Effect of Pyrolysis Temperature on Removal Efficiency and Mechanisms of Hg(II), Cd(II), and Pb (II) by Maize Straw Biochar

Pyrolysis temperature significantly affects the properties of biochar, which in turn can affect the removal of heavy metal ions and the underlying mechanism. In this work, biochars from the pyrolysis of maize straw at 300, 400, and 500 degrees C (BC300, BC400, and BC500, respectively) and wheat straw at 400 degrees C (WBC400) were investigated. The influence of production temperature on the adsorption of Hg2+, Cd2+, and Pb2+ by maize straw biochar was investigated by the characterization of the biochars and by adsorption tests. The adsorption capacities of maize and wheat straw biochar were compared in an adsorption experiment. Biochar BC400 showed the best physical and chemical properties and had the largest number of surface functional groups. The pseudo-second-order kinetic model was more suitable for describing the adsorption behavior of metal ions to biochar. The Langmuir model better fit the experimental data. Biochar BC400 had a higher adsorption speed and a stronger adsorption capacity than WBC400. The sorption of Pb2+ and Hg2+ to maize straw biochar followed the mechanisms of surface precipitation of carbonates and phosphates and complexation with oxygenated functional groups and delocalized pi electrons. The adsorption mechanism for Cd2+ was similar to those of Hg2+ and Pb2+, but precipitation mainly occurred through the formation of phosphate. In the multi-heavy-metal system, the adsorption of Cd2+ by BC400 was inhibited by Pb2+ and Hg2+. In summary, BC400 biochar was most suitable for the adsorption effect of heavy metals in aqueous solution.

Automated summary

Pyrolysis temperature has a significant impact on the properties of biochar, which in turn affects the adsorption of heavy metal ions. Comparing biochars from the pyrolysis of maize straw and wheat straw, it was found that the biochar produced at 400 degrees C from maize straw showed the best physical and chemical properties, as well as a higher adsorption rate and capacity. The adsorption mechanisms involve surface precipitation of carbonates and phosphates, as well as complexation with oxygenated functional groups and delocalized pi electrons.