| The Ag3PO4/g-C3N4,Ag3PO4/MFe2O4(M=Zn,Ni,Co)and Ag3PO4/rGO/CoFe2O4were synthesized and characterized by XRD,SEM,TEM,XPS,TG,UV-vis DRS,FT-IR,etc.The photocatalytic activities of as-synthesized composites were evaluated by degrading organic dyes and antibiotics,and the performance enhancement and photocatalytic mechanisms were also proposed.The main conclusions are as follows:The Z-scheme Ag3PO4/g-C3N4 was synthesized by a sample hydrothermal method.The photocatalytic performance of Ag3PO4/g-C3N4 for methyl orange degradation was higher than Ag3PO4,but was similar with Ag3PO4 for tetracycline degradation.In Ag3PO4/g-C3N4 system,h+and O2·-were the main reactive species for methyl orange degradation,while h+and H2O2 were the main reactive species for tetracycline removal.Magnetic Ag3PO4/MFe2O4(M=Zn,Ni,Co)composite was hydrothermally synthesized.The introduction of MFe2O4 can increase the surface area and visible light absorption ability of Ag3PO4.Among the three composites,Ag3PO4/CoFe2O4 exbibited the best photocatalytic performance for methyl orange,methylene blue,tetracycline and levofloxacin degradation.Due to the photo-generated electrons and holes of MFe2O4easily recombined,thus they cannot participate in the photocatalytic reaction.CoFe2O4promoted the separation and transfer of photo-induced carriers,which inhibited the reduction of Ag+,thereby improving the stability of Ag3PO4.Magnetic Ag3PO4/rGO/CoFe2O4 was synthesized via a solvothermal and precipitation method.The ternary catalyst showed an excellent adsorption-photocatalysis performance for removing levofloxacin due to rGO improved the adsorption ability and charge separation efficiency of the catalyst.The degradation efficiency of levofloxacin in river water,lake water and secondary effluent by the ternary catalyst reached to 90%.1O2was the main reactive species for levofloxacin degradation and four possible degradation routes of levofloxacin were proposed.After five cycles,the removal efficiency of levofloxacin from the real water matrices by the ternary catalyst was above 80%.Figure 57;Table 8;Reference 136... |