Back to Search Start Over

Kinetic Comparison of Photocatalysis with the Photo-Fenton Process on the Removal of Tetracycline Using Bismuth-Modified Lanthanum Orthoferrite Nanostructures.

Authors :
James, Anupriya
Rodney, John D.
N. K., Udayashankar
Source :
ACS Applied Nano Materials; 5/24/2024, Vol. 7 Issue 10, p11560-11574, 15p
Publication Year :
2024

Abstract

In this study, we investigate visible-light-driven photocatalytic and photo-Fenton degradation of tetracycline (TC) using bismuth-impregnated lanthanum orthoferrite (Bi<subscript>x</subscript>La<subscript>1–x</subscript>FeO<subscript>3</subscript> (x = 0, 0.01, 0.05, 0.07)) nanostructures. Bi doping significantly improves the removal of TC, with Bi<subscript>0.05</subscript>La<subscript>0.95</subscript>FeO<subscript>3</subscript> (LFO-Bi5) exhibiting optimal degradation. In both photocatalysis (PC) and photo-Fenton catalysis (PFC), the reaction follows pseudo-first-order kinetics, with LFO-Bi5 showing rate constants of 0.0065/min for PC and 0.02716/min for PFC, surpassing LaFeO<subscript>3</subscript> by 2.76 and 3.43 times, respectively. The long-term presence of photoexcited carriers in LFO-Bi5 is confirmed through transient PL, TRPL, and EIS studies. The superior degradation capabilities are attributed to radicals in photocatalysis and OH<superscript>•</superscript> radicals in photo-Fenton catalysis. The PFC exhibited faster kinetics due to the rapid production of OH<superscript>•</superscript> radicals via the Fe-redox cycle and direct dissociation of H<subscript>2</subscript>O<subscript>2</subscript> at oxygen vacancies. LFO-Bi5 demonstrates excellent photostability and reusability for up to six consecutive cycles. The degradation pathway and toxicological properties of the intermediates are analyzed, highlighting the potential of LFO-Bi5 catalysts in antibiotic-contaminated water treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
25740970
Volume :
7
Issue :
10
Database :
Complementary Index
Journal :
ACS Applied Nano Materials
Publication Type :
Academic Journal
Accession number :
177485496
Full Text :
https://doi.org/10.1021/acsanm.4c01145