TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery
This paper reports new solid materials based on TEGylated phenothiazine and chitosan, with a high capacity to recover mercury ions from aqueous solutions. They were prepared by hydrogelation of chitosan with a formyl derivative of TEGylated phenothiazine, followed by lyophilization. Their structural...
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-10-01
|
Series: | Gels |
Subjects: | |
Online Access: | https://www.mdpi.com/2310-2861/8/11/692 |
_version_ | 1827646525080076288 |
---|---|
author | Sandu Cibotaru Daniela Ailincai Bianca-Iustina Andreica Xinjian Cheng Luminita Marin |
author_facet | Sandu Cibotaru Daniela Ailincai Bianca-Iustina Andreica Xinjian Cheng Luminita Marin |
author_sort | Sandu Cibotaru |
collection | DOAJ |
description | This paper reports new solid materials based on TEGylated phenothiazine and chitosan, with a high capacity to recover mercury ions from aqueous solutions. They were prepared by hydrogelation of chitosan with a formyl derivative of TEGylated phenothiazine, followed by lyophilization. Their structural and supramolecular characterization was carried out by <sup>1</sup>H-NMR and FTIR spectroscopy, as well as X-ray diffraction and polarized light microscopy. Their morphology was investigated by scanning electron microscopy and their photophysical behaviour was examined by UV/Vis and emission spectroscopy. Swelling evaluation in different aqueous media indicated the key role played by the supramolecular organization for their hydrolytic stability. Mercury recovery experiments and the analysis of the resulting materials by X-ray diffraction and FTIR spectroscopy showed a high ability of the studied materials to bind mercury ions by coordination with the sulfur atom of phenothiazine, imine linkage, and amine units of chitosan. |
first_indexed | 2024-03-09T19:03:49Z |
format | Article |
id | doaj.art-b4bac9376bf0429a8b4b71e92f372f5f |
institution | Directory Open Access Journal |
issn | 2310-2861 |
language | English |
last_indexed | 2024-03-09T19:03:49Z |
publishDate | 2022-10-01 |
publisher | MDPI AG |
record_format | Article |
series | Gels |
spelling | doaj.art-b4bac9376bf0429a8b4b71e92f372f5f2023-11-24T04:46:12ZengMDPI AGGels2310-28612022-10-0181169210.3390/gels8110692TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury RecoverySandu Cibotaru0Daniela Ailincai1Bianca-Iustina Andreica2Xinjian Cheng3Luminita Marin4“Petru Poni” Institute of Macromolecular Chemistry, Gr. Ghica Voda Alley, 41A, 700487 Iasi, Romania“Petru Poni” Institute of Macromolecular Chemistry, Gr. Ghica Voda Alley, 41A, 700487 Iasi, Romania“Petru Poni” Institute of Macromolecular Chemistry, Gr. Ghica Voda Alley, 41A, 700487 Iasi, RomaniaSchool of Chemistry and Environmental Engineering, Wuhan Institute of Technology, Wuhan 430079, China“Petru Poni” Institute of Macromolecular Chemistry, Gr. Ghica Voda Alley, 41A, 700487 Iasi, RomaniaThis paper reports new solid materials based on TEGylated phenothiazine and chitosan, with a high capacity to recover mercury ions from aqueous solutions. They were prepared by hydrogelation of chitosan with a formyl derivative of TEGylated phenothiazine, followed by lyophilization. Their structural and supramolecular characterization was carried out by <sup>1</sup>H-NMR and FTIR spectroscopy, as well as X-ray diffraction and polarized light microscopy. Their morphology was investigated by scanning electron microscopy and their photophysical behaviour was examined by UV/Vis and emission spectroscopy. Swelling evaluation in different aqueous media indicated the key role played by the supramolecular organization for their hydrolytic stability. Mercury recovery experiments and the analysis of the resulting materials by X-ray diffraction and FTIR spectroscopy showed a high ability of the studied materials to bind mercury ions by coordination with the sulfur atom of phenothiazine, imine linkage, and amine units of chitosan.https://www.mdpi.com/2310-2861/8/11/692phenothiazinechitosaniminemercury recovery |
spellingShingle | Sandu Cibotaru Daniela Ailincai Bianca-Iustina Andreica Xinjian Cheng Luminita Marin TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery Gels phenothiazine chitosan imine mercury recovery |
title | TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery |
title_full | TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery |
title_fullStr | TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery |
title_full_unstemmed | TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery |
title_short | TEGylated Phenothiazine-Imine-Chitosan Materials as a Promising Framework for Mercury Recovery |
title_sort | tegylated phenothiazine imine chitosan materials as a promising framework for mercury recovery |
topic | phenothiazine chitosan imine mercury recovery |
url | https://www.mdpi.com/2310-2861/8/11/692 |
work_keys_str_mv | AT sanducibotaru tegylatedphenothiazineiminechitosanmaterialsasapromisingframeworkformercuryrecovery AT danielaailincai tegylatedphenothiazineiminechitosanmaterialsasapromisingframeworkformercuryrecovery AT biancaiustinaandreica tegylatedphenothiazineiminechitosanmaterialsasapromisingframeworkformercuryrecovery AT xinjiancheng tegylatedphenothiazineiminechitosanmaterialsasapromisingframeworkformercuryrecovery AT luminitamarin tegylatedphenothiazineiminechitosanmaterialsasapromisingframeworkformercuryrecovery |