| Literature DB >> 31009576 |
Xiaoli Wu1, Guoli Zhou1, Xulin Cui1, Yifan Li1, Jingtao Wang1, Xingzhong Cao2, Peng Zhang2.
Abstract
Polymeric thin film composite (TFC) membranes have been proven promising for a wide range of separation applications. However, their development is significantly hindered by low permeance (below 8.0 L m-2 h-1 bar-1). Here, we report the fabrication of new films with nanoparticle-assembled structure via interfacial polymerization using quantum dots (QDs) as building blocks. The tailored QDs with hydrophobic and hydrophilic regions permit cross-linking into nanoparticle-assembled defect-free thin films. Significantly, amphipathic QDs show good affinity to polar and nonpolar molecules, facilitating their fast dissolution into film. Meanwhile, the nanopores (∼1.4 nm) render fleet diffusion of molecules, which highly promotes the transfer of molecules within the film. This synergetic effect endows the resultant TFC membrane with high permeance, over 2 orders of magnitude higher than the conventional polyamide films. The permeances for acetonitrile and n-hexane reach 46.9 and 50.8 L m-2 h-1 bar-1, respectively. We demonstrate that films fabricated by hydrophilic and hydrophobic QDs exhibit different molecular transfer mechanisms, and the corresponding model equations are established. The film fabricated by amphipathic QDs shows a combination transfer mechanism of the two models. Furthermore, those QD-based TFC membranes display favorable structural and operational stability, holding promise for industrial separation applications.Entities:
Keywords: amphipathic nanopore; high solvent permeation; molecular transfer mechanism; nanoparticle-assembled film; organic solvent nanofiltration; quantum dot
Year: 2019 PMID: 31009576 DOI: 10.1021/acsami.9b03753
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229