Pharmaceuticals’ pervasive contamination of aquatic ecosystems underscores the urgent need for efficacious and innovative remediation strategies. This study introduces a highly selective and efficient approach for recovering Ibuprofen using molecularly imprinted polymers (MIPs). The cross-linked polymer was synthesized by reacting poly(2-oxazoline) with amino side chains and hexamethylene diisocyanate in the presence of Ibuprofen. Key parameters affecting Ibuprofen adsorption, including initial concentration, contact time, and MIP reusability, were thoroughly examined. The developed MIP exhibits a remarkable adsorption capacity, achieving a maximum Ibuprofen binding capacity of 92 mg g-1 and significantly outperforming the non-imprinted polymer’s 30 mg g-1. Moreover, kinetic studies reveal a rapid adsorption process predominantly following pseudo-first-order kinetics, indicating chemisorption as the primary mechanism. The MIPs demonstrate excellent reusability and maintain their efficacy in real-world scenarios, as evidenced by the successful recovery of Ibuprofen from lake water samples with significant removal percentages, instilling confidence in its potential application.

Molecularly Imprinted Poly(2-(3-(amino)propyl)-2-oxazoline) for the Selective Removal of Ibuprofen from Aqueous Solutions / Ricci, Agnese; Stefanuto, Luca; Del Galdo, Sara; Fardelli, Elisa; Pepi, Simone; Casciardi, Stefano; Capone, Barbara; Rossi, Claudio; Tofani, Daniela; Capellini, Giovanni; Iucci, Giovanna; Masci, Giancarlo; Gasperi, Tecla. - In: ACS APPLIED POLYMER MATERIALS. - ISSN 2637-6105. - 7:1(2025), pp. 42-53. [10.1021/acsapm.4c02576]

Molecularly Imprinted Poly(2-(3-(amino)propyl)-2-oxazoline) for the Selective Removal of Ibuprofen from Aqueous Solutions

Masci, Giancarlo
;
2025

Abstract

Pharmaceuticals’ pervasive contamination of aquatic ecosystems underscores the urgent need for efficacious and innovative remediation strategies. This study introduces a highly selective and efficient approach for recovering Ibuprofen using molecularly imprinted polymers (MIPs). The cross-linked polymer was synthesized by reacting poly(2-oxazoline) with amino side chains and hexamethylene diisocyanate in the presence of Ibuprofen. Key parameters affecting Ibuprofen adsorption, including initial concentration, contact time, and MIP reusability, were thoroughly examined. The developed MIP exhibits a remarkable adsorption capacity, achieving a maximum Ibuprofen binding capacity of 92 mg g-1 and significantly outperforming the non-imprinted polymer’s 30 mg g-1. Moreover, kinetic studies reveal a rapid adsorption process predominantly following pseudo-first-order kinetics, indicating chemisorption as the primary mechanism. The MIPs demonstrate excellent reusability and maintain their efficacy in real-world scenarios, as evidenced by the successful recovery of Ibuprofen from lake water samples with significant removal percentages, instilling confidence in its potential application.
2025
adsorption; molecularly imprinted polymers; pharmaceuticals; polyoxazoline; water remediation
01 Pubblicazione su rivista::01a Articolo in rivista
Molecularly Imprinted Poly(2-(3-(amino)propyl)-2-oxazoline) for the Selective Removal of Ibuprofen from Aqueous Solutions / Ricci, Agnese; Stefanuto, Luca; Del Galdo, Sara; Fardelli, Elisa; Pepi, Simone; Casciardi, Stefano; Capone, Barbara; Rossi, Claudio; Tofani, Daniela; Capellini, Giovanni; Iucci, Giovanna; Masci, Giancarlo; Gasperi, Tecla. - In: ACS APPLIED POLYMER MATERIALS. - ISSN 2637-6105. - 7:1(2025), pp. 42-53. [10.1021/acsapm.4c02576]
File allegati a questo prodotto
File Dimensione Formato  
Ricci_Molecularly_2025.pdf

solo gestori archivio

Note: articolo principale
Tipologia: Versione editoriale (versione pubblicata con il layout dell'editore)
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 4.82 MB
Formato Adobe PDF
4.82 MB Adobe PDF   Contatta l'autore
Ricci_supporting_Molecularly_2025.pdf

solo gestori archivio

Note: supporting information
Tipologia: Altro materiale allegato
Licenza: Tutti i diritti riservati (All rights reserved)
Dimensione 555 kB
Formato Adobe PDF
555 kB Adobe PDF   Contatta l'autore

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1736897
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 5
  • ???jsp.display-item.citation.isi??? 4
social impact