Atmospheric volatile organic compounds (VOCs) measurement was carried out using gas chromatography-flame ionization detector (GC-FID) technique (Airmo VOCs online analyzer) in a typical urban area in Beijing from April 2014 to January 2015. Ambient levels, variation characteristics and influential factors contributing to the formation of near-ground-ozone and secondary organic aerosols as well as health risk assessment of VOCs were analyzed. Based on these analyses, the important VOC species that should be given more attention for pollution control were identified and the source apportionment of VOCs was made. Suggestions for VOCs pollution control countermeasures were put forward. The annual average concentration of 84 VOCs was 119 μg·m⁻³ and the hourly mean concentration was 9.11–567 μg·m⁻³. Ambient level of VOCs in Beijing has been alleviated in recent years, but is still severe compared to some other cities. VOCs with the largest proportion were alkanes in spring and halogenated hydrocarbons in summer, autumn and winter. The variation of 84 VOCs concentrations was consistent with that of the ambient air quality index, indicating that VOCs had a strong influence on ambient air quality. Influenced by the concentration and activity of VOCs, the largest contribution to ozone formation potential and secondary organic aerosol formation potential came from alkenes and aromatic hydrocarbons, respectively. Five VOCs species such as benzene pose carcinogenic risk to exposed populations. Contrary to some previous studies, benzene was found to have potential cancer risk in some urban areas in China. The main sources of VOCs in the study area were vehicle exhaust, solvent usage, and industrial processes. In order to improve air quality in Beijing and reduce the infection rate of air pollutant related diseases, it is necessary to strengthen the control the emission of VOCs from those three sources.

Atmospheric carbonyls (aldehyde and ketone compounds) can be precursors for ozone and PM_2.5, and they play an essential role in atmospheric chemistry. Linfen is a basin between mountains on the east and west, and there are many coking plants on the north and south sides of its urban area. The special topography and unfortunate industrial layout have frequently contributed to serious air pollution in Linfen. In order to investigate the pollution characteristics of atmospheric carbonyls in winter in urban Linfen, the carbonyl compounds were collected from the Municipal Committee site (MC) and the Yaowangtai site (YWT) from 16 to 25 January 2019, and their concentrations were analyzed by a high performance liquid chromatography-ultraviolet detector (HPLC-UV). The results show that formaldehyde, acetaldehyde, and acetone were the most abundant compounds, accounting for more than 70% of the total mass concentration of carbonyls in urban Linfen. Levels of these three carbonyls increased during the morning and evening traffic rush hours. The mass concentration of formaldehyde at both sites reached peak values at around noon (10:00–14:00). In addition, the mass concentrations of formaldehyde, acetaldehyde, and acetone were positively correlated with CO mass concentrations, whereas only formaldehyde and acetaldehyde were positively correlated with temperature. Therefore, atmospheric formaldehyde in urban Linfen’s winter mainly came from vehicle exhaust emissions and the secondary generation of photochemical reactions. Most of the acetaldehyde came from vehicle exhaust emissions, and photochemical reactions also partially contributed to it. For acetone, vehicle exhaust emissions were the main source. In addition, coking industry emissions from Northern Linfen′s Hongtong County may also have contributed to the atmospheric carbonyls in the urban area of Linfen. For the first time, this study found that formaldehyde showed different behavior to acetaldehyde and acetone; that is, the nighttime decrease in formaldehyde mass concentration was greater than that of acetaldehyde and acetone.

To better evaluate the variations in concentration characteristics and source contributions of atmospheric volatile organic compounds (VOCs) during continuous haze days and non-haze days, hourly observations of atmospheric VOCs were conducted using a continuous on-line GC-FID (Airmo VOC GC-866) monitoring system during 1–15 March 2019, in urban areas of Beijing, China. The results showed that the total VOC concentrations during haze days and non-haze days were 59.13 ± 31.08 μg/m³ and 16.91 ± 7.19 μg/m³, respectively. However, the average O₃ concentrations during the two haze days were lower than those of non-haze days due to the extremely low concentrations at night instead of the reported lower photochemical reaction in daytime. The ratio of OH radical concentration during haze and non-haze days indicating that the rate of photochemical reaction during haze days was higher than those of non-haze days from 13:00–19:00. The stable air conditions and the local diesel emission at night were the main reasons for the decreased O₃ concentrations during haze days. Six major sources were identified by positive matrix factorization (PMF), namely, diesel exhaust, combustion, gasoline evaporation, solvent usage, gasoline exhaust, and the petrochemical industry, contributing 9.93%, 25.29%, 3.90%, 16.88%, 35.59% and 8.41%, respectively, during the whole observation period. The contributions of diesel exhaust and the petrochemical industry emissions decreased from 26.14% and 6.43% during non-haze days to 13.70% and 2.57%, respectively, during haze days. These reductions were mainly ascribed to the emergency measures that the government implemented during haze days. In contrast, the contributions of gasoline exhaust increased from 34.92% during non-haze days to 48.77% during haze days. The ratio of specific VOC species and PMF both showed that the contributions of gasoline exhaust emission increased during haze days. The backward trajectories, potential source contribution function (PSCF) and concentration weighted trajectory (CWT) showed that the air mass of VOCs during haze days was mainly affected by the short-distance transportation from the southwestern of Hebei province. However, the air mass of VOCs during non-haze days was mainly affected by the long-distance transportation from the northwest.

Twenty-three atmospheric volatile halogenated hydrocarbons (VHHs) were detected in a typical urban area of Beijing, China from 24 August to 4 September, 2012. The mean and range in daily mass concentrations of the 23 VHHs were 30.53 and 13.45–76.33 µg/m³, respectively. Seven of those VHHs were controlled ozone-depleting substances in China, with a mean of 12.95 µg/m³, accounting for 42.43% of the total. Compared with other national and international cities, the concentrations of the selected 11 VHHs in this study were relatively higher. Dichloroethane had the highest mass concentration, followed by difluorochloromethane. Maxima of total VHHs occurred within the period 8:30–9:00 a.m., while minima occurred during 1:30–2:00 p.m. Source apportionment suggested that the main sources of VHHs in the study area were solvents usage and industrial processes, leakage of chlorofluorocarbons banks, refrigerants, and fumigant usage. Among the selected 7 VHHs, trichloromethane, tetrachloromethane, 1,2-dichloroethane, and 1,4-dichlorobenzene posed potential carcinogenic risks to exposed populations, while none of the selected 11 VHHs posed appreciable non-carcinogenic risks to exposed populations. The carcinogenic risks from atmospheric VHHs in Beijing are higher than in other Chinese cities, indicating that it is necessary to implement immediate control measures for atmospheric VHHs in Beijing.

Solar radiation is the fundamental energy source of climate change, which has a significant impact on the generations of secondary fine particulate matter (PM_2.5) and ozone (O₃) in the atmosphere. Additionally, surface solar radiation is also affected by the concentration of PM_2.5, which in turn affects the generation of O₃. To clarify the relationships among the O₃, PM_2.5 and the total radiation intensity, this study analyzes their temporal and spatial variation trends from 2017 to 2019. Meanwhile, as a common precursor of O₃ and PM_2.5, concentration variations in nitrogen dioxide (NO₂) are discussed as well in this study. The results showed the following: (1) There are significant positive correlations between the O₃-8 h concentrations and the total radiation intensities in critical regions, especially in the “2 + 26” cities, Fen-Wei Plain and Yangtze River Delta. (2) The decrease in PM_2.5 concentrations is in good agreement with the trend of NO₂ concentrations, while the response of O₃ concentration to the NO₂ concentration variation differs in different regions, except in the Pearl River Delta. (3) In addition to the meteorological factors, changes in the concentrations and ratios of precursors such as NO₂ and volatile organic compounds (VOCs) likely contribute to the observed fluctuations in O₃ concentrations in recent years.