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使用基于活性炭的离子印迹吸附剂通过固相萃取法对痕量铜(II)进行预富集。

Preconcentration of trace amount Cu(II) by solid-phase extraction method using activated carbon-based ion-imprinted sorbent.

作者信息

Turan Kübra, Saygili Canlidinç Rukiye, Kalfa Orhan Murat

机构信息

Department of Chemistry, Science and Art Faculty, Kütahya Dumlupınar University, Kütahya, Turkey.

出版信息

Turk J Chem. 2021 Dec 24;46(2):550-566. doi: 10.3906/kim-2110-41. eCollection 2022.

Abstract

In this study, preconcentration conditions of trace amounts of copper ions were investigated with solid-phase extraction (SPE) method by synthesizing activated carbon-based ion-imprinted sorbent (Cu(II)-IAC) with a novel and selective approach. Flame atomic absorption spectrometry (FAAS) was used for the determination of metal ions concentrations. For the characterization of the sorbents, scanning electron microscopy, energy dispersive X-ray (SEM/EDX) analysis, and Fourier transform infrared spectroscopy (FTIR) were used. Optimum conditions for the SPE procedure, various parameters such as pH value, eluent type and concentration, sample volume, sample flow rate, adsorption capacity, and selectivity were studied. The adsorption isotherm was analyzed by Freundlich and Langmuir isotherm, and the maximum adsorption capacity was found to be 142.9 and 312.5 mg/g for activated carbon-based nonimprinted (Cu(II)-non-IAC) and Cu(II)-IAC sorbents, respectively from the Langmuir isotherm. Limit of determination (LOD) and limit of quantification (LOQ) values were found to be 0.038 and 0.113 μg/L, respectively for Cu(II)-IAC sorbent, and the results were compared with the literature. The accuracy and validity of the proposed method were evaluated by the determination of Cu(II) ions from tap water samples and certified reference materials (CRMs) (soft drinking water ERML-CA021e and NIST 1643e) analysis. Good and quantitative recoveries were obtained for the spiked analysis.

摘要

在本研究中,采用固相萃取(SPE)法,通过一种新颖且具有选择性的方法合成基于活性炭的离子印迹吸附剂(Cu(II)-IAC),研究痕量铜离子的预富集条件。采用火焰原子吸收光谱法(FAAS)测定金属离子浓度。使用扫描电子显微镜、能量色散X射线(SEM/EDX)分析和傅里叶变换红外光谱(FTIR)对吸附剂进行表征。研究了SPE程序的最佳条件,包括pH值、洗脱剂类型和浓度、样品体积、样品流速、吸附容量和选择性等各种参数。通过Freundlich和Langmuir等温线分析吸附等温线,根据Langmuir等温线,基于活性炭的非印迹(Cu(II)-non-IAC)和Cu(II)-IAC吸附剂的最大吸附容量分别为142.9和312.5 mg/g。Cu(II)-IAC吸附剂的测定限(LOD)和定量限(LOQ)值分别为0.038和0.113 μg/L,并将结果与文献进行了比较。通过对自来水样品和有证标准物质(CRMs)(软质饮用水ERML-CA021e和NIST 1643e)的分析测定Cu(II)离子,评估了所提出方法的准确性和有效性。加标分析获得了良好的定量回收率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df36/10734765/3326e74cfeac/turkjchem-46-2-550f1.jpg

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