Sustainability and Quality Group of Fruit and Vegetable Products, Murcia Institute of Agri-Food Research and Development, C/ Mayor S/n, La Alberca, 30150, Murcia, Spain.
Department of Agricultural Chemistry, Geology and Pedology, Faculty of Chemistry, University of Murcia, Campus Universitario de Espinardo, 30100, Murcia, Spain.
Chemosphere. 2021 Jul;274:129965. doi: 10.1016/j.chemosphere.2021.129965. Epub 2021 Feb 15.
This work assesses the behavior (adsorption, degradation and leaching) of four insecticides (chlorantraniliprole, thiametoxam, imidacloprid and pirimicarb) and their main reaction intermediates in a clay-loam textured soil (1.6% OM). Following the batch equilibrium method, the K (as log values) ranged from 1.2 to 3.9 (thiametoxam and pirimicarb, respectively). All the insecticides were moderately persistent (t = 39-100 days) in the following order: thiametoxam > imidacloprid > pirimicarb > chlorantraniliprole. Two major transformation products, desmethyl-formamido pirimicarb and desmethyl pirimicarb, were formed as consequence of dealkylation of the parent compound. Using disturbed soil columns only thiametoxam (93% of the initial amount) and imidacloprid (42% of the initial amount) were recovered from leachates. In the case of pirimicarb and chlorantraniliprole, 74% and 30%, respectively, were recovered from the soil. Thiametoxam and imidacloprid can be catalogued as mobile compounds, while pirimicarb and chlorantraniliprole are classified as immobile according to the screening indices used (GUS and ELI). Leachates containing thiametoxam and imidacloprid were subjected to photocatalytic treatment for 240 min using TiO/NaSO with the help of a photochemical reactor equipped with LED lamp. Both compounds had a very fast degradation rate (half-lives ≤ 0.5 min) in deionized water, while their half-lives were 112 min and 178 min, respectively, in leaching water. This implies a strong effect of the water matrix composition, mainly due to organic matter dissolved (quenching). Only traces of thiametoxam urea and hydroxy imidacloprid were detected during the photocatalytic experiment.
本研究评估了四种杀虫剂(氯虫苯甲酰胺、噻虫嗪、吡虫啉和吡丙醚)及其主要反应中间体在粘壤土质地土壤(1.6%有机质)中的行为(吸附、降解和淋溶)。采用批平衡法,K 值(以对数表示)范围为 1.2 至 3.9(分别为噻虫嗪和吡丙醚)。所有杀虫剂在土壤中的半衰期(t)为 39-100 天,降解顺序为:噻虫嗪>吡虫啉>吡丙醚>氯虫苯甲酰胺。由于母体化合物脱烷基化,形成了两种主要的转化产物,即脱甲酰胺基吡丙醚和脱甲醚吡丙醚。使用扰动土柱,仅从淋出液中回收噻虫嗪(初始量的 93%)和吡虫啉(初始量的 42%)。对于吡丙醚和氯虫苯甲酰胺,分别有 74%和 30%从土壤中回收。根据所用筛选指数(GUS 和 ELI),噻虫嗪和吡虫啉可归类为移动性化合物,而吡丙醚和氯虫苯甲酰胺则被归类为非移动性化合物。含有噻虫嗪和吡虫啉的淋出液在装有 LED 灯的光化学反应器的帮助下,使用 TiO/NaSO 进行了 240 分钟的光催化处理。这两种化合物在去离子水中都具有极快的降解速率(半衰期≤0.5 分钟),而在淋出水中的半衰期分别为 112 分钟和 178 分钟。这意味着水基质组成的强烈影响,主要是由于溶解的有机物(猝灭)。在光催化实验过程中仅检测到痕量的噻虫嗪脲和羟基吡虫啉。