Activation of peroxymonosulfate using metal-free in situ N-doped carbonized polypyrrole: A non-radical process.

Metal-free catalysts are widely considered as promising alternatives to traditional metal-based catalysts, which can effectively activate peroxymonosulfate (PMS). In this study, a novel metal-free catalyst, carbonized polypyrrole (CPPy) was synthesized through high-temperature carbonization of PPy, easily achieving the in situ N doping without the addition of nitrogen sources. Tetracycline (TC) was selected as the target contaminant to assess the catalytic activity of the CPPy/PMS system. Enhanced catalytic activity was observed in CPPy/PMS over a wide pH range (3.0–9.0), and the removal rate of TC by CPPy-3/PMS reached 91.3% after 10 min. After regenerating the used catalyst, the catalytic activity was refreshed, implying its stability and recyclability. The catalytic degradation of TC by CPPy/PMS was mainly attributed to a non-radical process. CPPy, as an intermediary, grabbed electrons from the electron-donating groups of TC and transferred them to the PMS molecule. Thereafter, TC that lost electrons was oxidized and degraded, and the O–O bonds of PMS were destroyed by the transferred electrons to form S O 4 2 − and OH−. Moreover, O ⋅ 2 − and 1O 2 were involved in TC degradation. TC degradation pathway was investigated through HPLC-MS analysis. These findings provide a promising strategy for the construction of catalysts for PMS and environmental remediation. Image 1 • Metal-free N-doped material CPPy was prepared without the addition of N sources. • CPPy/peroxymonosulfate showed excellent catalytic degradation of tetracycline. • The in-situ generation of graphitic N is the key of peroxymonosulfate activation. • The tetracycline degradation is mainly attributed to a non-radical process. [ABSTRACT FROM AUTHOR]