Unveiling the synergistic mechanism of magnesium hydroxide and silica in modulating polyethersulfone membrane structure and function

Q1 Environmental Science
Umi Fathanah , Abubakar Abubakar , Syawaliah Muchtar , Cut Meurah Rosnelly , Zuhra Zuhra , Mirna Rahmah Lubis , Sidik Marsudi
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引用次数: 0

Abstract

In this study, an environmentally benign dual-additive modification strategy was investigated by incorporating magnesium hydroxide and silica into PES membranes to simultaneously tailor surface chemistry and pore morphology during non-solvent-induced phase separation. Membranes were fabricated using a fixed Mg(OH)2 content with varying silica concentrations and characterized by FESEM, ATR-FTIR, gravimetric porosity analysis, water contact angle measurements, and filtration performance testing, including pure-water flux, humic acid rejection, and flux recovery ratio. All modified membranes retained the asymmetric structure of pristine PES but developed thinner selective layers and more elongated finger-like macrovoids as silica content increased up to the optimum composition (M-MS2.5). At this condition, porosity increased to 67.73 %, the O–H absorption band became more pronounced, and the water contact angle decreased from ∼80° to 53.4° (≈33 % reduction), indicating enhanced interfacial hydrophilicity. These structural and chemical enhancements led to improved transport and fouling behavior, with water flux approaching ∼80 L m−2 h−1 and the flux recovery ratio increasing to 90.91 %. Although humic acid rejection decreased from 79.8 % (pristine) to 69.19 % at the optimum silica loading (2.5 %), it remained within a reasonable ultrafiltration performance range. At higher silica concentrations, however, particle agglomeration and localized structural densification were observed, resulting in increased contact angle, reduced flux, and partial recovery of rejection, indicating a limited compositional window for effective synergy between silica and Mg(OH)2. Overall, the intermediate silica loading (2.5 wt%) provided the most favorable balance between permeability, antifouling stability, and rejection, suggesting strong potential for application in high-throughput treatment of NOM-rich waters.
揭示了氢氧化镁和二氧化硅协同调节聚醚砜膜结构和功能的机理
在这项研究中,研究了一种环境友好的双添加剂改性策略,将氢氧化镁和二氧化硅掺入PES膜中,同时调整非溶剂诱导相分离过程中的表面化学和孔隙形态。采用固定的Mg(OH)2含量和不同的二氧化硅浓度制备膜,并通过FESEM、ATR-FTIR、重量孔隙度分析、水接触角测量和过滤性能测试(包括纯水通量、腐植酸截留率和通量回收率)进行表征。所有改性膜都保留了原始PES的不对称结构,但随着二氧化硅含量的增加(M-MS2.5),选择性层变薄,手指状巨孔变长。在此条件下,孔隙率增加到67.73%,O-H吸收带变得更加明显,水接触角从~ 80°减小到53.4°(≈33%),表明界面亲水性增强。这些结构和化学的增强导致了输运和污染行为的改善,水通量接近~ 80 L m−2 h−1,通量回收率提高到90.91%。虽然在最佳二氧化硅负载(2.5%)下,腐植酸截留率从79.8%(原始)下降到69.19%,但仍在合理的超滤性能范围内。然而,在较高的二氧化硅浓度下,观察到颗粒团聚和局部结构致密化,导致接触角增加,通量降低和部分排斥恢复,这表明二氧化硅和Mg(OH)2之间有效协同作用的成分窗口有限。总体而言,中间二氧化硅负载(2.5 wt%)在渗透性、防污稳定性和截留性之间提供了最有利的平衡,表明在高通量处理富氮氧化物水方面具有很大的应用潜力。
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来源期刊
Case Studies in Chemical and Environmental Engineering
Case Studies in Chemical and Environmental Engineering Engineering-Engineering (miscellaneous)
CiteScore
9.20
自引率
0.00%
发文量
103
审稿时长
40 days
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