter (1.6×10 6 molec cm -3 s -1 averaged over 7:00−16:00) (Zheng et al, 2020). This indicates that high reactive VOC emissions over the NCP region can drive fast photochemistry in cold seasons on a regional scale by acting as radicals in addition to precursors.…”

Exploration of the atmospheric chemistry of nitrous acid in a coastal city of southeastern China: Results from measurements across four seasons

“…The ratio of HONO to NOx or the ratio of HONO to NO2 have been extensively applied to indicate heterogeneous conversion of NO2 to HONO (Li et al, 2012b;Liu et al, 2019c;Zheng et al, 2020). Compared with the HONO/NO2 ratio, the HONO/NOx ratio can better avoid the influence of primary emissions (Liu et al, 2019c).…”