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在电感耦合等离子体发射光谱法中采用切换阀实现外部标准校准自动化。

Employing a switching valve to automate external standard calibration in inductively coupled plasma optical emission spectrometry.

作者信息

Ingham Jesse R, Fontoura Beatriz M, Jones Bradley T, Donati George L

机构信息

Department of Chemistry, Wake Forest University, Salem Hall, Box 7486, Winston-Salem, NC, 27109, United States.

Department of Chemistry, Wake Forest University, Salem Hall, Box 7486, Winston-Salem, NC, 27109, United States.

出版信息

Talanta. 2024 Dec 1;280:126749. doi: 10.1016/j.talanta.2024.126749. Epub 2024 Aug 24.

Abstract

The traditional external standard calibration method (EC) is automated and simplified using a four-port switching valve (SV4) and a multi-signal approach that enables the generation of several calibration points from a single calibration solution. The SV4-EC method is applied to inductively coupled plasma optical emission spectrometry (ICP-OES) and is based on gradient dilution taking place within the instrument's sample introduction tubing. Both the calibration solution and the samples are diluted by a blank solution containing an internal standard species. Forty-five dilution points are collected over time while the solutions are mixed. Instrument responses from the calibration solution are then plotted against those from the samples, and the slope of the calibration curve is used to determine the unknown analyte concentrations in the samples. The method is used to determine Ba, Co, Cr, Cu, Fe, Mn, Ni, V and Zn in coconut water, creek water, green tea, mouthwash, soft drink, vinegar, and vodka. Limits of detection are in the 0.0002-0.009 mg L (n = 10) range, with precision on the order of 0.4 %-3 % RSD. Analyte percent recoveries from a 0.5 mg L spike are in the ranges of 88.4 %-111 %, 88.9 %-111 %, and 88.0 %-111 % for EC, SV4-EC, and the internal-standard-corrected method (SV4-EC/Sc), respectively. No statistically significant difference is observed between EC and SV4-EC recoveries for any of the sample matrices evaluated. Comparable results between EC and SV4-EC were also found for the analysis of two certified reference materials, Bovine Liver and Oyster Tissue. Based on a single calibration solution, the SV4-EC method requires caution when preparing the calibration standard to minimize measurement bias.

摘要

传统的外标校准方法(EC)通过一个四端口切换阀(SV4)和一种多信号方法实现了自动化和简化,该方法能够从单一校准溶液生成多个校准点。SV4-EC方法应用于电感耦合等离子体发射光谱法(ICP-OES),其基于在仪器进样管内进行的梯度稀释。校准溶液和样品均被含有内标物质的空白溶液稀释。在溶液混合过程中,随时间收集45个稀释点。然后将校准溶液的仪器响应与样品的仪器响应作图,校准曲线的斜率用于确定样品中未知分析物的浓度。该方法用于测定椰子水、溪水、绿茶、漱口水、软饮料、醋和伏特加中的钡、钴、铬、铜、铁、锰、镍、钒和锌。检测限在0.0002 - 0.009 mg/L(n = 10)范围内,精密度为0.4% - 3% RSD。对于0.5 mg/L加标,EC、SV4-EC和内标校正方法(SV4-EC/Sc)的分析物回收率分别在88.4% - 111%、88.9% - 111%和88.0% - 111%范围内。在所评估的任何样品基质中,EC和SV4-EC的回收率之间均未观察到统计学上的显著差异。在分析两种有证标准物质牛肝和牡蛎组织时,也发现EC和SV4-EC的结果具有可比性。基于单一校准溶液,SV4-EC方法在制备校准标准时需要谨慎操作,以尽量减少测量偏差。

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