{"title":"Unveiling the synergistic mechanism of magnesium hydroxide and silica in modulating polyethersulfone membrane structure and function","authors":"Umi Fathanah , Abubakar Abubakar , Syawaliah Muchtar , Cut Meurah Rosnelly , Zuhra Zuhra , Mirna Rahmah Lubis , Sidik Marsudi","doi":"10.1016/j.cscee.2026.101328","DOIUrl":null,"url":null,"abstract":"<div><div>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)<sub>2</sub> 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<sup>−2</sup> h<sup>−1</sup> 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)<sub>2</sub>. 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.</div></div>","PeriodicalId":34388,"journal":{"name":"Case Studies in Chemical and Environmental Engineering","volume":"13 ","pages":"Article 101328"},"PeriodicalIF":0.0000,"publicationDate":"2026-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Case Studies in Chemical and Environmental Engineering","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666016426000071","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/1/12 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"Environmental Science","Score":null,"Total":0}
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.