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印度北部城市地区大气颗粒碳组分的空间和季节变化及二次源识别

Spatial and seasonal variations of atmospheric particulate carbon fractions and identification of secondary sources at urban sites in North India.

作者信息

Behera Sailesh N, Sharma Mukesh

机构信息

Department of Civil and Environmental Engineering, National University of Singapore, Singapore, 117411, Singapore,

出版信息

Environ Sci Pollut Res Int. 2015 Sep;22(17):13464-76. doi: 10.1007/s11356-015-4603-7. Epub 2015 May 5.

Abstract

An intensive measurement campaign was undertaken to characterize eight fractions of organic carbon (OC) and elemental carbon (EC) in particulate matter (PM) at four urban sites with different pollution characteristics during summer, post-monsoon, and winter at Kanpur, India. Speciation samplers were used to collect particulate samples on quartz filters followed by analysis of OC and EC using Interagency Monitoring of Protected Visual Environments (IMPROVE)-based thermal/optical reflectance (TOR) method. Based on 24-h average results at each site, the highest levels of OC and EC were observed during winter as 96.7 ± 26.9 and 31.8 ± 9.8 μg/m(3) at residential site and traffic site, respectively. The levels of OC at residential sites during winter appeared to be more than twice of that during summer. The site close to the road traffic had the least value of OC/EC, as 1.77 ± 0.28 during post-monsoon, and the site influenced by emissions of domestic cooking and heating had the highest value of OC/EC, as 4.05 ± 0.79 during winter. The average abundances of OC1, OC2, OC3, OC4, OP, EC1, EC2, and EC3 in total carbon (TC) at all sites for three seasons were 10.03, 19.04, 20.03, 12.32, 10.53, 33.39, 3.21, and 1.99 %, respectively. A sharp increase in levels of OC1 and EC1-OP during winter at two residential sites revealed that biomass burning could be a significant contributor to carbonaceous aerosols. From the application of EC-tracer method, it was observed that contribution of secondary organic carbon (SOC) to PM mass increased from 5 % during post-monsoon to 16 % during winter at residential sites and from 2 % during post-monsoon to 7 % during winter at traffic sites. Therefore, it could be inferred that increase in primary emissions coupled with unfavorable meteorological conditions could cause particle agglomeration and hygroscopic growth, leading to unpleasant pollution episode during winter.

摘要

在印度坎普尔,于夏季、季风后和冬季期间,针对四个具有不同污染特征的城市地点,开展了一项密集测量活动,以表征颗粒物(PM)中有机碳(OC)和元素碳(EC)的八个组分。使用形态采样器在石英滤膜上采集颗粒物样本,随后采用基于保护视觉环境跨部门监测(IMPROVE)的热/光反射(TOR)方法对OC和EC进行分析。基于各站点的24小时平均结果,在冬季观测到的OC和EC最高水平分别为:居民区为96.7±26.9μg/m³,交通区为31.8±9.8μg/m³。冬季居民区的OC水平似乎是夏季的两倍多。靠近道路交通的站点OC/EC值最低,季风后为1.77±0.28,而受家庭烹饪和取暖排放影响的站点OC/EC值最高,冬季为4.05±0.79。三个季节中所有站点总碳(TC)中OC1、OC2、OC3、OC4、OP、EC1、EC2和EC3的平均丰度分别为10.03%、19.04%、20.03%、12.32%、10.53%、33.39%、3.21%和1.99%。两个居民区冬季OC1和EC1 - OP水平急剧上升,表明生物质燃烧可能是碳质气溶胶的重要来源。通过应用EC示踪法观察到,居民区二次有机碳(SOC)对PM质量的贡献从季风后的5%增加到冬季的16%,交通区从季风后的2%增加到冬季的7%。因此,可以推断,一次排放增加以及不利的气象条件可能导致颗粒物团聚和吸湿增长,从而在冬季引发令人不快的污染事件。

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