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Atmospheric sink of β-ocimene and camphene initiated by Cl atoms: kinetics and products at NO x free-air.


ABSTRACT: Rate coefficients for the gas-phase reactions of Cl atoms with β-ocimene and camphene were determined to be (in units of 10-10 cm3 per molecule per s) 5.5 ± 0.7 and 3.3 ± 0.4, respectively. The experiments were performed by the relative technique in an environmental chamber with FTIR detection of the reactants at 298 K and 760 torr. Product identification experiments were carried out by gas chromatography with mass spectrometry detection (GC-MS) using the solid-phase microextraction (SPME) method employing on-fiber carbonyl compound derivatization with o-(2,3,4,5,6-pentafluorobenzyl) hydroxylamine hydrochloride. An analysis of the available rates of addition of Cl atoms and OH radicals to the double bond of alkenes and cyclic and acyclic terpenes with a conjugated double bond at 298 K is presented. The atmospheric persistence of these compounds was calculated taking into account the measured rate coefficients. In addition, tropospheric chemical mechanisms for the title reactions are postulated.

SUBMITTER: Gaona-Colman E 

PROVIDER: S-EPMC9083264 | biostudies-literature | 2018 Jul

REPOSITORIES: biostudies-literature

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Atmospheric sink of β-ocimene and camphene initiated by Cl atoms: kinetics and products at NO <sub><i>x</i></sub> free-air.

Gaona-Colmán Elizabeth E   Blanco María B MB   Barnes Ian I   Wiesen Peter P   Teruel Mariano A MA  

RSC advances 20180731 48


Rate coefficients for the gas-phase reactions of Cl atoms with β-ocimene and camphene were determined to be (in units of 10<sup>-10</sup> cm<sup>3</sup> per molecule per s) 5.5 ± 0.7 and 3.3 ± 0.4, respectively. The experiments were performed by the relative technique in an environmental chamber with FTIR detection of the reactants at 298 K and 760 torr. Product identification experiments were carried out by gas chromatography with mass spectrometry detection (GC-MS) using the solid-phase microe  ...[more]

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