Abstract

Gas-phase reactions with the hydroxyl radical (OH) are expected to be an important removal pathway of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F) in the atmosphere. Our laboratory recently developed a system to measure the rate constants of the gas-phase reactions of OH with semivolatile organic compounds using on-line mass spectrometry. We have now incorporated electron capture mass spectrometry (EC-MS) into this system to increase its sensitivity to PCDD/F, which tend to have low vapor pressures. OH reaction rate constants were determined in helium for 1,2,3,4-tetrachlorodibenzo-p-dioxin at 373−432 K using a heated quartz reaction chamber. The photolysis of O3 in the presence of H2O and the photolysis of H2O2 (both at λ = 254 nm) served as OH sources. An extrapolation using the Arrhenius equation gives a 1,2,3,4-tetrachlorodibenzo-p-dioxin−OH reaction rate constant of 8.5 × 10-13 cm3 s-1 at 298 K, which is in excellent agreement with the value predicted by a structure−activity method. The predicted OH reaction rate constants for tetra- through octachlorodibenzo-p-dioxin and dibenzofuran isomers were used in a simple model of the atmospheric removal of PCDD/F. The results of our model indicate that atmospheric removal is a combination of gas-phase removal processes of lower chlorinated dioxins and furans and particle-phase removal processes of higher chlorinated ones.

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