This study proposed a novel closed-wet accelerated carbonation method based on ultrasonic chemistry for treating municipal solid waste incineration fly ash (MSWI FA), assessing various reaction parameters (time, temperature, CO2 pressure, ultrasonic power, and alkaline additives) on the detoxification and synergistic carbon fixation. The mechanisms of carbon sequestration, heavy metal migration-stabilization, and PCDD/Fs migration-degradation were elucidated. Key findings include the reaction kinetic of MSWI FA ultrasonic carbonation aligning with the surface coverage model (R2 > 0.999), achieving a carbonation efficiency of 29.4% within 30 min. Optimal conditions-room temperature, 1-2 MPa CO2 pressure, and 500 W ultrasonic power-enhanced carbon sequestration and heavy metal stabilization. The formation of fine calcium carbonate resulted in the co-precipitation of heavy metals, such as Ba, Pb, and Zn, avoiding liquid phase heavy metal pollution and reducing their leaching concentrations in solid samples well below the HJ 1134-2020 standard. The particle size reduction rate was 69.9% (18.6 μm) for non-ultrasonic carbonated FA compared to 89.2% (6.7 μm) for ultrasonic carbonated FA (UFA). NaOH and ammonia addition effectively decreased calcium concentration in the carbonation reaction solution (<200 mg/L) and calcium sulfate content in UFA. The ultrasonic carbonation process prevented PCDD/Fs from migrating into the reaction solution and achieved 35.0% PCDD/Fs degradation. This comprehensive evaluation supports the viability of ultrasonic carbonation for treating MSWI FA.
Keywords: Alkaline additive; CO(2) mineralization; Dioxin degradation; Heavy metal leaching risk; Resource recycling; Ultrasound excitation.
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