Abstract. Three water-dispersable composites have been synthesized by in situ chemical oxidative polymerization of aniline N-propanesulfonic acid (AnS) in reduced graphene oxide (r-GO) dispersion, in an ice bath at 0°C and in the absence of any surfactant. The mass ratio between r-GO and aniline monomer have been established as (m r-GO :m AnS ) = 1:1, 1:2 and 1:5 while in the composites, the mass ratio between r-GO and polyaniline was found: 1:0.3, 1:0.5 and 1:1, respectively. The molecular structure, morphology, and optical properties of the composites were analyzed through Fourier transform infrared (FTIR), Raman and ultraviolet-visible (UV-Vis) spectroscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM). Electrochemical performances for energy storage were evaluated by cyclic voltammetry and galvanostatic charge/discharge measurements with 1M H 2 SO 4 as electrolyte in a three-electrode cell. The composite with the mass ratio (m r-GO :m PAnS ) = 1:1 has showed good capacitive behavior with a specific capacitance of 1019 F/g at scan rate of 1 mV/s calculated from integrated area of cyclic voltammogram curve and a retention life of 80% after 100 cycles. These results indicate that the composites prepared by chemical oxidative polymerization are promising materials for electrode supercapacitors.

Nanoparticles are often used as fillers for enhancing various properties of polymer composites such as mechanical, electrical, or dielectric. Among them, polymer nanoparticles are considered ideal contenders because of their compatibility with a polymer matrix. For this reason, it is important that they are synthesized in a surfactant-free form, to obtain predictable surface and structural properties. Here, we synthesized a series of polystyrene nanoparticles (PS NPs), by emulsion polymerization of styrene, using varying amounts of divinylbenzene as a crosslinking agent and sodium 4-vinylbenzenesulfonate as a copolymerizing monomer surfactant—“surfmer”. Using “surfmers” we obtained surfactant-free nanoparticles that are monodisperse, with a high degree of thermal stability, as observed by scanning electron microscopy and thermogravimetric investigations. The prepared series of NPs were investigated by means of broadband dielectric spectroscopy and we demonstrate that by fine-tuning their chemical composition, fine changes in their dielectric and thermal properties are obtained. Further, we demonstrate that the physical transformations in the nanoparticles, such as the glass transition, can be predicted by performing the first derivative of dielectric permittivity for all investigated samples. The glass transition temperature of PS NPs appears to be inversely correlated with the dielectric permittivity and the average diameter of NPs.

Semiconducting polymers with amphiphilic properties can play an increasing role in future organic and unimolecular electronic devices, especially due to their excellent processability and ease of self-assembly into thin films, but they could also be used as intermediate layers to improve electron transport in metal-organic junctions. In this work, we synthesized a homologous series of amphiphiles by copolymerization of aniline with aniline-N-propanesulfonic acid. The polymerization was first initiated with aniline, and the latter monomer was added at different time intervals: 2, 10, 20, 30, 40, and 60 min, spaced from the time of initiation. Thus, the poly(aniline-co-aniline-N-propanesulfonic acid) (PANi-co-PANs) homologous series of copolymers obtained had the same length of the water soluble PANs chain, and a variable length of the water insoluble PANi chain. We demonstrated that there is a strong structure–activity relationship in the homologous series of PANi-co-PANs copolymers, evidenced in the tensiometry and wettability studies, as well as in-depth conductivity with frequency and temperature investigations. We observed a gradual change in solubility, interfacial activity, and conductivity in the homologous series of amphiphiles within the boundaries set by the electrically insulating, hydrophilic PANs chain and the semiconducting, hydrophobic PANi chains; representing a viable platform toward designing polymers with tunable conductivity.

Flexible materials that provide an electric, magnetic, or optic response upon deformation or tactile pressure could be important for the development of smart monitors, intelligent textiles, or in the development of robotic skins. In this work we demonstrate the capabilities of a flexible and electrically conductive polymer material that produces an electrical response with any deformation, namely the electrical resistance of the material changes proportionally with the deformation pressure. Furthermore, the material exhibits a memory effect. When compressed beyond the elastic regime, it retains the memory of the plastic deformation by increasing its resistance. The material was obtained by in situ polymerization of semiconducting polyaniline (PANi) in a polyvinyl alcohol/glycerol (PVA/Gly) hydrogel matrix at −17 °C. Upon drying of the hydrogel, an elastomer composite is obtained, with rubber-like characteristics. When compressed/decompressed, the electrical resistance of the material exhibits an unusually long equilibration/relaxation time, proportional with the load applied. These phenomena indicate a complex relaxation and reconfiguration process of the PANi/PVA elastomer matrix, with the shape change of the material due to mechanical stress.

In this work, we report the fabrication of sensors’ element for humidity or gases, prepared by in situ polymerization of aniline N‐propansulfonic acid using ammonium persulfate in acidic medium. The polymer is being used in the form of powder or deposited in multiple layers onto the PET film. Various techniques including Fourier Transform infrared (FTIR), ultraviolet‐–visible spectroscopy (UV–vis), X‐ray diffraction (XRD) and scanning electron microscopy (SEM) were employed to characterize the as‐prepared sensing materials. The film has been tested for humidity influence, where the significant variations in electrical characteristics were observed, suggesting its usefulness for humidity sensors. Also, for different organic and inorganic gases, a relatively low operating temperature and important sensitivity were observed that indicate its applicability as an active element for general gases sensors. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2019, 136, 47743.