Preparation of metal–organic framework nanosheets with electron-rich groups for SO2 adsorption

IF 3.8 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Hongsong Lian, Jin Huang, Yonghua Lai, Huixin Liu, Dongsheng Zheng, Song Xiao, Hongye Yuan
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引用次数: 0

Abstract

Metal–organic frameworks (MOFs), as a new type of porous crystalline materials, hold great promise for gas purification in electrical insulation equipment, especially for the selective capture of SO2 produced from the decomposition of SF6. However, challenges remain in the design and synthesis of MOF-based adsorbents with salient SO2 adsorption performance due to the limited effective interactions with SO2 molecules. This study reports the successful direct synthesis of two-dimensional (2D) MOFs nanosheets coordinated by Zr4+ and tridentate carboxylic organic ligands with nitrogen-containing electron-rich groups within the organic ligands. The resulting MOF nanosheets exhibit enhanced interactions with SO2 molecules due to the spatial location and electronic properties of the nitrogen groups, thereby conducing to the adsorption of SO2. Additionally, by precisely controlling the positioning of nitrogen groups, the Zr-BTB-NH2 (BTB-NH2: 1,1′:3′,1″-Terphenyl]-4,4″-dicarboxylic acid, 3,3″-diamino-5′-(3-amino-4-carboxyphenyl) and Zr-TPY (TPY: 4′-(4-carboxyphenyl)-[2,2′:6′,2″-terpyridine]-5,5″-dicarboxylic acid) MOFs synthesised in this study achieve differentiated SO2 adsorption capacities of 39.3 cm³·g⁻1 and 66.3 cm³·g⁻1, respectively, surpassing those of several previously reported MOFs. This strategy provides a novel design strategy for developing efficient SO2 absorbents and lays a foundation for the further development of absorbents promising for gas remediation in electrical insulation equipment.

Abstract Image

富电子基金属有机骨架纳米片的制备及其对二氧化硫的吸附
金属有机骨架(MOFs)作为一种新型多孔晶体材料,在电气绝缘设备的气体净化,特别是对SF6分解产生的SO2的选择性捕获方面具有很大的应用前景。然而,由于与SO2分子的有效相互作用有限,设计和合成具有显著SO2吸附性能的mof基吸附剂仍然存在挑战。本研究成功地直接合成了由Zr4+与有机配体中含氮富电子基团的三齿羧基有机配体配位的二维(2D) mof纳米片。由于氮基团的空间位置和电子性质,MOF纳米片与SO2分子的相互作用增强,从而促进了SO2的吸附。此外,通过精确控制氮基的定位,本研究合成的Zr-BTB-NH2 (BTB-NH2: 1,1 ':3 ',1″- terphenyl]-4,4″- dicarbolic acid, 3,3″- diam氨基-5 ' -(3-氨基-4-carboxyphenyl)和Zr-TPY (TPY: 4 ' -(4-carboxyphenyl)-[2,2 ':6 ',2″-terpyridine]-5,5″- dicarbolic acid) mfs分别达到39.3 cm³·g毒血症和66.3 cm³·g毒血症的吸附量,超过了之前报道的一些mfs。该策略为开发高效的SO2吸收剂提供了一种新的设计策略,为进一步开发有前途的电气绝缘设备气体修复吸收剂奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
IET Nanodielectrics
IET Nanodielectrics Materials Science-Materials Chemistry
CiteScore
5.60
自引率
3.70%
发文量
7
审稿时长
21 weeks
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