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Observations of nitrogen dioxide, total peroxy nitrates, total alkyl nitrates, and nitric acid in the mid-sierras and Sacramento plume using thermal dissociation - laser induced fluorescence.

机译:使用热解离-激光诱导的荧光观察中西拉和萨克拉曼多羽中的二氧化氮,总过氧硝酸盐,总硝酸烷基酯和硝酸。

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Nitrogen oxide radicals (NOx ≡ NO + NO2) control the rate of tropospheric ozone production and affect particle formation through production of HNO3 and organic nitrates. The chemistry affecting the fate of NOx while extensively studied in the laboratory, remains poorly documented in the atmosphere because of the difficulty of making simultaneous observations of NOx and NOx reaction products. Furthermore, it has been difficult to obtain such observations under conditions where chemistry occurs in a well understood transport regime. In Chapter 2 of this dissertation, I describe development of a new experimental technique, thermal dissociation-laser induced fluorescence (TD-LIF), capable of observing NO2, ΣPNs, ΣANs, and HNO3, and its applications to field measurements. The instrument's capabilities to measure HNO3 and ΣANs are unique. Also, as a result of progress that has been made at simplifying maintenance, it has a unique capacity to obtain long term records.; In Chapters 3 and 4, I describe nearly continuous measurements of NO2, total peroxy nitrates (ΣPNs), total alkyl nitrates (ΣANs), and HNO3 which were made from October 2000 to February 2002 at the University of California Research Station (UC-BFRS). ΣANs were observed to routinely comprise 10–20% of NOy, a much larger fraction than previously reported (typically 1–3%). In contrast to prior observations that suggested ΣANs are negligible, I demonstrate here that large abundances of ΣANs are consistent with simple chemical models of tropospheric ozone production and with the few prior comprehensive model studies. ΣANs were strongly correlated with O3 at the UC-BFRS. I illustrate how ΣANs production is directly linked to the HOx/NOx ozone production cycles. ΣANs were observed at similar concentrations (200–800 ppt), with a similar seasonal cycle (summer peak), and similar correlations with photochemical parameters (O 3, peroxy nitrates) to previous reports of ‘missing NOy’ at non-urban, mid-latitude continental sites. Comparison of the sum NO y as measured by TD-LIF (ΣNOyi) to observations of total NOy as measured by the catalysis chemiluminesence method showed good agreement. Observations of ΣANs at Granite Bay, California and La Porte, Texas also provide consistent insights, leading to the conclusion that ΣANs are most, if not all, of the ‘missing NOy’.; In Chapter 4, I describe and analyze the seasonal and diurnal cycles of ΣNOyi, NOx, ΣPNs, ΣANs, HNO 3, CO, and O3 observed at the UC-BFRS. The seasonal cycles (most peaked in summer) are attributed to a combination of changes in transport and chemical processing. (Abstract shortened by UMI.)
机译:氮氧化物自由基(NO x ≡NO + NO 2 )控制对流层臭氧的产生速率,并通过HNO 3 和HNO的产生影响颗粒形成有机硝酸盐。在实验室中广泛研究了影响NO x 命运的化学反应,但由于很难同时观察NO x 和NO x 反应产物。此外,在化学以众所周知的运输方式发生的条件下,很难获得这种观察结果。在本论文的第2章中,我描述了一种新的实验技术的发展,即热解离激光诱导荧光(TD-LIF),它能够观察NO 2 ,ΣPN,ΣAN和HNO 3 ,及其在现场测量中的应用。该仪器测量HNO 3 和ΣAN的能力是独一无二的。而且,由于简化维护方面取得了进展,因此它具有获得长期记录的独特能力。在第3章和第4章中,我描述了NO 2 ,总过氧硝酸盐(ΣPNs),总硝酸盐(ΣANs)和HNO 3 的近乎连续测量,这些测量是由2000年10月至2002年2月在加利福尼亚大学研究站(UC-BFRS)。观察到ΣAN通常占NO y 的10%至20%,比以前报道的要大得多(通常<1-3%)。与以前的建议ΣAN可以忽略不计的观察相反,我在这里证明了ΣAN的大量存在与对流层臭氧生产的简单化学模型是一致的,而很少有先前的综合模型研究。在UC-BFRS中,ΣAN与O 3 密切相关。我说明了ΣAN的生产如何与HO x / NO x 臭氧生产周期直接相关。与以前的“缺少NO”的报告相似,在浓度(200–800 ppt),季节性周期(夏季峰值)和与光化学参数(O 3 ,过氧硝酸盐)相似的相关性下观察到ΣAN。 y ”位于非城市中纬度大陆地区。 TD-LIF(ΣNO yi )测量的总NO y 与催化化学发光法测量的总NO y 的比较表现出良好的协议。在加利福尼亚州花岗岩湾和得克萨斯州拉波特的ΣAN观测也提供了一致的见解,得出的结论是ΣAN是“丢失NO y ”的大部分(即使不是全部)。在第4章中,我描述和分析了ΣNO yi ,NO x ,ΣPNs,ΣAN,HNO 3 ,CO, UC-BFRS观察到的是O 3 。季节周期(夏季最高峰)归因于运输和化学加工过程的变化。 (摘要由UMI缩短。)

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