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Environmental modeling of uranium interstitial compositions of non-stoichiometric oxides: experimental and theoretical analysis

机译:非化学计量氧化物铀间隙成分的环境模型:实验和理论分析

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Study of uranium interstitial compositions of non-stoichiometric oxides UO2+x (x a 0.1-0.02) in gas and condense phases has been presented, using various soft-ionization mass spectrometric methods such as ESI-, APCI-, and MALDI-MS at a wide dynamic temperature gradient (a 25-300 A degrees C). Linearly polarized vibrational spectroscopy has been utilized in order to assign unambiguously, the vibrational frequencies of uranium non-stoichiometric oxides. Experimental design has involved xUO(2.66)center dot yUO(2.33), xUO(2.66)center dot yUO(2.33)/SiO2, xUO(2.66)center dot yUO(2.33)/SiO2 (NaOH) and SiO2/x'NaOH center dot y'UO2(NO3)(2)center dot 6H(2)O, multicomponent systems (x = 1, y a 0.1-1.0 and x' = 1, y' a 0.1-0.6) as well as phase transitions UO2(NO3)(2)center dot 6H(2)O -> {U4O9(UO2.25)} -> U3O7(UO2.33) -> U3O8(UO2.66) -> {UO3}, thus ensuring a maximal representativeness to real environmental conditions, where diverse chemical, geochemical and biochemical reactions, including complexation and sorption onto minerals have occurred. Experimental factors such as UV-irradiation, pH, temperature, concentration levels, solvent types and ion strength have been taken into consideration, too. As far as uranium speciation represents a challenging analytical task in terms of chemical identification diverse coordination species, mechanistic aspects relating incorporation of oxygen into UO (2+x) form the shown full methods validation significantly impacts the field of environmental radioanalytical chemistry. UO2 is the most commonly used fuel in nuclear reactors around the globe; however, a large non-stoichiometric range a UO1.65-UO2.25 has occurred due to radiolysis of water on UO2 surface yielding to H2O2, OH center dot, and more. Each of those compositions has different oxygen diffusion. And in this respect enormous effort has been concentrated to study the potential impact of hazardous radionuclide on the environment, encompassing from the reprocessing to the disposal stages of the fuel waste, including the waste itself, the processes in the waste containers, the clay around the containers, and geological processes. In a broader sense, thereby, this study contributes to field of environmental analysis highlighting the great ability of various soft-ionization MS methods, particularly, MALDI-MS one, for direct assay of complex multicomponent heterogeneous mixtures at fmol-attomol concentration ranges, along with it the great instrumental features allowing, not only meaningful quantitative, but also structural information of the analytes, thus making the method indispensable for environmental speciation of radionuclides, generally.
机译:使用各种软电离质谱方法,例如ESI-,APCI-和MALDI-MS,在气相和冷凝态下研究了非化学计量的氧化物UO2 + x(xa 0.1-0.02)的铀间隙成分。宽动态温度梯度(25-300 A摄氏度)。为了明确地分配铀非化学计量的氧化物的振动频率,已经使用了线性极化振动光谱法。实验设计涉及xUO(2.66)中心点yUO(2.33),xUO(2.66)中心点yUO(2.33)/ SiO2,xUO(2.66)中心点yUO(2.33)/ SiO2(NaOH)和SiO2 / x'NaOH中心点y'UO2(NO3)(2)中心点6H(2)O,多组分系统(x = 1,ya 0.1-1.0和x'= 1,y'a 0.1-0.6)以及相变UO2(NO3 )(2)中心点6H(2)O-> {U4O9(UO2.25)}-> U3O7(UO2.33)-> U3O8(UO2.66)-> {UO3},从而确保了对实数的最大代表性环境条件,发生了多种化学,地球化学和生化反应,包括络合和吸附到矿物上。还考虑了诸如紫外线辐射,pH,温度,浓度水平,溶剂类型和离子强度等实验因素。就铀形态而言,就化学鉴定而言,不同的配位物种代表了一项具有挑战性的分析任务,涉及将氧掺入UO(2 + x)中的机制方面,已显示出完整的方法验证对环境放射分析化学领域产生了重大影响。 UO2是全球核反应堆中最常用的燃料;但是,由于水在UO2表面上的辐射分解产生H2O2,OH中心点等,因此出现了很大的非化学计量范围UO1.65-UO2.25。这些组合物中的每一个具有不同的氧扩散。在这方面,人们集中精力研究有害放射性核素对环境的潜在影响,包括从燃料废物的再处理到处置阶段,包括废物本身,废物容器中的过程,废物周围的粘土。容器和地质过程。因此,从更广泛的意义上讲,这项研究为环境分析领域做出了贡献,突出了各种软电离质谱方法(尤其是MALDI-MS)的强大能力,可直接测定fmol-attomol浓度范围内的复杂多组分非均质混合物。凭借其强大的仪器功能,不仅可以进行有意义的定量分析,而且还可以提供分析物的结构信息,因此通常使该方法对于放射性核素的环境形态分析必不可少。

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