Citation: Yang Xinping, Wang Haichao, Tan Zhaofeng, Lu Keding, Zhang Yuanhang. Observations of OH Radical Reactivity in Field Studies[J]. Acta Chimica Sinica, ;2019, 77(7): 613-624. doi: 10.6023/A19030094 shu

Observations of OH Radical Reactivity in Field Studies

Yang Xinping ^a,b ,
Wang Haichao ^a,b ,
Tan Zhaofeng ^a,b,c ,
Lu Keding ^a,b,, ,
Zhang Yuanhang ^a,b,d,e,,

a.
State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871
b.
International Joint Research Center for Atmospheric Research, Peking University, Beijing 100871
c.
Institute of Energy and Climate Research, IEK-8:Troposphere, Forschungszentrum Jülich GmbH, Jülich, Germany 52425
d.
CAS Center for Excellence in Regional Atmospheric Environment, Chinese Academy of Sciences, Xiamen 361021
e.
Beijing Innovation Center for Engineering Sciences and Advanced Technology, Peking University, Beijing 100871

Corresponding author: Lu Keding, k.lu@pku.edu.cn Zhang Yuanhang, yhzhang@pku.edu.cn
Received Date: 21 March 2019
Available Online: 3 July 2019
Fund Project: the National Natural Science Foundation of China 91544225Project supported by the National Natural Science Foundation of China (No. 91544225) and Integrative study on the key chemical mechanisms of the Air Pollution Complex in China (No. 91844301)Integrative study on the key chemical mechanisms of the Air Pollution Complex in China 91844301

Figures(6)

Observations of OH Radical Reactivity in Field Studies Yang, Xinpinga, b Wang, Haichaoa, b Tan, Zhaofenga, b, c Lu, Keding*, a, b Zhang, Yuanhang*, a, b, d, e (a State Key Joint Laboratory of Environmental Simulation and Pollution Control, College of Environmental Sciences and Engineering, Peking University, Beijing 100871) (b International Joint Research Center for Atmospheric Research, Peking University, Beijing 100871) (c Institute of Energy and Climate Research, IEK-8:Troposphere, Forschungszentrum Jülich GmbH, Jülich, Germany 52425) (d CAS Center for Excellence in Regional Atmospheric Environment, Chinese Academy of Sciences, Xiamen 361021) (e Beijing Innovation Center for Engineering Sciences and Advanced Technology, Peking University, Beijing 100871) Abstract The hydroxyl radical (OH) is the main source of atmospheric oxidation capacity, which oxidizes the primary pollutants into the secondary pollutants. Therefore, the measurements and characterization of source and sink of OH radical are critical to understand the formation mechanism of regional secondary pollution. However, the removal routes of OH radical still cannot be quantified accurately. OH radical reactivity can describe the OH total loss rate and the atmospheric oxidation, thus playing an important role in the OH budget analysis. The OH radical reactivity is defined as the total pseudo first-order rate coefficient for all atmospheric reactions of OH in an air parcel. It is challenging to accurately measure the OH radical reactivity due to the high activity and short life of OH radical. In this paper, we summarized all kinds of measurement techniques used in the field observations of OH radical reactivity, including Total OH Loss-rate Measurement (TOHLM), Laser flash Photolysis-Laser Induced Fluorescence (LP-LIF), Chemical Ionisation Mass Spectrometry (CIMS) and Comparative Reactivity Method (CRM). The techniques were reviewed on the aspects of measurement principles, instrument modules, and so on. Overall, LP-LIF is proposed to be the best technical approach. In addition, the measured OH radical reactivity and the major scientific findings of corresponding measurement campaigns conducted in typical tropospheric conditions as urban, forest and rural environments, etc. were outlined. The OH radical reactivity varies significantly in different conditions, ranging from less than 10 per second to hundreds. Comparison of measured OH radical reactivity and the calculated or modeling results reveals a significant missing reactivity, ranging from 20% to over 80% in some environments. Depending on the emission and pollution characteristics of the field observation sites, the sources of missing reactivity are generally attributed to the undetected or unknown organic species, i.e. primary organic species, secondary organic species or a combination of both. The accurate observation and the numerical modeling of the OH radical reactivity can provide a possibility for achieving numerical closure study of RO_x radicals. Finally, we discussed the current research difficulties and possible new directions for future studies of the OH radical reactivity.
- OH radical reactivity,
- measurement techniques,
- field observation,
- compositions of OH radical reactivity,
- missing reactivity
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沈阳化工大学材料科学与工程学院沈阳 110142