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Solid-phase extraction of Hg(Ⅱ) on creatine modified activated carbon and determination by ICP-OES in water samples

机译:肌酸修饰活性炭上固相萃取汞(Ⅱ)及ICP-OES测定

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摘要

A new sorbent was successfully prepared by immobilizing creatine on activated carbon and then used for separation/preconcentration of trace Hg(Ⅱ) prior to detection by inductively coupled plasma optical emission spectrometry (ICP-OES). Experimental conditions including pH, sample flow rate and volume, eluting variables and tolerance limit of interfering ions were evaluated and established. At pH 1.0 and flow rate of 2.5mLmin~(-1), Hg(Ⅱ) was adsorbed quantitatively on the column, then quantitatively eluted by 2.0 mL 0.1.mol L~(-1) nitric acid solution; other transition metal ions did not interfere with the determination of Hg(Ⅱ). An enrichment factor of 100 was obtained for Hg(II). The maximum adsorption capacity was 49.5 mg g~(-1). Under the optimal conditions, the value of the detection limit (3a) was 0.06 ng mL~(-1), and the relative standard deviation (RSD) calculated was lower than 3.0% (n = 8). The methodology was validated by analyzing certified reference materials and successfully applied to the determination of trace Hg(Ⅱ) in natural water samples with satisfactory results.
机译:通过将肌酸固定在活性炭上成功制备了一种新的吸附剂,然后用于电感耦合等离子体发射光谱法(ICP-OES)分离/预富集痕量的Hg(Ⅱ)。评估并建立了包括pH,样品流速和体积,洗脱变量和干扰离子耐受极限在内的实验条件。在pH值为1.0,流速为2.5mLmin〜(-1)的条件下,Hg(Ⅱ)被定量吸附在色谱柱上,然后用2.0mL 0.1mol L〜(-1)的硝酸溶液进行定量洗脱。其他过渡金属离子不影响Hg(Ⅱ)的测定。汞(II)的富集系数为100。最大吸附容量为49.5 mg g〜(-1)。在最佳条件下,检出限(3a)的值为0.06 ng mL〜(-1),计算出的相对标准偏差(RSD)低于3.0%(n = 8)。该方法通过对认证参考物质的分析得到验证,并成功应用于天然水样中痕量汞(Ⅱ)的测定,结果令人满意。

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