Magnetic solid-phase extraction for speciation of mercury based on thiol and thioether-functionalized magnetic covalent organic frameworks nanocomposite synthesized at room temperature

化学 吸附 固相萃取 检出限 Mercury(编程语言) 色谱法 解吸 萃取(化学) 共价有机骨架 纳米复合材料 样品制备 共价键 有机化学 化学工程 程序设计语言 工程类 计算机科学
作者
Ruixiang Bi,Fangli Li,Jingbo Chao,Houhuan Dong,Xiaolai Zhang,Zhenhua Wang,Bing Li,Ning Zhao
出处
期刊:Journal of Chromatography A [Elsevier BV]
卷期号:1635: 461712-461712 被引量:54
标识
DOI:10.1016/j.chroma.2020.461712
摘要

A simple and practical magnetic solid-phase extraction high-performance liquid chromatography-inductively coupled plasma mass spectrometry (MSPE-HPLC-ICP-MS) method for extraction and determination of trace mercury species, including inorganic mercury (IHg), monomethylmercury (MeHg) and ethylmercury (EtHg), was developed. The MSPE adsorbent, urchin-like thiol and thioether-functionalized magnetic covalent organic frameworks (Fe3O4@COF-S-SH), was synthesized by coating covalent organic frameworks (COFs) on the surface of Fe3O4 nanoparticles at room temperature and then easily grafting 1,2-Ethanedithiol on the COFs. The as-prepared Fe3O4@COF-S-SH has strong adsorption capacity for IHg, MeHg and EtHg, with excellent static adsorption capacity: 571, 559 and 564 mg g−1, respectively. The parameters influencing the extraction and enrichment had been optimized, including pH, adsorption and desorption time, composition and amount of the eluent, co-existing ions and dissolved organic materials etc. Under the optimized condition, the limit of detection (3δ) of the proposed method were 0.96, 0.17 and 0.47 ng L−1 for IHg, MeHg and EtHg, and the developed method has high actual enrichment factors of 370, 395, 365-fold for IHg, MeHg and EtHg based on 200 mL samples, respectively. The high accuracy and reproducibility has been proved by the spiked recoveries (96.0‒108 %) in real water samples and determination of the certified reference material. Both the adsorption and desorption process can be completed within 5 min. The proposed method with simple operation, short pre-concentration time and high sensitivity has been successfully applied to mercury speciation at trace levels in the samples with complicated matrices, including underground water, surface water, sea water and fish samples.
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