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Study reveals mechanism of Cl-initiated oxidation of methacrolein under NOx-free conditions

08.15.22 | Hefei Institutes of Physical Science, Chinese Academy of Sciences

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Chlorine atoms (Cl) have higher reactivity than other oxidants (OH radicals, O 3 , etc.) in the atmosphere. In recent years, researchers found increased concentrations of Cl precursors in the inland regions. The Cl-initiated atmospheric oxidation reactions become more and more important.

Methacrolein (MACR) is the key intermediate of the atmospheric oxidation of biogenic isoprene. The oxidation and degradation of MACR play an essential role in the formation of atmospheric ozone and secondary organic aerosols.

A team of researchers led by Prof. ZHANG Weijun from the Hefei Institutes of Physical Science (HFIPS) of the Chinese Academy of Sciences (CAS), recently investigated Cl-initiated oxidation reactions of MACR under NOx-free conditions, by using a home-made photoionization TOF mass spectrometer complemented with theoretical calculations.

In this study, scientists used a microwave discharge flow tube reactor to study the oxidation reaction of Cl + MACR. The key species such as intermediate radicals and products during the oxidation process were detected online and confirmed in photoionization mass spectra.

The results showed that the reaction of MACR with Cl atoms could generate the C 4 H 5 O and C 4 H 6 OCl radicals via hydrogen abstraction and the addition of Cl atom to the C=C double bond, respectively.

"This is the first time the transient C 4 H 5 O and C 4 H 6 OCl radicals were experimentally detected here," said LIN Xiaoxiao, first author of the paper.

She further explained the mechanism. The C 4 H 5 O and C 4 H 6 OCl radicals could react with O 2 to produce the corresponding peroxy radicals C 4 H 5 OO 2 and C 4 H 6 OClO 2 . Under low NOx conditions, these peroxy radicals would perform bimolecular reactions with themselves and the HO2 radicals.

Combined with theoretical calculations, the resulting specific products could be identified in the photoionization mass spectra.

At the end of the experiment, they measured the time evolutions of products by kinetic experiments and compared it with theoretical model results.

This work elucidated the chemical mechanisms of the Cl-initiated oxidation of MACR, which is helpful to understand the chemical behavior of MACR in the atmosphere.

Physical Chemistry Chemical Physics

10.1039/D2CP02101C

Cl-Initiated oxidation of methacrolein under NOx-free conditions studied by VUV photoionization mass spectrometry

5-Jul-2022

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Contact Information

Weiwei Zhao
Hefei Institutes of Physical Science, Chinese Academy of Sciences
annyzhao@ipp.ac.cn

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How to Cite This Article

APA:
Hefei Institutes of Physical Science, Chinese Academy of Sciences. (2022, August 15). Study reveals mechanism of Cl-initiated oxidation of methacrolein under NOx-free conditions. Brightsurf News. https://www.brightsurf.com/news/LPE5KE08/study-reveals-mechanism-of-cl-initiated-oxidation-of-methacrolein-under-nox-free-conditions.html
MLA:
"Study reveals mechanism of Cl-initiated oxidation of methacrolein under NOx-free conditions." Brightsurf News, Aug. 15 2022, https://www.brightsurf.com/news/LPE5KE08/study-reveals-mechanism-of-cl-initiated-oxidation-of-methacrolein-under-nox-free-conditions.html.