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dc.contributor.author
Straccia Cepeda, Vianni Giovanna
dc.contributor.author
Blanco, Maria Belen
dc.contributor.author
Teruel, Mariano Andres
dc.date.available
2024-02-14T13:49:34Z
dc.date.issued
2023-08
dc.identifier.citation
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
dc.identifier.uri
http://hdl.handle.net/11336/226852
dc.description.abstract
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.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Royal Society of Chemistry
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
Esteres insaturados
dc.subject
FTIR in situ
dc.subject
Mecanismos Químicos Atmosféricos
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Reactividad en fase gaseosa
dc.subject.classification
Físico-Química, Ciencia de los Polímeros, Electroquímica
dc.subject.classification
Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
OH and Cl radicals initiated oxidation of Amyl Acetate under atmospheric conditions: Kinetics, products and mechanisms
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2024-02-09T12:17:54Z
dc.identifier.eissn
2634-3606
dc.journal.volume
3
dc.journal.number
10
dc.journal.pagination
1485-1496
dc.journal.pais
Reino Unido
dc.description.fil
Fil: Straccia Cepeda, Vianni Giovanna. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Blanco, Maria Belen. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.description.fil
Fil: Teruel, Mariano Andres. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Córdoba. Instituto de Investigaciones en Físico-química de Córdoba. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas. Instituto de Investigaciones en Físico-química de Córdoba; Argentina
dc.journal.title
Environmental Science: Atmospheres
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2023/EA/D3EA00082F
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/D3EA00082F
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