Hydrophilic Properties Research Articles

Negative expansion induced anti-abrasive self-cleaning coatings for enhancing output of solar panels

Pollutants on solar panels impede sunlight absorption, leading to a reduction in their output power. Superhydrophilic coatings exhibit effective self-cleaning performance as droplets fully spread on their surfaces. However, one challenge for the commercial development of transparent superhydrophilic coatings is poor abrasion resistance. Frictional heating on the coatings’ surface causes the abrasion force to rise uncontrollably, which in turn causes the coatings to either fracture or wear catastrophically. A promising alternative is utilizing novel adaptive materials with a negative thermal expansion coefficient in the coating. The compressive stress on the surface of the coating with negative expansion will enhance its abrasion resistance. Here, we demonstrate a method to achieve compressive stress in the coating by incorporating halloysite (HNTs) nanotubes due to their negative expansive behavior. Hydrolyzed tetraethyl orthosilicate (TEOS) combines HNTs nanotubes with SiO2 nanoparticles, thus forming a hard nano-composite unit. Meanwhile, amino resin and acrylic resin as adhesives participate in constructing the coating’s three-dimensional network structure. The surfactant sodium alkenyl sulfonate (AOS) endows the coating with superhydrophilicity. As a result, the nano-composite (NC) coating shows superior superhydrophilicity and anti-abrasive properties. The NC coating retains good hydrophilicity and self-cleaning properties after 2000 cycles of Taber abrasion loading 250 g or 1000-line cycles of steel wool friction loading 500 g. The self-cleaning performance of the robust NC coating on solar panels can improve the output power by up to 33.65 % after 296 days. Hence, introducing shrinkage components such as HNTs may provide a general strategy for developing robust superhydrophilic coatings.

Sustainable lignosulfonate-modified PA6.6 fabrics to improve durable flame retardancy, hydrophilicity and mechanical performance

Creating durable flame retardancy, enhanced mechanical performance, and hydrophilic polyamide 6.6 (PA6.6) textiles via cost-effectiveness from sustainable renewable sources is a considerable challenge. This study introduces a pretreatment process involving the application of sodium lignosulfonate (LS) to the surface of PA6.6 fabrics, thereby enhancing their hydrophilic and flame-retardant properties. Subsequently, a layer-by-layer (LbL) nanocoating treatment is employed, utilizing renewable polyelectrolytes—chitosan (CS), LS, and poly (sodium phosphate) (PSP)—to create 8-bilayer (BL) and 4-quarda layer (QL) structures that further improve the hydrophilicity and durable flame resistance of PA6.6 fabrics. The combined LS-modified and LbL coatings notably increased the limiting oxygen index (LOI) values from 19.5 % to 22.5 %, eliminated melt dripping, and secured a V-1 rating in the vertical burning (UL-94) tests. Moreover, the treated fabrics exhibited a 43 % reduction in the peak heat release rate (PHRR) and a lower fire growth rate (FGR) of 0.84 W/g·s, with a significant increase in char yield% in both air and nitrogen (N2) atmospheres. A cross-linked network structure is responsible for the superior hydrophilicity, enhanced tensile strength, and fabric softening properties. The self-crosslinking of sulfur-containing radicals with amide units ensures an anti-dripping performance that can withstand up to 30 home laundering cycles, demonstrating remarkable washing durability. However, a convincing approach has been developed for sustainable and high-performance materials for the textile industry, and a simple LbL technique using renewable polyelectrolytes that have traditionally been utilized in water treatment and food processing has been developed.

Classical Simulations on Quantum Computers: Interface-Driven Peptide Folding on Simulated Membrane Surfaces

Background:Antimicrobial peptides (AMPs) are crucial in the fight against infections and play significant roles in various health contexts, including cancer, autoimmune diseases, and aging. A key aspect of AMP functionality is their selective interaction with pathogen membranes, which often exhibit altered lipid compositions. These interactions are thought to induce a conformational shift in AMPs from random coil to alpha-helical structures, essential for their lytic activity. Traditional computational approaches have faced challenges in accurately modeling these structural changes, especially in membrane environments, thereby opening and opportunity for more advanced approaches. Method:This study extends an existing quantum computing algorithm, initially designed for peptide folding simulations in homogeneous environments, to address the complexities of AMP interactions at interfaces. Our approach enables the prediction of the optimal conformation of peptides located in the transition region between hydrophilic and hydrophobic phases, resembling lipid membranes. The new method was tested on three 10-amino-acid-long peptides, each characterized by distinct hydrophobic, hydrophilic, or amphipathic properties, across different media and at interfaces between solvents of different polarity. Results:The developed method successfully modeled the structure of the peptides without increasing the number of qubits required compared to simulations in homogeneous media, making it more feasible with current quantum computing resources. Despite the current limitations in computational power and qubit availability, the findings demonstrate the significant potential of quantum computing in accurately characterizing complex biomolecular processes, particularly AMP folding at membrane models. Conclusions:This research highlights the promising applications of quantum computing in biomolecular simulations, paving the way for future advancements in the development of novel therapeutic agents. We aim to offer a new perspective on enhancing the accuracy and applicability of biomolecular simulations in the context of AMP interactions with membrane models.

Aminomethanesulfonic acid grafted polyamidoxime fibers with hydrophilicity, salt-tolerance and antimicrobial properties for highly efficient uranium extraction from seawater

Uranium extraction from seawater plays a key role in redefining the declining uranium reserves to afford sustainable nuclear power. However, it is an urgent need to develop adsorbents simultaneously possessing enhanced efficiency, collect ability, salt resistance, antibacterial properties and economy to massively extract uranium from seawater. Herein, aminomethanesulfonic acid grafted polyamidoxime fibers (PAO-AMS-A) with hydrophilicity, salt resistance and antibacterial properties were prepared. The resulting fibers display high salt resistance and high uranium uptake capacity, providing the fibers a very high adsorption efficiency of 554.09 mg g−1 in pure uranium solution, 205.43 mg g−1 and 473.44 mg g−1 in 8 ppm and 20 ppm uranium spiked seawater and 10.04 mg g−1 in real seawater, respectively. Furthermore, the material exhibited good salt tolerance, and the uranium adsorption capacity was still as high as 597.97 mg g−1 in high concentrations of NaCl solution. Note that PAO-AMS-A has also good antibacterial activity, the antibacterial rate against bacteriais cultured in seawater is up to 93.49 %. Overall, PAO-AMS-A fibers are promising in industrial uranium extraction from seawater due to their high adsorption efficiency, salt resistance and antimicrobial properties.

Anchoring ultrafine Au nanoclusters on sulfonate groups functionalized carbon matrix for efficient catalytic reduction of nitrophenol

Despite immense research efforts in the field of Au supported on carbon matrix, the rational design and fabrication of ultrafine Au/carbon matrix nanocatalysts with effective reactivity and high stability are still challenging. The main obstacles are faced with adjusting the size of Au nanoclusters and strengthening the bond of Au and carbon. In this work, sulfonate groups (−SO3H) introduced onto activated coke (AC) matrix was prepared for steadily anchoring ultrafine Au nanoclusters (∼2 nm). The obtained Au/SO3H-AC exhibited superior reactivity for 4-nitrophenol reduction within 3 min using NaBH4 as reducing agent. The superior performance and stability are attributed to the − SO3H groups with hydrophilic property, benefiting for substrates readily dispersion and for Au species (including oxidized Au+ and Au3+) bind and stabilization, possibly by tightly interacting with the O atoms bound to S atom of − SO3H. In addition, several lines of evidence demonstrate the oxidized Au species can serve as electron relay system, ensuring the sustained reaction. Given that the Au nanoclusters in this study have superior reactivity and stability, this work proposes a novel strategy for preparing other supported metal nanocomposites.

Oxygen plasma-modified polycaprolactone nanofiber membrane activates the biological function in cell adhesion, proliferation, and migration through the phosphorylation of FAK and ERK1/2, enhancing bone regeneration

Bone defects present significant clinical challenges in orthopedics, orthodontics, and maxillofacial surgeries. Accelerated bone regeneration can be facilitated by incorporating mesenchymal stem cells, but limitations in cell survival and growth remain concerns for complete bone repair. Biomaterial-based membranes have been developed to form biocompatible, degradable, and mechanically stable barriers in guided bone regeneration processes. Polycaprolactone (PCL) is a biodegradable polymer widely used as a bone regenerative material because of its favorable mechanical properties. However, its inherent hydrophobicity limits cell adhesion and proliferation, which are necessary for effective bone regeneration. To address this, we fabricated cell-regulatory PCL nanofiber membranes using plasma treatment to enhance induced pluripotent stem cell-derived mesenchymal stem cells and osteoblast growth. The plasma treatment parameters (gas type, flow rate, power, and exposure time) were optimized to enhance PCL’s surface hydrophilicity and protein adsorption properties while maintaining its mechanical integrity. The optimized oxygen plasma-modified PCL membrane demonstrated notable improvements in cell viability, adhesion, and proliferation. In addition, there was improved migration, regulated by cell surface markers and signaling proteins, of the induced pluripotent stem cell-derived mesenchymal stem cells and osteoblasts. In vivo studies in a rat calvarial defect model showed that the plasma-modified PCL membrane dramatically improved new bone formation, facilitating bone regeneration. These findings highlight the potential of plasma treatment of PCL nanofibers to produce effective cell-regulatory membranes for bone defect reconstruction.

Bioavailability of Acemanan: An Active Compound Found in Aloe Gel

Acemannan is said to be the biologically active substance in aloe vera (Aloe barbadensis). Many producers of aloe products utilize inadequate production and extraction methods, resulting in aloe products that contain little or no acemannan. This article outlines a systematic procedure for extracting the bioactive polysaccharide compound from the aloe plant. This paper also provides a description of the physical distinctive features of acemannan. The study also emphasized the determination of physical properties, such as the pKa and Log P values, of acemannan. The physical characteristics were used to evaluate the bioavailability and hydrophilicity of this chemical. The primary approach used to acquire these physical characteristics involves the extraction of acemannan from aloe vera, the creation of phosphate buffer with varying pH levels, the separation of acemannan between chloroform and buffer using the shake flask technique, and the utilization of spectrophotometric analysis. Chloroform was used as a representation of the lipid membrane in the experiment, whereas phosphate buffer was utilized to symbolize the blood. A buffer solution was used to maintain a steady pH at a desired value. The acemannan compound had a pKa value of 4.82 at a pH of 3.45, indicating its acidity. Additionally, the Log P value (chloroform/buffer) was determined to be -3.282, indicating its hydrophobicity. Thus, it was deduced that acemannan exhibited hydrophilic properties throughout the gastrointestinal system.

Enhancement of wound dressings through cerium canadate and hydroxyapatite-infused hyaluronic acide and PVA membranes: A comprehensive characterization and biocompatibility study

This study explores the emhancement of advanced wound dressings by enhancing traditional bandages with suitable biomedical materials. We utilized Hyaluronic Acid (HA) and Polyvinyl Alcohol (PVA) as a polymeric matrix to create a novel membrane. Employing a film casting technique, we incorporated varying ratios of biological nanoparticles—Hydroxyapatite (HAP) and Cerium Vanadate (Ce₃(VO₄)₄)—to improve the wound dressing's properties. Wettability assessments provided insights into the surface characteristics of the scaffolds, revealing a diverse range of contact angles that reflect varying hydrophilic properties. Notably, the pure PVA/HA sample exhibited a contact angle of approximately 31.2° ± 12.1°, indicating excellent hydrophilicity and a strong capacity for drug absorption. However, the doping of nanoparticles resulted in an raise in contact angles, suggesting a slight reduction in hydrophilicity. Specifically, the addition of HAP produced a contact angle of about 36.5° ± 6.7°, while the addition of Ce₃(VO₄)₄ resulted in a contact angle of approximately 38.6° ± 6.4°. A significant increase in contact angle to 42.23° ± 4.8° was observed when mixing the nanoparticles, though the introduction of Graphene Oxide (GO) reduced the angle to 37.4° ± 0.35°, enhancing the hydrophilic properties of the composite. Cell viability testing was conducted to confirm the biocompatibility and bioactivity of the fabricated scaffolds. The results confirmed the ability of the scaffolds to promote cell growth, with an increase of 88.4 % in cell growth ratio observed at a suitable drug concentration of approximately 0.68 μg/ml. These findings highlight the potential of the developed scaffolds to enhance the wound healing process.

Photo-Crosslinked Polyurethane-Containing Gel Polymer Electrolytes via Free-Radical Polymerization Method.

Using a novel technique, crosslinked gel polymer electrolytes (GPEs) designed for lithium-ion battery applications have been created. To form the photo crosslink via free-radical polymerization, a mixture of polyurethane acrylate (PUA), polyurethane methacrylate (PUMA), vinyl phosphonic acid (VPA), and bis[2-(methacryloyloxy)ethyl] phosphate (BMEP) was exposed to ultraviolet (UV) radiation during the fabrication process. The unique crosslinked configuration of the membrane increased its stability and made it suitable for use with liquid electrolytes. The resulting GPE has a much higher ionic conductivity (1.83 × 10-3 S cm-1) than the commercially available Celgrad2500 separator. A crosslinked structure formed by the hydrophilic properties of the PUA-PUMA blend and the higher phosphate content from BMEP reduced the leakage of the electrolyte solution while at the same time providing a greater capacity for liquid retention, significantly improving the mechanical and thermal stability of the membrane. GPP2 shows electrochemical stability up to 3.78 V. The coin cell that was assembled with a LiFePO4 cathode had remarkable cycling characteristics and generated a high reversible capacity of 149 mA h g-1 at 0.1 C. It also managed to maintain a consistent Coulombic efficiency of almost 100%. Furthermore, 91.5% of the original discharge capacity was maintained. However, the improved ionic conductivity, superior electrochemical performance, and high safety of GPEs hold great promise for the development of flexible energy storage systems in the future.

Enhancing electricity generation from water evaporation through cellulose-based multiscale fibers network

Harvesting energy from the water − solid interface through natural water evaporation provides a promising approach for generating sustainable electricity to power self-powered electronics. Advancing the bio-based hydrovoltaic materials enhances sustainability, with wood as a viable candidate due to the inherent hydrophilic and charged properties. However, current wood-based water evaporation-induced electricity generators (WEIGs) mainly depend on the “top-down” construction strategies. Wherein, the improvement of power density is constrained by the limited structural regulation, nondiverse building blocks, and monolithic enhancement mechanisms. Here, the high-performance wood-based WEIGs based on multiscale fibers network (MFN) are reported by embedding the Ti4O7 nanofibers (T4NF) inside the assemblies of TEMPO-oxidized cellulose nanofibrils (TOCNF) through a “bottom-up” route. Benefiting from the large specific surface area, high surface potential, and photothermal effect of conductive T4NF, the WEIG achieves a high short-circuit current of ∼13.7 μA while delivering ∼0.94 V open-circuit voltage. This work presents an efficient method to boost performance while understanding the impact of functional MFN on water evaporation.

Low-voltage organic field-effect transistors by using solution-processable high-κ inorganic-polymer hybrid dielectrics

Organic field-effect transistors (OFETs) incorporating hybrid high-κ inorganic Al2O3 and polymer dielectrics, including polyvinyl alcohol (PVA), polystyrene (PS), or polymethyl methacrylate (PMMA), through solution-processing techniques were fabricated. The analyses revealed that the high surface energy and hydrophilicity property of Al2O3 and PVA, and the relatively hydrophobic property of PS surface, hindered the performance of corresponding OFETs. The Al2O3/PMMA-based OFET achieved the optimized performance, with a threshold voltage of −2.7 V, a hole carrier mobility of 0.056 cm2/Vs, and a current on/off ratio of 1.0 × 104 at a low operating voltage of −5 V. Through analyzing the characteristics of leakage current, capacitance, contact resistance, and trap density of OFETs, we found that the PMMA-engaged films possessed the optimized electrical properties. The introduction of PMMA eliminated the interfacial trapping, thereby lowering the threshold voltage and enhancing the performance of the device. The COMSOL Multiphysics simulation was conducted to confirm the physical mechanism. The strategy of utilizing Al2O3/PMMA hybrid dielectric could simultaneously ensure the low operating voltage and good performance of OFET, while guaranteeing the low leakage current by the thick PMMA.

Physical, chemical, and biological property of silk reinforced polycaprolactone composites for bone tissue engineering

To develop a biodegradable implantable bone material with compatible mechanics with the bone tissue, providing a new biomaterial for clinical bone repair and regeneration. Silk reinforced polycaprolactone composites (SPC) containing 20%, 40%, and 60% silk were prepared by layer-by-layer assembly and hot-pressing technology. Macroscopic morphology was observed and microstructure were observed by scanning electron microscopy, compressive mechanical properties were detected by compression test, surface wettability was detected by surface contact angle test, degradation of materials was observed after soaking in PBS for 180 days, and proliferation of MC3T3-E1 cells was detected by cell counting kit 8 assay. Six Sprague Dawley rats were subcutaneously implanted with polycaprolactone (PCL) and 20%-SPC, respectively. Masson staining was used to analyze the in vivo degradation behavior and vascularization effect within 180 days. The pore defects of the three SPC sections were relatively few. In the range of 20% to 60%, as the silk content increased and the PCL content decreased, the interlayer spacing of silk fabric decreased, and the fibers almost covered the entire cross-section. The compressive modulus and compressive strength of SPC showed an increasing trend, and the compressive modulus of 60%-SPC was slightly lower than that of 40%-SPC. There were significant differences in compressive modulus and compressive strength between the materials ( P<0.05). In vitro simulated fluid degradation experiments showed that the mass loss of the three types of SPC after 180 days of degradation was within 5%, with the highest mass loss observed in 60%-SPC. The differences in mass loss between the materials were significant ( P<0.05). As the silk content increased, the static water contact angle of each material gradually decreased, and all could promote the proliferation of MC3T3-E1 cells. The subcutaneous degradation experiment in rats showed that 20%-SPC began to degrade at 30 days after implantation, and material degradation and vascularization were significant at 180 days, which was in sharp contrast to PCL. SPC has the mechanical and hydrophilic properties that are compatible with bone tissue. It maintains its mechanical strength for a long time in a simulated body fluid environment in vitro, and achieves dynamic synchronization of material degradation, tissue regeneration, and vascularization through the body's immune regulation mechanism in vivo. It is expected to provide a new type of implant material for clinical bone repair.

Role of surface roughness in determining surface energy and magnetic properties of Fe80Ce20 films during thermal processing on Si(100) and glass substrates

In this study, Fe80Ce20 films were deposited on Si(100) and glass substrates using sputtering in a high-vacuum environment and subsequently heat-treated in a vacuum annealing furnace. The films, with thicknesses ranging from 10 nm to 50 nm, were annealed at temperatures of 100 °C, 200 °C, and 300 °C. The objective was to investigate the effects of film thickness and annealing temperature on the structural, surface energy, and magnetic properties of the material. X-ray diffraction (XRD) analysis confirmed the crystalline nature of both Si(100)/Fe80Ce20 and Glass/Fe80Ce20 films. Atomic force microscopy (AFM) revealed a smooth film surface that became rougher after annealing. Contact angle measurements indicated hydrophilic properties, with the highest surface energy observed in the as-deposited films due to a higher density of defects and grain boundaries. The hysteresis loop demonstrated exceptional soft magnetic properties and a high saturation magnetization (Ms) of approximately 2000 emu/cm³. Annealing at 100 °C altered the magnetic domain structure from a striped labyrinthine configuration to an aligned pattern. At higher annealing temperatures, the films exhibited grain growth, increased surface roughness, and new grain formation. Following annealing, the grains in the Fe80Ce20 films became larger, surface roughness increased, and the water contact angle increased, rendering the films more hydrophobic. The as-deposited films displayed the highest surface energy due to the high density of defects and grain boundaries. Increased surface roughness led to more grain boundary defects and irregularities, which served as pinning points for magnetic domain walls, thus increasing coercivity (Hc). Rough surfaces induced local stress fields, increased magnetic anisotropy, and decreased saturation magnetization. Thermal perturbations from higher annealing temperatures further disrupted the alignment of the magnetic moments, leading to a reduction in saturation magnetization.

Investigation on Tensile Properties of Polylactide-Nanoclay (PLA/ MMT) Surface Modification Nanocomposites

Polylactic acid (PLA) has gained significant attention as an environmentally friendly biopolymer, but its limited mechanical properties have hindered broader applications. Nanoparticles such as montmorillonite (MMT) offer a promising approach to address this limitation. The intercalation of MMT with polymer chains can significantly impact the mechanical properties of the nanocomposites. Hence, this paper investigated the effect of surface-modified montmorillonite (MMT) nanoparticles on the mechanical properties of polylactic acid (PLA) nanocomposites. The acetylation process of MMT was carried out followed by neutralisation process with NaOH. PLA granules and acetylated-modified MMT were mixed, crushed into granular form, and moulded. The effect of varying concentrations of modified MMTs on the tensile strength, elongation at break, and maximum force of PLA/MMT nanocomposites was evaluated using the ASTM D638 standard. FTIR results showed shifts in peak intensities in regions 2750 cm-1- 2810 cm-1 led to changes in the aliphatic and aromatic regions, which confirmed the presence of acetylation. Controlled surface modification improved interfacial interactions and load distribution, enhancing overall mechanical performance. The incorporation of surface-modified MMT in PLA/MMT nanocomposite increased the maximum force, Young's modulus, elongation at breaks and tensile strength. PLA/1wt% MMT and the PLA/7wt% MMT compositions exhibited good mechanical properties. However, the PLA/5 wt% MMT blendis deemed more suitable for food applications, such as disposable cups, plates, and cutleries, due to its lower elongation point. In conclusion, the hydrophilic properties of MMT and the hydrophobic properties of PLA are compatible due to the synergistic effects during surface modification which enhance the overall performance of the nanocomposites.

Novel and stable carbon black/polyvinyl acetal aerogels efficiently harvesting solar energy for seawater desalination

A novel interfacial solar steam generators (ISSG) was prepared by a porous carbon black/polyvinyl acetal aerogel (CPA) with high light-absorbing hydrophilic properties, to achieve efficient solar-driven water evaporation and seawater desalination. The polyvinyl acetal was produced by the aldol condensation reaction of polyvinyl alcohol(PVA) and glutaraldehyde(GA). It was freeze-dried to create a hydrophilic porous structure that constructs an efficient hydrophilic channel. Carbon black (CB) exhibits high light absorption capabilities. Incident light undergoes multiple scattering within its porous network structure, effectively reducing reflected light energy loss and enabling efficient thermal conversion of sunlight. Benefited from its highly light-absorbing porous hydrophilic structure, CPA-40-3 evaporation rate achieves an impressive 3.23 kg·m−2·h−1 and an evaporation efficiency of 94 % under 1 sun irradiation, without obvious decay even during long-term use. Furthermore, CPA-40-3 demonstrates remarkable salt tolerance, the evaporation rate remains at 2.55 kg·m−2·h−1 although in simulated Dead Sea salt water under 1 sun irradiation. Compared to traditional ISSG, the CPA has advantages such as superior mechanical properties, prevention of surface salt precipitation, faster water supply, and a larger light absorption area. This design had tremendous promise for efficient solar desalination due to its extraordinarily high evaporation performance in high-salinity brine.

Development and characterization of bilayer chitosan/alginate cling film reinforced with essential oil based nanocomposite for red meat preservation

With a goal to finding suitable alternatives to plastic packaging in the food industry, we developed a multifunctional bio-based active packaging film to enhance the shelf life of red meat. A chitosan/alginate (Chi + Alg) bilayer film was developed through layer-by-layer (LBL) assembly and an active material i.e. lemongrass nanoemulsion with silver nanoparticles-based nanocomposite (NC1) was loaded into the alginate layer to improve the quality of the bio-based film (Chi + Alg + NC1). The Chi + Alg + NC1 film was characterized in terms of its microstructure, mechanical strength, thermal stability, and antimicrobial activity. Scanning electron microscopy (SEM) revealed a film (22.5 ± 1.44 μm thickness) with a smooth and even surface and a cross-sectional structure. The incorporation of NC1 improves the quality of the film by enhancing its mechanical strength and thermal stability. FT-IR spectra showed the successful interaction between chitosan and alginate in the LBL assembly and the incorporation of NC1 in the alginate layer. The red meat preservation test demonstrated that the shelf life improved when the meat was covered with the fabricated bio-based film. The color of the meat was retained for up to 7 days compared to that of the control (Chi alone and Chi + Alg). Additionally, a reduction in the microbial count in the Chi + Alg + NC1 film was observed, corroborating the shelf-life improvement. In addition to its inherent antimicrobial properties, NC1 induced hydrophilic properties to the film, which further aids in its antimicrobial activity against E. coli. These findings suggest that Chi + Alg + NC1 film could be a potent alternative to plastic packaging and can be used as a cling film to prolong the shelf life of red meat.

Comparison of Key Properties of Ag-TiO2 and Hydroxyapatite-Ag-TiO2 Coatings on NiTi SMA.

To functionalize the NiTi alloy, multifunctional innovative nanocoatings of Ag-TiO2 and Ag-TiO2 doped with hydroxyapatite were engineered on its surface. The coatings were thoroughly characterized, focusing on surface topography and key functional properties, including adhesion, surface wettability, biocompatibility, antibacterial activity, and corrosion resistance. The electrochemical corrosion kinetics in a simulated body fluid and the mechanisms were analyzed. The coatings exhibited hydrophilic properties and were biocompatible with fibroblast and osteoblast cells while also demonstrating antibacterial activity against E. coli and S. epidermidis. The coatings adhered strongly to the NiTi substrate, with superior adhesion observed in the hydroxyapatite-doped layers. Conversely, the Ag-TiO2 layers showed enhanced corrosion resistance.

Simple and reversible method to control the surface energy of ITO branched nanowires for tuning wettability of micro/nanoscale droplets

Reversible control of hydrophobic and hydrophilic surfaces has gained attention due to their potential applications in microfluidic devices, membranes for electrochemical cells, and sensors. While external stimuli such as temperature and electric field can regulate surface properties, they cannot be selectively applied to specific regions, which limits the patterning of areas with different surface energies. Here, we present a simple and reversible method for converting hydrophobic and hydrophilic properties through surface treatments involving nonpolar (−CFx) or polar groups (–OH) on indium tin oxide branched nanowires (ITO BRs). The formation of nonpolar groups results in superhydrophobic surface. Subsequent ultraviolet ozone treatment, using a shadow mask, induces the exposed area to transition into a superhydrophilic state, while the unexposed area retains superhydrophobicity. This demonstrates the potential for selective-area surface energy patterning. Furthermore, we investigate the wetting behavior of nanoscale Ag nanoparticles (NPs) on surface-modified ITO BRs. It is observed that size and shape of Ag NPs depend on the surface energy of ITO BRs. Consequently, controlling the surface energy leads to the formation of unique geometric structure of Ag NPs, enhancing plasmonic light absorption and scattering at specific resonant wavelengths.

Superhydrophobic Cellulose Nanofiber Aerogels for Efficient Hemostasis with Minimal Blood Loss.

Reducing unnecessary blood loss in hemostasis is a major challenge for traditional hemostatic materials due to uncontrolled blood absorption. Tuning the hydrophilic and hydrophobic properties of hemostatic materials provides a road to reduce blood loss. Here, we developed a superhydrophobic aerogel that enabled remarkably reduced blood loss. The aerogel was fabricated with polydopamine-coated and fluoroalkyl chain-modified bacterial cellulose via a directional freeze-drying method. Primarily, the hydrophobic feature prevented blood from uncontrolled absorption by the material and overflowing laterally. Additionally, the aerogel had a dense network of channels that allowed it to absorb water from blood due to the capillary effect, and fluoroalkyl chains trapped the blood cells entering the channels to form a compact barrier via hydrophobic interaction at the bottom of the aerogel, causing quick fibrin generation and blood coagulation. The animal experiments reveal that the aerogel reduced the hemostatic time by 68% and blood loss by 87 wt % compared with QuikClot combat gauze. The study demonstrates the superiority of superhydrophobic aerogels for hemostasis and provides new insights into the development of hemostatic materials.

Biofilm formation comparison of Vibrio parahaemolyticus on stainless steel and polypropylene while minimizing environmental impacts and transfer to grouper fish fillets

This study investigated the influence of food contact surface materials on the biofilm formation of Vibrio parahaemolyticus while attempting to minimize the impact of environmental factors. The response surface methodology (RSM), incorporating three controlled environmental factors (temperature, pH, and salinity), was employed to determine the optimal conditions for biofilm formation on stainless steel (SS) and polypropylene (PP) coupons. The RSM results demonstrated that pH was highly influential. After minimizing the impacts of environmental factors, initially V. parahaemolyticus adhered more rapidly on PP than SS. To adhere to SS, V. parahaemolyticus formed extra exopolysaccharide (EPS) and exhibited clustered stacking. Both PP and SS exhibited hydrophilic properties, but SS was more hydrophilic than PP. Finally, this study observed a higher transfer rate of biofilms from PP to fish fillets than from SS to fish fillets. The present findings suggest that the food industry should consider the material of food processing surfaces to prevent V. parahaemolyticus biofilm formation and thus to enhance food safety.