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测定硅酸钙水合物相中吸附的六价铀:激光诱导发光光谱法和批量吸附研究。

Determination of uranium(VI) sorbed species in calcium silicate hydrate phases: a laser-induced luminescence spectroscopy and batch sorption study.

机构信息

Paul Scherrer Institute, Waste Management Laboratory, CH-5232 Villigen-PSI, Switzerland.

出版信息

J Colloid Interface Sci. 2011 Jul 1;359(1):248-56. doi: 10.1016/j.jcis.2011.03.046. Epub 2011 Mar 21.

DOI:10.1016/j.jcis.2011.03.046
PMID:21489548
Abstract

Batch sorption experiments and time-resolved luminescence spectroscopy investigations were carried out to study the U(VI) speciation in calcium silicate hydrates for varying chemical conditions representing both fresh and altered cementitious environments. U(VI) uptake was found to be fast and sorption distribution ratios (R(d) values) were very high indicating strong uptake by the C-S-H phases. In addition a strong dependence of pH and solid composition (Ca:Si mol ratio) was observed. U(VI) luminescence spectroscopy investigations showed that the U(VI) solid speciation continuously changed over a period up to 6 months in contrast to the fast sorption kinetics observed in the batch sorption studies. Decay profile analysis combined with factor analysis of series of spectra of U(VI)-C-S-H suspensions, recorded with increasing delay times, revealed the presence of four luminescent U(VI) species in C-S-H suspensions, in agreement with the batch sorption data. Along with the aqueous UO(2)(OH)(4)(2-) species and a Ca-uranate precipitate, two different sorbed species were identified which are either bound to silanol groups on the surface or incorporated in the interlayer of the C-S-H structure.

摘要

开展了批式吸附实验和时间分辨荧光光谱研究,以研究在不同化学条件下(代表新鲜和改变的水泥环境)硅酸钙水合物中 U(VI) 的形态。发现 U(VI) 的吸附速度很快,分配比(R(d) 值)非常高,表明 C-S-H 相具有很强的吸附能力。此外,还观察到 pH 值和固体组成(Ca:Si 摩尔比)的强烈依赖性。U(VI) 荧光光谱研究表明,与批式吸附研究中观察到的快速吸附动力学相反,U(VI) 的固体形态在长达 6 个月的时间内不断变化。衰减曲线分析结合对 U(VI)-C-S-H 悬浮液的一系列光谱的因子分析,记录了随着延迟时间的增加,在 C-S-H 悬浮液中存在四种发光 U(VI) 物种,与批式吸附数据一致。除了水溶液中的 UO(2)(OH)(4)(2-)物种和钙铀酸盐沉淀外,还鉴定出两种不同的被吸附物种,它们要么与表面上的硅醇基团结合,要么掺入 C-S-H 结构的层间。

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