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Aunan K.,CICERO Center for International Climate and Environmental Research | Aunan K.,University of Oslo | Wang S.,Tsinghua University | Wang S.,State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex
Science of the Total Environment | Year: 2014

Exposure to fine particles ≤2.5μm in aerodynamic diameter (PM2.5) from incomplete combustion of solid fuels in household stoves, denoted household air pollution (HAP), is a major contributor to ill health in China and globally. Chinese households are, however, undergoing a massive transition to cleaner household fuels. The objective of the present study is to establish the importance of internal migration when it comes to the changing household fuel use pattern and the associated exposure to PM2.5 for the period 2000 to 2010. We also estimate health benefits of the fuel transition in terms of avoided premature deaths. Using China Census data on population, migration, and household fuel use for 2000 and 2010 we identify the size, place of residence, and main cooking fuel of sub-populations in 2000 and 2010, respectively. We combine these data with estimated exposure levels for the sub-populations and estimate changes in population exposure over the decade. We find that the population weighted exposure (PWE) for the Chinese population as a whole was reduced by 52 (36-70) μg/m3 PM2.5 over the decade, and that about 60% of the reduction can be linked to internal migration. During the same period the migrant population, in total 261million people, was subject to a reduced population weighted exposure (δPWE) of 123 (87-165) μg/m3 PM2.5. The corresponding figure for non-migrants is 34 (23-47) μg/m3. The largest δPWE was estimated for rural-to-urban migrants (138million people), 214 (154-283) μg/m3. The estimated annual health benefit associated with the reduced exposure in the total population is 31 (26-37) billion USD, corresponding to 0.4% of the Chinese GDP. © 2014 Elsevier B.V. Source


Wang L.T.,Hebei University of Engineering | Wang L.T.,State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex | Wang L.T.,North Carolina State University | Wei Z.,Hebei University of Engineering | And 11 more authors.
Atmospheric Chemistry and Physics | Year: 2014

Extremely severe and persistent haze occurred in January 2013 over eastern and northern China. The record-breaking high concentrations of fine particulate matter (PM2.5) of more than 700 μgm-3 on hourly average and the persistence of the episodes have raised widespread, considerable public concerns. During that period, 7 of the top 10 polluted cities in China were within the Hebei Province. The three cities in southern Hebei (Shijiazhuang, Xingtai, and Handan) have been listed as the top three polluted cities according to the statistics for the first half of the year 2013. In this study, the Mesoscale Modeling System Generation 5 (MM5) and the Models-3/Community Multiscale Air Quality (CMAQ) modeling system are applied to simulate the 2013 severe winter regional hazes in East Asia and northern China at horizontal grid resolutions of 36 and 12 km, respectively, using the Multi-resolution Emission Inventory for China (MEIC). The source contributions of major source regions and sectors to PM2.5 concentrations in the three most polluted cities in southern Hebei are quantified by aiming at the understanding of the sources of the severe haze pollution in this region, and the results are compared with December 2007, the haziest month in the period 2001-2010. Model evaluation against meteorological and air quality observations indicates an overall acceptable performance and the model tends to underpredict PM2.5 and coarse particulate matter (PM10) concentrations during the extremely polluted episodes. The MEIC inventory is proven to be a good estimation in terms of total emissions of cities but uncertainties exist in the spatial allocations of emissions into fine grid resolutions within cities. The source apportionment shows that emissions from northern Hebei and the Beijing-Tianjin city cluster are two major regional contributors to the pollution in January 2013 in Shijiazhuang, compared with those from Shanxi and northern Hebei for December 2007. For Xingtai and Handan, the emissions from northern Hebei and Henan are important. The industrial and domestic sources are the most significant local contributors, and the domestic and agricultural emissions from Shandong and Henan are non-negligible regional sources, especially for Xingtai and Handan. Even in the top two haziest months (i.e., January 2013 and December 2007), a large fraction of PM2.5 in the three cities may originate from quite different regional sources. These results indicate the importance of establishing a regional joint framework of policymaking and action system to effectively mitigate air pollution in this area, not only over the Beijing-Tianjin-Hebei area, but also surrounding provinces such as Henan, Shandong, and Shanxi. © 2014 Author(s). Source


Zheng B.,Tsinghua University | Zhang Q.,Tsinghua University | Zhang Q.,Collaborative Innovation Center for Regional Environmental Quality | Zhang Y.,Tsinghua University | And 10 more authors.
Atmospheric Chemistry and Physics | Year: 2015

Severe regional haze pollution events occurred in eastern and central China in January 2013, which had adverse effects on the environment and public health. Extremely high levels of particulate matter with aerodynamic diameter of 2.5 μm or less (PM2.5) with dominant components of sulfate and nitrate are responsible for the haze pollution. Although heterogeneous chemistry is thought to play an important role in the production of sulfate and nitrate during haze episodes, few studies have comprehensively evaluated the effect of heterogeneous chemistry on haze formation in China by using the 3-D models due to of a lack of treatments for heterogeneous reactions in most climate and chemical transport models. In this work, the WRF-CMAQ model with newly added heterogeneous reactions is applied to East Asia to evaluate the impacts of heterogeneous chemistry and the meteorological anomaly during January 2013 on regional haze formation. As the parameterization of heterogeneous reactions on different types of particles is not well established yet, we arbitrarily selected the uptake coefficients from reactions on dust particles and then conducted several sensitivity runs to find the value that can best match observations. The revised CMAQ with heterogeneous chemistry not only captures the magnitude and temporal variation of sulfate and nitrate, but also reproduces the enhancement of relative contribution of sulfate and nitrate to PM2.5 mass from clean days to polluted haze days. These results indicate the significant role of heterogeneous chemistry in regional haze formation and improve the understanding of the haze formation mechanisms during the January 2013 episode. © Author(s) 2015. Source


Bai B.,Tsinghua University | Li J.,Tsinghua University | Li J.,State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex
ACS Catalysis | Year: 2014

Three-dimensional (3D) ordered mesoporous Ag/Co3O4 and K-Ag/Co3O4 catalysts were successfully prepared on the basis of 3D-Co3O4. All catalysts possess 3D mesoporous structures, which are not affected due to Ag and K addition. Ag nanoparticles, uniformly dispersed and supported on the polycrystalline wall of K-Ag/Co 3O4, provide sufficient active sites for HCHO oxidation reaction. 1.7% K-Ag/Co3O4 has turnover frequencies (TOFs) of 0.22 s-1 at 60 °C and 2.62 s-1 at 100 °C, and its HCHO conversion at room temperature is 55% (HCHO 100 ppm and GHSV 30000 h-1). The addition of K+ ions obviously promotes the catalytic performance for HCHO oxidation due to surface OH- species provided by K+ ions and more abundant Ag(111) active faces, Co 3+ cations and surface lattice oxygen (O2-) species generated by stronger interaction between Ag and Co and anion lattice defects. Ag(111) faces, Co3+ ions, and O2- are active species. Combined with TOFs, at low temperature (<80 °C), the HCHO catalytic activity on K-Ag/Co3O4 catalyst largely depends on the surface OH- species at the perimeter of the Ag(111) facets; at relatively high temperature (>80 °C), the surface OH- species are consumed and replaced quickly, and their supplement relies on the migration of O2- species from 3D-Co3O4 support. The pathway of reaction for HCHO oxidation on the K-Ag/Co3O4 follows the HCHO → CHOO- + OH- → CO2 + H2O route. © 2014 American Chemical Society. Source


Wei W.,Beijing University of Technology | Wei W.,State Environmental Protection Key Laboratory of Sources and Control of Air Pollution Complex | Cheng S.,Beijing University of Technology | Li G.,Beijing University of Technology | And 2 more authors.
Atmospheric Environment | Year: 2014

This study made a field VOCs (volatile organic compounds) measurement for a petroleum refinery in Beijing by determining 56 PAMS VOCs, which are demanded for photochemical assessment in US, and obtained the characteristics of VOCs emitted from the whole refinery and from its inner main devices. During the monitoring period, this refinery brought about an average increase of 61ppbv in the ambient TVOCs (sum of the PAMS VOCs) at the refinery surrounding area, while the background of TVOCs there was only 10-30ppbv. In chemical profile, the VOCs emitted from the whole refinery was characteristic by isobutane (8.7%), n-butane (7.9%), isopentane (6.3%), n-pentane (4.9%%), n-hexane (7.6%), C6 branched alkanes (6.0%), propene (12.7%), 1-butene (4.1%), benzene (7.8%), and toluene (5.9%). On the other hand, the measurement for the inner 5 devices, catalytic cracking units (CCU2 and CCU3), catalytic reforming unit (CRU), tank farm (TF), and wastewater treatment(WT), revealed the higher level of VOCs pollutions (about several hundred ppbv of TVOCs), and the individual differences in VOCs chemical profiles. Based on the measured speciated VOCs data at the surrounding downwind area, PMF receptor model was applied to identify the VOCs sources in the refinery. Then, coupling with the VOCs chemical profiles measured at the device areas, we concluded that CCU1/3 contributes to 25.9% of the TVOCs at the surrounding downwind area by volume, followed by CCU2 (24.7%), CRU (18.9%), TF (18.3%) and WT (12.0%), which was accordant with the research of US EPA (2008). Finally, ozone formation potentials of the 5 devices were also calculated by MIR technique, which showed that catalytic cracking units, accounting for about 55.6% to photochemical ozone formation, should be given the consideration of VOCs control firstly. © 2014 Elsevier Ltd. Source

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