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首页> 外文期刊>Eurasian Journal of Analytical Chemistry >Micellar-Sensitized Spectrophotometric Determination of Magnesium in Drinking Water
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Micellar-Sensitized Spectrophotometric Determination of Magnesium in Drinking Water

机译:胶束增敏分光光度法测定饮用水中的镁

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A sensitive and relatively selective spectrophotometric method is proposed for the rapid determination of magnesium using Eriochrome black T (EBT) as a complexing agent in the presence of N-cetyl-N,N,N-trimethylammonium bromide (CTAB). The complex formation reaction between EBT and magnesium (II) is instantaneous in presence of NH3/NH4Cl buffer at pH 9.5 after CTAB adds as micellar-sensitized medium and the absorbance as analytical signal remains stable for over 6 h. N-cetyl N,N,N-trimethylammonium bromide as cationic surfactant and Triton X-100 as nonionic surfactant are used for improving the sensitivity and solubility of the analytical system, respectively. The surfactant-sensitizing method allows the determination of magnesium in the concentration range of 0.05-1.2 µg mL–1 with a molar absorption coefficient of 8928 L mol–1 cm–1 and Sandell’s sensitivity of 2.82 ng cm2-. The method has a detection limit of 0.012 µg mL–1 (DL=3Sb/m) and quantification limit of 0.054 µg mL–1 (QL=10Sb/m) at an analytical measurement wavelength of 640 nm with a bathochromic shift of 86 nm. The selectivity of chelating reagent was improved by the use of 1 mL masking agent solution containing 0.1 M EDTA, 0.01 M triethanolamine and 5000 µgNaF mL–1. The proposed method has been successfully applied to the determination of magnesium at trace levels in different drinking water samples. The precision (with CV of 2.35%) and the accuracy obtained were highly satisfactory.
机译:提出了一种灵敏且相对选择性的分光光度法,在N-十六烷基-N,N,N-三甲基溴化铵(CTAB)存在下,使用铬黑T(EBT)作为络合剂快速测定镁。在CTAB添加为胶束敏化介质且分析信号的吸光度保持稳定超过6小时后,在pH 9.5的NH3 / NH4Cl缓冲液存在下,EBT与镁(II)之间的络合物形成反应即刻发生。 N-鲸蜡基N,N,N-三甲基溴化铵作为阳离子表面活性剂和Triton X-100作为非离子表面活性剂分别用于提高分析系统的灵敏度和溶解度。表面活性剂敏化方法可测定浓度范围为0.05-1.2 µg mL-1的镁,摩尔吸收系数为8928 L mol-1 cm-1,Sandell的灵敏度为2.82 ng cm2-。该方法在640 nm的分析测量波长下的检出限为0.012 µg mL-1(DL = 3Sb / m),定量限为0.054 µg mL-1(QL = 10Sb / m),红移为86 nm 。通过使用含有0.1 M EDTA,0.01 M三乙醇胺和5000 µgNaF mL-1的1 mL掩蔽剂溶液,可以改善螯合剂的选择性。该方法已成功应用于不同饮用水样品中痕量镁的测定。精度(CV为2.35%)和获得的精度非常令人满意。

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