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In situ and denuder-based measurements of elemental and reactive gaseous mercury with analysis by laser-induced fluorescence – results from the Reno Atmospheric Mercury Intercomparison Experiment

机译:通过激光诱导荧光进行的元素和反应性气态汞的原位和剥蚀法测量–来自里诺大气汞比对实验的结果

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The University of Miami (UM) deployed a sequential two-photon laser-induced fluorescence (2P-LIF) instrument for the in situ measurement of gaseous elemental mercury, Hg(0), during the Reno Atmospheric Mercury Intercomparison Experiment (RAMIX) campaign. A number of extended sampling experiments, typically lasting 6–8?h but on one occasion extending to ~?24?h, were conducted, allowing the 2P-LIF measurements of Hg(0) concentrations to be compared with two independently operated instruments using gold amalgamation sampling coupled with cold vapor atomic fluorescence spectroscopic (CVAFS) analysis. At the highest temporal resolution, ~?5?min samples, the three instruments measured concentrations that agreed to within 10–25?%. Measurements of total mercury (TM) were made by using pyrolysis to convert total oxidized mercury (TOM) to Hg(0). TOM was then obtained by difference. Variability in the ambient Hg(0) concentration limited our sensitivity for measurement of ambient TOM using this approach. In addition, manually sampled KCl-coated annular denuders were deployed and analyzed using thermal dissociation coupled with single-photon LIF detection of Hg(0). The TOM measurements obtained were normally consistent with KCl denuder measurements obtained with two Tekran speciation systems and with the manual KCl denuder measurements but with very large uncertainty. They were typically lower than measurements reported by the University of Washington (UW) Detector for Oxidized Hg Species (DOHGS) system. The ability of the 2P-LIF pyrolysis system to measure TM was demonstrated during one of the manifold HgBrsub2/sub spikes but the results did not agree well with those reported by the DOHGS system. The limitations of the RAMIX experiment and potential improvements that should be implemented in any future mercury instrument intercomparison are discussed. We suggest that instrumental artifacts make a substantial contribution to the discrepancies in the reported measurements over the course of the RAMIX campaign. This suggests that caution should be used in drawing significant implications for the atmospheric cycling of mercury from the RAMIX results.
机译:迈阿密大学(UM)在里诺(Reno)大气汞比对实验(RAMIX)活动期间,部署了连续的两光子激光诱导荧光(2P-LIF)仪器,用于原位测量气态元素汞Hg(0)。进行了许多扩展的采样实验,通常持续6–8?h,但有一次扩展到〜?24?h,使Hg(0)浓度的2P-LIF测量结果与使用仪器的两个独立操作的仪器进行比较。金合并采样与冷蒸气原子荧光光谱法(CVAFS)分析结合。在最高的时间分辨率(〜5?min样品)下,这三台仪器测得的浓度在10–25 %%之内。通过使用热解将总氧化汞(TOM)转换为Hg(0)进行总汞(TM)的测量。然后通过差异获得TOM。环境Hg(0)浓度的变化限制了我们使用这种方法测量环境TOM的灵敏度。另外,使用热解离结合Hg(0)的单光子LIF检测,部署并手动采样了KCl涂层的环形剥蚀器并进行了分析。获得的TOM测量值通常与使用两个Tekran形态分析系统获得的KCl剥蚀剂测量值和手动KCl剥蚀剂测量值一致,但不确定性非常大。它们通常低于华盛顿大学(UW)氧化汞物种检测器(DOHGS)系统报告的测量值。在多个HgBr 2 峰之一期间证明了2P-LIF热解系统测量TM的能力,但结果与DOHGS系统报道的结果不一致。讨论了RAMIX实验的局限性以及将来在任何汞仪器比对中应采取的潜在改进措施。我们建议,在RAMIX运动过程中,仪器文物对报告的测量差异做出了重大贡献。这表明从RAMIX结果中得出汞对大气循环的重大影响时应谨慎行事。

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