密度泛函理论
水溶液
金属有机骨架
质子化
纳米颗粒
X射线光电子能谱
水溶液中的金属离子
金属
粉末衍射
无机化学
离子
化学
纳米技术
材料科学
物理化学
结晶学
计算化学
有机化学
化学工程
吸附
工程类
作者
Dongmei Jia,Yuejin Li,Huamin Cai,Yongzheng Duan,Jing Li,Ling Chen
出处
期刊:ACS applied nano materials
[American Chemical Society]
日期:2023-04-16
卷期号:6 (8): 6820-6830
被引量:12
标识
DOI:10.1021/acsanm.3c00544
摘要
Capture of heavy metal ions from aqueous solutions is a critical but challenging step in environmental treatment. In this work, NH2-MIL-101(Fe) nanoparticles were synthesized by simple solvothermal methods and applied to capture Cr(VI) anions from aqueous solutions. The results revealed that NH2-MIL-101(Fe) exhibited a high capture capacity (375.2 mg g–1) and an ultrafast capture rate (4 min reaching equilibrium). The competitive effects of coexisting ions such as Cl–, HCO3–, PO43–, Cd2+, Ca2+, and Cu2+ on Cr(VI) are very weak, suggesting that the adsorption selectivity significantly enhanced by loading amino groups on MIL-101(Fe). Density functional theory (DFT) calculation was performed to better understand the adsorption mechanism of Cr(VI), showing that the amino groups could increase the adsorption energy of Cr(VI) for enhancing the adsorption capacity. Based on powder X-ray diffraction, X-ray photoelectron spectroscopy, and DFT calculations, the Cr(VI) capture mechanism by NH2-MIL-101(Fe) nanoparticles was a combination of coordination between Fe and Cr(VI), electrostatic interaction between Cr2O72– and the protonated amino group, and reduction of Cr(VI) to Cr(III).
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