CH 2 OO +甲基乙烯基酮和CH 2 OO +甲基丙烯醛反应的直接动力学研究以及CH 2 OO + CO反应的上限测定<a href="#fn1" title="提供电子补充信息（ESI）。参见DOI：10.1039 / c8cp03606c">†</a>,Physical Chemistry Chemical Physics

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CH ₂ OO +甲基乙烯基酮和CH ₂ OO +甲基丙烯醛反应的直接动力学研究以及CH ₂ OO + CO反应的上限测定 †
Physical Chemistry Chemical Physics ( IF 2.9 ) Pub Date : 2018-07-03 00:00:00 , DOI: 10.1039/c8cp03606c
Arkke J. Eskola _{1,

2,

3,

4,

5} , Malte Döntgen _{4,

5,

6,

7} , Brandon Rotavera _{1,

2,

3} , Rebecca L. Caravan _{1,

2,

3} , Oliver Welz _{1,

2,

3} , John D. Savee _{1,

2,

3} , David L. Osborn _{1,

2,

3} , Dudley E. Shallcross _{8,

9,

10,

11} , Carl J. Percival _{11,

12,

13,

14,

15} , Craig A. Taatjes _{1,

2,

3}

Affiliation

甲基乙烯基酮（MVK）和甲基丙烯醛（MACR）是挥发性有机化合物（尤其是异戊二烯）在大气中降解的重要中间产物。这项工作使用多重光电离质谱法（MPIMS），结合来自先进光源或莱曼光谱仪的可调同步辐射，研究了最小的Criegee中间体CH ₂ OO与异戊二烯臭氧分解，MVK和MACR的副产物的反应。 α（10.2 eV）辐射用于光电离。在过量O ₂的存在下通过CH ₂ I _2的脉冲激光光解产生CH ₂ OO。进行时间分辨的反应物消失和产物形成的测量，以监测反应进程。一阶速率系数是从对CH ₂ OO衰减的指数拟合中获得的。在300 K和4 Torr下的双分子反应速率系数为k（CH ₂ OO + MVK）=（5.0±0.4）×10 ^-13 cm ³ s ^-1和k（CH ₂ OO + MACR）=（4.4±1.0） ×10 ^-13 cm ³ s ^-1，其中规定的± 2σ不确定性是统计不确定性。在两个反应中均观察到加合物的形成，这归因于形成了次级恶臭化物（1,2,4-三氧戊环），并由动力学的主方程计算以及绝热电离能之间的一致性所支持。还针对可能的双分子CH ₂ OO + CO反应以及CH ₂ OO与CF ₃ CHCH ₂在300 K和4 Torr下的反应进行了动力学测量。对于CH ₂ OO + CO，未观察到反应，并且确定了上限：k（CH ₂ OO + CO）<2×10 ^-16 cm ³ s ^-1。对于CH_通过2 OO + CF₃ CHCH₂，得到k的上限（CH₂ OO + CF₃ CHCH₂）＜2×10^-14 cm³ s^-1。

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Direct kinetics study of CH2OO + methyl vinyl ketone and CH2OO + methacrolein reactions and an upper limit determination for CH2OO + CO reaction†

Methyl vinyl ketone (MVK) and methacrolein (MACR) are important intermediate products in atmospheric degradation of volatile organic compounds, especially of isoprene. This work investigates the reactions of the smallest Criegee intermediate, CH₂OO, with its co-products from isoprene ozonolysis, MVK and MACR, using multiplexed photoionization mass spectrometry (MPIMS), with either tunable synchrotron radiation from the Advanced Light Source or Lyman-α (10.2 eV) radiation for photoionization. CH₂OO was produced via pulsed laser photolysis of CH₂I₂ in the presence of excess O₂. Time-resolved measurements of reactant disappearance and of product formation were performed to monitor reaction progress; first order rate coefficients were obtained from exponential fits to the CH₂OO decays. The bimolecular reaction rate coefficients at 300 K and 4 Torr are k(CH₂OO + MVK) = (5.0 ± 0.4) × 10⁻¹³ cm³ s⁻¹ and k(CH₂OO + MACR) = (4.4 ± 1.0) × 10⁻¹³ cm³ s⁻¹, where the stated ±2σ uncertainties are statistical uncertainties. Adduct formation is observed for both reactions and is attributed to the formation of a secondary ozonides (1,2,4-trioxolanes), supported by master equation calculations of the kinetics and the agreement between measured and calculated adiabatic ionization energies. Kinetics measurements were also performed for a possible bimolecular CH₂OO + CO reaction and for the reaction of CH₂OO with CF₃CHCH₂ at 300 K and 4 Torr. For CH₂OO + CO, no reaction is observed and an upper limit is determined: k(CH₂OO + CO) < 2 × 10⁻¹⁶ cm³ s⁻¹. For CH₂OO + CF₃CHCH₂, an upper limit of k(CH₂OO + CF₃CHCH₂) < 2 × 10⁻¹⁴ cm³ s⁻¹ is obtained.

更新日期：2018-07-03

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