Synthesis of N-A-S-H Gels via Sol–Gel and Hydrothermal Methods: Composition, Microstructure, and Dynamic Adsorption Characteristics for Sr2+
Artikel i vetenskaplig tidskrift, 2026

Fly ash-based geopolymers are widely used as solidification matrices for intermediate- and low-level radioactive waste liquids. Their performance relies heavily on the adsorption capacity of the primary component, N-A-S-H gels, which directly governs the long-term stability of the solidified waste form. This study prepared N-A-S-H gels using both the sol–gel synthesis and the hydrothermal synthesis method. The effects of the Si/Al ratio, alkalinity, and NaNO3 on the structure of N-A-S-H gels were analyzed using EDS, FT-IR, and XRD. Additionally, the dynamic adsorption capacity of N-A-S-H gels for Sr2+ under varying solution temperatures and alkaline conditions was evaluated and fitted using the Thomas and Yoon–Nelson models. For sol–gel-synthesized gels, a lower initial Si/Al ratio led to a higher theoretical maximum Sr2+ adsorption capacity of 121.71 mg/g at room temperature and neutral pH. For hydrothermally synthesized gels from raw fly ash, the high initial alkalinity reduced the Si/Al ratio but adversely decreased Sr2+ adsorption capacity. Raising the temperature to 60 °C improved Sr2+ uptake for all gel samples, with a maximum increase of 28.75 mg/g. Under alkaline conditions, Sr2+ uptake for all gels decreased significantly, with a minimum theoretical reduction of 31.55 mg/g. The findings of this study provide a theoretical foundation for understanding the radionuclide migration mechanisms of fly ash-based geopolymer solidification forms in complex geological environments.

Si/Al

N-A-S-H gels

dynamic adsorption capacity

sol–gel synthesis

hydrothermal synthesis

Författare

Zhao Zheng

SWUST

Xinpeng Ye

SWUST

Jun Yang

SWUST

Long Shi

SWUST

Xue Ma

SWUST

Luping Tang

Chalmers, Arkitektur och samhällsbyggnadsteknik, Byggnadsteknologi

Materials

19961944 (eISSN)

Vol. 19 19 4035

Ämneskategorier (SSIF 2025)

Keramiska och pulvermetallurgiska material

Oorganisk kemi

DOI

10.3390/ma19194035

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Senast uppdaterat

2026-10-23