4.7 Article

Graphene quantum dots (GQDs)-assembled membranes with intrinsic functionalized nanochannels for high-performance nanofiltration

期刊

CHEMICAL ENGINEERING JOURNAL
卷 420, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2020.127602

关键词

Thin-film composite membranes; Nanoparticle-assembled thin films; Interfacial polymerization; Nanofiltration; Graphene quantum dots

资金

  1. Special Coordination Funds for Promoting Science and Technology
  2. Creation of Innovation Centers for Advanced Interdisciplinary Research Areas from the Ministry of Education, Culture, Sports, Science, and Technology, Japan
  3. China Scholarship Council (CSC)

向作者/读者索取更多资源

Recent innovations have shown the significant potential of graphene quantum dots (GQDs) as ideal materials for advanced nanofiltration membranes. This study developed a novel thin-film composite (TFC) nanofiltration membrane using assembled GQDs as building blocks for highly selective water transport via interfacial polymerization, achieving improved water permeance without sacrificing membrane selectivity.
Recent innovations highlight the great potential of zero-dimensional materials of graphene quantum dots (GQDs) as attractive candidates for fabricating advanced nanofiltration membranes. In this study, a novel class of thinfilm composite (TFC) nanofiltration membranes derived from assembled GQDs with amino/sulfonic modification (GQDs_N/S) as building blocks directly, is developed to achieve highly selective water transport for highperformance nanofiltration via interfacial polymerization. Based on the transport behavior, the intrinsically hydrophilic sulfonic groups are introduced to endow the membrane with stronger internal polarity and more accessible sites for easier water molecules infiltration, while engineering the nanochannels by covalently immobilizing GQDs between the terminal amino groups and trimesoyl chloride. Furthermore, an enhanced interparticle space with enlarged free volumes between GQDs is obtained for rapidly transporting water molecules inside the membrane, owing to the intercalation of sulfonic groups acting as spacers to break up the tightly stacking structure of GQDs. The resultant GQDs_N/S TFC membrane exhibits superior separation properties with high water permeance of 9.82 L m-2h- 1 bar-1 and 97.4% rejection against Na2SO4, giving rise to more than 2fold higher water permeability without obviously sacrificing the membrane selectivity, and revealing an outperformed separation property when compared to state-of-the-art nanofiltration membranes. Simultaneously, the sulfonic and amino sites firmly anchored on GQDs with custom-tailored functionality further enables the GQDs_N/S TFC membrane to perform an outstanding antifouling property and durability over the long-term operation condition. The proposed approach opens new pathways to fabricate highly permeable-selective nanofiltration membranes.

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