Reaction of O(1D) with Methane

激进的 光解 分解 化学 甲烷 活化能 清除 光化学 反应速率常数 甲基自由基 分子 分析化学(期刊) 物理化学 动力学 有机化学 物理 抗氧化剂 量子力学
作者
W. B. DeMore,O. F. Raper
出处
期刊:Journal of Chemical Physics [American Institute of Physics]
卷期号:46 (7): 2500-2505 被引量:60
标识
DOI:10.1063/1.1841075
摘要

The reaction of O(1D) with CH4 has been studied by photolysis (2537 Å) of O3–CH4 mixtures dissolved in liquid argon at 87°K. The quantum yields of O3 decomposition and the product yields based on O3 decomposed were measured. The products found were CH3OH, CH2O, and H2. Added O2 was found to lower the quantum yields of O3 decomposition and to increase the product yields. Experiments with added 18O2 were carried out to trace the origin of the products. At 6000 Å, which can only give O (3P), no photo-reaction could be detected. The results indicate that the O(1D)—CH4 reaction has essentially zero activation energy and proceeds by three paths: O(1D)+CH4+M→CH3OH+M,O(1D)+CH4→CH2O+H2,O(1D)+CH4→CH3+OH. The effect of added O2 is attributed to scavenging of methyl radicals which otherwise react with O3. The reaction of CH3 with O3 has zero Ea and occurs at a rate approximately equal to the reaction of CH3 with O2. The magnitude of the scavenging effect shows that at least two O3 molecules are decomposed by each CH3. By contrast, OH radicals do not react with O3 in these experiments, indicating a nonzero activation energy for the reaction OH+O3→HO2+O2.
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