调节共价有机框架的表面化学以增强阳离子染料的去除和识别。

IF 3.8 2区 化学 Q1 BIOCHEMICAL RESEARCH METHODS
Analytical and Bioanalytical Chemistry Pub Date : 2025-02-01 Epub Date: 2024-12-09 DOI:10.1007/s00216-024-05687-x
Xiaoli Zhou, Wenjuan Lei, Xiaohuan Qin, Xiaofen Lai, Kun Hu, Shulin Zhao
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引用次数: 0

摘要

同时从水中去除和鉴定痕量阳离子染料污染物既重要又具有挑战性,因为它们具有高度极性和复杂的样品基质。以2,4,6 -三甲酰间苯三酚为原料,以溴化乙啶(EB)为正电荷基,3,5 -二氨基苯甲酸(DABA)为负电荷基,对苯二胺(Pa)为缺电荷基,合成了三个共价有机框架(COFs)。它们分别被命名为EB-COFs、TpPa-1和DP-COFs,并被用作提取和鉴定阳离子染料的吸附剂。考察了三种COFs对亚甲基蓝(MB)和结晶紫(CV)的吸附性能。通过将羧基加入到DP-COFs中,可以有效地调整吸附剂的表面化学性质,从而完全利用选择性阳离子位点。这促进了阳离子染料通过多种吸附机制的动态相互作用,包括静电、π-π和氢键相互作用。DP-COFs对MB和CV具有较高的吸附能力,分别达到383和326 mg g-1。利用吸附等温线、动力学和热力学进一步分析了吸附行为。此外,在激光解吸/电离飞行时间质谱(LDI-TOF MS)中,DP-COFs作为基质可以吸附和直接识别这两种阳离子染料,而不需要洗脱过程。该方法灵敏度高,重现性好,本底干扰小,耐盐性好。MB和CV的检出限分别为0.12和0.04 ng mL-1,与单独使用DP-COFs作为基质相比,分别提高了166倍和225倍。两种染料在加标工业废水和湖泊水样中的回收率为81.4 ~ 111.1%,rsd为1.9 ~ 6.3%。这些结果突出了该方法的高可靠性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulating the surface chemistry of covalent organic frameworks for enhancement cationic dye removal and identification.

Simultaneous removal and identification of trace-level cationic dye pollutants from water is both important and challenging owing to their highly polar and complex sample matrices. In this study, three covalent organic frameworks (COFs) were synthesized using 2, 4, 6-triformylphloroglucinol with ethidium bromide (EB) containing positively charged groups, 3, 5-diaminobenzoic acid (DABA) containing negatively charged groups, and p-phenylenediamine (Pa) lacking charged groups. These were named EB-COFs, TpPa-1, and DP-COFs, respectively, and were employed as adsorbents for the extraction and identification of cationic dyes. The adsorption performance of the three COFs toward methylene blue (MB) and crystal violet (CV) was investigated. By incorporating carboxyl groups into DP-COFs, the surface chemistry of the adsorbent was effectively tailored, enabling complete exploitation of selective cationic sites. This facilitated dynamic interactions with cationic dyes through multiple adsorption mechanisms, including electrostatic, π-π, and H-bonding interactions. DP-COFs exhibited high adsorption capacities for MB and CV, achieving 383 and 326 mg g-1, respectively. The adsorption behavior was further analyzed using adsorption isothermals, kinetics, and thermodynamics. Moreover, DP-COFs were employed as a matrix in laser desorption/ionization time-of-flight mass spectrometry (LDI-TOF MS) to adsorb and directly identify both cationic dyes without the need for an elution process. This approach demonstrated high sensitivity, high reproducibility, low background interference, and excellent salt tolerance. The limits of detection for MB and CV were 0.12 and 0.04 ng mL-1, respectively, representing improvements of 166-fold and 225-fold compared with using DP-COFs solely as a matrix. Recovery rates of both dyes in spiked industrial wastewater and lake water samples ranged from 81.4 to111.1% with RSDs of 1.9-6.3%. These results highlight the high reliability of the proposed method.

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来源期刊
CiteScore
8.00
自引率
4.70%
发文量
638
审稿时长
2.1 months
期刊介绍: Analytical and Bioanalytical Chemistry’s mission is the rapid publication of excellent and high-impact research articles on fundamental and applied topics of analytical and bioanalytical measurement science. Its scope is broad, and ranges from novel measurement platforms and their characterization to multidisciplinary approaches that effectively address important scientific problems. The Editors encourage submissions presenting innovative analytical research in concept, instrumentation, methods, and/or applications, including: mass spectrometry, spectroscopy, and electroanalysis; advanced separations; analytical strategies in “-omics” and imaging, bioanalysis, and sampling; miniaturized devices, medical diagnostics, sensors; analytical characterization of nano- and biomaterials; chemometrics and advanced data analysis.
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