Giulia Tameni , Diana Lago , Hana Kaňková , Lenka Buňová , Jozef Kraxner , Dušan Galusek , Daniel M. Dawson , Sharon E. Ashbrook , Enrico Bernardo
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引用次数: 0
摘要
本文主要研究了将废弃医药容器中的硼铝硅酸盐玻璃活化成细粉,悬浮在相对稀释的碱性溶液(2.5 M NaOH/KOH)中,然后在40°C下干燥7天。提出了玻璃硬化的具体分子机理。与地聚合物不同,硬化不是由广泛溶解产物的凝结引起的。相反,缩合反应发生在水合表面层,导致单个玻璃颗粒之间的强键(Si-O-Si, Al-O-Si等)。玻璃溶解产生的硅酸盐、硼酸盐和铝酸盐与碱性离子结合,产生额外的可溶相。固体核磁共振光谱和ICP-OES元素分析结果支持了这一机制。通过直接发泡或包含微球或商用膨胀玻璃(Poraver®)制备的稳定基质可用于制造轻质组件
Alkaline attack of boro-alumino-silicate glass: New insights of the molecular mechanism of cold consolidation and new applications
This paper focuses on the activation of boro-alumino-silicate glass from discarded pharmaceutical containers as fine powders suspended in relatively diluted alkaline solutions (2.5 M NaOH/KOH), followed by drying at 40 °C for 7 days. A specific molecular mechanism of glass hardening is proposed. Unlike geopolymers, the hardening does not result from the condensation of products of extensive dissolution. Instead, condensation reactions occur in hydrated surface layers, leading to strong bonds (Si-O-Si, Al-O-Si, etc.) between individual glass particles. Silicates, borates, and aluminates from glass dissolution combine with alkaline ions, yielding additional soluble phases. This mechanism is supported by the results of solid-state NMR spectroscopy and elemental analysis using ICP-OES. Stable matrices prepared by direct foaming or by the inclusion of cenospheres or commercial expanded glass (Poraver®) can be exploited for the fabrication of lightweight components