A Supramolecular Polymer Network Based on Chitosan and Porphyrin and Its Application as an Adsorbent for Selective Removal of Dyes from Water
Source abstract
Abstract
Abstract Environmentally friendly, high adsorption efficiency, and recyclable adsorbents meet the actual needs of organic dye wastewater treatment. Driven by noncovalent interactions between chitosan (CS) and 5,10,15,20‐tetra(4‐hydroxyphenyl) porphyrin sodium (THPPNa) under acidic conditions, a supramolecular polymer network is constructed. The supramolecular polymer network is applied as an excellent adsorbent for the removal of organic dyes from water with high efficiency. In addition, the supramolecular adsorbent shows excellent selectivity for the removal of organic anionic dyes from the mixtures of organic anionic and cationic dyes in water. Furthermore, the removal efficiency of anionic dyes of the network adsorbent keeps over 95% even after five adsorption–desorption cycles, indicating its reusability. This supramolecular polymer network shows its great potential as a low‐cost, effective, and selective adsorbent for removing organic dyes from water.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: Molecular Sensors and Ion Detection · Porphyrin and Phthalocyanine Chemistry · Supramolecular Self-Assembly in Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Scientific Instrument Center Shanxi University Taiyuan 030006 P. R. China
Institute of Molecular Science Shanxi University Taiyuan 030006 P. R. China
College of Materials Science and Engineering Taiyuan University of Technology Taiyuan 030006 P. R. China
References (41)
Show source-provided references
1. 10.1016/j.carbpol.2021.11860410.1016/j.carbpol.2021.118604 ↗
2. 10.1039/D1CC02373J10.1039/D1CC02373J ↗
3. 10.1021/acs.nanolett.3c0003410.1021/acs.nanolett.3c00034 ↗
4. 10.1016/j.supmat.2023.10003510.1016/j.supmat.2023.100035 ↗
5. 10.1039/C7TA08894A10.1039/C7TA08894A ↗
6. 10.1016/j.dyepig.2018.10.06110.1016/j.dyepig.2018.10.061 ↗
7. 10.1002/anie.20200911310.1002/anie.202009113 ↗
8. 10.1016/j.cej.2020.12811610.1016/j.cej.2020.128116 ↗
9. 10.1016/j.dyepig.2022.11057610.1016/j.dyepig.2022.110576 ↗
10. 10.1039/D3TA04885C10.1039/D3TA04885C ↗
11. 10.1007/s10311-023-01603-410.1007/s10311-023-01603-4 ↗
12. 10.1016/j.cej.2019.02.08910.1016/j.cej.2019.02.089 ↗
13. 10.1021/acs.chemrev.9b0083910.1021/acs.chemrev.9b00839 ↗
14. 10.1007/s42765-021-00103-w10.1007/s42765-021-00103-w ↗
15. 10.1002/adma.20230172110.1002/adma.202301721 ↗
16. 10.1021/ja506577g10.1021/ja506577g ↗
17. 10.1016/j.progpolymsci.2021.10148610.1016/j.progpolymsci.2021.101486 ↗
18. 10.1021/ma502607p10.1021/ma502607p ↗
19. 10.1016/j.carbpol.2022.11918910.1016/j.carbpol.2022.119189 ↗
20. 10.1021/acsbiomaterials.3c0021610.1021/acsbiomaterials.3c00216 ↗
21. 10.1016/j.carbpol.2018.08.07010.1016/j.carbpol.2018.08.070 ↗
22. 10.1016/j.jhazmat.2020.12488910.1016/j.jhazmat.2020.124889 ↗
23. 10.1016/j.ijbiomac.2022.09.21310.1016/j.ijbiomac.2022.09.213 ↗
24. 10.1039/C7CS00719A10.1039/C7CS00719A ↗
25. 10.1002/anie.20211251410.1002/anie.202112514 ↗
26. 10.1016/j.carbpol.2016.05.06010.1016/j.carbpol.2016.05.060 ↗
27. 10.3390/polym1307100710.3390/polym13071007 ↗
28. 10.1021/acsami.0c1872510.1021/acsami.0c18725 ↗
29. 10.1002/anie.20220184310.1002/anie.202201843 ↗
30. 10.1039/D2CS00275B10.1039/D2CS00275B ↗
31. 10.1039/D1RA08148A10.1039/D1RA08148A ↗
32. 10.1002/adfm.20230034810.1002/adfm.202300348 ↗
33. 10.1016/j.progpolymsci.2019.05.00210.1016/j.progpolymsci.2019.05.002 ↗
34. 10.1007/s00289-020-03331-z10.1007/s00289-020-03331-z ↗
35. 10.1016/j.cej.2021.13326210.1016/j.cej.2021.133262 ↗
36. 10.1039/D0TB00810A10.1039/D0TB00810A ↗
37. 10.1039/D0LC00621A10.1039/D0LC00621A ↗
38. 10.1021/acsami.9b1925310.1021/acsami.9b19253 ↗
39. 10.1039/C9DT01713E10.1039/C9DT01713E ↗
40. 10.1038/s41598-022-24303-510.1038/s41598-022-24303-5 ↗
41. 10.1039/C9PY01373C10.1039/C9PY01373C ↗