Influence of pesticide mixture on their heterogeneous atmospheric degradation by ozone and OH radicals.

Pesticides in the atmosphere can exist in both gaseous and particulate phases due to their semi-volatile properties. They can undergo degradation when exposed to atmospheric oxidants like ozone and hydroxyl radicals. The majority of studies on the atmospheric reactivity of pesticides study them in combination, without considering potential mixture effects that could induce uncertainties in the results. Therefore, this study aims to address this gap, through laboratory studies using a flow reactor, and by evaluating the degradation kinetics of pendimethalin mixed with folpet, tebuconazole, and S-metolachlor, which were simultaneously adsorbed on hydrophobic silica particles that mimic atmospheric aerosols. The comparison with other mixtures, including pendimethalin, from the literature has shown similar reactivity with ozone and hydroxyl radicals, indicating that the degradation kinetics of pesticides is independent of the mixture. Moreover, the degradation rates of the four pesticides under study indicate that they are not or slightly degraded by ozone, with half-lives ranging from 29 days to over 800 days. In contrast, when exposed to hydroxyl radicals, tebuconazole exhibited the fastest reactivity, with a half-life of 4 days, while pendimethalin had a half-life of 17 days.

Influence of pesticide concentration on their heterogeneous atmospheric degradation by ozone.

A fraction of the atmospheric pesticides can be adsorbed on particles surface according to their physicochemical properties. After adsorption, pesticides can undergo heterogeneous reactivity with atmospheric oxidants such as ozone, but the influence of the pesticide surface coating (i.e., the percentage of the particle surface covered by pesticide molecules) on the degradation kinetics is not well-understood. To estimate the importance of this phenomenon, the influence of the surface coating level in pesticides on the heterogeneous ozonolysis of cyprodinil, deltamethrin, permethrin, and pendimethalin adsorbed on hydrophobic and hydrophilic silicas was investigated. Surface coating level varied from 0.3% to 15% of a monolayer. Generally, the increase of the surface coating level induced a slower degradation of the pesticides above 1%-3% of a monolayer. This decrease was attributed to a shielding effect. More aggregates of pesticides form with increasing surface coating leading to lower accessibility for ozone to the adsorbed pesticide molecules. Moreover, it was observed that the particle type could play a role in the influence of the surface coating level on the degradation rates. Results obtained will contribute to a better understanding of the atmospheric fate of pesticides and semi-volatile organic compounds in the particulate phase and show the importance of working with consistent surface coating level in order to compare the obtained degradation constants.

Heterogeneous degradation of pesticides by OH radicals in the atmosphere: Influence of humidity and particle type on the kinetics.

Pesticides can be adsorbed on the surface of atmospheric aerosol, depending on their physicochemical properties. They can be degraded by atmospheric oxidants such as OH radicals but the influence of some environmental parameters on the degradation kinetics, especially relative humidity and particle surface type, is not well understood. Heterogeneous degradation by OH radicals of eight commonly used pesticides (i.e., difenoconazole, tetraconazole, cyprodinil, fipronil, oxadiazon, pendimethalin, deltamethrin, and permethrin) adsorbed on hydrophobic and hydrophilic silicas at a relative humidity ranging from 0% to 70% was studied. Under experimental conditions, only cyprodinil, deltamethrin, permethrin, and pendimethalin were degraded by OH radical in atmospheric relevant concentration. Second-order kinetic constants calculated for the pesticides degraded by OH radicals ranged from (1.93 ±â€¯0.61) × 10-13 cm3 molecule-1 s-1 (permethrin, hydrophobic silica, 30% RH) to (4.08 ±â€¯0.27) × 10-12 cm3 molecule-1 s-1 (pendimethalin, hydrophilic silica, 0% RH). Results obtained can contribute to improve the understanding of the atmospheric fate of pesticides and other semi-volatile organic compounds in the particulate phase and they highlight the importance of taking humidity and particle type into account for the determination of pesticides atmospheric half-lives.

Heterogeneous atmospheric degradation of pesticides by ozone: Influence of relative humidity and particle type.

In the atmosphere pesticides can be adsorbed on the surface of particles, depending on their physico-chemical properties. They can react with atmospheric oxidants such as ozone but parameters influencing the degradation kinetics are not clear enough. In this study the heterogeneous ozonolysis of eight commonly used pesticides (i.e., difenoconazole, tetraconazole, cyprodinil, fipronil, oxadiazon, pendimethalin, deltamethrin, and permethrin) adsorbed on hydrophobic and hydrophilic silicas, and Arizona dust at relative humidity ranging from 0% to 80% was investigated. Under experimental conditions, only cyprodinil, deltamethrin, permethrin and pendimethalin were degraded by ozone. Second-order kinetic constants calculated for the pesticides degraded by ozone ranged from (4.7 ±â€¯0.4) × 10-20 cm3 molecule-1 s-1 (pendimethalin, hydrophobic silica, 55% RH) to (2.3 ±â€¯0.4) × 10-17 cm3 molecule-1 s-1 (cyprodinil, Arizona dust, 0% RH). Results obtained can contribute to a better understanding of the atmospheric fate of pesticides in the particulate phase and show the importance of taking humidity and particle type into account for the determination of pesticides atmospheric half-lives.