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杂化聚集金属氧化物和粘土对氧化石墨烯吸附四环素的影响。

Effects of heteroaggregation with metal oxides and clays on tetracycline adsorption by graphene oxide.

机构信息

College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control, Ministry of Education, Hunan University, Changsha 410082, PR China.

College of Environmental Science and Engineering, Hunan University, Changsha 410082, PR China; Key Laboratory of Environmental Biology and Pollution Control, Ministry of Education, Hunan University, Changsha 410082, PR China.

出版信息

Sci Total Environ. 2020 Jun 1;719:137283. doi: 10.1016/j.scitotenv.2020.137283. Epub 2020 Feb 26.

Abstract

Multiple nanoparticles (NPs) often coexist in water with contaminants, which inevitably affect the fate and transport of coexisted contaminants and other types of nanoparticles in actual water. This research was devoted to examine the adsorption of tetracycline (TC) on graphene oxide (GO) in the presence of different amounts of model engineered and natural NPs (m-NPs), including metal oxides (ZnO and FeO), clays (kaolin and montmorillonite). The experimental results proved that the existence of m-NPs greatly enhanced the TC adsorption onto GO except for that at FeO/GO = 10:1 and lengthened the adsorption equilibrium time. The enhanced adsorption amount of TC with increasing m-NPs/GO ratio was primarily due to the adsorption of TC onto m-NPs. In contrast, the slightly inhibitory effects by 10:1 FeO/GO could be attributed to the blockage effect on GO surface by a small amount of FeO. Compared with five m-NPs/adsorbents, m-NPs/GO had the greatest promoting efficiency on TC removal. Moreover, the heteroaggregation of GO with different m-NPs was studied in aqueous phase by microscopic, spectroscopic, and computational methods. Analysis showed that the electrostatic attraction between negatively charged GO and positively charged ZnO were likely to first heteroaggregate in binary systems of GO and ZnO, while GO were prone to homoaggregate owing to electrostatic repulsion with the same negatively charged montmorillonite (or kaolin). Besides, FeO tended to first homoaggregate and then heteroaggregate with GO. In summary, this report elucidated complex interactions between GO and m-NPs, which was crucial to fundamentally understand towards a predictive framework for describing the fate and migration of GO and m-NPs in actual water.

摘要

多种纳米粒子(NPs)经常与污染物共存于水中,这不可避免地影响共存污染物以及实际水中其他类型纳米粒子的命运和迁移。本研究致力于考察四环素(TC)在不同量的模型工程纳米粒子和天然纳米粒子(m-NPs)存在下在氧化石墨烯(GO)上的吸附,包括金属氧化物(ZnO 和 FeO)、粘土(高岭土和蒙脱石)。实验结果证明,除了在 FeO/GO=10:1 时,m-NPs 的存在极大地增强了 TC 对 GO 的吸附,并延长了吸附平衡时间。随着 m-NPs/GO 比例的增加,TC 吸附量的增强主要归因于 TC 对 m-NPs 的吸附。相比之下,少量 FeO 对 10:1 FeO/GO 的轻微抑制作用可能归因于少量 FeO 对 GO 表面的堵塞作用。与五种 m-NPs/吸附剂相比,m-NPs/GO 对 TC 去除的促进效率最大。此外,通过微观、光谱和计算方法研究了不同 m-NPs 与 GO 的异质聚集。分析表明,带负电荷的 GO 与带正电荷的 ZnO 之间的静电吸引可能首先在 GO 和 ZnO 的二元体系中异质聚集,而由于与带相同负电荷的蒙脱石(或高岭土)之间的静电排斥,GO 更倾向于同聚。此外,FeO 倾向于首先同聚,然后与 GO 异质聚集。总之,本报告阐明了 GO 和 m-NPs 之间的复杂相互作用,这对于从根本上理解描述 GO 和 m-NPs 在实际水中的命运和迁移的预测框架至关重要。

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