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描述了硫酸铵溶液中铀矿坑水样品中铀的电沉积层特性。 电沉积液为10 ml 0.8 M的硫酸铵溶液, 电流密度0.6 A/cm2, pH值为2.5, 电镀1 h。 电沉积经化学分离后的水样品和电沉积的纯硝酸铀酰样品进行了比较, 并对二者分别做了红外(IR)光谱、 扫描电镜(SEM)、 元素分析以及α能谱测量。 IR谱上铀酰离子的反对称伸缩振动峰在887 cm-1附近, 使电沉积在不锈钢片上的铀主要以铀酰离子水合物的形式存在, 有一部分NH+4以NH3的形式替代水合物中的水, 使电沉积层中铀的化合物形式为UO2(OH)2·xNH3·yH2O或者UO2(OH)2-x·(ONH4)x·yH2O, 铀酰离子通过链的形式形成聚合结构。 SEM照片显示电沉积层均匀, 没堆积成团现象出现。 α谱表明电沉积层中铀的同位素主要是238U和234U, 相应的α能量峰4198和4773 keV很显著, 没其它峰的干扰。 Characteristics of electrodeposited uranium films of uranium ore water sample in ammonium sulphate was investigated in this work. The optimized electrodeposited conditions were as follows: electrolyte was ammonium sulphate of 0.8 M, and current density at the cathode was 0.6 A/cm2, electrolyte pH value was 2.5, the time of plating on the electrodeposition was 1 h. In this situation, the uniform, thin and adheresive films were produced by electrodeposition method. Two samples were made, one electrodeposition of pure uranyl nitrate, and another electrodeposition of uranium ore water sample after chemical separation. Characteristics of electrodeposited uranium films of uranium ore water sample after chemical separation was studied, making comparisons with electrodeposited films of uranyl nitrate. The analysis of film characteristics was done through infrared (IR) spectrum, scanning electron microscopy(SEM), element analysis and α spectrum measurment. According to Fourier transform infrared spectra, the asymmetric stretching vibration band of uranyl group is around 887 cm-1. In addition, according to IR spectrum, we know that uranium exists mainly as the form of hydrated polymeric compound in the film. Electrodeposited uranium films also included many NH+4. Polymeric structures of variable composition were present in the electrodeposited samples, with the unit monomeric formula UO2(OH)2·xNH3·yH2O or UO2(OH)2-x·(ONH4)x·yH2O. Scanning electron microscopy shows that the two samples have similar surface characteristics and no cluster is observed. The samples were also measured by spectrometer equipped with Passivated Implanted Planar Silicon(PIPS) detector. From the α spectrum, we know that isotopes of uranium in the film are 238U and 234U. 235U is not found in the α spectrum. It also shows that the chemical separation process can isolate uranium from other interfering elements effectively, the result of chemical separation is very satisfactory and electrodeposited process is rather efficient. Source electrodeposited in ammonium sulphate through optimized conditions satisfies the need of high resolution α spectrum. 相似文献
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用二-2-乙基己基磷酸(HDEHP)做萃取剂,Na2CO3做反萃剂,234Th为示踪剂,完成了从盐酸溶液中液-液萃取Th(IV)的实验研究。在不同萃取条件下(包括HDEHP和Na2CO3溶液浓度、震荡时间、有机相和水相比值等)对234Th百分萃取(或反萃取)作了一系列实验。发现,随HDEHP浓度的增加,234Th的萃取效率明显增加。当HDEHP的浓度≥20%时,234Th的萃取效率>97%;用Na2CO3溶液能有效地从有机相中反萃出234Th,当Na2CO3溶液的浓度≥0.5mol/L时,234Th的反萃效率>96%;反萃时,震荡周期长于4min时,两相能达到反萃平衡;随有机相和水相比值的增加,234Th的萃取效率也明显地增加,在合适的萃取条件下,有机相与水相比值≥4:1时,高达97%的234Th进入有机相。 相似文献
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利用14MeV中子轰击天然钨靶,通过^180,182,183,184,186W（n,2pxn）反应,产生铪的放射性同位素,以γ（X）谱学方法鉴别出铪,观测到了能量为75．2keV和88．7keV的2条新1射线,测定其半衰期为（3．6±0．6）min。 相似文献
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14MeV中子可以引起重核奇异的(n,2p)反应。中能较轻的重离子轰击重核,可以产生多核子转移反应,并以此为基础形成了我们合成和研究重丰中子新核素的一条物理思想和生成、分离鉴别技术路线。介绍了化学分离和X-γ符合方法(元素分离方法);先后合成了一些如185Hf、186Hf、237Th、238Th、239Pa、175Er和197Os等重丰中子新核素,并测定它们的半衰期分别为3.5min、2.6min、5.0min、9.4min、106min、2.8min和1.2min;还观测了它们其他的衰变性质,如新γ射线和衰变纲图等。 相似文献
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用^233Pa做示踪剂,分别使用ABS树脂、有机玻璃、聚乙烯和普通玻璃试管做吸附材料,研究了在不同浓度的HCL溶液中哪Pa在试管壁上的吸附。结果显示,^233Pa在试管壁上的吸附随盐酸浓度的增加而减少。当HCL浓度≥0．5mol／L时,同ABS树脂和有机玻璃比较,^233Pa在玻璃试管壁上的吸附最少。当HCL浓度≤0．25mol／L时,^233Pa在玻璃试管壁上的吸附反而比在ABS树脂和有机玻璃试管壁上的大。若^233Pa的HCL溶液在聚乙烯、ABS树脂和玻璃试管中存放较长的时间（24h）,聚乙烯试管壁对^233Pa的吸附量最少。 相似文献
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以TBP（磷酸三丁脂）为萃取剂,苯为稀释剂,以^233pa为示踪剂,研究盐酸溶液中Pa（V）的萃取行为。讨论了盐酸浓度、萃取剂浓度对Pa（V）萃取的影响。同时萃取时间对萃取的影响也进行了讨论。 相似文献
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