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Microextraction based on solidification of a floating organic drop followed by electrothermal atomic absorption spectrometry for the determination of ultratraces of lead and cadmium in waters

机译:基于浮选有机物凝固的微萃取-电热原子吸收光谱法测定水中的痕量铅和镉

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摘要

A procedure for the determination of ultratraces of lead and cadmium by liquid-phase microextraction based on solidification of a floating organic droplet (LPME-SFO) separation and electrothermal atomic absorption spectrometry (ETAAS) has been developed. For this purpose, 50 μL of pre-heated (50 °C) undecanoic acid (UA) are added to 25 mL of aqueous sample solution at pH 5. The mixture, maintained at 50 °C, is stirred at 1000 rpm for 10 min and then the vial is immersed in an ice-bath, which results in the solidification of the UA drop that is easily separated. Injection into the atomizer is carried out after a gentle heating. By impregnating the atomizer with tungstate as a permanent chemical modifier, the detection limits were 10 and 0.5 ng L~(-1) with enrichment factors of 380 and 420, for lead and cadmium, respectively. The relative standard deviation was in the 2.8-3.2% range (n = 5, 25-400 ng L~(-1) Pb(II) and 1-15 ng L~(-1) Cd(II)). The proposed method has been applied to the determination of lead and cadmium in bottled, tap and sea water samples, the reliability of the results being verified by means of recovery tests and by using ICP-MS.
机译:开发了一种基于悬浮有机液滴凝固(LPME-SFO)分离和电热原子吸收光谱法(ETAAS)的液相微萃取测定铅和镉超痕量的方法。为此,将50μL预热(50°C)十一酸(UA)添加到25 mL pH 5的水溶液中。将保持在50°C的混合物以1000 rpm的转速搅拌10分钟然后将小瓶浸入冰浴中,从而固化UA滴,使其易于分离。缓慢加热后,注入雾化器。通过用钨酸盐作为永久性化学改性剂浸渍雾化器,铅和镉的检出限分别为10和0.5 ng L〜(-1),富集系数分别为380和420。相对标准偏差在2.8-3.2%的范围内(n = 5、25-400 ng L〜(-1)Pb(II)和1-15 ng L〜(-1)Cd(II))。该方法已用于瓶装,自来水和海水样品中铅和镉的测定,结果的可靠性通过回收率测试和ICP-MS进行了验证。

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