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首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Simultaneous determination of trace amounts of borate, chloride and fluoride in nuclear fuels employing ion chromatography (IC) after their extraction by pyrohydrolysis
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Simultaneous determination of trace amounts of borate, chloride and fluoride in nuclear fuels employing ion chromatography (IC) after their extraction by pyrohydrolysis

机译:离子水解热解提取离子色谱法同时测定核燃料中痕量的硼酸,氯和氟

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An accurate and sensitive method based on the combination of pyrohydrolysis-ion chromatography (PH-IC) is proposed for the simultaneous separation and determination of boron as borate, chloride and fluoride in nuclear fuels such as U3O8, (Pu,U)C and Pu-alloys. The determination is based on the initial pyrohydrolytic extraction of B, Cl and F from the samples as boric acid, HCl and HF, respectively, which are Subsequently separated by ion chromatography (IC). The proposed method significantly improves the existing analytical methodology as it combines the determination of boron. a critical trace constituent in nuclear materials, along with F- and Cl- for chemical quality control measurements. Various experimental parameters were optimized to achieve maximum recoveries of the analytes during the pyrohydrolysis and to get better ion chromatographic (IC) separation of borate, F- and Cl- along with other anions such as CH3COO-, NO2-, NO3-, Br-, PO43- and SO42-. Recoveries of more than 93% could be obtained for all the analytes in the sample (0.5-1.5g) at 1200 +/- 25 K and distilled with pre-heated steam at the flow rate of 0.3 mL/min. An isocratic elution with a mobile phase of 0.56 M D-mannitol in 6.5 mM NaHCO3 was used for the IC separation. The detection limits for B (as borate), F- and Cl- were 24, 13 and 25 mu g L-1, respectively. Precision of about 5% was achieved for determination of boron, Cl- and F- in the samples containing 1-5 ppm(w) of boron, and 10-25 ppm(w) of Cl and F. The method was validated with reference materials and successfully applied to the nuclear fuels. The methodology is easy to adapt on routine basis. (C) 2008 Elsevier B.V. All rights reserved.
机译:提出了一种基于热水解-离子色谱法(PH-IC)的准确,灵敏的方法,用于同时分离和测定核燃料如U3O8,(Pu,U)C和Pu中的硼酸根,氯离子和氟离子-合金。该测定基于最初从样品中分别以硼酸,HCl和HF的形式对B,Cl和F进行热水解萃取,然后通过离子色谱法(IC)进行分离。该方法结合了硼的测定,大大改善了现有的分析方法。核材料中至关重要的痕量成分,以及用于化学质量控制测量的F-和Cl-。优化了各种实验参数,以实现热水解过程中分析物的最大回收率,并获得更好的硼酸根,F-和Cl-以及其他阴离子(如CH3COO-,NO2-,NO3-,Br-等)的离子色谱(IC)分离结果,PO43-和SO42-。在1200 +/- 25 K下,样品中所有分析物(0.5-1.5g)的回收率均超过93%,并用预热的蒸汽以0.3 mL / min的流速蒸馏。 IC分离采用在0.5 mM NaHCO3中具有0.56 M D-甘露醇流动相的等度洗脱。 B(硼酸盐),F-和Cl-的检出限分别为24、13和25μgL-1。测定含1-5 ppm(w)的硼和10-25 ppm(w)的Cl和F的样品中的硼,Cl-和F-的精密度约为5%。该方法已通过参考验证材料并成功地应用于核燃料。该方法易于常规调整。 (C)2008 Elsevier B.V.保留所有权利。

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