Search

Stringent emission controls during the Asia Pacific Economic Cooperation Summit (APEC; November 5–11, 2014) provide a valuable opportunity to examine the impact of such measures on the chemical properties of PM 2.5 and other air pollutants. Here, we measured the water-soluble inorganic ions (WSII) and carbonaceous species in PM 2.5 , NH 3 and NO 2 at multiple sites in Beijing between September and November 2014. Relative to the pre-APEC period (September and October 2014), significant reductions in the average concentrations of WSII (69% for NO 3 −, 68% for SO 4 2−, 78% for NH 4 +, and 29–71% for other species), elemental carbon (EC, 43%) and organic carbon (OC, 45%) in PM 2.5 were found during the APEC period. The contributions of secondary inorganic ions (SIA, including SO 4 2−, NO 3 −, and NH 4 +) to PM 2.5 were significantly lower during the APEC period (9–44%), indicating a combination of lower gaseous precursor emissions and a relative weak secondary aerosol formation. Ion-balance calculations indicated that the PM 2.5 sample in the pre-APEC period was alkaline but was acidic during the APEC period. Relatively lower mean concentrations of EC (1.5 μg m−3), OC (10.5 μg m−3), secondary organic carbon (SOC, 3.3 μg m−3), secondary organic aerosol (SOA, 5.9 μg m−3) and primary organic aerosol (POA, 10.0 μg m−3) appeared during the APEC period. The average concentrations of NH 3 and NO 2 at all road sites were significantly reduced by 48 and 60% during the APEC period, which is consistent with clear reductions in satellite NH 3 columns over Beijing city in the same period. This finding suggests that reducing traffic emissions could be a feasible method to control urban NH 3 pollution. During the APEC period, concentrations of PM 2. 5 , PM 10 , NO 2 , SO 2 and CO from the Beijing city monitoring network showed significant reductions at urban (20–60%) and rural (18–57%) sites, whereas O 3 concentrations increased significantly (by 93% and 53%, respectively). The control measures taken in the APEC period substantially decreased PM 2.5 pollution but can increase ground O 3 , which also merits attention. • Concentrations of PM 2.5 and components reduced significantly during the APEC period. • Major components in PM 2.5 and other pollutants were comparable with other cities. • Vehicle restrictions could lower atmospheric NH 3 concentration over Beijing. • Emission control measures significantly increased ground-level O 3 concentrations. [ABSTRACT FROM AUTHOR]

The Clean Air Action implemented by the Chinese government in 2013 has greatly improved air quality in the North China Plain (NCP). In this work, we report changes in the chemical components of atmospheric fine particulate matter (PM 2.5) at four NCP sampling sites from 2012/2013 to 2017 to investigate the impacts and drivers of the Clean Air Action on aerosol chemistry, especially for secondary inorganic aerosols (SIA). During the observation period, the concentrations of PM 2.5 and its chemical components (especially SIA, organic carbon (OC), and elemental carbon (EC)) and the frequency of polluted days (daily PM 2.5 concentration ≥ 75 μg m−3) in the NCP, declined significantly at all four sites. Asynchronized reduction in SIA components (large decreases in SO 4 2− with stable or even increased NO 3 − and NH 4 +) was observed in urban Beijing, revealing a shift of the primary form of SIA, which suggested the fractions of NO 3 − increased more rapidly than SO 4 2− during PM 2.5 pollution episodes, especially in 2016 and 2017. In addition, unexpected increases in the sulfur oxidation ratio (SOR) and the nitrogen oxidation ratio (NOR) were observed among sites and across years in the substantially decreased PM 2.5 levels. They were largely determined by secondary aerosol precursors (i.e. decreased SO 2 and NO 2), photochemical oxidants (e.g. increased O 3), temperature, and relative humidity via gas-phase and heterogeneous reactions. Our results not only highlight the effectiveness of the Action Plan for improving air quality in the NCP, but also suggest an increasing importance of SIA in determining PM 2.5 concentration and composition. [Display omitted] • PM 2.5 and its chemical components were reduced in North China Plain during 2012–2017. • Reduced air pollutant emissions contributed more to PM 2.5 decline than meteorology. • NO 3 − became increasingly important in the formation of secondary inorganic aerosols. • Both sulfur oxidation ratio and nitrogen oxidation ratio increased unexpectedly. [ABSTRACT FROM AUTHOR]

In order to cope with heavy haze pollution in Beijing, the Air Pollution Prevention and Control Action Plan was issued in 2013. In this study, we took January observations from 2014 to 2018 as a case study to assess wintertime air quality improvement in Beijing after five years of continuous emission control measures and to investigate the causes of haze formation. SO 2 and NO 2 concentrations in January 2018 decreased by 84% and 41% from January 2014, while NH 3 concentrations remained relatively stable during these years with an average of 7.28 μg m−3. The mean concentrations of PM 2.5 and water-soluble inorganic ions declined over the study period, while compared with 2014, decreased SO 4 2− ratio and increased NO 3 − contribution in PM 2.5 were observed, highlighting the importance of reactive nitrogen (Nr) pollution control. High concentrations of NH 3 , NO 2 , as well as NH 4 + and NO 3 − in PM 2.5 at roadside monitoring sites, indicated that vehicle sources played a vital role in local urban Nr emissions. Finally, we found most NH 3 existed in the gas phase in the Beijing atmosphere, even on polluted winter days, suggesting a considerable risk for additional secondary aerosol formation. Our findings demonstrate the effectiveness of the emissions control in alleviating Beijing's air pollution. Significant reductions of precursor emissions are needed to achieve the goals set by air quality standards in the future, especially for NH 3. It is especially crucial to jointly consider and control multiple pollution sources to effectively reduce the high levels of air pollution that remain in Beijing. • Significant improvements in Beijing air quality were observed during January 2014 to 2018. • The concentrations of SO 2 , NO 2 in air and SO 4 2−, NO 3 −, NH 4 + in PM 2.5 significantly decreased. • NH 3 concentrations remained stable during these 5 years. • Vehicle sources are vital contributors to NH 3 and NO 2 emissions. • The Beijing atmosphere is NH 3 -rich. [ABSTRACT FROM AUTHOR]