Photocatalytic degradation of propranolol hydrochloride using Nd–TiO2 nanoparticles under UV and visible light

Propranolol (PRO) hydrochloride is one of the most commonly used β-blockers for cardiovascular diseases that is frequently detected in aquatic environment. Photocatalytic removal of propranolol using an efficient UV and visible light responsive neodymium (Nd)-modified photocatalyst has been investig...

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Bibliographic Details
Published in:Journal of materials research Vol. 36; no. 7; pp. 1584 - 1599
Main Authors: Giordani, Thainá, Dose, Janaine, Kuskoski, Yassmin, Schultz, Juliana, Mangrich, Antonio Salvio, de Mello, Josiane Maria Muneron, Silva, Luciano Luiz, Zeferino, Rubieli Carla Frezza, Zanetti, Micheli, Fiori, Márcio Antônio, Colpani, Gustavo Lopes
Format: Journal Article
Language:English
Published: Cham Springer International Publishing 14-04-2021
Springer Nature B.V
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Summary:Propranolol (PRO) hydrochloride is one of the most commonly used β-blockers for cardiovascular diseases that is frequently detected in aquatic environment. Photocatalytic removal of propranolol using an efficient UV and visible light responsive neodymium (Nd)-modified photocatalyst has been investigated. Nd–TiO 2 nanoparticles were synthesized by a simple ultrasonic method with Nd-modified in the range of 0–1.0 mol% to evaluate the effects of Nd 3+ content in crystal structure and photocatalytic activity. The TiO 2 –Nd 0.10% sample was the most efficient photocatalyst to degrade PRO with 95% and 90% degradation after 60 min under UV and visible light radiation, respectively. The characterization analysis revealed that neodymium is dispersed on the surface semiconductor, where probably forming Ti–O–Nd bonds, which can induce oxygen vacancies and surface defects. The effective separation of the photogenerated electrons and holes was regarded as the main reason for the high photocatalytic activity. Graphic abstract The effective separation of the photogenerated electrons and holes was regarded as the main reason for the high photocatalytic activity.
ISSN:0884-2914
2044-5326
DOI:10.1557/s43578-021-00207-4