Membrane System Research Articles

Chemical modification of Pinus walliichiana sawdust: Application in membrane system for efficient purification of groundwater containing Cd(II) and Ni(II)

In the Sargodha region of Pakistan, the concentrations of Cd(II) and Ni(II) ions are very high as compared to WHO and US EPA standards and may be one of the leading reasons for water-borne diseases in the population of this area. In the current research work, an eco-friendly, low-cost, effective, and reusable filter membrane system is developed. The cellulose sawdust of Pinus walliichiana (PWC) was treated with succinic anhydride to form Pinus walliichiana cellulose succinate (PWCS) and finally converted to sodic form (PWCS-Na) by treating with saturated sodium bicarbonate. The PWCS and PWCS-Na as obtained were characterized using FTIR, pHZPC, SEM, PXRD, and Brunauer–Emmett–Teller (BET) analysis. The BET surface area of the PWCS-Na was found to be 579.5 m2/g. Maximum sorption capacity values in the batch study for Cd(II) (235.2 ± 10.3 mg g−1) and Ni(II) (195.6 ± 15.2 mg g−1) were observed at 298 K, pH 6, sorbent dosage of 30 mg, and metal ion concentration of 70 mg/L. The filter membrane system was designed and employed for the purification of the flowing water system. Theoretical calculations show that 1 L of filter membrane containing 138.0 g of the adsorbent PWCS-Na can purify 532.8 L solution with Cd(II) concentration 70 mg/L and 278.2 L solution of Ni(II) with concentration 70 mg/L. The regeneration study proved the efficient reusability of sorbent after five cycles with a slight change in sorption capacity.

Programmable Lipid Bilayer Tension-Control Apparatus for Quantitative Mechanobiology.

The biological membrane is not just a platform for information processing but also a field of mechanics. The lipid bilayer that constitutes the membrane is an elastic body, generating stress upon deformation, while the membrane protein embedded therein deforms the bilayer through structural changes. Among membrane-protein interplays, various channel species act as tension-current converters for signal transduction, serving as elementary processes in mechanobiology. However, in situ studies in chaotically complex cell membranes are challenging, and characterizing the tension dependency of mechanosensitive channels remains semiquantitative owing to technical limitations. Here, we developed a programmable membrane tension-control apparatus on a lipid bilayer system. This synthetic membrane system [contact bubble bilayer (CBB)] uses pressure to drive bilayer tension changes via the Young-Laplace principle, whereas absolute bilayer tension is monitored in real-time through image analysis of the bubble geometry via the Young principle. Consequently, the mechanical nature of the system permits the implementation of closed-loop feedback control of bilayer tension (tension-clamp CBB), maintaining a constant tension for minutes and allowing stepwise tension changes within a hundred milliseconds in the tension range of 0.8 to 15 mN·m-1. We verified the system performance by examining the single-channel behavior of tension-dependent KcsA and TREK-1 potassium channels under scheduled tension time courses prescribed via visual interfaces. The result revealed steady-state activity and dynamic responses to the step tension changes, which are essential to the biophysical characterization of the channels. The apparatus explores a frontier for quantitative mechanobiology studies and promotes the development of a tension-operating experimental robot.

A tuneable minimal cell membrane reveals that two lipid species suffice for life.

All cells are encapsulated by a lipid membrane which facilitates the interaction between life and its environment. How life exploits the diverse mixtures of lipids that dictate membrane property and function has been experimentally challenging to address. We introduce an approach to tune and minimize lipidomes in Mycoplasma mycoides and the Minimal Cell (JCVI-Syn3A) revealing that a 2-component lipidome can support life. Systematically reintroducing phospholipid features demonstrated that acyl chain diversity is more critical for growth than head group diversity. By tuning lipid chirality, we explored the lipid divide between Archaea and the rest of life, showing that ancestral lipidomes could have been heterochiral. Our approach offers a tunable minimal membrane system to explore the fundamental lipidomic requirements for life, thereby extending the concept of minimal life from the genome to the lipidome.

Characterization of genome-wide phylogenetic conflict uncovers evolutionary modes of carnivorous fungi.

Mass extinction has often paved the way for rapid evolutionary radiation, resulting in the emergence of diverse taxa within specific lineages. The emergence and diversification of carnivorous nematode-trapping fungi (NTF) in Ascomycota have been linked to the Permian-Triassic (PT) extinction, but the processes underlying NTF radiation remain unclear. We conducted phylogenomic analyses using 23 genomes that represent three NTF lineages, each employing distinct nematode traps-mechanical traps (Drechslerella spp.), three-dimensional (3D) adhesive traps (Arthrobotrys spp.), and two-dimensional (2D) adhesive traps (Dactylellina spp.), and the genome of one non-NTF species as the outgroup. These analyses revealed multiple mechanisms that likely contributed to the tempo of the NTF evolution and rapid radiation. The species tree of NTFs based on 2,944 single-copy orthologous genes suggested that Drechslerella emerged earlier than Arthrobotrys and Dactylellina. Extensive genome-wide phylogenetic discordance was observed, mainly due to incomplete lineage sorting (ILS) between lineages. Two modes of non-vertical evolution (introgression and horizontal gene transfer) also contributed to phylogenetic discordance. The ILS genes that are associated with hyphal growth and trap morphogenesis (e.g., those associated with the cell membrane system and polarized cell division) exhibited signs of positive selection.IMPORTANCEBy conducting a comprehensive phylogenomic analysis of 23 genomes across three NTF lineages, the research reveals how diverse evolutionary mechanisms, including ILS and non-vertical evolution (introgression and horizontal gene transfer), contribute to the swift diversification of NTFs. These findings highlight the complex evolutionary dynamics that drive the rapid radiation of NTFs, providing valuable insights into the processes underlying their diversity and adaptation.

Rapid polyamide membrane compatibility testing of potential anti-biofouling agents for reverse osmosis membrane systems

ABSTRACT The detrimental impacts of biofouling on reverse osmosis (RO) membrane (ROM) installations is one of the main technical barriers faced by RO technology to provide potable water. To unveil safer alternatives for biofouling prevention in ROM installations, this work assesses the ROM compatibility of three potential low-hazard anti-biofouling agents (lauroyl arginate ethyl (LAE), phenoxyethanol (PE), and sodium benzoate (SB)) via a proposed rapid membrane degradation test. This study offers a cost-effective screening tool to select biocides for extensive compatibility studies. Attenuated total reflectance – Fourier-transform infrared spectroscopy, atomic force microscopy, and scanning electron microscopy assessed ROM surface damage due to biocide exposure. LAE did not show significant morphological or chemical membrane damage at any experimental conditions (exposure time: 1, 8, and 24 h; pH: 4, 7, 9; concentration: 100 mg/L, 50 g/L, 100 g/L, and 150 g/L). However, results indicated that exposure to PE and SB led to membrane degradation. The proposed rapid membrane degradation test showed to be an excellent tool for improving current membrane compatibility testing practices. It identified two ROM-damaging biocides, SB and PE, streamlining large-scale testing efforts. Additionally, it identified a promising biocide, LAE, with the potential to address biofouling in RO systems, prompting further long-term compatibility studies.

Efficient Removal of PFASs Using Photocatalysis, Membrane Separation and Photocatalytic Membrane Reactors.

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are persistent compounds characterized by stable C-F bonds giving them high thermal and chemical stability. Numerous studies have highlighted the presence of PFASs in the environment, surface waters and animals and humans. Exposure to these chemicals has been found to cause various health effects and has necessitated the need to develop methods to remove them from the environment. To date, the use of photocatalytic degradation and membrane separation to remove PFASs from water has been widely studied; however, these methods have drawbacks hindering them from being applied at full scale, including the recovery of the photocatalyst, uneven light distribution and membrane fouling. Therefore, to overcome some of these challenges, there has been research involving the coupling of photocatalysis and membrane separation to form photocatalytic membrane reactors which facilitate in the recovery of the photocatalyst, ensuring even light distribution and mitigating fouling. This review not only highlights recent advancements in the removal of PFASs using photocatalysis and membrane separation but also provides comprehensive information on the integration of photocatalysis and membrane separation to form photocatalytic membrane reactors. It emphasizes the performance of immobilized and slurry systems in PFAS removal while also addressing the associated challenges and offering recommendations for improvement. Factors influencing the performance of these methods will be comprehensively discussed, as well as the nanomaterials used for each technology. Additionally, knowledge gaps regarding the removal of PFASs using integrated photocatalytic membrane systems will be addressed, along with a comprehensive discussion on how these technologies can be applied in real-world applications.

A single-atom manganese nanozyme mediated membrane reactor for water decontamination

Single-atom nanozymes possess high catalytic activity and selectivity, and are emerging as advanced heterogeneous catalysts for environmental applications. Herein, we present the innovative synthesis and characterization of a single-atom manganese-doped carbon nitride (SA-Mn-CN) nanozyme, integrated into a polyvinylidene fluoride (PVDF) membrane for advanced water treatment applications. The SA-Mn-CN nanozyme demonstrates high peroxidase-like activity, efficiently catalyzing the oxidation of 3,3′,5,5′-tetramethylbenzidine (TMB) and generating reactive oxygen species (ROS) for effective antibacterial action. Notably, the SA-Mn-CN/PVDF membrane showcases enhanced water permeability, superior antifouling properties, and ultra-fast degradation kinetics of organic pollutants. Mechanistic studies reveal that the nanozyme selectively generates Mn(IV)-oxo species via peroxymonosulfate (PMS) activation, crucial for the efficient oxidation processes. Our integrated membrane system effectively removes (within 1 min, > 92 % removal) a variety of organic micropollutants in continuous-flow operations, demonstrating excellent stability and minimal manganese leaching. Compared to conventional advanced oxidation process (AOPs)/membrane system, the SA-Mn-CN/PVDF/PMS system holds the advantages of high catalytic activity and selectivity for generation of reactive species, wide working pH range (pH3–11) and excellent stability and reusability under the backwashing conditions. The developed device-scale AOPs/membrane system was proven to be effective in bacterial inactivation and pollutants degradation, verifying the vast application potential of the SA-Mn-CN/PVDF membrane for practical water decontamination. This work pioneers the development of enzyme-mimicking nanozyme membranes, offering a sustainable and high-performance solution for wastewater treatment, and sets a new benchmark for the design of nanozyme-based catalytic membranes in environmental applications.

Advanced Two-Stage Nanocomposite Membrane System for Methane and Carbon Dioxide Separation from Atmospheric Air

This paper presents an advanced two-stage nanocomposite membrane system designed to efficiently separate and capture methane (CH4) and carbon dioxide (CO2) from atmospheric air and water sources. The membrane system comprises a CO2-selective primary membrane and a CH4-selective secondary membrane, utilizing a hierarchical nanomaterials and polymers structure. The proposed system demonstrates unprecedented versatility, operating effectively across an extensive range of gas concentrations (>20% to <0.02%) and reducing CH4 levels from 100-500 ppm to 5-10 ppm in both aerobic and anaerobic conditions. Performance metrics specify CO2 permeances of 200-2000 GPU and CO2/N2 selectivities of 30-500 at 57 °C and 1 atm feed pressure, surpassing the Robeson upper bound for traditional polymer membranes. The CH4-selective membrane achieves 500-2000 GPU permeances with CH4/CO2 selectivities >50. Furthermore, experimental validation over 1000 hours of continuous operation demonstrated 92% methane capture efficiency under challenging conditions (55 tons/hour methane content at 30 °C). The system's energy consumption of 0.3 kWh/kg of CH4 captured underscores its efficiency compared to traditional methods. This innovative membrane technology offers a promising solution for addressing critical ecological and industrial challenges associated with greenhouse gas emissions in the 21st century.

Techno-Economic Analysis of a Carbon Molecular Sieve-Based Xylene Isomer Purification Process.

The separation and purification of xylene isomers is critical to the production of polyethylene terephthalate (PET). These separations are complex to operate and demand tremendous amounts of energy and thus are an opportunity for reducing industrial energy consumption. Membranes provide a low-energy footprint technology with simpler operation, and recently, membrane materials have been developed that are capable of separating xylene isomers. While these materials have demonstrated the ability to separate xylenes, they have yet to be commercially deployed. This work conducts a techno-economic analysis (TEA) to provide insight on the commercial attractiveness of a p-xylene selective carbon molecular sieve (CMS) membrane from both a cost and energy standpoint. This TEA was conducted through the pairing of a Maxwell-Stefan transport framework for rigid microporous materials with process modeling. Single-stage organic solvent reverse osmosis (OSRO) and pervaporation processes were used to evaluate the effects of recovery, selectivity, and diffusivity on the energy intensity and cost of the xylene separation. The final analysis used two systems, a single pervaporation stage followed by two OSRO stages, which was compared against a three-stage OSRO cascade. These were benchmarked against the commercial Parex process. We estimate that the membrane processes have the potential to enable impressive cost savings compared to the Parex process. While both systems outperformed the Parex process in terms of cost, the pervaporation/OSRO hybrid process was able to achieve the lowest cost of all due to its reduced membrane surface area compared to standalone OSRO. These findings demonstrate the potential of membrane systems in the field of difficult small molecule solvent separations.

Morphological, structural, and ultrastructural key features of hyperhydricity in Beta vulgaris L. var. saccharifera

Abstract Hyperhydricity, as a phenomenon specific to in vitro plants, triggers a series of changes at the cell and tissue level, which modify the plants’ physiological processes. For a better understanding of this phenomenon, we found it useful to present here the fundamental research on establishing the steps of structural and ultrastructural degradation of cells and tissues, observed by light microscopy (LM) and transmission electron microscopy (TEM) analyses, in the leaves of Beta vulgaris var. saccharifera, at 30 days of secondary culture, and their correlation with viability in the third culture. Comparative with control (non-hyperhydric plants), three degradation steps of hyperhydricity were identified in plants regenerated on a culture medium with 2.5 mg·L-1 6-benzyladenine. The first step involved cell wall deformation, which lost its rigidity and became sinuous, causing the enlargement of the intercellular spaces. In the second step, these spaces formed gaps through their union, and the whole membrane system suffered: both chloroplasts and tonoplast were broken (the cytoplasm and vacuolar composition were mixed), the nuclear membrane presented undulations, just before the damage to the tonoplast, and the nucleus became pyknotic. In step 3, the cell showed the beginning of lysis, which leads to necrosis, the cell had nothing in common with a normal ultrastructure. For in vitro plants in this final step, there was no chance of surviving but in steps I and II, the viability was 55-75%. These features can be useful to producers to calculate the level of culture damage and start measures to prevent losses.

Genome-wide identification and expression analysis of SlKFB gene family (Solanum lycopersicum) and the molecular mechanism of SlKFB16 and SlKFB34 under drought

Environmental stress significantly affects plant growth and productivity. The effects of drought stress on plants are reflected primarily in enzyme activity, membrane systems, and cell-water loss. Here, the Kelch repeat F-box (KFB) protein family in tomato was systematically identified and analysed. Using bioinformatics, we identified 37 SlKFB family members in the tomato genome and analysed their protein structure, phylogenetic relationships, chromosome distribution, and expression under drought or biotic-stress conditions. Transcriptome data revealed that SlKFB members exhibit differential responses to drought stress, with significant differences in SlKFB16 and SlKFB34 expression. Functional analysis revealed that SlKFB16 functions in the cytoplasm and SlKFB34 in the nucleus and cytoplasm. Under drought stress, SlKFB16 and SlKFB34-silencing significantly reduced reactive oxygen species scavenging and resistance to drought stress. These findings provide a reference for further studies of the mechanisms of SlKFB16 and SlKFB34 in drought stress in tomato as well as a foundation for enhancing their resistance to drought stress.

Exploring the Membrane-Active Interactions of Antimicrobial Long-Chain Fatty Acids Using a Supported Lipid Bilayer Model for Gram-Positive Bacterial Membranes.

The dynamic nature of bacterial lipid membranes significantly impacts the efficacy of antimicrobial therapies. However, traditional assay methods often fall short in replicating the complexity of these membranes, necessitating innovative approaches. Herein, we successfully fabricated model bacterially supported lipid bilayers (SLBs) that closely mimic the characteristics of Gram-positive bacteria using the solvent-assisted lipid bilayer (SALB) technique. By employing a quartz crystal microbalance with dissipation and fluorescence microscopy, we investigated the interactions between these bacterial mimetic membranes and long-chain unsaturated fatty acids. Specifically, linolenic acid (LNA) and linoleic acid (LLA) demonstrated interaction behaviors correlated with the critical micelle concentration (CMC) on Gram-positive membranes, resulting in membrane remodeling and removal at concentrations above their respective CMC values. In contrast, oleic acid (OA), while showing similar membrane remodeling patterns to LNA and LLA, exhibited membrane insertion and CMC-independent activity on the Gram-positive membranes. Particularly, LNA and LLA demonstrated bactericidal effects and promoted membrane permeability and ATP leakage in the bacterial membranes. OA, characterized by a CMC-independent activity profile, exhibited potent bactericidal effects due to its robust penetration into the SLBs, also enhancing membrane permeability and ATP leakage. These findings shed light on the intricate molecular mechanisms governing the interactions between long-chain unsaturated fatty acids and bacterial membranes. Importantly, this study underscores the potential of using biologically relevant model bacterial membrane systems to develop innovative strategies for combating bacterial infections and designing effective therapeutic agents.

Computational Analysis of Permeance Prediction for Gas Separation Membrane Using Countercurrent Flow Model

Gas separation polymeric membranes have gained significant attention in various industries, including gas processing, petrochemicals, and environmental applications. Accurately predicting the permeance of these membranes is crucial for optimizing their design and performance. This paper presented a numerical prediction model for the permeance of a binary gas mixture under various process conditions, using only algebraic equations to minimize the calculation effort. The model considers input parameters such as feed and permeate flow rates, feed pressure, feed and permeate mole fraction, and membrane area. It demonstrates the behavior of permeance and selectivity in this study. The study also presented two case studies that utilize predicted selectivity to model counter-current flow and compare the results with experimental data from the literature. The first case study involves recovering helium from natural gas using an asymmetric high-flux membrane. The second case study separates air using nano-porous carbon as the membrane material. The numerical analysis successfully accurately predicted the permeance of gas separation polymeric membranes. The model accounted for variations in membrane thickness, feed composition, and operating conditions, providing valuable insights into the overall performance of the membrane system. It also allowed for the optimization of membrane design and operational parameters to enhance separation efficiency and productivity. The study showcased the effectiveness of numerical techniques in accurately predicting membrane performance. The developed model can be a valuable tool for membrane designers and engineers, enabling them to optimize the design and operation of gas separation systems.

Constructing the high-efficiency “celluveyor conveyor” transport systems in membranes by IL@ZIF-8 for efficient CO2/CH4 separation

Inspired by the high-efficiency transport systems combined the “conveyor” transport pathways with the “celluveyor” transport pathways, the ionic liquid imide modified ZIF-8 (IL@ZIF-8) was prepared as a filler and incorporated into the self-polymerization-confined Pebax/polyethylene glycol methyl ether acrylate matrix (SPM) to prepare mixed matrix membranes (MMMs) for efficient CO2/CH4 separation. The incorporated IL@ZIF-8 can construct the high-efficiency “celluveyor conveyor” transport systems that consisted of the “celluveyor” transport pathways and the “conveyor” transport pathways, and it played important roles in MMMs. Therein, the “celluveyor” transport pathways can be constructed with the help of CO2 carriers (Zn2+) in oriented and ordered pore channels of IL@ZIF-8, contributing to promoting rapid CO2 transport in multiple direction. IL was uniformly distributed on ZIF-8, and it acted as “binder” between adjacent ZIF-8 in IL@ZIF-8. IL in IL@ZIF-8 can adsorb CO2 molecules as a consequence of its strong chemical affinity for CO2, and the “conveyor” transport pathways can be constructed with the help of CO2 carriers ([Tf2N]-) in IL for rapid CO2 transport between the adjacent ZIF-8, improving CO2 separation performance of MMMs. Consequently, it was possible to enhance the performance of CO2 separation by constructing the high-efficiency “celluveyor conveyor” transport systems in SPM/IL@ZIF-8 MMMs. Therefore, SPM/IL@ZIF-8 MMMs were endowed with the excellent CO2 separation performance. It showed an enhanced permeability for CO2, which increased by 96.9 %, and a better CO2/CH4 selectivity, which improved by 56.6 %, when compared to the performance of the pure SPM membrane. It implied that the constructed high-efficiency “celluveyor conveyor” transport systems in MMMs were a promising strategy for efficient CO2 separation.

An Overview of Different Water Electrolyzer Types for Hydrogen Production

While fossil fuels continue to be used and to increase air pollution across the world, hydrogen gas has been proposed as an alternative energy source and a carrier for the future by scientists. Water electrolysis is a renewable and sustainable chemical energy production method among other hydrogen production methods. Hydrogen production via water electrolysis is a popular and expensive method that meets the high energy requirements of most industrial electrolyzers. Scientists are investigating how to reduce the price of water electrolytes with different methods and materials. The electrolysis structure, equations and thermodynamics are first explored in this paper. Water electrolysis systems are mainly classified as high- and low-temperature electrolysis systems. Alkaline, PEM-type and solid oxide electrolyzers are well known today. These electrolyzer materials for electrode types, electrolyte solutions and membrane systems are investigated in this research. This research aims to shed light on the water electrolysis process and materials developments.

Characterization of two Plasmodium falciparum lipid transfer proteins of the Sec14/CRAL-TRIO family

Invasion of human red blood cells by the malaria parasite Plasmodium falciparum is followed by dramatic modifications of erythrocytes properties, including de novo formation of new membrane systems. Lipid transfer proteins from both the parasite and the host cell are most likely an important part of those membrane remodeling processes. Using bioinformatics and in silico structural analysis, we have identified five P. falciparum potential lipid transfer proteins containing cellular retinaldehyde binding – triple functional domain (CRAL-TRIO). Two of these proteins, C6KTD4, encoded by the PF3D7_0629900 gene and Q8II87, encoded by the PF3D7_1127600 gene, were studied in more detail. In vitro lipid transfer assays using recombinant C6KTD4 and Q8II87 confirmed that these proteins are indeed bona fide lipid transfer proteins. C6KTD4 transfers sterols, phosphatidylinositol 4,5 bisphosphate, and, to some degree, also phosphatidylcholine between two membrane compartments. Q8II87 possesses phosphatidylserine transfer activity in vitro. In the yeast model, the expression of P. falciparumQ8II87 protein partially complements the absence of Sec14p and its closest homologue, Sfh1p. C6KTD4 protein can substitute for the collective essential function of oxysterol-binding related proteins. According to published whole genome studies in P. falciparum, absence of C6KTD4 and Q8II87 proteins has severe consequences for parasite viability. Therefore, CRAL-TRIO lipid transfer proteins of P. falciparum are potential targets of novel antimalarials, in search for which the yeast model expressing these proteins could be a valuable tool.

Interfacial insights: [6]-Gingerol monolayers at the air-water interface and beyond

Ginger is a culinary spice with a millennia-old tradition due to its extensive therapeutic applications, recently validated by scientific studies. In particular [6]-Gingerol, a key active molecule in ginger, exhibits extraordinary capabilities in addressing a wide spectrum of health issues. However, its therapeutic potential is limited by its rather low bioavailability. The incorporation of [6]-Gingerol into membrane systems of liposomes, micelles, or exosomes is a promising strategy to overcome this limitation. In this contribution, we report the hitherto unexplored surface properties of [6]-Gingerol at the air-water interface. Our comprehensive study, which includes a detailed analysis of surface pressure and surface potential vs. area per molecule isotherms, surface compression modulus, and Brewster Angle Microscopy, demonstrates the capability of [6]-Gingerol to form Langmuir films. These films can be transferred onto solid substrates, forming remarkably homogeneous Langmuir-Blodgett films which have been characterized by Quartz Crystal Microbalance and Atomic Force Microscopy. This study may be of interest as it paves the way for future research on introducing [6]-Gingerol into membrane systems and transporting it into living cells.

Quorum sensing on the activated performances of gravity-driven membrane (GDM) system at low temperatures: Ammonia removal and flux stabilization

Gravity-driven membrane (GDM) filtration technology offers a low-energy, low-maintenance solution for water purification due to its powerful bio-cake, but faces predicament in contaminant removal under low temperatures. Quorum sensing (QS), a microbial communication process mediated by signaling molecules such as C6-HSL (N-Hexanoyl-L-homoserine lactone), has been shown to influence microbial behavior and enhance biofilm formation, with promising potential for consolidation of GDM operation at low temperature. This study investigates the application of C6-HSL to enhance ammonia nitrogen and organics removal in low-temperature GDM systems. C6-HSL was administered at varying dosages (0/50/250/500 nM/d) at 5 °C, with further experiments conducted at 25 °C to assess the impact of QS regulation on GDM performance under room temperature. The results demonstrated that the optimized presence of C6-HSL (500 nM/d) improved the removal efficiency of dissolved organic carbon, ammonia nitrogen, and raised the stable normalized flux (increase ratios at low vs. room temperature: ∼19 % vs. ∼7 %, ∼38 % vs. ∼9 %, and ∼22 % vs. ∼12 %, respectively). Analysis of the biofouling layer’s structural characteristics, composition, and biological activity indicated that the increased C6-HSL effectively promoted microbial growth and migration/movement, increased the production of extracellular polymeric substances (EPS) and soluble microbial products (SMP), and accelerated biofilm formation. The resulting thicker (∼172.98 vs. ∼119.21 μm), rougher (∼62.1 vs. ∼55.0 nm) cake layer, equipped with abundant channels for water penetration, contributed to increased contaminant degradation, but also stabilized the flux with slight growth (∼3.26 vs. ∼3.02 LMH) under low temperature. Notably, the enhancement effect of QS regulation was more pronounced at low temperature than at room temperature, attributing to the optimized release and diffusion of signal molecules and the more substantial stimulation of metabolic and enzymatic activity in nitrifying bacteria. This study provides valuable insights and technical support for decentralized water treatment in winter via reliable GDM process operation in challenging temperature conditions.

From enzyme dispersion to purification: Optimizing biocatalytic membranes for high-purity ginsenoside Rd production

This study presents a novel biocatalytic membrane (BM) system for the continuous production of high-purity ginsenoside Rd. Recognizing that enzymes concentrated on one side of BM caused by reverse filtration hinder substrate access and catalytic efficiency, polyethyleneimine (PEI) and polyallylamine hydrochloride (PAH) were added during dopamine (DA) deposition. They effectively disrupted the clustering of enzyme molecules, enabling a more homogeneous enzyme distribution within BMs, as confirmed by microscopy, activity assays, and simulations. This controlled dispersion, facilitated by Protein-Polyelectrolyte Complexes (PPCs) formation, significantly improved substrate accessibility and catalytic performance. Exceptional catalytic performance was exhibited by the optimized PDA/PEI BM (using 1800 Da PEI), enabling highly efficient conversion of Rb1 to Rd. This high conversion efficiency, coupled with the inherent temperature-dependent solubility of Rd, enables a remarkably simple purification process. By exploiting Rd precipitation upon cooling, high-purity (93.1 %) Rd was achieved at a 55.6 % recovery from a 70 % purity Rb1 feed using a simple solid–liquid separation, eliminating the need for other separation techniques. This study provides new insights into the preparation of BMs and offers innovative strategies for the transformation and purification of ginsenosides.

Experimental study on current density distribution characteristics in a novel oxygen recirculation system of dead-ended proton exchange membrane fuel cell

ABSTRACT Dead-ended proton exchange membrane fuel cells (PEMFCs) using pure hydrogen and oxygen can improve fuel efficiency and cell performance, making them widely applicable in enclosed spaces. However, dead-ended PEMFCs are prone to flooding, which reduces cell performance and service life. To address this issue, an oxygen recirculation system utilizing oscillating flow generated by pressure differences is designed in this study. This system not only achieves close to 100% fuel utilization but also optimizes water management and enhances current density uniformity. The optimal oxygen cycling conditions were selected based on current density uniformity and cell performance enhancement. The results show that a larger pressure difference amplitude improves water removal from the cell; however, excessively large pressure differences can lead to unstable cell operation. The oscillating flow generated by pressure differences significantly improved current density uniformity, particularly at higher output load currents. Current density uniformity improved by 16.29% at a current of 75 A. The experiment demonstrates that the best current density uniformity is achieved when managing water using a pressure difference at 4-minute intervals, as longer or shorter oscillation intervals are unsuitable for dead-ended performance.