Dynamics of the reaction CH2I + O2 probed via infrared emission of CO, CO2, OH and H2CO

被引:6
作者
Chen, Ting-Yu [1 ,2 ]
Lee, Yuan-Pern [1 ,2 ,3 ,4 ]
机构
[1] Natl Chiao Tung Univ, Dept Appl Chem, Hsinchu 30010, Taiwan
[2] Natl Chiao Tung Univ, Inst Mol Sci, Hsinchu 30010, Taiwan
[3] Natl Chiao Tung Univ, Ctr Emergent Funct Matter Sci, Hsinchu 30010, Taiwan
[4] Acad Sinica, Inst Atom & Mol Sci, Taipei 10617, Taiwan
关键词
CRIEGEE INTERMEDIATE CH2OO; ABSORPTION CROSS-SECTIONS; POTENTIAL-ENERGY SURFACE; GAS-PHASE OZONOLYSIS; EQUAL-TO 13); PHOTODISSOCIATION DYNAMICS; VIBRATIONAL-RELAXATION; INFRARED-EMISSION; TRIPLET METHYLENE; RATE CONSTANTS;
D O I
10.1039/d0cp01940b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The reaction CH2I + O(2)has been widely employed recently for the production of the simplest Criegee intermediate CH2OO in laboratories, but the detailed dynamics of this reaction have been little explored. Infrared emission of several products of this reaction, initiated on irradiation of CH(2)I(2)and O-2(similar to 8 Torr) in a flowing mixture at 308 or 248 nm, was recorded with a step-scan Fourier-transform spectrometer; possible routes of formation were identified according to the observed vibrational distribution of products and published theoretical potential-energy schemes. Upon irradiation at 308 nm, Boltzmann distributions of CO (v <= 5,J <= 19) with an average vibrational energy of 32 +/- 3 kJ mol(-1)and OH (v <= 3,J <= 5.5) with an average vibrational energy of 29 +/- 4 kJ mol(-1)were observed and assigned to the decomposition of HCOOH* to form CO + H2O and OH + HCO, respectively. The broadband emission of CO(2)was simulated with two vibrational distributions of average energies (91 +/- 4) and (147 +/- 8) kJ mol(-1)and assigned to be produced from the decomposition of HCOOH* and methylene bis(oxy), respectively. Upon irradiation of samples at 248 nm, the emission of OH and CO(2)showed similar distributions with slightly greater energies, but the distribution of CO (v <= 11,J <= 19) became bimodal with average vibrational energies of (23 +/- 4) and (107 +/- 29) kJ mol(-1), and branching (56 +/- 5) : (44 +/- 5). The additional large-vcomponent is assigned to be produced from a secondary reaction HCO + O(2)to form CO + HO2; HCO is a coproduct of OH. The branching between CO and OH is (50 +/- 5) : (50 +/- 5) at 308 nm and (64 +/- 5) : (36 +/- 4) at 248 nm, consistent with the mechanism according to which an additional channel to produce CO opens at 248 nm. Highly internally excited H2CO was also observed. With O(2)at 16 Torr, the extrapolated nascent internal distributions are similar to those with O(2)at 8 Torr except for a slight quenching effect.
引用
收藏
页码:17540 / 17553
页数:14
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