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Carbonyls have attracted continuous attention due to their critical roles in atmospheric chemistry and their potential hazards to the ecological environment and human health. In this study, atmospheric carbonyls were measured during several ground-level-ozone (O 3 ) pollution episodes at three urban sites (CRAES, IEP and BJUT) in Beijing in 2019 and 2020. Comparative analysis revealed that the carbonyl concentrations were 20.25 ± 6.91 ppb and 13.43 ± 5.13 ppb in 2019 and 2020 in Beijing, respectively, with a significant spatial trend from north to south, and carbonyl levels in urban Beijing were in an upper-intermediate range in China, and higher than those in other countries reported in the literature. A particularly noteworthy phenomenon is the consistency of carbonyl concentrations with variations in O 3 concentrations. On O 3 polluted days, the carbonyl concentrations were 1.3-1.5 times higher than those on non-O 3 polluted days. Secondary formation contributed more to formaldehyde (FA) and acetaldehyde (AA) on O 3 polluted days, while the anthropogenic emissions were more significant for acetone (AC) on non-O 3 polluted days. Vehicle exhaust and solvent utilization were the main primary contributors to carbonyls. Due to reduced anthropogenic emissions caused by the COVID-19 lockdown and the "Program for Controlling Volatile Organic Compounds in 2020" in China, the contributions of primary emissions to carbonyls decreased in 2020 in Beijing. Human cancer risks to exposed populations from FA and AA increased with elevated O 3 levels, and the risks still remained on non-O 3 polluted days. The residents around the BJUT site might experience relatively higher human cancer risks than those around the other two sites. The findings in this study confirmed that atmospheric carbonyl pollution and its potential human health hazards cannot be ignored in urban Beijing; therefore, more strict control strategies for atmospheric carbonyls are urgently needed to better protect human health in Beijing in the future., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Polycyclic aromatic hydrocarbons (PAHs) and their nitrated derivatives (NPAHs) attract continuous attention due to their distinct carcinogenicity and mutagenicity. To investigate the characteristics, sources, formation mechanism and health risk assessment of PAHs and NPAHs, PM 2.5 were collected at an urban site in Beijing from 2017 to 2018. The highest PAHs and NPAHs concentrations were 77.92 ± 54.62 ng/m 3 and 963.71 ± 695.06 pg/m 3 in the winter campaign, which were several times larger than those in other seasonal campaigns. Distinct diurnal variations of nocturnal levels higher than daytime levels were shown for PAHs and NPAHs. Source analysis indicated that besides vehicle exhaust, biomass burning and coal combustion were important sources of PAHs and NPAHs in the fall and winter campaigns. Secondary formation in atmosphere was another source of NPAHs especially in the spring and summer campaigns. NO 2 and RH could positively influence the heterogeneous formation of NPAHs when RH was less than 60%. Quantum calculation results confirmed the formation pathway of 2N-FLA from the OH/NO 3 -initiated oxidation of FLA. The results of health risk assessment showed the potential health risks for the residents, especially in the winter campaign. These results indicated that PAHs and NPAHs still deserve attention following with the decrease concentrations of particulate matter., (Copyright © 2022 Elsevier B.V. All rights reserved.)

Nitrated aromatic compounds (NACs) constitute a key segment of brown carbon (BrC), thereby contributing to the light-absorbing characteristics of aerosols in the atmosphere. However, until recently, there is a scarcity of research on their generation in the urban environment. The current study is based upon an extensive field study of NACs from fine particle samples obtained at an urban location in Beijing in the spring and summer of 2017, which was characterized by both high anthropogenic volatile organic compounds (VOCs) and high-NO x dominated conditions. The mean total concentration of the nine NACs was 8.58 ng m -3 in spring and 8.54 ng m -3 in summer. In the spring, the most abundant NACs were 4-nitrophenol (33.7%) and 4-nitrocatechol (19.3%), while in the summer, the most abundant NACs were 4-nitroguaiacol (34.9%) and 2, 4-dinitrophenol (23%). Atmospheric NACs were primarily produced from coal combustion (52%) and biomass burning (32%) in spring, and originated from the secondary formation (37%) and traffic (35%) in summer. NO 2 could promote the formation of NACs with a significant effect on their compositions, especially for nitrophenols and nitrocatechols. It can also affect the formation of nitrated aerosols and their existing form. Inorganic nitrates were increased to conversion in the daytime when NO 2 concentrations were higher than 30 ppb, but the corresponding oxidation products shifted to primarily organic ones at night. The transition was VOC-sensitive regimes for NAC formation, and nitration of toluene was a more important pathway during the campaign in Beijing., (Copyright © 2021 Elsevier Inc. All rights reserved.)

Volatile halogenated hydrocarbons (VHCs) have attracted wide attention in the atmospheric chemistry field since they not only affect the ecological environment but also damage human health. In order to better understand the characteristics, sources and health risks of VHCs in typical urban areas in Beijing, and also verify the achievement in implementing the Montreal Protocol (MP) in Beijing, observational studies on 22 atmospheric VHCs species were conducted during six air pollution episodes from December 2016 to May 2017. The range in daily mixing ratios of the 6 MP-regulated VHCs was 1000-1168 pptv, and the 16 MP-unregulated VHCs was 452-2961 pptv. The 16 MP-unregulated VHCs accounted for a relatively high concentration proportion among the 22 VHCs with a mean of 70.25%. Compared with other regions, the mixing ratios of MP-regulated VHCs were in the middle concentrations. The mixing ratios of the MP-regulated VHCs remained the same concentrations during the air pollution episodes, while the concentrations of MP-unregulated VHCs were generally higher on polluted days than on clean days and increased with the aggravation of the pollution episodes. The mixing ratios of dichlorodifluoromethane and trichlorofluoromethane were higher than Northern Hemisphere (NH) background values, while the mixing ratios of the other 4 MP-regulated VHCs were moderate and similar to the NH background values. All the 9 VHCs with carcinogenic risk might pose potential carcinogenic risks to the exposed populations in the six pollution episodes, while none of the 12 VHCs might pose appreciable non-carcinogenic risks to the exposed populations. Considering the higher concentration levels and higher risk values of 1,2-dichloropropane, 1,2-dichloroethane, carbon tetrachloride and trichloromethane, Beijing needs to further strengthen the control of these VHCs. The analysis of air mass transportation and PMF model showed that regional transportation and leakage of CFCs banks were important sources of VHCs in Beijing, and the contribution of industrial process and solvent usage should not be neglected. The results revealed the effective implementation of the MP in Beijing and its surrounding areas, while further measures are suggested to control the emissions of important VHCs especially from regional transportation and leakage of CFCs banks to reduce the possible health risks to the exposed population., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2021 Elsevier B.V. All rights reserved.)