Piezoelectric properties of zinc oxide/iron oxide filled polyvinylidene fluoride nanocomposite fibers

Piezoelectric nanogenerators (PENG) with flexible and simple design have pronounced significance in fabricating sustainable devices for self-powering electronics. This study demonstrates the fabrication of electrospun nanocomposite fibers from polyvinylidene fluoride (PVDF) filled zinc oxide (ZnO)/iron oxide (FeO) nanomaterials. The nanocomposite fiber based flexible PENG shows piezoelectric output voltage of 5.9 V when 3 wt% of ZnO/FeO hybrid nanomaterial is introduced, which is 29.5 times higher than the neat PVDF. No apparent decline in output voltage is observed for almost 2000 s attributed to the outstanding durability. This higher piezoelectric output performance is correlated with the β-phase transformation studies from the Fourier transformation infrared spectroscopy and the crystallinity studies from the differential scanning calorimetry. Both these studies show respective enhancement of 3.79 and 2.16% in the β-phase crystallinity values of PVDF-ZnO/FeO 3 wt% composite. Higher dielectric constant value obtained for the same composite (three times higher than the neat PVDF) confirms the increased energy storage efficiency as well. Thus the proposed soft and flexible PENG is a promising mechanical energy harvester, and its good dielectric properties reveals the ability to use this material as good power sources for wearable and flexible electronic devices.

     

Curing enhancement and network effects in multi‐walled carbon nanotube‐filled vulcanized natural rubber: evidence for solvent sensing

Electrically and thermally conductive polymer composites offer great possibilities in various electronic fields because of their low weight and ease of processing. This paper addresses the curing behaviour and network properties of conducting multi‐walled carbon nanotube (MWCNT)‐reinforced natural rubber (NR) nanocomposites, emphasizing the sensing and diffusion performances. NR/MWCNT composites were prepared following a special master batch technique which allows the appropriate distribution of nanotubes within the elastomer. The sensing responses of the composites towards solvents were observed as variations in electrical resistance. Thermal resistance and glass transition behaviour were examined and correlated with the swelling measurements as evidence for solvent sensing. An optimum level of 3 phr of MWCNTs is understood to lead to the best properties for the NR/MWCNT composites. Finally, the structural morphology and interfacial interactions were found to have correlations with cure reactions, glass transition temperatures and sensing responses of all compositions. © 2017 Society of Chemical Industry     

Graphene oxide reinforced polyvinyl alcohol/polyethylene glycol blend composites as high-performance dielectric material

Novel flexible dielectric composites composed of polyvinyl alcohol (PVA), polyethylene glycol (PEG), and graphene oxide (GO) with high dielectric constant and low dielectric loss have been developed using facile and eco-friendly colloidal processing technique. The structure and morphology of the PVA/PEG/GO composites were evaluated using Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, UV-vis spectroscopy (UV-vis), X-ray diffraction (XRD), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The dielectric behavior of PVA/PEG/GO composites was investigated in the wide range of frequencies from 50 Hz to 20 MHz and temperature in the range 40 to 150 °C using impedance spectroscopy. The dielectric constant for PVA and PVA/PEG (50/50) blend film was found to be 10.71 (50 Hz, 150 °C) and 31.22 (50 Hz, 150 °C), respectively. The dielectric constant for PVA/PEG/GO composite with 3 wt% GO was found to be 644.39 (50 Hz, 150 °C) which is 60 times greater than the dielectric constant of PVA and 20 times greater than the dielectric constant of PVA/PEG (50/50) blend film. The PVA/PEG/GO composites not only show high dielectric constant but also show low dielectric loss which is highly attractive for practical applications. These findings underline the possibilities of using PVA/PEG/GO composites as a flexible dielectric material for high-performance energy storage applications such as embedded capacitors.     

Investigation of antimicrobial properties and in-vitro bioactivity of Ce3+-Sr2+dual-substituted nano hydroxyapatites

Dual doped calcium apatite has been widely focused as it enhances the osteoconductive property for the possible applications in orthopedic and dental implants. In this work, we investigate the antimicrobial and bioactive properties of cerium/strontium (Ce³⁺/Sr²⁺) co-substituted hydroxyapatite (HA) nanoparticles synthesized by sol-gel assisted precipitation method. The structure, morphology, functional groups, photoluminescence, and thermal stability of the developed systems are examined. The comparative studies performed among the pure HA, Sr²⁺, and Ce³⁺-substituted HA nanoparticles illustrate higher antibacterial activity with lowered apatite-forming ability and biocompatibility for the Ce³⁺-substituted HA. However, the Ce³⁺/Sr²⁺co-substituted HA exhibits better biocompatibility, apatite-forming ability, and good antimicrobial properties. Sr²⁺ ion inclusion leads to better biological properties and compromise the cytotoxic nature of the Ce³⁺-HA. In addition, the Ce³⁺/Sr²⁺-HA nanoparticles prevent thermal decomposition up to 700°C, pointing also toward the possibility of this co-substituted HA in bone implant applications.     

Fumed SiO2 nanoparticle reinforced biopolymer blend nanocomposites with high dielectric constant and low dielectric loss for flexible organic electronics

In the present study, fumed silica (SiO₂) nanoparticle reinforced poly(vinyl alcohol) (PVA) and poly(vinylpyrrolidone) (PVP) blend nanocomposite films were prepared via a simple solution‐blending technique. Fourier transform infrared spectroscopy (FTIR), ultraviolet–visible spectroscopy (UV–vis), X‐ray diffraction (XRD), and scanning electron microscopy (SEM) were employed to elucidate the successful incorporation of SiO₂ nanoparticles in the PVA/PVP blend matrix. A thermogravimetric analyzer was used to evaluate the thermal stability of the nanocomposites. The dielectric properties such as dielectric constant (?) and dielectric loss (tan δ) of the PVA/PVP/SiO₂ nanocomposite films were evaluated in the broadband frequency range of 10^?2 Hz to 20 MHz and for temperatures in the range 40–150 °C. The FTIR and UV–vis spectroscopy results implied the presence of hydrogen bonding interaction between SiO₂ and the PVA/PVP blend matrix. The XRD and SEM results revealed that SiO₂ nanoparticles were uniformly dispersed in the PVA/PVP blend matrix. The dielectric property analysis revealed that the dielectric constant values of the nanocomposites are higher than those of PVA/PVP blends. The maximum dielectric constant and the dielectric loss were 125 (10^?2 Hz, 150 °C) and 1.1 (10^?2 Hz, 70 °C), respectively, for PVA/PVP/SiO₂ nanocomposites with 25 wt % SiO₂ content. These results enable the preparation of dielectric nanocomposites using a facile solution‐casting method that exhibit the desirable dielectric performance for flexible organic electronics. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134 , 44427.     

Microton irradiation induced tuning of dielectric properties of nano ZnO–natural rubber disks

The effect of electron beam irradiation of dielectric and conductivity properties of nano ZnO–natural rubber (NR) disks was investigated here. It is revealed that electric properties such as AC conductivity, dielectric constant, and loss tangent of the irradiated samples were improved significantly as compared to the non-irradiated samples, which have been associated with defects in the composites. The total number of dipoles was generated inside the polymer matrix upon irradiation depends on the dislocations formed inside the matrix. From the experiments, we observe that in the amorphous region electron beam irradiation fetches crosslinking and breakdown at the same time. The enhancement of the dielectric and conductivity properties demonstrates that nano ZnO–NR disks will be a promising candidate for the optoelectronic industry. Finally, we also examined the influences of temperature on the electrical conductivity of irradiated samples.     

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.     

Vapor sensing performances of PVDF nanocomposites containing titanium dioxide nanotubes decorated multi-walled carbon nanotubes

Inorganic nanocarbon hybrid materials are good alternatives for superior electrochemical performance and specific capacitance to their traditional counterparts. Nanocarbons act as a good template for the growth of metal nanoparticles on it and their hybrid combinations enhance the charge transport and rate capability of electrochemical materials without sacrificing the specific capacity. In this study, titanium dioxide nanotubes (TNT) are synthesized hydrothermally in the presence of multi-walled carbon nanotubes (MWCNT) where the latter acts as base template material for the metal oxide nanotube growth. The MWCNT–TNT hybrid material possesses very high dielectric strength and this is used to enhance the dielectric property of the polymer polyvinyledene fluoride (PVDF). Solution mixing was used to prepare the PVDF/MWCNT–TNT nanocomposites by varying the filler concentrations from 0.5 to 2.5 wt%. Excellent vapor sensing was noticed for the PVDF nanocomposites with different rate of response towards commonly used laboratory solvents. The composites and the fillers were characterized for its morphology and structural properties using scanning and transmission electron microscopy, X-ray diffraction studies and infrared spectroscopy. Vapor sensing was measured as relative resistance variations against the solvent vapors, and the dielectric properties of the composites were measured at room temperature during the frequency 10²–10⁷ Hz. Experimental results revealed the influence of filler synergy on the properties of PVDF and the enhancement in the solvent vapor detectability and dielectric properties reflects the ability of these composite films in flexible vapor sensors and in energy storage.     

Investigation on the thermal and crystallization behavior of high density polyethylene/acrylonitrile butadiene rubber blends and their composites

The properties of a blend containing a crystallizable component depend largely on the extent of crystallinity and the crystallization behavior of that component in presence of the other. Here, the semi crystalline high density polyethylene (HDPE) is blended with the amorphous elastomer, acrylonitrile butadiene rubber (nitrile rubber or NBR) and we focus mainly on the crystallinity of HDPE/NBR immiscible blends and its variation in the presence of compatibilizer and filler. The effect of blend ratio, compatibilizer concentration, dynamic vulcanization, and filler incorporation were carefully evaluated from the crystallinity measurements using differential scanning calorimeter and the basic aim of this work lies in tuning these conditions. This study allows the elucidation of the influence of crosslink density in regulating the crystallinity of thermoplastic elastomer blends. The scanning electron micrographs provide blend morphology from which the reduced domain size and the influence of NBR particles as heterogeneous nuclei for crystallization are evidenced especially at 5% compatibilizer concentration. The crystallinity of blends was observed to be high at 30 phr carbon black filler addition. Finally, the thermal stability of blends and their composites are also addressed and correlated with the crystallization effect. POLYM. ENG. SCI., 55:1203–1210, 2015. © 2014 Society of Plastics Engineers     

Effect of nanostructured polyhedral oligomeric silsesquioxane on the physical properties of poly(vinyl alcohol)

An effective amphiphilic polyhedral oligomeric silsesquioxane (POSS) encapsulated poly(vinyl alcohol) (PVA) nanocomposite was successfully fabricated by solution blending method. Anionic octa(tetramethylammonium) (Octa‐TMA) and poly(ethylene glycol) (PEG) were used as cage side groups in POSS (Octa‐TMA‐POSS and PEG‐POSS) for the present study. Transmission electron microscopic analysis revealed the uniform dispersion of POSS in the PVA matrix. Crystallinity of PVA/POSS system was computed from differential scanning calorimetric studies. The effect of POSS on the mechanical, dynamic mechanical, and dielectric properties of PVA has been analyzed and discussed in detail with respect to the weight percentage of POSS. The incorporation of POSS in PVA matrix remarkably enhances the Young's modulus of the matrix. The viscoelastic properties such as storage modulus, loss modulus, damping behavior, and glass transition temperature of the membranes were evaluated. The relaxation corresponding to the crystal–crystal slippage characteristic of semicrystalline polymers were observed in storage modulus curves of PVA/POSS system, suggesting the crystalline nature of matrix even in the presence of POSS. Less polar, inert, and stiff inorganic center core of POSS contributes to the reduced energy dissipation and dielectric constant of PVA/POSS system. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45447.