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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Determination of cobalt in biological samples by line-source and high-resolution continuum source graphite furnace atomic absorption spectrometry using solid sampling or alkaline treatment
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Determination of cobalt in biological samples by line-source and high-resolution continuum source graphite furnace atomic absorption spectrometry using solid sampling or alkaline treatment

机译:固体进样或碱处理的线源和高分辨率连续谱源石墨炉原子吸收光谱法测定生物样品中的钴

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Two procedures for the determination of Co in biological samples by graphite furnace atomic absorption spectrometry (GF AAS) were compared:solid sampling (SS) and alkaline treatment with tetramethylammonium hydroxide (TMAH) using two different instruments for the investigation:a conventional line-source (LS) atomic absorption spectrometer and a prototype high-resolution continuum source atomic absorption spectrometer.For the direct introduction of the solid samples,certified reference materials (CRM) were ground to a particle size <=50 mum.Alkaline treatment was carried out by placing about 250 mg of the sample in polypropylene flasks,adding 2 mL of 25% m/v tetramethylammonium hydroxide and de-ionized water.Due to its unique capacity of providing a 3-D spectral plot,a high-resolution continuum source (HR-CS) graphite furnace atomic absorption spectrometry was used as a tool to evaluate potential spectral interferences,including background absorption for both sample introduction procedures,revealing that a continuous background preceded the atomic signal for pyrolysis temperatures lower than 700 deg C.Molecular absorption bands with pronounced rotational fine structure appeared for atomization temperatures >1800 deg C probably as a consequence of the formation of PO.After optimization had been carried out using high resolution continuum source atomic absorption spectrometry,the optimized conditions were adopted also for line-source atomic absorption spectrometry.Six biological certified reference materials were analyzed,with calibration against aqueous standards,resulting in agreement with the certified values (according to the t-test for a 95% confidence level) and in detection limits as low as 5 ng g-~(-1).
机译:比较了两种通过石墨炉原子吸收光谱法(GF AAS)测定生物样品中Co的方法:固体进样(SS)和使用两种不同的研究仪器用氢氧化四甲基铵(TMAH)进行碱处理:传统的线源(LS)原子吸收光谱仪和原型高分辨率连续谱源原子吸收光谱仪。为直接引入固体样品,将经过认证的参考材料(CRM)研磨成粒径小于等于50微米的颗粒。将约250 mg的样品放入聚丙烯烧瓶中,加入2 mL 25%m / v的四甲基氢氧化铵和去离子水。由于其具有提供3-D光谱图的独特能力,因此具有高分辨率连续谱源(HR -CS)石墨炉原子吸收光谱法用作评估潜在光谱干扰的工具,包括两种样品引入过程的背景吸收res,揭示了在低于700摄氏度的热解温度下原子信号之前存在连续的背景。对于大于1800摄氏度的雾化温度,可能出现了具有明显旋转精细结构的分子吸收带,这可能是由于PO的形成。经过优化后使用高分辨率连续谱源原子吸收光谱法进行分析,对线源原子吸收光谱法也采用了优化条件。分析了六种经过生物认证的参考物质,并根据水标准品进行了校准,结果与认证值一致(根据t检验的置信水平为95%),检出限低至5 ng g-〜(-1)。

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