Green and Mild Fabrication of Magnetic Poly(trithiocyanuric acid) Polymers for Rapid and Selective Separation of Mercury(II) Ions in Aqueous Samples.

IF 4.7 3区 工程技术 Q1 POLYMER SCIENCE Polymers Pub Date : 2024-10-31 DOI:10.3390/polym16213067
Qianqian Li, Boxian Ruan, Yue Yu, Linshu Ye, Aoxiong Dai, Sasha You, Bingshan Zhao, Limin Ren
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Abstract

The removal and detection of highly toxic mercury(II) ions (Hg2+) in water used daily is essential for human health and monitoring environmental pollution. Efficient porous organic polymers (POPs) can provide a strong adsorption capacity toward heavy metal ions, although the complex synthetic process and inconvenient phase separation steps limit their application. Hence, a combination of POPs and magnetic nanomaterials was proposed and a new magnetic porous organic polymer adsorbent was fabricated by a green and mild redox reaction in the aqueous phase with trithiocyanuric acid (TA) and its sodium salts acting as reductive monomers and iodine acting as an oxidant. In the preparation steps, no additional harmful organic solvent is required and the byproducts of sodium iodine are generally considered to be non-toxic. The resulting magnetic poly(trithiocyanuric acid) polymers (MPTAPs) are highly porous, have large surface areas, are rich in sulfhydryl groups and show easy magnetic separation ability. The experimental results show that MPTAPs exhibit good adsorption affinity toward Hg2+ with high selectivity, rapid adsorption kinetics (10 min), a large adsorption capacity (211 mg g-1) and wide adsorption applicability under various pH environments (pH 2~8). Additionally, MPTAPs can be reused for up to 10 cycles, and the magnetic separation step of MPTAPs is fast and convenient, reducing energy consumption compared to centrifugation and filtration steps required for non-magnetic adsorbents. These results demonstrate the promising capability of MPTAPs as superior adsorbents for effective adsorption and separation of Hg2+. Based on this, the prepared MPTAPs were adopted as magnetic solid-phase extraction (MSPE) materials for isolation of trace Hg2+ from aqueous samples. Under optimized conditions, the extraction and quantification of trace Hg2+ in water samples were accomplished using inductively coupled plasma mass spectrometry (ICP-MS) detection after MSPE procedures. The proposed MPTAPs-based MSPE-ICP-MS method is efficient, rapid, sensitive and selective for the determination of trace Hg2+, and was successfully employed for the accurate analysis of trace Hg2+ in tap water, wastewater, lake water and river water samples.

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绿色低成本制造磁性聚(三硫氰尿酸)聚合物,用于快速选择性分离水样中的汞(II)离子。
去除和检测日常用水中的剧毒汞(II)离子(Hg2+)对人类健康和监测环境污染至关重要。高效多孔有机聚合物(POPs)对重金属离子具有很强的吸附能力,但其复杂的合成过程和不便的相分离步骤限制了其应用。因此,有人提出将持久性有机污染物与磁性纳米材料相结合,并以三硫氰尿酸(TA)及其钠盐作为还原单体,以碘作为氧化剂,通过水相中绿色温和的氧化还原反应制备出一种新型磁性多孔有机聚合物吸附剂。在制备步骤中,不需要额外的有害有机溶剂,碘钠的副产物通常被认为是无毒的。制备出的磁性聚(三硫氰尿酸)聚合物(MPTAPs)多孔性强、比表面积大、富含巯基,并且易于磁分离。实验结果表明,MPTAPs 对 Hg2+ 具有良好的吸附亲和力,选择性高,吸附动力学快(10 分钟),吸附容量大(211 mg g-1),在各种 pH 环境(pH 2~8)下都有广泛的吸附适用性。此外,MPTAPs 可重复使用多达 10 次,而且与非磁性吸附剂所需的离心和过滤步骤相比,MPTAPs 的磁性分离步骤快捷方便,降低了能耗。这些结果表明,MPTAPs 具有良好的吸附能力,可有效吸附和分离 Hg2+。在此基础上,制备的 MPTAPs 被用作磁性固相萃取(MSPE)材料,用于分离水样中的痕量 Hg2+。在优化的条件下,采用电感耦合等离子体质谱法(ICP-MS)检测了 MSPE 程序后水样中的痕量 Hg2+。所提出的基于 MPTAPs 的 MSPE-ICP-MS 方法具有高效、快速、灵敏和选择性强等特点,可用于自来水、废水、湖水和河水样品中痕量 Hg2+ 的准确分析。
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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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