Crosslinked Poly Vinyl Alcohol Research Articles

Low-cost and durable polyvinyl alcohol modified polyethylene separator for vanadium redox flow battery

Porous separators are considered a viable alternative to the high cost Nafion membrane for vanadium redox flow battery (VRFB) commercialization. However, the porous separators suffer from high vanadium ion crossover due to the presence of large micron size pores, which leads to decay in capacity of the VRFB system. To tackle the same, a composite separator is synthesized wherein a cross-linked polyvinyl alcohol (PVA) layer is coated on to the porous polyethylene silica separator (PE separator) to mitigate the vanadium ion crossover rate and employed in the VRFB application. Scanning electron microscopy (SEM) analysis confirmed the successful coating of the PVA film on to the PE separator. Synthesized PE-PVA separator showed a significant decrease in the vanadium ion crossover by 31.44 times compared to the pristine PE separator. Consequently, the self-discharge time increases by 8 and 1.66 times compared to the pristine PE separator and the Nafion117 membrane, respectively. VRFB cell equipped with the synthesized separator showed better capacity retention with a capacity fade rate of 0.2 % Ah·cycle−1 than the Nafion117 membrane (0.5 % Ah·cycle−1). In-situ and ex-situ oxidative stability of the separator is explored in detail and a degradation mechanism of the cross-linked PVA membrane is proposed accordingly. The synthesized single side coated PE-PVA´ separator exhibits higher coulombic efficiency of 99 % and comparable energy efficiency of 71 % at a current density of 120 mA·cm−2 and demonstrated excellent lifetime durability tested up to 1600 charge-discharge cycles at 80 mA·cm−2.

P16-07 Toxicological evaluation of anisotropic cross-linked polyvinyl alcohol hydrogels intended for humic substances immobilization and topical skin disease treatment

P16-07 Toxicological evaluation of anisotropic cross-linked polyvinyl alcohol hydrogels intended for humic substances immobilization and topical skin disease treatment

Research on the Thermal Aging Mechanism of Polyvinyl Alcohol Hydrogel.

Polyvinyl alcohol (PVA) hydrogels find applications in various fields, including machinery and tissue engineering, owing to their exceptional mechanical properties. However, the mechanical properties of PVA hydrogels are subject to alteration due to environmental factors such as temperature, affecting their prolonged utilization. To enhance their lifespan, it is crucial to investigate their aging mechanisms. Using physically cross-linked PVA hydrogels, this study involved high-temperature accelerated aging tests at 60 °C for 80 d and their performance was analyzed through macroscopic mechanics, microscopic morphology, and microanalysis tests. The findings revealed three aging stages, namely, a reduction in free water, a reduction in bound water, and the depletion of bound water, corresponding to volume shrinkage, decreased elongation, and a "tough-brittle" transition. The microscopic aging mechanism was influenced by intermolecular chain spacing, intermolecular hydrogen bonds, and the plasticizing effect of water. In particular, the loss of bound water predominantly affected the lifespan of PVA hydrogel structural components. These findings provide a reference for assessing and improving the lifespan of PVA hydrogels.

Experimental study for the decontamination of various surfaces from 99Mo using PVA/Borax/Al(OH)3 strippable hydrogel

Polyvinyl alcohol (PVA) is a beneficial polymer capable of forming hydrogels helpful in a wide range of applications. Hydrogels based on cross-linking of PVA with borax, and able to incorporate with a decontaminating agent have been used in the decontamination of 99Mo from contaminated surfaces. Aluminum hydroxide has been introduced in the formulations of PVA-borax, to increase the gel efficiency for 99Mo decontamination from surfaces. The formulations were investigated with glass, stainless steel, and wood as examples of different surfaces. When the hydrogel is sprayed on different surfaces, it forms rapidly and adheres well. Moreover, the hydrogel was shown to efficiently decontaminate surfaces contaminated with 99Mo by a maximum value of decontamination factor (D.F) for glass, stainless steel, and wood to be 43.5, 31.3, and 19.6 respectively.

Crosslinking of polyvinyl alcohol with di, tri, and tetracarboxylic acids: an experimental investigation

Crosslinking of polyvinyl alcohol with di, tri, and tetracarboxylic acids: an experimental investigation

Antibacterial Properties of Dandelion Extract-Based PVA/CTS/DAN/CuNP Composite Gel

Dandelion extract is a reducing agent, and CuSO4∙5H2O was used as a carrier to create copper nanoparticles (CuNPs). A novel polyvinyl alcohol–chitosan–dandelion–CuNP (PVA/CTS/DAN/CuNP) gel was acquired by cross-linking Polyvinyl alcohol (PVA) and chitosan (CTS) solution. Its structure was analyzed using Fourier transform infrared spectroscopy, Scanning electron microscopy, and X-ray diffraction. The PVA/CTS/DAN/CuNP gels manifested good stability, recycling ability, swelling properties, and biocompatibility. Using the agar diffusion method, the diameters of the inhibition zone of the composite gel against Escherichia coli, Staphylococcus aureus, and Pseudomonas aeruginosa could be over 21 mm. In conclusion, the PVA/CTS/DAN/CuNP composite gel had good antibacterial performance, which has a high potential for application in microbial contamination treatment and environmental protection.

Enhancing the performance of nanostructured PVA/SA scaffolds through incorporation of macromolecules: From synergistic effects to advanced multifunctionalities

The increasing use of biomaterial scaffolds in tissue engineering applications demands a comprehensive understanding and precise control of their overall properties. This work analyzes the synergy of naturally occurring biological macromolecules on the swelling, and thermal and mechanical properties of ionically crosslinked polyvinyl alcohol (PVA)/sodium alginate (SA) fibrous scaffolds. The presence of collagen (COL) or hyaluronic acid (HA) contributed not only to increasing the hydrogen-bond density but also to induce the crystalline PVA phase formation. Consequently, the swelling, thermal degradation, elastic modulus, and nanohardness of the scaffolds were significantly enhanced. By considering COL and HA the relevance in diverse cellular processes and tissue functions, the PVA-scaffolds here introduced are promising materials by providing advanced multifunctionalities.

Harnessing pomegranate rind waste to develop novel bioactive packaging films using citric acid crosslinked polyvinyl alcohol (PVA)/starch-based polymer matrix

Harnessing pomegranate rind waste to develop novel bioactive packaging films using citric acid crosslinked polyvinyl alcohol (PVA)/starch-based polymer matrix

Gel beads prepared by polyvinyl alcohol cross-linking with phytic acid and Fe as novel microbial carriers for simultaneous partial nitrification, anammox and denitrification

Enhancing the stability of biomass and ensuring a stable activity of anaerobic ammonia oxidizing bacteria are crucial for successful operation of the simultaneous partial nitrification, Anammox, and denitrification (SNAD) process. In this study, gel beads of polyvinyl alcohol/phytic acid (PVA/PA) and polyvinyl alcohol/phytic acid/Fe (PVA/PA/Fe) were prepared as innovative bio-carriers. Theoretical simulations and analyses revealed that these carriers are predominantly connected via hydrogen and borate bonds, with PVA/PA/Fe also featuring metal coordination bonds. The total nitrogen removal efficiency of reactors with PVA/PA/Fe and PVA/PA increased by 13.5 % and 9.0 %, respectively, compared to reactor without carriers. The iron-enriched PVA/PA/Fe carriers significantly improve SNAD by promoting Anammox, Feammox, and nitrate-dependent Fe2+ oxidation reactions, leading to faster nitrogen conversion and higher nitrogen removal rate than reactor without carriers and with PVA/PA. Using of PVA/PA and PVA/PA/Fe gel beads as bio-carriers offers benefits to the SNAD process, including cost-effective and low carbon requirement.

Coal tar pitch porous carbon-based bimolecular crosslinked hydrogel evaporator for solar-driven efficient water purification

Hydrogel evaporators have been widely used in solar-driven interfacial water evaporation due to their good thermal insulation, strong hydrophilicity, and rich internal pores. However, the occlusion pores in the hydrogel with a single molecule chain not only limit water transportation but also lead to serious salt crystallization. Hence, we developed a hydrogel evaporator (NSC-PVA/8CMC) with an abundant and open pore structure by cross-linking polyvinyl alcohol (PVA) and carboxymethyl cellulose (CMC). In which, the low-cost amorphous coal tar pitch porous carbon (NSC) is used to absorb light and improve light-to-heat conversion. The porous structure and thermal insulation (0.37 W m−1 K−1) of NSC-PVA/8CMC are conducive to excellent light absorption (≈99.02 %) and minimizing heat loss, finally leading to excellent photothermal conversion (1.44 kg m−2 h−1, 72.96 %, 1 sun). More significantly, NSC-PVA/8CMC with a strong desalination capacity can provide a self-purifying performance in seawater and brackish water. At the same time, the innovative attempt to use coal tar pitch as the photothermal conversion material has expanded the application scope of coal tar pitch.

Promoting the healing of infected diabetic wound by nanozyme-containing hydrogel with anti-bacterial inflammation suppressing, ROS-scavenging and oxygen-generating properties.

Bacterial infections already pose a significant threat to skin wounds, especially in diabetic patients who have difficulty healing wounds. However, wound or bacterial infections are known to produce excess reactive oxygen species (ROS), and hypoxia may further hinder wound healing and the development of chronic wounds. In this study, a multifunctional hydrogel for ROS scavenging and bacterial inhibition was developed by cross-linking polyvinyl alcohol (PVA) and sodium alginate (SA) with graphene oxide (GO) loaded with silver-platinum hybrid nanoparticles (GO@Ag-Pt). The PVA/SA hydrogel loaded with GO@Ag-Pt exhibited the ability to scavenge different types of ROS, generate O2, and kill a broad spectrum of bacteria in vitro. The silver-platinum hybrid nanoparticles significantly increased the antibacterial ability against Escherichia coli and Staphylococcus aureus compared with silver nanoparticles (AgNps). GO@Ag-Pt loaded hydrogel was effective in treating infections caused by S.aureus, thereby significantly promoting wound healing during the inflammatory phase. Hydrogel therapy significantly reduced the level of ROS and alleviated inflammation levels. Notably, our ROS-scavenging, antibacterial hydrogels can be used to effectively treat various types of wounds, including difficult-to-heal diabetic wounds with bacterial infections. Thus, this study proposes an effective strategy for various chronic wound healing based on ROS clearance and bacteriostatic hydrogels.

Engineering the nanozyme hydrogel beads by polyvinyl alcohol/chitosan encapsulation with recyclable and sustainable catalytic activity for visual analysis of hydrogen peroxide

BackgroundHydrogen peroxide (H2O2) plays a vital role in human health and have been regarded as a crucial analyte in metabolic processes, redox transformations, foods research and medical fields. Especially, the long-time and excessive digestion of H2O2 may even cause severe diseases. Although conventional instrumental methods and nanozymes-based colorimetric methods have been developed to accomplish the quantitative analysis of H2O2, the drawbacks of instrument dependence, cost-effectiveness, short lifespan, non-portable and unsustainable detection efficacies will limit their applications in different detection scenarios. ResultsHerein, to address these challenges, we have proposed a novel strategy for nanozyme (RuO2) hydrogel preparation by the solid support from cross-linked polyvinyl alcohol (PVA) and chitosan (CS) to both inherit the dominant peroxidase-like (POD) activity and protect the RuO2 from losing efficacies. Taking advantages from the hydrogel, the encapsulated RuO2 were further prepared as the regularly spherical beads (PCRO) to exhibit the sustainable, recyclable, and robust catalysis. Moreover, the intrinsic color interferences which originated from RuO2 can be avoided by the encapsulation strategy to promote the detection accuracy. Meanwhile, the high mechanical strength of PCRO shows the high stability, reproducibility, and cyclic catalysis to achieve the recyclable detection performance and long lifetime storage (40 days), which enables the sensitively detection of H2O2 with the detection limit as lower to 15 μM and the wide detection linear range from 0.025 to 1.0 mM. SignificanceOn the basis of the unique properties, PCRO has been further adopted to construct a smartphone detection platform to realize the instrument-free and visual analysis of H2O2 in multi-types of milk and real water samples through capturing, processing, and analyzing the RGB values from the colorimetric photographs. Therefore, PCRO with the advanced detection efficacies holds the great potential in achieving the portable and on-site analysis of targets-of-interest.

Charge-patterned nanofiltration membranes with polystyrene sulfonate particles and polyethyleneimine in cross-linked polyvinyl alcohol

Removing salinity has always been a challenge for wastewater treatment. Utilizing nanofiltration (NF) membranes is a promising approach. However, currently available NF membranes are less effective in monovalent salt removal. In this study, work toward the initial aim of fabricating charge mosaic membranes led to charge-patterned NF-selective films on polyether sulfone (PES) or polyacrylonitrile (PAN) support membranes, with similar rejection for mono- and divalent salts. The membranes were fabricated by a two-step layer assembly of first negatively charged polystyrene sulfonate (PSS) particles immobilized in a polyvinyl alcohol (PVA) layer, followed by coating a positively charged polyethyleneimine (PEI) layer. Both PVA and PEI were crosslinked using glutaraldehyde that had initially been impregnated into the support membrane. The type of support membrane, nanoparticle, PVA, and PEI concentrations during fabrication, as well as feed pH and salt concentration, play significant roles in separation performance of obtained composite membranes. Charge-patterned NF membranes fabricated using 0.5 wt.% PVA and 0.05 wt.% PSS for assembly of the first layer followed by coating 0.5 wt.% PEI solution had even somewhat higher rejection for monovalent salt (NaCl; ∼82%) compared to multivalent salts (Na2SO4, MgSO4, and MgCl2; ∼74%), at a permeance of 5.5 LMH/bar on the PES and 3.1 LMH/bar on the PAN support membrane.

Development of novel proton exchange membranes based on cross-linked polyvinyl alcohol (PVA)/5-sulfosalicylic acid (SSCA) for fuel cell applications

The proton-conducting and methanol permeation behaviors of polymeric electrolyte membranes (PEMs), as well as the expensive nature of direct methanol fuel cell (DMFC) components, pose major concerns in DMFC performance and commercialization. As a result, this research aimed to develop low-cost polyelectrolyte membranes based on cross-linked poly(vinyl alcohol)/5-sulfosalicylic acid dehydrate (PVA/SSCA) composite. Chemical cross-linkers and modifiers offer the essential chemical and mechanical stability of the developed membranes for usage as polyelectrolyte membranes (PEMs). The manufactured composite proton exchange membranes provide several benefits, including significant thermal, chemical, and mechanical stability. The results revealed that extending the SSCA molar concentration increased IEC outcomes of the synthesized membranes, reaching an elevated level of (3.31 meq g−1) compared to (0.91 meq g−1) for the Nafion 117 membrane. The proton conductivity of a composite membrane (102 μm thick) measured by impedance spectroscopy was relatively (0.078 S cm−1) and found comparable to other PVA-based composite membranes reported in the literature. Other key parameters, such as methanol permeability, were measured for constructed composite proton exchange membranes (2.52 × 10–7 cm2 s−1), which were much lower than Nafion 117 (3.39 × 10–6 cm2 s−1). The Fourier transform infrared (FT-IR), Raman scattering spectroscopy, scanning electron microscopy (SEM), energy-dispersive X-ray (EDX) spectroscopy, elemental analysis, and thermal gravimetric analysis (TGA) were among the techniques used to characterize the synthesized membranes. These characterizations confirm the structural interaction between the membrane components’ crystalline nature, and no signs of phase separation or cracks were found; surface morphology and good membrane homogeneity, elemental analysis, and the membranes’ thermal stability (up to 290 °C). The membranes were also mechanically characterized using a universal testing machine (UTM), which revealed good mechanical stability. The findings demonstrate that a low-cost proton exchange membrane could potentially be synthesized for DMFC applications.

Processing physically crosslinked polyvinyl alcohol hydrogel into solid foams via freeze-drying: The role of hydrogel state

Processing hydrogels into solid foams or aerogels via freeze-drying broaden their applications. However, one challenge is its inherent processing instability, often leading to dimensional shrinkage and structural collapse of the resultant solid foams. To address this, our study investigated the role of hydrogel state in the solid foam formation. Specifically, polyvinyl alcohol (PVA) hydrogel, synthesized through repeated freeze-thaw (FT) cycles, was investigated. It was found that PVA concentration and FT cycles played a vital role; specifically, higher PVA concentration and more FT cycles negatively affected solid foam formation. These hydrogels exhibited an increase in hydrogel viscoelasticity and crystallizability of the most flexible chains, indicative of strong and denser network structure. We proposed that the final solid foam structure was determined by a balance between the volumetric expansion due to water-to-ice transition during freezing and the intense inter-polymeric chain attractions within the denser network during sublimation.

Ionic Interactions of NaCl in Aqueous Polyvinyl Alcohol and Cross-Linked Polyvinyl Alcohol with Glutaraldehyde

Ionic Interactions of NaCl in Aqueous Polyvinyl Alcohol and Cross-Linked Polyvinyl Alcohol with Glutaraldehyde

Tartaric Acid Cross-Linking Polyvinyl Alcohol as Degradable Separators for Rechargeable Lithium Ion Batteries.

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.

Detection of H2O2 and catalase on a paper-based flow sensor constructed with borate cross-linked PVA hydrogel

The detections of H2O2 and catalase play an important role in daily life. This study introduces a paper-based flow sensor that is specifically designed to detect H2O2 and catalase. The sensor utilizes a hydrogel composed of cross-linked 4-carboxyphenylboronic acid and polyvinyl alcohol. When H2O2 is in contact with the hydrogel, the B–C bonds of the hydrogel undergo a reactive process, causing decomposition of the hydrogel. The pH indicator strip enables the visual monitoring of the viscosity change that occurs during the gel-sol transition. The quantification of H2O2 is accomplished by assessing the proportion of water coverage on the pH indicator strip. The sensor shows a detection limit of 0.077 wt% and is applicable for the quantitative measurement of H2O2 in routinely used disinfectants. Furthermore, the presence of catalase is effectively identified and the detection of catalase in milk is successfully fulfilled. In summary, this work proposes a simple, user-friendly, label-free, and cost-effective method for constructing a paper-based flow sensor using borate cross-linked polyvinyl alcohol hydrogel, showing great potential for detecting H2O2 and catalase in various practical scenarios.

Tough and biodegradable C-lignin cross-linked polyvinyl alcohol supramolecular composite films with closed-looping recyclability

Catechyl lignin (C-lignin) is a unique natural biopolymer that is considered to be the best alternative to conventional lignin due to its linear homogeneous molecular structure. Based on the structural properties of C-lignin, the development of a new biodegradable plastic to replace traditional petroleum-based plastics is a sustainable route. However, the maximum filling fraction of lignin is required to achieve excellent biodegradability of lignin-based bio-plastics, yet resulting in decreased mechanical strength of composites. Herein, we report a novel strategy to fabricate a closed-loopling recyclability supramolecular composite films through casting and dry molding process of intermolecular covalent-noncovalent cross-linking networks with polyvinyl alcohol by the epoxidation of C-lignin. The intermolecular cross-linking mechanism analyses reveal that the resultant bio-material not only display improved mechanical properties (maximum tensile strength of 133.5 MPa and strain at break of 690.2 %), but also show UV-resistant, antimicrobial, thermally stable, and rapid biodegradable properties. Notably, the fabricated films demonstrate the characteristics of closed-loop recyclability, which paves a new way toward rational design of bioplastics using renewable lignin. These integrated properties make the lignin-based biocomposites a promising alternative to traditional plastics.

Cover Image, Volume 141, Issue 22

The cover image is based on the Research Article Development of crosslinked polyvinyl alcohol nanofibrous membrane for microplastic removal from water by Anandu Nair Gopakumar et al., https://doi.org/10.1002/app.55428image