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基于磁性肼连接共价有机骨架的磁性固相萃取-高效液相色谱-电感耦合等离子体质谱联用同时富集和形态分析铅和汞

Simultaneous enrichment and speciation of lead and mercury by magnetic solid-phase extraction coupled to HPLC-ICP-MS based on magnetic hydrazine-linked covalent organic frameworks.

作者信息

Zhang Xiaolai, Li Fangli, Chao Jingbo, Li Zhicai, Zhang Guimin, Zhai Lihai, Hu Ligang, Jiao Heping, Wang Zhenhua

机构信息

College of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, China.

Shandong public health clinic center, Jinan, 250021, China.

出版信息

Anal Chim Acta. 2024 Jun 8;1307:342622. doi: 10.1016/j.aca.2024.342622. Epub 2024 Apr 21.

Abstract

BACKGROUND

Trace levels of organic and inorganic lead and mercury species in the environment, including divalent lead (Pb), trimethyllead (TML), divalent mercury (Hg), monomethylmercury (MeHg), and ethylmercury (EtHg), are highly toxic to humans and ecology. It is of great importance for speciation of lead and mercury to evaluate the toxicity of lead and mercury and their biogeochemistry in the environment. However, simultaneous multi-elemental enrichment and speciation at trace level remains a challenge. There are few reports of simultaneous magnetic solid-phase extraction (MSPE) of organic and inorganic lead and mercury species at trace level in the real water.

RESULTS

In this work, a novel core-shell magnetic hydrazine-linked covalent organic frameworks (FeO@COF-TCH) was prepared for the first time by grafting hydrazine-linked COFs on the FeO nanoparticles. FeO@COF-TCH with abundant thione and imino groups has strong adsorption for lead and mercury species. Based on it, a simple and practical magnetic solid-phase extraction high-performance liquid chromatography-inductively coupled plasma mass spectrometry (MSPE-HPLC-ICP-MS) method was developed for extraction and determination of trace lead and mercury species, including Hg, MeHg, EtHg, Pb and TML. The limits of detection (3δ) of the developed method were 0.08, 0.81, 0.90, 0.56 and 0.88 ng L with the enrichment factors (EFs) of 384, 376, 379, 389 and 360-fold for Pb, TML, Hg, MeHg and EtHg, respectively. The high accuracy and reproducibility have been proved by the spiked recoveries (94.4-103 %) in real samples.

SIGNIFICANCE

The proposed method with simple operation and high sensitivity has been successfully applied to simultaneous speciation of lead and mercury at trace levels in the water samples with complicated matrices, including underground water, surface water, sea water. Meanwhile, it has the advantages of cost-saving, labor-saving and time-saving and is suitable for the investigation and risk assessment in water. The development of MSPE-HPLC-ICP-MS method provides ideas and guidance for the simultaneous multi-elemental enrichment and speciation.

摘要

背景

环境中的痕量有机和无机铅汞物种,包括二价铅(Pb)、三甲基铅(TML)、二价汞(Hg)、一甲基汞(MeHg)和乙基汞(EtHg),对人类和生态具有高毒性。铅汞的形态分析对于评估铅汞的毒性及其在环境中的生物地球化学过程至关重要。然而,痕量水平下的同时多元素富集和形态分析仍然是一个挑战。在实际水样中痕量水平同时进行有机和无机铅汞物种的磁性固相萃取(MSPE)的报道很少。

结果

在这项工作中,首次通过将肼连接的共价有机框架(COF)接枝到FeO纳米颗粒上制备了一种新型的核壳磁性肼连接共价有机框架(FeO@COF-TCH)。具有丰富硫酮和亚氨基的FeO@COF-TCH对铅汞物种具有很强的吸附作用。基于此,开发了一种简单实用的磁性固相萃取高效液相色谱-电感耦合等离子体质谱(MSPE-HPLC-ICP-MS)方法,用于萃取和测定痕量铅汞物种,包括Hg、MeHg、EtHg、Pb和TML。所开发方法的检测限(3δ)分别为0.08、0.81、0.90、0.56和0.88 ng/L,Pb、TML、Hg、MeHg和EtHg的富集因子(EFs)分别为384、376、379、389和360倍。实际样品中的加标回收率(94.4-103%)证明了该方法具有高准确性和重现性。

意义

所提出的方法操作简单、灵敏度高,已成功应用于复杂基质水样(包括地下水、地表水、海水)中痕量铅汞的同时形态分析。同时,它具有节省成本、省力和省时的优点,适用于水体调查和风险评估。MSPE-HPLC-ICP-MS方法的开发为同时多元素富集和形态分析提供了思路和指导。

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