电热汽化icp -质谱法测定固体塑料中钯的含量

F. Vanhaecke, Marieke Verstraete, L. Moens, R. Dams
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引用次数: 17

摘要

采用电热汽化电感耦合等离子体质谱法(ETV-ICPMS)测定固体脂肪族聚酮中Pd的含量。这种材料中Pd的存在是由于在生产过程中使用了含Pd的均相催化剂。通过应用多步加热程序,可以在分析物元素汽化之前选择性地完全去除有机基质。当使用(i)外部校准和(ii)使用水标准溶液的单一标准添加时,可达到的精度通过与中子活化分析(NAA)方法获得的参考值进行比较来评估。基于其相似的炉内行为,Ir被证明完全适合用作内部标准。此外,氩二聚体信号(Ar2+)显示出用作内部标准的一些潜力。当使用Ir或Ar2+作为内标和单标添加物进行校准时,ETV-ICPMS结果(~ 5µg - 1)每次与NAA结果的一致性在10%以内(ETV-ICPMS平均结果与参考值之间的偏差~ 2%)。观察到检测的绝对限(3s标准)为~ 1 pg,对应于以1 mg为典型样品质量的相对值为~ 1 ng g-1。然而,当使用Ir作为内标时,由于在Ir标准溶液中存在可测量量的Pd,确定了检测限恶化到~ 20pg。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of the palladium content in a solid plastic material by electrothermal vaporization ICP-mass spectrometry (ETV-ICPMS)
Electrothermal vaporization inductively coupled plasma mass spectrometry (ETV-ICPMS) was used for the determination of the Pd content in a solid aliphatic polyketone. The presence of Pd in this material has to be attributed to the use of a Pd-containing homogeneous catalyst for its production. By application of a multi-step heating programme, the organic matrix could be selectively and completely removed prior to the vaporization of the analyte element. The accuracy attainable when using (i) external calibration and (ii) single standard addition using an aqueous standard solution was evaluated by comparison of the results obtained with a reference value obtained by means of neutron activation analysis (NAA). On the basis of its similar furnace behaviour, Ir was shown to be perfectly suited to be used as an internal standard. Also the argon dimer signal (Ar2+) shows some potential to be used as an internal standard. When using Ir or Ar2+ as an internal standard and single standard addition for calibration, the ETV-ICPMS result (∼5 µg g–1) agreed within 10% with the NAA result on each occasion (deviation between average ETV-ICPMS result and reference value ∼2%). The absolute limit of detection (3s-criterion) was observed to be ∼1 pg, corresponding to a relative value of ∼1 ng g–1, taking 1 mg as a typical sample mass. However, when using Ir as an internal standard, it was established that the detection limit deteriorated to ∼20 pg, due to the presence of a measurable amount of Pd in the Ir standard solution.
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