Aqueous Solution Of Polyvinyl Alcohol Research Articles

Preparation of a PVA/Chitosan/Glass Fiber Composite Membrane and the Performance in CO2 Separation.

In this study, a novel composite membrane was developed by casting the mixed aqueous solution of chitosan (CS) and polyvinyl alcohol (PVA) on a glass fiber microporous membrane. The polymeric coating of a composite membrane containing amino groups and hydroxyl groups has a favorable CO2 affinity and provides an enhanced CO2 transport mechanism, thereby improving the permeance and selectivity of CO2. A series of tests for the composite membranes were taken to characterize the chemical structure, morphology, strength, and gas separation properties. ATR-FTIR spectra showed that the chemical structure and functional group of the polymer coating had no obvious change after the heat treatment under 180 °C, while SEM results showed that the composite membranes had a dense surface. The gas permeance and selectivity of the composite membrane were tested using single gases. The results showed that the addition of chitosan can increase the CO2 permeance which could reach 233 GPU. After a wetting treatment, the CO2 permeance (454 GPU) and gas selectivity (17.71) were higher than that of dry membranes because moisture promotes the composite membrane transmission. After a heat treatment, the permeance of N2 decreased more significantly than that of CO2, which led to an increase in CO2/N2 selectivity (10.0).

Effect of spraying polyvinyl alcohol solution on the surface of liquid film on the structure and antifouling properties of polyvinylidene membrane

Abstract Polyvinylidene fluoride (PVDF) membrane was prepared by a two-step method of surface gelation-immersion precipitation. The surface of the scraping solution film was sprayed with polyvinyl alcohol (PVA) aqueous solution to gel the film surface first, and then the liquid film was immersed in a coagulation bath for phase transformation to obtain the surface modified PVDF membrane. The effects of PVA solution with different mass fraction on the structure and properties of PVDF membrane were studied. The results showed that with the increase of spraying PVA mass fraction, the contact angle of the upper surface of PVDF membranes gradually decreased, the porosity and mean pore size of PVDF membranes gradually increased, and the crystallinity of PVDF membranes gradually decreased. The pores on upper surface of the membranes first increased and then decreased, and the finger-like macropore structure appeared inside the membranes, the water flux first increased and then decreased, and the rejection rate increased. Dynamic cycle filtration experiment of bovine serum protein (BSA) solution showed an increase in membrane flux recovery from 68.31 to 95.08% and a decrease in the irreversible fouling rate from 31.69 to 4.92%, indicating an improvement in the hydrophilicity and antifouling properties of the modified PVDF membrane.

Nanofiber production from rose water and mate plant extract solutions using environmentally friendly electrospinning

In this study, it was aimed to produce nanofibers from polyvinyl alcohol (PVA) polymer using natural solvents such as rose water, rose extract and mate plant extract by the environmentally friendly electrospinning or green electrospinning technique in other words and it was also aimed to investigate the morphological properties of produced nanofibers. For this purpose, nanofibers having 7 different morphologies were produced from 4% PVA aqueous solutions. The morphologies of the produced nanofibers were analysed by scanning electron microscopy (SEM). As a result of these analyses, it was observed that uniform nanofiber morphology was formed in nanofiber productions made with distilled water, while in the others, dense bead structure was formed at low voltages and nanofiber morphology with reduced bead amount at high voltages was observed. In all electrospinning experiments, it was observed that the nanofibers were randomly collected on the collector plate. It was observed that the nanofibers obtained from the solutions prepared from solvents other than distilled water, especially the one from the mate plant extract, had a low bead structure and a smooth morphology. These results showed that environmentally friendly nanofibers can be produced from natural solvents by electrospinning technique and their morphological properties can be improved via modification in process conditions. It is thought that the nanofibers produced within the scope of the study are candidate materials especially for health, hygiene and food applications since they are produced in pure properties without using any other additives.

Green immobilization and efficient proliferation of Escherichia coli cells in polyvinyl alcohol hydrogel membranes by unidirectional nanopore dehydration

BackgroundThe immobilized technology for microbial or cells has the advantages of high microbial activity, high microbial density per unit space, good tolerance, strong shock, load resistance, high processing efficiency, and high reuse rate. It is now widely used in environmental remediation, water quality treatment, biodegradation, food industry, chemical analysis, energy development, medicine and pharmaceuticals, and other fields.ResultsA novel Escherichia coli cell-immobilizing polyvinyl alcohol hydrogel membrane (ECI-PVAHM) was prepared by unidirectional nanopore dehydration (UND) from a 10% polyvinyl alcohol (PVA) aqueous solution containing enhanced green fluorescent protein-labeled E. coli. This bacteria-loaded film has high water stability, flexibility, transparency, and mechanical robustness. Its tensile strength, elongation rate, and swelling rate are in the ranges 0.66–0.90 MPa, 300–390%, and 330–800%, respectively. The effective bacterial load of ECI-PVAHM is 2.375 × 109–1010 CFU/g (dry weight), which does not affect the original crystal structure of the PVAHM. This biofilm has a porous network structure with pore sizes between 0.2 and 1.0 μm, and these cells are embedded in the PVAHM network. When the immobilized cells were continuously cultured for 20 days, and the medium was renewed twice daily, their relative proliferation efficiency after 40 cycles could still be maintained at ~ 91%.ConclusionThe above results show that the cell division, proliferation ability, and metabolic activity of immobilized E. coli were not affected by the physical barrier of the porous network structure of the hydrogel. This UND-based ECI-PVAHM has potential applications in molecular biology, biopharmaceutical expression and production, bioreactors, and fuel cells.

Unidirectional Nanopore Dehydration Induces an Anisotropic Polyvinyl Alcohol Hydrogel Membrane with Enhanced Mechanical Properties.

As a biocompatible, degradable polymer material, polyvinyl alcohol (PVA) can have a wide range of applications in the biomedical field. PVA aqueous solutions at room temperature can be cast into very thin films with poor mechanical strength via water evaporation. Here, we describe a novel dehydration method, unidirectional nanopore dehydration (UND). The UND method was used to directly dehydrate a PVA aqueous solution to form a water-stable, anisotropic, and mechanically robust PVA hydrogel membrane (PVAHM), whose tensile strength, elongation at break, and swelling ratio reached values of up to ~2.95 MPa, ~350%, and ~350%, respectively. The film itself exhibited an oriented arrangement of porous network structures with an average pore size of ~1.0 μm. At 70 °C, the PVAHMs formed were even more mechanically robust, with a tensile strength and elongation at break of 10.5 MPa and 891%, almost 3.5 times and 2 times greater than the PVAHM prepared at 25 °C, respectively. The processing temperature affects the velocity at which the water molecules flow unidirectionally through the nanopores, and could, thus, alter the overall transformation of the PVA chains into a physically crosslinked 3D network. Therefore, the temperature setting during UND can control the mechanical properties of the hydrogel membrane to meet the requirements of various biomaterial applications. These results show that the UND can induce the ordered rearrangement of PVA molecular chains, forming a PVAHM with superior mechanical properties and exhibiting a greater number of stronger hydrogen bonds. Therefore, the novel dehydration mode not only induces the formation of a mechanically robust and anisotropic PVA hydrogel membrane with a porous network structure and an average pore size of ~1.0 μm, but also greatly enhances the mechanical properties by increasing the temperature. It may be applied for the processing of water-soluble polymers, including proteins, as novel functional materials.

Formation of beryllium oxide nanofibers by polyvinyl alcohol/beryllium sulfate/polyethyleneimine composite precursors

Polyvinyl alcohol (PVA)/beryllium sulfate (BeSO4) precursor nanofibers are fabricated by electrospinning technique, mixing PVA aqueous solution with BeSO4 salt. The productivity is increased by adding polyethyleneimine (PEI) with PVA/BeSO4 spinning solution. The beryllium oxide (BeO) nanofibers are obtained by calcinating the PVA/BeSO4/PEI precursor nanofiber heated at 1000 °C or above. The crystallographic structure of BeO nanofibers is examined by X-ray diffraction. The thermal behaviors of the pure PVA nanofibers, BeSO4 salt, and PVA/BeSO4/PEI precursor nanofibers are studied by thermogravimetry analysis. The BeO nanofiber diameters are reduced with the increase in calcination temperatures. The specific surface area of the PVA/BeSO4/PEI precursor nanofibers is around 36.9 m2 g−1, and that of the BeO nanofibers calcined at 1200 °C is about 11.9 m2 g−1. The pore properties deteriorate due to sintering and blockage as the calcination temperature increases. This work introduces mesoporous BeO nanofibers for the very first time.

Design and Fabrication of a Robust Chitosan/Polyvinyl Alcohol-Based Humidity Sensor energized by a Piezoelectric Generator

Due to their rapid growth in industrial and environmental applications, there is a need to develop self-powered humidity sensor systems with improved sensitivity, a wide detection range, and an eco-friendly nature. In this study, an aqueous solution of chitosan (CS) and polyvinyl alcohol (PVA) was blended to yield a composite film material with enhanced humidity detection properties. Meanwhile, a polyvinylidene difluoride (PVDF)-loaded chitosan composite film was developed and employed as a piezoelectric generator. Moreover, the developed composite materials for both devices (the piezoelectric generator and the humidity sensor) were optimized based on output performance. The piezoelectric generator generates a maximum of 16.2 V when a force of 10 N is applied and works as a power source for the humidity-sensing film. The sensing film swells in response to changes in relative humidity, which affects film resistance. This change in resistance causes a change in voltage through the piezoelectric generator and allows the precise measurement of relative humidity (RH). The fabricated sensor showed a linear response (R2 = 0.981) with a reasonable sensitivity (0.23 V/% RH) in an environment with an RH range of 21–89%. In addition, the device requires no external power, and therefore, it has numerous sensing applications in various fields.

Adsorptive separation of dye by filled polymeric FIPN hydrogel

ABSTRACT Acrylic acid (AA) and Acrylamide (AM) are copolymerised to produce copolymer of Poly-acrylic acid-co-acrylamide (PAA) in the aqueous solution of Polyvinyl alcohol (PVA). Both the polymers PVA and PAA were cross-linked in situ by glutaraldehyde and N, N O-methylene bis acrylamide (MBA) respectively using 2 mass% of polymer basis for both of them. Thus, three different full interpenetrating network (FIPN) hydrogels were synthesised varying the mass ratio of PVA to PAA. The hydrogel of PVA: PAA = 1:0.50 composition designated as PAA50 found competitive for separating Malachite green from its 50 ppm aqueous solution by adsorption compared to the other two. PAA50 was further modified by incorporating 2, 5, 8 and 10 mass% nano size sodium monomontellite filler and produced four filled FIPN hydrogels designated as PAA52, PAA55, PAA58 and PAA510, respectively. These four nano-filled FIPN hydrogels along with unfilled PAA50 and pure nano size sodium monomontellite were used for adsorption in same dye solution of 5, 10, 25, 50, 75 and 100 ppm concentrations and different pH of 4, 7, 9, 10 & 11. Highest 98.039% dye removal was done by PAA58 from 75 ppm feed at 9 pH. 93.7% recovery was observed at 3 pH in desorption study.

Effect of Hydrogen Bonding on Dynamic Rheological Behavior of PVA Aqueous Solution.

The rheological behavior of polyvinyl alcohol (PVA) aqueous solution is crucial to optimizing the processing technology and performance of PVA products. In this paper, the dynamic rheological behavior of PVA aqueous solution was investigated in detail. PVA solution with a concentration of 10 wt% showed unnormal rheological behaviors, that is, the liquid-like behavior in the high frequency (ω) region and the solid-like behavior in the low ω region. A storage modulus (G′) plateau appears in the relatively low ω region as a gel with a network structure. Different from conventional hydrogel, this plateau has a low modulus, and the corresponding size of the relaxation unit is estimated to be 554 nm, being higher than the size of a whole PVA chain. It is believed that the network mesh is formed by the intermolecular hydrogen bonding interactions among PVA chains. The relaxation time of these meshes is longer than the reptation time of a PVA chain. Based on the relaxation spectrum and calculation analysis, it is found that the destruction of intermolecular hydrogen bonds, such as by heating up, adding sodium dodecyl sulfate, and shear operation, will make the relaxation unit (mesh) larger and lead to the left shift of the intersection of G′ and loss modulus (G″). In a PVA solution with a high concentration, multiple meshes of various sizes could be formed and thus generate multiple relaxation peaks. The large-sized meshes mainly contribute to the left shift of the intersection of G′ and G″, and the small-sized meshes contribute to the high plateau modulus. The results in this paper offer a new angle to analyze polymer solutions with strong intermolecular interaction.

Kinetics of Stability of Foams from Aqueous Solutions of Polyvinyl Alcohol with Different Molecular Weight

Kinetics of Stability of Foams from Aqueous Solutions of Polyvinyl Alcohol with Different Molecular Weight

Acoustically induced birefringence in polymer aqueous solutions: The case of polyvinyl alcohol

Transient and stationary ultrasonically induced birefringence traces of various relatively dilute poly-vinyl alcohol aqueous solutions were measured over a range 500–1400 kHz of ultrasonic frequencies and 0.02–0.13 W/cm2 of acoustic field amplitudes. The intrinsic value of the stationary birefringence for all polymer solutions investigated in this study was found to be proportional to the solution mass concentration, the square root of the ultrasonic intensity and the frequency of the ultrasound in agreement with theoretical predictions. Systematic analysis of the transient birefringence signals caused by the applied ultrasonic field has been performed in order to evaluate the orientational relaxation times from the viewpoint of dynamics of polymer chain orientation and anisotropy changes in polarizability. The results are discussed in the context of recent experimental studies and theoretical predictions of the ultrasonically induced birefringence in terms of transport phenomena.

РЕОЛОГИЯ ВОДНОГО РАСТВОРА НИЗКОМОЛЕКУЛЯРНОГО ПОЛИВИНИЛОВОГО СПИРТА

The rheology of aqueous solutions of polyvinyl alcohol (PVA) was studied by the method viscometry. The values of the verification coefficients were estimated depending on both the concentration of PVA, and on the average molecular weight of the PVA itself. It is shown that in water a solution of low molecular weight PVA (70-140 kDa) with a concentration of up to 0.035% dominant is the interaction of polymer chains with water (the first belief coefficient), and above 0.035% PVA, the interaction of polymer chains between itself (the second confidence factor).

Conducting Polymer Hydrogel Driven By Sodium Chloride as High Performance Flexible Supercapacitor Electrode

With the rapid development of the wearable devices and flexible supercapacitors (FSCs), urgent demand for electrodes with high specific capacitance and excellent flexibility have been put forward. Herein, a self-standing conducting polymer hydrogel electrode has been successfully synthesized by in situ polymerization of aniline (ANI) in aqueous solution of polyvinyl alcohol (PVA), phytic acid (PA) and sodium chloride (NaCl). The prepared PANI/PVA/NaCl (PPN) hydrogel electrode shows high specific capacitance (1544 mF cm−2 at current density of 1 mA cm−2), good flexibility (elongation at fracture of 110%), satisfactory electrochemical stability (92% capacitance retention after 500 repeated bending cycles) and excellent cycling stability (78.2% capacitance retention after 10000 cycles) due to the uniform 3D interconnected structure driven by NaCl pseudo template. In order to further explore the potential application prospects of the synthesized hydrogel in flexible devices, a series of all-hydrogel-state FSCs are assembled based on the prepared PPN hydrogel electrodes and typical PVA/H2SO4 electrolyte. The assembled FSCs exhibit high energy density of 51.1 μWh cm−2 at power density of 250 μW cm−2 and long-life stability of 81.10% capacitance retention after 10000 charge/discharge cycles. This work provides a new synthesis strategy for the high performance energy storage electrodes and devices.

Modification of Thin Film Composite PVA/PAN Membranes for Pervaporation Using Aluminosilicate Nanoparticles.

The effect of the modification of the polyvinyl alcohol (PVA) selective layer of thin film composite (TFC) membranes by aluminosilicate (Al2O3·SiO2) nanoparticles on the structure and pervaporation performance was studied. For the first time, PVA-Al2O3·SiO2/polyacrylonitrile (PAN) thin film nanocomposite (TFN) membranes for pervaporation separation of ethanol/water mixture were developed via the formation of the selective layer in dynamic mode. Selective layers of PVA/PAN and PVA-Al2O3·SiO2/PAN membranes were formed via filtration of PVA aqueous solutions or PVA-Al2O3·SiO2 aqueous dispersions through the ultrafiltration PAN membrane for 10 min at 0.3 MPa in dead-end mode. Average particle size and zeta potential of aluminosilicate nanoparticles in PVA aqueous solution were analyzed using the dynamic light scattering technique. Structure and surface properties of membranes were studied using scanning electron microscopy (SEM), atomic force microscopy (AFM) and water contact angle measurements. Membrane performance was investigated in pervaporation dehydration of ethanol/water mixtures in the broad concentration range. It was found that flux of TFN membranes decreased with addition of Al2O3·SiO2 nanoparticles into the selective layer due to the increase in selective layer thickness. However, ethanol/water separation factor of TFN membranes was found to be significantly higher compared to the reference TFC membrane in the whole range of studied ethanol/water feed mixtures with different concentrations, which is attributed to the increase in membrane hydrophilicity. It was found that developed PVA-Al2O3·SiO2/PAN TFN membranes were more stable in the dehydration of ethanol in the whole range of investigated concentrations as well as at different temperatures of the feed mixtures (25 °C, 35 °C, 50 °C) compared to the reference membrane which is due to the additional cross-linking of the selective layer by formation hydrogen and donor-acceptor bonds between aluminosilicate nanoparticles and PVA macromolecules.

A biomimetic compound eye lens for photocurrent enhancement at low temperatures

In this study, an artificial compound eye lens (ACEL) was fabricated using a laser cutting machine and polyvinyl alcohol (PVA) solution. A laser cutter was used to punch micro-sized holes (500 μm diameter—the smallest possible diameter) into an acrylic plate; this punched plate was then placed on the aqueous PVA solution, and the water was evaporated. The plate was used as the mold to obtain a polydimethylsiloxane (PDMS) micro lens array film, which was fixed to a dome-shaped three-dimensional-printed mold for further PDMS curing, and a hemispherical compound eye lens was obtained. Using a gallium nitride (GaN) photodetector, a light detection experiment was performed with the ACEL, bare lens, and no lens by irradiating light at various angles under low temperatures. The photodetector with the ACEL generated a high photocurrent under several conditions. In particular, when the light was irradiated at 0° and below −20 °C, the photocurrent of the GaN sensor with the ACEL increased by 61% and 81% compared with the photocurrent of the GaN sensor with the bare lens and without a lens, respectively. In this study, a sensor for detecting light with ACEL was demonstrated in low-temperature environments, such as indoor refrigerated storages and external conditions in Antarctica and Arctic.

Strain-sensitive alginate/polyvinyl alcohol composite hydrogels with Janus hierarchy and conductivity mediated by tannic acid

To construct conductive hydrogels with a conductive and a non- or weakly conductive layer for comfortable and safe electronic application, marine biobased anionic polysaccharide sodium alginate (SA) and neutral polyvinyl alcohol (PVA) were employed as the hydrogel matrixes. Tannic acid (TA) was exploited to mediate the demixing of the miscible aqueous solution of SA and PVA in view of the much larger interaction strength of TA with PVA than both of TA with SA and PVA with SA calculated from the density functional theory (−40.21, −29.77 and −21.00 kcal·mol−1 respectively). The finally-fabricated alginate/PVA composite hydrogels not only possess a “Janus” hierarchy but manifest asymmetrical conductivity, i.e., one layer strongly conductive and another weakly conductive. The strongly conductive layer achieves a conductivity of more than 2.95 S·m−1, facilitating their application in soft electronic areas like human-machine interfaces, smart wearable devices and soft robots. The weakly conductive layer with the conductivity less than 0.60 S·m−1 and the thickness adjustable, constitutes a protective screen for another layer. The Janus hydrogels exhibit good mechanical performance, excellent strain-sensing performance and fatigue-resistant mechanics, conductivity and sensitivity.

Use of Thermal Boron Technique to Determine Optimum Synthesis Parameters for Zirconium and Hafnium Diborides

Zirconium and hafnium diborides were synthesized. The process of obtaining zirconium and hafnium diborides was carried out by reduction of zirconium and hafnium dioxides with amorphous boron at high temperature in a vacuum furnace with a residual pressure of 10 Pa. The synthesis of metal diborides included the following stages: preparation of charge, pressing, annealing of tablets, milling, and classification. The initial components were mixed in a drum-type apparatus; an aqueous solution of polyvinyl alcohol was used as a plasticizer. Tableting was performed on an OYSTAR Manesty FlexiTab tablet press with a punch diameter of 13 mm at a pressure of 218.7 MPa. The thickness of the obtained tablets was 3 mm. The obtained tablets were annealed in a Nabertherm VHT/GR vacuum furnace. A graphite crucible with zirconium oxide or hafnium oxide backfill, respectively, was used for annealing. The furnace was vacuumized with a forevacuum pump to a residual pressure of 10 Pa. The morphology of ZrB2 and HfB2 particles was investigated using the QUANTA 200 3D electron and focused-beam system. The phase composition and structural parameters of the samples were investigated on a Shimadzu XRD-6000 diffractometer with Cu Kα radiation. We determined the optimal parameters for the synthesis of zirconia and hafnium diborides: the optimal temperature for the synthesis of zirconia diboride was 1800 оС, for the synthesis of hafnium diboride — 1850 оС, the heating rate was 8.5 оС/min. The highest yield of zirconium and hafnium diborides was achieved in samples with a molar ratio of MeO2:B = = 1:6 at a synthesis time of 60 minutes. The yield of metal diborides was 99%.The authors who contributed to this paper include V. I. Sachkov, R. A. Nefedov, R. O. Medvedev, A. S. Sachkova, D. A. Biryukov.The authors would like to thank the Tomsk Regional Centre of Shared Knowledge for their support of this research work. This research was funded by the Ministry of Education and Science of the Russian Federation under the Governmental Assignment no. FSWM-2020-0028.

Investigation of the fabrication of nanofibers from aqueous polyvinyl alcohol solutions by electrospinning

Polyvinyl alcohol (PVA) refers to polymers that have great potential for medical and technical applications. Especially, the possibility of its medical application in nanofibres is of great interest due to its good water solubility, high biocompatibility and non-toxicity. PVA is used for various pharmaceutical and biomedical purposes, as a carrier for the delivery of proteins and drugs, as dressings, filter materials, and as artificial organs. Currently, many drug delivery systems have been developed, such as hydrogels or complex electronic microchips. Nanostructural materials are particularly advantageous for rapid drug release due to their high surface area to volume ratio. Both natural and synthetic polymers can be used to produce nanofiber materials, but the combination of different polymers (synthetic and natural) and the incorporation of various biologically active substances into them provides special properties to the finished materials. In this work, the properties of aqueous solutions based on polyvinyl alcohol were investigated: electrical conductivity, viscosity and pH. The influence of technological parameters of electroforming process on obtaining nanofibers from aqueous solutions of PVA. The optimum PVA concentration for the formation of nanostructures was determined equal to 8 wt.%. At this concentration, the PVA solution has electrical conductivity, viscosity and pH equal to 571 µS/cm, 107.23 mPa·s and 6.14 respectively. As part of the study, the electroforming process parameters were obtained to enable the production of nanofibers with a diameter of about 170 nm: distance between needle and collector 140 mm, spinning solution feed rate 0.2 ml/h and voltage between needle and collector 30 kV.

A high strength, low friction, and biocompatible hydrogel from PVA, chitosan and sodium alginate for articular cartilage

Developing articular cartilage substitutes required a combination of high compressive strength, excellent biocompatibility and low friction. Despite great success in tough hydrogels, this combination was hardly realized. Herein, a high strength, low friction, and biocompatible hydrogel was obtained by freezing-thawing polyvinyl alcohol and chitosan aqueous solutions three times, followed with soaking in sodium alginate aqueous solution. Owing to the synergy of crystalline domains, hydrogen bonds, and ionic interactions, the obtained hydrogel exhibited high strength (maximum compressive strength = 141 MPa). Because of the reversible linkages, the gel was also creep-resistant (recovery efficiency = 93%). Benefitted from the negative carboxyl groups from sodium alginate, the water lubrication layer between the gel and the opposing surface was thickened greatly, resulting in a low coefficient of friction (0.044). The biocompatible materials and green progress led to excellent cell compatibility. All these merits made it an ideal substitute for articular cartilage.

POTENTIAL EFFECT OF UV RADIATION ON THE OPTICAL AND ANTI-MICROBIAL PROPERTIES OF PVA/METAL-SALT NANOCOMPOSITES

Polymer/metals nanocomposite films were investigated from aqueous solutions of polyvinyl alcohol (PVA)/acrylic acid (AAc) using UV radiation. The formation of metal nanoparticles (NPs) was characterized by transmission electron microscopy (TEM), Fourier-transform infrared spectrometry (FTIR) and UV-vis spectroscopy. It was found that UV radiation induced the reduction of the metal ions in the polymer matrix into metal nanoparticles. The electrical properties and the anti-microbial efficiency were carried out for the prepared compositions. The maximum AC conductivity was observed in the composites containing Ag NPs. Finally, a green method has been suggested for the development of conductive nano polymer/metal composites that can be used in biomedical applications.