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腐殖酸增强胶体和磷在饱和多孔介质中的共迁移。

Humic acid enhances the co-transport of colloids and phosphorus in saturated porous media.

机构信息

College of Land Science and Technology, China Agricultural University, Beijing, 100083, PR China.

College of Land Science and Technology, China Agricultural University, Beijing, 100083, PR China.

出版信息

Chemosphere. 2024 Sep;364:143300. doi: 10.1016/j.chemosphere.2024.143300. Epub 2024 Sep 7.

Abstract

Phosphorus (P) has been widely recognized as a substance that is difficult to transport due to its tendency to become easily fixed in the soil. However, many reports demonstrate that groundwater P pollution is rising in humus-rich areas. Research is urgently needed to confirm (or reject) the hypothesis that increased P pollution is related to humus, as there is currently limited quantitative research on this topic. In this study, we conducted a series of batch equilibrium adsorption-desorption experiments and column experiments to quantify the effects of montmorillonite colloids (MCs) and humic acids (HCs, the main components of humus) on the P transport behavior. The results indicate that P's adsorption and desorption behavior on MCs can be well simulated using the Langmuir and Temkin models (R > 0.91). Compared to the non-HC treatments, HCs significantly increased MCs' P adsorption and desorption capacity 5.18 and 7.21 times, respectively. Moreover, HCs facilitated the transport ability of the MC-P mixture through the saturated quartz sand column. In a 0.1 M NaCl solution, the MC-P mixture is nearly completely adsorbed on the surface of quartz sand, with a penetration rate of only 0.5%. In contrast, the HC-MC-P mixture can evidently penetrate further at a rate of 26.1%. The transport parameters fitted using HYDRUS-1D further indicated that the presence of humic acids significantly decreased the deposition coefficients of colloids, thereby enhancing the co-transport of colloids and P through the quartz sand porous medium. The potential mechanism of P pollution in humus-rich areas is likely enhanced by the formation of an HC-colloid-P mixture, which greatly increases the adsorption amount of P on colloids and enhances the electrostatic and spatial repulsion between colloids as well as between colloids and quartz sand. It reduces the aggregation and adsorption of colloids, ultimately transferring P into groundwater through colloid-facilitated co-transport. The findings of this study clarified the relationship between the transport of P, colloids, and HCs, which provides a theoretical basis for explaining the P pollution mechanism in humus-rich areas.

摘要

磷(P)由于其在土壤中易固定的倾向而被广泛认为是一种难以迁移的物质。然而,许多报告表明,富含有机质地区的地下水 P 污染正在上升。需要进行研究来确认(或否定)增加的 P 污染与腐殖质有关的假说,因为目前针对这一主题的定量研究有限。在这项研究中,我们进行了一系列批平衡吸附-解吸实验和柱实验,以量化蒙脱石胶体(MCs)和腐殖酸(HCs,腐殖质的主要成分)对 P 迁移行为的影响。结果表明,P 在 MCs 上的吸附和解吸行为可以用 Langmuir 和 Temkin 模型很好地模拟(R>0.91)。与非 HC 处理相比,HCs 分别显著增加了 MCs 的 P 吸附和解吸容量 5.18 倍和 7.21 倍。此外,HCs 促进了 MC-P 混合物在饱和石英砂柱中的传输能力。在 0.1 M NaCl 溶液中,MC-P 混合物几乎完全被吸附在石英砂表面,穿透率仅为 0.5%。相比之下,HC-MC-P 混合物的穿透率明显更高,为 26.1%。使用 HYDRUS-1D 拟合的传输参数进一步表明,腐殖酸的存在显著降低了胶体的沉积系数,从而增强了胶体和 P 通过石英砂多孔介质的共传输。富含有机质地区 P 污染的潜在机制可能是由于形成 HC-胶体-P 混合物而增强,这大大增加了胶体对 P 的吸附量,并增强了胶体之间以及胶体与石英砂之间的静电和空间排斥作用。它减少了胶体的聚集和吸附,最终通过胶体促进的共传输将 P 转移到地下水中。本研究结果阐明了 P、胶体和 HCs 传输之间的关系,为解释富含有机质地区 P 污染机制提供了理论依据。

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