Abstract
The development of efficient solar driven catalyst for the degradation of antibiotics has become increasingly important in environmental protection. However, the reported efficient photocatalysts for antibiotic degradation are limited. In this work, porous Fe3+-doped graphitic carbon nitride (g-C3N4) with outstanding photocatalytic ability is synthesized and then used as the photocatalyst for the efficient degradation of sulfadiazine (SDZ) under visible light. A series of characterization results indicate that Fe3+ is successfully doped into the interlayer of g-C3N4 and is stabilized in g-C3N4 by Fe-N coordination bond. The SEM, DRS and ESI and transient photocurrent results demonstrated that Fe3+-doped g-C3N4 has a porous structure, a low band gap, improved separation efficiency of photogenerated electron and holes as well as a wider light absorption range. Such improved physical and chemical properties greatly enhanced the photocatalytic ability. Using Fe3+-doped g-C3N4 for photocatalytic degradation of SDZ under white light, almost complete degradation of SDZ was achieved with a degradation efficiency as high as 99.8% (whereas only 52.1% for bulk g-C3N4) within 90min. The degradation was mainly ascribe to 1O2 during the irradiation, and also a small amount of •O2-, OH• and h+ are involved in the degradation process. The Fe3+-doped g-C3N4 was applicable for the degradation of a wide range of antibiotic pollutants.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Environmental science and pollution research international
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.