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用于从二次资源中高效回收金(III)的MIL-161金属有机框架:性能、机理及密度泛函理论计算

MIL-161 Metal-Organic Framework for Efficient Au(III) Recovery from Secondary Resources: Performance, Mechanism, and DFT Calculations.

作者信息

Hu Guangyuan, Wang Zhiwei, Zhang Weiye, He Hongxing, Zhang Yi, Deng Xiujun, Li Weili

机构信息

Department of Chemical Science and Technology, Kunming University, Kunming 650214, China.

出版信息

Molecules. 2023 Jul 17;28(14):5459. doi: 10.3390/molecules28145459.

Abstract

The recovery of precious metals from secondary resources is significant economically and environmentally. However, their separation is still challenging because they often occur in complex metal ion mixtures. The poor selectivity of adsorbents for gold in complicated solutions prevents further application of adsorption technology. In this study, a Zr-based MOF adsorbent, MIL-161, was synthesized using s-tetrazine dicarboxylic acid (HSTz) as an organic ligand. MIL-161 demonstrated a high adsorption capacity of up to 446.49 mg/g and outstanding selectivity for gold(III) in a simulated electronic waste solution as a result of the presence of sulfur- and nitrogen-containing groups. In addition, the MIL-161 adsorbents were characterized using Fourier transform infrared (FT-IR), field emission scanning electron microscopy (FESEM), thermogravimetric analysis (TG), Brunner-Emment-Teller (BET), and X-ray photoelectron spectroscopy (XPS). Additionally, the adsorption kinetics, isotherms, and thermodynamics of the MOF adsorbents were also thoroughly examined. More importantly, the experimental results and DFT calculations indicate that chelation and electrostatic interactions are the main adsorption mechanisms.

摘要

从二次资源中回收贵金属在经济和环境方面都具有重要意义。然而,它们的分离仍然具有挑战性,因为它们经常存在于复杂的金属离子混合物中。吸附剂在复杂溶液中对金的选择性较差,这阻碍了吸附技术的进一步应用。在本研究中,以均四嗪二羧酸(HSTz)为有机配体合成了一种锆基金属有机框架吸附剂MIL-161。由于含硫和含氮基团的存在,MIL-161在模拟电子废物溶液中表现出高达446.49 mg/g的高吸附容量和对金(III)的出色选择性。此外,使用傅里叶变换红外光谱(FT-IR)、场发射扫描电子显微镜(FESEM)、热重分析(TG)、布鲁诺尔-埃米特-泰勒(BET)和X射线光电子能谱(XPS)对MIL-161吸附剂进行了表征。此外,还对金属有机框架吸附剂的吸附动力学、等温线和热力学进行了深入研究。更重要的是,实验结果和密度泛函理论(DFT)计算表明,螯合作用和静电相互作用是主要的吸附机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f64/10384270/3bb1fe7c3351/molecules-28-05459-sch001.jpg

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