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Heterogeneous kinetics of the OH-initiated degradation of fenthion and parathion.

TLDR
In this paper , the authors investigated the heterogeneous kinetics of the OH-initiated degradation of surface-bound fenthion and parathion using a flow reactor, and they showed that OH radicals played an important role in the atmospheric degradation of Fenthion.
Abstract
Fenthion and parathion are two representative kinds of organophosphorus pesticides and widely used in agriculture. They are directly or indirectly released into the atmosphere by spraying or volatilization processes. However, their heterogeneous reactivity toward OH radicals has not yet been well understood. Therefore, this work investigated the heterogeneous kinetics of the OH-initiated degradation of surface-bound fenthion and parathion using a flow reactor. The results showed that OH radicals played an important role in the atmospheric degradation of fenthion and parathion. Their average rate constants were (7.20 ± 0.77) × 10−12 and (10.40 ± 0.60) × 10−12 cm3 molecule−1 s−1 at a relative humidity (RH) and temperature of 35% and 20 °C, respectively, suggesting that they have relatively short lifetimes in the atmosphere. In addition, a negative RH dependence and a positive temperature dependence of the rate constants were observed. The Arrhenius expressions of fenthion and parathion were k2 = (1.34 ± 0.48) × 10−9exp[−(1432.59 ± 105.29)/T] and k2 = (1.96 ± 1.38) × 10−9exp[−(1619.98 ± 222.02)/T], respectively, and their overall activation energy was estimated to be (11.88 ± 0.87) and (13.48 ± 1.83) kJ mol−1. The experimental results will update the kinetic data of fenthion and parathion in the atmosphere and be helpful to further understand their atmospheric transportation processes.

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Sulfur-functionalized porphyrin-based covalent organic framework as a metal-free dual-functional catalyst for photodegradation of organophosphorus pesticides under visible-LED-light.

TL;DR: In this paper , a polysulfide-functionalized porphyrinic covalent organic framework (COF) with elemental sulfur under solvent-free conditions was used for the degradation of diazinon and parathion using visible-LED-light.
References
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Journal ArticleDOI

Chemistry of secondary organic aerosol: Formation and evolution of low-volatility organics in the atmosphere

TL;DR: A review of the chemistry of the formation and continuing transformation of low-volatility species in the atmosphere can be found in this article, where the primary focus is chemical processes that can change the volatility of organic compounds: oxidation reactions in the gas phase, reaction in the particle phase, and reaction in either phase over several generations.
Journal ArticleDOI

Elucidating severe urban haze formation in China

TL;DR: A periodic cycle of PM episodes in Beijing is demonstrated that is governed by meteorological conditions and characterized by two distinct aerosol formation processes of nucleation and growth, but with a small contribution from primary emissions and regional transport of particles.
Journal ArticleDOI

Tropospheric ozone: Seasonal behavior, trends, and anthropogenic influence

TL;DR: In this paper, two modes of seasonal behavior are noted for surface ozone at mid-latitudes: a broad summer maximum within a few hundred km of industrial/urban areas in Europe and the U.S., and a minimum in summer or autumn in sparcely populated regions that are remote from industrial activity.
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