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 铀 硼 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 Zhao,Yu Yang,Mingzhang Lin
出处
期刊:Separation and Purification Technology [Elsevier BV]
卷期号:305: 122538-122538 被引量:10
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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