Compound-specific stable isotope analysis for characterization of the transformation of γ-HCH induced by biochar

The role of biochar as the redox catalyst in the removal of reductive pollutants from soil and water system has been extensively studied recently, but there is still a lack of qualitative description of its specific mechanisms in redox processes. In this study, the mechanism of biochar in the transformation process of γ-HCH under anoxic condition was revealed by the compound-specific isotope analysis. The concentration and carbon isotopic composition (δ¹³C) of γ-HCH were detected in the treatments with different initial concentrations of γ-HCH and biochar materials with different redox properties and varied doses. The surface functional groups and electrochemical properties of biochar before and after the reaction were also characterized. The addition amount of biochar could affect the reduction of γ-HCH concentration, which were 59.1%, 34.6% and 22.4% in treatments with the addition of 5%, 1% and 0.2% biochar, respectively. Meanwhile, the δ¹³C value of γ-HCH also increased from -26.6 ± 0.2‰ to -23.8 ± 0.2‰ with the addition amount of biochar, especially in the treatment with 5% biochar. As evidenced by X-ray diffraction analysis and electrochemical analysis, biochar promoted the adsorption and transformation of γ-HCH simultaneously, and the oxygen-containing functional groups on the surface of biochar played an important role in the redox process. The isotopic fractionation value (ε_C) of γ-HCH transformation by biochar was first reported as -3.4 ± 0.4‰. The results will enable the quantitative description of the transformation degree of organic pollutants induced by biochar, and provide a new approach for evaluating the in-situ remediation effects of biochar in a complex environment.