...
首页> 外文期刊>The Science of the Total Environment >Assessing the emission sources of atmospheric mercury in wet deposition across Illinois
【24h】

Assessing the emission sources of atmospheric mercury in wet deposition across Illinois

机译:评估伊利诺伊州湿沉降中大气汞的排放源

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

From August 4, 2007 to August 31, 2009, we collected event-based precipitation samples for mercury (Hg) and trace element analyses at four sites in Illinois (IL), USA. The objectives of these measurements were to quantify Hg wet deposition across the state, and to assess the contributions to Hg in precipitation from major local and regional emission sources. Monitoring sites were located, from north to south, in Chicago, Peoria, Nilwood, and Carbondale, IL Measurements from these four sites demonstrated that a dear spatial gradient in Hg wet deposition was not evident across the state. Each site received > 10 µg m~(-2) of Hg wet deposition annually, and these observed values were comparable to annual Hg wet deposition measurements from other event-based precipitation monitoring sites in source-impacted areas of the Midwestern US. We applied the multivariate statistical receptor model. Positive Matrix Factorization (EPA PMF v3.0), to the measured Hg and trace element wet deposition amounts at the four sites. Results suggested that 50% to 74% of total Hg wet deposition at each site could be attributed to coal combustion emissions. The other source signatures identified in the precipitation compositions included cement manufacturing, mixed metal smelting/waste incineration, iron-steel production, and a phosphorus source. We also applied a hybrid receptor model, Quantitative Transport Bias Analysis (QTBA), to the Hg wet deposition datasets to identify the major source regions associated with the measured values. The calculated QTBA probability fields suggested that transport from urban/industrial areas, such as Chicago/Gary, St. Louis, and the Ohio River Valley, resulted in some of the highest estimated event-based Hg wet deposition amounts at the four sites (potential mass transfer of up to 032 µg m~(-2)). The combined application of PMF and QTBA supported the hypothesis that local and regional coal combustion was the largest source of Hg wet deposition in Illinois.
机译:从2007年8月4日到2009年8月31日,我们在美国伊利诺伊州(IL)的四个地点收集了基于事件的汞(Hg)降水样品和微量元素分析。这些测量的目的是量化全州的汞湿沉降,并评估主要本地和区域排放源对汞在降水中的贡献。监测点从北到南位于伊利诺伊州芝加哥,皮奥里亚,尼尔伍德和卡本代尔,这四个站点的测量结果表明,全州汞湿沉降的空间梯度并不明显。每个站点每年接受的汞湿沉降量> 10 µg m〜(-2),这些观测值可与美国中西部受源影响地区其他基于事件的降水监测站点的年度汞湿沉降测量值相媲美。我们应用了多元统计受体模型。正矩阵分解(EPA PMF v3.0),用于测量四个位置处的汞和痕量元素湿沉降量。结果表明,每个站点汞湿沉降总量的50%至74%可归因于燃煤排放。沉淀成分中确定的其他来源特征包括水泥生产,混合金属冶炼/废物焚烧,钢铁生产和磷源。我们还对汞湿沉降数据集应用了混合受体模型,即定量迁移偏向分析(QTBA),以识别与测量值相关的主要来源区域。计算得出的QTBA概率字段表明,从城市/工业区(例如芝加哥/加里,圣路易斯和俄亥俄河谷)的运输,导致在这四个地点估算出的基于事件的汞湿沉降量最高(潜在传质高达032 µg m〜(-2))。 PMF和QTBA的组合应用支持以下假设:局部和区域燃煤是伊利诺伊州汞湿沉降的最大来源。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号