有机磷农药在土壤中的降解,特别是在非需氧土壤条件下。

Environmental quality and safety Pub Date : 1975-01-01
C Tomizawa
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引用次数: 0

摘要

有机磷农药通常通过氧化、还原、水解、羟基化、脱氯化氢、脱烷基、甲基化、异构化和共轭形成等反应转化。虽然农药在土壤中的降解过程是复杂的,但主要因素可能是土壤成分、土壤微生物区系和农药的化学结构。化学结构对有机磷农药的土壤代谢尤为重要,因为上述反应的优先级是决定的。虽然有机磷农药通常是可水解的,但水解的顺序因化学结构而异。可以说,分子的水解速率越慢,受到非水解反应攻击的可能性就越大。在这种情况下,氧化和还原对有机磷农药的降解至关重要。水田淹水土壤为硝基等不稳定取代基有机磷农药的减少提供了有利的环境。淹水土壤的还原阈值表示为氧化还原电位。水稻土的Eh随季节和土壤类型,特别是有机质含量的不同,有较大的波动。通过对倍硫磷、二硫磷、Kitazin P(0,0-二异丙基S-苄基磷硫代盐)、edifenphos(0-乙基S-二苯基磷硫代盐)和amprophos(0-乙基0-(2-硝基对甲苯基)n -异丙基磷硫代盐)的室内实验表明,上述几种因素参与了有机磷农药的降解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Degradation of organophosphorus pesticides in soils with special reference to unaerobic soil conditions.

Organophosphorus pesticides are generally transformed by the reactions including oxidation, reduction, hydrolysis, hydroxylation, dehydrochlorination, dealkylation, methylation, isomerization, and conjugate formation. Although the degradation process of pesticides in soils is complicated, main factors may be soil constituents, soil microflora, and chemical structures of pesticides. Chemical structures are especially important for soil metabolism of organophosphorus pesticides, because the priority of the reactions mentioned above is decided. Although organophosphorus pesticides are generally hydrolyzable, the order of hydrolysis varies with chemical structures. It might be said that the slower the hydrolysis rate of the molecule, the more the possibility to be attacked by reactions other than hydrolysis. In such cases, oxidation and reduction are primarily important for the degradation of organophosphorus pesticides. Flooded soils in paddy fields give a favourable environment for the reduction of organophosphorus pesticides having labile substituents such as nitro groups. The threshold of reduction in-flooded soil is expressed as redox potential. Eh, the Eh of paddy soil fluctuates to a great extent, depending on seasons and soil types, especially organic matter content. The result of laboratory experiments with fenthion, disulfoton, Kitazin P (0,0-diisopropyl S-benzyl phosphorothiolate), edifenphos (0-ethyl S,S-diphenyl phosphorodithiolate) and amiprophos (0-ethyl 0-(2-nitro-p-tolyl) N-isopropyl phosphoramidothionate) suggested the participation of several factors mentioned above in the degradation of organophosphorus pesticides.

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