Co-pyrolysis of sewage sludge as additive with phytoremediation residue on the fate of heavy metals and the carbon sequestration potential of derived biochar

Abstract

Considering the characteristics of municipal sewage sludge (MS) and Sedum alfreddi L. (SA, a hyperaccumulator plant), we attempted to use MS to enhance the enrichment and stability of heavy metals (HMs) in pyrolysis residue during SA pyrolysis. The effects of pyrolysis temperature (400–800 °C) and co-pyrolysis on migration behavior, chemical speciation, long-term leaching toxicity of HMs, and the environmental risk and carbon sequestration potential of biochar were systematically investigated. Besides, thermodynamic equilibrium simulations were performed to study the transformation of HM compounds during pyrolysis. When the pyrolysis temperature increased from 400 °C to 800 °C, the unstable fractions (F1+F2) of Cd, Pb, Cu, and Cr in MS1SA3 800 had decreased to less than 6% and Zn to 20.4%, and long-term leachability of HMs decreased continuously. Meanwhile, biochar's ecological risk was reduced to a low level, while its carbon sequestration potential improved with little released HMs. Compared with SA pyrolysis alone, adding MS increased the relative residue content of Cd and Zn in biochar, whereas no apparent effect on Pb, Cu, and Cr, and the proportion of stable fractions (F3+F4) increased. Co-pyrolysis enhanced the carbon sequestration potential of biochar, attributed to the inherent minerals of MS. Equilibrium calculations showed that the influence of MS on the fate of HMs during SA pyrolysis is mainly attributed to its high sulfur content, while Si and Al preferentially combine with alkali metal (K)/alkaline earth metal (Ca) and then interact with Zn. The findings in this paper suggest that co-pyrolysis of MS as an additive with hyperaccumulator plants is a feasible proposal, and the co-pyrolysis biochar obtained at suitable temperatures has the potential for safe application.