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以新型铁包裹聚酰胺-胺-羟基磁性纳米粒子作为固相萃取吸附剂进行预富集后,用火焰原子吸收光谱法测定不同茶叶样品中痕量铜和钴。

Determination of copper and cobalt in different tea samples at trace levels by FAAS after preconcentration with a novel iron PAMAM-OH-encapsulated magnetic nanoparticle as SPE sorbent.

作者信息

Yılmaz Özge, Koyuncu İkbal

机构信息

Faculty of Arts and Sciences, Department of Chemistry, Yıldız Technical University, Esenler, İstanbul, Türkiye.

出版信息

Anal Sci. 2024 Apr;40(4):633-641. doi: 10.1007/s44211-023-00495-2. Epub 2024 Jan 22.

Abstract

Environmental contamination caused by heavy metals is a significant global concern. The presented study investigated the efficiency of iron PAMAM-OH encapsulated magnetic nanoparticles (Fe-MNP-G2-OH) as sorbent for the preconcentration of copper and cobalt from tea samples. High metal-chelating ethylenediamine core polyamidoethanol generation-2 (PAMAM-G2-OH) was encapsulated with iron oxide (FeO) to synthesize the sorbent. Limit of detection (LOD) values for copper and cobalt extracted and detected by the developed Fe-MNP-G2-OH -SPE-FAAS method were 0.52 and 1.1 μg L, respectively. There were 230- and 101-fold improvement in detection limits for copper and cobalt, respectively, when compared to direct FAAS measurement. The percent recovery results for the analytes in green and black tea samples ranged from 93 to 107%, with low relative standard deviation (%RSD) values. The synthesis of nanoparticle was carried out through a unique method, which was characterized by thermogravimetric analysis (TGA), scanning electron microscope (SEM), and Fourier transform infrared spectroscopy (FTIR) methods. The analytical results demonstrated the applicability and effectiveness of Fe-MNP-G2-OH nanoparticles on the preconcentration of copper and cobalt from tea samples and the developed method is suitable for the trace detection of heavy metals by FAAS method. To the best our knowledge, this is the first study where copper and cobalt in green and black tea samples were extracted by Fe-MNP-G2-OH adsorbent and precipitation of the adsorbent during its synthesis was carried out in acetone medium rather than aqueous one.

摘要

重金属造成的环境污染是一个重大的全球问题。本研究调查了铁包裹的聚酰胺-胺羟基磁性纳米颗粒(Fe-MNP-G2-OH)作为从茶叶样品中预富集铜和钴的吸附剂的效率。将具有高金属螯合能力的乙二胺核心第二代聚酰胺乙醇(PAMAM-G2-OH)用氧化铁(FeO)包裹以合成吸附剂。采用所开发的Fe-MNP-G2-OH -SPE-FAAS方法萃取并检测铜和钴,其检测限(LOD)值分别为0.52和1.1 μg/L。与直接火焰原子吸收光谱法(FAAS)测量相比,铜和钴的检测限分别提高了230倍和101倍。绿茶和红茶样品中分析物的回收率结果在93%至107%之间,相对标准偏差(%RSD)值较低。纳米颗粒的合成通过一种独特的方法进行,该方法通过热重分析(TGA)、扫描电子显微镜(SEM)和傅里叶变换红外光谱(FTIR)方法进行表征。分析结果证明了Fe-MNP-G2-OH纳米颗粒在从茶叶样品中预富集铜和钴方面的适用性和有效性,所开发的方法适用于通过FAAS法对重金属进行痕量检测。据我们所知,这是第一项使用Fe-MNP-G2-OH吸附剂萃取绿茶和红茶样品中的铜和钴且在合成吸附剂时沉淀过程在丙酮介质而非水介质中进行的研究。

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