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磁性纳米粒子与腐殖酸的相互作用:在表面活性剂存在的情况下。

Magnetic Nanoparticles Interaction with Humic Acid: In the Presence of Surfactants.

机构信息

State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences , Beijing 100012, China.

Key Laboratory of Integrated Regulation and Resources Development on Shallow Lakes, Ministry of Education, College of Environment, Hohai University , Nanjing 210098, People's Republic of China.

出版信息

Environ Sci Technol. 2016 Aug 16;50(16):8640-8. doi: 10.1021/acs.est.6b01749. Epub 2016 Jul 27.

Abstract

Adsorbed humic acid (HA) on surfaces of nanoparticles (NPs) will affect their transport, transfer, and fate in the aquatic environment, especially in the presence of surfactants, and thereby potentially alter exposures and bioavailable fractions of NPs and surfactants. This study investigated adsorption of HA on Fe3O4 NPs in the presence or absence of surfactant. Surfactant established a bridge connecting HA and Fe3O4 NPs, and significantly changed adsorption behavior of HA on NPs. Adsorption of HA in the absence of surfactant was 120.3 mg/g, but 350.0 mg/g and 146.5 mg/g in the present of CTAB (hexadecyl trimethylammonium bromide) and SDS (sodium dodecyl sulfate), respectively. Surfactants can form different stages (hemimicelles, mixed hemimicelles and admicelles) on Fe3O4 NPs by electrostatic and hydrophobic interactions, adsorption of HA was different for each of those stages. Adsorption of HA on surface of Fe3O4 NPs/CTAB was codetermined by hydrophobic, electrostatic interactions and ligand exchange. The presence of CTAB or SDS changed mechanisms for adsorption and effects of functional groups. Results of Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) indicated that carbohydrate carbon was important in adsorption of HA on Fe3O4 NPs in the presence of surfactants.

摘要

吸附在纳米颗粒(NPs)表面上的腐殖酸(HA)会影响它们在水环境中的迁移、转化和归宿,特别是在存在表面活性剂的情况下,从而可能改变 NPs 和表面活性剂的暴露和生物可利用分数。本研究调查了在存在或不存在表面活性剂的情况下,HA 在 Fe3O4 NPs 上的吸附。表面活性剂在 HA 和 Fe3O4 NPs 之间建立了桥梁,并显著改变了 HA 在 NPs 上的吸附行为。在不存在表面活性剂的情况下,HA 的吸附量为 120.3mg/g,但在存在 CTAB(十六烷基三甲基溴化铵)和 SDS(十二烷基硫酸钠)的情况下,分别为 350.0mg/g 和 146.5mg/g。表面活性剂可以通过静电和疏水相互作用在 Fe3O4 NPs 上形成不同的阶段(半胶束、混合半胶束和混合胶束),HA 的吸附对每个阶段都不同。HA 在 Fe3O4 NPs/CTAB 表面上的吸附是由疏水、静电相互作用和配体交换共同决定的。CTAB 或 SDS 的存在改变了吸附的机制和官能团的作用。傅里叶变换红外(FTIR)和 X 射线光电子能谱(XPS)的结果表明,在存在表面活性剂的情况下,碳水化合物碳在 HA 吸附到 Fe3O4 NPs 上的过程中起着重要作用。

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