Water Transport Mechanisms Research Articles

Tragacanth Gum/Trimethyl Chitosan‐Derived Polyelectrolyte Complex as Potential Carriers in Drug Delivery Applications

ABSTRACTA three‐step procedure described in the literature has been used to create N,N,N‐trimethyl Ct a chitosan derivative that is extremely soluble in water. By combining two polymers in aqueous media, this derivative and tragacanth gum were able to form a new polyelectrolyte complex. The TGA, FTIR, and DSC analysis established the development of TMC/XG‐PEC. SEM was used to describe the TMC/TG‐PEC's surface morphology. The features of diffusion and swelling, such as the theoretical equilibrium ratio, initial swelling rate constant, and the process of water transportation into TMC/TG‐PEC, were established. The TMC/TG‐PEC swelling is seen to be pH‐dependent. It swells in the subsequent order: pH 7.4 > 6.8 > 1.2. At pH 1.2, 6.8, and 7.4, the TMC/TG‐PEC swelling ratio was found to be 6.5, 7.7, and 9.6 g/g, respectively. The second‐order kinetics of the swelling process is indicated by the linearity of the plot “t/SR” versus “t”. The TMC/TG‐PEC's n values under various pH circumstances ranged from 0.12 to 0.16, suggesting the Fickian water transport mechanism. The utility of complex as a matrix for KP formulations for sustained‐release tablets was investigated. It was discovered that 90.5% of KP was loaded into PEC. There is evidence that pH influences how much medicine is released. When the medium's pH was altered from acidic to neutral, the KP release was considerably boosted. The TMC/TG‐PEC demonstrated a maximum drug release of 7% in a pH 1.2 medium and between 85% and 90% in a pH 7.4 medium, demonstrating the TMC/TG‐PEC's potential as a matrix substance for the drug's prolonged release formulations of KP. The Fickian drug transport mechanism was indicated by the release exponent n, which was less than 0.5.

Water transport through carbon nanotubes with a peanut-shaped cross-section

Carbon nanotubes are typically characterized by a circular cross-section. However, under hydrostatic pressure, their cross-section can deform into a peanut-like shape. In this study, we explore water transport in carbon nanotubes that exhibit the peanut-shaped cross-section. Our findings reveal that the axial separation in the peanut-shaped carbon nanotube significantly impacts water transport. We attribute these effects to changes in water molecule occupancy, average water velocity, and the order parameter of water, all of which are finely influenced by the axial separation. These results enhance our understanding of the water transport mechanisms in carbon nanotubes with peanut-shaped cross-sections.

Design of nature-inspired patterns on knitted fabrics for directional transportation of sweat and study of their performances

The human body in a hot environment or during intense training will sweat a lot. Traditional cotton fabrics are soft and breathable, but they tend to absorb moisture easily and evaporate it slowly, which makes people feel cold and wet. Sweat staying on fabrics for a long time could also cause bacteria to grow. Thus, it is necessary to transport the excessive sweat from the gathering section to the collection points along the surface paths in time to minimize such problems. The mechanism of directional water transport of desert beetles, cacti, nepenthes, and river meanders was referenced in this paper. The paths in dot, tree, V-shape, and river meander patterns were designed and manufactured from the inspiration of these natural architectures. The paths were coated on the surfaces of selected knitted fabrics with different structures through a one-step coating process. The optimal recipe of hydrophobic solution was determined when 0.1 g hydroxyethyl-cellulose (HEC) was added into MS-S002 solution. The results showed that sweat movement is mainly influenced by FL, FWD, FG, and knitted structure. The continuous and enclosed paths such as tree and river contribute to a better sweat moving track than those of dot and V-shape ones. Terry structure is more suitable for surface sweat transport than plain and pique. The highest movement speed of the terry structure with a tree pattern reaches 0.43 cm/s, followed by that of the terry structure with river pattern 0.35 cm/s. The coated fabrics also have ideal moisture and air permeability for wearing.

Multifunctional Janus nanofibrous membrane with unidirectional water transport and pH-responsive color-changing for wound dressing

Chronic wounds often produce a significant volume of exudate, posing a substantial obstacle to healing. Consequently, there is a pressing demand for a versatile dressing capable of effectively managing exudate in chronic wounds. In this context, a Janus smart dressing is proposed, featuring unidirectional water transport and a pH-responsive color-changing for exudate management and wound monitoring. The dressing’s mechanisms for unidirectional water transport and color changing are elucidated. The Janus dressing consists of a polyacrylonitrile (PAN)/sodium polyacrylate (SPA)/anthocyanin (An) hydrophilic layer with antioxidant and pH-sensitive functions and a poly (3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) hydrophobic layer, enabling unidirectional exudate drainage without reverse osmosis. Studies indicate that the Janus dressing exhibits excellent air permeability, moisture permeability, mechanical properties, cytocompatibility, and antioxidant performance while promptly responding to color variations in solutions of varying pH levels. In vivo studies demonstrated the excellent wound healing ability of Janus PHBV-PAN/SPA/An membrane. Consequently, this study provides a promising solution to develop wound dressings that can effectively manage excessive wound exudate and dressing changes.

A practical method for the in-situ estimation of the effective thermal resistance of gas diffusion layers in PEMFC

The membrane electrode assembly of a PEM fuel cell is hotter than the gas feeding plates because heat is generated within it, and the diffusion layers are thermally resistive. The temperature gradient created, which increases as a function of the current density, is useful for evacuating the water produced in vapor form. This water transport mechanism is known as the “heat pipe effect”. The temperature gradient produces a saturation vapour pressure gradient, which in turn produces a diffusive vapor flow. Mastering water management, coupled with heat management, requires knowledge of the temperature of the MEA and therefore the effective thermal resistance of the diffusion layers. In this paper, we present an original method for estimating this thermal resistance in situ, without using heat flux sensors or directly measuring the temperature of the MEA. The method requires the ability to impose a temperature gradient between the anode and cathode plates, and to perform a hot-side water balance. Thermal resistance is deduced from the coupling between heat and water transfer. Two diffusion layers widely used by the community are tested. The GDL Sigracet 22 BB (from SGL Carbon) has a lower effective thermal resistance than the GDL Freudenberg H15C14. Variations in these thermal resistances are measured as a function of the temperature gradient imposed and of the compression ratio.

Liquid water transport mechanism inside fuel cells with orderly graded perforation microporous layer

Liquid water transport mechanism inside fuel cells with orderly graded perforation microporous layer

Modeling Water Transport in Polymer Electrolyte Membrane Electrolyzers Using a One-Dimensional Transport Model

In this work, we present a water transport model to quantify the movement of water across Nafion® membranes in a proton exchange membrane electrolyzer as a function of varying operating conditions and membrane parameters. This physics-based model is based on the three main water transport mechanisms: diffusion, electro-osmotic drag, and pressure-driven flow. Three sets of equations are obtained to model the movement of water on the cathode side – I. Material balances for hydrogen and water in the flow channel (z-direction), II. Water movement across the membrane in the x-direction, and III. Expressions for variable membrane properties to serve as model inputs. The condensation of water at the cathode is also modeled to understand the respective transport contributions from the vapor and liquid phases. The coupled equation sets are solved numerically with appropriate boundary conditions. An analytical solution is also obtained for the governing differential equation for the mole fraction of water in the vapor phase. This study is perhaps the first effort for a detailed physics-based transport model to predict the water transport in the electrolyzer in one dimension using the actual measured values for the physical parameters of the system. The model results are compared with the experimental data available for water transport, and a good agreement is observed over the wide range of current, temperature and pressure differentials. Further, with the help of this simple transport model, the numerical analysis is performed to delineate the effect of electrolyzer operating conditions on the net water transport across the membrane, water condensation at the cathode, individual contribution of the transport fluxes, and electrolyzer design. Finally, the model is exercised to simulate the dependence of water transport as a function of membrane thickness. This confirms the validity of the current approach of using thin reinforced membranes by electrolyzer fabricators. Figure 1

Thermo-adaptive interfacial solar evaporation enhanced by dynamic water gating

Solar-driven evaporation offers a sustainable solution for water purification, but efficiency losses due to heat dissipation and fouling limit its scalability. Herein, we present a bilayer-structured solar evaporator (SDWE) with dynamic fluidic flow mechanism, designed to ensure a thin water supply and self-cleaning capability. The porous polydopamine (PDA) layer on a nickel skeleton provides photothermal functionality and water microchannels, while the thermo-responsive sporopollenin layer on the bottom acts as a switchable water gate. Using confocal laser microscopy and micro-CT, we demonstrate that this unique structure ensures a steady supply of thin water layers, enhancing evaporation by minimizing latent heat at high temperatures. Additionally, the system initiates a self-cleaning process through bulk water convection when temperature drops due to salt accumulation, thus maintaining increased evaporation efficiency. Therefore, the optimized p-SDWE sample achieved a high evaporation rate of 3.58 kg m−2 h−1 using 93.9% solar energy from 1 sun irradiation, and produces 18–22 liters of purified water per square meter of SDWE per day from brine water. This dynamic water transport mechanism surpasses traditional day-night cycles, offering inherent thermal adaptability for continuous, high-efficiency evaporation.

Resolving micro-scale water potential gradients within leaves

Many questions in leaf physiology, from mechanisms of water transport and stomatal responses to interpretation of gas exchange measurements, hinge on distributions of water potential among compartments in the leaf. A new tool, AquaDust, offers the possibility of quantifying those distributions at unprecedentedly small scales of organization

Molecular simulations of organic solvent transport in dense polymer membranes: Solution-diffusion or pore-flow mechanism?

We employed non-equilibrium molecular dynamics simulations and theoretical predictions to elucidate organic solvent and water transport mechanisms in dense polymer membranes. Our study investigated the transport of water and 14 organic solvents across 16 dense polymer membranes with varying fractional free volumes. Simulations demonstrated that the dependence of organic solvent or water flux on applied pressure exhibited minimal deviation from linearity, contrary to the prediction of a “ceiling flux” at high pressures, based on the solution-diffusion model. Notably, our findings underscore the paramount influence of solvent size and membrane pore size on solvent permeance, significantly diverging from the solvent solubility-based predictions of the solution-diffusion model. Overall, our results agree with the solution-friction model for characterizing water and organic solvent transport in dense polymer membranes such as reverse osmosis and organic solvent nanofiltration. These fundamental insights into the transport mechanisms of water and organic solvents offer molecular-level guidance for designing next-generation high-performance polymer membranes for various separation applications.

Liquid Water Visualization in the Pt‐Loading Cathode Catalyst Layers of Polymer Electrolyte Fuel Cells Using Operando Synchrotron X‐ray Radiography

Water management is important for addressing the challenges posed by next‐generation fuel cell electric vehicles. Although X‐ray imaging techniques are useful for probing the mechanism of water transport in the gas diffusion layer of polymer electrolyte fuel cells, they cannot be easily applied to the Pt‐loading catalyst layer because of its low X‐ray transmittance due to the high absorption coefficient of Pt. Herein, a method to realize the high‐resolution X‐ray imaging of a 30 μm‐thick cathode catalyst layer in polymer electrolyte fuel cells using synchrotron X‐ray radiography is proposed, thus bridging the above gap. The results of operando synchrotron X‐ray radiography measurements reveal that water accumulation in the cathode catalyst layer depends on the cell temperature, feed gas humidity, and cell voltage, while time‐slice analysis shows that the water accumulation rate in the cathode catalyst layer immediately after the power generation is faster than that in the cathode gas diffusion layer. The proposed imaging method can be used to evaluate the water storage capacity of the catalyst layer and thus deepen the understanding of flooding phenomena and cold‐start behavior at subzero temperatures.

Tree-Inspired Structurally Graded Aerogel with Synergistic Water, Salt, and Thermal Transport for High-Salinity Solar-Powered Evaporation

HighlightsInspired by transport system in trees, a two-way water and salt transport mechanism is realized in a structurally graded aerogel, enabling simultaneous fast water uptake and salt rejection.The horizontally aligned pore channels near the surface achieve excellent heat localization by maximizing solar absorption and minimizing heat loss.The integrated water, salt, and thermal transports impart an impressive evaporation rate of 1.94 kg m−2 h−1 in a 20 wt% NaCl solution for 8 h without salt accumulation.

A bamboo 'PeSAPK4-PeMYB99-PeTIP4-3' regulatory model involved in water transport.

Water plays crucial roles in expeditious growth and osmotic stress of bamboo. Nevertheless, the molecular mechanism of water transport remains unclear. In this study, an aquaporin gene, PeTIP4-3, was identified through a joint analysis of root pressure and transcriptomic data in moso bamboo (Phyllostachys edulis). PeTIP4-3 was highly expressed in shoots, especially in the vascular bundle sheath cells. Overexpression of PeTIP4-3 could increase drought and salt tolerance in transgenic yeast and rice. A co-expression pattern of PeSAPK4, PeMYB99 and PeTIP4-3 was revealed by WGCNA. PeMYB99 exhibited an ability to independently bind to and activate PeTIP4-3, which augmented tolerance to drought and salt stress. PeSAPK4 could interact with and phosphorylate PeMYB99 in vivo and in vitro, wherein they synergistically accelerated PeTIP4-3 transcription. Overexpression of PeMYB99 and PeSAPK4 also conferred drought and salt tolerance in transgenic rice. Further ABA treatment analysis indicated that PeSAPK4 enhanced water transport in response to stress via ABA signaling. Collectively, an ABA-mediated cascade of PeSAPK4-PeMYB99-PeTIP4-3 is proposed, which governs water transport in moso bamboo.

Tuning physicomechanical properties of PEG-interpenetrated anionically modified semi-IPN cryogels functionalized with carboxylate groups

Anionically modified interpenetrated polymer network (semi-IPN) cryogels containing linear polyethylene glycol chains (PEG) were prepared via in situ synthesis and directed assembly of the negatively charged copolymer poly(acrylamide-co-sodium acrylate) (PAN) network template. The influence of reaction conditions; the concentration of linear PEG chains, and polymerization temperature on the elasticity and swelling of these IPNs was analyzed in detail. The interpenetrating structure of PEG chains and PAN host network have been confirmed by FTIR, TGA and XRD analysis. The equilibrium water content, oscillatory swelling/deswelling kinetics, and water transport mechanism were analyzed as a function of PEG content. The results showed that semi-IPN gels exhibited different swelling behavior as the reaction conditions varied. Addition of 13.9% (w/v) PEG resulted in a 25-fold increase in the swelling ratio of semi-IPN hydrogels. By performing compression tests on semi-IPN gels to determine the change of compression properties, the effective cross-linking density of semi-IPN PAN/PEG was expressed as a second-order polynomial depending on the amount of PEG. The swollen modulus of semi-IPN cryogels was much higher than that of semi-IPN hydrogels for all PEG concentrations. Semi-IPNs showed reversible on-off switching with remarkable sensitivity to external pH stimulus. Structural parameters, degree of swelling, volume fraction of cross-linked polymer in the swollen state, and diffusion coefficients due to pH-induced swelling of semi-IPN gels were determined. The presence of linear PEG chains in the structure promoted swelling by both increasing the swelling rate and significantly reducing the time required to reach the equilibrium-state. The swelling process was Fickian diffusion, and the diffusion coefficients for swelling of PEG-interpenetrated semi-IPNs increased with PEG content. The effectiveness of removing methylene blue (MB) dye from aqueous solutions by semi-IPNs was evaluated. Batch adsorption experiments were performed as a function of the gelation temperature, amount of PEG, contact time, and initial dye concentration. The adsorption isotherm and kinetics were described well by Langmuir isotherm model and pseudo-second-order model, respectively. Adsorption of MB was a multi-step process involving surface adsorption followed by intra-particle diffusion. Semi-IPN PAN/PEG cryogels prepared under cryocondition with high adsorption capacities and fast adsorption rates have been developed as new adsorbents effective in removing dyes and other toxic substances with higher mechanical strength in water and wastewater treatment.

Hybrid Banana Pseudo Stem biochar- poly (N-hydroxyethylacrylamide) hydrogel and its magnetic nanocomposite for effective remediation of dye from wastewater

A hybrid hydrogel based on Banana Pseudo Stem, an agricultural waste material, has been developed as an adsorbent for use in wastewater treatment. The Biochar obtained from Banana Pseudo Stem was modified by graft copolymerization with N-hydroxyethylacrylamide (HEAAm). The graft copolymer was made by microwave irradiation of an aqueous mixture containing BPSBC, N-hydroxyethylacrylamide (HEAAm), N,N-methylenebisacrylamide (MBA), and potassium peroxodisulphate (KPS). The magnetite (Fe3O4) nanoparticles have been incorporated into the gel by in-situ diffusion of Fe2+ and Fe3+ followed by a reaction with ammonia solution. FTIR, SEM, EDS, TGA, VSM, BET, and XRD techniques were used to characterize the gel and its nanocomposite. The swelling process appeared to be a second-order kinetic process and the mechanism of water transport is found to be non-Fickian. The hybrid gel and nanocomposite were evaluated for the adsorptive removal of cationic dyes using Methylene Blue (MB) and Crystal Violet (CV) as model dyes. The adsorption capacities of the graft copolymer gel for MB and CV were 200 mg g−1 and 183 mg g−1 respectively. A considerable increase in adsorption capacities was observed in nanocomposite formation, with adsorption capacity values of 235 and 202 mg g−1 for MB and CV respectively. The pseudo-second-order kinetic model and Freundlich adsorption isotherm model provide the best fit of the dye sorption data. Thermodynamic studies revealed adsorption to be a spontaneous and endothermic process. Effective desorption under acidic conditions illustrated the possibility of reuse of the developed adsorbent materials in repeated cycles during the wastewater treatment process.

The solution-diffusion model for water transport in reverse osmosis: What went wrong?

Reverse osmosis (RO) stands as the state-of-the-art desalination technology, owing to its high energy efficiency and low cost. Further improvements in the performance of this technology require a fundamental understanding of transport mechanisms in RO membranes. For decades, the solution-diffusion model has been the prevalent approach to describe water transport mechanism in RO membranes. In this model, water first partitions into the membrane and then diffuses down a concentration gradient of water within the RO membrane. However, recent experimental and theoretical findings pose serious challenges to the fundamental assumptions of this theory. In this perspective, we discuss seven critical flaws in the solution-diffusion model and explain why the model fails to describe water transport in RO membranes. Instead, through our careful analyses, we determine that the pore-flow model, in which a pressure gradient drives water flow through membrane pores or interconnected free volumes, represents the true mechanism for water transport. We conclude by highlighting the need for research efforts to better understand the frictional interactions between water, salt, and membrane and their impact on water transport. Overall, a fundamental understanding of the water transport mechanism will inform the development of next-generation RO desalination membranes.

Unveiling transport mechanisms of cesium and water in operando zero-gap CO2 electrolyzers

Unveiling transport mechanisms of cesium and water in operando zero-gap CO2 electrolyzers

Expression and functional analysis of a recombinant aquaporin Z from Antarctic Pseudomonas sp. AMS3.

Aquaporin (AQP) is a water channel protein from the family of transmembrane proteins which facilitates the movement of water across the cell membrane. It is ubiquitous in nature, however the understanding of the water transport mechanism, especially for AQPs in microbes adapted to low temperatures, remains limited. AQP also has been recognized for its ability to be used for water filtration, but knowledge of the biochemical features necessary for its potential applications in industrial processes has been lacking. Therefore, this research was conducted to express, extract, solubilize, purify, and study the functional adaptations of the aquaporin Z family from Pseudomonas sp. AMS3 via molecular approaches. In this study, AqpZ1 AMS3 was successfully subcloned and expressed in E. coli BL21 (DE3) as a recombinant protein. The AqpZ1 AMS3 gene was expressed under optimized conditions and the best optimized condition for the AQP was in 0.5 mM IPTG incubated at 25°C for 20 h induction time. A zwitterionic mild detergent [(3-cholamidopropyl) dimethylammonio]-1-propanesulfonate was the suitable surfactant for the protein solubilization. The protein was then purified via affinity chromatography. Liposome and proteoliposome was reconstituted to determine the particle size using dynamic light scattering. This information obtained from this psychrophilic AQP identified provides new insights into the structural adaptation of this protein at low temperatures and could be useful for low temperature application and molecular engineering purposes in the future.

Modeling water transport in polymer electrolyte membrane electrolyzers using a one-dimensional transport model

In this paper, we present a one-dimensional transport model for water transport across Nafion® membranes in a proton exchange membrane electrolyzer. This physics-based model is based on the three main water transport mechanisms: diffusion, electro-osmotic drag, and pressure-driven flow. A good agreement is obtained between the model predictions using the measured values of the physical parameters as inputs and the previously reported experimental data. Further, with the help of this simple transport model, the numerical analysis is performed to delineate the effect of electrolyzer operating conditions on the net water transport across the membrane, water condensation at the cathode, individual contribution of the transport fluxes, and electrolyzer design. Finally, the model is exercised to simulate the dependence of water transport as a function of membrane thickness. This confirms the validity of the current approach of using thin reinforced membranes by electrolyzer fabricators.

Ion and Water Dynamics in the Transition from Dry to Wet Conditions in Salt-Doped PEG.

The influence of the water content on ion and water transport mechanisms in polymer membranes under low to moderate hydration conditions remains poorly understood. In this study, we combine ion and water diffusivity (PFG-NMR) measurements with atomistic molecular dynamics simulations to better understand transport processes in hydrated salt-doped poly(ethylene glycol). Above the water percolation threshold, the experimental and simulated diffusivities are in good agreement with the free volume transport models. At low hydration levels, unlike dry systems, ion diffusion cannot be described by polymer segmental dynamics alone. We rationalize such observations by the interplay between ion-water and ion-polymer solvation of cations and between ion-water and cation-anion interactions for anions. Further, we demonstrate that a two-state model combining ion-water solvation and free volume transport can describe water dynamics across the entire hydration range of interest. Our findings provide a more encompassing analysis of ion and water transport in hydrated polyelectrolytes, specifically in the low hydration regime.