Mechanism of the OH-initiated oxidation of glycolaldehyde over the temperature range 233-296 K

被引:52
作者
Butkovskaya, Nadezhda I.
Pouvesle, Nicolas
Kukui, Alexandre
Le Bra, Georges
机构
[1] CNRS, Lab Combust & Syst React, F-45071 Orleans 2, France
[2] Russian Acad Sci, Inst Chem Phys, Moscow, Russia
关键词
RADICALS; KINETICS; CL; CHEMISTRY; ISOPRENE; ACID;
D O I
10.1021/jp064993k
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 mechanism of the gas-phase OH-initiated oxidation of glycolaldehyde (HOCH2CHO) was studied in the 233-296 K temperature range using a turbulent flow reactor coupled with a chemical ionization mass spectrometer. In the presence of O-2, formaldehyde, CO2, formic acid, and glyoxal were observed at room temperature with the yields of 80, 34, 18, and 14%, respectively. Decrease of temperature to 233 K led to significant changes in the yields of the stable products: those of formaldehyde and glyoxal decreased to 50 and 4%, respectively, whereas that of formic acid increased to 52%. It was also found that the OH + glycolaldehyde + O-2 reaction proceeds with considerable reformation of OH radicals (by 25% at 296 K). The observed product yields are explained by a mechanism including formation of short-lived intermediate adducts of the primary radicals with O-2. The implication of the obtained results for the HOx budget in the upper troposphere is discussed.
引用
收藏
页码:13492 / 13499
页数:8
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