PVA Membranes Research Articles

One-Pot Fabrication of Highly Flexible Fluorine-Free Lubricant-Infused Poly(vinyl alcohol) Films with Superior Antifouling Properties.

In clinical settings, biofluid-contacting devices can suffer from biofouling, leading to thrombus formation and bacterial biofilm buildup, which impair device function and pose health risks. Traditional antifouling methods, including the use of hydrophilic polymers and heparin coatings, often suffer from instability and reduced bioactivity over time. Lubricant-infused surfaces (LIS) have emerged as a promising alternative due to their long-term stability and broad-spectrum repellency. However, current LIS technologies typically involve complex, multistep processes that restrict their application to surface layers, potentially compromising performance under mechanical stress. This study introduces a novel method for bulk modification of poly(vinyl alcohol) (PVA) films, creating flexible lubricant-infused PVA membranes with superior antifouling properties. These films are fabricated by cross-linking the PVA chains using n-propyltrichlorosilane (n-PTCS) and subsequent infusion with silicone oil as a lubricant. The modified PVA films significantly prevent bacterial adhesion and prolong blood and plasma clot formation. Additionally, these films exhibit enhanced mechanical properties, particularly in elasticity and flexibility compared to unmodified PVA films. The developed technique provides a straightforward method for creating flexible, super-repellent biointerfaces with the potential to prevent blood adhesion and bacterial biofilm formation, which are common complications associated with biofluid-contacting devices and medical implants.

Investigation of the Effects of Different Phases of TiO2 Nanoparticles on PVA Membranes

Introduction: PVA/TiO2 nanocomposite membranes are prepared by solution casting technique where different phases of TiO2 nanoparticles like brookite, brookiterutile and rutile are dispersed in PVA matrix. Sol-gel method was employed to prepare TiO2 nanoparticles, while different phases of TiO2 have been obtained by controlling the calcination temperature. Methods: PVA/TiO2 nanocomposite membranes were characterized by XRD, FTIR, AFM, TEM, UV-visible and PL techniques. XRD results confirmed the presence of different phases of TiO2, exhibiting 3.3 nm, 8.4 nm, and 35.7 nm mean crystalline size. The XRD studies also confirmed that TiO2 nanoparticles became properly dispersed to the PVA matrix, leading to increased PVA crystallinity after doping of different phases of TiO2 nanoparticles. UV-visible analysis revealed an increase in absorption intensity and peak position shifts slightly towards longer wavelengths, which indicates that nanofillers tuned the band gap of PVA. The doping of the TiO2 (brookite) phase in the PVA matrix results in a decreased in PL intensity. Results: This suggests that the PVA/TiO2 (brookite) membrane exhibits a greater degree of photocatalytic activity in comparison to the other two composites. According to the FTIR investigation, the hydroxyl (OH) groups present in PVA interact with the dopants Ti+ ions via intra- and intermolecular hydrogen bonds to produce charge transfer complexes (CTC). The AFM study shows surface roughness details for PVA and PVA/TiO2 composite membranes. The average grain size of TiO2 nanoparticles calculated from TEM images is in good agreement with the grain size calculated by XRD. Conclusion: By adjusting the phase of TiO2 nanoparticles into PVA matrix, composites can be developed that are optimized for a variety of applications such as water purification, UV protection, self-cleaning surfaces, lithium-ion batteries, and optoelectronic devices.

Fabrication of a ZIF-8/PVA Membrane on PVDF Fiber by Spray for the Highly Efficient Separation of Oil-in-Water Emulsions.

In human life and production, excessive oily wastewaters containing detergents are produced and discharged, causing severe environmental pollution and water resource problems. A metal-organic framework (MOF)-based membrane is an economical and environmentally friendly tool for emulsion separation but is limited by a complex preparation process and poor flexibility. Herein, we developed a simple method to synthesize a MOF-based mixed-matrix membrane (MMM) by spray and fabricated the membrane on poly(vinylidene fluoride) (PVDF) fibers via postdeposition and in situ growth manners. The prepared ZIF-8/PVA MMMs have uniform distribution of ZIF-8 particles and poly(vinyl alcohol) (PVA) on the PVDF fibers. PVA improved the adhesion between the ZIF-8 particles and between the MOF layer and PVDF fiber, endowing the separation membrane with high flexibility and bendability. The prepared ZIF-8/PVA membrane exhibited hydrophilicity and underwater superoleophobicity, which showed high separation efficiency and considerable water flux for emulsions, emulsion containing dye, and surfactant-stabilized emulsion. In addition, the fabricated ZIF-8/PVA/PVDF fibers exhibited good antifouling property and flexibility and can maintain stable separation efficiency after working several times and even under bending, demonstrating the stability and potentiality of the ZIF-8/PVA/PVDF fibers in practical applications. This work paves a new avenue for the synthesis and application of MOF-based MMMs.

Enhancement of the energy dissipation capacity C-S-H gel through self-crosslinking the poly (vinyl alcohol)

Damping cementitious materials have been widely used in engineering structures for vibration control. However, achieving a balance between the mechanical strength and damping capacity of cementitious materials remains a challenge. Herein, we utilized an initiator (APS) to initiate the self-crosslinking reaction of PVA molecules in C3S paste, then successfully introduced the viscoelastic PVA membranes into C-S-H gel to enhance its energy dissipation capacity. Results showed that the self-crosslinking PVA (scPVA) increased the loss modulus (E′′) of C-S-H gel by about 158 %, increased loss tangent (tanδ) by 85 % and increased the compressive strength by 24 %. Nano-microscopic tests and molecular dynamics (MD) simulation confirmed that scPVA was introduced into C-S-H gel via the hydrogen-bonding interaction, and then formed the viscoelastic PVA membranes, which promoted C3S hydration, reduced the pore size of C-S-H gel and increased the mean chain length (MCL) of C-S-H gel. This study proposes a novel approach for designing high-damping cementitious materials.

Application of biohybrid membranes for arsenic and chromium removal and their impact on pollutant accumulation in soybean (Glycine max L.) seedlings.

Chromium and arsenic are among the priority pollutants to be controlled by regulatory and health agencies due to their ability to accumulate in food chains and the harmful effects on health resulting from the ingestion of food contaminated with metals and metalloids. In the present work, four biohybrid membrane systems were developed as alternatives for the removal of these pollutants, three based on polyvinyl alcohol polymeric mesh (PVA, PVA-magnetite, PVA L-cysteine) and one based on polybutylene adipate terephthalate (PBAT), all associated with bioremediation agents. The efficiency of the bioassociation process was assessed through count methods and microscopy. The removal capacity of these systems was evaluated in synthetic liquid medium, both in the absence and in the presence of soybean (Glycine max L.) seedlings. The content of chromium and arsenic was also analyzed in aerial and hypogeous tissues of seedlings grown on contaminated solid substrate. PVA and PVA-magnetite biohybrid membranes showed the highest removal rates, between 57 and 75% of the initial arsenic content and more than 80% of the initial chromium content after 48h of treatment, when evaluated in synthetic liquid media with initial concentrations of 2.5ppm of pentavalent arsenic and 5ppm of hexavalent chromium, both in presence and absence of seedlings. PVA and PBAT promoted a significant reduction of arsenic translocation to the aerial parts, generally edible, of this crop of agronomic interest. The systems tested showed a high potential for biotechnological applications in matrices affected by the presence of arsenic and chromium.

Development of Polyvinyl Alcohol/Chitosan Nanoparticles Mixed-Matrix Membrane

The blend of PVA-CSNP is widely used in many industries and research fields such as packaging in the food industry, medical and pharmaceutical industries, as well as separation industries. Polymer blending can improve the membrane by combining two or more polymers in suitable ratios. CSNP was blended with PVA membrane to improve its properties. In this study, the CSNP polymer and PVA/CSNP membrane were synthesized and characterized. The synthesis of CSNP involved the application of CS at 0.5 wt.% and 1.0 wt.% at 1:1 and 1:2 ratios to STPP. The particle size and zeta potential for the 0.5 wt.% ratios showed significant outcomes for the study. The particle sizes were 892 nm and 975 nm, whereas the zeta potential showed significant cation values of +50.4 and +43.7 mV for the 1:1 and 1:2 ratios, respectively. The PVA membrane was developed using these nanofillers, and the functional group analysis showed molecular bonding throughout the membrane. The developed membrane also exhibited a smooth and dense structure, supporting good dispersion of CSNP within the membrane. To evaluate the physical strength of the membrane, the swelling index was measured, and a low degree of swelling confirmed the forecast that CSNP would reduce the hydrophilicity of the PVA membrane, subsequently providing good membrane strength.

Preparation of Free-Standing Defect-Free ZIF-8/PVA Membranes via Confined Reaction at the Quasi-Interface.

Developing a facile strategy to synthesize free-standing defect-free metal-organic framework (MOF) membranes with high separation selectivity and good mechanical stability is very appealing but challenging. Herein, by confining the reaction of metal and ligand at the quasi-interface, a representative membrane composed of a continuous ZIF-8 layer and poly(vinyl alcohol) (PVA) was fabricated. The continuous ZIF-8 layer endowed the membrane with high separation efficiency, while PVA acted as a filler to eliminate the defection, synergistically achieving high selective ion transport and good mechanical stability. The continuous defect-free ZIF-8/PVA membrane showed excellent separation performance of selective ion transport with high Li+ permeance of 17.83 mol·m-2·h-1 as well as decent Li+/Mg2+ and Li+/Ca2+ selectivities of 24.60 and 244.58, respectively. The separation performance of the ZIF-8/PVA membrane remained stable after 10% strain, indicating its good mechanical stability. This work will promote the development of MOF-based membranes in practical applications.

Application of Principal Component Analysis for the Elucidation of Operational Features for Pervaporation Desalination Performance of PVA-Based TFC Membrane

Principal Component Analysis (PCA) serves as a valuable tool for analyzing membrane processes, offering insights into complex datasets, identifying crucial factors influencing membrane performance, aiding in design and optimization, and facilitating monitoring and fault diagnosis. In this study, PCA is applied to understand operational features affecting pervaporation desalination performance of PVA-based TFC membranes. PCA-biplot representation reveals that the first two principal components (PCs) accounted for 62.34% of the total variance, with normalized permeation with selective layer thickness (Pnorm), water permeation flux (P), and operational temperature (T) contributing significantly to PC1, while salt rejection dominates PC2. Membrane clustering indicates distinct influences, with membranes grouped based on correlation with operational factors. Excluding outliers increases total variance to 74.15%, showing altered membrane arrangements. Interestingly, the adopted strategy showed a high discrepancy between P and Pnorm, indicating the relevance of comparing between PVA membranes with specific layers and those with none. PCA results showed that Pnorm is more important than P in operational features, highlighting its significance in both research and practical applications. Our findings show that even know P remains a key performance property; Pnorm is critical for developing high-performance, efficient, and economically viable pervaporation desalination membranes. Subsequent PCA for membranes without specific layers (M1 to M6) and with specific layers (M7 to M11) highlights higher total variance and influence of variables, aiding in understanding membranes’ behavior and suitability under different conditions. Overall, PCA effectively delineates performance characteristics and potential applications of PVA-based TFC membranes. This study would confirm the applicability of the PCA approach in monitoring the operational efficiency of pervaporation desalination via these membranes.

Slow‐release fertilizer behavior of polyvinyl alcohol (PVA)/urea/TiO2 nanofiber membrane

AbstractNanofiber is a material used as a drug carrier matrix in drug release materials. Its morphology has high porosity and good flexibility, making it suitable for this purpose. The use of nanofiber as a carrier matrix in slow‐release fertilizer (SRF) material is expected to provide a solution for releasing fertilizer into the soil more measurably and efficiently In this study, PVA/Urea/TiO2 nanofibers were fabricated using the electrospinning method. PVA/Urea/TiO2 SRFs were prepared using varying urea mass percentages (10%, 15%, and 20% of PVA mass) and the concentration of titanium dioxide suspension solution (0, 0.2, and 0.4 mL). Every sample was analyzed using scanning electron microscopy (SEM) and Fourier transform infrared (FTIR) and tested using contact angle and slow‐release tests. From SEM characterizations, all samples showed the ability to form nanofiber. It was found that the membrane diameter sizes for each sample A, B, C, D, E, and F were 341 ± 5, 309 ± 12, 109 ± 3, 313 ± 10, 109 ± 3, and 158 ± 6 nm, respectively. The FTIR characterizations showed that all the matrix samples successfully contained the nitrogen group, which was found at wave number 1605 cm−1 (NH deformation), 1574 cm−1 (CN stretching), and 3430 cm−1 (NH stretching). The SEM mapping images confirmed the presence of titanium dioxide (green dots). The contact angle test showed that all samples had hydrophilic properties (the contact angle value lower than 90°), and the greatest value of contact angle measurement was 31.08° for sample C/E (sample with the most presence of TiO2 suspension solution 0.4 mL). The sample with the greatest TiO2 suspension concentration (0.4 mL) had the longest urea release time, lasting 8 days. This result indicates the addition of TiO2, can potentially suppress the hydrophilic properties of the PVA membrane. It is found that the addition of TiO2 influenced the membrane's hydrophilicity, consequently increasing the release rate. This study used the Korsmeyer–Peppas mathematical kinetic model to show that diffusion and swelling are release mechanisms for SRF membranes.

Plasma Surface Treatment and Application of Polyvinyl Alcohol/Polylactic Acid Electrospun Fibrous Hemostatic Membrane

In this study, an improved PVA/PLA fibrous hemostatic membrane was prepared by electrospinning technology combined with air plasma modification. The plasma treatment was used to modify PLA to enhance the interlayer bonding between the PVA and PLA fibrous membranes first, then modify the PVA to improve the hemostatic capacity. The surfaces of the PLA and PVA were oxidized after air plasma treatment, the fibrous diameter was reduced, and roughness was increased. Plasma treatment enhanced the interfacial bond strength of PLA/PVA composite fibrous membrane, and PLA acted as a good mechanical support. Plasma-treated PVA/PLA composite membranes showed an increasing liquid-enrichment capacity of 350% and shortened the coagulation time to 258 s. The hemostatic model of the liver showed that the hemostatic ability of plasma-treated PVA/PLA composite membranes was enhanced by 79% compared to untreated PVA membranes, with a slight improvement over commercially available collagen. The results showed that the plasma-treated PVA/PLA fibers were able to achieve more effective hemostasis, which provides a new strategy for improving the hemostatic performance of hemostatic materials.

Ammonia permeation and plasticization of glassy polymeric membranes

Ammonia (NH3) is a vital industrial chemical and a potential clean fuel, whose production is increasing globally. The permeation of ammonia through glassy polymeric membranes demonstrates considerable variability, due to hydrogen bonding with both the polymer and residual water. This study reveals the underlying mechanisms for ammonia permeability within membranes, which is strongly correlated with the presence of water and the polymer's chemistry. Three polymers with varying water/ammonia affinity were studied: poly (vinyl alcohol) (PVA), polysulfone (PSU), and Teflon AF 1600. Ammonia was found to readily plasticize PVA, with sorption isotherms that follow Henry's law at conditions below the nominal glass transition temperature. Residual water within the PVA membranes increased ammonia permeability by an order of magnitude greater than that observed for well-dried PVA, due to water-induced swelling. PSU, being hydrophobic, was unaffected by residual water, though ammonia permeability was clearly time-dependent with a 50 % reduction over 4 days. This was attributed to ammonia clustering within the ammonia phobic PSU, which resulted in pore-blocking. The superhydrophobic Teflon AF 1600 membrane demonstrated the same time dependent permeability behaviour, but at a much faster timescale of minutes rather than days. It is suggested that this relates to the rate of formation of ammonia clusters, which is dependent on the degree of ammonia sorption within the polymer.

Transdermal delivery system to release phthalocyanine photosensitizers for the potential treatment of skin cancer with PDT.

This research aims to examine the transdermal release of water-soluble indium and zinc metallo phthalocyanine (InPc and ZnPc) compounds from the poly(vinyl alcohol) (PVA) membrane and the cytotoxicity effect of these Pcs on normal mouse fibroblasts (L929 fibroblast) and human melanoma (SK-MEL-30) cells. For this purpose, the effects of temperature, pH, drug concentration and membrane thickness on transdermal release were investigated in order to obtain the optimum transdermal release profile by preparing PVA membranes with different thicknesses and crosslinked by heat treatment. Optimum drug release was found to be 85.36% using 6 μm thick PVA membrane at 37 ± 0.5 °C, when upper cell pH 1.2 and lower cell pH 5.5, for 3 mg/mL InPc drug concentration. Under the same conditions, the drug release value for ZnPc was found to be 69.78%. In addition, in vitro studies were performed on L929 and SK-MEL-30 cells. under optimized drug (InPc and ZnPc) and membrane conditions. It was found that no significant cytotoxic effect was observed in L929 and SK-MEL-30 cells in the dark. Photodynamic tests were also carried out with InPc and ZnPc. The results show that cell viability decreases in SK-MEL-30 cells at concentrations of 10 μg/mL and above. In addition, while the InPc IC50 value was determined as 4.058 μg/mL, this value was determined as 11.574 μg/mL for ZnPc.

Influence of Process Parameters on the Efficiency of Pervaporation Pilot ECO-001 Plant for Raw Ethanol Dehydration.

Pervaporation is a membrane-based process used for the separation of liquid mixtures. As this membrane process is governed by the differences in the sorption and diffusivities of separated components, close boiling mixtures and azeotropic mixtures can effectively be separated. The dehydration of ethanol is the most common application of hydrophilic pervaporation. The pilot scale properties of hydrophilic composite poly(vinyl alcohol) PVA membrane (PERVAPTM 2200) in contact with wet raw bioethanol are presented. The wet raw bioethanol was composed of ethanol (82.4-89.6 wt%), water (5.9-8.5 wt%), methanol (2.3-6.9 wt%), cyclohexane (0.2-2.4 wt%), higher alcohols (0.2-1.3 wt%), and acetaldehyde (0.004-0.030 wt%). All experiments were performed using a SULZER ECO-001 plant equipped with a 1.5 m2 membrane module. The efficiency of the dehydration process (i.e., membrane selectivity, permeate flux, degree of dehydration) was discussed as a function of the following parameters: the feed temperature, the feed composition, and the feed flow rate through the module. It was found that the low feed flow rate influenced the dehydration efficiency as the enthalpy of evaporation caused a high temperature drop in the module (around 25 °C at a feed flow rate equal to 5 kg h-1). The separation coefficient during pervaporation was in the range of 600-1200, depending on the feed composition. The increase in temperature augmented the permeation flux and shortened the time needed to reach the assumed level of dehydration. It was revealed that dehydration by pervaporation using ECO-001 pilot plant is an efficient process, allowing also to investigate the influence of various parameters on the process efficiency.

Practical organic electronic noses using semi-permeable polymer membranes

Electronic noses (E-noses) mimic olfactory organs and quantify volatile organic compounds (VOCs), emulating the sense of smell, with applications in real-time monitoring of VOCs in food, healthcare, and law enforcement industries. Organic field-effect transistor (OFET) based sensors can be fabricated in large arrays by economical processes, however, lack the selectivity necessary to differentiate wide varieties of VOCs. Here, we explore the use of permeable polymer membranes with OFET sensors to improve their selectivity. Acylated poly(vinyl alcohol) (PVA) derivatives were synthesized, characterized, and evaluated in OFET vapor sensors as tunable membranes. Sensors with and without acylated PVA membranes were tested with VOC analytes. By monitoring drain current over time, we found that membranes dramatically changed responses to different analytes. We show that VOCs including methanol, ethanol, hexane, toluene, tetrahydrofuran, methyl ethyl ketone, and ethyl acetate can all be detected and differentiated with much greater selectivity than sensors without membranes. In particular, methanol and ethanol, which are difficult to differentiate in vapor sensors, showed significant quantitative differences in the initial slope (0.0403 s−1 vs 0.0192 s−1 respectively; 6 σ) and decay constants (5.5 s vs 15.9 s respectively; 26 σ) of their current vs time responses, allowing methanol and ethanol to be differentiated with 100 % confidence. This approach enables the economical fabrication of large varieties of unique organic vapor sensors by simply changing the membrane layer and results in an outstanding level of selectivity for OFET vapor sensors.

Dialdehyde polyethylene glycol cross‐linked poly(vinyl alcohol) membranes with enhanced CO2/N2 separation performance

AbstractThe development of carbon dioxide (CO2) separation technology is crucial for mitigating global climate change and promoting sustainable development. In this study, we successfully synthesized an array of cross‐linked poly(vinyl alcohol) (PVA) membranes, xALD‐PEG‐ALD‐c‐PVA, with enhanced CO2/N2 separation performance by employing dialdehyde polyethylene glycol (ALD‐PEG‐ALD) as a cross‐linker. The formation of the cross‐linked network structure not only inhibits the crystallization of PVA but also disrupts hydrogen bonding and thus increases fractional free volume of PVA chains. Under the synergistic effect of these multiple factors, the cross‐linked PVA membranes exhibit a significantly improved CO2 permeability. Moreover, they maintain high CO2/N2 selectivity, attributing to the CO2‐philic characteristic of ethylene oxide groups in the cross‐linked structure. At the ALD‐PEG‐ALD content of 1.6 mmol g−1, the xALD‐PEG‐ALD‐c‐PVA membrane demonstrates a CO2 permeability of 41.4 barrer and a CO2/N2 selectivity of 57.4 at 2 bar and 25°C. Furthermore, compared with the pristine PVA membrane, xALD‐PEG‐ALD‐c‐PVA membranes manifest superior mechanical properties and outstanding separation performance for a CO2/N2 (15/85, vol%) gas mixture. The excellent combination of permeability and selectivity makes xALD‐PEG‐ALD‐c‐PVA membranes highly promising for various CO2 separation applications.

Reinforcement using undoped carbon quantum dots (CQDs) with a partially carbonized structure doubles the toughness of PVA membranes.

Nano-carbon-reinforced polymer composites have gained much consideration in functional applications due to their attractive mechanical strength and cost-effectiveness. The surface chemistry and associated mechanical strength of carbon nanotubes (CNTs), graphene, and other carbon derivative-based nanocomposites are well understood. While CQDs are considered emerging carbon derivatives, their surface chemistry, unique physio-chemical properties, and dispersion behavior in polymers are yet to be explored. Therefore, in this work, CQDs with different structures were synthesized from lemon pulp and urea, and their rheology and mechanical strength were studied in the PVA matrix. The surface chemistry and structure of CQDs were controlled using different solvents and reaction temperatures, respectively. CQDs possessed a circular shape, with a size of <10 nm, having a suitable carbon core and functional groups, as confirmed by TEM and FTIR spectroscopy. The dynamic viscosity and particle size of PVA/CQDs films peaked at 4% inclusion due to the maximum crosslinking of U-CQDs with reinforcement at 180 °C. Compared with pure PVA, the optimized composite showed an 80% larger particle size with 67% better tensile strength at 4% U-CQDs concentration. In addition to enhanced mechanical strength, CQDs exhibited antibacterial activity in composites. These CQDs-reinforced PVA composites may be suitable for different functional textile applications (shape memory composites and photo-active textiles).

Assessing the Dehydration Pervaporation Performance for Purification of Industrially Significant 1, 2 Hexanediol/Water Mixtures Using Crosslinked PVA Membrane

Assessing the Dehydration Pervaporation Performance for Purification of Industrially Significant 1, 2 Hexanediol/Water Mixtures Using Crosslinked PVA Membrane

Fabrication of Zr-MOF filled PVA/CS blended membranes for high efficiency CO2 separation

In the present work, a series of PVA and CS blend membranes were studied. These prepared membranes were evaluated by binary mixture gases of CO2/N2 and CO2/CH4. The optimum ratio of PVA/CS for CO2 permeance was achieved at 5:5. It recorded a CO2 permeability of 20.8 GPU (1 GPU = 1 × 10-6·cm3 (STP)·cm−2·s−1·cmHg−1) with CO2/N2 selectivity of 89.7, as well as CO2 permeability of 10.2 GPU and CO2/CH4 selectivity of 56.3. Secondly, two kinds of nanoparticle UiO-66 and UiO-66-NH2 were used to prepare mixed matrix membranes. The effects of nanofiller content and chemical groups on gas permselectivity were investigated. Results show that the addition of nanoparticles can effectively improve the permselectivity of membrane. The mixed matrix membranes addition with UiO-66-NH2 achieved the optimum CO2 performance and these were following the order of PVA(5)/CS(5)-UiO-66-NH2 > PVA(5)/CS(5)-UiO-66 > PVA(5)/CS(5). For all these membranes, the permeance and selectivity present initial increased and then decreased. Mixed matrix membranes addition UiO-66-NH2 (containing 3.75 wt%) exhibits a CO2 permeance of 32.77 GPU and CO2/N2 selectivity of 93.47, as well as CO2 permeance of 25.57 GPU and CO2/CH4 selectivity of 70.1, which was beyond the 2008 Robeson upper bound.

Novel Physically-Crosslinked Caffeine and Vitamin C-Loaded PVA/Aloe Vera Hydrogel Membranes for Topical Wound Healing: Synthesis, Characterization and In-Vivo Wound Healing Tests

Novel physically-crosslinked PVA membranes blended with Aloe vera extract were fabricated by solution-casting method. Physically-crosslinking process is depending on the rearrangement of PVA chains forming intermolecular hydrogen bonding with removal of water molecules using propanol as a stabilizing agent. The structure of crosslinked membranes was characterized by FT-IR, SEM, TGA, and XRD analyses and confirmed via gel faction and swelling ratio studies. Caffeine and vitamin C loaded-PVA/Aloe vera membranes were bio-assessed in terms of their impact on the wound healing using Wistar albino rats as an animal model. In vitro evaluation includes protein adsorption showed that the fabricated membranes improved significantly the wound healing ability via enhancing the tissue platelet aggregation. In addition, resulting adequate in vitro release behavior for the loaded ingredients in the potential application. In-vivo results displayed that rats full-thickness wounds were remarkably reduced after PVA/Aloe vera/Vitamin C membranes treatment, as shown by a reduction in the area of the wounds when compared to wounds treated with cotton gauze and PVA/Aloe vera membranes. Furthermore, the treated wounds with PVA/Aloevera/caffeine show more wound closer comparing to that incorporate vitamin C and the PVA/Aloevera incorporated both caffeine and vitamin C give the most significant healing that show reappearance of hair covered the wound area. Histological examinations of wounds covered in membranes showed a successful re-epithelialization, demonstrating caffeine's and vitamin C’s efficacy. These results demonstrated that, PVA/Aloe Vera/Caffeine and PVA/Aloe vera/vitamin C membrane have remarkable wound healing and skin regeneration properties.Graphical

Synergistic pervaporation dehydration of ethanol/water mixture: Exploring the potential of a covalently designed hybrid membrane structure of polyacrylic acid grafted carbon nitride and polyvinyl alcohol

Polyacrylic acid (PAA) grafted CN sheet (P-g-CN) was synthesized to enhance the dispersive properties of carbon nitride (CN) in the membrane. A successful PAA grafting to the CN was confirmed from FTIR, TGA, and Zeta potential and XRD analyses. The A PVA membrane embedded P-g-CN, including a covalently constructed polymer-filler network, was developed to separate ethanol-water mixtures using pervaporation (PV). XPS study has confirmed a covalent attachment of P-g-CN sheets to the PVA matrix. Thereby, a defect-free membrane matrix was observed in the FESEM analysis. A 10 wt% loaded PVA-P-g-CN10 composite membrane was compared to the pristine PVA membrane, demonstrating improved PV dehydration performance. The flux decreased from 0.21 kg/m2h of pristine PVA membrane to 0.17 kg/m2h of PVA-P-g-CN10 membrane, while the separation factor improved from 49 to 176 in a 90/10 wt % ethanol/water feed at 40 °C. This improvement can be attributed to the selective diffusion of water through the P-g-CN interlayer spacing and tiny triangular nanopores in the s-triazine network, along with their dispersibility in the PVA matrix, resulting in well-ordered membrane morphology. Furthermore, PVA-P-g-CN10 exhibited higher water permeance (43.31–86.07 GPU) than ethanol (1.18–10.47 GPU) as the feed temperature increased from 30 to 70 °C, suggesting P-g-CN successfully inhibits swelling in the feed solution through proper interaction with PVA. In a long-term PV test lasting 250 h, the PVA-P-g-CN10 membrane displayed excellent structural stability and maintained its performance.