Brandt Felix, Caes Sébastien, Klinkenberg Martina, Barthel Juri, Liu Sanheng, Lemmens Karel, Bosbach Dirk, Ferrand Karine
Institute of Fusion Energy and Nuclear Waste Management (IFN-2), Forschungszentrum Jülich GmbH 52425 Jülich Germany
Institute of Sustainable Waste & Decommissioning, SCK CEN B-2400 Mol Belgium.
RSC Adv. 2024 Nov 4;14(47):35114-35127. doi: 10.1039/d4ra04936e. eCollection 2024 Oct 29.
Long-term static dissolution experiments, lasting up to ∼1500 days, were conducted on International Simple Glass (ISG) and SON68 glass under hyperalkaline pH, at 70 °C, and at a very high glass surface area to solution volume ratio. The study compared (1) glass dissolution kinetics, (2) secondary phase formation, and (3) the microstructure of the altered glass and secondary phase interface. Boron release indicated rapid initial dissolution followed by a slowdown mainly due to a significant pH drop. ISG reached a residual rate regime, while SON68 approached this regime near the experiment's end, with both glasses having similar final dissolution rates. Electron microscopy (SEM, TEM, EDS) of the reacted glass surfaces and the alteration products revealed nontronite formation on SON68, while C(A)SH phases and later rhodesite appeared on ISG, in addition to phillipsite-type zeolite formation observed in both experimental series. TEM observations revealed a porous, foam-like surface altered layer (SAL) near the pristine glass. SON68's SAL nanostructure, more complex than ISG's, had two porous zones, hindering water transfer and glass constituent release, in addition to a pH drop reducing silica network hydrolysis. TEM-EDS showed cation exchange and iron depletion in SON68's SAL, leading to nontronite formation. Secondary phases at the SAL-solution interface did not destabilize the SAL, and no alteration resumption was observed due to the pH drop below the threshold necessary for an alteration resumption due to zeolite formation. In conclusion, the combination of alkaline conditions and very high reaction progress does not lead to the dissolution of the glass by a dissolution-reprecipitation mechanism, as typically observed at much lower SA/V ratios. At the relatively mildly alkaline pH reached within the first year of the experiments, the diffusion of cations through the SAL becomes rate-controlling.
在高碱性pH值、70°C以及非常高的玻璃表面积与溶液体积比条件下,对国际简单玻璃(ISG)和SON68玻璃进行了长达约1500天的长期静态溶解实验。该研究比较了(1)玻璃溶解动力学、(2)次生相形成以及(3)蚀变玻璃和次生相界面的微观结构。硼释放表明初始溶解迅速,随后减缓,主要是由于pH值显著下降。ISG达到了残余速率状态,而SON68在实验接近尾声时接近该状态,两种玻璃的最终溶解速率相似。对反应后的玻璃表面和蚀变产物进行电子显微镜(SEM、TEM、EDS)观察发现,SON68上形成了绿脱石,而ISG上除了在两个实验系列中均观察到的钙十字沸石型沸石形成外,还出现了C(A)SH相和后来的蔷薇辉石。TEM观察显示,在原始玻璃附近有一个多孔的、泡沫状的表面蚀变层(SAL)。SON68的SAL纳米结构比ISG的更复杂,有两个多孔区域,除了pH值下降降低了硅氧网络水解外,还阻碍了水的传输和玻璃成分的释放。TEM-EDS显示SON68的SAL中存在阳离子交换和铁耗尽,导致绿脱石形成。SAL-溶液界面处的次生相并未使SAL不稳定,并且由于pH值降至因沸石形成而恢复蚀变所需的阈值以下,未观察到蚀变恢复。总之,碱性条件和非常高的反应进程的结合并不会像在低得多的SA/V比下通常观察到的那样,通过溶解-再沉淀机制导致玻璃溶解。在实验的第一年达到的相对温和的碱性pH值下,阳离子通过SAL的扩散成为速率控制因素。