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氨氯吡啶酸和氯氨吡啶酸的吸附、解吸和淋溶比较。

Comparative sorption, desorption and leaching potential of aminocyclopyrachlor and picloram.

机构信息

Departamento de Agronomia, Universidade Estadual de Maringá (UEM), Maringá, Paraná, Brazil.

出版信息

J Environ Sci Health B. 2013;48(12):1049-57. doi: 10.1080/03601234.2013.824291.

Abstract

Sorption and desorption of aminocyclopyrachlor (6-amino-5-chloro-2-cyclopropylpyrimidine-4-carboxylic acid) were compared to that of the structurally similar herbicide picloram (4-amino-3,5,6-trichloro-2-pyridinecarboxylic acid) in three soils of differing origin and composition to determine if picloram data is representative of aminocyclopyrachlor behavior in soil. Aminocyclopyrachlor and picloram batch sorption data fit the Freundlich equation and was independent of concentration for aminocyclopyrachlor (1/n = 1), but not for picloram (1/n = 0.80-0.90). Freundlich sorption coefficients (K f) for aminocyclopyrachlor were lowest in the eroded and depositional Minnesota soils (0.04 and 0.12 μmol ((1-1/n)) L(1/n) kg(-1)) and the highest in Molokai soil (0.31 μmol ((1-1/n)) L(1/n) kg(-1)). For picloram, K f was lower in the eroded (0.28 μmol ((1-1/n)) L(1/n) kg(-1)) as compared to the depositional Minnesota soil (0.75 μmol ((1-1/n)) L(1/n) kg(-1)). Comparing soil to soil, K f for picloram was consistently higher than those found for aminocyclopyrachlor. Desorption of aminocyclopyrachlor and picloram was hysteretic on all three soils. With regard to the theoretical leaching potential based on groundwater ubiquity score (GUS), leaching potential of both herbicides was considered to be similar. Aminocyclopyrachlor would be ranked as leacher in all three soils if t1/2 was > 12.7 days. To be ranked as non-leacher in all three soils, aminocyclopyrachlor t1/2 would have to be <3.3 days. Calculated half-life that would rank picloram as leacher was calculated to be ∼15.6 d. Using the current information for aminocycloprachlor, or using picloram data as representative of aminocycloprachlor behavior, scientists can now more accurately predict the potential for offsite transport of aminocycloprachlor.

摘要

比较了 3 种不同来源和组成的土壤中氨氯吡啶酸(6-氨基-5-氯-2-环丙基嘧啶-4-羧酸)和类似结构的除草剂草甘膦(4-氨基-3,5,6-三氯-2-吡啶羧酸)的吸附和解吸情况,以确定草甘膦数据是否能代表氨氯吡啶酸在土壤中的行为。氨氯吡啶酸和草甘膦的批量吸附数据符合 Freundlich 方程,且氨氯吡啶酸的浓度不影响 1/n 值(1/n = 1),而草甘膦的 1/n 值为 0.80-0.90(1/n = 0.80-0.90)。氨氯吡啶酸在侵蚀和沉积的明尼苏达州土壤中的 Freundlich 吸附系数(K f)最低(0.04 和 0.12 μmol(1-1/n)L(1/n)kg(-1)),在莫洛凯土壤中的最高(0.31 μmol(1-1/n)L(1/n)kg(-1))。草甘膦在侵蚀土壤中的 K f (0.28 μmol(1-1/n)L(1/n)kg(-1))低于沉积的明尼苏达州土壤(0.75 μmol(1-1/n)L(1/n)kg(-1))。相比之下,土壤对土壤,草甘膦的 K f 始终高于氨氯吡啶酸。在所有 3 种土壤中,氨氯吡啶酸和草甘膦的解吸均表现出滞后性。根据地下水普遍得分(GUS),基于理论淋溶潜力,这两种除草剂的淋溶潜力被认为是相似的。如果半衰期(t1/2)大于 12.7 天,氨氯吡啶酸将在所有 3 种土壤中被归类为淋溶物。如果要在所有 3 种土壤中被归类为非淋溶物,氨氯吡啶酸的半衰期(t1/2)必须小于 3.3 天。半衰期为 15.6 d,可将草甘膦归类为淋溶物。使用氨氯吡啶酸的当前信息,或使用草甘膦数据作为氨氯吡啶酸行为的代表,科学家现在可以更准确地预测氨氯吡啶酸场外迁移的可能性。

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