4.7 Article

A novel method of calcium dissolution-crystallization-polymerization for stabilization/solidification of MSWI fly ash

Journal

CHEMOSPHERE
Volume 326, Issue -, Pages -

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2023.138465

Keywords

Carbon dioxide; Carbonation; Heavy metals; pH -dependent leaching; Polymers; Geochemical model

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Municipal solid waste incineration fly ash (MSWI FA) stabilization/solidification using calcium carbonate (CaCO3) oligomer is an efficient, low-carbon disposal method. This method converts insoluble calcium in FA to free calcium, which is then utilized for CaCO3 oligomer preparation. The CaCO3 oligomers effectively stabilize and solidify potentially toxic elements (PTEs) such as lead (Pb) and zinc (Zn). Experimental results show that the weakly alkaline acid-leaching suspension provides an excellent condition for the generation of CaCO3 oligomers, with Pb and Zn immobilization reaching over 99.4%. The use of ethanol as a solvent and triethylamine (TEA) as a capping agent promotes the synthesis of CaCO3 oligomers.
Municipal solid waste incineration fly ash (MSWI FA) stabilization/solidification using calcium carbonate (CaCO3) oligomer is an efficient, low-carbon disposal method. The insoluble Ca in FA was converted to free-Ca, utilizing for CaCO3 oligomer preparation, which was crystallized and polymerized by thermal induction to develop continuous cross-link or bulk structures for stabilization/solidification of potentially toxic elements (PTEs, e.g., lead (Pb) and zinc (Zn)). Experimental results showed that the weakly alkaline acid-leaching sus-pension provided an excellent condition for the generation of CaCO3 oligomers, with Pb and Zn immobilization reaching over 99.4%. With the acid strengthening of the suspension, H+ took the lead in protonating with TEA and limiting the capping action of TEA, which was harmful to the synthesis of CaCO3 oligomers. Ethanol with a low dielectric constant was considered an ideal solvent for oligomer production, and triethylamine (TEA) as a capping agent established hydrogen bonds (NMIDLINE HORIZONTAL ELLIPSISH) with protonated CaCO3. H2O molecules competed with the protonated CaCO3 molecules for TEA with ethanol concentration decreasing, resulting in erratic precipitation of CaCO3 molecules and significantly elevated leaching risk of Pb and Zn. The sequential extraction procedure, pH -dependent leaching, and geochemical analysis results revealed that the dissolution/precipitation of Ca, Pb, and Zn in treated FA was mostly controlled by the carbonate mineral phases. Moreover, the low boiling points of ethanol and TEA can be recovered for recycling. The gel-like, flexible combination of CaCO3 oligomers and FA particles formed by FA offers great resource utilization potential via a controlled crystallization polymerization process.

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