Abstract

In recent works, many industrial by-products were employed as solid precursors for the synthesis of alkali-activated binders and as alternatives to Portland cement for the immobilization of hazardous, toxic and nuclear wastes. Among industrial wastes, alkali-activated brick was found to be an interesting porous composite for removing very toxic heavy metals (Pb2+, Cd2+, Co2+) and radio-nuclides (Sr2+, Cs+, Rb+) from aqueous solutions. The starting material is very attractive due to the presence of metakaolinite as a geo-polymer precursor and silica for increasing material permeability and facilitating water filtration. The alkaline reaction gave rise to geo-polymerization followed by partial zeolitization. Elemental surface micro-analysis was performed by Scanning Electron Microscopy (SEM) equipped with an Energy-Dispersive X-ray Spectrometer (EDS). The formation of crystalline phases was corroborated by X-ray diffraction (XRD) analysis. Information about 29Si, 27Al and 1H nuclei environments in crystallized and amorphous aluminosilicates was obtained by 29Si, 27Al and 1H MAS NMR. 27Al–1H dipolar-mediated correlations were investigated by employing dipolar hetero-nuclear multiple quantum coherence (D-HMQC) NMR, highlighting Al–O–H bonds in bridging hydroxyl groups (Si–OH–Al) that are at the origin of adsorptive properties. Aqueous structural stability and cationic immobilization characteristics before and after material calcination were investigated from acid-leaching experiments.

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