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      The contribution of new particle formation and subsequent growth to haze formation

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      Environmental Science
      RSC

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          Abstract

          We investigated the contribution of atmospheric new particle formation (NPF) and subsequent growth of the newly formed particles, characterized by high concentrations of fine particulate matter (PM 2.5). In addition to having adverse effects on visibility and human health, these haze particles may act as cloud condensation nuclei, having potentially large influences on clouds and precipitation. Using atmospheric observations performed in 2019 in Beijing, a polluted megacity in China, we showed that the variability of growth rates (GR) of particles originating from NPF depend only weakly on low-volatile vapor – highly oxidated organic molecules (HOMs) and sulphuric acid – concentrations and have no apparent connection with the strength of NPF or the level of background pollution. We then constrained aerosol dynamic model simulations with these observations. We showed that under conditions typical for the Beijing atmosphere, NPF is capable of contributing with more than 100 μg m −3 to the PM 2.5 mass concentration and simultaneously >10 3 cm −3 to the haze particle (diameter > 100 nm) number concentration. Our simulations reveal that the PM 2.5 mass concentration originating from NPF, strength of NPF, particle growth rate and pre-existing background particle population are all connected with each other. Concerning the PM pollution control, our results indicate that reducing primary particle emissions might not result in an effective enough decrease in total PM 2.5 mass concentrations until a reduction in emissions of precursor compounds for NPF and subsequent particle growth is imposed.

          Abstract

          We investigated the contribution of atmospheric new particle formation (NPF) and subsequent growth of the newly formed particles, characterized by high concentrations of fine particulate matter (PM 2.5).

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          Most cited references52

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          High secondary aerosol contribution to particulate pollution during haze events in China.

          Rapid industrialization and urbanization in developing countries has led to an increase in air pollution, along a similar trajectory to that previously experienced by the developed nations. In China, particulate pollution is a serious environmental problem that is influencing air quality, regional and global climates, and human health. In response to the extremely severe and persistent haze pollution experienced by about 800 million people during the first quarter of 2013 (refs 4, 5), the Chinese State Council announced its aim to reduce concentrations of PM2.5 (particulate matter with an aerodynamic diameter less than 2.5 micrometres) by up to 25 per cent relative to 2012 levels by 2017 (ref. 6). Such efforts however require elucidation of the factors governing the abundance and composition of PM2.5, which remain poorly constrained in China. Here we combine a comprehensive set of novel and state-of-the-art offline analytical approaches and statistical techniques to investigate the chemical nature and sources of particulate matter at urban locations in Beijing, Shanghai, Guangzhou and Xi'an during January 2013. We find that the severe haze pollution event was driven to a large extent by secondary aerosol formation, which contributed 30-77 per cent and 44-71 per cent (average for all four cities) of PM2.5 and of organic aerosol, respectively. On average, the contribution of secondary organic aerosol (SOA) and secondary inorganic aerosol (SIA) are found to be of similar importance (SOA/SIA ratios range from 0.6 to 1.4). Our results suggest that, in addition to mitigating primary particulate emissions, reducing the emissions of secondary aerosol precursors from, for example, fossil fuel combustion and biomass burning is likely to be important for controlling China's PM2.5 levels and for reducing the environmental, economic and health impacts resulting from particulate pollution.
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            Elucidating severe urban haze formation in China.

            As the world's second largest economy, China has experienced severe haze pollution, with fine particulate matter (PM) recently reaching unprecedentedly high levels across many cities, and an understanding of the PM formation mechanism is critical in the development of efficient mediation policies to minimize its regional to global impacts. We demonstrate a periodic cycle of PM episodes in Beijing that is governed by meteorological conditions and characterized by two distinct aerosol formation processes of nucleation and growth, but with a small contribution from primary emissions and regional transport of particles. Nucleation consistently precedes a polluted period, producing a high number concentration of nano-sized particles under clean conditions. Accumulation of the particle mass concentration exceeding several hundred micrograms per cubic meter is accompanied by a continuous size growth from the nucleation-mode particles over multiple days to yield numerous larger particles, distinctive from the aerosol formation typically observed in other regions worldwide. The particle compositions in Beijing, on the other hand, exhibit a similarity to those commonly measured in many global areas, consistent with the chemical constituents dominated by secondary aerosol formation. Our results highlight that regulatory controls of gaseous emissions for volatile organic compounds and nitrogen oxides from local transportation and sulfur dioxide from regional industrial sources represent the key steps to reduce the urban PM level in China.
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              Severe haze in northern China: A synergy of anthropogenic emissions and atmospheric processes

              Significance Severe haze events with large temporal/spatial coverages have occurred frequently in wintertime northern China. These extremes result from a complex interplay between emissions and atmospheric processes and provide a unique scientific platform to gain insights into many aspects of the relevant atmospheric chemistry and physics. Here we synthesize recent progress in understanding severe haze formation in northern China. In particular, we highlight that improved understanding of the emission sources, physical/chemical processes during haze evolution, and interactions with meteorological/climatic changes are necessary to unravel the causes, mechanisms, and trends for haze pollution. This viewpoint established on the basis of sound science is critical for improving haze prediction/forecast, formulating effective regulatory policies by decision makers, and raising public awareness of environmental protection.
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                Author and article information

                Journal
                Environ Sci Atmos
                Environ Sci Atmos
                EA
                ESANC9
                Environmental Science
                RSC
                2634-3606
                22 March 2022
                19 May 2022
                22 March 2022
                : 2
                : 3
                : 352-361
                Affiliations
                [a] Aerosol and Haze Laboratory, Beijing Advanced Innovation Center for Soft Matter Sciences and Engineering, Beijing University of Chemical Technology (BUCT) Beijing China
                [b] Institute for Atmospheric and Earth System Research (INAR)/Physics, Faculty of Science, University of Helsinki Finland markku.kulmala@ 123456helsinki.fi
                [c] Joint International Research Laboratory of Atmospheric and Earth System Sciences, School of Atmospheric Sciences, Nanjing University Nanjing China
                [d] Laboratory of Atmospheric Chemistry, Paul Scherrer Institute Villigen Switzerland
                [e] State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University Beijing China
                Author information
                https://orcid.org/0000-0003-3464-7825
                https://orcid.org/0000-0003-1105-9043
                https://orcid.org/0000-0002-1881-9044
                https://orcid.org/0000-0001-6172-190X
                Article
                d1ea00096a
                10.1039/d1ea00096a
                9119031
                35694136
                52cf8578-1fe5-4b1e-ad68-b9bf2d10fbef
                This journal is © The Royal Society of Chemistry
                History
                : 22 November 2021
                : 21 March 2022
                Page count
                Pages: 10
                Funding
                Funded by: Academy of Finland, doi 10.13039/501100002341;
                Award ID: 337549
                Award ID: 302958
                Award ID: 1325656
                Award ID: 316114
                Award ID: 325647
                Funded by: H2020 European Research Council, doi 10.13039/100010663;
                Award ID: 742206
                Funded by: Jane ja Aatos Erkon Säätiö, doi 10.13039/501100004012;
                Award ID: Unassigned
                Funded by: Horizon 2020 Framework Programme, doi 10.13039/100010661;
                Award ID: 895875
                Categories
                Chemistry
                Custom metadata
                Paginated Article

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