Polyvinyl Alcohol Research Articles

Load‐Bearing Structure Inspired Cellulose‐Based Aerogel With High Resilience and Water Tolerance

AbstractCellulose‐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.

Emulsification in nearly Newtonian and non-Newtonian media of wormlike micelles

Emulsification experiments with four silicone oils, having viscosities ranging from 0.01 to 30 Pa.s, were conducted in two types of media: nearly Newtonian polyvinyl alcohol (PVA) solutions and non-Newtonian mixtures induced by worm-like micelles in solutions of sodium laureth sulfate and cocoamidopropyl betaine (BS) with NaCl. The increased viscosity of BS solutions upon the addition of NaCl did not significantly affect the drop size in the formed emulsions. In contrast, the increased viscosity of solutions with higher PVA concentrations significantly reduced the drop sizes for all silicone oils. A theoretical expression predicting the maximum drop size in both types of media (nearly Newtonian and non-Newtonian) was derived and validated against experimental data. The expression accounts for shear-thinning behavior in both the aqueous and oil phases. Interfacial stress dominates the breakage of less viscous oils, while viscous stress inside the breaking drop plays a leading role for more viscous oils. The formation of emulsions with similar sizes in non-Newtonian solutions of BS with different NaCl concentrations was explained by their strongly shear-thinning behavior, which leads to nearly similar viscosity at high shear rates, despite their zero-shear viscosities differing by more than two orders of magnitude.

Preparation of Polyvinyl Alcohol–Chitosan Nanocellulose–Biochar Nanosilver Composite Hydrogel and Its Antibacterial Property and Dye Removal Capacity

In this research, silver-loaded biochar (C-Ag) was acquired from a waste fish scale, and nanocellulose (CNF) was prepared from the waste wheat stalk. Then C-Ag was loaded into chitosan-polyvinyl alcohol hydrogel (CTS-PVA) with CNC as a reinforcement agent, and a novel nanocomposite material was acquired, which could be efficiently applied for antibacterial and dye removal. By plate diffusion analysis, the inhibition areas of C-Ag-CTS-PVA-CNF (C/CTS/PVA/CNF) hydrogel against E. coli ATCC25922, S. aureus ATCC6538, and P. aeruginosa ATCC9027 could reach 22.5 mm, 22.0 mm, and 24.0 mm, respectively. It was found that the antibacterial rate was 100% in the water antibacterial experiment for 2 h, and the antibacterial activity was more than 90% within 35 days after preparation, and the antibacterial rate was more than 90% after repeated antibacterial tests for five times. Through swelling, water adsorption, water loss rate, and water content tests, the hydrogel manifested good moisturizing properties and could effectually block the loss of water and improve the stability of the C/CTS/PVA/CNF hydrogel. The pseudo-first-order and pseudo-second-order models were built, and the adsorption capacity of hydrogel to dye was analyzed, and the dye removal was more consistent with the pseudo-first-order kinetic model. The best removal effect for Congo red was 96.3 mg/g. The C/CTS/PVA/CNF hydrogel had a remarkable removal efficacy on Malachite green, Methyl orange, Congo red, and Methylene blue. As a result, the C/CTS/PVA/CNF hydrogels had robust antibacterial properties and reusability. In addition, the present research developed a facile strategy for effectual dyes removal from the aqueous medium.

Use of aqueous polyvinyl alcohol in binder jetting of Inconel 718

AbstractBinders used in binder jetting often pose health and environmental risks during processing and post processing operations. The print-heads which are used to deposit binder selectively on the feedstock are prone to clogging, despite the trend of print-heads being highly customised to suit different kinds of binders. These factors often hide the advantages of binder jetting as an additive manufacturing process, especially its scalability and its faster printing rates in comparison to powder bed fusion methods. The work presented here takes a step back and focuses on the development of an aqueous, polyvinyl alcohol (PVA)-based liquid binder that is easy to manufacture and store, safe to handle, and can be reliably jetted to print parts. The feedstock considered was Inconel 718, a nickel-based super alloy which can be effectively processed by binder jetting without niobium segregation. PVA was added to the Inconel 718 powder in dry, granular form to manufacture a modified feedstock. The study also investigated the role of molecular weight of the PVA used, sintering environments and post-processing methods like hot isostatic pressing (HIP) on process responses like part densification, tensile strength, and hardness. Three different types of PVA were chosen which had molecular weights 10,000 g/mol (low molecular weight or LMW), 26,000 g/mol (medium molecular weight or MMW), and 84,000 g/mol (high molecular weight or HMW). The compatibility of the liquid, aqueous PVA-based binders with virgin Inconel 718 was examined by measuring the contact angle. The liquid, aqueous binder having MMW PVA reported better wetting with the Inconel 718 powder with a wetting angle of 26.6 which was lower than the wetting angle of 42.4°, seen in case of a commercial resin-based binder. The green strength reported by the MMW PVA liquid binder was 220 kPa which was higher than the other two PVA-based liquid binders. Green parts, upon successful printing, were sintered at 1260 °C. It was observed that a part printed using MMW PVA had a densification of 96.16% when sintered in 99.98% by volume argon gas, which increased to 98.96% after undergoing HIP. The same part reported a densification of 88.69% when sintered in a 95% by volume N2 and 5% by volume H2 gaseous environment, which was later attributed to the uptake of nitrogen by the chromium present in Inconel 718, which prevented necking between particles. Tensile specimens printed using MMW PVA, sintered in a 99.98% argon environment, showed the highest ultimate tensile strength of 220 MPa, which increased to 1010 MPa after the HIP process, which can be compared to commercially available Inconel 718.

Embolization of posterior fossa meningiomas supplied with meningohypophyseal trunk by using n-BCA and dual balloon protection.

Efficacy of tumor embolization for posterior fossa meningioma is controversial due to the lack of adequate embolization for dangerous feeders. Of these, a meningohypophyseal trunk (MHT) has high therapeutic value despite the high risks associated with embolization. To analyze the utility of preoperative MHT embolization for posterior fossa meningiomas using n-BCA with dual balloon protection, a single center retrospective record review was performed on eight consecutive patients who underwent preoperative tumor embolization via the MHT for posterior fossa meningiomas between 2020 and 2024. All patients successfully embolized the MHT using n-BCA. Complete obliteration was achieved in five cases, which is related to the tentorial artery alone as the feeding vessel. None of the patients had cerebral infarction associated with distal embolization. One patient experienced worsening of preoperatively observed abducens nerve palsy due to cranial nerve ischemia. Gross total resection was achieved in seven of eight cases. The mean estimated blood loss during surgical resection was 186 mL (range, 39-392 mL). The mean operative time was 431 min (range, 317-767 min). The MHT embolization of posterior fossa meningiomas by using n-BCA is technically feasible with a high success rate and an acceptable complication rate. MHT=meningohypophyseal trunk; ILT=inferolateral trunk; CPA=Cerebellopontine angle; BGC=balloon guide catheter; PVA=polyvinyl alcohol; GTR=Gross Total Resection; CN=Cranial nerve.

Heat-Resistant Covalent Organic Framework (COF) PVA-Hybridized Gel Electrolyte for the Preparation of Dendrite-Free Zinc-Ion Batteries.

High-performance zinc-ion batteries (ZIBs) have attracted a great deal of attention due to their high theoretical capacity and high level of safety. Herein, we propose a covalent organic framework (COF) hybrid poly(vinyl alcohol) (PVA)-based gel electrolyte, which can induce the uniform deposition of Zn2+ and achieve dendrite-free formation. By grafting sulfonic acid groups on the surface of COFs to absorb Zn2+, we can strengthen the interaction between strong ions and dipoles in the electrolyte, improve the ionic conductivity, and achieve stable Zn2+ electroplating and stripping. Due to the good thermal stability of the COF material itself, the gel electrolyte hybrid with the PVA hydrogel shows high mechanical strength and good heat resistance and is capable of stable cycling for >1000 h at 50 °C, with a capacity retention rate of ≤75%. This study provides a new approach for developing high-temperature-resistant and highly stable dendrite-free ZIBs.

Hybrid composite beads of chitosan/graphene oxide for dye adsorption: characterizations, kinetic modeling and toxicity study

The current study aimed to the preparation of graphene oxide impregnated chitosan– polyvinyl alcohol hybrid beads (GO/CS-PVA) for the removal of Reactive Black 5 (RB5) dye from wastewater solutions, presenting them as a cost-effective alternative for wastewater treatment. These hybrid beads were fabricated using a dripping technique in an aqueous solution. The surface and structure of the material before and after adsorption process were studied by analyzing FTIR spectroscopy and Scanning electron microscope (SEM) as well as adsorption capacity was also evaluated. The results proved the successful synthesis of GO/CS-PVA beads and elucidated the physical adsorption mechanism of RB5. SEM images revealed uniform spherical beads with a rough surface, approximately 752 μm in diameter. Additionally, the evaluation of adsorption capacity showed that the optimum condition for RB5 adsorption is at pH = 3 while the kinetic investigations revealed that the adsorption process adhered to the pseudo-second-order model, indicating a chemisorption reaction. Furthermore, an increase in temperature from 25 to 65 °C enhanced the maximum adsorption capacity of GO/CS-PVA beads by 34%. The cytotoxic effect of the hybrid as measured on adipose derived stem cells via the MTT assay was negligible. In conclusion, it was proved that the eco-friendly GO/CS-PVA beads adsorbents can efficiently remove RB5 from wastewater in practical applications.

Assessing suitability and stability of materials for a head and neck anthropomorphic multimodality (MRI/CT) phantoms for radiotherapy.


This study aims to identify and evaluate suitable and stable materials for developing a head and neck anthropomorphic multimodality phantom for radiotherapy purposes. These materials must mimic human head and neck tissues in both computed tomography (CT) and magnetic resonance imaging (MRI) and maintain stable imaging properties over time and after radiation exposure, including the high levels associated with linear accelerator (linac) use.
Approach:
Various materials were assessed by measuring their CT numbers and T1 and T2 relaxation times. These measurements were compared to literature values to determine how closely the properties of the candidate materials resemble those of human tissues in the head and neck region. The stability of these properties was evaluated monthly over a year and after radiation exposure to doses up to 1000 Gy. Statistical analyses were conducted to identify any significant changes over time and after radiation exposure.
Main Results:
10% and 12.6% Polyvinyl alcohol cryogel (PVA-c) both exhibited T1 and T2 relaxation times and CT numbers within the range appropriate for brain grey matter. 14.3% PVA-c and some plastic-based materials matched the MRI properties of brain white matter, with CT numbers close to the clinical range. Additionally, some plastic-based materials showed T1 and T2 relaxation times consistent with MRI properties of fat, although their CT numbers were not suitable. Over time and after irradiation, 10% PVA-c maintained consistent properties for brain grey matter. 12.6% PVA-c's T1 relaxation time decreased beyond the range after the first month.
Significance:
This study identified 10% PVA-c as a substitute for brain grey matter, demonstrating stable imaging properties over a year and after radiation exposure up to 1000 Gy. However, the results highlight a need for further research to find additional materials to accurately simulate a wider range of human tissues.&#xD.

High-Strength PVA/Cellulosic hydrogels with Acid/Base and thermo dual-responsive fluorescence

Fluorescent polymer hydrogels (FPHs) with tunable luminous features have attracted immense interest. Nevertheless, until now, the development of most FPHs had been hindered by their poor mechanical properties and limited application range. This study presents a novel strategy to fabricate high-strength, multi-application cellulosic fluorescent hydrogels using polyvinyl alcohol (PVA) and fluorescent nanocellulose (containing pyrene tetracarboxylic acid) through a salting-out process. Such strategy enables cellulosic hydrogels with high tensile strength and toughness (26.45 MPa and 201.27 MJ/m3), compressive strength (165.58 MPa), dual-responsive fluorescence (acid/base and temperature), and multiple applications. Specifically, cellulosic hydrogels exhibit fluorescence switching through the utilization of lanthanide metals (Eu3+/Tb3+), acid/base, and temperature, owing to the presence of perylene tetracarboxylic acid as a fluorescent moiety with an aggregation-caused quenching (ACQ) effect. Based on this, the resulting hydrogels were utilized in rewritable display systems, temperature monitoring, and encrypted QR codes. This study envisions opening new possibilities for the development of high-strength fluorescent hydrogels with multiple applications.

Microneedle created in skin in situ forming gels depot; an alternate approach to the sustained transdermal delivery of colchicine

Colchicine (CLC) is a commonly used medication in prevention and treatment of acute gout condition via oral route. However its oral administrations pose several gastrointestinal (GI) adverse effects. In current study, an alternate combinatorial approach of microneedles patch and in skin forming gel depots were evaluated for sustained CLC delivery through skin using CLC loaded non-ionic amphiphilic triblock pluronic-127 thermoresponsive poloxamers. In first phase, to validate the development of in situ forming depots, the phase transition of pluronic-127 from the sol-gel state was examined using AR2000 rheometer. In second phase, microneedles patches (MAPs) were fabricated via casting method utilizing (19 × 19) laser-engineered silicone micromoulds from varied biocompatible polymer blends such as Gantrez S-97, Poly-vinyl alcohol, Polyethelene glycol 10000 and Poly (vinylpyrollidone) at various concentrations. For optimized MAPs, the mechanical strength, in skin dissolution kinetics and moisture contents were determined. From mechanical testing PVP and PVA MAPs showed more brittle nature and highest loss of MAPs reduction in comparison to Gantrez® MAPs. Optimized MAPs (Gantrez®) based on high mechanical strength were utilized as a microporation source in rabbit skin. In comparison to PVA and PVP, Gantrez® MAPs showed slow dissolution kinetics and resist dissolution for 540 s. Optical coherence tomography (OCT) quantified the penetration depth of Gantrez® MAPs in newborn rabbit skin at 591 μm. Increased in TEWL values after Gantrez® MAPs treatment confirmed the pores formation in skin. Ex-vivo permeation analysis showed that 25 % w/w CLC loaded PF127® gel showed controlled and prolonged drug permeation across microporated skin for 84 h in comparison to untreated skin. The distribution of PF127 gel solution in treated skin samples was confirmed by tracking fluorescence using confocal microscopy. Results shows that MAPs created in skin micropores can be used as CLC depots and sustained effects can be achieved by successfully avoiding oral route and GI adverse effects.

Biogas purification using cellulose nanocrystals/polyvinyl alcohol coated facilitated transport hollow fiber membranes with L‐arginine as CO2 carrier

AbstractThe composition of biogas consists mainly of CH4 (~60%) and CO2 (40%). To be considered a clean fuel, CH4 concentration in biogas must be increased to over 95%. In this study, membranes which were stacked in a chamber were utilized to purify biogas by passing biogas over them. These membranes were composed of polyethersulfone hollow fiber substrate coated with a “selective layer” made of cellulose nanocrystals (CNC‐0–2 wt) in polyvinyl alcohol (PVA) and l‐arginine as a CO2 carrier. Of the different CNC concentrations in PVA‐LA, CNC1/PVA‐LA (1.0 wt% CNC in PVA‐LA) displayed the lowest water contact angle of 17° (corresponding to higher moisture absorbing ability). With further increase in CNC concentration, even though CNC1.5/PVA‐LA showed the higher crystallinity (66%), and water contact angle increased (20°); reducing the chances of facilitated transport of CO2 through it. Biogas separation experiments were conducted at 90% RH and different feed pressures (0.8–1 bar) for various CNC concentrations. Increasing the CNC concentration led to a thicker selective layer, enhancing the CO2 permeability and selectivity up to CNC1/PVA‐LA. However, with the further addition of CNC, both permeability and selectivity decreased. At 90% RH and 1 bar feed pressure, the CNC1/PVA‐LA setup demonstrated a CO2 permeability of 20,522 Barrer and a selectivity of 33, making it suitable for low‐pressure biogas storage systems with lower energy requirements.

Mechanism and Performance Evaluation of a Strain Sensor Made from a Composite Hydrogel Containing Conductive Fibers of Thermoplastic Polyurethane and Polyvinyl Alcohol

Mechanism and Performance Evaluation of a Strain Sensor Made from a Composite Hydrogel Containing Conductive Fibers of Thermoplastic Polyurethane and Polyvinyl Alcohol

MoS2 nanosheet assisted poly vinyl alcohol cross-linked with carboxylated acryl-amido-2-methyl-1-propanesulfonic acid in medium temperature proton exchange membrane fuel cell application

ABSTRACT Initially, the carboxylated-acryl amido propane sulfonic acid (C-AMPSA) was synthesized through the thiol-ene reaction using 2-acrylamido-2-methylpropane sulfonic acid and 3-mercapto propane sulfonic acid monomers. The C-AMPSA was cross-linked with polyvinyl alcohol to create a non-perfluorinated membranes were of these acid group-containing monomers. Using a cross-linking technique, a poly vinyl alcohol cross-linked C-AMPSA (PVA-C-AMPSA) polymer was prepared. Following that, the MoS2 nanosheets (NSs) were synthesized through the one-pot hydrothermal method, and their phase purity, functionality, and morphology were evaluated by p-XRD, FT-IR, and FE-SEM analyses. These nanosheets were then incorporated into PVA-C-AMPSA polymer nanocomposite membranes at various concentrations (0%, 1%, 2%, 3%, and 5% by weight). In addition, the physicochemical properties of bare and MoS2 nanosheets incorporated PVA-C-AMPSA polymer nanocomposite membranes were assessed, including water uptake, swelling ratio, and ion-exchange capacity. Remarkably, the membrane with 5% of MoS2 NSs in PVA-C-AMPSA displayed an ion-exchange capacity of 1.13 mmol g−1 and a proton conduction of 1.8 × 10−3 S cm−1 at 110°C. The Arrhenius plot indicated that the proton transport was involved in both Grotthuss and vehicular mechanisms. In the fuel cell testing, the PVA-C-AMPSA polymer nanocomposite membrane containing MoS2 NSs demonstrated superior performance, achieving a peak power density (PD) exceeding 0.7 W cm−2 and an open-circuit voltage (OCV) surpassing 0.93 V at 110°C. In contrast, the pure PVA-C-AMPSA membrane exhibited a peak PD of over 0.4 W cm−2 and an OCV of around 0.6 V at the same temperature. Additionally, the 5% of MoS2 NSs incorporated PVA-C-AMPSA polymer nanocomposite membrane exhibited outstanding oxidative stability with 87.7% of degradation when exhibited to a Fenton reagent at 80°C for 8 h.

Copper selenide as a facile nanomaterial for triboelectric nanogenerator: Self-powered Braille code keyboard

The development of triboelectric nanogenerators (TENGs) for sustainable energy harvesting has garnered significant interest, especially in integrating advanced materials to enhance device performance and exploring applications. Herein, the present study investigates the use of copper selenide (Cu2Se) as a robust material for TENGs fabrication. Cu2Se nanorods are synthesized using a facile hydrothermal method and subsequently embedded in a polyvinyl alcohol (PVA) matrix to form a nanocomposite, which is then utilized as tribopositive film. The procured Cu2Se and nanocomposites with varying filler quantities (0.1, 0.2, 0.4, and 0.8 wt%) are analyzed using powder X-ray diffraction, scanning electron microscopy, dielectric measurements, Fourier transform infrared spectroscopy, and ultraviolet–visible spectroscopy to evaluate their structural, morphological, dielectric, and optical properties, and their impact on TENG performance. Interestingly, the device with 0.2 wt% Cu2Se generated peak-to-peak voltage and current of 394.35 V and 83.45 µA respectively, which is about 2.5- and 41-times higher output compared to pristine PVA-TENG. Integrating Cu2Se as filler enhances charge generation, transfer, and retention, due to increased surface roughness, and ability to facilitate better charge separation within the polymer matrix leading to more efficient energy conversion in TENGs. In practical demonstration, the optimized PVA@ Cu2Se-TENG is employed as a self-powered Braille keyboard to generate electrical signals from mechanical interactions, offering a promising solution for energy-efficient, user-friendly Braille technology. Thus, the current study highlights the synergistic effects of integrating Cu2Se with polymer, resulting in enhanced triboelectric performance for innovative energy harvesting applications and self-powered sensory devices.

Corrosion resistance and biocompatibility of magnesium alloy with bioactive glass-reinforced hydrogel composite coatings

Magnesium (Mg) alloy is a promising candidate for biodegradable implants; however, its rapid degradation can create an unstable physiological environment that hampers tissue regeneration. To address this challenge, a polyvinyl alcohol (PVA) hydrogel composite reinforced with bioactive glass (BG) particles was developed as a coating for Mg alloy pellets, which underwent laser surface texturing (LST) and salting-out processes. results demonstrate that these treatments significantly enhance both the adhesiveness and swelling of the hydrogel coating. Notably, electrochemical corrosion assessments reveal a marked improvement in corrosion resistance, with the Mg–B1-L-S specimen exhibiting the highest performance after salting-out treatment. Electrochemical corrosion assessments revealed a significant enhancement in corrosion resistance for Mg alloy with the hydrogel coating, with the Mg–B1-L-S specimen showing superior performance following salting-out treatment. Immersion tests in simulated body fluid (SBF) confirmed the protective effect of the coatings, indicating that the addition of BG particles and salting-out treatment reduced mass loss and maintained pH stability. Biocompatibility evaluations through in vitro viability tests and osteogenic differentiation assays indicate that the Mg–B1-L and Mg–B1-L-S specimens exhibit superior cell activity, surface adhesion, and osteogenic potential. These findings highlight the effectiveness of PVA-BG hydrogel composite coatings in enhancing the corrosion resistance and biocompatibility of Mg alloy implants, positioning this approach as a significant advancement in the development of biodegradable materials for biomedical applications.

Synthetic and Natural Polymers Enhancing Drug Delivery and Their Treatment: A Comprehensive Review

Polymers, both synthetic and natural, play a critical role in modern drug delivery systems by enhancing the efficacy, targeting, and release profiles of therapeutic agents. This comprehensive review delves into the various types of synthetic polymers such as poly (lactic-co-glycolic acid) (PLGA), polyethylene glycol (PEG), and polyvinyl alcohol (PVA), as well as natural polymers like chitosan, alginate, and gelatin. These polymers are explored for their potential to improve solubility, bioavailability, and controlled release of drugs. Moreover, their application in targeted drug delivery, particularly for cancer, cardiovascular, and inflammatory diseases, is highlighted. The review also compares the advantages and limitations of synthetic versus natural polymers, discussing their biodegradability, biocompatibility, and regulatory considerations. Advances in polymer-based drug delivery platforms such as nanoparticles, hydrogels, and micelles are also examined, offering insights into future directions in personalized medicine. The highlights of provide in the review article, initially basics of drug delivery, polymer, polymerization with role of polymer in polymerization. At intermediate, classification, sources of polymer with that some advanced approached in drug delivery and lastly, marketed, recent available products with future challenges and current status in the drug delivery. Keywords: Biodegradable polymer; natural; compatible; drug delivery; treatment; enhancing; polymers.

Properties and mechanism analysis of a novel construction dust suppressant based on polymer blending

To address the poor suppression efficacy and limited mechanical properties enhancement of traditional dust suppressants in relation to construction dust, this study adopted polymer blending to prepare binding agent SA-PVA-CMC (SPC) utilizing sodium alginate (SA), polyvinyl alcohol (PVA), and carboxymethyl cellulose (CMC). Using a response surface methodology, the optimal mass concentrations of SPC, dodecyl dimethyl betaine (BS-12), and carboxymethyl chitosan (CMCS) were determined to be 0.317 %, 0.197 %, and 0.626 %, respectively, and a novel dust suppressant (SPC/CMCS/BS-12) was developed. The performance testing revealed the outstanding capabilities of the dust suppressant in binding, wetting, water retention, and moisture absorption. Dust treated with SPC/CMCS/BS-12 attained a compressive strength of 313.93 kPa, experiencing only a 2.73 % wind erosion rate under strong wind conditions (12 m/s). Furthermore, the dust suppressant achieved an 86.67 % efficiency in removing respirable dust and up to 93.21 % for total dust. The hydrogen bonding between polymer molecular chains and the adsorption between SPC/CMCS/BS-12 and the surface of construction dust enhance the mechanical properties of the construction dust.

Development of zeolite 5A-incorporated polyvinyl alcohol membrane for desalination by pervaporation

Abstract With the rapid depletion of potable and useable water resources globally due to population growth and the effects of global warming, the desalination of seawater – the world’s largest source of water – to acceptable quality levels is critical to meeting future water needs. This study investigates the use of zeolite 5A-incorporated polyvinyl alcohol membranes to produce fresh water from seawater for industrial and domestic use and evaluates the application of the pervaporation process on the separation performance. Polyvinyl alcohol and polyvinyl alcohol/zeolite 5A mixed matrix membranes were prepared by solution-casting technique, and their morphological, structural, and mechanical properties were analyzed by field emission scanning electron microscopy, thermogravimetric analysis, Fourier transform infrared spectroscopy, and tensile strength tests. The swelling behavior and pervaporation performance of the membranes were investigated at different temperatures (30, 45, and 60 °C) using synthetic seawater containing 35 g L−1 NaCl, and membrane–solvent interactions were determined using data from sorption experiments. The membrane produced water flux and salt rejection values at 60 °C of 5.82 kg m−2 h−1 and >99.9 %, respectively.

High-Performance Dual-Redox-Mediator Supercapacitors Based on Buckypaper Electrodes and Hydrogel Polymer Electrolytes.

In recent years, the demand for solid, thin, and flexible energy storage devices has surged in modern consumer electronics, which require autonomy and long duration. In this context, hybrid supercapacitors have become strategic, and significant efforts are being made to develop cells with higher energy densities while preserving the power density of conventional supercapacitors. Motivated by these requirements, we report the development of a new high-performance dual-redox-mediator supercapacitor. In this study, cells were constructed using fully moldable buckypapers (BPs), composed of carbon nanotubes and cellulose nanofibers, as electrodes. We evaluated the compatibility of BPs with hydrogel polymer electrolytes, based on 1 mol L-1 H2SO4 and polyvinyl alcohol (PVA), supplemented with different redox species: methylene blue, indigo carmine, and hydroquinone. Solid cells were constructed containing two active redox species to maximize the specific capacity of each electrode. Considering the main results, the dual-redox-mediator supercapacitor exhibits high energy density of 32.0 Wh kg-1 (at 0.8 kW kg-1) and is capable of delivering 25.9 Wh kg-1 at high power demand (4.0 kW kg-1). Stability studies conducted over 10,000 galvanostatic cycles revealed that the PVA polymer matrix benefits the system by inhibiting the crossover of redox species within the cell.

The Development of a Flexible Humidity Sensor Using MWCNT/PVA Thin Films.

The exponential demand for real-time monitoring applications has altered the course of sensor development, from sensor electronics miniaturization, e.g., resorting to printing techniques, to low-cost, flexible and functional wearable materials. Humidity sensing has been used in the prevention and diagnosis of medical conditions, as well as in the assessment of physical comfort. This paper presents a resistive flexible humidity sensor composed of silver interdigitated electrodes (IDTs) screen printed onto polyimide film and an active layer of multiwall carbon nanotubes (MWCNT) dispersed in a water-soluble polymer, polyvinyl alcohol (PVA). Different MWCNT/PVA sensor sizes and MWCNT percentages are tested to study their effect on the initial electrical resistance (Ri) values and sensor response at different humidity percentages. The results show that the Ri values decrease with the increase in % MWCNT. The sensor size did not influence the sensor response, while the % MWCNT affected the sensor behavior upon relative humidity (RH) increments. The 1% MWCNT/PVA sensor showed the best response, reaching a relative electrical resistance, ΔR/R0, of 509% at 99% RH. Comparable with other reported sensors, the produced MWCNT/PVA flexible sensor is simpler, greener and shows a good sensitivity to humidity, being easily incorporated in wearable monitoring applications, from sports to medical fields.