Robust Hilly Polyamide Membrane for Fast Desalination
Source abstract
Abstract
Tailoring the microstructure of a selective layer is a highly attractive way to improve the water flux of a reverse osmosis (RO) membrane by forming a crumpled surface without altering its chemical structure required for high salt rejection. However, it is challenging to maintain its structural integrity and stability and high flux at high pressure during desalination. Herein, a robust hilly thin-film composite (TFC) polyamide (PA) membrane is developed based on composite substrates made of cellulose nanofibers (CNFs) and metal–organic frameworks (MOFs). Water-stable, highly crystalline, submicrometer-sized MOF crystals, NH2-MIL-53(Al), are integrated with CNFs to form a robust and highly porous intermediate layer for the formation of a hilly PA layer. The resulting TFC RO membrane exhibits an excellent water permeance of 5.55 LMH/bar and a NaCl rejection of ∼94.8%. The strategy reported here has great potential for the fabrication of polyamide desalination membranes with enhanced flux and mechanical stability.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Membrane Separation Technologies · Membrane-based Ion Separation Techniques · Electrohydrodynamics and Fluid Dynamics
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical Engineering, Monash University, Clayton, Victoria 3800, Australia
CSIRO Manufacturing, Private Bag 10, Clayton South, Victoria 3169, Australia
Department of Materials Science and Engineering, Monash University, Clayton, Victoria 3800, Australia
Funding
Australian Research Council
References (36)
Show source-provided references
1. 10.1038/s41565-018-0203-210.1038/s41565-018-0203-2 ↗
2. 10.1021/acs.nanolett.9b0322510.1021/acs.nanolett.9b03225 ↗
3. 10.1038/s41565-018-0067-510.1038/s41565-018-0067-5 ↗
4. 10.1021/acsnano.8b0418710.1021/acsnano.8b04187 ↗
5. 10.1021/acsnano.9b0461210.1021/acsnano.9b04612 ↗
6. 10.1038/s41467-019-10132-010.1038/s41467-019-10132-0 ↗
7. 10.1016/j.jcis.2017.09.06210.1016/j.jcis.2017.09.062 ↗
8. 10.1038/s41467-018-06097-110.1038/s41467-018-06097-1 ↗
9. 10.1021/acsnano.8b0976110.1021/acsnano.8b09761 ↗
10. 10.1016/j.memsci.2019.03.04210.1016/j.memsci.2019.03.042 ↗
11. 10.1016/j.memsci.2018.11.07510.1016/j.memsci.2018.11.075 ↗
12. 10.1016/j.memsci.2013.09.01410.1016/j.memsci.2013.09.014 ↗
13. 10.1002/anie.20160150910.1002/anie.201601509 ↗
14. 10.1016/j.memsci.2019.11738610.1016/j.memsci.2019.117386 ↗
15. 10.1039/C9TA00031C10.1039/C9TA00031C ↗
16. 10.1016/j.progpolymsci.2016.03.00310.1016/j.progpolymsci.2016.03.003 ↗
17. 10.1016/j.desal.2017.05.02710.1016/j.desal.2017.05.027 ↗
18. 10.1021/mz300163h10.1021/mz300163h ↗
19. 10.1038/s41467-018-04467-310.1038/s41467-018-04467-3 ↗
20. 10.1126/science.aar630810.1126/science.aar6308 ↗
21. 10.1039/C9SC03088C10.1039/C9SC03088C ↗
22. 10.1016/j.crci.2019.08.00110.1016/j.crci.2019.08.001 ↗
23. 10.1016/j.memsci.2019.11736310.1016/j.memsci.2019.117363 ↗
24. 10.1039/C0NR00583E10.1039/C0NR00583E ↗
25. 10.1002/adfm.20120008410.1002/adfm.201200084 ↗
26. 10.1039/c3dt51322j10.1039/c3dt51322j ↗
27. 10.1080/15422119.2014.88235510.1080/15422119.2014.882355 ↗
28. 10.1016/j.memsci.2015.04.01010.1016/j.memsci.2015.04.010 ↗
29. 10.1016/j.watres.2015.04.03710.1016/j.watres.2015.04.037 ↗
30. 10.1016/j.desal.2017.04.01910.1016/j.desal.2017.04.019 ↗
31. 10.1016/j.memsci.2006.11.01910.1016/j.memsci.2006.11.019 ↗
32. 10.3390/polym1006068610.3390/polym10060686 ↗
33. 10.1016/j.memsci.2014.06.04910.1016/j.memsci.2014.06.049 ↗
34. 10.1016/j.desal.2017.06.02910.1016/j.desal.2017.06.029 ↗
35. 10.1021/acs.est.8b0410210.1021/acs.est.8b04102 ↗
36. 10.1002/adma.20140578310.1002/adma.201405783 ↗