A novel solid digestate-derived biochar-Cu NP composite activating H2O2 system for simultaneous adsorption and degradation of tetracycline

Solid digestate, a by-product of anaerobic digestion systems, has led to a range of environmental issues . In the present study, a novel composite based on a solid digestate-biochar-Cu NP composite was synthesized for tetracycline removal from an aqueous medium. The removal efficiency values for tetracycline (200 mg L −1 ) were 31.5% and 97.8%, respectively, by the biochar-Cu NP composite (0.5 g L −1 ) in the absence and presence of hydrogen peroxide (H 2 O 2 , 20 mM) within 6 h of reaction time. The possible degradation pathway of tetracycline was investigated using liquid chromatography-mass spectrometry. The desorption experiment results suggested that no significant concentration of tetracycline was detected on the composite after the reaction, but a small amount of intermediates in terms of total organic carbon (TOC) accounting for 3.1%, and 23.3% of the end-product NH 4 + was adsorbed onto the biochar sheets. The dispersive Cu NPs on the biochar resulted in an increase in the surface area and pore volume of the biochar-Cu NP composite, which enhanced tetracycline adsorption as well as the degradation efficiency. Relative tetracycline removal mechanisms were dominantly ascribed to ·OH generation from the Cu(II)/Cu(I) redox reaction with H 2 O 2 and the electron-transfer process of free radicals (FRs) in biochar. The proposed approach serves dual purposes of waste digestate reuse and treatment of antibiotic pollutants. This study highlights the activation of H 2 O 2 by the dispersive Cu NPs coupling with biochar derived from a waste solid digestate for tetracycline treatment.