Biochar-supported nanoscale zero-valent iron as an efficient catalyst for organic degradation in groundwater

[Display omitted] •The porous biochar carrier can facilitate the TCE removal by alleviating aggregation of iron nanoparticles and enhancing PMS activation.•The biochar catalysts manifested a superior catalytic performance of PMS activation for TCE degradation.•The catalytic performance of Fe-CB600 out-performed other fabricated catalysts.•The superoxide radical and singlet oxygen were validated as predominant ROSs and oxygen containing group played the key role in PMS activation. High-efficiency and cost-effective catalysts are critical to completely mineralization of organic contaminants for in-situ groundwater remediation via advanced oxidation processes (AOPs). The engineered biochar is a promising method for waste biomass utilization and sustainable remediation. This study engineers maize stalk (S)- and maize cob (C)-derived biochars (i.e., SB300, SB600, CB300, and CB600, respectively) with oxygen-containing functional groups as a carbon-based support for nanoscale zero-valent iron (nZVI). Morphological and physiochemical characterization showed that nZVI could be impregnated within the framework of the synthesized Fe-CB600 composite, which exhibited the largest surface area, pore volume, iron loading capacity, and Fe0 proportion. Superior degradation efficiency (100% removal in 20 min) of trichloroethylene (TCE, 0.1 mM) and fast pseudo-first-order kinetics (kobs =22.0 h−1) were achieved via peroxymonosulfate (PMS, 5 mM) activation by the Fe-CB600 (1 g L−1) under groundwater condition (bicarbonate buffer solution at pH = 8.2). Superoxide radical and singlet oxygen mediated by Fe0 and oxygen-containing group (i.e., CO) were demonstrated as the major reactive oxygen species (ROSs) responsible for TCE dechlorination. The effectiveness and mechanism of the Fe/C composites for rectifying organic-contaminated groundwater were depicted in this study.