动力学
产量(工程)
化学
化学动力学
氘
光谱学
燃烧
反应机理
大气压力
光化学
分析化学(期刊)
物理化学
热力学
催化作用
原子物理学
有机化学
物理
地质学
海洋学
量子力学
作者
Bryce Bjork,Thinh Bui,Oliver H. Heckl,P. Bryan Changala,Ben Spaun,Paula Heu,David Follman,C. Deutsch,Garrett D. Cole,Markus Aspelmeyer,Mitchio Okumura,Jun Ye
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2016-10-27
卷期号:354 (6311): 444-448
被引量:115
标识
DOI:10.1126/science.aag1862
摘要
The kinetics of the hydroxyl radical (OH) + carbon monoxide (CO) reaction, which is fundamental to both atmospheric and combustion chemistry, are complex because of the formation of the hydrocarboxyl radical (HOCO) intermediate. Despite extensive studies of this reaction, HOCO has not been observed under thermal reaction conditions. Exploiting the sensitive, broadband, and high-resolution capabilities of time-resolved cavity-enhanced direct frequency comb spectroscopy, we observed deuteroxyl radical (OD) + CO reaction kinetics and detected stabilized trans-DOCO, the deuterated analog of trans-HOCO. By simultaneously measuring the time-dependent concentrations of the trans-DOCO and OD species, we observed unambiguous low-pressure termolecular dependence of the reaction rate coefficients for N2 and CO bath gases. These results confirm the HOCO formation mechanism and quantify its yield.
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