Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/112907
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dc.contributorDepartment of Applied Physics-
dc.creatorYang, L-
dc.creatorZhan, Z-
dc.creatorZhao, L-
dc.creatorZhang, C-
dc.creatorWang, S-
dc.creatorHu, W-
dc.creatorZhu, G-
dc.date.accessioned2025-05-15T06:58:54Z-
dc.date.available2025-05-15T06:58:54Z-
dc.identifier.issn2041-6520-
dc.identifier.urihttp://hdl.handle.net/10397/112907-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rights© 2025 The Author(s). Published by the Royal Society of Chemistryen_US
dc.rightsThis article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence (https://creativecommons.org/licenses/by-nc/3.0/).en_US
dc.rightsThe following publication Yang, L., Zhan, Z., Zhao, L., Zhang, C., Wang, S., Hu, W., & Zhu, G. (2025). Efficient construction of high-quality sulfonated porous aromatic frameworks by optimizing the swelling state of porous structures [10.1039/D4SC05329J]. Chemical Science, 16(2), 775-783 is available at https://dx.doi.org/10.1039/d4sc05329j.en_US
dc.titleEfficient construction of high-quality sulfonated porous aromatic frameworks by optimizing the swelling state of porous structuresen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage775-
dc.identifier.epage783-
dc.identifier.volume16-
dc.identifier.issue2-
dc.identifier.doi10.1039/d4sc05329j-
dcterms.abstractConventional post-modification methods usually face the fundamental challenge of balancing the high content of functional groups and large surface area for porous organic polymers (POPs). The reason, presumably, stems from ineffective and insufficient swelling of the porous structure of POP materials, which is detrimental to mass transfer and modification of functional groups, especially with large-sized ones. It is important to note that significant differences exist in the porous structures of POP materials in a solvent-free state after thermal activation and solvent swelling state. Herein, we propose that the improvement of the swelling state of the porous structure of POP materials is more conducive to obtaining high-quality sulfonated POP materials, and employ a one-pot modification strategy for preparing sulfonated porous aromatic frameworks (PAFs) to prove the proposal. These results show that the specific surface area of the resulting polymer is 580 m2 g−1 with a sulfur content of up to 13.2 wt%, which is superior to most sulfonated porous materials and the control sample. More importantly, we have also shown that the same conclusion is reached by performing similar treatments on hyper-crosslinked polymers (HCPs) and conjugated microporous polymers (CMPs), proving that our hypothesis is effective and feasible when compared to the conventional post-sulfonation method. The excellent hydrophilicity, rich content of sulfonic acid groups, high specific surface area and hierarchical pore structure make the resulting polymer an ideal adsorbent for micro-pollutants in water. The maximum adsorption capacities for Rhodamine B (RhB), Methylene Blue (MB), Tetracycline (TC) and Ciprofloxacin (CIP) are 1075 mg g−1, 1020 mg g−1, 826 mg g−1 and 1134 mg g−1, respectively. This study not only demonstrates the preparation of efficient sulfonated porous adsorbents for the efficient removal of cationic dyes and antibiotics but also illustrates an effective method for constructing high-quality functional POP materials by optimizing the swelling state of the porous structure.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationChemical science, Jan. 2024, v. 16, no. 2, p. 775-783-
dcterms.isPartOfChemical science-
dcterms.issued2025-01-
dc.identifier.scopus2-s2.0-85211017386-
dc.identifier.eissn2041-6539-
dc.description.validate202505 bcrc-
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_Scopus/WOSen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNational Natural Science Foundation of China; Fundamental Research Funds for the Central Universitiesen_US
dc.description.pubStatusPublisheden_US
dc.description.oaCategoryCCen_US
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