Synthesis,characterization, and conductivity studies of polypyrrole/copper sulfide nanocomposites

Nanocomposites of polypyrrole (PPy) containing copper sulfide (CuS) were synthesized by an in situ chemical oxidative polymerization. The nanocomposites were characterized by FTIR, SEM, XRD, DSC, TGA, and conductivity studies. The FTIR spectra ascertained the chemical interlinking of polypyrole with metal sulfide nanoparticles. Morphological analysis showed that the nanoparticles were uniformly covering the entire substrate. The XRD pattern reveals that the nanoparticle incorporated polypyrrole showed a crystalline nature and the crystallinity of the polymer increases with increase in concentration of CuS nanoparticles. From DSC, an increase in glass transition temperature shows the increased orderness in the polymer composite than in the pure polypyrrole. Thermal analysis (TGA) of the composite showed a progressive increase in the thermal stability with increase in content of CuS. The frequency dependent electrical properties (a.c. conductivity) of the nanocomposites were higher than that of polypyrrole. The d.c. electrical conductivity increased with increase in amount of nanoparticles in the polymer matrix. The results obtained for these composites have greater scientific and technological interest. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013     

Synthesis and characterization of conducting polypyrrole-polymannuronate nanocomposites

Polypyrrole-polymannuronate (PPy-PM) composite films were studied by preparing the composites via in situ deposition techniques. These studies on the chemical interactions, structural morphology, and thermal properties of the films support the formation of PPy-PM composites, and suggest that the ratio of pyrrole to PM is tailored to optimize the potential crosslinking inside the composite. The room temperature current–voltage characteristics and the frequency-dependent AC conductivity of the PPy-PM composites were studied within the frequency range of 10² to 10⁶ Hz. Based on the aforementioned properties, the synthesis of PPy-PM composite films may suggest the future development of biomimetic materials that can be used to create new multicomponent and multifunctional bionanocomposite materials.     

Synthesis and dielectric properties of polyaniline/titanium dioxide nanocomposites

Two series of polyaniline–TiO₂ nanocomposite materials were prepared in base form by in situ polymerization of aniline with inorganic fillers using TiO₂ nanoparticles (P25) and TiO₂ colloids (Hombikat), respectively. The effect of particle sizes and contents of TiO₂ materials on their dielectric properties was evaluated. The as-synthesized polyaniline–TiO₂ nanocomposite materials were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR), thermal analysis (DTA/TGA), and X-ray diffraction (XRD). Dielectric properties of polyaniline–TiO₂ nanocomposites in the form of films were measured at 1 KHz–1 MHz and a temperature range of 35–150 °C. Higher dielectric constants and dielectric losses of polyaniline–TiO₂ nanocomposites than those of neat PANI were found. PANI–TiO₂ nanocomposites derived from P25 exhibited higher dielectric constants and losses than those from Hombikat TiO₂ colloids. Electrical conductivity measurements indicate that the conductivity of nanocomposites is increased with TiO₂ content. The dielectric properties and conductivities are considered to be enhanced due to the addition of TiO₂, which might induce the formation of a more efficient network for charge transport in the base polyaniline matrix.     

Synthesis and properties of novel conducting polyaniline copolymers

A novel copolymer based on aniline and N‐β‐cyanoethylaniline was chemically prepared and characterized by a number of techniques including UV–vis, FTIR, ESR, XRD, and TGA. According to the systematic studies on the physical properties, it was found that the copolymers had excellent solubility in common organic solvents especially in DMF and pyridine, while the conductivity and yield decreased as the content of cyanoethyl group increased in the system. Moreover, an increase in the feed ratio of N‐β‐cyanoethylaniline induced a blue‐shift of the absorption bands in the UV–vis and IR region and significant line broadening of ESR signals together with a reduction in spin density. The XRD patterns of the copolymers lost the characteristic diffraction peaks of emeraldine salt as the ratio of cyanoethyl group increased. The thermal stability of the copolymer was increased with increasing the feed molar ratio of N‐β‐cyanoethylaniline. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 140–147, 2007     

Synthesis,characterization, and application of fluorescent electrically conducting copolymer/metal-oxide nanocomposites

ABSTRACT

Solution polymerization of aniline in the presence of fluorescent organic dyes was carried out at 0–5°C for 2 h under nitrogen atmosphere with FeCl₃ as an initiator. The copolymers were prepared under different experimental conditions. The prepared copolymers were characterized by various analytical tools. The electrical conductivity was measured. From the absorbance and emission intensity values the order of reaction was calculated. Further, its application toward the reduction of nitrophenol was done and the apparent rate constant (K_app) was calculated. The Fourier Transform Infra Red (FTIR) spectrum confirmed the presence of benzenoid, quinonoid, and azo functionalities.     

Polyindene/organo‐montmorillonite conducting nanocomposites. I. Synthesis,characterization, and electrokinetic properties

In this study, Na‐montmorillonite was organically modified with cetyltrimethylammoniumbromide (CTAB) and intercalated with in‐situ polymerized indene. Polyindene(PIn)/Organo‐MMT nanocomposites were obtained with three different compositions and coded as: K1: [PIn(94.5%)/O‐MMT(5.5%)], K2: [PIn(92.8%)/O‐MMT(7.2%)], and K3: [PIn(87.9%)/O‐MMT(12.1%)]. These nanocomposites were subjected to full characterization with various techniques. Electrokinetic studies were conducted to reveal the zeta (ζ)‐potential characteristics of the nanocomposites. ζ‐potentials of the materials were observed to decrease with increasing O‐MMT content. The cationic (CTAB) and anionic (sodium dodecylsulfate) surfactants were shifted the ζ‐potentials of the colloidal dispersions to more positive and more negative regions, respectively whereas nonionic surfactant (Triton X‐100) caused almost no change. The pH and temperature were observed to shift the ζ‐potential values of the nanocomposites to more negative and slightly more positive regions, respectively. With the addition of mono (NaCl), di (BaCl₂) and three (AlCl₃) valent salts, the ζ‐potential of the nanocomposites were shifted to more negative, more positive, and much more positive regions, respectively. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

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     

Synthesis and characterization of conducting gas barrier polyacrylonitrile/graphite nanocomposites

Graphite platelets were expanded by functionalization with inorganic acids followed by strong thermal treatment. The expanded graphite (EG) was exfoliated on the polyacrylonitrile (PAN) matrix through in situ emulsion sonication technique with different proportions of EG. The Ultraviolet‐visible (UV) spectroscopy revealed the interaction between EG and PAN matrix. In Fourier Transform Infrared spectroscopy (FTIR), the chemical interaction between EG and the cyanide group of PAN was evidenced to the formation of PAN/EG composites. The X‐ray diffraction pattern of raw graphite (RG), expanded graphite (EG), polyacrylonitrile (PAN), and PAN/EG nanocomposites were evidenced the dispersion of EG with the PAN matrix. The morphology of EG, PAN, and PAN/EG composites were studied by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). The tensile strength of PAN/EG nanocomposite was measured and found to be increased with increase in EG concentrations. The conductivity and impedance of composites were measured as function of EG concentration. It was found that, conductivity of composites gradually increased with the increase in EG loading. Oxygen permeability of PAN/EG was reduced substantially with rise of EG proportion. To investigate the flame retardancy behavior of PAN/EG nanocomposites, the limiting oxygen indexes were calculated. POLYM. COMPOS., 2011. © 2011 Society of Plastics Engineers     

One-dimensional conducting polymer nanocomposites: Synthesis, properties and applications

Intrinsically conducting polymers have been studied extensively due to their intriguing electronic and redox properties and numerous potential applications in many fields since their discovery in 1970s. To improve and extend their functions, the fabrication of multi-functionalized conducting polymer nanocomposites has attracted a great deal of attention because of the emergence of nanotechnology. This article presents an overview of the synthesis of one-dimensional (1D) conducting polymer nanocomposites and their properties and applications. Nanocomposites consist of conducting polymers and one or more components, which can be carbon nanotubes, metals, oxide nanomaterials, chalcogenides, insulating or conducting polymers, biological materials, metal phthalocyanines and porphyrins, etc. The properties of 1D conducting polymer nanocomposites will be widely discussed. Special attention is paid to the difference in the properties between 1D conducting polymer nanocomposites and bulk conducting polymers. Applications of 1D conducting polymer nanocomposites described include electronic nanodevices, chemical and biological sensors, catalysis and electrocatalysis, energy, microwave absorption and electromagnetic interference (EMI) shielding, electrorheological (ER) fluids, and biomedicine. The advantages of 1D conducting polymer nanocomposites over the parent conducting polymers are highlighted. Combined with the intrinsic properties and synergistic effect of each component, it is anticipated that 1D conducting polymer nanocomposites will play an important role in various fields of nanotechnology.     

A study on the synthesis,characterization and properties of polyaniline/magnesium boride nanocomposites

The present paper reports the novel synthesis of polyaniline/magnesium boride (PAni/MgB₂) nanocomposites. Nanowires 50–100 nm in diameter grown by the sol–gel technique were incorporated in the PAni to prepare PAni/MgB₂ nanocomposites, which yielded an enhancement of conductivity by 5 orders of magnitude. PAni was synthesized through the chemical oxidative polymerization method. The composition of the prepared nanocomposites was tunable, i.e. the amount of dopant was varied and the effects on various parameters were observed by different techniques. The morphology of PAni/MgB₂ nanocomposites was determined using SEM. The temperature dependence of the conductivity of all composites was measured in the temperature range 300–450 K and it was observed that samples having a high concentration of MgB₂ show the highest conductivity. The molecular structure of the nanocomposites was further characterized by Fourier Transform IR spectroscopy which showed small structural changes in the backbone of PAni. I?V measurements showed that the current increases on increasing MgB₂ content. UV?visible spectra exposed the occurrence of an indirect optical transition in the composite. © 2013 Society of Chemical Industry     

聚苯胺/镍纳米复合材料的制备及其表征

以苯胺（An）、氯化镍（NiCl2×6H2O）为原料,原位聚合法合成聚苯胺/镍纳米复合微粒。采用X射线衍射仪、扫描电镜、傅里叶变换红外光谱仪、振动样品磁强计（VSM）及四探针测试仪技术表征了复合微粒的结构、形貌和电磁性能。结果表明：复合微粒在室温外加磁场下表现出铁磁性物质具有的磁滞现象,饱和磁化强度为9.44 emu/g,复合微粒在室温下的电导率为5×10-3 S/cm。     

Synthesis,characterization, and thermal aging behavior of HCl‐doped polyaniline/TRGO nanocomposites

In this article polyaniline (PANI) nanocomposites containing thermally reduced graphene oxide (TRGO) were synthesized and characterized before and after thermal aging. The nanocomposites were prepared through in situ oxidative polymerization of aniline in the presence of TRGO nanoplatelets. FTIR and Raman spectroscopies, XRD, FESEM, and electrical conductivity measurements were used to characterize synthesized materials. PANI/TRGO nanocomposites showed considerably higher electrical conductivity when compared to pure PANI, which was associated with the higher electrical conductivity of TRGO and increased crystallinity of PANI in the presence of TRGO. Pure PANI and PANI/TRGO nanocomposites were thermally aged at 70, 80, 90, and 100 °C. The results showed that the characteristic time of thermal aging process is higher for PANI/TRGO nanocomposites and increases with TRGO loading, which indicates better stability of conductivity during thermal aging process. On the other hand, the characteristic time of thermal aging reduced with aging temperature and a fast decrease was observed from 80 to 90 °C. Improved resistance over thermal aging can be attributed to the barrier effect of TRGO nanoplatelets to the dopant molecules, which retards conductivity degradation in the thermal aging process. Furthermore, TRGO increases PANI crystallinity and it can also prevent crystallinity reduction during thermal aging process. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 44635.     

Synthesis,characterization, and colloidal properties of polythiophene/borax conducting composite

In this study, synthesis of polythiophene (PT) and polythiophene/borax pentahydrate (PT/borax) conducting composite were carried out by in‐situ oxidative polymerization. The composite was subjected to various characterization techniques namely: FTIR, particle size, magnetic susceptibility, density, conductivity, dielectric, TGA, XRD, SEM, and zeta (ζ)‐potential measurements. The effects of time, pH, various surfactants, electrolytes and temperature on the ζ‐potential of PT and PT/borax composite were investigated. In a basic medium the ζ‐potential of the composite was observed to decrease up to ζ = −66.5 mV. The most effective surfactant on the ζ‐potential of the composite was sodium dodecyl sulfate, which reduced the value of ζ‐potential to ζ = −39.2 mV. It was concluded that the presence of mono‐valent (NaCl) salt has no impact on ζ‐potential whereas, di‐valent (BaCl₂) salt shifted the ζ‐potential value to more positive regions. Elevated temperatures caused almost no change on the ζ‐potential of the composite. Also an electrorheological effect (a tremendous viscosity increase) was determined from the PT/borax colloidal systems under an externally applied electric field, and the results obtained will be discussed in the forthcoming article. POLYM. COMPOS., 2011. © 2010 Society of Plastics Engineers     

Fabrication and characterization of conducting nanomaterials composed of copper sulfide and polyindole

Conducting polymer nanocomposites of polyindole (PIN)/copper sulfide (CuS) were fabricated by in situ polymerization of indole with different concentration of CuS nanoparticles. These composites were examined by X‐ray diffraction (XRD), Fourier transform infrared spectrometer (FTIR), scanning electron microscopy (SEM), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), and electrical studies. XRD analysis confirmed that the composite began to crystallize by the incorporation of CuS nanoparticles. The IR spectrum shows the intermolecular interaction between PIN and CuS. SEM images revealed that the nanoparticles were uniformly embedded in the entire substrate. Glass transition temperature was found to be increased with increase in concentration of nanoparticles, which showed an ordered structure of the samples. TGA results indicated that the fabricated PIN/CuS composite attains better thermal stability than pure PIN. The dc conductivity of nanocomposite was significantly increased with increase in content of CuS nanoparticle. An increase in ac electrical conductivity and dielectric properties of the composite were observed with increase in molar concentration of CuS nanoparticles. Thus, enhancements in these properties suggest that the fabricated PIN/CuS nanocomposite has potential application in the field of nanotechnology. POLYM. COMPOS., 2012. © 2012 Society of Plastics Engineers     

Comparative study of conducting polyaniline/copper and polyaniline/nickel composites in the presence of surfactants

Polyaniline/copper and polyaniline/nickel composites were synthesized in the presence and absence of surfactants using ammonium persulfate as an initiator. The structural and surface characteristics of the composites were studied and compared using different techniques. The interfacial interactions and thermal stability of the composites were characterized using X‐ray diffraction and thermogravimetric analysis. Surface properties were investigated using scanning electron microscopy and energy‐dispersed X‐ray spectroscopy. The results indicate significant changes in the morphological and physicochemical properties of the composites when incorporating surfactants. The surfactant‐induced surface characteristics also have an effect on conductivity. Copyright © 2010 Society of Chemical Industry     

Electrochemical synthesis and in situ spectroelectrochemistry of conducting polymer nanocomposites. I. polyaniline/TiO2, polyaniline/ZnO,and polyaniline/TiO2+ZnO

The polyaniline (PAn), polyaniline/titanium dioxide (PAn/TiO₂), polyaniline/zinc oxide (PAn/ZnO), and a novel conducting polymer nanocomposites, polyaniline/titanium dioxide + zinc oxide (PAn/TiO₂+ZnO), were synthesized by in situ electropolymerization and potential cycling on gold electrode. The PAn and nanocomposite films were characterized by cyclic voltammetry, Fourier transform infra‐red (FTIR) spectroscopy, in situ resistivity measurements, in situ UV–Visible, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). The differences between cathodic and anodic peaks of three redox couples were obtained for PAn and polymeric nanocomposite films. During cathodic and anodic scans, the shift of potential was observed for polymer nanocomposite films. The characteristic FTIR peaks of PAn were found to shift to lower wavelengthsin polymer nanocomposite films. These observed effects have been attributed to interaction of TiO₂, ZnO, and TiO₂+ZnO particles with PAn molecular chains. Significant differences from in situ resistivity of PAn and nanocomposite films were obtained. The resistance of PAn/TiO₂, PAn/ZnO, and PAn/TiO₂+ZnO films were found to be smaller than the PAn film. The in situ UV–Visible spectra for Pan and polymer nanocomposite films were studied. The results show the intermediate spectroscopic properties between PAn and polymer nanocomposite films. The morphological analyses of PAn and nanocomposite films have been investigated. The nanocomposites SEM and TEM micrographs suggest that the inorganic semiconductor particles were incorporated in organic conducting polymer, which consequently modifies the morphology of the films significantly. POLYM. COMPOS., 35:351–363, 2014. © 2013 Society of Plastics Engineers     

Synthesis and characterization of conducting polyaniline‐activated carbon nanocomposites

Conducting polyaniline (PAni)/activated carbon (AC) nanocomposites were synthesized by the in situ chemical polymerization method. The resultant shell–core PAni–AC nanocomposites were characterized by elemental analysis, Fourier transform infrared, scanning electron microscopy, thermal gravimetric analysis, X‐ray diffraction, and transmission electron microscopy. We did not observe any significant chemical interaction between the PAni and AC, only core–shell coupling between the AC and the tightly coated polymer chain was revealed. Measurement of the physical properties showed that the incorporation of conducting PAni on to AC particles during chemical synthesis increased electrical conductivity and thermal stability by several orders of magnitude to that of the pristine PAni powders. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 1973–1977, 2007     

Synthesis and characterization of a conducting polyaniline/TiO2−SiO2 composites

Polyaniline/TiO₂?SiO₂ composites were prepared by an in situ chemical oxidation polymerization approach in the presence of hybrid TiO₂?SiO₂ fillers. The obtained polyaniline/TiO₂?SiO₂ composites were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectrometer (FTIR), X‐ray diffraction (XRD), thermogravimetry (TG), and current?voltage (I?V) measurements. SEM picture shows a variation in morphology of polyaniline (PANI) from fiber shape to relatively regular particle shape with increasing TiO₂?SiO₂ contents in the composites. The floccule‐like structures were observed by high resolution TEM, which may help improve the efficiency of conductive network. SEM, XRD, TG, and FTIR spectra all reveal that a relatively strong interaction exist between TiO₂?SiO₂ and PANI. The I?V characteristics in such composites indicate that the charge transport is mainly governed by the space charge effects, which occurs at the interface between the conducting PANI and TiO₂?SiO₂. Meanwhile, PANI/TiO₂?SiO₂ composites exhibit significant increase in conductivity than PANI/TiO₂ or PANI/SiO₂. The reasons about high conductivity of PANI/TiO₂?SiO₂ have also been discussed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 2288–2295, 2013     

Synthesis and characterization of water‐soluble conducting polyaniline by enzyme catalysis

Enzymatic synthesis of a water‐soluble, conducting polyaniline (PANI) was studied, using horseradish peroxidase as the biocatalyst and H₂O₂ as the initiator, in the presence of a poly(vinylsulfonic acid, sodium salt) (PVS) polyanion template. The effects of the buffer, concentration of H₂O₂, and the molar ratio of aniline to PVS on the polymerization were particularly investigated. The products were characterized by UV–vis/near‐IR and FTIR spectroscopy, thermogravimetric analysis, and four‐point probe conductivity measurement. The results showed that PVS could be chosen as a new template in the synthesis of PANI. The proper conditions of polymerization were obtained as follows: pH of the buffer was pH 4.0–5.0, the concentration of H₂O₂ was around 20 mM, and the molar ratio of PVS to aniline was 1–1.5. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 814–817, 2005     

Synthesis,characterization, and comparative study of conducting polyaniline/lead titanate and polyaniline–dodecylbenzenesulfonic acid/lead titanate composites

To study the effect of a surfactant on the properties of polyaniline (PANI)/metal oxide composites, PANI/lead titanate (PbTiO₃) composites were synthesized with different weight percentages (10, 20, 30, 40, and 50 wt %) of PbTiO₃ in both the absence and presence of dodecylbenzenesulfonic acid (DBSA) by the polymerization of aniline with ammonium persulfate as an initiator. The structural characteristics and stability, surface characteristics, and electric properties of PANI/PbTiO₃ and PANI–DBSA/PbTiO₃ were studied and compared. The interfacial interactions and thermal stability of these composites were characterized with X‐ray diffraction, scanning electron microscopy, transmission electron microscopy, and thermogravimetry techniques. The results indicate significant changes in the physicochemical properties of the composites with the incorporation of DBSA. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci, 2008