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A composite of cobalt tetracarboxyl phthalocyanine and amino-functionalized manganese octahedral molecular sieve (CNOMS-2) was synthesized in a simple way, and applied for degrading diclofenac in aqueous media by catalyzing of peroxymonosulfate heterogeneously. The experiment results revealed that the CNOMS-2/PMS system was highly efficient for DCF degradation in the pH range of 5-9, and the mechanism involved the generation of OH, SO4⁻ and 1O2 by the activation of PMS. The main reactive oxygen species was found to be 1O2 by radical scavenging experiments and electron paramagnetic resonance (EPR) spectroscopy. Further, a carboxylation product of DCF at m/z 340 was found to be a prominent intermediate of the reaction in this system specially, as determined by LC-MS/MS. The reusability and ion leaching concentrations under different pH were also examined to determine the application prospects of the catalyst.

Diclofenac (DCF) control measures have become an area of increased interest for environmental researchers due to the high environmental concentration and risk of DCF. Adsorption seems to be promising for DCF removal from the aqueous phase because of its specific superiority in comparison with biodegradation, membrane separation, and advanced oxidation or reduction. In this study, OMS-2 and metal-doped OMS-2 ((Me-OMS-2, with Me = Co, Cu or Ce) were prepared and tested as adsorbents for the removal of DCF. It was evident that the maximum adsorption capacity and rate of Ce-OMS-2 were much higher than those of the other adsorbents, which could be attributed to its large specific surface area and stereoscopic aperture structure. The experimental data are fitted the pseudo-second-order model, the Elovich equation and the Langmuir model well; moreover, the process is an endothermic and spontaneous thermodynamic process, during which the entropy increased, based on the experimental results, indicating that chemisorption was dominant during the DCF adsorption process onto Ce-OMS-2. By the integral of the peak deconvoluted from the XPS spectrum, the ratio of Mn3+/Mn4+ increased from 0.393 to 0.407, revealing that Mn(IV) is rarely reduced into Mn(III) during the DCF adsorption process.