Abstract

Pharmaceutical effluents in water bodies pose hazards to the ecosystem because of their potent biological toxicity. Focusing on the removal of such toxic complicated pharmaceutical residues, an innovative LaTiO2N/g-C3N4@Fe3O4 heterojunction photocatalyst was assembled by a simplistic route for visible and solar light degradation of anti-inflammatory drug indomethacin (IDM). The LCF-20 catalyst (with LaTiO2N:g-C3N4 -0.2:1) shows excellent performance for visible light photodegradation of IDM, as evidenced by 97.3 % removal in just 45 min exposure which is about 13 times faster than bare g-C3N4. 83.4 % of total organic carbon removal was achieved by LVF-20 under visible light. Also, with natural sunlight, nearly 80 % of IDM was removed in 90 min irradiation. The heterojunction’s extensive intimate interfacial interactions amid LaTiO2N and g-C3N4 reduce the shortcomings of the two for a better photo-activity. The high visible activity, diminished recombination, high charge transfer is attributed to effective Z-scheme transfer facilitated by Fe3O4 nanoparticles. Scavenging experiments prove the importance of superoxide radicals as the dominant species responsible for photodegradation reaction. By mass spectrometry and total organic carbon analysis, a reaction mechanism was also reasonably proposed. The photocatalytic mechanism was discussed in light of conventional and Z-scheme transfer for better insight. The catalyst is stable, recyclable and magnetically separable. This investigation offers a new perspective in the rational design and manufacture of organic-inorganic nitrides based magnetically recoverable heterojunctions as LaTiO2N/g-C3N4@Fe3O4. Such heterojunctions present a new class of robust hierarchical photocatalytic materials which are capable of remediation of pharmaceutical residues under practical conditions.

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