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dc.contributor.author
Blanco, Maria Belen
dc.contributor.author
Barnes, Ian
dc.contributor.author
Wiesen, Peter
dc.contributor.author
Teruel, Mariano Andres
dc.date.available
2018-08-09T21:26:41Z
dc.date.issued
2016-05-20
dc.identifier.citation
Blanco, Maria Belen; Barnes, Ian; Wiesen, Peter; Teruel, Mariano Andres; Atmospheric sink of methyl chlorodifluoroacetate and ethyl chlorodifluoroacetate: Temperature dependent rate coefficients, product distribution of their reactions with Cl atoms and CF2ClC(O)OH formation; Royal Society of Chemistry; RSC Advances; 6; 57; 20-5-2016; 51834-51844
dc.identifier.issn
2046-2069
dc.identifier.uri
http://hdl.handle.net/11336/54900
dc.description.abstract
Rate coefficients as a function of temperature have been measured for the first time for the gas-phase reactions of chlorine atoms with methyl chlorodifluoracetate (k1) and ethyl chlorodifluoroacetate (k2) using the relative rate technique. The experiments were carried out in a 1080 L photoreactor over the temperature range 287-313 K at a total pressure of 1000 ± 10 mbar of synthetic air using in situ FTIR spectroscopy to monitor reactants and products. The following Arrhenius expressions were obtained: k(MCDFA+Cl) = (9.6 ± 5.1) × 10-12exp[-(1363 ± 79)/T] and k(ECDFA+Cl) = (64.4 ± 29.7) × 10-12exp[-(1110 ± 68)/T]. The kinetic results are compared with previous experimental and theoretical studies. In addition, a product study of the reactions of Cl with methyl chlorodifluoracetate and ethyl chlorodifluoroacetate is reported. The results indicate that in the absence of NOx the main fate of the alkoxy radicals formed after H-atom abstraction by Cl from the -CH3 group in methyl chlorodifluoroacetate is reaction of the radical with O2 to form the mixed anhydride CF2ClC(O)OC(O)H. In the case of ethyl chlorodifluoroacetate the main fate of the alkoxy formed via H-atom abstraction by Cl from the -CH2- entity in the ethyl group is α-ester rearrangement to produce chlorodifluoroacetic acid and the corresponding radical. The yields of chlorofluoracetic acid (CF2ClC(O)OH) obtained were as follows: (34 ± 5)% and (86 ± 8)% for the reactions of Cl with CF2ClC(O)OCH3 and CF2ClC(O)OCH2CH3, respectively. The measured yields are rationalized in terms of mechanisms consisting of competitive reaction channels for the formed products in the oxidation, i.e. reaction with O2, α-ester rearrangement and a decomposition pathway. Atmospheric implications are discussed according to the rate coefficients obtained as a function of temperature and altitude, and regarding the formation of chlorofluorocarboxylic acid.
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/2.5/ar/
dc.subject
Cfcs Replacements
dc.subject
Clorofluoroacetates
dc.subject
Kinetics
dc.subject
Mechanisms
dc.subject.classification
Otras Ciencias Químicas
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Ciencias Químicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Atmospheric sink of methyl chlorodifluoroacetate and ethyl chlorodifluoroacetate: Temperature dependent rate coefficients, product distribution of their reactions with Cl atoms and CF2ClC(O)OH formation
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2018-07-30T15:22:39Z
dc.journal.volume
6
dc.journal.number
57
dc.journal.pagination
51834-51844
dc.journal.pais
Reino Unido
dc.journal.ciudad
Cambridge
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: Barnes, Ian. Bergische Universität Wuppertal; Alemania
dc.description.fil
Fil: Wiesen, Peter. Bergische Universität Wuppertal; Alemania
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
RSC Advances
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra03454c
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1039/C6RA03454C
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