Ion Permeability Research Articles

Interlayer Cohesion in 3D Printed Concrete: The Role of Width-to-Height Ratio in Modulating Transport Properties and Pore Structure

Due to the extrusion-based printing and layer-to-layer deposition characteristics, the interlayer cohesion of 3D printed concrete is highly sensitive to the geometry of the printed layers, significantly influencing both mechanical performance and long-term durability. In this study, the width-to-height (W/H) ratio was employed as a geometric parameter to explore its relationship with interlayer transport and pore morphology. The research began by optimizing mix proportions through fluidity and printability tests. Subsequently, chloride ion permeation, mercury intrusion porosimetry, and micro-CT were used to analyze interfacial transport and pore distribution, revealing the influence of the W/H ratio on these properties. The results demonstrate that the W/H ratio plays a crucial role in densification and interfacial defect formation in 3D printed concrete. While the extrusion process enhances matrix compaction, a higher W/H ratio generally promotes stronger interlayer cohesion and reduces chloride ion permeability. However, an excessively large W/H ratio, especially when coupled with air entrainment, can introduce defects and increase porosity at the layer interfaces. The study concludes that maintaining a W/H ratio between 1.5 and 2.0 effectively strengthens interlayer cohesion. These results offer valuable theoretical insights and technical support for the design and application of 3D printed concrete materials.

Effect of a novel negative temperature early-strength agent in improving concrete performance under varying curing temperatures

This study investigates the effect of a novel negative temperature early-strength agent (NEA) in enhancing concrete performance under varying curing temperatures, with a discussion on the underlying mechanism through analysis of hydration products and microstructure.The results indicate NEA markedly accelerates early cement hydration, reduces setting time, and enhances compressive strength. Moreover, the efficacy of NEA is more pronounced at lower temperatures. With an optimal dosage of 3%, the incorporation of NEA leads to a remarkable 285.9% increase in compressive strength at 28 days under -5°C curing temperature. Despite accelerating cement hydration can induce increased chemical shrinkage, NEA effectively mitigates early freezing expansion under negative temperature and significantly diminishes chloride ion permeability. Higher temperatures facilitate early cement hydration but also compromise long-term hydration continuity. Consequently, the highest hydration degree and loweast porosity are observed at 28 days under 5°C curing temperature. NEA's air-entraining component introduces numerous superfine pores into the paste, augmenting early pore volume while optimizing pore structure. As the early-strength component fosters hydration, these pores undergo further filling and refinement, ultimately reducing the total pore volume at 28 days. This study provides insights into optimizing concrete performance in cold environments.

Transmembrane Ion Channels: From Natural to Artificial Systems.

Natural channel proteins allow the selective permeation of ions, water or other nutritious entities across bilayer membranes, facilitating various essential physiological functions in living systems. Inspired by nature, chemists endeavor to simulate the structural features and transport behaviors of channel proteins through biomimetic strategies. In this review, we start from introducing the inherent traits of channel proteins such as their crystal structures, functions and mechanisms. Subsequently, different kind of synthetic ion channels including their design principles, dynamic regulations and therapeutic applications were carefully reviewed. Finally, the potential challenges and opportunities in this research field were also carefully discussed. It is anticipated that this review could provide some inspiring ideas and future directions towards the construction of novel bionic ion channels with higher-level structures, properties, functions and practical applications.

Transmembrane Ion Channels: From Natural to Artificial Systems

Natural channel proteins allow the selective permeation of ions, water or other nutritious entities across bilayer membranes, facilitating various essential physiological functions in living systems. Inspired by nature, chemists endeavor to simulate the structural features and transport behaviors of channel proteins through biomimetic strategies. In this review, we start from introducing the inherent traits of channel proteins such as their crystal structures, functions and mechanisms. Subsequently, different kind of synthetic ion channels including their design principles, dynamic regulations and therapeutic applications were carefully reviewed. Finally, the potential challenges and opportunities in this research field were also carefully discussed. It is anticipated that this review could provide some inspiring ideas and future directions towards the construction of novel bionic ion channels with higher‐level structures, properties, functions and practical applications.

Prediction Model for the Chloride Ion Permeability Resistance of Recycled Aggregate Concrete Based on Machine Learning

The chloride ion permeability resistance of recycled aggregate concrete (RAC) is influenced by multiple factors, and the prediction model for this resistance based on machine learning is still limited. In the paper, six impact factors (IFs), including the carbonation of recycled coarse aggregates (YN), the replacement ratio of recycled coarse aggregates (r), the bending load level (L), the carbonation time (t) and temperature (T) of RAC, and the replacement ratio of carbonated recycled fine aggregates (f), were considered to conduct a chloride penetration test on RAC. Based on the experimental data, four algorithms, including artificial neural network (ANN), support vector machine (SVM), random forest (RF) and extreme gradient boosting (XGBoost), were adopted to establish the machine learning prediction models and study the relationships between the electric flux of RAC and the IFs. The results showed that the predicted values of all four models were in good agreement with the experimental values, and the XGBoost model had the best prediction performance on the testing set. Based on the XGBoost model, the LIME method was adopted to solve the interpretability problem in the prediction process. The importance ranking of IFs on the electric flux was r > t > f > T > L > YN. A graphical user interface (GUI) was developed based on Python 3.8 software to facilitate the use of machine learning models for the chloride ion permeability resistance of RAC. The research results can provide an accurate prediction of the electric flux of RAC.

The Donnan equilibrium is still valid in high-volume HDF.

Clinical studies have shown that hemodiafiltration reduces morbidity and mortality of dialysis patients compared to hemodialysis alone. This is attributed to its superior middle molecule clearance compared to standard hemodialysis. However, doubts arose as to whether a high convective flux through the dialyzer membrane has an influence on the equilibrium concentration of small ions, especially that of sodium. Due to the presence of negatively charged impermeable proteins on the blood side, the Gibbs-Donnan effect leads to an asymmetric distribution of membrane permeable ions on both sides of the membrane. In thermodynamic equilibrium, the concentrations of those ions can easily be calculated. However, the convective fluid flow leads to deviations from thermodynamic equilibrium. In this article, the effect of a convective flow on the ion distribution across a semipermeable membrane is analyzed in a theoretical model. Starting from the extended Nernst-Planck equation, including diffusive, convective, and electrostatic effects, a set of differential equations is derived. An approximate solution for flow speeds up to 0.1 ms-1 as well as a numerical solution are given. The results show that in any practical dialysis setting the convective flow has negligible influence on the electrolyte concentrations.

Isoleucine gate blocks K+ conduction in C-type inactivation.

Many voltage-gated potassium (Kv) channels display a time-dependent phenomenon called C-type inactivation, whereby prolonged activation by voltage leads to the inhibition of ionic conduction, a process that involves a conformational change at the selectivity filter toward a non-conductive state. Recently, a high-resolution structure of a strongly inactivated triple-mutant channel kv1.2-kv2.1-3m revealed a novel conformation of the selectivity filter that is dilated at its outer end, distinct from the well-characterized conductive state. While the experimental structure was interpreted as the elusive non-conductive state, our molecular dynamics simulations and electrophysiological measurements show that the dilated filter of kv1.2-kv2.1-3m is conductive and, as such, cannot completely account for the inactivation of the channel observed in the structural experiments. The simulation shows that an additional conformational change, implicating isoleucine residues at position 398 along the pore lining segment S6, is required to effectively block ion conduction. The I398 residues from the four subunits act as a state-dependent hydrophobic gate located immediately beneath the selectivity filter. By mutating I398 to Asparagine, ion permeation can be resumed in the kv1.2-kv2.1-3m channel, which was not a reversion C-type inactivation, since AgTxII fails to block the ionic permeation of kv1.2-kv2.1-3m_I398N. As a critical piece of the C-type inactivation machinery, this structural feature is the potential target of a broad class of QA blockers and negatively charged activators thus opening new research directions towards the development of drugs that specifically modulate gating-states of Kv channels.

Synaptic-like plasticity in 2D nanofluidic memristor from competitive bicationic transport.

Synaptic plasticity, the dynamic tuning of signal transmission strength between neurons, serves as a fundamental basis for memory and learning in biological organisms. This adaptive nature of synapses is considered one of the key features contributing to the superior energy efficiency of the brain. Here, we use molecular dynamics simulations to demonstrate synaptic-like plasticity in a subnanoporous two-dimensional membrane. We show that a train of voltage spikes dynamically modifies the membrane's ionic permeability in a process involving competitive bicationic transport. This process is shown to be repeatable after a given resting period. Because of a combination of subnanometer pore size and the atomic thinness of the membrane, this system exhibits energy dissipation of 0.1 to 100 aJ per voltage spike, which is several orders of magnitude lower than 0.1 to 10 fJ per spike in the human synapse. We reveal the underlying physical mechanisms at molecular detail and investigate the local energetics underlying this apparent synaptic-like behavior.

A High-Performance Polyimide Composite Membrane with Flexible Polyphosphazene Derivatives for Vanadium Redox Flow Battery.

A sulfonated polyimide, S-F-abSPI, with alkyl sulfonic acid side chains, and a polyphosphonitrile derivative, poly[4-methoxyphenoxy (4-fluorophenoxy) phosphazene] (PFMPP), were designed and synthesized. Composite modification of the S-F-abSPI membrane was carried out using PFMPP, resulting in the preparation of composite membranes with different composite ratios, which were then subjected to performance testing and characterization. Experimental results revealed a significant enhancement in the proton conductivity of the S-F-abSPI membrane, reaching 0.116 S cm-1, slightly higher than that of the N212 membrane. The S-F-abSPI/1% PFMPP composite membrane exhibited the optimal comprehensive performance, with a surface resistance as low as 0.54 Ω cm2, comparable to that of the N212 membrane. At a high current density of 200 mA cm-2 during charge-discharge, the composite membrane achieved a voltage efficiency (VE) of 83.12% and an energy efficiency (EE) of 81.95%. Cycling tests over 200 cycles demonstrated the composite membrane's excellent long-term cycling stability. The alkyl sulfonic acid side chains enhanced the proton conductivity of the membrane, while electrostatic potential distribution calculations indicated strong interactions between PFMPP and the base membrane, enhancing the membrane's mechanical strength, reducing vanadium ion permeability, and improving chemical stability and vanadium ion selectivity. This composite membrane holds promise for high-performance VRFB applications.

Enhanced Stability of N‐Type Organic Electrochemical Transistors Via Small‐Molecule Passivation

AbstractOrganic electrochemical transistors (OECTs) are of great interest owing to their potential applications in bioelectronics and neuromorphic systems. However, n‐type OECTs suffer from poor stability and facile degradation, mainly due to the oxygen reduction reactions in organic mixed ionic‐electronic conductors during device operation. In this study, a small‐molecule passivation strategy is introduced to greatly improve the stability of poly(benzobisimidazobenzophenanthroline) (BBL)‐based n‐type OECTs. 6,6‐Phenyl‐C61‐butyric acid methyl ester (PCBM) is spin‐coated onto the BBL layer to form a smooth and hydrophobic passivation layer, which effectively inhibits the oxygen reduction reactions while enabling ion permeation in aqueous electrolytes. Consequently, the OECTs employing the PCBM/BBL bilayers with an optimized PCBM thickness exhibit significantly improved operational stability at various electrolyte conditions (0.1 m NaCl or NaOH) and over a wide gate‐voltage sweep range (from −0.7 to 0.7 V). Owing to the high electron mobility of PCBM, the carrier mobility and switching speed of the PCBM/BBL OECTs are also improved compared with those of the pristine BBL OECTs. This study demonstrates the beneficial effects of simple surface passivation in organic mixed ionic‐electronic conductors and provides valuable insights for the design of high‐performance and stable OECTs for more specialized and advanced applications.

TMEM16 and OSCA/TMEM63 proteins share a conserved potential to permeate ions and phospholipids.

The calcium-activated TMEM16 proteins and the mechanosensitive/osmolarity-activated OSCA/TMEM63 proteins belong to the Transmembrane Channel/Scramblase (TCS) superfamily. Within the superfamily, OSCA/TMEM63 proteins, as well as TMEM16A and TMEM16B, are thought to function solely as ion channels. However, most TMEM16 members, including TMEM16F, maintain an additional function as scramblases, rapidly exchanging phospholipids between leaflets of the membrane. Although recent studies have advanced our understanding of TCS structure-function relationships, the molecular determinants of TCS ion and lipid permeation remain unclear. Here, we show that single mutations along the transmembrane helix (TM) 4/6 interface allow non-scrambling TCS members to permeate phospholipids. In particular, this study highlights the key role of TM 4 in controlling TCS ion and lipid permeation and offers novel insights into the evolution of the TCS superfamily, suggesting that, like TMEM16s, the OSCA/TMEM63 family maintains a conserved potential to permeate ions and phospholipids.

TMEM16 and OSCA/TMEM63 proteins share a conserved potential to permeate ions and phospholipids

The calcium-activated TMEM16 proteins and the mechanosensitive/osmolarity-activated OSCA/TMEM63 proteins belong to the Transmembrane Channel/Scramblase (TCS) superfamily. Within the superfamily, OSCA/TMEM63 proteins, as well as TMEM16A and TMEM16B, are thought to function solely as ion channels. However, most TMEM16 members, including TMEM16F, maintain an additional function as scramblases, rapidly exchanging phospholipids between leaflets of the membrane. Although recent studies have advanced our understanding of TCS structure–function relationships, the molecular determinants of TCS ion and lipid permeation remain unclear. Here, we show that single mutations along the transmembrane helix (TM) 4/6 interface allow non-scrambling TCS members to permeate phospholipids. In particular, this study highlights the key role of TM 4 in controlling TCS ion and lipid permeation and offers novel insights into the evolution of the TCS superfamily, suggesting that, like TMEM16s, the OSCA/TMEM63 family maintains a conserved potential to permeate ions and phospholipids.

Histidine containing dipeptides protect epithelial and endothelial cell barriers from methylglyoxal induced injury

Integrity of epithelial and endothelial cell barriers is of critical importance for health, barrier disruption is a hallmark of numerous diseases, of which many are driven by carbonyl stressors such as methylglyoxal (MG). Carnosine and anserine exert some MG-quenching activity, but the impact of these and of other histidine containing dipeptides on cell barrier integrity has not been explored in detail. In human proximal tubular (HK-2) and umbilical vein endothelial (HUVEC) cells, exposure to 200 µM MG decreased transepithelial resistance (TER), i.e. increased ionic permeability and permeability for 4-, 10- and 70-kDa dextran, membrane zonula occludens (ZO-1) abundance was reduced, methylglyoxal 5-hydro-5-methylimidazolones (MG-H1) formation was increased. Carnosine, balenine (ß-ala-1methyl-histidine) and anserine (ß-ala-3-methyl-histidine) ameliorated MG-induced reduction of TER in both cell types. Incubation with histidine, 1-/3-methylhistidine, but not with ß-alanine alone, restored TER, although to a lower extent than the corresponding dipeptides. Carnosine and anserine normalized transport and membrane ZO-1 abundance. Aminoguanidine, a well-described MG-quencher, did not mitigate MG-induced loss of TER. Our results show that the effects of the dipeptides on epithelial and endothelial resistance and junction function depend on the methylation status of histidine and are not exclusively explained by their quenching activity.

Guanidinium‐Based Covalent Organic Framework Membranes for Superior Mono‐ and Divalent Cations Separation

Biological membranes exhibit extraordinary efficiency in processing ion permeability and selectivity. However, creating artificial membranes for an ideal ion separation is still challenging due to the subtle distinctions in valence and size among different ions. In the realm of biological recognition, the ultimate selectivity of ion channels is considered to stem from the specific binding interactions and appropriate charge density. Designing artificial membranes to achieve similar performance not only helps the understanding of complex ion transport in bioprocesses but also facilitates critical industrial separations. Inspiring by the remarkable performance in biological systems, a guanidinium‐based covalent organic framework membrane is designed, which exhibits an excellent capability to recognize mono‐/divalent cations, achieving K+/Mg2+ selectivity up to 202 in a mixed salt solution. Furthermore, the membrane displays rapid ion transport owing to the uniform sub‐2 nm channels. The experimental results and molecular dynamics simulations illustrate that the charge‐assisted hydrogen bonding sites and the Cl− counter ions within 1D channels play critical roles in cations sieving. Specifically, divalent ions passing through the positively charged channels need to overcome higher energy barriers than monovalent ions. These findings offer promising avenues for the development of advanced multifunctional membranes for efficient ion separation and sustainable water‐related separations.

Citicoline eluting hydrogels for therapeutic contact lenses intended to treat neurodegenerative diabetic ocular diseases

Ophthalmic neurodegenerative diseases related to diabetes, such as glaucoma and retinopathy, are among the major causes of blindness in the world. Citicoline (CIT) in the form of eye drops is currently used for the treatment/prevention of these diseases, which affect the posterior segment of the eye. To ensure the drug penetration into the back of the eye, frequent instillations of highly concentrated drug solutions are required with potential side effects. Drug-loaded soft contact lenses (SCLs) may be an effective alternative to the conventional eye drop treatment, since they may enable a sustained drug release during daily wear, ensuring a higher drug bioavailability, and avoiding drug waste. In this work, one 2-hydroxyethyl methacrylate (HEMA) based hydrogel was functionalised with N-(3-aminopropyl) methacrylamide hydrochloride (APMA), molecularly imprinted with CIT and loaded with the same drug. The material was extensively characterised, in terms of morphology, optical, mechanical, and physical–chemical properties, namely, equilibrium water content, wettability, oxygen and ionic permeability, Young’s modulus, shear deformation, transmittance and refractive index, before and after steam sterilisation. Additionally, the tendency of the material to adsorb proteins of the lachrymal fluid was evaluated and its biocompatibility was assessed by irritation and cytotoxicity assays. Comparison with the non-functionalised and non-imprinted hydrogel showed that the modified hydrogel led to a sustained in vitro release of a much higher amount of CIT than the original one, while keeping typical values for physical–chemical properties of SCLs. The drug-loaded material resisted steam sterilisation and proved to be biocompatible, demonstrating adequate properties to be used in therapeutic SCLs for the prophylaxis/treatment of neurodegenerative diabetic ocular diseases. The neuroprotective effect of the released drug was confirmed with tests using porcine retinal explants.

Segmental-porosity regulation of nanochannel membranes with anomalously improved ion selectivity for enhanced osmotic power generation

Nanochannel-based osmotic energy conversion can directly convert salinity gradient energy between solutions with different ion concentrations into electric energy. In the energy conversion process, the high-concentration side of the nanochannel membrane has high ion permeability but low ion selectivity, whereas the low-concentration side exhibits opposite properties, which is the inherent limitation of osmotic power. However, the relationship between ion selectivity and permeability is unclear, which hinders the improvement of the output power density. This paper reports a segmental-porosity regulation method to break through the inherent constraints of the ion selectivity–permeability trade-off. The nanochannel membrane was divided into three regions along the ion transport direction as upstream, midstream, and downstream. The porosities of these three regions were separately regulated to optimize the structures for ion selectivity–permeability matching. When a high porosity was adopted for the downstream region and a small and mediate porosity combination was used for the upstream and midstream regions, the highest output power density was achieved, which was 78.44% higher than that of a straight nanochannel with homogeneous porosity under a 100-fold concentration ratio. The outstanding osmotic power generation performance of the optimized segmental structure was attributed to the alleviated ion concentration polarization and unexpectedly improved ion selectivity. Finally, the process and underlying mechanisms of segmental-porosity regulation are also proposed. This paper reports a novel methodology for designing the structure and porosity of nanochannel membranes to enhance osmotic power generation.

Ion and water permeation through claudin-10b and claudin-15 paracellular channels

Ion and water permeation through claudin-10b and claudin-15 paracellular channels

Heterojunction-structured Ni0.85Se/CoSe nanoparticles anchored on holey graphene for performance-enhanced sodium-ion batteries

Graphene-based metal selenides, are increasingly recognized for their potential in sodium-ion battery applications due to their superior electrochemical properties. The unique structure of graphene facilitates rapid in-plane transport of sodium ions, but the interlayer diffusion remains a significant challenge. The Ni0.85Se@CoSe heterojunctions, strategically grown adjacent to the graphene pores, offer a novel solution by creating in-plane holes that serve as direct channels for vertical ion transport, thereby enhancing cross-layer sodium ion permeation. The incorporation of Ni0.85Se@CoSe heterojunctions with holey graphene (NCS/HG) significantly enhances the reaction dynamics between sodium ions and anode material. These heterojunctions not only promote easier sodium ion insertion/extraction process by reducing the Na+ adsorption energy, but also improve the electrical conductivity by adjusting the band gap. The configuration supports high current density applications (573.5 mAh/g at 5.0 A/g), and ensures robust cycle stability with a capacity retention rate of 97 % after 1000 cycles at 2.0 A/g. Therefore, the development and etching techniques employed in engineering the Ni0.85Se@CoSe/HG graphene-based anodes exemplify a significant advancement in anode material design, highlighting the importance of material architecture in the development of high-performance energy storage devices.

Experimental study on chloride ion permeability of carbonated recycled aggregate concrete considering the effects of multiple factors

The chloride ion permeability is an important index of durability of carbonated recycled aggregate concrete (CRAC), but the resistance to chloride ion permeability of CRAC is affected by many factors and has yet been fully explored, which needs further systematic study. Considering the effects of the replacement ratio of carbonated recycled coarse aggregate (CRCA), the carbonation time of CRAC, the bending load level, the carbonation temperature of CRAC, and the replacement ratio of carbonated recycled fine aggregate (CRFA), the resistance to chloride ion permeability of CRAC was investigated by conducting tests in this paper. The results indicated that, compared with the non-carbonated recycled aggregate concrete (NCRAC), the electric flux of CRAC decreased by 9.14% to 37.34%. An increase in the replacement ratio of CRCA could reduce the resistance to chloride ion permeability of CRAC, while an increase in CRAC carbonation time had a significant effect on improving the resistance to chloride ion permeability. When the replacement ratio of CRCA was 100%, as the carbonation time increased from 0 to 14 days, the maximum reduction in electric flux of CRAC was 31.66%. With the same replacement ratio of CRCA, as the bending load level increased, the decrease in electric flux of CRAC showed an increasing trend compared to that of NCRAC. The resistance to chloride ion permeability of CRAC could be improved with an increase in carbonation temperature. Compared with the CRAC with carbonation temperature of 20 °C, the electric flux of the CRAC with carbonation temperature of 40 °C decreased by 11.03%. When the replacement ratio of CRFA was in the range of 0 to 20%, the resistance to chloride ion permeability of CRAC could be improved by incorporating CRFA, but the improvement effect was not significant. Therefore, compared with the NCRAC, the resistance to chloride ion permeability of CRAC is enhanced, and the research results can provide data support for the engineering application of CRAC.

Effect of Waste PET Fiber on the Mechanical Properties and Chloride Ion Penetration of Emergency Repair Concrete for Road Pavement.

This study evaluated the effects of adding waste PET fibers on the mechanical properties and chloride ion penetration of latex-modified ultra-rapid hardening cement concrete used for emergency road pavement repairs. The primary experimental variable was the content of waste PET fibers. The mechanical properties of the concrete were evaluated through compressive strength, flexural strength, and splitting tensile strength tests. Its durability was evaluated through chloride ion penetration, surface resistivity, and abrasion resistance tests. The experimental results were compared with the quality standards for emergency repair concrete set by the Korea Expressway Corporation. As a result, this study has enhanced the strength and resistance to chloride ions of latex-modified concrete by incorporating waste PET fibers. In the mixture with 3.84 kg/m3 of waste PET fibers, the compressive strength was 29.9 MPa at 4 h and 42.5 MPa at 28 curing days. The flexural strength was 6.0 MPa at 4 curing hours and 7.0 MPa at 28 days, and the splitting tensile strength was 4.5 MPa at 28 days of curing. The chloride ion permeability amount and abrasion depth were 1081C and 0.82 mm, respectively. The mixture with 3.84 kg/m3 of waste PET fibers has superior compressive strength, flexural strength, splitting tensile strength, chloride ion penetration, and surface resistivity compared to the mixture with 7.68 kg/m3. This result means that the waste PET fibers caused poor dispersion and fiber-balling within the concrete, leading to loose internal void structures when incorporated at 3.84 kg/m3. However, the abrasion resistance test showed better results for the mixture with 7.68 kg/m3 of waste PET fibers than the 3.84 kg/m3 mixture. Therefore, the test results indicated that 3.84 kg/m3 of waste PET fibers is the most effective for latex-modified concrete used in emergency road pavement repairs.