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制备亚氨基二乙酸功能化多壁碳纳米管及其作为用于分离和预浓缩重金属离子的吸附剂的应用。

Preparation of iminodiacetic acid functionalized multi-walled carbon nanotubes and its application as sorbent for separation and preconcentration of heavy metal ions.

机构信息

Key Laboratory of Food Nutrition and Safety, Ministry of Education, Tianjin University of Science & Technology, Tianjin 300457, China.

出版信息

J Hazard Mater. 2011 Feb 28;186(2-3):1985-92. doi: 10.1016/j.jhazmat.2010.12.087. Epub 2010 Dec 25.

Abstract

In this paper, a novel material was prepared with functionalizing multi-walled carbon nanotubes (MWCNTs) using iminodiacetic acid (IDA) and characterized by FT-IR. Isotherm and kinetics of adsorption were studied and the experimental data fitted the Langmuir model and pseudo-second-order equation very well. An on-line method for simultaneous determination of trace V (V), Cr (VI), Pb (II), Cd (II), Co (II), Cu (II) and As (III) in biological samples was developed using this material as sorbent coupled with inductively coupled plasma mass spectrometry (ICP-MS). A series of experimental parameters, including sample pH, sample flow rate and loading time, eluting solution and the effect of interfering ions have been investigated systematically. Under the optimum experimental conditions, the enrichment factors for above metal ions were ranged from 66 to 101. Detection limit (3 s) was achieved at 1.3, 1.2, 0.70, 0.40, 2.5, 3.4, 0.79 ng L(-1), respectively. At the 1.0 μg L(-1) level, the precision (RSD, %) for 11 replicate measurements was from 1.0 to 4.0. In spiked biological samples, good recoveries (n=3) were obtained in the range of 90-110%. These results had proved that the proposed method was with good accuracy and could be applied to the analysis of trace metal ions in biological samples.

摘要

本文采用亚氨基二乙酸(IDA)对多壁碳纳米管(MWCNTs)进行功能化,制备了一种新型材料,并通过傅里叶变换红外光谱(FT-IR)进行了表征。研究了吸附的等温线和动力学,实验数据非常好地符合朗缪尔模型和准二级方程。采用该材料作为吸附剂,结合电感耦合等离子体质谱(ICP-MS),建立了一种同时在线测定生物样品中痕量 V(V)、Cr(VI)、Pb(II)、Cd(II)、Co(II)、Cu(II)和 As(III)的方法。系统研究了一系列实验参数,包括样品 pH 值、样品流速和加载时间、洗脱溶液以及干扰离子的影响。在最佳实验条件下,上述金属离子的富集因子范围为 66-101。在 1.3、1.2、0.70、0.40、2.5、3.4、0.79ng L(-1)时,检测限(3s)分别达到。在 1.0μg L(-1)水平下,11 次重复测量的精密度(RSD,%)为 1.0-4.0。在加标生物样品中,回收率(n=3)在 90-110%范围内良好。这些结果证明了该方法具有良好的准确性,可用于生物样品中痕量金属离子的分析。

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