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首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >Evaluation of Medicinal Plant Decomposition Efficiency Using Microwave Ovens and Mini-Vials for Cd Determination by TS-FF-AAS
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Evaluation of Medicinal Plant Decomposition Efficiency Using Microwave Ovens and Mini-Vials for Cd Determination by TS-FF-AAS

机译:TS-FF-AAS用微波炉和小瓶测定镉对药用植物的分解效率评估

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摘要

Sample preparation is an important step in the analytical process because it can introduce different error sources.Its efficiency is checked based on the quality and reliability of the data obtained,and the time spent on this'task.This work evaluates medicinal plant decomposition parameters using polypropylene mini-vials heated by microwave radiation,applying the single vessel concept.As an example,sample mass amount(5 mg),mixture of oxidant agents(200 uL cone.HNO_3+150muL 30% v/v H_2O_2),microwave time and power were evaluated by heating 24 mini-vials in both closed-vessel(CV)and focused(F)microwave ovens.In order to achieve the best-optimised condition for sample preparation,cadmium and residual carbon determinations were carried out for all experiments.The residual carbon(between 0.30 and 0.45%)was determined by CHN elemental analysis and the cadmium concentration(up to 0.80 mug g~(-1))by thermospray flame furnace atomic absorption spec-trometry(TS-FF-AAS)in three different medicinal plants.The accuracy of the proposed methods was assessed using certified reference materials(rye grass,BCR 281 and bovine liver,NIST 1577b)as well as conventional microwave assisted decomposition.The new method used a minium sample amount(5 mg)and reagent volume(ca.400 uL)and only 4 and 10 min of microwave sample decomposition for CV and F ovens,respectively.In addition,the capacity of both microwave ovens was increased up to 4 times while contamination risks were inherently reduced with the single vessel concept.
机译:样品制备是分析过程中的重要步骤,因为它会引入不同的误差源。它的效率是根据获得的数据的质量和可靠性以及完成此任务所花费的时间来检查的。这项工作使用以下方法来评估药用植物的分解参数:微波辐射加热的聚丙烯小瓶,采用单容器概念。例如,样品质量(5 mg),氧化剂混合物(200 uL浓,HNO_3 +150μL30%v / v H_2O_2),微波时间和通过在封闭容器(CV)和聚焦(F)微波炉中加热24个小瓶来评估功率。为了达到最佳的样品制备条件,对所有实验进行了镉和残留碳的测定。通过CHN元素分析确定残留碳(0.30至0.45%),并通过热喷雾火焰炉原子吸收光谱法(TS-FF-AAS)测定镉的浓度(最高0.80马克杯〜(-1))。不同的医学l植物。使用认证的参考物质(黑麦草,BCR 281和牛肝,NIST 1577b)以及常规微波辅助分解方法评估了所提出方法的准确性。新方法使用的样品量最少(5 mg)和试剂CV和F烤箱的容积分别约为400 uL和仅4和10分钟微波样品分解。此外,两个微波炉的容量提高了4倍,而单个容器固有地降低了污染风险概念。

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