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合成磷酸化超交联聚合物及其在水中对铀的高效吸附。

Synthesis of phosphorylated hyper-cross-linked polymers and their efficient uranium adsorption in water.

机构信息

Key Laboratory of Superlight Materials & Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China.

Key Laboratory of Superlight Materials & Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, China; Yantai Research Institute and Graduate School of Harbin Engineering University, Yantai 264006, China.

出版信息

J Hazard Mater. 2021 Oct 5;419:126538. doi: 10.1016/j.jhazmat.2021.126538. Epub 2021 Jun 29.

Abstract

Uranium (U) is hazardous and radioactive, wastewater containing U(VI) should be treated before being discharged. Here, two novel uranium adsorbents, phosphorylated hyper-cross-linked bisphenol A (PHCP-1) and fluorene-9-bisphenol (PHCP-2) were separately synthesized via Friedel-Crafts reaction followed by phosphorylation using phosphorus oxychloride. PHCPs had a BET surface area (up to 564 m/g) with pore sizes of 2.2-2.8 nm. These adsorbents were used for the first time for uranium adsorption from water and demonstrated outstanding adsorption performance. PHCP-2 had a great uranium adsorption capacity (297.14 mg/g) and a very fast sorption rate (85% removal rate within 5 min). The adsorption data were well fitted with Freundlich isotherm and the pseudo-second-order kinetic model. PHCPs displayed selective adsorption capacity for U(VI) from solution that including a variety of competing metal ions. The reusability was confirmed through three regeneration cycles. Based on a series of spectroscopic analyses, the mechanism of action between PHCPs and U(VI) is primarily derived from the complex between phosphate functional groups and U (VI). The sorption performance of PHCPs is attributed to their huge specific surface area and the strong complex between phosphate groups and U(VI). These findings suggest that PHCPs could be useful in the effective adsorption of uranium from water.

摘要

铀(U)是一种危险的放射性物质,含六价铀(U(VI))的废水在排放前应进行处理。在此,我们通过 Friedel-Crafts 反应分别合成了两种新型铀吸附剂:磷酰化超交联双酚 A(PHCP-1)和芴-9-双酚(PHCP-2),然后使用三氯氧磷进行磷酰化。PHCPs 的比表面积(高达 564 m/g),孔径为 2.2-2.8 nm。这些吸附剂首次被用于从水中吸附铀,并表现出优异的吸附性能。PHCP-2 具有很大的铀吸附容量(297.14 mg/g)和非常快的吸附速率(5 分钟内去除率达到 85%)。吸附数据与 Freundlich 等温线和拟二级动力学模型拟合良好。PHCPs 对包括多种竞争金属离子在内的溶液中 U(VI)表现出选择性吸附能力。通过三个再生循环证实了其可重复使用性。基于一系列光谱分析,PHCPs 与 U(VI)之间的相互作用机制主要源于磷酸根官能团与 U(VI)之间的络合。PHCPs 的吸附性能归因于其巨大的比表面积和磷酸基团与 U(VI)之间的强络合作用。这些发现表明,PHCPs 可能在从水中有效吸附铀方面具有应用潜力。

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