A new approach for studying aqueous phase OH kinetics: application of Teflon waveguides

Bimolecular rate coefficients for the reactions of the hydroxyl radical, OH, with methanol, ethanol, tetrahydrofuran, dimethylmalonate [CH3OC(O)CH2C(O)OCH3], dimethylsuccinate [CH3OC(O)CH2CH2C(O) OCH3], dimethylcarbonate [CH3OC(O)OCH3] and diethylcarbonate [CH3CH2OC(O) OCH2CH3] in aqueous solutions have been measured using a novel experimental approach. The centrepiece of the new experimental technique reported in this work is a Te on AF 2400 liquid core waveguide. The physical properties of the Te on AF 2400 liquid core waveguide allow for the construction of a micro-flowtube reaction photolysis cell with an extremely low volume and a very long optical pathway. Such a reaction system allows for a very sensitive detection of chemical transients in the aqueous phase. The micro-flowtube experiments involved competition kinetics of the OH radical with the organic reactant of interest and an SCN- anion, (k(OH+SCN-) = 1.29 +/- 10(10) M-1 s(-1)).(1) The (SCN)(-)(2) anion was detected using UV-visible spectroscopy following a medium pressure mercury lamp photolysis (lambdagreater than or equal to 366 nm) of H2O/H2O2 /reactant/ KSCN mixtures. All experiments were carried out at room temperature. Measured rate coefficients for the reaction of the OH radical with methanol, ethanol, tetrahydrofuran, dimethylmalonate, dimethylsuccinate, dimethylcarbonate and diethylcarbonate are (units are 10(8) M-1 s(-1)) : k(OH+methanol) = 13 +/- 4, k(OH+ethanol) = 19 +/- 5, k(OH+THF) = 38 +/- 10, k(OH+dimethylmalonate) = 2.7 +/- 0.9, k(OH+dimethylsuccinate) = 5.3 +/- 2.9, k(OH+dimethylcarbonate) = 0.51 +/- 0.22, k(OH+diethylcarbonate) = 7.9 +/- 3.2. Uncertainties in the above expressions are +/- 2sigma and represent precision only. The reported rate coefficients for the reactions of OH with ethanol, methanol and THF agree very well with the currently recommended values. To date, there is no kinetic data reported in the literature for the OH radical reaction with dimethylmalonate, dimethylsuccinate, dimethylcarbonate and diethylcarbonate. The reaction mechanism is briefly discussed as a function of bond energies.