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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Hybrid mesoporous materials for on-line preconcentration of Cr(VI) followed by one-step scheme for elution and colorimetric determination at ultratrace levels
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Hybrid mesoporous materials for on-line preconcentration of Cr(VI) followed by one-step scheme for elution and colorimetric determination at ultratrace levels

机译:在线预富集六价铬(Cr)的混合介孔材料,然后一步法进行超痕量洗脱和比色测定

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摘要

An hybrid mesoporous material synthesised in our laboratories for solid phase extraction (SPE) in flow through systems has been used for analytical purposes. The solid was obtained from mesoporous silica MCM-41 functionalized with 3-aminopropyltriethoxy silane by Sol-Gel methodology. In order to exploit the large sorption capacity of the material together with the possibility of modeling it for anions retention. a microcolumn (MC) filled with the solid was inserted in a flow system for preconcentration of Cr(VI) and its determination at ultratrace levels in natural waters. The analytical methodology involved a reverse flow injection system (rFI) holding a MC filled with the solid for the analyte extraction. Elution and colorimetric detection were carried out with 1-5 diphenylcarbazide (DPC) in sulfuric acid. DPC produced the reduction of Cr(VI) to Cr(III) together with the generation of a cationic red complex between Cr(Ill) and 1-5 diphenylcarbazone which was easily eluted and detected with a visible spectro photo meter. Moreover, the filling material got ready for the next sample loading remaining unspoiled for more than 300 cycles. The effect of several variables on the analytical signal as well as the influence of cationic and anionic interferences were discussed. Particular attention was given to sulfuric acid interference since it is the required media for the complex generation. Under optimal conditions, 99.8% of Cr(VI) recovery was obtained for a preconcentration time of 120 s (sample and DPC flow rates = 1 mL min(-1)) and an elution volume of 250 mu L. The limit of detection (3s) was found to be 0.09 mu g L-1 Cr(VI) with a relative standard deviation (n = 10, 3 mu g L-1) of 1.8. Since no Cr(III) was retained by the solid material and Cr(VI) was completely adsorbed, electrothermal atomic absorption spectrometry (ET AAS) determinations of Cr(III) were also performed by simply measuring its concentration at the end of the microcolumn after Cr(VI) retention by the mesoporous solid. Applications to the determination of Cr(VI) and Cr(III) in natural waters and the validation of the methodology were also studied. (C) 2008 Elsevier B.V. All rights reserved.
机译:在我们的实验室中合成的杂化介孔材料用于流过系统的固相萃取(SPE)已用于分析目的。通过Sol-Gel方法从用3-氨基丙基三乙氧基硅烷官能化的中孔二氧化硅MCM-41获得固体。为了利用该材料的大吸附能力以及对它进行阴离子保留建模的可能性。将充满固体的微柱(MC)插入流动系统中以进行Cr(VI)的预浓缩,并在天然水中以超痕量水平进行测定。该分析方法涉及一个反向流动注射系统(rFI),该系统装有一个充满固体的MC以便进行分析物提取。洗脱和比色检测是在硫酸中用1-5二苯卡巴肼(DPC)进行的。 DPC可以将Cr(VI)还原为Cr(III),并在Cr(III)和1-5二苯基卡巴zone之间生成阳离子红色络合物,可以很容易地用可见分光光度计洗脱和检测。此外,填充材料已准备好用于下一个样品加载,并且在300个以上的循环中保持不变。讨论了几个变量对分析信号的影响以及阳离子和阴离子干扰的影响。特别注意硫酸干扰,因为它是生成复杂化合物的必需介质。在最佳条件下,以120 s的预浓缩时间(样品和DPC流速= 1 mL min(-1))和250μL的洗脱体积可获得99.8%的Cr(VI)回收率。 3s)为0.09微克L-1 Cr(VI),相对标准偏差(n = 10,3微克L-1)为1.8。由于固体材料中没有残留的Cr(III)且Cr(VI)被完全吸附,因此还可以通过简单地测量后的微柱末端的浓度来进行Cr(III)的电热原子吸收光谱法(ET AAS)测定。 Cr(VI)被中孔固体保留。还研究了在天然水中测定Cr(VI)和Cr(III)的应用以及方法学的验证。 (C)2008 Elsevier B.V.保留所有权利。

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