Polyvinyl Alcohol Research Articles

Immobilization and characterization of β-galactosidase from Aspergillus oryzae in polyvinyl alcohol hydrogels.

One of the main goals of contemporary biotechnology has been the development of novel immobilized enzyme formulations. In the present study, the industrially important β-galactosidase was trapped in a polyvinyl alcohol (PVA) gel to immobilize it. The optimization of immobilization method and characterization of the immobilized enzyme were studied. The results were compared with free enzymes. The results indicate that the optimal temperature range for the enzyme to be at following immobilization is between 40°C and 50°C. At pH 7, the optimal pH, the activity increased, the Vmax value increased from 1.936 to 2.495 Umg‒1, and the Km value decreased from 4.861 to 0.982mM.Depending on how stable the immobilized enzyme when stored, β-galactosidases immobilized on PVA gels showed 52.87% activity at the end of the seventh week and 58.86% activity at the end of the fifth week. Their initial activity subsided after three reuses. The final result was 66%. Therefore, one may argue that it increases the catalytic effect of the enzyme. As a result, it has been found that immobilized β-galactosidase has more potent enzymatic properties than free β-galactosidase, which may make it more advantageous for industrial processes. Further studies could delve deeper into the mechanistic aspects of the immobilization process in an effort to improve optimization and tailor the immobilized enzyme to specific industrial needs.

Temperature-Governed Microstructure of Poly(vinyl alcohol) Hydrogels Prepared through Mixed-Solvent-Induced Phase Separation.

The formation of phase-separated structures in hydrogels plays a crucial role in determining their optical and mechanical properties. Traditionally, phase-separated hydrogels are prepared through a two-step process involving initial hydrogel synthesis followed by post-treatment. In this study, we present an approach for temperature-governed phase separation microstructure modulation in hydrogels, harnessing the cononsolvency effect. This method allows the phase-separated structure to develop during hydrogel synthesis, significantly simplifying the preparation process. Importantly, we found that the preparation temperature has a substantial effect on the internal structure of the phase-separated hydrogel. We systematically investigated how the temperature influences the phase structure, optical properties, and mechanical performance of these hydrogels. The resulting hydrogels demonstrate excellent moisturizing and antifreezing capabilities. Additionally, the incorporation of sodium chloride imparts remarkable electrical conductivity to the hydrogels, making them suitable for strain sensing applications across a wide temperature range.

Synthesis and evaluation of self‐healing polyvinyl alcohol‐tannic acid membranes for skin bio‐applications

AbstractAutonomic self‐healing films have shown limited mechanical strength, hindering their application as biomaterials, particularly in skin bioengineering. To address this challenge, we developed polyvinyl alcohol (PVA)‐tannic acid (TA)‐based membranes with improved self‐healing properties and strong mechanical performance. Using a blade coating method and freeze–thaw cycles (−10°C for 1 h, followed by room temperature thawing), the synthesized membranes demonstrated a tensile strength of 8.8 MPa before healing and 7.6 MPa after healing, achieving an 88% healing efficiency. Membrane thickness showed a slight reduction from 465 to 432 μm posthealing. After 3000 bending cycles at a 1 cm radius, the membranes maintained flexibility with no significant changes in water vapor transmission rate (WVTR) (7.66 g/m2·day) or oxygen transmission rate (OTR) (0.13 cm3/m2·day·bar). These results underscore the membranes' suitability for dynamic skin environments, combining robust mechanical properties with excellent self‐healing capabilities. The PVA‐TA membranes present a promising solution for advanced skin bioengineering applications.

Tailoring the mechanical properties of macro-porous PVA hydrogels for biomedical applications

Polyvinyl alcohol (PVA) is a biocompatible biopolymer with superior dimensional and mechanical stability when compared to naturally available biomaterials such as collagen and gelatin. Furthermore, PVA in hydrogel form behaves non-linearly during mechanical loading, generating a response like soft biological tissues. Generally, PVA hydrogels are fabricated using freeze-thaw cycles (FTCs) and changing the number of FTCs gives control over its mechanical properties. Porosity of the hydrogel is another important factor which determines its mechanical properties and is also evident in biological soft tissues. Incorporating macro-pores in PVA hydrogels substantially reduces the stiffness of the material and can mimic some porous tissues such as lung, liver, bone marrow, kidneys, urethra and penile tissues (corpus cavernosa). Within this study, we developed macro-porous PVA hydrogels using the freeze-thaw process followed by particulate leaching of sacrificial 3D-printed and milled PVA (m-PVA) filler particles. This fabrication method enables control over the porosity in macro-porous PVA hydrogels, which is crucial not only for tuning mechanical properties but also for mimicking the structure of spongy tissues, such as liver tissue and corpus cavernosum in the penile tissue, for example. We investigated the level of porosity in the specimen using optical microscopy to understand the distribution of the pores and the pore size. The tunability of the mechanical properties of PVA hydrogels is, a key finding of this study and is achieved using three factors: (i) weight percentage of sacrificial fillers, (ii) number of FTCs and (iii) concentration of PVA. These macro-porous PVA specimens have wide ranging biomedical applications as biological soft tissue analogues, or tissue engineering scaffolds, where the PVA hydrogel can be tuned to match the mechanical properties of these soft biological tissues.

Polyvinyl alcohol and alginate bio-composite film containing titanium dioxide nanotubes for skin injury repair

This study explores the potential of polyvinyl alcohol (PVA) and alginate (SA) blend polymer films with embedded titanium dioxide nanotubes (TiO2NT) for wound healing applications. The nanocomposite film (PVA+SA@TiO2NT) was fabricated via a simple solvent casting process. The synergistic interaction between PVA and alginate significantly enhanced the film's stability in aqueous environments without compromising its weight. After 24 hours of immersion, the film exhibited a substantial swelling capacity (836±6%) and good WVTR ((282±4%). Scanning electron microscopy (SEM) revealed the formation of a smooth and random pore structure within the film. Fourier-transform infrared spectroscopy (FTIR) confirmed the successful formation of hydrogen bonds between PVA and alginate, along with the presence of Ti-O bonds, indicating successful incorporation of TiO2NT into the PVA+SA matrix. X-ray diffraction (XRD) analysis further corroborated the presence of TiO2NT. In vitro biocompatibility studies demonstrated the non-cytotoxic nature of the PVA+SA@TiO2NT bio-composite film. Additionally, in vitro wound healing studies suggest its potential as a promising biomaterial for wound dressing applications. These findings warrant further investigation to elucidate the complete mechanisms of action and optimize the nanocomposite's properties for clinical translation.

Fabrication and characterization of novel electrospun nanofibers based on grass pea (Lathyrus sativus L.) protein isolate loaded with sumac (Rhus coriaria L.) extract

In this study, sumac extract was utilized as an active ingredient and combined with grass pea protein isolate and polyvinyl alcohol to produce novel active nanofiber mats using an electrospinning technique. First, nanofiber mats were fabricated by different ratios (100:0, 90:10, 70:30, 50:50, 30:70, 10:90, 0:100) of grass pea protein isolate and polyvinyl alcohol. The characterization of nanofiber mats revealed that the nanofibers with a polymer ratio of 50:50 had appropriate mechanical properties and presented a fibrous and uniform morphology. Therefore, the 50:50 polymer solution ratio was selected to produce active nanofibers by adding different amounts (0%, 2%, and 4% (w/v)) of sumac extract. The average diameters of nanofibers decreased from 150 ± 31 to 122 ± 25, and 105 ± 19 nm, by increasing the concentration of sumac extract. Based on the SEM results, the electrospun nanofibers exhibited a bead-free and smooth surface. The FTIR and XRD analyses indicated the presence of intermolecular hydrogen bonds between the components. The antioxidant activity of the nanofibers was confirmed by DPPH analysis and ranged between 3.33% and 68.75%. Additionally, the antimicrobial test results indicated that the nanofibers with the highest sumac concentration (4%) displayed inhibitory activity against Staphylococcus aureus, resulting in an inhibition zone of 10 mm. The optimal treatment of this study was grass pea protein isolate: polyvinyl alcohol ratio of 50:50 containing 4% sumac extract which can be used as a natural antimicrobial and antioxidant agent.

Fabrication and characterization of double-layer active intelligent film based on chitosan, polyvinyl alcohol, grape skin anthocyanin and selenium nanoparticle

This study involved the fabrication of double-layer intelligent films using chitosan (CS), polyvinyl alcohol (PVA), grape skin anthocyanin (GSA), gellan gum (GG) and selenium nanoparticles (SeNPs). The CS/PVA/GSA layer functioned as the internal indicator layer, and the GG/SeNPs layer acted as the external layer for antioxidant and antimicrobial purposes. SEM, FTIR, XRD, and TGA results confirmed the successful fabrication of double-layer films as well as the presence of hydrogen bonding interaction between the two layers. The tensile strength of double-layer films (8.06 MPa–9.61 MPa) fallen between that of single-layer CS/PVA/GSA film (12.51 MPa) and GG/SeNPs film (1.50 MPa–7.67 MPa). The double-layer films demonstrated good UV-blocking abilities, as well as outstanding antioxidant (ABTS scavenging rate can be up to ~80 %) and antimicrobial properties. Compared with single-layer CS/PVA/GSA film, the double-layer film incorporated with 6.6 wt% SeNPs (CPG/GS2 film) possessed a more rapid and stronger response towards NH3/acetic acid as well as enhanced storage stability. Furthermore, the CPG/GS2 film can increase the shelf life of strawberries at 25 °C by 4 days, and its visible color change showed strong correlation with the weight loss rate (R2 = 0.99) and hardness (R2 = 0.98) of strawberries.

Bio-inspired chitosan/polyvinyl alcohol/tannic acid hydrogels as plant grafting wood adhesives

Recently, there has been growing interest in plant-inspired materials for various biological, medical, and industrial applications. Notably, tannic acid-based materials exhibit remarkable adhesive properties and can be used in a variety of applications, particularly biomedical applications. In addition, mixtures composed of tannic acid and polymers (e.g., polyvinyl alcohol) exhibit excellent adhesion to various substrates. In this study, we developed gallol-containing chitosan (G-CS), polyvinyl alcohol (PVA), and tannic acid (TA) composite (G-CPT) hydrogels as wood adhesive materials. G-CPT hydrogels were immediately formed by mixing the G-CS/PVA solution with the TA solution. Rheological analysis revealed an increase in the elastic modulus (G′) with the addition of small amounts of G-CS. In addition, the detachment stress of wood sticks attached using G-CPT hydrogels was 142.2 ± 7.2 MPa, which was substantially higher than that of G-CS (5.3 ± 1.4 kPa), PVA (2.2 ± 0.2 kPa), TA (0.4 ± 0.1 kPa), and PVA/TA hydrogels (106.5 ± 2.5 MPa). Furthermore, G-CPT hydrogels can be used as wood adhesives for scion grafting into the rootstock of English ivy. These findings highlight the importance of G-CPT hydrogels as eco-friendly wood adhesives with enormous potential for various industrial and agricultural applications.

Ease-of-manufacture highly transparent thin polyvinyl alcohol aerogel

The earliest silicon-based aerogels attracted attention due to their nanoscale porous structure and high transparency. Still, they need to be more balanced with the poor mechanical properties. Their brittle structure limits the development of this promising new material. Therefore, the goal of this work is to optimize the mechanical properties of aerogels while maintaining transparency. The good mechanical properties of polymers have made them the material of choice for this work. Polyvinyl alcohol (PVA), which can undergo self-crosslinking through side-chain hydroxyl groups forming hydrogen bonds, was chosen as the raw material to simplify and expedite the production process. The production process was experimented with, analyzed, and refined. Considering the time efficiency of the experimental process, a one-step gelling method was invented to facilitate the sol-gel transition. The one-step gelling method maintained the high transparency of PVA aerogels and reduced the time required for the gelation process compared to the freeze-thawing method. This work employs carbon dioxide supercritical drying to ensure minimal structural collapse and maximize the porous structure’s retention. The transmittance of PVA aerogels can reach up to 93.67% at a wavelength of 1333 nm. The internal structure of aerogels with different PVA concentrations was observed using a Scanning electron microscope. Applying Beer-Lambert’s Law eliminated the effect of sample thickness on transparency. The relationship between the transparency of PVA aerogels, their microstructure, and macroscopic concentration was studied and analyzed for the first time. While ensuring light transmittance, the modulus of the PVA aerogel reached as high as 6.18 ± 0.56 MPa at 13 wt%.

Incorporation of polyvinyl alcohol in bacterial cellulose/polypyrrole flexible conductive films to enhance the mechanical and conductive performance

The integration of polypyrrole (PPy) into bacterial cellulose (BC) has provided significant conductivity and cost benefits. However, this combination has led to a reduction in mechanical properties, particularly in terms of elongation at break and tensile strength. This study investigated the enhancement of BC/PPy composite films by incorporating polyvinyl alcohol (PVA). The resulting BC/PPy/PVA films demonstrated improvements in flexibility, tensile strength and thermal stability. Specifically, with 7 % PVA, the flexible films exhibited remarkable enhancements: tensile strength increased from 11.01 MPa (for BC/PPy) to 25.27 MPa and elongation at break rose from 5.81 % to 11.54 %. Additionally, the electrical conductivity of the BC/PPy/PVA films with a resistance of 38.5 Ω, surpassed that of the BC/PPy films. Furthermore, the equilibrium swelling water absorption rates of BC/PPy and BC/PPy/PVA films were 30.6 % and 81.4 %, respectively, with corresponding resistances of 530 Ω and 540 Ω. The variation in resistance between the dry and swollen states of the BC/PPy/PVA flexible conductive film resulted in differences in the brightness of the small light bulb. These findings highlighted the synergistic effects of PVA within the BC/PPy matrix, presenting a promising avenue for developing high-performance conductive materials suitable for flexible electronics and wearable devices.

A closed-loop sustainable method for the fabrication of electrospun nanofiber using food waste for filtration of particulate matters (PMs) and volatile organic matter (VOCs) from air

Indoor air pollution significantly impacts human health and the environment. Humans suffer the greatest health burden due to inefficient combustion technologies and polluted fuels. Therefore, air filtration is essential for a healthy and prosperous household. This study aims to develop a sustainable approach for the fabrication of biodegradable electrospun nanofibers (ENs) as air filters from food waste materials and offer a closed-loop circular solution and potential replacement for non-biodegradable HEPA air filters. We have tested banana peel extract (BPE), eggshell membrane, chitosan, and starch blended with polyvinyl alcohol (PVA) for fabricating ENs. Among the nanofibers investigated for air filtration application, BPE/PVA nanofiber shows the best performance in terms of maximum particulate matter (PM) removal efficiency and minimum pressure drop while incorporating > 50 % of the food waste into the electrospinning solution. Adding BPE into a 10 % PVA solution leads to a reduction in the hydrophilic behavior of the BPE/PVA nanofiber as compared to neat 10 % PVA ENs. The BPE/PVA nanofiber shows minimum pressure drop (156–160 Pa) and highest quality factor (Qf) in comparison with other waste-derived nanofibers with > 98 % filtration efficiency of PM2.5. Further, BPE/PVA nanofiber shows the highest adsorption of xylene vapor among other food waste derived nanofibers studied. Based on the above results, it can be concluded that BPE based nanofiber shows the best performance as air filter media among all other food waste-based ENs. The study demonstrates a successful regeneration and reuse of the BPE/PVA filter up to 3 cycles. The leftover material from banana peels after BPE extraction was utilized as a soil ameliorant. It showed 55 % soil water retention (SWR) capacity, making it possible to apply in arid regions or crops with high water requirements.

Suspension-washcoat optimization for preparing copper-manganese oxide structured catalyst towards flue gas CO purification

Structured catalysts play significant role in nowaday environmental industry. The copper-manganese oxide (Cu-Mn) is a low cost and efficient catalyst for CO purification from flue gas, for which a robust preparation regarding stabilized suspension and washcoat process is still lacked. This work addressed this challenge by constructing the catalyst suspension by introducing absorbent polymer (SAP), polyvinyl alcohol (PVA), and nano-silica sol (SiO2-NA). The effects of the dosage of SAP, PVA, and SiO2-NA on suspension properties including viscosity, water-retention capacity and stability were systematically studied. The combined effect of the three additives regarding electrostatic-sterical stability and regionalized coating is demonstrated to avoids the destruction of connection between SiO2-NA and Cu-Mn due to the thermal stress during the drying process. After calcination, SiO2-NA is efficiently utilized, evenly distributed and tightly bonded to Cu-Mn catalyst, rendering strongly-attached, crack-free and compact washcoated layer. The optimized structured catalyst shows appreciable balance of loading (up to 182kg/m3) and strength (powder shedding rate <1wt%) without blockage. The potential of practical application was verified by CO purification from realistic iron-ore sintering flue gas with catalytic efficiency of above 90% for 240h. These findings indicated a promising strategy to design Cu-Mn structured catalysts efficient for industrial use.

Fluorescence Enhancement of Nonemissive Monodeprotonated Luteolin in a Poly(vinyl alcohol) Film.

Solid polymer matrixes can modulate the electronic states of embedded chromophores and have been widely used in flexible optoelectronic and optical materials. Luteolin is one of the most common natural flavonoids, and its neutral and monodeprotonated forms are nonemissive in aqueous solution induced by ultrafast excited-state proton transfer (ESPT) followed by nonradiative relaxation. In this study, we have incorporated luteolin into poly(vinyl alcohol) (PVA) films and studied their fluorescence behaviors. Neutral and one monodeprotonated luteolin coexist in the PVA film. Weak steady-state fluorescence of neutral luteolin peaking at about 440 nm is observed for the first time. In addition, the monodeprotonated luteolin in PVA film exhibits obvious fluorescence peaking at 500 nm, with a fluorescence quantum yield of as high as 0.4 and a fluorescence lifetime of as long as 2.4 ns. Time-dependent density functional theory calculations have determined that the ESPT of neutral luteolin is barrierless but that of monodeprotonated luteolin needs to surmount a barrier, explaining their distinct emission properties. These results indicate the modulation ability of the PVA film in both ground-state deprotonation and ESPT, broadening the application areas of the solid polymer matrix.

Construction and characterization of sodium alginate/polyvinyl alcohol double-network hydrogel beads with surfactant-tailored adsorption capabilities for efficient tetracycline hydrochloride removal

The extensive use of tetracycline (TC) for disease control and the residuals in wastewater has resulted in the spread and accumulation of antibiotic resistance genes, posing a severe threat to the human health and environmental safety. To solve this problem, a series of double-network hydrogel beads based on sodium alginate and polyvinyl alcohol were constructed with the introduction of various surfactants to modulate the morphology. The results showed that the introduction of surfactants can modulate the surface morphology and internal structure, which can also regulate the adsorption ability of the hydrogel beads. The SDS-B beads with SDS as surfactant exhibited highest adsorption efficiency for removal of TC with a maximum adsorption capacity up to 121.6 mg/g, which possessed a resistance to various cations and humic acid. The adsorption mechanism revealed that the superior adsorption performance of the hydrogel beads was primarily attributed to hydrogen bonding, electrostatic attraction, and π-π EDA interactions. Adsorption kinetics demonstrated that the pseudo-second-order model fitted the adsorption process well and adsorption isotherm showed the adsorption of TC occurred through both chemical and physical interactions. Moreover, the adsorption efficiency remained approximately 87.5 % after three adsorption-desorption cycles, which may have potential application and practical value in TC adsorption.

Enhanced photocatalytic performance of (Mg, Cu) Dual-Doped ZnS nanosheets for Solar-Driven water treatment and embedded with PVA polymer membrane for reusability

Photocatalysis uses semiconductor materials to solar energy effectively purify to water by eliminating pollutants. Organic Dye degradation serves as a standard to assess the photocatalytic effects of the materials. In this study Mg, Cu dual-doped ZnS nanosheets were synthesized using the coprecipitation method. The impact of the concentration on the structural, morphology, optical, and degradation efficiency was investigated with XRD, XPS, TEM with EDAX, and UV spectroscopy. The pure ZnS and Zn0.98-xCu0.02MgxS (x = 0, 0.01, 0.02) (ZCM1, ZCM2, ZCM3, and ZCM4) nanosheets, exhibited cubic structure with high phase purity. The average crystalline size was calculated as 1.66, 1.60, 1.45, and 1.47 nm for the ZCM1, ZCM2, ZCM3, and ZCM4 nanosheets, respectively. TEM analysis revealed the presence of crumpled nanosheets. The bandgap of the ZCM1, ZCM2, ZCM3, and ZCM4 nanosheets were 3.99, 3.78, 4.03, and 4.09 eV respectively. This study investigated the photocatalytic activity of crystal violet dye when exposed to natural sunlight irradiation. Notably, ZCM3 nanosheets exhibited a high degradation rate of 99 % over 120 min under sunlight. Furthermore, the proposed dye degradation mechanism, effect of dosage, effect of dye variation, reusability, scavenging activity, and hemolytic activity were comprehensively discussed. The nanosheets embedded with the Polyvinyl alcohol (PVA) polymer membrane for reusability.

A ratiometric indicator pad utilizing Alz/BRI-PVA for visual assessment of fish freshness

In this study, a novel intelligent water-absorbent cellulose pad with a specified area was developed for the visual and non-destructive monitoring of fish freshness. The pad’s substrate was composed of wood pulp cellulose (WPC), and the specified area contained a ratiometric mixture of brilliant blue (BRI) and alizarin (Alz)., fixed with Polyvinyl alcohol (PVA). During the freshness monitoring process, the Alz/BRI-PVA WPC pad exhibited a color transition from green to brown, followed by a shift to purple-red, corresponding to the increasing levels of total volatile base nitrogen (TVB-N) and total viable count (TVC). After testing, a BRI/Alz ratio of 1:8 was selected as the optimal ratio. Compared to the volatile gas-based sensing tags, the pad developed in this study demonstrated a high sensitivity of 53.4% by interacting with the sample exudate to produce signal changes. This study demonstrates the feasibility of using the developed dual-functional pad for water absorption and freshness indications.

Tetrapanax papyriferus lignocellulosic skeleton aerogel enhanced with polyvinyl alcohol of high mechanical performance and thermal insulating

Biodegradable and renewable biomass aerogel has attracted significant attention because of its excellent characteristics. However, most aerogels were limited by poor mechanical strength and complex fabrication process. Herein, two delignified Tetrapanax papyriferus (TP) lignocellulosic samples (TP-SC, TP-FA/HAC) served as renewable porous skeletons with polyvinyl alcohol (PVA) modification to prepare high performance aerogels. The excellent pore structure facilitates the penetration of polyvinyl alcohol, which enhances the mechanical property and thermal stability of the resulting aerogel. The SC-8 h exhibited excellent mechanical strength with a bending stress of 102.9 MPa, 26.7 % increase in strain and 2.5 % in bending modulus compared to the TP-SC. The maximum thermal decomposition temperature of the FA/HAC-4 h was 358.6 °C, which was showed an outstanding thermal stability of the aerogel. Furthermore, these aerogels exhibited thermal insulating properties, and the maximum surface heating temperature after impregnation modification is lower than that of the original wood. This performance has a development prospect in the field of thermal insulation packaging and building structural materials. The high strength lignocellulosic skeleton aerogel could be prepared by a simple and effective strategy that preserved the original distinctive structure, offering a novel approach to the efficient utilization of TP.

Effect of surface-active substances on the macrodispersion behavior of thermal stress-modified multi-wall carbon nanotubes in cryogenic environments

In the preparation of nanocomposites, the agglomeration of multi-walled carbon nanotubes (MWCNTs) in the composite due to their low colloidal stability limits their use in industrial areas. To overcome these problems, it is important to develop simpler, economical, high-yield and non-hazardous techniques to replace existing techniques with low yields, expensive additional equipment or hazardous liquids. This study explores how surfactants affect the macrodispersion of thermal stress-modified MWCNTs in cryogenic environments, focusing on their application in polymer film preparation. Firstly, optimal conditions for modifying MWCNTs through thermal stress were identified using liquid nitrogen. Parameters assessed included the number of cycles (2, 4, and 6), duration in liquid nitrogen (10, 20, and 30 min), and subsequent waiting time at room temperature (5, 12, and 20 min). Results showed that the highest surface area was obtained with 2 cycles, 20 min in liquid nitrogen, and 5 min at room temperature. Analytical techniques such as Brunauer-Emmett-Teller (BET), X-Ray Diffraction (XRD), High Contrast Transmission Electron Microscopy (CTEM) and Raman spectroscopy were used to evaluate the functionalization process's effects on MWCNTs' internal graphitic structure and physicochemical properties. CTEM micrographs indicated that thermal stress reduced the length of MWCNTs, while Raman analysis showed improved graphite quality. The modification process, carried out with 100 % efficiency and no sample loss, increased the BET surface area from 297.551 m2/g to 397.295 m2/g. The study also investigated the impact of surfactants (polyethylene glycol sorbitan monooleate-Tween 80, sodium dodecyl sulfate-SDS, and hexadecyltrimethylammonium bromide-CTAB) on MWCNTs' macrodispersion degrees (DM%) and energy band gaps via UV–visible (UV–Vis) absorption spectroscopy. CTAB provided the highest and most stable macrodispersion, reducing the energy band gaps of MWCNTs from 5.65 to 5.75 eV to 3.53–3.60 eV. CTAB showed excellent colloidal stability with a zeta potential of 44.2 mV, while SDS had −49.9 mV. Polyvinyl alcohol (PVA) polymer films, created using MWCNT solutions with optimal macrodispersion, were confirmed by Scanning Electron Microscope (SEM), Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimeters (DSC), and BET surface area analyses to have successfully and homogeneously incorporated MWCNTs. In addition to the superior properties of MWCNTs modified with the functionalization technique developed within the scope of this study by increasing their specific surface area and porosity, the excellent colloidal stability provided may have various effects in many industrial areas. These advantages enable MWCNTs functionalized with the developed technique to have a wider range of applications in industrial applications and provide more efficient and sustainable solutions.

Enhancing nanofiltration performance with tannic acid and polyvinyl alcohol interlayers for improved water permeability and selective solute rejection

Global water shortages have significantly intensified the demand for efficient and sustainable water purification technologies. Nanofiltration (NF) plays a crucial role in desalination, providing distinct advantages by removing a variety of pollutants including heavy metals and organic compounds, all while consuming minimal energy. Traditional NF membranes often struggle to balance high rejection with satisfactory permeability. This study advances NF technology by utilizing polysulfone as a durable substrate and introducing tannic acid (TA)-polyvinyl alcohol (PVA) interlayer to enhance structural robustness and functional capabilities of membranes. Through streamlined one-step coating followed by precise interfacial polymerization, this approach optimizes monomer piperazine storage and dispersion on substrate, effectively controlling its diffusion rate, resulting in a thinner polyamide (PA) layer. These strategic enhancements not only lead to a significant increase in permeability to 216.3 L·m−2·h−1·MPa−1 and an impressive rejection for Na2SO4 of 99.04 % but also ensure enhanced long-term operational stability. The innovative TA-PVA interlayer sets new benchmarks for high-performance NF membranes by combining environmental friendliness with cost-effectiveness, making it ideal for large-scale industrial applications. This unique composition promotes sustainability and economic efficiency in water treatment technologies, and underscoring the vast potential for expanding the production and application of advanced NF systems.

Cubosomes hydrogel containing silver based organometallic compounds for enhanced wound healing of burns: In vitro and in vivo studies

The aim of this study is to investigate the treatment of burn wounds and bacterial infections, specifically focusing on silver(I) N-heterocyclic carbene (Ag-NHC) loaded into cubosomes. Ag-NHC is an organometallic complex of silver (Ag) and can be considered an active pharmaceutical ingredient for the topical treatment of burns. A novel nanoparticle system, cubosome dispersions, was formulated using high pressure homogenization methods with different concentrations of lipid phase glyceryl monooleate (GMO), surfactants such as poloxamer 407 (F-127), and polyvinyl alcohol (PVA). The optimized formulation (U6) was characterized by in vitro drug release profile (90.54 ± 1.17 %), particle size (126.7 ± 0.98 nm), zeta potential (−21.6 ± 6.83 mV), entrapment efficiency (89.30 ± 1.46 %), and morphology as observed by transmission electron microscopy (TEM). The U6 formulation was incorporated into a hydrogel containing Carbopol 940 to form a cubosomal hydrogel (cubogel). The cubogel was characterized by the in vitro release of Ag-NHC (92 %), entrapment efficiency (>90 %), pH (5.3), viscosity (1.2 cP), spreadability, and TEM. From the in vitro drug release pattern, it was concluded that the U6 formulation showed slow and sustained drug release over 24 h, and demonstrated superior burn healing compared to marketed products. The in vivo wound healing study revealed that the cubogel demonstrated a superior burn healing rate compared to commercially available products (Quench® and Clotrimazole®). The in vivo histopathological results showed that the prepared cubogel was effective in treating second-degree burns, with no side effects or skin irritation, compared to commercial products. Additionally, Ag-NHC-loaded cubogel facilitated sustained release for treating burn wounds without any bacterial infections. The current findings provide a strong basis for the initiating phase 0 clinal trials, highlighting significant potential for the further research to benefit the pharmaceutical industry.