Efficient and selective adsorption of uranium by diamide-pyridine-functionalized hierarchically porous boron nitride

介孔材料 铀酰 氮化硼 吸附 吡啶 单层 人体净化 化学工程 选择性 材料科学 无机化学 核化学 化学 离子 有机化学 催化作用 冶金 工程类 核物理学 物理 生物化学
作者
Peng Zhang,Yizhi Chen,Qiqi Guo,Liu Y,Hanbao Chong,Hanqin Weng,Xing Ling Zhao,Yu Yang,Mingzhang Lin
出处
期刊:Separation and Purification Technology [Elsevier]
卷期号:305: 122538-122538 被引量:8
标识
DOI:10.1016/j.seppur.2022.122538
摘要

• Hierarchically porous boron nitride (HPBN) was modified with diamide pyridine (DAPy). • Assistance of radiation-induced hydroxylation was essential to modify inert HPBN. • Hierarchically porous structure endowed HPBN-DAPy ultrafast adsorption kinetics. • HPBN-DAPy selectively adsorbed U due to the strong affinity between uranyl and DAPy. • HPBN-DAPy retained 86% of the original adsorption amount after 5 cycles. Uranium (U) released by nuclear accident raises concerns about human health owing to its long half-life and toxicity. Diamide-pyridine-modified hierarchically porous boron nitride (HPBN-DAPy) was prepared for efficient removal of U. HPBN, which could hardly adsorb U, gained the ability to uptake U only after functionalization with diamide pyridine (DAPy) groups. The hierarchically mesoporous structure with bimodal mesopores around 20 and 3 nm endowed HPBN-DAPy with unique adsorption kinetic. Uranyl ions (UO 2 2+ ) easily approached the adsorption sites in those large mesopores and thus the adsorption rapidly reached temporary equilibrium within 0.5 min with a relatively high adsorption of amounts ( q e ) of 87.5 mg g −1 (adsorbent dosage = 0.4 g L −1 , [U] 0 = 100 mg L −1 , pH = 4.0 ± 0.1, T = 298 ± 1 K), which was beneficial for rapid decontamination. Small mesopores and the inner large mesopores, which were connected through small mesopores, provided extra adsorption sites, leading to a further increased q e of 115.7 mg g −1 after achieving final equilibrium. Investigation of adsorption mechanism showed that UO 2 2+ were chemically adsorbed in monolayer at a low initial concentration while they were physically adsorbed in the form of polynuclear complexes at a high initial concentration. Benefited from the strong affinity between UO 2 2+ and DAPy, HPBN-DAPy performed excellent selectivity for UO 2 2+ toward other most concerned radionuclide ions. Furthermore, HPBN-DAPy also exhibited adequate salt tolerance and outstanding reusability, which should be promising in removal of U from contaminated water.
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