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Immobilization of (Aqueous) Cations in Low pH M-S-H Cement

Department of Physical Chemistry, University of Konstanz, 78457 Konstanz, Germany
Institute of Geological Sciences, University of Bern, 3012 Bern, Switzerland
Department of Civil and Environmental Engineering, Imperial College London, South Kensington, Skempton Building, London SW7 2AZ, UK
Laboratory for Waste Management, Paul Scherrer Institute, 5232 Villigen, Switzerland
Author to whom correspondence should be addressed.
Academic Editor: Martínez-García Carmen
Appl. Sci. 2021, 11(7), 2968;
Received: 18 February 2021 / Revised: 18 March 2021 / Accepted: 19 March 2021 / Published: 26 March 2021
(This article belongs to the Special Issue Sustainable Construction Materials)
Incorporation of heavy metal ions in cement hydrates is of great interest for the storage and immobilization of toxic, hazardous, and radioactive wastes using cementitious matrix. Magnesium silicate hydrate (M-S-H) is a low pH alternative cementitious binder to commonly used Portland cement. Low pH cements have been considered as promising matrix for municipal and nuclear waste immobilization in the last decades. It is however crucial to assure that the incorporation of secondary ions is not detrimental for the formation of the hydration products. Herein, we investigate the early stages of formation of M-S-H from electrolyte solutions in presence of a wide range of metal cations (LiI, BaII, CsI, CrIII, FeIII, CoII, NiII, CuI, ZnII, PbII, AlIII). The final solid products obtained after 24 h have been characterized via powder X-ray diffraction (PXRD), attenuated total reflectance-Fourier transformed infrared spectroscopy (FTIR-ATR), elemental analysis via energy-dispersive X-ray spectroscopy (EDX), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HR-TEM). In all the experiments, the main precipitated phase after 24 h was confirmed to be M-S-H with a ratio (total metal/Si) close to one. The obtained M-S-H products showed strong immobilization capacity for the secondary metal cations and can incorporate up to 30% of the total metal content at the early stages of M-S-H formation without significantly delaying the nucleation of the M-S-H. It has been observed that presence of Cr, Co, and Fe in the solution is prolonging the growth period of M-S-H. This is related to a higher average secondary metal/total metal ratio in the precipitated material. Secondary phases that co-precipitate in some of the experiments (Fe, Pb, Ni, and Zn) were also effectively trapped within in the M-S-H matrix. Barium was the only element in which the formation of a secondary carbonate phase isolated from the M-S-H precipitates was detected. View Full-Text
Keywords: low pH cement; magnesium-silicate-hydrate (M-S-H); waste immobilization low pH cement; magnesium-silicate-hydrate (M-S-H); waste immobilization
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MDPI and ACS Style

Marsiske, M.R.; Debus, C.; Di Lorenzo, F.; Bernard, E.; Churakov, S.V.; Ruiz-Agudo, C. Immobilization of (Aqueous) Cations in Low pH M-S-H Cement. Appl. Sci. 2021, 11, 2968.

AMA Style

Marsiske MR, Debus C, Di Lorenzo F, Bernard E, Churakov SV, Ruiz-Agudo C. Immobilization of (Aqueous) Cations in Low pH M-S-H Cement. Applied Sciences. 2021; 11(7):2968.

Chicago/Turabian Style

Marsiske, Maximilian R., Christian Debus, Fulvio Di Lorenzo, Ellina Bernard, Sergey V. Churakov, and Cristina Ruiz-Agudo. 2021. "Immobilization of (Aqueous) Cations in Low pH M-S-H Cement" Applied Sciences 11, no. 7: 2968.

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