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Daytime radiative cooling material provides a low‐energy way of cooling because it can reflect sunlight and radiate heat without consuming any energy. However, there are still great difficulties in manufacturing low‐cost, high‐efficiency, sustainable, and biodegradable daytime radiative cooling materials. In this paper, poly (vinyl alcohol)/boron nitride (PVA/BN) composite aerogels were prepared by freeze‐drying technology. By adjusting the PVA concentration and BN content, the aerogel can achieve high sunlight reflectivity (96%), high mid‐infrared emissivity (96%) and good thermal insulation performance. Therefore, the temperature of the aerogel can be reduced to 12.5°C lower than the ambient temperature at night, and 5.5°C lower than the ambient temperature under the direct sunlight of 900 W/m2. This aerogel opens an environmentally sustainable pathway for radiative cooling applications. [ABSTRACT FROM AUTHOR]

A hydrogel that is expected as a biomedical load‐bearing material remains a substantial challenge. In this work, a multi‐solvent‐induced gradient aggregation state strategy is developed to construct lignin‐based supramolecular hydrogels that feature superstrong, tough, stretchable, and fatigue‐resistant properties. The multi‐solvent high‐temperature annealing induces the gradient crystallization of polyvinyl alcohol and the self‐assembly of lignin. The interior strong hydrogen‐binding and the external weak non‐covalent‐binding forms a gradient aggregation state microstructure and compact macrostructure, where lignin acts as an interfacial molecular bridge. By sharing interconnection points to collaboratively dissipate energy, the developed hydrogels demonstrate high modulus (74.4 MPa), toughness (90 MJ m−3), tear (34,000 J m−2), tensile (24.8 MPa), and compressive strength (60 MPa). Moreover, such lignin‐based supramolecular hydrogels also exhibit extraordinary fatigue resistance, biocompatibility, and reactive oxygen species scavenging activity. This gradient non‐covalent conjoined‐network caused by multi‐solvent high‐temperature annealing provides a new design strategy and potential for developing biomaterials that mimic biomedical load‐bearing materials (e.g., natural tendons and ligaments). [ABSTRACT FROM AUTHOR]

ABSTRACT In this study, chitosan (C)‐polyvinyl alcohol (P) edible film containing bio‐fabricated nanosilver particles (nAg) (as antimicrobial agent) and beetroot peel extract (BRPE) (as antioxidant agent and pH indicator) was used as spoilage indicator in cold‐stored rainbow trout fillets. DPPH (2,2‐diphenyl‐1‐picrylhydrazyl) radical scavenging activity (43.02%), reducing power (2.87), and total phenolic content (360.50 mg GAE/g) of ethanolic BRPE were higher than aqueous extract. Silver nanoparticles were biosynthesized using silver nitrate reduction by chitosan, confirmed by UV–Visible spectroscopy, optical and scanning electron microscope images, and X‐ray diffraction analysis. The highest tensile strength (4.20 MPa) and elongation at break (118%) belonged to the CP‐BRPE film, and the lowest water vapor permeability (2.45 10−5 g/s/m/P) was related to the CP‐nAg film. Also, the lowest total viable count (6.17 log CFU/g), psychrotrophic bacteria (6.27 log CFU/g), Enterobacteriaceae (4.9 log CFU/g), pH (5.66), total volatile basic‐nitrogen (TVB‐N) (22.1 mg/100 g of fish), and thiobarbituric acid reactive substances (TBARS) (0.705 mg MDA/kg of fish) values of the packaged trout fillets were significantly (p ≤ 0.05) observed in CP‐BRPE‐gnAg treatment among the other treatments at the end of the storage period, and CP‐gnAg, CP‐BRPE, and CP treatments were in the next ranks, respectively. Colorimetric analysis of the used films showed that the films containing BRPE depicted color spectra of red to yellow at the same time as the spoilage symptoms initiated in the packaged fillets. It is concluded that BRPE not only increased the preservative effects of chitosan‐polyvinyl alcohol film containing green silver nanoparticles but also can be considered as a natural cost‐effective spoilage indicator of the rainbow trout fillets during cold storage time. [ABSTRACT FROM AUTHOR]

In this study, guest carriers, composed of magnetic‐directed hydrogel particles with near‐infrared (NIR)‐light‐triggered guest‐release properties, are prepared via the one‐pot method. The gel particles contain photostable NIR‐responsive polypyrrole nanoparticles with temperature‐sensitive poly(N‐isopropyl acrylamide), the combination of which can induce the accelerated release of encapsulated drugs by 337% upon 5 minutes of NIR light irradiation based on the release profile of NRMG‐1 at 10–15 min. Additionally, with magnetic iron oxide particles crosslinking the polyvinyl alcohol frames, these gel particles can form a physical barrier that decreases the release rate by 20% under an external magnetic field over 24 h. The magnetic iron oxide particles also enable the gel particles to reach their target destination without extra drug losses. [ABSTRACT FROM AUTHOR]

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 U mg‒1, and the Km value decreased from 4.861 to 0.982 mM. 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. [ABSTRACT FROM AUTHOR]

In this study, a novel biodegradable polymer electrolyte membrane with reduced fuel crossover, high selectivity, and high conductivity compared with Nafion 117 membrane in direct ethanol fuel cells (DEFCs) has been reported. Herein, polyvinyl alcohol/epoxidized natural rubber (PVA/ENR) blend membranes were synthesized via a simple solution casting method and applied in DEFCs. The structural and physicochemical features of the PVA/ENR blend membranes were examined using FESEM, FTIR, XRD, water absorption, ethanol uptake, swelling ratio and oxidative stability. ENR enhances the chemical, structural, and mechanical characteristics of PVA, making it a valuable material in fuel cell applications. The incorporation of ENR into the PVA matrix results in a compact morphology, excessive multifunctional groups, low fuel crossover, and high selectivity. The optimum membrane thickness achieves the highest selectivity, reaching up to 12.32 × 104 S s cm−3 at 30°C. Additionally, the maximum power density achieved is 19.52 mW cm−2, surpassing that of the Nafion membrane, which is only 14.55 mW cm−2 at 90°C. Furthermore, this biodegradable membrane can sustain operation for 1000 h at 90°C, owing to its ability to maintain hydration for an extended period. This study represents the first attempt to combine PVA and ENR in fuel cells. [ABSTRACT FROM AUTHOR]

The present study aims to improve the mechanical strength of hydrogels via a simplified method, involving the creation of a nanocomposite hydrogel using polyvinyl alcohol (PVA) incorporated with un‐modified multiwalled carbon nanotubes (um‐MWCNTs). Departing from conventional freezing–thawing cycles, our research employs a facile approach, in which high‐shear mixing along with solvent exchange with deionized water was utilized. Morphological analysis unveiled a compact and dense microstructure within the nanocomposite hydrogel in correlation with MWCNT concentration. Attenuated total reflection‐Fourier transform infrared spectroscopy (ATR‐FTIR) elucidated the chemical structure of PVA/um‐MWCNTs hydrogel nanocomposite. Rheological studies on the viscoelastic properties indicated the formation of more "solid‐like" structure in the developed hydrogel nanocomposite. Broadband dielectric spectroscopy revealed alterations in dielectric properties of the fabricated PVA/um‐MWCNTs hydrogel nanocomposite corresponding to MWCNTs content in the PVA matrix. This comprehensive investigation highlights the impact of minimal MWCNTs concentration on the rheology, mechanical, and dielectric properties of developed PVA/um‐MWCNTs hydrogel nanocomposite. [ABSTRACT FROM AUTHOR]

Highly sensitive strain sensors have been widely used in human motion monitoring, medical treatment, soft robots, and human–computer interaction, and the recycling of functional materials is in a huge demand for eco‐friendly and sustainable electronics. However, the manufacturing of recyclable strain sensors still remains challenging. Here, a semi‐wrapped structure based on silver nanowires and polyvinyl alcohol is proposed to realize a recyclable and stable strain sensor. It has shown excellent sensitivity, fast response, high stretchability and good environmental stability, and is successfully applied for human motion monitoring. In addition, a simple strategy is developed to effectively recycle silver nanowires in an eco‐friendly manner. The recyclable and stable strain sensor demonstrates potential applications in wearable and stretchable electronics, and the recycling strategy can be extended to other noble metal nanomaterials. [ABSTRACT FROM AUTHOR]

With the rapid development of industrialization and population surge in modern society, noise pollution has been considered as a serious threat to human beings. In order to effectively reduce noise, the application of sound absorbing textile materials has gradually increased, also the rapid development of acoustic coating consists of conventional fiber layers and polymers. In this work, the surface morphology, micro‐structure and sound absorption properties of polyvinyl alcohol coated fabric and its composites were studied. It was found that the addition of nano‐TiO2 particles can obviously improve the sound absorption properties, and the absorption coefficient is related to fabric thickness. Furthermore, the surface of the coated fabric was compounded with melt‐blown nonwoven fabric, thus to fabricate composite sound absorber. This work indicates the good feasibility and promising application prospect of lightweight polyvinyl alcohol coated fabrics in noise reduction engineering. Highlights: Combination of fiber layers and polymers for acoustic coating materials.Adding inorganic nano‐TiO2 particles with different contents.Different modification methods to improve the dispersion of coating.Composite structure with reduced thickness and increased sound absorption. [ABSTRACT FROM AUTHOR]

Flexible sensors are garnering substantial interests for various promising applications, including medical electronics, environmental monitoring, and wearable devices. Developing a flexible sensor with high compliance, high sensitivity, and high reliability through the construction of a novel composite conductive hydrogel based on the synergistic enhancement effect of conductive polymers and metal ions is a remarkable achievement. Herein, an electronic/ionic‐conductive double network hydrogel (polypyrrole (PPy)/carboxymethyl cellulose (CMC)‐Al3+/polyvinyl alcohol (PVA)) with soft compliance, highly conductivity, and stability is presented. Moreover, owing to the synergistic reinforcement effect of the relatively immobilized "islands" of PPy particles and large amounts of movable "bridges" of aluminum ions (Al3+) within the double network hydrogel, the as‐optimized PPy/CMC‐Al3+/PVA composite gels exhibit excellent conductivity (σ = 3.47 ± 0.25 S m−1) and mechanical properties (E = 18.53 ± 0.67 kPa). Furthermore, it has been developed as strain sensors with relatively high linear sensitivity (gauge factor = 2.58) within a broad linearity range (0–400%). It can also be served as a monitoring devices for subtle physiological signals emanating from various parts of the human body. The robust sensor has great potential to be developed as wearable electronic devices and applied in healthcare monitoring fields. [ABSTRACT FROM AUTHOR]

In this study, polyvinyl alcohol/Nafion nanofibrous composite membranes were produced to investigate their possible application as a polymer electrolyte membrane (PEM) in direct methanol fuel cells. Electrospinning method was used for nanofibrous membrane production, in which the mixture of polyvinyl alcohol (PVA) and Nafion solutions was directly electrospun. Produced nanofibers were subjected to physical stabilization, filler application, and sulfonating to produce composite nanofibrous membranes. PVA and Nafion polymers were used also as filler materials. The properties of resultant composite membranes were compared in terms of water swelling, weight loss in water and methanol solution, thermal stability, morphology, proton conductivity, and methanol permeability. Proton conductivity of the membranes depending on the humidity was also investigated. TGA analysis showed that the membranes had adequate thermal properties regardless of the filler material. The nanofibrous structure was shown to be preserved by scanning electron microscopy (SEM) after treatment with water and methanol solution. It was shown that PVA/Nafion nanofibers displayed proton conductivity after filling process. The use of PVA as a filler material led to higher proton conductivity at 100 RH%. It was reported that proton conductivity could only be obtained at higher relative humidity values (>80% RH). A lower methanol permeability of PVA‐filled membranes was reported. Highlights: PVA/Nafion nanofibrous membranes were produced by electrospinning.PVA and Nafion were also used as pore filling materials.PVA‐filled membranes had higher proton conductivity and lower methanol permeability.Proton conductivity could only be obtained at higher RH% values. [ABSTRACT FROM AUTHOR]

In this study, chromium‐based metal–organic framework (MIL‐101(Cr)) was incorporated into polyvinyl alcohol nanofibers (PVA NFs) via green electrospinning followed by heat treatment to fabricate MIL‐101(Cr)@PVA NFs composite without the need for any organic solvent or other dispersants. The fabricated MIL‐101(Cr)@PVA NFs were comprehensively characterized using a suite of common techniques. Morphological characteristics of MIL‐101(Cr)@PVA NFs showed a fibrous structure with an average diameter of 228 ± 37 nm and decorated with MIL‐101(Cr) particles arranged in a nanoneedle‐like pattern. Subsequently, its adsorption efficiency towards the cationic crystal violet dye (CV) was evaluated through batch adsorption experiments. The influence of various experimental parameters on CV removal efficiency was systematically optimized using a factorial design approach. The Langmuir isotherm and kinetic pseudo‐second‐order (PSO) model provided an excellent fit to the adsorption equilibrium data, indicating a maximum adsorption capacity (qmax) of 344.18 mg/g for MIL‐101(Cr)@PVA NFs compared with 83.94 mg/g for pristine PVA NFs. Furthermore, the MIL‐101(Cr)@PVA NFs composite demonstrated excellent reusability and stability, maintaining a significant portion of its removal capacity even after six adsorption–desorption cycles. These findings highlight the potential of the fabricated composite as a highly efficient and reusable adsorbent for CV removal from wastewater treatment applications. Highlights: The MIL‐101(Cr)@PVA NFs nanocomposite fabricated by electrospinning technique.The MIL‐101(Cr) particle arranged in a nanoneedle‐like pattern in the PVA NFs.Incorporation of MIL‐101(Cr) improved qmax of PVA by 391.5%.The MIL‐101(Cr)@PVA NFs membrane has excellent stability and reusability. [ABSTRACT FROM AUTHOR]

The blockage of gas transmission pipelines due to gas hydrates poses a significant challenge for the gas industry. Low‐dosage hydrate inhibitors (LDHI) are utilized to influence the kinetics of hydrate formation, including nucleation, growth, and/or agglomeration. In the current study, a series of batch, isochoric, and isothermal tests were carried out to investigate the impacts of two LDHIs, poly N‐vinylpyrrolidone (PVP) and polyvinyl alcohols (PVA). This study examined the influence of these inhibitors on nucleation and growth of ethane+propane mixture in the presence of kaolin nanoparticles. In laboratory studies and using pure constituents, the rate of hydrate formation is low to investigate the inhibitors effect. To enhance the rate of hydrate formation, kaolin nanoparticles were utilized as they serve as a suitable representative for solid minerals commonly found in pipelines. The gas phase's compositional change were measured using a gas chromatograph. The results revealed that the growth stage of mixed‐gas exhibited two distinct steps, attributed to the formation of two different structures known as structure II and structure I. During the first step, structure II was formed, and the cavities were occupied by both gas components. In the second stage, structure I was formed by ethane. The effect of temperature on the induction time (nucleation rate) and the growth rate during the second stage was lower than that at the first stage. The increase in PVA concentration resulted in an increase in the induction time and a decrease in the rate of growth during the first stage. The performance of PVA was found to be affected by temperature. Lower temperatures resulted in the formation of less foam, providing improved performance for PVA at −0.5°C. PVP had a stronger impact on induction time and both growth steps compared to PVA, indicating stronger inhibitory impact of PVP on nucleation of hydrates initiated by propane and the growth of both propane and ethane hydrates. [ABSTRACT FROM AUTHOR]

Food packaging that impedes microbial growth and can be safely used is critical to attenuate food spoilage. Herein, a green berberine/phytate salt (BPA) is successfully synthesized and aggregated in polyvinyl alcohol (PVA) film to impart fluorescent and photodynamic antimicrobial properties. Compared to berberine hydrochloride (BHL), BPA exhibited stronger fluorescence because intramolecular motions and intermolecular π–π accumulation of BHL are restricted by phytic acid (PA). Molecular dynamics simulation indicate that aggregation of BHL and PA formed through electrostatic interactions in the PVA matrix due to the change of the binding energy during the drying process. With increasing BPA content, the films exhibited increased ultraviolet, water vapor, and oxygen barriers and fluorescent properties, but reduced tensile strength and elongation at break. After radiated, PVA‐BPA9 film showed the highest antimicrobial rates against Staphylococcus aureus, Escherichia coli, P. citrinum, and Aspergillus niger reached 100%, 100%, 86.14%, and 66.24%, respectively, due to the increased reactive oxygen species production. The total number of microbial colonies in cooked chicken and oranges packaged by PVA‐BPA9 film with irradiation ARE 87.54% and 29.21% of those by PVA film. The findings indicate a new and feasible strategy to obtain a green photodynamic‐mediated film for safe and effective food packaging. [ABSTRACT FROM AUTHOR]

Wearable strain transducers are poised to transform the field of healthcare owing to the promise of personalized devices capable of real‐time collection of human physiological health indicators. For instance, monitoring patients' progress following injury and/or surgery during physiotherapy is crucial but rarely performed outside clinics. Herein, multifunctional liquid‐free ionic elastomers are designed through the volume effect and the formation of dynamic hydrogen bond networks between polyvinyl alcohol (PVA) and weak acids (phosphoric acid, phytic acid, formic acid, citric acid). An ultra‐stretchable (4600% strain), highly conducting (10 mS cm−1), self‐repairable (77% of initial strain), and adhesive ionic elastomer is obtained at high loadings of phytic acid (4:1 weight to PVA). Moreover, the elastomer displayed durable performances, with intact mechanical properties after a year of storage. The elastomer is used as a transducer to monitor human motions in a device comprising an ESP32‐based development board. The device detected walking and/or running biomechanics and communicated motion‐sensing data (i.e., amplitude, frequency) wirelessly. The reported technology can also be applied to other body parts to monitor recovery after injury and/or surgery and inform practitioners of motion biomechanics remotely and in real time to increase convalescence effectiveness, reduce clinic appointments, and prevent injuries. [ABSTRACT FROM AUTHOR]

Integrating superior mechanical performance, anisotropic conductivity, and biocompatibility into conductive hydrogels as all‐in‐one human‐machine interaction device remains challenging. Herein, by mimicking the anisotropic structures of human muscles, a robust anisotropic conductive hydrogel is developed by initially aligning polyvinyl alcohol with polypyrrole decorated cellulose nanofibrils to form an anisotropically oriented polymer networks, followed by post‐crosslinking with tannic acid (TA). Introducing TA into hydrogel network permanently secures its hierarchically anisotropic structure through multiple hydrogen bonds, thus endowing the hydrogel with exceptional mechanical properties (tensile strength of 11.41 MPa, toughness of 12.44 MJ m−3), anisotropic adhesive property, and direction‐dependent conductivity. With these attributes, a hydrogel strain sensor with excellent multidirectional sensitivity is developed, enabling stable monitoring of multi‐degrees of freedom joint movements in the human body and facilitating the control of a multiaxial virtual robot manipulator. Moreover, the in vitro/vivo tests demonstrate exceptional biocompatibility and anti‐biofouling properties of the as‐prepared hydrogel sensor, maintaining stable electronic response signals for over 14 days after successful implantation into the Achilles tendon of mice. Overall, this study presents a promising approach for designing conductive hydrogels with superior mechanical properties and anisotropic functionality for emerging applications in both in vitro and in vivo human‐machine interface materials. [ABSTRACT FROM AUTHOR]

Polyvinyl alcohol (PVA) was crosslinked with a homologous series of four different dicarboxylic acids, HOOC(CH2) n‐2COOH (n = 2 to 5) viz. oxalic acid (OA; C2), malonic acid (MA; C3), succinic acid (SA; C4) and glutaric acid (GA; C5) containing odd and even number of carbon atoms. The characterization and assessment of synthesized crosslinked films were done using ATR‐FTIR, XRD, SEM, AFM, DSC, rheology, percent swelling and sessile drop contact angle. The odd‐even effect of dicarboxylic acids was observed to significantly influence the physicochemical properties of PVA when employed as a crosslinker. PVA films crosslinked using dicarboxylic acids containing an even number of carbon atoms, displayed translucency, roughness, and an irregular matrix. In contrast, films incorporating an odd number of carbon atoms were transparent, homogenous, and densely packed. Furthermore, films containing even acids exhibited relatively lower crystallinity, lower melting temperature (Tm) and displayed an unexpected irregular trend in swelling as crosslinker concentration increased compared to films containing dicarboxylic acids with an odd number of carbon atoms which exhibits a consistent swelling with increasing crosslinker concentration. These results are attributed to the difference in the solubility and crystal structures of the odd‐even series of dicarboxylic acids. [ABSTRACT FROM AUTHOR]

Cellulose‐based aerogels possess satisfactory sustainability, porosity, and resilience, which are promising materials to replace traditional petroleum‐based foams. However, the viscous aggregation formed between hydrophilic fibers and the pore collapse caused by weak support force pose challenges for their further applications. Here, a load‐bearing structure‐inspired cellulose‐based aerogel is innovatively developed with excellent elasticity and water tolerance through surface‐interface modulation. Specifically, cellulose and polyvinyl alcohol (PVA) form interwoven skeletons by non‐directional freeze drying. Crucially, the rhamnolipid surfactant assists in forming stable and uniform bubbles, and drives the regularization of frame structure during the freezing process, promoting the construction of refined mechanical structures. Besides, the interfacial enhancement by esterification reaction of citric acid and the encapsulation by hydrophobic silane via chemical vapor deposition endow aerogels with better resilience and water tolerance. The as‐prepared aerogels can withstand intensive compression cycle tests and possess the ability to rebound over 10 times underwater. Even after 12 h wet treatment, the strain and stress loss respectively decrease by ≈55.5% and ≈14% compare with the initial unregulated aerogels after 500 cycles of 80% compression. Surprisingly, they have excellent cushioning performance beyond expanded polystyrene (EPS) and expanded polyethylene (EPE) in simulated road transportation packaging applications, indicating their potential in new‐generation cushioning materials. [ABSTRACT FROM AUTHOR]

Poly(3,4‐ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT: PSS) is a promising material for organic thermoelectric (TE) applications. However, it is challenging to achieve PEDOT: PSS composites with stretchable, self‐healable, and high TE performance. Furthermore, some existing self‐healing TE materials employ toxic reagents, posing risks to human health and the environment. In this study, a novel intrinsically self‐healable and wearable composite is developed by incorporating environmentally friendly, highly biocompatible, and biodegradable materials of polyvinyl alcohol (PVA) and citric acid (CA) into PEDOT: PSS. This results in the formation of double hydrogen bonding networks among CA, PVA, and PEDOT: PSS, inducing microstructure alignment and leading to simultaneous enhancements in both TE performance and stretchability. The resulting composites exhibit a high electrical conductivity and power factor of 259.3 ± 11.7 S·cm−1, 6.9 ± 0.4 µW·m−1·K−2, along with a tensile strain up to 68%. Furthermore, the composites display impressive self‐healing ability, with 84% recovery in electrical conductivity and an 85% recovery in tensile strain. Additionally, the temperature and strain sensors based on the PEDOT: PSS/PVA/CA are prepared, which exhibit high resolution suitable for human–machine interaction and wearable devices. This work provides a reliable and robust solution for the development of environmentally friendly, self‐healing and wearable TE thermoelectrics. [ABSTRACT FROM AUTHOR]

Flexible electrochromic devices (FECDs) are widely explored for diverse applications including wearable electronics, camouflage, and smart windows. However, the manufacturing process of patterned FECDs remains complex, costly, and non‐customizable. To address this challenge, a strategy is proposed to prepare integrated FECDs via multi‐material direct writing 3D printing. By designing novel viologen/polyvinyl alcohol (PVA) hydrogel inks and systematically evaluating the printability of various inks, seamless interface integration can be achieved, enabling streamlined manufacturing of patterned FECDs with continuous production capabilities. The resultant 3D‐printed FECDs exhibit excellent electrochromic and mechanical properties, including high optical contrast (up to 54% at 360 nm), nice cycling stability (less than 5% electroactivity reduction after 10 000 s), and mechanical stability (less than 19% optimal contrast decrease after 5000 cycles of bending). The potential applications of these 3D‐printed hydrogel‐based FECDs are further demonstrated in wearable electronics, camouflage, and smart windows. [ABSTRACT FROM AUTHOR]

Multi‐level anticounterfeiting tags have been developed using a combination of different materials. Polyvinyl alcohol (PVA) mixed with titanium dioxide (TiO2) is used to produce flexible substrates. Fluorescent Opuntia Ficus‐indica (OFI) extract dissolved with polymethyl methacrylate (PMMA) is then sprayed over the substrate to create a random, yet unique deposition of droplets. Photographs of the tags are taken under UV illumination at different angles and analyzed through the scale‐invariant feature transform (SIFT) algorithm to extract their unique features. The SIFT analysis reveals hundreds to thousands of matched features when a given tag is compared with itself, whereas this number drops to tens for different tags. To enhance the security of the tags, ITO is sputtered onto one of them in the form of a pattern formed by a patch array exhibiting a specific fingerprint at terahertz (THz) frequencies. The evaluation of ITO reflectance shows that each patch array has a unique and unpredictable response stemming from its distinct electro‐optical characteristics. The non‐deterministic response of sprayed dye droplets and ITO patches enables the realization of two‐level authentication, which is difficult to replicate at a reasonable cost. The simple manufacturing process and inexpensive materials involved make the proposed tags easily integrable into packaging. [ABSTRACT FROM AUTHOR]

The increasing demand for portable and flexible energy storage devices drives the rapid development of flexible electrodes and electrolytes. Meanwhile, the free‐standing polymer electrodes face great chance and challenge. In this work, the stretchable and flexible polyaniline/carbon nanotube/poly(vinyl alcohol) electrode (PANI/CNT/PVA‐E) was fabricated by in‐situ polymerization of aniline in CNT/PVA‐E substrate, where CNT was used to enhance the conductivity and mechanical properties of the polymer electrodes. Compared with PANI/PVA, the comprehensive performance of PANI/CNT/PVA‐E was improved. In addition, the electrochemical performance and tensile property of the electrodes depended on the CNT content. The nanocomposite electrode with 0.25% of CNT possessed optimal properties with high capacitance of 248.69 mF cm−2, and 75.29% of capacity retention over 4000 charge–discharge cycles at 1 mA cm−2. It also exhibited outstanding tensile strength of 3.88 MPa and elongation up to 462.3%. Interestingly, the electrode possessed good heat driven shape memory effect. The temporary shape could be fixed at 70°C under extra force, and the fixed shape recovered within 10 s when it was reheated to the same temperature. It is concluded that the present work may contribute to the development and fabrication of flexible energy‐storage devices, portable and highly stretchable electric devices. [ABSTRACT FROM AUTHOR]

Nanofibrous membranes were developed by combining chitosan (CS), polyvinyl alcohol (PVA), and calcium chloride (CC) to incorporate curcumin (CCM) through a co‐axial electro‐spinning method to improve CCM bioavailability. The optimal parameters were PVA/CS ratio of 7:3 v/v, PVA/CCM ratio of 8:2 v/v, CC amount of 0.5 g, fiber collection distance of 15 cm, voltage value of 18 kV, and injection flow of 0.1 mL/h (both core and shell layer). The prepared PVA/CCM@CS/PVA/CC nanofiber showed smooth surfaces and uniform bead‐free morphology with core‐shell structure. The average fiber diameter was 301.55 ± 76.77 nm with a narrow distribution. Using the Korsmeyer‐Peppas kinetic release model, the nanofiber membrane effectively released ∼85% CCM at pH 7.4 over 96 h via Fickian diffusion transport mechanism. In vitro antibacterial tests demonstrated that the membrane was efficient against both Gram‐positive (Staphylococcus aureus) and Gram‐negative (Pseudomonas aeruginosa) bacteria. When compared to free CCM, the membrane improved cell survival due to its nontoxic and cytobiocompatible features. In vivo tests found that the membrane significantly improved healing in incised‐wound rats, reducing inflammation, fibroblast proliferation, and collagen deposition. These findings indicate that the novel PVA/CCM@CS/PVA/CC nanofiber membrane, which has numerous biological functions, could be a promising candidate for wound dressing therapeutic applications. [ABSTRACT FROM AUTHOR]

Although a variety of functional polyvinyl alcohol hydrogels (PVAHG) with attractive mechanical and electrochemical properties have been fabricated using traditional freeze‐thaw cycling, this approach is usually relatively complicated, time‐consuming and relies essentially on the use of PVA chains with a weight‐average molecular weight above 60000. Here a new strategy capable of assembling relatively low‐molecular‐weight (≈30000) polyvinyl alcohol (PVA) into highly crosslinked physical hydrogels is developed. By exploiting ammonium persulfate as a simple and versatile oxidant to simultaneously provide oxidizing and salting‐out effects to the polymeric building blocks, PVAHG with excellent and tailorable elasticity, conductivity and sensitivity can be achieved building on the strong intermolecular hydrogen bonding between the newly formed ─COOH and ─CHO terminations and the inclusion of abundant inorganic ions. The hydrogels cannot only act as effective wearable wireless sensors for detecting output resistance signals but also be further employed to construct a motion‐mapped self‐propelled robotic arm that is able to instantly and accurately map the motion of human bodies. This study may provide new insights into polymer chemistry, hydrogel sensing, and soft robotics. [ABSTRACT FROM AUTHOR]

Summary This study aims to develop a novel active food packaging material from hybrid micro‐nanofibrous mats fabricated from gelatin (G)–chitosan (Ch)–polyvinyl alcohol (PVA)–Origanum elongatum essential oil (EO), (G‐Ch‐PVA‐EO) through electro‐blowing. The fibrous mats were characterised to assess their morphologies, shelf life efficiency, antimicrobial and antioxidant properties, surface‐wetting, and thermal, chemical, and physical interactions, among other factors. Results showed that the antioxidant activity was improved with the addition of EO, this enhancement is potentially linked to its rich content of phenolic components; carvacrol and P‐cymene. In addition, G‐Ch‐PVA‐EO showed higher firmness measurements compared to the control samples. Herein, low microbial counts were noted for both mesophilic aerobic bacteria (3.76 log CFU g−1) and yeast/mould (3.91 log CFU g−1) even at day 20. To conclude, the G‐Ch‐PVA‐EO microfibrous mat exhibits great promise in preserving the freshness of tomatoes. [ABSTRACT FROM AUTHOR]

The escalating focus on environmental concerns and the swift advancement of eco‐friendly biodegradable batteries raises a pressing demand for enhanced material design in the battery field. The traditional polypropylene (PP) that is monopolistically utilized in the commercial LIBs is hard to recycle. In this work, we prepare a novel water degradable separators via the cross‐linking of polyvinyl alcohol (PVA) and dibasic acid (tartaric acid, TA). Through the integration of non‐solvent liquid‐phase separation, we successfully produced a thermally stable PVA‐TA membrane with tunable thickness and a high level of porosity. These specially engineered PVA‐TA separators were implemented in LiFePO4 (LFP)|separator|Li cells, resulting in superior multiplicative performance and achieving a capacity of 88 mAh g−1 under 5 C. Additionally, the straightforward small molecule cross‐linking technique significantly reduced the crystalline region of the polymer, thereby enhancing ionic conductivity. Notably, after cycling, the PVA‐TA separators can be easily dissolved in 95 °C hot water, enabling its reutilization for the production of new PVA‐TA separators. Therefore, this work introduces a novel concept to design green and sustainable separators for recyclable lithium batteries. [ABSTRACT FROM AUTHOR]

The crucial point of solar thermal utilization makes solar heat collector gathering much attention. In this study, imitating polar bears' fur structure, fluorescent materials are modified into a solar heat collector, and the photothermal conversion is evaluated to examine the influence of polyvinyl alcohol concentration, fluorescent luminescence type and fluorescence concentration. The test results indicate that fluorescent materials that has a greater Stokes shift show the greater photothermal effect. Moreover, when composed of a PVA concentration being 5.0% and a fluorescent concentration being 0.50%, the composites exhibit the maximal photothermal conversion temperature (99.4°C) that is 17.9% higher than that of the solar heat collectors without fluorescent materials. This study proposes creating solar heat collector with modified fluorescent materials, and the new perspective of which demonstrates that the composites have a great potential and application prospect in the solar photothermal field. [ABSTRACT FROM AUTHOR]

This paper presents the development of the blend polymer solid electrolyte films (BPSE) for potential applications in electrochemical devices. Two host polymers, polyvinyl alcohol (PVA) and polymethyl methacrylate (PMMA), along with the salt KI, are employed to create the solid polymer electrolytes (SPEs). The synthesis involves varying the weight percentage of salt within the SPEs to investigate its impact on the material properties. Conductivity measurements are conducted using AC impedance spectroscopy, unveiling the conductivity behavior of the BPSEs. Additionally, surface morphology is characterized using polarized optical microscopy (POM) at 10 pixel resolution, offering a detailed examination of the film's microstructure. This comprehensive study not only contributes to the understanding of the fundamental properties of BPSEs but also opens avenues for their utilization in various electrochemical applications. [ABSTRACT FROM AUTHOR]

To overcome the two main obstacles of large‐scale application of superspreading material, self assembly is used to prepare superspreading polymer membrane (SPPM) in this work. An amphiphilic SPPM is prepared by capillary force‐driven self assembly using PP melt‐blown nonwovens and polyvinyl alcohol (PVA). The prepared SPPM has low preparation cost and stable performance since self assembly needs low energy consumption, and the production is thermodynamically stable. By using cryo‐electron microscopy, transmission electron microscopy, X‐ray photoelectron spectrum and scanning electron microscope with energy dispersive X‐ray spectroscopy. It is proved that PVA is successfully assembled on the fiber surface of PP melt‐blown nonwovens. The prepared SPPM has excellent spreading performance, the "spreading times" of both water and oil are less than 0.5 s. They showed much superior performance compared to traditional materials when applied in oil‐water separation, seawater desalination, and ion separation. This work will definitely promote the development of self assembly, superspreading materials, and related sciences. [ABSTRACT FROM AUTHOR]

Developing dynamic color‐tunable ultra‐long room temperature phosphorescence (URTP) polymers with afterglow of over 1 s, photo‐chromism, and multi‐stimuli response for practical anti‐counterfeiting and information security applications is attractive but very challenging. Herein, by doping multicolor phosphorescence pyridinium bromide L block or viologen‐based photo‐chromic V block into polyvinyl alcohol matrixes, the water‐stimuli‐responsive color‐tunable URTP polymer films with afterglow of up to 8 s and the reversible viologen‐based photochromic polymer films have been developed. More significantly, a series of dynamic color‐tunable URTP polymer films with ultra‐long afterglow of over 6 s, photo‐chromism, and water‐stimuli response have been successfully exploited by integrating L and V blocks into one polymer system. Mechanistic investigations have revealed that their photo‐chromism mainly comes from the photo‐generated viologen free radicals. Furthermore, their dynamic multilevel anti‐counterfeiting applications have been demonstrated. These results pave the way to develop smarter multifunctional URTP materials for anti‐counterfeiting and optical sensing. [ABSTRACT FROM AUTHOR]

This study is aimed at fabricating composite films by cross‐linking polyvinyl alcohol (PVA) and dialdehyde cellulose (DAC) in varying ratios using citric acid as a catalyst. The acetal formation between the two components was studied using FTIR. Characterizations of the physiochemical properties revealed that increasing the DAC ratio of the composite film improved the hydrophobicity, tensile strength and barrier properties (water vapour, UV and oxygen) of the films while reducing elongation at break (flexibility), swelling and solubility of the film in water. When the DAC ratio was elevated to 50%, the tensile strength was enhanced to 98 MPa. In comparison, flexibility diminished to 29%, the solubility of the film reduced to 10% and water vapour permeability was lower by two orders of magnitude than that of the control PVA film. The peroxide value of linoleic acid decreased from 21.2% ± 7.6 (packed with PVA film) to 9.9% ± 0.9 (packed with 50% DAC composite film) after 15 days. Furthermore, the composite films demonstrated effective absorption of UV radiation, with the order of effectiveness being UV‐C > UV‐B > UV‐A radiation. No significant difference in biodegradability was detected in the composite films with an increase in DAC ratio during indoor soil burial tests for 30 days. This study implies that the composite film could serve as an alternative sustainable packaging option, especially when transparency and high oxygen barrier properties are desired. [ABSTRACT FROM AUTHOR]

A new triple‐network organo‐hydrogel with high anti‐freezing and thermally‐stable performance is prepared for application in all‐temperature flexible supercapacitor. It is composed of boric acid/graphene/polyvinyl alcohol matrix and H2SO4/dimethyl sulfoxide mixing solution. The incorporation of graphene and boric acid into polymer matrix can improve thermal stability and ionic conductivity of organo‐hydrogel. The H2SO4 and dimethyl sulfoxide are key roles for improving anti‐freezing of organo‐hydrogel. The organo‐hydrogel exhibits high ionic conductivity of 1.6 and 3.1 S/m at −80 and 90°C, respectively. As a result, the assembled supercapacitor delivers a high capacitance retention of 84.5% and 113.3% at ultra‐low temperature (−80.0°C) and high temperature (90.0°C), respectively. The work provides a new route to design and prepare flexible supercapacitor with wide temperature range. [ABSTRACT FROM AUTHOR]

As family members of polycyclic aromatic hydrocarbons, compound anthracene (Ant) and phenanthrene (Phe) as isomers are widely used in organic optical materials and electronic materials. But their photochemical and physical properties are very different. In this work, the room temperature phosphorescence (RTP) properties of PVA−B‐Ant and PVA−B‐Phe are discussed carefully which are prepared by B−O click reaction through polyvinyl alcohol (PVA) with 9‐anthraceneboronic acid (B‐Ant) and 9‐phenanthrenylboronic acid (B‐Phe), respectively. PVA−B‐Phe 1 % film exhibits excellent fluorescence (FL) emission at 374 nm and RTP emission at 523 nm with green afterglow and around 1.9 s phosphorescence lifetime. However, PVA−B‐Ant 1 % film only shows strong blue FL emission at 414 nm, and the emission intensity decreases seriously with the extension of irradiation time. Experimental and theoretical calculations results suggest that the photodimer of Ant which is formed in PVA matrix under the UV light irradiation would be competitive with the process of RTP emission. This work demonstrates that the RTP properties of organic molecules might be probably affected by the photostability of the organic phosphor under UV irradiation. [ABSTRACT FROM AUTHOR]

Super macroporous (SMP) hydrogels have garnered significant attention in biomedical applications due to their high permeability and biomimetic pore structure. However, maintaining toughness in highly porous materials remains a formidable challenge. This study introduces a facile one‐step preparation method for fabricating tough alginate hydrogels with an SMP structure by blending polyvinyl alcohol (PVA) and sodium alginate cross‐linked with calcium chloride. By capitalizing on the phase separation effect, this method bypasses traditional requirements such as cryogelation and templating that necessitate low temperatures or solvent etching. The presence of PVA molecules promotes the regional aggregation of alginates, leading to enhanced toughness, and also occupies larger interstitial spaces between the densely packed alginate phases, facilitating pore formation. The resulting SMP structure, featuring pore sizes ranging from 50 µm to 700 µm, forms during the polymer cross‐linking process and achieves a porosity exceeding 85%. These hydrogels exhibit superior toughness compare to their non‐macroporous counterparts. Additionally, this method allows for flexible adjustments in the porous structure and overall gel shape, making it adaptable to various applications. This simple yet effective approach holds great potential for developing novel SMP materials with enhanced toughness. [ABSTRACT FROM AUTHOR]

As human exploration of marine continues to expand, the demand for underwater devices is also increasing. The unique properties of hydrogel materials make them well‐suited for underwater applications. We propose a multi‐functional polyvinyl alcohol (PVA) – NaCl @ Polyaniline (PANI) (PNP) hydrogel, which is characterized by easy fabrication, integrated structure, and flexibility, and can be directly applied in the fields of underwater energy storage and underwater sensing. Solid‐state supercapacitors fabricated by the PNP hydrogel, due to integrated and all‐solid‐state design, can be charged and discharged underwater without encapsulation. What's more, the PNP supercapacitor can maintain a capacitance retention rate of over 90 % after 5,000 cycles in simulated seawater, eliminating concerns about the hydrogel's dehydration when used underwater. The PNP hydrogel with an integrated three‐layer structure can also be applied to the capacitive pressure sensors, which can also be directly used in underwater environments without the need for encapsulation, significantly reducing the structural complexity and preparation steps of the device. Finally, we demonstrate a “supercapacitor module” with a voltage window greater than 1.6 V created by directly connecting multiple PNP supercapacitors in series, as well as an underwater intelligent glove, providing new solutions for underwater energy storage and underwater wearable sensing applications. [ABSTRACT FROM AUTHOR]

The objective of this study was to explore the applicability of biocompatible quince seed mucilage hydrogel as a promising material for drug delivery systems. In this investigation, the hydrogel was synthesized through the graft copolymerization of acrylic acid and allyl polyvinyl alcohol onto quince seed mucilage in an aqueous solution under an argon atmosphere. Characterization of the synthesized hydrogel was performed using Fourier‐transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FE‐SEM), and thermogravimetric analysis (TGA). Subsequently, the developed hydrogel served as a carrier for ceftriaxone antibiotic release in both distilled water and a buffer solution with a pH of 7.4. The results demonstrated an impressive encapsulation efficiency of 96.1% for ceftriaxone within the hydrogel matrix. Additionally, the adsorption properties of ceftriaxone onto the proposed hydrogel structures (I, II, and III) were theoretically investigated in the aqueous phase using Monte Carlo adsorption locator calculations in Materials Studio2017. Our findings revealed strong adsorption on structure (III) compared to structures (I and II), with respective theoretical energies of −2.836 kcal/mol, −2.840 kcal/mol, and −2.127 kcal/mol. Therefore, the proposed hydrogel structure (III) emerges as a promising candidate for drug delivery applications, emphasizing its potential as an efficient carrier system. [ABSTRACT FROM AUTHOR]

Aqueous Zn metal batteries show promise for large‐scale energy storage but face challenges including dendrite formation, volume changes, and side reactions. This study introduces a novel anti‐swelling supramolecule‐crosslinked hydrogel (SCH) interphase to stabilize Zn metal anodes. The SCH, composed of cyclodextrin molecules crosslinked with polyvinyl alcohol, offers a multifaceted approach to enhance anode stability. It homogenizes ion flux and suppresses Zn dendrite growth by creating well‐defined pathways for Zn2+ movement. The supramolecular structure selectively traps SO42− ions, effectively desolvating Zn2+ and enabling fast ion transportation. Additionally, by disrupting water cluster hydrogen bonds, SCH reduces free water activity, mitigating corrosion at the Zn surface. Electrochemical tests demonstrate the excellent performance of SCH‐Zn, with symmetric cells achieve lifespans of 1800 h at 4 mA cm−2/2 mAh cm−2 and 1100 h at 10 mA cm−2/5 mAh cm−2. Zn||Cu half‐cells maintain 99.7% Coulombic efficiency over 500 cycles, while full cells with polyaniline cathodes exhibit stable cycling for 1500 cycles at 5 A g−1 with no apparent capacity decay. These results highlight the effectiveness of the SCH in stabilizing Zn anodes. This study provides a new interfacial engineering strategy for high‐performance aqueous Zn batteries, potentially accelerating their practical implementation in large‐scale energy storage. [ABSTRACT FROM AUTHOR]

Highlights Highly filled polymer fibers offer huge promise for radiation protection safety and wear comfort of personal protective equipment (PPE) in radiation environments. However, it usually sacrifices mechanical properties that directly related to practical usability. Here, as high as 75 wt% PbWO4 (PWO) particles have been filled in polyvinyl alcohol (PVA) fiber via tailoring their size and shape for enhanced γ‐rays shielding and good mechanical properties. Clearly shown that 0 dimensional (0‐D) PWO exhibits better dispersion and compatibility between the interfaces than 1‐D PWO in highly filled PVA fibers. In addition, 70 wt% 0‐D PWO/PVA fibers display better mechanical properties than 70 wt% 1‐D PWO/PVA fibers. Note that 75 wt% 0‐D PWO/PVA fibers show 1.02 cN/dtex of tensile strength. However, 75 wt% 1‐D PWO/PVA fibers fail to be fabricated smoothly. Importantly, the overlapped fabrics with 75 wt% 0‐D PWO/PVA fibers display 43.05% of γ‐ray shielding (105 keV) meanwhile it offers good air and water vapor permeability for wear comfort. The superior γ‐ray shielding ascribes the polymer fibers with the higher filling in comparison with its counterpart, which provides a practical means to design radiation protection safety and wear comfort of articles. This work breaks the upper limit of filling in polymer fibers Filler structure can weigh the integrated properties of polymer fibers. 0‐D PWO particles promote interfacial compatibility in highly filled fibers. Radiation protection safety and wear comfort of articles tend to be designed. [ABSTRACT FROM AUTHOR]

Real‐time monitoring of respiration plays a very important role in human health assessment, especially in monitoring and analyzing respiration during exercise and sleep. However, traditional humidity sensors still have problems in flexibility, sensitivity, and durability, so there is an urgent need to develop humidity sensors with high sensitivity, stretchability, and environmental resistance as respiratory monitoring applications. Here, based on the double network hydrogel structure of polyvinyl alcohol and polyacrylamide, a highly sensitive, highly stretchable, and environmentally stable organic hydrogel humidity sensor has been manufactured by using the synergistic effect of lithium chloride and MXene. The hydrogel humidity sensor shows rapid response in the humidity range of 40–85% RH, and has a high sensitivity of −103.4%/% RH. In addition, it exhibits more than 3000% mechanical strain and excellent environmental resistance, which is attributed to the chemical cross‐linking in the hydrogel network and the synergistic effect of multiple hydroxyl groups in glycerol forming rich hydrogen bonds with water and polymer chains. The hydrogel humidity sensor is used for real‐time monitoring of breathing and sleep processes. This work provides a new strategy for preparing high‐performance, extensibility, and environmental stability hydrogel‐based sensors for respiratory monitoring. [ABSTRACT FROM AUTHOR]

This study introduces a technique for decontaminating radioactive surfaces by employing a gel, herein termed as radiation decontamination gel with eutectic liquids (RADGEL), composed of a deep eutectic solvent and polyvinyl alcohol, with the goal of enabling reuse of the surface post‐decontamination. The decontamination effectiveness of RADGEL underwent thorough evaluation through trials conducted on different simulated surfaces, achieving decontamination efficiency up to 99.9% for alpha as well as gamma radionuclides. The various parameters influencing decontamination factors such as amount of complexing agent used, polymer film thickness, nature, and magnitude of radioactivity, as well as surface characteristics of substrates to be decontaminated were optimized. Additionally excellent mechanical strength of RADGEL, affirms its potential as practically efficient, cost‐effective, and safe option for surface decontamination. The Fourier‐transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM) analysis suggest RADGELs capability for both physical and chemical interactions with contaminants, thus highlighting its comprehensive decontamination efficacy. The outcomes of this study carry substantial implications for the decontamination of surfaces contaminated with various types of radionuclides. [ABSTRACT FROM AUTHOR]

Flexible pressure sensors have attracted much attention because of their application prospects in wearable devices, electronic skin, and health monitoring. However, it is still difficult to obtain pressure sensors with excellent performance simply and efficiently. Indium tin oxide (ITO) is a widely used transparent conductive material, and polyvinyl alcohol (PVA) is an elastic insulating material with the advantages of easy processing and stable mechanical properties. ITO nano‐crystalline particles are dispersed into PVA polymers to form an ITO nanocrystalline‐PVA composite film with good electrical conductivity as a piezorestoresistive material, fabricating a pressure sensor with excellent performance. The pressure sensor possesses superior sensitivity (641.15 kPa−1), wide detection range (0–80 kPa), fast response time (10.93 ms), and recovery time (8.05 ms), and excellent stability (more than 1500 cycles). The pressure sensor shows excellent performance in a variety of applications, such as pulse testing, speech recognition, and detection of various joint movements of the human body (such as knees, fingers, elbows, etc.). The sensor has application prospects in health monitoring and motion perception. [ABSTRACT FROM AUTHOR]

With the aim of producing a photomechanical material for incorporation in soft microrobots, a one‐dimensional diene coordination polymer (CP) [Cd(F‐bpeb)(3‐CBA)2]n (CP1, F‐bpeb=4,4′‐((1E,1′E)‐(2,5‐difluoro‐1,4‐phenylene)bis(ethene‐2,1‐diyl))dipyridine, 3‐HCBA=3‐chlorobenzoic acid) was synthesized and characterized. Irradiation of CP1 with ultraviolet (UV) or visible light causes [2+2] photocycloaddition reactions resulting in the introduction of crystal strain which triggers various types of crystal movements. Composite films of CP1‐PVA (SC) fabricated by dispersing CP1 crystals into polyvinyl alcohol (PVA) solution allow amplification of the crystal movement so that the film strips exhibit fast and flexible curling upon photoirradiation. The composite films may be cut into long rectangular strips and folded to simulate soft microrobots which exhibit a variety of fast, flexible and continuous photomechanical movements resembling a human performing various gymnastic exercises. [ABSTRACT FROM AUTHOR]

Photoconductors featuring an individual micro/nano‐crystal as the photoactive channel hold the great promise for next‐generation integrated optoelectronics. Meanwhile, the gain aiming for signal amplification without an extra amplifier, the fast response for fast data transfer, and low dark current for weak signal acquisition are highly desirable in integrated optoelectronics, but are inherent trade‐off in traditional photoconductors. Herein, the study demonstrates a single‐microplate MAPbI3 photoconductor based on polyvinyl alcohol‐filled planar electrodes that can simultaneously achieve excellent performance on these parameters. The superior performance can be attributed to the exquisite design of filling the device channel gap with polyvinyl alcohol. This deep‐work‐function transparent polyvinyl alcohol can not only passivate surface defects of the perovskite microplate by hydrogen bonding, but also form a heterojunction with top perovskites to induce a depleted channel. Resultant single‐microplate photodetectors exhibit exceptional performance characteristics including ultra‐low noise‐equivalent power of 0.19 fW Hz−1/2, high specific detectivity of 3.68 × 1014 Jones, fast response of 3.2 µs, high EQE‐bandwidth over 107 Hz, as well as excellent stability. More importantly, single‐microplate MAPbI3 photoconductors demonstrate ultra‐weak‐light imaging ability surpassing silicon counterparts. Furthermore, the successful integration of their microplate pixels showcases the promising prospect for integrated optoelectronics. [ABSTRACT FROM AUTHOR]

Stimuli‐responsive hydrogels (HGs) have shown promise for smart drug delivery applications. Specifically, glucose‐responsive HGs having phenylboronic acid (PBA) functional groups are extensively pursued for insulin delivery in hyperglycemia. Current polymeric glucose‐responsive HGs are cumbersome to fabricate and show a limited insulin release profile. Herein, we develop a straightforward fabrication of glucose‐responsive multipolymer HGs (MPHGs) using a three‐component in situ mixing. Molecular cargo, such as insulin, was loaded during the gelation. Heterobifunctional formylphenylboronic acid (FPBA) crosslinkers were used to interconnect polyvinyl alcohol (PVA) and branched polyethyleneimine (PEI) via boronate ester and imine bonds, respectively. Three positional isomers of FPBA (2FPBA, 3FPBA, and 4FPBA) resulted in HGs with distinct viscoelastic behaviors under the same conditions. HGs derived from 4FPBA exhibited more solid‐like properties compared to 2FPBA and 3FPBA due to a higher crosslinking density. All the HGs exhibited glucose‐responsive dissolution and release of embedded insulin cargo without disrupting the native structure. Insulin release profiles show a higher glucose‐responsive release from 4FPBA‐derived MPHGs. All the HGs were injectable, self‐healing, and noncytotoxic below 10 μg/ml concentrations. The MPHGs developed in this study uncover new directions in creating glucose‐responsive matrices for self‐regulating drug delivery applications. In the future, detailed in vivo studies will be performed for clinical applications. [ABSTRACT FROM AUTHOR]

Summary The white button mushroom is a significant vegan food with a limited shelf‐life. To prolong the shelf‐life of mushrooms, certain treatment must be implemented. The current investigation is involved in the development of biocomposite film (BCF) by employing cellulose nano crystal (CNC), dispersed in a polyvinyl alcohol (PVA) matrix. The CNC extracted from aloe vera rind exhibited a sharp crystalline peak and rod‐shaped structures with a particle size of ~322.7 nm. Among the various concentrations of the CNC, incorporated in the BCF, the 8% CNC (BCF‐8%)‐loaded film showed the highest mechanical strength of ~166.73 MPa and a best crystallinity pattern. The study examined the synergistic impact of BCF along with neroli and palmarosa essential oil vapours, which effectively preserved the overall physiochemical properties and sensory characteristics of white button mushrooms for up to 8 days of storage. Hence, these innovative packaging systems are suitable substitute for the commercial food grade packaging to maintain the quality of mushrooms during postharvest storage. [ABSTRACT FROM AUTHOR]

Renewable osmotic energy between seawater and river water shows great potential in meeting global energy demand. Reverse electrodialysis (RED) technique using ion‐selective membrane is particularly outstanding for its easy operation. Preparing low‐cost and large‐area ion‐selective membranes with excellent ion transport characteristics is particularly important to promote commercial applications. Herein, large‐area ion‐selective membrane is prepared by scraping slurry of flocculated GO (graphene oxide)/PAAS (sodium polyacrylate) solution and then coated with PVA (polyvinyl alcohol)/SA (sodium alginate) gel layer. The PVA/SA molecules can penetrate into the membrane through the unique micro/meso‐pores, which together increase the ion selectivity, membrane permeability, and stability. This ion‐selective membrane can achieve a power density of 8.65 W m−2 under a 50‐fold salinity gradient (NaCl) simulating the sea/river junction environment (with the testing area of 0.0314 mm2). This work significantly promotes the application of GO in large‐area preparation of low‐cost ion‐selective membrane. [ABSTRACT FROM AUTHOR]

The increased usage and misuse of antibiotics cause antimicrobial resistance, which makes it necessary to develop new antibiotic agents. Antimicrobial peptides (AMPs) could be a significant solution to addressing this issue. Antimicrobial temporin 1Ta and temporin 1Tb peptides, derived from frog skin secretions, exhibit notable activity against Gram (+) bacteria; on the other hand, apidaecin 1b peptide, obtained from honeybees, is effective against Gram (−) bacteria. In this study, hybrid AMPs were synthesized by merging temporin 1Ta and temporin 1Tb with apidaecin 1b to produce peptides that are active against a broad spectrum of microorganisms. Furthermore, the hybrid peptides were mixed with polyvinyl alcohol (PVA) polymer to produce bioactive nanofibers by electrospinning. The synthesized peptides and the nanofibers were tested on various Gram (+) and Gram (−) bacteria (E. coli ATCC 25922, P. aeruginosa ATCC 27853, S. aureus ATCC 29213, and E. faecalis ATCC 29212). As a result, the hybrid peptides were found to have a reasonable antibacterial effect on both bacterial groups. In addition, peptide‐containing nanofibers preserved the antibacterial activity as well. The hemolytic activities of the peptides were also examined, and it was found that the hybrid peptides were not lethal to red blood cells at a concentration of 16 μM. [ABSTRACT FROM AUTHOR]

Fluorescent hydrogel as an advanced material has been used for anti‐counterfeiting, probe detection, and optical devices. A facile strategy to prepare fluorescent hydrogel is developed by carboxymethyl cellulose (CMC) with Europium(III) and polyvinyl alcohol (PVA). The hydrogel forms a physical cross‐linking network under mild reaction conditions without using volatile organic chemicals. The addition of CMC‐Eu(III) improves the mechanical properties of the hydrogel. At 15% CMC‐Eu(III), the hydrogel reaches its maximum tensile and compressive stress, which are 47.25 ± 10.35 and 10.14 ± 1.90 kPa, respectively. Meanwhile, the hydrogels exhibit a 5D0→7F2 characteristic emission peak assigned to Eu3+, which emits stable red fluorescence under 254 nm ultraviolet (UV) light. When this hydrogel is applied to paper, the paper showed hidden fluorescent dots under UV light. This additive also enhances the mechanical properties of the paper, which reveals the multifunctionality of this fluorescent hydrogel for anti‐counterfeiting and reinforcement. [ABSTRACT FROM AUTHOR]

Chitosan (CS) has attracted substantial attention as a sustainable biopolymer in drug delivery applications, in recent years, because of its nontoxicity, biocompatibility, and accessibility. This study develops chitosan/polyvinyl alcohol/carboxymethylcellulose (CS/PVA/CMC) ternary hydrogel with excellent efficacy as a potential delivery vehicle for the antidiabetic drug metformin hydrochloride. The incorporation of carboxymethylcellulose (CMC) in the blend remarkably improves the swelling properties of the hydrogel. Metformin hydrochloride is loaded in the CS/PVA/CMC ternary blend by ultrasonication method. The prepared hydrogel beads are characterized by, Fourier‐transform infrared spectroscopy (FT‐IR), Scanning electron microscopy (SEM), and X‐ray diffraction (XRD) techniques and confirm the presence of the drug in the beads. The loading and release of metformin from the CS/PVA/CMC hydrogel beads are followed by UV–visible spectroscopy at 233 nm. Different formulations are prepared by varying the compositions of chitosan and carboxymethylcellulose. α‐Glucosidase inhibitory studies reveal that metformin loaded CS/PVA/CMC hydrogel beads show excellent antidiabetic activity. The maximum value of inhibitory activity observed is 89%. Cytotoxic analysis proves that the beads prepared are nontoxic. [ABSTRACT FROM AUTHOR]

The purpose of this research was to use polyvinyl alcohol (PVOH) 18‐88 as a case study to evaluate the environmental fate, ecotoxicity, and overall safety profile of water‐soluble, nonmodified PVOH polymers used in detergent films. An OECD 303A Wastewater Treatment Plant Simulation Study was conducted with dissolved organic carbon as the analytical endpoint to evaluate the removal of PVOH 18‐88 during wastewater treatment. During the plateau phase, high levels of removal due to biodegradation were observed (average 97.4 ± 7.1, range: 88%–116%). The OECD 303A study quantitatively verified that surface water is the dominant receiving compartment for PVOH 18‐88 post wastewater treatment. Acute algae, invertebrate, and fish embryo (fish embryo acute toxicity test [FET]) ecotoxicity studies quanitified the 50% lethal/effect concentration (L/EC50) for PVOH 18‐88. Due to the potential for the chorion to impact PVOH 18‐88 bioavailability, both chorionated and dechorionated FET tests were conducted. L/EC50 > 1000 mg/L for FET (chorionated and dechorionated), invertebrate, and algae were observed. The Sustainable Futures (US) and REACH (EU) frameworks were used to evaluate environmental risk. For the US assessment, the Exposure and Fate Assessment Screening Tool was used to predict the single day lowest flow over a 10‐year period (1Q10) surface water concentration and the seven consecutive days of lowest flow over a 10‐year period (7Q10) surface water concentration and compared with acute and chronic concentrations of concern. For the EU assessment, the European Union System for the Evaluation of Substances was used to predict local and regional exposure concentrations and compared to the predicted no effect concentration. For both regulatory assessments, the exposure concentrations were >2 orders of magnitude below the effect concentrations. Integr Environ Assess Manag 2024;20:1693–1705. © 2024 The Authors. Integrated Environmental Assessment and Management published by Wiley Periodicals LLC on behalf of Society of Environmental Toxicology & Chemistry (SETAC). Key Points: Polyvinyl alcohol (PVOH) 18‐88 was used as a case study to evaluate the environmental fate, ecotoxicity, and overall safety profile of water‐soluble, nonmodified PVOH polymers used in detergent films.Polyvinyl alcohol 18‐88 was biodegraded extensively during wastewater treatment.Low ecotoxicity was observed with measured LC/EC50s > 1000 mg/L.The US and EU environmental risk assessments predicted exposure concentrations were >2 orders of magnitude below effect concentrations, providing significant assurance of safety for PVOH 18‐88 as a representative test substance for nonmodified PVOH polymers used in detergent films. [ABSTRACT FROM AUTHOR]