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一种用于从环境水样和土壤样品中固相微萃取硝基芳香族化合物的三维富氮共轭微孔聚合物。

A three-dimensional nitrogen-rich conjugated microporous polymer for solid-phase microextraction of nitroaromatic compounds from environmental water and soil samples.

作者信息

Zhang Qing, Liu Weihua, Zang Xiaohuan, Zhang Shuaihua, Wang Chun, Wang Zhi

机构信息

Department of Chemistry, College of Science, Hebei Agricultural University, Baoding, 071001, China.

Department of Chemistry, College of Science, Hebei Agricultural University, Baoding, 071001, China; College of Food Science and Technology, Hebei Agricultural University, Baoding, 071001, China.

出版信息

Talanta. 2025 Feb 1;283:127101. doi: 10.1016/j.talanta.2024.127101. Epub 2024 Oct 24.

DOI:10.1016/j.talanta.2024.127101
PMID:39476794
Abstract

Nitroaromatic compounds (NACs), as a kind of important chemical intermediates, are widely used in industrial productions. However, NACs have carcinogenic effect and their residues may pose harm to human health. Therefore, there is necessity to set up effective analytical method to monitor them in some environmental samples. However, because of their low concentrations in real samples, they need to be enriched by an effective adsorbent before the subsequent instrumental detection. In this work, a three-dimensional nitrogen-rich conjugated microporous polymer (DCT-Try-CMP) was synthesized with 3,6-dichloro-1,2,4,5-tetrazine and triptycene as monomers via Friedel-Crafts reaction. It presented a good adsorption capability for the NACs. After optimization, a solid-phase microextraction with DCT-Try-CMP fiber combined with gas chromatography-flame ionization detection for the quantitation of trace NACs in environmental water and soil samples was developed. The limits of detection of the method (S/N = 3) for environmental water and soil samples were 0.08-0.30 μg L and 1.00-5.00 ng g, and the limits of quantification (S/N = 9) were 0.27-0.90 μg L and 3.00-15.0 ng g, respectively. The linear quantification response ranges for the analytes were 0.27-200 μg L and 3.00-1000 ng g for water and soil samples, respectively. For water samples at the analytes concentrations of 5.00, 50.0 and 100 μg L, the method recoveries ranged from 82.2 % to 120 % and for soil samples at the concentrations of 15.0, 200 and 400 ng g, the method recoveries fell in the range from 80.2 % to 120 %. The method provides a sensitive and effective approach for monitoring trace NACs in environmental water and soil samples.

摘要

硝基芳香族化合物(NACs)作为一类重要的化学中间体,被广泛应用于工业生产中。然而,NACs具有致癌作用,其残留可能对人体健康造成危害。因此,有必要建立有效的分析方法来监测某些环境样品中的NACs。然而,由于它们在实际样品中的浓度较低,在后续仪器检测之前需要用有效的吸附剂进行富集。在本研究中,以3,6-二氯-1,2,4,5-四嗪和三蝶烯为单体,通过傅克反应合成了一种三维富氮共轭微孔聚合物(DCT-Try-CMP)。它对NACs表现出良好的吸附能力。经过优化,建立了一种基于DCT-Try-CMP纤维的固相微萃取结合气相色谱-火焰离子化检测法,用于定量分析环境水和土壤样品中的痕量NACs。该方法对环境水和土壤样品(信噪比S/N = 3)的检出限分别为0.08 - 0.30 μg/L和1.00 - 5.00 ng/g,定量限(信噪比S/N = 9)分别为0.27 - 0.90 μg/L和3.00 - 15.0 ng/g。分析物在水样和土壤样品中的线性定量响应范围分别为0.27 - 200 μg/L和3.00 - 1000 ng/g。对于分析物浓度为5.00、50.0和100 μg/L的水样,该方法回收率在82.2%至120%之间;对于浓度为15.0 ng/g、200 ng/g和400 ng/g的土壤样品,该方法回收率在80.2%至120%之间。该方法为监测环境水和土壤样品中的痕量NACs提供了一种灵敏有效的方法。

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