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首页> 外文期刊>Spectrochimica Acta, Part B. Atomic Spectroscopy >Diffusion vapour transfer modelling for an end-capped atomizer. Part 1. Atomizer with closed injection port
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Diffusion vapour transfer modelling for an end-capped atomizer. Part 1. Atomizer with closed injection port

机译:封端雾化器的扩散蒸气传递模型。第1部分。封闭注入口的雾化器

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For end-cap equipped transverse-heated graphite atomizers (THGA) with integrated contacts used for analytical atomic spectrometry, a model equation describing the diffusional losses of analyte atomic vapour through the tube ends was constructed. The model assumes that the atomic density distribution is stepwise linear, along the tube axis and the absence of a sample injection hole. With a quartz tube system, providing controlled experimental conditions at room temperature, the time constant of the diffusion removal function (TR) of mercury vapour was determined for various open and end-capped tube geometries. These results were also described by an empirical multiple regression equation with a residual standard deviation of 5%. The theoretically predicted τ_R values, corrected with an empirical factor of 1.33, agreed well (correlation coefficient = 0 996) with the experimentally obtained τ_R values for the end-capped quartz tubes. For the Perkin-Elmer THGA tubes, the diffusional transfer model was evaluated using the integrated atomic absorbance ratio between various end-capped and open tubes. This is meaningful because the signal ratio tor graphite atomizers is closely equal to the corresponding τ_R ratio. For recommended atomization temperatures the average deviation between these experimental signal ratios and the theoretically predicted ratios for the elements Ag, In, Cd, Co, Hg and Cu was 1-5% for various end-capped tube geometries The results for the individual elements deviated more from the theoretically predicted ratios mainly because of small differences in the mean gas-phase temperature between open and end-capped tubes For elements which tend to form molecules in the gas phase at low temperatures and for which the atomization efficiency is increased with the atomization temperature, the experimental ratios tended to be higher than the theoretically predicted values (In, Al, Se, Sn, As), whereas experimental ratios were slightly lower for other elements (Cd, Co, Cu).
机译:对于配备有集成触点的端盖配备的横向加热石墨雾化器(THGA),用于分析原子光谱法,构建了一个模型方程,该方程描述了分析物原子蒸气通过管端的扩散损失。该模型假设原子密度分布沿管轴呈逐步线性,并且没有样品注入孔。使用石英管系统(可在室温下提供受控的实验条件),针对各种开放式和封端式管几何结构,确定了汞蒸气扩散消除功能(TR)的时间常数。这些结果也用经验标准多元回归方程描述,剩余标准偏差为5%。理论上预测的τ_R值(用1.33的经验系数校正)与通过实验获得的端盖石英管的τ_R值吻合良好(相关系数= 0 996)。对于Perkin-Elmer THGA管,使用各种封端的和敞开的管之间的积分原子吸收率评估了扩散转移模型。这是有意义的,因为石墨雾化器的信号比与相应的τ_R比非常接近。对于推荐的雾化温度,对于各种封端的管几何形状,这些实验信号比率与元素Ag,In,Cd,Co,Hg和Cu的理论预测比率之间的平均偏差为1-5%。单个元素的结果有所偏差与理论上预测的比率相比更多,主要是因为敞开式管和端盖式管之间的平均气相温度差异很小,对于那些在低温下易于在气相中形成分子并且随着雾化作用雾化效率提高的元素温度下,实验比率往往高于理论预测值(In,Al,Se,Sn,As),而其他元素(Cd,Co,Cu)的实验比率则稍低。

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