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Frontiers of Chemical Science and Engineering

ISSN 2095-0179

ISSN 2095-0187(Online)

CN 11-5981/TQ

邮发代号 80-969

2019 Impact Factor: 3.552

Frontiers of Chemical Science and Engineering  2023, Vol. 17 Issue (10): 1555-1567   https://doi.org/10.1007/s11705-023-2338-4
  本期目录
Tailoring the microstructure and properties of PES/SPSf loose nanofiltration membranes using SPES as a hydrophilic polymer for the effective removal of dyes via steric hindrance and charge effect
Xiaowei Liu1, Christine Matindi1, Sania Kadanyo1, Mengyang Hu1, Shuqian Yang1, Gansheng Liu1, Ran Tao1, Zhenyu Cui1, Xiaohua Ma1, Kuanjun Fang2, Jianxin Li1,3()
1. State Key Laboratory of Separation Membranes and Membrane Processes, National Center for International Joint Research on Separation Membranes, School of Materials Science and Engineering, Tiangong University, Tianjin 300387, China
2. Collaborative Innovation Center for Eco-Textiles of Shandong Province, Qingdao 266071, China
3. Institute for Nanotechnology and Water Sustainability College of Science Engineering and Technology, University of South Africa, Science Campus, Florida 1710, Johannesburg, South Africa
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Abstract

Herein, polyethersulfone (PES) and sulfonated polysulfone (SPSf) blend membranes were prepared with addition of sulfonated polyethersulfone (SPES) as a hydrophilic polymer and adipic acid as a porogen via non-solvent induced phase separation method for effective fractionation of dyes based on the influence of steric hindrance and charge effect. Raman spectroscopy and molecular dynamic simulation modeling confirmed that hydrogen bonds between PES, SPSf, SPES, and adipic acid were crucial to membrane formation and spatial arrangement. Further addition of hydrophilic SPES resulted in a membrane with reduced pore size and molecular weight cut-off as well as amplified negative charge and pure water permeance. During separation, the blend membranes exhibited higher rejection rates for nine types of small molecular weight (269.3–800 Da) dyes than for neutral polyethylene glycol molecules (200–1000 Da). This was attributed to the size effect and the synergistic effect between steric hindrance and charge repulsion. Notably, the synergistic impact decreased with dye molecular weight, while greater membrane negative charge enhanced small molecular dye rejection. Ideal operational stability and anti-fouling performance were best observed in M2 (PES/SPSf/SPES, 3.1 wt %). Summarily, this study demonstrates that SPES with –SO3 functional groups can be applied to control the microstructure and separation of membranes.

Key wordsadipic acid    loose nanofiltration membrane    dye/salt selective separation    steric hindrance    charge effect
收稿日期: 2022-12-31      出版日期: 2023-10-07
Corresponding Author(s): Jianxin Li   
 引用本文:   
. [J]. Frontiers of Chemical Science and Engineering, 2023, 17(10): 1555-1567.
Xiaowei Liu, Christine Matindi, Sania Kadanyo, Mengyang Hu, Shuqian Yang, Gansheng Liu, Ran Tao, Zhenyu Cui, Xiaohua Ma, Kuanjun Fang, Jianxin Li. Tailoring the microstructure and properties of PES/SPSf loose nanofiltration membranes using SPES as a hydrophilic polymer for the effective removal of dyes via steric hindrance and charge effect. Front. Chem. Sci. Eng., 2023, 17(10): 1555-1567.
 链接本文:  
https://academic.hep.com.cn/fcse/CN/10.1007/s11705-023-2338-4
https://academic.hep.com.cn/fcse/CN/Y2023/V17/I10/1555
Dye MW/(g?mol?1) Charge Max. absorption wavelength/nm Molecular structure
MR 269.3 ?1 410
MO 327.3 ?1 463
AC25 416.4 ?1 630
OG 452.4 ?2 478
IC 466.4 ?2 608
AF 585.5 ?2 546
CR 696.7 ?2 488
DR23 813.7 ?2 508
EB 960.8 ?4 611
Tab.1  
MembranePES/gSPES/gSPES/(wt %)SPSf/gDMAc/gAA/g
M016.0582.173.13.47248.30
M118.228003.47248.37.7
M216.0582.173.13.47248.37.7
M313.8884.345.583.47248.37.7
Tab.2  
Fig.1  
Fig.2  
Fig.3  
Fig.4  
MembraneMembrane thickness/μmAverage porosity/%Contact angle/(° )PWP/(L?m?2?h?1?bar?1)Breaking strength/MPa
M1120.8 ± 3.365.3 ± 2.253.2 ± 2.958.3 ± 0.49.1 ± 0.1
M2132.7 ± 3.773.2 ± 1.541.3 ± 3.676.2 ± 0.216.4 ± 0.3
M3140.9 ± 4.178.1 ± 1.928.7 ± 3.765.5 ± 0.316.7 ± 0.1
Tab.3  
Fig.5  
Fig.6  
Fig.7  
Fig.8  
Fig.9  
Fig.10  
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