The Change of Structural,Optical and Thermal Properties of a PVDF/PVC Blend Containing ZnO Nanoparticles

Nanocomposites consisting of a polyvinylidene fluoride (PVDF)/polyvinyl chloride (PVC) blend containing zinc oxide (ZnO) nanoparticles were prepared. The changes of the structural, optical and thermal properties of the PVDF/PVC blend before and after addition of ZnO were studied. The shift of intensity in IR bands suggested an interaction and compatibility between the blend and ZnO. The structural properties, crystallinity and grain size of the samples were studied using X-ray diffraction. The average grain size was approximately 16 nm confirmed by TEM observations. The X-ray peak positions of ZnO in doped samples were located in the same positions as those of pure ZnO indicating the crystal structure of ZnO was not altered by its incorporation into PVDF/PVC. The estimated values of the optical energy gap from UV/Vis spectra for indirect transition decrease with increasing ZnO due to charge transfer between PVDF/PVC and ZnO nanoparticles. The thermogravimetric analysis curves showed nearly identical behaviors for all samples. Samples that contained ZnO exhibited less weight loss compared to the pure blend attributed to crosslinking formation between the blend and ZnO. Transmission electron microscopy (TEM) images revealed that ZnO was uniformly distributed inside PVDF/PVC polymeric matrices and was superimposed on an amorphous background.     

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     

Role of copper alumina nanoparticles on the performance of polyvinylchloride nanocomposites

Poly(vinyl chloride) (PVC) nanocomposites with different contents of copper alumina (Cu-Al₂O₃) nanoparticles were prepared by the solution casting method. The effects of the nanoparticles on structural, thermal, electrical, contact angle and mechanical properties were thoroughly examined. The presence of Cu-Al₂O₃ in the macromolecular chain was confirmed through Fourier transform infrared (FTIR) spectroscopy. The X-ray diffraction (XRD) analysis of PVC nanocomposites showed the systematic arrangement of Cu-Al₂O₃ nanoparticles within the polymer, which indicated the higher crystallinity of the nanocomposites. The surface morphology of PVC was changed into hemispherical shaped particles by the inclusion of nanofiller was analyzed from SEM images. The glass transition temperature of the nanocomposites obtained from differential scanning calorimetry (DSC) was found to be increased with an increase in loading of nanoparticles in the polymer. The AC conductivity and dielectric studies revealed that the inclusion of nanofiller increases the electrical properties of the material and the composite with 7 wt.% sample showed the maximum conductivity and dielectric constant. The mechanical properties such as modulus, tensile strength, hardness, and impact properties of the PVC nanocomposites were significantly enhanced by the reinforcement of nanoparticles into the PVC matrix. The reinforcing mechanism behind the increase in tensile strength with the addition of nanoparticles was correlated with different theoretical models. The highest mechanical and electrical properties were observed for 7 wt.% Cu-Al₂O₃ loaded nanocomposite. Contact angle measurements of PVC with various loadings of Cu-Al₂O₃ nanofillers demonstrated that the nanoparticle attachment increased the hydrophobicity of the polymer matrix.     

Structural,electrical, thermal,and gas sensing properties of new conductive blend nanocomposites based on polypyrrole/phenothiazine/silver‐doped zinc oxide

The main aim of this study is to investigate the effect of silver‐doped zinc oxide (Ag‐ZnO) loading on the structural, morphological, thermal and electrical properties, and gas sensing behavior of polypyrrole (PPy)/phenothiazine (PTZ)‐blend nanocomposites. The composites are characterized by FTIR, XRD, SEM, TEM, DSC, TGA, and impedance studies. FTIR spectra exhibit the presence of Ag‐ZnO in the PPy/PTZ blend. XRD analysis shows that the semicrystalline behavior of the polymer blend is greatly enhanced by the addition of Ag‐doped ZnO particles. Uniform dispersion of nanoparticles in the polymer is obtained from SEM analysis. The TEM images confirm the presence of spherically shaped nanoparticles in PPy/PTZ blend with a size of 10–25 nm. The DSC measurement indicates that the glass transition temperature of PPy/PTZ blend was significantly improved in the presence of Ag‐doped ZnO nanoparticles. The thermal decomposition temperature of nanocomposite obtained from TGA shows an increase with increase in the content of Ag‐ZnO particles. The incorporation of Ag‐doped ZnO nanoparticles to PPy/PTZ blend exhibit increase in the AC conductivity and dielectric properties of the nanocomposite, due to the pilling of charges at the extended interface of the composite system. The DC conductivity of the nanocomposite increases with the loading of nanoparticles. The ammonia gas sensing performance of PPy/PTZ/Ag‐ZnO nanocomposite is analyzed, and the result shows that the fabricated blend composite can be used as a promising candidate for the easy access of gas molecules. J. VINYL ADDIT. TECHNOL., 26:187–195, 2020. © 2019 The Authors. Journal of Vinyl and Additive Technology published by Wiley Periodicals, Inc. on behalf of Society of Plastics Engineers.     

Morphological,structural, dielectric and electrical properties of PEO–ZnO nanodielectric films

The morphological, structural, dielectric and electrical properties of aqueous solution-cast prepared poly(ethylene oxide)–zinc oxide (PEO–ZnO) nanocomposite films have been investigated as a function of ZnO nanoparticle concentrations up to 5 wt%. Scanning electron microscopy (SEM) images of these films show that the morphology of pristine PEO aggregated spherulites changes into fluffy, voluminous and highly porous with dispersion of ZnO nanoparticles into the PEO matrix. X-ray diffraction (XRD) study confirms that the crystalline phase of PEO greatly reduces at 1 wt% ZnO, and it again increases gradually with further increase of ZnO concentration. The dielectric relaxation spectroscopy (DRS) over the frequency range 20 Hz–1 MHz reveals that the real part of complex dielectric permittivity at audio frequencies decreases non-linearly whereas it remains almost constant at radio frequencies for these polymeric nanocomposites. Dispersion of nanosize ZnO particles into the PEO matrix reduces the values of dielectric permittivity which also exhibits a correlation with the dispersivity of ZnO nanoparticles. The relaxation peaks observed in the dielectric loss tangent and electric modulus spectra reveal that the electrostatic interactions of nanoscale ZnO particles with the ethylene oxide functional dipolar group of PEO monomer units decrease the local chain segmental dynamics of the polymer. Real part of ac conductivity spectra of these films have been analyzed by power law fit over the audio and radio frequency regions, respectively, and the obtained dc conductivity values for these regions differ by more than two orders of magnitude. The temperature dependent relaxation time and dc conductivity values of the nanodielectric material obey the Arrhenius relation of activation energies and confirm a correlation between dc conductivity and PEO chain segmental motion which is exactly identical to the characteristics of solid polymer electrolytes. Results imply that these nanocomposite materials can serve as low permittivity flexible nanodielectric for radio frequency microelectronic devices and also as electrical insulator for audio frequency operating conventional devices in addition to their suitability in preparation of solid polymer electrolytes.     

Impact of vanadium-, sulfur-, and dysprosium-doped zinc oxide nanoparticles on various properties of PVDF/functionalized-PMMA blend nanocomposites: Structural,optical, and morphological studies

The polymeric blend was fabricated with crystalline poly(vinylidene fluoride) (PVDF)/amorphous functionalized-poly(methyl methacrylate) (PMMA) in 70/30 w/w ratio by chemical mixing method. Functionalization of PMMA was achieved with 2-amino-5-nitrobenzoic acid. The prepared polymer blend was used as a matrix to synthesize nanocomposites with undoped/doped zinc oxide (ZnO) nanoparticles. Doping in ZnO was achieved with vanadium, sulfur, and dysprosium elements as a dopant. The structural, optical, electronic, and morphological properties of undoped/doped nanosized ZnO and blended nanocomposites were accessed through sophisticated analytical techniques, that is, Fourier transform infrared (FTIR), ultraviolet–visible (UV–vis), UV–vis–diffuse reflectance spectra, nuclear magnetic resonance, fluorescence spectroscopy, X-ray diffraction (XRD), transmission electron microscopy, and scanning electron microscopy. The FTIR band at 1165–1176 cm⁻¹ in functionalized-PMMA indicate the formation of aliphatic C-N bond along with aromatic ¹H chemical shift (δ) at 7.134, 7.829 and 8.210 ppm confirm the successfully functionalization of PMMA. The prominent XRD peak at 2θ = 20.8° in nanocomposites shown improvement in β-phase of PVDF. The results show that Dy doped ZnO nanoparticles create remarkable effect on various properties of nanocomposites. © 2018 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019 , 136, 47116.     

An Efficient Preparation and Characterization of Nanocomposite Films Based on Poly(vinyl chloride) and Modified ZnO Quantum Dot with an Optically Active Diacid Containing Amino Acid as Coupling Agent

The nanocomposites were manufactured by the incorporation of modified ZnO into the poly(vinyl chloride). ZnO nanoparticles were modified with diacid containing alanine amino acid. Ultrasonic irradiation was used for all process. The PVC/ZnO@DA nanocomposites were investigated by field emission scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, UV–visible spectroscopy, thermogravimetric, and mechanical analysis. Results showed the uniform dispersion of particles in the polymer matrix and ZnO@DA nanoparticles in quantum dot size. The optical properties of PVC were affected by the incorporation of modified quantum dot ZnO; also mechanical properties of PVC/ZnO@DA nanocomposites were improved.     

Thermophysical properties of foliated graphite/nickel reinforced polyvinyl chloride nanocomposites

A novel, polymer‐based foliated graphite/nickel nanocomposites with high thermal conductivity, mechanical properties, and low dielectric constant was developed. The network structure of polyvinyl chloride (PVC) reinforced foliate graphite and nickel nanoparticles (GN) were tested in terms of X‐ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive x‐ray analysis (EDX), and thermal‐gravimetric analyses (TGA). Thermogravimetric analysis revealed a large improvement in the thermal stability of PVC/GN nanocomposites. Thermal conductivity and diffusivity of the composites increased with increasing GN content and temperature. The obtained experimental thermal conductivity result are compared with the existing theoretical models. The measured values of thermal conductivity were in excellent agreement with those calculated from the Agari model. In addition, specific heat, coefficient of thermal expansion (TEC), micro porosity, and crosslinking density (CLD) of composites were investigated. The mechanical properties such as tensile strength, tensile modulus, hardness, and elongation at break of the nanocomposites were improved with inclusion GN which is proportional to GN content. Finally, the dielectric properties of PVC/GN nanocomposites as a function of frequency have been investigated in details. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012     

Studies on synergistic effect of CNT and CB nanoparticles on PVDF

Poly(vinylidene fluoride) (PVDF) nanocomposites with different loading of carbon nanotubes (CNT) and carbon black (CB) were prepared by melt blending method. The conductivity and mechanical properties of the nanocomposites were investigated. The results showed that percolation threshold of CNT/CB/PVDF nanocomposites appeared at a lower concentration (1.25 vol% CNT) than that of CNT/PVDF (>2.08 vol% CNT). The tensile strength of CNT/CB/PVDF nanocomposites was also improved, with 32.1% increase compared to PVDF and 18.0% increase compared to CNT/PVDF at loading of 1.25 vol% CNT/0.96 vol% CB. To explore the synergistic effect of CNT and CB, nonisothermal crystallization and isothermal crystallization behaviors of PVDF and its nanocomposites were studied by differential scanning calorimetry, and the crystallization morphology of them was observed under the three dimensional digital microscope with the polarized model. The crystallization rate of PVDF was speeded up markedly because of heterogeneous nucleation effect of nanoparticles, and CNT and CB nanoparticles had a synergistic effect on nucleation. Polarized microscope observation confirmed that spherulite size of PVDF became smaller owing to the accelerating of crystallization, which influenced the distribution of nanoparticles. The dispersion of nanofillers in matrix was observed by scanning electron microscope. It was revealed that CB could make CNT disperse more evenly in the PVDF matrix. The synergies network of CNT and CB is suggested to build in matrix, which improved conductivity and mechanical properties of PVDF nanocomposites. POLYM. COMPOS., 36:2248–2254, 2015. © 2014 Society of Plastics Engineers     

Solution-processed white graphene-reinforced ferroelectric polymer nanocomposites with improved thermal conductivity and dielectric properties for electronic encapsulation

The recent surge in graphene research has stimulated interest in the investigation of various two-dimensional (2D) nanomaterials, including 2D boron nitride (BN) nanostructures. Among these, hexagonal boron nitride nanosheets (h-BNNs; also known as white graphene, as their structure is similar to that of graphene) have emerged as potential nanofillers for preparing thermally conductive composites. In this work, hexagonal boron nitride nanoparticles (h-BNNPs) approximately 70 nm in size were incorporated into a polyvinylidene fluoride (PVDF) matrix with different loadings (0–25 wt.%). The PVDF/h-BNNP nanocomposites were prepared by a solution blending technique and characterized using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), polarized optical microscopy (POM) and scanning electron microscopy (SEM). In addition, the thermal conductivity and dielectric properties of the nanocomposites were investigated. The incorporation of h-BNNPs in the PVDF matrix resulted in enhanced thermal conductivity. The highest value, obtained at 25 wt.% h-BNNP loading, was 2.33 W/mK, which was five times that of the neat PVDF (0.41 W/mK). The thermal enhancement factor (TEF) at 5 wt.% h-BNNP loading was 78%, increasing to 468% at 25 wt.% h-BNNP loading. The maximum dielectric constant of approximately 36.37 (50Hz, 150 °C) was obtained at 25 wt.% h-BNNP loading, which was three times that of neat PVDF (11.94) at the same frequency and temperature. The aforementioned results suggest that these multifunctional and high-performance nanocomposites hold great promise for application in electronic encapsulation.     

Conducting nanocomposites of polyaniline/nylon 6,6/zinc oxide nanoparticles: preparation,characterization and electrical conductivity studies

Nanocomposites of polyaniline as a conducting polymer and main matrix, zinc oxide nanoparticles as inorganic filler and nylon 6,6 as supporting matrix were prepared by solution mixing process in a common solvent. DC electrical conductivity and its thermal stability at different temperatures under ambient atmospheric conditions were studied for the nanocomposites. The stability studies were carried out by two slightly different techniques, i.e., cyclic ageing and isothermal ageing. The results showed that the DC electrical conductivity of the nanocomposites decreased with increase in the content of zinc oxide nanoparticles whereas the thermal stability in terms of DC electrical conductivity retention was slightly improved in few cases but not for all samples. The advance analytical techniques such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy, transmission electron microscopy, thermogravimetric analysis and X-ray diffraction (XRD) were also used to characterize the selected samples. It was also observed that zinc oxide nanoparticles in the nanocomposites were homogeneously distributed; however, some clusters/aggregates were also present. The FTIR results showed the existence of some interaction between the individual components of the nanocomposites as evident from the little shift in the peaks of FTIR spectra. This result was also supported by XRD data.     

Direct writing polyvinylidene difluoride thin films by intercalation of nano-ZnO

Polyvinylidene fluoride (PVDF) is a preeminent pyrolytic and piezoelectric polymer. It has been widely studied as an ideal material for wearable flexible sensors or low-power electronic equipment. PVDF/ZnO thin films were prepared by direct writing method, which promoted the ordered arrangement of PVDF molecular chains under the action of electric field and thus improved the crystallinity of the β phase. Meanwhile, the effects of intercalation of ZnO nanoparticles on the crystallinity of PVDF thin films were explored. The results show that appropriate addition of nano-ZnO as nucleating agent can induce the crystallinity of the PVDF film obviously. While the additive amount of nanoparticles was 0.02 wt%, the relative β phase content of the PVDF film can reach 88.92%. Under the double action of adding ZnO nanoparticles and electric field assistance, the dielectric constant of the composite film increases from 6.9 (pure PVDF) to 12.4 (0.03 wt% ZnO) at a frequency of 1 kHz. The d₃₃ value of the film without polarization is up to −9.1 pC/N, the output voltage is increased to 351 mV, and the conductivity of the composite film has been improved.     

Study of alternating current impedance analysis and dielectric properties of carbon nanotube‐based polysulfone nanocomposites

Polysulfone (PSU)/multiwalled carbon nanotubes (MWCNTs) nanocomposites containing 0.5–3 wt% of MWCNTs were prepared by solution casting technique. To understand the dispersion behavior of MWCNTs inPSU matrix, high resolution transmission electron microscopy (HRTEM) and field emission scanning electron microscopy (FESEM) were used. Electrical properties of nanocomposites were investigated by analyzing alternating current (AC) impedance spectra. The real part of complex impedance was decreased with increasing carbon nanotubes loading in the PSU matrix, which may be due to increase in conductive networks in the nanocomposite. The complex impedance Nyquist plots for PSU/MWCNTs nanocomposites were characterized by the appearance of a single semicircular arc, whose radii of curvature decreases with increasing MWCNTs loading. The polarization mechanism and the AC conduction mechanism were studied by designing equivalent circuit from impedance data. The dielectric response of PSU/MWCNTs nanocomposite was investigated over a wide range of frequency from 10 Hz to 10⁻⁶ Hz. Dielectric constant of PSU/MWCNTs nanocomposite was enhanced significantly from 2 to 6 × 10¹⁰ at 10 Hz when the addition of MWCNTs was increased from 0 to 3 wt%. The enhancement of dielectric property might be due to the interfacial polarization between carbon nanotubes and polysulfone. POLYM. COMPOS., 2012. © 2011 Society of Plastics Engineers     

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     

Structural and electrical properties of ZnO:Ag core-shell nanoparticles synthesized by a polymer precursor method

Monodispersed core-shell type ZnO:Ag nanoparticles were synthesized by a polymer precursor method and their structural and electrical properties were reported in detail. The synthesis technique involves a sol-gel type chemical reaction between aqueous solutions of poly-vinyl alcohol (PVA), sucrose and Zn²⁺ salt. The Zn²⁺-PVA-sucrose polymer precursor powders so obtained after the reaction was further explored for the synthesis of ZnO:Ag nanoparticles. The key part of the work lies in the use of polymer coated ZnO nanoparticles as templates to obtain the ZnO core-Ag shell type nanostructures. Structural and spectroscopic analyses of the derived samples were performed with X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS). The XRD patterns of the ZnO:Ag nanoparticles consist of distinct peaks corresponding to the hexagonal wurtzite type (space group P63mc) crystal structure of ZnO along with the typical peaks of face centered cubic crystal structure of metallic silver. EDS and XPS analyses confirmed the chemical composition and surface structure of the core-shell nanoparticles. Microstructural analysis revealed the monodispersed platelet shaped ZnO nanoparticles with a thin layer of Ag coating on the surface. UV–visible diffuse reflectance studies revealed the effects of Ag coating on the optical properties of the samples. Detail analysis of the dielectric properties of the samples were performed as a function of frequency (1 Hz to 10 MHz) and temperature (300–528 K) to investigate the electrical conduction mechanism in the samples.     

Effect of imidazole based polymer blend electrolytes for dye-sensitized solar cells in energy harvesting window glass applications

The exploration of polymer electrolyte in the field of dye sensitized solar cell (DSSC) can contribute to increase the invention of renewable energy applications. In the present work, the influence of imidazole on the poly (vinylidene fluoride) (PVDF)-poly (methyl methacrylate) (PMMA)-Ethylene carbonate (EC)-KI-I₂ polymer blend electrolytes has been evaluated. The different weight percentages of imidazole added into polymer blend electrolytes have been prepared by solution casting. The prepared films were characterized by Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), UV-visible spectra, photoluminescence spectra and impedance spectroscopy. The surface roughness texture of the film was analyzed by atomic force microscopy (AFM). The ionic conductivity of the optimized polymer blend electrolyte was determined by impedance measurement, which is 1.95×10^-3 S·cm^-1 at room temperature. The polymer electrolyte containing 40 wt% of imidazole content exhibits the highest photo-conversion efficiency of 3.04% under the illumination of 100 mW·cm^-2. Moreover, a considerable enhancement in the stability of the DSSC device was demonstrated.     

Thermal,thermomechanical, and morphological characterization of poly(vinyl chloride) (PVC)/ZnO nanocomposites: PVC molecular weight effect

Poly(vinyl chloride) (PVC)‐based nanocomposites containing 2 wt% zinc oxide (ZnO) nanoparticles were prepared by solution casting and the effect of the PVC molecular weight (MW) on the morphology, thermal properties, and thermogravimetric behavior was studied. The addition of ZnO nanoparticles to PVCs of different MWs increased the glass transition temperature (T_g) of the resulting nanocomposites, the extent of which was dependent upon the MW of the PVC matrix. The nanocomposite samples exhibited broadened transition zones as compared with their unfilled PVC matrices. The extent of transition zone broadening was also controlled by the MW of the PVC matrix in the nanocomposites. In the absence of ZnO nanoparticles, the increase in MW of PVC had no effect on the breadth of the transition zone. The TGA results showed that the incorporation of ZnO nanoparticles into PVC matrices of different MWs accelerated the first stage weight loss via the nanoparticle catalytic effect through removal of HCL from the polymeric chains. The presence of ZnO nanoparticles lowered the second stage weight loss, and the char yield obtained for nanocomposites samples was significantly greater than that obtained for neat PVC samples. At low MWs, the presence of ZnO nanoparticles had no effect on the first stage of thermal degradation process. The presence of ZnO nanoparticles in the matrix in different nanocomposites was revealed by SEM observations, and the EDX analysis demonstrated a progressive improvement in the distribution and dispersion state of ZnO nanoparticles in the PVC‐based nanocomposites as the MW of PVC matrix gradually increased. J. VINYL ADDIT. TECHNOL., 25:E63–E71, 2019. © 2018 Society of Plastics Engineers     

PVDF-HFP型凝胶聚合物固体电解质的结构与离子导电性能

以PVDF-HFP为基体聚合物，制备了一系列凝胶聚合物固体电解质膜，其中有机极性介质为碳酸丙烯酯(PC)，电解质盐为LiClO4。通过红外光谱分析、差示扫描量热分析、复阻抗分析等手段对凝胶聚合物固体电解质的结构与离子导电性能进行了研究。结果表明，PC与阳离子之间存在较强的络合作用，PC对基体聚合物有很强的增塑作用。锂盐和PC含量对材料的离子导电性能有较大的影响。随着锂盐和PC含量的增加，材料的离子电导率呈上升趋势。     

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.