Wojtal Paul K, Miller David J, O'Conner Mary, Clark Sydney C, Hastings Meredith G
Department of Chemistry, Brown University; Institute at Brown for Environment and Society, Brown University.
Institute at Brown for Environment and Society, Brown University; Department of Earth, Environmental, and Planetary Sciences, Brown University.
J Vis Exp. 2016 Dec 20(118):54962. doi: 10.3791/54962.
Nitrogen oxides (NOx = NO + NO2) are a family of atmospheric trace gases that have great impact on the environment. NOx concentrations directly influence the oxidizing capacity of the atmosphere through interactions with ozone and hydroxyl radicals. The main sink of NOx is the formation and deposition of nitric acid, a component of acid rain and a bioavailable nutrient. NOx is emitted from a mixture of natural and anthropogenic sources, which vary in space and time. The collocation of multiple sources and the short lifetime of NOx make it challenging to quantitatively constrain the influence of different emission sources and their impacts on the environment. Nitrogen isotopes of NOx have been suggested to vary amongst different sources, representing a potentially powerful tool to understand the sources and transport of NOx. However, previous methods of collecting atmospheric NOx integrate over long (week to month) time spans and are not validated for the efficient collection of NOx in relevant, diverse field conditions. We report on a new, highly efficient field-based system that collects atmospheric NOx for isotope analysis at a time resolution between 30 min and 2 hr. This method collects gaseous NOx in solution as nitrate with 100% efficiency under a variety of conditions. Protocols are presented for collecting air in urban settings under both stationary and mobile conditions. We detail the advantages and limitations of the method and demonstrate its application in the field. Data from several deployments are shown to 1) evaluate field-based collection efficiency by comparisons with in situ NOx concentration measurements, 2) test the stability of stored solutions before processing, 3) quantify in situ reproducibility in a variety of urban settings, and 4) demonstrate the range of N isotopes of NOx detected in ambient urban air and on heavily traveled roadways.
氮氧化物(NOx = NO + NO2)是一类对环境有重大影响的大气微量气体。NOx浓度通过与臭氧和羟基自由基的相互作用直接影响大气的氧化能力。NOx的主要汇是硝酸的形成和沉积,硝酸是酸雨的一个组成部分,也是一种可生物利用的养分。NOx来自自然源和人为源的混合排放,其在空间和时间上各不相同。多种排放源的并存以及NOx的短寿命使得定量限制不同排放源的影响及其对环境的影响具有挑战性。有人提出,不同来源的NOx氮同位素有所不同,这是了解NOx来源和传输的一个潜在有力工具。然而,以前收集大气中NOx的方法是在较长(从一周到一个月)的时间跨度内进行综合采样,并且在相关的、多样的野外条件下未经验证能否高效收集NOx。我们报告了一种新的、高效的基于野外的系统,该系统能以30分钟至2小时的时间分辨率收集大气中的NOx用于同位素分析。这种方法在各种条件下都能100%有效地将气态NOx收集到溶液中形成硝酸盐。文中给出了在城市环境中固定和移动条件下采集空气的方案。我们详细说明了该方法的优点和局限性,并展示了其在野外的应用。来自几次部署的数据用于:1)通过与现场NOx浓度测量结果进行比较来评估基于野外的收集效率;2)在处理之前测试储存溶液的稳定性;3)量化各种城市环境中的现场重现性;4)展示在城市环境空气中以及交通繁忙道路上检测到的NOx氮同位素范围。