Wu ZJ, Wang Y, Tan TY, Zhu YS, Li MR, Shang DJ, Wang HC, Lu KD, Guo S, Zeng LM, et al. Aerosol Liquid Water Driven by Anthropogenic Inorganic Salts: Implying Its Key Role in Haze Formation over the North China Plain. Environmental Science & Technology Letters. 2018;5:160-166.
AbstractThis study reveals aerosol liquid water content (ALWC) in PM2.5 ranged from 2% up to 74%, and the associated secondary inorganic fraction rose from 24% to 55%, while ambient relative humidity (RH) increased from 15% to 83% in the atmosphere over Beijing. Unexpectedly, the secondary inorganic fraction in PM2.5 increased with an increase in the ambient RH, which is a meteorological parameter independent of anthropogenic activities, indicating the presence of a feedback mechanism driven by Henry's law and thermodynamic equilibrium. During haze episodes, simultaneously elevated RH levels and anthropogenic secondary inorganic mass concentrations resulted in an abundant ALWC. The condensed water could act as an efficient medium for multiphase reactions, thereby facilitating the transformation of reactive gaseous pollutants into particles and accelerating the formation of heavy haze. ALWC was well correlated with the mass concentrations of both nitrate and sulfate, indicating both nitrate and sulfate salts play key roles in determining ALWC. Coincident with a significant reduction in SO2 emissions throughout China, nitrates will become a dominant anthropogenic inorganic salt driving ALWC. Thus, the abundance of ALWC and its effects on the aerosol chemistry and climate should be reconsidered.
Su R, Lu KD, Yu JY, Tan ZF, Jiang MQ, Li J, Xie SD, Wu YS, Zeng LM, Zhai CZ, et al. Exploration of the formation mechanism and source attribution of ambient ozone in Chongqing with an observation-based model. Science China-Earth SciencesScience China-Earth SciencesScience China-Earth Sciences. 2018;61:23-32.
AbstractAn intensive field campaign was conducted in Chongqing during the summer of 2015 to explore the formation mechanisms of ozone pollution. The sources of ozone, the local production rates, and the controlling factors, as well as key species of volatile organic compounds (VOCs), were quantified by integrating a local ozone budget analysis, calculations of the relative incremental reactivity, and an empirical kinetic model approach. It was found that the potential for rapid local ozone formation exists in Chongqing. During ozone pollution episodes, the ozone production rates were found to be high at the upwind station Nan Quan, the urban station Chao Zhan, and the downwind station Jin-Yun Shan. The average local ozone production rate was 30x10(-9) V/V h(-1) and the daily integration of the produced ozone was greater than 180x10(-9) V/V. High ozone concentrations were associated with urban and downwind air masses. At most sites, the local ozone production was VOC-limited and the key species were aromatics and alkene, which originated mainly from vehicles and solvent usage. In addition, the air masses at the northwestern rural sites were NO (x) -limited and the local ozone production rates were significantly higher during the pollution episodes due to the increased NO (x) concentrations. In summary, the ozone abatement strategies of Chongqing should be focused on the mitigation of VOCs. Nevertheless, a reduction in NO (x) is also beneficial for reducing the regional ozone peak values in Chongqing and the surrounding areas.
Li ZY, Zhu R, Xie PH, Wang HC, Lu KD, Wang D.
Intercomparison of in situ CRDS and CEAS for measurements of atmospheric N2O5 in Beijing, China. Science of the Total Environment. 2018;613:131-139.
AbstractDinitrogen pentoxide (N2O5) is one of the basic trace gases which plays a key role in nighttime atmosphere. An intercomparison and validation of different N2O5 measurement methods is important for determining the true accuracy of these methods. Cavity ring down spectroscopy (CRDS) and cavity enhanced absorption spectrometer (CEAS) were used to measure N2O5 at the campus of the University of Chinese Academy of Sciences (UCAS) from February 21, 2016 to March 4, 2016. The detection limits were 1.6 ppt (1 sigma) at 30 s intervals for the CEAS instrument and 3.9 ppt (1 sigma) at 10 s time resolution for the CRDS instrument respectively. In this study, a comparison of the 1 min observations from the two instruments was presented. The two data sets showed a good agreement within their uncertainties, with an absolute shift of 15.6 ppt, slope of 0.94 and a correlation coefficient R-2 = 0.97. In general, the difference between the CRDS and CEAS instruments for N2O5 measurement can be explained by their combined measurement uncertainties. However, high relative humidity (> 60%) and high PM2.5 concentration (> 200 mu g/m(3)) may contribute to the discrepancies. The excellent agreement between the measurement by the CRDS and CEAS instruments demonstrates the capability of the two instruments for accurately measuring N2O5 with high sensitivity. (C) 2017 Elsevier B.V. All rights reserved.
梁昱, 刘禹含, 王红丽, 李莉, 段玉森, 陆克定*.
基于主成分分析的上海春季近地面臭氧污染区域性特征研究. 环境科学学报. 2018;38(10):3807-3815.
Duan J, Qin M, Ouyang B, Fang W, Li X, Lu K, Tang K, Liang S, Meng F, Hu Z.
Development of an incoherent broadband cavity-enhanced absorption spectrometer for in situ measurements of HONO and NO 2. Atmospheric Measurement Techniques. 2018;11(7).
Le Breton M *, Hallquist AM, Pathak RK, Simpson D, Wang YJ, Johansson J, Zheng J, Yang YD, Shang DJ, Wang HC, et al. Chlorine oxidation of VOCs at a semi-rural site in Beijing: significant chlorine liberation from ClNO 2 and subsequent gas-and particle-phase Cl–VOC production. Atmospheric Chemistry and Physics. 2018;18(17):13013-13030.
Wang L, Wang X, Gu R, Wang H, Yao L, Wen L, Zhu F, Wang W, Xue L, Yang L, et al. Observations of fine particulate nitrated phenols in four sites in northern China: concentrations, source apportionment, and secondary formation. Atmospheric Chemistry and Physics [Internet]. 2018;18:4349–4359.
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