Due to the synergistic redox coupling between the two metals, cobalt ferrite-based materials demonstrate stable degradation properties for organic pollutants by activating peroxomonosulfate (PMS). However, the challenge lies in developing the simplest and fastest methods to construct and modulate cobalt ferrite composites. In this study, CoFe2O4 nanoparticle-integrated carbon black composite catalysts (CoFe2O4-CB-x) were prepared using an environmentally friendly solid-state microwave method. The CoFe2O4-CB-120 catalyst showed excellent efficiency in degrading tetracycline (TC) through PMS activation, achieving a removal rate of nearly 90 % in 30 min with an apparent rate constant of 0.1232 min−1. The catalyst also effectively degraded various organic compounds and real-life wastewater by almost 80 %, promising application potential. Furthermore, CoFe2O4-CB-120 maintained its high activity after five cycles, attributed to its its magnetic properties facilitating good separation and preventing catalyst loss during cycling tests. The degradation mechanism of the CoFe2O4-CB-120/PMS system was thoroughly investigated, identifying key active species such as SO4•−, •OH, and 1O2, with proposed pathways for TC degradation. This study presents an innovative, simple, and efficient strategy for producing spinel cobalt ferrite and carbon composites for PMS activation in organic pollutant degradation.