Atmospheric chemistry of (CF3)2CCH2: OH radicals, Cl atoms and O3 rate coefficients, oxidation end-products and IR spectra. Issue 38 (15th September 2015)
- Record Type:
- Journal Article
- Title:
- Atmospheric chemistry of (CF3)2CCH2: OH radicals, Cl atoms and O3 rate coefficients, oxidation end-products and IR spectra. Issue 38 (15th September 2015)
- Main Title:
- Atmospheric chemistry of (CF3)2CCH2: OH radicals, Cl atoms and O3 rate coefficients, oxidation end-products and IR spectra
- Authors:
- Papadimitriou, Vassileios C.
Spitieri, Christina S.
Papagiannakopoulos, Panos
Cazaunau, Mathieu
Lendar, Maria
Daële, Véronique
Mellouki, Abdelwahid - Abstract:
- Abstract : OH, Cl and O3 kinetics and IR spectra of (CF3 )2 CCH2 utilized to estimate tropospheric lifetimes, radiative efficiencies, global warming potentials, estimated photochemical ozone creation potentials and tropospheric oxidation end-products. Abstract : The rate coefficients for the gas phase reactions of OH radicals, k 1, Cl atoms, k 2, and O3, k 3, with 3, 3, 3-trifluoro-2(trifluoromethyl)-1-propene ((CF3 )2 CCH2, hexafluoroisobutylene, HFIB) were determined at room temperature and atmospheric pressure employing the relative rate method and using two atmospheric simulation chambers and a static photochemical reactor. OH and Cl rate coefficients obtained by both techniques were indistinguishable, within experimental precision, and the average values were k 1 = (7.82 ± 0.55) × 10 −13 cm 3 molecule −1 s −1 and k 2 = (3.45 ± 0.24) × 10 −11 cm 3 molecule −1 s −1, respectively. The quoted uncertainties are at 95% level of confidence and include the estimated systematic uncertainties. An upper limit for the O3 rate coefficient was determined to be k 3 < 9.0 × 10 −22 cm 3 molecule −1 s −1 . In global warming potential (GWP) calculations, radiative efficiency (RE) was determined from the measured IR absorption cross-sections and treating HFIB both as long (LLC) and short (SLC) lived compounds, including estimated lifetime dependent factors in the SLC case. The HFIB lifetime was estimated from kinetic measurements considering merely the OH reaction, τ OH = 14.8 days andAbstract : OH, Cl and O3 kinetics and IR spectra of (CF3 )2 CCH2 utilized to estimate tropospheric lifetimes, radiative efficiencies, global warming potentials, estimated photochemical ozone creation potentials and tropospheric oxidation end-products. Abstract : The rate coefficients for the gas phase reactions of OH radicals, k 1, Cl atoms, k 2, and O3, k 3, with 3, 3, 3-trifluoro-2(trifluoromethyl)-1-propene ((CF3 )2 CCH2, hexafluoroisobutylene, HFIB) were determined at room temperature and atmospheric pressure employing the relative rate method and using two atmospheric simulation chambers and a static photochemical reactor. OH and Cl rate coefficients obtained by both techniques were indistinguishable, within experimental precision, and the average values were k 1 = (7.82 ± 0.55) × 10 −13 cm 3 molecule −1 s −1 and k 2 = (3.45 ± 0.24) × 10 −11 cm 3 molecule −1 s −1, respectively. The quoted uncertainties are at 95% level of confidence and include the estimated systematic uncertainties. An upper limit for the O3 rate coefficient was determined to be k 3 < 9.0 × 10 −22 cm 3 molecule −1 s −1 . In global warming potential (GWP) calculations, radiative efficiency (RE) was determined from the measured IR absorption cross-sections and treating HFIB both as long (LLC) and short (SLC) lived compounds, including estimated lifetime dependent factors in the SLC case. The HFIB lifetime was estimated from kinetic measurements considering merely the OH reaction, τ OH = 14.8 days and including both OH and Cl chemistry, τ eff = 10.3 days. Therefore, GWP(HFIB, OH) and GWP(HFIB, eff) were estimated to be 4.1 (LLC) and 0.6 (SLC), as well as 2.8 (LLC) and 0.3 (SLC) for a hundred year time horizon. Moreover, the estimated photochemical ozone creation potential ( ε POCP ) of HFIB was calculated to be 4.60. Finally, HCHO and (CF3 )2 C(O) were identified as final oxidation products in both OH- and Cl-initiated oxidation, while HC(O)Cl was additionally observed in the Cl-initiated oxidation. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 17:Issue 38(2015)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 17:Issue 38(2015)
- Issue Display:
- Volume 17, Issue 38 (2015)
- Year:
- 2015
- Volume:
- 17
- Issue:
- 38
- Issue Sort Value:
- 2015-0017-0038-0000
- Page Start:
- 25607
- Page End:
- 25620
- Publication Date:
- 2015-09-15
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c5cp03840e ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1814.xml