首页> 外文期刊>The Science of the Total Environment >An evaluation of direct measurement techniques for mercury dry deposition
【24h】

An evaluation of direct measurement techniques for mercury dry deposition

机译:汞干法沉积直接测量技术的评估

获取原文
获取原文并翻译 | 示例
           

摘要

In this project, several surrogate surfaces designed to directly measure Hg dry deposition were investigated. Static water surrogate surfaces (SWSS) containing deionized (DI), acidified water, or salt solutions, and a knife-edge surrogate surface (KSS) using quartz fiber filters (QFF), KCl-coated QFF and gold-coated QFF were evaluated as a means to directly measure mercury (Hg) dry deposition. The SWSS was hypothesized to collect deposited elemental mercury (Hg°), reactive gaseous/oxidized mercury (RGM), and mercury associated with paniculate matter (Hg_((p))) while the QFF, KCl-coated QFF, and gold-coated QFF on the KSS were hypothesized to collect Hg_((p)). RGM + Hg_((p)), and Hg° + RGM + Hg_((p)), respectively. The Hg flux measured by the DI water was significantly smaller than that captured by the acidified water, probably because Hg° was oxidized to Hg~(2+) which stabilized the deposited Hg and decreased mass transfer resistance. Acidified BrCl, which efficiently oxidizes Hg°, captured significantly more Hg than other solutions. However, of all collection media, gold-coated QFFs captured 6 to 100 times greater Hg mass than the other surfaces, probably because there is no surface resistance for Hg° deposition to gold surfaces. In addition, the Hg~° concentration is usually 100-1000 times higher than RGM and Hg_((p)). For all other media, co-located samples were not significantly different, and the combination of daytime plus nighttime results were comparable to 24-h samples, implying that Hg°, RGM and Hg_((p)) were not released after they deposited nor did the surfaces reach equilibrium with the atmosphere. Based on measured Hg ambient air concentrations and fluxes, dry deposition velocities of RGM and Hg° to DI water and other surfaces were 5.6 ± 5.4 and 0.005-0.68cms~(-1) in this study, respectively. These results suggest surrogate surfaces can be used to measure Hg dry deposition; however, extrapolating the results to natural surface can be challenging.
机译:在该项目中,研究了一些旨在直接测量汞干沉降的替代表面。含有去离子(DI),酸化水或盐溶液的静态水替代表面(SWSS)以及使用石英纤维滤纸(QFF),KCl涂层QFF和金涂层QFF的刀口替代表面(KSS)被评估为一种直接测量汞(Hg)干沉降的方法。假设SWSS会收集沉积的元素汞(Hg°),反应性气态/氧化汞(RGM)以及与颗粒物质相关的汞(Hg _((p))),而QFF,KCl涂层QFF和金涂层假设在KSS上的QFF收集Hg _((p))。 RGM + Hg _((p))和Hg°+ RGM + Hg _((p))。去离子水测得的汞通量明显小于酸化水所捕获的汞通量,这可能是因为Hg°被氧化成Hg〜(2+)从而稳定了沉积的Hg并降低了传质阻力。有效氧化Hg°的酸化BrCl捕获的汞比其他溶液多得多。但是,在所有收集介质中,镀金的QFF捕获的汞质量比其他表面大6至100倍,这可能是因为Hg°沉积到金表面没有表面电阻。此外,Hg〜°的浓度通常比RGM和Hg _((p))高100-1000倍。对于所有其他媒体,同一地点的样本没有显着差异,并且白天和夜间结果的组合与24小时样本相当,这意味着Hg°,RGM和Hg _((p))在沉积后也不会释放表面是否与大气达到平衡。根据测得的汞周围空气浓度和通量,本研究中RGM和Hg°对去离子水和其他表面的干沉降速度分别为5.6±5.4和0.005-0.68cms〜(-1)。这些结果表明,替代表面可用于测量汞的干沉降。但是,将结果外推到自然表面可能会很困难。

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