PVA Blend Research Articles

PPY: PVA Blend Enhanced with Metal Salt for Gas Sensing Applications

PPY: PVA Blend Enhanced with Metal Salt for Gas Sensing Applications

Aloe vera Gel–Reinforced Biodegradable Starch–PVA Blends for Sustainable Packaging of Green Chillies

ABSTRACTThe objective of the current study was to evaluate the feasibility of Aloe vera gel as a plasticizer and crosslinker in improving the properties of starch–polyvinyl alcohol blends that could find applications in packaging. The concentration of Aloe vera gel was varied (1%, 3%, 5% and 7% wt/wt) to produce SPA‐1, SPA‐3, SPA‐5 and SPA‐7 films, respectively. The plasticizing and crosslinking characteristics associated with Aloe vera gel had a positive influence on the mechanical properties of the films. Addition of Aloe vera gel increased the tensile strength of films from 27.45 MPa (control) to 32.98, 32.53 and 32.32, for SPA‐1, SPA‐3 and SPA‐5 films, respectively. Among all the films, highest elongation at break (20.62%) was observed for SPA‐3 films. Due to crosslinking, degree of swelling, water solubility and water vapour permeability for SPA‐3 films decreased by 5.58%, 38.29% and 21.44%, respectively, compared to control films. The contact angle of the SPA‐3 film significantly increased by 49.25% when compared to control samples. Scanning electron microscope images revealed compact and smooth surface microstructure of control films, and crosslinking was evident in presence of Aloe vera gel. The rate of degradation for SPA‐3 films in soil after 40 days was enhanced by 32.25% compared to control films. SPA‐1 and SPA‐3 films were tested for use as packaging material for storage of green chillies. Chillies under unpacked conditions, in control and SPA‐1 films, turned red in 3 days. Those stored in films with 3% Aloe vera gel began to change colour later (after 5 days) with no visual evidence of microbial or fungal growth. In summary, starch–polyvinyl alcohol matrix films with 3% Aloe vera gel (SPA‐3) were effective as a sustainable alternative in increasing shelf life of foodstuff.

Silicon Vacancies Diamond/Silk/PVA Hierarchical Physical Unclonable Functions for Multi-Level Encryption.

Physical unclonable functions (PUFs) have emerged as a promising encryption technology, utilizing intrinsic physical identifiers that offer enhanced security and tamper resistance. Multi-level PUFs boost system complexity, thereby improving system reliability and fault tolerance. However, crosstalk-free multi-level PUFs remain a persistent challenge. In this study, a hierarchical PUF system that harnesses the spontaneous phase separation of silk fibroin /PVA blend and the random distribution of silicon-vacancy diamonds within the blend is presented. The thermodynamic instability of phase separation and inherent unpredictability of diamond dispersion gives rise to intricate random patterns at two distinct scales, enabling time-efficient hierarchical authentication for cryptographic keys. These patterns are complementary yet independent, inherently resistant to replication and damage thus affording robust security and reliability to the proposed system. Furthermore, customized authentication algorithms are constructed: visual PUFs authentication utilizes neural network combined structural similarity index measure, while spectral PUFs authentication employs Hamming distance and cross-correlation bit operation. This hierarchical PUF system attains a high recognition rate without interscale crosstalk. Additionally, the coding capacity is exponentially enhanced using M-ary encoding to reinforce multi-level encryption. Hierarchical PUFs hold significant potential for immediate application, offering unprecedented data protection and cryptographic key authentication capabilities.

Comparative Study on Structural, Dielectric Behavior and AC Conductivity of PPY-PVA Incorporated with TiO2 Fine and Nano Particles

Abstract An in-situ oxidative chemical polymerization technique to prepare thin films of PPY, PVA, and PPY-PVA blend doped with variable concentrations of TiO2 fine- and nano-particles was further investigated by X-ray diffractometer (XRD) and impedance spectrometer to study structural, dielectric, and AC conducting behavior. XRD spectra established that sharp and high intense peaks of PPY-PVA- fine TiO2 films indicated more crystallinity, which might be due to higher compactness and modification in interplanar spacing. Dielectric plots revealed that PPY-PVA-nano TiO2 films exhibited higher dielectric constants and lower dielectric loss compared to films of PPY-PVA- fine TiO2 in shorter frequency region, suggesting that these films are more suitable for charge storage devices. Conductivity plots revealed that AC conductivity of pure PPY was low (4.8 x10-3 S/cm at 313 0K) and was increased to 5.3 x10-3 S/cm by addition of PVA. AC conductivities of PPY-PVA-nano TiO2 thin films are relatively higher (7.43x10-3 S/cm to 1.14x10-2 S/cm) than PPY-PVA-fine TiO2 films (6.35x10-3 to 9.78x10-3 S/cm) with increasing frequency and temperature, which could be due to large surface area to volume ratio of nano-size dopant. This suggests that PPY-PVA-nano TiO2 thin films may be used for sensing various gasses.

Influence of the Type of Biocompatible Polymer in the Shell of Magnetite Nanoparticles on Their Interaction with DPPC in Two-Component Langmuir Monolayers.

Magnetite nanoparticles (MNPs) are attractive nanomaterials for applications in magnetic resonance imaging, targeted drug delivery, and anticancer therapy due to their unique properties such as nontoxicity, wide chemical affinity, and intrinsic superparamagnetism. Their functionalization with polymers such as chitosan or poly(vinyl alcohol) (PVA) can not only improve their biocompatibility and biodegradability but it also plays an important role in their interactions with biological cells. In this work, the effect of the functionalization of MNPs with chitosan, PVA, and their blend on model cell membranes formed from 1,2-dipalmitoyl-sn-glycerol-3-phosphocholine (DPPC) using a Langmuir technique was studied. The studies performed showed that the type of biocompatible polymer in the MNP shell plays a crucial role in the effectiveness of its adsorption process into the model cell membrane. Modification of MNPs with chitosan facilitates significantly more effective adsorption than coating them with PVA or with a chitosan and PVA blend. The presence of all the investigated MNPs in the DPPC monolayer at low concentrations does not affect its thermodynamic state, fluidity, or morphology, which is promising in terms of their biocompatibility. On the other hand, their high concentration (molar fraction above ≈0.05) exerts a disruptive effect on the model cell membrane and results in their aggregation, leading probably to the loss of their superparamagnetic properties essential for nanomedicine.

Activated Carbon Nanofiber Sheets Derived from Electrospun Lignin: PVA Blend for Flexible Supercapacitors

The present investigation reports the performance of ultra-flexible activated carbon nanofiber sheets (ACNF) as a flexible electrode for supercapacitors application. ACNF was fabricated by pre-carbonization at 600 °C and then by activation using potassium hydroxide (KOH) at 800 °C.These ACNF sheets prepared via the facile electrospinning technique possess the morphology of the nanofiber network with the diameter range (600-1400 nm) of the carbon. The findings demonstrate that the activation method not only enhances the sheet's surface area (806.9 m2/g) and total pore volume (0.519 cc/g) but also eliminates the lignin polymer's inherent sodium (Na) impurity through washing. This interconnected nanofiber sheet possesses high electrical conductivity of 8.40 S/cm. These sheets exhibit cloth-like flexibility with high electrical conductivity and porosity, making them suitable candidates for flexible electrodes. Raman spectroscopy was also carried out to get information about sp2 carbon. Cyclic Voltammetry (CV), Galvanostatic Charge-Discharge (GCD), and Electrochemical Impedance Spectroscopy (EIS) were performed to understand the electrochemical performance of the sheets as electrodes. This ACNF sheet demonstrate a higher specific capacitance of 203.29 F/g at a current density of 1 A/g in a three-electrode configuration. Furthermore, a flexible supercapacitor device was fabricated using an ACNF sheet due to its high flexibility, stand-alone character, and excellent performance as an electrode. The device exhibits a high energy density of 65.52 Wh/kg and a power density of 1036.27 W/kg with high coulombic efficiency (99.6%) after 10,000 cycles. Also, the prepared device illuminated the seven-segment display in various bending conditions showing its flexibility.

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.

Investigation of KOH‐doped PVA‐based membrane electrolytes cross‐linked with tartaric acid for DMAFCs

AbstractThis research focused on the development of anion exchange membrane electrolytes suitable for direct methanol alkaline fuel cells (DMAFC) by employing a straightforward blending and solution casting process complemented by subsequent heat treatment. Tartaric acid (TA) was employed as a cross‐linking agent to enhance the heat resistance and structural integrity of the PVA matrix. The distinctive attributes of the PT (PVA and tartaric acid blend) samples, including water absorption and swelling capacity, were comprehensively investigated with respect to variations in both TA content (expressed as wt. % relative to the PVA matrix) and alterations in the duration of thermal treatment. Cross‐link formation between the polymer chains and TA was determined using FTIR analysis. The samples were subjected to comprehensive analysis, encompassing the determination of crystallinity via X‐ray diffraction (XRD), assessment of thermal stability using thermogravimetric analysis (TGA), investigation of morphology through scanning electron microscopy (SEM), and measurement of ionic conductivity using AC Impedance spectroscopy. The methanol permeability was measured to determine the selectivity values of the membranes. Subsequently, within the DMAFC system, the performances of the PT30‐3, PT40‐2, and PT40‐3 membranes, which exhibited the highest selectivities, were assessed. The contribution of the crosslinking process to the resistance of the membranes to oxidative conditions, as represented by the Fenton solution, was evaluated to assess the chemical stability of the membranes. The maximum power densities for PT30‐3 and PT40‐3 membranes reached 15.29 and 12.53 mW/cm2 at 30°C, respectively. These figures exhibited a notable increase, reaching 32.73 mW/cm2 for PT30‐3 and 31.72 mW/cm2 for PT40‐3 when the temperature was elevated to 60°C. This study confirmed that the crosslinking strategy using TA assisted by thermal treatment is very simple and competitive compared with other techniques reported in the literature. PT membranes are promising candidates for commercialization and utilization in DMAFC owing to their environment‐friendly nature, cost‐effectiveness, and high efficiency.Highlights TA cross‐linking improved the thermal and dimensional stability of PVA. The PT membrane properties varied with TA content and thermal treatment time. Some electrolytes in this study outperformed those previously reported for DMAFC. PT membranes offer efficiency, cost‐effectiveness, and eco‐friendliness for DMAFCs.

Studies on Agrochemical Controlled Release Behavior of Copolymer Hydrogel with PVA Blends of Natural Polymers and Their Water-Retention Capabilities in Agricultural Soil.

Agricultural technical development relies exclusively on the effective delivery of agrochemicals and water to plants and on reducing the harmful effects of agrochemicals on useful organisms in the soil. In this study, super-absorbent hydrogels were prepared in the form of microspheres using gum Arabic (GA), which was copolymerized once with chitosan (CS) and once with poly (vinyl alcohol) (PVA). To impart mechanical strength to the hydrogel microspheres, a covalent cross-linker (N,N'-methylenebisacrylamide (MBA)) was used for the PVA/GA hydrogel, and an ionic cross-linker (sodium hexametaphosphate (SHMP)) was used for the CS/GA hydrogel. The prepared PVA/GA-CH and CS/GA-PH hydrogel microspheres showed different degrees of swelling (DSs) in the following solution media: deionized water (DW), river water (RW), and buffered solutions (pH 4; pH 9). The PVA/GA-CH hydrogel microspheres showed a maximum DS of 84 g/g in the RW, while the CS/GA-PH hydrogel microspheres showed a maximum DS of 63 g/g in the buffered solution at a pH 9. The water-retention capabilities of the hydrogels were studied using a mixture of 0.5% (w/w) hydrogel microspheres in agricultural soil; the composite showed an additional 20 days of water retention in comparison with a control sample consisting of soil alone. The hydrogels were loaded with urea, which is an important fertilizer in the field of agriculture. The PVA/GA-CH hydrogel microspheres showed a maximum loading percentage (Lmax%) of 89% (w/w), while the CS/GA-PH hydrogel microspheres showed an Lmax% = 79.75% (w/w) for urea. The urea-release behaviors of the hydrogel microspheres were studied under different release media and temperature conditions. In practice, the PVA/GA-CH hydrogel microspheres showed a better release profile in the RW at 10 °C, while the CS/GA-PH hydrogel microspheres showed a more controlled release in media at a pH 9 and at 30 °C. The urea-loaded microspheres, aside from those following the release, were characterized via FTIR and SEM. In contrast, virgin microspheres were characterized using XRD,1H NMR, (TGA and DSC), and the maximum degree of swelling, in addition to being subjected to SEM and FTIR analyses.

Effect of dopant on ion-dynamics of sodium ion-based flexible polyblend electrolyte for electrochemical device application

This work examines the impact of NaNO3 salt on a NaAlg: PVA blend polymer, focusing on charge carrier properties, such as number density (n), mobility (μ), and diffusion coefficient (D). It is found that the addition of NaNO3 increased the room temperature conductivity from (6.12±0.15) × 10−8 S cm−1 (PNN0, salt-free) to (6.50±0.03) × 10−6 S cm−1 (PNN15, 15 wt.% NaNO3), influenced by increasing n compared to µ. Temperature-dependent conductivity revealed a significant influence of both n and μ on electrolyte conductivity, and the ion dynamics were explored using various formalisms. XRD studies showed reduced crystallinity owing to the interaction of Na+ and NO3− with -OH groups, as confirmed by IR spectroscopy. Scanning electron microscopy confirmed salt deposits at higher concentrations. However, sufficient mechanical strength was observed for the optimally conducting sample. Obtained results showed the potential applications of the sample in electrochemical devices.

Thermo-mechanical performance of nanostructured electrospun composites produced from poly(vinyl alcohol) and cellulosic compounds for potential uses as wound dressings

The purpose of this research was to analyze the morphology, thermal and mechanical properties of poly(vinyl alcohol) (PVA)-based electrospun mats reinforced with cellulose acetate (CA) or cellulose nanocrystalline (CNC) for potential applications in wound dressings. Bead-free and water-stable electrospun nanofibers made of blends of PVA and CA or CNC were successfully produced and crosslinked with glutaraldehyde vapor. Crosslinking slightly increased the nanofibers' diameters in order of 43 and 13% for 80/20 PVA/CA and PVA/CNC electrospun mats, respectively, while maintaining their bead-free morphology. Thermogravimetry (TGA) and differential scanning calorimetry (DSC) evaluations were employed to determine the miscibility and the thermal response of the uncrosslinked and crosslinked mats, reporting a reduction in mass loss upon addition of CA and CNC and upon crosslinking process. Polymers' powder and mats (before and after crosslinking) crystallinity was assessed by X-ray diffraction analysis (XRD). Crosslinked mats experienced a slight reduction in crystallinity compared to the uncrosslinked. Static and dynamic tensile strength tests revealed that CA and CNC doped mats enhanced the Young's modulus and lowered deformation at failure compared to pristine PVA electrospun mats. Data from storage modulus (E′) demonstrated the strength of the physical interactions formed between PVA and the cellulosic derivatives (either before and after crosslinking), highlighting the stiffness of CA (231.58 MPa for the 80/20 mat) and, particularly, CNC (742.04 MPa for the 80/20 mat). This research uncovered important information concerning the chemical and physical relation between polymeric matrices and additives, essential for the proper selection of materials for wound dressings production.

Linear and Nonlinear Optical Properties of PVA:SA Blend Reinforced by TiO2 Nanoparticles Prepared by Flower Extract of Aloe Vera for Optoelectronic Applications

In this study, a polyvinyl alcohol–sodium alginate blend, PVA:SA 3:1 (w:w), was doped with different contents of TiO2 nanoparticles (NPs) prepared by aloe vera leaf extract to form the investigated nanocomposites. The nonlinear parameters of third-order susceptibility (χ(3)) and refractive index (n2) were detected by using UV-Vis spectroscopy and Z-scan techniques. Some different optical parameters were also determined, including the refractive index (n), optical dielectric parameters, volume and surface energy loss functions, and some others. The best solar skin protection factor (SSPF) was investigated by 5 wt.% of TiO2 NPs doped in PVA:SA 3:1, which was about 84.6% compared to the corresponding value of the host blend (41%). The studied nanocomposites were examined for their utility in the optical limiting of CUT-OFF laser filters utilizing a continuous He-Ne laser working at 632.2 nm. As a result, our finding demonstrated that TiO2 NPs doped in the host blend of PVA:SA positively influences a laser light blocking for the investigated laser source. Using the estimated gap energies values, different models were used to deduce theoretical values of the linear refractive index (n). The presence of Ti peaks in the EDX spectrum confirmed the doping of TiO2 NPs in the nanocomposites. SEM showed that the TiO2 NPs are homogeneously dispersed through the host blend with some agglomerates. XRD spectra showed that the values of the lattice strain εstr. detected at 2ϴ = 19.78° are 0.058, 0.055, and 0.060, corresponding to 1, 3, and 5 wt.% of TiO2 NPs doped in the PVA:SA blend.

Abstract Number ‐ 127: Poly(vinyl alcohol) grafts of brain aneurysms with patient‐specific morphologies

Introduction Current animal models of brain aneurysms used for testing neuro‐interventional devices have highly simplistic vascular anatomy in comparison with human aneurysm‐parent vessel complexes. Poly(vinyl alcohol) (PVA) is a leading biomaterial for manufacture of artificial vascular grafts because of its biocompatibility, hemocompatibility, availability, low cost, moldability/castability, and tunable mechanical properties to match arterial compliance [1,2]. However, PVA is non‐cell adhesive and requires modification with additives to promote endothelialization of the luminal surface to maintain long‐term graft patency [1,3]. We have previously studied the biocompatibility of resorcinol bis(diphenyl phosphate) (RDP) coated clays blended with polymers and have found excellent cell adhesion and proliferation with human dermal fibroblasts as well as dental pulp stem cells [4]. Our overall goal is to develop a new in vivo model of brain aneurysms by manufacturing patient‐specific aneurysm anatomies with a blend of PVA and RDP clay and grafting them into animals. Here, we evaluate the casting of PVA in the shape of patient‐specific aneurysms. Methods 10% PVA (w/w) (99% hydrolyzed, 85–124K molecular weight, Sigma Aldrich) was dissolved in deionized water, to which 1% RDP clay (ICL Industrial Products, Be’er Sheva, Israel) was added. The PVA was crosslinked using 15% (w/w) of sodium trimetaphosphate and 30% (w/w) of sodium hydroxide, after which rheological studies (stress sweeps using a Bohlin Gemini rheometer) were conducted. In the casting procedure, negative molds of both simple tubes and complex aneurysm geometries were designed using Rhinoceros 3D software (Robert McNeel & Associates, Seattle, WA) and 3D printed in ABS plastic. The negative mold was then filled with beeswax, resulting in a positive wax mold that was dip‐coated 8 times in PVA solution, and spun on a two‐axis spinner in between each dip to ensure even coverage. After overnight drying in a fume hood, the model was placed in heated water, allowing the wax to melt out and leaving behind the luminal PVA cast. Results Rheology on the crosslinked polymers showed that the PVA/RDP blend exhibited over twice the elastic modulus of unblended PVA (Figure A). Such enhanced mechanical properties are consistent with previous studies [5]. Both simple tubular geometries and patient‐specific anatomies were able to be successfully cast using the methodology developed here (Figure B). Conclusions This proposed casting methodology demonstrates a realistic, efficient way to replicate complex aneurysm geometries with comparatively inexpensive materials and short time frame. Future endeavors will include further exploration of the PVA/RDP biocompatibility as well as completing the casting procedure with a PVA/RDP blend.

Hemp cellulose nanocrystals for functional chitosan/polyvinyl alcohol-based films for food packaging applications.

Hemp is known for its swift growth and remarkable sustainability, requiring significantly less water, an adaptable cultivation to a wide range of climates when compared to other fibers sources, making it a practical and environmentally friendly choice for packaging materials. The current research seeks to extract cellulose nanocrystals (CNCs) from hemp fibers using alkali treatment followed by acid hydrolysis and assess their reinforcing capacity in polyvinyl alcohol (PVA) and chitosan (CS) films. AFM analysis confirmed the existence of elongated, uniquely nanosized CNC fibers. The length of the isolated CNCs was approximately 277.76 ± 61 nm, diameter was 6.38 ± 1.27 nm and its aspect ratio was 44.69 ± 11.08. The FTIR and SEM analysis indicated the successful removal of non-cellulosic compounds. Furthermore, the study explored the impact of adding CNCs at varying weight percentages (0, 0.5, 1, 2.5, and 5 wt%) as a strengthening agent on the chemical composition, structure, tensile characteristics, transparency, and water solubility of the bionanocomposite films. Adding CNCs to the CS/PVA film, up to 5 wt%, resulted in an improvement in both the Young's modulus and tensile strength of the bionanocomposite film, which are measured at (412.46 ± 10.49 MPa) and (18.60 ± 3.42 MPa), respectively, in contrast to the control films with values of (202.32 ± 22.50 MPa) and (13.72 ± 2.61 MPa), respectively. The scanning electron microscopy (SEM) images reveal the creation of a CS/PVA/CNC film that appears smooth, with no signs of clumping or clustering. The blending and introduction of CNCs have yielded transparent and biodegradable CS/PVA films. This incorporation has led to a reduction in the gas transmission rate (from 7.013 to 4.159 cm3 (m2 day·0.1 MPa))-1, a decrease in transparency (from 90.23% to 82.47%), and a lowered water solubility (from 48% to 33%). This study is the inaugural effort to propose the utilization of hemp-derived CNC as a strengthening component in the development of mechanically robust and transparent CS/PVA-CNC bio-nanocomposite films, holding substantial potential for application in the field of food packaging.

Investigation of Transport Mechanism and Nanostructure of Nylon-6,6/PVA Blend Polymers

A casting technique was used to prepare poly(vinyl alcohol) (PVA) blend polymers with different concentrations of Nylon-6,6 to increase the free-volume size and control the ionic conductivity of the blended polymers. The thermal activation energy for some blends is lower than that of pure polymers, indicating that their thermal stability is somewhere in between that of pure Nylon-6,6 and pure PVA. The degree of crystallinity of the blend sample (25.7%) was lower than that of the pure components (41.0 and 31.6% for pure Nylon-6,6 and PVA, respectively). The dielectric properties of the blended samples were investigated for different frequencies (50 Hz-5 MHz). The σac versus frequency was found to obey Jonscher's universal power law. The calculated values of the s parameter were increased from 0.53 to 0.783 for 0 and 100 wt.% Nylon-6,6, respectively, and values less than 1 indicate the hopping conduction mechanism. The barrier height (Wm) was found to increase from 0.33 to 0.72 for 0 and 100 wt.% Nylon-6,6, respectively. The ionic conductivity decreases as the concentration of Nylon-6,6 is blended into PVA because increasing the Nylon-6,6 concentration reduces the number of mobile charge carriers. Positron annihilation lifetime (PAL) spectroscopy was used to investigate the free volume's nanostructure. The hole volume size grows exponentially with the concentration of Nylon-6,6 mixed with PVA. The Nylon-6,6/PVA blends' free-volume distribution indicates that there is no phase separation in the blended samples. Mixing PVA and Nylon-6,6 resulted in a negative deviation (miscible blends), as evidenced by the interaction parameter's negative value. The strong correlation between the free-volume size and other macroscopic properties like ionic conductivity suggests that the free-volume size influences these macroscopic properties.

Chitosan/PVA Nanofibrous Membranes as Air Filter Material

Nanofiber membranes made of polymer materials are being extensively investigated and developed as air filter materials. This research aims to make and characterize the nanofiber membranes as filter materials capable of filtering gaseous pollutants from cigarette smoke. The electrospinning method manufactured the chitosan (CS)/PVA blend nanofiber membranes with CS/PVA ratios of (0/100, 20/80, 30/70, and 40/60 w/w) using low molecular weight (LMw) PVA and the ratios of (0/100, 10/90, 20/80, and 30/70 w/w) with high Mw (HMw) PVA. The CS concentration increased the CS-PVA solution‘s electrical conductivity and decreased the membrane‘s average fiber diameter and tensile properties. The filtration test on neat PVA and CS/LMw PVA (20/80) membranes set on the metallic substrate with a 0.08 mm hole size was conducted by varying membrane thickness (20, 35, and 45 µm). The filtration efficiency increased with the membrane thickness because membrane pores tend to be smaller, indicating that reducing the fiber diameter by adding CS increases pore size. The filtration test on CS/HMw PVA (20/80) membranes with 45 µm thickness on different substrate¢s hole sizes of (0.08, 1.19, and 1.41 mm) showed that the larger the hole size, the lower the filtration efficiency. By similar CS/PVA ratio, membrane thickness, and substrate size hole, the CS/HMw PVA's filtration efficiency (87.15%) is higher than CS/LMw PVA (85.79%). However, the CS/LMw PVA membrane showed higher tensile strength, low stiffness, and more economical air filtration material than CS/HMw PVA.

Development of active packaging films based on liquefied shrimp shell chitin and polyvinyl alcohol containing β-cyclodextrin/cinnamaldehyde inclusion

To maintain the freshness of fruits and to meet environmental and consumer needs, a biobased packaging film with long-lasting antimicrobial activity was developed in this article. Liquefied ball-milled shrimp shell chitin/polyvinyl alcohol (LBSC/PVA) blend films containing varying concentrations (0, 1, 2, 3, 4, 5 wt%) of the β-cyclodextrin/cinnamaldehyde (β-CD/CA) inclusion were prepared and characterized. The association between β-CD and CA and the sustained release behavior of CA were explored. The physicochemical property, antimicrobial activity and food preservation performance of the films were investigated. Results showed that CA was successfully encapsulated into the cavity of CD by host-guest interactions, which greatly improved the sustained release of CA. The 3 wt% β-CD/CA/LBSC/PVA blend film showed optimized mechanical properties with a tensile strength of 41.5 MPa and an elongation at break of 810 %. In addition, the incorporation of β-CD/CA inclusion significantly enhanced the antimicrobial activity and food preservation performance of the blend films. Moreover, the 3 wt% β-CD/CA/LBSC/PVA blend film exhibited evidently longer lasting antimicrobial activity and cherry tomato preservation performance than the 3 wt% CA/LBSC/PVA blend film, further demonstrating the critical role of β-CD in delaying CA release. These novel β-CD/CA/LBSC/PVA blend films may have a potential use in active food packaging.

Effect of thermal crosslinking process on membrane structure and PEM fuel cell applications performed with SPEEK-PVA blend membranes

One of the promising options in the pursuit of clean and sustainable energy is fuel cell technology. PEM fuel cell stands out among fuel cell technologies due to its high efficiency, compactness, and ability to be used in portable applications. SPEEK (with different sulfonation degrees) and PVA blend membranes, which are thought to create a good synergy for PEM fuel cell, were prepared by using the solution casting method. As a result of the weight loss experiments, it was understood that the membranes dissolve in water regardless of the degree of sulfonation. Thermal crosslinking was carried out to prevent the membrane dissolution in water, which is in continuous contact with water in the fuel cell. Dissolution was mostly prevented by means of the thermal crosslinking process. Changes in the physical, chemical, and mechanical structure of the membrane after thermal crosslinking were comparatively determined by fourier transform infrared (FTIR), thermogravimetric analysis – differential thermal analysis (TGA-DTA), differential scanning calorimetry (DSC), water uptake capacity, swelling property, ion exchange capacity (IEC), dynamic mechanical analysis (DMA), electrochemical impedance analysis and oxidative stability. In addition, single-cell performance tests were performed with the membrane that gave the best results in the characterization analyses. Analysis results showed that thermal crosslinking prevented the dissolution of membranes in water ingreat extent. In addition, it was determined that the thermally crosslinked membranes had a more stable structure.

Evaluation of Antimicrobial and Anti-Biofilm Formation Activities of Novel Poly(vinyl alcohol) Hydrogels Reinforced with Crosslinked Chitosan and Silver Nano-Particles.

Novel hydrogels were prepared by blending chitosan and poly(vinyl alcohol), PVA, then crosslinking the resulting blends using trimellitic anhydride isothiocyanate at a concentration based on chitosan content in the blends. The weight ratios of chitosan: PVA in the blends were 1:3, 1:1, and 3:1 to produce three hydrogels symbolized as H13, H11, and H31, respectively. For a comparison, H10 was also prepared by crosslinking pure chitosan with trimellitic anhydride isothiocyanate. For further modification, three H31/silver nanocomposites (AgNPs) were synthesized using three different concentrations of silver nitrate to obtain H31/AgNPs1%, H31/AgNPs3% and H31/AgNPs5%. The structures of the prepared samples were emphasized using various analytical techniques. PVA has no inhibition activity against the tested microbes and biofilms. The antimicrobial and anti-biofilm formation activities of the investigated samples was arranged as: H31/AgNPs5% ≥ H31/AgNPs3% > H31/AgNPs1% > H10 > H31 > H11 > H13 > chitosan. H31/AgNPs5% and H31/AgNPs3% were more potent than Vancomycin and Amphotericin B against most of the tested microbes. Interestingly, H31 and H31/AgNPs3% were safe on the normal human cells. Consequently, hydrogels resulting from crosslinked blends of chitosan and PVA loaded with AgNPs in the same structure have significantly reinforced the antimicrobial and inhibition activity against the biofilms of PVA.

Homogeneous and highly photoluminescent composites based on in-situ formed fluorophores in PVA blends

There is a strong demand for developing a simple, scalable, and transferable method to prepare homogeneous and highly photoluminescent composite for diverse applications. Herein, homogeneous composites were successfully synthesized by thermal annealing blends of polyvinyl alcohol, citric acid, and ethylenediamine. The composites exhibited intensive photoluminescence under excitation around 350 nm. Infrared, nuclear resonance, and optical characterizations suggest that diverse structures involving 5-oxo-1,2,3,5-tetrahydroimidazo-[1,2-α]-pyridine-7-carboxylic acid (IPCA) accounts for the high photoluminescence of the composites.