1.Key Laboratory of Middle Atmosphere and Global environment Observation (LAGEO), Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China 2.Key Laboratory of Regional Climate-Environment for Temperate East Asia (RCE-TEA), Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China 3.Beijing Weather Modification Office, Beijing 100089, China 4.Xianghe Observatory of Whole Atmosphere, Institute of Atmospheric Physics, Chinese Academy of Sciences, Xianghe 065400, China 5.University of Chinese Academy of Sciences, Beijing 100049, China Manuscript received: 2020-01-14 Manuscript revised: 2020-04-03 Manuscript accepted: 2020-04-15 Abstract:Aerosols in the atmosphere not only degrade visibility, but are also detrimental to human health and transportation. In order to develop a method to estimate PM2.5 mass concentration from the widely measured visibility, a field campaign was conducted in Southwest China in January 2019. Visibility, ambient relative humidity (RH), PM2.5 mass concentrations and scattering coefficients of dry particles were measured. During the campaign, two pollution episodes, i.e., from 4?9 January and from 10?16 January, were encountered. Each of the two episodes could be divided into two periods. High aerosol hygroscopicity was found during the first period, when RH was higher than 80% at most of the time, and sometimes even approached 100%. The second period experienced a relatively dry but more polluted condition and aerosol hygroscopicity was lower than that during the first period. An empirical relationship between PM2.5 mass concentration and visibility (ambient aerosol extinction) under different RH conditions could thus be established. Based on the empirical relationship, PM2.5 mass concentration could be well estimated from visibility and RH. This method will be useful for remote sensing of PM2.5 mass concentration. Keywords: visibility, hygroscopic growth, PM2.5 mass concentration 摘要:大气气溶胶不仅降低能见度,也危害人体健康和交通运输。基于2019年1月在西南地区外场观测中的能见度、环境湿度、PM2.5质量浓度和干气溶胶散射系数,本文发展了一套利用能见度估算PM2.5质量浓度的方法。观测期间,经历了两个污染过程(1月4-9日及10-16日),每个过程都可以分为两个阶段:第一阶段相对湿度大部分时间都高于80%,有时候接近100%,且气溶胶吸湿性较强;第二阶段相对湿度相对较低,污染更严重,且气溶胶吸湿性弱于第一阶段。基于外场观测数据,本文建立了PM2.5质量浓度与能见度(或环境气溶胶消光系数)在不同相对湿度下的关系。基于该关系,可以利用能见度和相对湿度很好地估算PM2.5质量浓度。该方法也可以用于改进PM2.5质量浓度的遥感反演。 关键词:能见度, 吸湿增长, PM2.5质量浓度
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2.1. Site and instruments
The experiment was conducted from 4?19 January 2019 in Changshou, Chongqing, in Southwest China. The site (29°49'N, 107°00'E; 266 m above sea level) is located in Yanjia Industrial Park surrounded by busy highways. It is about 51 km away from the city center of Chongqing. A dust monitor (EDM 180, Grimm Aerosol) and an ambient particulate monitor (FH62C14, Thermo Scientific) were used to jointly measure the aerosol mass concentration. The FH62C14 instrument provided PM2.5 mass concentrations at 1-h intervals. The EDM 180 instrument measured aerosol number concentrations in 31 particle size channels, and mass concentrations including PM10, PM2.5 and PM1.0, with a temporal resolution of 6 s. The isothermal inlet was integrated with a nafion dryer, which was turned on at ambient RH above 55%. Several studies have reported the errors in the measurements of GRIMM EDM 180 (Ding et al., 2014; Xu, 2017). Thus, the GRIMM EDM 180 measurements were validated using FH62C14 measurements at a 1-h temporal resolution. A good correlation between PM2.5 mass concentrations from GRIMM EDM 180 and FH62C14 was found. Then, the GRIMM EDM 180 data were corrected using the regression fit function and reported at a temporal resolution of 10 min. A polar nephelometer (Aurora-4000, Ecotech) was used to measure the aerosol scattering coefficients at seven angle ranges at the wavelengths of 635 nm, 525 nm, and 450 nm at relatively dry RH (~35%). Full scattering coefficients were corrected based on the measurements for the angle range 9°?170° using the method proposed by Müller et al. (2011). Black carbon (BC) mass concentration was measured by an aethalometer (model AE31, MAGEE) (Hansen et al., 1984; Collaud Coen et al., 2010) at seven wavelengths of 370, 470, 520, 590, 680, 880 and 950 nm. Loading effects were corrected and absorption coefficients were obtained following the method in Ran et al. (2016). However, data availability was only 35% due to instrument malfunction. Visibility was measured by a PWD20 instrument (Vaisala Co.) at an interval of 1 min. Ambient RH was observed by the sensor attached to the Grimm EDM 180 instrument. The Grimm EDM 180 and FH62C14 instruments were calibrated before and after the campaign. The results showed that the instruments were stable throughout the campaign. Aurora-4000 was calibrated routinely and zero-checked every day for the correction of the zero point. All data were filtered according to measurement logs and data consistency between instruments. A flow chart of the steps involved in the method, which will be detailed in section 2.2, is presented in Fig. 1. Figure1. Flow chart for data processing and parameterization.
Aerosol scattering coefficient and complex refractive index are related to ambient RH. Measurements of total scattering coefficient and the simultaneous RH are used to indicate aerosol hygroscopic growth. Several studies have defined the hygroscopic enhancement factor for aerosol total scattering, f(RH), and aerosol back scattering, fb(RH), in different cases (Sun et al., 2016). The hygroscopic enhancement factor, which considers light extinction by scattering and absorption of both aerosol and gas, is defined as follows: where bsp,λ (RH) and bsp,λ (dry) are the aerosol scattering coefficient at wavelength λ in the ambient environment and under dry conditions; bext,λ (RH) is the ambient extinction coefficient; bap,λ is the aerosol absorption coefficient; bag,λ is the gas absorption coefficient; and bsg,λ is the gas scattering coefficient. Since the gas extinction contribution to total light extinction is much less than that of particles in such polluted regions (Chan et al., 1999) and aerosol absorption is usually much smaller than aerosol scattering, Eq. (1) can be simplified to: It is calculated from the measurements of ambient extinction coefficient, bext,λ(RH), at a certain RH and aerosol scattering coefficient, bsp,λ(dry), under dry conditions (RH < 40%). The bext,λ(RH) at a certain wavelength (λ) is calculated from visibility (V) by the following equation: where the coefficient q is determined by experiments. Two fit functions, the dual-parameter fit equation (H?nel, 1976, 1980; Carrico, 2003; Zieger et al., 2011; Liu et al., 2019) and single-parameter equation (H?nel, 1980; Kotchenruther and Hobbs, 1998; Gassó et al., 2000; Liu et al., 2019), were used to establish the relationship between fλ(RH) and RH. Aerosols that are metastable or on the upper branch of the hygroscopic growth hysteresis curve typically follow the dual-parameter power lower fit equation described by Kasten (1969): where $\alpha $ is a scale factor that normalizes the hygroscopic growth and $\gamma $ represents the magnitude of the hygroscopic growth. During the observational period, RH was frequently above 60%, with few records at low RH. Curve fitting will be misleading under such a condition. Thus, f(RH) under dry conditions, which is the ratio of dry extinction and scattering from the aethalometer and nephelometer, was added for the curve fitting.
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3.1. Overview of the experiment
Figure 2 shows the time series of PM2.5 mass concentration, visibility, and RH during the experiment. It can be clearly seen that there were two episodes according to PM2.5 mass concentrations, i.e., one from 4?9 January with a continuous increase from 75 μg m?3 to 200 μg m?3, and the other from 10?16 January with an increase from 25 μg m?3 to 150 μg m?3. A linear correlation between PM2.5 mass concentration and dry aerosol scattering coefficient was found, with a correlation coefficient of about 0.98 (Fig. 3). However, there was no obvious decrease in visibility along with the increase in PM2.5 mass concentration during either of the two episodes, as is often expected. No correlation between the mass concentration of PM2.5 and visibility was found, with the correlation coefficient found to be 0.21. During the whole campaign, visibility ranged from 2 km to 15 km, with 86.4% lower than 10 km. It was notable that RH was higher than 70% at most of the time, and even up to 85%?100% during 53% of the whole time. Aerosol hygroscopic growth in such a highly humid environment may greatly influence the scattering properties of aerosol and thereby visibility. Figure2. Observation of PM2.5, visibility, RH and ${d_{80\% {\rm{,24h}}}}$.
Figure3. Linear relationship between PM2.5 mass concentration and scattering coefficient at three wavelengths.
2 3.2. Aerosol hygroscopic growth under different RH conditions -->
3.2. Aerosol hygroscopic growth under different RH conditions
The effect of water vapor on aerosol scattering was examined, in order to explain the difference in the variations of PM2.5 mass concentrations and visibility. A new empirical relationship between RH and f550nm(RH), the ratio of ambient extinction coefficient to aerosol dry scattering coefficient, was built to characterize the aerosol hygroscopicity. Considering the large variation in RH and the duration of high RH during the experiment, the observational period was classified into different periods according to the ambient RH condition. A distinct diurnal cycle of RH can be seen in Fig. 2. To analyze the high RH condition and its impact on aerosol hygroscopic growth, a new parameter, ${d_{80{\rm{\%,24h}}}}$, was defined to quantitatively characterize the occurrence of high humidity conditions (> 80%) during the last 24 h: where ${\rm{RH}}\left({{\rm{RH}} > {\rm{R}}{{\rm{H}}_0}{\rm{,}}t{\rm{ - }}\Delta t < T \leqslant t} \right)$ is the RH above a threshold RH (${\rm{R}}{{\rm{H}}_0}$) during the previous $\Delta t$ period, overbar represents average throughout the given period, and the fraction on the right ensures that the result is within the RH range, i.e., 0%?100%. A high ${d_{{\rm{R}}{{\rm{H}}_0}{\rm{,}}\Delta t}}$ might suggest a favorable situation for heterogeneous reactions at high RH for a long time. As a result, trace gases such as SO2 and NOx from industries near the experimental site and other emission sources could be more easily heterogeneously oxidized to form sulfates and nitrates. In other words, a high ${d_{{\rm{R}}{{\rm{H}}_0}{\rm{,}}\Delta t}}$ means a long duration of high moisture leading to a stronger hygroscopic growth ability of aerosol. Each of the two pollution episodes could be further divided into two periods (Fig. 2c). It was noted that ${d_{{\rm{R}}{{\rm{H}}_0}{\rm{,}}\Delta t}}$ decreased similarly from the first period to the second period during each episode, showing that aerosols firstly went through a humid condition and then a relatively dry condition. Figure 4 shows the simplified hygroscopic enhancement factor, f550nm(RH), which was typically below 1.2, representing very weak hygroscopic growth when RH was below 60%. The f550nm(RH) increased steeply with RH above 80%. The scattering of particles could be enhanced by 1.5?3 times when ambient RH was above 90%. The dual-parameter fit [Eq. (4)] was applied and the fit parameters of γ were 0.201, 0.180, 0.222 and 0.174 for the four periods, respectively. Clearly, γ was higher for the periods with high ${d_{80\% {\rm{,24h}}}}$ (Ⅰ and Ⅲ), indicating efficient aging due to multi-phase reactions and the production of soluble inorganic salts. The ${d_{80\% {\rm{,24h}}}}$ was lower for the other two periods (Ⅱ and Ⅳ), indicating less efficient aging by soluble inorganic salts. However, the aerosol mass concentration could still accumulate via condensation of organic species, which was the main emission of the surrounding industrial park and might have resulted in smaller aerosol hygroscopicity. Figure4.f(RH) in four periods and the fitted function.
Pan et al. (2009) reported f525nm (80%) values of 1.20, 1.31 and 1.57 during dust, clean and pollution episodes over a rural area near the megacity of Beijing. Zhao et al. (2019) performed a survey of fλ(RH) studies in China for the past seven years. In winter, the f550nm (80%) of Gucheng, f525nm (80%) of Beijing and f525nm (80%) of Guangzhou was 1.29 ± 0.10, 1.47 ± 0.16, and 1.58 ± 0.07, respectively. In this study, the f550nm (80%) for the above mentioned four segments ranged from 1.28?1.46, which was a similar range to other studies.
2 3.3. Relationship between PM2.5 mass concentration and visibility -->
3.3. Relationship between PM2.5 mass concentration and visibility
The relationship between PM2.5 mass concentration and visibility is subject to the RH conditions owing to the hygroscopic growth of aerosols. The establishment of an empirical relationship between PM2.5 mass concentration and visibility under different RH conditions would be useful for estimating PM2.5 mass concentrations based on visibility—a widely measured parameter. In the IMPROVE algorithm, the computed aerosol light extinction coefficients include contributions from PM2.5 species such as ammonium sulfate, ammonium nitrate, organic matter, elemental carbon, fine soil, coarse mass, and Rayleigh scattering, as well as the hygroscopic enhancement factor fλ(RH) (Ryan et al., 2005). The equation requires knowledge of mass concentrations of different components, which are not always available or only measured at low temporal resolution. Since the light extinction at the observational site is mainly contributed by PM2.5, we can simply calculate the extinction coefficient at ambient RH using the following equation: where the contribution of PM2.5 mass concentration is considered using a mass scattering efficiency, ${\alpha _{{\rm{PM}_{2.5}}{\rm{,}}\lambda }} $, and others are written as ε. The linear relationship between PM2.5 mass concentration and the dry scattering coefficient, bsp, is built based on the observation. Figure 3 shows the linearly fitted results at three wavelengths (450, 525 and 635 nm). The mass scattering efficiency at the site is 4.127 m2 g?1 (550 nm), which is close to but a little higher than that in the IMPROVE equation. From the combination of Eqs. (2) and (5), the relationship between PM2.5 mass concentration and measured visibility under a given RH can be obtained as Eq. (7): Figure 5 compares the measured and regressed PM2.5 mass concentrations in two ways—one using fλ(RH) in four periods, and the other using the average fλ(RH) during the whole observational period, 1.030 / (1 ? RH)0.183. The results show that simulated PM2.5 mass concentrations from both methods coincide well with the measurements. The slopes of the two methods are 0.93 and 0.94 respectively, and the intercepts are 6.6 and 8. The correlation coefficient of the first method is 0.89, which is better than the second one at 0.81. Figure5. Comparison between measured PM2.5 mass concentration and regressed PM2.5 mass concentration via two methods (black solid line—using four fitted equations; black dotted line—using averaged fitted equation).