<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yi R</submitter><funding>Zhejiang A and F University</funding><funding>National Natural Science Foundation of China</funding><pagination>40397-40403</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9076233</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(69)</volume><pubmed_abstract>Cross-linking with large flexible molecules is a common method to improve the stability and control the interlayer spacing of graphene oxide (GO) membranes, but it still suffers from the limitation of low water flux. Herein, a novel high flux GO membrane was fabricated using a pressure-assisted filtration method, which involved a synergistic chemical cross-linking of divalent magnesium ions and 1,6-hexanediamine (HDA) on a polyethersulfone (PES) support. The membrane cross-linked with magnesium ions and HDA (GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> ) exhibited a high water flux up to 144 L m&lt;sup>-2&lt;/sup> h&lt;sup>-1&lt;/sup> bar&lt;sup>-1&lt;/sup>, about 7 times more than that of cross-linked GO membranes without adding magnesium ions (GO&lt;sub>HDA&lt;/sub>), while keeping excellent rejection performance. The GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> membrane also showed an outstanding stability in water for a long time. The effects of magnesium ions on the GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> membrane were analyzed using several characterization methods, including Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The results indicated that magnesium ions not only promoted reasonable cross-linking, but also improved the stacking of GO sheets to give lower mass transfer resistance channels for water transport in the membranes, resulting in the ultrahigh permeance of the GO membranes.</pubmed_abstract><journal>RSC advances</journal><pubmed_title>Ultrahigh permeance of a chemical cross-linked graphene oxide nanofiltration membrane enhanced by cation-π interaction.</pubmed_title><pmcid>PMC9076233</pmcid><funding_grant_id>11875236</funding_grant_id><funding_grant_id>U1832150</funding_grant_id><funding_grant_id>2017FR032</funding_grant_id><pubmed_authors>Wu M</pubmed_authors><pubmed_authors>Yu R</pubmed_authors><pubmed_authors>Chen J</pubmed_authors><pubmed_authors>Chen L</pubmed_authors><pubmed_authors>Yi R</pubmed_authors><pubmed_authors>Yang R</pubmed_authors><pubmed_authors>Wang Z</pubmed_authors><pubmed_authors>Lan J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ultrahigh permeance of a chemical cross-linked graphene oxide nanofiltration membrane enhanced by cation-π interaction.</name><description>Cross-linking with large flexible molecules is a common method to improve the stability and control the interlayer spacing of graphene oxide (GO) membranes, but it still suffers from the limitation of low water flux. Herein, a novel high flux GO membrane was fabricated using a pressure-assisted filtration method, which involved a synergistic chemical cross-linking of divalent magnesium ions and 1,6-hexanediamine (HDA) on a polyethersulfone (PES) support. The membrane cross-linked with magnesium ions and HDA (GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> ) exhibited a high water flux up to 144 L m&lt;sup>-2&lt;/sup> h&lt;sup>-1&lt;/sup> bar&lt;sup>-1&lt;/sup>, about 7 times more than that of cross-linked GO membranes without adding magnesium ions (GO&lt;sub>HDA&lt;/sub>), while keeping excellent rejection performance. The GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> membrane also showed an outstanding stability in water for a long time. The effects of magnesium ions on the GO&lt;sub>HDA-Mg&lt;sup>2+&lt;/sup>&lt;/sub> membrane were analyzed using several characterization methods, including Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD). The results indicated that magnesium ions not only promoted reasonable cross-linking, but also improved the stacking of GO sheets to give lower mass transfer resistance channels for water transport in the membranes, resulting in the ultrahigh permeance of the GO membranes.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Dec</publication><modification>2024-11-14T19:56:29.94Z</modification><creation>2024-11-14T19:56:29.94Z</creation></dates><accession>S-EPMC9076233</accession><cross_references><pubmed>35542666</pubmed><doi>10.1039/c9ra07109a</doi></cross_references></HashMap>