In this paper, a two dimensional/two dimensional (2D/2D) heterostructure of TiC/g-CN (T/CN) was constructed and used to activate peroxymonosulfate (PMS) for the degradation of diclofenac (DCF) in water in the presence of light illumination. Compared with single photocatalytic process by T/CN (0.040/min) and with pure g-CN nanosheets in PMS system (0.071/min), 5.0 and 3.0 times enhanced activities were achieved in the T/CN-PMS system at optimum TiC (1.0 wt%) loading under light illumination (0.21/min). Moreover, the decomposing processes of DCF in T/CN-PMS system were applicable in a wide initial pH range (3∼14), therefore, overcoming the limitation of pH dependence in traditional PMS system. Based on the synergistic effect of photocatalysis and PMS oxidation processes, the O was generated as primary reactive species for the removal of DCF in T/CN-PMS system. The DCF degradation mechanism was further proposed through the results of liquid chromatography-mass spectrometry (LC-MS) and density functional theory (DFT) calculations.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.chemosphere.2020.127339 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!