State Key Laboratory of Water Environment Simulation, School of Environment, Beijing Normal University, Beijing 100875, China; State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China.
State Key Laboratory of Atmospheric Boundary Layer Physics and Atmospheric Chemistry, Institute of Atmospheric Physics, Chinese Academy of Sciences, Beijing 100029, China; Collaborative Innovation Center on Forecast and Evaluation of Meteorological Disasters, Nanjing University of Information Science & Technology, Nanjing 210044, China.
Environ Pollut. 2016 Dec;219:957-966. doi: 10.1016/j.envpol.2016.09.077. Epub 2016 Oct 14.
Size-segregated aerosol samples were collected in New Delhi, India from March 6 to April 6, 2012. Homologous series of n-alkanes (CC), n-fatty acids (CC) and n-alcohols (CC) were measured using gas chromatography/mass spectrometry. Results showed a high-variation in the concentrations and size distributions of these chemicals during non-haze, haze, and dust storm days. In general, n-alkanes, n-fatty acids and n-alcohols presented a bimodal distribution, peaking at 0.7-1.1 μm and 4.7-5.8 μm for fine modes and coarse modes, respectively. Overall, the particulate matter mainly existed in the coarse mode (≥2.1 μm), accounting for 64.8-68.5% of total aerosol mass. During the haze period, large-scale biomass burning emitted substantial fine hydrophilic smoke particles into the atmosphere, which leads to relatively larger GMDs (geometric mean diameter) of n-alkanes in the fine mode than those during the dust storms and non-haze periods. Additionally, the springtime dust storms transported a large quantity of coarse particles from surrounding or local areas into the atmosphere, enhancing organic aerosol concentration and inducing a remarkable size shift towards the coarse mode, which are consistent with the larger GMDs of most organic compounds especially in total and coarse modes. Our results suggest that fossil fuel combustion (e.g., vehicular and industrial exhaust), biomass burning, residential cooking, and microbial activities could be the major sources of lipid compounds in the urban atmosphere in New Delhi.
2012 年 3 月 6 日至 4 月 6 日,在印度新德里采集了按粒径分段的气溶胶样本。采用气相色谱/质谱法对同系物正构烷烃(CC)、正脂肪酸(CC)和正醇(CC)进行了测量。结果表明,在无霾、霾和沙尘天气期间,这些化学物质的浓度和粒径分布变化很大。总体而言,正构烷烃、正脂肪酸和正醇呈双峰分布,细模态和粗模态的峰值分别为 0.7-1.1μm 和 4.7-5.8μm。总体而言,颗粒物主要存在于粗模态(≥2.1μm)中,占总气溶胶质量的 64.8-68.5%。在霾期间,大规模的生物质燃烧将大量细亲水烟尘颗粒排放到大气中,导致细模态中正构烷烃的 GMD(几何平均直径)相对较大,而在沙尘和无霾期间则较小。此外,春季沙尘天气将大量粗颗粒从周边或当地地区输送到大气中,增加了有机气溶胶浓度,并导致明显的向粗模态的粒径分布转移,这与大多数有机化合物,特别是在总模式和粗模式下的较大 GMD 一致。我们的结果表明,化石燃料燃烧(例如车辆和工业废气)、生物质燃烧、居民烹饪和微生物活动可能是新德里城市大气中脂类化合物的主要来源。