Using MXene as substrate, CoOOH@MXene with different mass content of CoOOH were prepared and used to active peroxymonosulfate (PMS) for the sulfamethoxazole (SMX) degradation. The sample characterizations demonstrated the successful… Click to show full abstract
Using MXene as substrate, CoOOH@MXene with different mass content of CoOOH were prepared and used to active peroxymonosulfate (PMS) for the sulfamethoxazole (SMX) degradation. The sample characterizations demonstrated the successful preparation of CoOOH@MXene. CoOOH@MXene possessed much higher BET surface area (183.82 m2/g) than CoOOH (85.36 m2/g) and MXene (6.89 m2/g) due to the good dispersibility of CoOOH particles on MXene. Due to its large surface area, 1.3CoOOH@MXene displayed the best catalytic performance for the degradation of SMX. With 0.2 g/L of 1.3CoOOH@MXene and 0.5 mM of PMS, 20 μM of SMX was completely eliminated in 10 min. The degradation followed pseudo-first-order kinetic model well, with rate constants of 0.33 min−1 for 1.3CoOOH@MXene and 0.054 min−1 for CoOOH. Influencing factors of initial pH, catalyst dosage, PMS concentration, SMX concentration, and co-existing anions on SMX degradation were assessed systematically. Recycling tests verified the excellent reusability and stability of the catalyst. Quenching experiments and electron paramagnetic resonance analysis substantiated that 1O2 played a leading role. Moreover, the intermediates were identified, and degradation pathways and activation mechanism of CoOOH@MXene for PMS were proposed. This work may highlight the application of MXene with transition metals in PMS activation.
               
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