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首页> 外文期刊>Analytical and bioanalytical chemistry >Direct determination of selenium in urine samples by electrothermal atomic absorption spectrometry using a Zr plus Rh-treated graphite tube and co-injection of Rh as chemical modifier
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Direct determination of selenium in urine samples by electrothermal atomic absorption spectrometry using a Zr plus Rh-treated graphite tube and co-injection of Rh as chemical modifier

机译:使用Zr加Rh处理的石墨管并共注入Rh作为化学改性剂,通过电热原子吸收光谱法直接测定尿液样品中的硒

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Different chemical modifiers for use with electrothermal atomic absorption spectrometry (ET AAS) were investigated in relation to determining the selenium in human urine samples. The samples were diluted in a solution containing 1% v/v HNO3 and 0.02% m/v cetyltrimethylammonium chloride (CTAC). Studying the modifiers showed that the use of either Ru or Ir as the permanent modifier gave low sensitivity to Se and the peak shape was very noisy, while Zr or Rh gave no peak at all. The same occurred when Zr was used in solution. For mixtures of permanent modifiers, Ir plus Rh or Zr plus Rh gave very low sensitivity, Zr plus Rh with co-injection of Ir in solution was also not efficient, Zr plus Rh in solution gave good sensitivity, but the best results were obtained with a mixture of Zr and Rh as the permanent modifier and co-injection of Rh in solution. Using this last modifier, the following dilutions with the HNO3 and CTAC were studied: 1:1, 1:2, 1:3 and 1:4. The best dilution was 1:1, which promoted good sensitivity and a more defined peak shape and made it possible to correct for the background using a deuterium arc lamp. Under these conditions, a characteristic mass of 26 +/- 0.2 pg was obtained for Se in aqueous solution. Six certified urine samples were analyzed using matrix matching calibration and the measured concentrations were in agreement with the certified values, according to a t-test at the 95% confidence level. Recovery tests were carried out and the recoveries were in the range 100-103%, with relative standard deviation better than 9%. The limit of detection (LOD, 3 sd, n=10) was 3.0 mu g L-1 in the sample. The treated graphite tube could be used for at least 600 atomization cycles without significant alteration of the analytical signal.
机译:研究了与电热原子吸收光谱法(ET AAS)一起使用的不同化学改性剂,以确定人类尿液样品中的硒。将样品在含有1%v / v HNO3和0.02%m / v十六烷基三甲基氯化铵(CTAC)的溶液中稀释。对改性剂的研究表明,使用Ru或Ir作为永久性改性剂对Se的敏感性低,峰形非常嘈杂,而Zr或Rh根本没有峰。在溶液中使用Zr时也会发生同样的情况。对于永久性改性剂的混合物,Ir加Rh或Zr加Rh的灵敏度非常低,Zr加Rh与溶液中Ir的共注入效率也不高,Zr加Rh溶液具有很好的灵敏度,但是在Zr和Rh的混合物作为永久性改性剂,并将Rh共同注入溶液中。使用该最后的改性剂,研究了以下用HNO3和CTAC稀释的比例:1:1、1:2、1:3和1:4。最佳的稀释比例为1:1,这可以提高灵敏度和峰形,并且可以使用氘弧灯校正背景。在这些条件下,水溶液中的硒的特征质量为26 +/- 0.2 pg。根据95%置信水平下的t检验,使用基质匹配校准法分析了六份经认证的尿液样本,测量的浓度与经认证的值一致。进行了回收率测试,回收率在100-103%范围内,相对标准偏差优于9%。样品中的检出限(LOD,3 sd,n = 10)为3.0μg L-1。经处理的石墨管可用于至少600个雾化循环,而不会明显改变分析信号。

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