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原位锚定磁黄铁矿于石墨相氮化碳纳米片以实现铀的高效固定

In Situ Anchoring of Pyrrhotite on Graphitic Carbon Nitride Nanosheet for Efficient Immobilization of Uranium.

机构信息

Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, Harbin Engineering University, Harbin, 150001, P.R. China.

College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin, 150001, P.R. China.

出版信息

Chemistry. 2019 Jan 7;25(2):590-597. doi: 10.1002/chem.201804289. Epub 2018 Dec 11.

Abstract

Enrichment of U is an urgent project for nuclear energy development. Herein, magnetic graphitic carbon nitride nanosheets were successfully prepared by in situ anchoring of pyrrhotite (Fe S ) on the graphitic carbon nitride nanosheet (CNNS), which were used for capturing U . The structural characterizations of Fe S /CNNS-1 indicated that the CNNS could prevent the aggregation of Fe S and the saturation magnetization was 4.69 emu g , which meant that it was easy to separate the adsorbent from the solution. Adsorption experiments were performed to investigate the sorption properties. The results disclosed that the sorption data conformed to the Langmuir isotherm model with the maximum adsorption capacity of 572.78 mg g at 298 K. The results of X-ray photoelectron spectroscopy (XPS) demonstrated that the main adsorption mechanism are as follows: U is adsorbed on the surface of Fe S /CNNS-1 through surface complexation initially, then it was reduced to insoluble U . Thereby, this work provided an efficient and easy to handle sorbent material for extraction of U .

摘要

铀的富集成了核能发展的当务之急。在此,通过将磁硫铁矿(FeS)原位锚定在石墨相氮化碳纳米片(CNNS)上,成功制备了磁性石墨相氮化碳纳米片(FeS/CNNS-1),用于捕获 U。FeS/CNNS-1 的结构特征表明,CNNS 可以防止 FeS 的聚集,饱和磁化强度为 4.69 emu g,这意味着它很容易从溶液中分离出吸附剂。进行了吸附实验以研究吸附性能。结果表明,吸附数据符合 Langmuir 等温线模型,在 298 K 时最大吸附容量为 572.78 mg g。X 射线光电子能谱(XPS)的结果表明,主要的吸附机制如下:U 最初通过表面络合吸附在 FeS/CNNS-1 的表面上,然后被还原为不溶性 U。因此,这项工作为提取 U 提供了一种高效、易于处理的吸附材料。

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