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Solid Phase Extraction Using a Sulfoxide Adsorbent for Preconcentration and Separation of Hg(II) in Natural Water Followed by ICP-MS Measurements

机译:固相萃取使用亚砜吸附剂对天然水中的Hg(II)进行预浓缩和分离,然后进行ICP-MS测量

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A separation and preconcentration method based on solid-phase extraction using sulfoxide adsorbent was developed for the determination of Hg(II) in natural water samples by inductively coupled plasma mass spectrometry (ICP-MS). The sulfoxide adsorbent was packed into a commercially available syringe-driven column (with a bed volume of 1.0 mL), which permitted off-line sample loading and on-line elution/measurement. The optimized operating conditions were as follows: sample condition for Hg(II) adsorption, 0.5% HCl; sample-loading flow rate, 10 mL min~(?1); eluent for recovering Hg(II), 1% cysteine water solution. A test using multi-element mixed solution showed that most trace elements in natural water, except for Bi, could be completely separated from Hg(II). The recoveries of Hg(II) were 99.0 ± 3.2 and 100.7 ± 4.3%, respectively, when 0.64 and 0.16 ng mL~(?1) of Hg(II) were added into the test sample. The detection limit of Hg(II) using a quadrupole ICP-MS after 10-fold preconcentration was 1.5 pg mL~(?1). The blank value was 2.8 ± 0.5 pg mL~(?1).
机译:建立了基于亚砜吸附剂固相萃取的分离富集方法,通过电感耦合等离子体质谱法(ICP-MS)测定天然水样中的汞(II)。将亚砜吸附剂装填到市售的注射器驱动柱(床体积为1.0 mL)中,可以进行离线样品加载和在线洗脱/测量。优化的操作条件如下:Hg(II)吸附的样品条件:0.5%HCl;样品加载流速,10 mL min〜(?1);回收Hg(II),1%半胱氨酸水溶液的洗脱液。使用多元素混合溶液进行的测试表明,除Bi外,天然水中的大多数微量元素都可以与Hg(II)完全分离。当将0.64和0.16 ng mL〜(?1)的Hg(II)添加到测试样品中时,Hg(II)的回收率分别为99.0±3.2和100.7±4.3%。预富集10倍后,使用四极杆ICP-MS对Hg(II)的检出限为1.5 pg mL〜(?1)。空白值为2.8±0.5pgmL·(Δ1)。

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