Polyvinyl Alcohol Research Articles

Highly conductive and sensitive alginate hydrogel strain sensors fabricated using near-field electrohydrodynamic direct-writing process

Hydrogel flexible sensors have attracted considerable attention because of their wearability, biocompatibility, and precision signal transmission capability. However, the hydrogel strain sensors fabricated by conventional printing or hand-injection methods have difficulty balancing their mechanical strength and sensing characteristics, limiting the application of hydrogel strain sensors. Herein, polyvinyl alcohol and polyacrylamide were loosely crosslinked with sodium alginate through chemical cross-linking. Subsequently, MXene nanosheets were introduced for doping, the crosslinked hydrogel conductive network was constructed, and the hydrogel strain sensors were fabricated using the electrohydrodynamic (EHD) printing method. The ions in the EHD-printed hydrogel undergo directional movement under an externally enhanced electric field, causing the formation of more uniform and dense porous conductive networks inside the hydrogel, and high electrical conductivity (0.49 S m−1) is obtained. These hydrogel strain sensors have excellent mechanical properties (tensile strength: 0.17 MPa at 787 % strain), high sensitivity (gauge factor: 1.54 at 0–100 % strain), and low detection limits (1 % strain). Furthermore, demonstrations of real-time Morse code tapping information transmission, handwriting recognition during writing, and human physiological behavior monitoring demonstrations using the fabricated sensors indicate that the EHD-printed hydrogel strain sensor method has significant potential for wearable devices and human-computer interaction applications.

Adhesive lipophilic gels delivering rapamycin prevent oral leukoplakia from malignant transformation

Oral leukoplakia (OLK) is the most emblematic oral potentially malignant disorder that may precede the diagnosis of oral squamous cell carcinoma (OSCC) and has an overall malignant transformation rate of 9.8 %. Early intervention is crucial to reduce the malignant transformation rate from OLK to OSCC but the lack of effective local pharmaceutical preparations poses a challenge to clinical management. Rapamycin is speculated to prevent OLK from carcinogenesis and its inherent lipophilicity facilitates its penetration into stratum corneum. Nevertheless, hydrophilic hydrogels frequently encounter challenges when attempting to deliver lipophilic drugs. Furthermore, the oral cavity presents a complex environment defined by oral motor functions, saliva secretion cycles, dynamic fluctuations, and protective barriers comprising mucus and lipid layers. Consequently, addressing issues of muco-penetration and muco-adhesion is imperative for developing an effective drug delivery system aiming at delivering rapamycin to target oral potentially malignant disorders.Here, a dual-function hydrogel drug delivery system integrating adhesion and lipophilicity was successfully developed based on polyvinyl alcohol (PVA) and dioleoyl phosphatidylglycerol (DOPG) via dynamic boronic ester bonds. Rheological experiments based on orthogonal design revealed that PVA-DOPG hydrogels exhibited ideal adhesive strength (around 6 kPa) and could adhere to various surfaces in both dry and wet conditions. PVA-DOPG hydrogels also significantly promoted lipophilic molecules’ penetration into stratum corneum (integrated fluorescence density of 6.95 ± 0.52 × 106 and mean fluorescence depth of 0.96 ± 0.07 mm) of ex-vivo porcine buccal mucosa (p < 0.001). Furthermore, PVA-DOPG hydrogels incorporating rapamycin inhibited malignant transformation of OLK mouse model induced by 4-Nitroquinoline N-oxide (4-NQO), distinct improvements in survival (the neoplasm incidence density at the 40th day is 0.0091) (p < 0.05), decrease in neoplasm incidence density of 36.36 % and inhibition rate in neoplasm volume of 75.04 ± 33.67 % have been demonstrated, suggesting the hydrogels were valuable candidates for potential applications in the management of OLK.

Separator‐Supported Electrode Configuration for Ultra‐High Energy Density Lithium Secondary Battery

AbstractSignificant efforts are being made to develop high‐performance battery materials, particularly active materials. However, material‐dependent strategies for increasing energy density face challenges such as raw material costs and supply limitations, reducing their versatility to some extent. In this regard, the development of efficient battery designs can be a universal approach to increasing the energy density of lithium‐ion batteries with relatively low dependence on material properties. Herein, a novel configuration of an electrode‐separator assembly is presented, where the electrode layer is directly coated on the separator, to realize lightweight lithium‐ion batteries by removing heavy current collectors. Even on the hydrophobic separator, a poly(vinyl alcohol) binder enables uniform and scalable coating of aqueous electrode slurries through molecular interactions with the separator surface. Moreover, carbon nanotubes are utilized to reinforce the electronic conduction of the electrode, providing consistent electronic pathways regardless of SEI formation. Furthermore, owing to the superior permeability of liquid electrolytes through this electrode‐separator assembly, a multilayered electrode‐separator assembly can be suggested to further increase energy density when combined with a lithium metal anode. This lithium metal battery can achieve an areal capacity of ≈30 mAh cm−2 and an enhanced energy density of over 20% compared to conventional battery configurations.

Effect of Morphology and Concentration of CeO2 Nanoceria on the Thermal Stability of Polyvinyl Alcohol Films

Objective: To determine the thermal stability of polyvinyl alcohol films under different concentrations of CeO2 nanoceria. Method: Cerium Oxide doped polyvinyl alcohol (PVA) nano-composites were synthesized by the traditional solution casting method for various concentrations of nano CeO2 by solution combustion method. The thermal properties of prepared PVA-2.5 wt% CeO2, PVA-7.5 wt% CeO2 , PVA-12.5 wt% CeO2, and PVA-25 wt% CeO2 composite films were elucidated by using techniques such as Differential Scanning Calorimetry, Thermogravimetry analysis and Differential Thermal analysis. Findings: The glass transition temperature of the pure PVA is found to be 114°C, whereas it varies between 110°C-120°C for composite films. The melting temperature of the composite films is the same as that of pure PVA except in the case of 7.5wt% CeO2 and 25wt% CeO2 composites. The reduced melting point of these composites elicits a decrease in crystallinity. A 12.5 wt % and 25 wt% CeO2-PVA nano-composite films exhibit an increase in the final degradation temperature, a high specific heat capacity, low mass loss, and a larger residual weight, indicating their potential applicability in thermal coating and thermal sensing applications. Polyvinyl alcohol (PVA) films are being used routinely as a dielectric layer for electrical applications due to the good physiochemical and dialectic properties of the material. An incorporation of CeO2 nanoceria improves not only the thermal but also the mechanical properties of PVA and extends its application for electrical and optical operation. Here in the present study, different concentrations of CeO2 were incorporated with the PVA and analysed for the thermal properties. The study showed that 12.5 wt % and 25 wt% CeO2-PVA nano-composite enhanced PVA film thermal stability. Keywords: PVA-CeO2 Nanocomposites; Differential Scanning Calorimetry; Thermogravimetry Analysis and Differential Thermal Analysis; Physical properties and thermal properties

Biocompatible and hydrophilic copper-complexed polyvinyl alcohol coating for antifogging surfaces

Visibility is decreased when fog accumulates on the clear surface of optical devices. It is quite desirable to design the surface with antifogging properties. The current study used a dip coating process to prepare copper-incorporated polyvinyl alcohol (PVA) hydrophilic coating on the hydroxylated glass substrate. The formation of the PVA-Cu complex by the hydroxyl group was determined by FTIR and XPS methods. The surface morphology, adhesion test, wettability behavior, and cytotoxicity were investigated by SEM, cross-cut tape, contact angle measurement, and MTT experiment. By varying the CuCl2 concentration (0.0125–0.0625 M), the durability and adhesion of the coating were improved, as evidenced by its minimal mass loss and water uptake. The optimum coating condition showed a thickness of about 24.0 ± 0.7 μm and a good optical transmittance of over 90 %. Below 0.0375 M, the coating stability and water resistance could not be achieved due to the weak complexation of Cu with the PVA coating. In contrast, the PVA-Cu3 coating (0.0375 M, Cu2+ ions) was identified as an optimized condition for improved antifogging performance due to the effective complexation of Cu with the PVA matrix while maintaining the hydrophilicity and wettability behavior. Furthermore, no cytotoxicity was observed by L929 cell lines in response to the prepared coating. The current study results revealed that the adhesive, hydrophilic PVA-Cux coating with a contact angle of less than 62° might demonstrate strong antifogging properties and find its usage for endoscopic applications.

An Experimental Investigation on Synthesis, Characterization, and Photothermal Conversion Efficiency of Stable Aqueous Nanofluids Containing Multiwalled Carbon Nanotubes for Direct Absorption Solar Collectors

The nanofluids are the potential substitute in solar collectors as working fluids for better photothermal conversion efficiency. The present investigation focuses on the development of aqueous‐based nanofluids comprising multiwalled carbon nanotubes (MWCNTs) with and without surfactants to enhance the capacity of photothermal conversion in direct absorption solar collectors. To improve the stability of the nanofluid, the gum Arabic (GA) and polyvinyl alcohol (PVA) are used as the surfactants. The stable nanofluid was characterized using UV‐visible spectroscopy, zeta potential, fourier‐transform infrared spectroscopy, field emission scanning electron microscopy, and energy dispersive X‐ray spectroscopy (EDS) analysis. The results indicated that the thermal conductivity was enhanced by 94.57% and 91.19% for the MWCNT/GA/deionized (DI) water and MWCNTs/PVA/DI water based nanofluids in presence of surfactants at 90 °C and 0.02 wt%. The presence of surfactant in MWCNTs/DI water nanofluids exhibit excellent stability and enhanced MWCNTs dispersion. In the photothermal response analysis, the highest temperature of 62.8 °C, which is 16 °C higher than the base fluid, is obtained from 0.02wt% MWCNT/GA nanofluid. The highest efficiency of 27.94% is recorded when 0.02wt% MWCNT/GA nanofluid is used, which shows 71.24% enhancement as compared to the DI water after exposure of 30 minutes under solar irradiation. The use of MWCNTs/GA nanofluid as light‐absorbing working fluids in solar collectors is encouraged in the present investigation.

Polymer-Modified Fertilizers for Mitigating Strawberry Root Burn

Polymer-modified fertilizers (PMFs) with prolonged nutrient release present a promising solution to address the challenges associated with conventional fertilization practices, particularly for sensitive crops such as strawberries. This study investigates the effectiveness of biodegradable PMFs in maintaining nutrient availability at optimal levels while minimizing root burn and nutrient losses. In a factorial field experiment, we obtaineda total of 3780 sets of parallel measured time series for soil EC, moisture, and temperature as well as two sets of harvest data to evaluate the impact of varying concentrations of polyvinyl alcohol (PVA) on the nutrient release rates from complex NPK fertilizer and monoammonium phosphate. Results indicate that polymer modifications significantly slow down nutrient release, leading to optimal salt levels and maximizing yield while remaining low enough to prevent the risk of root burn (EC of soil solution below 1 mS/cm). Consequently, the application of PMFs enhances strawberry yield surplus (on average 2.8 times in the second harvest) by ensuring a steady supply of nutrients throughout the growing season without inducing stress, which reduces the yield by nearly half. This research provides valuable insights into the development of more effective fertilization strategies for strawberry cultivation and other sensitive crops using PMFs.

SCC/PVA Hydrogel with Self‐Healing Capability for Electrochromic Device

AbstractCracking caused by aging or repeated bending can severely affect the lifetime of electrochromic devices. In this work, a self‐healing electrochromic hydrogel was developed with poly (vinyl alcohol) (PVA)‐sodium carboxymethyl chitosan (SCC) semi‐inter transfer network as the matrix, viologen bromide (HPV2+2Br−) as the electrochromic substance, and borax as the cross‐linking agent. The self‐healing properties of hydrogel stem from the dynamic and reversible borate bonds between borax and PVA molecular chains. As the voltage changes, the color of the device transitions from colorless to light purple and then to dark purple. The optical contrast at 600 nm reaches approximately 51 %. At room temperature, the disconnected hydrogel can fully restore its original state after 30 minutes of contact, effectively addressing issues related to cracks and damage in flexible electrochromic devices. This research holds significant implications for enhancing the reliability and stability of flexible electrochromic devices.

High-Performance Supercapacitive Pressure Sensors via Height-Grading Micro-Domes of Ionic Conductive Elastomer.

Soft capacitive sensors present numerous appealing characteristics, including simple structure, low power consumption, and fast response. However, they often suffer from low sensitivity and a limited linear sensing range. Herein, a concept is presented to enhance the sensitivity and linearity of supercapacitive pressure sensors by functionally grading the heights of macrodomes constructed from a highly elastic and ionic conductive elastomer made of poly(vinyl alcohol) and phosphoric acid (PVA/H3PO4). The resultant supercapacitive sensors exhibit a high sensitivity (423.42 kPa-1), wide linear sensing range (0-400 kPa), ultralow limit of detection (0.48 Pa), and high durability (stable signal outputs up to 5000 cycles of loading/unloading). Additionally, the sensors can maintain consistent sensing performance within a temperature range of 25-40 °C. The potential of the sensor in health monitoring is demonstrated through ultrahigh-resolution weight measurement, pulse detection, and respiration monitoring.

Direct Ink Writing of Cephalopod Skin‐Like Core‐Shell Fibers From Cholesteric Liquid Crystal Elastomers and Dyed Solutions

AbstractDirect ink writing (DIW) of core‐shell structures allows for patterning hollow or composite structures for shape morphing and color displays. Cholesteric liquid crystal elastomers (CLCEs) with liquid crystal mesogens assembled in a helix superstructure are attractive for generating tunable iridescent structural colors. Here, by fine‐tuning the rheology of the core and shell materials, respectively, this study creates droplets or a continuous filament in the core from the precursors of polydimethylsiloxane (PDMS) or poly(vinyl alcohol), whereas CLCE forms the outer shell. By introducing a dye in the droplets, the skin structures of cephalopods, consisting of chromatophores and iridocytes, are mimicked for enhanced color saturation, lightness, and camouflage. After removal of the core material, a CLCE hollow fiber is obtained, which can switch colors upon mechanical stretching and pneumatic actuation, much like papilla along with iridocytes. Further, liquid crystal mesogens assembled in the bulk of the fiber are in polydomain. Thus, the skin appears opalescent at room temperature, much like how leucophores enhance reflectins. Upon heating above the nematic to isotropic transition temperature, the skin becomes transparent. Lastly, a cephalopod model is constructed, where different parts of the model can change colors independently based on different mechanisms.

A Highly Sensitive, Conductive, and Flexible Hydrogel Sponge as a Discriminable Multimodal Sensor for Deep‐Learning‐Assisted Gesture Language Recognition

AbstractFlexible multimodal sensors have gained increasing popularity for applications in healthcare and extreme environment operations owing to their all‐around environmental perception and data acquisition capabilities. However, fabricating a magnetism‐mechanics‐humidity multimodal sensor that possesses high sensitivity without signal overlapping while in a facile methodology remains a great challenge. Herein, a highly sensitive, conductive, and flexible hydrogel sponge sensor with discriminable magnetism, mechanics, and humidity sensing capability is proposed, which shows stable pore size (19.30 µm) and satisfactory mechanical properties based on the synergistic hydrogen bonding among sodium alginate, poly(vinyl alcohol) and glycerol. The proposed sensors can not only display favorable humidity sensing ability with rapid response/recovery time (2.5/4 s) but also possess enhanced sensitivities (a gauge factor of 0.46 T−1 for magnetic field, −1.16 kPa−1 for pressure), superior stability and durability (over 8000 cycles). Benefiting from the separated capacitive and resistive response signals, the sensors can precisely distinguish the magnetic, mechanical, and humidity stimuli without cross‐talk. Further, the sensor arrays assisted by the deep learning algorithm are developed to realize gesture language recognition with a high accuracy of 99.17%. It can be believed that this high‐performance sensor will have good prospects in future soft electronics and human‐machine interaction systems.

Positional Isomerism Toward Tunable Organic Afterglow and Reversible Photoactivation Behavior for Anti‐Counterfeiting and Encryption

AbstractAchieving amorphous polymers with ultralong room‐temperature phosphorescence (RTP), tunable organic afterglow, and reversible photoactivation behavior is highly desirable for practical applications but challenging. Herein, simple positional isomers with three carboxyl groups located in the ortho, meta, and para positions of the triphenylamine skeleton are designed and synthesized. By physically blending with the poly(vinyl alcohol) matrix, these isomers show ultralong RTP properties, among which the meta‐isomer has the longest RTP lifetime (620.1 ms). Theoretical calculations reveal that the more efficient intersystem crossing, the slower radiative decay rate of the lowest triplet excitons, and stronger intermolecular hydrogen‐bonding interactions should be responsible for the superior RTP property of meta‐isomer. Furthermore, the tunable organic afterglow is readily realized via a triplet‐to‐singlet energy transfer process. More impressively, the meta and para isomers exhibit reversible photoactivated ultralong RTP properties after embedding into the rigid poly(methyl methacrylate) matrix. Finally, amorphous and flexible polymer films prepared from these positional isomers show potential applications in advanced anti‐counterfeiting and multilevel encryption through subtly combining ultralong RTP lifetime, tunable organic afterglow, and reversible photoactivation behavior.

Gel polymer electrolytes containing SiO2 spheres with tuned sizes to increase rechargeability of quasi-solid-state Zn-air batteries

Rechargeable zinc–air batteries (RZABs) with high energy densities and low costs have attracted tremendous interest for meeting the ever-growing demand for flexible and portable applications. In these batteries, the quasi-solid/solid-state electrolyte plays a critical role in the battery performance, such as the cycling performance rate and power output. In this study, porous poly (vinyl alcohol) (PVA) and poly (acrylic acid) (PAA) composite gel polymer electrolytes (GPEs) were modified by incorporating SiO2 as a water retainer. For this reason, SiO2 spheres of different sizes were synthesized by varying the temperature (5, 20, 60, and 80 °C) and reaction time (2, 6, 18, and 24 h). According to the SEM micrographs, the average size ranged from 107 to 710 nm depending on the conditions. The porous PVA/PAA–SiO2 GPEs obtained by selecting three SiO2 sizes (107, 425, and 630 nm) exhibited higher water retention capability than the unmodified GPE. Among them, the GPE with SiO2–630 nm displayed the highest battery performance (1.46 V, 85 mWcm−2 @ 0.8 V). This was achieved using CoMn2O4 spinel as a bifunctional electrocatalyst, with a catalyst loading of 2 mg cm−2. The quasi-solid-state RZAB displayed twice the rechargeability of the RZAB assembled with Pt/C+IrO2/C (120 vs. 62 cycles). According to post-mortem tests, this can be related to the improved water retention, the decrease in the size of the formed Zn dendrites, and the stability of the bifunctional material. Thus, fine-tuning of the electrocatalyst/electrolyte interface strongly affects the rechargeability.

A hybrid 3D-printed and electrospun bilayer pharmaceutical membrane based on polycaprolactone/chitosan/polyvinyl alcohol for wound healing applications

Skin injuries resulting from physical trauma pose significant health risks, necessitating advanced wound care solutions. This investigation introduces an innovative bilayer wound dressing composed of 3D-printed propolis-coated polycaprolactone (PCL/PP) and an electrospun composite of polyvinyl alcohol, chitosan, polycaprolactone, and diltiazem (PVA/CTS/PCL/DTZ). SEM analysis revealed a bilayer structure with 89.23 ± 51.47 % porosity and uniformly distributed nanofibers. The scaffold tensile strength, with pore sizes of 100, 300, and 500 μm, was comparable to native skin. However, smaller pore sizes reduced water vapor transmission from 4211.59 ± 168.53 to 2358.49 ± 203.63 g/m2. The incorporation of DTZ lowered the contact angle to 35.23 ± 3.65°, while the addition of PCL reduced the degradation rate and modulated the release of DTZ by approximately 50 %. Moreover, lower pH increased the degradation rate and decreased swelling. The inclusion of propolis enhanced antibacterial activity, and 10 % DTZ promoted the viability, proliferation, and migration of fibroblasts and adipose-derived stem cells. However, increasing DTZ concentration to 12 % reduced cell viability. In vivo tests on rats demonstrated effective wound healing and anti-inflammatory properties of the bilayer samples. Regarding the aforementioned results, the PCL/PP-PVA/CTS/PCL/DTZ (10 % w/w) bilayer wound dressing is a promising candidate for wound healing applications.

Enhancing concrete beam performance with PVA fibers, coal ash, and graphene fabric: a comprehensive structural analysis

ABSTRACT This study evaluates the structural performance of Polyvinyl Alcohol Cementitious Composites (PVCC)-layered reinforced concrete beams with coal ash under static loading. Experimental investigations included first crack load, ultimate load, load-deflection behavior, ductility, stiffness, and energy absorption. Results highlight the influence of Polyvinyl Alcohol-(PVA) fiber dosage on structural behavior. The control specimen exhibited an initial crack load of 80kN, with subsequent specimens showing varied crack initiation loads influenced by PVA fiber content. Optimal performance was observed at 1.2% PVA fiber dosage, with higher dosages leading to earlier crack initiation. Ultimate load carrying capacity increased with PVA fiber addition, reaching a peak at 1.2% dosage before slight decreases occurred with higher dosages. Load-deflection behavior demonstrated the superior performance of PVCC layered beams, particularly specimen BP3, attributed to optimal fiber content. Ductility, stiffness, and energy absorption increased with PVA fiber reinforcement, with 1.2% dosage yielding optimal results. Excessive fiber content led to diminishing returns. Energy index analysis revealed superior energy dissipation in specimens with higher PVA fiber content, emphasizing the effectiveness of fiber reinforcement in enhancing structural performance. Overall, the study underscores the importance of optimizing PVA fiber dosage to maximize structural resilience and load-bearing capacity in PVCC-layered concrete beams with coal ash.

Experimental Study on the Protective Effect of High Alcoholysis Polyvinyl Alcohol (PVA) Solution Spraying on Loess Fill Slopes

Loess has high water sensitivity and exhibits poor characteristics such as weak cementation and high porosity. Under heavy rainfall, loess fill slopes are prone to erosion and landslides, posing serious threats to public safety and property. In light of these serious threats, this study employed the method of spraying polyvinyl alcohol (PVA) solution to improve loess fill slopes and systematically examine its protective effects. Through field investigations and combined laboratory and outdoor tests, this study comprehensively evaluated the mechanical properties, anti-aging and anti-erosion performance of loess after PVA solution spraying. Scanning electron microscopy was used to reveal the mechanism of PVA action at the microscopic level. The results showed that after treatment with PVA solutions of varying concentrations, the mechanical properties of loess samples were significantly enhanced, while also exhibiting excellent anti-aging and water resistance performance. Additionally, PVA-treated loess fill slopes exhibited excellent rain erosion resistance. A microscopic structural analysis showed that PVA fills the internal pores of loess, strengthens inter-particle bonding, and uses its hydrophobic groups’ water-repellent action to effectively enhance slope stability and erosion resistance. In conclusion, PVA treatment not only significantly enhances the protective effects of loess fill slopes but also holds important value in improving soil sustainability and environmental protection.

Development of Polyvinyl Alcohol Hydrogels for Controlled Glucose Release in Biomedical Applications.

Polyvinyl alcohol (PVA) hydrogels have a wide range of applications in the pharmaceutical and biomedicine fields due to their exceptional biophysical properties. The study focuses on preparing and characterizing capsule-shaped PVA hydrogels to enhance their biocompatibility and porosity for controlled glucose release and cell proliferation. The hydrogels were prepared using different concentrations (Cs) and molecular weights (MWs) of PVA, with two different lengths, A (10 mm) and B (20 mm), to control glucose release over 60 min. The preparation process involved PVA gel preparation and PVA hydrogel formation. A total of 500 µL of glucose was injected into all dehydrated hydrogels in groups A and B. Glucose release was studied by immersing the hydrogels in saline at 37 °C with stirring at 500 rpm. The SUP-B15 cell line was grown in six A1 hydrogels for biocompatibility testing. The results indicate that all hydrogels remained stable at 37 °C without degrading. Those with a higher C and MW exhibited a denser and less porous structure, lower glucose storage capacity, and higher elongation at break. Significant differences in glucose release, diffusion speed, and flux were observed, which were more evident in A1 > A4, B1 > B4, and B1 > A1 over 60 min. A1 and B1 had higher values because their higher porosity distribution allowed glucose to diffuse more easily. B1, being larger, has more glucose due to its increased length. The cell growth response and viability at 48 h in contact with the hydrogels was similar to that of the control (4.5 × 105 cells/mL, 98.5% vs. 4.8 × 105 cells/mL, 99.7% viability), thus demonstrating biocompatibility. The hydrogels effectively released glucose over 60 min, with variations based on porosity, C, MW, and length, and demonstrated good biocompatibility with the cell line.

Aminated ZIF‐8 to facilitate CO2 sieving through polyvinyl alcohol/ionic liquid membranes

AbstractCO2 separation technology at low pressure is most desirable in carbon capture projects to mitigate global warming. Facilitated transport membranes offer selective and effective CO2 permeation using a wide range of carbon carriers at low pressure. Porous fillers were recently included as they can carry abundant fixed carriers besides offering open channels for CO2 permeation. This study investigates the effects of amine‐modified zeolitic imidazolate framework‐8 (ZIF‐8) with well‐defined micropores and gas sieving ability in polyvinyl alcohol (PVA) membranes containing an ionic liquid that worked as mobile carriers. The effects of amine‐modified ZIF‐8 and silica nanoparticles on membrane properties and separation performance were also compared. Fourier transform infrared spectra confirmed the incorporation of ZIF‐8, secondary amine, IL anions, and silica nanoparticles in PVA membranes. Energy dispersive analysis showed the good dispersion of inorganic fillers. The amine‐modified silica nanoparticles resulted in higher thermal stability compared to the amine‐modified ZIF‐8 in PVA membranes containing [bmin][Ac] ionic liquid, as shown in the thermogravimetric analysis. However, the CO2 separation performance of PVA membranes containing [bmim][Ac] ionic liquid was improved more significantly by the amine‐modified ZIF‐8 with microporous structure. A CO2/N2 ideal selectivity of 85.65 and CO2 permeance up to 4,502.91 GPU were attained. Unlike the CO2/N2 ideal selectivity, the CO2 permeance was not significantly affected either using [bmin][Ac] or [bmin][BF4]. The humid gas greatly enhanced the CO2 permeance without much changes in the CO2/N2 ideal selectivity due to the promotion of facilitated transport. © 2024 Society of Chemical Industry and John Wiley &amp; Sons, Ltd.

Development and evaluation of biocompatible coated microneedle array for controlled insulin delivery: Fabrication, characterization, in vitro, and in vivo investigations

Traditional insulin administration for people with diabetes often involves painful injections, leading to discomfort and challenges with patient compliance. A promising alternative to these conventional methods is transdermal insulin delivery using microneedle arrays, which offer a more comfortable way to deliver insulin through the skin. This study introduces an innovative approach using 3D-printed microneedle arrays coated with insulin via a dip-coating process. These microneedles present a compelling alternative to traditional injections, particularly due to their ability to gently pierce the stratum corneum, the outermost layer of skin, while minimizing discomfort. The microneedle arrays were fabricated using biocompatible resin polymers through 3D printing, creating solid conical needles with a length of 1200 µm, a base diameter of 200 µm, a tip diameter of 80 µm, and a needle spacing of 1.2 mm. The insulin coating was achieved by dip-coating the microneedles in a solution of insulin and polyvinyl alcohol (PVA), with careful optimization of the solution concentration, immersion time, and withdrawal speed to ensure a uniform and controlled coating thickness. Mechanical stability and skin penetration capabilities of the microneedles were assessed using skin models such as parafilm and porcine skin. The tests confirmed that the coated microneedles are robust enough to consistently penetrate the skin. In vivo studies with diabetic rats were conducted to evaluate skin irritation, penetration, and drug delivery efficiency. The insulin-coated microneedle arrays successfully penetrated the skin and delivered the drug with approximately 90 % efficiency. The study also showed that the microneedles provided consistent drug delivery, and the skin recovered without any signs of injury. Additionally, the hypoglycemic effect of the insulin-coated microneedles was comparable to that of traditional subcutaneous insulin injections. These findings underscore the potential of microneedle arrays as a painless and effective method for insulin delivery, maintaining stable glucose levels over an extended period. The demonstrated safety and efficacy of the coated microneedles open the door for clinical trials and potential use in diabetic patients, offering a promising advancement in diabetes management.

Improvement of the physical properties of poly vinyl alcohol nanofibers by adding carbon nanotubes

في هذه الدراسة تم تحضير عينات من ألياف نانوية من كحول البولي فينيل وأنابيب الكربون النانوية بطريقة الغزل الكهربائي. تم استخدام نسب مختلفة من الانابيب النانوية الكربونية ، وهي 2 و4 و6% نسبة وزنية . تمت دراسة الخصائص الضوئية والكهربائية والحرارية. تم استخدام المجهر الالكتروني الماسح لدراسة مورفولوجية الالياف النانوية . تم استخدام التحليل الطيفي لفوريير لدراسة اواصر العينات المحضرة .تم استخدام المسعر الحراري التفاضلي لدراسة الخواص الحرارية المتمثلة بدرجة الانتقال الزجاجي ونقطة الأنصهار. أظهرت النتائج أن إضافة انابيب الكربون النانوية بنسب صغيرة 6% بالوزن يؤدي إلى تحسن في الخواص الحرارية حيث تزداد درجة الانتقال الزجاجي من 85.17 درجة مئوية إلى 107 درجة مئوية مع. نسبة تقوية 6% بالوزن . ترتفع الموصلية الكهربائية بإضافة 6% بالوزن من الأنابيب النانوية الكربونية من ( 14.28 الى 20 اوم -1 سم -1 تشير نتائج طيف الأشعة فوق البنفسجية إلى إمكانية التحكم في فجوة نطاق الطاقة بإضافة الأنابيب النانوية الكربونية وتقليل قيمتها من 3.25 الكترون .فولت الى 0.75 الكترون .فولت بإضافة 6% نسبة وزنية من المادة النانوية . كما ان خواص الامتصاصية ومعامل الامتصاص تزداد بإضافة انابيب الكاربون النانوية ، حيث اثبتت النتائج ان افضل نتيجة في تحسين الخواص كانت بالضافة 6% من انابيب الكاربون النانوية.