物理选矿方法降低富硼渣中铀含量的可行性

研究了铀在硼铁矿原矿及富硼渣中的赋存状态，并利用物理选矿方法进行了硼铁矿原矿、硼铁矿矿产品及富硼渣降铀试验，以最终解决富硼渣中铀含量高的难题。研究结果否定了这种可能性。     

含铀砂岩中铀与有机质、油气和煤的关系——以鄂尔多斯盆地东胜地区和吐哈盆地十红滩地区为例

目的探讨油、气、煤与铀的综合研究对于含油气盆地内多种能源的成因机制及盆地资源的开发利用。方法对鄂尔多斯盆地东胜地区和吐哈盆地十红滩地区砂岩型铀矿的岩石学特征、地质构造、含矿建造与古水文地质条件及铀矿的成矿特点等进行了综合分析与研究。结果源区火成岩和泥岩可能为铀的物质来源之一,铀矿化是成岩—后生阶段介质条件及环境改变的产物,受氧化-还原界面的控制;构造作用使目的层的抬升掀斜与暴露以及水动力环境是形成层间氧化带和铀矿化的重要条件;铀矿石带中黄铁矿表面及其附近存在吸附铀α径迹,有机质碎屑胞腔中沥青铀矿和黄铁矿共生,含铀砂岩中可见含沥青质的镜煤。结论铀的富集和铀矿的形成可能与黄铁矿、油气、煤等有机质有密切的成因关系。     

夹竹桃(Nerium indicum)等四种植物放射性核素U、226Ra的含量研究

对铀尾矿生长的夹竹桃、狗芽根、假俭草和蕨及土壤中的U、^226Ra的含量进行了测定。结果表明，夹竹桃、狍芽根、假检草和蕨对U、^226Ra具有一定的积累，并且植物体地上部分U、6226Ra的含量小于地下部分U、^226Ra的含量；四种植物为铀尾矿的耐性植物，可用于尾矿地的生态恢复。     

用地球化学特征判别川北含铀砂岩

文章阐述了川北砂岩型铀矿床的地球化学特征。根据能谱测量，用Ｕ，Ｔｈ，Ｋ元素的丰度和比值，获得铀富集的有利条件、不利条件。通过伽马能谱法（测Ｕ，Ｔｈ，Ｋ）和Ｘ射线荧光法（测Ａｓ，Ｂａ），区分含铀浅色砂岩和不含铀浅色砂岩，区分红色砂岩（红色泥岩）与浅色砂岩，缩小川北砂岩找铀矿的范围。     

铀(Ⅵ)的二溴水杨醛缩二胺类双希夫碱及溶剂三元配合物的合成和表征

Nine new complexes [UO₂(Dbsal-o-Phdn)L][UO₂(Dbsalen)L] and [UO₂(Dbsalpn)L] [Dbsal-o-PhdnH 2=N,N′-o-phenylenebis-(3,5-dibromosalicylideneimine), DbsalenH₂=N,N′-ethylenebis (3,5-dibromosalicylideneimine), DbsalpnH₂=N,N′-1,2-propanylenebis (3,5-dibromosalicylideneimine), L=MeOH, EtOH, py] have been synthesized and characterized by elemental analysis, IR, UV, TG-DTA and molar conductance analysis. These complexes are proposed to have seven coordinate environment.     

SIMS Analysis of Uranium and Actinides in Microparticles of Different Origin

In the framework of the projects Environmental Sampling and High Performance Trace Analysis in support to the International Atomic Energy Agency (IAEA) and the Euratom Safeguards Office (ESO), the research has been focused on the identification and characterisation of particles of interest containing mainly U and other actinides.Multiple analyses, elemental and isotopic, of single radioactive particles in the µm-size range are key-tools in environmental research and in nuclear forensics. The main purpose in the analysis of single particles by SIMS is the determination of their isotopic composition that has been demonstrated successfully for uranium and plutonium particles. From these results, the enrichment of the material produced, the process used for the enrichment as well as the starting material employed (natural or reprocessed uranium) can be identified.     

Bonding of multiple noble-gas atoms to CUO in solid neon: CUO(Ng)n (Ng=Ar, Kr, Xe; n=1, 2, 3, 4) complexes and the singlet-triplet crossover point

Laser-ablated U atoms co-deposited with CO in excess neon produce the novel CUO molecule, which forms distinct Ng complexes (Ng=Ar, Kr, Xe) with the heavier noble gases. The CUO(Ng) complexes are identified through CO isotopic and Ng reagent substitution and comparison to results of DFT frequency calculations. The U[bond]C and U[bond]O stretching frequencies of CUO(Ng) complexes are slightly red-shifted from neon matrix (1)Sigma(+) CUO values, which indicates a (1)A' ground state for the CUO(Ng) complexes. The CUO(Ng)(2) complexes in excess neon are likewise singlet molecules. However, the CUO(Ng)(3) and CUO(Ng)(4) complexes exhibit very different stretching frequencies and isotopic behaviors that are similar to those of CUO(Ar)(n) in a pure argon matrix, which has a (3)A" ground state based on DFT vibrational frequency calculations. This work suggests a coordination sphere model in which CUO in solid neon is initially solvated by four or more Ne atoms. Up to four heavier Ng atoms successively displace the Ne atoms leading ultimately to CUO(Ng)(4) complexes. The major changes in the CUO stretching frequencies from CUO(Ng)(2) to CUO(Ng)(3) provides evidence for the crossover from a singlet ground state to a triplet ground state.     

Photoconversion and photocatalytic activity of uranyl in acetone solutions

We have studied the effect of irradiation on the uranyl nitrate — acetone and uranyl perchlorate — acetone systems. We have established that when the uranyl perchlorate — acetone system is irradiated, polymerization of the acetone occurs and the catalyst for the process is excited uranyl complexes. In the polymer, uranium is found in the form of nanoclusters of pentavalent and tetravalent uranium, formed as a result of photochemical reactions. Polymerization does not occur in the uranyl nitrate — acetone system. We consider possible factors responsible for the noted differences. __________ Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 74, No. 5, pp. 565–568, September–October, 2007.