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腐殖酸诱导富勒烯 nC 纳米颗粒的弱附着,以及随后在饱和多孔介质中溶液离子强度降低时的脱附。

Humic acid induced weak attachment of fullerene nC nanoparticles and subsequent detachment upon reduction of solution ionic strength in saturated porous media.

机构信息

Department of Soil and Water Sciences, China Agricultural University, Beijing 100193, China.; College of Land and Environment, Shenyang Agricultural University, Shenyang, Liaoning 110866, China.

Department of Soil and Water Sciences, China Agricultural University, Beijing 100193, China.

出版信息

J Contam Hydrol. 2020 May;231:103630. doi: 10.1016/j.jconhyd.2020.103630. Epub 2020 Feb 21.

Abstract

Sand column experiments were performed under saturated conditions to investigate impact of humic acid (HA) on attachment of nC nanoparticles (NPs) in NaCl and CaCl at ionic strengths (ISs) from 1 mM to 100 mM and subsequent detachment via reducing solution IS. The attachment increased with increasing IS due to reduced repulsive Derjaguin-Landau-Verwey-Overbeek (DLVO) interaction energy and accordingly increased retention in primary energy wells. More attachments occurred in CaCl compared to NaCl because Ca exhibited greater charge screen ability and served as a bridging agent between the NPs and sand surfaces. The presence of HA significantly reduced nC NPs attachment on sand surfaces (especially on nanoscale physical heterogeneities) in 10 mM NaCl and 1 mM CaCl because of enhanced electrostatic and steric repulsions. Interestingly, although the HA did not cause reduction of attachment in 100 mM NaCl and 10 mM CaCl compared to the case in absence of HA, the HA caused weak attachment of nC on sand surfaces and then much more significant detachment by decreasing IS. The HA did not alter both attachment and detachment in 100 mM CaCl, because the Ca at the high concentration caused formation of very stable complex of HA and NPs, and strong interaction of the complex with the sand surfaces via cation bridge. Our study highlighted that the HA can not only enhance the transport of NPs by inhibiting attachment as revealed in the literature, but also by the continuous capture and release of the NPs from surfaces in subsurface environments.

摘要

在饱和条件下进行沙柱实验,研究腐殖酸(HA)对 nC 纳米颗粒(NPs)在 NaCl 和 CaCl 中的附着的影响,离子强度(IS)从 1 mM 到 100 mM,随后通过降低溶液 IS 进行脱附。由于排斥德加古林-兰德沃维尔-奥弗贝克(DLVO)相互作用能降低,附着随 IS 的增加而增加,因此在初级能量阱中的保留增加。与 NaCl 相比,CaCl 中发生更多的附着,因为 Ca 表现出更大的电荷屏蔽能力,并在 NPs 和沙表面之间充当桥接剂。由于静电和空间排斥的增强,HA 的存在显著降低了 nC NPs 在 10 mM NaCl 和 1 mM CaCl 中的沙表面附着(特别是在纳米级物理不均匀性上)。有趣的是,尽管与没有 HA 的情况相比,HA 没有导致 100 mM NaCl 和 10 mM CaCl 中的附着减少,但 HA 通过降低 IS 导致 nC 在沙表面的弱附着,然后导致更显著的脱附。HA 没有改变 100 mM CaCl 中的附着和脱附,因为高浓度的 Ca 导致 HA 和 NPs 的非常稳定的复合物的形成,以及通过阳离子桥与沙表面的复合物的强相互作用。我们的研究强调,HA 不仅可以通过抑制附着来增强 NPs 的迁移,如文献中所揭示的那样,还可以通过在地下环境中从表面连续捕获和释放 NPs 来增强。

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