Atmospheric chemistry of CCl₂FCH₂CF₃(HCFC‐234fb): Kinetics and mechanism of reactions with Cl atoms and OH radicals

The atmospheric chemistry of CCl₂FCH₂CF₃ (HFCF-234fb) was examined using FT-IR/relative-rate methods. Hydroxyl radical and chlorine atom rate coefficients of k(CCl₂FCH₂CF₃+OH)= (2.9 ± 0.8) × 10⁻¹⁵ cm³ molecule^–1 s^–1 and k(CCl₂FCH₂CF₃+Cl)= (2.3 ± 0.6) × 10⁻¹⁷ cm³ molecule^–1 s^–1 were determined at 297 ± 2 K. The OH rate coefficient determined here is two times higher than the previous literature value. The atmospheric lifetime for CCl₂FCH₂CF₃ with respect to reaction with OH radicals is approximately 21 years using the OH rate coefficient determined in this work, estimated Arrhenius parameters and scaling it to the atmospheric lifetime of CH₃CCl₃. The chlorine atom initiated oxidation of CCl₂FCH₂CF₃ gives C(O)F₂ and C(O)ClF as stable secondary products. The halogenated carbon balance is close to 80% in our system. The integrated IR absorption cross-section for CCl₂FCH₂CF₃ is 1.87 × 10⁻¹⁶ cm molecule⁻¹ (600–1600 cm⁻¹) and the radiative efficiency was calculated to 0.26 W m⁻² ppb¹. A 100-year Global Warming Potential (GWP) of 1460 was determined, accounting for an estimated stratospheric lifetime of 58 years and using a lifetime-corrected radiative efficiency estimation.