Co-pyrolysis with pine sawdust reduces the environmental risks of copper and zinc in dredged sediment and improves its adsorption capacity for cadmium.

Proper treatment of heavy metal-contaminated dredged sediment (DS) is crucial to avoid secondary pollution. Effective and sustainable technologies are desired for the treatment of Zn- and Cu-contaminated DS. Due to the advantages of low energy consumption and time saving, co-pyrolysis technology was innovatively applied to treat Cu- and Zn-polluted DS in this study, and the effects of the co-pyrolysis conditions on Cu and Zn stabilization efficiencies, potential stabilization mechanisms, and the possibility for resource utilization of co-pyrolysis product were also investigated. The results showed that pine sawdust is an appropriate co-pyrolysis biomass for the stabilization of Cu and Zn based on the leaching toxicity analysis. The ecological risks of Cu and Zn in DS were reduced after co-pyrolysis treatment. The total concentrations of Zn and Cu in co-pyrolysis products were decreased by 5.87%-53.45% and 8.61%-57.45% of that in DS before co-pyrolysis. However, the total concentrations of Zn and Cu in DS remained basically unchanged after co-pyrolysis, which indicating the decreases in total concentrations of Zn and Cu in co-pyrolysis products were mainly related to dilution effect. Fraction analysis indicated that co-pyrolysis treatment contributed to transforming weakly bound Cu and Zn into stable fractions. The co-pyrolysis temperature and mass ratio of pine sawdust/DS had a greater influence than co-pyrolysis time on the fraction transformation of Cu and Zn. The leaching toxicity of Zn and Cu from the co-pyrolysis products was eliminated when the co-pyrolysis temperature reached 600 and 800 °C, respectively. Analysis of the X-ray photoelectron spectroscopy and X-ray diffraction results demonstrated that co-pyrolysis treatment could transform mobile Cu and Zn in DS into metal oxides, metal sulfides, phosphate compounds, etc. Batch adsorption procedures suggested that the co-pyrolysis product possessed a high adsorption capacity for Cd (95.70 mg/g at 318 K). The formation of CdCO3 precipitates and the complexation effects of oxygen-containing functional groups were the principal adsorption mechanisms of the co-pyrolysis product. Overall, this study provides new insights into sustainable disposal and resource utilization for heavy metal-contaminated DS.