首页> 外文期刊>Applied Geochemistry: Journal of the International Association of Geochemistry and Cosmochemistry >Behaviour of actinides (Th, U, Np and Pu) and rare earths (La, Ce and Nd) during aqueous leaching of a nuclear glass under geological disposal conditions
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Behaviour of actinides (Th, U, Np and Pu) and rare earths (La, Ce and Nd) during aqueous leaching of a nuclear glass under geological disposal conditions

机译:地质处置条件下核玻璃水浸过程中act系元素(Th,U,Np和Pu)和稀土(La,Ce和Nd)的行为

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Leaching experiments in aqueous media were carried out on non-radioactive and radioactive nuclear waste glasses to investigate the release behaviour of 4 actinides (Th, U, Np and Pu) and 3 lanthanides (La, Ce and Nd) from the solid into solution. The experiments were conducted under Rowing conditions using synthetic aqueous solutions. The lanthanide and actinide concentrations were measured in the leachates before and after filtration to 0.45 mu m and 1.8 nm. Over 98.5% of the lanthanides and Th released from the glass were retained in the alteration products on the glass surface, probably coprecipitated with a siliceous gel. The retention was enhanced by the presence in the gel of 20 wt% P oxides from the initial 5 x 10(-3) M PO4 solution. In the leachates, more than 90% of the lanthanides and Th were associated with colloidal particles. Uranium and Np retention varied from 40% in a 5 x 10(-3) M CO, medium to 95% in a 5 x 10(-3) PO4 medium. In the CO3 medium, U and Np formed stable CO3 complexes that diminished the formation of precipitates: in the PO4 medium, precipitation of PO4 or more complex phases may have occurred. Pu exhibited atypical behaviour to the extent that it was strongly bonded to colloidal particles in solution, concentrated in the fraction exceeding 0.45 mu m, and modifyed the calculated Pu leach rates. These particles may be the result of limited disaggregation of the alteration film. As most of the Pu was found at valence IV, it may be strongly retained in the alteration layer by precipitation or coprecipitation. Under oxidizing conditions, Np and U are found at high valences as Np(V) and U(VI), yielding charged forms in solution (NpO2+ and UO2+). The ianthanides, Th and Pu were present at lower valences as Ln(III), Th(IV) and Pu(IV), yielding Ln(3+), Th4+ and Pu4+ in oxidizing media. The different behaviour of U and Np compared with the lanthanides, Th or Pu, observed during these experiments shows that the valence is the determining factor, and must be taken into account in assessing the evolution of radionuclides during the alteration of nuclear waste glass. (C) 1998 Elsevier Science. All rights reserved. [References: 97]
机译:在非放射性和放射性核废玻璃上进行了水介质中的浸出实验,以研究4种act系元素(Th,U,Np和Pu)和3种镧系元素(La,Ce和Nd)从固体中释放到溶液中的行为。使用合成水溶液在划船条件下进行实验。在过滤至0.45μm和1.8nm之前和之后,在渗滤液中测量镧系元素和act系元素的浓度。从玻璃中释放出的98.5%的镧系元素和Th被保留在玻璃表面的蚀变产物中,可能与硅质凝胶共沉淀。通过在凝胶中存在20 wt%的P氧化物(来自最初的5 x 10(-3)M PO4溶液),可以提高保留率。在渗滤液中,超过90%的镧系元素和Th与胶体颗粒相关。铀和Np的保留量从5 x 10(-3)M CO介质中的40%到5 x 10(-3)PO4介质中的95%不等。在CO3介质中,U和Np形成了稳定的CO3复合物,从而减少了沉淀物的形成:在PO4介质中,可能发生了PO4或更复杂相的沉淀。 Pu表现出非典型的行为,即它与溶液中的胶体颗粒牢固结合,并浓缩到超过0.45μm的部分,从而改变了计算得出的Pu浸出率。这些颗粒可能是蚀变膜有限度分解的结果。由于大多数Pu的价位为IV,因此可能通过沉淀或共沉淀而强烈保留在蚀变层中。在氧化条件下,Np和U以高价形式被发现为Np(V)和U(VI),在溶液中产生带电形式(NpO2 +和UO2 +)。镧系元素,Th和Pu的化合价较低,分别为Ln(III),Th(IV)和Pu(IV),在氧化介质中生成Ln(3 +),Th4 +和Pu4 +。在这些实验中观察到的U和Np与镧系元素Th或Pu的不同行为表明,化合价是决定性因素,在评估核废料玻璃更换过程中放射性核素的演变时必须将其考虑在内。 (C)1998 Elsevier科学。版权所有。 [参考:97]

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