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Online standard additions calibration of transient signals for inductively coupled plasma mass spectrometry

机译:电感耦合等离子体质谱的瞬态信号在线标准添加校准

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An online standard additions calibration method for transient signals in ICPMS is demonstrated in which a small volume of standard is injected as a spike into the sample/carrier stream, overlaying the analyte peak. This technique provides the advantages of conventional standard additions but requires only a single sample run. The method corrects for matrix effects and is suitable for transient signals in which the severity of the matrix effect changes over the analyte peak. The method uses a peak-fitting program to determine the area of the underlying peak and is shown to be effective for the determination of trace metal concentrations in both a high ionic strength matrix and in a biological matrix (urine). Eight analytes with concentrations in the range of 0.82-233.2 mu g L-1 in urine were simultaneously determined using a standard spiking solution of 75 mu g L-1 injected through a 100-mu L loop. The measured concentrations for analytes free of spectral interferences agreed with the certified values, and the precision achieved was comparable to that achieved by the certifying agency. Using a conventional cross-flow nebulizer and Scott-type spray chamber, the accuracy obtained for online standard additions calibration was within 2%, and the precision was within 5%.
机译:展示了在线ICPMS中用于瞬变信号的在线标准加标校准方法,其中将少量标准液作为尖峰注入样品/载流中,覆盖了分析物峰。该技术具有常规标准品添加的优点,但只需要运行一次样品即可。该方法可校正基质效应,适用于瞬态信号,在瞬态信号中,基质效应的严重性会随着分析物峰的变化而变化。该方法使用峰拟合程序确定潜在峰的面积,并被证明可有效测定高离子强度基质和生物基质(尿液)中的痕量金属。使用通过100μL定量环注入的75μg L-1的标准加标溶液,同时测定了8种尿液中浓度在0.82-233.2μg L-1之间的分析物。不含光谱干扰的分析物的测得浓度与认证值一致,并且所达到的精度与认证机构所达到的精度相当。使用常规的错流雾化器和Scott型雾化室,在线标准添加校准所获得的精度在2%以内,精度在5%以内。

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