Gil Junsu, Kim Jeonghwan, Lee Meehye, Lee Gangwoong, An Joonyeong, Lee Dongsoo, Jung Jinsang, Cho Seogju, Whitehill Andrew, Szykman James, Lee Jeonghoon
Department of Earth and Environmental Science, Korea University, Seoul, South Korea.
Department of Environmental Science, Hankuk University of Foreign Studies, Yongin, South Korea.
Atmos Environ (1994). 2021;247. doi: 10.1016/j.atmosenv.2020.118182.
Photolysis of nitrous acid (HONO) is recognized as an early-morning source of OH radicals in the urban air. During the Korea-US air quality (KORUS-AQ) campaign, HONO was measured using quantum cascade - tunable infrared laser differential absorption spectrometer (QC-TILDAS) at Olympic Park in Seoul from 17 May, 2016 to 14 June, 2016. The HONO concentration was in the range of 0.07-3.46 ppbv, with an average of 0.93 ppbv. Moreover, it remained high from 00:00-05:00 LST. During this time, the mean concentration was higher during the high-O episodes (1.82 ppbv) than the non-episodes (1.20 ppbv). In the morning, the OH radicals that were produced from HONO photolysis were 50% higher (0.95 pptv) during the high-O episodes than the non-episodes. Diurnal variations in HO and O concentrations were simulated by the F0AM model, which revealed a difference of ~20 ppbv in the daily maximum O concentrations between the high-O episodes and non-episodes. Furthermore, the HONO concentration increased with an increase in relative humidity (RH) up to 80%; the highest HONO was associated with the top 10% NO in each RH group, confirming that NO is one of the main precursors of HONO. At night, the conversion ratio of NO to HONO was estimated to be 0.88×10 h; this ratio was found to increase with an increase in RH. The Aitken mode particles (30-120 nm), which act as catalyst surfaces, exhibited a similar tendency with a conversion ratio that increased along with RH, indicating the coupling of surfaces with HONO conversion. Using an artificial neural network (ANN) model, HONO concentrations were successfully simulated with measured variables (r = 0.66 as an average of five models). Among these variables, NO, aerosol surface area, and RH were found to be the main factors affecting the ambient HONO concentrations. The results reveal that RH facilitates the conversion of NO to HONO by constraining the availability of aerosol surfaces. This study demonstrates the coupling of HONO with the HO-O cycle in the Seoul Metropolitan Area (SMA) and provides practical evidence of the heterogeneous formation of HONO by employing the ANN model.
亚硝酸(HONO)的光解被认为是城市空气中清晨羟基自由基的来源。在美韩空气质量(KORUS - AQ)行动期间,于2016年5月17日至2016年6月14日在首尔奥林匹克公园使用量子级联 - 可调谐红外激光差分吸收光谱仪(QC - TILDAS)对HONO进行了测量。HONO浓度范围为0.07 - 3.46 ppbv,平均为0.93 ppbv。此外,在当地标准时间00:00 - 05:00期间其浓度一直较高。在此期间,高臭氧事件期间的平均浓度(1.82 ppbv)高于非事件期间(1.20 ppbv)。在早晨,高臭氧事件期间由HONO光解产生的羟基自由基比非事件期间高50%(0.95 pptv)。利用F0AM模型模拟了HO和O浓度的日变化,结果显示高臭氧事件和非事件期间每日最大O浓度相差约20 ppbv。此外,HONO浓度随相对湿度(RH)增加至80%而升高;每个RH组中最高的HONO与前10%的NO相关,证实NO是HONO的主要前体之一。在夜间,NO向HONO的转化率估计为0.88×10⁻³ h⁻¹;该转化率随RH增加而升高。作为催化剂表面的艾肯模态颗粒(30 - 120 nm)表现出类似趋势,其转化率随RH升高,表明表面与HONO转化存在耦合。使用人工神经网络(ANN)模型,利用测量变量成功模拟了HONO浓度(五个模型的平均值r = 0.66)。在这些变量中,NO、气溶胶表面积和RH被发现是影响环境HONO浓度的主要因素。结果表明,RH通过限制气溶胶表面的可用性促进了NO向HONO的转化。本研究证明了首尔大都市区(SMA)中HONO与HO - O循环的耦合,并通过采用ANN模型为HONO的非均相形成提供了实际证据。