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氢氧化四甲铵消解后采用流动注射冷蒸气发生原子吸收光谱法测定生物组织中的总汞

Determination of total mercury in biological tissues by flow injection cold vapour generation atomic absorption spectrometry following tetramethylammonium hydroxide digestion.

作者信息

Tao G, Willie S N, Sturgeon R E

机构信息

Institute for National Measurement Standards, National Research Council of Canada, Ottawa, Ontario, Canada.

出版信息

Analyst. 1998 Jun;123(6):1215-8. doi: 10.1039/a802000k.

Abstract

A simple, rapid and reliable method was developed for the determination of total mercury in biological samples. Samples were solubilized using tetramethylammonium hydroxide (TMAH). The organically bound mercury was cleaved and converted to inorganic mercury by on-line addition of KMnO4. The decomposed mercury together with inorganic mercury originally present in samples was determined by flow injection cold vapour atomic absorption spectrometry after reduction to elemental mercury vapour using NaBH4. A sample throughput of 100 measurements per hour was achieved after a 30 min dissolution with TMAH. The relative standard deviation for 20 micrograms l-1 Hg was 1.3% (n = 11) and the limit of detection was 0.1 microgram l-1 (3 sigma). The proposed method was validated by the analysis of a suite of certified marine biological reference materials, DORM-2 (dogfish muscle), DOLT-2 (dogfish liver) and TORT-2 (lobster hepatopancreas), with calibration against simple HgII standards.

摘要

开发了一种简单、快速且可靠的方法来测定生物样品中的总汞。使用氢氧化四甲铵(TMAH)溶解样品。通过在线添加KMnO₄将有机结合汞裂解并转化为无机汞。样品中原本存在的分解汞和无机汞在使用NaBH₄还原为元素汞蒸气后,通过流动注射冷蒸气原子吸收光谱法进行测定。用TMAH溶解30分钟后,每小时可实现100次测量的样品通量。20微克/升汞的相对标准偏差为1.3%(n = 11),检测限为0.1微克/升(3σ)。通过分析一系列经认证的海洋生物参考物质DORM - 2(鲨鱼肌肉)、DOLT - 2(鲨鱼肝脏)和TORT - 2(龙虾肝胰腺),并以简单的HgII标准进行校准,验证了所提出的方法。

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