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Artículo

OH and Cl radicals initiated oxidation of Amyl Acetate under atmospheric conditions: Kinetics, products and mechanisms

Straccia Cepeda, Vianni GiovannaIcon ; Blanco, Maria BelenIcon ; Teruel, Mariano AndresIcon
Fecha de publicación: 08/2023
Editorial: Royal Society of Chemistry
Revista: Environmental Science: Atmospheres
e-ISSN: 2634-3606
Idioma: Inglés
Tipo de recurso: Artículo publicado
Clasificación temática:
Físico-Química, Ciencia de los Polímeros, Electroquímica

Resumen

The relative rate coefficients of the gas-phase reaction of amyl acetate, (AA), CH3COO(CH2)4CH3 with OH radicals and Cl atoms were determined at (298 ± 2) K and 1000 mbar of pressure. The experiments were developed in two different atmospheric Pyrex chambers coupled with “in situ” Fourier Transform Infrared (FTIR) spectroscopy and Gas Chromatography equipped with flame ionization detection (GC-FID). The rate coefficients obtained from the average of different experiments were (in units of cm3 molecule−1 s−1): kAA+OH-FTIR = (6.00 ± 0.96) × 10−12; kAA+OH-GC-FID = (6.37 ± 1.50) × 10−12 and kAA+Cl-GC-FID = (1.35 ± 0.14) × 10−10. Additionally, product studies were completed for the Cl-initiated oxidation of AA, in similar conditions of the kinetic experiments by Gas Chromatography coupled with a mass detector (GC-MS) with Solid Phase Micro Extraction (SPME). Acetic acid, formaldehyde, acetaldehyde, propionaldehyde, and butyraldehyde were the main products identified. Complementary Structure Activity Relationships (SAR) were developed to compare with the experimental kinetic results and to clarify the individual reactivity sites of the ester. The atmospheric oxidation pathways of the AA are postulated and discussed taking into account the observed products and the SAR estimations. The initial pathway for the degradation of AA initiated by Cl atoms and OH radicals occurs via H-atom abstraction at -C(O)OCH2- (C1); -CH2- (C2); -CH2- (C3); and -CH2CH3- (C4) moieties. The atmospheric implications of the reactions studied were evaluated by the estimation of their tropospheric lifetimes toward OH radicals and Cl atoms to be: τOH = 22 and τCl = 62 hours. Consequently, the estimated average ozone production ([O3] = 2.15) suggests a potential contribution of these compounds emission to the formation of photochemical smog. On the other hand, the Photochemical Ozone Creation Potential (POCP) for AA was calculated to be POCP = 70.2. A moderate risk of photochemical smog production suggests that this ester could be harmful to the health and the biota in urban environments.
Palabras clave: Esteres insaturados , FTIR in situ , Mecanismos Químicos Atmosféricos , Reactividad en fase gaseosa
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info:eu-repo/semantics/openAccess Excepto donde se diga explícitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)
Identificadores
URI: http://hdl.handle.net/11336/226852
URL: http://pubs.rsc.org/en/Content/ArticleLanding/2023/EA/D3EA00082F
DOI: http://dx.doi.org/10.1039/D3EA00082F
Colecciones
Articulos(INFIQC)
Articulos de INST.DE INVESTIGACIONES EN FISICO- QUIMICA DE CORDOBA
Citación
Straccia Cepeda, Vianni Giovanna; Blanco, Maria Belen; Teruel, Mariano Andres; OH and Cl radicals initiated oxidation of Amyl Acetate under atmospheric conditions: Kinetics, products and mechanisms; Royal Society of Chemistry; Environmental Science: Atmospheres; 3; 10; 8-2023; 1485-1496
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