Search

The study and control of air pollution involves measuring the structure of the atmospheric boundary layer (ABL) to understand the mechanisms of the interactions occurring between the atmospheric boundary layer and air pollution. Beijing, the capital of China, experienced heavy haze pollution in December 2016, and the city issued its first red-alert air pollution warning of the year (the highest PM 2.5 concentrations were later found to exceed 450 µgm-3). In this paper, the vertical profiles of wind, temperature, humidity and the extinction coefficient (reflecting aerosol concentrations), as well as ABL heights and turbulence quantities under heavy haze pollution conditions, are analyzed, with data collected from lidar, wind profile radar (WPR), radiosondes, a 325 m meteorological tower (equipped with a 7-layer ultrasonic anemometer and 15-layer low-frequency wind, temperature, and humidity sensors) and ground observations. The ABL heights obtained by three different methods based on lidar extinction coefficient data (Hc) are compared with the heights calculated from radiosonde temperature data (Hθ), and their correlation coefficient can reach 72 %. Our results show that Hθ measured on heavy haze pollution days was generally lower than that measured on clean days without pollution, but Hc increased from clean to heavy pollution days. The time changes in friction velocity (u*) and turbulent kinetic energy (TKE) were clearly inversely correlated with PM 2.5 concentration. Momentum and heat fluxes varied very little with altitude. The nocturnal sensible heat fluxes close to the Earth surface always stay positive. In the daytime of the haze pollution period, sensible heat fluxes were greatly reduced within 300 m of the ground. These findings will deepen our understanding of the boundary layer structure under heavy pollution conditions and improve the boundary layer parameterization in numerical models. [ABSTRACT FROM AUTHOR]

The effectiveness of national policies for air pollution control has been demonstrated, but the relative effectiveness of short-term emission reduction measures in comparison with national policies has not. Here we show that short-term abatement measures during important international events substantially reduced PM2.5 concentrations, but air quality rebounded to pre-event levels after the measures ceased. Long-term adherence to strict emission reduction policies led to successful decreases of 54% in PM2.5 concentrations in Beijing, and 23% in atmospheric nitrogen deposition in China from 2012 to 2020. Incentivized by "blue skies" type campaigns, economic development and reactive nitrogen pollution are quickly decoupled, showing that a combination of inspiring but aggressive short-term measures and effective but durable long-term policies delivers sustainable air quality improvement. However, increased ammonia concentrations, transboundary pollutant flows, and the complexity to achieving reduction targets under climate change scenarios, underscore the need for the synergistic control of multiple pollutants and inter-regional action. In response to the rebound of air pollution during large events in China, the authors propose that a combination of ambitious short-term measures and enduring long-term pollution control policies is a sustainable solution for improving air quality. [ABSTRACT FROM AUTHOR]

As major chemical components of airborne fine particulate matter (PM 2.5), organic carbon (OC) and elemental carbon (EC) have vital impacts on air quality, climate change, and human health. Because OC and EC are closely associated with fuel combustion, it is helpful for the scientific community and policymakers assessing the efficacy of air pollution control measures to study the impact of control measures and regional transport on OC and EC levels. In this study, hourly mass concentrations of OC and EC associated with PM 2.5 were semi-continuously measured from March 2013 to February 2018. The results showed that annual mean OC and EC concentrations declined from 14.0 to 7.7 µgm-3 and from 4.0 to 2.6 µgm-3 , respectively, from March 2013 to February 2018. In combination with the data of OC and EC in previous studies, an obvious decreasing trend in OC and EC concentrations was found, which was caused by clean energy policies and effective air pollution control measures. However, no obvious change in the ratios of OC and EC to the PM 2.5 mass (on average, 0.164 and 0.049, respectively) was recorded, suggesting that inorganic ions still contributed a lot to PM 2.5. Based on the seasonal variations in OC and EC, it appeared that higher OC and EC concentrations were still observed in the winter months, with the exception of winter of 2017–2018. Traffic policies executed in Beijing resulted in nighttime peaks of OC and EC, caused by heavy-duty vehicles and heavy-duty diesel vehicles being permitted to operate from 00:00 to 06:00 (China standard time, UTC + 8, for all times throughout the paper). In addition, the fact that there was no traffic restriction in weekends led to higher concentrations on weekends compared to weekdays. Significant correlations between OC and EC were observed throughout the study period, suggesting that OC and EC originated from common emission sources, such as exhaust of vehicles and fuel combustion. OC and EC levels increased with enhanced SO2 , CO, and NOx concentrations while the O3 and OC levels were enhanced simultaneously when O3 concentrations were higher than 50 µgm-3. Non-parametric wind regression analysis was performed to examine the sources of OC and EC in the Beijing area. It was found that there were distinct hot spots in the northeast wind sector at wind speeds of approximately 0–6 km h -1 , as well as diffuse signals in the southwestern wind sectors. Source areas further away from Beijing were assessed by potential source contribution function (PSCF) analysis. A high-potential source area was precisely pinpointed, which was located in the northwestern and southern areas of Beijing in 2017 instead of solely in the southern areas of Beijing in 2013. This work shows that improvement of the air quality in Beijing benefits from strict control measures; however, joint prevention and control of regional air pollution in the regions is needed for further improving the air quality. The results provide a reference for controlling air pollution caused by rapid economic development in developing countries. [ABSTRACT FROM AUTHOR]

From 1990 to 2017, the number of vehicles in China increased sharply from 5 million to 310 million, and vehicle emissions became one of the major sources of air pollution. Among the main sources of PM 2.5 in Beijing, the contributions from vehicle sources increased from 5.6% (2000) to 31.1% (2012) to 45% (2017). In 2010, the CO, hydrocarbon (HC), NO x , and particulate matter (PM) emissions of yellow-label vehicles (YLVs) accounted for 46.1%, 47.9%, 63.1% and 86.1% of the total emissions from on-road vehicles. In recent years, China has been implementing a YLV scrappage subsidy policy to control air pollution, and this policy has cost several hundred billion yuan nationwide. However, China has not evaluated the costs and benefits of the policy. Many people question whether the YLV scrappage subsidy policy is worthwhile, but all the stakeholders involved complicate the process of accurately evaluating the true value of the policy. In this study, we evaluated and compared the costs and benefits of the policy in the Beijing-Tianjin-Hebei (BTH) region based on 1.362 million YLVs from 2008 to 2015. Because of the implementation of the policy, the PM 2.5 , PM 10 , NO x , CO and HC emissions in the BTH region decreased by 16.46, 18.12, 174.44, 669.11, and 91.64 kt, respectively, in 2008–2015. The results show that the policy played an important role in reducing pollutant emissions and improving environmental quality in the BTH region. The costs, benefits, and net benefits of the policy were 13.69, 34.03, and 20.34 billion yuan , respectively. The cost-benefit ratio in the BTH region was 1:2.49; at the city scale, Beijing ranked first (1:7.27), and the cost-benefit ratios of Tianjin and Hebei Province were 1:2.06 and 1:1.14, respectively. Of the 13 cities in the BTH region, Beijing had the highest net benefits, amounting to 16.43 billion yuan , while Handan City has the lowest net benefits, amounting to −0.58 billion yuan. The results may provide scientific support for the promotion of older vehicle and diesel vehicle scrappage subsidy policies, the development of cost-benefit analysis (CBA), and effective environmental decision-making in China. • Based on net number of scrappage YLVs, net benefits of the policy are calculated. • This paper estimates costs and benefits of the policy based on 1.27 million YLVs. • The costs, benefits, and net benefits are 13.69, 34.03, and 20.34 billion yuan. • The results help China promote vehicle scrappage subsidy policy on a large scale. • The results promote the development of the cost-benefit analysis in China. [ABSTRACT FROM AUTHOR]

Currently, air pollution is primarily characterized by PM 2.5 and O 3. Therefore, the co-control of PM 2.5 and O 3 has become an important task of atmosphere pollution prevention and control in China. However, few studies have been conducted on the emissions from vapor recovery and processes, which is an important source of VOCs. This paper analyzed the VOC emissions of three vapor process technologies in service stations and first proposed key pollutants for priority control based on the coordinated reactivity of O 3 and SOA. The concentration of VOCs emitted from the vapor processor was 3.14–9.95 g m−3, compared to 631.2–717.8 g m−3 for uncontrolled vapor. Alkanes, alkenes, and halocarbons accounted for a high proportion of the vapor both before and after control. Among the emissions, i -pentane, n -butane, and i -butane were the most abundant species. Then, the species of OFP and SOAP were calculated through the maximum incremental reactivity (MIR) and fractional aerosol coefficient (FAC). The average source reactivity (SR) value of the VOC emissions from three service stations was 1.9 g g−1, while the OFP ranged from 8.2 to 13.9 g m−3 and SOAP ranged from 0.18 to 0.36 g m−3. By considering the coordinated chemical reactivity of O 3 and SOA, a comprehensive control index (CCI) was proposed for the control of key pollutant species that have multiplier effects on environment. For adsorption, trans -2-butene and p -xylene were the key co-control pollutants, while toluene and trans -2-butene were the most important for membrane and condensation + membrane control. A 50% emission reduction of the top two key species that emission account for 4.3% averagely will reduce O 3 by 18.4% and SOA by 17.9%. [Display omitted] • The organized emissions of VOCs from three vapor processors were studied in service stations. • The species composition of VOCs before and after control were analyzed. • The OFP and SOAP were calculated to evaluate the secondary pollution. • The co-control of key pollutants based on SOA and O 3 has great environmental benefits. [ABSTRACT FROM AUTHOR]

China has made great efforts to monitor and control air pollution in the past decade. Comprehensive characterization and understanding of pollutants in three-dimensions are, however, still lacking. Here, we used data from an observation network consisting of 13 aerosol lidars and more than 1000 ground observation stations combined with a data assimilation technique to conduct a comprehensive analysis of extreme heavy aerosol pollution (HAP) over the North China Plain (NCP) from November–December 2017. During the studied period, the maximum hourly mass concentration of surface PM 2.5 reached ∼390 µ g m -3. After assimilation, the correlation between model results and the independent observation sub-dataset was ∼50 % higher than that without the assimilation, and the root mean square error was reduced by ∼40 %. From pollution development to dissipation, we divided the HAP in the NCP (especially in Beijing) into four phases: an early phase (EP), a transport phase (TP), an accumulation phase (AP), and a removal phase (RP). We then analyzed the evolutionary characteristics of PM 2.5 concentration during different phases on the surface and in 3-D space. We found that the particles were mainly transported from south to north at a height of 1–2 km (during EP and RP) and near the surface (during TP and AP). The amounts of PM 2.5 advected into Beijing with the maximum transport flux intensity (TFI) were through the pathways in the relative order of the southwest > southeast > east pathways. The dissipation of PM 2.5 in the RP stage (with negative TFI) was mainly from north to south with an average transport height of ∼1 km above the surface. Our results quantified the multi-dimensional distribution and evolution of PM 2.5 concentration over the NCP, which may help policymakers develop efficient air pollution control strategies. [ABSTRACT FROM AUTHOR]

The implementation of the Air Pollution Prevention and Control Action Plan in China since 2013 has profoundly altered the ambient pollutants in the Beijing–Tianjin–Hebei (BTH) region. Here we show observations of substantially increased O3 concentrations (about 30 %) and a remarkable increase in the ratio of organic carbon (OC) to elemental carbon (EC) in BTH during the autumn from 2013 to 2015, revealing an enhancement in atmospheric oxidizing capacity (AOC) and secondary organic aerosol (SOA) formation. To explore the impacts of increasing AOC on the SOA formation, a severe air pollution episode from 3 to 8 October 2015 with high O3 and PM 2.5 concentrations is simulated using the WRF-Chem model. The model performs reasonably well in simulating the spatial distributions of PM 2.5 and O3 concentrations over BTH and the temporal variations in PM 2.5 , O3 , NO2 , OC, and EC concentrations in Beijing compared to measurements. Sensitivity studies show that the change in AOC substantially influences the SOA formation in BTH. A sensitivity case characterized by a 31 % O3 decrease (or 36 % OH decrease) reduces the SOA level by about 30 % and the SOA fraction in total organic aerosol by 17 % (from 0.52 to 0.43, dimensionless). Spatially, the SOA decrease caused by reduced AOC is ubiquitous in BTH, but the spatial relationship between SOA concentrations and the AOC is dependent on the SOA precursor distribution. Studies on SOA formation pathways further show that when the AOC is reduced, the SOA from oxidation and partitioning of semivolatile primary organic aerosol (POA) and co-emitted intermediate volatile organic compounds (IVOCs) decreases remarkably, followed by those from anthropogenic and biogenic volatile organic compounds (VOCs). Meanwhile, the SOA decrease in the irreversible uptake of glyoxal and methylglyoxal on the aerosol surfaces is negligible. [ABSTRACT FROM AUTHOR]