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Fabrication of monovalent cation perm-selective membranes via quaternized poly(aryl ether sulfone) modification for efficient Li+/Mg2+ separation 季铵化聚芳醚砜改性制备一价阳离子双选择性膜,用于Li+/Mg2+的高效分离
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-11 DOI: 10.1016/j.desal.2026.119971
Shuting Zhang, Yunxiang Ouyang, Khalznkhuu Otgonlkhagva, Jiaze Li, Jialin Lv, Na Li, Zhaoxia Hu, Shouwen Chen
Optimizing the structural and physicochemical attributes of monovalent cation perm-selective membranes (MCPMs) is crucial to achieve high selectivity, flux, and durability, which are essential for the efficient extraction of lithium through electrodialysis from salt-lake brines with a high Mg2+/Li+ ratio. In this study, MCPMs derived from sulfonated poly(aryl ether sulfone) (SPAES) first were solution cast and subsequently coated with quaternized poly(aryl ether sulfone) (QPAES). The modification layer of QPAES was simply adjusted by varying the ion exchange capacity (IEC) level and the number of coating applications. Their selectivity, flux and stability were systematically evaluated. The results demonstrate that for the SPAES/Q-1.17-3 membrane, which has a modified layer of IEC 1.17 mmol/g and 3 times of coating, the selectivity of Li+/Mg2+ is above 1000, while concurrently achieving a Li+ flux of 0.167 mol/(m2 h). Additionally, the perm-selectivity remained virtually unchanged over five cycling tests, thereby showcasing its considerable potential for ion separation.
优化一价阳离子膜(mcpm)的结构和物理化学性质是实现高选择性、通量和耐久性的关键,这是通过电渗析从高Mg2+/Li+比的盐湖盐水中高效提取锂的必要条件。在这项研究中,由磺化聚芳醚砜(SPAES)衍生的mcpm首先被溶液铸造,然后被季铵盐化聚芳醚砜(QPAES)包裹。通过改变离子交换容量(IEC)水平和镀膜次数,可以简单地调整QPAES的修饰层。系统评价了它们的选择性、通量和稳定性。结果表明:采用IEC为1.17 mmol/g的改性层和3次涂层的SPAES/Q-1.17-3膜,Li+/Mg2+的选择性在1000以上,同时Li+通量为0.167 mol/(m2 h)。此外,在五次循环测试中,烫发选择性几乎保持不变,从而显示出其相当大的离子分离潜力。
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引用次数: 0
Cryo-engineered macroporous adsorbent with synergistic adsorption-reduction for efficient gold recovery from e-waste 具有协同吸附-还原作用的低温工程大孔吸附剂用于从电子垃圾中高效回收金
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-09 DOI: 10.1016/j.desal.2026.119955
Xianshuang Zhu , Wenjie Li , Abdul Haleem , Hao Li
Recycling gold from e-waste mitigates pollution and delivers greater economic benefits than extracting it from ore. This study reports the first fabrication of a customizable macroporous thiourea-based adsorbent via low-temperature UV-assisted ice-templated polymerization, an approach that enables simple, time-efficient, and large-scale production. With exceptional structural properties (16.36 g g−1 water uptake, 92.33% porosity, 5.209 m2 g−1 total pore area), the adsorbent exhibits superior Au(III) adsorption: maximum capacity of 2558.7 ± 35.7 mg g−1 at pH 4 and 318 K (800 mg L−1 Au(III)), fitting the Freundlich model. It retains high performance after heat/acid/alkali treatments, achieving >98% Au(III) removal in spiked actual leachate and 1679.2 ± 16.3 mg g−1 saturated capacity. XPS confirms Au(III) adsorption via allylthiourea groups, while sponge-like metallic gold formation post-calcination validates thiourea's reduction capability. This adsorbent offers outstanding Au(III) affinity, selectivity, and extreme-condition stability, providing a reliable basis for harsh industrial precious metal recovery and valuable insights for soft polymeric materials in environmental applications.
与从矿石中提取黄金相比,从电子垃圾中回收黄金可以减轻污染,并带来更大的经济效益。本研究报告首次通过低温紫外线辅助冰模板聚合制备了可定制的大孔硫脲基吸附剂,这种方法可以实现简单、高效和大规模的生产。该吸附剂具有优异的结构性能(吸水性为16.36 g g−1,孔隙率为92.33%,总孔面积为5.209 m2 g−1),对Au(III)具有优异的吸附性能:在pH为4,温度为318 K (800 mg L−1 Au(III))时,最大吸附量为2558.7±35.7 mg g−1,符合Freundlich模型。经过热/酸/碱处理后,它仍保持高性能,在加标的实际渗滤液中达到98%的Au(III)去除率和1679.2±16.3 mg g−1的饱和容量。XPS证实了金(III)通过烯丙基硫脲基团吸附,而焙烧后形成的海绵状金属金证实了硫脲的还原能力。这种吸附剂具有出色的Au(III)亲和力、选择性和极端条件稳定性,为苛刻的工业贵金属回收提供了可靠的基础,并为环境应用中的软聚合物材料提供了宝贵的见解。
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引用次数: 0
Growth behavior and desalination performance of Chlorella vulgaris under different seawater concentrations 不同海水浓度下普通小球藻的生长行为及脱盐性能
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-07 DOI: 10.1016/j.desal.2026.119951
Azin Nematkhah , Maryam Nazarinia , Toraj Mohammadi , Soheil Zarghami , Mehdi Mohammadi
Water scarcity is one of the most critical global challenges, and with growing demand for freshwater, desalination has emerged as a promising solution. However, conventional desalination technologies are limited by high energy consumption, substantial capital costs and environmental concerns. As an alternative, biological desalination has been gained attention as an efficient and eco-friendly method. In this study, microalgae-based desalination using Chlorella vulgaris (C. vulgaris) was investigated as a sustainable approach to reduce seawater salinity. Mixtures of seawater and BG-11 culture medium were prepared in different ratios, and the effect of algal inoculation levels (10%, 15%, and 20%) on cell growth and desalination performance was evaluated over 21-day period. Optical density (OD) and biomass dry weight were measured as growth indicators, while total dissolved solids (TDS) served as the desalination parameter. The results of a steady increment in OD across all samples confirmed the adaptation of C. vulgaris to the saline conditions. The highest OD (1.744) was obtained for the 15% inoculation on day 21. Significant reductions in TDS were achieved for all treatments, with greater desalination at higher inoculation levels. The maximum reduction occurred with the 20% inoculation on day 13, reaching 32% and 30% for the 75% and 100% seawater treatments, respectively. The results were further supported by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and Fourier transform infrared (FTIR) spectroscopy analyses. Overall, C. vulgaris demonstrated strong potential as an environmentally friendly and innovative strategy for seawater desalination, providing a sustainable complement to conventional methods and new opportunities in industrial water treatment.
水资源短缺是全球最严峻的挑战之一,随着对淡水需求的不断增长,海水淡化已经成为一种有希望的解决方案。然而,传统的海水淡化技术受到高能耗、大量资本成本和环境问题的限制。作为一种替代方法,生物脱盐作为一种高效且环保的方法受到了人们的关注。本研究研究了利用小球藻(Chlorella vulgaris)进行微藻脱盐作为降低海水盐度的可持续途径。将不同比例的海水与BG-11培养基混合配制,在21 d的时间内,观察接种量(10%、15%和20%)对细胞生长和脱盐性能的影响。以光密度(OD)和生物量干重为生长指标,以总溶解固形物(TDS)为脱盐参数。所有样品的OD均呈稳定增长的趋势,证实了寻常草对盐水环境的适应。接种15%时,第21天OD值最高,为1.744。所有处理的TDS均显著降低,接种水平越高,脱盐程度越高。在第13天,20%的接种量最大,75%和100%的海水处理分别达到32%和30%。扫描电镜(SEM)、能量色散x射线能谱(EDX)和傅里叶变换红外(FTIR)光谱分析进一步支持了研究结果。总体而言,C. vulgaris作为一种环境友好型和创新的海水淡化策略显示出强大的潜力,为传统方法提供了可持续的补充,并为工业水处理提供了新的机遇。
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引用次数: 0
LP single-driving RERD with inner shaft supporting for SWRO desalination system: structure design and performance optimization SWRO海水淡化系统内轴支撑LP单驱动rrd:结构设计与性能优化
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-01-19 DOI: 10.1016/j.desal.2026.119885
Hongshan Xu , Junqi Wang , Xinmiao Hou , Xiaobo Feng , Yuhao Yan , Liangjuan Ouyang , Yue Wang
To reduce the effect of energy loss caused by RERD on SWRO desalination system, the LP single-driving RERD with inner shaft supporting is innovatively proposed with a rated operating pressure of 6.0 MPa and capacity of 15.0 m3/h. Firstly, compared with outer sleeve supporting, the inner shaft supporting exhibits lower resisting moment. Compared with double-driving, LP single-driving with lower HP pressure loss performs lower driving moment to match the inner shaft supporting. Secondly, the backflow ratio is reduced by firstly decreasing the central angle of driving-flow part from 67.50° to 33.75°and secondly moving the LP brine nozzle close to the driving-flow part. As the result, the backflow optimization reduces the LP pressure loss and volumetric mixing. Additionally, increasing the rotor length from 100 mm to 150 mm further reduces the still high volumetric mixing. Finally, over the optimum flowrate range of 8.2 m3/h-17.1 m3/h, the LP single-driving RERD after structure optimization performs the volumetric mixing of 0.85%–2.03% and the energy recovery efficiency range of 97.9%–98.8%. The competitive performances of LP single-driving RERD compared to commercial products exhibit the potential for reducing the energy consumption of SWRO desalination system from the perspective of ERD.
为减少rrd对SWRO海水淡化系统能量损失的影响,创新提出了内轴支撑的LP单驱动rrd,额定工作压力为6.0 MPa,容量为15.0 m3/h。首先,与外套筒支承相比,内轴支承的阻力矩更小。与双驱动相比,低压单驱动的压力损失更小,驱动力矩更小,与内轴支撑相匹配。其次,将驱动流部分中心角从67.50°减小到33.75°,将LP盐水喷嘴移至驱动流部分附近,降低了回流比。结果表明,回流优化降低了低压压力损失和体积混合。此外,将转子长度从100毫米增加到150毫米,进一步减少了仍然高体积的混合。最终,在最佳流量8.2 m3/h-17.1 m3/h范围内,经结构优化后的低压单驱rrd的体积混合率为0.85% ~ 2.03%,能量回收效率为97.9% ~ 98.8%。LP单驱动rrd与商业产品相比的竞争性能显示了从ERD的角度降低SWRO海水淡化系统能耗的潜力。
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引用次数: 0
Multivalent intercalation in Prussian blue analogues as a novel recovery method from spent Li-ion batteries 普鲁士蓝类似物多价插层回收废锂离子电池新方法
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-02 DOI: 10.1016/j.desal.2026.119938
Victoria Carnero-Roldan , Adrián Licari , Alejandro López-Chías , Ángela Fernández-Merino , Fabio La Mantia , Rafael Trócoli
Finding alternative extraction sources of principal components for the manufacturing of Li-ion batteries has become of great interest owing to the ubiquitous presence of this storage system, from mobile to electric vehicles. Battery recycling has the potential to reduce reliance on conventional raw sources; however, current technologies suffer from numerous drawbacks, including environmental issues and low selectivity. The use of an intercalation material, a Prussian Blue Analogue, for the recovery of multivalent cations (Ni2+ and Co2+) from spent Li-ion batteries is demonstrated for the first time in this work. Firstly, the capacity of the material to intercalate the cations of interest in aqueous media was proven by a combination of electrochemical, structural, and composition analysis of the electrode and electrolyte, subsequently a novel electrochemical approach to extract Ni and Co from a NMC leachate was developed, being able to produce a recovered solution with a purity of 99.99% in Ni and Co in a single step owing to the extraordinary selectivity of Nickel Hexacyanoferrate towards these cations. These performances, combined with the reversibility of the material and the well-known low cost of Prussian Blue Analogues, open a promising new alternative for battery recycling.
寻找制造锂离子电池的主要成分的替代提取来源已经变得非常有趣,因为这种存储系统无处不在,从移动到电动汽车。电池回收有可能减少对传统原材料的依赖;然而,目前的技术存在许多缺点,包括环境问题和低选择性。在这项工作中,首次展示了使用插层材料普鲁士蓝类似物从废锂离子电池中回收多价阳离子(Ni2+和Co2+)。首先,通过对电极和电解质的电化学、结构和成分分析,证明了该材料在水介质中插入感兴趣阳离子的能力,随后开发了一种从NMC渗滤液中提取Ni和Co的新型电化学方法。由于六氰高铁镍对这些阳离子具有非凡的选择性,因此能够在一步中产生纯度为99.99%的镍和钴的回收溶液。这些性能,再加上材料的可逆性和众所周知的普鲁士蓝类似物的低成本,为电池回收开辟了一个有前途的新选择。
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引用次数: 0
Biomass-derived modifiers customize polymeric nanofiltration membranes for enhanced lithium/magnesium ion selectivity 生物质衍生改性剂定制聚合物纳滤膜,增强锂/镁离子的选择性
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-01-30 DOI: 10.1016/j.desal.2026.119923
Xin-Xi Ding , Cheng Jiang , Jia-Wang Wang , Zi-Hui Wu , Rui Luo , Yue Zhao , Yue Wang , Dan-Dan Shao
Driven by the rapid expansion of the battery industry, lithium extraction from salt lake brines has emerged as a promising strategy to address the growing global demand for lithium. However, the selective separation of Li+ from Mg2+ remains difficult due to their similar hydrated radii and the typically high Mg2+/Li+ ratios in natural brines. Polymeric nanofiltration membranes provide an attractive approach for selective ion separation by tuning surface charge and pore size, enabling low-pressure operation and continuous processing. Herein, we present a sustainable strategy that incorporates biomass-derived waste jujube extract (JE), rich in functional moieties such as polyphenols and carboxylic groups, into the interfacial polymerization process to construct sub-nanometer channels in nanofiltration membranes. This bio-based modification effectively regulates membrane structure and surface chemistry, significantly enhancing water permeability (8.96 L·m−2·h−1·bar−1) and Li+/Mg2+ selectivity (up to 38.28). The resulting membranes exhibit excellent long-term stability, maintaining separation performance over 60 h of continuous operation. This work provides new insights into designing functionalized sub-nanometer channels for precise ion sieving and offers a green and cost-effective approach to valorizing agricultural biomass for the development of high-performance nanofiltration membranes.
在电池行业快速扩张的推动下,从盐湖盐水中提取锂已成为解决全球锂需求不断增长的一种有前景的策略。然而,由于它们相似的水合半径和天然盐水中典型的高Mg2+/Li+比,Li+和Mg2+的选择性分离仍然很困难。聚合物纳滤膜通过调节表面电荷和孔径,实现低压操作和连续处理,为选择性离子分离提供了一种有吸引力的方法。在此,我们提出了一种可持续的策略,将富含多酚和羧基等功能基团的生物质来源的废枣提取物(JE)纳入界面聚合过程,在纳滤膜中构建亚纳米通道。这种生物基改性有效地调节了膜的结构和表面化学,显著提高了膜的透水性(8.96 L·m−2·h−1·bar−1)和Li+/Mg2+的选择性(高达38.28)。所得到的膜表现出优异的长期稳定性,在60小时的连续操作中保持分离性能。这项工作为设计用于精确离子筛选的功能化亚纳米通道提供了新的见解,并为开发高性能纳滤膜提供了一种绿色和经济有效的方法。
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引用次数: 0
Molecular dynamics simulation of polyamide based reverse osmosis for boron removal 聚酰胺反渗透除硼的分子动力学模拟
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-06 DOI: 10.1016/j.desal.2026.119943
Yawei Du , Mengru Cui , Jingxin Wei , Yanping Li , Yize Liu , Shizhao Wang , Zhiyong Ji
The inadequate boron removal performance of Polyamide (PA) based reverse osmosis (RO) membrane is one of the bottlenecks restricting its use as drinking water. Therefore, it is of importance to investigate the trans-membrane mechanism of PA membranes at the atomic level. In this work, an all-atom solution-membrane-pure water sandwich RO model was built. Non-equilibrium molecular dynamics (NEMD) simulations were employed to explore the transmembrane behaviors of water, ions, H₃BO₃, H₄BO₄, and D-gluconate borate complex (referred to Complex). The influences of transmembrane pressure difference, temperature, and chlorination of the PA membrane were investigated. The results indicate that an increase in transmembrane pressure difference and feed temperature facilitates the RO process by increasing the diffusion coefficients of all components. Both factors reduce the number of hydrogen bonds between boron-containing species and water while increasing those with the PA membrane, which benefits water molecule permeation. Pressure difference has little effect on salt rejection but impacts boron rejection ability, whereas higher temperatures decrease salt rejection. Chlorination enlarges PA membrane pores and increases component diffusivity, while weakening interactions with both water and boron species (H₃BO₃ and H₄BO₄) and reducing associated hydrogen bonding. These changes enhance water permeability but affect boron rejection differently: H₃BO₃ rejection remains less impacted due to its weak membrane affinity, whereas H₄BO₄ rejection declines markedly as chlorination disrupts its strong electrostatic/hydrogen-bonding interaction with the membrane. Among boron species, Complex exhibits the highest removal rate and is least affected by these factors, leading to the recommendation of adding polyhydroxylic substances to form hydroxyl borate complexes for optimal boron removal.
聚酰胺(PA)基反渗透(RO)膜除硼性能不佳是制约其作为饮用水应用的瓶颈之一。因此,在原子水平上研究PA膜的跨膜机理具有重要意义。本文建立了全原子溶液-膜-纯水夹层反渗透模型。采用非平衡分子动力学(NEMD)模拟研究了水、离子、H₃BO₃、H₄BO₄−和d -葡萄糖酸硼酸盐配合物(简称配合物)的跨膜行为。考察了跨膜压差、温度和氯化对PA膜性能的影响。结果表明,膜间压差和进料温度的升高通过提高各组分的扩散系数来促进反渗透过程的进行。这两个因素都减少了含硼物质与水之间的氢键数量,而增加了与PA膜之间的氢键数量,这有利于水分子的渗透。压差对脱盐影响不大,但会影响脱硼能力,而温度升高会降低脱盐能力。氯化作用扩大了PA膜的孔隙,增加了组分的扩散率,同时减弱了与水和硼的相互作用(H₃BO₃和H₄BO₄−),并降低了相关的氢键。这些变化提高了水的渗透性,但对硼的吸附性有不同的影响:H₃BO₃吸附性受到的影响较小,因为它的膜亲和力较弱,而H₄BO₄−吸附性显著下降,因为氯化破坏了它与膜的强静电/氢键相互作用。在硼种中,配合物的去除率最高,受这些因素的影响最小,因此建议添加多羟基物质形成羟基硼酸盐配合物以达到最佳的脱硼效果。
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引用次数: 0
High-strength sulfonated cellulose nanofiber membranes with high pore density for efficient osmotic power generation 具有高孔隙密度的高强度磺化纤维素纳米纤维膜,用于高效渗透发电
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-02 DOI: 10.1016/j.desal.2026.119940
Jiale Zhou , Yangning Zhao , Haiyu Dong , Yi Mi , Yun Zhang
Osmotic energy, as a clean and renewable energy source derived from the salinity gradient between seawater and river water, holds great potential for alleviating global energy shortages. However, the development of high-performance nanofluidic membranes with both high ion selectivity and ion flux remains a critical bottleneck for its practical application. Herein, we report a sulfonated cellulose nanofibers (SCNF) membranes constructed with three-dimensional (3D) nanochannels featuring high charge density and pore density (2 × 1010 cm−2). Under a 50-fold salinity gradient, the SCNF membrane exhibits an exceptional cation selectivity of up to 0.977. These superior ion transport properties directly translate into outstanding osmotic energy conversion performance: the maximum power densities reach 14.85 W m−2 and 111.06 W m−2 under 50-fold and 500-fold concentration gradients, respectively. Notably, the SCNF membrane maintains its power density stably for 60 days, demonstrating remarkable long-term operational durability. When mixing seawater and real river, the membrane achieves a maximum output power density of up to 16.37 W m−2; even upon scaling up the active testing area to 7.07 mm2, a considerable output power density of 1.64 W m−2 is still attained. This work provides a promising green membrane material for advancing the commercialization of osmotic energy technology.
渗透能作为一种从海水和河水之间的盐度梯度中提取的清洁可再生能源,在缓解全球能源短缺方面具有巨大潜力。然而,高离子选择性和高离子通量的高性能纳米流控膜的开发仍然是其实际应用的关键瓶颈。在此,我们报道了一种由三维(3D)纳米通道构建的磺化纤维素纳米纤维(SCNF)膜,具有高电荷密度和孔隙密度(2 × 1010 cm−2)。在50倍盐度梯度下,SCNF膜的阳离子选择性高达0.977。这些优异的离子传输性能直接转化为优异的渗透能转换性能:在50倍和500倍浓度梯度下,最大功率密度分别达到14.85 W m−2和111.06 W m−2。值得注意的是,SCNF膜可在60天内稳定保持其功率密度,表现出卓越的长期运行耐久性。当与真实河水混合时,膜的最大输出功率密度可达16.37 W m−2;即使将有效测试区域扩大到7.07 mm2,仍然可以获得1.64 W m−2的可观输出功率密度。本研究为推进渗透能技术的商业化提供了一种有前景的绿色膜材料。
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引用次数: 0
Two-dimensional nanomaterials in membrane-based water purification: Advances, challenges, and future perspectives 二维纳米材料在膜基水净化中的应用:进展、挑战和未来展望
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-02-01 DOI: 10.1016/j.desal.2026.119935
Masoud Rahbari-Sisakht , Ahmad Fauzi Ismail , Pei Sean Goh , Mohd Sohaimi Abdullah , Yanuardi Raharjo
Global shortages of safe water continue to push research beyond standard purification practices, especially where energy use and removal efficiency matter. Membrane separation is widely used. Still, common polymer membranes face clear limits, including the permeability–selectivity trade-off, fouling, and gradual loss of performance during long operation. Two-dimensional nanomaterials are being studied as alternative membrane components because their sheets are only atoms thick, their lateral size is large, and their surface chemistry can be adjusted. These traits change how water and ions move across a membrane. This review examines recent progress in water purification membranes that incorporate 2D materials such as graphene oxide, MXenes, transition metal dichalcogenides like MoS₂, hexagonal boron nitride, and layered double hydroxides. Attention is given to transport mechanisms that control separation behavior. These include diffusion through slit-like channels between stacked layers, control of interlayer spacing, transport through engineered nanopores, steric size exclusion, electrostatic interactions at charged surfaces, and Donnan-type exclusion effects. Fabrication routes are discussed in detail, with focus on mixed-matrix membranes, thin-film nanocomposites, and laminated multilayer structures, alongside their links to flux, rejection, scalability, and stability during operation. Performance comparisons with commercial membranes are presented to show where 2D-based systems outperform existing materials and where problems remain, especially regarding fouling resistance, mechanical strength, and long-term durability. Key barriers to practical deployment are identified. These include swelling in aqueous environments, loss of structural order, difficulty controlling defects, and reduced selectivity in complex water compositions. The discussion closes by outlining research directions aimed at improving reliability and translating laboratory results into workable membrane technologies for water purification.
全球安全用水短缺继续推动标准净化实践之外的研究,特别是在能源使用和去除效率很重要的地方。膜分离应用广泛。尽管如此,普通聚合物膜仍然面临着明显的限制,包括渗透率与选择性的权衡、结垢以及在长期使用过程中性能的逐渐丧失。二维纳米材料正被研究作为替代膜组件,因为它们的薄片只有原子厚,它们的横向尺寸很大,而且它们的表面化学性质可以调整。这些特性改变了水和离子在膜上的移动方式。本文综述了水净化膜的最新进展,包括二维材料,如氧化石墨烯、MXenes、过渡金属二硫族化合物,如MoS 2、六方氮化硼和层状双氢氧化物。关注控制分离行为的传输机制。这些包括通过堆叠层之间的裂隙状通道扩散、层间间距控制、通过工程纳米孔传输、空间尺寸排斥、带电表面的静电相互作用以及donnan型排斥效应。详细讨论了制造路线,重点是混合基质膜、薄膜纳米复合材料和层压多层结构,以及它们在运行过程中与通量、排斥、可扩展性和稳定性的联系。通过与商业膜的性能比较,可以看出基于2d的系统在哪些方面优于现有材料,以及存在的问题,特别是在抗污性、机械强度和长期耐用性方面。确定了实际部署的主要障碍。这些问题包括在水环境中膨胀,结构秩序的丧失,难以控制缺陷,以及在复杂的水成分中选择性降低。讨论结束时概述了旨在提高可靠性和将实验室结果转化为可行的水净化膜技术的研究方向。
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引用次数: 0
High-vacuum multi-effect desalination system with barometric ejector-condensation for simultaneous water and cooling production 高真空多效海水淡化系统,带气压喷射器-冷凝,同时进行水和冷却生产
IF 9.8 1区 工程技术 Q1 ENGINEERING, CHEMICAL Pub Date : 2026-05-01 Epub Date: 2026-01-29 DOI: 10.1016/j.desal.2026.119908
C.A. Casares-De la Torre , N. Velázquez-Limón , R. López-Zavala , J. Ríos-Arriola , G.E. Dévora-Isiordia , S. Islas-Pereda , J.A. Aguilar-Jiménez
This paper evaluates the technical feasibility of a desalination system for the simultaneous production of water and cooling, developed from a novel high-vacuum multi-effect distillation (MED-HV) system (28.3–0.8 kPa). The innovation lies in leveraging the operating conditions to use the product water directly as a refrigerant. The system integrates a barometric ejector-condenser and a three-way valve that regulates the product water flow to an evaporator, allowing the cooling capacity to be adjusted according to demand. The study was conducted in Aspen Plus and validated with experimental results reported in the literature. The MED-HV system achieves a water production of 96.03 m3/d and a cooling capacity of 700 TR (2460 kW). The effect of cooling capacity variation on the ejector-condenser performance and the system's global indicators was analyzed. Compared to commercial desalination and cooling technologies operating in a hybrid manner, the proposed system achieves a Global Coefficient of Performance (COPG) of 9.22 —20.73% higher— and accomplishes a 17.15% reduction in global specific energy consumption, for both desalination (SECG_D: 127.15 kWh/m3) and cooling (SECG_C: 0.73 kWh/TR). These results confirm the potential of the proposed system to efficiently and simultaneously meet water and space conditioning needs.
本文评估了在新型高真空多效蒸馏(MED-HV)系统(28.3-0.8 kPa)基础上开发的同时生产水和冷却的海水淡化系统的技术可行性。创新之处在于利用操作条件将产品水直接用作制冷剂。该系统集成了一个气压喷射器-冷凝器和一个三通阀,该三通阀调节产品水流向蒸发器,允许根据需求调整冷却能力。该研究在Aspen Plus中进行,并通过文献中报道的实验结果进行验证。MED-HV系统的产水量为96.03 m3/d,制冷量为700 TR (2460 kW)。分析了制冷量变化对喷射-凝汽器性能和系统整体指标的影响。与以混合方式运行的商业海水淡化和冷却技术相比,所提出的系统实现了9.22 - 20.73%的全球性能系数(COPG),并实现了17.15%的全球比能耗降低,海水淡化(SECG_D: 127.15 kWh/m3)和冷却(SECG_C: 0.73 kWh/TR)。这些结果证实了所提出的系统的潜力,有效地同时满足水和空间调节需求。
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Desalination
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