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首页> 外文期刊>Analytical and bioanalytical chemistry >Chromatographic behavior of cadmium in an ion-pair reversed-phase micro HPLC system and its application to the determination of bio-available cadmium in soil samples
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Chromatographic behavior of cadmium in an ion-pair reversed-phase micro HPLC system and its application to the determination of bio-available cadmium in soil samples

机译:离子对反相微HPLC系统中镉的色谱行为及其在测定土壤样品中生物有效性镉中的应用

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摘要

A novel reversed phase ion-pair micro HPLC system with on-line fluorescence detection has been developed systematically and studied for the determination of cadmium in its bio-available fractions of soil samples. In this system, a micro ODS column of 1.0 mm i.d.x150 mm length and a mobile phase containing 6 mmol L~(-1) 8-hydroxyaquinoline 5-sulphonic acid (HQS), 3 mmol L~(-1) cetyltrimethylammonium bromide (CTMABr), 10 mmol L~(-1) acetic acid-acetate buffer (pH 5.1) as well as 50% acetonitrile at 50 μL min~(-1) flow rate were employed to determine cadmium with a 2 μL flow cell through its fluorescence at 518 nm under 338 nm excitation. Furthermore, the composition of Cd-HQS chelate formed on the column was confirmed to be [Cd(HQS)_2]~(2-) through a log-log plot method, and then combined with the ion-pair reagent by the electrostatic force under the chromatographic condition proposed. With such a method, the detection limit of cadmium was 8.48 ng mL~(-1) (3σ) with 1 μL sample injection, and the linear range for the determination of cadmium was 30-800 ng mL~(-1) (R~2=0.992). This method has been successfully applied to determination of cadmium in its bio-available fractions of BCR-483 and soil samples without interference from other coexistent metal ions. The RSD (n=6) was less than 7.3%. The results were in agreement with the indicative value for BCR-483 and those for the soil samples obtained by ICP-MS with a pretreatment of bis(1,1,3,3-tetramethylbutyl) phosphinic acid extraction.
机译:系统地开发了一种新型的具有在线荧光检测功能的反相离子对微型HPLC系统,并进行了测定土壤样品生物可利用部分中镉的研究。在该系统中,使用长度为1.0 mm idx150 mm的微型ODS色谱柱和流动相,其中包含6 mmol L〜(-1)8-羟基喹啉5-磺酸(HQS),3 mmol L〜(-1)十六烷基三甲基溴化铵( CTMABr),10 mmol L〜(-1)乙酸-醋酸盐缓冲液(pH 5.1)和50%乙腈(流速50μLmin〜(-1))用于通过2μL流通池测定镉在338 nm激发下在518 nm发出荧光。此外,通过对数对数图法确认在柱上形成的Cd-HQS螯合物的组成为[Cd(HQS)_2]〜(2-),然后通过静电力与离子对试剂结合在建议的色谱条件下。通过这种方法,进样量为1μL时,镉的检出限为8.48 ng mL〜(-1)(3σ),测定镉的线性范围为30-800 ng mL〜(-1)(R 〜2 = 0.992)。该方法已成功地用于测定BCR-483和土壤样品中生物可利用部分中的镉,而不受其他共存金属离子的干扰。 RSD(n = 6)小于7.3%。结果与BCR-483的指示值和通过ICP-MS进行双(1,1,3,3-四甲基丁基)次膦酸萃取预处理的土壤样品的指示值一致。

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