4.6 Article

Kinetics of CF3CH2OCH3 (HFE-263fb2), CHF2CF2CH2OCH3 (HFE-374pcf), and CF3CF2CH2OCH3 (HFE-365mcf3) with OH radicals, IR absorption cross sections, and global warming potentials

Journal

PHYSICAL CHEMISTRY CHEMICAL PHYSICS
Volume 24, Issue 23, Pages 14354-14364

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cp00160h

Keywords

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Funding

  1. regional government of Castilla-La Mancha through CINEMOL project [SBPLY/19/180501/000052]
  2. University of Castilla-La Mancha - UCLM (Ayudas para la financiacion de actividades de investigacion dirigidas a grupos) [2020-GRIN-29016, 2021-GRIN-31279]
  3. UCLM (Plan Propio de Investigacion)
  4. European Regional Development Fund
  5. CINEMOL project

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Hydrofluoroethers (HFEs) have been proposed as third-generation replacements for perfluorocarbons (PFCs) and hydrofluorocarbons (HFCs) due to their environmental benefits. This study focuses on the temperature and pressure dependencies of the reaction rate coefficients of three HFEs. The results show that there is no pressure dependence observed within the range studied, and the reaction rates can be described by mathematical models. Additionally, the impact of these HFEs on climate change is found to be negligible.
Hydrofluoroethers (HFEs), such as CF3CH2OCH3 (HFE-263fb2), CHF2CF2CH2OCH3 (HFE-374pcf), and CF3CF2CH2OCH3 (HFE-365mcf3), have been proposed in the last few decades as the third-generation replacements for perfluorocarbons (PFCs) and hydrofluorocarbons (HFCs) because of their zero stratospheric ozone depletion potentials and relatively low global warming potentials (GWPs). These GWPs depend on the radiative efficiency (RE) and the atmospheric lifetime (tau(OH)) of HFEs due to the reaction with hydroxyl (OH) radicals. The temperature and pressure dependencies of the OH-rate coefficient (k(OH)(T)) for HFE-263fb2, HFE-374pcf, and HFE-365mcf3 are not known. Therefore, in this paper, we present the first study on the temperature (263-353 K) and pressure (50-500 torr of helium) dependence of k(OH)(T) for the titled HFEs. No pressure dependence of k(OH)(T) was observed in the investigated range. From k(OH)(298 K), estimated tau(OH) are 17 days (for HFE-263fb2), 12 days (for HFE-374pcf), and 13 days (for HFE-365mcf3). The observed T-dependencies of k(OH)(T) (in cm(3) molecule(-1) s(-1)) are well described by (3.88 +/- 0.89) x 10(-12) exp[-(508 +/- 69)/T] for HFE-263fb2, (2.81 +/- 0.33) x 10(-12) exp[-(312 +/- 35)/T] for HFE-374pcf, and (2.60 +/- 0.31) x 10(-12) exp[-(319 +/- 35)/T] for HFE-365mcf3. A correlation between log k(OH)(298 K) and the activation energy (E-a) of the process is presented, allowing the prediction of E-a for OH-reactions with other HFEs, exclusively investigated at room temperature. In addition to the kinetic measurements, the infrared absorption cross sections of HFE-263fb2, HFE-374pcf, and HFE-365mcf3 were determined between 520 and 3100 cm(-1). Lifetime corrected REs and GWPs relative to CO2 at 100 years' time horizon were reexamined. The impact of the investigated HFEs on the radiative forcing of climate change would be negligible.

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