Optical,electrical, and electrochemical properties of graphene based water soluble polyaniline composites

Polyaniline (PANI) is one of the most common polymers known for its conducting properties. However, poor water solubility limits its applications. In this work, PANI has been functionalized with sulfonic acid groups to produce sulfonated PANI (SPANI) offering excellent solubility in water. To compensate for the decrease of electrical conductivity due to functionalization, SPANI was combined with reduced graphene oxide (RGO) to form SPANI/RGO composites with interesting optical, thermal, and electrical properties. The composites have been characterized using X‐ray diffraction (XRD), field emission scanning electron microscopy, UV–vis absorption spectroscopy, Raman spectroscopy, Fourier‐transform infrared spectroscopy, X‐ray photoelectron spectroscopy, thermogravimetric analysis, cyclic voltammetry, and four probe electrical conductivity measurement. The SPANI/RGO composites show increased thermal stability, reduced optical band gap and improved electrochemical properties compared with the pure polymer. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42766.     

Synthesis,spectral analysis,and catalytic activity of poly(aniline‐co‐congored)–metal oxide nanocomposites

Electrically conducting, water‐soluble fluorescent copolymer nanocomposites were synthesized by a solution polymerization method under different experimental conditions in the presence of CuO and V₂O₅ nanoparticles. The prepared copolymer nanocomposites were characterized with analytical tools, including Fourier transform infrared spectroscopy, ultraviolet–visible (UV–vis) spectroscopy, and fluorescence emission spectroscopy. The order of copolymerization was determined on the basis of the UV–vis absorption spectra and fluorescence emission spectra. The copolymer–CuO nanocomposite system exhibited the highest electrical conductivity. The scanning electron microscopy image showed the presence of more CuO nanoparticles on the surface of the copolymer. Furthermore, the catalytic activity of the copolymer nanocomposites was tested for the reduction of p‐nitrophenol. All three types of polymer systems exhibited almost the same apparent rate constant values. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46469.     

Optical and electrical properties of polyaniline‐cadmium sulfide nanocomposite

Polyaniline‐cadmium sulfide nanocomposite has been synthesized by the chemical oxidative polymerization of aniline with ammonium peroxodisulfate as an initiator in presence of cadmium sulfide nanoparticles. TEM, XRD, FTIR, TGA, UV–vis spectroscopy, and photoluminescence studies were done for the structural, thermal and optical characterization of the samples. The particle size of nanocomposites lies in between 7 and 10 nm. XRD spectrum shows that polyaniline is amorphous, but peaks present in the spectrum of polymer nanocomposites are for cadmium sulfide nanoparticles. TGA result shows that nanocomposite is more thermally stable. The band gap of nanocomposite decreases with increasing content of cadmium sulfide nanoparticles. An enhancement in photoluminescence has been observed in the nanocomposite than that in pure polyaniline. The dc and ac electronic transport property of polyaniline cadmium sulfide composites has been investigated within a temperature range 77 ≤ T ≤ 300 K and in the frequency range 20 Hz–1 MHz. The dc conductivity follows variable range hopping (VRH) model. The ac conductivity follows a power law whereas the temperature dependence of frequency exponent s can be explained by correlated barrier hopping (CBH) model. The dielectric behavior of the samples has been explained in terms of the grain and grain boundary resistance and capacitance. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Nanocomposites of silver nanoparticle and dinonylnaphthalene disulfonic acid‐doped thermoreversible polyaniline gel

Silver/polyaniline‐dinonylnaphthalene disulfonic acid (PANI‐DNNDSA) gel nanocomposites are prepared from the reduction of silver salt by polyaniline in formic acid medium. Scanning electron micrographs (SEM) indicate the presence of three‐dimensional fibrillar network structure and the silver nanoparticles remain dispersed within the PANI‐DNNDSA fibrillar network. Differential scanning calorimetric (DSC) study shows reversible first‐order phase transition characterizing the composite to behave as a thermoreversible gel. Transmission electron micrographs (TEM) show a decrease of nanoparticle size with increasing AgNO₃ concentration. Wide angle X‐ray scattering (WAXS) patterns show lamellar structure in the gel as well as in the gel metal nanocomposites (GMNCs) and the two melting peaks in the DSC patterns correspond to the melting of monolayer and bilayer crystals produced from the interdigitation of DNNDSA tails anchored from PANI chains within the PANI lamella. The above melting points are greater in the GMNCs than that of pure gel indicating the formation of complex melting thermogram with crystallites produced from the anchored surfactants tails at the surface of Ag nanoparticles. The GMNCs show a higher thermal stability than that of pure PANI‐DNNDSA gel. PANI‐DNNDSA gel has an emission peak at 354 nm but fluorescence quenching occurs in the GMNCs and the emission peak becomes red shifted. Also in the UV–vis spectra the π band‐polaron band transition peak shows a red shift and the DC conductivity increases with increasing Ag nanoparticle concentration in the GMNCs. The current (I)–voltage (V) characteristic curves indicate Ohmic nature of conductivity of the gel and the current at the same voltage increases appreciably with increasing Ag nanoparticle concentration. These GMNCs are easily processible due to its thermoreversible nature. So, an easily processible, thermally stable and highly conducting DNNDSA‐doped PANI‐Ag gel nanocomposite with interesting photoluminescent property has been successfully developed suitable for optoelectronic applications. POLYM. ENG. SCI., 2010. © 2009 Society of Plastics Engineers     

The Meyer‐Neldel rule in layered silicone‐silver nanocomposites

X‐Ray diffraction and X‐ray photoelectron spectroscopy studies, applied on some silicone‐silver nanocomposites, revealed the influence of the solvent used in preparation on the morphology of the resulted materials. It has been emphasized that dimethylformamide solvent favors the formation of silver nanoparticles and their migration at the surface, while water solvent favors the formation of a homogeneous composite with small silver nanoparticles. The places occupied by Ag nanoparticles (some prevent their oxidation and others that favor the oxidation process) are dependent on the mixture used in sol‐gel technique and have influence on the nanocomposite electrical conductivity. The temperature dependence of the electrical conductivity is investigated. A linear relationship between the pre‐exponential factor (σ₀) and activation energy (E_a) was observed, in the high temperature range (T > 315 K), for all the samples, indicating that the conductivity data obey Meyer‐Neldel rule. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Compatibilization of polyethylene/polyaniline blends with polyethylene‐graft‐maleic anhydride

The use of compatibilizers as interfacial agents in composites can offer a convenient way to improve the mechanical properties of immiscible polymer blends. The aim of this article is to illustrate the compatibilization effect of polyethylene‐graft‐maleic anhydride (PEgMA) in blends of low‐density polyethylene (LDPE) and n‐dodecylbenzene sulfonate doped polyaniline (PANIDBSA) prepared by extrusion. Films with different compositions of the coupling agent were evaluated with optical spectroscopy and thermomechanical, electrical, mechanical, and morphological techniques. The incorporation of PEgMA into the LDPE/PANIDBSA composites resulted in an improvement of their electrical conductivity and changes in the mechanical and morphological properties of the films. When 5 wt % of the coupling agent was added to a 30 wt % of the polyaniline‐containing film, the conductivity increased by more than three orders of magnitude, and the ductility also improved qualitatively. The morphology analysis also indicated that the addition of PEgMA produced a strengthening of the filler–matrix interfacial region. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Synthesis of nano‐sized ZnO and polyaniline‐zinc oxide composite: Characterization,stability in terms of DC electrical conductivity retention and application in ammonia vapor detection

Nano‐sized particles of Zinc oxide (ZnO) were synthesized using a new chemical rout. The chemical oxidative polymerization of aniline in the presence of nano ZnO was employed to synthesize a polyaniline‐zinc oxide (PANI‐ZnO) nanocomposite. The material was characterized by using transmission electron microscopy, XRD, scanning electron microscopy (SEM), fourier transform infrared spectroscopy (FTIR), and Thermogravimetric analysis (TGA). The conductivity measurements showed the resulting composites possessed higher conductivity as compared to pure polyaniline (PANI). The nanocomposite exhibited fairly sensitive towards solution of aqueous ammonia (NH₃), when it was exposed to various concentrations of NH₃ in an ambient room temperature. The results show that the sensor has good sensitivity and good repeatability upon repeated exposure to NH₃. PANI‐ZnO nanocomposite was also used to study electrical conductivity under isothermal conditions in the temperature range 50–130°C. The composite was found stable under ambient conditions below 90°C in terms of DC electrical conductivity retention. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2010     

Semiconductive poly[N1,N4‐bis(thiophen‐2‐ylmethylene)benzene‐1,4‐diamine]‐nickel oxide nanocomposite based ethanol sensor

This study aims to use the conductivity of a synthetic polymer as the sensing probe for ethanol. In order to enhance the sensitivity of the sensor, a composite of the polymer and nickel oxide (NiO) nanoparticles was formed as it improved the conductivity. This composite exhibited 100 times more conductivity than the neat polymer. The semiconductive nanocomposite of poly [N¹,N⁴‐bis(thiophen‐2‐ylmethylene)benzene‐1,4‐diamine]‐nickel oxide (PBTMBDA‐NiO) was prepared by in situ chemical oxidative polymerization. The monomer was N¹,N⁴‐bis(thiophen‐2‐ylmethylene)benzene‐1,4‐diamine (BTMBDA). The monomer (BTMBDA), polymer (PBTMBDA), and NiO nanoparticles used in this study were synthesized. The monomer was prepared by refluxing together 2‐thiophene carboxaldehyde, benzene‐1,4‐diamine, and few drops of glacial acetic acid in ethanol medium for 3 h. The polymer, PBTMBDA, was formed by the chemical oxidative polymerization of BTMBDA in chloroform by FeCl₃. NiO nanoparticles were prepared by slow addition of aqueous ammonia to anhydrous nickel chloride at room temperature (28 ± 2 °C), and at a pH of 8 under constant stirring condition. The composite was formed by in situ chemical oxidative polymerization of BTMBDA in chloroform by FeCl₃ in the presence of the dispersed NiO nanoparticles. The molecular structure of BTMBDA and PBTMBDA were confirmed by nuclear magnetic resonance (NMR) (¹H, ¹³C, and Dept‐90°), Fourier transform infrared spectroscopy, and ultraviolet (UV)–visible spectroscopy. The PBTMBDA and PBTMBDA‐NiO nanocomposite were characterized by X‐ray diffraction, thermogravimetric analysis, field emission scanning electron microscopy, and energy‐dispersive X‐ray spectroscopy analysis. The results of characterization studies indicate the strong interaction between PBTMBDA and NiO in the nanocomposite. The broadness of ¹H NMR peaks in PBTMBDA was due to the increased number of monomer units. The disappearance of the peak of α‐hydrogens on thiophene confirms the polymerization involving the fifth position of thiophene part of BTMBDA. The Fourier transform infrared spectroscopy spectra revealed that position of the characteristic peaks of the functional groups in the monomer shifted toward lower wave numbers in PBTMBDA and PBTMBDA‐NiO nanocomposite. This shifting confirms the presence of extended conjugation along the polymer backbone. Electronic spectra of these compounds showed three absorption bands corresponding to π→π*, n→π* and n→π* transitions of π electron of carbon, lone pair electrons of S, and lone pair electrons of N (imine) groups, respectively. From the Tafel plot, the exchange current density evaluated for the BTMBDA and PBTMBDA are 0.2815 × 10⁻⁸ and 1.1508 × 10⁻⁸ A cm⁻², respectively. PBTMBDA is evaluated to be a better electrode material than the BTMBDA. The X‐ray diffraction plots showed that the characteristic peak of NiO in PBTMBDA‐NiO nanocomposite suggested successful incorporation of NiO in PBTMBDA‐NiO nanocomposite. The thermogravimetric analysis revealed the improved thermal stability of the composite. Field emission scanning electron microscopy and energy‐dispersive X‐ray spectroscopy analysis confirmed the presence of the NiO in the composite. Incorporation of nickel oxide nanoparticles improved the electrical conductivity and stability of PBTMBDA. The conductivity of the polymer was found to be of the order of 10⁻⁵ S cm⁻¹ while that of the composite was of the order of 10⁻³ S cm⁻¹. The nanocomposite was found to be thermally more stable than PBTMBDA and exhibited better direct‐current electrical conductivity and isothermal stability than the PBTMBDA as revealed by the four‐probe study. The electrical conductivity as inferred from the four‐probe method was used as the parameter to study the isothermal stability of the composite. The PBTMBDA‐NiO nanocomposite based vapor sensor was constructed for the sensing of ethanol vapor in commercial ethanol and real samples (alcoholic drinks: Beer, Wine, Brandy, Vodka, Whisky, and Rum) It was observed that on exposure to ethanol vapor at ambient temperature, the electrical resistivity of the nanocomposite increased indicating suppression of charge carriers. The interaction of ethanol vapor with PBTMBDA in PBTMBDA‐NiO nanocomposite was confirmed by IR spectral technique. The change in the structure of the PBTMBDA on interaction with ethanol was highlighted by the changes in the infrared spectrum. The conductivity of the polymer was explained using the structure‐activity relationship of the monomer evaluated using Gaussian 09 software. This study also analyzed the total electron density with electrostatic potential of the monomer and its correlation with chemical reactivity in order to explain the ethanol vapor sensing‐property of the nanocomposite. A new method of ethanol vapor sensing by a conducting polymer composite is hereby reported. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45918.     

Thermal stability of HCl‐doped‐polyaniline and TiO2 nanoparticles‐based nanocomposites

Electrically conductive HCl doped polyaniline (Pani) : titanium dioxide (TiO₂) nanocomposites thin films were prepared by in‐situ oxidative polymerization of aniline in the presence of different amounts of TiO₂ nanoparticles. Later film casting was done using N‐Methyl‐2‐pyrrolidone (NMP) as a solvent. The formation of Pani : TiO₂ nanocomposites were characterized by Fourier Transform Infra‐Red spectroscopy (FTIR), x‐ray diffraction (XRD) and thermogravimetric analysis (TGA). The stability of the nanocomposites in terms of direct‐current electrical conductivity retention was studied in air by isothermal and cyclic techniques. The films of Pani : TiO₂ nanocomposites were observed thermally more stable under ambient environmental conditions than pure polyaniline film. The stability was seen to be highly dependent on the content of TiO₂ nanoparticles in the nanocomposite films. Due to their high stability, such type of nanocomposites can find place as a replacement material for pure polyaniline in electrical and electronic devices. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Reversed micelle Synthesis of Ag/polyaniline nanocomposites via an in situ ultraviolet photo‐redox mechanism

Silver/polyaniline nanocomposites were synthesized in reversed micellar solution, and the reaction was performed via in situ reduction of silver nitrate in aniline by photolysis. The nanocomposites were characterized by ultraviolet‐visible spectroscopy, Fourier transform infrared spectroscopy, X‐ray diffraction, scanning electron microscopy, transmission electron microscopy, thermo‐gravimetric analysis, differential scanning calorimetric analysis, and electrochemical methods. The results showed that the Ag/polyaniline nanocomposites are composed of nano‐sized particles of 15–30 nm that contain Ag domains of 10–15 nm. The electrical conductivity of an Ag/polyaniline pellet is 95.89 S cm⁻¹, whereas a polyaniline pellet is found to be 3.1 × 10⁻² S cm⁻¹. Ag/polyaniline composites also have a higher degradation temperature and specific capacitance, when compared with pure polyaniline. Potentiodynamic polarization showed the anodic shifting of the zero current potential and a lower exchange current density for the Ag/polyaniline composite. Compared with polyaniline, the Ag/polyaniline nanocomposite is a promising candidate for coatings with improved anticorrosion performance. POLYM. COMPOS.,, 2012. © 2012 Society of Plastics Engineers     

A convenient approach to synthesize stable silver nanoparticles and silver/polystyrene nanocomposite particles

In this study, silver nanoparticles were prepared by the reduction of silver nitrate in SDS+ isopentanol/styrene/H₂O reverse microemulsion system using sodium citrate as reducing agent. The Ag/PS nanocomposite particles were prepared by in situ emulsion polymerization of the styrene system containing silver nanoparticles that did not separate from the reaction solution. The polymerization dynamic characteristic was studied, at the same time, silver nanparticles and the encapsulation of composite particles were characterized by Fourier‐transform‐infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X‐ray diffraction (XRD) measurement, UV–vis diffuse reflectance spectroscopy, and X‐ray photoelectron spectroscopy (XPS). The results of TEM and UV–vis absorption spectra showed that well‐dispersed silver nanoparticles have a narrow size distribution. XRD showed that Ag and Ag/PS nanocomposite particles were less than 10 and 20 nm in size, which is similar to those observed by TEM. The results of XPS spectra revealed that the microemulsion system can stabilize the silver nanoparticles from aggregation and provided supporting evidence for the polystyrene encapsulated silver nanoparticle structure. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008.     

Electrochemical preparation of poly(2‐bromoaniline) and poly(aniline‐co‐2‐bromoaniline) in acetonitrile

Electrochemical preparation of poly(2‐bromoaniline) (PBrANI) and poly(aniline‐co‐2‐bromoaniline) [P(An‐co‐2‐BrAn)] was carried out in an acetonitrile solution containing tetrabutylammonium perchlorate (TBAP) and perchloric acid (HClO₄). The cyclic voltammograms during the copolymerization had many features similar to those for the usual polymerization of aniline. The copolymer exhibits a higher dry electrical conductivity value than that of PBrANI and a lower one than that of PANI. The observed decrease in the conductivity of the copolymer relative to PANI is attributed to the incorporation of bromine moieties into the polyaniline chain. The structure and properties of the polymer and copolymer were elucidated using cyclic voltammetry (CV), FTIR, and UV‐vis spectroscopy. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 90: 2460–2468, 2003     

Molecular composites created by the solution blending of polyaniline and sulfonated poly(ether sulfone)

New conducting thermally stable blends of polyaniline (PANi) with sulfonated poly(ether sulfone) as a matrix were prepared by a solution‐blending method. Camphorsulfonic acid (CSA) was used as a protonic agent for PANi. A sulfonyl group was introduced into the poly(ether sulfone) to enhance the coulomb interaction among the blends. The influence of the sulfonated group in poly(ether sulfone) was monitored with electrical property measurements. Ultraviolet–visible spectra of the blend compositions showed a well‐developed polaron band. The compatibility of the blends, that is, hydrogen bonding and dispersion at the molecular level, was ascertained with X‐ray diffraction and Fourier transform infrared (FTIR) spectroscopy; these supported intermolecular interaction. A smooth and uniform morphology was observed in the blends. The electrical conductivity of the blends increased up to 14 S/cm with the protonation of the PANi complex with CSA, and the percolation threshold was found to be 2 wt % PANi. These new blends showed increases in conductivity and compatibility over other PANi–poly(ether sulfone) blends. © 2010 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Conducting polymerized high‐internal‐phase emulsion/single‐walled carbon nanotube nanocomposite foams: Effect of the aqueous‐phase surfactant type on the morphology and conductivity

Poly(styrene‐co‐divinylbenzene)/single‐walled carbon nanotubes (SWCNTs) polymerized high‐internal‐phase emulsion (polyHIPE) nanocomposite foams were successfully synthesized with various types of aqueous‐phase surfactants. The effects of anionic, cationic, nonionic, and mixed surfactants on the morphology and electrical conductivity of the resulting nanocomposite foams were investigated. The use of an anionic surfactant, sodium dodecylbenzesulfonate (SDBS), did not completely result in the typical polyHIPE nanocomposite foam microstructure because of the partial instability of the high‐internal‐phase emulsion. The nanocomposite foams synthesized by nonionic surfactants, that is, Pluronic F127 and Triton X‐100, and the cationic/anionic mixture, cetyltrimethylammonium bromide/SDBS, exhibited the proper morphology, but the resulting nanocomposite foams were electrically insulators. Interestingly, the use of a Gemini‐like surfactant, sodium dioctylsulfosuccinate (SDOSS), significantly improved both the typical morphology and electrical properties of the resulting nanocomposite foams because of the probable stronger interactions of SDOSS molecules with SWCNTs. The typical morphology of the nanocomposite foam synthesized with the SDOSS/F127 mixed surfactant was significantly improved, but the electrical conductivity decreased to some extent compared with the SDOSS‐synthesized nanocomposite foams. This behavior was attributed to an increase in the tunneling length of the electrons between adjacent SWCNTs. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43883.     

Preparation and corrosion resistance of nanostructured PVC/ZnO–polyaniline hybrid coating

ZnO–polyaniline nanocomposite with core–shell nanostructure was prepared by in situ polymerization of aniline monomer in the presence of ZnO nanoparticles. Fourier transform infrared spectroscopy, X-ray diffraction patterns, field emission scanning electron microscopy and transmission electron microscopy techniques were used to characterize the composition and structure of ZnO–polyaniline nanocomposite. d.c. electrical conductivity measurement showed that the electrical conductivity of ZnO–polyaniline nanocomposite pellets is higher than that of pristine polyaniline and ZnO nanoparticles pellets. The addition of ZnO nanoparticles causes to the increasing of polyaniline electrical conductivity. ZnO–polyaniline nanocomposite was mixed with polyvinyl chloride (PVC) through a solution mixing method and the three components PVC/ZnO–polyaniline hybrid material was applied as coating on iron coupon by the solution casting method. Corrosion protection efficiency of PVC/ZnO–polyaniline hybrid coating on iron coupons was studied by open circuit potential and Tafel techniques in 3.5% NaCl solution as corrosive environment. According to the results, PVC/ZnO–polyaniline hybrid nanocomposite coating showed dramatically increased corrosion protection effect on iron samples compared to that of uncoated iron coupon and pure polyaniline anticorrosive coating. It was found that ZnO nanoparticles improve the barrier and electrochemical anticorrosive properties of polyaniline and the addition of polyvinyl chloride increases the barrier effect of polyaniline coating.     

Preparation of antibacterial temperature‐sensitive silver‐nanocomposite hydrogels from N‐isopropylacrylamide with green tea

This article reports the temperature‐sensitive, green tea (GT)‐based silver‐nanocomposite hydrogels for bacterial growth inactivation. The temperature‐sensitive hydrogels were prepared via free‐radical polymerization using temperature‐sensitive N‐isopropylacrylamide (NIPAM) monomer with GT as the hydrogel matrix. The nanocomposite hydrogels were encapsulated with silver ions via swelling method, which was later reduced to silver nanoparticles using Azadirachta indica leaf extract. The temperature‐sensitive silver nanocomposite hydrogels were analyzed by using Fourier transforms infrared, UV–visible spectroscopy, differential scanning calorimetry–thermogravimetric analysis, X‐ray diffraction, scanning electron microscopy, and transmission electron microscopy. The prepared hydrogels exhibited higher phase volume transition temperature than the NIPAM. The inhibition zone study of the inactivation of bacteria on the developed hydrogels was carried out against Gram negative (Escherichia coli) and Gram positive (Staphylococcus aureus), which revealed that the prepared hydrogels are helpful for the inactivation of these bacteria due to the high stabilization of antibacterial properties of the silver nanoparticles. The developed hydrogels are promising for biomedical applications. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 45739.     

Few‐layer‐graphene/polycarbonate nanocomposites as dielectric and conducting material

An attempt is taken to develop a flexible and light weight polycarbonate‐based nanocomposite system which could be successfully used as a dielectric material below percolation and as conducting material beyond percolation. The nanocomposite system has been prepared by solution mixing method in which few layer graphene was incorporated as conductive filler. X‐ray diffractometry, Raman spectroscopy, transmission electron microscopy, scanning electron microscopy techniques were employed for characterization studies. The dielectric constant and conductivity were evaluated using precision impedance analyzer. Percolation threshold has been observed to occur at 3.5 wt % of few layer graphene. Dielectric constant of the nanocomposite system, in the smearing region, has been found to increase from ～3.3 (without filler) to ～70 (at 5 wt % FLG) with a dissipation factor of 0.07. The conductivity of the system was increased from 10^?9 S/cm without FLG to 10^?2 S/cm with 7 wt % of few layer graphene. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42443.     

Room temperature preparation,electrical conductivity,and thermal behavior evaluation on silver nanoparticle embedded polyaniline tungstophosphate nanocomposite

An advanced nanocomposite, polyaniline tungstophosphate (PANI‐WP) cation exchanger, was synthesized by simple solution method and treated with silver nitrate resulting silver embedded PANI‐WP (PANI‐WP/Ag). Spectroscopic characterization of PANI‐WP/Ag was carried out by scanning electron microscopy, fourier transform infrared spectroscopy, UV‐Visible spectroscopy, and X‐ray diffraction. Electrical conductivity measurements and thermal effect on conductivity of PANI‐WP/Ag was studied after acid treatment. The dc electrical conductivity was found 3.06 × 10⁻³ S cm⁻¹ for HCl doped, measured by 4‐in line‐probe dc electrical conductivity measuring technique. Thermal conductivity is stable with all temperatures in isothermal studies showing excellent stability of PANI‐WP/Ag material. Hybrid showed better linear Arrhenius electric conducting response for semiconductors, stable upto 120°C. It was observed that conductivity is at the border of metallic and semiconductor region. POLYM. COMPOS., 37:2460–2466, 2016. © 2015 Society of Plastics Engineers     

Characterization of polymer systems based on sulfonated poly(2,6‐dimethyl‐1,4‐phenylene oxide)

The sulfonation reaction of poly(2,6‐dimethyl‐1,4‐phenylene oxide) (PPO) has been carried out, incorporating the resulting product into pure PPO to study, in forthcoming research, the electrical and mechanical features of the composites with regard to their performance in fuel cells. Pure sulfonated polymers and their blends have been characterized from a microstructural and electrical point of view, by means of X‐ray photoelectron spectroscopy (XPS), differential scanning calorimetry (DSC) and complex impedance spectroscopy. Membranes have been manufactured with excellent ionic conductivity at room temperature. © 2000 Society of Chemical Industry     

Microemulsion route to fabrication of silver and platinum‐polymer nanocomposites

Polymethylmethacrylate (PMMA)‐platinum and PMMA‐silver nanocomposites have been produced using polymerization of W/O microemulsions. MMA monomer was used as the oil or continues phase of the microemulsion system and polymerized following formation of Pt and Ag nanoparticles in the fluid medium. The UV‐vis absorption spectra have been used to trace the growth process of the nanoparticles in the microemulsion system. Scanning electron microscopy and transmission electron microscopy (TEM) have been used to determine the morphology and particle size of the Pt and Ag particles in the synthesized nanocomposites. Image analyses of TEM micrographs confirm that the Pt and Ag particles in the synthesized nanocomposites have a narrow size distribution. Meanwhile, Fourier‐transform infrared spectroscopy was used to verify polymer‐nanoparticles interaction in nanocomposite bulk. POLYM. COMPOS., 35:2023–2028, 2014. © 2014 Society of Plastics Engineers