Wang Kun, Han Yong-Ming, Ho Steven Sai Hang, Zhang Ting, Liu Sui-Xin, Cao Jun-Ji
Key Laboratory of Aerosol Chemistry and Physics, State Key Laboratory of Loess and Quaternary Geology, Institute of Earth Environment, Chinese Academy of Sciences, Xi'an 710061, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Huan Jing Ke Xue. 2017 Jul 8;38(7):2679-2687. doi: 10.13227/j.hjkx.201611045.
PM samples were collected in Xi'an, China during haze(2015-11-30-2015-12-9) and clean days(2016-01-13-2016-01-22). PM mass, organic carbon(OC), elemental carbon(EC), and water-soluble ions(i.e., NH, NO, and SO) were measured to investigate the characteristics of the two typical pollution processes. The result showed that PM masses were(170±47.5) μg·m and(48.6±17.9) μg·m for the haze and clean days, respectively, with the haze accompanied by low visibility, high humidity, calm wind, and other adverse weather conditions. The secondary inorganic aerosol(SIA) including NH, NO, and SO accounted for 49.8%±13.1% and 19.4%±5.95% of the PM mass for the haze and clean days, respectively. sulfur and nitrogen oxidation ratios(SOR and NOR) on haze days were 0.282±0.157 and 0.269±0.124, respectively, which were much higher than those measured on the clean days(0.189±0.057 and 0.077±0.046). The average concentration of secondary organic carbon(SOC) for the haze days(6.22±3.87) μg·m was 5 times of that measured in the clean days(1.44±1.63) μg·m. Secondary pollution and adverse weather conditions were the main reasons for the heavy haze. Finally, the level of particulate-Reactive Oxygen Species(ROS)was measured by the 2',7'-dichlorofluorescin diacetate(2',7'-DCFH) fluorescence method, and the average ROS concentration (as HO) was(4.99±1.54) nmol·m during haze days and(0.492±0.356) nmol·m during clean days. Accumulation effect and secondary oxidation process may be the main reasons for the increase of ROS concentration under the heavy haze conditions in Xi'an. Positive correlations(<0.05) between the concentrations of ROS and the ions of NO and SO indicated that ROS may participate in secondary oxidation process of SIA.
在中国西安,于雾霾天(2015年11月30日至2015年12月9日)和清洁天(2016年1月13日至2016年1月22日)采集了颗粒物(PM)样本。测量了PM质量、有机碳(OC)、元素碳(EC)和水溶性离子(即NH₄⁺、NO₃⁻和SO₄²⁻),以研究这两个典型污染过程的特征。结果表明,雾霾天和清洁天的PM质量分别为(170±47.5)μg·m⁻³和(48.6±17.9)μg·m⁻³,雾霾天伴有低能见度、高湿度、静风及其他不利天气条件。包括NH₄⁺、NO₃⁻和SO₄²⁻在内的二次无机气溶胶(SIA)分别占雾霾天和清洁天PM质量的49.8%±13.1%和19.4%±5.95%。雾霾天的硫和氮氧化率(SOR和NOR)分别为0.282±0.157和0.269±0.124,远高于清洁天测量值(0.189±0.057和0.077±0.046)。雾霾天二次有机碳(SOC)的平均浓度(6.22±3.87)μg·m⁻³是清洁天测量值(1.44±1.63)μg·m⁻³的5倍。二次污染和不利天气条件是重度雾霾的主要原因。最后,采用2',7'-二氯荧光素二乙酸酯(2',7'-DCFH)荧光法测量了颗粒物活性氧(ROS)水平,雾霾天的平均ROS浓度(以HO·计)为(4.99±1.54)nmol·m⁻³,清洁天为(0.492±0.356)nmol·m⁻³。累积效应和二次氧化过程可能是西安重度雾霾条件下ROS浓度升高的主要原因。ROS浓度与NO₃⁻和SO₄²⁻离子浓度之间呈正相关(<0.05),表明ROS可能参与了SIA的二次氧化过程。