Onel Lavinia, Lade Rachel, Mortiboy Jennifer, Blitz Mark A, Seakins Paul W, Heard Dwayne E, Stone Daniel
School of Chemistry, University of Leeds, Leeds, LS2 9JT, UK.
National Centre for Atmospheric Science, University of Leeds, Leeds, LS2 9JT, UK.
Phys Chem Chem Phys. 2021 Sep 15;23(35):19415-19423. doi: 10.1039/d1cp02932k.
The kinetics of the gas phase reaction of the Criegee intermediate CHOO with SO have been studied as a function of temperature in the range 223-344 K at 85 Torr using flash photolysis of CHI/O/SO/N mixtures at 248 nm coupled to time-resolved broadband UV absorption spectroscopy. Measurements were performed under pseudo-first-order conditions with respect to SO, revealing a negative temperature dependence. Analysis of experimental results using the Master Equation Solver for Multi-Energy well Reactions (MESMER) indicates that the observed temperature dependence, combined with the reported lack of a pressure dependence in the range 1.5-760 Torr, can be described by a reaction mechanism consisting of the formation of a pre-reaction complex leading to a cyclic secondary ozonide which subsequently decomposes to produce HCHO + SO. The temperature dependence can be characterised by = (3.72 ± 0.13) × 10 (/298) cm molecule s. The observed negative temperature dependence for the title reaction in conjunction with the decrease in water dimer (the main competitor for the Criegee intermediate) concentration at lower temperatures means that Criegee intermediate chemistry can play an enhanced role in SO oxidation in the atmosphere at lower temperatures.
利用248 nm波长下CHI/O/SO/N混合物的闪光光解结合时间分辨宽带紫外吸收光谱,在85 Torr压力下,研究了Criegee中间体CHOO与SO的气相反应动力学随温度在223 - 344 K范围内的变化。在相对于SO的准一级条件下进行测量,结果显示出负温度依赖性。使用多能阱反应主方程求解器(MESMER)对实验结果进行分析表明,观察到的温度依赖性,结合报道的在1.5 - 760 Torr范围内不存在压力依赖性的情况,可以用一个反应机理来描述,该机理包括形成一个预反应复合物,导致生成环状二级臭氧化物,随后该臭氧化物分解生成HCHO + SO。温度依赖性可以用 = (3.72 ± 0.13) × 10 (/298) cm molecule s来表征。观察到的标题反应的负温度依赖性,结合较低温度下水二聚体(Criegee中间体的主要竞争物)浓度的降低,意味着Criegee中间体化学在较低温度下的大气SO氧化中可以发挥增强作用。