Artículo

Atmospheric degradation of chloroacetoacetates by Cl atoms: Reactivity, products and mechanism in coastal and industrialized areas

Straccia Cepeda, Vianni Giovanna Icon; Lugo Garcia, Pedro Luis Icon; Rivela Fretes, Cynthia Beatriz Icon; Blanco, Maria Belen Icon; Teruel, Mariano Andres Icon

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Fecha

09/2023

Editorial

Pergamon-Elsevier Science Ltd

Revista

Atmospheric Environment

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Institución organizadora

ISSN

1352-2310

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ISBN

Idioma

Inglés

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Clasificación temática

Resumen

Kinetic studies of the reaction of Cl atoms with ethyl 2-chloroacetoacetate, CH3C(O)CHClC(O)OCH2CH3, (k1) and methyl 2-chloroacetoacetate, CH3C(O)CHClC(O)OCH3, (k2) have been developed for the first time using SPME/GC-FID and in situ FTIR spectroscopy at (298 ± 2) K and 1000 mbar in glass atmospheric chambers. Relative rate coefficients obtained by Fourier Transform Infrared Spectroscopy (FTIR) using different reference compounds, were the following (in cm3.molecule−1.s−1): kE2CAA-FTIR= (2.41 ± 0.57) × 10−10 and kM2CAA-FTIR= (2.16 ± 0.85) × 10−10. Similar and reproducible values were obtained using Gas Chromatography equipped with Flame Ionization Detection coupled with Solid Phase Micro Extraction (SPME), kE2CAA-GC-FID = (2.54 ± 0.81) × 10−10 and kM2CAA-GC-FID = (2.34 ± 0.87) × 10−10 all values in units of cm3.molecule−1.s−1. In addition, product studies were performed in similar conditions to the kinetic experiments to identify the reaction products and postulate their tropospheric degradation mechanisms. The reaction of Cl atoms with saturated esters initiates via H-atom abstraction from the alkyl groups of the molecule. Formyl chloride, chloroacetone, and acetyl chloride were positively identified as reaction products by FTIR. On the other hand, acetyl chloride, 1,1,1-trichloropropan-2-one, 1,1-dichloropropan-2-one, 1-chloropropan-2-one, ethyl chloroformate, and methyl chloroformate were identified by the GC-MS technique. Structure–Activity Relationship (SAR), calculations were also performed to estimate the more favorable reactions pathways in agreement with the products observed. The atmospheric implications of these reactions were assessed by the estimation of the residence times of the chloroesters studied as following: τCl-E2CAA = 1.47 days, and τCl-M2CAA = 1.57 days. Additionally, the possible impact of the emission of chloro acetoacetates in rain acidification was evaluated from the moderate Acidification Potentials (AP), 0.19, and 0.21 obtained for E2CAA and M2CAA, respectively.

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