Insight into radical-nonradical coupling activation pathways of peroxymonosulfate by CuxO for antibiotics degradation

In this work, a heterogeneous catalyst of CuxO was rationally designed by using Cu-based metal organic frameworks (marked Cu-BDC) as the template, and was used to degrade tetracycline (TC) via activation of peroxymonosulfate (PMS). The optimal CuxO-350 showed excellent catalytic efficiency for TC degradation, and the reaction rate constant (0.104 min -1) was 8 times higher than that (0.013 min -1) of raw Cu-BDC. The characterization observations confirmed that CuxO-350 possessed multiple valence states (CuO and Cu2O) and oxygen vacancies (Ov), both of which were favorable for the activation of PMS, resulting in promoting the generation of active species in the CuxO-350 + PMS system. Different from the free radical pathway in Cu-BDC + PMS system, a radical-nonradical coupling process was detected in the CuxO-350 + PMS system, which was confirmed by quenching experiments and EPR measurements. Moreover, the toxicity prediction showed that the toxicity of degradation intermediates declined compared with TC. This work not only opened up a new strategy for the rational design and preparation of high-efficient catalysts by employing metal organic frameworks pre-cursors, but also offered an insight into the reaction mechanism of PMS activation through a radical-nonradical coupling process catalyzed by CuxO-350 derived from Cu-BDC.

Automated summary

A heterogeneous catalyst of CuxO was designed by using Cu-based metal organic frameworks as the template and was used to degrade tetracycline via activation of peroxymonosulfate. The optimal CuxO-350 showed excellent catalytic efficiency and a reaction rate constant 8 times higher than that of raw Cu-BDC. Characterization confirmed that CuxO-350 possessed multiple valence states and oxygen vacancies, favorable for PMS activation and generation of active species.