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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  
dc.subject
Reactividad en fase gaseosa  
dc.subject.classification
Físico-Química, Ciencia de los Polímeros, Electroquímica  
dc.subject.classification
Ciencias Químicas  
dc.subject.classification
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