Studies on Fourier transform infrared spectroscopy,scanning electron microscope,and direct current conductivity of polyaniline doped zinc ferrite

In situ polymerization of aniline was carried out in the presence of zinc ferrite to synthesize polyaniline/ZnFe₂O₄ composites (PANI/ZnFe₂O₄) by chemical oxidation method. The composites have been synthesized with various compositions (10, 20, 30, 40, and 50 wt %) of zinc ferrite in PANI. From the Fourier transform infrared spectroscopy (FTIR) studies on polyaniline/ZnFe₂O₄ composites, the peak at 1140 cm⁻¹ is considered to be measure of the degree of electron delocalization. The surface morphology of these composites was studied with scanning electron micrograph (SEM). The dc conductivity has been studied in the temperature range from 40–160°C and supports the one‐dimensional variable range hopping (1DVRH) model proposed by Mott. The results obtained for these composites are of scientific and technological interest. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011     

Ferromagnetic polyaniline/TiO2 nanocomposites

Novel ferromagnetic semiconducting polyaniline PANI/TiO₂ nanocomposites were synthesized by the oxidative polymerization of aniline with ammonium peroxydisulfate in an aqueous medium, in the presence of colloidal TiO₂ nanoparticles (d ∼ 4.5 nm), without added acid. The morphological, magnetic, structural, and optical properties of the PANI/TiO₂ nanocomposites prepared at initial aniline/TiO₂ mole ratios 80, 40, and 20 were studied by scanning electron microscopy, superconducting quantum interference device, X‐ray powder diffraction, FTIR, Raman, and UV‐Vis spectroscopies. The emeraldine salt form of linear PANI chains as well as the presence of phenazine units, branched PANI chains, and anatase crystalline structure of TiO₂ in PANI/TiO₂ nanocomposites was confirmed by FTIR and Raman spectroscopies. The electrical conductivity of synthesized composites was ∼10⁻³ S cm⁻¹. The room temperature ferromagnetic response with coercive field of H_c ∼ 300 Oe and the remanent magnetization of M_r ∼ 4.35 × 10⁻⁴ emu/g was detected in all investigated PANI/TiO₂ nanocomposites. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Improvement of microwave absorption for PAni/HA/TiO2/Fe3O4 nanocomposite after chemical treatment

In order to obtain efficient microwave absorbers that possess high conductivity, dielectric and magnetic properties, hexanoic acid doped polyaniline (PAni) nanocomposites which contain different ratios of ferum (II) oxide (Fe₃O₄) and titanium dioxide (TiO₂) nanoparticles were successfully prepared by in situ chemical polymerization through template free method. Chemical structure, conductivity, morphology, thermal stability, magnetic properties, and amorphous/crystalline behavior of PAni nanocomposites were characterized by Fourier transform infrared spectrometer (FTIR), four point probe, field emission scanning electron microscope (FESEM), thermal gravimetric analysis (TGA), vibrating samples magnetometer (VSM), and X‐ray diffractometer (XRD), respectively. From this study, conductivity was significantly improved from 8.48 × 10⁻⁴−1.23 × 10⁻² S/cm for PAni nanocomposites without any chemical treatment (during addition of Fe₃O₄) to 3.58 × 10⁻²−4.77 × 10⁻² S/cm for those with chemical treatment. PAni nanocomposites with chemical treatment show a narrow sharp reflection loss (RL) peak with high absorption (−48.9 dB) at lower frequency due to the limited individual Fe₃O₄ nanoparticles outside the nanorods/nanotubes as proved by the new proposed mechanism (Fig. 5 ), while it shows a broad RL peak with poor absorption (−13 dB) at higher frequency for those without chemical treatment. The novelty of this research has been focused on PAni with chemical treatment which yield better microwave absorption property (99.999% absorption), combination of high conductivity (3.58 × 10⁻²−4.77 × 10⁻² S/cm), high heterogeneity and moderate magnetization (Ms = 8.87–28.49 emu/g) compare to the PAni without chemical treatment. POLYM. COMPOS., 34:1186–1194, 2013. © 2013 Society of Plastics Engineers     

Polyaniline grafted chitosan/GO-CNT/Fe3O4 nanocomposite as a superior electrode material for supercapacitor application

Developing appropriate stable electroactive electrode materials for supercapacitor application is the challenging issue, which attracts enormous attention in recent decades. In this regard, Fe₃O₄ nanoparticles are firstly synthesized on chitosan/graphene oxide-multiwall carbon nanotubes (CS/GM/Fe₃O₄). Then, polyaniline (PANI) is grafted on it via in situ chemical polymerization and named as CS/GM/Fe₃O₄/PANI. The as-prepared nanocomposites are characterized by Field emission scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and energy dispersive X-ray spectroscopy. The capacitive properties of the electrodes are investigated in a three electrode configuration in 0.5 M Na₂SO₄ electrolyte by various electrochemical techniques. The specific capacitance of CS/GM/Fe₃O₄/PANI electrode is 1513.4 Fg⁻¹ at 4 Ag⁻¹ which is 1.9 times higher than that of CS/GM/Fe₃O₄ (800 Fg⁻¹). Meanwhile, the electrodes exhibit appropriate cycle life along with 99.8% and 93.95% specific capacitance at 100 Ag⁻¹ for chitosan/GO-CNT/Fe₃O₄ and polyaniline grafted chitosan/GO-CNT/Fe₃O₄, respectively.     

Preparation,characterization and electromagnetic properties of polyaniline/carbon nanotubes/nickel ferrite nanocomposites

New electromagnetic nanocomposites were prepared from polyaniline (PANI)/oxidized single‐walled carbon nanotubes (OxSWCNTs)/NiFe₂O₄ by in situ polymerization of aniline using hexanoic acid as a soft template. OxSWCNT and NiFe₂O₄ were prepared first so as to be used in the formulation of PANI composites. Transmission electron microscope (TEM) results revealed the formation of PANI nanoparticles of 60 nm diameter, OxSWCNT of 24 nm, and NiFe₂O₄ of 54 nm. Also, TEM image of the ternary composite indicated agglomerative coating of PANI appearing as a gray shells and black core of NiFe₂O₄ with widening the diameter of OxSWCNT to be around 66 nm. Dc conductivity was measured as a function of temperature. Magnetic susceptibility was measured as a function of temperature and magnetic field intensity. All samples revealed NiFe₂O₄‐dependent ferromagnetism. The activation energies for dc conductivity suggest that the conductivity is owing to hopping conduction mechanism. A synergistic effect between NiFe₂O₄ and PANI/OxSWCNT is observed. POLYM. COMPOS.,, 2012. © 2012 Society of Plastics Engineers     

Novel electrically conductive and ferromagnetic composites of poly(aniline‐co‐aminonaphthalenesulfonic acid) with iron oxide nanoparticles: Synthesis and characterization

Nanocomposites of iron oxide (Fe₃O₄) with a sulfonated polyaniline, poly(aniline‐co‐aminonaphthalenesulfonic acid) [SPAN(ANSA)], were synthesized through chemical oxidative copolymerization of aniline and 5‐amino‐2‐naphthalenesulfonic acid/1‐amino‐5‐naphthalenesulfonic acid in the presence of Fe₃O₄ nanoparticles. The nanocomposites [Fe₃O₄/SPAN(ANSA)‐NCs] were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X‐ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, elemental analysis, UV–visible spectroscopy, thermogravimetric analysis (TGA), superconductor quantum interference device (SQUID), and electrical conductivity measurements. The TEM images reveal that nanocrystalline Fe₃O₄ particles were homogeneously incorporated within the polymer matrix with the sizes in the range of 10–15 nm. XRD pattern reveals that pure Fe₃O₄ particles are having spinel structure, and nanocomposites are more crystalline in comparison to pristine polymers. Differential thermogravimetric (DTG) curves obtained through TGA informs that polymer chains in the composites have better thermal stability than that of the pristine copolymers. FTIR spectra provide information on the structure of the composites. The conductivity of the nanocomposites (～ 0.5 S cm^?1) is higher than that of pristine PANI (～ 10^?3 S cm^?1). The charge transport behavior of the composites is explained through temperature difference of conductivity. The temperature dependence of conductivity fits with the quasi‐1D variable range hopping (quasi‐1D VRH) model. SQUID analysis reveals that the composites show ferromagnetic behavior at room temperature. The maximum saturation magnetization of the composite is 9.7 emu g^?1. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007     

Fabrication and characterization of poly(vinyl alcohol)—Glycerol—Spinel ferrites flexible membranes

Polymer membranes of ferrites nanoparticles, glycerol, and poly(vinyl alcohol) (PVA) were fabricated using a solution casting method. Spinel ferrites nanoparticles, CuFe₂O₄ or ZnFe₂O₄, and glycerol were used as dopants to control the membranes' electrical conductivity. The morphology, composition, and interaction between PVA and the dopants were investigated byscanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), differentialscanning calorimeter (DSC), and thermal gravimetric analysis (TGA). Electrical characterization of the membranes was conducted by impedance spectroscopy using frequencies between 1 and 10⁶ Hz and variable temperatures. The results revealed a negative temperature coefficient of the resistance of the membranes. Additionally, membranes with ZnFe₂O₄ nanoparticles exhibit higher electrical impedance than those with CuFe₂O₄ nanoparticles. Therefore, electrical conductivity could be controlled using a suitable dopant's composition and concentration. The membranes presented in this study exhibit semiconducting properties, thus, they have potentials to be utilized in multiple applications including the flexible organic-based device. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48821.     

Electrical transport and magnetic properties of PEDOT‐ferrite nanocomposites

We have studied the temperature‐dependent transport and magnetic properties of the nanocomposites, containing varied amounts of CoFe₂O₄, NiFe₂O₄, and Fe₃O₄ nanoparticles embedded in the conducting poly(3,4‐ethylenedioxythiophene) or PEDOT matrix, in the temperature range 77–300 K. Resistivities of all the composites, including pure PEDOT follows the Mott VRH relation ρ = ρ₀ T^−1/4 over the studied temperature range. This suggests that hopping is the mechanism of transport in these systems. Plots of (lnρ − lnρ₀)/A as a function of temperature for all the studied samples are found to collapse on a single curve. Although, the conduction mechanism does not change with nanoparticle inclusions in the polymer matrix, the hopping parameters change in the nanocomposites. Magnetic studies of ferrite nanoparticles and nanocomposites show signature of superparamagnetic blocking, with a distribution of particle size. The spin structure on the surface of any particle is different from that of the core. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

Synthesis and characterization of tanninsulfonic acid doped polyaniline–metal oxide nanocomposites

Composites of conducting polymers and metal oxides have a potential role in electronic devices because of their enhanced physical and electronic properties. An in situ synthesis of metal oxide nanocomposites of polyaniline (PANI) and tanninsulfonic acid doped PANI was carried out at ?10°C with two different ratios of aniline to sodium persulfate (oxidant) and the simultaneous incorporation of TiO₂, Al₂O₃, and ZnO nanopowders. The products were characterized by X‐ray diffraction (XRD), thermal analysis, spectroscopy, and electrical conductivity measurements. XRD and thermogravimetric analysis confirmed the presence of the metal oxide in the final product, whereas the spectroscopic characterization revealed interactions among the tannin, metal oxides, and PANI. The electrical properties were determined by four‐point‐probe bulk conductivity measurements. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

ZnFe2O4@Polypyrrole nanocomposites as an efficient broadband electromagnetic wave absorber at 2–40 GHz

In this work, polypyrrole-coated ZnFe₂O₄ (ZnFe₂O₄@PPy) nanocomposites were successfully synthesized via a simple in-situ polymerization process, then evaluated as electromagnetic wave (EMW) absorbers over the 2–40 GHz frequency range. The ZnFe₂O₄@PPy nanocomposites exhibited excellent EMW absorption properties, including very low reflection losses (−42.31 dB at 30.24 GHz and a thickness of 2.5 mm) and a broad absorption bandwidth of 28.20 GHz (from 9.66 to 37.86 GHz). The EMW absorption properties of the ZnFe₂O₄@PPy nanocomposites could be adjusted by changing the PPy shell thickness and also the thickness of the absorber (1–2.5 mm). The excellent microwave absorption performance of the ZnFe₂O₄@PPy nanocomposites is attributable to the synergistic effects of magnetic losses (ZnFe₂O₄ nanoparticles), dielectric losses (ZnFe₂O₄ and PPy) and interfacial relaxation losses at ZnFe₂O₄-PPy interfaces.     

Development of polyaniline/zinc oxide nanocomposite impregnated fabric as an electrostatic charge dissipative material

The paper presents the electrostatic charge dissipative performance of conducting polymer nanocomposite impregnated fabric based on polyaniline (PANI) and zinc oxide nanoparticles (ZnO NPs). Conducting polymer nanocomposites (PANI‐ZnO NPs) were synthesized by in situ chemical oxidative polymerization of aniline by using sodium dodecyl sulfate as surfactant and HCl as dopant. Coating of PANI‐ZnO nanocomposites on the cotton fabric was carried out during polymerization. The interaction of ZnO NPs with the PANI matrix was determined by Fourier transform infrared spectra (FTIR), TGA, XRD, scanning electron Microscopy (SEM), high resolution transmission electron microscopy (HRTEM) and conductivity measurements. The conductivity of PANI‐ZnO NP coated fabric was found to be in the range 10^?3 ? 10^?6 S cm^?1 depending on the loading concentration of ZnO NPs in the polymer matrix. TEM and HRTEM images showed that the PANI‐ZnO nanocomposites had an average diameter of 25–30 nm and were nicely dispersed in the polymer matrix. Antistatic performance of the nanocomposite impregnated fabric was investigated by static decay meter and John Chubb instrument. The static decay time of the film was in the range 0.5 ? 3.4 s on recording the decay time from 5000 V to 500 V. This indicated that the nanocomposite based on PANI‐ZnO nanocomposites has great potential to be used as an effective antistatic material. © 2015 Society of Chemical Industry     

Electrospinning combined with hydrothermal synthesis and lithium storage properties of ZnFe2O4-graphene composite nanofibers

ZnFe₂O₄-graphene composite nanofibers were prepared through electrospinning technique, then with graphene oxide by the facile solvothermal method to get the final products for the first time. The obtained ZnFe₂O₄ nanofibers composed of numerous same size nanoparticles wrapped by graphene sheets to form a unique nanostructure. When the ZnFe₂O₄-graphene electrode was evaluated as anode for lithium-ion batteries, good rate capability and long-term cycling stability could be achieved. The ZnFe₂O₄-graphene electrode exhibited a first discharge capacity of 2166 mAh g⁻¹ cycling at 0.05 C, remained an average reversible capacity of 1000 mAh g⁻¹ after 50 cycles, and kept the high rate capacities of 899, 822, 760 and 711 mAh g⁻¹ at the current rates of 0.5, 1, 2 and 5 C, respectively. The excellent electrochemical performance could be ascribed to the following reasons: the large electrochemical active surface area provided by the composite nanofibers; the graphene sheets decreased the internal resistance of the lithium-ion batteries, which resulted from the electrical conductivity of the graphene sheets; the graphene sheets as conductive network could effectively restrain the agglomeration of ZnFe₂O₄ nanopaiticals.     

A comparative study on camphorsulphonic acid modified montmorillonite clay based conducting polymer nanocomposites

Nanotechnology has emerged as a subject of immense academic interest and excitement in the past few decades. The immediate goal of this science aims at the production of high performance nanomaterials. The present study reports comparative investigations on the in situ polymerization of polyaniline (PANI), and its derivatives poly(1‐naphthylamine) (PNA) and poly(o‐toluidine) (POT) within the camphor sulphonic acid (CSA) modified montmorillonite (MMT) layers. The polymerization as well as intercalation of the conducting polymers was confirmed by FT‐IR, UV‐visible spectroscopies, and XRD studies, whereas the morphology of the nanocomposites was analyzed by TEM studies. It was found that the PANI derivatives (PNA and POT) revealed higher intercalation as compared with PANI. The morphology of nanocomposites was found to be governed by the type of conducting polymer intercalated. A large variation in the morphology as well as particle size was observed between the nanocomposites of PANI and its derivatives. The conductivity was found to be in the range of 10⁻³–10⁻² S·cm⁻¹. POLYM. COMPOS., 2010. © 2009 Society of Plastics Engineers     

Synthesis of new electromagnetic nanocomposite based on modified Fe3O4 nanoparticles with enhanced magnetic,conductive, and catalytic properties

A new method for the fabrication of an electromagnetic nanocomposite based on Fe₃O₄ and polyaniline (PANI) is offered. The authors focused on improvement of the physical and electromagnetic properties of the nanocomposite using a new synthetic method. Supermagnetic Fe₃O₄ nanoparticles were synthesized through coprecipitation method. As a chemical modification, the third generation of poly (amidoamine) dendrimer was grafted on the surface of the nanoparticles. PANI was grafted from –NH₂ functional groups of dendrimer via in situ polymerization of aniline. Finally, Au nanoparticles were loaded on the nanocomposite and its catalytic activity for reduction reactions was studied.     

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     

Magnetoresistive polyaniline-magnetite nanocomposites with negative dielectrical properties

Magnetic polyaniline (PANI) polymer nanocomposites (PNCs) reinforced with magnetite (Fe₃O₄) nanoparticles (NPs) have been successfully synthesized using a facile surface initiated polymerization (SIP) method. The chemical structures of the PANI/Fe₃O₄ PNCs are characterized by Fourier transform infrared (FT-IR) spectroscopy. The thermal stability of the PANI/Fe₃O₄ PNCs is performed by thermogravimetric analysis (TGA). Both transmission electron microscopy (TEM) and scanning electron microscopy (SEM) are used to characterize the morphologies of the PANI, Fe₃O₄ nanoparticles (NPs) and the PNCs. X-ray diffraction (XRD) shows a significant effect of the Fe₃O₄ NPs on the crystallization structure of the formed PANI. The dielectrical properties of these PNCs are strongly related to the Fe₃O₄ nanoparticle loadings and unique negative permittivity is observed in all the samples. Temperature dependent resistivity analysis from 50 to 290 K reveals a quasi 3-dimension variable range hopping (VRH) electron conduction mechanism for the nanocomposite samples. The PNCs do not show hysteresis loop with zero coercivity, indicating the superparamagnetic behavior at room temperature. The PNCs with 30 wt% Fe₃O₄ NP loading exhibit a larger positive magnetoresistance (MR = 95%) than 53% of the pure PANI.     

Polyaniline–organoclay nanocomposites as curing agent for epoxy: Preparation and characterization

Polyaniline (PANI)–organoclay/Epoxy (EP) nanocomposites were prepared. PANI–organoclay nanocomposites were used as curing agent for EP. Organoclay was prepared by an ion exchange process between sodium cations in MMT and NH₃⁺ groups in polyoxypropylene (D₂₃₀). PANI–organoclay nanocomposite was synthesized by in situ polymerization of aniline in (14 wt%) organoclay. Infrared spectra and differential scanning calorimetry confirm the curing of EP. The absence of d₀₀₁ diffraction band of organoclay in the nanocomposites was observed by X‐ray diffraction. The structure argument was further supported by scanning electron microscopy and transmission electron microscopy. Electrical conductivity of the nanocomposites within the range 2.1 × 10⁻⁷–3.2 × 10⁻⁷ S/cm depending on the concentration of the PANI/D₂₃₀‐MMT. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Fabrication of PMMA/PANI/Fe3O4 as a Novel Conducting Hybrid Coating

In this paper, an excellent new hybrid coating including poly(methyl methacrylate) (PMMA), polyaniline (PANI), and magnetite nanoparticles (Fe₃O₄) was obtained. Fe₃O₄ nanoparticles were synthesized using coprecipitation method, and then magnetite nanoparticles have been dispersed into the PANI to increase compatibility with PMMA. Also, PANI/Fe₃O₄ nanocomposites were synthesized through in situ emulsion polymerization, and then PMMA/PANI/Fe₃O₄ hybrid coating was successfully synthesized using batch emulsion polymerization method. Structure, morphology and thermal stability of the samples were characterized using Fourier transform infrared, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and thermal gravimetric analysis (TGA). The synthesized samples were well distributed with an average diameter smaller than 20?nm. Microscopy and X-ray photoelectron spectroscopy results illustrated a great dispersion of magnetite nanoparticles in hybrid matrix. Moreover, the TGA results demonstrated that the PMMA/PANI/Fe₃O₄ hybrid coating nanoparticle is an excellent hybrid coating with high thermal resistance.     

Polyaniline/FE3O4 magnetic nanocomposite prepared by ultrasonic irradiation

Ultrasonic irradiation is employed to assist the chemical oxidative polymerization of aniline in the presence of Fe₃O₄ nanoparticles in order to prepare a polyaniline (PANI)/Fe₃O₄ magnetic nanocomposite. In the chemical oxidative polymerization of aniline in the initially neutral medium, the optimum molar ratio of the oxidant ammonium persulfate to the monomer aniline is 2 : 1. The prepared PANI is in the emeraldine form and is doped by sulfate anions. Fe₃O₄ particles are encapsulated by PANI and dispersed well in PANI. Fe₃O₄ increases the doping level and decreases the crystallinity of PANI. The PANI/Fe₃O₄ nanocomposite possesses conductivity and magnetic properties. Increasing the Fe₃O₄ content increases the magnetization of the PANI/Fe₃O₄ composite but decreases its conductivity. © 2006 Wiley Periodicals Inc. J Appl Polym Sci 102: 2107–2111, 2006     

In-Situ Infrared Study of the Synthesis of Polyaniline Under Acid and Neutral pH

In-situ infrared study of polyaniline (PANI) synthesis showed that the reaction initiated at pH = 1.5 produced a granule PANI microstructure via para-linked dimers of 4-aminodiphenylamine, exhibiting γ(C–H) at 802 cm⁻¹; the reaction initiated at pH = 5.0 and 7.0 produce fiberous, and planar microstructures via ortho-linked dimers of 1,2-aminodiphenylamine and phenazine, exhibiting γ(C–H) at 738 and ν(C=N) at 1446 cm⁻¹. The doped PANI that was produced at pH less than 5.0 showed a feature-less IR background absorption above 1600 cm⁻¹. This absorption could correspond to π-electron delocalization as an indicative of polyaniline conductivity.