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Evaluation of extraction techniques for the determination of butyltin compounds in sediments using isotope dilution-GC/ICPMS with Sn-118 and Sn-119-enriched species

机译:同位素稀释-GC / ICPMS富集Sn-118和Sn-119物种的萃取技术对沉积物中丁基锡化合物测定的评价

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Different liquid-solid extraction techniques, including room-temperature leaching with mechanical shaking, ultrasonic, and microwave-assisted extractions, have been evaluated for the quantitative speciation of tin for mono-, di-, and tributyltin (MBT, DBT, and TBT, respectively) in PACS-2 and BCR-646 certified reference materials. A methanol-acetic acid mixture was used as the extractant reagent in all cases. For this purpose, a mixed spike containing Sn-119-enriched MBT (79.7 At%), Sn-118-enriched DBT (86.7 At%), and Sn-119-enriched TBT (83.1 At%), was synthesized, characterized, and used for isotope dilution analysis. The isotopic composition of the mixed spike was determined by gas chromatography/ICPMS after aqueous ethylation using sodium tetraethylborate, and the determination of the concentration of the different species in the spike was performed by means of reverse isotope-dilution analysis using natural MBT, DBT, and TBT standards. In the analysis of the certified sediments, the sample was spiked with the mixed spike, extracted under different conditions, derivatized with sodium tetraethylborate, and extracted into hexane, and the isotope ratios 120/118 and 120/119 were measured as peak area ratios for all butyltin species after GC/ICPMS. Mass bias was corrected using a derivatized natural standard every three sample injections. Sequential degradation reactions during extraction (from TBT to DBT, from DBT to MBT, and from MBT to inorganic tin) were assumed, and mathematical equations were developed that allowed the determination of the correct species concentration and the decomposition factor for each of the transformation reactions. For ultrasonic extraction and mechanical shaking, negligible degradation reactions were observed. However, for microwave assisted extractions, degradation factors up to 7% (M to DBT) and 16% (DBT to MBT) were obtained for both reference materials when high-MW energy was applied in the extraction step. For the three extraction techniques tested, the DBT and TBT concentration values obtained for PACS-2 closely matched the certified values. However, for MBT the concentrations found by microwave and ultrasonic extraction were much higher than the certified value. This was not the case for mechanical shaking. The results obtained for BCR-646 using microwave assisted extraction were in good agreement with the certified values for all tin species. [References: 31]
机译:对于单丁基锡,二丁基锡和三丁基锡的锡(MBT,DBT和TBT)的定量形态分析,已经评估了不同的液固萃取技术,包括采用机械摇动的室温浸提,超声和微波辅助萃取。分别在PACS-2和BCR-646认证的参考材料中)。在所有情况下,将甲醇-乙酸混合物用作萃取剂。为此,合成了一个混合尖峰,其中包含富含Sn-119的MBT(79.7 At%),富含Sn-118的DBT(86.7 At%)和富含Sn-119的TBT(83.1 At%),并用于同位素稀释分析。使用四乙基硼酸钠水溶液进行乙基化后,通过气相色谱/ ICPMS确定混合尖峰的同位素组成,并使用天然MBT,DBT,反相同位素稀释法对尖峰中不同物质的浓度进行测定。和TBT标准。在对合格沉积物进行分析时,将样品掺入混合掺加物,在不同条件下萃取,用四乙基硼酸钠衍生化,然后萃取至己烷中,并测量同位素比120/118和120/119作为峰面积比。 GC / ICPMS之后的所有丁基锡种类。每三个样品进样,使用衍生化的自然标准品校正质量偏差。假设萃取过程中发生顺序降解反应(从TBT到DBT,从DBT到MBT,从MBT到无机锡),并且建立了数学方程式,可以确定每种转化反应的正确物种浓度和分解因子。对于超声提取和机械摇动,观察到的降解反应可忽略不计。但是,对于微波辅助提取,当在提取步骤中施加高MW能量时,两种参考材料的降解因子分别达到7%(M到DBT)和16%(DBT到MBT)。对于测试的三种提取技术,为PACS-2获得的DBT和TBT浓度值与认证值非常匹配。但是,对于MBT,通过微波和超声提取发现的浓度远高于认证值。机械震动不是这种情况。使用微波辅助萃取获得的BCR-646的结果与所有锡物种的认证值高度吻合。 [参考:31]

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