BaTiO3 incorporation effect on the dielectric properties of polymer from aqueous emulsion: An enhanced dispersion technique

An economic and environment friendly process was adapted to synthesize new dielectric composite materials. Using ethylene vinyl acetate (EVA)/vinyl ester of versatic acid (VeoVa) terpolymer as an aqueous emulsion provides a homogenous dispersion of BaTiO₃ (BT) particles, due to the high viscosity and polarity of the vinyl resin (VR). Composites films were obtained from these dispersions by water evaporation. The evolution of the dielectric properties as a function of the BaTiO₃ content, was correctly fitted by a Maxwell‐Garnett model. This fitting of the experimental curve shows a good dispersion of filler in the vinyl resin and the particles separation by a layer of resin as expected for the preparation method used in this study. The VR/BT composites show good synergy between the dielectric properties of the different phases of the composites due to the formation of macrodipoles and to the strong interactions between polar EVA/VeoVa groups and the BaTiO₃ particles surface. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44333.     

Polymeric piezoelectric fiber with metal core produced by electrowetting‐aided dry spinning method

An electrowetting‐aided dry spinning method is developed to produce morphologically stable polymeric piezoelectric fibers with a metal core covered by a beta‐phase poly(vinylidene fluoride) [or poly(vinylidene‐trifluoroethylene)] layer. Each fiber consists of a 100 μm copper core (enameled with 6 μm polyester‐imide), a 3–10 μm piezoelectric layer, and a sputtered 100 nm gold electrode. The morphological properties of the fibers are analyzed with scanning electron microscopy, X‐ray diffraction, and a step profiler. The piezoelectric properties are tested in a vibration‐detecting application. Both morphological observation and piezoelectric testing demonstrate that the electrowetting‐aided dry spinning helps in forming high‐quality polymeric piezoelectric fibers. Moreover, this method can also be applied in different fabrications, where adhesion between a liquid and solid surface needs to be enhanced. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43968.     

Disposable potentiometric citrate sensor based on polypyrrole‐doped films for indirect determination of sildenafil in pharmaceuticals formulations

A new sensitive and selective disposable potentiometric sensor based on polypyrrole (PPy) films for determination of sildenafil citrate (SC) was proposed. The pyrrole polymerization was performed in presence of citrate ions under galvanostatic conditions which resulted in a membrane of PPy doped with citrate anion at graphite pencil electrode surface. Experimental conditions (e.g., pH and conditioning time) and instrumental parameters (e.g., current density and electrical charge) were evaluated in order to reach the best potentiometric response for the proposed sensor. Under optimized conditions, the device presented a linear dynamic range (LDR) for citrate ions concentrations varying from 0.034 to 1.7 mmol L^?1 with a Nernstian slope of 57.2 mV dec^?1 and a limit of detection (LOD) of 30 µmol L^?1. The developed potentiometric sensor was applied for sildenafil citrate (SC) determination (pharmaceutical formulations) and results compared with an official spectrophotometric method indicating a good agreement for a confidence level of 95%. Effect of concomitants species on the potentiometric response of the proposed device and morphologic characterization using microscopy of atomic force (AFM) were realized. The surface roughness of PPy films (synthesized in citrate solution and chloride) showed poorly affected by changing the doping anion, probably because the polypyrrole nodules grow three‐dimensionally simultaneously. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 43762.     

Fabrication of oriented electrospun cellulose nanocrystals–polystyrene composite fibers on a rotating drum

Nitrobenzene (CNC-1), trifluoromethyl benzene (CNC-2) modified and polystyrene-grafted (CNC-g) cellulose nanocrystals in polystyrene (PS)-N,N dimethylformamide (DMF) solutions were electrospun and collected as stretched and aligned fibers on a rotating drum. Scanning electron microscope pictures showed significant alignment in the case of unmodified and nitrobenzene-modified CNC-1/PS nanocomposite fibers once the linear speed of rotor reached to 15 m s⁻¹. Fiber diameter decrease was more strong with rotor speed increase in the case of trifluoromethyl benzene modified (CNC-2) and polystyrene-grafted (CNC-g) cellulose nanocrystals/PS systems. Dynamic mechanical analysis including storage and elastic modulus of electrospun-oriented fibers were performed on surface-modified and polymer-grafted CNC/PS samples. According to α transition peak, the increase in the glass-transition temperature with filler concentration was the highest in polymer-grafted CNC-g/PS composite fibers. It was due to the interpenetration of grafted polymer brushes and free polymer chains in continuous phase and resulted in restrictions of motions of polymer chains in the PS matrix. The elastic moduli of nitrobenzene (CNC-1) and trifluoromethyl benzene (CNC-2)-modified CNC-filled PS composite fibers agreed well with percolation model, which indicates the CNC–CNC interactions and network formation with an increase in concentration. Magnitude of the elastic modulus of polymer grafted CNC-g at 0.33 vol % in PS was significantly higher than the prediction from percolation theory. It was due the immobilized polymer chains around CNC-g particles. However, grafted polymer chains, at higher CNC concentrations acted like stickers among CNC particles and caused CNC agglomerates with entrapped free polystyrene from the matrix, thus caused a decrease in the elastic modulus. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48942.     

Synthesis and characterization of novel hyperbranched fluorescent polymers that can be precisely used for metal ion detection and quantification

Four novel hyperbranched polymers with 4 or 5 ring-closed rhodamine units in each were achieved through RAFT polymerization followed by modification with rhodamine moieties. The solubility, thermostability, and photophysical properties of the polymers were studied. The polymers showed high selectivity and sensitivity to Fe³⁺ among various metal ions in CH₃CN/H₂O (75/25, v/v) and could signal Fe³⁺ through multichannels: emerging a new absorption around 558 nm, over 30 nm fluorescence redshift and significant fluorescence enhancement (including 33–37 folds in intensity and 8.3–12.8 folds in quantum yield), accompanied by visual and fluorescent color changes. The polymers could be applied in the analysis of Fe³⁺ in real water samples. © 2020 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48933.     

Electrochemical inspection of polypyrrole/chitosan/zinc oxide hybrid composites

Polymer nanocomposite composed of polypyrrole, chitosan, and zinc oxide nanoparticles has been synthesized and it has been evaluated for various electrochemical aspects of the current electrochemical industry. The polypyrrole (PPy) was synthesized by the chemical oxidative polymerization reaction by employing ammonium persulfate as oxidizing agent. Composites of polypyrrole/chitosan (PPy/Chy) and polypyrrole/chitosan/ZnO (PCZ) composites were synthesized by the solution blending method. Detailed structural, morphological, thermal characterization of PPy, PPy/Chy, and PCZ were performed to characterize the specific features of the systems. The composites exhibit better thermal stability and high surface area and the addition of ZnO nanoparticle increase the crystallinity of the composite. Electrochemical characterization of the ITO electrodes modified with PPy, PPy/Chy, and PCZ were performed using cyclic voltammetry, electrochemical impedance spectroscopy, and amperometry techniques. The present study highlights the role of a bio-compatible material with high surface area and conductive constituent for designing of various high performing electronic noninvasive sensors, biosensors, and so forth.     

Improvement of actuation performance of dielectric elastomers by barium titanate and carbon black fillers

Dielectric elastomers are promising materials for actuators resembling human muscle. Among elastomers, acrylic rubbers (ACM) have shown good actuation performance but its use is limited by the high operating voltages required. The present work demonstrates that simultaneous incorporation of nanostructured carbon black and dielectric fillers offers an increase in a dielectric permittivity and a suitable modulus of the elastomers matrix, enabling an improved electro‐mechanical actuation performance at low voltages. By the use of reinforcing carbon black and barium titanate in an acrylic elastomer matrix a sixfold increase in the dielectric permittivity was realized. A fine tuning of the actuation stress and, consequently, actuation strain can be done by a judicial selection of the different filler concentrations in the soft rubber matrix. Finally, a synergistic effect of the fillers was observed in the improved actuation performance of the developed materials. This work may pave the way to design dielectric elastomers for actuator fabrication. © 2016 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2016 , 133, 44116.