Membrane Structure Research Articles

Effects of FMWCNT inclusions on PVDF/FMWCNT membranes structure and characteristics

Effects of FMWCNT inclusions on PVDF/FMWCNT membranes structure and characteristics

Histomorphological and Histochemical Study of Esophagus and Stomach in Adult Guinea Pigs (Cavia porcellus)

This study was performed to examine and compare the esophagus and stomach histomorphological and histochemical characteristics during adulthood to clarify micromorphological alterations. In addition to the importance of this animal species as a model in many scientific experiments and due to some of its unique anatomical and physiological features. It also supports further studies on vital processes of the digestive system, such as food processing and absorption. To conduct such a project, ten heathy adult guinea pigs at 2 months age and weighing 461.8±8.3g were gathered from the public spinning market. The animals were euthanized and dissected, then the organs were topographically investigated in situ, and samples were collected from the ten animals and was kept in 10% neutral buffered formalin for routine histological procedures. The esophagus is a musculo – membranous tube structure extended from the pharynx to the stomach, measured about 10.54±0.14 cm in length and 0.35±0.01 g in weight, and segmented according to its position in the body into three sections: the cervical, thoracic, and abdominal. The stomach is a simple unilocular transverse grayish white sac-like structure of the digestive system; it connects the esophagus to the intestine; its mean length was 4.39±0.11 cm; its capacity was 17.01±0.22 ml; and its weight was 7.07±0.05 gm. It lacks an outward demarcation-limiting ridge between its divisions and appears relatively smooth. Histologically, the esophagus is devoid of glands, while the stomach's three interior sections are dotted with glands, and both organs consist of the same four basic histological layers.

Predictive modeling of pH on the transport of Co(II) Ions from aqueous solutions through supported ceramic polymer membrane

Optimal pH is essential for efficient cobalt extraction from polymeric membrane systems, with D2EHPA used as an extractant for Co(II) at pH < 7, achieving 47% efficiency. The pH of piperazine as a stripping agent increases to a concentration of 0.48 M, and the extraction efficiency of Co(II) > 80%. Depending on the functional group of (C4H10N2), the optimal pH for separation was 9.8. The study revealed that pKa value was calculated to predict the ideal pH, and its value was 9.73, which is nearly to the pH, since the pH of the strip concentration and the properties of the membrane affect the extraction of cobalt at 30 °C. The partition ratio indicates the high distribution of the extract in supported ceramic polymer membrane (SCPM). The ceramic component provides mechanical strength and rigidity to the overall membrane structure, allowing it to withstand high pressures and temperatures during operation Study various factors such as the effect of pH on the ionization of the extract; effect of pH on band ionization; effect of pH on the temperature in the extract, effect of pH on the solute, effect of the band at different pH ranges and a comparison was made between the predictive model and experimental data that was proven through mathematical modeling using the MATLAB program.

Knockdown of motility-related genes of Komagataeibacter xylinus and its effect on bacterial cellulose synthesis

Bacterial cellulose (BC) is a biopolymer synthesized by bacteria, which possess excellent characteristics such as high water holding capacity, high crystallinity, and high purity. It is widely used in food, medical, cosmetics, and functional films. Komagataeibacter xylinus is a model strain used in BC synthesis research. In bacteria, motility-related genes are associated with BC synthesis, whereas in Komagataeibacter xylinus CGMCC 2955, the functions of motility-related genes and their effects on BC synthesis are not known. To address this gap, we used the λ Red recombinant system to individually knock out motA, motB, and mot2A respectively, and constructed the knockout strains K. x-ΔmotA, K. x-ΔmotB, and K. x-Δmot2A. Additionally, both motA and motB were disrupted to construct the K. x-ΔmotAB mutant. The results demonstrated that knockout strain K. x-ΔmotAB exhibited the highest BC yield, reaching (5.05±0.26) g/L, which represented an increase of approximately 24% compared to wild-type strains. Furthermore, the BC synthesized by this strain exhibited the lowest porosity, 54.35%, and displayed superior mechanical properties with a Young's modulus of up to 5.21 GPa. As knocking out motA and motB genes in K. xylinus CGMCC 2955 did not reduce BC yield; instead, it promoted BC synthesis. Consequently, this research further deepened our understanding of the relationship between motility and BC synthesis in acetic acid bacteria. The knockouts of motA and motB genes resulted in reduced BC porosity and improved mechanical properties, provides a reference for BC synthesis and membrane structure regulation modification.

Impact of end groups of small molecules grafted to reverse osmosis membranes on their separation and antifouling performance

In this study, surface hydroxylation and methoxylation were employed to fabricate polyamide (PA) reverse osmosis (RO) membranes with enhanced permeability and antifouling performance. Diethanolamine (DEA) and bis(2-methoxyethyl) amine (BMEA) were grafted onto PA of RO membranes, and the impact of their end groups of hydroxyls and methoxyls on PAs were investigated. Benefiting from the increased surface hydrophilicity (particularly for the DEA-grafted RO) and the tailored cross-linking structure of PA layers, both DEA- and BMEA-grafted membranes showed high water permeance (1.58-fold than the pristine RO membrane) with highly competitive NaCl rejection of 99 %. The DEA-grafted membrane exhibited the enhanced antifouling performance against both positively and negatively charged foulants, while the BMEA-grafted membrane exhibited exceptional performance against small cationic foulants. Quantum chemistry simulations reveal that hydroxyl groups grafted on PA possess a relatively low binding energy with both positively and negatively charged small foulants, whereas methoxyl groups grafted on PA exhibited an exceptionally low binding energy with positively charged small foulants, which rendered them less likely to be adsorbed onto the corresponding grafted PA and to form a loose cake layer. Our study provides new insights into design of small molecules with different end groups used for the simple and effective modification of antifouling RO membranes.

Influence and mechanism of typical transition metal ions on the denitrification performance of heterotrophic nitrification-aerobic denitrification bacteria

To investigate the inhibitory effects of various transition metal ions on nitrogen removal and their underlying mechanisms, the single and combined effects of Cu2+ Ni2+ and Zn2+ on Heterotrophic nitrification-aerobic denitrification (HN-AD) bacteria Acinetobacter sp. TAC-1 were studied in a batch experiment system. The results revealed that increasing concentrations of Cu2+ and Ni2+ had a detrimental effect on the removal of ammonium nitrogen (NH4+-N) and total nitrogen (TN). Specifically, Cu2+ concentration of 10 mg/L, the TN degradation rate was 55.09%, compared to 77.60% in the control group. Cu2+ exhibited a pronounced inhibitory effect. In contrast, Zn2+ showed no apparent inhibitory effect on NH4+-N removal and even enhanced TN removal at lower concentrations. However, when the mixed ion concentration of Zn2++Ni2+ exceeded 5 mg/L, the removal rates of NH4+-N and TN were significantly reduced. Moreover, transition metal ions did not significantly impact the removal rates of chemical oxygen demand (COD). The inhibition model fitting results indicated that the inhibition sequence was Cu2+ > Zn2+ > Ni2+. Transcriptome analysis demonstrated that metal ions influence TAC-1 activity by modulating the expression of pivotal genes, including zinc ABC transporter substrate binding protein (znuA), ribosomal protein (rpsM), and chromosome replication initiation protein (dnaA) and DNA replication of TAC-1 under metal ion stress, leading to disruptions in transcription, translation, and cell membrane structure. Finally, a conceptual model was proposed by us to summarize the inhibition mechanism and possible response strategies of TAC-1 bacteria under metal ion stress, and to address the lack of understanding regarding the influence mechanism of TAC-1 on nitrogen removal in wastewater co-polluted by metal and ammonia nitrogen. The results provided practical guidance for the management of transition metal and ammonia nitrogen co-polluted water bodies, as well as the removal of high nitrogen.

How to understand the effect of relative humidity on the morphology and performance of polypiperazine-amide NF membrane during heat curing process

Recent studies have shown that the temperature and time of the heat curing process have important effects on the nanofiltration (NF) membrane structure and properties. However, the mechanism of the relative humidity (RH), as one of the important factors in the heat curing of NF membranes, is still unclear. To analyze the specific effect of RH, we compared the heat curing results of the NF polyamide (PA) membranes fabricated with different monomer concentrations at various RH. The nanofiltration performance of the membranes appeared to be non-uniform when the RH was in the range of 40 %–60 %. Within the appropriate RH range, the rejection of Na2SO4 was preserved at about 98.5 % for the manufactured NF membranes. At high concentrations, the increasing RH created a discontinuous condensate layer on the PA layer surface, which affected the morphology and physicochemical properties of the NF membrane causing a doubling of pure water permeability (PWP) to 8.33 L m−2 h−1·bar−1. At low concentrations, the PA layer was not significantly changed with the increase of RH, but the evaporation of water from the smaller capillary pores in its PES substrate was slowed down, which reduced the capillary stress on the substrate and prevented the collapse of the substrate pore size, resulting in a nearly 20 times increase in its PWP to 39.7 L m−2 h−1·bar−1. This work reveals the effect of RH during heat curing and gives significant guidance to the design and synthesis of high-performance NF membranes.

The life cycle assessment of temporary reusable membrane structures: Case study analysis

Membrane structures represent lightweight spatial structures composed of a primary framework combined with tensioned membranes. Their popularity has increased due to their lightweight, flexible, and durable characteristics. However, as all constructions, their production and use come with an environmental impact. This study aims to assess the life cycle assessment of membrane structures with temporary use, specially focusing on the Global Warming Potential, a well-recognised indicator of greenhouse gas emissions.Using Life Cycle Assessment methodology, this research evaluates the environmental impact of membrane structures from raw material extraction to disposal. The investigation concentrates on temporary membrane structures installed multiple times across different locations within a 25-year lifespan. Two case studies, Nomad ADD-ON rental sails and Wolke Marienfeld, are analysed. The LCA of a temporary structure involves three distinct LCAs: one for the initial installation, one for each intermediate installation, and a final assessment for the end installation.Results indicate that temporary reusable membrane structures demonstrate a significant environmental impact, primarily due to the high energy consumption during manufacturing and transportation. It is essential to consider the effects of the ‘End-of-Life’ stages and the ‘benefits and loads beyond the system boundaries’ stage, particularly for temporary structures.This research aims to raise awareness about the environmental impact of temporary membrane structures and offers a framework for sustainable design and construction methods. Additionally, it explores potential strategies to reduce the environmental impact including thoughtful material choices, innovative construction practices and effective End-of-Life management.

Highly efficient and selective nitrate and Hg(II) removal from wet oxidation flue gas purification wastewater using bifunctional MXene nanofiltration membrane

The wet oxidation process is a promising method for simultaneously removing SO2, NO, and Hg0 from coal-fired flue gas. However, the resource utilization of the resulting wastewater, which is enriched with complex ions such as Hg2+, NH4+, NO3−, and SO42−, remains a significant challenge. To achieve the simultaneous goals of concentrating NH4+/NO3−/SO42− ions, adsorbing and separating Hg2+ ions, and reusing wastewater, a bifunctional MXene composite nanofiltration membrane with large interlayer spacing and excellent electrostatic repulsion was developed. The membrane was prepared by co-depositing MXene nanosheets, carboxylated multi-walled carbon nanotubes (MWCNTs), and sodium dodecyl sulfate (SDS) onto an NF-90 membrane. The resulting MXene-MWCNTs-SDS (MMS-COOH) composite membrane demonstrated exceptional salt rejection of 84.4 % for NO3−, 89.0 % for NH4+, 99.8 % for SO42−, and 99.7 % for Hg2+. After 30 cycles, the membrane structure remained stable, maintaining good reusability, with NH4+ and SO42− rejection still reaching 90.0 %. Moreover, the maximum adsorption capacity for Hg2+ was 2869.6 mg g−1, while the capacities for Cr6+ and Pb2+ were 577.6 and 316.8 mg g−1, respectively. The MMS-COOH composite membrane introduces an innovative method for the benign treatment of wet oxidation flue gas purification wastewater and facilitates the recovery of (NH4)2SO4 and NH4NO3 as fertilizers, holding a promising application prospect.

Design an in-situ anti-bacterial structure of nanofiltration membrane with a novel bisimidazoline aqueous monomer

Bio-fouling is a key issue for the nanofiltration operation. In this study, 1, 2-bis (N-aminoethyl imidazoline) ethane (BAIE) firstly was used as a novel bisimidazoline aqueous monomer to prepare the anti-bacterial nanofiltration (NF) membranes. A novel nanofiltration (BAIE-TMC NF) membrane with in-situ anti-bacterial structure and anti-fouling property was fabricated via interfacial polymerization (IP) with trimesoyl chloride (TMC), basing on a polyethersulfone (PES) substrate. Protonated imidazole endowed the surface of BAIE-TMC NF membrane with weak electronegativity, and its salt rejection sequence was MgSO4 > Na2SO4 > MgCl2 > NaCl > LiCl. Meantime, the BAIE-TMC NF membrane with 0.5 wt% BAIE (M-0.5) exhibited a high rejection for bivalent ions, with a high MgSO4 rejection (94.7 %). Notably, BAIE-TMC NF membrane containing an in-situ anti-bacterial imidazole structure showed significant anti-fouling and anti-bacterial properties. After BSA or HA filtration process, the flux recovery rates of all BAIE-TMC NF membranes were higher than 95 %, and M-0.5 exhibited high inhibition performance against Escherichia coli (98.5 %) and Staphylococcus aureus (98.4 %). Furthermore, M-0.5 exhibited excellent long-term separation stability during the three weeks separation experiment. BAIE can serve as an effective aqueous monomer for fabricating in-situ anti-bacterial and anti-fouling NF membrane to achieve the rejection of organic pollutant and bivalent ions.

Cell-Impermeable Buffering Fluorogenic Probes for Live-Cell Super-Resolution Imaging of Plasma Membrane Morphology Dynamics.

Super-resolution fluorescence imaging has emerged as a potent tool for investigating the nanoscale structure and function of the plasma membrane (PM). Nevertheless, the challenge persists in achieving super-resolution imaging of PM dynamics due to limitations in probe photostability and issues with cell internalization staining. Herein, we report assembly-mediated buffering fluorogenic probes BMP-14 and BMP-16 exhibiting fast PM labeling and extended retention time (over 2 h) on PM. The incorporation of alkyl chains proves effective in promoting the aggregation of BMP-14 and BMP-16 into nonfluorescent nanoparticles to realize fluorogenicity and regulate the buffering capacity to rapidly replace photobleached probes ensuring stable long-term super-resolution imaging of PM. Utilizing these PM-buffering probes, we observed dynamic movements of PM filopodia and continuous shrinkage, leading to the formation of extracellular vesicles (EVs) using structured illumination microscopy (SIM). Furthermore, we discovered two distinct modes of EV fusion: one involving fusion through adjacent lipids and the other through filamentous lipid traction. The entire process of EV fusion outside the PM was dynamically tracked. Additionally, BMP-16 exhibited a unique capability of inducing single-molecule fluorescence blinking when used for cell membrane staining. This property makes BMP-16 suitable for the PAINT imaging of cell membranes.

Structure and positive charge regulation in nanofiltration membrane by novel nanomaterial g-C3N5 for efficient Li+/Mg2+ separation

The positively charged nanofiltration (NF) membrane prepared via interfacial polymerization (IP) of polyethyleneimine (PEI) and trimesoyl chloride (TMC) has drawn considerable attention for lithium-magnesium separation, particularly crucial for lithium recovery from salt lakes with high Mg2+/Li+ mass ratios. However, NF membranes prepared solely from amine monomers have not achieved efficient Li+ and Mg2+ separation. In this study, PEI-g-C3N5/TMC composite NF membranes were successfully fabricated by mixing amino-rich graphitic carbon nitride (g-C3N5) with PEI, followed by the IP reaction of the mixed solution with TMC. Molecular dynamics (MD) simulation results showed that g-C3N5 had an attractive effect on PEI, which led to a decrease in the diffusion rate of PEI, thereby resulting in a thinner separation layer. Density functional theory (DFT) revealed that g-C3N5 competed with PEI, leading to a reduction in the crosslinking within the polyamide (PA) layer and subsequently causing an increase in the surface pore size of the membrane. Besides, the hydrophilicity and positive charge of the modified membrane were both improved. MD simulations, transition state theory, and DLVO principles indicated that the modification of the PA layer by g-C3N5 enhanced the repulsion of Mg2+ and the transport of Li+ during the NF process. This breakthrough effectively overcame the trade-off effect between membrane separation and permeability, especially at a g-C3N5 content of 0.06 wt%, where the lithium-magnesium selectivity coefficient (SLi, Mg = 18.18) and pure water flux (Flux = 58.59 L m−2 h−1) reached the optimum values. Meanwhile, the PEI-g-C3N5/TMC membrane demonstrated stable separation performance during prolonged filtration and in solutions with varying Mg2+/Li+ mass ratios. This study not only provides an effective strategy for the design of NF membranes but also expands the application prospects of nanomaterials in the field of membrane separation.

Self-Healing Conductive Hydrogels with Dynamic Dual Network Structure Accelerate Infected Wound Healing via Photothermal Antimicrobial and Regulating Inflammatory Response.

Wound infections are an escalating clinical challenge with continuous inflammatory response and the threat of drug-resistant bacteria. Herein, a series of self-healing conductive hydrogels were designed based on carboxymethyl chitosan/oxidized sodium alginate/polymerized gallic acid/Fe3+ (CMC/OSA/pGA/Fe3+, COGFe) for promoting infected wound healing. The Schiff base and catechol-Fe3+ chelation in the dynamical dual network structure of the hydrogels endowed dressings with good toughness, conductivity, adhesion, and self-healing properties, thus flexibly adapting to the deformation of skin wounds. In terms of ultraviolet (UV) resistance and scavenging of reactive oxygen species (ROS), the hydrogels significantly reduced oxidative stress at the wound site. Additionally, the hydrogels with photothermal therapy (PTT) achieved a 95% bactericidal rate in 5 min of near-infrared (NIR) light radiation by disrupting the bacterial cell membrane structure through elevated temperature. Meanwhile, the inherent antimicrobial properties of GA could reduce healthy tissue damage caused by excessive heat. The composite hydrogels could effectively promote the proliferation and migration of fibroblasts and possess good biocompatibility and hemostatic effect. In full-thickness infected wound repair experiments in rats, the COGFe5 hydrogel combined with NIR effectively killed bacteria, modulated macrophage polarization (M1 to M2 phenotype) to improve the immune microenvironment of the wound, and shortened the repair time by accelerating the expression of collagen deposition (TGF-β) and vascular factors (CD31). This combined therapy might provide a prospective strategy for infectious wound treatment.

Fluid energy theory of membrane

Membrane science is the key strategy to solve water shortage in the future, and its essence is energy and mass transfer. Due to the complexity and variety of the internal structure of membrane, the energy transfer theory of membrane is still a black box theory. Herein, a new fluid mechanics principle is introduced to establish the energy fluid theory of membrane, which is translated into the energy formula: such as the initial total pressure difference (ΔP), the flow rate of fluid exiting the membrane (v1 and v2), fluid density (ρ), and energy consumption by salt resistance (NSR): {ΔP2ΔPρ=ΔP2ΔPρ[1−v1ρ2ΔP]+NSR+[ΔPv1(v2v1)2−12ρv23]+12ρv23}. The theoretical framework is not only helpful for the data analysis of the energy transfer process of membranes, but also helps to allow for more in-depth and specific theoretical research. For instance, the relationship between NSR and the concentration difference (C) of salt can be expressed as NSR = aCb (a-product constant, b-exponential constant, R2>0.99). Hence, the basic theory can not only be widely applied to a variety of membranes with complex internal structure, but also have a profound impact on the application and research of membrane science.

Mechanisms of Triton X-100 reducing the Ag+-resistance of Enterococcus faecalis.

To investigate the mechanism of Triton X-100 (TX-100) reducing the Ag+-resistance of Enterococcus faecalis (E. faecalis), and evaluate the antibacterial effect of TX-100+Ag+ against the induced Ag+-resistant E. faecalis (AREf). The minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) of AgNO3 against E. faecalis with/without TX-100 were determined to verify the enhanced antibacterial activity. Transmission electron microscopy (TEM) was used to observe the morphological changes of E. faecalis after treatment. The intra- and extracellular concentration of Ag+ in treated E. faecalis was evaluated using inductively coupled plasma mass spectrometer (ICP-MS). The changes in cell membrane potential and integrity of treated E. faecalis were also observed using the flow cytometer. Moreover, AREf was induced through continuous exposure to sub-MIC of Ag+ and the antibacterial effect of TX-100+Ag+ on AREf was further evaluated. The addition of 0.04% TX-100 showed maximal enhanced antibacterial effect of Ag+ against E. faecalis. The TEM and ICP-MS results demonstrated that TX-100 could facilitate Ag+ to enter E. faecalis through changing the membrane structure and integrity. Flow cytometry further showed the effect of TX-100 on membrane potential and permeability of E. faecalis. In addition, the enhanced antibacterial effect of TX-100+Ag+ was also confirmed on induced AREf. TX-100 can facilitate Ag+ to enter E. faecalis through disrupting the membrane structure and changing the membrane potential and permeability, thus reducing the Ag+-resistance of E. faecalis and enhancing the antibacterial effect against either normal E. faecalis or induced AREf.

X-ray scatterings to probe the structure and assembly of biomimetic membranes

X-ray scatterings to probe the structure and assembly of biomimetic membranes

Plant Flavonoids with Antimicrobial Activity against Methicillin-Resistant Staphylococcus aureus (MRSA).

Methicillin-resistant Staphylococcus aureus (MRSA) has become a serious threat to human public health and global economic development, and there is an urgent need to develop new antimicrobial agents. Flavonoids are the largest group of plant secondary metabolites, and the anti-S. aureus and anti-MRSA activities of flavonoids have now been widely reported. The aim of this Review is to describe plant-derived flavonoid active ingredients and their effects and mechanisms of inhibitory activity against MRSA in order to provide insights for screening novel antimicrobial agents. Here, 85 plant-derived flavonoids (14 flavones, 21 flavonols, 26 flavanones, 9 isoflavones, 12 chalcones, and 3 other classes) with anti-MRSA activity are reviewed. Among these flavonoids, flavones and isoflavones generally showed the most significant anti-MRSA activity (MICs: 1-8 μg/mL). The results of the present Review display that most of the flavonoids with excellent anti-MRSA activity were derived from Morus alba L. and Paulownia tomentosa (Thunb.) Steud. The antibacterial mechanism of flavonoids against MRSA is mainly achieved by disruption of membrane structures, inhibition of efflux pumps, and inhibition of β-lactamases and bacterial virulence factors. We hope this Review can provide insights into the development of novel antimicrobials based on natural products for treating MRSA infections.

Study on pervaporation performance of hydrophobically modified carbon-based membrane materials

Abstract Based on the appropriate pore size, the surface of the carbon membrane was hydrophobically modified to preferentially adsorb alcohols, so as to achieve the purpose of enriching alcohols in the penetrant. This operation is significant for expanding the application of carbon membranes for gas separation. In this work, a hydrophobic silica sol was synthesized using tetraethyl orthosilicate (TEOS) and methyltriethoxysilane (MTES) as mixed silicon sources, and it was impregnated and coated on a rolled carbon membrane. The material was then dried and thermally treated to obtain the hydrophobic carbon membrane. The preparation procedure of silica sol was also investigated, and the surface chemical structure and morphology of the hydrophobic carbon membrane were characterized by contact angle (CA), Fourier Transform infrared spectroscopy (FTIR), and scanning electron microscope (SEM). The pervaporation performance of the hydrophobic carbon membrane was inspected with both ethanol/water and isopropanol/water mixed solution. The results showed that the hydrophobic carbon membrane has favorable pervaporation performance. With the elevation of temperature, the total flux significantly increased while the selectivity slightly decreased. The increase of alcohol (ethanol and isopropanol) content also enhanced total flux, but the selectivity reduced prominently. The phenomena indicated that a relatively ideal effect had been achieved.

Laminated graphene oxide and hydrotalcite membranes via alternating spray-deposition with stable desalting performance

Laminated graphene oxide (GO) membrane has great potential for desalination, but achieving good stability in salt retention and water permeation is still a challenge. The “compact” sieving structure and the “loose” permeating structure of the GO membranes offer synergetic effects for high-performance desalination. Here, a composite desalination membrane involving two two-dimensional layered nanomaterials with opposite charges has been reported. The multi-layered GO (MLGO) and hydrotalcite (HT) were then alternated in a spray-coating on a PDA-modified substrate to construct multiple structures. Different assembly regions were identified by in-situ morphology monitoring, which showed that MLGO and HT were connected by electrostatic attractions. Also, the composite membrane showed high salt retention, permeability and long-term performance stability. The water flux of the composite membrane increased from 2.8 L m−2 h−1 bar−1 to 3.6–5.2 L m−2 h−1, which was due to the increases in the interlayer spacing distances and the introduction of new permeable spaces. After a 400 h continuous filtration test, the Na2SO4 retention remained stable. The water fluxes were in the range of 2.0–3.0 L m−2 h−1 bar−1, which corresponded to an increase by 42.9 %–114.3 % in comparison with the pure MLGO membrane. As compared with the MLGO membrane, molecular dynamics (MD) simulations revealed that more water molecules passed through the MLGO-HT membrane with a shorter pathway length and higher speed than MLGO membrane. The present study demonstrated the potential of a composite with 2D materials for desalination applications.

Zr-BTB nanosheets assist in optimizing the structure of forward osmosis membranes to enhance the lithium concentration performance

Recently, low-energy forward osmosis (FO) technology has been employed in the lithium concentration stage during the extraction of lithium from brine sources. The interlayer FO membrane is renowned for its exceptional structural characteristics; however, challenges remain in selecting suitable interlayer materials and exploring their control mechanisms on amine monomers. As interlayer materials, traditional 3D nanomaterials are prone to detachment, while traditional 2D materials without micropores can increase the transmission resistance of water molecules. This study introduces a novel FO membrane utilizing Zr-BTB nanosheets with 5.4 Å micropores as the interlayer material. Based on detection and simulation calculations, it was found that the increase in steric hindrance and interaction forces jointly slowed the diffusion of amine monomers in the presence of the Zr-BTB interlayer. This results in a thinner separation layer, facilitating water transport. The interlayer also plays crucial roles in preventing defective pore formation in the separation layer and assisting in intercepting salt ions. The Zr-BTB interlayer membrane exhibited a water flux of 29.14 L m−2 h−1 and a reverse salt flux of 0.16 g m−2 h−1, which are superior to those of many FO membranes reported in the field. The prepared membrane also has excellent performance in lithium concentration applications, and its separation mechanism was explored by MD simulations.