Miao Qing-Qing, Jiang Nan, Zhang Rui-Qin, Zhao Xiao-Nan, Qi Jing-Wen
College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
School of Ecology and Environment, Zhengzhou University, Zhengzhou 450001, China.
Huan Jing Ke Xue. 2021 Jan 8;42(1):19-29. doi: 10.13227/j.hjkx.202005333.
To study the characteristics of PM pollution and the potential sources of its main components in the central plain urban agglomeration in autumn and winter, PM samples were collected continually in the four typical cities of Zhengzhou, Luoyang, Anyang, and Xinxiang from October 2018 to January 2019. X-ray fluorescence spectrometry, carbon analysis methods, and ion chromatography were used to determine 18 kinds of inorganic elements, organic carbon (OC)/elemental carbon (EC), and 9 kinds of water-soluble inorganic ions. According to the daily PM concentration, three pollution levels were divided, and the comparative analysis for the spatial and temporal variation of PM and its main components, i.e., NO, OC, and 18 kinds of inorganic elements, were studied via the calculation of the nitrogen oxidation rate (NOR), secondary organic carbon (SOC), and enrichment factor. The emission sources and their contribution rates of PM pollution level in the four cities were calculated by a chemical mass balance (CMB) model; the potential pollution sources of PM and its main components, NO and OC, in the four cities were analyzed by a backward trajectory model (HYSPLIT) and potential source contribution factor method (PSCF). The results showed that the means of PM in Zhengzhou, Luoyang, Anyang, and Xinxiang were (82.1±45.5), (84.7±39.8), (96.8±46.1), and (81.1±36.6) μg·m, respectively, during the sampling period, and the maximum daily mean values were 3.3, 2.6, 3.0, and 2.3 times, respectively, of the Chinese national secondary standard; the main components of PM in the four cities were NO and SOC, and the concentration of NO, the ratio of NO/EC, and NOR all increased significantly with the rising of pollution levels, generally showing that the mean values of NO/EC and NOR of Zhengzhou and Luoyang were a little higher than those of Anyang and Xinxiang; the concentration of SOC, the proportion of SOC in OC, and the ratio of SOC/EC all increased with the rising of pollution levels. From the concentration and enrichment degree of inorganic elements, As was the highest in Zhengzhou; Mn and Fe were the highest in Luoyang; Zn, Ni, and Cr were the highest in Anyang; and Cu and Pb were the highest in Xinxiang. Secondary nitrate, secondary sulfate, organic matter, coal combustion, motor vehicle, dust, biomass burning, and industrial processes were the main PM pollution sources in the four cities, with the highest contribution rate of secondary nitrate in Zhengzhou (37.7%), the highest contribution rate of vehicle sources in Xinxiang (14.1%), and a relatively high contribution rate of industrial process source in Luoyang (7.0%) and Anyang (6.8%). The northwest direction of airflow contributed 51.6%, 49.2%, 49.6%, and 46.3% of the total airflow in Zhengzhou, Luoyang, Anyang, and Xinxiang, respectively. From the potential pollution area of each city, the Zhengzhou area was mainly concentrated in Henan province, the Luoyang area was mainly concentrated in the south of Henan province and Fen-wei plain, and the Anyang and Xinxiang areas were mainly concentrated in Henan province and the Beijing-Tianjin-Hebei transport belt. The pollution levels of OC in Anyang and Xinxiang were also affected by the northwest Anhui, southwest Shandong, southeast Shanxi, and north Shaanxi.
为研究中原城市群秋冬季细颗粒物(PM)污染特征及其主要组分的潜在来源,于2018年10月至2019年1月在郑州、洛阳、安阳和新乡4个典型城市连续采集PM样本。采用X射线荧光光谱法、碳分析方法和离子色谱法测定18种无机元素、有机碳(OC)/元素碳(EC)以及9种水溶性无机离子。根据每日PM浓度划分3个污染等级,通过计算氮氧化率(NOR)、二次有机碳(SOC)和富集因子,对PM及其主要组分(即NO、OC和18种无机元素)的时空变化进行对比分析。利用化学质量平衡(CMB)模型计算4个城市PM污染水平的排放源及其贡献率;通过后向轨迹模型(HYSPLIT)和潜在源贡献因子法(PSCF)分析4个城市PM及其主要组分NO和OC的潜在污染源。结果表明,采样期间郑州、洛阳、安阳和新乡的PM均值分别为(82.1±45.5)、(84.7±39.8)、(96.8±46.1)和(81.1±36.6)μg·m,日均值最大值分别为国家二级标准的3.3、2.6、3.0和2.3倍;4个城市PM的主要组分为NO和SOC,NO浓度、NO/EC比值和NOR均随污染等级升高而显著增加,总体上郑州和洛阳的NO/EC和NOR均值略高于安阳和新乡;SOC浓度、SOC在OC中的占比以及SOC/EC比值均随污染等级升高而增加。从无机元素的浓度和富集程度来看,郑州的As最高;洛阳的Mn和Fe最高;安阳的Zn、Ni和Cr最高;新乡的Cu和Pb最高。二次硝酸盐、二次硫酸盐、有机物、煤炭燃烧、机动车、扬尘、生物质燃烧和工业过程是4个城市PM的主要污染源,郑州二次硝酸盐贡献率最高(37.7%),新乡机动车源贡献率最高(14.1%),洛阳(7.0%)和安阳(6.8%)工业过程源贡献率相对较高。气流西北方向对郑州、洛阳、安阳和新乡总气流的贡献率分别为51.6%、49.2%、49.6%和46.3%。从各城市的潜在污染区域来看,郑州地区主要集中在河南省,洛阳地区主要集中在河南省南部和汾渭平原,安阳和新乡地区主要集中在河南省和京津冀传输带。安阳和新乡的OC污染水平还受皖西北、鲁西南、晋东南和陕北的影响。