Abstract
AbstractIn this study, the gas phase reaction of chlorine atoms with three first‐generation oxidation products of monoterpene: (myrtenal C10H14O, nopinone C9H14O, and ketolimonene C9H14O) were investigated using a relative technique method. These compounds result from the atmospheric oxidation of monoterpene compounds such as α/β – pinene and limonene. Experiments were performed at temperature range 298–353 K and atmospheric pressure in synthetic air bath gas. Cl atoms were generated by UV photolysis of dichloride (Cl2). The reaction was followed using a proton‐transfer reaction mass spectrometer (PTR‐MS) and/or Fourier‐transform infrared spectroscopy (FTIR) to monitor the concentrations of the investigated species simultaneous with several reference compounds as a function of time. The rate constants were obtained and the Arrhenius expressions (cm3 molecule−1 s−1) obtained were established over the temperature range of 298–353 K:knopinone + Cl = (5.0 ± 1.2) × 10−10 exp ( − (406 ± 78) /T)kketolimonene + Cl = (8.88 ± 1.3) × 10−10 exp( − (246 ± 46)/T)kmyrtenal + Cl = (13.5 ± 6.4) × 10−10 exp( − (535 ± 153)/T)Based on rate constants, the atmospheric lifetimes (τ) of targeted compounds with respect to reaction with chlorine atoms were estimated and expected to be less than 1 day. There results led to conclude that the reaction with chlorine atoms can be an effective tropospheric loss pathway mainly in regions presenting relatively high chlorine concentrations.
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