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Enhancing reverse osmosis membrane performance via interfacial diffusion control using porous graphene oxide

Authors
Kim, Young JaeLee, Byung KwanPark, InhoYoun, ChaewonLee, Myung-SeokLee, Jung-HyunPark, Ho Bum
Issue Date
May-2025
Publisher
Elsevier BV
Keywords
Additional water channel; Desalination; Highly crosslinked membrane; Interfacial diffusion modulation; Porous graphene oxide
Citation
Journal of Membrane Science, v.726, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Journal of Membrane Science
Volume
726
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/207225
DOI
10.1016/j.memsci.2025.124040
ISSN
0376-7388
1873-3123
Abstract
The development of polyamide (PA) thin-film composite (TFC) membranes with enhanced water permeance and salt rejection is essential for energy-efficient desalination. This study introduces a reverse osmosis (RO) membrane that achieves rapid water transport and high salt rejection through precise control of interfacial polymerization (IP), enabled by porous graphene oxide (PGO) with optimally sized nanopores. These nanopores act as diffusion pathways for m-phenylenediamine (MPD) during IP in a confined space, reducing residual unreacted MPD and creating additional water transport channels. This process facilitates the formation of a highly crosslinked and permeable PA selective layer. The thin-film nanocomposite (TFN) membrane incorporating PGO etched for 3 h exhibited outstanding water permeance of 3.57 L m−2 h−1 bar−1 and NaCl rejection of 98.7 %, surpassing state-of-the-art GO-modified RO membranes. Additionally, the membrane demonstrated superior antifouling performance and long-term operational stability. Structural and performance comparisons with TFN membranes incorporating PGO with varying nanopore sizes, controlled via etching time, elucidated the transport mechanism across the membrane. This work highlights a robust strategy for manufacturing high-performance TFC membranes by modulating interfacial diffusion during IP.
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