Svoboda | Graniru | BBC Russia | Golosameriki | Facebook
Next Article in Journal
Pulse Oximetry with Two Infrared Wavelengths without Calibration in Extracted Arterial Blood
Previous Article in Journal
A Quadrature Single Side-Band Mixer with Passive Negative Resistance in Software-Defined Frequency Synthesizer
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Satellite-Based Estimation of Hourly PM2.5 Concentrations Using a Vertical-Humidity Correction Method from Himawari-AOD in Hebei

1
State Key Laboratory of Remote Sensing Science, Institute of Remote Sensing and Digital Earth of Chinese Academy of Sciences, Beijing 100101, China
2
University of Chinese Academy of Sciences, Beijing 100049, China
3
Chongqing Institute of Meteorological Sciences, Chongqing 401147, China
4
Remote Sensing Monitoring, Beijing Municipal Environmental Monitoring Center, Beijing 100048, China
5
Environmental Emergency and Heavy Pollution Weather Warning Center, Shijiazhuang 050051, China
*
Authors to whom correspondence should be addressed.
Sensors 2018, 18(10), 3456; https://doi.org/10.3390/s18103456
Submission received: 14 August 2018 / Revised: 29 September 2018 / Accepted: 11 October 2018 / Published: 14 October 2018
(This article belongs to the Section Remote Sensors)

Abstract

:
Particulate matter with an aerodynamic diameter less than 2.5 μm (PM2.5) is related to various adverse health effects. Ground measurements can yield highly accurate PM2.5 concentrations but have certain limitations in the discussion of spatial-temporal variations in PM2.5. Satellite remote sensing can obtain continuous and long-term coverage data, and many previous studies have demonstrated the relationship between PM2.5 and AOD (aerosol optical depth) from theoretical analysis and observation. In this study, a new aerosol product with a high spatial-temporal resolution retrieved from the AHI (the Advance Himawari Imager) was obtained using a vertical-humidity correction method to estimate hourly PM2.5 concentrations in Hebei. The hygroscopic growth factor ( f ( RH ) ) was fitted at each site (in a total of 137 matched sites). Meanwhile, assuming that there was little change in f ( RH ) at a certain scale, the nearest f ( RH ) of each pixel was determined to calculate PM2.5 concentrations. Compared to the correlation between AOD and PM2.5, the relationship between the “dry” mass extinction efficiency obtained by vertical-humidity correction and the ground-measured PM2.5 significantly improved, with r coefficient values increasing from 0.19–0.47 to 0.61–0.76. The satellite-estimated hourly PM2.5 concentrations were consistent with the ground-measured PM2.5, with a high r (0.8 ± 0.07) and a low RMSE (root mean square error, 30.4 ± 5.5 μg/m3) values, and the accuracy in the afternoon (13:00–16:00) was higher than that in the morning (09:00–12:00). Meanwhile, in a comparison of the daily average PM2.5 concentrations of 11 sites from different cities, the r values were approximately 0.91 ± 0.03, and the RMSEs were between 13.94 and 31.44 μg/m3. Lastly, pollution processes were analyzed, and the analysis indicated that the high spatial-temporal resolution of the PM2.5 data could continuously and intuitively reflect the characteristics of regional pollutants (such as diffusion and accumulation), which is of great significance for the assessment of regional air quality.

1. Introduction

Many researchers have demonstrated that particulate matter with an aerodynamic diameter less than 2.5 μm (PM2.5) is related to various adverse health effects, such as respiratory mortality, lung diseases, and cardiovascular disease [1,2,3,4,5]. With the rapid development of industrialization and urbanization, PM2.5 increasingly leads to terrible air quality and has been a hot research topic for public health. Donkelaar et al. [2] suggested that China is one of the most important regions in the world with respect to air pollutants; thus, many environmental monitoring stations have been built in China since 2013. Ground-based stations can measure PM2.5 concentrations and compositions with a relatively high accuracy. However, these stations are mainly located in cities, and the distribution of stations is sparse and asymmetrical; therefore, research on the spatial-temporal variation in PM2.5 has certainly limitations [6]. Conversely, satellite remote sensing can obtain seamless and long-term coverage data, and the aerosol optical depth (AOD) of retrieval has been widely used to predict PM2.5 concentrations [7,8,9,10,11,12]. AOD is the column integration of light extinction (scattering and absorption) in the atmosphere and is relative to the physicochemical properties of particles (e.g., radius, composition, and refraction index). Many previous studies have demonstrated the relationship between PM2.5 and AOD from theoretical analysis and observation. Methods for demonstrating this relationship are mainly classified into two categories: observation-based methods and simulation-based methods [9]. Observation-based methods include the proportional factor method [13,14,15], semi-empirical formula method [16,17,18], and statistical model method [8,19,20,21,22], which rely on ground-measured and meteorological parameters and have a relatively high PM2.5 estimation accuracy, while observation-based methods do not consider the effect of chemical composition. The effects of meteorology and particle properties are considered in simulation-based methods at global or regional scales, but these methods have some uncertainties (e.g., emission uncertainties) that can lead to inaccurate results [23,24,25].
The correlation between AOD and PM2.5 is highly influenced by the vertical distribution of AOD and the relative humidity (RH). These two parameters are concerned with atmospheric profiles, ambient conditions, and aerosol sizes, which might have large spatiotemporal variations. Many scholars have studied physicochemical impacts on the AOD-PM relationship and have improved the accuracy of PM2.5 estimation. Li et al. [6] indicated that the correlation between AOD and PM10 was improved by up to 0.54 after being corrected by the vertical-and-RH correction method. Koelemeijer et al. [26] demonstrated that this scaling of the AOD with planetary boundary layer height (PBLH) and RH improved the time-correlation with PM2.5 (r = 0.6). Guo et al. [27] studied the correlation between RH-corrected AOD and PM2.5 in Eastern China in 2007 and found a higher correlation with hourly average PM2.5 concentrations (r = 0.61) and daily average PM2.5 concentrations (r = 0.58). Wang et al. [28] used the vertical-humidity correcting method to estimate the PM in Beijing, with R2 increasing from 0.35 to 0.56 (from 0.35 to 0.66) for PM2.5 after vertical (RH) correction. Wang et al. [10] collected visibility (VIS), RH and PM10 data to discuss the impact of RH correction on PM10 estimation and suggested that the monthly correlation between aerosol extinction coefficients and PM10 increased from 0.26–0.63 to 0.49–0.82 after RH correction. Lin et al. [9] considered the effects of aerosol characteristics (aerosol composition and size distribution) to quantify the PM2.5 distribution in Eastern China, and this consideration improved the correlation between satellite-estimated and ground-measured annual and monthly PM2.5 averages, with r values of 0.90 and 0.76, respectively. He et al. [29] analyzed the effect of RH in East China and concluded that higher hygroscopic growth regions can relate to more sulfates and nitrates, and the correlation between satellite estimations and ground measurements was more than 0.85.
However, most studies have obtained a limited number of ground-measured PM2.5 data and have developed correlative linear models between AOD and PM2.5 to estimate regional PM2.5 concentrations with insufficient accuracy, and few studies have fit the hygroscopic growth function at each ground-measured site. Furthermore, the temporal resolution of these studies is relatively low, which prevents the adequate monitoring of the spread and accumulation of pollutants. Due to economic development, Hebei province is the most polluted area in China, and more dense sites are being established. A geostationary satellite (Himawari-8) has provided hourly resolution data since 2015, making it feasible to estimate hourly PM2.5 concentrations with relatively high accuracy and robust validation. This study proposes a new vertical-RH correcting method to estimate hourly PM2.5 concentration in Hebei province by fitting the hygroscopic growth function at each ground-measured site, which both temporal and spatial resolution are improved compared with previous studies. This paper is structured as follows: descriptions of the observational dataset are reported in Section 2; Section 3 describes the theoretical basis of the vertical-RH correcting method and proposes an equation for PM2.5 estimation. Section 4 presents the hygroscopic model fitting results and evaluates the estimated PM2.5 accuracy at different time scales and stations. Finally, the conclusions are given.

2. Study Area and Data

2.1. Study Area

The study area is Hebei province, which has a spatial extent of 36°05′ to 42°40′ N latitude and 113°27′ to 119°50′ E longitude (Figure 1). Hebei is the only province in China with highlands, mountains, hills, basins, plains, grassland, and seashores and has a total area of 188,800 km2 and a permanent population of approximately 75 million. Hebei includes 11 cities, and the northernmost part of the province belongs to the Mongolian Plateau, with high altitudes; the southern part of the province comprises plains with a low altitude. Hebei has a temperate monsoon climate and is dry with little rain in winter. The air pressure is low, and the air does not flow. Hebei has important steel and coal sites in the north. The unfavorable climatic conditions and massive pollutant emissions of this province lead to poor air quality, so Hebei is one of the most polluted provinces in the China.

2.2. Data

2.2.1. AHI AOD

Himawari-8, a geostationary satellite launched by the Japan Meteorology Agency (JMA) on 7 October 2014, carries the primary instrument of the Advance Himawari Imager (AHI). AHI is a 16-channel multispectral imager with wavelengths spanning a range from 0.47 to 13.3 μm, including 3 visible (VIS), 3 near-infrared (NIR), and 10 infrared (IR) bands. The imager has the highest spatial resolution at 0.5 km and provides observations approximately every 30 min over China. In this study, the AHI_AOD, which were retrieved by the method of Yang et al. [30], provided AOD data. They used the AHI and Moderate Resolution Imaging Spectroradiometer (MODIS) spectral response functions to make the relationship more suitable for AHI, and a new dark target algorithm was proposed to retrieve the AOD at 1 km resolution over Mainland China. Yang et al. downloaded the Himawari-8 level three hourly AOD (AOD_JAXA) data from the Japan Aerospace Exploration Agency (JAXA) for comparison with their retrieval results (http://www.eorc.jaxa.jp/ptree/index.html), and extracted satellite data and Aerosol Robotic NETwork (AERONET) data from 02:00 to 07:00 (UTC). Except for that at 02:00 (UTC), the R2 of AHI_AOD is higher than that of AOD_JAXA. Meanwhile, seasonal averages showed that their product is more similar to MODIS Collection 6 (C6) Dark Target (DT) [31] AOD than AOD_JAXA.

2.2.2. Meteorological Data

A total of 142 meteorological sites, with data including visibility (VIS), RH, and wind direction, were obtained from the Hebei Province Meteorological Bureau. The temporal resolution was 1 h from January to June 2017, which can be matched with the AHI AOD and PM2.5 data. To reduce errors, visibility data were omitted when the daily average visibility was less than 1/3 of the values in the next and previous days [32].

2.2.3. PM2.5 Data

The ground-level PM2.5 observations over Hebei from January to June 2017 were obtained from the Hebei Province Environmental Monitoring Center and had a temporal resolution of 1 h. PM2.5 concentrations are measured using the tapered element oscillating microbalance (TEOM) approach or beta-attenuation approach, both of which comply with the National Standard for Environmental Air Quality (GB3095-2012) [33]. The PM2.5 data need be somewhat regular to avoid affecting the fitting results of aerosol hygroscopic growth. (1) PM2.5 levels less than the 3rd percentile or more than the 97th percentile within 3 h were not used for calculations. (2) Data with humidity less than 70% when the extinction coefficients exceeded the 80th percentile were omitted. (3) The distances between pairs of meteorological sites and environmental monitoring sites had to be within 10 km; therefore, there were 198 PM2.5 observation sites that could be matched with 137 meteorological sites.

3. Methodology

AOD is the integration of the extinction coefficients absorbed and scattered by aerosols in an atmospheric column; thus, to obtain the surface aerosol extinction coefficient from AOD, vertical correction is needed. The physicochemical characteristics of an aerosol particle are changed because of absorbing or evaporating water vapor in the atmosphere, so humidity correction is needed to obtain the “dry” aerosol extinction coefficient.

3.1. Vertical Correction

By assuming that the plane atmosphere is homogeneous, AOD is the integral of the extinction coefficient ( σ a ) at all altitudes along the vertical orientation [34]. Assuming the vertical distribution of σ a is the negative exponent form, AOD can be expressed by Equation (1) [9,28,35,36]
AOD = 0 σ a , 0 · e z / H dz = σ a , 0 · H
where σ a , 0 stands for the surface aerosol extinction coefficient at the wavelength of 550 μm, Z is the vertical height, and H is the scale height of aerosols. H can be approximately replaced by the boundary layer height [26,37]. Koschmieder [38] assumed that the impact of air molecules can be neglected when the threshold contrast of human eyes takes the common value of 0.02; thus, the σ a ( λ ) can be expressed as
σ a ( λ ) = 3.912 VIS 32 π 3 ( n 1 ) 2 3 N λ 4
where VIS is visibility, and n and N represent the atmospheric refractive index and the number density of molecules (n − 1 = 293 × 10−6 and N = 266 × 1019 at the sea level), respectively. λ stands for wavelength. Thus, H can be calculated by AOD and VIS at each meteorology station. Under the assumption of relatively smooth scale height changes within a certainty scale, the spatial distribution of H can be obtained by inverse distance weighted (IDW) interpolation method, and the σ a , 0 at each pixel can be calculated by Equation (1).

3.2. Relativity Correction

Based on the Mie theory, the extinction coefficient is proportional to the PM concentrations in the ambient air and can be expressed using the following equation [26,28]:
σ a ( λ ) = 3 · Q ext 4 · r eff · ρ · PM x
where Q ext is the size-distribution-integrated extinction efficiency, which is closely related to the aerosol composition and particle spectrum distribution [34]. r eff is the effective radius, and ρ is the averaged mass density of the particles, which are related to RH [39,40]. PM x is the mass concentration of PM. The parameters are affected by the environmental humidity due to the existence of a large number of hygroscopic components in particles.
Wang et al. [10] defined the average mass extinction efficiency ( E ext ) for an aerosol as the ratio of σ a ( λ ) to the PM x concentrations. Hand and Malm [41] summarized that E ext could be related to RH and expressed as a function of RH. Meanwhile, assuming that the chemical composition and aerosol distribution of aerosols would change little during a certain period, Liu [40] proposed that E ext can be regarded as a function of ambient RH, and E ext ( RH ) can be translated to Equation (4):
E ext ( RH ) = σ a ( λ ) PM x = 3 · Q ext 4 · r eff · ρ .
Importantly, σ a is the integration of the extinction coefficients of aerosol, but the PM2.5 concentrations were used to calculate the average mass extinction efficiency in this paper, which overestimated the ability of extinction and could lead to some uncertainty. Therefore, the average mass extinction efficiency describes the mean state of the extinction ability of particles for different properties.
To obtain the “dry” extinction coefficient, many studies have investigated the hygroscopic properties of aerosol particles [10,40,42,43,44]. An aerosol particle is influenced by water vapor in the atmosphere via a process called aerosol hygroscopic growth [28,45]. The aerosol hygroscopic growth factor f ( RH ) is defined as the ratio of aerosol extinction in ambient humidity to “dry” aerosol extinction under relatively dry conditions (RH less than 30%). In this study, the f ( RH ) can be described by Equation (5) [17,27,44,46,47,48,49].
f ( RH ) = σ a ( λ ) σ dry ( λ ) = E ext ( RH ) E dry = a + b × ( RH 100 ) c
where σ dry is the extinction coefficient when RH is set below 30%. In this study, RH represents the relative humidity of the atmosphere, and a, b, and c are the parameters of f ( RH ) and can be obtained by fitting. Assuming that RH varies smoothly at a certain scale, the spatial map of RH can be obtained by IDW interpolation method from metrological sites. We assumed that the f ( RH ) demonstrates little change at a certain scale; hence, each pixel can find a nearest f ( RH ) to calculate PM2.5 concentrations.
PM 2.5 = σ a ( λ ) E ext ( RH ) = AOD H ( a + b × ( RH 100 ) c ) × E dry

4. Results and Discussion

The physical and chemical properties of particles have large spatial and temporal variations; therefore, the capacity of hygroscopic growth differs. In this study, we selected three PM2.5 sites with different sources of pollution, which are in Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiakou-Huaian (as indicated in Figure 1 by blue points), to analyze aerosol hygroscopic growth. The pollutants of Xingtai, which is one of the most polluted cities in China and is located to the east of Taihang Mountain, mainly come from anthropogenic activities and industry. Qinhuangdao is near the Bohai Sea, and sea salt represents part of pollutants. Taihang Mountain and Yanshan block pollutant transmission to Zhangjiakou, and the air quality of Zhangjiakou is relatively good. Therefore, the three sites can reflect spatial differences in aerosol hygroscopic growth.

4.1. Descriptive Statistics

The summary statistics of factors (PM2.5, VIS, and RH) are listed in Table 1, and histograms of PM2.5 are presented in Figure 2. According to Table 1, the mean, median, and standard deviation (std) of the PM2.5 concentrations in Xingtai-Nanhe are 86.96 μg/m3, 57 μg/m3, and 81.93 μg/m3, respectively, indicating that the PM2.5 concentrations demonstrated a large change over the study period. Compared to Xingtai-Nanhe, Qinhuangdao-Changli has significantly low PM2.5 concentrations (mean, median, and std are 64.32 μg/m3, 51.50 μg/m3, and 46.53 μg/m3, respectively). Zhangjiakou-Huaian has the best air quality of the three sites, with a mean value of 29.34 μg/m3. The visibility of Qinhuangdao-Changli, with a mean value of 13.38 km, is relatively low compared to that of the other two sites due to the influence of water vapor from the sea. Compared to Qinhuangdao-Changli, Xingtai-Nanhe, and Zhangjiakou-Huaian have improved visibility (22.14 and 23.15 km, respectively). The study area is located in North China, which has a low-rainfall period and accordingly low RH in spring and winter [50] (RH of 57.21%, 59.19%, and 44.54% in Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiakou-Huaian, respectively).
According to Figure 2, the means of the monthly and maximum PM2.5 concentrations of the three sites gradually decreased from January to June 2017. This decrease can be attributed to the following reason: a large amount of pollutants were discharged into the atmosphere during coal heating in January and February, and the static stability weather conditions, such as the relatively low boundary layer height and rainfall, were not conducive to pollutant diffusion, resulting in higher PM2.5 concentrations. However, in spring and summer, the PM2.5 concentrations were relatively low because the atmosphere was relatively active, thus favoring pollutant diffusion, and coal heating was stopped, thus reducing the source of pollutants. The air quality of Xingtai-Nanhe was more likely to be “heavily” and “severely” polluted in January than in other months, and the maximum PM2.5 value reached 573 μg/m3. The number of high PM2.5 concentrations decreased after January, with a maximum monthly value of only 219 μg/m3 in February. There were more good air quality cases in May and June than in other months. In general, the PM2.5 concentrations were lower in Qinhuangdao-Changli than in Xingtai-Nanhe, and the highest PM2.5 value was 359 μg/m3. However, the air quality in Qinhuangdao-Changli was most commonly “moderately” polluted in April. The air quality of Zhangjiakou-Huaian was better than that of the other sites, and the PM2.5 concentrations were generally less than 50 μg/m3, except for in January.

4.2. E e x t ( R H ) Fitting and f ( R H ) Analysis

The relationships between E ext ( RH ) and RH of the three stations were adequately fitted by Equation (5), as shown in Figure 3, Figure 4 and Figure 5. In general, E ext ( RH ) grows slowly when RH is low and increases rapidly under higher RH. However, there were differences in RH among the three sites, showing the following: (1) The scatter distribution had the most concentrations and the best fitting ability at Xingtai-Nanhe, and the R2 was higher than 0.5 (except for in February). At Qinhuangdao-Changli, the fitting ability was the worst in January and the best in April (R2 of 0.3 and 0.9, respectively). The hygroscopic growth capacity was stronger at Qinhuangdao-Changli than at the other two sites because Qinhuangdao-Changli is close to the coast, the aerosol compositions of this coastal site contain salt particles, and the E ext ( RH ) rapidly grows with RH when RH is more than 70%. The fitting result in Zhangjiakou-Huaian was not ideal, and the R2 was generally less than 0.5 in each month. (2) At Xingtai-Nanhe, the fitting curve from January to June was relatively flat when RH was less than 90% and increases slightly when RH was more than 90%, which shows that the capacity of hygroscopic growth was weak. Compared with the fitting curve of Xingtai-Nanhe, the Qinhuangdao-Changli curve increased more rapidly when RH exceeded 90%. The data from both March and May presented obvious hygroscopic behavior, and a deliquescent point with an RH of approximately 90% occurred in April, while a hygroscopic and deliquescent phenomenon occurred in January and June. At Zhangjiakou-Huaian, the humidographs from January to June had flat growths at a medium RH (40–80%), with sharp increases under high RH (>80%) in March and June, which shows that both hygroscopic and deliquescent behaviors occurred simultaneously. Therefore, there were significant differences in the physical and chemical characteristics of aerosols in the three regions. (3) There was little variation in the fitting curve of Xingtai-Nanhe, which indicates that the aerosol sources and environmental conditions in the area varied little from month to month. The capacity of hygroscopic growth had a high monthly variation at Qinhuangdao-Changli, indicating that the site experienced large environmental changes or had complex aerosol sources because of aerosol transmission from other areas. Although the existence of outliers within the fitting results can generate an uncertainty for humidity correction, the results were able to reflect the average variation of E ext ( RH ) with RH. It is helpful to correct the influence of humidity to obtain near-surface particle concentrations.
The monthly and half-year mean humidification factor values at RH = 80%, f ( 80 % ) were calculated for the three sites by Equation (5), as listed in Table 2. The f ( 80 % ) value in Qinhuangdao-Changli was generally higher than those of the other two sites (except in February), with a range from 1.39 to 2.39, which shows hygroscopic growth has a stronger capacity with RH. The mainly reason for this trend is that aerosol particles near coastal sites have a relatively high proportion of sea salt components, and their overall hygroscopic growth ability is the strongest. The proportion of sea salt particles at inland sites such as Zhangjiakou-Huaian and Xingtai-Nanhe is small, and the proportion of black carbon aerosols is large; thus, hygroscopic growth at inland areas is relatively weak. However, the capacity of hygroscopic growth can have great variations over different months at the same site. For example, at Xingtai-Nanhe, the f ( 80 % ) value was the highest in February and the lowest in March, with values of 2.23 and 1.01, respectively. At Qinhuangdao-Changli, the highest (lowest) value of f ( 80 % ) was 2.39 (1.39) in May (February). At Zhangjiakou-Huaian, the highest (lowest) value of f ( 80 % ) was 4.34 (1.35) in February (June). According to the above analysis, the hygroscopic growth of particles in different regions and at different times varies greatly with the RH. Therefore, it is necessary to perform hygroscopic correction at each site in this paper in order to improve the estimation accuracy of PM2.5 concentrations.

4.3. The Results of PM2.5 Estimation

4.3.1. Vertical-Humidity Correction on AOD

According to the matching data of the environmental monitoring stations and meteorological stations in Hebei province, vertical and humidity corrections were made to each site to estimate the PM2.5 concentrations. Both the scatterplots of PM2.5 vs. AOD and PM2.5 vs. the “dry” extinction coefficient ( σ dry ) are shown in Figure 6 (colorbar indicates RH). The first and third rows represent the scatterplots between AHI AOD and PM2.5 from 09:00 to 16:00, and the second and fourth rows represent σ dry and PM2.5. The scatter distributions of AOD and PM2.5 are relatively discrete, and their correlations are low (the lowest r is 0.18 at 10:00, and the highest r is only 0.47 at 15:00). Compared to the poor correlation between AOD and PM2.5, a better, relatively high correlation was obtained by vertical-humidity correction between σ dry and PM2.5, with the hour correlation r increasing from 0.19–0.47 to 0.61–0.76.

4.3.2. PM2.5 Estimation Validation

The relationship between the near-surface “dry” extinction coefficient and PM2.5 concentrations improved after vertical-humidity correction; therefore, the PM2.5 concentrations were calculated by Equation (6). The satellite-estimated PM2.5 and all ground-measured data from January to June 2017, in which there are a total of 153,482 points, are shown in Figure 7. According to the fitting results, the correlation was relatively high (r = 0.82), the root mean square error (RMSE) was 30.08 μg/m3, the slope was close to 1, and the intercept was 2.48. The accuracy of PM2.5 estimation was verified on a daily, monthly, and by site.
(1) Monthly PM2.5 Validation
To analyze the accuracy of PM2.5 estimation at the monthly scale, the scatterplot for each month is shown in Figure 8. The r value of each month was approximately 0.8 (except for June, r is 0.68), and the slope was between 0.99 and 1.03. Hebei was “heavily” polluted and had high PM2.5 concentrations in January and February. After vertical-humidity correction, the r value increased (r = 0.81 and 0.82 in January and February, respectively), but the dispersion of some scattered points was relatively large, and the RMSE increased (45.29 and 42.63 μg/m3 in January and February, respectively). The air was relatively dry in winter, and the capacity of hygroscopic growth was weak; hence, humidity correction had no obvious effect at some sites. The r values in March, April, and May were 0.8 ± 0.1, and the PM2.5 concentrations and RMSE values (RMSEs of 19.16, 24.13, and 29.54 μg/m3, respectively) were lower than those in both January and February. The points were relatively concentrated in March and April, but some high values were dispersed in May. The RMSEs were the lowest in June (RMSE = 18.09 μg/m3), and the slope was equal to 1.
(2) Daily PM2.5 Validation
Figure 9 presents hourly daytime PM2.5 scatter plots from January to June 2017. The correlation increased from 09:00 to 16:00, and the r increased from 0.73 to 0.86, with the maximum (minimum) RMSE of 38.58 μg/m3 (24.18 μg/m3) at 10 a.m. (15 p.m.) and higher PM2.5 concentrations in morning than in afternoon, which might be attributed to the following two factors. (1) In the morning, the solar azimuth and water vapor level are relatively high, and sunlight reaches the ground after a longer path through the atmosphere, which can affect the accuracy of AOD retrieval. (2) The higher RH can cause deliquescent behaviour, which has an influence on the humidity correction. In June 2017, the correlation was relatively low, with r = 0.68, which might have occurred because the atmosphere was more active, with higher wind speeds and increases in rainfall. Consequently, the physical and chemical properties of particulates in local areas were more complex and varied greatly.
(3) Site-Based PM2.5 Validation
To evaluate the accuracy of the PM2.5 vertical-humidity correction at each site, we selected 11 sites from different cities in Hebei and respectively drew a time series diagram of the daily mean PM2.5 concentrations, as shown in Figure 10. According to the ground-measured PM2.5, in January and February 2017, there was “heavy” pollution weather (PM2.5 > 150 μg/m3) at Baoding, Changzhou, Handan, Hengshui, Xingtai, and Shijiazhuang, where the air quality was very poor. There were low PM2.5 concentrations at Zhangjiakou, Tangshan, and Chengde, where there were few pollutants from industry and vehicle emissions. At all sites, except for on 4, May 2017 (PM2.5 > 200 μg/m3), the mean daily PM2.5 concentrations from March to June were generally less than 100 μg/m3, which shows good air quality. The decrease in PM2.5 was mainly related to meteorological conditions and decreases in pollution from coal heating. According to Figure 11, the correlation between ground-measured PM2.5 and satellite estimation was relatively high overall. The r values were generally ±0.9, and the RMSEs were between 13.94 and 31.44 μg/m3. However, PM2.5 concentrations were overestimated (underestimated) when the PM2.5 concentrations was low (high). Interestingly, satellite estimation commonly underestimated the PM2.5 of Qinghuandao-Changli, as the PM2.5 of this site has complex physical and chemical characteristics, but the particle component were not considered in this paper, which may have a certain influence on the accuracy of PM2.5 estimation.

4.3.3. Hourly Patterns of PM2.5 Concentration

Assuming that particle composition and weather condition are basically stable, the f ( RH ) of each pixel can be matched by the nearest neighbour searching principle in order to estimate the spatial distribution of PM2.5. The larger daily variation of PM2.5 in this section is selected to analyze the hourly change process on 10 January 2017, as shown in Figure 11 (the classification standard adopts the ambient air quality standard of China). Except for a few stations with underestimated results, the satellite-estimated PM2.5 concentrations at the air quality level agreed well with the ground-based measurements, so the satellite data can clearly reflect the spatial distribution of pollution. Clouds covered a larger area (blank area) at 09:00 over Hebei, but the ground-measured PM2.5 concentrations show that the air quality was poor, and Baoding, Shijiazhuang, Hengshui, and Xingtai were especially heavily polluted. From 09:00 to 12:00, the wind direction changed from an east wind from the Bohai Sea to Hengshui to mainly northerly winds and southerly winds; accordingly, the pollution over Cangzhou, Langfang, and Hengshui migrated to the southern regions, leading to high PM2.5 concentrations in Xingtai and Handang. The south wind predominated over Shijiazhuang and Baoding at 13:00, and pollutants migrated from Handan to Xingtai, Shijiazhuang, and Baoding along the Taihang Mountain range, forming an obvious pollution zone. Therefore, the high spatial-temporal resolution PM2.5 data can continuously and intuitively reflect the characteristics of regional pollutants (such as diffusion and accumulation), which is of great significance for the assessment of regional air quality.

5. Conclusions

This study analyzed the hygroscopic growth characteristics of particulate matter in different regions of Hubei province, improved the estimation method of PM2.5, obtained high spatial-temporal resolution AHI AOD data to estimate hourly PM2.5 concentrations, and evaluated the estimated accuracy. The main conclusions include the following:
  • Three sites located in different regions of Hebei province were selected to analyze the capacity of hygroscopic growth. Qinhuangdao-Changli, with a sea salt pollutant component, has the highest hygroscopic growth ability, while Zhangjiakou-Huaian has the second highest hygroscopic growth ability, and Xingtai-Nanhe, with a high black carbon pollutant component, has the lowest hygroscopic growth ability; these results indicate that the physicochemical characteristics of the particles in different regions are inconsistent. Thus, vertical-humidity correction is helpful to improve the accuracy of PM2.5 estimation in different regions.
  • Compared to the relationship between AOD and PM2.5, the relationship between σ a , dry and PM2.5 significantly improved, with the coefficient r increasing from 0.19–0.47 to 0.61–0.76. The accuracy of PM2.5 estimation is verified at the hourly, daily, and monthly scales, respectively. The hourly PM2.5 estimation is relatively high r (0.8 ± 0.07), with a low RMSE (30.4 ± 5.5 μg/m3), and the accuracy in the afternoon (13:00 to 16:00) is higher than that in the morning (09:00 to 12:00). In a comparison of the daily average PM2.5 concentrations at 11 sites, the r value is approximately 0.9, and the RMSE is between 13.94 and 31.44 μg/m3. The result suggested that the new method in this study is useful to improve the accuracy of PM2.5 estimation.
  • The spatial distribution of PM2.5 concentrations from 09:00 to 16:00 is estimated for 10 January 2017, and the process of pollution accumulation and dissipation is clearly presented over space and time. This type of estimation is conducive to the evaluation and control of air quality.
The use of the vertical-humidity method to estimate the spatial distribution of PM2.5 yielded results with a relatively high accuracy, but obtaining the hygroscopic growth factor far from the ground monitoring site can impact the estimation accuracy when the meteorological conditions change greatly. The particulate composition, which affects the accuracy of PM2.5 estimation, was not considered in this study. Therefore, obtaining more ground-based data and research on the composition of particles will help improve the PM2.5 inversion accuracy in future research.

Author Contributions

Q.Z. proposed the method, collected data, and wrote this paper; Z.W. performed the method; L.C. and J.T. analyzed the data; J.X. and Y.W. offered the AOD data; H.Z., X.W., and M.T. processed the data.

Funding

This study was supported by the Major Research Plan of the National Natural Science Foundation of China (Grant No. 91644216), the National Key Research and Development Program of China (Grant No. 2016YFC0200404), the National Natural Science Foundation of China (Grant No. 41571347).

Acknowledgments

The authors are grateful to the China Meteorological Data Sharing Service System (http://data.cma.cn/), NASA (https://pmm.nasa.gov/), CMDSSS (http://data.cma.cn/), SRTM (http://srtm.csi.cgiar.org/), European Center (http://www.ecmwf.int/), CNEMC (http://106.37.208.233:20035/), AERONET (http://aeronet.gsfc.nasa.gov/), and the Data Center for Resource and Environmental Sciences, Chinese Academy of Sciences (http://www.resdc.cn) scientific team for the provision of satellite data and in situ measurement data utilized in this study.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Wu, J.; Zhu, J.; Li, W.; Xu, D.; Liu, J. Estimation of the PM2.5 health effects in China during 2000–2011. Environ. Sci. Pollut. Res. 2017, 24, 1–13. [Google Scholar] [CrossRef] [PubMed]
  2. Donkelaar, A.V.; Martin, R.V.; Brauer, M.; Kahn, R.; Levy, R.; Verduzco, C.; Villeneuve, P.J. Global estimates of ambient fine particulate matter concentrations from satellite-based aerosol optical depth: Development and application. Environ. Health Perspect. 2010, 118, 847. [Google Scholar] [CrossRef] [PubMed]
  3. See, S.W.; Balasubramanian, R. Chemical characteristics of fine particles emitted from different gas cooking methods. Atmos. Environ. 2008, 42, 8852–8862. [Google Scholar] [CrossRef]
  4. Pope, R.C.; Dockery, D.W. Health effects of fine particulate air pollution: Lines that connect. J. Air Waste Manag. Assoc. 2006, 56, 1368–1380. [Google Scholar] [CrossRef]
  5. World Health Organization (WHO). Air Quality Guidelines for Europe, 2nd ed.; European Series; WHO Regional Office for Europe: Copenhagen, Denmark, 2000; Volume 91. [Google Scholar]
  6. Li, C.C.; Mao, J.T.; Liu, Q.H. Application of modis aerosol product in the study of air pollution in Beijing. Sci. China Ser. D Earth Sci. 2005, 35, 177–186. [Google Scholar]
  7. Zhang, M.; Ma, Y.; Wang, L.; Gong, W.; Hu, B.; Shi, Y. Spatial-temporal characteristics of aerosol loading over the yangtze river basin during 2001–2015: Aerosol loading in the yangtze river basin. Int. J. Climatol. 2018, 38, 2138–3252. [Google Scholar] [CrossRef]
  8. Xiao, Q.Y.; Wang, Y.J.; Howard, H.; Meng, X.; Geng, G.; Lyapustin, A.; Liu, Y. Full-coverage high-resolution daily PM2.5 estimation using maiac aod in the yangtze river delta of China. Remote. Sens. Environ. 2017, 199, 437–446. [Google Scholar] [CrossRef]
  9. Lin, C.; Li, Y.; Yuan, Z.; Lau, A.K.H.; Li, C.; Fung, J.C.H. Using satellite remote sensing data to estimate the high-resolution distribution of ground-level PM2.5. Remote. Sens. Environ. 2015, 156, 117–128. [Google Scholar] [CrossRef]
  10. Wang, Z.; Chen, L.; Tao, J.; Liu, Y.; Hu, X.; Tao, M. An empirical method of RH correction for satellite estimation of ground-level pm concentrations. Atmos. Environ. 2014, 95, 71–81. [Google Scholar] [CrossRef]
  11. Hoff, R.; Christopher, S. Remote sensing of particulate pollution from space: Have we reached the promised land? J. Air Waste Manag. Assoc. 2009, 59, 645–675. [Google Scholar] [CrossRef] [PubMed]
  12. Van, A.D.; Martin, R.V.; Brauer, M.; Boys, B.L. Use of satellite observations for long-term exposure assessment of global concentrations of fine particulate matter. Environ. Health Perspect. 2015, 123, 135. [Google Scholar]
  13. Donkelaar, A.V.; Martin, R.V.; Brauer, M.; Hsu, N.C.; Kahn, R.A.; Levy, R.C.; Lyapustin, A.; Sayer, A.M.; Winker, D.M. Global estimates of fine particulate matter using a combined geophysical-statistical method with information from satellites, models, and monitors. Environ. Sci. Technol. 2016, 50, 3762. [Google Scholar] [CrossRef] [PubMed]
  14. Tilson, H.A. Ehp paper of the year, 2011. Environ. Health Perspect. 2013, 121, A322. [Google Scholar] [CrossRef] [PubMed]
  15. Liu, Y.; Park, R.J.; Jacob, D.J.; Li, Q.; Kilaru, V.; Sarnat, J.A. Mapping annual mean ground-level PM2.5 concentrations using multiangle imaging spectroradiometer aerosol optical thickness over the contiguous united states. J. Geophys. Res. Atmos. 2004, 109, D22. [Google Scholar]
  16. He, Q.; Geng, F.; Li, C.; Yang, S.; Wang, Y.; Mu, H.; Zhou, G.; Liu, X.; Gao, W.; Cheng, T. Long-term characteristics of satellite-based PM2.5 over east China. Sci. Total. Environ. 2017, 612, 1417. [Google Scholar] [CrossRef] [PubMed]
  17. Lin, C.; Li, Y.; Lau, A.K.H.; Deng, X.; Tse, T.K.T.; Fung, J.C.H.; Li, C.; Li, Z.; Lu, X.; Zhang, X. Estimation of long-term population exposure to PM2.5 for dense urban areas using 1-km modis data. Remote. Sens. Environ. 2016, 179, 13–22. [Google Scholar] [CrossRef]
  18. Zhang, Y.; Li, Z. Remote sensing of atmospheric fine particulate matter (PM2.5) mass concentration near the ground from satellite observation. Remote. Sens. Environ. 2015, 160, 252–262. [Google Scholar] [CrossRef]
  19. Yao, F.; Si, M.; Li, W.; Wu, J. A multidimensional comparison between modis and viirs aod in estimating ground-level PM2.5 concentrations over a heavily polluted region in China. Sci. Total. Environ. 2018, 618, 819–828. [Google Scholar] [CrossRef] [PubMed]
  20. Wang, W.; Mao, F.; Du, L.; Pan, Z.; Gong, W.; Fang, S. Deriving hourly PM2.5 concentrations from himawari-8 aods over beijing–tianjin–hebei in China. Remote. Sens. 2017, 9, 858. [Google Scholar] [CrossRef]
  21. Hu, X.; Waller, L.A.; Al-Hamdan, M.Z.; Crosson, W.L.; Jr, M.G.E.; Estes, S.M.; Quattrochi, D.A.; Sarnat, J.A.; Liu, Y. Estimating ground-level PM2.5 concentrations in the southeastern U.S. Using geographically weighted regression. Environ. Res. 2013, 121, 1–10. [Google Scholar] [CrossRef] [PubMed]
  22. Liu, Y.; Franklin, M.; Kahn, R.; Koutrakis, P. Using aerosol optical thickness to predict ground-level PM2.5 concentrations in the St. Louis area: A comparison between misr and modis. Remote Sens. Environ. 2007, 107, 33–44. [Google Scholar] [CrossRef]
  23. Zheng, J.; Zhang, L.; Che, W.; Zheng, Z.; Yin, S. A highly resolved temporal and spatial air pollutant emission inventory for the pearl river delta region, China and its uncertainty assessment. Atmos. Environ. 2009, 43, 5112–5122. [Google Scholar] [CrossRef]
  24. Tiwary, A.; Colls, J. Air Pollution: Measurement, Modelling and Mitigation, 3rd ed.; CRC Press: Boca Raton, FL, USA, 2009. [Google Scholar]
  25. Kukkonen, J.; Olsson, T.; Schultz, D.M.; Baklanov, A.; Klein, T.; Miranda, A.I.; Monteiro, A.; Hirtl, M.; Tarvainen, V.; Boy, M. A review of operational, regional-scale, chemical weather forecasting models in europe. Atmos. Chem. Phys. Discuss. 2012, 11, 1–87. [Google Scholar] [CrossRef] [Green Version]
  26. Koelemeijer, R.; Homan, C.; Matthijsen, J. Comparison of spatial and temporal variations of aerosol optical thickness and particulate matter over europe. Atmos. Environ. 2006, 40, 5304–5315. [Google Scholar] [CrossRef]
  27. Guo, J.P.; Zhang, X.Y.; Che, H.Z.; Gong, S.L.; An, X.; Cao, C.X.; Jie, G.; Zhang, H.; Wang, Y.Q.; Zhang, X.C. Correlation between PM concentrations and aerosol optical depth in Eastern China. In Proceedings of the Geoscience and Remote Sensing Symposium, Vancouver, BC, Canada, 24–29 July 2011; pp. 5876–5886. [Google Scholar]
  28. Wang, Z.; Chen, L.; Tao, J.; Zhang, Y.; Su, L. Satellite-based estimation of regional particulate matter (PM) in beijing using vertical-and-rh correcting method. Remote Sens. Environ. 2010, 114, 50–63. [Google Scholar] [CrossRef]
  29. He, Q.; Zhou, G.; Geng, F.; Gao, W.; Yu, W. Spatial distribution of aerosol hygroscopicity and its effect on PM2.5 retrieval in east China. Atmos. Res. 2016, 170, 161–167. [Google Scholar] [CrossRef]
  30. Yang, F.; Wang, Y.; Tao, J.; Wang, Z.; Fan, M.; Leeuw, G.D.; Chen, L. Preliminary investigation of a new ahi aerosol optical depth (AOD) retrieval algorithm and evaluation with multiple source aod measurements in China. Remote. Sens. 2018, 10, 748. [Google Scholar] [CrossRef]
  31. Kaufman, Y.J.; Tanré, D.; Remer, L.A.; Vermote, E.F.; Chu, A.; Holben, B.N. Operational remote sensing of tropospheric aerosol over land from eos moderate resolution imaging spectroradiometer. J. Geophys. Res. Atmos. 1997, 102, 17051–17067. [Google Scholar] [CrossRef]
  32. Husar, R.B.; Jd, M.L.H. Distribution of continental surface aerosol extinction based on visual range data. Atmos. Environ. 2000, 34, 5067–5078. [Google Scholar] [CrossRef]
  33. Ouyang, S.H. Summarization on PM2.5 online monitoring technique. China Environ. Prot. Ind. 2012, 4, 013. [Google Scholar]
  34. Liou, K.N.; Bohren, C. An introduction to atmospheric radiation. Phys. Today 1981, 34, 66–67. [Google Scholar] [CrossRef]
  35. Emili, E.; Popp, C.; Petitta, M.; Riffler, M.; Wunderle, S.; Zebisch, M. PM 10 remote sensing from geostationary seviri and polar-orbiting modis sensors over the complex terrain of the european alpine region. Remote Sens. Environ. 2010, 114, 2485–2499. [Google Scholar] [CrossRef]
  36. Busen, R.; Hänel, G. Radiation budget of the boundary layer. Part i: Measurement of absorption of solar radiation by atmospheric particles and water vapor. Beiträge Zur Physik Der Atmosphäre 1987, 60, 229–240. [Google Scholar]
  37. Liu, Y.; Sarnat, J.A.; Kilaru, V.; Jacob, D.J.; Koutrakis, P. Estimating ground-level PM2.5 in the eastern united states using satellite remote sensing. Environ. Sci. Technol. 2005, 39, 3269. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  38. Koschmieder, H. Theorieder horizontalen sichtweite ii: Kontrast und sichtweite beitrage zurphysik derfreien. Beiträge Zur Physik Der Freien Atmosphäre 1925, 12, 171–181. [Google Scholar]
  39. Tang, I.N. Chemical and size effects of hygroscopic aerosols on light scattering coefficients. J. Geophys. Res. Atmos. 1996, 101, 19245–19250. [Google Scholar] [CrossRef]
  40. Liu, X.; Cheng, Y.; Zhang, Y.; Jung, J.; Sugimoto, N.; Chang, S.Y.; Kim, Y.J.; Fan, S.; Zeng, L. Influences of relative humidity and particle chemical composition on aerosol scattering properties during the 2006 prd campaign. Atmos. Environ. 2008, 42, 1525–1536. [Google Scholar] [CrossRef]
  41. Hand, J.L.; Malm, W.C. Review of aerosol mass scattering efficiencies from ground-based measurements since 1990. J. Geophys. Res. Atmos. 2007, 112, D16. [Google Scholar] [CrossRef]
  42. Nessler, R.; Weingartner, E.; Baltensperger, U. Effect of humidity on aerosol light absorption and its implications for extinction and the single scattering albedo illustrated for a site in the lower free troposphere. J. Aerosol Sci. 2005, 36, 958–972. [Google Scholar] [CrossRef]
  43. Lai, L.Y.; Sequeira, R. Visibility degradation across hong kong: Its components and their relative contributions. Atmos. Environ. 2001, 35, 5861–5872. [Google Scholar] [CrossRef]
  44. Kotchenruther, R.A.; Hobbs, P.V.; Hegg, D.A. Humidification factors for atmospheric aerosols off the mid-atlantic coast of the united states. J. Geophys. Res. Atmos. 1999, 104, 2239–2251. [Google Scholar] [CrossRef]
  45. Lee, A.K.Y.; Ling, T.Y.; Chan, C.K. Understanding hygroscopic growth and phase transformation of aerosols using single particle raman spectroscopy in an electrodynamic balance. Faraday Discuss. 2008, 137, 245. [Google Scholar] [CrossRef] [PubMed]
  46. Kotchenruther, R.A.; Hobbs, P.V. Humidification factors of aerosols from biomass burning in brazil. J. Geophys. Res. Atmos. 1998, 103, 32081–32089. [Google Scholar] [CrossRef]
  47. Im, J.S.; Saxena, V.K.; Wenny, B.N. An assessment of hygroscopic growth factors for aerosols in the surface boundary layer for computing direct radiative forcing. J. Geophys. Res. Atmos. 2001, 106, 20213–20224. [Google Scholar] [CrossRef] [Green Version]
  48. Randriamiarisoa, H.; Chazette, P.; Couvert, P.; Sanak, J.; Mégie, G. Relative humidity impact on aerosol parameters in a paris suburban area. Atmos. Chem. Phys. 2006, 6, 1389–1407. [Google Scholar] [CrossRef]
  49. Zieger, P.; Kienast-Sjogren, E.; Starace, M.; Bismarck, J.V. Spatial variation of aerosol optical properties around the high-alpine site jungfraujoch (3580 m a.S.L.). Atmos. Chem. Phys. Discuss. 2012, 12, 7231–7249. [Google Scholar] [CrossRef] [Green Version]
  50. Zeng, Q.; Wang, Y.; Chen, L.; Wang, Z.; Zhu, H.; Li, B. Inter-comparison and evaluation of remote sensing precipitation products over China from 2005 to 2013. Remote Sens. 2018, 10, 168. [Google Scholar] [CrossRef]
Figure 1. Study region with environmental monitoring stations and meteorological stations.
Figure 1. Study region with environmental monitoring stations and meteorological stations.
Sensors 18 03456 g001
Figure 2. Histogram statistics of PM2.5 concentrations from Jan. to Jun. 2017 in Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiakou-Huaian, respectively.
Figure 2. Histogram statistics of PM2.5 concentrations from Jan. to Jun. 2017 in Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiakou-Huaian, respectively.
Sensors 18 03456 g002
Figure 3. E ext ( RH ) fitting at Xingtai-Nanhe.
Figure 3. E ext ( RH ) fitting at Xingtai-Nanhe.
Sensors 18 03456 g003
Figure 4. E ext ( RH ) fitting at Qinhuangdao-Changli.
Figure 4. E ext ( RH ) fitting at Qinhuangdao-Changli.
Sensors 18 03456 g004
Figure 5. E ext ( RH ) fitting at Zhangjiakou-Huaian.
Figure 5. E ext ( RH ) fitting at Zhangjiakou-Huaian.
Sensors 18 03456 g005
Figure 6. Scatterplots of both AOD with PM2.5 and σ dry with PM2.5 for different hours (09:00–16:00 local times) in Hebei (colorbar represents RH).
Figure 6. Scatterplots of both AOD with PM2.5 and σ dry with PM2.5 for different hours (09:00–16:00 local times) in Hebei (colorbar represents RH).
Sensors 18 03456 g006aSensors 18 03456 g006b
Figure 7. Scatterplots of satellite-retrieved and ground-measured PM2.5 from January to June 2017 in Hebei.
Figure 7. Scatterplots of satellite-retrieved and ground-measured PM2.5 from January to June 2017 in Hebei.
Sensors 18 03456 g007
Figure 8. Monthly PM2.5 of satellite-retrieved and ground-measured data in Hebei.
Figure 8. Monthly PM2.5 of satellite-retrieved and ground-measured data in Hebei.
Sensors 18 03456 g008
Figure 9. Hourly PM2.5 of satellite-retrieved and ground-measured PM2.5 data in Hebei.
Figure 9. Hourly PM2.5 of satellite-retrieved and ground-measured PM2.5 data in Hebei.
Sensors 18 03456 g009
Figure 10. Daily averaged PM2.5 of satellite-retrieved and ground-measured PM2.5 data at Baoding-Zhuozhou, Cangzhou-Potou, Tangshan-Qianxi, Handan-Wuan, Hengshui-Jinzhou, Langfang-Sanhe, Xingtai-Nanggong, Zhangjiakou-Xuanhuaqu, Shijiazhaung-Jingjing, Chengde-Xinglong, and Qinhuangdao-Changli.
Figure 10. Daily averaged PM2.5 of satellite-retrieved and ground-measured PM2.5 data at Baoding-Zhuozhou, Cangzhou-Potou, Tangshan-Qianxi, Handan-Wuan, Hengshui-Jinzhou, Langfang-Sanhe, Xingtai-Nanggong, Zhangjiakou-Xuanhuaqu, Shijiazhaung-Jingjing, Chengde-Xinglong, and Qinhuangdao-Changli.
Sensors 18 03456 g010
Figure 11. Hourly PM2.5 concentrations of satellite-retrieved and ground-measured from 09:00 to 16:00 on 10 January 2017, in Hebei.
Figure 11. Hourly PM2.5 concentrations of satellite-retrieved and ground-measured from 09:00 to 16:00 on 10 January 2017, in Hebei.
Sensors 18 03456 g011aSensors 18 03456 g011b
Table 1. Statistical hourly PM2.5 data from January to June 2017.
Table 1. Statistical hourly PM2.5 data from January to June 2017.
VariableValueXingtai-NanheQinhuangdao-ChangliZhangjiakou-Huaian
PM2.5 (μg/m3)mean86.9664.3229.34
median57.0051.5019.00
std81.9346.5328.88
VIS (km)mean22.1413.3823.15
median25.5611.5524.26
std12.608.6211.08
RH (%)mean57.2159.1944.54
median56.0066.0040.00
std24.1424.9224.52
Table 2. Hygroscopic growth ability of f ( 80 % ) at Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiankou-Huaian.
Table 2. Hygroscopic growth ability of f ( 80 % ) at Xingtai-Nanhe, Qinhuangdao-Changli, and Zhangjiankou-Huaian.
MonthXingtai-NanheQinhuangdao-ChangliZhangjiakou-Huaian
January1.131.611.78
February2.231.394.34
March1.011.812.13
April1.062.08 1.96
May1.182.392.23
June1.202.031.35
Half-year1.321.841.28

Share and Cite

MDPI and ACS Style

Zeng, Q.; Chen, L.; Zhu, H.; Wang, Z.; Wang, X.; Zhang, L.; Gu, T.; Zhu, G.; Zhang, Y. Satellite-Based Estimation of Hourly PM2.5 Concentrations Using a Vertical-Humidity Correction Method from Himawari-AOD in Hebei. Sensors 2018, 18, 3456. https://doi.org/10.3390/s18103456

AMA Style

Zeng Q, Chen L, Zhu H, Wang Z, Wang X, Zhang L, Gu T, Zhu G, Zhang Y. Satellite-Based Estimation of Hourly PM2.5 Concentrations Using a Vertical-Humidity Correction Method from Himawari-AOD in Hebei. Sensors. 2018; 18(10):3456. https://doi.org/10.3390/s18103456

Chicago/Turabian Style

Zeng, Qiaolin, Liangfu Chen, Hao Zhu, Zifeng Wang, Xinhui Wang, Liang Zhang, Tianyu Gu, Guiyan Zhu, and Yang Zhang. 2018. "Satellite-Based Estimation of Hourly PM2.5 Concentrations Using a Vertical-Humidity Correction Method from Himawari-AOD in Hebei" Sensors 18, no. 10: 3456. https://doi.org/10.3390/s18103456

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop