首页> 外文期刊>Journal of Analytical Atomic Spectrometry >Ti-containing mesoporous silica packed microcolumn separation/preconcentration combined with inductively coupled plasma-mass spectrometry for the determination of trace Cr, Cu, Cd and Pb in environmental samples
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Ti-containing mesoporous silica packed microcolumn separation/preconcentration combined with inductively coupled plasma-mass spectrometry for the determination of trace Cr, Cu, Cd and Pb in environmental samples

机译:含钛的介孔二氧化硅填充微柱分离/预浓缩-电感耦合等离子体质谱法测定环境样品中的痕量Cr,Cu,Cd和Pb

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摘要

Ti-containing mesoporous silica was prepared and characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), ultraviolet-visible spectrometry (UV-Vis) and the N_2 adsorption technique. The adsorption behaviours of Cr(Ⅲ), Cu(Ⅱ), Cd(Ⅱ) and Pb(Ⅱ) on Ti-containing mesoporous silica were studied and the adsorption mechanism was also investigated by FT-IR and X-ray photoelectron spectroscopy (XPS). With Ti-containing mesoporous silica as the adsorbent, a new method of microcolumn solid phase extraction (SPE) combined with inductively coupled plasma-mass spectrometry (ICP-MS) was established for the determination of Cr(Ⅲ), Cu(Ⅱ), Cd(Ⅱ) and Pb(Ⅱ) in environmental samples. The parameters affecting extraction and desorption of the target analytes, such as pH, sample flow rate, desorption reagent, desorption flow rate and sample volume, were investigated. Under optimized conditions, the limits of detection (LODs) of Cr(Ⅲ), Cu(Ⅱ), Cd(Ⅱ) and Pb(Ⅱ) were 19, 39, 7 and 13 pg mL~(-1) with a preconcentration factor of 10, respectively, and the relative standard deviations (RSDs) varied from 6.1 to 7.3% (n = 7, c = 1 ng mL~(-1)). The developed method was applied to analyze environmental water and soil samples with recovery in the range of 85-119% for the spiked samples. In order to validate the accuracy of the method, certified reference materials of GSBZ50009-88 (environmental water), GBW07429 and GBW07425 (soil sample) were analyzed and the determined values were in good agreement with the certified values. The developed method is simple, rapid, sensitive and suitable for the analysis of trace elements in environmental samples with complex matrices.
机译:制备了含钛的介孔二氧化硅,并通过扫描电子显微镜(SEM),透射电子显微镜(TEM),X射线衍射(XRD),傅里叶变换红外光谱(FT-IR),紫外可见光谱(UV-Vis)对其进行了表征。 )和N_2吸附技术。研究了Cr(Ⅲ),Cu(Ⅱ),Cd(Ⅱ)和Pb(Ⅱ)在含Ti介孔二氧化硅上的吸附行为,并通过FT-IR和X射线光电子能谱(XPS)研究了其吸附机理。 )。以含钛的介孔二氧化硅为吸附剂,建立了微柱固相萃取-电感耦合等离子体质谱法(ICP-MS)测定铬(Ⅲ),铜(Ⅱ),环境样品中的Cd(Ⅱ)和Pb(Ⅱ)。研究了影响目标分析物提取和解吸的参数,例如pH,样品流速,解吸试剂,解吸流速和样品量。在优化条件下,Cr(Ⅲ),Cu(Ⅱ),Cd(Ⅱ)和Pb(Ⅱ)的检出限(LOD)为19、39、7和13 pg mL〜(-1),且具有预富集因子的相对标准偏差(RSD)分别从10%下降到6.1%至7.3%(n = 7,c = 1 ng mL〜(-1))。该方法用于分析环境水和土壤样品,加标样品的回收率在85-119%之间。为了验证该方法的准确性,对GSBZ50009-88(环境水),GBW07429和GBW07425(土壤样品)的认证参考材料进行了分析,测定值与认证值高度吻合。该方法简便,快速,灵敏,适用于复杂基质环境样品中痕量元素的分析。

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  • 来源
    《Journal of Analytical Atomic Spectrometry》 |2015年第6期|1386-1394|共9页
  • 作者单位

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

    Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, P. R. China;

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