DesalinationPub Date : 2025-09-29DOI: 10.1016/j.desal.2025.119460
Wenyu Jia , Lei Sun , Xuewei Wang , Bo Xiong , Lijing Wang , Weilong Shi , Yan Sun , Feng Guo
{"title":"Janus-structured bilayer textile enabling high-efficiency salt-resistant solar desalination through directional water transport","authors":"Wenyu Jia , Lei Sun , Xuewei Wang , Bo Xiong , Lijing Wang , Weilong Shi , Yan Sun , Feng Guo","doi":"10.1016/j.desal.2025.119460","DOIUrl":"10.1016/j.desal.2025.119460","url":null,"abstract":"<div><div>Interfacial solar evaporation technology offers a green and sustainable approach to solving the global freshwater shortage, but salt accumulation at the evaporation interface reduces the light absorption efficiency and hinders the escape of water vapor, thereby significantly degrading the evaporation performance, which poses a key obstacle to long-term practical applications. Herein, a Janus-structured double-layer photothermal evaporator (CDs-SA-CT/DC) was designed in this study, integrating carbon dots (CDs) and sodium alginate (SA)-functionalized cotton textile (CT) photothermal layer with a directional water-transferring dustless cloth (DC), which displays an asymmetric bilayer structure of combining efficient broadband solar energy absorption with hydrodynamic conditioning. Experimental results presented that the CDs-SA-CT/DC evaporator possesses an evaporation rate of 1.82 kg m<sup>−2</sup> h<sup>−1</sup> at 1 solar irradiation (1 kW m<sup>−2</sup>) and a photothermal conversion efficiency of 79.28 %. Most importantly, the directional transport mechanism of water enabled salt ions to migrate and selectively deposit at the edges of the DC, effectively preventing interface blockage. By combining the photothermal interface with directional water transport, this Janus structural system provides a scalable salt-resistant strategy for efficient solar desalination.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"618 ","pages":"Article 119460"},"PeriodicalIF":9.8,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145265233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-29DOI: 10.1016/j.desal.2025.119459
Jiangmei Zhao , Shuyi Yang , Changlong Bi , Chong Peng , Yuanfei Wang , Tao E
{"title":"Enhanced ciprofloxacin removal from water by chitosan/Mn-modified biochar: Synergistic adsorption at multi-site active centers","authors":"Jiangmei Zhao , Shuyi Yang , Changlong Bi , Chong Peng , Yuanfei Wang , Tao E","doi":"10.1016/j.desal.2025.119459","DOIUrl":"10.1016/j.desal.2025.119459","url":null,"abstract":"<div><div>The widespread contamination of water resources by ciprofloxacin (CIP) necessitates efficient remediation technologies. While biochar (BC) is a promising adsorbent, its practical application is hindered by limited adsorption capacity. To bridge this gap, this study presents a novel chitosan-manganese co-modified biochar (CS-MBC) engineered through a coupled impregnation-pyrolysis method. This strategic modification significantly enhanced the adsorption performance, with CS-MBC achieving a maximum CIP capacity of 167.08 mg·g<sup>-1</sup>, vastly outperforming pristine BC. The novelty of this work lies in the synergistic integration of chitosan biopolymer and manganese oxides, which created multiple active sites for CIP binding. Crucially, CS-MBC demonstrated exceptional robustness and practicality in complex environments, maintaining high efficiency across varying ionic strengths, in the presence of humic acid, and in real water matrices. A combination of advanced characterization and theoretical calculations (DFT and MD) elucidated the enhanced adsorption mechanisms: (1) coordination between Mn species and the piperazine group of CIP, (2) optimized π-π electron donor-acceptor interactions, and (3) hydrogen bonding and electrostatic interactions facilitated by surface amino/hydroxyl groups. This work not only provides a highly effective and sustainable adsorbent for antibiotic removal but also offers deep mechanistic insights that can guide the future design of advanced functionalized materials for environmental remediation.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119459"},"PeriodicalIF":9.8,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217763","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"A review on the mediated role of peroxymonosulfate in contaminated water remediation","authors":"Siwen Cheng , Ruiren Zhou , Pei Zhou , Fude Liu , Qixing Zhou","doi":"10.1016/j.desal.2025.119456","DOIUrl":"10.1016/j.desal.2025.119456","url":null,"abstract":"<div><div>With the increasing complexity of eco-environmental issues and the growing demand for technological effectiveness at all levels, traditional treatment technologies and many existing remediation methods for contaminated water are becoming ineffective. In this context, improved remediation for contaminated water mediated by peroxymonosulfate (PMS) has being emerged and become an important trend for future development in this field. In this review, recent researching progresses made in the emerging technology, namely the PMS mediated remediation for contaminated water including contaminated saline water with tricky pollutants (PAHs, pesticides, and heavy metals) and emerging micropollutants (antibiotics and microplastics), were firstly summarized. Moreover, coupling PMS activation with other technical means including emerging membrane materials for desalination, UV method, microwave method, electrochemical method, heat and alkali method, transition metals method, carbon-based materials method, and photo-electrons method has been overviewed. Then, the reaction pathways (free radical and non-radical) and influencing factors (organic matter, pH, temperature and inorganic anions) of the PMS mediated contaminated water remediation were also discussed. Finally, the focus of the future research and development directions on emerging advanced technologies aimed at more cost-effective, environmentally friendly, non-destructive, safe, stable, and sustainable remediation strategy were prospected.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119456"},"PeriodicalIF":9.8,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217788","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-29DOI: 10.1016/j.desal.2025.119454
Qibiao Chen , Chao Qian , Shaodong Zhou
{"title":"Theory-guided design of high-efficiency lithium extraction system for high Mg/Li ratio brines","authors":"Qibiao Chen , Chao Qian , Shaodong Zhou","doi":"10.1016/j.desal.2025.119454","DOIUrl":"10.1016/j.desal.2025.119454","url":null,"abstract":"<div><div>Global demand for lithium necessitates efficient extraction technologies, especially from low-quality brines with high magnesium-to‑lithium (Mg/Li) ratios, where conventional methods falter. This study presents a novel, quantum chemistry-guided methodology for the rational design of solvent extraction systems to address this challenge. By evaluating lithium binding affinities, triisopropylphenyl phosphate (TiPPP) was identified as a superior extractant. When formulated into an TiPPP-FeCl<sub>3</sub> system, it demonstrated exceptional performance under optimized conditions (90 % vol extractant, Fe/Li molar ratio of 1.2, O/A ratio of 1). In a single stage, the system achieved a lithium extraction efficiency of 92.8 %, corresponding to a remarkable Li/Mg separation factor of 1699. After scrubbing and stripping, the Mg/Li mass ratio in the final product was reduced to 0.0199, a 4156-fold decrease from the initial brine (82.7), outperforming the conventional tributyl phosphate (TBP)-FeCl<sub>3</sub> system. A combination of DFT calculations and spectroscopic analyses (Infrared spectroscopy, Ultraviolet spectroscopy, Raman spectroscopy, and electrospray ionization mass spectrometry) confirmed that the high selectivity is governed by both the electronic environment of the phosphoryl (P=O) group and the steric hindrance effects. This study not only presents a high-performance system for direct lithium extraction but also establishes a rational design paradigm for developing advanced extractants for challenging separation tasks.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119454"},"PeriodicalIF":9.8,"publicationDate":"2025-09-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217815","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-28DOI: 10.1016/j.desal.2025.119449
Chao Li , Zaixing Li , Xueqing Xu , Hong Mo , Haitang Wang , Jiaxuan Deng , Shenghuan Liu , Yunzhi Qian , Mengfei Liu , Shilong He , Haijiao Xie
{"title":"Overcoming hydroxyl radical quenching in high-salinity wastewater: Electrostatically shielded porous perovskite boosts adsorption-oxidation of organic contaminants","authors":"Chao Li , Zaixing Li , Xueqing Xu , Hong Mo , Haitang Wang , Jiaxuan Deng , Shenghuan Liu , Yunzhi Qian , Mengfei Liu , Shilong He , Haijiao Xie","doi":"10.1016/j.desal.2025.119449","DOIUrl":"10.1016/j.desal.2025.119449","url":null,"abstract":"<div><div>Free radicals are severely quenched by ubiquitous anions (e.g., Cl<sup>−</sup>) in high-salinity organic wastewater, which severely impedes the application of advanced oxidation processes. To address this, a free radical protection microzone (FRPM) is created on a catalyst through synergistic electrostatic repulsion (between the anionic group and anion) and physical adsorption. Specifically, poly (sodium 4-styrenesulfonate) was used to modify three-dimensionally ordered macroporous perovskite-ceria composite to introduce a surface negative layer, where anions are difficult to enter due to electrostatically repelled by the sulfonic acid group (-SO<sub>3</sub><sup>−</sup>) and avoid free radical quenching. Porous perovskites with large specific surface area and strong adsorption capacity enrich organic pollutants in FRPM through physical adsorption process and remove them by free radicals. The anionic porous perovskite composite (A-3DLFC) can completely remove tetracycline (TC) within 30 min with the k value over 0.1664 min<sup>−1</sup> in a variety of high-salinity environments. Quenching experiments and EPR tests showed that surface-bounded hydroxyl radical (·OH) is the main reactive oxygen species. Crucially, density functional theory (DFT) calculations quantitatively substantiate the FRPM mechanism, revealing an exceptionally high energy barrier (+8.19 eV) for the quenching reaction between Cl<sup>−</sup> and ·OH on the A-3DLFC surface, with the Cl<sup>−</sup> adsorption process being the primary limiting step (+7.09 eV).</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119449"},"PeriodicalIF":9.8,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217720","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Simultaneous capacitive removal of nitrate and phosphate pollutants via Zr-BTB@CNTs electrode for remediation of aquatic eutrophication","authors":"Chenxin Ding , Jianguo Zhou , Zhen Jin , Hongjian Zhou","doi":"10.1016/j.desal.2025.119451","DOIUrl":"10.1016/j.desal.2025.119451","url":null,"abstract":"<div><div>The excessive influx of nitrogen and phosphorus, driven by accelerated urbanization, has become a predominant contributor to aquatic eutrophication and water quality deterioration. Herein, Zr-BTB@CNTs (ZB@C), a layered nanoscale metal-organic framework (MOF) material synthesized through a hydrothermal method coupled with carbon nanotubes, was comprehensively evaluated as capacitive deionization (CDI) anode for simultaneous capacitive removal of nitrate (NO<sub>3</sub><sup>−</sup>) and phosphate (PO<sub>4</sub><sup>3−</sup>) pollutants from water. The optimized ZB@20C exhibited electrosorption capacities of 222.1 mg g<sup>−1</sup> for NO<sub>3</sub><sup>−</sup> and 159.9 mg g<sup>−1</sup> for PO<sub>4</sub><sup>3−</sup> within 120 min, under an applied voltage of 1.2 V. Furthermore, ZB@20C retained high electrosorption capacities for both nitrate and phosphate across a wide pH range (3−11) and maintained over 80 % removal efficiency for both pollutants after 10 consecutive electrosorption-desorption cycles. Through DFT calculations, XPS, and FTIR analyses, the electrosorption mechanisms of ZB@20C were further elucidated: nitrate electrosorption primarily involves coordination interactions with Zr<sub>6</sub> clusters, while phosphate electrosorption mainly stems from lattice oxygen coordination and hydroxyl exchange. Finally, ZB@20C demonstrates strong resistance to ionic interference, effectively reducing nitrate and phosphate concentrations to below 10 mg L<sup>−1</sup> and 1.0 mg L<sup>−1</sup>, respectively, in samples from Chaohu River, Nanfei River, and industrial wastewater, thereby meeting WHO standards.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119451"},"PeriodicalIF":9.8,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217819","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-28DOI: 10.1016/j.desal.2025.119445
Jiahui Du , Jian Xiao , Xiaohua Ma , Jianxin Li
{"title":"Crown ether-functionalized polyimide nanofiber membranes fabricated by in-situ grafting and electrospinning for efficient selective adsorption of cesium","authors":"Jiahui Du , Jian Xiao , Xiaohua Ma , Jianxin Li","doi":"10.1016/j.desal.2025.119445","DOIUrl":"10.1016/j.desal.2025.119445","url":null,"abstract":"<div><div>A nanofiber membrane (18C6-g-18C6PI) containing crown ethers in both the main and side chains was fabricated via in-situ grafting and electrospinning through amidation between 18-crown-6 polyimide (18C6PI, Mₙ = 93 kDa) and di(aminobenzo)18-crown-6 (DAB18C6). The goal of this study is to enhance the loading amount of crown ethers so as to improve the adsorption capacity for cesium (Cs<sup>+</sup>) from salt lakes. Results showed that the nanofiber membrane with a fiber diameter of 310–340 nm was obtained by precisely controlling the viscosity of the spinning system (650–700 mPa·s) and the grafting reaction time (10 h). The grafting degree of crown ether was enhanced from 17.3 % (18C6PI) to 84.8 % after DAB18C6 grafting. Dynamic cyclic adsorption experiments revealed that the 18C6-g-18C6PI nanofiber membrane achieved a Cs<sup>+</sup> adsorption capacity of 85.23 mg g<sup>−1</sup>, which is significantly higher than that of the 18C6PI nanofiber membrane (68.21 mg g<sup>−1</sup>). In addition, the 18C6-g-18C6PI nanofiber membrane showed a high selective separation for Cs<sup>+</sup>, with separation factors for Cs<sup>+</sup>/Rb<sup>+</sup>, Cs<sup>+</sup>/K<sup>+</sup>, Cs<sup>+</sup>/Na<sup>+</sup>, Cs<sup>+</sup>/Ca<sup>2+</sup>, and Cs<sup>+</sup>/Mg<sup>2+</sup> of 10.3, 6.5, 29.5, 17.6, and 21.4, respectively. The 18C6-g-18C6PI nanofiber membrane maintained 96.3 % of the initial capacity after five regeneration cycles. Furthermore, density functional theory (DFT) calculations demonstrated that 18C6-g-18C6PI exhibited a stronger Cs<sup>+</sup> binding energy (−436.89 kJ mol<sup>−1</sup>) than 18C6PI (−360.41 kJ mol<sup>−1</sup>). This enhancement was ascribed to the higher crown ether loading in 18C6-g-18C6PI, which intensified the ion-dipole interaction with Cs<sup>+</sup>. In summary, this work provides insights into the development of crown ether-functionalized nanofiber membranes for efficient and selective recovery of cesium.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"618 ","pages":"Article 119445"},"PeriodicalIF":9.8,"publicationDate":"2025-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145264322","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-26DOI: 10.1016/j.desal.2025.119438
Shehriyar , Arslan Khurram , Abdul Jabbar , Muhammad Asim Khan , Wenhao Liu , Sadaf Mutahir , Akhtar Munir , Sameerah I. Al-Saeedi
{"title":"pH-responsive MIL-101(Fe)/NiFe-LDH composite membranes for high-flux removal of cationic and anionic dyes in wastewater treatment","authors":"Shehriyar , Arslan Khurram , Abdul Jabbar , Muhammad Asim Khan , Wenhao Liu , Sadaf Mutahir , Akhtar Munir , Sameerah I. Al-Saeedi","doi":"10.1016/j.desal.2025.119438","DOIUrl":"10.1016/j.desal.2025.119438","url":null,"abstract":"<div><div>Synthetic dyes, known for their toxicity, mutagenicity, and carcinogenicity, pose severe threats to aquatic ecosystems and human health. Membrane filtration offers an energy-efficient solution, but achieving simultaneously high selectivity, permeability, and stability for both cationic and anionic dyes remain challenging. Here, we design a hierarchical composite membrane by integrating MIL-101(Fe), a high-porosity metal-organic framework (MOF), with NiFe-layered double hydroxide (LDH) nanosheets. The MIL-101(Fe) matrix provides a large surface area (∼19.2 m<sup>2</sup>/g) and tailored pore architecture for size-selective adsorption. At the same time, the NiFe-LDH enhances electrostatic interactions via its pH-tunable surface charge (isoelectric point = 3.16). This synergy enables exceptional removal efficiencies for methyl green (MG, 88 %) and methyl orange (MO, 91 %) at ultrahigh water flux (>100 L·m<sup>−2</sup>·h<sup>−1</sup>·bar<sup>−1</sup>), outperforming conventional membranes (Table S1). The membrane's pH-responsive selectivity, driven by zeta potential reversal, allows targeted removal of cationic (e.g., MG at pH > 3.16) and anionic (e.g., MO at pH < 3.16) dyes. Density functional theory (DFT) simulations reveal that MG adsorption occurs via π-π stacking with MIL-101's benzene linkers and electrostatic attraction to LDH hydroxyl groups. In contrast, MO uptake involves anion exchange with LDH interlayers. With excellent recyclability (>80 % efficiency after 5 cycles) and antifouling properties (flux recovery >90 %), this work advances the design of multifunctional membranes for scalable wastewater treatment.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119438"},"PeriodicalIF":9.8,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217765","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-26DOI: 10.1016/j.desal.2025.119447
Hongyuan Yin, Fenghua Zhang, Zongkai Ma, Xiangyu Wang, Xusheng Wang, Feihang Long, Maoqian Xie, Jianyun He, Ying An, Weimin Yang
{"title":"Recent advances on enhancing the solar distillation systems through the condensate-side","authors":"Hongyuan Yin, Fenghua Zhang, Zongkai Ma, Xiangyu Wang, Xusheng Wang, Feihang Long, Maoqian Xie, Jianyun He, Ying An, Weimin Yang","doi":"10.1016/j.desal.2025.119447","DOIUrl":"10.1016/j.desal.2025.119447","url":null,"abstract":"<div><div>Solar distillation has attracted widespread attention as an environmentally friendly and easy-to-operate water treatment technology. While significant research efforts have been devoted to optimizing the structural design of solar stills and improving photothermal conversion efficiency, relatively limited attention has been paid to the enhancement of the condensation process. The low condensation efficiency often results in a substantial gap between the actual water collection rate and the theoretical yield or evaporation rate. We review current strategies and mechanisms for enhancing condensation in solar stills and analyse their critical role in the overall performance of solar distillation systems. Key topics include surface design strategies for condensation, optimization of surface wettability, the impact of micro/nanostructures on condensation efficiency, as well as structural innovations and the integration of advanced cooling technologies to enhance condensation. Furthermore, we examine the balance between enhanced condensation and evaporation processes based on the internal heat and mass transfer dynamics of the distillation system. Finally, we recommend that future research on solar distillation systems focus on the integration of efficient passive and active cooling technologies, bioinspired micro/nanostructured designs, hybrid wettability surface engineering, modular system architectures, and AI-assisted optimization. These strategies aim to enhance condensation efficiency, system flexibility, and environmental adaptability, ultimately enabling the development of high-performance, intelligent, and sustainable solar distillation solutions.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119447"},"PeriodicalIF":9.8,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145218263","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
DesalinationPub Date : 2025-09-26DOI: 10.1016/j.desal.2025.119439
Shuwei Jia , Jun Wei , Xinyu Ma , Zhi Wang
{"title":"Fabrication of enhanced Mg2+/Li+-selective membranes via aminoacetonitrile-modulated PEI/TMC interfacial polymerization","authors":"Shuwei Jia , Jun Wei , Xinyu Ma , Zhi Wang","doi":"10.1016/j.desal.2025.119439","DOIUrl":"10.1016/j.desal.2025.119439","url":null,"abstract":"<div><div>High-efficiency lithium extraction from salt lakes is pivotal to meet escalating lithium demand driven by energy storage and electric vehicle industries. In this study, the small-molecule aminoacetonitrile (AAN) was introduced as an aqueous-phase <em>co</em>-monomer to modulate the interfacial polymerization process between polyethyleneimine (PEI) and trimesoyl chloride (TMC). Specifically, the primary amine in AAN molecules reacted with acyl chloride moieties in TMC, occupying reaction sites and thereby preserving a larger fraction of unreacted primary amine groups on the PEI chains within the separation layer, which significantly enhanced the membrane's surface positive charge. Simultaneously, the nitrile groups of AAN preferentially coordinated with Li<sup>+</sup> ions to effectively counteract the repulsive effect of the strongly positively charged membrane surface on Li<sup>+</sup>. This “charge-coordination” synergistic mechanism enabled precise control over the separation process. When treating mixed salt solution with a Mg<sup>2+</sup>/Li<sup>+</sup> mass ratio of 100, the optimized membrane achieved a separation factor of 74.7, along with enhanced MgCl<sub>2</sub> rejection of 99.3 % compared to virgin membrane's 93.9 %, and reduced LiCl rejection from 56.3 % to 49.3 %. Notably, upon treatment of simulated salt lake brine, the membrane manifested a pronounced Li<sup>+</sup> enrichment effect, with a LiCl rejection rate of −8.8 % while retaining a high MgCl<sub>2</sub> rejection capacity. This study employed a simple preparation process with industrialization potential, providing a guiding strategy for constructing high-selectivity membranes for Mg<sup>2+</sup>/Li<sup>+</sup> separation.</div></div>","PeriodicalId":299,"journal":{"name":"Desalination","volume":"617 ","pages":"Article 119439"},"PeriodicalIF":9.8,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145217760","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}