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机构地区:[1]核工业总公司第六研究所
出 处:《原子能科学技术》1989年第4期29-33,共5页Atomic Energy Science and Technology
摘 要:U_3O_8样品用HNO_3溶解,用TBP-CCl_4溶液萃取以分离铀,水相用HClO_4蒸干,残渣溶于0.05mol/l的HClO_4和0.03mol/l的酒石酸混合底液中,用方波阳极伏安法测定铅,峰电位为-0.376 V,然后加入氨水使溶液pH约为9.5,用方波阴极伏安法测定铁,峰电位为-1.426V。方法的准确度和精密度都较好。The U_3O_8 sample is dissolved in nitric acid and uranium is removed by ex-traction with TBP-carbon tetrachloride three times. The aqueous solution is evapo-rated to dryness with perchloric acid and the residue is dissolved in 5 ml mixturecontaining 0.05 mol/l perchloric acid and 0.03 mol/l tartaric acid. The Pb isdetermined by square wave anodic stripping voltammetry in the range -0.5~0.15 V (vs. S. C. E.) with a peak potential at -0.376 V. The solution isfurther treated with ammonium hydroxid to make the pH about 9.5. The Fe isdetermined by square wave cathodic voltammetry in the range -1.30~-1. 65 Vwith a peak potential at -1. 426V. Simultaneous determination of 1-0. 01ppm ofthe above elements are possible.
分 类 号:TL271[核科学技术—核燃料循环与材料]
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