A transdermal diltiazem hydrochloride delivery device using multi-walled carbon nanotube/poly(vinyl alcohol) composites

Membranes with high strength and elasticity are of great demand in patch therapy. Similar membranes have been developed by combining carboxy-functionalized multiwalled carbon nanotube (c-MWCNT) with different poly(vinyl alcohol) (PVA) as potential diltiazem delivery device through aqueous mixing. High molecular weight PVA (PVA_H) produced stronger interaction with c-MWCNT than low molecular weight PVA (PVA_L) preferably at low concentration. Positive changes in favor of PVA_H in infrared and solid state ¹³C nuclear magnetic resonance spectroscopy, wide angle X-ray scattering, thermal stability, morphology and dry and wet mechanical properties clearly demonstrate that. Fibrillar c-MWCNT array at 1 wt.% in PVA_H (PVA_H/1) has drastically improved PVA crystalline cell dimension, tensile strength (201%) and elongation (196%) than neat PVA_H whereas the similar improvement is much less (100% and 185%) in PVA_L (PVA_L/1) due to globular morphology. Instead, c-MWCNT performed better at 0.5 wt.% in PVA_L (PVA_L/0.5). The kinetic data reflects better encapsulation and slower release by PVA_H (5.87%) than PVA_L (10.17%) due to greater interfacial interaction.     

Polyvinyl alcohol-based fiber membranes with high strength and ultraviolet shielding properties for enhancing the shelf life of grapes

Currently, the rising environmental concerns caused by nonbiodegradable food packaging materials have promoted the research and development of biodegradable alternatives. Polyvinyl alcohol (PVA) was selected as the substrate, and zinc oxide nanoparticles (ZnONPs) and titanium dioxide nanoparticles (TiO₂NPs) were blended and modified with PVA, respectively. Based on the electrostatic spinning technology to prepare fiber membranes with high strength and UV blocking properties for grapes preservation. The study indicated that the tensile strength of PVA fiber membranes increased by 243% and 209% when ZnONPs and TiO₂NPs were added at 1%, respectively. Under UV radiation, the PVA/ZnO composite membranes exhibited superior UV absorption than the PVA/TiO₂ composite membranes. After conducting TG tests, it was found that the addition of ZnONPs decreased the thermal stability of the fiber membranes, while TiO₂NPs could improve the thermal stability. Both composite membranes could extend grapes' shelf life, but the PVA/ZnO composite membranes were more effective at maintaining freshness than the PVA/TiO₂ composite membranes.     

Properties of polyamide 612/poly(vinyl alcohol) blends and their impact on free volume and oxygen barrier properties

Oxygen transmission rates and free volume properties (i.e. average volumes of free-volume-cavities (V_f), mean number of the free volume cavities per unit volume (I₃) and fractional free volume (F_v)) values of bio-based polyamide 612 (PA612)/poly(vinyl alcohol) (PVA) (i.e. PA612_xPVA⁰³_y, PA612_xPVA⁰⁵_y, PA612_xPVA⁰⁸_y and PA612_xPVA¹⁴_y) blend films were reduced to a minimum value, when their PVA content reached corresponding optimal values of 25, 20, 15 and 10 wt%, respectively. The minimum oxygen transmission rate, V_f, I₃ and F_v value obtained for the best PA612₉₀PVA¹⁴₁₀, PA612₈₅PVA⁰⁸₁₅, PA612₈₀PVA⁰⁵₂₀ and PA612₇₅PVA⁰³₂₅ bio-based blown films reduced considerably with decreasing PVA degrees of polymerization. As evidenced by the results of dynamical mechanical analysis, differential scanning calorimetry, wide angle X-ray diffraction and Fourier transform infrared spectroscopic experiments, PA612 and PVA are miscible to some extent at the molecular level when their PVA contents are ≤ the corresponding optimal values. The significantly improved oxygen barrier and free volume properties for the PA612_xPVA^z_y blend films with optimized compositions is at least in part to the enhanced intermolecular interactions between PA612 carbonyl groups and PVA hydroxyl groups.     

Preparation of PFSA‐PVA/PSf hollow fiber membrane for IPA/H2O pervaporation process

Using Na⁺ form of perfluorosulfonic acid (PFSA) and poly(vinyl alcohol) (PVA) as coating materials, polysulfone (PSf) hollow fiber ultrafiltration membrane as a substrate membrane, PFSA‐PVA/PSf hollow fiber composite membrane was fabricated by dip‐coating method. The membranes were post‐treated by two methods of heat treatment and by both heat treatment and chemical crosslinking. Maleic anhydride (MAC) aqueous solution was used as chemical crosslinking agent using 0.5 wt % H₂SO₄ as a catalyst. PFSA‐PVA/PSf hollow fiber composite membranes were used for the pervaporation (PV) separation of isopropanol (IPA)/H₂O mixture. Based on the experimental results, PFSA‐PVA/PSf hollow fiber composite membrane is suitable for the PV dehydration of IPA/H₂O solution. With the increment of heat treatment temperature, the separation factor increased and the total permeation flux decreased. The addition of PVA in PFSA‐PVA coating solution was favorable for the improvement of the separation factor of the composite membranes post‐treated by heat treatment. Compared with the membranes by heat treatment, the separation factors of the composite membranes post‐treated by both heat treatment and chemical crosslinking were evidently improved and reached to be about 520 for 95/5 IPA/water. The membranes post‐treated by heat had some cracks which disappeared after chemical crosslinking for a proper time. Effects of feed temperature on PV performance had some differences for the membranes with different composition of coating layer. The composite membranes with the higher mass fraction of PVA in PFSA‐PVA coating solution were more sensitive to temperature. It was concluded that the proper preparation conditions for the composite membranes were as follows: firstly, heated at 160°C for 1 h, then chemical crosslinking at 40°C for 3 h in 4% MAC aqueous solution. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008     

State of water in chitosan–PVA hydrogel

The bound water fraction (X_BW) of a newly‐ developed pH‐sensitive, biodegradable chitosan‐polyvinyl alcohol (PVA) hydrogel crosslinked with glutaraldehyde (GA) was investigated as a function of the chitosan/PVA molar ratio, GA concentration (C_GA), and ionization state. Differential scanning calorimetry (DSC) was used to determine the X_BW of the initial hydrogel, and of the hydrogel equilibrated in pH 3 and pH 7 buffers. Changes in X_BW during swelling and shrinking of hydrogel were also investigated. In the initial state of hydrogel, X_BW increased with increasing PVA concentration (C_PVA), without being significantly affected by C_GA. In the buffer‐equilibrated hydrogels, X_BW decreased with increasing C_PVA and decreasing C_GA. The amount of bound water based on dry mass (C_BW) was substantially higher when the hydrogel was in the ionized (swollen) state compared to its unionized counterpart. This may be due to the association of a large quantity of water molecules with ? NH₃⁺ groups of chitosan when the gel swelled in the acidic environment. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 3227–3232, 2006     

Characteristics and sensing behavior of electrochemically codeposited polypyrrole–poly(vinyl alcohol) thin film exposed to ethanol vapors

Polypyrrole–poly(vinyl alcohol) (PPy–PVA) composite films were prepared electrochemically by means of codeposition at a constant potential. Their sensing behaviors to various ethanol-vapor concentrations were investigated. Increasing the molar fraction of PVA up to PPy_0.964PVA_0.036 showed an increase of the sensitivity of the composite sensors. However, the sensitivity decreased if further PVA was incorporated. The ethanol-sensing behaviors were also largely dependent upon the electropolymerization charge, ranging from 50 to 200 mC in this investigation. Higher sensitivity was measured from the composite film prepared with a lower electrical charge. For example, a sensitivity of 7.70 mΩ mg⁻¹ L, about 3.3 times the sensitivity of the pristine PPy sensor, was measured by the PPy_0.964PVA_0.036 composite film prepared at 50 mC. However, incorporating PVA into the conducting polymer was at the sacrifice of the response speed as well as the stability of the composite as it was under continuous exposure to ethanol vapor. An adsorption model based on the Langmuir isotherm was used to interpret the sensing behaviors and the equation derived from this model correlated well with the measured sensitivities. The sensing parameters including the adsorption equilibrium constant, K_m, and the resistance change caused by a pseudomonolayer, [m(r₁ − r₂)]/n, were determined and found to decrease with increasing polymerization charge. © 1999 John Wiley & Sons, Inc. J Appl Polym Sci 73: 2079–2087, 1999     

Silicon dioxide/poly(vinyl alcohol) composite hydrogels with high mechanical properties and low swellability

Poly(vinyl alcohol) (PVA) hydrogels with tissue-like viscoelasticity, excellent biocompatibility, and hydrophilicity have been considered as promising cartilage replacement materials. However, the low mechanical properties of pure PVA hydrogels limit their applications for bearing complicated loads. Herein, we report silicon dioxide (SiO₂)/PVA composite hydrogels fabricated by fabricated cyclically freezing/thawing the aqueous mixture of PVA and methyltrimethoxysilane (MTMS). MTMS hydrolyzes and forms SiO₂ particles in situ to reinforce PVA hydrogel. Meanwhile, silanol group condenses with hydroxyl groups of PVA and chemically bonds with PVA. The resulting SiO₂/PVA hydrogels exhibit much better mechanical properties than bare PVA hydrogel. In addition, the composite hydrogels keep very low swellable property. This prepared composite hydrogels are promising in a variety of biomedical applications such as artificial articular cartilage, drug delivery, and biosensors. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 46895.     

Photosensitive antibacterial and cytotoxicity performances of a TiO2/carboxymethyl chitosan/poly(vinyl alcohol) nanocomposite hydrogel by in situ radiation construction

Nano‐TiO₂/carboxymethyl chitosan (CMCS)/poly(vinyl alcohol) (PVA) ternary nanocomposite hydrogels were prepared by freezing–thawing cycles and electron‐beam radiation with PVA, CMCS, and nano‐TiO₂ as raw materials. The presence of nano‐TiO₂ nanoparticles in the composite hydrogels was confirmed by thermogravimetry, Fourier transform infrared spectroscopy, and X‐ray powder diffraction. Field emission scanning electron microscopy images also illustrated that the TiO₂/CMCS/PVA hydrogel exhibited a porous and relatively regular three‐dimensional network structure; at the same time, there was the presence of embedded nano‐TiO₂ throughout the hydrogel matrix. In addition, the nano‐TiO₂/CMCS/PVA composite hydrogels displayed significant antibacterial activity with Escherichia coli and Staphylococcus aureus as bacterial models. The antibacterial activity was demonstrated by the antibacterial circle method, plate count method, and cell density method. Also, with the Alamar Blue assay, the cytotoxicity of the composite hydrogel materials to L929 cells was studied. The results suggest that these materials had no obvious cytotoxicity. Thus, we may have developed a novel, good biocompatibility hydrogel with inherent photosensitive antibacterial activity with great potential for applications in the fields of cosmetics, medical dressings, and environmental protection. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44150.     

Polyvinyl alcohol/polysulfone (PVA/PSF) hollow fiber composite membranes for pervaporation separation of ethanol/water solution

Polysulfone (PSF) hollow fiber membranes were spun by phase‐inversion method from 29 wt % solids of 29 : 65 : 6 PSF/NMP/glycerol and 29 : 64 : 7 PSF/DMAc/glycol using 93.5 : 6.5 NMP/water and 94.5 : 5.5 DMAc/water as bore fluids, respectively, while the external coagulant was water. Polyvinyl alcohol/polysulfone (PVA/PSF) hollow fiber composite membranes were prepared after PSF hollow fiber membranes were coated using different PVA aqueous solutions, which were composed of PVA, fatty alcohol polyoxyethylene ether (AEO₉), maleic acid (MAC), and water. Two coating methods (dip coating and vacuum coating) and different heat treatments were discussed. The effects of hollow fiber membrane treatment methods, membrane structures, ethanol solution temperatures, and MAC/PVA ratios on the pervaporation performance of 95 wt % ethanol/water solution were studied. Using the vacuum‐coating method, the suitable MAC/PVA ratio was 0.3 for the preparation of PVA/PSF hollow fiber composite membrane with the sponge‐like membrane structure. Its pervaporation performance was as follows: separation factor (α) was 185 while permeation flux (J) was 30g/m²·h at 50°C. Based on the experimental results, it was found that separation factor (α) of PVA/PSF composite membrane with single finger‐void membrane structure was higher than that with the sponge‐like membrane structure. Therefore, single finger‐void membrane structure as the supported membrane was more suitable than sponge‐like membrane structure for the preparation of PVA/PSF hollow fiber composite membrane. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 247–254, 2005     

Properties of polyamide 6,10/poly(vinyl alcohol) blends and impact on oxygen barrier performance

The oxygen transmission rate, average volume of free‐volume cavities (V_f) and fractional free volume (F_v) of polyamide 6,10 (PA610)/poly(vinyl alcohol) (PVA) (i.e. PA610_xPVA⁰⁵_y, PA610_xPVA⁰⁸_y and PA610_xPVA¹⁴_y) blend films reduced to minimum values when their PVA contents reached corresponding optimal values. Oxygen transmission rate, V_f and F_v values obtained for optimal PA610_xPVA^z_y blown films were reduced considerably with decreasing PVA degrees of polymerization. The oxygen transmission rate of the optimal bio‐based PA610₈₀PVA⁰⁵₂₀ blown film was only 2.4 cm³ (m²·day·atm)^?1, which is about the same as that of the most often used high‐barrier polymer, ethylene–vinyl alcohol copolymer. Experimental findings from dynamic mechanical analysis, differential scanning calorimetry, wide‐angle X‐ray diffraction and Fourier transform infrared spectroscopy of the PA610_xPVA^z_y blends indicate that PA610 and PVA in the blends are miscible to some extent at the molecular level when the PVA contents are less than or equal to the corresponding optimal values. The considerably enhanced oxygen barrier properties of the PA610_xPVA^z_y blend films with optimized compositions are attributed to the significantly reduced local free‐volume characteristics. © 2017 Society of Chemical Industry     

Enhancing interfacial adhesion performance by using poly(vinyl alcohol) in (low‐density polyethylene)/(natural rubber)/(water hyacinth fiber) composites

The effects of (a) the chemical modification of water hyacinth fiber by poly(vinyl alcohol) (WHF‐_PVA) and (b) loading on the properties of low‐density polyethylene (LDPE)/(natural rubber (NR))/(water hyacinth fiber (WHF)) composites were studied. Mechanical properties, water absorption behavior, morphology, and thermal properties were examined; X‐ray diffraction and infrared spectroscopic analysis were done. The results indicated that LDPE/NR/WHF‐_PVA composites had higher values of tensile strength, Young's modulus, melting temperature, and water absorption resistance but lower elongation at break than LDPE/NR/WHF composites. The LDPE/NR/WHF‐_PVA composites had better interfacial adhesion between the matrix and the fibers than LDPE/NR/WHF composites, as shown by SEM results. The LDPE/NR/WHF‐_PVA composites exhibited lower interparticle spacing than LDPE/NR/WHF composites, a feature which enhanced the interparticle interaction between the water hyacinth fibers and the LDPE/NR matrix. J. VINYL ADDIT. TECHNOL., 19:47–54, 2013. © 2012 Society of Plastics Engineers     

PFSA-TiO2(or Al2O3)-PVA/PVA/PAN difunctional hollow fiber composite membranes prepared by dip-coating method

PFSA-TiO₂(or Al₂O₃)-PVA/PVA/PAN difunctional hollow fiber composite membranes with separation performance and catalytic activity have been prepared by dip-coating method. The good separation performance was brought about by the glutaraldehyde (GA) surface cross-linked PVA/PAN composite membrane, and the good catalytic activity of the membrane was achieved by the perfluorosulphonic acid (PFSA) used. The difunctional hollow fiber membranes were characterized by XRD, TGA, EDX, SEM, and FTIR. The separation performance was measured by dehydration of azeotropic top product of ethanol-acetic acid esterification, and the catalytic activity was obtained by investigating the esterification of ethanol and acetic acid. The FTIR spectra and the morphologies of difunctional hollow fiber composite membranes were similar for samples prior to esterification and post-esterification with ethanol and acetic acid for 24?h. Difunctional hollow fiber composite membranes with 2% PFSA, 8% TiO₂ (named as DM-T1), and 2% PFSA, 8% Al₂O₃ (named as DM-A1) (all by weights) showed the best catalytic activity. They displayed fluxes of 165 and 173?g/m^2?h, separation factors of water to ethanol of 279 and 161, PFSA contents in difunctional hollow fiber composite membrane of 3.2 and 2.4%, the ratios of PFSA to feed solution (acetic acid?Cethanol) of 0.031 and 0.023%, and the equilibrium conversion of ethanol at 53.5 and 57.6%, in the given order for TiO₂ and Al₂O₃ containing samples.     

Effects of poly (vinyl alcohol) (PVA) content on preparation of novel thiol-functionalized mesoporous PVA/SiO2 composite nanofiber membranes and their application for adsorption of heavy metal ions from aqueous solution

Thiol-functionalized mesoporous poly (vinyl alcohol)/SiO₂ composite nanofiber membranes and pure PVA nanofiber membranes were synthesized by electrospinning. The results of Fourier transform infrared (FTIR) indicated that the PVA/SiO₂ composite nanofibers were functionalized by mercapto groups via the hydrolysis polycondensation. The surface areas of the PVA/SiO₂ composite nanofiber membranes were >290 m²/g. The surface areas, pore diameters and pore volumes of PVA/SiO₂ composite nanofibers decreased as the PVA content increased. The adsorption capacities of the thiol-functionalized mesoporous PVA/SiO₂ composite nanofiber membranes were greater than the pure PVA nanofiber membranes. The largest adsorption capacity was 489.12 mg/g at 303 K. The mesoporous PVA/SiO₂ composite nanofiber membranes exhibited higher Cu²⁺ ion adsorption capacity than other reported nanofiber membranes. Furthermore, the adsorption capacity of the PVA/SiO₂ composite nanofiber membranes was maintained through six recycling processes. Consequently, these membranes can be promising materials for removing, and recovering, heavy metal ions in water.     

Oxygen barrier,free volume,and blending properties of fully bio-based polyamide 11/poly(vinyl alcohol) blends

Fully bio-based polyamide 11 (PA11) was melt-blended with poly(vinyl alcohol) (PVA) with varying degrees of polymerization (DP) to prepare PA11_xPVA^z_y. The PA11_xPVA^z_y films demonstrated the lowest oxygen transmission rates (OTR) and free volume characteristics, when PVA contents of each PA11_xPVA^z_y series reached a corresponding critical concentration. The minimum OTR and free volume characteristics obtained for the optimal PA11_xPVA^z_y films reduced significantly with decreasing PVA DPs. The OTR of the optimal PA11_xPVA^z_y blown film was 1.07 cm³ m⁻² day⁻¹ atm⁻¹, which is near to that of the ethylene-vinyl alcohol copolymer high-barrier polymer. The results of dynamical, mechanical, and other experimental characterizations demonstrated that PA11 and PVA are compatible to some extent when PVA concentrations are less-than or equal to the respective critical values. The enhanced oxygen permeation resistance and free volume characteristics for optimal PA11_xPVA^z_y films are at least partly ascribed to the improved hydrogen-bonded molecular interactions between PA11 CO groups and PVA O─H groups. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48562.     

Study on the Crystallization Kinetic and Characterization of Poly(lactic acid) and Poly(vinyl alcohol) Blends

In this study, poly(lactic acid) (PLA) and poly(vinyl alcohol) (PVA) blends, with PLA/PVA mass ratios of 100/0, 90/10, 80/20, 70/30, 60/40, 50/50, and 40/60, were prepared by means of the melt blending method. The result of torque measurements and thermal gravimtric analysis tests showed that the addition of PLA can decrease the melt viscosity of PVA and that the second degradation step of PVA nearly disappeared for the PLA₈₀/PVA₂₀ blend. The absorbance peaks of the carbonyl group and the hydroxyl group in the Fourier transform infrared spectra of PLA/PVA blends had significant shifts to lower wave numbers, indicating that there were interactions between these two groups. Combined with the result of the differential scanning calorimetry curves, this interaction would be favorable for improving miscibility. The X-ray diffraction patterns and the polarized light microscope (PLM) micrographs showed that PVA can serve as a nucleating agent to promote the crystallization of PLA in PLA/PVA blends. Moreover, the PLA₈₀/PVA₂₀ blend gave the highest growth rate of PLA spherulite.     

Mechanical properties of films of poly(vinyl alcohol) derived from vinyl trifluoroacetate

In order to study the influence of the stereoreguralities of polymer chains on the mechanical properties of films of poly(vinyl alcohol) (PVA)_(VTFA) derived from vinyl trifluoroacetate, the strength of the film was measured. In the case of undrawn PVA_(VTFA) films, Young's modulus and strength at break were the smallest at the annealing temperature of about 100°C. It is considered to be due to the melt of small microcrystals and the increase in mobility of chains in amorphous parts. Young's moduli of undrawn PVA_(VTFA) films were in the range of 1.50–3.75 GPs and the values were higher than that (0.17–0.36 GPa) of undrawn film of commercial PVA with the low concentration of syndiotacticity and the high concentration of head-to-head bounds. In the case of drawn, annealed PVA_(VTFA) films, the maximum Young's modulus was about 20 GPa.     

Electrospinning fabrication and characterization of poly(vinyl alcohol)/layered double hydroxides composite fibers

Nanofibers of poly(vinyl alcohol) (PVA)/layered double hydroxide (Mg‐Al LDH) composites are prepared by the electrostatic fiber spinning using water as the solvent at a high voltage of 21 kV. Either inorganic LDH carbonate (LDH‐CO₃) or L ‐lactic acid‐modified LDH (Lact‐LDH) is used for incorporating with PVA. Scanning electron microscopy SEM investigations on the nanofibers suggest that the average diameters of PVA/LDH composite fibers are smaller than that of neat PVA. Transmission electron microscopy (TEM) investigations indicate that the dispersity of the LDH in PVA matrix is much improved after modification with L ‐lactic acid. The mechanical properties of the PVA/LDH fibers are obviously enhanced compared to that of neat PVA. For example, the tensile stress and elongation at break of the PVA/Lact‐LDH electrospun fibrous mat with 5 wt % Lact‐LDH are 31.7 MPa and 36.7%, respectively, which are significantly higher than those of neat PVA, and also higher than those of PVA/LDH‐CO₃ owing to the better dispersity of Lact‐LDH nanoparticles. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Effect of degree of cross-linking on swelling and on drug release of low viscous chitosan/poly(vinyl alcohol) hydrogels

In the present work, a series of cross-linked LVCS/PVA hydrogels with various feed compositions were prepared using glutaraldehyde as cross-linking agent. The prepared hydrogels were used for dynamic and equilibrium swelling studies. The swelling behavior of these hydrogels was investigated as functions of effect of pH, polymeric compositions and degree of cross-linking. Swelling studies were performed in 0.05 M USP phosphate buffer solutions of varying pH 1.2, 5.5, 6.5 and 7.5. Results showed that swelling increased by increasing PVA contents in the structure of hydrogels in solutions of higher pH values. This is due to the presence of more hydroxyl groups (–OH) in the PVA structure. On the other hand, by increasing LVCS contents, swelling increased in a solution of acidic pH and it is due to ionization of amino groups (–NH₂), but this swelling was not significant. Swelling of hydrogels was decreased with increase in cross-linking ratio due to tighter hydrogel structure. Porosity and sol–gel fraction were also investigated. It was found that with increase in LVCS and PVA contents porosity and gel fraction increased, whereas by increasing glutaraldehyde content gel fraction increased and porosity decreased. Diffusion coefficient (D) and network parameters, i.e., the average molecular weight between cross-links (M _C), solvent interaction parameters (χ), polymer volume fraction in swollen state (V _2S) and cross-linked density (q) were calculated using Flory–Rehner theory. Selected samples were loaded with model drug diphenhydramine HCl. The release of diphenhydramine HCl was studied for 12 h period in 0.05 M USP phosphate buffer solutions of varying pH 1.2, 5.5 and 7.5. It was observed that drug release increased with increasing PVA contents in the hydrogels, while release of drug decreased as the ratio of cross-linking agent increased in the hydrogel structure owing to strong physical entanglements between polymers. The release mechanisms were studied by fitting experimental data to model equations like zero order, first order, Higuchi and Peppas. Results showed that the kinetics of drug release from hydrogels in buffer solutions of pH 1.2, 5.5 and 7.5 was mainly non-fickian diffusion. Hydrogels were characterized by Fourier transform infrared and X-ray diffraction to confirm the structure and study the crystallinity of hydrogel, respectively.     

Preparation of poly(vinyl alcohol)/poly(acrylic acid)/TiO2/carbon nanotube composite nanofibers and their photobleaching properties

The composite nanofibers of poly(vinyl alcohol) (PVA)/poly(acrylic acid) (PAAc)/titanium(IV) oxide (TiO₂) were prepared by electrospinning for a novel photocatalytic treatment of waste water. To improve the photoelectronic properties of PVA/PAAc/TiO₂ composite nanofibers, carbon nanotubes (CNTs) were used as an additive. The TiO₂ and CNTs were immobilized in the PVA/PAAc hydrogels as electrospun nanofibers for an easier recovery after the wastewater treatment. The improved efficiency of pollutant dye removal was observed at pH 10 due to the pH-sensitive swelling behavior of the PVA/PAAc/TiO₂/CNTs composite nanofibers. The photocatalytic activity of TiO₂ was improved noticeably by applying electric field to the CNTs-embedded composite nanofibers.     

Preparation of a PVA/HAP composite polymer membrane for a direct ethanol fuel cell (DEFC)

A novel PVA/Hydroxyapatite (HAP) composite polymer membrane was prepared by the direct blend process and solution casting method. The characteristic properties of the PVA/HAP composite polymer membranes were investigated using thermal gravimetric analysis (TGA), X-ray diffraction (XRD), scanning electron microscopy (SEM), micro-Raman spectroscopy and the AC impedance method. An alkaline direct ethanol fuel cell, consisting of an air cathode with MnO₂ carbon inks based on Ni-foam, an anode with PtRu black on Ni-foam, and the PVA/HAP composite polymer membrane, was assembled and investigated. It was found that the alkaline direct ethanol fuel cell comprising of a novel cheap PVA/HAP composite polymer membrane showed an improved electrochemical performance in ambient temperature and air. As a result, the maximum power density of the alkaline DEFC, using a PtRu anode based on Ni-foam (10.74 mW cm⁻²), is higher than that of DEFC using an E-TEK PtRu anode based on carbon (7.56 mW cm⁻²) in an 8M KOH + 2M C₂H₅OH solution at ambient temperature and air. These PVA/HAP composite polymer membranes are a potential candidate for alkaline DEFC applications.