4.7 Article

Control over the Hydrophilicity in the Pores of Covalent Organic Framework Membranes for High-Flux Separation of Dyes from Water

期刊

ACS APPLIED NANO MATERIALS
卷 5, 期 12, 页码 17632-17639

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsanm.2c03392

关键词

covalent organic framework; membrane; hydrophilic; water treatment; dye separation

资金

  1. Japan Society for the Promotion of Science (JSPS) KAKENHI [20H02698, 20H02552, 18H05178, 20H05115, 21H00027, 22H04562]
  2. JST Adaptable and Seamless Technology Transfer Program through Target-driven RD (A-STEP) [JPMJTM20MS]
  3. Yazaki Memorial Foundation for Science and Technology
  4. Ogasawara Foundation for the Promotion of Science and Engineering
  5. Kao Foundation for Arts and Sciences
  6. TEPCO Memorial Foundation
  7. Japan Science Society
  8. Takahashi Industrial and Economic Research Foundation
  9. Kobe University Strategic International Collaborative Research Grant (Type B Fostering Joint Research)
  10. Kubota Corporation

向作者/读者索取更多资源

Membrane separation plays a crucial role in water purification, and pore-size control is essential for molecular sieving. In this study, a covalent organic framework (COF) membrane called TUS-46 was precisely designed with appropriate pore metrics and functionalities. The TUS-46 COF membrane exhibited excellent rejection performance for anionic dyes due to its suitable pore sizes and negative electrostatic pore walls. Furthermore, the presence of free aldehyde functionalities in the framework resulted in a 10-fold higher water permeance compared to a similar COF membrane without these functionalities. The unique construction of hydrophilic and hydrophobic nanospaces within the TUS-46 COF structure enabled high water flux, making it a promising material for water separation applications.
Membrane separation is making substantial contributions to water purification. Particularly important is the pore-size control designed for molecular sieving. Regarding water permeation, filtration experiments accentuate the importance of hydrophilic pores in enhancing the water adsorption capacity, while hydrophobic pores enable low-friction water diffusion. To reach both the criteria, we herein precisely design the pore metrics and pore functionalities to prepare a covalent organic framework (COF), termed TUS-46, membrane. Credited with pore sizes befitting for size-selective molecular exclusion and negative electrostatic pore walls, the TUS-46 COF membrane shows excellent rejection performance toward anionic dyes. Attributed to the free aldehyde functionalities in the framework resulting from unbalanced stoichiometry, the TUS-46 COF membrane also shows a 10-fold higher water permeance compared to the analogue COF membrane without free aldehyde functionalities. In particular, the in situ construction of hydrophilic nanospaces partaking in high water uptake and hydrophobic nanospaces facilitating fast water diffusion in a single COF structure endows the TUS-46 membranes with unprecedentedly high water flux. The stoichiometric imbalance approach presented herein offers a different route to COF membrane fabrication and may impart with an unprecedented control handle on the permeability and separation selectivity of COF membranes.

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