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AUTOMATED IN-LINE EXTRACTION OF URANIUM(VI) FROM RAFFINATE STREAMS WITH ON-LINE DETECTION BY CATHODIC STRIPPING VOLTAMMETRY

机译:阴极溶出伏安法在线检测残液中铀(VI)并在线检测

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An automated method for on-site monitoring of uranium(VI) in raffinate streams originating from nuclear fuel reprocessing plants is described. An in-line stripping procedure (based on liquid/liquid extraction) was developed to extract U(VI) from this stream, a solvent mixture of 20% tributyl phosphate and nitric acid in kerosene, into an aqueous sodium sulfate solution, Degradation products in the solvent mixture, especially dibutyl phosphate, give rise to very strong complexes and are responsible for moderate but constant U(VI) recoveries (similar to 50%), Optimal conditions for in-line stripping comprise a mixing ratio of extractant (0.5 M sodium sulfate in water)/solvent mixture of similar to 3 and a pumping rate of similar to 0.4 mL min(-1) of the solvent mixture. The determination of U(VI) was by on-line cathodic stripping voltammmetry (CSV), preceded by adsorptive collection of the U(VL) as an oxine complex onto a hanging mercury drop electrode, Quantities of 1-2 mL of the aqueous extract were pumped into the voltammmetric cell and diluted (1/5 to 1/10) with a background electrolyte containing 0.1 M PIPES buffer, 2 x 10(-4) M oxine, 10(-4) M EDTA, and 0.2 M hydrazine hydrate (pH 9.0), The CSV peak for U(VI) was obtained at -0.68 V with a detection limit of 20 nM in the raffinate stream using an adsorption time of 120 s, Both the inline stripping procedure and the on-line measurement were fully automated, with a relative standard deviation in the measurements of < 5%. [References: 11]
机译:描述了一种用于现场监测源自核燃料后处理厂的提余液中铀(VI)的自动化方法。开发了在线汽提程序(基于液/液萃取),从该物流,煤油中20%磷酸三丁酯和硝酸的溶剂混合物中萃取U(VI)到硫酸钠水溶液中,溶剂混合物(尤其是磷酸二丁酯)会形成非常牢固的配合物,并负责中等但恒定的U(VI)回收率(约50%)。在线汽提的最佳条件包括萃取剂(0.5 M钠)的混合比硫酸盐在水)/溶剂混合物中的溶解度与3相似,并且抽速与溶剂混合物的0.4 mL min(-1)相似。 U(VI)的测定是通过在线阴极溶出伏安法(CSV)进行的,然后将U(VL)作为一种含氧配合物吸附收集到悬挂的汞滴电极上,水提取液的量为1-2 mL将其泵入伏安法池中,并用背景电解液稀释(1/5至1/10),该电解液包含0.1 M PIPES缓冲液,2 x 10(-4)M牛磺酸,10(-4)M EDTA和0.2 M水合肼(pH 9.0),U-VI的CSV峰是在-0.68 V处获得的,使用120 s的吸附时间在萃余物流中的检出限为20 nM,在线汽提过程和在线测量均达到完全自动化,相对标准偏差小于5%。 [参考:11]

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