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Determination of Ultratrace Beryllium in Natural Water by Electrothermal Atomic Absorption Spectrometry after Preconcentration with One-Drop Solvent

机译:一滴溶剂预浓缩-电热原子吸收法测定天然水中的痕量铍

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摘要

An effective method for the determination of beryllium at sub ng dm~(-3) levels in natural water is described. Beryllium is extracted with acetylacetone into chloroform. The organic phase is transferred to a Teflon beaker containing a micro volume of dimethyl sulfoxide (DMSO, a high boiling-point solvent); chloroform is then removed by evaporation in a water bath (ca. 35 deg C). Beryllium is concentrated in the residual DMSO and determined by electrothermal atomic absorption spectrometry. The sensitivity and stability of beryllium atomic absorption were enhanced in the presence of palladium as a matrix modifier. The detection limit (3#sigma#) for beryllium was 0;050 ng dm~(-3), based on a 400-fold preconcentration using 40 cm~3 of the sample water; the relative standard deviation was 1.8% (2.0 ng dm~(-3), n=8). The concentration of dissolved beryllium in natural water was found to be 0.25-0.63 nag dm~(-3) by the proposed method.
机译:介绍了一种测定天然水中亚ng dm〜(-3)含量的铍的有效方法。用乙酰丙酮将铍萃取到氯仿中。将有机相转移到含有微量二甲基亚砜(DMSO,高沸点溶剂)的特氟龙烧杯中;然后通过在水浴(约35℃)中蒸发除去氯仿。铍浓缩在残留的DMSO中,并通过电热原子吸收光谱法测定。在钯作为基质改性剂的存在下,铍原子吸收的灵敏度和稳定性得到了提高。基于使用40 cm〜3的样品水进行400倍的预浓缩,铍的检出限(3#sigma#)为0; 050 ng dm〜(-3)。相对标准偏差为1.8%(2.0 ng dm〜(-3),n = 8)。所提出的方法发现天然水中溶解的铍浓度为0.25-0.63 nag dm〜(-3)。

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