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鼎湖山秋季大气细粒子及其二次无机组分的污染特征及来源
摘要点击 3723  全文点击 2500  投稿时间:2011-01-08  修订日期:2011-03-07
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中文关键词  PM2.5  二次无机组分  污染特征  形成机制  珠三角地区
英文关键词  PM2.5  secondary inorganic compounds  pollution characteristic  formation mechanism  PRD region
作者单位
刘子锐 中国科学院大气物理研究所LAPC北京 100029 
王跃思 中国科学院大气物理研究所LAPC北京 100029 
刘全 中国科学院大气物理研究所LAPC北京 100029 
刘鲁宁 中国科学院大气物理研究所LAPC北京 100029 
张德强 中国科学院华南植物园广州 510650 
中文摘要
      利用大气颗粒物质量浓度分析仪(TEOM)及大气细粒子快速捕集及其化学成分自动在线分析系统(RCFP-IC)于2008年10~11月在中国科学院华南植物园鼎湖山定位站进行了大气细粒子(PM2.5)及其二次无机组分(SO2-4、 NH+4和NO-3)与相关污染气体组分的同步观测与分析,同时结合主成分分析和HYSPLIT轨迹模式对颗粒物的来源和传输过程进行了探讨.结果表明,观测期间PM2.5的日平均浓度为76.9 μg·m-3 ,PM2.5中SO2-4、 NH+4和NO-3的日均浓度分别为20.0、 6.8和2.6 μg·m-3 .二次无机组分浓度之和超过PM2.5质量浓度的35%,为鼎湖山地区大气细粒子的主要组成部分;细粒子中SO2-4和NH+4浓度日变化表现出与PM2.5相一致的“双峰”型分布特征,峰值分别出现在10:00和16:00;而NO-3仅在10:00出现单一峰值.细粒子中SO2-4浓度的日变化与大气中SO2浓度的日变化特征相似,SO2-4主要由SO2转化而来;而NO-3浓度的日变化特征则异于NO2,NO2的二次转化率(NOR)远低于SO2的二次转化率(SOR).细粒子中NH+4主要以硫酸盐、 硝酸盐及氯盐的形式存在.主成分分析结合后向轨迹推算,鼎湖山地区大气细粒子污染主要来自于珠江三角洲地区城市群如广州和惠州等的区域输送,同时本地二次硫酸盐的贡献较大而一次排放的贡献较小.
英文摘要
      Real-time measurements of PM2.5, secondary inorganic compounds in PM2.5 (SO2-4, NH+4, and NO-3) and related gaseous pollutants were conducted at Mount Dinghu, a regional background station of the Pearl River Delta (PRD), in October and November 2008 by using a conventional R&P TEOM and a system of rapid collection of fine particles and ion chromatography (RCFP-IC). Sources and transportation of atmospheric particles during the experiment were discussed with principal component analysis and backward trajectories calculated using HYSPLIT model. The average daily mass concentrations of PM2.5 were 76.9 μg·m-3 during sampling period, and average daily mass concentrations of SO2-4, NH+4, and NO-3 were 20.0 μg·m-3 , 6.8 μg·m-3 and 2.6μg·m-3 , respectively. The sum of these three secondary inorganic compounds accounted for more than one third of the PM2.5 mass concentration, which had become the major source of atmospheric fine particles at Mount Dinghu. The diurnal variation of PM2.5, SO2-4, and NH+4 all showed a “bimodal” distribution with two peaks appeared at 10:00 am and at 16:00 pm, respectively, whereas NO-3showed “single peak” distribution peaked at 10:00 am. The mass concentrations of SO2-4 in PM2.5 had the similar diurnal variation with that of SO2, SO2-4 in PM2.5 was mainly transformed from SO2, whereas NO-3showed difference diurnal variation with that of NO2, and the second conversion rate of NO2 was far lower than that of SO2. NH+4 in PM2.5 existed mainly in the form of sulfate, nitrate and chloride. Both of principal component analysis and back trajectory analysis showed that the variations of PM2.5 and secondary inorganic compounds at Mount Dinghu were mainly affected by the long-range transport air mass passed over Guangzhou, Huizhou and other highly industrialized areas which carried air pollutants to the observation site, at the same time local sulfate originated from secondary formation also contributed an important part of atmospheric fine particles and the contribution from local direct emission was little.

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