Abstract

Fabricating heterojunction catalysts is a promising strategy for improving the performance in heterogeneous photo-Fenton reaction (PFR). Herein, a Z-scheme heterostructured α-Fe2O3@g-C3N4 catalyst was successfully synthesized through the co-calcination of melamine and Fe-based MOF. The characterization results demonstrated that α-Fe2O3 nanoparticles anchored on the surface of g-C3N4 successfully. The degradation of tetracycline (TC) in visible-light/H2O2 system was adopted to evaluate the photo-Fenton activity of the catalysts. About 92% of TC was degraded by the optimum composite FOCN-0.45 in 60 min; the degradation rate (0.042 min−1) of TC by the FOCN-0.45 is 6, 7 and 14 times higher than that by pristine MIL-53 (Fe) (0.007 min−1), α-Fe2O3 (0.006 min−1) and g-C3N4 (0.003 min−1), respectively. The prepared FOCN-0.45 composite exhibited excellent performance and high stability in a wide range of pH value. The promoted photo-Fenton catalytic efficiency benefited from the Z-scheme heterojunctions of α-Fe2O3@g-C3N4, which enhanced the separation ability of photo-generated charge carriers and increased the electrons that participated in Fe2+/Fe3+ cycle. The boosting OH radicals degraded organic pollutants as main reactive radicals. This work presents a feasible path to design and synthesize heterogeneous photo-Fenton catalysts for the removal of organic pollutants.

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