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Since the first isolation of graphene, the importance of van der Waals (vdW) interactions has become increasingly recognized in the burgeoning field of layered materials. In this work, infrared nanoimaging techniques and theoretical modeling are used to unravel the critical role played by interfacial vdW interactions in governing the stability of violet phosphorus (VP)—a recently rediscovered wide bandgap p‐type semiconductor—when exfoliated on different substrates. It is demonstrated that vdW interactions with the underlying substrate can have a profound influence on the stability of exfoliated VP flakes and investigate how these interactions are affected by flake thickness, substrate properties (e.g., substrate hydrophilicity, surface roughness), and the exfoliation process. These findings highlight the key role played by interfacial vdW interactions in governing the stability and physical properties of layered materials, and can be used to guide substrate selection in the preparation and study of this important class of materials. [ABSTRACT FROM AUTHOR]

Benzophenone (BP) and N‐vinylpyrrolidone (NVP) were used to modify the surface of polylactide (PLA) films by UV grafting method. The effects of light distance, temperature, reaction time, and modifier concentration on the structure and properties of PLA films were investigated by Fourier transform infrared spectroscopy, X‐ray photoelectron spectroscopy (XPS), nuclear magnetic resonance spectroscopy, differential scanning calorimetry (DSC), and universal testing machine (UTM). With BP and NVP UV grafting, the hydrophilicity of PLA films is improved, but their thermal and mechanical properties are reduced under different surface modification condition. Base on the principle of good surface hydrophilicity, better mechanical and thermal properties, the hydrolytic degradation performance of modified PLA films in artificial seawater at 70°C was studied by scanning electron microscopy, XPS and DSC. The research results show that the degradation of modified PLA films mainly occurs in the amorphous region, and the degradation process conforms to surface hydrolysis mechanism. The grafting modification of NVP is better than BP to accelerate the degradation process of PLA films in artificial seawater. The degradation of modified PLA undergoes water molecule erosion and autocatalytic degradation reaction. The degradation of BP‐PLA obeys the first‐order kinetics in part, while the degradation of NVP‐PLA is more complex. Therefore, surface hydrophilicity modification is an effective technique for improving the degradability of PLA. [ABSTRACT FROM AUTHOR]

Heterostructured interfaces are crucial to electrocatalysts for water splitting. Herein, coral‐like multiheterostructured NixB/Mo0.8B3 (NMB) nanorods encapsulated by a boron‐rich amorphous layer are prepared for water splitting. Density‐functional theory (DFT) calculations indicate that the NMB interface adjusts the d‐band center and electronic structure of the molybdenum sites. Owing to the strong electronic coupling between Ni, Mo, and B at the heterojunction, large number of exposed catalytic active sites, as well as the special hydrophilic characteristics endowed by the surrounding amorphous layer, the NMB catalyst exhibits remarkable universal‐pH hydrogen evolution reaction (HER) activity with low overpotentials (η) of 15, 26, and 83 mV to deliver 10 mA cm−2 in basic, acid, and neutral media, respectively, and outstanding oxygen evolution reaction (OER) characteristics in the basic medium with η10 and η500 of 170 and 420 mV, respectively. The unique self‐supporting 3D hierarchical interconnected structure facilitates mass transport thus leading to high mechanical stability for 450 and 200 h in HER and OER at ≈1000 mA cm−2. More importantly, the NMB exhibits excellent performance toward overall‐water electrolysis as a bifunctional catalyst with ultralow cell voltages of 1.45/1.56/1.85 V @ 10/100/1000 mA cm−2, demonstrating the large potential in industrial water splitting applications. [ABSTRACT FROM AUTHOR]

Replacing the sluggish oxygen evolution reaction with the oxidation of benzyl alcohol to construct the hybrid water electrolysis system has been attractive for its merits of environmentally friendly and economically efficient. However, the activity of the catalyst to oxidize alcohols needs to be further improved. Tailoring the d-band center (E d) has been proven as an effective method to promote the hydrogen evolution reaction (HER). How feasible is this strategy in the oxidation of benzyl alcohol? Here, using Co 2 C as a research platform, the doping nonmetal heteroatom (P, S, N) engineering is adopted to promote its electrocatalytic BA oxidation and HER performance. The results of electrochemical tests show that the P-doped Co 2 C (P–Co 2 C) only requires a low potential of 1.33 and 1.38 V vs. RHE to achieve current densities of 20 and 100 mA cm−2 for BA oxidation, which is superior to that of S–Co 2 C, N–Co 2 C, and pristine Co 2 C. The conversation and faradaic efficiency for BA is up to 98.1% and 93.8% during ten consecutive cycle tests. The P–Co 2 C also exhibited outstanding activity and stability toward HER. The density functional theory (DFT) calculation revealed that specified P doping could modify the d-band center of Co 2 C approaching the peak of the volcano map (electrochemical overpotentials ∼ E d). The Gibbs free energy of the BA oxidation was also reduced, thus optimizing the adsorption and desorption process of intermediates. On the other hand, the catalyst surface physical properties of Co 2 C such as hydrophilicity was promoted by the doped heteroatoms which was favorable for the gas-liquid-solid triphase electrocatalytic reaction. This work offers a facial perception of regulating the d-band to design advanced bifunctional electrocatalysts for organic matter oxidation and HER. The d-band center engineering was employed to boost the bifunctional electrocatalytic performance of X–Co 2 C (X = P, S, N). [Display omitted] • The X-doped Co 2 C (X = P, S, N) electrocatalysts were designed for BA oxidation and HER. • Among the prepared samples, the P–Co 2 C exhibited superior hydrophilicity and catalytic performance. • The P doping could change the d-band center of Co 2 C and optimize the adsorption/desorption process of intermediates. • The Gibbs free energy derived from the DFT was consistent with the order of electrochemical activity. [ABSTRACT FROM AUTHOR]

The detection of explosive materials, particularly nitroaromatic compounds such as 2,4,6‐trinitrotoluene (TNT), is critical for public safety and national security. Existing detection methods often require complex instrumentation, limiting their applicability for real‐time or in‐field use. Fluorescent sensors, which offer rapid and sensitive detection through fluorescence quenching, present a promising alternative. This study evaluates the performance of two pentiptycene‐based polymers, P‐1 and P‐2, in detecting explosive vapors, with a specific focus on their behavior under high‐humidity conditions. P‐2, modified with triethylene glycol groups, demonstrated significantly increased hydrophilicity compared to the commonly studied P‐1, as confirmed by contact angle measurements. Spectroscopic analysis revealed a blue shift in P‐2's UV–Vis absorption and photoluminescence spectra, indicating electronic property changes due to structural modifications. The enhanced hydrophilicity of P‐2 enabled it to maintain stable sensing performance under moist conditions, showing less than a 10% reduction in sensitivity, compared to the 20% decrease observed in P‐1. This superior moisture resistance suggests that P‐2 is a more robust and practical sensor for explosive detection in environments with variable humidity levels. [ABSTRACT FROM AUTHOR]

In this work, the structure of silica thin films synthesized with three different SiO2 precursors and obtained by the sol–gel method and dip coating technique was studied. Additionally, the influence of Ag addition on the obtained silica sols and then gel structure was investigated. Silica coatings show antireflective properties and high thermal resistance, as well as hydrophobic or hydrophilic properties. Three different silica precursors, TEOS (tetraethylorthosilicate), DDS (dimethyldietoxysilane) and AerosilTM, were selected for the synthesis. DDS added to silica sol act as a pore size modifier, while Ag atoms are known for their antibacterial activity. Coatings were deposited on two different substrates: steel and titanium, dried and annealed at 500 °C in air (steel substrate) and in argon (titanium substrate). For all synthesized films, IR (infrared) spectroscopic studies were performed together with GID and XRD (Grazing Incidence Diffraction, X-ray Diffraction) measurements. The topography and morphology of the surface were traced by SEM and AFM microscopic methods, providing information on the samples' roughness, particle sizes and thickness of the particular layers. The wetting angle values were also measured. GID and XRD measurements pointed to the distinct contribution of an amorphous phase in the samples, allowing us to recognize the crystalline phases and calculate the silver crystallite sizes. The FTIR spectra gave information on the first coordination sphere of the studied samples. [ABSTRACT FROM AUTHOR]

In order to prevent catheter-associated urinary tract infections caused by biofilm, in this study, polydopamine (PDA) was polymerized in the presence of ammonia on the surface of the silicone samples selected from the urinary catheters used in medicine. The OH groups in polydopamine were alpha-brominated by nucleophilic substitution reaction in the presence of α-bromoisobutyryl bromide. Then, poly (2-hydroxyethyl methacrylate) (PHEMA) was polymerized on the functionalized polydopamine by ATRP polymerization. PHEMA-PDA-coated catheter was evaluated at each step using attenuated total reflection-Fourier transform infrared (ATR-FTIR), scanning electron microscope, thermal gravimetric analysis, and atomic force microscopy, and its hydrophilicity was assessed by water contact angle. The contact angle of water decreases from 115° for uncoated catheter to 84° for PHEMA-PDA-catheter. PHEMA-PDA-coated catheter prevented Pseudomonas aeruginosa adhesion and colonization during 24 and 48 h and Escherichia coli during 24 h compared to the uncoated sample. It is concluded that functionalization of catheters with PDA-PHEMA appears as a favorable candidate for indwelling urinary catheters. [ABSTRACT FROM AUTHOR]

This study aimed to use a carboxybetaine methacrylate (CBMA) copolymer solution to surface treat 3D printed clear aligners at different fabrication stages, to impart antifouling properties, and assess the surface treatment at various fabrication stages' impact on physico-mechanical characteristics. Surface treatments using a blend of 2-hydroxyethyl methacrylate (HEMA) and CBMA, termed CCS, were performed at various stages of 3D printed clear aligner fabrication. Experimental groups, CB1, CB2, and CB3, were determined by the stage of surface treatment during post-processing. CB1, CB2, and CB3 received treatment before post-curing, after post-curing, and after post-processing, respectively. Untreated samples served as controls. Physical and mechanical properties were assessed through tensile testing, Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), and UV-Vis spectroscopy. The surface was further characterized through scanning electron microscopy and contact angle measurements. The cytotoxicity was assessed with 7-day elution and agar diffusion assays. Lastly, bacterial biofilm resistance was evaluated using confocal laser scanning microscopy. Crystal violet assay was performed using Streptococcus mutans. Surface treatment during CB1 stage exerted the most significantly unfavorable influence on properties of the 3D printed aligner resin. CB2 samples showed the maximum preservation of translucency even after 7-day aging. CB2 and CB3 phases showed enhanced hydrophilicity of sample surfaces with reduced adhesion of multispecies biofilm and S. mutans. Application of CCS surface treatment immediately after post-curing (CB2) can enhance the biofilm resistance of 3D printed clear aligners while maintaining high fidelity to optical translucency and constituent mechanical properties. [ABSTRACT FROM AUTHOR]

To evaluate the effects of dentin biomodification agents (Proanthocyanidin (PAC), Cardol (CD) and Cardol-methacrylate (CDMA) on dentin hydrophilicity by contact angle measurement, viability of dental pulp stem cells (DPSCs) and nanomechanical properties of the hybrid layer (HL). CDMA monomer was synthesized from cardol through methacrylic acid esterification. Human extracted third molars were used for all experiments. For nanomechanical tests, specimens were divided in four groups according to the primer solutions (CD, CDMA, PAC and control) were applied before adhesive and composite coating. Nanomechanical properties of the HL were analyzed by nanoindentation test using a Berkovich probe in a nanoindenter. Wettability test was performed on dentin surfaces after 1 min biomodification and measured by contact angle analysis. Cytotoxicity was assessed by a MTT assay with DPSCs after 48 and 72 h. Data were analyzed with Student's t test or Two-way ANOVA and Tukey HSD test (p < 0.05). CD and CDMA solutions achieved greater hydrophobicity and increased the water-surface contact angles when compared to PAC and control groups (p < 0.05). PAC group showed a greater reduction of elastic modulus in nanoindentation experiments when compared to CD and CDMA groups (p < 0.05) after 4 months of aging. CD inhibited cell proliferation compared to all further materials (p < 0.05), whilst CDMA and PAC indicated no cell cytotoxicity to human DPSCs. Cardol-methacrylate provided significantly higher hydrophobicity to dentin and demonstrated remarkable potential as collagen crosslinking, attaining the lowest decrease of HL's mechanical properties. Furthermore, such monomer did not affect pulp cytotoxicity, thereby highlighting promising feasibility for clinical applications. • Cell viability and dentin nanomechanical properties were surveyed for first time with collagen crosslinkers from CNSL. • Cardol and cardol-methacrylate as biomodification agents showed relevant reduction on dentin hydrophilicity. • Cardol and Cardol-methacrylate demonstrated promising reduction of hydrolytic degradation of the hybrid layer over time. • Cardol-methacrylate demonstrated no cell cytotoxicity in human DPSCs after 72 h. [ABSTRACT FROM AUTHOR]

This research aimed to synthesize polyvinyl fluoride membranes and coat them with tannic acid (TA) nanoparticles and polyethylene glycol (PEG) additives so that the membrane's removal efficacy for humic acid (HA) pollutant from agricultural wastewater was investigated. Thus, six membranes with PEG:TA ratios of 0:0, 1:0, 0:1, 1:1, 4:1, and 1:4 were synthesized. Then, the membranes' characteristics were identified by FTIR-ATR, FESEM, and AFM analysis, and HA's particle size and zeta potential were also investigated. Based on optimizing effective parameters, the operating pressure of 1.5 bar and HA concentration of 80 ppm were selected as optimal values. The membrane with PEG:TA = 4:1, as the optimally modified membrane, had a pure water flux of 446.03 L/m2.h, effluent flux of 72.43 L/m2.h, and pollutant removal rate of 86.62% at pH = 7 after 60 min had passed. These values for the pristine membrane (PEG:TA = 0:0) were 265.64 L/m2.h, 89.39 L/m2.h, and 75.59%, respectively. The results showed that although the effluent flux was lower in the optimized modified membrane than in the pristine membrane, HA removal percentage was increased. [ABSTRACT FROM AUTHOR]

Batteries play a crucial role in our daily lives, with separators being a key component influencing their functionality. The separators based on petrochemical for example polythene and polypropylene have been long favored for their chemical and thermal stability, their drawbacks in terms of sustainability, eco‐efficiency, and associated environmental risks are undeniable. In pursuit of sustainable development, there is a growing demand for biopolymer composite separators that offer a compelling combination of low cost, high mechanical and thermal stability, biodegradability, and renewability. Among these alternatives, cellulose‐derived separators have garnered significant attention from the scientific community. This review delivers a brief overview of cellulose's chemical structure, their types, delving into the intricate interplay of various electrodes and electrolytic solutions. The focus is then directed towards exploring diverse preparatory methods for cellulose‐derived separators, along with highlighting the promising factors associated with their adoption. Special attention is given to cellulose composite separators and the challenges they present. Highlights: Cellulose‐based composite separators in LIB/SIB batteries are discussed.Preparatory methods for eco‐friendly cellulose‐derived composite battery separators.Prominent affecting factors of separator performance have been elaborated.Special attention to the challenges cellulose composite separators present. [ABSTRACT FROM AUTHOR]

The complicated reaction pathway and slow electron-transfer kinetics of the oxygen evolution reaction (OER) have been identified as a critical bottleneck that restricts the overall performance of electrochemical water splitting. Metal oxyhydroxides have emerged as viable alternative catalysts as compared to the precious metal-based commercial benchmarks. Yet, the activity may be compromised by the instability of the layered structures. Herein, a simple two-step method is developed for the synthesis of Co–FeOOH electrocatalysts by thermal treatment of cobalt-containing zeolitic imidazolate framework (ZIF-L) deposited on the skeleton of NF (nickel foam) in the presence of FeSO 4 and urea. Co–FeOOH/NF, the thin nanosheet arrays exhibit a high specific surface area and high hydrophobicity. The addition of Co regulates the electronic environment around the Fe center, which optimizes the adsorption energy of intermediates and enhances the inherent OER activity of active sites. The Co–FeOOH nanoarrays show excellent OER performance and 99.7% Faradaic efficiency (FE). At current densities of 10 and 100 mA cm−2, there is a low overpotential of 208 and 249 mV, respectively at 1 M KOH. This kind of synthesis method will provide a promising approach for the construction of catalysts featuring stable structures for alkaline water oxidation. Promoting the decomposition of ZIF-L/NF to generate the thin nanoarrays Co–FeOOH/NF through in situ growth and ions exchange for high-performing and stable OER catalysts. [Display omitted] • Co–FeOOH was prepared by sacrificing ZIF templates through in situ growth and ions exchange. • Co–FeOOH/NF exhibits effective activity and stability at high current density of 100 mA cm−2. • Co–FeOOH/NF exhibits the thin structure of nanosheets with a high specific surface area, porosity and superhydrophobicity. • Partial amorphization of Co–FeOOH provides unsaturated sites promoting OER reaction from in situ Raman spectroscopy. [ABSTRACT FROM AUTHOR]

Polylactic acid (PLA) is one of promising biocompatible and biodegradable polyester. Poly(2-hydroxyethyl methacrylate) (PHEMA) is a polymer with good hydrophilicity. The hydrophilic PHEMA may improve PLA's amphiphilic properties. Hence, directly starting from hydroxyethyl methacrylate (HEMA), lactic acid (LA), maleic anhydride (MAH) and 2,2'-azobis(2-methyl-propionitrile) (AIBN), a series of new amphiphilic copolymers PLA20MHn were obtained through direct melt polycondensation (DMP) and subsequent free radical polymerization (FRP) in one pot. The results show that PLA20MHn can self-assemble in aqueous solution to form stable spherical micelles and dissolve hydrophobic pyrene molecules. What's more, The CMC value can be adjusted by the polymerization ratio. Therefore, this method is expected to further realize the encapsulation and controlled release of hydrophobic drug molecules for systemic circulation in vivo. [ABSTRACT FROM AUTHOR]

The microstructure and chemical properties of the corona discharge process could provide an effective method for predicting the performance of high-voltage cable insulation materials. In this work, the depth profile of the microstructure and chemical characteristics of corona discharge-treated PE were extensively investigated using Doppler broadening of position annihilation spectroscopy accompanied with positron annihilation lifetime spectroscopy, attenuated total reflectance Fourier transform infrared spectra, Raman spectra and contact angle measurement. By increasing corona discharge duration, the oxygen-containing polar groups, including hydroxyl, carbonyl and ester groups, strongly contribute to the deterioration of hydrophobicity and the enhancement of hydrophilicity. And the mean free volume size, with a broadening distribution, decreases slightly. The line shape S parameter decreases because of the decrease in free volume elements and the appearance of oxygen-containing groups. Also, the thickness of the degradation layer, determined from the S parameter with positron injection depth, increases and diffuses into the PE matrix. A linear S-W plot within the degradation layer of different corona treatment duration samples indicates the defect type does not change. The S parameter decreases and the W parameter increases with an increasing corona duration. Using a slow positron beam, the nondestructive probe can be used to profile the microstructure and chemical environment across the corona discharge damage depth, which is beneficial for investigating the surface and interfacial insulation materials. [ABSTRACT FROM AUTHOR]

The utilization of biopolymers incorporated with antimicrobial agents is extremely interesting in the development of environmentally friendly functional materials for food packaging and other applications. In this study, the effect of calcium oxide (CaO) on the morphological, mechanical, thermal, and hydrophilic properties as well as the antimicrobial activity of carboxymethyl chitosan (CMCH) bio-composite films was investigated. The CMCH was synthesized from shrimp chitosan through carboxymethylation, whereas the CaO was synthesized via a co-precipitation method with polyethylene glycol as a stabilizer. The CMCH-CaO bio-composite films were prepared by the addition of synthesized CaO into the synthesized CMCH using a facile solution casting method. As confirmed by XRD and SEM, the synthesized CaO has a cubic shape, with an average crystalline size of 25.84 nm. The synthesized CaO exhibited excellent antimicrobial activity against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) (>99.9% R). The addition of CaO into CMCH improved the mechanical and hydrophobic properties of the CMCH-CaO films. However, it resulted in a slight decrease in thermal stability. Notably, the CMCH-CaO10% films exhibited exceptional antimicrobial activity against E. coli (98.8% R) and S. aureus (91.8% R). As a result, such bio-composite films can be applied as an active packaging material for fruit, vegetable, or meat products. [ABSTRACT FROM AUTHOR]

Growing concerns regarding the presence of pharmaceuticals in wastewater necessitate their removal. Membrane filtration offers a promising approach. This study explores the development of biochar incorporated mixed matrix membranes (MMMs) for ciprofloxacin removal from water. Biochar, derived from the pyrolysis of agricultural waste, was blended with polyether sulfone (PES) and polyvinylpyrrolidone in varying ratios. The resulting MMMs exhibited progressively improved properties with increasing biochar content. Notably, membrane M11, comprising equal parts PES and biochar, displayed the highest porosity, lowest surface roughness (12.0), and lowest contact angle (31.05°), indicating enhanced hydrophilicity (increased by 58.19% compared to the biochar-free membrane). M11 effectively removed ciprofloxacin along with three additional antibiotics from different classes. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses corroborated the removal of ciprofloxacin. Furthermore, M11 demonstrated excellent regenerability, retaining over 57% removal efficiency after four cycles. These findings highlight the potential of M11 as a sustainable and cost-effective membrane for pharmaceutical removal from wastewater. [ABSTRACT FROM AUTHOR]

The slip behavior of crustal faults is known to be controlled by the composition of the fault gouge, but the exact mechanisms, especially considering the role of water‐rock interactions, are still under investigation. Here, we use a geochemical approach measuring the cation exchange capacity (CEC) of several phyllosilicate minerals and non‐clays, using CEC as a proxy for the ability to bind water to the mineral surfaces and/or develop electrostatic forces between particles. Laboratory shearing experiments show that low CEC materials (<3 mEq/100 g) tend to exhibit high friction, low cohesion, and velocity‐weakening frictional behavior. Phyllosilicate minerals exhibit CEC values up to 78 mEq/100 g and correspondingly lower friction coefficients, higher cohesion, and a tendency for velocity‐strengthening friction. Zeolite behavior is atypical, exhibiting a high CEC value typical of phyllosilicates but the strength and frictional characteristics of a non‐clay with low CEC. This suggests that the structure of the mineral is important for non‐phyllosilicates. For phyllosilicates, our results can be explained by water bound to mineral surfaces, creating bridges of hydrogen or van der Waals bonds between particles. The enhanced particle bonding for high CEC materials is consistent with high cohesion under zero effective stress conditions, and lowered friction by trapping bound water between the mineral surfaces under normal load. Bound water may explain the tendency for velocity‐strengthening friction in high CEC materials by hindering a Dieterich‐type time‐dependent frictional strengthening mechanism. Plain Language Summary: How faults in the Earth move and their potential for earthquakes is controlled by the types of minerals in the fault, but exactly how is still being studied. Here, we measured the cation exchange capacity (CEC) of several different minerals, including various platy‐shaped minerals, where CEC is used to measure a very small electrical charge on the mineral surfaces and how strongly the minerals attract and hold water. Laboratory shearing experiments show that low CEC materials tend to be strong, and become weaker when sheared faster. Platy minerals exhibit large CEC values and lower strength, and tend to become stronger when sheared faster. We suggest that mineral surface chemistry controls fault movement because high CEC materials have a stronger electrical charge, meaning they can hold large amounts of water on their surfaces. This water becomes trapped and reduces fault strength but can also hold the particles together depending on the stresses on the fault. The mineral zeolite does not fit the pattern shown by the other materials, having a high CEC seen in platy minerals, but the strength characteristics of a non‐platy mineral with low CEC. This suggests that grain shape is also important along with mineral surface charge. Key Points: For a wide range of mineral types, large cation exchange capacity (CEC) correlates with low friction, high cohesion, and velocity‐strengthening frictionThe mechanism for the observed patterns may be strong bond bridges between particles formed by water in high CEC materialsZeolite is an exception and is strong and velocity‐weakening despite high CEC, indicating that grain shape is also important [ABSTRACT FROM AUTHOR]

Polystyrene (PS) finds diverse applications across various fields, often necessitating a hydrophilic PS surface. In this study, the PS films were prepared using PS–toluene solutions of 15, 20, and 25 mass percentage concentrations (% w/v). Here, the main focus is on the influence of concentration on the hydrophilization of the prepared PS thin films under atmospheric pressure air dielectric barrier discharge plasma treatment. The contact angle, surface energy measurements, atomic force microscopy, and Fourier‐transform infrared spectroscopy analysis were conducted to evaluate the PS surface properties. Our results demonstrate, for the first time, the significant role of concentration in altering surface properties; the lower concentration of PS films leads to the most hydrophilic surface. Fourier‐transform infrared spectroscopy analysis confirms an increase in the OH functional group on the PS surface. atomic force microscopy analysis reveals needle‐shaped surface morphology, increased roughness and an expanded effective surface area. Surface energy analysis confirms an increase in the polar sector of surface energy. Overall, the findings from this research underscore the increase in film hydrophilicity with a decrease in PS–toluene concentration. Highlights: Polystyrene (PS)–toluene solutions with different concentrations were prepared.PS–toluene films were spin‐coated and were been treated with dielectric barrier discharge plasma.The contact angle, surface energy measurements, atomic force microscopy, and Fourier‐transform infrared spectroscopy analysis were conducted.PS films with lower concentration have more impact from plasma treatment.Concentration, impact the hydrophilicity and roughness of treated PS films. [ABSTRACT FROM AUTHOR]

Nanoparticles, considered building blocks of nanotechnology, are a topic of widespread research due to their extraordinary properties that are useful in diverse sectors. Among all nanoparticle types, TiO2 (anatase) has drawn the most attention, primarily because of its superhydrophilic properties and effective antibacterial actions. Its applications include self-cleaning of solid surfaces, treatment of water and air, production of clean energy, treatment of microbial infections, pesticide management, etc. making TiO2 a focal point of research in materials science. However, the lack of photosensitivity to visible light (>390 nm) reduces the scope for utilising TiO2 in photocatalytic processes. Therefore, most studies on TiO2 nanoparticles have focused on broadening their spectral sensitivity through band gap manipulation for effective photocatalysis under visible light. Researchers have doped/co-doped metals and non-metals, such as N, C, F, S, B, Cu, Fe, V, Pt, etc. to nano-TiO2 to shorten its band gap with varying degrees of success. This review paper mainly focuses on the mechanism and effectivity of N and Fe co-doped TiO2 nanoparticles. The progress of scientific research on TiO2 photocatalysis has introduced an array of new applications using TiO2 nanoparticles, and these applications have also been discussed in this article. [ABSTRACT FROM AUTHOR]

Inevitable leaching and corrosion under anodic oxidative environment greatly restrict the lifespan of most catalysts with excellent primitive activity for oxygen production. Here, based on Fick’ s Law, we present a surface cladding strategy to mitigate Ni dissolution and stabilize lattice oxygen triggering by directional flow of interfacial electrons and strong electronic interactions via constructing elaborately cladding‐type NiO/NiS heterostructure with controlled surface thickness. Multiple in situ characterization technologies indicated that this strategy can effectively prevent the irreversible Ni ions leaching and inhibit lattice oxygen from participating in anodic reaction. Combined with density functional theory calculations, we reveal that the stable interfacial O−Ni−S arrangement can facilitate the accumulation of electrons on surficial NiO side and weaken its Ni−O covalency. This would suppress the overoxidation of Ni and simultaneously fixing the lattice oxygen, thus enabling catalysts with boosted corrosion resistance without sacrificing its activity. Consequently, this cladding‐type NiO/NiS heterostructure exhibits excellent performance with a low overpotential of 256 mV after 500 h. Based on Fick's law, this work demonstrates the positive effect of surface modification through precisely adjusting of the oxygen‐sulfur exchange process, which has paved an innovative and effective way to solve the instability problem of anodic oxidation. [ABSTRACT FROM AUTHOR]

The graphite-resin composite bipolar plates prepared by the traditional hybrid pressing process exhibit poor conductivity, processability, and wettability due to the graphite flake layer being covered by resin, hindering the formation of a continuous conductive network, which significantly constrains their promotion and application in the field of proton exchange membrane fuel cells (PEMFC). In this paper, an ultra-thin flexible graphite/epoxy composite bipolar plates (BPs) with a thickness of only 0.775 mm is prepared followed by a process of flexible graphite preforming and impregnation curing. The hydrophilicity-modified BPs surface has a contact angle of 59.01° as well as flexural and compressive strengths of 11 MPa and 4 MPa and possesses a high in-plane conductivity of 380 S/cm and a low in-plane specific resistance of 6 mΩ cm2. The electrostack test results show that the hydrophilic runner channel is more conducive to the diffusion and spreading of H 2 O generated from the cathode-side reduction reaction in the flow channel, so that O 2 smoothly passes through the gas diffusion layer to participate in the reduction reaction of O 2 , and exhibits higher electric power at high current density, while the hydrophobically modified BPs has relatively poor overall performance due to ohmic losses. [Display omitted] • A hydrophilic flexible graphite bipolar plate with a contact angle of 59.01° is prepared. • The bipolar plates with excellent flexural strength of 11 MPa and a high in-plane conductivity of 380 S/cm. • The Electricstack has the best overall monolithic voltage and total power when the current density over 1800 mA/cm2. [ABSTRACT FROM AUTHOR]

Aqueous rechargeable Zn batteries offer a promising technological route as a safe and low‐cost energy storage system for grid energy storage. However, major challenges of Zn dendrites and parasitic side reactions upon cycling in aqueous environments remain unsolved. Here, a design of a bifunctional electrode interface consisting of heterostructured zinc hydroxide chloride (ZHC) and Cu, as well as their synergy in promoting high‐efficiency and low‐polarization Zn deposition is reported. Hydrophilic/zincophobic ZHC promotes the desolvation of hydrated Zn2+ prior to Zn nucleation, meanwhile adjacent Cu acts as a zincophilic site for subsequent nucleation and deposition. Consequently, the reduction polarization of Zn2+ at the bifunctional layer (ZHC‐Cu) features ten times lower nucleation overpotential of 3 mV than bare Zn. Meanwhile, the water‐induced hydrogen evolution side reactions on Zn are significantly hindered by the bifunctionality of the electrode interface. Accordingly, the ZHC‐Cu@Zn symmetric cells exhibit a superior cycling stability for over 3500 cycles at 10 mA cm−2/3 mAh cm−2. The ZHC‐Cu@Zn full‐cell with MnO2 cathode can stably operate for low C‐rate cycling with a high average Coulombic efficiency of 99.5% over 600 cycles. This work provides an effective approach to rational design of heterostructured bifunctional electrode interfaces to obtain high‐efficiency and low‐polarization Zn anodes. [ABSTRACT FROM AUTHOR]

Wettability is recognized as an important property of implant surfaces for ensuring improved biological responses. However, limited information exists on how bone grafting procedures including materials influence the hydrophilic behavior of implant surfaces. This in vitro study aimed to investigate the influence of two bovine grafting materials after hydration on the wettability of four different disk surfaces: commercially pure titanium (CP-Ti), titanium–zirconium dioxide (TiZrO2-Cerid®), zirconia (SDS®), and niobium. Wettability tests were performed on each of the four implant surfaces with a solution of 0.9% sodium chloride after mixture with W-boneTM (Group A) or Bio-Oss® (Group B) or 0.9% sodium chloride alone (Group C). In total, 360 contact angle measurements were completed with n = 30 per group. Statistical analysis was performed using a one-way analysis with variance (ANOVA) test with a significant mean difference at the 0.05 level. For pure titanium, Group A demonstrated increased hydrophilicity compared to Group B. Both TiZrO2 and zirconia showed significant differences for Groups A, B and C, exhibiting a decrease in hydrophilicity after the use of bovine grafting materials compared to titanium surfaces. Niobium remained consistently hydrophobic. In summary, this study revealed that bovine grafting materials may diminish the hydrophilicity of zirconia surfaces and exert varied effects on titanium and niobium. These findings contribute to the understanding of implant surface interactions with grafting materials, offering insights for optimizing biological responses in implantology. [ABSTRACT FROM AUTHOR]

The medical device market is a high-growth sector expected to sustain an annual growth rate of over 5%, even in developed countries. Daily, numerous patients have medical devices implanted or inserted within their bodies. While medical devices have significantly improved patient outcomes, as foreign objects, their wider use can lead to an increase in device-related infections, thereby imposing a burden on healthcare systems. Multiple materials with significant societal impact have evolved over time: the 19th century was the age of iron, the 20th century was dominated by silicon, and the 21st century is often referred to as the era of carbon. In particular, the development of nanocarbon materials and their potential applications in medicine are being explored, although the scope of these applications remains limited. Technological innovations in carbon materials are remarkable, and their application in medicine is expected to advance greatly. For example, diamond-like carbon (DLC) has garnered considerable attention for the development of antimicrobial surfaces. Both DLC itself and its derivatives have been reported to exhibit anti-microbial properties. This review discusses the current state of DLC-based antimicrobial surface development. [ABSTRACT FROM AUTHOR]

All‐day passive daytime radiative coolers (PDRC) offer a promising solution for energy‐free cooling of buildings and devices. This study investigates the use of various cellulose‐derivative networks to achieve optimal and stable cooling performance. These results showed that the mixed cellulose ester network has a maximum solar reflectance of 97%. While cellulose acetate network has a maximum infrared emissivity of 96% in the atmospheric transparency window band, which is a near‐perfect infrared emitter, the nitrocellulose network shows the highest cooling temperature, with a significant reduction of 14 °C from the ambient temperature and a power of 124 W·m−2 during the daytime and at night of 7.7 °C and 72.8 W·m−2. This study also analyzes the dampness's effect on the cooling performance of cellulose‐derivative networks. The cooling performance of the nitrocellulose network drops ≈ 3 °C (from 14 to 11.3 °C) when the relative humidity of the day exceeds ≈ 30% is observed. These findings indicate that the capacity of a material to absorb water from the surrounding air significantly influences its performance as a passive cooler, primarily due to changes in its optical properties. This is an important insight, as it highlights the need to consider environmental factors like relative humidity and sample hydrophobicity for PDRC systems. [ABSTRACT FROM AUTHOR]

The objective of this study was to evaluate the coating integrity performance and corrosion protection property of trimethylsilane (TMS) plasma nanocoatings that were directly deposited onto cobalt chromium (CoCr) L605 cardiovascular stents. Hydrophilic surfaces were achieved for the TMS plasma nanocoatings that were deposited onto the coronary stents through NH3/O2 (2:1 molar ratio) plasma post-treatment. With a coating thickness of approximately 20–25 nm, the TMS plasma nanocoatings were highly durable and able to resist delamination and cracking from crimping and expansion by a Model CX with a J-Crimp Station. The stent surface that was evaluated by Scanning Electron Microscopy (SEM) and Energy-Dispersive X-ray Spectroscopy (EDS) showed no indications of pitting, corrosion, or adsorption products on either the luminal or abluminal surfaces of the stents, in contrast to the uncoated stent surface. The TMS plasma nanocoatings significantly enhanced the stent's corrosion resistance in immersion experiments that followed the ASTM F2129-15 corrosion protocol, evident in the increase of the open circuit potential (OCP) from 0.01 V for the uncoated L605 stent to 0.18 V for the plasma-nanocoated L605 stent, reducing potential cytotoxic metal ion release. Cyclic polarization (CP) curves show that the corrosion rate (density level) observed in plasma-nanocoated L605 stents was approximately half an order of magnitude lower than that of the uncoated stents, indicating improved corrosion protection of the stents. CP curves of the TMS plasma-nanocoated stents with different coating thicknesses show that, in the range of 20–65 nm, the coating thickness does not result in any difference in the corrosion resistance of the stents. [ABSTRACT FROM AUTHOR]

This study introduces an innovative approach for enhancing oil–water emulsion separation using a polyethersulfone (PES) membrane embedded with a nanocomposite of graphene oxide (GO) and silver oxide (AgO). The composite membrane, incorporating PES and polyvinyl chloride (PVC), demonstrates improved hydrophilicity, structural integrity and resistance to fouling. Physicochemical characterization confirms successful integration of GO and AgO, leading to increased tensile strength, porosity and hydrophilicity. Filtration tests reveal substantial improvements in separating various oils from contaminated wastewater, with the composite membrane exhibiting superior efficiency and reusability compared to pristine PES membranes. This research contributes to the development of environmentally friendly oil–water separation methods with broad industrial applications. [ABSTRACT FROM AUTHOR]

Copyright of Advanced Textile Technology is the property of Zhejiang Sci-Tech University Magazines and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Advanced Textile Technology is the property of Zhejiang Sci-Tech University Magazines and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Abstract Batteries play a crucial role in our daily lives, with separators being a key component influencing their functionality. The separators based on petrochemical for example polythene and polypropylene have been long favored for their chemical and thermal stability, their drawbacks in terms of sustainability, eco‐efficiency, and associated environmental risks are undeniable. In pursuit of sustainable development, there is a growing demand for biopolymer composite separators that offer a compelling combination of low cost, high mechanical and thermal stability, biodegradability, and renewability. Among these alternatives, cellulose‐derived separators have garnered significant attention from the scientific community. This review delivers a brief overview of cellulose's chemical structure, their types, delving into the intricate interplay of various electrodes and electrolytic solutions. The focus is then directed towards exploring diverse preparatory methods for cellulose‐derived separators, along with highlighting the promising factors associated with their adoption. Special attention is given to cellulose composite separators and the challenges they present. Highlights Cellulose‐based composite separators in LIB/SIB batteries are discussed. Preparatory methods for eco‐friendly cellulose‐derived composite battery separators. Prominent affecting factors of separator performance have been elaborated. Special attention to the challenges cellulose composite separators present.

Abstract This research aimed to synthesize polyvinyl fluoride membranes and coat them with tannic acid (TA) nanoparticles and polyethylene glycol (PEG) additives so that the membrane’s removal efficacy for humic acid (HA) pollutant from agricultural wastewater was investigated. Thus, six membranes with PEG:TA ratios of 0:0, 1:0, 0:1, 1:1, 4:1, and 1:4 were synthesized. Then, the membranes’ characteristics were identified by FTIR-ATR, FESEM, and AFM analysis, and HA’s particle size and zeta potential were also investigated. Based on optimizing effective parameters, the operating pressure of 1.5 bar and HA concentration of 80 ppm were selected as optimal values. The membrane with PEG:TA = 4:1, as the optimally modified membrane, had a pure water flux of 446.03 L/m2.h, effluent flux of 72.43 L/m2.h, and pollutant removal rate of 86.62% at pH = 7 after 60 min had passed. These values for the pristine membrane (PEG:TA = 0:0) were 265.64 L/m2.h, 89.39 L/m2.h, and 75.59%, respectively. The results showed that although the effluent flux was lower in the optimized modified membrane than in the pristine membrane, HA removal percentage was increased.

Abstract Growing concerns regarding the presence of pharmaceuticals in wastewater necessitate their removal. Membrane filtration offers a promising approach. This study explores the development of biochar incorporated mixed matrix membranes (MMMs) for ciprofloxacin removal from water. Biochar, derived from the pyrolysis of agricultural waste, was blended with polyether sulfone (PES) and polyvinylpyrrolidone in varying ratios. The resulting MMMs exhibited progressively improved properties with increasing biochar content. Notably, membrane M11, comprising equal parts PES and biochar, displayed the highest porosity, lowest surface roughness (12.0), and lowest contact angle (31.05°), indicating enhanced hydrophilicity (increased by 58.19% compared to the biochar-free membrane). M11 effectively removed ciprofloxacin along with three additional antibiotics from different classes. Fourier-transform infrared spectroscopy and X-ray photoelectron spectroscopy analyses corroborated the removal of ciprofloxacin. Furthermore, M11 demonstrated excellent regenerability, retaining over 57% removal efficiency after four cycles. These findings highlight the potential of M11 as a sustainable and cost-effective membrane for pharmaceutical removal from wastewater.

[Display omitted] • Three pyrene-based COFs are developed for the overall photosynthesis of H 2 O 2. • The wettability and charge separation are optimized by the introduction of functional groups into the COF skeleton. • PyCOF-OH exhibits superior H 2 O 2 production efficiency compared to PyCOF-F and PyCOF-H. • Further, the photocatalytic mechanism is clarified with both the ORR and WOR pathways. • Remarkably, good recyclability has been demonstrated for the PyCOF-OH photocatalyst. Covalent organic frameworks (COFs) have shown great potential in the photocatalytic production of hydrogen peroxide (H 2 O 2) due to their precisely designed and customized ability. Nevertheless, the quest for efficient overall photosynthesis of H 2 O 2 in pure water without sacrificial agents using COF photocatalysts remains a formidable challenge. Herein, three pyrene-based covalent organic frameworks are synthesized using an advanced interfacial design strategy. By incorporating functional groups of F, H, and OH into a COF skeleton, their wettability and charge-separation properties are fine-tuned. These COFs show great performances as photocatalysts for H 2 O 2 production from water and air by utilizing both the oxygen reduction reaction and water oxidation reaction pathways. Compared to PyCOF-F and PyCOF-H, PyCOF-OH demonstrates superior H 2 O 2 production efficiency due to its improved hydrophilicity and enhanced carrier separation, achieving a remarkable rate of 2961 µmol g−1 h−1 from 25 mL pure water and air. Further, the mechanism of H 2 O 2 production over PyCOF-OH is clarified by combining a series of control experiments, in situ characterizations, and theoretical calculations. This study offers valuable insights into the interfacial design of high-performance photocatalysts for H 2 O 2 synthesis. [ABSTRACT FROM AUTHOR]

Hydrogen is a renewable and environmentally friendly energy carrier and is considered a viable alternative to fossil fuels. Consequently, developing electrodes with excellent hydrogen evolution electrocatalysis is a top priority in research. However, the use of flat electrodes as cathode substrates by most researchers limits the electrocatalytic active area of the prepared electrode. To address this issue, it is essential to prepare a micro-nano structure on a cathode substrate before electrodeposition. This study introduced a novel Ni nanocone/Grid electrode, obtained through a combined laser-electrodeposition process to investigate its electrocatalytic activity and stability for the hydrogen evolution reaction (HER). Various techniques, including linear sweep voltammetry (LSV), electrochemical impedance spectra (EIS), cyclic voltammetry (CV), and chronopotentiometry (CP) in 1 M KOH solution, were employed to assess the HER electrocatalytic performance of the Ni nanocone/Grid electrodes. The experimental results demonstrated that the electrodes could achieve current densities of -10, -20, and -100 mA/cm2 with corresponding overpotentials of -281, -308, and -390 mV, respectively. Additionally, the Tafel slope of these electrodes was found to be only -82.05 mV/dec. The enhanced catalytic performance of the electrode was attributed to the synergistic effect of the grid-like and nanocone structures, which significantly increased the electrocatalytically active area and improved surface hydrophilicity, thereby boosting electrocatalytic performance. The simplicity of the preparation method and the exceptional performance of the electrode provide a promising new avenue for future research on HER electrocatalysts. • A new laser-electrodeposition combined process was proposed to prepare the catalytic electrode for hydrogen evolution. • Ni nanocone/Grid showed low overpotential and Tafel slope for hydrogen evolution. • The combination of grid structure and nanocone can significantly increase the ECSA of the electrode. • The electrode shows excellent hydrophilicity and extraordinary durability. [ABSTRACT FROM AUTHOR]

Factors affecting the swelling of cellulosic fibers are considered in this review. Emphasis is placed on aqueous systems and papermaking fibers, but the review also considers cellulose solvent systems, nanocellulose research, and the behavior of cellulosic hydrogels. The topic of swelling of cellulosic fibers ranges from effects of humid air, continuing through water immersion, and extends to hydrogels and the dissolution of cellulose, as well as some of its derivatives. The degree of swelling of cellulose fibers can be understood as involving a balance between forces of expansion (especially osmotic pressure) vs. various restraining forces, some of which involve the detailed structure of layers within the fibril structure of the fibers. The review also considers hornification and its effects related to swelling. The expansive forces are highly dependent on ionizable groups, pH, and the ionic strength of solution. The restraining forces depend on the nature of lignin, cellulose, and their detailed structural arrangements.

Polyvinylidene Fluoride (PVDF) membranes were modified with quaternized graphene oxide (QGO) synthesized from graphene oxide and quaternized ammonium groups. PVDF/QGO membranes were created by blending PVDF and 0.01-0.05 g QGO via phase inversion. FTIR confirmed the successful QGO incorporation. PVDF/QGO membranes exhibited increased mechanical stiffness. Meanwhile, SEM revealed asymmetric morphology with surface and internal pores. AFM showed the membrane with 0.05 g and QGO had the highest surface roughness of 101.2 nm, which increased filtration area and flux. QGO improved hydrophilicity through hydroxyl and quaternary ammonium groups, enhancing water flux up to 1208 Lm?2h?1 for 0.05 g QGO. Cu2+ rejection increased to 75% for 0.05 g QGO membrane due to chelation and adsorption effects. PVDF/QGO membranes displayed bacterial growth inhibition, unlike pristine PVDF. The inhibition zone diameter increased with more QGO, indicating improved antibacterial activity. Overall, this study demonstrated that QGO improved PVDF membranes' hydrophilicity, antibacterial properties, and mechanical strength.

The study of the properties of clay minerals and the creation of innovative drilling fluids based on them are extremely important aspects for improving the processes of extraction of natural resources, reducing operating costs, and increasing the energy efficiency of industrial operations. The purpose of this study was to explore the possibilities of developing a composition of drilling fluids based on the investigation of the properties of clay minerals for drilling and maintenance of wells in the conditions of the Gubadag deposit located in Turkmenistan. Statistical methods, experiments, and analysis were used in the course of the work. The results of the study showed that clay from the Gubadag deposit is characterised by low hydrophilicity and weakened structural stability, which is manifested in limited hydration energy and high filtration permeability. This leads to low viscosity, rheological, and structural-mechanical parameters of natural solutions. It follows from this that Gubadag clay is classified as a low-quality material. The prepared solutions from the above samples on different types of water have volumes in the range of 2-3 m³. However, after treating sea water with caustic soda, sample No. 2 generates more than 4 m³ of solution, significantly different from other samples. This highlights the need for additional research to optimise drilling fluid formulae, since it is important to determine the effect of clay materials on the properties of solutions and develop more adapted formulae that consider the specifics of the material and the conditions of its use in drilling wells. The practical significance of the results obtained lies in a significant improvement in the efficiency of drilling and maintenance of wells in regions with difficult geological conditions, offering new methods for preparing drilling fluids.

Abstract Background Hemodialyzers should efficiently eliminate small and middle molecular uremic toxins and possess exceptional hemocompatibility to improve well-being of patients with end-stage kidney disease. However, performance and hemocompatibility get compromised during treatment due to adsorption of plasma proteins to the dialyzer membrane. Increased membrane hydrophilicity reduces protein adsorption to the membrane and was implemented in the novel FX CorAL dialyzer. The present randomized controlled trial compares performance and hemocompatibility profiles of the FX CorAL dialyzer to other commonly used dialyzers applied in hemodiafiltration treatments. Methods This prospective, open, controlled, multicentric, interventional, crossover study randomized stable patients on post-dilution online hemodiafiltration (HDF) to FX CorAL 600, FX CorDiax 600 (both Fresenius Medical Care) and xevonta Hi 15 (B. Braun) each for 4 weeks. Primary outcome was β2-microglobulin removal rate (β2-m RR). Non-inferiority and superiority of FX CorAL versus comparators were tested. Secondary endpoints were RR and/or clearance of small and middle molecules, and intra- and interdialytic profiles of hemocompatibility markers, with regards to complement activation, cell activation/inflammation, platelet activation and oxidative stress. Further endpoints were patient reported outcomes (PROs) and clinical safety. Results 82 patients were included and 76 analyzed as intention-to-treat (ITT) population. FX CorAL showed the highest β2-m RR (76.28%), followed by FX CorDiax (75.69%) and xevonta (74.48%). Non-inferiority to both comparators and superiority to xevonta were statistically significant. Secondary endpoints related to middle molecules corroborated these results; performance for small molecules was comparable between dialyzers. Regarding intradialytic hemocompatibility, FX CorAL showed lower complement, white blood cell, and platelet activation. There were no differences in interdialytic hemocompatibility, PROs, or clinical safety. Conclusions The novel FX CorAL with increased membrane hydrophilicity showed strong performance and a favorable hemocompatibility profile as compared to other commonly used dialyzers in clinical practice. Further long-term investigations should examine whether the benefits of FX CorAL will translate into improved cardiovascular and mortality endpoints. Trial registration eMPORA III registration on 19/01/2021 at ClinicalTrials.gov (NCT04714281).

In this research, a straightforward template method was utilized to fabricate a superhydrophilic ethylene-vinyl acetate copolymer (EVA)/nitrile-butadiene rubber (NBR) thermoplastic vulcanizate (TPV) surface where the paper sheet was used as template. Organic modified montmorillonite (OMMT) powder was introduced in order to improve the superhydrophilic response rate of the TPV surface. Investigations were conducted to research the durability and the self-cleaning behavior of the TPV surface, as well as to explore its potential application in the separation of oil-water and oil-oil mixtures. Experimental results demonstrated that the EVA/NBR/OMMT TPV (mass ratio 20/80/7) surface molded with No. 1000 paper sheet exhibited the excellent superhydrophilic property, which could achieve a contact angle of 0.0° within 5.5 s and had a surface energy of 35.6 mN·m–1. The superhydrophilic surface displayed the remarkable durability and the evident self-cleaning behavior; moreover, it could exhibit the significant difference in the critical pressure data for various liquids, suggesting the promising application in the field of oil-water and oil-oil separation.

Introduction: Wet oral environment may have deleterious effects on performance of the composites due to influences of water sorption and solubility. The study evaluated the hydrolytic degradation caused because of water sorption and solubility of silorane and methacrylate-based dental composites. Methods: Ten disc samples (2 mm × 10 mm) were prepared. Samples were analyzed for water solubility and sorption according to ISO 4049:2000 regulations and tested for mass gain or loss following immersion in water or in artificial saliva at 1 day, 15 days, and 30 days period. Student’s ‘t’ test, repeated measures analysis of variance (ANOVA), and Tukey’s post-hoc tests determined statistical significance of the experimental results with global significance set at P = 0.05. Results: Considerable sorption and solubility was observed with time in both materials on immersion. Silorane composites showed lower water sorption and solubility than methacrylate-based composite (MBC). Artificial saliva demonstrated higher sorption and solubility compared to distilled water. Conclusion: Silorane composites display enhanced hydrolytic stability even after a month of immersion in contrast to conventional methacrylate-based composites (MBCs), making it a better alternative to MBC resins clinically.

The problem of membrane fouling remains a significant concern in ultrafiltration, a commonly employed method in water treatment due to its high efficacy and minimal energy consumption. This study made a nanocomposite ultrafiltration membrane out of MXene Ti3C2 nanosheets, a new two-dimensional material, to improve the antifouling properties of PVDF membranes. It was possible to incorporate the nanosheets into the membrane structure through in situ embedment during the phase inversion process. To learn more about them, the study investigated the membranes using FESEM, FTIR, water contact angle (CA), and porosity measurements. The application of common flux and rejection tests assessed the manufactured membranes' performance. Adding MXene Ti3C2 to membranes made them less hydrophobic than the original membrane that wasn't mixed with anything else. The porosity and pore size of the membrane exhibit an increase in the MXene ratio. The mixed matrix membrane containing 0.5 wt% of Ti3C2 (M3) exhibited the lowest contact angle (CA). The modification of membrane characteristics has a positive impact on their overall performance. The membrane exhibiting the greatest porosity, specifically 0.5 wt% of Ti3C2, N5, demonstrated the highest flux rates for pure water and protein solution, measuring 538 L/m2.h and 467.8 L/m2.h, respectively. The membrane with the highest hydrophilicity, which was labeled as M3, had much better protein rejection and flux recovery rates than the pure membrane. Specifically, the recorded values for M3 were 96.6, whereas the corresponding values for the pristine membrane were 59.6. MXene Ti3C2 has some interesting properties, such as better water permeability, protein rejection, and excellent antifouling abilities, which makes it a possible material for changing antifouling membranes.

Bone tissue engineering shows potential for regenerating or replacing damaged bone tissues by utilizing biomaterials renowned for their biocompatibility and structural support capabilities. Among these biomaterials, polycaprolactone (PCL) and polylactic acid (PLA) have gained attention due to their biodegradability and versatile applications. However, challenges such as low degradation rates and poor mechanical properties limit their effectiveness. Dimethyl sulfone (DMSO2) has emerged as a potential additive to address these limitations, offering benefits such as reduced viscosity, increased degradation time, and enhanced surface tension. In this study, we investigate tailored composites comprising PLA, PCL, and DMSO2 to enhance mechanical properties and hydrophilicity. Through material characterization and mechanical testing, we found that the addition of DMSO2 led to improvements in the yield strength, modulus, and hydrophilicity of the composites. PCL and DMSO2 10, 20, and 30 wt% were premixed, and 20 wt% PCL + 10, 20, and 30 wt% DMSO2 were mixed with PLA. Specifically, PLA/PCL/DMSO2 composites exhibited higher yield strengths and moduli compared to pure PLA, pure PCL, and PLA/PCL composites. Moreover, the hydrophilicity of the composites increased with DMSO2 concentration, facilitating cell attachment. Fourier-transform infrared spectroscopy (FTIR) confirmed the presence of –COOH and –COH bands in PLA/PCL/DMSO2 composites, indicating chemical interactions between DMSO2 and the polymer matrix. Fractography analysis revealed enhanced interface adhesion in PLA/PCL/DMSO2 composites due to the hydrogen bonding. Overall, this study demonstrates the potential of PLA/PCL/DMSO2 composites in bone tissue engineering applications, offering improved mechanical properties and enhanced cell compatibility. The findings contribute to the advancement of biomaterials for additive manufacturing in tissue engineering and regenerative medicine. [ABSTRACT FROM AUTHOR]

Background: Hemodialyzers should efficiently eliminate small and middle molecular uremic toxins and possess exceptional hemocompatibility to improve well-being of patients with end-stage kidney disease. However, performance and hemocompatibility get compromised during treatment due to adsorption of plasma proteins to the dialyzer membrane. Increased membrane hydrophilicity reduces protein adsorption to the membrane and was implemented in the novel FX CorAL dialyzer. The present randomized controlled trial compares performance and hemocompatibility profiles of the FX CorAL dialyzer to other commonly used dialyzers applied in hemodiafiltration treatments. Methods: This prospective, open, controlled, multicentric, interventional, crossover study randomized stable patients on post-dilution online hemodiafiltration (HDF) to FX CorAL 600, FX CorDiax 600 (both Fresenius Medical Care) and xevonta Hi 15 (B. Braun) each for 4 weeks. Primary outcome was β2-microglobulin removal rate (β2-m RR). Non-inferiority and superiority of FX CorAL versus comparators were tested. Secondary endpoints were RR and/or clearance of small and middle molecules, and intra- and interdialytic profiles of hemocompatibility markers, with regards to complement activation, cell activation/inflammation, platelet activation and oxidative stress. Further endpoints were patient reported outcomes (PROs) and clinical safety. Results: 82 patients were included and 76 analyzed as intention-to-treat (ITT) population. FX CorAL showed the highest β2-m RR (76.28%), followed by FX CorDiax (75.69%) and xevonta (74.48%). Non-inferiority to both comparators and superiority to xevonta were statistically significant. Secondary endpoints related to middle molecules corroborated these results; performance for small molecules was comparable between dialyzers. Regarding intradialytic hemocompatibility, FX CorAL showed lower complement, white blood cell, and platelet activation. There were no differences in interdialytic hemocompatibility, PROs, or clinical safety. Conclusions: The novel FX CorAL with increased membrane hydrophilicity showed strong performance and a favorable hemocompatibility profile as compared to other commonly used dialyzers in clinical practice. Further long-term investigations should examine whether the benefits of FX CorAL will translate into improved cardiovascular and mortality endpoints. Trial registration: eMPORA III registration on 19/01/2021 at ClinicalTrials.gov (NCT04714281). [ABSTRACT FROM AUTHOR]

Climate change incurred by the increasing amount of CO2 released into the atmosphere has become a global priority, and triggers the development of carbon capture, utilization, and storage. Low energy requirement and cost by employing moisture swing process make quaternary ammonium-based materials applicable for CO2 capture. The moisture-sensitive sorbents suffer decreased CO2 affinity and cyclic capacities with moderate or high humidity, while water vapor ubiquitously exists in flue gas or ambient air. The effect of applying electric field on CO2 adsorption, especially the water-involved proton transfer step, by quaternary ammonium-based sorbents in the existence of water, is analyzed. The discrepancy in the hydrophilicity between reactant and product species is enhanced by the electric field, which indicates more favorable chemisorption. Thermodynamics of CO2 adsorption coupling interfacial water evaporation under the electric field are depicted with changes of enthalpy and free energy calculated. Therefore, the rationality of electric field enhanced CO2 capture of quaternary ammonium-based sorbents in moist circumstance is theoretically validated, providing the methodology of optimizing moisture swing adsorption from process intensification apart from material design. [ABSTRACT FROM AUTHOR]

Factors affecting the swelling of cellulosic fibers are considered in this review. Emphasis is placed on aqueous systems and papermaking fibers, but the review also considers cellulose solvent systems, nanocellulose research, and the behavior of cellulosic hydrogels. The topic of swelling of cellulosic fibers ranges from effects of humid air, continuing through water immersion, and extends to hydrogels and the dissolution of cellulose, as well as some of its derivatives. The degree of swelling of cellulose fibers can be understood as involving a balance between forces of expansion (especially osmotic pressure) vs. various restraining forces, some of which involve the detailed structure of layers within the fibril structure of the fibers. The review also considers hornification and its effects related to swelling. The expansive forces are highly dependent on ionizable groups, pH, and the ionic strength of solution. The restraining forces depend on the nature of lignin, cellulose, and their detailed structural arrangements. [ABSTRACT FROM AUTHOR]

The surface treatment for a polymer‐ceramic composite is additionally performed in advanced material industries. To prepare the composite without a surface treatment, the simplest way to manufacture an advanced ceramic‐particle is devised. The method is the formation of a nanocrystalline composite layer through the simple liquid‐phase sintering. Using magnesia (MgO) which shows hydrophilicity, a nanocrystalline surface layer is realized by liquid‐phase sintering. The amorphous matrix of nanocrystalline composite layer makes MgO hydrophobic and ensures miscibility with polymers, and the nanocrystalline MgO ensures high thermal conductivity. In addition, the liquid phase removes the open pores and makes the surface morphology smooth MgO with smooth surface (MgO‐SM). Thermal interface materials (TIM) prepared with MgO‐SM and epoxy show a high thermal conductivity of ≈7.5 W m−1K−1, which is significantly higher than 4.5 W m−1K−1 of pure MgO TIM. Consequently, the formation process of a nanocrystalline surface layer utilizing simple liquid‐phase sintering is proposed as a fabrication method for a next‐generation ceramic‐filler. In addition, it is fundamentally identified that the thermal conductivity of MgO depends on the Mg deficiency, and therefore a poly‐crystal MgO‐SM (produced at a low temperature) has a higher thermal conductivity than a single‐crystal MgO (produced at a high temperature). [ABSTRACT FROM AUTHOR]

The present study investigates the effects of Er3+ doping content on the microstructure and up-conversion emission properties of CaTiO3: Er3+ phosphors as a potential material in biomedical applications. The CaTiO3: x%Er3+ (x = 0.5, 1.0, 1.5, 2.0, 2.5, and 3.0%) films were synthesized on Ti substrates by a hydrothermal reaction at 200 °C for 24 h. The SEM image showed the formation of cubic nanorod CaTiO3: Er3+ films with a mean edge size value of (1–5) μm. When excited with 980 nm light, the CaTiO3: Er3+ films emitted a strong green band and a weak red band of Er3+ ions located at 543, 661, and 740 nm. The CaTiO3: Er3+ film exhibited excellent surface hydrophilicity with a contact angle of ~zero and good biocompatibility against baby hamster kidney (BHK) cells. CaTiO3: Er3+ films emerge as promising materials for different applications in the biomedical field. [ABSTRACT FROM AUTHOR]

In this work, an effort has been made to show that a cold atmospheric pressure plasma (CAPP) can be applied to promote the growth and development of wheat seedlings. A dielectric barrier discharge (DBD) plasma-based reactor has been developed having two-roller conveyor rollers running on sprockets to generate cold plasma. Wheat seeds (Triticum aestivum) are treated with cold plasma for shorter durations to examine their germination parameters. In the cold plasma, reactive oxygen and nitrogen species (RONS) are generated which alter the surface of the seeds. This results in enhanced germination, growth, and enduring vitality of the plants enhance seed germination. After plasma treatment, the germination rate was enhanced from 84% to 98%. Also, after treatment surfaces of wheat seeds became more hydrophilic, as confirmed by a decrease in the water contact angle which results in higher seed germination. It is inferred that plasma is a viable alternative to the conventional pre-sowing seed treatment for germination due to its uniform treatment without degradation and the use of pesticides. [ABSTRACT FROM AUTHOR]