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Successive digestions for pre-concentration and ultra-trace determination of Br and I by plasma-based atomic spectrometry and ion chromatography

机译:基于等离子体基原子光谱和离子色谱法,连续消化Br和I的预浓度和超痕量测定

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摘要

This study demonstrates the feasibility of successive digestions as a strategy for Br and I pre-concentration and ultra-trace determination by ion chromatography and plasma-based spectrometric techniques. Digestion and pre-concentration steps were performed by using microwave-induced combustion (MIC), and milk powder samples for adult and infant nutrition were used as an example of application. Samples were pressed as pellets (up to 0.7 g) and combusted in closed quartz vessels pressurized with oxygen. Up to 5 combustion cycles were sequentially performed using the same vessel without changing the absorbing solution. In each cycle, a new filter paper, igniter, and sample pellet (0.7 g) were used allowing digestion and pre-concentration. Ammonium hydroxide solutions (100 to 300 mmol L-1) were evaluated for analytes absorption. Using 300 mmol L-1 NH4OH as absorbing solution, up to 5 digestion cycles (0.7 g each cycle, total mass of 3.5 g) can be applied while keeping a suitable relative standard deviation ( < 5%). The accuracy of the proposed MIC method was evaluated by using a whole milk powder reference material (RM NIST 8435) and results were in agreement with reference values (better than 95%). The digestion efficiency was demonstrated by the low residual carbon in digests ( < 25 mg L-1), allowing Br and I determination virtually free of interferences caused by the presence of dissolved organic matter. The limits of detection (LODs) for Br and I were 1.25 and 0.15 ng g(-1), respectively, which are 5 times lower than the LOD obtained using the conventional MIC method. Taking into account the very low LODs obtained, the proposed sequential digestion and pre-concentration MIC method can be recommended for further Br and I determination in ultra-trace levels by inductively coupled plasma mass spectrometry or even by less sensitive techniques, such as inductively coupled plasma optical emission spectrometry or ion chromatography.
机译:本研究表明,连续消化的可行性作为BR的策略和通过离子色谱和基于等离子体的光谱技术的预浓缩和超痕量测定。通过使用微波诱导的燃烧(MIC)进行消化和预浓缩步骤,并使用用于成人和婴儿营养的乳粉样品作为应用的实例。将样品作为粒料(高达0.7g)压制,并在用氧气加压的闭合石英血管中燃烧。使用相同的容器顺序地执行最多5个燃烧循环,而不改变吸收溶液。在每个循环中,使用新的滤纸,点火剂和样品颗粒(0.7g),允许消化和预浓度。评估氢氧化铵溶液(100至300mmol L-1)以进行分析物吸收。使用300mmol L-1 NH4OH作为吸收溶液,可以在保持合适的相对标准偏差(<5%)的同时施加高达5个消化循环(每循环0.7g,每循环,3.5g)。通过使用全奶粉参考物质(RM NIST 8435)评价所提出的MIC方法的准确性,结果与参考值(优于95%)一致。消化效率通过消化物(<25mg L-1)中的低残留碳,允许BR和我几乎没有由溶解的有机物存在引起的干扰。 Br和I的检测限率分别为1.25和0.15ng(-1),分别比使用传统的MIC方法获得的床单低5倍。考虑到非常低的床皂床,所提出的顺序消化和预浓度的MIC方法可以推荐用于进一步的BR,并且我通过电感耦合等离子体质谱法或甚至通过较少敏感的技术确定超轨道水平,例如电感耦合等离子体光发射光谱法或离子色谱法。

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