Polymer Membranes for Separation Processes

A special issue of Polymers (ISSN 2073-4360). This special issue belongs to the section "Polymer Applications".

Deadline for manuscript submissions: 15 September 2024 | Viewed by 5176

Special Issue Editor

Chongqing Institute of Green and Intelligent Technology, Chinese Academy of Sciences, Chongqing, China
Interests: functional polymers; membranes; coatings; composites; separation; nanomaterials; carbon materials

Special Issue Information

Dear Colleagues,

Membrane-based technologies have been regarded as important sustainable strategies in separation processes to address global issues of water security and supply. In particular, polymer membranes are increasingly being developed and utilized due to their good processability, high flexibility, multi-functionality and low cost. However, the development of high-performance polymer membranes is still restricted by their inherent limitations, including a permeability/selectivity trade-off and a high fouling propensity. This Special Issue focuses on membrane structure design at the molecular and multi-scale level, as well as membrane fabrication for separation processes including, but not limited to, microfiltration (MF), ultrafiltration (UF), nanofiltration (NF), reverse osmosis (RO), forward osmosis (FO) and membrane distillation (MD). Reports on novel membrane/materials design and formation are preferred. In this Special Issue, I sincerely invite you to submit cutting-edge research works on the design, synthesis, characterization, mechanism, performance and application of polymer membranes for separation processes, in the form of a communication, full paper, or review. 

Dr. Xiao Wang
Guest Editor

Manuscript Submission Information

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Keywords

  • polymer membranes
  • hybrid membranes
  • (nano)composites
  • membrane separation processes
  • membrane performance
  • permeability/selectivity
  • membrane fouling
  • structure–properties relationship

Published Papers (3 papers)

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Research

23 pages, 10414 KiB  
Article
Evaluating Post-Treatment Effects on Electrospun Nanofiber as a Support for Polyamide Thin-Film Formation
by Anniza Cornelia Augusty, Ratthapol Rangkupan and Chalida Klaysom
Polymers 2024, 16(5), 713; https://doi.org/10.3390/polym16050713 - 5 Mar 2024
Viewed by 639
Abstract
Poly(acrylonitrile-co-methyl acrylate) (PAN-co-MA) electrospun nanofiber (ENF) was used as the support for the formation of polyamide (PA) thin films. The ENF support layer was post-treated with heat-pressed treatment followed by NaOH hydrolysis to modify its support characteristics. The influence of heat-pressed conditions and [...] Read more.
Poly(acrylonitrile-co-methyl acrylate) (PAN-co-MA) electrospun nanofiber (ENF) was used as the support for the formation of polyamide (PA) thin films. The ENF support layer was post-treated with heat-pressed treatment followed by NaOH hydrolysis to modify its support characteristics. The influence of heat-pressed conditions and NaOH hydrolysis on the support morphology and porosity, thin-film formation, surface chemistry, and membrane performances were investigated. This study revealed that applying heat-pressing followed by hydrolysis significantly enhances the physicochemical properties of the support material and aids in forming a uniform polyamide (PA) thin selective layer. Heat-pressing effectively densifies the support surface and reduces pore size, which is crucial for the even formation of the PA-selective layer. Additionally, the hydrolysis of the support increases its hydrophilicity and decreases pore size, leading to higher sodium chloride (NaCl) rejection rates and improved water permeance. When compared with membranes that underwent only heat-pressing, those treated with both heat-pressing and hydrolysis exhibited superior separation performance, with NaCl rejection rates rising from 83% to 98% while maintaining water permeance. Moreover, water permeance was further increased by 29% through n-hexane-rinsing post-interfacial polymerization. Thus, this simple yet effective combination of heat-pressing and hydrolysis presents a promising approach for developing high-performance thin-film nanocomposite (TFNC) membranes. Full article
(This article belongs to the Special Issue Polymer Membranes for Separation Processes)
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16 pages, 4882 KiB  
Article
Developing Mixed Matrix Membranes with Good CO2 Separation Performance Based on PEG-Modified UiO-66 MOF and 6FDA-Durene Polyimide
by Kavya Adot Veetil, Asmaul Husna, Md. Homayun Kabir, Insu Jeong, Ook Choi, Iqubal Hossain and Tae-Hyun Kim
Polymers 2023, 15(22), 4442; https://doi.org/10.3390/polym15224442 - 17 Nov 2023
Cited by 1 | Viewed by 1786
Abstract
The use of mixed matrix membranes (MMMs) comprising metal–organic frameworks (MOFs) for the separation of CO2 from flue gas has gained recognition as an effective strategy for enhancing gas separation efficiency. When incorporating porous materials like MOFs into a polymeric matrix to [...] Read more.
The use of mixed matrix membranes (MMMs) comprising metal–organic frameworks (MOFs) for the separation of CO2 from flue gas has gained recognition as an effective strategy for enhancing gas separation efficiency. When incorporating porous materials like MOFs into a polymeric matrix to create MMMs, the combined characteristics of each constituent typically manifest. Nevertheless, the inadequate dispersion of an inorganic MOF filler within an organic polymer matrix can compromise the compatibility between the filler and matrix. In this context, the aspiration is to develop an MMM that not only exhibits optimal interfacial compatibility between the polymer and filler but also delivers superior gas separation performance, specifically in the efficient extraction of CO2 from flue gas. In this study, we introduce a modification technique involving the grafting of poly(ethylene glycol) diglycidyl ether (PEGDE) onto a UiO-66-NH2 MOF filler (referred to as PEG-MOF), aimed at enhancing its compatibility with the 6FDA-durene matrix. Moreover, the inherent CO2-philic nature of PEGDE is anticipated to enhance the selectivity of CO2 over N2 and CH4. The resultant MMM, incorporating 10 wt% of PEG-MOF loading, exhibits a CO2 permeability of 1671.00 Barrer and a CO2/CH4 selectivity of 22.40. Notably, these values surpass the upper bound reported by Robeson in 2008. Full article
(This article belongs to the Special Issue Polymer Membranes for Separation Processes)
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19 pages, 5016 KiB  
Article
Electrospinning Novel Sodium Alginate/MXene Nanofiber Membranes for Effective Adsorption of Methylene Blue
by Meng Li, Pingxiu Zhang, Qianfang Wang, Ningya Yu, Xiaomin Zhang and Shengpei Su
Polymers 2023, 15(9), 2110; https://doi.org/10.3390/polym15092110 - 28 Apr 2023
Cited by 8 | Viewed by 1899
Abstract
Understanding how to develop highly efficient and robust adsorbents for the removal of organic dyes in wastewater is crucial in the face of the rapid development of industrialization. Herein, d-Ti3C2Tx nanosheets (MXene) were combined with sodium alginate (SA), [...] Read more.
Understanding how to develop highly efficient and robust adsorbents for the removal of organic dyes in wastewater is crucial in the face of the rapid development of industrialization. Herein, d-Ti3C2Tx nanosheets (MXene) were combined with sodium alginate (SA), followed by electrospinning and successive Ca2+-mediated crosslinking, giving rise to a series of SA/MXene nanofiber membranes (NMs). The effects of the MXene content of the NMs on the adsorption performance for methylene blue (MB) were investigated systemically. Under the optimum MXene content of 0.74 wt.%, SA/MXene NMs possessed an MB adsorption capacity of 440 mg/g, which is much higher than SA/MXene beads with the same MXene content, pristine MXene, or electrospinning SA NMs. Furthermore, the optimum SA/MXene NMs showed excellent reusability. After the adsorbent was reused ten times, both the MB adsorption capacity and removal rate could remain at 95% of the levels found in the fresh samples, which indicates that the electrospinning technique has great potential for developing biomass-based adsorbents with high efficiency. Full article
(This article belongs to the Special Issue Polymer Membranes for Separation Processes)
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